US20110070285A1 - Method of making flexible bioresorbable hemostatic packing and stent having a preselectable in-vivo residence time - Google Patents
Method of making flexible bioresorbable hemostatic packing and stent having a preselectable in-vivo residence time Download PDFInfo
- Publication number
- US20110070285A1 US20110070285A1 US12/956,709 US95670910A US2011070285A1 US 20110070285 A1 US20110070285 A1 US 20110070285A1 US 95670910 A US95670910 A US 95670910A US 2011070285 A1 US2011070285 A1 US 2011070285A1
- Authority
- US
- United States
- Prior art keywords
- hyaluronic acid
- making flexible
- flexible bioresorbable
- bioresorbable foam
- foam
- 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
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
- A61K31/726—Glycosaminoglycans, i.e. mucopolysaccharides
- A61K31/728—Hyaluronic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L24/00—Surgical adhesives or cements; Adhesives for colostomy devices
- A61L24/04—Surgical adhesives or cements; Adhesives for colostomy devices containing macromolecular materials
- A61L24/043—Mixtures of macromolecular materials
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
- A61L2/0005—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor for pharmaceuticals, biologicals or living parts
- A61L2/0011—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor for pharmaceuticals, biologicals or living parts using physical methods
- A61L2/0029—Radiation
- A61L2/0035—Gamma radiation
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L24/00—Surgical adhesives or cements; Adhesives for colostomy devices
- A61L24/001—Use of materials characterised by their function or physical properties
- A61L24/0036—Porous materials, e.g. foams or sponges
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L24/00—Surgical adhesives or cements; Adhesives for colostomy devices
- A61L24/001—Use of materials characterised by their function or physical properties
- A61L24/0042—Materials resorbable by the body
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/04—Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2202/00—Aspects relating to methods or apparatus for disinfecting or sterilising materials or objects
- A61L2202/20—Targets to be treated
- A61L2202/21—Pharmaceuticals, e.g. medicaments, artificial body parts
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2400/00—Materials characterised by their function or physical properties
- A61L2400/04—Materials for stopping bleeding
Definitions
- the present invention relates generally to the field of bioresorbable packing and stents, and more specifically to a method of making flexible bioresorbable foam, useful for post-operative or drug delivery use, having both hemostatic properties and a preselectable in-vivo residence time.
- sterile packing and stents are used in the medical and surgical fields for keeping tissues apart or preventing adhesion.
- Such uses include, but are not limited to, nasal packing and sinus stents, packing for inner ear surgery, tympanoplasty, exostosis, orbital decompression, as well as various orifice restenosis prevention uses.
- Personal uses such as tampons, bandaging and the like also involve sterile packing materials.
- Such packing and stents have been made from gauzes, microfibers, non-fibrous expandable packing, such as tampons, and the like. These types of packing are not bioresorbable and can cause injury or discomfort upon removal, as well as causing toxic shock syndrome if left internally for more than a day or two.
- HA hyaluronic acid
- salts of hyaluronic acids which are naturally occurring mucopolysaccharides found in various body fluids and connective tissues.
- HA is biocompatible. It has been adapted for use as a surgical aid to prevent tissue contact and adhesion formation.
- HA has a very high solubility, and thus poor liquid absorption, and tends to quickly disperse when exposed to such liquids. This reduces HA materials' effectiveness in areas such as surgical wounds that exude blood and other fluids. Crosslinking has created somewhat insoluble HA materials.
- biocompatible materials such as polysaccharides, especially methylcellulosic materials have been combined with the hyaluronic acid to produce packing materials that are resorbable but are also insoluble and have a longer in-vivo residence time before they dissolve into gels and are absorbed by the body tissues. These materials also have increased fluid absorption capabilities. Such materials stop bleeding only by effect of compression and packing and do not have any inherent hemostatic properties.
- Collagen is also known for use in the medical field. It is a major protein constituent of connective tissue and is widely used in medical and surgical applications such as sutures, grafts and surgical prostheses. Typical sources include calfskin, bovine Achilles tendons, cattle bones, porcine tissue, human cadaver tissue, and rat tails. Collagen, as an animal protein, is bioresorbable, even when crosslinked to reasonable levels. Collagen is available in a variety of forms including powders and fibrils, and in aqueous solution. Collagen may be provided in insoluble or soluble forms.
- a flexible bioresorbable foam for packing, post-operative use, and other medical uses may be created having both hemostatic properties and a variable preselectable resorption time (also known as an in-vivo residence time).
- the foam is formed from a blend of collagen and hyaluronic acid or derivative thereof.
- the foam is crosslinked using a chemical crosslinking agent.
- bioresorbable means capable of being absorbed by the body.
- hemostat means a device or material which stops blood flow.
- tissue means a material or device used for separating tissue and holding it in such separated position.
