CA2309413A1 - Novel detergent compositions with enhanced depositing, conditioning and softness capabilities - Google Patents

Novel detergent compositions with enhanced depositing, conditioning and softness capabilities Download PDF

Info

Publication number
CA2309413A1
CA2309413A1 CA002309413A CA2309413A CA2309413A1 CA 2309413 A1 CA2309413 A1 CA 2309413A1 CA 002309413 A CA002309413 A CA 002309413A CA 2309413 A CA2309413 A CA 2309413A CA 2309413 A1 CA2309413 A1 CA 2309413A1
Authority
CA
Canada
Prior art keywords
percent
composition
agent
comprised
mixtures
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
CA002309413A
Other languages
French (fr)
Inventor
Susan M. Niemiec
Hsing Yeh
Regina Gallagher
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Johnson and Johnson Consumer Inc
Original Assignee
Johnson and Johnson Consumer Companies LLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Johnson and Johnson Consumer Companies LLC filed Critical Johnson and Johnson Consumer Companies LLC
Publication of CA2309413A1 publication Critical patent/CA2309413A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89Polysiloxanes
    • A61K8/891Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • A61K8/894Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone modified by a polyoxyalkylene group, e.g. cetyl dimethicone copolyol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89Polysiloxanes
    • A61K8/891Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • A61K8/731Cellulose; Quaternized cellulose derivatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • A61K8/737Galactomannans, e.g. guar; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8158Homopolymers or copolymers of amides or imides, e.g. (meth) acrylamide; Compositions of derivatives of such polymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89Polysiloxanes
    • A61K8/891Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • A61K8/892Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone modified by a hydroxy group, e.g. dimethiconol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/08Antiseborrheics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/10Anti-acne agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/14Drugs for dermatological disorders for baldness or alopecia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/02Preparations for care of the skin for chemically bleaching or whitening the skin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/08Anti-ageing preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/10Washing or bathing preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/006Antidandruff preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/02Preparations for cleaning the hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/12Preparations containing hair conditioners
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q7/00Preparations for affecting hair growth
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/54Polymers characterized by specific structures/properties
    • A61K2800/542Polymers characterized by specific structures/properties characterized by the charge
    • A61K2800/5426Polymers characterized by specific structures/properties characterized by the charge cationic

Abstract

Novel "two-in-one" detergent compositions comprised of at least one water soluble silicone agent, at least one cationic conditioning agent, and a detergent. These compositions are suitable for use in shampoos, baths, and shower gels. Also described is a novel delivery system for depositing benefit agents into and onto the skin, nails, and/or hair comprised of at least one water soluble silicone and at least one cationic conditioning agent.

Description

JBP 452 CIP (patent) NOVEL DETERGENT COMPOSITIONS WITH ENHANCED
DEPOSITING, CONDITIONING AND SOFTNESS CAPABILITIES
BACKGROUND OF THE INVENTION
1. Field of Invention The present invention relates to detergent compositions that not only effectively cleanse the hair but also impart superior wet stage and dry stage conditioning properties to the hair in a single application.
The present invention is further directed to a novel delivery system for delivering benefit agents onto and/or into the surface of the skin, nails, and/or hair, and methods of using such systems.
2. Background of the Invention and Prior Art Consumers often desire to have a hair shampoo that not only effectively cleanses the hair, but that also imparts other desirable properties, such as conditioning and lathering, to the hair. Because nonionic, amphoteric and zwitterionic surfactants are relatively inferior cleansing surfactants in comparison to anionic surfactants, hair shampoos generally are formulated with the latter, which thoroughly cleanses as opposed to conditions the hair. Hence, hair that has been shampooed with an anionic surfactant-based composition usually appears unconditioned and is considered to be cosmetically unappealing.
Furthermore, anionic surfactants adversely leave the hair with an undesirable harsh and "dry to the touch"
feel, which is difficult to comb in either the wet or dry state. Even after complete drying, such thoroughly cleansed hair remains unsatisfactory in hair softness and "flyaway"
properties. Thus, it is usually necessary to perform a post-shampoo conditioning step to such hair in order to ameliorate these undesirable physical characteristics.
With the advent of so-called "two-in-one" conditioning shampoos, it became possible to condition and cleanse hair simultaneously. However, it is well known that the formulation of such "two-in-one"
conditioning shampoos is difficult due to the inherent incompatibility between the cleansing anionic surfactants and the cationic conditioning agents. Unfortunately, those known "two-in-one" conditioning shampoos that have overcome the incompatibility problem disadvantageously possess inferior cleansing and conditioning properties.

One known method for reducing the incompatibility between the anionic surfactants and the cationic conditioning agents is through the use of alternative, non-anionic surfactants and improved cationic conditioning agents. However, such alternative, non-anionic surfactants possess relatively inferior cleansing properties.
Other efforts have concentrated on varying the types of conditioners. Cationic conditioning agents disadvantageously do not generally provide optimal overall conditioning benefits, particularly in the areas of " softness" and " wetldry combing", when delivered as an ingredient in a shampoo composition. Water-insoluble conditioning agents, such as the non-volatile silicones that are well recognized in the art as providing a degree of softness to the hair, often results in unstable "two-in-one" formulations. See U.S.
Patent 4,704,272; U.S. Patent 4,741,855; and U.S. Patent RE 34,584.
Substantive cationic polymers, which are capable of depositing on the hair shaft during shampooing to impart the desired degree of manageability, disadvantageously result in formulations that give the hair a greasy feeling or "build-up" on hair. See U.S. Patent 5,221,530; U.S. Patent 5,417,965; U.S. Patent 4,292,212;
and U.S. Patent 4,472,297.
Another important property of cleansing compositions that is desired by consumers is lathering.
Consumers often associate high lathering with effective cleansing, and typically prefer high lathering shampoos to low lathering shampoos from an aesthetic standpoint.
Unfortunately, many therapeutic shampoos, in particular those possessing therapeutic agents such as anti-dandruff agents, contain active agents that tend to adversely affect lathering performance. It is well known that the deposition of therapeutic agents on the hair or skin may be improved via significantly increasing the levels of therapeutic agents in the shampoo compositions. However, not only does the use of such high levels therapeutic agents disadvantageously increase raw materials costs, but also it also reduces the latherability of the shampoo and deleteriously affects product stability. The presence of detergents in the anti-dandruff shampoos also interferes with the ability of therapeutic agents to deposit onto the hair because the detergents are designed to carry or remove oil, grease, dirt, and particulate matter from the hair and scalp during rinsing.
Accordingly, it would be highly desirable to find a "two-in-one" cleansing composition capable of effectively cleansing and detangling the hair while imparting superior wet and dry combing and softness thereto, without creating "build-up". It would also be desirable to have a high-lathering "two-in-one"
cleansing composition that not only effectively cleansed the hair but also deposited a significant amount of therapeutic agents onto the hair and skin.
SUMMARY OF THE INVENTION
In accordance with this invention, there is provided a cleansing composition comprising, consisting essentially of, andlor consisting of:
a) at least one water soluble silicone agent;
b) at least one cationic conditioning agent; and c) at least one detergent.
Another embodiment of the present invention is directed to a delivery system for delivering benefit agents into and/or onto the hair, nails, and scalp comprised of, consisting essentially of, andlor consisting of:
a) at least one water soluble silicone agent; and b) at least one cationic conditioning agent.
Another embodiment of the present invention is directed to a method for enhancing the deposition of benefit agents which comprises, consists essentially of, and/or consists of topically administering to a human or animal a composition comprised of, consists essentially of, andlor consists of:
a) a delivery system comprised of i) at least two cationic conditioning compounds selected from the group consisting of guar hydroxypropyltrimonium chloride, acrylaminopropyltrimonium chloridelacrylamide copolymer, and mixtures thereof;
ii) at least one water soluble silicone compound comprised of silicone quaternium-13; and b) an effective amount of a benefit agent to a desired location on the skin, hair, andlor nails.
Yet another embodiment is directed to a method for depositing a thin coating of conditioner on a hair fiber, comprised of, consisting essentially of, andlor consisting of:
a) topically applying an effective amount of a delivery system composition comprised of i) at least two cationic conditioning compounds selected from the group consisting of guar hydroxypropyltrimonium chloride, acrylaminopropyltrimonium chloride/acrylamide copolymer, and mixtures thereof;
ii) at least one water soluble silicone compound comprised of cetyl triethylmonium dimethicone copolyol phthalate; and iii) a hydrophilic benefit agent to a desired location on the hair of a human or animal.
Yet another embodiment is directed to a method for treating hair loss comprising, consisting essentially of, andlor consisting of topically administering to a human or animal at a desired area for treating hair loss a composition comprised of, consisting essentially of, and/or consisting of based upon the total weight of the composition,:
A. a delivery system comprised of i.) at least one water soluble silicone agent;
ii) at least one cationic conditioning agent; and B. an effective amount of a hair loss treatment agent.
Another embodiment is directed to a method for inhibiting hair growth comprising, consisting essentially of, andlor consisting of topically administering to a human or animal at a desired area for inhibiting hair growth a composition comprised of, consisting essentially of, and/or consisting of, based upon the total weight of the composition,:
A. a delivery system comprised of i.) at least one water soluble silicone agent;
ii) at least one cationic conditioning agent; and B. an effective amount of a hair growth inhibiting agent.
Another embodiment of the present invention is directed to a method for treating or minimizing the effects of aging comprising, consisting essentially of, andlor consisting of topically administering to a human or animal at a desired area a composition comprised of, consisting essentially of, and/or consisting of based upon the total weight of the composition,:
A. a delivery system comprised of i.) at least one water soluble silicone agent;
ii) at least one cationic conditioning agent; and B. an effective amount of an anti-aging active agent.
Another embodiment of the present invention is directed to a method for treating acne comprising, consisting essentially of, andlor consisting of topically administering to a human or animal at a desired area a composition comprised of, consisting essentially of, and/or consisting of, based upon the total weight of the composition,:
A. a delivery system comprised of i.) at least one water soluble silicone agent;
ii) at least one cationic conditioning agent; and B. an effective amount of an anti-acne active agent.
Another embodiment of the present invention is directed to a method for depigmenting skin comprising, consisting essentially of, and/or consisting of topically administering to a human or animal at a desired area a composition comprised of, consisting essentially of, andlor consisting of based upon the total weight of the composition,:
A. a delivery system comprised of i.) at least one water soluble silicone agent;
ii) at least one cationic conditioning agent; and B. an effective amount of a depigmentation active agent.
In yet another embodiment of the present invention is a method for treating the diseases of dandruff, seborrheic dermatitis, and psoriasis andlor the symptoms associated therewith comprising, consisting essentially of, and/or consisting of topically administering to a human or animal at a desired area a composition comprised of, consisting essentially of, andlor consisting of based upon the total weight of the composition,:
A. a delivery system comprised of i.) at least one water soluble silicone agent;
ii) at least one cationic conditioning agent; and B. an effective amount of a benefit agent selected from the group consisting of an anti-dandruff agent, an anti-seborrheic dermatitis agent, an anti-psoriasis agent, and mixtures thereof.
The composition of this invention, when used in a shampoo or body cleanser, possesses one or more of the following properties: lathering, cleansing, wet detangling, wet combining, dry combing, conditioning, softness, manageability, rinseability, and ability to significantly deposit therapeutic agents.
Moreover, the delivery system of the present invention is capable of effectively depositing benefit agents into andlor onto the skin, hair and nails.
BRIEF DESCRIPTION OF THE DRAWINGS
The above and other aspects and novel features of the present invention will become apparent from the following detailed description of the preferred embodiments, as illustrated in the accompanying figures showing the improved hair conditioning properties imparted by using the method and composition of the present invention, wherein:
FIG. 1 (a) is a mass spectrometric representation of a hair fiber previously treated with Pantene Pro-V
shampoo.
FIG. 1 (b) is a mass spectrometric representation of a hair fiber previously treated with a cleansing composition of the present invention as described in Example 11.
DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS
In one embodiment of the present invention, the cleansing composition may suitably comprise, consist of, or consist essentially of : a) at least one water soluble silicone agent; b) at least one cationic conditioning agent; and c) at least one detergent. Preferably, the cleansing composition contains, based upon the total weight of the cleansing composition, a) from about 0.001 percent to about 20 percent, and preferably from about 0.01 percent to about 5 percent of water soluble silicone agents; b) from about 0.01 percent to about 10 percent, and preferably from about 0.1 percent to about 5 percent of cationic conditioning agents; and c) from about 0.01 percent to about 30 percent, and preferably from about 5 percent to about 20 percent detergent.
The first component of the cleansing composition is a water soluble or insoluble silicone agent, with water soluble silicone agents being preferred. Examples of suitable water soluble silicone agents nonexclusively include the water soluble dimethicones substituted with fatty acid moieties, water soluble silicone quaterniums, and mixtures thereof. Either volatile or nonvolatile water soluble silicones are suitable for use in the present invention, with the latter being preferred.
Preferably, the water soluble dimethicones are substituted with fatty acid moieties selected from fatty acids having from about 5 carbon atoms to about 30 carbon atoms and the silicone quatemiums contain about 6 carbon atoms to about 20 carbon atoms.
Examples of suitable water soluble volatile silicone agents nonexclusively include polydimethylsiloxane, hexamethyldisiloxane, cyclomethicone fluids such as polydimethylcyclosiloxane available commercially from Dow Corning Corporation of Midland, Michigan under the tradename, "DC-345"
and mixtures thereof, with the cyclomethicone fluids being preferred.
Examples of suitable water soluble nonvolatile silicone agents nonexclusively include cetyl triethylmonium dimethicone copolyol phthalate, stearalkonium dimethicone copolyol phthalate, dimethicone copolyol having the following structure I.:
I
SI(CH3)s C-~ SI(CH3)2~~ q' ~ SI-O-]q.- SI(CH3)3 R9 I .
Wherein:
q' is an integer from about 1 to about 7000;
q" is an integer from about 1 to about 5000;
R9 may be any water soluble group such as:
a) a fatty alcohol having from about 8 carbon atoms to about 30 carbon atoms;
b) a fatty acid having from about 8 carbon atoms to about 30 carbon atoms, and derivatives thereof;
c) a crosslinked water soluble polymer such as mercaptol propyl copolymer;
d) a cationic moiety, e.g. trimonium chloride;
e) propyl PG- Betaine;
f) polypeptides such as polysarcosine, and e) mixtures thereof, dimethicone copolyol acetate, dimethicone copolyol lactate, dimethicone copolyol laurate, dimethicone copolyol methyl ether, dimethicone copolyol octyl dodecyl citrate, hydrolyzed soy proteinldimethicone copolyol acetate, dimethiconol, and mixtures thereof.
Examples of suitable water soluble silicone quaterniums nonexclusively include silicone quaternium 13, silicone quaternium 40, quaternium 80 and mixtures thereof, as well as those silicone quaterniums disclosed in United States Patent No. 5,098,979, which is incorporated by reference herein in its entirety.
More preferred water soluble silicone agents include silicone quaternium 13, cetyl triethylmonium dimethicone copolyol phthalate, stearalkonium deimethicone copolyol phthalate, and mixtures thereof.
The second component in the composition of the present invention is a cationic conditioning agent such as a cationic cellulose derivative; a cationic guar derivative; a homopolymer or copolymer of a cationic monomer selected from:
a. a monomer having the formula II.

R
O
Y
I

R- ~Q+-R XO

II.
wherein R is H or CH3, YisOorNH, R, is an alkylene group having from about 2 to about 6 carbon atoms, Rz, R3 and R4 are each independently an alkyl group or hydroxyalkyl group having from about 1 to about 22 carbon atoms, and X is a monovalent anion selected from halide and alkyl sulfate having from about 1 to about 4 carbon atoms, or b. diallyldimethylammonium chloride, or mixtures thereof.
A suitable cationic cellulose derivative is the polymeric quaternary ammonium salt derived from the reaction of hydroxyethyl cellulose with a trimethylammonium substituted epoxide. The material known as Polyquaternium-10, commercially available from Amerchol Corporation of Edison, New Jersey as "Polymer JR-400," is especially useful in this regard.
The cationic guar derivative is preferably a guar hydroxypropyltrimonium chloride, available commercially from Rhone-Poulenc Inc., of Cranbury, New Jersey under the tradename, "Jaguar C-17:' Another suitable cationic polymer includes those compounds derived from acrylamidopropyl trimonium chloride which has the formula IIL:
O~H3 O
~N N-CH3 X
2o H CH3 I I I.
and more preferably is the copolymer of this monomer with acrylamide, the latter of which is available commercially from Allied Colloids, of Suffolk, Virginia under the tradename, "Salcare SC60."

