CA2018825A1 - Phospholipidic liposomes containing active principles and a process for the production thereof - Google Patents
Phospholipidic liposomes containing active principles and a process for the production thereofInfo
- Publication number
- CA2018825A1 CA2018825A1 CA 2018825 CA2018825A CA2018825A1 CA 2018825 A1 CA2018825 A1 CA 2018825A1 CA 2018825 CA2018825 CA 2018825 CA 2018825 A CA2018825 A CA 2018825A CA 2018825 A1 CA2018825 A1 CA 2018825A1
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- active principles
- hydrophilic
- liposomes
- phospholipidic
- hydrophobic
- Prior art date
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Abstract
ABSTRACT
Phospholipidic liposomes containing active principles which can be released in a regulated manner and a process for the production of some phospholipidic liposomes are described.
Phospholipidic liposomes containing active principles which can be released in a regulated manner and a process for the production of some phospholipidic liposomes are described.
Description
-. ~` 2n~ss~s P~OiPHOLIPI~IC LIPOSOMES CONTAINING ACTIVE PRINCIPLES AND A
PROCESS FOR T~E PRODUCTION T~BREOF
SPECIFICATION
The present invention relates to phospholipidic liposomes containing hydrophilic and hydrophobic active principles and a process for their production. i One of the topical purposes of cosmetics nowadays is not only an improvement in the appearance of our body but also an improvement in our health. If we focus our observations to the cutis, for instance, we notice it can be subject to alterations which can have either a "physiological" origin (such as aging) or a "pathological"
origin. The origin of these alterations may be internal or external to our body, the latter having mainly a physico-chemical origin related to the environment we live in.
Stressful environmental conditions (intense cold or heat), variations in relative humidity or in ventilation, such as exposure to solar rays or to atmospheric chemical pollutants are clear examples. Dermatologic cosmetics is no longer limited to simple aesthetical interventions but is increasingly pursuing the aim of better protecting the cutis, particularly in re-establishing the status of hydration and elasticity (trophism) which is necessary for its optimal functioning. When the above referred alterations affect mainly the outermost layer of the cutis, the epidermis, in order to re-establish its functional status, local applications of substances which can counterbalance the negative effect of aggressive agents are carried out. Therefore dry skins are treated with fatty creams, that is those containing a high percentage of natural oils, neutral fats or neutralized saturated fatty acids. Where dryness is mainly determined by dehydration, the moisturising creams used contain substances which can absorb water (saccharopolymers or polyoxyethylenic polymers) which then transfer the water to the cutis after application. However, one of the most complex problems in the formulation of a cream for dermatologic cosmetics is however the introduction of active principles showing, for instance, chemical instabllity or low solubility limits, . . . .. .. .. .
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PROCESS FOR T~E PRODUCTION T~BREOF
SPECIFICATION
The present invention relates to phospholipidic liposomes containing hydrophilic and hydrophobic active principles and a process for their production. i One of the topical purposes of cosmetics nowadays is not only an improvement in the appearance of our body but also an improvement in our health. If we focus our observations to the cutis, for instance, we notice it can be subject to alterations which can have either a "physiological" origin (such as aging) or a "pathological"
origin. The origin of these alterations may be internal or external to our body, the latter having mainly a physico-chemical origin related to the environment we live in.
Stressful environmental conditions (intense cold or heat), variations in relative humidity or in ventilation, such as exposure to solar rays or to atmospheric chemical pollutants are clear examples. Dermatologic cosmetics is no longer limited to simple aesthetical interventions but is increasingly pursuing the aim of better protecting the cutis, particularly in re-establishing the status of hydration and elasticity (trophism) which is necessary for its optimal functioning. When the above referred alterations affect mainly the outermost layer of the cutis, the epidermis, in order to re-establish its functional status, local applications of substances which can counterbalance the negative effect of aggressive agents are carried out. Therefore dry skins are treated with fatty creams, that is those containing a high percentage of natural oils, neutral fats or neutralized saturated fatty acids. Where dryness is mainly determined by dehydration, the moisturising creams used contain substances which can absorb water (saccharopolymers or polyoxyethylenic polymers) which then transfer the water to the cutis after application. However, one of the most complex problems in the formulation of a cream for dermatologic cosmetics is however the introduction of active principles showing, for instance, chemical instabllity or low solubility limits, . . . .. .. .. .
: :.
, . . : :
. : , ,, . ' :
:, . : :
. ' , : - :
i; ~' ''~ .~ ' .