- lyophilizing means freeze-drying.
- resorption time and “in-vivo residence time” are used interchangeably, and refer to the time between insertion into the body and the time at which the material has been substantially absorbed into the tissues.
- adheresion refers to the sticking together of tissues which are in intimate contact for extended periods.
- preselectable in-vivo residence time means that foams of the invention may be formed that will have different in-vivo residence times to be useful for different applications.
- the bioresorbable hemostatic packing provided herein may be used in any manner in which sterile packing and/or stents are normally used in the surgical or medical fields, including uses for which control of low weight bleeding and adhesion prevention are important. Such uses include, but are not limited to, nasal packing and sinus stents, packing for inner ear surgery, tympanoplasty, exostosis, orbital decompression, as well as various orifice restenosis prevention uses.
- the packing materials may also be used as single or combination drug delivery systems for humans or mammals.
- Bioresorbable foams of an embodiment of the invention are formed from a blend of a hyaluronic acid component and collagen. Varying ratios of the components may be used in the blends according to the application desired, e.g., 50/50, 60/40 etc.
- a typical blend may comprise from about 70 to about 90 weight percent of the hyaluronic acid component, and correspondingly from about 10 to about 30 weight percent of collagen.
- the blend contains from about 70 to about 80 weight percent of the hyaluronic acid or derivative thereof.
- the ratios of such blends can be selected by the particular application anticipated. For example, higher amounts of collagen will increase the hemostatic effect somewhat.
- Collagen materials useful in blends of an embodiment of the invention are absorbable collagen materials from any source, e.g., corium collagen, tendon collagen, and the like, available commercially from such companies as Datascope® and Fibrogen, Inc.
- the blends are formed of a microfibrillar collagen foam that includes a collagen flour.
- Such collagen materials are available from Davol Inc., a subsidiary of C. R. Bard, Inc., as Avitene®.
- Useful hyaluronic acid components include hyaluronic acid, derivatives thereof, and mixtures thereof.
- One particularly useful derivative is esterified hyaluronic acid.
- Useful ester derivatives may be partial or total esters of hyaluronic acid; e.g., hyaluronic acid esterified with aliphatic or araliphatic esters such as ethyl esters, octadecyl esters, benzyl esters and mixtures thereof.
- the blend comprises a partial esterified hyaluronic acid; especially, an esterified HA having an esterification of at least about 60%.
- One useful esterified hyaluronic acid has an esterification level of from about 60% to about 70%. Such materials are available commercially from Fidia Advanced Biopolymers, S.r.l. under the trade name Hyaff®.
- the in-vivo residence times of flexible foams of an embodiment of the invention may be selected to be from about 5 days to about 28 days; in some embodiments, the foam will have an in-vivo residence time of from about 5 days to about 14 days.
- the in-vivo residence time for the flexible bioresorbable foams of an embodiment of the invention is controlled by adjusting the re-suspension shear parameters, the level of crosslinking of the foam ingredients to produce the desired level; the sterilization bombardment must also be controlled in order to control the chain scission caused by such bombardment.
- the foams are formed by a method that includes the formation of a suspension of the collagen and the esterified hyaluronic acid in water.
- the suspension is formed by mixing with conventional mixers until suspended.
- the suspension is mixed at a shear rate of from about 0.25 minutes/liter to about 3.0 minutes/liter, and at a speed of from about 7,000 rpm to about 10,000 rpm.
- the suspension is then metered into lyophilization trays with a series of cavities. Typical trays have cavities nominally about 4 cm by 1.3 cm by 1 cm.
- the suspended solution is then freeze-dried into solid foam blocks using well known procedure involving vacuum conditions at temperatures that are less than the freezing temperature of water, i.e., less than 0° C. After 0° C. is reached, the temperature is then reduced further over time, and cycled; e.g., the temperature is reduced by a few degrees then maintained at the lower temperature for a period of time, and then reduced again.
- the temperature reaches a low of about ⁇ 45° C. where it is maintained for the period required to complete the lyophilization.
- the lyophilization can be more than 10 hours, and perhaps as much as 24-30 hours.
- the drying portion of the lyophilization is performed at a vacuum set point of about 75 mm of mercury (Hg) with the temperature being raised to about 0° C. and maintained there for at least about 2 hours, and up to about 6 hours, then raised to at least about 25° C. to a period of from about 4 hours to about 40 hours.
- the foam Upon completion of lyophilization, the foam is then ready to be crosslinked.
- Crosslinking may be accomplished by dehydrothermal crosslinking, or by exposure to a chemical crosslinking agent.
- dehydrothermal crosslinking the foam is dehydrated to reduce the moisture content to the temperature at which crosslinking occurs, typically to less than about 1%.