_g_ Other suitable cationic conditioning polymers are those derived from the monomer diallyldimethylammonium chloride. The homopolymer of this monomer is Polyquaternium-6, which is available commercially from Allied Colloids of Suffolk, Virginia under the tradename, "Salcare SC30." The copolymer of diallyldimethylammonium chloride with acrylamide is known as Polyquaternium-7, and is also available from Allied Colloids under the tradename "Salcare SC10." Other suitable polymers include polyquaternium-47, which is available from Calgon Corporation under the tradename, "MERQUAT
2001 N."
Most preferred cationic conditioning agents include acrylamidopropyltrimonium chloridelacrylamide copolymer, guar hydroxypropyltrimonium chloride, and mixtures thereof.
The third component in the composition of the present invention is a detergent. By "detergent," it is meant any known surfactant and/or soap that is compatible with the silicone agents and the cationic agents of the cleansing composition, and may nonexclusively include anionic surfactants, nonionic surfactants, cationic surfactants, amphoteric surfactants (including betaine surfactants and zwitterionic surfactants) and mixtures thereof.
Examples of suitable anionic surfactants include, but are not limited to, compounds in classes known as alkyl sulfates, sulfate esters of an alkylphenoxy polyoxyethylene ethanol, alpha-olefin sulfonates, betaalkyloxy alkane sulfonates, alkyl arylsulfonates, alkyl carbonates, alkyl ether carboxylates, fatty acids, sulfosuccinates, alkyl ether sulfosuccinates, sarcosinates, octoxynol phosphates, nonoxynol phosphates, taurates, fatty taurides, sulfated monoglycerides, fatty acid amido polyoxyethylene sulfates, and isethionates and mixtures thereof. Many additional surfactants are described in WO 07126860 and in McCUTCHEON'S DETERGENTS AND EMULSIFIERS (1989), which are both incorporated herein by reference. These anionic surfactants are generally present in the composition as a neutralized salt in the form of sodium salts, potassium salts, ammonium salts, lithium salts, alkyl ammonium salts, or hydroxyalkyl ammonium salts. Preferred anionic surfactants are alkyl sulfates, alkyl ether sulfates, alkyl phosphates, amino acid salts such as N-acyl-L-glutamate, a-olefin sulfonates, alkyl sarcosinates, alkyl benzene sulfonates, acyl isethionates, alkyl sulfosuccinates, acyl methyl taurides, and mixtures thereof, with sodium C14 -16 olefin sulfonate, ammonium lauryl sulfate, sodium trideceth sulfate, sodium laureth sulfate, disodium laureth sulfosuccinate being most preferred.
Examples of suitable nonionic surfactants include, but are not limited to, those set forth in WO
07/26860, with polysorbate 20, long chain alkyl glucosides having alkyl groups containing about 8 carbon atoms to about 22 carbon atoms; coconut fatty acid monoethanolamides such as cocamide MEA; coconut fatty acid diethanolamides, and mixtures thereof, being most preferred. Any amount of cationic surfactants or non-ionic surfactants employed in the detergent base are in addition to the amount of the non-ionic surfactant or cationic surfactant, respectively, that may be included in the vesicle bilayer.
Examples of suitable cationic surfactants include, but are not limited to, those set forth in WO
07126860, as well as the quaternary ammonium surfactants and quaternary amine surfactants that are not only positively charged at the pH of the shampoo composition, which generally is about pH 10 or lower, but also are soluble in the shampoo composition. Preferred cationic surfactants nonexclusively include the n-acylamidopropyl dimethylamine oxides such as cocamidopropylamine oxide sold commercially under the tradename °Incromine Oxide CH available from Croda Inc.
Parsippany, New Jersey.
Examples of suitable amphoteric surfactants include, but are not limited to, those set forth in WO
07126860, i.e., amphocarboxylates, alkyl betaines, amidoalkylbetaines, amidoalkylsultaines, amphophosphates, phosphobetaines, pyrophosphobetaines, carboxyalkyl alkyl polyamines, and mixtures thereof. Preferred amphoteric surfactants include amidoalkylbetaines such as cocamidopropyl betaine available commercially from Goldschmidt Chemical Corporation of Hopewell, Virginia under the tradename "Tegobetaine E"; alkyl imidazoline having from about 8 carbon atoms to about 18 carbon atoms in the alkyl group such as Sodium Cocoamphopropionate available commercially from Mona Industries Inc. of Paterson, New Jersey under the tradename "Monateric CA-35".
Examples of suitable soaps include fatty acids reacted with potassium, sodium, ammonium, lithium, or a triethanol amine base to form soaps such as, e.g., sodium cocoate or triethanolamine cocoate.
In a preferred embodiment, the detergent is comprised of a mixture of, based upon the total weight of the detergent, from about 0.1 percent to about 30 percent, and preferably from about 1 percent to about 20 percent anionic surfactants, from about 0 percent to about 10 percent, and preferably from about 1 percent to about 7 percent nonionic surfactants, from about 0 percent to about 10 percent, and preferably from about 0 percent to about 4 percent cationic surfactants, and from about 0 percent to about 15 percent, and preferably from about 1 percent to about 10 percent amphoteric surfactants.
In another preferred embodiment, the cleansing composition is comprised of, based upon the total weight of surfactant, from about 50 percent to about 99 percent, and preferably from about 80 percent to about 95 percent, of anionic surfactants preferably selected from the group consisting of alkyl sulfates, alkyl ether sulfates, and mixtures thereof wherein the alkyl group has from about 8 carbon atoms to about 18 carbon atoms, and from about 1 percent to about 20 percent, and preferably from about 5 percent to about 15 percent of amphoteric surfactants, preferably cocamidopropyl betaine.
In another preferred embodiment, the cleansing composition is comprised of, based upon the total weight of surfactant, from about 50 percent to about 99 percent, and preferably from about 70 percent to about 90 percent, of anionic surfactants, preferably those selected from the group consisting of sodium PEG-7 olive oil carboxylate, alkyl sulfates, alkyl ether sulfates, and mixtures thereof wherein the alkyl group has from about 8 carbon atoms to about 18 carbon atoms; from about 1 percent to about 30 percent, and preferably from about 10 percent to about 25 percent of an amphoteric surfactant preferably selected from the group consisting of cocamidopropyl betaine and mixtures thereof; and optionally, from about 0 percent to about 15 percent, and preferably from about 2 percent to about 10 percent of a cationic surfactant such as cocammoniumcarbomoyl chloride.
In embodiments wherein a particulate compound, such as several of the anti-dandruff agents, e.g.
zinc pyrithione, that tends to precipitate out of the solution is combined with the cleansing composition, the surfactant is preferable employed in conjunction with a suspending agent, with the latter having the ability - to -of suspending the particulate compound. In those embodiments, the suspending agent-containing cleansing composition may be made by either 1 ) simultaneously combining the suspending agent with the detergent, the silicone agents, and the cationic conditioners, or preferably, 2) pre-mixing the suspending agent with the detergent component, then combining the resulting mixture with the silicone agents and the cationic conditioners.
Examples of suitable suspending agents nonexclusively include: 1 ) acrylate polymers and copolymers thereof such as the AcrylateslAminoacrylates C10-30 Alkyl PEG-20 Itaconate copolymer available commercially from National Starch and Chemical Corporation of Bridgewater, New Jersey under the trade name "Structure Plus'; 2) fatty acyl derivatives, wherein the acyl group has the structure IV:
l0 Q
I I
R,oC- IV.
wherein R,o comprises a carbon chain having from about 7 carbon atoms to about 21 carbon atoms that is either saturated or unsaturated and is either substituted or unsubstituted with, for example, hydroxyl 15 groups; 3) esters of long chain fatty acids, wherein the fatty acids have the structure V:
O
II
R"C OR,2 V
20 wherein R" is an alkyl group having from 8 carbon atoms to about 30 carbon atoms, and R,z is an alkyl group having from 8 carbon atoms to about 30 carbon atoms, such as stearyl stearate ; 4) alkyl dimethylamine oxides wherein the alkyl group has from about 8 carbon atoms to about 18 carbon atoms as disclosed in U.S. Patent Re. 34,584, which is incorporated by reference herein in its entirety; 5) methylvinyletherlmaleic anhydride copolymer crosslinked with 1,9-decadiene PoIyVMIMA (PVMIMA
25 decadiene crosspolymer) available from International Specialty Products under the tradename, "Stabileze 06 & QM;" 6) cellulose derivatives such as methylcellulose, hydroxybutyl methylcellulose, hydroxypropylcellulose, hydroxypropyl methylcellulose, hydroxyethyl ethylcellulose, hydroxyethyl cellulose, and mixtures thereof; 7) Distearyl Phthalic Amide available from Stepan Company under the tradename "Stepan SAB-2," 8) Di(hydrogenated) Tallow Phthalic Amide available from Stepan Company 30 under the tradename "Stepan TAB-2"; 9) primary amines having a fatty alkyl group with at least about 16 carbon atoms such as palmitate amine and stearamine; 10) polyacrylic acids such as carbomers, which are available from B. F. Goodrich Company under the tradename, "Carbopol"; 11 ) polysaccharide gums such as xanthan gum; 12) colloidal clays such as benzyl dimethyl hydrogenated tallow ammonium montmorillonite (Bentone 27); 13) colloidal silica; and 14) mixtures thereof.
Examples of suitable fatty acyl 35 derivatives include ethylene glycol distearate, ethylene glycol monostearate, and alkanolamides such as cocamide MEA, and mixtures thereof.
Preferred suspending agents include carbomer, hydroxyethyl cellulose, methylvinylether/maleic anhydride copolymer crosslinked with 1,9-decadiene PoIyVM/MA (PVMIMA decadiene crosspolymer), and AcrylateslAminoacrylates C10-30 Alkyl PEG-20 Itaconate Copolymer, with AcrylateslAminoacrylates C10-30 Alkyl PEG-20 Itaconate Copolymer being most preferred.
The suspending agent is preferably used in an amount effective for suspending the particulate compound. Although such amount may vary dependent upon, for example, the type of particulate compound selected, the viscosity of the formulation desired, and the stability of the formulation, typically the amount of suspending agent may range, based upon the total weight of the detergent, from about 0 percent to about 5 percent, and preferably from about 0.01 percent to about 1 percent.
Other optional ingredients that may be included in the cleansing composition nonexclusively include commercially available pearlescent or opacifying agents, thickeners, chelating agents, colorants, fragrances, preservatives, pH adjustors, conditioning agents, and mixtures thereof.
Suitable pearlescent or opacifying agents which are respectively present in an amount, based upon the total weight of the composition, of from about 0 percent to about 3 percent, preferably from about 0.25 percent to about 2.5 percent, and more preferably, from about 0.5 percent to about 1.5 percent. Examples of suitable pearlescent or opacifying agents include, but are not limited to mono or diesters of (a) fatty acids having from about 16 to about 22 carbon atoms and (b) either ethylene or propylene glycol; mono or diesters of (a) fatty acids having from about 16 to about 22 carbon atoms (b) a polyalkylene glycol of the formula X.:
HO-(JO)a H X.
wherein J is an alkylene group having from about 2 to about 3 carbon atoms; and a is 2 or 3;
fatty alcohols containing from about 16 to about 22 carbon atoms; fatty esters of the formula XI:
KCOOCHZL XI.
wherein K and L independently contain from about 15 to about 21 carbon atoms;
inorganic solids insoluble in the shampoo composition, and mixtures thereof.
In a preferred embodiment, the pearlescent or opacifying agent is introduced to the shampoo composition as a pre-formed, stabilized aqueous dispersion, such as that commercially available from Henkel Corporation of Hoboken, New Jersey under the tradename, "Euperlan PK-3000."
This material is a combination of glycol distearate (the diester of ethylene glycol and stearic acid), Laureth-4 (CH3(CH2),aCH2(OCHZCH2)aOH) and cocamidopropyl betaine and preferably is in a weight percent ratio of from about 25 to about 30: about 3 to about 15: about 20 to about 25, respectively.
Examples of suitable chelating agents include those which are capable of protecting and preserving the compositions of this invention. Preferably, the chelating agent is EDTA, and more preferably is tetrasodium EDTA available commercially from Dow Chemical Company of Midland, Michigan under the tradename, "Versene 100XL" and is present in an amount, based upon the total weight of the composition, from about 0 to about 0.5 percent, and preferably from about 0.05 percent to about 0.25 percent. Other suitable chelating agents include parabens such as methyl paraben, propyl paraben, butyl paraben, isomethyl paraben, isopropyl paraben, isobutyl paraben, sodium benzoate, iodopropynyl butylcarbamate which is commercially available as "Glycacil L" from Lonza, Inc., and mixtures thereof. Suitable preservatives include Quaternium-15, available commercially as "Dowicil 200" from the Dow Chemical Corporation of Midland, Michigan, and are present in the composition in an amount, based upon the total weight of the composition, from about 0 to about 0.2 percent, and preferably from about 0.05 percent to about 0.10 percent.
The above described cleansing composition may be prepared by combining the desired components in a suitable container and mixing them under ambient conditions in any conventional mixing means well known in the art, such as a mechanically stirred propeller, paddle, and the like. Although the order of mixing is not critical, it is preferable to pre-blend certain components, such as the fragrance and the nonionic surfactant before adding such components into the main mixture.
The composition of this invention can be formulated in a variety of dosage forms for topical application that include, but are not limited to, for example, washes, baths, lotions, creams, ointments, sprays, aerosols, skin patches, soap, mousses, tonics, gels, solids (e.g.
sticks) or the like which is designed to be left on the skin and not washed shortly after application.
Alternatively, the composition may be applied to the desired area in the form of, for example, a lotion, cream, gel, soap, shampoo or the like which is designed to be rinsed off within a given amount of time after application.
Another preferred embodiment of the present invention is directed to a delivery system for delivering benefit agents to the hair, nails, and scalp comprised of a) at least one water soluble silicone agent; and b) at least one, and more preferably at least two cationic conditioning compounds. Preferably, the delivery system is comprised of, based upon the total weight of the delivery system, a) from about 0.001 percent to about 10 percent, and preferably from about .01 percent to about 5 percent of at least one water soluble silicone agent; and b) from about 0.001 percent to about 5 percent, and preferably from about 0.01 percent to about 2 percent of at least one, and preferably at least two cationic conditioning compounds.
In embodiments wherein it is desirable to deposit hydrophilic benefit agents, e.g. salicylic acid, alpha hydroxy acids, vitamins, proteins, and peptides, onto andlor into the skin, hair, and nails, it is preferable to apply thereto the benefit agent in the delivery system composition comprised of at least two cationic conditioning compounds, which preferably are guar hydroxypropyltrimonium chloride and acrylaminopropyltrimonium chloride/acrylamide copolymer; and more preferably with the combination of at least 2 cationic conditioning compounds, which are preferably guar hydroxypropyltrimonium chloride and acrylaminopropyltrimonium chloridelacrylamide copolymer, and at least one water soluble silicone compound, which preferably is a silicone quaternium-13. It is most preferable to apply the hydrophilic benefit agent in a delivery system comprised of at least 2 cationic conditioning compounds, which preferably are guar hydroxypropyltrimonium chloride and acrylamidopropyltrimonium chloridelacrylamide copolymer, and at least two water soluble silicone compounds, one of which is preferably a silicone quaternium-13.
In embodiments wherein it is desirable to deposit hydrophobic benefit agents, i.e. elubiol, ketoconazole, retinol and derivatives thereof, onto and/or into the skin, nails, andlor hair, it is preferable to apply thereto the hydrophobic benefit agent in a delivery system composition comprised of at least 2 cationic conditioning compounds, which preferably are guar hydroxypropyltrimonium chloride and acrylamiiopropyltrimonium chloridelacrylamide copolymer and at least one water soluble silicone compound, which preferably is a silicone quaternium-13. It is more preferable to apply the hydrophobic benefit agent in a delivery system comprised of at least 2 cationic conditioning compounds, which preferably are guar hydroxypropyltrimonium chloride and acrylamidopropyltrimonium chloridelacrylamide copolymer, and at least two water soluble silicone compounds, one of which is preferably a silicone quaternium-13.
In embodiments wherein it is desirable to deposit a thin coating of conditioner on the hair fiber, it is desirable to apply thereto a composition comprised of at least two cationic agents and at least one water soluble silicone, the latter of which preferably is cetyl triethylmonium dimethicone copolyol phthalate. Suitable depositing conditioners nonexclusively include the silicone agents and cationic conditioning agents described herein as well as other known conditioners.
In addition to combining a benefit agent along with the delivery system, another embodiment of the present invention is directed to combining an optional benefit agent along with the above-described cleansing composition. By "benefit agent," it is mean any active ingredient that is to be delivered into andlor onto the skin at a desired location, such as a cosmetic agent or a pharmaceutical agent. By "cosmetic agent," it is meant any ingredient that is appropriate far cosmetically treating, providing nutrients to, and/or conditioning the hair andlor skin via topical application. By "pharmaceutical agent," it is mean any drug that is either hydrophobic or hydrophilic in nature and appropriate for topical use. As used herein °medicament agents" include those agents capable of promoting recovery ftom injury and illness.
Examples of suitable benefit agents include, but are not limited to, depigmentation agents;
reflectants; thickening agents; detanglinglwet combing agents; film forming polymers; humectants; amino acid agents; antimicrobial agents; allergy inhibitors; anti-acne agents; anti-aging agents; anti-wrinkling agents, antiseptics; analgesics; antitussives; antipruritics; local anesthetics; anti-hair loss agents; hair growth promoting agents; hair growth_inhibitor agents, antihistamines;
antiinfectives; inflammation inhibitors; anti-emetics; anticholinergics; vasoconstrictors; vasodilators;
wound healing promoters;

peptides, polypeptides and proteins; deodorants and anti-perspirants;
medicament agents; skin emollients and skin moisturizers; hair conditioners; hair softeners; hair moisturizers;
vitamins; tanning agents; skin lightening agents; antifungals such as antifungals for foot preparations;
depilating agents; shaving preparations; external analgesics; perfumes; counterirritants; hemorrhoidals;
insecticides; poison ivy products; poison oak products; burn products; anti- diaper rash agents;
prickly heat agents; make-up preparations; vitamins; amino acids and their derivatives; herbal extracts;
retinoids; tlavoids; sensates;
anti-oxidants; skin conditioners; hair lighteners; chelating agents; cell turnover enhancers; coloring agents;
pigments; sunscreens and the like, and mixtures thereof. The amount of certain cleansing compositionldelivery system compounds for the benefit agent purposes set forth below is in addition to the amount of the same compound that may be desired for use in the cleansing composition/delivery system therefor.
Examples of suitable reflectants nonexclusively include mica, alumina, calcium silicate, glycol dioleate, glycol distearate, silica, sodium magnesium tluorosilicate, and mixtures thereof.
Examples of suitable UV absorbers include benzophenone, bornelone, butyl paba, cinnamidopropyl trimethyl ammonium chloride, disodium distyrylbiphenyl disulfonate, paba, potassium methoxycinnamate, and mixtures thereof.
Commercially available thickening agents that are capable of imparting the appropriate viscosity to the conditioning shampoo compositions are suitable for use in this invention.
If used, the thickener should be present in the shampoo compositions in an amount sufficient to raise the Brookfield viscosity of the composition to a value of between about 500 to about 10,000 centipoise, Examples of suitable thickening agents nonexclusively include: mono or diesters of polyethylene glycol of formula VI.
HO-(CHzCH20)ZH Vl.
wherein z is an integer from about 3 to about 200;
fatty acids containing from about 16 to about 22 carbon atoms; fatty acid esters of ethoxylated polyols;
ethoxylated derivatives of mono and diesters of fatty acids and glycerine;
hydroxyalkyl cellulose; alkyl cellulose; hydroxyalkyl alkyl cellulose; and mixtures thereof. More specifically, suitable thickening agents nonexclusively include behenalkonium chloride; cetyl alcohol, quaternium 46, PG-hydroxyethyl cellulose, cocodimonium chloride, polyquaternium 6, polyquaternium 7, quaternium 18, PEG-18 glycerol oleate/cocoate, a mixture of acrylateslspirit 50 acrylate copolymer, laureth 3 and propylene glycol, which is commercially available from Goldschmidt under the tradename "Antil 208," a mixture of cocamidopropylbetaine and glyceryl laurate which is commercially available from Goldschmidt under the tradename, "Antil HS60," a mixture of propylene glycol, PEG 55, and propylene glycol oleate, which is commercially available from Goldschmidt under the tradename, "Antil 414 liquid," and mixtures thereof.
Preferred thickeners include polyethylene glycol ester, and more preferably PEG-150 distearate which is available from the Stepan Company of Northfield, Illinois or from Comiel, S.p.A. of Bologna, Italy under the tradename, "PEG 6000 DS".

Suitable detangling/wet combing agents nonexclusively include dioleoylamidoethyl hydroxythylmonium methosulfate, di (soyoylethyl) hydroxyethylmonium methosulfate, hydroxyethyl behenamidopropyl dimonium chloride, olealkonium chloride, polyquaternium 47, stearalkonium chloride, tricetylmonium chloride, and mixtures thereof.
Suitable film forming polymers include those that, upon drying, produce a substantially continuous coating or film on the hair, skin, or nails. Nonexclusive examples of suitable film forming polymers include acrylamidopropyl trimonium chloride/acrylamide copolymer; corn starchl acrylamidel sodium acrylate copolymer; polyquaternium 10; polyquaternium 47; polyvinylmethyllmaleic anhydride copolymer;
styrenelacrylates copolymers; and mixtures thereof.
Commercially available humectants which are capable of providing moisturization and conditioning properties to the cleansing composition are suitable for use in the present invention. The humectant is preferably present in an amount of from about 0 percent to about 10 percent, more preferably from about 0.5 percent to about 5 percent, and most preferably from about 0.5 percent to about 3 percent, based on the overall weight of the composition. Examples of suitable humectants nonexclusively include: 1 ) water soluble liquid polyols selected from the group comprising glycerine, propylene glycol, hexylene glycol, butylene glycol, pentylene glycol, dipropylene glycol, and mixtures thereof;
2) polyalkylene glycol of the formula VII:
HO-(R"O)b-H VII.
wherein R° is an alkylene group having from about 2 to about 4 carbon atoms and b is an integer of from about 1 to about 10, such as PEG 4; 3) polyethylene glycol ether of methyl glucose of formula VIII:
CH3-C6H,o05-(OCHZCHZ)~ OH VIII.
wherein c is an integer from about 5 to about 25;
4) urea; 5) fructose; 6) glucose; 7) honey; 8) lactic acid; 9) maltose; 10) sodium glucuronate; and 11 ) mixtures thereof, with glycerine being the preferred humectant.
Suitable amino acid agents include amino acids derived from the hydrolysis of various proteins as well as the salts, esters, and acyl derivatives thereof. Examples of such amino acid agents nonexclusively include amphoteric amino acids such as alkylamido alkylamines, i.e. stearyl acetyl glutamate, capryloyl silk amino acid, caprylol collagen amino acids; capryloyl kertain amino acids;
capryloyl pea amino acids;
cocodimonium hydroxypropyl silk amino acids; corn gluten amino acids;
cysteine; glutamic acid; glycine;
hair keratin amino acids; hair amino acids such as aspartic acid, threonine, serine, glutamic acid, proline, glycine, alanine, half cystine, valine, methionine, isoleucine, leucine, tyrosine, phenylalanine, cysteic acid, lysine, histidine, arginine, cysteine, tryptophan, citrulline; lysine; silk amino acids, wheat amino acids; and mixtures thereof Suitable proteins include those polymers that have a long chain, i.e. at least about 10 carbon atoms, and a high molecular weight, i.e. at least about 1000, and are formed by self-condensation of amino acids. Nonexclusive examples of such proteins include collagen, deoxyribonuclease, iodized corn protein; keratin; milk protein; protease; serum protein; silk; sweet almond protein; wheat germ protein;
wheat protein; wheat protein, alpha and beta helix of keratin proteins; hair proteins, such as intermediate filament proteins, high-sulfur proteins, ultrahigh-sulfur proteins, intermediate filament-associated proteins, high-tyrosine proteins, high-glycine tyrosine proteins, tricohyalin, and mixtures thereof.
Examples of suitable vitamins nonexclusively include vitamin B complex;
including thiamine, nicotinic acid, biotin, pantothenic acid, choline, riboflavin, vitamin B6, vitamin B12, pyridoxine, inositol, carnitine; vitamins A,C,D,E,K and their derivatives such as vitamin A
palmitate and pro-vitamins, e.g. (i.e.
panthenol (pro vitamin B5) and panthenol triacetate) and mixtures thereof.
Examples of suitable antibacterial agents nonexclusively include bacitracin, erythromycin, neomycin, tetracycline, chlortetracycline, benzethonium chloride, phenol, and mixtures thereof.
Examples of suitable skin emollients and skin moisturizers nonexclusively include mineral oil, lanolin, vegetable oils, isostearyl isostearate, glyceryl laurate, methyl gluceth 10, methyl gluceth 20 chitosan, and mixtures thereof.
Examples of suitable hair conditioners nonexclusively include quaternized compounds such as behenamidopropyl PG-dimonium chloride, tricetylammonium chloride, dihydrogenated tallowamidoethyl hydroxyethylmonium methosulfate, and mixtures thereof as well as lipophilic compounds like cetyl alcohol, stearyl alcohol, hydrogenated polydecene, and mixtures thereof.
An example of a suitable hair softener nonexclusively includes silicone compounds, such as those that are either non-volatile or volatile and those that are water soluble or water insoluble. Examples of suitable silicones include organo-substituted polysiloxanes, which are either linear or cyclic polymers of monomeric siliconeloxygen monomers and which nonexclusively include cetyl dimethicone; cetyl triethylammonium dimethicone copolyol phthalate; cyclomethicone; dimethicone copolyol; dimethicone copolyol lactate; hydrolyzed soy proteinldimethicone copolyol acetate;
silicone quaternium 13;
stearalkonium dimethicone copolyol phthalate; stearamidopropyl dimethicone;
and mixtures thereof.
Examples of suitable hair moisturizers nonexclusively include panthenyl ethyl ether, phytantriol, and mixtures thereof.
Examples of sunscreen agents nonexclusively include butyl methoxydibenzoylmethane, octyl methoxycinnamate, oxybenzone, octocrylene, octyl salicylate, phenylbenzimidazole sulfonic acid, ethyl hydroxypropyl aminobenzoate, menthyl anthranilate, aminobenzoic acid, cinoxate, diethanolamine methoxycinnamate, glyceryl aminobenzoate, titanium dioxide, zinc oxide, oxybenzone, padimate o, red petrolatum, and mixtures thereof.
An example of a suitable tanning agent nonexclusively includes dihydroxyacetone.
Examples of skin lightening agents nonexclusively include hydroquinone, catechol and its derivatives, ascorbic acid and its derivatives, and mixtures thereof.