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2()ll5 825 high hydrophobicity or hydrophilicity and so forth. This difficulty increases when such compounds must reach the deepest layers of the cutis ~the "derma") to improve its vital conditions. As a matter of fact the derma is responsible for maintaining the elasticity and proper functioning of the outermost layers. It has already been described in scientific literature what difficulties exist for very hydrophilic substances to reach the derma, which can be explained considering that our skin is mainly waterproof. In the cosmetic formulations known from the state of art in order to reach the derma with more hydrophilic compounds, it has been necessary to make compromises, such as the removal of the outermost lipophilic barrier by means of organic solvents or by the introduction of the hydrophilic compounds in carriers containing emulsifiers or surface active agents such as Tween or Triton.
It has been now found, surprisingly, that liposomes can play a new role in allowing highly hydrophilic substances to reach the derma. Liposomes are microscopical blisters having a variable size (starting from some nanometers to some micrometers) and are artificially formed, mostly from phospholipidic mixtures which are the same phisiological components of the animal or vegetal cell membranes. The importance of these blisters relates to their tridimensional structure which, in turn, relates to the particular chemical composition of its components, the phospholipids. These biological compounds, having a lipidic origin, are substantially made of glycerin esters where an hydroxy group has been esterified by an ortophosphoric group and the other two hydroxy groups are esterified by fatty acids having chains of variable length which can also be branched. The phosphoric moiety is characterized by being electrostatically charged and it is called polar head; said polar head is therefore highly hydrophilic while the hydrocarbon chains are highly hydrophobic. In an aqueous environment and as a function of their concentration with regard to the solvent, these compounds spontaneously form blister structures where the polar head , -.
- : : . ..................... .
Z~ 82,~
faces other polar heads (multiple layers) or the water, while the hydrophobic regions in turn face one another so as to repel water. The liposomes are uni- or multilamellas stuctures where one or more double concetric layers are formed, each double layer being in turn formed by two single layers where the polar heads are turned towards the ;i hydrophilic phase, while the hydrophobic tails are in mutual contact so that after the liposome has formed the water can not enter the liposome. A very interesting application of the liposomes is that according which both the hydrophobic substances (in the layer between hydrophobic tails) and the hydrophilic substances (in the water volume entrapped within the liposome as between concentric lamellas) may. be brought about by the same liposome. Moreover it is to be stressed that the chemical (natural) origin of phospholipids from biological membranes makes it possible for them to be re-absorbed from the epidermis into the deepest layers.
It has already been proposed in the state of art to use such structures in view of their biological origin which shows the great advantage of non-toxicity. However the processes making use of such structures have encountered drawbacks of a twofold nature, which made difficult the application of same structures:
a) the phospholipids which are commonly used to form liposome with fixed characteristics (shape, size, internal volumes, number of layers and so on) must be handled in physico-c~emical conditions which are compatible with their biological origin and therefore at temperatures between 20 to 37 C and pH between 6 to 8;
b) after their formation, particularly in the case of multilamellar liposomes, they are very stable and as a L
consequence, it will be very difficult to add new compounds or active principles. These compounds or active principle, particularly in case of h~drophobic substances, find an almost insuperable obstacle in the outermost polar heads exposed to water; in case of hydrophilic compounds and/or active principles, also considering their charge and their degree of ionization, they will mostly adhere : '' ' '; ,' . ` ' ' ~, :~
'` ` ' ~n~ s electrostatically to the polar heads of the outermost layer.
In view of the above stated difficulties in the state of the art, liposomes are used in cosmetics only additioned as preformed co-principles, to the cosmetic mixtures or as carriers of hydrolized animal elastin and of total hydrophilic extracts of spleen (oxydermin~. Liposomes containing active principles and particularly produced in situ before the application are not presently disclosed in the state of the art.
Subject of the present invention are therefore phospholipidic uni- or multilamellar liposomes in suspension in an aqueous solvent, said liposomes containing hydrophilic and/or hydrophobic active principles, each of said lamellas being substantially formed by a double layer of phospholipids showing a hydrophilic polar head and a hydrophobic tail, in said double layer said hydrophilic heads being disposed toward the hydrophilic phase (the outer part) said hydrophobic tails reciprocally faced (toward the inner part) and no water being present inside said double layer, so that a tridimensional, substantially concentric structure is formed, wherein double layers without water in the inside alternate to aqueous layer, characterized in that the hydrophilic active principles are localized within the aqueous layer while the hydrophobic principles are localized within double layers.