- the product is subjected to elevated temperatures and/or vacuum conditions until crosslinking occurs.
- Useful combinations of such conditions include vacuum of at least about 10 ⁇ 5 mm of mercury, and temperatures of at least about 35° C. Naturally, if vacuum is not used, much higher temperatures are required, e.g., above 75° C.
- the conditions are maintained for at least about 10 hours, typically for about 24 hours until the desired molecular weight has been achieved.
- useful chemical crosslinking agents include aldehydes, e.g., formaldehyde vapor, which can be used by pumping it into a room containing the lyophilized foam and allowed to contact the foam for at least about 2 hours, preferably at least about 5 hours. After the desired exposure time is complete, the crosslinking agent is evacuated from the room.
- aldehydes e.g., formaldehyde vapor
- the foam is then ready for compression, packaging and sterilization, typically by bombardment with gamma rays or electron beam bombardment.
- the bombardment both kills bacteria and performs chain scission on the foam. It is important that the sterilization/chain scission procedure and the crosslinking procedure be balanced to produce the desired crosslinking level to achieve the in-vivo residence time desired.
- the bioresorbable foam of the invention is flexible and does not require any rehydration.
- the bioresorbable foam of the invention can be easily handled either wet or dry and may be squeezed, and/or cut to required size.
- the foam will contour to the body cavity or wound as required, and provides chemical hemostasis as well as preventing adhesion, and minimizing swelling and edema.
Abstract
The invention provides a method of making flexible bioresorbable foam having hemostatic properties and a preselectable in-vivo residence time. A blend of crosslinked collagen blended and a hyaluronic acid component is prepared. The blend is mixed with water to form a suspension. The blend is freezed and lyophilized at less than about 0° C. Next, the blend is crosslinked. The product is then sterilized and chain scission is performed by bombardment with gamma rays or a beam of electrons.
Description
- This application claims priority to U.S. Provisional Application No. 10/938,999, which was filed on Sep. 10, 2004, the contents of which are incorporated herein by reference.
- The present invention relates generally to the field of bioresorbable packing and stents, and more specifically to a method of making flexible bioresorbable foam, useful for post-operative or drug delivery use, having both hemostatic properties and a preselectable in-vivo residence time.
- Various types of sterile packing and stents are used in the medical and surgical fields for keeping tissues apart or preventing adhesion. Such uses include, but are not limited to, nasal packing and sinus stents, packing for inner ear surgery, tympanoplasty, exostosis, orbital decompression, as well as various orifice restenosis prevention uses. Personal uses such as tampons, bandaging and the like also involve sterile packing materials.
- Such packing and stents have been made from gauzes, microfibers, non-fibrous expandable packing, such as tampons, and the like. These types of packing are not bioresorbable and can cause injury or discomfort upon removal, as well as causing toxic shock syndrome if left internally for more than a day or two.
- In an attempt to prevent such reactions, while continuing to prevent adhesion and tissue necrosis, resorbable packing and stent devices have been developed. Such packing materials have typically included hyaluronic acid (HA), or salts of hyaluronic acids, which are naturally occurring mucopolysaccharides found in various body fluids and connective tissues. Thus, HA is biocompatible. It has been adapted for use as a surgical aid to prevent tissue contact and adhesion formation.
- However, HA has a very high solubility, and thus poor liquid absorption, and tends to quickly disperse when exposed to such liquids. This reduces HA materials' effectiveness in areas such as surgical wounds that exude blood and other fluids. Crosslinking has created somewhat insoluble HA materials.
- Further, other biocompatible materials such as polysaccharides, especially methylcellulosic materials have been combined with the hyaluronic acid to produce packing materials that are resorbable but are also insoluble and have a longer in-vivo residence time before they dissolve into gels and are absorbed by the body tissues. These materials also have increased fluid absorption capabilities. Such materials stop bleeding only by effect of compression and packing and do not have any inherent hemostatic properties.
- Collagen is also known for use in the medical field. It is a major protein constituent of connective tissue and is widely used in medical and surgical applications such as sutures, grafts and surgical prostheses. Typical sources include calfskin, bovine Achilles tendons, cattle bones, porcine tissue, human cadaver tissue, and rat tails. Collagen, as an animal protein, is bioresorbable, even when crosslinked to reasonable levels. Collagen is available in a variety of forms including powders and fibrils, and in aqueous solution. Collagen may be provided in insoluble or soluble forms.
- It has now been discovered that a flexible bioresorbable foam for packing, post-operative use, and other medical uses may be created having both hemostatic properties and a variable preselectable resorption time (also known as an in-vivo residence time). The foam is formed from a blend of collagen and hyaluronic acid or derivative thereof.
