WO2005061611A1 - Compositions of semi-interpenetrating polymer network - Google Patents
Compositions of semi-interpenetrating polymer network Download PDFInfo
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- WO2005061611A1 WO2005061611A1 PCT/GB2004/005443 GB2004005443W WO2005061611A1 WO 2005061611 A1 WO2005061611 A1 WO 2005061611A1 GB 2004005443 W GB2004005443 W GB 2004005443W WO 2005061611 A1 WO2005061611 A1 WO 2005061611A1
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- 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
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/50—Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
- A61L27/52—Hydrogels or hydrocolloids
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
- C08B37/0006—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
- C08B37/0024—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid beta-D-Glucans; (beta-1,3)-D-Glucans, e.g. paramylon, coriolan, sclerotan, pachyman, callose, scleroglucan, schizophyllan, laminaran, lentinan or curdlan; (beta-1,6)-D-Glucans, e.g. pustulan; (beta-1,4)-D-Glucans; (beta-1,3)(beta-1,4)-D-Glucans, e.g. lichenan; Derivatives thereof
- C08B37/0027—2-Acetamido-2-deoxy-beta-glucans; Derivatives thereof
- C08B37/003—Chitin, i.e. 2-acetamido-2-deoxy-(beta-1,4)-D-glucan or N-acetyl-beta-1,4-D-glucosamine; Chitosan, i.e. deacetylated product of chitin or (beta-1,4)-D-glucosamine; Derivatives thereof
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/24—Crosslinking, e.g. vulcanising, of macromolecules
- C08J3/246—Intercrosslinking of at least two polymers
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L5/00—Compositions of polysaccharides or of their derivatives not provided for in groups C08L1/00 or C08L3/00
- C08L5/08—Chitin; Chondroitin sulfate; Hyaluronic acid; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2303/00—Characterised by the use of starch, amylose or amylopectin or of their derivatives or degradation products
- C08J2303/02—Starch; Degradation products thereof, e.g. dextrin
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2305/00—Characterised by the use of polysaccharides or of their derivatives not provided for in groups C08J2301/00 or C08J2303/00
- C08J2305/02—Dextran; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2305/00—Characterised by the use of polysaccharides or of their derivatives not provided for in groups C08J2301/00 or C08J2303/00
- C08J2305/04—Alginic acid; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2305/00—Characterised by the use of polysaccharides or of their derivatives not provided for in groups C08J2301/00 or C08J2303/00
- C08J2305/08—Chitin; Chondroitin sulfate; Hyaluronic acid; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/02—Applications for biomedical use
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/04—Polymer mixtures characterised by other features containing interpenetrating networks
Definitions
- the present invention relates to hydrogel compositions comprising crosslinked basic polysaccharides formed as semi interpenetrating networks where the basic polysaccharide is crosslinked in the presence of an acidic polysaccharide.
- the basic polysaccharide is chitosan or a derivative thereof and the acidic polysaccharide is hyaluronic acid (HA) or a derivative thereof.
- Biocompatible polysaccharide compounds are widely used in the biomedical field. To achieve extended residence times in vivo, these compounds are often chemically modified, usually by crosslinking, to form a polymer network.
- HA hyaluronic acid
- Hyaluronic acid is an extremely important component of connective tissue and because of its excellent biocompatibility, it has been the subject of many attempts to crosslink the molecule through both its hydroxyl and carboxyl moieties.
- crosslinking does change the chemical structure of the polymer and, for example when used in soft tissue augmentation, cells in the connective tissue which are influenced in their development, migration and proliferation by the milieu in which they are found are exposed to a hyaluronic acid polymer network which is not normally found there.
- biomaterial could have application as a mimetic of the extra cellular matrix if other polysaccharide components of the natural extra cellular matrix such as chondroitin, dermatan and keratin sulphates were incorporated into the polymer network.
- Chitosan an amino group containing basic polysaccharide, a derivative of the biopolymer chitin, is well reported in the scientific literature as having excellent biocompatibility and is used in a number of biomedical applications.
- US patent No 6,379,702 discloses a blend of chitosan and a hydrophilic poly(N- vinyl lactam). This document does not disclose any crosslinking of the chitosan or the formation of a semi IPN.
- US patent No 6,224,893 discloses compositions for forming a semi interpenetrating or interpenetrating polymer networks for drug delivery and tissue engineering whereby the semi IPN is prepared from synthetic and/or natural polymers with a photoinitiator where crosslinking is initiated by free radical generation by electromagnetic radiation.
- US patent No 5,644,049 discloses a biomaterial comprising an interpenetrating polymer network whereby one of the components, an acidic polysaccharide, is crosslinked to a second component, a synthetic chemical polymer to create an infinite network. There is no disclosure of crosslinking of acidic polysaccharides with basic polysaccharides.
- US patent No 5,620,706 discloses a biomaterial comprising a polyionic complex of xanthan and chitosan for encapsulation and controlled release of biologically active substances. There is no disclosure of covalently crosslinking basic polysaccharides with acidic polysaccharides.