A further subject of the present invention is a process for the production of phospholipidic liposomes in suspension in an aqueous solvent at room temperature containing hydrophilic and/or hydrophobic active principles characterized by the fact of comprising the following steps:
a) solubilization of hydrophilic active principles in said aqueous solvent;
b) homogeneous dispersion of hydrophobic active principles in said aqueous solvent containing said hydrophilic active principles and c) addition of phospholipids at concentrations between 40:1 and 10:1, referring to the weight of the added active .. ~. , , ~ , . ', .
principles, so that after 1~4 hours phospholipidic liposomes containing said active principles are formed.
In respect to the state of art it is to be emphasized that the liposomes are formed in the milieu which contains in a solubilized or dispersed form, all the active principles to be used, in this way overcoming one of the problems of the state of the art, that is the introduction of the active principle or principles inside an already formed liposome.
Among the active principles which can be carried within the liposomes according to the present invention, ialuronic acid, which is used as a normalizer for the collagen structures of the derma, and coenzyme Q10 (ubiquinone), are to be particularly considered in view of the particular role they play in cosmetic applications. Coenzyme Q10 is a physiological redox exchanger which is present in the mitochondrial respiratory chain of our cutis cells.
Moreover, coenzyme Q10 has the double advantage of not only being a necessary physiological component of our cutis, but also, as a consequence of its perfect solubility in the hydrophobic liposome chains and of its redox properties, a very good stabilizer of the same liposome structure. In fact, coenzyme Q10 keeps constant the level of optimal unsaturation of the double bonds carbon-carbon in the phospholipidic hydrocarbon chains.
It goes without saying that according to the present invention other active principles which may or may not have a cosmetic importance, can be carried; among these hydrolized nucleic acids, catalase, superoxidodismutase, fitotherapic extracts and organ extracts, and minoxidil can be cited.
In order to improve the ease of application of the suspensions of phospholipidic liposomes according to the present invention containing active principles, it is also possible to add a further step to the production process (this is also part of the present invention) in which a thickening agent is added in order to produce a cream containing said phospholipidic liposomes which in turn contain the active principles.
' ' ' In the process according to the present invention the ratio between phospholipids and active principles will vary from 40:1 to 10:1, preferably 12:1, and the time necessary for the formation of liposomes will be of 1-4 hours, pr/~erably 2 hours. The process is carried out at room temperature preferably between 20 to 37 C and a pH between 6 to 8. A further object of the present invention is the use in cosmetics of phospholipidic liposomes according to the present invention for the transport of active principles.
In the following examples, which are non-limitinq, the production of liposomes according to the present invention will be listed, which are used in the production of two anti-wrinkle creams and a moisturizing cream.
Example 1 Production of a f irst anti-wrinkle cream The active principles used are: coenzyme Q10 (Esperis Spa-M);
vitamin A (hydrodispersed solution, vitamin A 100.000 IU/g, Istituto delle Vitamine - Milano);
vitamin E (DL-alpha-tocopherol, Merck Bracco Milano) purified soya-lecitins (Sigma Chemical Co. St. Louis, USA);
oxydermin (proteic extract of spleen, Sederma Variati -Milano).
Preservers (antibacterial, antimycotic agents) Prevan (hydroxyethyliden-methyl-pirandion, dehydroacetate sodic, NIPA - Genova);
Methylparaben (methyl-paraoxy-benzoate, NIPA - Genova);
Propilparaben (propil-paraoxy-benzoate, NIPA - Genova);
glycerin (Merck Bracco - Milano) Germall li5 (imidazolin-urea AGRAR - Roma) Carriers and solubilizinq phases phosphate buffer 10 M pH 7,0 (Merck Bracco - Milano);
corn germ oil (Esperis Spa - Milano~
Thickeninq aqents Carbopol g34*(neutralized carboxymethylpolimer Biochim -Milano).
Two reacting mixtures are prepared into separated 50 1 stainless steel containers at 20 C.
* Trade-mark -- 7 ~
A) Formation of liposomes: 0.05 kg of Qlo, 300 mIU of vitamin A together with o.l kg of vitamin E are dissolved in 1 kg of corn germ oil. Such a homogeneous oil solution is emulsified at 25-30 g through agitation (emulsifier equipped with a stirrer, Totalia 150, Mambretti - Milano) in 44.6 kg of phosphate buffer solution lO mM pH 7.0; 1.25 kg of purified granulated soya-lecitins are added to the solution under continuous agitation. The resulting suspension is left under uniform agitation for a period between 2 to 4 hours at a.temperature of 20 C. This time is necessary for the formation of liposomes and the presence of active principles. The final suspension is kept at 4C in a stainless steel container before its use in the process of production of the cream.