Examples of suitable insecticides (including insect repellents, anti-scabies and anti-lice treatments) nonexclusively include permethrin, pyrethrin , piperonyl butoxide, imidacloprid, N,N-diethyl toluamide, which refers to the material containing predominantly the meta isomer, i.e., N,N-diethyl-m-toluamide, which is also known as DEET; compounds of the formula IX

~~C~N-CH2-CH-K
O
IX.
wherein RS is a branched or unbranched alkyl group having about 1 to about 6 carbon atoms;
Fts is H, methyl or ethyl;
R~ is a branched or unbranched alkyl or alkoxy group having from about 1 to about 8 carbon atoms; and K is a -CN or a -COORS group, wherein RB is a branched or unbranched alkyl group having from about 1 to about 6 carbon atoms, natural or synthetic pyrethroids, whereby the natural pyrethroids are contained in pyrethrum, the extract of the ground flowers of Chrysanthemum cinerariaefolium or C coccineum; and mixtures thereof. Within the structure of Formula IX. are ethyl 3-(N-butylacetamido)propionate, wherein R, is a CH3 group, R5 is an n-butyl group, R6 is H, K is COORS and RB is ethyl, which is available commercially from Merck KGaA of Darmstadt, Germany under the name, "Insect Repellent 3535."
An example of an anti fungal for foot preparations nonexclusively includes tolnaftate.
Examples of suitable depilating agents nonexclusively include calcium thioglycolate, magnesium thioglycolate, potassium thioglycolate, strontium thioglycolate, and mixtures thereof.
Examples of suitable external analgesics and local anesthetics nonexclusively include benzocaine, dibucaine, benzyl alcohol, camphor, capsaicin, capsicum, capsicum oleoresin, juniper tar, menthol, methyl nicotinate, methyl salicylate, phenol, resorcinol, turpentine oil, and mixtures thereof.
Examples of suitable antiperspirants and deodorants nonexclusively include aluminium chlorohydrates, aluminium zirconium chlorohydrates, and mixtures thereof.
Examples of suitable counterirritants nonexclusively include camphor, menthol, methyl salicylate, peppermint and clove oils, ichtammol, and mixtures thereof.
An example of a suitable inflammation inhibitor nonexclusively includes hydrocortisone.

- is -Examples of suitable hemorrhoidal products nonexclusively include the anesthetics such as benzocaine, pramoxine hydrochloride, and mixtures thereof; antiseptics such as benzethonium chloride;
astringents such as zinc oxide, bismuth subgallate, balsam Peru, and mixtures thereof; skin protectants such as cod liver oil, vegetable oil, and mixtures thereof.
Examples of suitable make-up preparations nonexclusively include components for lipstick, rouge, blush, eye liner, eyeshadow powder, mascara, face powder, and mixtures thereof.
One preferred type of benefit agent includes those therapeutic components that are effective in the treatment of dandruff, seborrheic dermatitis, and psoriasis as well as the symptoms associated therewith. Examples of such suitable benefits agents nonexclusively include zinc pyrithione, shale oil and derivatives thereof such as sulfonated shale oil, selenium sulfide, sulfur;
salicylic acid; coal tar; povidone-iodine, imidazoles such as ketoconazole, dichlorophenyl imidazolodioxalan, which is commercially available from Janssen Pharmaceutica, N.V., under the tradename, "Elubiol", clotrimazole, itraconazole, miconazole, climbazole, tioconazole, sulconazole, butoconazole, tluconazole, miconazolenitrite and any possible stereo isomers and derivatives thereof such as anthralin; piroctone olamine (Octopirox); selenium sulfide; ciclopirox olamine; anti-psoriasis agents such as vitamin D analogs, e.g. calcipotriol, calcitriol, and tacaleitrol; vitamin A analogs such as esters of vitamin A, e.g. vitamin A
palmitate, retinoids, retinols, and retinoic acid; corticosteroids such as hydrocortisone, clobetasone, butyrate, clobetasol propionate and mixtures thereof.
Most preferred benefit agents nonexclusively include sulfonated shale oil, elubiol, 6-(1-piperidinyl)-2,4-pyrimidinediamine-3-oxide, finasteride, ketoconazole, salicylic acid, zinc pyrithione, coal tar, benzoyl peroxide, selenium sulfide, hydrocortisone, sulfur, menthol, pramoxine hydrochloride, tricetylammonium chloride, polyquaternium 10, panthenol, panthenol triacetate, vitamin A and derivatives thereof, vitamin B
and derivatives thereof, vitamin C and derivatives thereof, vitamin D and derivatives thereof, vitamin E and derivatives thereof, vitamin K and derivatives thereof, keratin, lysine, arginine, hydrolyzed wheat proteins, hydrolyzed silk proteins, octyl methoxycinnamate, oxybenzone, minoxidil, titanium dioxide, zinc dioxide, retinol, erthromycin, tretinoin, and mixtures thereof.
The amount of benefit agent to be combined with the cleansing composition or the delivery system may vary depending upon, for example, the resulting benefit desired and the sensitivity of the user to the benefit agent. Unless otherwise expressed herein, preferably the benefit agent is present in the cleansing composition or delivery system in an amount, based upon the total weight of the composition or delivery system, from about 0.001 percent to about 20 percent, and preferably from about 0.001 percent to about 10 percent, and more preferably from about 0.001 percent to about 5 percent.
Another embodiment of the present invention is directed to a method for enhancing the deposition of benefit agents which comprises topically administering to a desired location on a human or animal the delivery system composition as described above combined with an effective amount of a benefit agent and an optional detergent. While the frequency and amount of the delivery system to be applied will depend upon, for example, the type and amount of benefit agent available, the intended usage of the final composition, i.e. therapeutic versus maintenance regimen, the amount and type of detergent present, and the sensitivity of the individual user to the delivery system, typically the delivery system of the present invention should be topically applied to affected body parts at regular intervals, and preferably from about 2 to about 14 times per week. More preferably, the delivery system composition is applied more frequently during the initial stages of treatment, e.g. from about 5 to about 7 times per week until the desired effect is achieved, then less frequently when maintenance is desired, e.g. from about 2 to about 5 times per week.
In a preferred embodiment wherein the delivery system composition containing a benefit agent is incorporated into a shampoo, the shampoo is applied to wet hair, then the hair is washed in accordance with known practices. More preferably, the composition remains on the hair for greater than about 0 to about 10 minutes, and preferably from about 1 to about 5 minutes before rinsing.
An alternative preferred embodiment of the present invention is directed to a method for treating hair loss, such as hair loss resulting from alopecia, comprising topically applying the above-described delivery system composition, the hair loss benefit agent, and the optional detergent, to a desired location on an animal or human, wherein the benefit agent is comprised of an effective amount of a hair loss treatment agent such as minoxidil or mixture thereof. As used herein, "hair loss treatment agents" shall include agents capable of growing hair and/or agents capable of preventing the loss of hair. By "effective amount," it is meant an amount effective for treating hair loss and preferably may range from, based upon the total weight of the cleansing composition/delivery system, from about 0.001 percent to about 20 percent, and preferably from about 1 percent to about 5 percent.
Examples of benefit agents suitable for treating hair loss include, but are not limited to potassium channel openers or peripheral vasodilators such as minoxidil, diazoxide, and compounds such as N"-cyano-N-(tert-pentyl)-N'-3-pyridinyl-guanidine ("P-1075") as disclosed in United States Patent No.:
5,244,664, which is incorporated herein by reference; vitamins, such as vitamin E and vitamin C, and derivatives thereof such as vitamin E acetate and vitamin C palmitate;
hormones, such as erythropoietin, prostaglandins, such as prostaglandin EI and prostaglandin F2-alpha; fatty acids, such as oleic acid;
diruretics such as spironolactone; heat shock proteins ('HSP"), such as HSP 27 and HSP 72; calcium channel blockers, such as verapamil HCL, nifedipine, and diltiazemamiloride;
immunosuppressant drugs, such as cyclosporin and Fk-506; 5 alpha-reductase inhibitors such as finasteride; growth factors such as, EGF, IGF and FGF; transforming growth factor beta; tumor necrosis factor; non-steroidal anti-inflammatory agents such as benoxaprofen; retinoids such as tretinoin;
cytokines, such as IL-6, IL-1 alpha, and IL-1 beta; cell adhesion molecules such as /CAM; glucorcorticoids such as betametasone;
botanical extracts such as aloe, clove, ginseng, rehmannia, swertia, sweet orange, zanthoxylum, Serenoa repens (saw palmetto), Hypoxis rooperi, stinging nettle, pumpkin seeds, and rye pollen; other botanical extracts including sandlewood, red beet root, chrysanthemum, rosemary, burdock root and other hair growth promoter activators which are disclosed in DE 4330597 which is incorporated by reference in its entirety herein; homeopathic agents such as Kalium Phosphoricum D2, Azadirachta indica D2, and Joborandi DI; genes for cytokines, growth factors, and male-pattered baldness;
antifungals such as ketoconazole and elubiol; antibiotics such as streptomycin; proteins inhibitors such as cycloheximide;

acetazolamide; benoxaprofen; cortisone; diltiazem; hexachlorobenzene;
hydantoin; nifedipine;
penicillamine; phenothaiazines; pinacidil; psoralens, verapamil; zidovudine;
alpha-glucosylated rutin having at least one of the following rutins: quercetin, isoquercitrin, hespeddin, naringin, and methylhesperidin, and flavonoids and transglycosidated derivatives thereof which are all disclosed in JP
7002677, which is incorporated by reference in its entirety herein; and mixtures thereof.
Preferred hair loss treatment agents include 6-(I-piperdinyl)-2,4-pyrimidinediamine-3-oxide, N'-cyano-N-(tert-pentyl)-N'-3-pyridinyl-guanidine, finasteride, retinoids and derivatives thereof, ketoconazole, elubiol or mixtures thereof.
Another embodiment of the present invention is directed to a method for inhibiting hair growth comprising topically applying the above-described delivery system composition combined with a benefit agent and an optional detergent, to a desired area on an animal or human for inhibiting hair growth, wherein the benefit agent is comprised of an effective amount of a hair growth inhibiting agent. In a preferred embodiment, the delivery system composition contains, based upon the total weight of the composition, from about 0.001 percent to about 20 percent, and preferably from about 0.01 percent to about 5 percent hair growth inhibiting agent.
Examples of benefit agents suitable for use in inhibiting hair growth include:
serine proteases such as trypsin; vitamins such as alpha-tocophenol (vitamin E) and derivatives thereof such as tocophenol acetate and tocophenol palmitate; antineoplastic agents, such as doxorubicin, cyclophosphamide, chlormethine, methotrexate, tluorouracil, vincristine, daunorubicin, bleomycin and hydroxycarbamide;
anticoagulants, such as heparin, heparinoids, coumaerins, detran and indandiones; antithyroid drugs, such as iodine, thiouracils and carbimazole; lithium and lithium carbonate;
interferons, such as interferon alpha, interferon alpha-2a and interferon alpha-2b; retinoids, such as retinol (vitamin A), isotretinoin:
glucocorticoids such as betamethasone, and dexamethosone; antihyperlipidaemic drugs, such as triparanol and clofibrate; thallium; mercury; albendazole; allopurinol;
amiodarone; amphetamines;
androgens; bromocriptine; butyrophenones; carbamazepine; cholestyramine;
cimetidine; clofibrate;
danazol; desipramine; dixyrazine; ethambutol; etionamide; tluoxetine;
gentamicin, gold salts; hydantoins;
ibuprofen; impramine; immunoglobulins; indandiones; indomethacin;
intraconazole; levadopa; maprotiline;
methysergide; metoprolol; metyrapone; nadolol; nicotinic acid; potassium thiocyanate; propranolol;
pyridostimine; salicylates; sulfasalazine; terfenadine; thiamphenicol;
thiouracils; trimethadione; troparanol;
valproic acid; and mixtures thereof.
Preferred hair growth inhibitory agents include serene proteases, retinol, isotretinoin, betamethoisone, alpha-tocophenol and derivatives thereof, or mixtures thereof.
Another preferred embodiment of the present invention is directed to a method for treating acne and for reducing the signs of aging, i.e. wrinkles, fine lines, and other manifestations of photodamage, comprising topically applying the above-described delivery system composition, the relevant benefit agent, and the optional detergent to the skin of an animal or human at a desired area, wherein the benefit agent is comprised of an effective amount of an anti-acne agent or an anti-aging agent, respectively.

Examples of suitable anti-aging agents include, but are not limited to inorganic sunscreens such as titanium dioxide and zinc oxide; organic sunscreens such as octyl-methyl cinnamates and derivatives thereof; retinoids; vitamins such as vitamin E, vitamin A, vitamin C, vitamin B, and derivatives thereof such as vitamin E acetate, vitamin C palmitate, and the like; antioxidants including beta carotene, alpha hydroxy acid such as glycolic acid, citric acid, lactic acid, malic acid, mandelic acid, ascorbic acid, alpha-hydroxybutyric acid, alpha-hydroxyisobutyric acid, alpha-hydroxyisocaproic acid, atrrolactic acid, alpha-hydroxyisovaleric acid, ethyl pyruvate, galacturonic acid, glucopehtonic acid, glucopheptono 1,4-lactone, gluconic acid, gluconolactone, glucuronic acid, glucurronolactone, glycolic acid, isopropyl pyruvate, methyl pyruvate, mucic acid, pyruvia acid, saccharic acid, saccaric acid 1,4-lactone, tartaric acid, and tartronic acid; beta hydroxy acids such as beta-hydroxybutyric acid, beta-phenyl-lactic acid, beta-phenylpyruvic acid; botanical extracts such as green tea, soy, milk thistle, algae, aloe, angelica, bitter orange, coffee, goldthread, grapefruit, hoellen, honeysuckle, Job's tears, lithospermum, mulberry, peony, puerarua, nice, safflower, and mixtures thereof.
Preferred anti-aging agents include retinoids, anti-oxidants, alpha-hydroxy acids and beta-hydroxy IS acid with retinol and tretinoin being most preferred.
Suitable amounts of anti-aging agents include, based upon the total weight, of the delivery system composition and optional detergent, from about 0.01 percent to about 10 percent, and preferably from about 0.04 percent to about 5 percent.
Examples of suitable anti-acne agents include, but are not limited to topical retinoids (tretinoin, isotretinoin, motretinide, adapalene, tazarotene, azelaic acid, retinol);
salicylic acid; benzoyl peroxide;
resorcinol; antibiotics such as tetracycline and isomers thereof, erythromycin, and the anti-inflammatory agents such as ibuprofen, naproxen, hetprofen; botanical extracts such as alnus, arnica, artemisia capillaris, asiasarum root, birth, calendula, chamomile, cnidium, comfrey, fennel, galla rhois, hawthrom, houttuynia, hypericum, jujube, kiwi, licorice, magnolia, olive, peppermint, philodendron, salvia, sasa albo-marginata; imidazoles such as ketoconazole and elubiol, and those described in Gollnick, H et al. 196(1) Dermatology Sebaceous Glands, Acne and Related Disorders, 119-157 (1998), which is incorporated by reference herein, and mixtures thereof.
Preferred anti-acne agents include benzoyl peroxide, retinol, elubiol, antibiotics, and salicylic acid, with retinol and tretinoin being most preferred.
Suitable amount of anti-acne agents include, based upon the total weight of the delivery system composition and optional detergent, from about 0.01 percent to about 10 percent, and preferably from about 0.04 percent to about 5 percent.
Another preferred embodiment of the present invention is directed to a method for depigmenting the skin comprising topically applying to skin at a desired area the above-described delivery system composition, the optional detergent, and an effective amount of the depigmentation benefit agent.
Suitable effective amounts of depigmentation agents include, based upon the total weight of the delivery system, from about 0.01 percent to about 10 percent, and preferably from about 0.04 percent to about 5 percent.

Examples of suitable depigmentation agents include, but are not limited to retinoids such as retinol; Kojic acid and its derivatives such as, for example, kojic dipalmitate; hydroquinone and it derivatives such as arbutin; transexamic acid; vitamins such as niacin, vitamin C and its derivatives;
azelaic acid; placertia; licorice; extracts such as chamomile and green tea, and mixtures thereof, with retinol, Kojic acid, and hydroquinone, being preferred.
An alternative preferred embodiment of the present invention is directed to a method for treating the symptoms and/or the diseases of dandruff, seborrheic dermatitis and/or psoriasis, comprising topically applying the above-described delivery system composition, the benefit agent, and the optional detergent, to a location desired wherein the benefit agent is comprised of an effective amount of a dandruff treatment agent, a seborrheic dermatitis treatment agent, or a psoriasis treatment agent, respectively. As used herein, "dandruff treatment agent," "seborrheic dermatitis treatment agent,"
or a "psoriasis treatment agent," respectively, shall include agents capable of treating the symptoms andlor the diseases of dandruff, seborrheic dermatitis, and psoriasis, respectively. By "effective amount," it is meant an amount effective for treating the disease and/or the symptoms associated therewith and preferably may range from, based upon the total weight of the vesicle delivery system and optional detergent, from about 0.001 percent to about 10 percent, and preferably from about 0.01 percent to about 5 percent.
Examples of benefit agents suitable for treating the symptoms and/or the diseases of dandruff, seborrheic dermatitis andJor psoriasis, respectively, nonexclusively include those set forth above with shale oil and derivatives thereof, elubiol, ketoconazole, coal tar, salicylic acid, zinc pyrithione, selenium sulfide, hydrocortisone, sulfur, menthol, pramoxine hydrochloride, and mixtures thereof being particularly preferred.
Another embodiment of the present invention is directed to a method for removing hair comprising topically applying to skin the above-described delivery system composition, the benefit agent, and the optional detergent, to a location desired wherein the benefit agent is comprised of an effective amount of a depilatory agent, such as thioglycolade. In a preferred embodiment, the composition contains, based upon the total weight of the composition, from about 0.001 percent to about 20 percent, and preferably from about 0.01 percent to about 5 percent hair depilatory agent.
We have unexpectedly found that the above-described cleansing compositionl delivery system is capable of efficiently mediating the deposition and permeation of various benefit agents, such as antidandruff agents, onto and into the skin following topical administration thereto.
We have surprisingly found that the cleansing composition of the present invention is sufficiently stable to resist phase separation even though both an anionic surfactant and cationic components may be present in the composition. Furthermore, the cleansing composition not only effectively cleanses the hair due to the ability to include an anionic surfactant therein, but it also effectively deposits conditioning agents on the hair without exhibiting an excessive build-up thereon, even after repeated shampooing.

Consequently, the hair is left in a more manageable, softer, shiny and overall more esthetically pleasing state after only a single application of the composition to the hair.
We have further unexpectedly found that the above-described delivery system is capable of efficiently mediating the deposition and permeation of various benefit agents, such as antidandruff agents, onto and into the skin, hair, and nails, following topical administration thereto.
The invention illustratively disclosed herein suitably may be practiced in the absence of any component, ingredient, or step which is not specifically disclosed herein.
Several examples are set forth below to further illustrate the nature of the invention and the manner of carrying it out. However, the invention should not be considered as being limited to the details thereof.
EXAMPLES
Example 1: Preparation of Cleansing Shampoo containing Two Cationic Agents Shampoos comprised of the following components as set forth in Table 1 were prepared:

Table 1: Cleansin sham oo with two cationic de ositin enhancin a ents.

Trade Name CTFA % wt/wt Su lier 1 DI Water DI Water 72.965 2 Salcare SC 60 Acrylamidopropylltrimoniumchloride0.08 Ciba Specialties Ac lamide Ca of mer 3 Jaguar C 17 Guar Hydroxypropyl Trimonium0.15 Rhone-Poulenc Chloride 4 Citric Acid Anh Citric Acid 0.025 Roche Elubiol Dichloro hen I Imidazoldioxolan0.50 Janssen Pharm.