- the present invention provides a composition consisting of a semi interpenetrating polymer network, which comprises at least one crosslinked water soluble derivative of a basic polysaccharide, which has primary and/or secondary amine groups, and a non crosslinked component, which comprises at least one anionic polysaccharide, wherein the anionc polysaccharide resides within the semi interpenetrating polymer network.
- a semi interpenetrating polymer network is a combination of at least two polymers formed by covalently crosslinking at least one of the polymers in the presence of but not to the other polymer(s) and having at least one of the polymers in the network as a linear or branched uncrosslinked polymer.
- a basic cationic polysaccharide is a polysaccharide containing at least one functional group which is capable of undergoing ionisation to form a cation, eg a protonated amine group
- an acidic anionic polysaccharide is a polysaccharide containing at least one functional group which is capable of undergoing ionisation to form an anion, eg a carboxylate or sulphate ion.
- compositions of the present invention find use as biomaterials, which can be formulated for instance as hydrogels, which in turn can be placed in soft tissue as a mimetic of the extra cellular matrix.
- the water soluble derivative of a basic polysaccharide is a derivative of chitosan, in particular, N-Carboxy methyl chitosan, O-Carboxy methyl chitosan or O-Hydroxy ethyl chitosan or a partially N- acetylated chitosan.
- the partially N-acetylated chitosan can be produced by partially deacetylating chitin or by reacetylating chitosan.
- the partially N-acetylated chitosan has a degree of acetylation in the range of 45% to 55%.
- the non crosslinked component is hyaluronic acid.
- other anionic polysaccharide components of the extra cellular matrix may be included.
- the crosslinked component of the composition can be crosslinked using crosslinking agents such as diglycidyl ethers, diisocyanates or aldehydes.
- crosslinking agents such as diglycidyl ethers, diisocyanates or aldehydes.
- 1,4- Butanedioldiglycidyl ether (BDDE) can be used.
- BDDE 1,4- Butanedioldiglycidyl ether
- the reaction between the epoxide rings at either end of the BDDE molecule and the amine groups on the chitosan chains occurs by nucleophilic attack by the reactive amine groups with subsequent epoxide ring opening as described in "Chitin in Nature and Technology", R. A. Muzarelli, C. Jeuniaux and G. W. Godday, Plenum Press, New York, 1986, p303.
- compositions of the present invention can be formed into films, sponges, hydrogels, threads or non woven matrices.
- the present invention provides a method for the preparation of a composition of the invention which comprises crosslinking at least one water soluble derivative of a basic polysaccharide containing primary and/or secondary amine groups, in the presence of at least one anionic polysaccharide, under conditions which avoid protonation of said primary or secondary amine groups on the basic polysaccharide and which also avoid reaction of any other functional group on the water soluble anionic polysaccharide.
- compositions of the present invention can be formed into various forms of biomaterials for use in medical applications.
- an injectible hydrogel for use in medical applications.
- aqueous solution of a water soluble derivative of a basic polysaccharide containing primary and/or secondary amine groups is formed, to which is added a water soluble anionic polysaccharide.
- Crosslinking of the basic polysaccharide is then initiated in the presence of a polyfunctional crosslinking agent, under essentially neutral conditions which will only crosslink the primary or substituted amines leaving the anionic polysaccharide entrapped within the crosslinked polymer network.
- aqueous solution of a water soluble derivative of a basic polysaccharide containing primary and/or secondary amine groups is formed, to which is added a water soluble anionic polysaccharide.
- a polyfunctional crosslinking agent is then added and the mixture is allowed to evaporate to dryness to allow the crosslinking reaction to take place.
- Chitosan becomes soluble in aqueous solutions only when protonated with acids.
- the polymer thus formed is positively charged and so will interact with negatively charged species such as hyaluronic acid and other polyanions.
- Such ionic complexes must be avoided in order to form the semi IPN, which is the subject of the present invention.
- chitosan must be solubilised either as an anionic polyelectrolyte or as a non ionic polymer in either a neutral or mildly alkaline medium.
- suitable derivatives include N-Carboxy methyl chitosan, O-Carboxy methyl chitosan, O-Hydroxy ethyl chitosan or partially N-acetylated chitosan.
- approximately 50% re-acetylated chitosan is used since it can be solubilised in neutral media without protonation of the amine groups.
- the re-acetylated chitosan has a degree of deacetylation in the range of 45% to 55% in order to achieve water soluble properties.
- the crosslinking reaction in the presence of the polyfunctional crosslinking agent is generally performed under neutral or mildly alkaline conditions, pH range 7 to 8, which ensures that essentially only the primary or secondary amine groups of the basic polysaccharide can react with the crosslinking agent.
- the degree of crosslinking can be controlled by varying the molar feed ratio of the basic polysaccharide to crosslinking agent. In this way, the release profile of the entrapped anionic polysaccharide can be altered/modified to suit the particular biomedical application in which it is to be used.
- the crosslinking reaction will be carried out around pH 7, preferably between PH 6.8 and 8.
- the present invention provides a biomaterial comprising a composition of the invention.
- the present invention provides the use of a composition or of a biomaterial of the invention in medicine.
- the present invention provides the use of a composition of the invention in the preparation of a biomaterial.