B) Formation of the support gel: 0.01 kg of Prevan, 0.1 kg of propilparaben, 0.1 kg of methylparaben, 3.0 kg of glycerin, 0.2 kg of Germall 115, 3.0 kg of oxydermin are dissolved in 43.0 kg of a neutralized solution of Carbopol 934 (1 %). During the process the emulsifier equipped with a stirrer referred to above is used; the carboxymethylpolimer (Carbopol 934) has been selected for its water absorbtion properties; as a consequence a thickening effect occurs without any solubilization effect (cleansing) on the liposome structures formed. As a function of the required thickness, from 0.5 to 2.0 kg of neutralized carboxymethylpolimer are added. The thickened solution is kept in a 50 l stainless steel container at room temperature before use.
C) Formation of the cream Two phases A and B are sucked in one after the other in the emulsifier referred to above. The mixing takes place in the following conditions: mixture A is sucked in first;
then mixture B is sucked in under quick agitation (about 1000 rpm) at a temperature of 20 C and a pressure of 400 mmHg. The process lasts about 60 minutes in conditions -, referred to above. At this stage the cream is perfumed with ~j essence (Crema test Ciprosia, Dragogo - GDR Milano).
Example 2 \ Production of a second anti-wrinkle cream l , ~ !
`
'' .' "- ~;
;zn~ 5 Following the procedure indicated in example 1, but dissolving 0.01 kg of ialuronic acid under the form of a sodic salt in the 10 mM a phophate buffer solution at pH
7.0 before of the emulsion step and before the addition of the granulated purified soya-lecitins, a new formulation of an anti-wrinkle cream containing both the co-enzyme Q10 and the ialuronic acid is obtained.
Example 3 Production of a moisturizina cream Startin~ material used Active principles Collastin (hydrolized animal elastin, CRODA - Milano) vitamin A (hydrodispersed solution (vitamin A, 100,000 IU/g, Istituto delle Vitamine - Milano) vitamin E (DL-alpha-to~opherol, Merck Bracco - Milano) purified soya lecitins (Sigma Chem. Co. St. Louis -USA) alpha-bisabol (active principle of chamomile, Dragogo GDR - Milano) ialuronic acid (Lambrokim - Milano) Preservers (antibacterial - antimycotal agents):
Bronopol (bromonitropropandiol Formenti - Milano) methylparaben (methyl-paraoxy-benzoate, NIPA - Genova) Propilparaben (propil-paraoxybenzoate, NIPA - Genova) Carriers and solubilizina phases Phosphate buffer 10 mM pH 7.0 Thickening aaents Carbopol 934 (neutralized carboxymethylpolimer, Biochim - Milano) Methodo~oaic sequence Two reactive mixtures into two different 50 1 stainless steel containers at 20 ~C are prepared.
A) Formation of the liposomes: 300 mIU of vitamin A, together with 0.1 kg of vitamin E, 0.02 kg of ialuronic acid and 1 kg of Collastin are dissolved in 45~3 kg of lO
mM phosphate buffer solution at pH 7.0 in the emulsifier of example 1. After the solubilization, 0.6 kg of granulated purified soya-lecitins are added under continuous agitation to the mixture. The resulting suspension is kept under .
.::
' ~ .
Z~ 8'~,5 g uniform agitation for a period between 2 to 4 hours at a temperature of 20 C. The final suspension is kept at 4 C
in a 50 1 stainless steel container before the process of cream production.
B) Formation of the support gel: 0.1 kg of Prevan, 0.1 kg of Propilparaben, 0.1 kg of Methylparaben, 3.0 kg of glycerin, 0.2 kg of Bronopol are dissolved in 46 kg of a neutralized solution of Carbopol 934 (1 %). According to the required density from 0.5 to 2.0 kg of neutralized carboxymethylpolymer are added. The thickened solution is kept in a 50 1 stainless steel container at room temperature before use.
C) Formation of the cream The two phases A and B are sucked in one after the other in the emulsifier of example 1. The mixing takes place in the following conditions:
as a first step mixture A is sucked in; then mixture B
is sucked in under quick agitation (about 1000 rpm) at a temperature of 20 ~C and a pressure of 400 mmHg. The process lasts about 60 minutes in conditions referred to above. The cream is then perfumed with "Crema test Ciprosia" essence.