- An embodiment of the invention provides a method of making flexible bioresorbable foam having hemostatic properties and a variable preselectable resorption time comprising the steps of:
-
- providing a blend of collagen and an hyaluronic acid component comprising from about 70 to about 90 weight percent of the esterified hyaluronic acid;
- mixing with water to form a suspension;
- freezing and lyophilizing the blend at 0° C. or below;
- crosslinking to form a flexible crosslinked product; and
- sterilizing and performing chain scission on the crosslinked product by means of bombardment with gamma rays or electrons.
- In one method of making the bioresorbable flexible foam of an embodiment of the invention, the foam is crosslinked using a chemical crosslinking agent.
- These terms when used herein have the following meanings.
- The term “bioresorbable” as used herein, means capable of being absorbed by the body.
- The term “ hemostat” means a device or material which stops blood flow.
- The term “stent” means a material or device used for separating tissue and holding it in such separated position.
- The term “lyophilizing” means freeze-drying.
- The term “resorption time” and “in-vivo residence time” are used interchangeably, and refer to the time between insertion into the body and the time at which the material has been substantially absorbed into the tissues.
- The term “adhesion” as used herein, refers to the sticking together of tissues which are in intimate contact for extended periods.
- The term “preselectable in-vivo residence time” means that foams of the invention may be formed that will have different in-vivo residence times to be useful for different applications.
- The following detailed description describes certain embodiments and is not to be taken in a limiting sense. The scope of the present invention is defined by the appended claims.
- The bioresorbable hemostatic packing provided herein may be used in any manner in which sterile packing and/or stents are normally used in the surgical or medical fields, including uses for which control of low weight bleeding and adhesion prevention are important. Such uses include, but are not limited to, nasal packing and sinus stents, packing for inner ear surgery, tympanoplasty, exostosis, orbital decompression, as well as various orifice restenosis prevention uses. The packing materials may also be used as single or combination drug delivery systems for humans or mammals.
- Bioresorbable foams of an embodiment of the invention are formed from a blend of a hyaluronic acid component and collagen. Varying ratios of the components may be used in the blends according to the application desired, e.g., 50/50, 60/40 etc. A typical blend may comprise from about 70 to about 90 weight percent of the hyaluronic acid component, and correspondingly from about 10 to about 30 weight percent of collagen. In one embodiment, the blend contains from about 70 to about 80 weight percent of the hyaluronic acid or derivative thereof. The ratios of such blends can be selected by the particular application anticipated. For example, higher amounts of collagen will increase the hemostatic effect somewhat.
- Collagen materials useful in blends of an embodiment of the invention are absorbable collagen materials from any source, e.g., corium collagen, tendon collagen, and the like, available commercially from such companies as Datascope® and Fibrogen, Inc. In one embodiment, the blends are formed of a microfibrillar collagen foam that includes a collagen flour. Such collagen materials are available from Davol Inc., a subsidiary of C. R. Bard, Inc., as Avitene®.
- Useful hyaluronic acid components include hyaluronic acid, derivatives thereof, and mixtures thereof. One particularly useful derivative is esterified hyaluronic acid. Useful ester derivatives may be partial or total esters of hyaluronic acid; e.g., hyaluronic acid esterified with aliphatic or araliphatic esters such as ethyl esters, octadecyl esters, benzyl esters and mixtures thereof. In one embodiment the blend comprises a partial esterified hyaluronic acid; especially, an esterified HA having an esterification of at least about 60%. One useful esterified hyaluronic acid has an esterification level of from about 60% to about 70%. Such materials are available commercially from Fidia Advanced Biopolymers, S.r.l. under the trade name Hyaff®.
- The in-vivo residence times of flexible foams of an embodiment of the invention may be selected to be from about 5 days to about 28 days; in some embodiments, the foam will have an in-vivo residence time of from about 5 days to about 14 days. The in-vivo residence time for the flexible bioresorbable foams of an embodiment of the invention is controlled by adjusting the re-suspension shear parameters, the level of crosslinking of the foam ingredients to produce the desired level; the sterilization bombardment must also be controlled in order to control the chain scission caused by such bombardment.
- In one embodiment, the foams are formed by a method that includes the formation of a suspension of the collagen and the esterified hyaluronic acid in water. The suspension is formed by mixing with conventional mixers until suspended. The suspension is mixed at a shear rate of from about 0.25 minutes/liter to about 3.0 minutes/liter, and at a speed of from about 7,000 rpm to about 10,000 rpm. The suspension is then metered into lyophilization trays with a series of cavities. Typical trays have cavities nominally about 4 cm by 1.3 cm by 1 cm.
- The suspended solution is then freeze-dried into solid foam blocks using well known procedure involving vacuum conditions at temperatures that are less than the freezing temperature of water, i.e., less than 0° C. After 0° C. is reached, the temperature is then reduced further over time, and cycled; e.g., the temperature is reduced by a few degrees then maintained at the lower temperature for a period of time, and then reduced again.