6 Salic lic Acid Salic lic Acid 1.00 Rhone-Poulenc 7 Cutina AGS GI col Distearate 1.75 Henkel 8 Meth I Paraben Meth I Paraben 0.20 Ni a Hardwicke Inc .
9 Em icot EAC 70 Ammonium Laureth Sulfate3.6 Albri ht &
Wilson 10Em icol AL 70 Ammonium Lau I Sulfate 11.8 Albri ht &
Wilson 11Te o Betaine Cocamido ro I Betaine 2.43 Goldschmidt E

12Te o Betaine Cocamido ro I Betaine 3.00 Goldschmidt 13Pol ox WSR-205 PEG 14M 0.05 Amerchol 14Ninol LMP Lauramide MEA 1.00 Ste han 15DL-Panthenol-50%Panthenol 0.15 Roche 16Ph antriol Ph tantriol 0.025 Roche 17H drotriticum Wheat Amino Acid 0.22 Croda WAA

18Sodium Benzoate Sodium Benzoate 0.20 EM Industries 19Versene 100XL Tetrasodium EDTA 0.20 Dow Chemical 20BHT But lated H drox toluene0.10 EM Industries 21Lorena Fragrance 0.50 Creation Aromati ues 22GI cacil L lodo ro n I bu Icarbamate0.05 Lonza 23NaOH 25% Sodium H droxide QS Mallinckrodt Total 100.00 Shampoo Process:
A vessel was charged with 3/ amount of deionized water (component 1 ).
Components 2, 3 and 4 were 5 added sequentially thereto, both with ten minute intervals between the additions and with mixing at 500 rpm under constant conditions. The resulting mixture was then heated to about 63 to 67°C with mixing at 500 rpm. Component 5 was then to the mixture. After all the elubiol had dissolved, salicylic acid (component 6) was added thereto with mixing for 15-20 minutes at constant conditions. The resultant mixture was then heated to 70-75°C and components 7, 8, 9 and 10 were sequentially added under mixing. Component 9 through 13 were sequentially added thereto with mixing under constant conditions.
The resultant primary mixture was then cooled to 50°C.
Components 15, 16, 20 and 21 were combined in a separate beaker at 25-30°C to form a premixture. After cooling the primary mixture to 50°C, component 14, component 17, the premixture, component 18, component 19 and component 22 were sequentially added thereto with mixing. Sodium hydroxide was added thereto with mixing to adjust the pH to about 5.3-5.7. The mixture was then continuously mixed and cooled to about 25-30°C. The remaining amount of deionized water was added to the final volume and was mixed at 500 rpm until uniform.
Example 2: Preparation of Cleansing Sham~aoo containing Three Cationic Agents Shampoos comprised of the following components as set forth in Table 2 were prepared:
Table 2: CI6anSlno shampoo with three cationic rle~nncifinn onl,~m~i.,., ~.,s.,*~
Trade Name CTFA % wtlwt Su lier 1 DI Water DI Water 72.665 2 Salcare SC Acrylamidopropylltrimoniumchloride_ Ciba Specialty 60 Ac lamide Co of mer 0.08 3 Jaguar C 17 Guar Hydroxypropyl Trimonium0.15 Rhone-Poulenc Chloride 4 Citric Acid Citric Acid 0.025 Roche Anh 5 Cutina AGS GI col Distearate 1.75 Henkel Cor oration 6 Meth I ParabenMeth I Paraben 0.20 Ni a Hardwicke Inc.

7 Mer uat 2001 Pol uaternium 47 0.30 Cal on 8 Em icol EAC Ammonium Laureth Sulfate3.6 Albri ht & Wilson 9 Em icol AL Ammonium Lau I Sulfate 11.8 Albri ht & Wilson 10Te o Betaine Cocamido ro I Betaine 2.43 Goldschmidt E

11Te o Betaine Cocamido ro I Betaine 3.00 Goldschmidt 12Elubiol Dicholorohen I Imidazoldioxolan0.50 Janssen Pharm.

13Salic lic AcidSalic lic Acid 1.00 Rhone-Poulenc 14Pol ox WSR-205PEG 14M 0.05 Amerchol 15Ninol LMP Lauramide MEA 1.00 Ste an 16DL-Panthenol-50%Panthenol 0.15 Roche 17Ph tantriol Ph tantriol 0.025 Roche 18H drotriticum Wheat Amino Acid 0.22 Croda WAA

19Sodium BenzoateSodium Benzoate 0.20 EM Industries 20Versene 100XL Tetrasodium EDTA 0.20 Dow Chemical 21BHT Bu lated H drox oluene 0.10 EM Industries 22Lorena Fra rance 0.50 Creation Aromati ues 23GI cacil L lodo ro n I bu Icarbamate0.05 Lonza 24NaOH 25% Sodium H droxide QS Mallinckrodt 100.00 Shampoo Process:
A vessel was charged with'/. amount of deionized water (component 1 ).
Components 2, 3 and 4 were added sequentially, with ten minute intervals between the additions and with mixing at 500 rpm under constant conditions. The resulting mixture was then heated to about 70 to 75°C with mixing at 500 rpm. Component 5 and 6 were added and mixed at 500 rpm until dispersed for about 15 to 25 minutes. At 70 to 75°C, components 9 through 11 were added with mixing.
After cooling the resultant mixture to about 63 to 67°C, elubiol, salicylic acid (component 6) and component 14 were added sequentially thereto with mixing until the latter three components were completely dispersed. The resultant primary mixture was then cooled to 50°C.

Components 15, 16, 20 and 21 were combined in a separate beaker at 25-30°C to form a premixture. After cooling the primary mixture to 50°C, components 15 and 18 were added thereto. The premixture followed by components 19, 20 and 23 were then added thereto sequentially with mixing.
Sodium hydroxide was then added thereto with mixing to adjust the pH to about 5.3-5.7. The mixture was continuously mixed and cooled to about 25-30°C. The remaining amount of deionized water was added to the final volume and was mixed at 500 rpm until uniform.
Example 3: Preparation of Cleansins~ Shampoo containing Two Cationic Agents and One Silicone Quaternaryr Comb ound.
Shampoos comprised of the following components as set forth in Table 3 were prepared:
Table 3: Cleansing shampoo with two cationic deposition enhancing agents and a silicone compound.
Trade Name CTFA % wtlwt Su lier 1 DI Water DI Water 72.765 2 Salcare SC 60 Acrylamidopropylltrimoniumchloride0.08 Ciba Industries Ac lamide Co of mer 3 Jaguar C 17 Guar Hydroxypropyl Trimonium0.15 Rhone-Poulenc Chloride 4 Citric Acid Citric Acid 0.025 Anh 5 Cutina AGS GI col Distearate 1.75 Henkel Cor oration 6 Meth I Paraben Meth I Paraben 0.20 Ni a Hardwicke 7 Em icol EAC Ammonium Laureth Sulfate3.6 Inc 70 Albri ht & Wilson 8 Em icol AL 70 Ammonium Lau I Sulfate 11.8 Albri ht & Wilson 9 Te o Betaine Cocamido ro I Betaine 2.43 Goldschmidt E
10 Te o Betaine Cocamido ro I Betaine 3.00 Goldschmidt 11 Elubiol Dicholorohen I Imidazoldioxolan0.50 Janssen Pharm .
12 Salic lic Acid Salic lic Acid 1.00 Rhone-Poulenc 13 Pol ox WSR-205 PEG 14M 0.05 Amerchol 14 Ninol LMP Lauramide MEA 1.00 Ste an DL-Panthenol-50%Panthenol 0.15 Roche 16 Ph tantriol Ph antriol 0.025 Roche 17 Biosil Basics Silicone Quaternium-13 0.20 Biosil SPQ

18 H drotriticum Wheat Amino Acid 0.22 Croda WAA

19 Sodium BenzoateSodium Benzoate 0.20 EM Industries Versene 100XL Tetrasodium EDTA 0.20 Dow Chemical 21 BHT Bu lated H drox toluene 0.10 EM Industries 22 Lorena Fra rance 0.50 Creation Aromati 23 GI cacil L l odo ro n I but Icarbamate0.05 ues Lonza 24 NaOH (25%) Sodium Hydroxide QS Mallinckrodt 100.00 Shampoo Process:
A vessel was charged with'/ amount of deionized water (component 1 ).
Components 2, 3 and 4 were added sequentially, with ten minute intervals between the additions and with mixing at 500 rpm 20 under constant conditions. The resulting mixture was then heated to about 70 to 75°C with mixing at 500 rpm. Component 5 and 6 were added and mixed at 500 rpm until dispersed for about 15 to 25 minutes. At 70 to 75°C, components 7 through 11 were added with mixing.
After cooling the resultant mixture to about 63 to 67°C, elubiol, salicylic acid (component 6) and component 14 were added sequentially thereto with mixing until the latter three components were completely dispersed. The resultant primary mixture was then cooled to 50°C.
Components 15, 16, 21 and 22 were combined in a separate beaker at 25-30°C to form a premixture. After cooling the primary mixture to 50°C, components 14, 17 and 18 were added. The premixture followed by components 19, 20 and 23 were added thereto sequentially with mixing. Sodium _ hydroxide was added thereto with mixing to adjust the pH to about 5.3-5.7. The mixture was continuously mixed and cooled to about 25-30°C. The remaining amount of deionized water was added to the final volume and was mixed at 500 rpm until uniform.
Example 4: Preparation of Cleansing Shampoo containin~t Three Cationic Additives and Two Silicone Quaternar~r Compounds.
Shampoos comprised of the following components as set forth in Table 4 were prepared:

Table 4: Cleansing shampoo with three cationic deposition enhancing agents and two silicone compounds.
Trade Name CTFA % wtlwt Su lier 1 DI Water DI Water 72.32 2 Salcare SC 60 Acrylamidopropylltrimoniumchloride0.08 Ciba Specialty Ac lamide Co of mer 3 Ja uar C 17 Guar H drox ro I Trimonium0.15 Rhone-Poulenc Chloride 4 Citric Acid Anh Citric Acid 0.025 Cutina AGS Glycol Distearate 1.75 Henkel Cor oration 6 Methyl Paraben Methyl Paraben 0.20 Nipa Hardwicke Inc.

7 Mer uat 2001 Pol uaternium 47 0.30 Cal on 8 Em icol EAC 70 Ammonium Laureth Sulfate 3.60 Albri ht & Wilson 9 Em icol AL 70 Ammonium Lau I Sulfate 11.8 Albri ht & Wilson 10Te o Betaine Cocamido ro I Betaine 2.43 Goldschmidt E

11Te o Betaine Cocamido ro I Betaine 3.00 Goldschmidt 12Elubiol Dicholorohen I Imidazoldioxolan0.50 Janssen Pharm.

13Salic lic Acid Salic lic Acid 1.00 Rhone-Poulenc 14Pol ox WSR-205 PEG 14M 0.05 Amerchol 15Ninol LMP Lauramide MEA 1.00 Ste an 16Biosil Basics Silicone Quaternium-13 0.20 Biosil SPQ Technol ies Inc.

17Biosil Basics Cetyl Triethylmonium-Dimethicone0.15 Biosil Cetylsil Co of of Phthalate Technolo ies Inc.

18DL-Panthenol-50%Panthenol 0.15 Roche 19Ph antriol Ph antriol 0.025 Roche 20H drotriticum Wheat Amino Acid 0.22 Croda WAA

21Sodium Benzoate Sodium Benzoate 0.20 EM Industries 22Versene 100XL Tetrasodium EDTA 0.20 Dow Chemical 23BHT Bu lated H drox toluene 0.10 EM Industries 24Lorena Fragrance 0.50 Creation Aromati ues I

25GI cacil L l odo ro 0.05 Lonza n I but Icarbamate 26NaOH 25% Sodium H droxide QS Mallinckrodt 100.00 Shampoo Process:
5 A vessel was charged with '/. amount of deionized water (component 1 ).
Components 2, 3 and 4 were added sequentially, with ten minute intervals between the additions and with mixing at 500 rpm under constant conditions. The resulting mixture was then heated to about 70 to 75°C with mixing at 500 rpm. Component 5 and 6 were added thereto and mixed at 500 rpm until dispersed, i.e., for about 15 to 25 minutes. At 70 to 75°C, components 7 through 11 were added thereto with mixing.

After cooling the resultant mixture to about 63 to 67°C, elubiol, salicylic acid (component 13) and component 14 were added sequentially thereto with mixing until the latter three components were completely dispersed therein. The resultant primary mixture was then cooled to 50°C.
Components 18, 19,23 and 24 were combined in a separate beaker at 25-30°C to form a premixture. After cooling the primary mixture to 50°C, components 15, 16, 17 and 20 were added thereto.
The premixture followed by components 21, 22 and 25 added thereto sequentially with mixing. Sodium hydroxide was then added thereto with mixing to adjust the pH to about 5.3-5..
The mixture was continuously mixed and cooled to about 25-30°C. The remaining amount of deionized water was added to the final volume and was mixed at 500 rpm until uniform.
Example 5: Preparation of Cleansing Shampoo containing Three Cationic Additives and One Silicone Quaternary Compounds.
Shampoos comprised of the following components as set forth in Table 5 were prepared:

Table 5: Cleansing shampoo with three cationic deposition enhancing agents and one silicon compound.
Trade Name CTFA % wtlwtSu lier 1 DI Water DI Water 72.82 2 Salcare SC Acrylamidopropylltrimoniumchlo0.08 Ciba Specialities 60 ride Ac lamide Co of mer 3 Jaguar C17 Guar Hydroxypropyl 0.15 Rhone-Poulenc Trimonium Chloride 4 Citric Acid Citric Acid 0.025 Roche Anh Cutina AGS GI col Distearate 1.75 Henkel Cor oration 6 Meth I ParabenMeth I Paraben 0.20 Ni a Hardwicke Inc.

7 Em icol EAC Ammonium Laureth 3.6 Albri ht & Wilson 70 Sulfate 8 Em icol AL Ammonium Lau I Sulfate11.8 Albri ht 8 Wilson 9 Te o BetaineCocamido ro I Betaine2.43 Goldschmidt E

10Tego BetaineCocamidopropyl Betaine3.00 Goldschmidt F

11Elubiol Dichlorophenyl 0.500 Janssen Pharm.
Imidazoldioxolan 12Salic lic Salic lic Acid 1.000 Rhone-Poulenc Acid 13Pol ox WSR-205PEG 14M 0.05 Amerchol 14Ninol LMP Lauramide MEA 1.00 Ste an 15Biosil BasicsCetyl Triethylmonium-0.15 Biosil Technologies Cetylsil Dimethicone Copolyol Inc.
Phthalate 16HydrotriticumWheat Amino Acid 0.220 Croda WAA

17DL-Panthenol-Panthenol 0.15 Roche 50%

18Ph tantriol Ph antriol 0.025 Roche 19Sodium BenzoateSodium Benzoate 0.20 EM Industries 20Versene 100XLTetrasodium EDTA 0.20 Dow Chemical 21BHT Bu lated H drox toluene0.10 M Industries E

22Lorena Fra rance 0.50 reation Aromati C ues 23GI cacil odo ro n I but Icarbamate0.05 onza L l L

24Citric Acid Citric Acid 50% QS Mallinckrodt [ Total ~ 100 Shampoo Process:
5 A vessel was charged with'/. amount of deionized water (component 1 ).
Components 2, 3 and 4 were added sequentially, with ten minute intervals between the additions and with mixing at 500 rpm under constant conditions. The resulting mixture was then heated to 70 to 75°C with mixing at 500 rpm.
Components 5 and 6 were then to the mixture with mixing for about 15 to 25 minutes. The resultant mixture was maintained at 70-75°C, and components 7 through 10 were sequentially added thereto with mixing.

After the resultant mixture was cooled to about 63-67°C, elubiol (component 11 ) was added thereto with mixing under constant conditions. Salicylic acid was then added thereto followed by component 13 under constant mixing to form a primary mixture.
Components 15, 16, 21 and 22 were combined in a separate beaker at 25-30°C to form a premixture. After cooling the primary mixture to 50°C, components 14, 17, and 18 were sequentially added thereto with mixing. The premixture was then added thereto. Sodium hydroxide was then added thereto with mixing to adjust the pH to about 5.3-5.7. The mixture was continuously mixed and cooled to about 25-30°C. The remaining amount of deionized water was added to the final volume and was mixed at 500 rpm until uniform.
Example 6: Preparation of Cleansing Shamn~oo Shampoos comprised of the following components as set forth in Table 6 were prepared:

Table 6: Cleansing shampoo.
Trade Name CTFA_ % wt/wt Su lier 1 DI Water DI Water 73.225 2 Cutina AGS GI col Distearate 1.75 Henkel Cor oration 3 Meth I ParabenMeth I Paraben 0.20 Ni a Hardwicke Inc.

4 Em icol EAC Ammonium Laureth Sulfate3.60 Albri ht & Wilson Em icol AL Ammonium Lau I Sulfate11.80 Albri ht & Wilson 6 Te o BetaineCocamido ro I Betaine 2.43 Goldschmidt E

7 Te o BetaineCocamido ro I Betaine 3.00 Goldschmidt 8 Elubiol Dichloro hen I Imidazoldioxolan0.50 Janssen Pharm.

9 Salic lic Salic lic Acid 1.00 Rhone-Poulenc Acid 10Pol ox WSR-205PEG 14M 0.05 Amerchol 11Ninol LMP Lauramide MEA 1.00 Ste an 12HydrotriticumWheat Amino Acid 0.22 Croda WAA

13DL-Panthenol-Panthenol 0.15 Roche 50%

14Ph antriol Ph tantriol 0.025 Roche 15Sodium BenzoateSodium Benzoate 0.20 EM Industries 16Versene 100XLTetrasodium EDTA 0.20 Dow Chemical 17BHT Bu lated H drox toluene0.10 EM Industries 18Lorena ~ Fra rance 0.50 Creation Aromati ues 19GI cacil lodo ro n I but Icarbamate0.05 Lonza L

20NaOH NaOH 25% QS Mallinckrodt Total ~ 100.00 Shampoo Process:
A vessel was charged with'/. amount of deionized water (component 1 ) and heated to about 70 to 5 75°C. Components 2 and 3 were added thereto with mixing at 500 rpm under constant conditions for 15 to 20 minutes. Component 4 through 7 were added sequentially thereto with mixing under constant conditions. After the resultant mixture was then cooled to 63-67°C, elubiol (component 11 j was added thereto with mixing under constant conditions. Salicylic acid was then added thereto followed by component 10 under constant mixing to form a primary mixture.
Components 13, 14, 17 and 18 were combined in a separate beaker at 25-30°C to form a premixture. After cooling the primary mixture to 50°C, the premixture was added thereto, then components 15, 16 and 19 were sequentially added thereto with mixing. Sodium hydroxide was then added thereto with mixing to adjust the pH to about 5.3-5.7. The mixture was then continuously mixed and cooled to about 25-30°C. The remaining amount of deionized water was added to the final volume and was mixed at 500 rpm until uniform.

Example 7: Preuaration of Cleansing Shampoo Containing One Water Soluble Silicone Compound Shampoos comprised of the following components as set forth in Table 7 were prepared:
Table 7: Cleansing shamnee wifih nna wator cnlmhle cilim,~s ~le....~u:....
..~.~._.-_:__ _ Trade Name CTFA % wt/wt ~ Su ' lier ..