It must be emphasized that solubilization or monodispersion of the active principle in aqueous solvents is a function of the coefficient of hydrophobic/hydrophilic ripartition. Upon formation of the liposomes the active principles will be distributed in different percentages within the hydrophobic layers or in the zone the water is found. These active principles, particularly for the cosmetic treatment, are vitamin complexes A, and E, hydrolized animal elastin, ialuronic acid, co-enzyme Q10 and so forth. This list is to be considered only as examplificative and non-limiting, because different active principles can be introduced before application with the liposomes of the present invention.
'`
.... .
.
-.
It has been now found, surprisingly, that liposomes can play a new role in allowing highly hydrophilic substances to reach the derma. Liposomes are microscopical blisters having a variable size (starting from some nanometers to some micrometers) and are artificially formed, mostly from phospholipidic mixtures which are the same phisiological components of the animal or vegetal cell membranes. The importance of these blisters relates to their tridimensional structure which, in turn, relates to the particular chemical composition of its components, the phospholipids. These biological compounds, having a lipidic origin, are substantially made of glycerin esters where an hydroxy group has been esterified by an ortophosphoric group and the other two hydroxy groups are esterified by fatty acids having chains of variable length which can also be branched. The phosphoric moiety is characterized by being electrostatically charged and it is called polar head; said polar head is therefore highly hydrophilic while the hydrocarbon chains are highly hydrophobic. In an aqueous environment and as a function of their concentration with regard to the solvent, these compounds spontaneously form blister structures where the polar head , -.
- : : . ..................... .
Z~ 82,~
faces other polar heads (multiple layers) or the water, while the hydrophobic regions in turn face one another so as to repel water. The liposomes are uni- or multilamellas stuctures where one or more double concetric layers are formed, each double layer being in turn formed by two single layers where the polar heads are turned towards the ;i hydrophilic phase, while the hydrophobic tails are in mutual contact so that after the liposome has formed the water can not enter the liposome. A very interesting application of the liposomes is that according which both the hydrophobic substances (in the layer between hydrophobic tails) and the hydrophilic substances (in the water volume entrapped within the liposome as between concentric lamellas) may. be brought about by the same liposome. Moreover it is to be stressed that the chemical (natural) origin of phospholipids from biological membranes makes it possible for them to be re-absorbed from the epidermis into the deepest layers.
It has already been proposed in the state of art to use such structures in view of their biological origin which shows the great advantage of non-toxicity. However the processes making use of such structures have encountered drawbacks of a twofold nature, which made difficult the application of same structures:
a) the phospholipids which are commonly used to form liposome with fixed characteristics (shape, size, internal volumes, number of layers and so on) must be handled in physico-c~emical conditions which are compatible with their biological origin and therefore at temperatures between 20 to 37 C and pH between 6 to 8;
b) after their formation, particularly in the case of multilamellar liposomes, they are very stable and as a L
consequence, it will be very difficult to add new compounds or active principles. These compounds or active principle, particularly in case of h~drophobic substances, find an almost insuperable obstacle in the outermost polar heads exposed to water; in case of hydrophilic compounds and/or active principles, also considering their charge and their degree of ionization, they will mostly adhere : '' ' '; ,' . ` ' ' ~, :~
'` ` ' ~n~ s electrostatically to the polar heads of the outermost layer.
In view of the above stated difficulties in the state of the art, liposomes are used in cosmetics only additioned as preformed co-principles, to the cosmetic mixtures or as carriers of hydrolized animal elastin and of total hydrophilic extracts of spleen (oxydermin~. Liposomes containing active principles and particularly produced in situ before the application are not presently disclosed in the state of the art.
Subject of the present invention are therefore phospholipidic uni- or multilamellar liposomes in suspension in an aqueous solvent, said liposomes containing hydrophilic and/or hydrophobic active principles, each of said lamellas being substantially formed by a double layer of phospholipids showing a hydrophilic polar head and a hydrophobic tail, in said double layer said hydrophilic heads being disposed toward the hydrophilic phase (the outer part) said hydrophobic tails reciprocally faced (toward the inner part) and no water being present inside said double layer, so that a tridimensional, substantially concentric structure is formed, wherein double layers without water in the inside alternate to aqueous layer, characterized in that the hydrophilic active principles are localized within the aqueous layer while the hydrophobic principles are localized within double layers.