- Finally, the temperature reaches a low of about −45° C. where it is maintained for the period required to complete the lyophilization. In certain embodiments, the lyophilization can be more than 10 hours, and perhaps as much as 24-30 hours. The drying portion of the lyophilization is performed at a vacuum set point of about 75 mm of mercury (Hg) with the temperature being raised to about 0° C. and maintained there for at least about 2 hours, and up to about 6 hours, then raised to at least about 25° C. to a period of from about 4 hours to about 40 hours.
- Upon completion of lyophilization, the foam is then ready to be crosslinked. Crosslinking may be accomplished by dehydrothermal crosslinking, or by exposure to a chemical crosslinking agent. In dehydrothermal crosslinking, the foam is dehydrated to reduce the moisture content to the temperature at which crosslinking occurs, typically to less than about 1%. The product is subjected to elevated temperatures and/or vacuum conditions until crosslinking occurs. Useful combinations of such conditions include vacuum of at least about 10−5 mm of mercury, and temperatures of at least about 35° C. Naturally, if vacuum is not used, much higher temperatures are required, e.g., above 75° C. The conditions are maintained for at least about 10 hours, typically for about 24 hours until the desired molecular weight has been achieved.
- If chemical crosslinking is desired, useful chemical crosslinking agents include aldehydes, e.g., formaldehyde vapor, which can be used by pumping it into a room containing the lyophilized foam and allowed to contact the foam for at least about 2 hours, preferably at least about 5 hours. After the desired exposure time is complete, the crosslinking agent is evacuated from the room.
- After crosslinking, the foam is then ready for compression, packaging and sterilization, typically by bombardment with gamma rays or electron beam bombardment. The bombardment both kills bacteria and performs chain scission on the foam. It is important that the sterilization/chain scission procedure and the crosslinking procedure be balanced to produce the desired crosslinking level to achieve the in-vivo residence time desired. The bioresorbable foam of the invention is flexible and does not require any rehydration.
- The bioresorbable foam of the invention can be easily handled either wet or dry and may be squeezed, and/or cut to required size. The foam will contour to the body cavity or wound as required, and provides chemical hemostasis as well as preventing adhesion, and minimizing swelling and edema.
- Although specific embodiments have been illustrated and described herein for purposes of description of the preferred embodiment, it will be appreciated by those of ordinary skill in the art that a wide variety of alternate and/or equivalent implementations calculated to achieve the same purposes may be substituted for the specific embodiments shown and described without departing from the scope of the present invention. Those with skill in the chemical, mechanical, biomedical, and biomaterials arts will readily appreciate that the present invention may be implemented in a very wide variety of embodiments. This application is intended to cover any adaptations or variations of the preferred embodiments discussed herein. Therefore, it is manifestly intended that this invention be limited only by the claims and the equivalents thereof.
Claims (21)
1. A method of making a flexible bioresorbable foam having a preselectable in-vivo residence time comprising the steps of:
preparing a blend consisting of crosslinked collagen blended with a hyaluronic acid component,
mixing the blend with water to form a suspension;
freezing and lyophilizing the suspension at less than about 0° C.;
crosslinking the suspension to form a crosslinked product, and
sterilizing and performing chain scission on the product by means of bombardment with gamma rays or a beam of electrons.
2. The method of making flexible bioresorbable foam of claim 1 , wherein the lyophilization is performed at a temperature of less than about −40° C.
3. The method of making flexible bioresorbable foam of claim 1 , wherein the crosslinking is achieved by means of a method selected from dehydrothermal crosslinking and chemical crosslinking.
4. The method of making flexible bioresorbable foam of claim 1 , wherein crosslinking is achieved by use of formaldehyde vapor.
5. The method of making flexible bioresorbable foam of claim 4 , wherein the formaldehyde vapor is evacuated after a period of between about 2 hours and about 7 hours.
6. The method of making flexible bioresorbable foam of claim 1 , wherein the blend comprises between about 70 percent and about 90 percent by weight of the esterified hyaluronic acid.
7. The method of making flexible bioresorbable foam composition of claim 1 , wherein the sterilizing is performed by bombardment with gamma rays.
8. The method of making flexible bioresorbable foam of claim 1 , wherein the hyaluronic acid component is selected from hyaluronic acid, esterified hyaluronic acid and mixtures thereof.
9. The method of making flexible bioresorbable foam of claim 8 , wherein the esterified hyaluronic acid has an esterification level of between about 60 percent and about 70 percent.
10. The method of making flexible bioresorbable foam of claim 9 , wherein the esterified hyaluronic acid is selected from the group consisting of a benzyl ester of hyaluronic acid, an ethyl ester of hyaluronic acid and mixtures thereof.