1 DI Water DI Water 73.00 2 Citric Acid Citric Acid 0.025 Roche Anh 3 Cutina AGS GI col Distearate 1.75 Henkel 4 Meth I Paraben Meth I Paraben 0.20 Mallinckrodt 5 Em icol EAC Ammonium Laureth Sulfate3.6 Albri ht &
70 Wilson 6 Em icol AL 70 Ammonium Lau I Sulfate 11.8 Albri ht &
Wilson 7 Te o Betaine Cocamido ro I Betaine 2.43 Goldschmidt E

8 Te o Betaine Cocamido ro I Betaine 3.00 Goldschmidt 9 Elubiol Dichloro hen I Imidazoldioxolan0.50 Janssen Pharm.

10Salic lic Acid Salic lic Acid 1.00 Rhone-Poulenc 11Pol ox WSR-205 PEG 14M 0.05 Amerchol 12Ninol LMP Lauramide MEA 1.00 Ste han 13DL-Panthenol-50%Panthenol 0.15 Roche 14Ph tantriol Ph tantriol 0.025 Roche 15Biosil Basic Silicone Quaternium 13 0.20 Biosil SPQ

16H drotriticum Wheat Amino Acid 0.22 Croda WAA

17Sodium BenzoateSodium Benzoate 0.20 EM Industries 18Versene 100XL T etrasodium EDTA 0.20 Dow Chemical 19BHT But lated H drox toluene0.10 EM Industries 20Lorena Fragrance 0.50 Creation Aromati ues 21GI cacil L lodo ro n I bu Icarbamate0.05 Lonza 22NaOH 25% Sodium H droxide QS Mallinckrodt Total 100.00 Shampoo Process:
A vessel was charged with'/, amount of deionized water (component 1 ).
Components 2 was then added thereto. The resultant mixture was then heated to 70-75°C, and components 3 & 4 were sequentially added thereto with mixing at 500 rpm under constant conditions.
Component 5 through 8 were then sequentially added thereto with mixing under constant conditions.
The resulting mixture was cooled to about 63 to 67°C with mixing at 500 rpm. Component 9 was then added to the mixture. After all the elubiol had dissolved therein, salicylic acid (component 10) was added thereto with mixing for 15-20 minutes at constant conditions; component 11 then was added thereto. The resultant primary mixture was then cooled to 50°C.
Components 13, 14, 19 and 20 were combined in a separate beaker at 25-30°C to form a premixture. After cooling the primary mixture to 50°C, component 12, component 15, component 16 , the premixture , component 17, component 18 and component 21 were sequentially added thereto with mixing. Sodium hydroxide was added thereto with mixing to adjust the pH to about 5.3-5.7. The mixture was continuously mixed and cooled to about 25-30°C. The remaining amount of deionized water was added to the final volume and mixed at 500 rpm until uniform.
Example 8: Preiaaration of CleansinASham~~oo Containing Two Water Soluble Silicone Compounds.
Shampoos comprised of the following components as set forth in Table 8 were prepared:
Table 8: Cleansins~ shamcoo with two water soluble silicone denositien enhant~inn anrsn~c Trade Name CTFA % wtlwt Su lier 1 DI Water DI Water 73.00 2 Citric Acid Citric Acid 0.025 Roche Anh 3 Cutina AGS GI col Distearate 1.75 Henkel 4 Meth I Paraben Meth I Paraben 0.20 5 Em icol EAC Ammonium Laureth Sulfate3.6 Albri ht &
70 Wilson 6 Em icol AL 70 Ammonium Lau I Sulfate 11.8 Albri ht &
Wilson 7 Te o Betaine Cocamido ro I Betaine 2.43 Goldschmidt E

8 Te o Betaine Cocamido ro I Betaine 3.00 Goldschmidt 9 Elubiol Dichloro hen I Imidazoldioxolan0.50 Janssen Pharm.

Salic lic Acid Salic lic Acid 1.00 Rhone-Poulenc 11 Pol ox WSR-205 PEG 14M 0.05 Amerchol 12 Ninol LMP Lauramide MEA 1.00 Ste han 13 DL-Panthenol-50%Panthenol 0.15 Roche 14 Ph antriol Ph tantriol 0.025 Roche Biosil Basic Silicone Gluaternium 0.20 Biosil 16 Biosil Basic Cetyl Triethylammonium 0.15 Biosil Cetylsil Dimethicone Co of of Phthalate 17 H drotriticum Wheat Amino Acid 0.22 Croda WAA
18 Sodium BenzoateSodium Benzoate 0.20 EM Industries 19 Versene 100XL T etrasodium EDTA 0.20 Dow Chemical BHT Bu lated H dro toluene 0.10 EM Industries 21 Lorena Fragrance 0.50 Creation Aromati ues 22 GI cacil L lodo ro n I but Icarbamate0.05 Lonza 23 NaOH 25% Sodium H droxide QS Mallinckrodt Total ~ 100.00 Shampoo Process:
A vessel was charged with'/. amount of deionized water (component 1 ).
Components 2 was then added thereto. The resultant mixture was then heated to 70-75°C and components 3 and 4 were sequentially added thereto with mixing at 500 rpm under constant conditions.
Component 5 through 8 15 were sequentially added thereto with mixing under constant conditions.
After cooling the resulting mixture to about 63 to 67°C with mixing at 500 rpm, component 9 was then added to the mixture. After all the elubiol had dissolved therein, salicylic acid (component 10) was added thereto with mixing for 15-20 minutes at constant conditions; component 11 was then added thereto. The resultant primary mixture was then cooled to 50°C.
Components 13, 14, 20 and 21 were combined in a separate beaker at 25-30°C to form a premixture. After cooling the primary mixture to 50°C, component 12, component 15, component 16, component 17 the premixture, component 18, component 19 and component 22 were sequentially added thereto with mixing. Sodium hydroxide was then added thereto with mixing to adjust the pH to about 5.3-5.7. The mixture was continuously mixed and cooled to about 25-30°C.
The remaining amount of deionized water was added to the final volume and was mixed at 500 rpm until uniform.
Example 9: Multiple Attribute Assessment Studv A large-scale consumer study was conducted to assess a variety of attributes such as cleansing ability; hair combing attributes (e.g. wet combing and dry combing); hair softness; and lather attributes (e.g. the amount of lather and the creaminess of the lather). The four formulations tested in this study included: 1 ) the formulation prepared in accordance with Example 3; 2) "Pantene Pro-V" regular shampoo for normal hair commercially available from Procter & Gamble; 3) "Johnson's pH 5.5" regular shampoo for normal hair commercially available from Johnson & Johnson Consumer Companies, Inc.;
and 4) "Johnson's pH 5.5" regular shampoo modified with a different fragrance.
For each of the four above-mentioned test products, 250 female subjects between the age of 16-65 who use regular shampoos for normal hair were selected to participate in a blinded, monadic in-home use study. After using the test product for 2 weeks, each subject completed a questionnaire which asked them to rate the overall performance of the test product as well as and various attributes associated therewith.
The following table is a summary of the results from study:

ante o a roduct each attributelisted.
rn pH 5.5 pH 5.5 Example #3 Pantene with modified(base wl 2 cationic fragrance agents & 1 silicone a ent Attributesa b c a Cleanin 88% 86% 4 91 % 3 88%

Wet combin71 % 2 66% 2 83% 1 3 77% 4 D combin 72% 2 78% 2 86% 1 g3%

Hair Softness78% 2 78% 2 90% 1 g6%

Amount 41 % 37% (2) 47% (1 ) (3) 38% (4) of lather Creaminess14% (2) 11 % (2) 27% (1 ) (3) 21 % (4) of lather (Very cream Table 9. % of sub'ects satisfied with the erform f th (1 ): formulations identified with a "(1 )" are significantly higher than those formulations identified with a "(2)"
at 95% two tailed level of confidence;
(3): formulations identified with a "(3)" are significantly higher than those formulations identified with a "(4)"
at 80% two tail level of confidence This Example showed that the formulation of Example 3 ranked superior with respect to the subject's satisfaction in all the attributes listed above. More specifically, the formulation of Example 3 performed significantly better relative to the performance of the pH 5.5 product with either the original and modified fragrance with respect to the following attributes: wet combing, dry combing, hair softness, cleansing, amount of lather and creaminess of the lather. The formulation of Example 3 also performed significantly superior relative to the performance of Pantene with respect to wet combing, amount of lather and creaminess of the lather. This Example showed that the subjects perceived that the formulation of Example 3 pertormed the best overall with respect to the attributes tested.
Example 10: Hair Softness Assessment 80 Caucasian females between the ages of 18 and 65 years old were selected to participate in a blind hair softness assessment study conducted by professional hair stylists.
Prior to participating in the study, each subject did not wash their hair for a period of 24 hours prior to the study entry. All of the subjects as well as the stylist completed two different questionnaires relating to the hair quality and hair softness of each panelist before the study commenced.
The following three methods were used for purposes of assessing hair softness:
1 ) pat and compress hair with hands; 2) run fingers through the hair; and 3) feel the hair fibers/strands with fingers.

After 3 cc of the formulation of Example 3 was applied via a syringe onto the hair on each respective subject's head, the stylist then shampooed the hair of each respective subject. After this procedure was repeated twice per subject, the hair of each subject was then blown until the hair was completely dried. No other styling aides were used on hair or scalp of any of the subjects. After the drying procedure, bath the respective subject as well as the stylist conducted an independent evaluation of the respective subject's hair softness, using the Softness scale as set forth in Table 10 below. The results of the evaluations are set forth ip Table 11 below.
Table 10. Softness Scale Number ScoreSoftness Assessment 0 Not At all Soft 1 Just Barel Soft 2 Between Just Barely and Slightly Soft 3 Sli htl Soft 4 Sli htl to Moderatel Soft 5 Moderatel Soft 6 Moderatel to Considerabl Soft 7 Considerable Soft 8 Considerabl to Ve Soft 9 Ve Soft Extremel Soft 10 Table 11. Softness assessments determine by the subject and stylist.
The numbers represent tha mwan ~ernrp frnm Rf1 m~hinw~c EvaluatorPre-wash softnessPost-Wash Scorep-value score S list 2.74 7.44 0.0001 Sub'ect 3.50 7.58 0.0001 It is evident from the data above that the formulation of Example 3 significantly increased the softness of the hair as determined independently by the stylist and the subjects.
Each respective subject as well as the stylist also conducted an independent, post-drying evaluation of the degree of softness of each respective subject's hair, using the Hair Softness Quantification Scale as set forth in Table 12 below. The results of the evaluations are set forth in Table 13 below.

Table 12. Hair Softness Qualification Scale Number Distinction Scale -1 Less Soft 0 The Same 1 Somewhat Softer 2 Twice as Soft 3 Three times as soft 4 More than Three times as soft Table 13. Qualification of the hair softness.

The numbers below re resent mean score values from 80 subjects.
~

EvaluatorMean Times Softer -value Score S list 2.44 0.0001 Sub'ect 2.33 0.0001 From the data above, it is evident that the formulation of Example 3 was approximately two to three times more soft as a result of shampooing with this cleansing base.
Example 11: $econdarv Ion Mass Saectrometryr (SIMS) to Assess Si Deposition A formulation was prepared in accordance with the procedure set forth in Example 3, except that:
a) the Biosil SPQ silicone agent was used instead at a concentration of 1 weight percent as opposed to 0.2 weight percent; b) the Salcare cationic agent was used instead at a concentration of 0.05 weight percent as opposed to 0.08 weight percent; and c) the Jaguar cationic agent was used instead at a concentration of 0.1 weight percent as opposed to 0.15 weight percent.
One hair tress was independently washed five times, followed by complete drying of the tress in between washings, with Pantene Pro-V 2-in-1 shampoo for normal hair that is commercially available from The Procter and Gamble Company, and another hair tress was similarly washed with the formulation of Example 3 as modified in Example 11 and dried.
Scanning SIMS (secondary ion mass spectrometry) was then used to characterize the distribution of silicone ions from the silicone-containing polymers that were deposited on the hair. Details of SIMS
may be found in, for example, Sibilia, John, "A Guide to Material Characterization and Chemical Analysis,"
Ch. 8, 185 -192 (1988)(hereinafter "Sibilia"), which is incorporated by reference herein. After placing one fiber of each tress in a Physical Electronics SIMS spectrometer, a primary ion beam was then scanned across the hair surface in order to ionize the Si molecules from the hair surface. The spectrometer then generated images revealing the distribution of Si ions on the surface of the hair.

This procedure was repeated with several hair fibers from each tress, and representative mass spectrometer images were taken of each set of hair fibers.
It is evident from FIG 1, which illustrates the distribution of Si ions on the hair surface that was washed with the Pantene Pro-V shampoo, that the Si ions were distributed over the surface hair fiber;
however, the ions were primarily concentrated only under the scale ridge of the hair fiber. By contrast, it is evident from FIG. 2, which illustrates the distribution of Si ions on the hair surface that was washed with the modified Example 3 formulation, that the distribution of the Si ions is comparatively more homogenous than the distribution shown by the hair fibers washed with the Pantene Pro-V
shampoo.
This Example showed that the cleansing composition of the present invention yielded a more homogeneous distribution of the Silicone polymers, which thereby significantly contributed to the improved softness and body of the treated hair fibers.
Example 12: X- Rayr Photoelectron S~~ectrometer (XPS)~ to Assess Polymer Thickness After each tress of Example 11 was placed into a Physical Electronics x-ray photoelectron spectrometer, a beam of X-rays were scanned onto the surface of the hair fibers. Details of XPS may be found in, for example, Sibilia at 197 - 199, which is incorporated by reference herein.
From the percentage of Carbon and Oxygen atoms on the hair fiber and the atomic ratios of Si:C
and Si:O as determined by XPS, the thickness of the silicone polymer layer on the hair surface was estimated as shown in Table 14 below:
Table 14. Thickness of Silicone molecules on the hair as determined by XPS.
Formulation Thickness of Si moleculesNumber of monolayers An stroms Pantene Pro-V 40-50 7-g Modified Exam 3 1 le 3 It is evident from the results of Table 14 that the Pantene shampoo left substantially higher levels of silicon molecular residue on the hair surface in comparison to the amount of such residue left by the modified Example 3 formulation. We believe that the higher levels of silicon deposition along the hair surface may contribute to the perception of high conditioning build-up on the hair, reduction in body, and limpness. By contrast, since the hair treated with the modified Example 3 formulation left only one or two layers of silicon molecular residue on the surface of the hair fibers, we believe that hair treated with this formulation will likely possess attributes, such as enhanced wet and dry comb, improved rinsing performance and enhanced softness, that are superior relative to such properties possessed by hair treated with the Pantene shampoo.

Since the performance of a hair care product largely depends upon on how the product interacts with the outermost layer of the hair fiber, this example indicated that the modified Example 3 shampoo will have a superior performance relative to that of the Pantene shampoo based upon a chemical and elemental analysis of the respective shampoo's residue left at the interface between the hair surface and the air.
Example 13: Instron Rina Compression Study to Assess Hair Softness and Bodv The ring compression technique, which measures the energy required to pull hair tresses through various sized rings both before and after the tresses are shampooed, is a well known technique as described in Wergmann & Kamuth, Principles of Polymer Science and Technology in Cosmetics and Personal Care, Chapter 12 °Evaluation Methods for Conditioned Hair "
554 - 556 (1999), which is incorporated herein by reference, for assessing hair softness and body. See, e.g., Garcia et al, "Measurement of Bulk Compressibility and Bulk Resiliency of a Hair Mass," 10'"
IFTSCC Congress, Sidney, Australia (1978), which is incorporated by reference herein. The apparatus used in this technique consisted of an Instron tensile tester, model 1122, which is connected to ring devices of varying diameters.
After 15 brown European hair tresses were permed with a tight perm, each tress was pulled through a metal ring having a 1.5" inner diameter twice. The energy required to pull the tress through the ring was then recorded via the Instron tester. The tresses were then manually loosened and pulled through a second metal ring having a 1.0" inner diameter twice. The energy required to pull the tress through this second ring was then recorded via the Instron tester.
The °Dry Pull Energy" required to pull a tress through a given ring may be expressed in terms of the difference between the energy exerted to pull a tress through the same ring twice. This value is a measure of the degree of body or rebound of the hair tress after compression.
Higher values of Dry Pull Energy indicate greater hair body.
The difference between the Dry Pull Energies required to pull each tress through the 1.0" and the 1.5" diameter rings, respectively, is an indication of the softness of the hair tress. The greater the difference between the difference in the Dry Pull Energies indicates that the respective hair tress is relatively more compressible or softer. The difference in the Dry Pull Energies resulting from the tress being pulled through a 1.0" inch ring and then through a 1.5" inch diameter ring are shown in Table 15 and 16 below for the dry permed hair.
The tresses were then shampooed once with one of the following products: 1 ) the formulation of Example 3; 2) "Pantene Pro-V" shampoo for normal hair; and 3) "Shiseido Super Mild" shampoo commercially available from Shiseido Fine Toiletries Co., LTD. A minimum of 3 tresses was used for each product. After the tresses were shampooed and blown completely dry, the tresses were manually loosened to separate the individual hair fibers. The tresses were then pulled through the rings in accordance with the procedures as described above.
The difference in the Dry Pull Energies resulting from the tress being pulled through the same size ring twice, i..e. a 1.0" diameter ring and independently a 1.5" diameter ring, both before the hair is shampooed as well as after the hair is both shampooed and dried are shown in the Table 17 below.
Table 15. Drv Pull Enerav (mJl Test Product Dry Pull Dry Pull Difference Between Dry Energy Energy AfterPull Energy Before and Before Shampooing After treatments Sham ooin Exarn le 3 16.0 10.0 6.0 Pantene Pro V 20.3 16.8 3.5 Shiseido Su er 7.99 7.90 0.09 Mild Table 16. Statistical significance of represented by p-values determined by the Student's t.test *_ Formulations p-value Example 3 vs. Pantene >0.000 Exam le 3 vs. Shiseido 0.026 It is evident from the data above that the formulation of Example 3 showed the greatest difference in Dry Pull Energies, which indicates that this formulation is superior with respect to the other two tested commercial formulations with respect to delivering softness to the hair fibers.

Table 17. Dry Pull Energy (mJ) Test ProductDry Pull Dry Pull DifferenceDry Pull Dry Pull Difference Energy Energy between Energy Energy between After Dry After Dry Before ShampooingPull Before ShampooingPull shampooingPulled Energies shampooingPulled Energies Pulled through before Pulled through Before 1.0" and 1.5" and through Ring after through Ring After 1.0" 1.5"

Ring shampooingRing Shampooing 1.0" rin 1.5" rin Exam le 2.76 1.31 1.45 2.20 1.07 1.13 Pantene 2.39 1.56 0.83 2.19 1.43 0.76 Pro V

Shiseido 1.26 1.05 0.21 1.34 0.93 0.41 Su er Mild It is evident from the data in Table 17 above that the formulation of Example 3 showed the greatest difference in Dry Pull Energy before and after shampooing regardless of the ring size employed.
This indicates that the formulation of Example 3 exhibited the greatest amount of body andlor rebound relative to that possessed by the other two commercial products.
Example 14: Dynamic Va~~or Sorption Studies to Determine Moisture Uptake Dynamic Vapor Sorption (DVS), Surface Measurement Systems, Ltd., was used to determine the water absorption and moisture desorption on hair fibers after application of a composition thereto.
Four hair tresses were individually shampooed twice with 3 g of one of the formulations prepared in accordance with one of the following examples as shown in Table 18 below: 1 ) modified Example 3; 2) Example 6; 3) modified Example 7; and 4) modified Example 6. After blow drying the hair tresses for 2 minutes, the tresses were then cut into segments 5-7 mm in length and weighed using a DVS Caln microbalance. The weights of the hair samples ranged between approximately 30 mg to 40 mglsample.
The hair samples were then placed into the DVS humidity chamber and equilibrated at 0% relative humidity at 25°C overnight. The relative humidity in the chamber was then increased to 10% RH until equilibration occurred. The relative humidity was then increased to 95% RH in approximately 10% RH
intervals. The weight of the hair samples was then measured at each interval after each equilibration using the Caln microbalance. The relative humidity was then reduced back to 10% RH in -10% RH
intervals. The weight of the hair fibers at each 10% RH interval is an indication of the water moisture absorbed and of the moisture retained by the hair samples. The water retaining capacity is the difference between the measured weight of water retained by the hair fibers at a given relative humidity during the ascent of the relative humidity versus measured weight of water retained by the hair fibers at a given relative humidity during the descent of the relative humidity. Higher values of water retaining capacity indicate the presence of surface water on the hair fiber, which tends to create limpness of the hair or increase interfiber adhesion. Lower values water retaining capacity indicated the reduction of water by the hair fiber, which tend to increase the body of the hair. A summary of the water retaining capacities is shown in Table 19 below.
Table 18. Summa of formulations tested and modifications Formulations Number Number of Modifications of Silicones in Cationic Formulation Modified Example 2 1 Jaguar is 0.10 3 wt%
instead of 0.15 wt%

Exam le 6 0 0 No modifications Modified Exam 0 1 No PEG 14M
le 7 Modified Exam 0 0 No PEG 14M
le 6 Table 19. Water Retaining Capacities Test Products Moderate Relative High Relative Humidity (calculated at Humidity (calculated 50% RH at 80% RH

Untreated 2.34 1.g0 Modified exam 2.14 1.65 le 3 Exam le 6 2.53 1.88 Modified Exam 2.34 1.82 le 7 Modified exam 2,47 1.99 le 6 It is evident from the data above that the formulation of Example 3 as modified above in Table 18 possessed superior body properties at both moderate and high relative humidity conditions. By contrast, the formulations that did not contain a cationic agent andlor a silicone agent did not perform relatively as well. This Example showed that formulations exhibiting superior body preferably contain both at least two cationic agents as well as one silicone agent.
Example 15: Determination of Skin Permeation Experiments were conducted to determine the deposition of actives into the skin from various shampoo compositions. To determine penetration of actives, in vitro skin permeation studies were conducted using non-occluded Franz diffusion chambers.
Human cadaver skin, microtomed to 400 Nm, were mounted on Franz diffusion cells containing a receptor medium composed of a citric acid phosphate buffer or a phosphate buffered solution (depending on the active being monitored). The receptor capacity was 5 ml and the cell surface was 0.636 cmz. The receptor compartment was maintained at 37°C during the experiment.
In a tube, 50 NI of each formulation as shown in Tables 1 and 2 through 6 were diluted with 50 NI
of 37°C water. This solution was then rubbed onto the epidermal surface of the mounted skin for 30 seconds and allowed to sit thereon for 5 minutes. The solution was then rinsed from the surface three times with 37°C water, and then swabbed twice with dry cotton swabs. At 24 hours after the topical application of the formulation, the surface of the skin was rinsed three times with methanol or distilled water soaked cotton swabs (depending on the active to be monitored), and then swabbed three times with three dry cotton swabs. After removing the skin from the diffusion cell, the epidermis and dermis were separated, chopped and placed into separate vials containing an extraction solution and sonicated in a bath sonicator for 30 minutes. After sonication of the epidermis, dermis and swabs, respectively, each sonicated sample was assayed using a Waiters high pressure liquid chromatography ("HPLC").
Penetration of the active into the skin was calculated based upon a percentage of the applied dose and the amount of active delivered into the epidermis or dermis per surface area.
For these studies, the penetration of a lipophilic agent, elubiol was investigated. Also the penetration of a hydrophilic agent, salicylic acid was investigated.
As shown in Table 20 below, the formulations investigated were the formulations prepared in accordance with the procedures set forth in Example 1, and Examples 3 through 8. Table 21 shows the amount of elubiol penetrated into the skin (epidermis and dermis ) after topical application of the formulations set forth in Table 20 in accordance with the procedure set forth above.
Table 20. Summa of De ~ositin A ents in each corn ositions Example Depositing Agents (Additives)Number Number Of of Silicones Cationic 1 Ja uar, Salcare 2 0 3 Ja uar, Salcare, Biosil 2 1 SPQ

4 Jaguar, Salcare, Merquat, 3 2 Biosil SPQ, Biosil Cetyl 6 None 0 0 7 Biosil Basic SPQ 0 1 8 Biosil SPQ, Biosil Ce I 0 2 Table 21. Levels of elubiol in the skin (epidermis and dermis) after topical application of various shampoo formulations.