A further subject of the present invention is a process for the production of phospholipidic liposomes in suspension in an aqueous solvent at room temperature containing hydrophilic and/or hydrophobic active principles characterized by the fact of comprising the following steps:
a) solubilization of hydrophilic active principles in said aqueous solvent;
b) homogeneous dispersion of hydrophobic active principles in said aqueous solvent containing said hydrophilic active principles and c) addition of phospholipids at concentrations between 40:1 and 10:1, referring to the weight of the added active .. ~. , , ~ , . ', .
principles, so that after 1~4 hours phospholipidic liposomes containing said active principles are formed.
In respect to the state of art it is to be emphasized that the liposomes are formed in the milieu which contains in a solubilized or dispersed form, all the active principles to be used, in this way overcoming one of the problems of the state of the art, that is the introduction of the active principle or principles inside an already formed liposome.
Among the active principles which can be carried within the liposomes according to the present invention, ialuronic acid, which is used as a normalizer for the collagen structures of the derma, and coenzyme Q10 (ubiquinone), are to be particularly considered in view of the particular role they play in cosmetic applications. Coenzyme Q10 is a physiological redox exchanger which is present in the mitochondrial respiratory chain of our cutis cells.
Moreover, coenzyme Q10 has the double advantage of not only being a necessary physiological component of our cutis, but also, as a consequence of its perfect solubility in the hydrophobic liposome chains and of its redox properties, a very good stabilizer of the same liposome structure. In fact, coenzyme Q10 keeps constant the level of optimal unsaturation of the double bonds carbon-carbon in the phospholipidic hydrocarbon chains.
It goes without saying that according to the present invention other active principles which may or may not have a cosmetic importance, can be carried; among these hydrolized nucleic acids, catalase, superoxidodismutase, fitotherapic extracts and organ extracts, and minoxidil can be cited.
In order to improve the ease of application of the suspensions of phospholipidic liposomes according to the present invention containing active principles, it is also possible to add a further step to the production process (this is also part of the present invention) in which a thickening agent is added in order to produce a cream containing said phospholipidic liposomes which in turn contain the active principles.
' ' ' In the process according to the present invention the ratio between phospholipids and active principles will vary from 40:1 to 10:1, preferably 12:1, and the time necessary for the formation of liposomes will be of 1-4 hours, pr/~erably 2 hours. The process is carried out at room temperature preferably between 20 to 37 C and a pH between 6 to 8. A further object of the present invention is the use in cosmetics of phospholipidic liposomes according to the present invention for the transport of active principles.
In the following examples, which are non-limitinq, the production of liposomes according to the present invention will be listed, which are used in the production of two anti-wrinkle creams and a moisturizing cream.
Example 1 Production of a f irst anti-wrinkle cream The active principles used are: coenzyme Q10 (Esperis Spa-M);
vitamin A (hydrodispersed solution, vitamin A 100.000 IU/g, Istituto delle Vitamine - Milano);
vitamin E (DL-alpha-tocopherol, Merck Bracco Milano) purified soya-lecitins (Sigma Chemical Co. St. Louis, USA);
oxydermin (proteic extract of spleen, Sederma Variati -Milano).
Preservers (antibacterial, antimycotic agents) Prevan (hydroxyethyliden-methyl-pirandion, dehydroacetate sodic, NIPA - Genova);
Methylparaben (methyl-paraoxy-benzoate, NIPA - Genova);
Propilparaben (propil-paraoxy-benzoate, NIPA - Genova);
glycerin (Merck Bracco - Milano) Germall li5 (imidazolin-urea AGRAR - Roma) Carriers and solubilizinq phases phosphate buffer 10 M pH 7,0 (Merck Bracco - Milano);
corn germ oil (Esperis Spa - Milano~
Thickeninq aqents Carbopol g34*(neutralized carboxymethylpolimer Biochim -Milano).
Two reacting mixtures are prepared into separated 50 1 stainless steel containers at 20 C.
* Trade-mark -- 7 ~
A) Formation of liposomes: 0.05 kg of Qlo, 300 mIU of vitamin A together with o.l kg of vitamin E are dissolved in 1 kg of corn germ oil. Such a homogeneous oil solution is emulsified at 25-30 g through agitation (emulsifier equipped with a stirrer, Totalia 150, Mambretti - Milano) in 44.6 kg of phosphate buffer solution lO mM pH 7.0; 1.25 kg of purified granulated soya-lecitins are added to the solution under continuous agitation. The resulting suspension is left under uniform agitation for a period between 2 to 4 hours at a.temperature of 20 C. This time is necessary for the formation of liposomes and the presence of active principles. The final suspension is kept at 4C in a stainless steel container before its use in the process of production of the cream.