11. The method of making flexible bioresorbable foam of claim 1 , wherein the crosslinked collagen is a microfibrillar collagen.
12. The method of making flexible bioresorbable foam of claim 1 , wherein the preselectable residence time ranges between about 5 days and about 14 days.
13. A method of making a flexible bioresorbable foam having a preselectable in-vivo residence time, wherein the method comprises the steps of:
preparing a blend consisting of crosslinked collagen blended with a hyaluronic acid component,
mixing the blend with water to form a mixture;
freezing the mixture;
lyophilizing the mixture;
crosslinking the mixture to form a crosslinked product, and
sterilizing and performing chain scission the product.
14. The method of making flexible bioresorbable foam of claim 13 , wherein crosslinking is achieved using formaldehyde vapor.
15. The method of making flexible bioresorbable foam of claim 14 , wherein the formaldehyde vapor is evacuated after a period of between about 2 hours and about 7 hours.
16. The method of making flexible bioresorbable foam of claim 13 , wherein the blend comprises between about 70 percent and about 90 percent by weight of the esterified hyaluronic acid.
17. The method of making flexible bioresorbable foam composition of claim 13 , wherein the sterilizing is performed by bombardment with gamma rays.
18. The method of making flexible bioresorbable foam of claim 13 , wherein the hyaluronic acid component is selected from hyaluronic acid, esterified hyaluronic acid and mixtures thereof.
19. The method of making flexible bioresorbable foam of claim 18 , wherein the esterified hyaluronic acid has an esterification level of between about 60 percent and about 70 percent.
20. The method of making flexible bioresorbable foam of claim 19 , wherein the esterified hyaluronic acid is selected from the group consisting of a benzyl ester of hyaluronic acid, an ethyl ester of hyaluronic acid and mixtures thereof.
21. The method of making flexible bioresorbable foam of claim 13 , wherein the crosslinked collagen is a microfibrillar collagen.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12/956,709 US20110070285A1 (en) | 2004-09-10 | 2010-11-30 | Method of making flexible bioresorbable hemostatic packing and stent having a preselectable in-vivo residence time |
US15/403,419 US20170119920A1 (en) | 2004-09-10 | 2017-01-11 | Method of making flexible bioresorbable hemostatic packing and stent having a preselectable in-vivo residence time |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/938,999 US7858107B2 (en) | 2004-09-10 | 2004-09-10 | Flexible bioresorbable hemostatic packing and stent having a preselectable in-vivo residence time |
US12/956,709 US20110070285A1 (en) | 2004-09-10 | 2010-11-30 | Method of making flexible bioresorbable hemostatic packing and stent having a preselectable in-vivo residence time |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/938,999 Division US7858107B2 (en) | 2004-09-10 | 2004-09-10 | Flexible bioresorbable hemostatic packing and stent having a preselectable in-vivo residence time |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US15/403,419 Continuation US20170119920A1 (en) | 2004-09-10 | 2017-01-11 | Method of making flexible bioresorbable hemostatic packing and stent having a preselectable in-vivo residence time |
Publications (1)
Publication Number | Publication Date |
---|---|
US20110070285A1 true US20110070285A1 (en) | 2011-03-24 |
Family
ID=36034279
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/938,999 Active 2028-06-02 US7858107B2 (en) | 2004-09-10 | 2004-09-10 | Flexible bioresorbable hemostatic packing and stent having a preselectable in-vivo residence time |
US12/956,709 Abandoned US20110070285A1 (en) | 2004-09-10 | 2010-11-30 | Method of making flexible bioresorbable hemostatic packing and stent having a preselectable in-vivo residence time |
US15/403,419 Abandoned US20170119920A1 (en) | 2004-09-10 | 2017-01-11 | Method of making flexible bioresorbable hemostatic packing and stent having a preselectable in-vivo residence time |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/938,999 Active 2028-06-02 US7858107B2 (en) | 2004-09-10 | 2004-09-10 | Flexible bioresorbable hemostatic packing and stent having a preselectable in-vivo residence time |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US15/403,419 Abandoned US20170119920A1 (en) | 2004-09-10 | 2017-01-11 | Method of making flexible bioresorbable hemostatic packing and stent having a preselectable in-vivo residence time |