FormulationsE idermis Dermis Total Skin Delive Number testedAmtISurface AmtISurface Amt/Surf Percentage Percentage Percentage of Area of Area (Ng/cmZ) ace Applied Applied Area Dose of Applied {Nglcm~) % (Nglcmz) Dose Dose #1 1.849 0.510 t 0.139 t 0.0580.038 t 1.988 0.549 t 0.363 0.016 1.316 #3 3.471 1.039 t 0.173 t 0.0510.052 t 3.644 1.091 t 0.601 0.015 2.009 #4 8.70 t 2.433 t 0.121 t 0.0210.034 t 8.822 2.466 3.35 0.936 0.006 #6 0.412 0.111 t 0.089 t 0.0230.024 t 0.502 0.135 t 0.014 0.006 0.051 #7 0.50 t 0.127 t 0.398 t 0.0670.101 t 0.899 0.227 0.14 0.036 0.017 #8 0.25 t 0.064 t 0.034 t 0.0060.009 t 0.279 0.072 0.02 0.06 0.002 Table 22. Statistical significance of elubiol permeation as represented by p-values determined b the Student's t-test '.
Formulations Epidermis Dermis 4 Vs 6 One Tail= 0.001One Tail= 0 Two Tail= 0.003Two Tail= 0 4 Vs 3 One Tail= 0.011One Tail= 0 Two Tail= 0.022Two Tail= 0 4 Vs 1 One Tail= 0.002One Tail= 0 Two Tail= 0.004Two Tail= 0 p-vawes>u.u5 are not significant The results of Table 21 are summarized below in Table 23.
Table 23. Ranking (from best to worst) of the formulations with respect to elubiol delivery into the skin (epidermis and dermis).
Ranked Example Number of CationicNumber Of SiliconsTotal /a of Elubiol Number Agents in in Composition Delivered into Com osition the Skin 4 3 2 2.466 3 2 1 1.091 0.549 7 0 1 0.227 6 0 0 0.135 8 0 2 0.072 This Example showed that a formulation (Formulation 4) containing 3 cationic agents and 2 silicones delivered 2.466% of the applied dose of elubiol into the skin.
However, when a formulation (Formulation 3) containing 2 cationic agents and 1 silicone were incorporated with the cleansing shampoo base, the percentage of elubiol delivered decreased to 1.091 %, over a 2.2 fold decrease in delivery.
When no cationic agents were incorporated into the cleansing base (Formulation 6), the elubiol permeation surprisingly decreased to 0.135 %, an 18.2 fold decrease over the delivery exhibited by Formulation 4.
It is also evident from this Example that there is a synergistic effect on the permeation of hydrophobic benefit agents in combination with cationic agents and water-soluble silicones. Formulations that contain either a cationic agent alone or a siliconeagent alone did not achieve the desired effect of enhanced permeation of the benefit agent. This Example showed that the combination of two or more cationic agents with one or more water soluble silicone agents was superior with respect to permeation of hydrophobic actives into the skin.
The amount of salicylic acid penetrated into the skin (epidermis and dermis) after topical application of the Formulations is set forth in Table 24, wherein the formulations were prepared in accordance with the procedure set forth above.
Table 24. Levels of salicylic acid in the skin after topical application of various shampoo formulations.
FormulationE idermis Dermis Total in Delive Sk Number AmtlSurfacePercentageAmtISurfacePercentageAmtISurtacPercentage of Tested Area of AppliedArea Applied a Area of Applied Dose (Nglcm') Dose (Nglcm~) % (uglcmZ) Dose #4 11.50 t 1.508 t 0.412 t 0.054 t 11.912 1.562 5.07 0.664 0.222 0.029 #6 4.83 t 2.520.604 t 0.195 t 0.024 t 5.027 0.629 0.315 0.141 0.018 #3 9.67 t 5.611.326 t 0.419 t 0.057 t 10.093 1.383 0.769 0.170 0.023 #1 5.23 t 1.270.675 t 0.473 t 0.061 t 5.707 0.700 0.293 0.200 0.026 #7 2.36 t 0.370.303 t 0.137 t 0.018 t 2.493 0.321 0.048 0.028 0.004 #8 0.93 t 0.200.118 t 0.022 t 0.003 t 0.95 0.121 0.025 0.022 0.003 Table 25. Statistical significance of salicylic acid permeation as represented by p-values determined b the Student's t-test *.
Formulations Epidermis Dermis 4 Vs. 6 One Tail= 0.011One Tail= 0 Two Tail= 0.021Two Tail= 0 4 Vs. 3 One Tail= 0.373One Tail= 0 Two Tail= 0.746Two Tail= 0 4 Vs. 1 One Tail= 0.066One Tail= 0 Two Tail= 0.132Two Tail= 0 The results of Table 24 are summarized below in Table 26.

Table 26. Ranking (from best to worst) of the formulations with respect to salicylic acid delivery into the skin ~BDIClArt111s anri rlermi~l Ranking Best Number of . Number Of Total % of Salcyclic to acid Worst Cationic A Silicones Delivered into the ents Skin 3 2 1 .

1 2 0 .

6 0 0 .

7 0 1 .

8 0 2 .
0.121 It is evident from Tables 24 and 26 above that Formulation 4, which contained a cleansing base incorporated with three cationic agents and two water-soluble silicones agents (Example 4), delivered the highest levels of salicylic acid into the skin. It is further evident that in the formulation containing only silicone agents incorporated with the cleansing base (Example 7 and 8), the level of salicylic acid delivered into the skin was comparatively low. Notably, the cleansing base without the cationic agents and silicone agents (Example 6) possessed superior salicylic acid delivery capabilities in comparison with formulations containing only silicone agents (Example 7 and 8). Formulation 4, which contained both cationic agents and silicone agents, performed 4.9 times better than formulations without cationic agents (Example 6) and 1.62 times better than formulations containing only cationic agents (Example 1 ).
This example demonstrated that the combination of elubiol and salicylic acid in a cleansing shampoo with 2 or more cationic agents and 1 or water soluble silicone agents performed superior with respect to delivering the elubiol and salicylic acid into the skin. Thus, the composition of this invention affords a method of regulating the delivery of both hydrophobic and hydrophilic actives into the skin.

Claims (66)

1. A cleansing composition comprised of:
a) at least one water soluble silicone agent;
b) at least one cationic conditioning agent; and c) at least one detergent.
2. The composition of claim 1 wherein the water soluble silicone agents are selected from water soluble dimethicones substituted with fatty acid moieties, water soluble silicone quaterniums, and mixtures thereof.
3. The composition of claim 1 wherein the dimethicones are substituted with fatty acid moieties selected from fatty acids having from about 5 carbon atoms to about 30 carbon atoms and the silicone quaterniums contain about 6 carbon atoms to about 20 carbon atoms.
4. The composition of claim 1 wherein the water soluble volatile silicone agents are selected from the group consisting of polydimethylsiloxane, hexamethyldisiloxane, cyclomethicone fluids, and mixtures thereof.
5. The composition of claim 1 wherein the water soluble non-volatile silicone agents are selected from the group consisting of cetyl triethylmonium dimethicone copolyol phthalate, stearalkonium dimethicone copolyol phthalate, dimethicone copolyol having the following structure:
Wherein:
q' is an integer from about 1 to about 7000;
q" is an integer from about 1 to about 5000;
R9 may be any water soluble group such as:
a) a fatty alcohol having from about 8 carbon atoms to about 30 carbon atoms;
b) a fatty acid having from about 8 carbon atoms to about 30 carbon atoms, and derivatives thereof;
c) a crosslinked water soluble polymer such as mercaptol propyl copolymer;
d) a cationic moiety, e.g. trimonium chloride;
e) propyl PG- Betaine;

f) polypeptides such as polysarcosine, and e) mixtures thereof, dimethicone copolyol acetate, dimethicone copolyol lactate, dimethicone copolyol laurate, dimethicone copolyol methyl ether, dimethicone copolyol octyl dodecyl citrate, hydrolyzed soy protein/dimethicone copolyol acetate, dimethiconol, and mixtures thereof.
6. The composition of claim 2 wherein the water soluble silicone quaterniums are selected from the group consisting of silicone quaternium 13, silicone quaternium 40, quaternium 80, and mixtures thereof.
7. The composition of claim 1 wherein the water soluble silicone agents include silicone quaternium 13, cetyl triethylmonium dimethicone copolyol phthalate, stearalkonium dimethicone copolyol phthalate; and mixtures thereof.
8. The composition of claim 1 comprised of, based upon the total weight of the composition, a) from about 0.001 percent to about 20 percent of water soluble silicone agents;
b) from about 0.01 percent to about 10 percent of cationic conditioning agents; and c) from about 0.01 percent to about 30 percent of detergent.
9. The composition of claim 1 comprised of, based upon the total weight of the composition, a) from about 0.01 percent to about 5 percent of water soluble silicone agents;
b) from about 0.1 percent to about 5 percent of cationic conditioning agents;
and c) from about 5 percent to about 20 percent of detergent.
10. The composition of claim 1 wherein the cationic conditioning agent is selected from the group consisting of a cationic cellulose derivative; a cationic guar derivative; a homopolymer or copolymer of a cationic monomer selected from:
a. a monomer having the formula wherein R is H or CH3, YisOorNH, R1 is an alkylene group having from about 2 to about 6 carbon atoms, R2, R3 and R4 are each independently an alkyl group or hydroxyalkyl group having from about 1 to about 22 carbon atoms, and X is a monovalent anion selected from halide and alkyl sulfate having from about 1 to about 4 carbon atoms, or b. diallyldimethylammonium chloride, and mixtures thereof.
11. The composition of claim 10 wherein the cationic conditioning agent is selected from the group consisting of polyquaternium-10, guar hydroxypropyltrimonium chloride, compounds derived from acrylamidopropyl trimonium chloride/acrylamide copolymer, polyquaternium-6, polyquaternium-7, polyquaternium-47, and mixtures thereof.
12. The composition of claim 11 wherein the cationic conditioning agent is selected from the group consisting of acrylamidopropyltrimonium chloride/acrylamide copolymer, guar hydroxypropyltrimonium chloride, and mixtures thereof.
13. The composition of claim 1 wherein the detergent is a surfactant, soap, or mixture thereof.
14. The composition of claim 1 wherein the surfactant is comprised of at least one anionic surfactant.
15. The composition of claim 1 wherein the detergent is comprised of, based upon the total weight of the detergent, a) from about 1 percent to about 20 percent of an anionic surfactant;
b) from about 1 percent to about 10 percent of an amphoteric surfactant;
c) from about 0 percent to about 4 percent of a cationic surfactant; and d) from about 1 percent to about 7 percent of a nonionic surfactant.
16. The composition of claim 1 wherein the detergent is comprised of, based upon the total weight of the detergent, a) from about 80 percent to about 95 percent of an anionic surfactant selected from the group consisting of alkyl sulfates, alkyl ether sulfates, and mixtures thereof wherein the alkyl groups have from about 8 carbon atoms to about 18 carbon atoms; and b) from about 5 percent to about 15 percent of an amphoteric surfactant containing at least a cocamidopropyl betaine.
17. The composition of claim 1 wherein the detergent is comprised of, based upon the total weight of the detergent, a) from about 70 percent to about 90 percent of an anionic surfactant selected from the group consisting of sodium PEG-7 olive oil carboxylate, alkyl sulfates, alkyl ether sulfates, and mixtures thereof wherein the alkyl group has from about 8 carbon atoms to about 18 carbon atoms;
b) from about 10 percent to about 25 percent of an amphoteric surfactant containing at least a cocamidopropyl betaine; and c) from about 2 percent to about 10 percent of a cationic surfactant.
18. The composition of claim 1 further comprising at least one benefit agent.
19. The composition of claim 18 wherein the benefit agent is selected from the group consisting of elubiol, 6-(1-piperidinyl)-2,4-pyrimidinediamine-3-oxide, shale oil and derivatives thereof, finasteride, ketoconazole, salicylic acid, zinc pyrithione, coal tar, benzoyl peroxide, selenium sulfide, hydrocortisone, sulfur, menthol, pramoxine hydrochloride, tricetylammonium chloride, polyquaternium 10, panthenol, panthenol triacetate, vitamin A and derivatives thereof, vitamin B and derivatives thereof, vitamin C and derivatives thereof, vitamin D and derivatives thereof, vitamin E and derivatives thereof, vitamin K and derivatives thereof, keratin, lysine, arginine, hydrolyzed wheat proteins, hydrolyzed silk proteins, octyl methoxycinnamate, oxybenzone, minoxidil, titanium dioxide, zinc dioxide, retinol, erthromycin, tretinoin, and mixtures thereof.
20. The composition of claim 18 further comprising, based upon the total weight of the composition, from about 0.001 percent to about 20 percent of the benefit agent
21. The composition of claim 18 further comprising a suspending agent.
22. The composition of claim 21 wherein the composition is comprised of, based upon the total weight of the composition, from about 0.01 percent to about 5 percent of the suspending agent.
23. The composition of claim 21 wherein the suspending agent is selected from the group consisting of carbomer, hydroxyethyl cellulose, methylvinylether/maleic anhydride copolymer crosslinked with 1,9-decadiene PolyVM/MA (PVM/MA decadiene crosspolymer), Acrylates/Aminoacrylates C10-30 Alkyl PEG-20 Itaconate Copolymer, and mixtures thereof.
24. The composition of claim 1 in the form of a shampoo, a gel, a bath, a cream, a lotion, or a mousse.
25. The use of the composition of claim 1 to cleanse the skin, hair and/or nails.
26. A delivery system for delivering benefit agents into and/or onto the hair, nails, and scalp comprised of:
a) at least one water soluble silicone agent; and b) at least one cationic conditioning agent.
27. The delivery system of claim 26 wherein the delivery system is comprised of, based upon the total weight of the delivery system:
a) from about 0.001 percent to about 10 of at least one water soluble silicone agent; and b) from about 0.001 percent to about 5 percent of at least one cationic conditioning compounds.
28. The delivery system of claim 26 wherein the water soluble silicone agent contains at least a silicone quaternium-13, a cetyl triethylmonium dimethicone copolyol phthalate, or a mixture thereof and the cationic conditioning agent contains at least a guar hydroxypropyltrimonium chloride, an acrylaminopropyltrimonium chloride/acrylamide copolymer, or a mixture thereof.
29. A method for enhancing the deposition of benefit agents which comprises topically administering to a human or animal a composition comprised of:
a) a delivery system comprised of i) at least two cationic conditioning compounds selected from the group consisting of guar hydroxypropyltrimonium chloride, acrylaminopropyltrimonium chloride/acrylamide copolymer, and mixtures thereof;
ii) at least one water soluble silicone compound comprised of silicone quaternium-13; and b) an effective amount of a benefit agent to a desired location on the skin, hair, and/or nails.
30. The method of claim 29 wherein the benefit agent is elubiol, shale oil and derivatives thereof, 6-(1-piperidinyl)-2,4-pyrimidinediamine-3-oxide, finasteride, ketoconazole, salicylic acid, zinc pyrithione, coal tar, benzoyl peroxide, selenium sulfide, hydrocortisone, sulfur, menthol, pramoxine hydrochloride, tricetylammonium chloride, polyquaternium 10, panthenol, panthenol triacetate, vitamin A and derivatives thereof, vitamin B and derivatives thereof, vitamin C and derivatives thereof, vitamin D and derivatives thereof, vitamin E and derivatives thereof, vitamin K and derivatives thereof, keratin, lysine, arginine, hydrolyzed wheat proteins, hydrolyzed silk proteins, octyl methoxycinnamate, oxybenzone, minoxidil, titanium dioxide, zinc dioxide, retinol, erthromycin, tretinoin, and mixtures thereof.
31. The method of claim 29 wherein the composition is further comprised of a detergent.
32. A method for depositing a thin coating of conditioner on a hair fiber, comprised of:
a) topically applying an effective amount of a delivery system composition comprised of i) at least two cationic conditioning compounds selected from the group consisting of guar hydroxypropyltrimonium chloride, acrylaminopropyltrimonium chloride/acrylamide copolymer, and mixtures thereof;
ii) at least one water soluble silicone compound comprised of cetyl triethylmonium dimethicone copolyol phthalate; and iii) a hydrophilic benefit agent to a desired location on the hair of a human or animal.
33. A method for treating hair loss comprising topically administering to a human or animal at a desired area for treating hair loss a composition comprised of , based upon the total weight of the composition,:
A. a delivery system comprised of i.) at least one water soluble silicone agent;
ii) at least one cationic conditioning agent; and B. an effective amount of a hair loss treatment agent.
34. The method of claim 33 wherein the composition is further comprised of a detergent.
35. The method of claim 33 wherein the hair loss treatment agent is selected from minoxidil, N"-cyano-N-(tert-pentyl)-N'-3-pyridinyl-guanidine, diazoxide, vitamin E, vitamin C, vitamin E acetate, vitamin C palmitate; erythropoietin; prostaglandin E1, prostaglandin F2-alpha; oleic acid; heat shock protein 27 ('HSP 27"), heat shock protein 72 ("HSP 72"); verapamil HCL, nifedipine, diltiazemamiloride, cyclosporin, Fk-506; finasteride, 17-beta estradiol, EGF, FGF, benoxaprofen, tretinoin, IL-6, IL-1alpha, and IL-1beta ICAM, betametasone, aloe, clove, ginseng, rehmannia, swertia, sweet orange, zanthoxylum, elubiol, ketoconazole, zinc pyrithione; streptomycin; cycloheximide; or mixtures thereof.
36. The method of claim 33 wherein the hair loss treatment agent is 6-(1-piperidinyl)-2,4-pyrimidinediamine-3-oxide, N"-cyano-N-(tert-pentyl)-N'-3-pyridinyl-guanidine, a retinoid and derivatives thereof, finasteride, minoxidil, ketoconazole, or mixtures thereof.
37. The method of claim 33 wherein the hair loss treatment agent is present in an amount, based upon the total weight of the composition, from about 0.001 percent to about 20 percent.
38. A method for inhibiting hair growth comprising topically administering to a human or animal at a desired area for inhibiting hair growth a composition comprised of, based upon the total weight of the composition,:
A. a delivery system comprised of i.) at least one water soluble silicone agent;
ii) at least one cationic conditioning agent; and B. an effective amount of a hair growth inhibiting agent.
39. The method of claim 38 wherein the hair growth inhibiting agent is selected from antineoplasitc agents; anticoagulants; antithyroid drugs; lithium; lithium carbonate;
interferons; retinoids;
antihyperlipidaemic drugs; thallium; mercury; albendazole; allopurinol;
amiodarone; amphetamines;
androgens; bromocriptine; butyrophenones; carbamazepine; cholestyramine;
cimetidine; clofibrate;
danazol; desipramine; dixyrazine; ethambutol; etionamide; fluoxetine;
gentamicin; gold salts; hydantoins;
ibuprofen; impramine; immunoglobulins; indandiones; indomethacin;
intraconazole; levadopa; maprotiline;
methysergide; metoprolol, metyrapone; nadolol;, nicotinic acid; potassium thiocyanate; propranolol, pyridostimine; salicylates; sulfasalazine; terfenadine; thiamphenicol;
thiouracils; trimethadione; troparanol;
valproic acid or mixtures thereof.
40. The method of claim 38 wherein the hair growth inhibiting agent is a serine protease, retinol, isotretinoin, betamethisone, alpha-tocophenol and derivatives thereof, or a mixture thereof.
41. The method of claim 38 wherein the hair growth inhibiting agent is present in an amount, based upon the total weight of the composition, from about 0.001 percent to about 20 percent.
42. The method of claim 38 further comprising a detergent.
43. A method for treating or minimizing the effects of aging comprising topically administering to a human or animal at a desired area a composition comprised of, based upon the total weight of the composition,:
A. a delivery system comprised of i.) at least one water soluble silicone agent;
ii) at least one cationic conditioning agent; and B. an effective amount of an anti-aging active agent.
44. The method of claim 43 wherein the anti-aging active agent is selected from sunscreens;
retinoids and derivatives thereof; vitamins and derivatives thereof;
antioxidants; hydrocarboxy acids;
botanical extracts; or mixtures thereof.
45. The method of claim 43 wherein the anti-aging active agent is retinol, tretinoin, or mixtures thereof.
46. The method of claim 43 wherein the anti-aging active agent is present in an amount, based upon the total weight of the composition, from about 0.01 percent to about 10 percent.
47. The method of claim 43 wherein the composition is further comprised of a detergent.
48. A method for treating acne comprising topically administering to a human or animal at a desired area a composition comprised of, based upon the total weight of the composition,:
A. a delivery system comprised of i.) at least one water soluble silicone agent;
ii) at least one cationic conditioning agent; and B. an effective amount of an anti-acne active agent.
49. The method of claim 48 wherein the anti-acne active agent is selected from imidazoles;
retinoids; salicylic acid; benzoyl peroxide; antibiotics; antiandrogens; 5-alpha-reductase isotypes;
anti-inflammatory agents; botanical extracts; or mixtures thereof.
50. The method of claim 48 wherein the anti-acne active agent is retinol, elubiol, an antibiotic, salicylic acid or mixtures thereof.
51. The method of claim 48 wherein the anti-acne active agent is present in an amount, based upon the total weight of the composition, from about 0.01 percent to about 10 percent.
52. The method of claim 48 wherein composition is further comprised of a detergent.
53. A method for depigmenting skin comprising topically administering to a human or animal at a desired area a composition comprised of, based upon the total weight of the composition,:
A. a delivery system comprised of i.) at least one water soluble silicone agent;
ii) at least one cationic conditioning agent; and B. an effective amount of a depigmentation active agent.
54. The method of claim 53 wherein the depigmentation active agent is selected from retinoids and derivatives thereof; kojic acid and its derivatives; hydroquinone and derivatives thereof; transexamic acid; vitamins; azelaic acid; botanical extracts or mixtures thereof.
55. The method of claim 53 wherein the depigmentation active agent is kojic acid, retinol, hydroquinone, transexamic acid or mixtures thereof.
56. The method of claim 53 wherein the depigmentation active agent is present in an amount, based upon the total weight of the composition, from about 0.01 percent to about 10 percent.
57. The method of claim 53 wherein the composition is further comprised of a detergent.
58. A method for treating the diseases of dandruff, seborrheic dermatitis, and psoriasis and/or the symptoms associated therewith comprising topically administering to a human or animal at a desired area a composition comprised of, based upon the total weight of the composition,:
A. a delivery system comprised of i.) at least one water soluble silicone agent;
ii) at least one cationic conditioning agent; and B. an effective amount of a benefit agent selected from the group consisting of an anti-dandruff agent, an anti-seborrheic dermatitis agent, an anti-psoriasis agent, and mixtures thereof.
59. The method of claim 58 wherein the anti-dandruff agent, the anti-seborrheic dermatitis agent, and the anti-psoriasis agent are selected from zinc pyrithione, selenium sulfide, sulfur; sulfonated shale oil;
salicylic acid; coal tar; povidone-iodine, imidazoles such as ketoconazole, dichlorophenyl imidazolodioxalan, clotrimazole, itraconazole, miconazole, climbazole, tioconazole, sulconazole, butoconazole, tluconazole, miconazolenitrite and any possible stereo isomers and derivatives thereof such as anthralin; piroctone olamine (Octopirox); selenium sulfide; ciclopirox olamine; anti-psoriasis agents;
vitamin A analogs; corticosteroids and mixtures thereof.
60. The method of claim 58 wherein the anti-dandruff agent, the anti-seborrheic dermatitis agent, and the anti-psoriasis agent are selected from elubiol, ketoconazole, coal tar, salicylic acid, zinc pyrithione, selenium sulfide, hydrocortisone, sulfur, menthol, pramoxine hydrochloride and mixtures thereof.
61. The method of claim 58 wherein the anti-dandruff agent, the anti-seborrheic dermatitis agent, and the anti-psoriasis agent are present in an amount, based upon the total weight of the composition, from about 0.001 percent to about 10 percent.
62. The method of claim 58 wherein the composition is further comprised of a detergent.
63. A method for removing hair comprising topically administering to a human or animal at a desired area a composition comprised of, based upon the total weight of the composition,:
A. a delivery system comprised of i.) at least one water soluble silicone agent;
ii) at least one cationic conditioning agent; and B. an effective amount of a depilartory benefit agent.
64. The method of claim 63 wherein the depilatory agent is thioglycolade.
65. The method of claim 63 wherein the depilatory agent is present in an amount, based upon the total weight of the composition, from about 0.001 percent to about 20 percent.
66. The method of claim 63 wherein the composition is further comprised of a detergent.
CA002309413A 1999-05-27 2000-05-24 Novel detergent compositions with enhanced depositing, conditioning and softness capabilities Abandoned CA2309413A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US09/321,074 1999-05-27
US09/321,074 US6495498B2 (en) 1999-05-27 1999-05-27 Detergent compositions with enhanced depositing, conditioning and softness capabilities