B) Formation of the support gel: 0.01 kg of Prevan, 0.1 kg of propilparaben, 0.1 kg of methylparaben, 3.0 kg of glycerin, 0.2 kg of Germall 115, 3.0 kg of oxydermin are dissolved in 43.0 kg of a neutralized solution of Carbopol 934 (1 %). During the process the emulsifier equipped with a stirrer referred to above is used; the carboxymethylpolimer (Carbopol 934) has been selected for its water absorbtion properties; as a consequence a thickening effect occurs without any solubilization effect (cleansing) on the liposome structures formed. As a function of the required thickness, from 0.5 to 2.0 kg of neutralized carboxymethylpolimer are added. The thickened solution is kept in a 50 l stainless steel container at room temperature before use.
C) Formation of the cream Two phases A and B are sucked in one after the other in the emulsifier referred to above. The mixing takes place in the following conditions: mixture A is sucked in first;
then mixture B is sucked in under quick agitation (about 1000 rpm) at a temperature of 20 C and a pressure of 400 mmHg. The process lasts about 60 minutes in conditions -, referred to above. At this stage the cream is perfumed with ~j essence (Crema test Ciprosia, Dragogo - GDR Milano).
Example 2 \ Production of a second anti-wrinkle cream l , ~ !
`
'' .' "- ~;
;zn~ 5 Following the procedure indicated in example 1, but dissolving 0.01 kg of ialuronic acid under the form of a sodic salt in the 10 mM a phophate buffer solution at pH
7.0 before of the emulsion step and before the addition of the granulated purified soya-lecitins, a new formulation of an anti-wrinkle cream containing both the co-enzyme Q10 and the ialuronic acid is obtained.
Example 3 Production of a moisturizina cream Startin~ material used Active principles Collastin (hydrolized animal elastin, CRODA - Milano) vitamin A (hydrodispersed solution (vitamin A, 100,000 IU/g, Istituto delle Vitamine - Milano) vitamin E (DL-alpha-to~opherol, Merck Bracco - Milano) purified soya lecitins (Sigma Chem. Co. St. Louis -USA) alpha-bisabol (active principle of chamomile, Dragogo GDR - Milano) ialuronic acid (Lambrokim - Milano) Preservers (antibacterial - antimycotal agents):
Bronopol (bromonitropropandiol Formenti - Milano) methylparaben (methyl-paraoxy-benzoate, NIPA - Genova) Propilparaben (propil-paraoxybenzoate, NIPA - Genova) Carriers and solubilizina phases Phosphate buffer 10 mM pH 7.0 Thickening aaents Carbopol 934 (neutralized carboxymethylpolimer, Biochim - Milano) Methodo~oaic sequence Two reactive mixtures into two different 50 1 stainless steel containers at 20 ~C are prepared.
A) Formation of the liposomes: 300 mIU of vitamin A, together with 0.1 kg of vitamin E, 0.02 kg of ialuronic acid and 1 kg of Collastin are dissolved in 45~3 kg of lO
mM phosphate buffer solution at pH 7.0 in the emulsifier of example 1. After the solubilization, 0.6 kg of granulated purified soya-lecitins are added under continuous agitation to the mixture. The resulting suspension is kept under .
.::
' ~ .
Z~ 8'~,5 g uniform agitation for a period between 2 to 4 hours at a temperature of 20 C. The final suspension is kept at 4 C
in a 50 1 stainless steel container before the process of cream production.
B) Formation of the support gel: 0.1 kg of Prevan, 0.1 kg of Propilparaben, 0.1 kg of Methylparaben, 3.0 kg of glycerin, 0.2 kg of Bronopol are dissolved in 46 kg of a neutralized solution of Carbopol 934 (1 %). According to the required density from 0.5 to 2.0 kg of neutralized carboxymethylpolymer are added. The thickened solution is kept in a 50 1 stainless steel container at room temperature before use.
C) Formation of the cream The two phases A and B are sucked in one after the other in the emulsifier of example 1. The mixing takes place in the following conditions:
as a first step mixture A is sucked in; then mixture B
is sucked in under quick agitation (about 1000 rpm) at a temperature of 20 ~C and a pressure of 400 mmHg. The process lasts about 60 minutes in conditions referred to above. The cream is then perfumed with "Crema test Ciprosia" essence.