Country Status (1)
Country | Link |
---|---|
US (3) | US7858107B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106880872A (en) * | 2016-12-23 | 2017-06-23 | 北京大清生物技术股份有限公司 | Natural extracellular matrix biomembrane and preparation method and application |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7858107B2 (en) * | 2004-09-10 | 2010-12-28 | Medtronic Xomed, Inc. | Flexible bioresorbable hemostatic packing and stent having a preselectable in-vivo residence time |
US8313762B2 (en) | 2006-07-05 | 2012-11-20 | Medtronic Xomed, Inc. | Flexible bioresorbable hemostatic packing and stent |
KR101047510B1 (en) | 2009-04-07 | 2011-07-08 | (주)다림티센 | Method for preparing anti-adhesion agent using esterified atelocollagen and hyaluronic acid |
US8617240B2 (en) | 2010-11-17 | 2013-12-31 | Charles D. Hightower | Moldable cushion for implants |
KR101047512B1 (en) | 2011-04-20 | 2011-07-08 | (주)다림티센 | The method of producing an anti-adhesion using non-chemical cross-linking of the esterified atelocollagen and hyaluronic acid |
WO2020197955A1 (en) | 2019-03-22 | 2020-10-01 | Dsm Ip Assets B.V. | Nasal dressings and stents |
CN114191609A (en) * | 2021-12-09 | 2022-03-18 | 成都汉丁新材料科技有限公司 | Collagen microfiber sponge and preparation method thereof |
Citations (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4140537A (en) * | 1975-10-22 | 1979-02-20 | Collagen Corporation | Aqueous collagen composition |
US4280954A (en) * | 1975-07-15 | 1981-07-28 | Massachusetts Institute Of Technology | Crosslinked collagen-mucopolysaccharide composite materials |
US4448718A (en) * | 1983-09-13 | 1984-05-15 | Massachusetts Institute Of Technology | Method for the preparation of collagen-glycosaminoglycan composite materials |
US4851521A (en) * | 1985-07-08 | 1989-07-25 | Fidia, S.P.A. | Esters of hyaluronic acid |
US4937270A (en) * | 1987-09-18 | 1990-06-26 | Genzyme Corporation | Water insoluble derivatives of hyaluronic acid |
US4957744A (en) * | 1986-10-13 | 1990-09-18 | Fidia, S.P.A. | Cross-linked esters of hyaluronic acid |
US5017229A (en) * | 1990-06-25 | 1991-05-21 | Genzyme Corporation | Water insoluble derivatives of hyaluronic acid |
US5527893A (en) * | 1987-09-18 | 1996-06-18 | Genzyme Corporation | Water insoluble derivatives of polyanionic polysaccharides |
US5658582A (en) * | 1993-02-12 | 1997-08-19 | Fidia Advanced Biopolymers S.R.L. | Multilayer nonwoven tissue containing a surface layer comprising at least one hyaluronic acid ester |
US5824335A (en) * | 1991-12-18 | 1998-10-20 | Dorigatti; Franco | Non-woven fabric material comprising auto-crosslinked hyaluronic acid derivatives |
US6294202B1 (en) * | 1994-10-06 | 2001-09-25 | Genzyme Corporation | Compositions containing polyanionic polysaccharides and hydrophobic bioabsorbable polymers |
US6458889B1 (en) * | 1995-12-18 | 2002-10-01 | Cohesion Technologies, Inc. | Compositions and systems for forming crosslinked biomaterials and associated methods of preparation and use |
US20030091646A1 (en) * | 2001-06-21 | 2003-05-15 | Shokyu Gen | Medical materials sterilized by radiation and their ways in use |
US20030187381A1 (en) * | 2001-12-28 | 2003-10-02 | Genzyme Corporation | Bioresorbable foam packing device and use thereof |
US6632802B2 (en) * | 1996-08-29 | 2003-10-14 | Fidia Advanced Biopolymers S.R.L. | Hyaluronic acid esters, threads and biomaterials containing them, and their use in surgery |
US6723709B1 (en) * | 1995-08-29 | 2004-04-20 | Fidia Advanced Biopolymers, S.R.L. | Biomaterials for preventing post-surgical adhesions comprised of hyaluronic acid derivatives |
US20060057182A1 (en) * | 2004-09-10 | 2006-03-16 | Medtronic Xomed, Inc. | Flexible bioresorbable hemostatic packing and stent having a preselectable in-vivo residence time |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1238043A (en) | 1983-12-15 | 1988-06-14 | Endre A. Balazs | Water insoluble preparations of hyaluronic acid and processes therefor |
US6732709B1 (en) * | 2002-12-06 | 2004-05-11 | Caterpillar Inc | Dynamic engine timing control |
-
2004
- 2004-09-10 US US10/938,999 patent/US7858107B2/en active Active
-
2010
- 2010-11-30 US US12/956,709 patent/US20110070285A1/en not_active Abandoned
-
2017
- 2017-01-11 US US15/403,419 patent/US20170119920A1/en not_active Abandoned