Publications (1)

Publication Number Publication Date
CA2309413A1 true CA2309413A1 (en) 2000-11-27

Family

ID=23249078

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002309413A Abandoned CA2309413A1 (en) 1999-05-27 2000-05-24 Novel detergent compositions with enhanced depositing, conditioning and softness capabilities

Country Status (11)

Country Link
US (3) US6495498B2 (en)
EP (1) EP1080714A3 (en)
JP (1) JP2001002535A (en)
KR (1) KR100766731B1 (en)
CN (1) CN1277836A (en)
AU (1) AU782857B2 (en)
BR (1) BR0002284A (en)
CA (1) CA2309413A1 (en)
MX (1) MX221734B (en)
PH (1) PH12000000280B1 (en)
TW (1) TWI291875B (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015176161A1 (en) * 2014-05-23 2015-11-26 Triple Hair Inc. Compositions for reducing hair loss and/or increasing hair regrowth
US10039703B2 (en) 2015-07-08 2018-08-07 Triple Hair Inc. Composition comprising resveratrol and melatonin for reducing hair loss and/or increasing hair regrowth
US11696883B2 (en) 2014-05-23 2023-07-11 Triple Hair Inc. Compositions for reducing hair loss and/or increasing hair regrowth
US20230414478A1 (en) * 2022-06-22 2023-12-28 K18, Inc. Hair cleanser composition, methods and uses thereof

Families Citing this family (181)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6495498B2 (en) 1999-05-27 2002-12-17 Johnson & Johnson Consumer Companies, Inc. Detergent compositions with enhanced depositing, conditioning and softness capabilities
EP1064938A1 (en) * 1999-06-28 2001-01-03 Sanofi-Synthelabo Pharmaceutical dosage forms for controlled release producing at least a timed pulse
KR20020039528A (en) * 2000-11-22 2002-05-27 조명재 Use of cyclosporin 7-thioamide derivatives for hair growth
US20050143267A1 (en) * 2001-02-06 2005-06-30 Playtex Products, Inc. Pearlized cleanser composition with milk protein and aromatherapy and method of making same
US6780825B2 (en) * 2001-02-06 2004-08-24 Playtex Products, Inc. Cleansing compositions with milk protein and aromatherapy
KR100681670B1 (en) * 2001-02-14 2007-02-09 주식회사 엘지생활건강 Use of [ ?-hydroxy-N-methyl-L-leucine9 ] cyclosporin A for hair growth
US20020172650A1 (en) * 2001-03-30 2002-11-21 Cannell David W. Heat activated durable conditioning compositions comprising C1 to C22 substituted C3 to C5 monosaccharides and methods for using same
KR100695610B1 (en) * 2001-05-15 2007-03-14 주식회사 엘지생활건강 Topical compositions containing nonimmunosuppressive cyclosporin derivatives for treating hair loss
KR100695611B1 (en) * 2001-05-17 2007-03-14 주식회사 엘지생활건강 The use of Nonimmunosuppressive [?-hydroxy-N-methyl -L-leucine4] cyclosporin derivatives for treating hair loss
FR2829384B1 (en) * 2001-09-11 2003-11-14 Oreal COSMETIC COMPOSITIONS CONTAINING A METHACRYLIC ACID COPOLYMER, A SILICONE AND A CATIONIC POLYMER AND USES THEREOF
US7025952B1 (en) 2005-01-31 2006-04-11 Aquea Scientific Corporation Methods of preparation and use of bodywashes containing additives
US20060173709A1 (en) * 2005-01-31 2006-08-03 Traynor Daniel H Bodywash additive business methods
US6998113B1 (en) * 2005-01-31 2006-02-14 Aquea Scientific Corporation Bodywashes containing additives
US7037513B1 (en) 2005-01-31 2006-05-02 Aquea Scientific Corporation Bodywash additives
EP1458337B1 (en) 2001-12-21 2016-05-04 Solvay USA Inc. Stable surfactant compositions for suspending components
DE10224024A1 (en) * 2002-05-31 2003-12-11 Beiersdorf Ag Tarnished care shampoo
DE10224022A1 (en) * 2002-05-31 2003-12-11 Beiersdorf Ag Mild care shampoo
FR2841467B1 (en) * 2002-06-28 2006-01-20 Oreal COSMETIC COMPOSITION COMPRISING QUATERNARY SILICONE, A CATION, TWO CATIONIC POLYMERS AND COSMETIC PROCESSING PROCESS
EP1396535B1 (en) * 2002-09-05 2004-12-15 The Procter & Gamble Company Structured liquid fabric treatment compositions
KR100681739B1 (en) 2002-09-20 2007-02-15 더 프록터 앤드 갬블 캄파니 Striped liquid personal cleansing compositions containing a cleansing phase and a separate benefit phase
US7511003B2 (en) 2002-11-04 2009-03-31 The Procter & Gamble Company Striped liquid personal cleansing compositions containing a cleansing phase and a separate benefit phase with improved stability
WO2004041983A1 (en) * 2002-11-04 2004-05-21 The Procter & Gamble Company Liquid laundry detergent
ES2260695T3 (en) * 2002-11-12 2006-11-01 Unilever N.V. COMPOSITIONS FOR WASHING AND CONDITIONING THE HAIR.
KR20040051869A (en) * 2002-12-13 2004-06-19 주식회사 엘지생활건강 Composition of Liquid Cleaner having Excellent Viscosity and Detergency
CN100558338C (en) 2003-05-01 2009-11-11 宝洁公司 By cleansing phase and the striped liquid personal cleansing compositions that comprises the separate benefit phase composition of High Internal Phase Emulsion
AU2004237615B2 (en) 2003-05-01 2007-06-14 The Procter & Gamble Company Visually distinctive multiple liquid phase compositions
US6743760B1 (en) 2003-05-29 2004-06-01 Colgate-Palmolive Company Transparent conditioning shampoo
JP4018032B2 (en) * 2003-06-17 2007-12-05 高砂香料工業株式会社 Hair and body cleaning composition
US20050129643A1 (en) * 2003-06-20 2005-06-16 Lepilleur Carole A. Hydrocolloids and process therefor
US7214391B2 (en) * 2003-06-30 2007-05-08 Usana Health Sciences, Inc. Botanical extract compositions and process for preparing same
US7326677B2 (en) 2003-07-11 2008-02-05 The Procter & Gamble Company Liquid laundry detergent compositions comprising a silicone blend of non-functionalized and amino-functionalized silicone polymers
AU2003260455A1 (en) * 2003-08-25 2005-04-11 Merz Pharma Gmbh And Co. Kgaa Detergent-containing preparation with a combination of polysaccharide polymers and tetra-copolymers and use thereof for example for personal cleaning
US20050095215A1 (en) * 2003-11-03 2005-05-05 Popp Karl F. Antimicrobial shampoo compositions
US8951947B2 (en) 2003-12-24 2015-02-10 The Procter & Gamble Company Multi-phase personal cleansing compositions comprising a lathering cleansing phase and a non-lathering structured aqueous phase
US7541320B2 (en) * 2004-01-23 2009-06-02 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Mild, viscous cleansing composition with versatile compatibility and enhanced conditioning
US7390478B2 (en) 2004-02-23 2008-06-24 Sebastian International, Inc. Hair thickening composition and method
US8314054B2 (en) 2004-02-27 2012-11-20 The Procter & Gamble Company Mild multi-phased personal care composition
US20080161230A1 (en) * 2004-04-23 2008-07-03 Novexin Limited Methods and Kits for Stabilising, Protecting and Solubilising Proteins
US7645730B2 (en) * 2004-04-29 2010-01-12 Advanced Biocatalytics Corp. Surfactant composition with a reduction of surface tension, interfacial tension, and critical micelle concentration using a protein-based surfactant synergist
US20080269094A1 (en) * 2004-05-07 2008-10-30 Ici Americas, Inc. Solvated Nonionic Surfactants
US7456139B2 (en) * 2004-05-07 2008-11-25 Croda Uniqema, Inc. Solvated nonionic surfactants
US20060057075A1 (en) * 2004-08-02 2006-03-16 Moshe Arkin Pharmaceutical and cosmeceutical wash-off mousse shampoo compositions, processes for preparing the same and uses thereof
US20060034779A1 (en) * 2004-08-02 2006-02-16 Agis Industries (1983) Ltd. Foamable compositions containing vitamin D3 analogues, processes for preparing same and methods of treatment utilizng same
US8642564B2 (en) * 2004-08-25 2014-02-04 Aegis Therapeutics, Llc Compositions for drug administration
US8268791B2 (en) * 2004-08-25 2012-09-18 Aegis Therapeutics, Llc. Alkylglycoside compositions for drug administration
US20060046969A1 (en) * 2004-08-25 2006-03-02 Aegis Therapeutics Llc Antibacterial compositions for drug administration
US20090047347A1 (en) * 2005-07-29 2009-02-19 Aegis Therapeutics, Inc. Compositions for Drug Administration
US20060046962A1 (en) * 2004-08-25 2006-03-02 Aegis Therapeutics Llc Absorption enhancers for drug administration
US9895444B2 (en) 2004-08-25 2018-02-20 Aegis Therapeutics, Llc Compositions for drug administration
US9114069B2 (en) * 2004-08-25 2015-08-25 Aegis Therapeutics, Llc Antibacterial compositions for drug administration
US20140162965A1 (en) 2004-08-25 2014-06-12 Aegis Therapeutics, Inc. Compositions for oral drug administration
US7704522B2 (en) 2004-09-08 2010-04-27 Clyde Morgan Topical medicament
RU2007125164A (en) * 2004-12-04 2009-01-10 Унилевер Н.В. (NL) SHAMPOO COMPOSITIONS CONTAINING A CATYOGENIC POLYMER AND A MIXTURE OF ANIONOGENIC SURFACE-ACTIVE SUBSTANCES
MX2007006426A (en) * 2004-12-08 2007-07-19 Galderma Sa Clobetasol propionate shampoos for the treatment of seborrheic dermatitis of the scalp.
US7001592B1 (en) 2005-01-31 2006-02-21 Aquea Scientific Corporation Sunscreen compositions and methods of use
US8147853B2 (en) 2005-02-15 2012-04-03 The Procter & Gamble Company Personal care compositions containing hydrophobically modified non-platelet particles
US20080112904A1 (en) * 2005-03-08 2008-05-15 Daniel Henry Traynor Sunscreen Compositions And Methods Of Use
WO2006113117A1 (en) 2005-04-13 2006-10-26 The Procter & Gamble Company Mild, structured, multiphase personal cleansing compositions
US7820609B2 (en) 2005-04-13 2010-10-26 The Procter & Gamble Company Mild, structured, multi-phase personal cleansing compositions comprising density modifiers
US20060286058A1 (en) * 2005-06-16 2006-12-21 Conopco, Inc., D/B/A Unilever System for cleaning and conditioning hair
US20070027152A1 (en) * 2005-07-27 2007-02-01 Clark Kathleen L Topical anti-pruritic compositions and methods of action of same
US8778369B2 (en) 2005-07-29 2014-07-15 Delaval Holding Ab Barrier film-forming compositions and methods of use
US8153613B2 (en) 2006-05-24 2012-04-10 Delaval Holding Ab Barrier film-forming germicidal composition for controlling mastitis
US8277788B2 (en) 2005-08-03 2012-10-02 Conopco, Inc. Quick dispersing hair conditioning composition
US20070037726A1 (en) * 2005-08-11 2007-02-15 Brooker Alan T Solid detergent comprising A C1-C3 alkyl carbonate salt
US20070059268A1 (en) * 2005-09-09 2007-03-15 Laura Magee Compositions, methods and kits for treating allergic dermatitis of skin
US20070059679A1 (en) * 2005-09-09 2007-03-15 Michelle Garay Method for demonstrating efficacy of a topically applied active ingredient
US20070071705A1 (en) * 2005-09-29 2007-03-29 De Oliveira Monica A M Topical anti-microbial compositions
US20070141001A1 (en) 2005-12-15 2007-06-21 The Procter & Gamble Company Non-migrating colorants in multi-phase personal cleansing compositions
US20080213207A1 (en) * 2006-12-14 2008-09-04 Avon Products, Inc. Shaving Preparation and Method for Shaving
US8104616B2 (en) * 2006-02-11 2012-01-31 The Procter & Gamble Company Clamshell package for holding and displaying consumer products
US8153144B2 (en) 2006-02-28 2012-04-10 The Proctor & Gamble Company Stable multiphase composition comprising alkylamphoacetate
EP2010133B1 (en) 2006-03-31 2016-05-04 Stiefel Research Australia Pty Ltd Foamable suspension gel
CA2545768A1 (en) * 2006-05-04 2007-11-04 Richard Wachsberg Shampoo composition
AU2007253775B2 (en) 2006-05-19 2012-02-02 Mary Kay, Inc. Glyceryl and glycol acid compounds
US8226949B2 (en) 2006-06-23 2012-07-24 Aegis Therapeutics Llc Stabilizing alkylglycoside compositions and methods thereof
DE102006030083A1 (en) * 2006-06-28 2008-01-03 Beiersdorf Ag Hair care cleansing composition with special dry hair sensor
US20080019939A1 (en) * 2006-07-20 2008-01-24 Alberto-Culver Company Conditioner formulation
US20080059313A1 (en) * 2006-08-30 2008-03-06 Oblong John E Hair care compositions, methods, and articles of commerce that can increase the appearance of thicker and fuller hair
BRPI0809314A2 (en) 2007-03-23 2014-10-14 Rhodia STRUCTURED SURFACE COMPOSITIONS
US8158566B2 (en) 2007-03-30 2012-04-17 The Procter & Gamble Company Multiphase personal care composition comprising a structuring system that comprises an associative polymer, a low HLB emulsifier and an electrolyte
US8105996B2 (en) 2007-03-30 2012-01-31 The Procter & Gamble Company Multiphase personal care composition comprising a structuring
WO2008130752A2 (en) 2007-04-19 2008-10-30 Mary Kay Inc. Magnolia extract containing compositions
CN101730518A (en) * 2007-05-21 2010-06-09 阿奎耶科技公司 Highly charged microcapsule
MX2010009371A (en) * 2008-02-29 2010-09-14 Procter & Gamble Hair care compositions and methods for increasing hair diameter.
KR101441025B1 (en) * 2008-03-05 2014-09-17 주식회사 엘지생활건강 Hair conditioning composition
CA2756690C (en) 2008-03-28 2016-08-16 Hale Biopharma Ventures, Llc Administration of benzodiazepine compositions
US20090312224A1 (en) * 2008-06-13 2009-12-17 Conopco, Inc., D/B/A Unilever Method of Reducing Viscosity of Concentrated Liquid Cleansers by Selection of Perfume Components
DE102008041020A1 (en) 2008-08-06 2010-02-11 Evonik Goldschmidt Gmbh Use of polysiloxanes with quaternary ammonium groups to protect animal or human hair from heat damage
US8440631B2 (en) 2008-12-22 2013-05-14 Aegis Therapeutics, Llc Compositions for drug administration
US8871698B2 (en) * 2009-02-09 2014-10-28 Advanced Biocatalytics Corporation Cleaning compositions and methods for reducing burnt-on food and oil residues
US20100209368A1 (en) * 2009-02-11 2010-08-19 Walsh Joseph F Method and preparation for treating baldness
WO2010101742A2 (en) 2009-03-05 2010-09-10 Ciba Corporation Ampholytic ter-polymers for use in personal care compositions
US8343469B2 (en) 2009-07-02 2013-01-01 Hercules Incorporated Cationic synthetic polymers with improved solubility and performance in surfactant-based systems and use in personal care and household applications
US8568701B2 (en) 2009-07-02 2013-10-29 Hercules Incorporated Cationic synthetic polymers with improved solubility and performance in phosphate surfactant-based systems and use in personal care and household applications
DE102009027965A1 (en) * 2009-07-23 2011-01-27 Henkel Ag & Co. Kgaa Hair conditioning agents containing selected cationic silicones and a B-series vitamin
US20110076312A1 (en) * 2009-09-29 2011-03-31 Ethicon, Inc. Antimicrobial/antibacterial medical devices coated with traditional chinese medicines
US8399590B2 (en) * 2009-10-07 2013-03-19 Akzo Nobel Chemicals International B.V. Superhydrophilic amphiphilic copolymers and processes for making the same
US11173106B2 (en) * 2009-10-07 2021-11-16 Johnson & Johnson Consumer Inc. Compositions comprising a superhydrophilic amphiphilic copolymer and a micellar thickener
US8258250B2 (en) * 2009-10-07 2012-09-04 Johnson & Johnson Consumer Companies, Inc. Compositions comprising superhydrophilic amphiphilic copolymers and methods of use thereof
WO2011071712A2 (en) * 2009-12-08 2011-06-16 The Procter & Gamble Company Hair conditioning composition comprising quaternized silicone polymer, silicone copolyol, and carbamate
JP5562820B2 (en) * 2009-12-08 2014-07-30 花王株式会社 Skin cleanser
US8470833B2 (en) * 2009-12-15 2013-06-25 Mcneil-Ppc, Inc. Hair growth and/or regrowth compositions
US8470880B2 (en) 2009-12-15 2013-06-25 Mcneil-Ppc, Inc. Methods of reducing hair loss and/or facilitating hair growth and/or regrowth
DE102010000993A1 (en) 2010-01-19 2011-07-21 Evonik Goldschmidt GmbH, 45127 Novel polysiloxanes with quaternary ammonium groups, process for their preparation and their use in cleansing and conditioning formulations
CA2786906A1 (en) 2010-01-29 2011-08-04 The Procter & Gamble Company Novel linear polydimethylsiloxane-polyether copolymers with amino and/or quaternary ammonium groups and use thereof
DE102010001350A1 (en) 2010-01-29 2011-08-04 Evonik Goldschmidt GmbH, 45127 Novel linear polydimethylsiloxane-polyether copolymers having amino and / or quaternary ammonium groups and their use
DE102011004122A1 (en) * 2011-02-15 2012-08-16 Henkel Ag & Co. Kgaa Nourishing cosmetic cleanser
DE102011110921A1 (en) 2011-02-23 2012-08-23 Evonik Goldschmidt Gmbh Novel polysiloxanes with betaine groups, their preparation and use
WO2012174158A2 (en) 2011-06-14 2012-12-20 Hale Biopharma Ventures, Llc Administration of benzodiazepine
EP2723452A2 (en) 2011-06-22 2014-04-30 Vyome Biosciences Pvt Ltd Conjugate-based antifungal and antibacterial prodrugs
WO2013050241A1 (en) * 2011-10-03 2013-04-11 Unilever N.V. Anti-dandruff composition comprising an azole active
CN103841955B (en) 2011-10-07 2016-08-17 宝洁公司 Personal care composition and the method preparing them
MX339327B (en) 2011-10-07 2016-05-20 Procter & Gamble Method of achieving improved hair feel.
DE102011086635A1 (en) * 2011-11-18 2013-05-23 Henkel Ag & Co. Kgaa Hair care products containing anti-dandruff and cationic silicones
DE102011086636A1 (en) * 2011-11-18 2013-05-23 Henkel Ag & Co. Kgaa Hair care products containing amino acids and cationic silicones
BR112014027633A2 (en) 2012-05-22 2017-06-27 Unilever Nv personal care composition, methods for providing a refreshing feel and use of a copolymer
US11724134B2 (en) 2012-11-06 2023-08-15 CoLabs International Corporation Compositions containing a cellulose derived capsule with a sunscreen active agent
US9456966B2 (en) 2012-11-06 2016-10-04 CoLabs International Corporation Composition containing a cellulose derived capsule with a sunscreen
US11690793B2 (en) 2012-11-06 2023-07-04 Colabs Int'l Corp. Composition containing a cellulose derived capsule with a sunscreen
US10322301B2 (en) 2012-11-06 2019-06-18 CoLabs International Corporation Compositions containing a cellulose derived capsule with a sunscreen active agent
US11707421B2 (en) 2012-11-06 2023-07-25 Colabs Int'l Corp. Compositions containing a flexible derived capsule with an active agent
US11491088B2 (en) 2012-11-06 2022-11-08 CoLabs International Corporation Compositions containing a capsule with a moisturizing agent
MX352380B (en) * 2013-02-08 2017-11-17 Procter & Gamble Hair care composition comprising antidandruff agent and polyquaternium-6.
CA2905121C (en) 2013-03-12 2021-10-26 Mary Kay Inc. Preservative system
CN105188850A (en) 2013-05-16 2015-12-23 宝洁公司 Hair thickening compositions and methods of use
KR101305349B1 (en) * 2013-05-16 2013-09-06 (주) 제이티 Composition of hydrogel soap, hydrogel soap and preparing method thereof
MX2015015909A (en) 2013-05-22 2016-03-09 Procter & Gamble Method of achieving improved product rheology, cosmetic consumer acceptance and deposition.
BR112015030501A2 (en) 2013-06-04 2017-07-25 Vyome Biosciences Pvt Ltd coated particles and compositions comprising them
EP3035909B2 (en) * 2013-08-21 2020-06-10 Unilever PLC, a company registered in England and Wales under company no. 41424 Hair treatment compositions
EP3079654B1 (en) * 2013-12-11 2020-10-14 Hercules LLC Sulfate-free personal care cleansing compositions
US11642353B2 (en) 2014-02-06 2023-05-09 The Procter & Gamble Company Hair care composition comprising antidandruff agent and polyquaternium-6
US9642787B2 (en) 2014-04-25 2017-05-09 The Procter & Gamble Company Method of inhibiting copper deposition on hair
US9642788B2 (en) 2014-04-25 2017-05-09 The Procter & Gamble Company Shampoo composition comprising gel matrix and histidine
US9586063B2 (en) 2014-04-25 2017-03-07 The Procter & Gamble Company Method of inhibiting copper deposition on hair
JP6462120B2 (en) 2014-06-17 2019-01-30 ザ プロクター アンド ギャンブル カンパニー Composition for reducing hair curling
IL301676A (en) 2014-10-24 2023-05-01 Garuhda Llc Combined hair loss inhibition treatment
WO2016077325A1 (en) 2014-11-10 2016-05-19 The Procter & Gamble Company Personal care compositions with two benefit phases
WO2016077327A1 (en) 2014-11-10 2016-05-19 The Procter & Gamble Company Personal care compositions with two benefit phases
US10966916B2 (en) 2014-11-10 2021-04-06 The Procter And Gamble Company Personal care compositions
WO2016090206A1 (en) 2014-12-05 2016-06-09 The Procter & Gamble Company Composition for hair frizz reduction
US10632054B2 (en) 2015-04-02 2020-04-28 The Procter And Gamble Company Method for hair frizz reduction
US10660835B2 (en) 2015-04-02 2020-05-26 The Procter And Gamble Company Method for hair frizz reduction
US10688025B2 (en) 2015-10-29 2020-06-23 Conopco, Inc. Personal cleansing compositions comprising a cationic polymer mixture
US10561591B2 (en) 2015-12-04 2020-02-18 The Procter And Gamble Company Hair care regimen using compositions comprising moisture control materials
US10258555B2 (en) 2015-12-04 2019-04-16 The Procter And Gamble Company Composition for hair frizz reduction
US10610473B2 (en) 2016-03-24 2020-04-07 The Procter And Gamble Company Hair care compositions comprising malodor reduction compositions
WO2017173050A1 (en) 2016-04-01 2017-10-05 The Procter & Gamble Company Composition for fast dry of hair
DE102016209122A1 (en) * 2016-05-25 2017-11-30 Beiersdorf Ag Transparent silicone-containing shampoo
US11246816B2 (en) 2016-06-30 2022-02-15 The Procter And Gamble Company Shampoo compositions comprising a chelant
US20180000706A1 (en) 2016-06-30 2018-01-04 The Procter & Gamble Company Conditioner Composition Comprising a Chelant
US20180000715A1 (en) 2016-06-30 2018-01-04 The Procter & Gamble Company Hair Care Compositions For Calcium Chelation
US20180000705A1 (en) 2016-06-30 2018-01-04 The Procter & Gamble Company Shampoo Compositions Comprising a Chelant
US11786447B2 (en) 2016-06-30 2023-10-17 The Procter & Gamble Company Conditioner composition comprising a chelant
EP3296945A1 (en) * 2016-09-15 2018-03-21 Henkel AG & Co. KGaA Individualized cleaning agent
KR101998102B1 (en) * 2016-09-27 2019-07-09 (주)아모레퍼시픽 Composition for hair care
CN110352232A (en) 2017-02-13 2019-10-18 荷兰联合利华有限公司 Laundry composition additive
CN110291179B (en) * 2017-02-13 2021-11-16 联合利华知识产权控股有限公司 Laundry adjunct composition
PL3580318T3 (en) 2017-02-13 2023-10-02 Unilever Ip Holdings B.V. Method of delivering a laundry composition
US10980723B2 (en) 2017-04-10 2021-04-20 The Procter And Gamble Company Non-aqueous composition for hair frizz reduction
JP2020517586A (en) * 2017-04-26 2020-06-18 ユニリーバー・ナームローゼ・ベンノートシヤープ Antidandruff hair care composition containing pyrithione
GB2571696B (en) 2017-10-09 2020-05-27 Compass Pathways Ltd Large scale method for the preparation of Psilocybin and formulations of Psilocybin so produced
WO2019074993A1 (en) 2017-10-10 2019-04-18 The Procter & Gamble Company Sulfate free clear personal cleansing composition comprising low inorganic salt
WO2019079409A1 (en) 2017-10-20 2019-04-25 The Procter & Gamble Company Aerosol foam skin cleanser
EP3697374B1 (en) 2017-10-20 2022-02-16 The Procter & Gamble Company Aerosol foam skin cleanser
JP7408546B2 (en) * 2017-12-21 2024-01-05 ユニリーバー・アイピー・ホールディングス・ベスローテン・ヴェンノーツハップ personal cleansing composition
MX2018001546A (en) 2018-02-06 2019-08-07 Centro Int De Cosmiatria S A P I De C V Mx/a/2018/001546formulation and method for the treatment of androgenic alopecia.
WO2019209481A1 (en) * 2018-04-27 2019-10-31 Dow Global Technologies Llc Personal care composition
CN112218614B (en) * 2018-06-12 2023-08-01 花王株式会社 Cleaning agent
AU2019291885A1 (en) 2018-06-27 2021-02-04 CoLabs International Corporation Compositions comprising silicon dioxide-based particles including one or more agents
WO2020112486A1 (en) 2018-11-29 2020-06-04 The Procter & Gamble Company Methods for screening personal care products
WO2020181395A1 (en) 2019-03-14 2020-09-17 Crescita Therapeutics Inc. Rinse-off compositions and uses thereof for delivery of active agents
CA3138100A1 (en) 2019-04-17 2020-10-22 Compass Pathfinder Limited Treatment of depression and other various disorders with psilocybin
MD3886799T2 (en) 2019-08-07 2024-01-31 Aneira Pharma Inc Compositions for the treatment of hair loss
EP4027965A1 (en) 2019-09-10 2022-07-20 The Procter & Gamble Company Personal care compositions comprising anti-dandruff agents
MX2022009191A (en) 2020-02-27 2022-08-18 Procter & Gamble Anti-dandruff compositions with sulfur having enhanced efficacy and aesthetics.
FR3113242B1 (en) * 2020-08-10 2022-12-02 Oreal COMPOSITION COMPRISING A PARTICULAR SILICONE EMULSION, A PARTICULAR (METH)ACRYLAMIDE POLYMER, SURFACTANTS AND A CATIONIC POLYSACCHARIDE
WO2021259973A1 (en) * 2020-06-26 2021-12-30 L'oreal Composition comprising a particular silicone emulsion, a particular (meth)acrylamide polymer, surfactants and a cationic polysaccharide
US11819474B2 (en) 2020-12-04 2023-11-21 The Procter & Gamble Company Hair care compositions comprising malodor reduction materials
US20220378684A1 (en) 2021-05-14 2022-12-01 The Procter & Gamble Company Shampoo Compositions Containing a Sulfate-Free Surfactant System and Sclerotium Gum Thickener
KR102571226B1 (en) * 2022-03-22 2023-08-25 주식회사 엘지생활건강 Composition for improving scalp condition comprising gluconolactone and climbazole as active ingredients