It must be emphasized that solubilization or monodispersion of the active principle in aqueous solvents is a function of the coefficient of hydrophobic/hydrophilic ripartition. Upon formation of the liposomes the active principles will be distributed in different percentages within the hydrophobic layers or in the zone the water is found. These active principles, particularly for the cosmetic treatment, are vitamin complexes A, and E, hydrolized animal elastin, ialuronic acid, co-enzyme Q10 and so forth. This list is to be considered only as examplificative and non-limiting, because different active principles can be introduced before application with the liposomes of the present invention.
'`
.... .
.
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Claims (9)
1. Phospholipidic uni- or multilamellar liposomes in suspension in an aqueous solvent, containing hydrophilic and/or hydrophobic active principles, said lamellas being substantially formed by a double layer of phospholipids, which shows a hydrophilic polar head and a hydrophobic tail, in said double layer said hydrophilic polar heads being directed toward the hydrophilic phase and said hydrophobic tails facing one to another and no water being present within said double layer, so that a concentric tridimensional structure is formed where double layers without any water alternate to aqueous layers, characterized in that said hydrophilic active principles are localized in the aqueous layers while said hydrophobic principles are localized within said double layers.
2. Phospholipidic liposomes according to claim 1, wherein said active principles are selected from the group comprising ialuronic acid, co-enzyme Q10 and their mixtures.
3. Phospholipidic liposomes according to claim 2, wherein active principles selected from the group formed by vitamin complexes A, vitamin complexes E, oxydermin, alphabisabol and their mixtures are also contained.
4. Cream containing phospholipidic liposomes as claimed in claims 1, 2 or 3, together with usual cosmetic carriers and excipients.
5. A process for the production of phospholipidic liposomes in suspension in an aqueous solvent at room temperature and containing hydrophilic and/or hydrophobic active principles, characterized by the fact of comprising the following steps:
A) solubilization of said hydrophilic active principles in said aqueous solvent;
B) homogeneous dispersion of the hydrophbic active principles in said aqueous solvent containing said hydrophilic active principles, and C) addition of phospholipids to concentrations between 42:1 to 10:1 with reference to the weight of the added active principles, so that after 1-4 hours phospholipidic liposoms containing said active principles are obtained.
A) solubilization of said hydrophilic active principles in said aqueous solvent;
B) homogeneous dispersion of the hydrophbic active principles in said aqueous solvent containing said hydrophilic active principles, and C) addition of phospholipids to concentrations between 42:1 to 10:1 with reference to the weight of the added active principles, so that after 1-4 hours phospholipidic liposoms containing said active principles are obtained.
6. The process according to claim 5, further comprising the step of adding a thickening agent compatible with the phospholipidic liposomes to be obtained in order to produce a cream containing said phospholipidic liposomes which contain said hydrophilic and/or hydrophobic active principles.
7. Cream obtained from the process as claimed in claim 6.
8. Cream according to claim 7, wherein said active principles are selected from the group comprising ialuronic acid, co-enzyme Q10 and their mixtures.
9. Cream according to claim 8, wherein said liposomes further contain active principles selected from the group formed by vitamin complexes A, vitamin complexes E, oxydermin, alphabisabol and their mixtures.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA 2018825 CA2018825A1 (en) | 1990-06-12 | 1990-06-12 | Phospholipidic liposomes containing active principles and a process for the production thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA 2018825 CA2018825A1 (en) | 1990-06-12 | 1990-06-12 | Phospholipidic liposomes containing active principles and a process for the production thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2018825A1 true CA2018825A1 (en) | 1991-12-12 |
Family
ID=4145200
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA 2018825 Abandoned CA2018825A1 (en) | 1990-06-12 | 1990-06-12 | Phospholipidic liposomes containing active principles and a process for the production thereof |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA2018825A1 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5853755A (en) * | 1993-07-28 | 1998-12-29 | Pharmaderm Laboratories Ltd. | Biphasic multilamellar lipid vesicles |
-
1990
- 1990-06-12 CA CA 2018825 patent/CA2018825A1/en not_active Abandoned
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5853755A (en) * | 1993-07-28 | 1998-12-29 | Pharmaderm Laboratories Ltd. | Biphasic multilamellar lipid vesicles |
| US5993851A (en) * | 1993-07-28 | 1999-11-30 | Pharmaderm Laboratories, Ltd. | Method for preparing biphasic multilamellar lipid vesicles |
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