Patent Citations (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4280954A (en) * | 1975-07-15 | 1981-07-28 | Massachusetts Institute Of Technology | Crosslinked collagen-mucopolysaccharide composite materials |
US4140537A (en) * | 1975-10-22 | 1979-02-20 | Collagen Corporation | Aqueous collagen composition |
US4448718A (en) * | 1983-09-13 | 1984-05-15 | Massachusetts Institute Of Technology | Method for the preparation of collagen-glycosaminoglycan composite materials |
US4851521A (en) * | 1985-07-08 | 1989-07-25 | Fidia, S.P.A. | Esters of hyaluronic acid |
US4957744A (en) * | 1986-10-13 | 1990-09-18 | Fidia, S.P.A. | Cross-linked esters of hyaluronic acid |
US4937270A (en) * | 1987-09-18 | 1990-06-26 | Genzyme Corporation | Water insoluble derivatives of hyaluronic acid |
US5527893A (en) * | 1987-09-18 | 1996-06-18 | Genzyme Corporation | Water insoluble derivatives of polyanionic polysaccharides |
US5017229A (en) * | 1990-06-25 | 1991-05-21 | Genzyme Corporation | Water insoluble derivatives of hyaluronic acid |
US5824335A (en) * | 1991-12-18 | 1998-10-20 | Dorigatti; Franco | Non-woven fabric material comprising auto-crosslinked hyaluronic acid derivatives |
US5658582A (en) * | 1993-02-12 | 1997-08-19 | Fidia Advanced Biopolymers S.R.L. | Multilayer nonwoven tissue containing a surface layer comprising at least one hyaluronic acid ester |
US6294202B1 (en) * | 1994-10-06 | 2001-09-25 | Genzyme Corporation | Compositions containing polyanionic polysaccharides and hydrophobic bioabsorbable polymers |
US6723709B1 (en) * | 1995-08-29 | 2004-04-20 | Fidia Advanced Biopolymers, S.R.L. | Biomaterials for preventing post-surgical adhesions comprised of hyaluronic acid derivatives |
US6458889B1 (en) * | 1995-12-18 | 2002-10-01 | Cohesion Technologies, Inc. | Compositions and systems for forming crosslinked biomaterials and associated methods of preparation and use |
US6632802B2 (en) * | 1996-08-29 | 2003-10-14 | Fidia Advanced Biopolymers S.R.L. | Hyaluronic acid esters, threads and biomaterials containing them, and their use in surgery |
US20030091646A1 (en) * | 2001-06-21 | 2003-05-15 | Shokyu Gen | Medical materials sterilized by radiation and their ways in use |
US20030187381A1 (en) * | 2001-12-28 | 2003-10-02 | Genzyme Corporation | Bioresorbable foam packing device and use thereof |
US20060057182A1 (en) * | 2004-09-10 | 2006-03-16 | Medtronic Xomed, Inc. | Flexible bioresorbable hemostatic packing and stent having a preselectable in-vivo residence time |
Non-Patent Citations (1)
Title |
---|
The Free Dictionary, available at http://www.thefreedictionary.com/foam. * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106880872A (en) * | 2016-12-23 | 2017-06-23 | 北京大清生物技术股份有限公司 | Natural extracellular matrix biomembrane and preparation method and application |
Also Published As
Publication number | Publication date |
---|---|
US20060057182A1 (en) | 2006-03-16 |
US20170119920A1 (en) | 2017-05-04 |
US7858107B2 (en) | 2010-12-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US8313762B2 (en) | Flexible bioresorbable hemostatic packing and stent | |
US20170119920A1 (en) | Method of making flexible bioresorbable hemostatic packing and stent having a preselectable in-vivo residence time | |
US20230270914A1 (en) | Haemostatic material | |
US9533005B2 (en) | Modified starch material of biocompatible hemostasis | |
JP6720279B2 (en) | Denatured collagen | |
US11712495B2 (en) | Hemostatic mixture of cellulose-based short and long fibers | |
KR101649792B1 (en) | Polymer Foam Composition for Noncompression Hemostasis, Method Of Producing Polymer for Noncompression Hemostasis Foam Using The Same, And Polymer Foam for Packing Noncompression Hemostasis Therefrom | |
CZ20032198A3 (en) | Process for preparing collagen sponge, apparatus for separating a portion of collagen foam and elongate collagen sponge | |
KR20020011955A (en) | A conglutination inhibitor | |
WO2020021499A1 (en) | Haemostatic gel composition and its process of preparation | |
GB2553260A (en) | A ready-to-use, hydrophilic, self-dispersive, fragmentable and biodegradable porous sponge matrix and a method of manufacturing thereof | |
JP2011046749A (en) | Fragmented polymeric hydrogel for adhesion prevention, and preparation thereof | |
CZ20003631A3 (en) | Sterilization process of native collagen in a liquid medium, obtained sterile native collagen, preparations containing thereof and its use |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- AFTER EXAMINER'S ANSWER OR BOARD OF APPEALS DECISION |