Family Cites Families (53)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US34584A (en) * 1862-03-04 Improvement in rakes for harvesters
US77256A (en) * 1868-04-28 Jacob clakk
US176303A (en) * 1876-04-18 Improvement in hat-holders
US4292212A (en) 1978-11-29 1981-09-29 Henkel Corporation Shampoo creme rinse
US4298494A (en) 1979-03-27 1981-11-03 Lever Brothers Company Shampoo
DE2912484A1 (en) * 1979-03-29 1980-10-16 Henkel Kgaa NEW QUARTAERE POLYSILOXAN DERIVATIVES, THEIR USE IN HAIR COSMETICS, AND THEIR WASHING AND TREATMENT PRODUCTS CONTAINING THEM
FR2460133B1 (en) 1979-07-02 1986-11-07 Bristol Myers Co COMPOSITION FOR HAIR CARE AND METHOD OF APPLICATION
CH645653A5 (en) 1980-08-01 1984-10-15 Ciba Geigy Ag QUATERNAERE, COPOLYMERE, HIGH MOLECULAR AMMONIUM SALTS ON ACRYLIC BASE, THE PRODUCTION AND USE THEREOF AS ACTIVE COMPONENTS IN COSMETIC AGENTS.
DE3172768D1 (en) 1980-09-05 1985-12-05 Ciba Geigy Ag Mixtures of polymeric high-molecular acrylic quaternary ammonium salts and detergents, their preparation and use in cosmetic formulations
DE3273489D1 (en) 1981-11-30 1986-10-30 Ciba Geigy Ag Mixtures of quaternary polymeric acrylic ammonium salts, quaternary mono- or oligomeric ammonium salts and surfactants, their preparation and their use in cosmetic compositions
US4472297A (en) 1982-03-01 1984-09-18 The Procter & Gamble Company Shampoo compositions containing hydroxypropyl guar gum
LU84463A1 (en) * 1982-11-10 1984-06-13 Oreal POLYQUATERNARY POLYSILOXANE POLYMERS
GR850600B (en) 1984-03-15 1985-07-02 Procter & Gamble
GB2161172B (en) 1984-07-03 1988-06-02 Beecham Group Plc Conditioning shampoo compositions
USRE34584E (en) 1984-11-09 1994-04-12 The Procter & Gamble Company Shampoo compositions
CA1261276A (en) 1984-11-09 1989-09-26 Mark B. Grote Shampoo compositions
US4704272A (en) 1985-07-10 1987-11-03 The Procter & Gamble Company Shampoo compositions
US4720353A (en) * 1987-04-14 1988-01-19 Richardson-Vicks Inc. Stable pharmaceutical w/o emulsion composition
US5244664A (en) 1988-01-21 1993-09-14 Leo Pharmaceutical Products Ltd. Topical preparation for treatment of alopecia
US4954335A (en) 1989-05-31 1990-09-04 Helene Curtis, Inc. Clear conditioning composition and method to impart improved properties to the hair
US5344643A (en) * 1990-12-21 1994-09-06 Dowbrands L.P. Shampoo-conditioning composition and method of making
US5098979A (en) 1991-03-25 1992-03-24 Siltech Inc. Novel silicone quaternary compounds
CA2066885C (en) 1991-04-29 2002-07-23 Michele Duffy Hair shampoo composition to impart improved hair conditioning properties
US5221530A (en) 1991-06-24 1993-06-22 Helene Curtis, Inc. Mild conditioning shampoo with a high foam level containing an anionic surfactant-cationic acrylate/acrylamide copolymer conditioning agent
US5417965A (en) 1991-06-24 1995-05-23 Helene Curtis, Inc. Stable conditioning shampoo having a high foam level containing a silicone conditioner, a cationic quaternary acrylate copolymer, an anionic surfactant and polyethyleneimine
CA2072319C (en) 1991-06-28 2005-11-22 Shih-Ruey T. Chen Ampholyte terpolymers providing superior conditioning properties in skin and nail care products
NZ243273A (en) 1991-06-28 1995-02-24 Calgon Corp Hair care compositions comprising ampholytic terpolymers
ATE205075T1 (en) 1991-12-13 2001-09-15 Vitachlor Corp MEANS AND METHOD FOR REMOVAL OF MINERALS FROM HAIR
DE4207046A1 (en) 1992-03-06 1993-09-09 Goldwell Ag shampoo
JP3148365B2 (en) 1992-06-29 2001-03-19 花王株式会社 Keratinous fiber modifier kit
DE4330597A1 (en) 1992-10-14 1995-03-16 Ahmad Khalil Hair tonic system and hair lotion for hair loss
GB9303889D0 (en) 1993-02-26 1993-04-14 Boots Co Plc Toiletries composition
US5328685A (en) 1993-03-30 1994-07-12 Helene Curtis, Inc. Clear conditioning composition
DE4315405A1 (en) 1993-05-08 1994-11-10 Wella Ag Hair treatment products
JPH072677A (en) 1993-06-18 1995-01-06 Toyo Seito Kk Peroral hair-growing agent
GB9316323D0 (en) * 1993-08-06 1993-09-22 Procter & Gamble Cosmetic compositions
US5391368A (en) 1993-08-09 1995-02-21 Revlon Consumer Products Corporation Hair styling shampoos
US6025311A (en) 1993-12-17 2000-02-15 Aqualon Company Fluid suspension of polysaccharides for personal care and household applications
GB9404550D0 (en) 1994-03-09 1994-04-20 Unilever Plc Hair conditioning composition
DE4426794C1 (en) 1994-07-28 1995-07-06 Goldwell Ag Agent for treating damaged hairs which is easily washed out
DE59600011D1 (en) 1995-08-01 1997-08-21 Goldwell Gmbh Hair treatment products
FR2738482B1 (en) 1995-09-07 1997-10-24 Oreal CONDITIONING AND DETERGENT COMPOSITION FOR HAIR USE
KR100234547B1 (en) * 1995-12-26 1999-12-15 손경식 Shampoo compositions containing capsule filled with oil material
CN1214628A (en) 1996-01-29 1999-04-21 庄臣消费者有限公司 Detergent compositions
US5776443A (en) * 1996-03-18 1998-07-07 Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. Hair care compositions
GB9607963D0 (en) 1996-04-17 1996-06-19 Unilever Plc Cleansing composition
DE19622968C2 (en) 1996-06-07 2000-08-17 Cognis Deutschland Gmbh Aqueous pearlescent concentrates
WO1998029094A1 (en) * 1996-12-30 1998-07-09 The Procter & Gamble Company Conditioning shampoo compositions
US5989533A (en) * 1997-07-21 1999-11-23 Revlon Consumer Products Corporation Hair conditioning compositions containing alpha or beta hydroxy acid esters
US6024952A (en) * 1997-09-12 2000-02-15 The Andrew Jergens Company Anionic/cationic moisturizing complex
WO1999023901A2 (en) 1997-11-10 1999-05-20 Eddie Majerfeld Jacket with drop down pants
US5977036A (en) * 1998-02-03 1999-11-02 The Procter & Gamble Company Styling shampoo compositions
US6495498B2 (en) * 1999-05-27 2002-12-17 Johnson & Johnson Consumer Companies, Inc. Detergent compositions with enhanced depositing, conditioning and softness capabilities

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015176161A1 (en) * 2014-05-23 2015-11-26 Triple Hair Inc. Compositions for reducing hair loss and/or increasing hair regrowth
US10470992B2 (en) 2014-05-23 2019-11-12 Triple Hair Inc. Compositions for reducing hair loss and/or increasing hair regrowth
US11696883B2 (en) 2014-05-23 2023-07-11 Triple Hair Inc. Compositions for reducing hair loss and/or increasing hair regrowth
US10039703B2 (en) 2015-07-08 2018-08-07 Triple Hair Inc. Composition comprising resveratrol and melatonin for reducing hair loss and/or increasing hair regrowth
US20230414478A1 (en) * 2022-06-22 2023-12-28 K18, Inc. Hair cleanser composition, methods and uses thereof

Also Published As

Publication number Publication date
CN1277836A (en) 2000-12-27
MXPA00005244A (en) 2002-04-01
MX221734B (en) 2004-07-26
US6495498B2 (en) 2002-12-17
US6858202B2 (en) 2005-02-22
AU782857B2 (en) 2005-09-01
US20020077256A1 (en) 2002-06-20
US20040157755A1 (en) 2004-08-12
JP2001002535A (en) 2001-01-09
TWI291875B (en) 2008-01-01
EP1080714A3 (en) 2002-10-30
US20030176303A1 (en) 2003-09-18
KR20010029752A (en) 2001-04-16
US6908889B2 (en) 2005-06-21
PH12000000280B1 (en) 2006-04-07
KR100766731B1 (en) 2007-10-15
AU3646500A (en) 2000-11-30
BR0002284A (en) 2001-01-23
EP1080714A2 (en) 2001-03-07

Similar Documents

Publication Publication Date Title
US6908889B2 (en) Detergent composition with enhanced depositing, conditioning and softness capabilities
US20040091443A1 (en) Compositions for application to the skin or hair
US6524594B1 (en) Foaming oil gel compositions
CA2351925C (en) Cleansing compositions
US7262158B1 (en) Cleansing compositions comprising a liquid silicone and ester mixture
US20030069148A1 (en) Mild cleansing composition having stable foam
US10463597B2 (en) Personal care composition
US6762158B2 (en) Personal care compositions comprising liquid ester mixtures
US6284234B1 (en) Topical delivery systems for active agents
US20140065088A1 (en) Combined stable cationic and anionic surfactant compositions
US20050009717A1 (en) Foaming make-up removing cleansing compositions
EP1284135A2 (en) Mild cleansing composition having stable foam
JPH0699285B2 (en) Hair cosmetics
CA2482584A1 (en) Hair conditioning compositions
AU2007201504A1 (en) Cleansing compositions

Legal Events

Date Code Title Description
EEER Examination request
FZDE Discontinued

Effective date: 20130315