- the biomaterial is for use in dermatology, plastic surgery, urology and in the field of orthopaedics.
- Such biomaterials can be formed into films, sponges, hydrogels, threads or non-woven matrices;
- HA (2g, prepared by fermentation, Hyaltech Ltd) was dissolved in water to give a solution which had a final concentration of 5% weight of polymer. The two solutions were refrigerated overnight to assist the dissolution of the polymers.
- the two polymer solutions were then mixed together on a high shear mixer and 1,4-butanediol diglycidyl ether (2.5g, Sigma) was added and stirred into the polymer mixture using a mechanical stirrer.
- the solution was then crosslinked with mild stirring in a water bath at 50°C for 3 hours.
- the gel formed was then immersed in de-ionised water and allowed to swell until it reached constant weight, during which time the water was replaced 4-5 times to remove unreacted residual crosslinker.
- the water absorption capacity of the gel was 9654% and had a concentration of lOmg/ml of each polymer.
- the sample was homogenised on the high shear mixer to enable the gel to be injected from a syringe through a 30G needle.
- the mean particle size (D4,3) was 302 ⁇ m.
- the sample had a G' elastic modulus value of 500 to 600 Pa measured in oscillatory shear over the frequency range from 0.01 - 10 Hz.
- An in vitro test was carried out to monitor the release of HA from the gel over a prolonged time period. The same experiment was also carried out in the presence of lysozyme. The results are shown below:
- HA (lg, prepared by fermentation, Hyaltech Ltd) was dissolved in water to give a solution which had a concentration of 5% weight of polymer. The two solutions were refrigerated overnight to assist the dissolution of the polymers.
- the two polymer solutions were then mixed together on a high shear mixer and 1,4-butanediol diglycidyl ether (2.5g, Sigma) was added and was stirred into the polymer mixture using a mechanical stirrer.
- the solution was then crosslinked with stirring in a water bath at 50°C for 3 hours.
- the gel formed was subsequently immersed in de-ionised water and allowed to swell until it reached constant weight, during which time the water was replaced 4-5 times to remove any unreacted residual crosslinker.
- the water absorption capacity of the gel was 4551% and gave a concentration of 22mg/ml for re-acetylated chitosan and 12mg/ml for HA.
- the sample was homogenised on the high shear mixer to enable the gel to be injected from a syringe through a 30G needle.
- the mean particle size (D4,3) was 255 ⁇ m.
- the sample had a G' elastic modulus of 2000 to 3000 Pa measured in oscillatory shear over the frequency range from 0.01 - 10 Hz.
- An in vitro test was carried out to monitor the release of HA from the gel over a prolonged time period. The same experiment was also carried out in the presence of lysozyme. The results are shown below:
- HA (2g, prepared by fermentation, Hyaltech Ltd) was dissolved in water to give a solution which had a final concentration of 5% weight of polymer. The two solutions were refrigerated overnight to assist the dissolution of the polymers.
- the two polymer solutions were then mixed together on a high shear mixer and 1,4-butanediol diglycidyl ether (1.7g, Fluka) was added and was stirred into the polymer mixture using a mechanical stirrer.
- the solution was then crosslinked with gentle stirring in a water bath at 50°C for 3 hours.
- the gel formed was subsequently immersed in de-ionised water and allowed to swell until it reached constant weight, during which time the water was replaced 4-5 times to remove unreacted residual crosslinker.
- the water absorption capacity of the gel was 12652% and gave a concentration of 7.9mg/ml for re-acetylated chitosan and 7.5mg/ml for HA.
- O-Hydroxy ethyl chitosan (lg, Sigma) was dissolvedhydrated in de-ionised water to give a solution which had a final concentration of 5% weight of polymer.
- HA (lg, prepared by fermentation, Hyaltech Ltd) was dissolved in water to give a solution which had a final concentration of 5% weight of polymer.
- the two solutions were refrigerated overnight to assist the dissolution of the polymers.
- the two polymer solutions were then mixed together on a high shear mixer and 1,4-butanediol diglycidyl ether (1.5g, Fluka) was added and was stirred into the polymer mixture using a mechanical stirrer.
- the solution was then crosslinked with mild stirring in a water bath at 50°C for 3 hours.
- the gel formed was subsequently immersed in de- ionised water and allowed to swell until it reached constant weight, during which time the water was replaced 4-5 times to wash away the residual crosslinker.
- the water absorption capacity of the gel was 8525% and gave a final concentration of 11.7mg/ml for O-Hydroxy ethyl chitosan and 12.7mg/ml for HA.
- the sample was homogenised using a high shear mixer to enable the gel to be injected from a syringe through a 30G needle.
- the particle size (D4,3) was 205 ⁇ m.
- the sample had a G' elastic modulus of 1000 to 2000 Pa measured in oscillatory shear over the frequency range from 0.01 - 10 Hz.
- HA (0.6g, produced by fermentation, Hyaltech Ltd) was dissolved in water to give a solution which had a final concentration of 5% weight of polymer.
- the two solutions were refrigerated overnight to assist the dissolution of the polymers.
- the two polymer solutions were then mixed together on a high shear mixer and 1,4-butanediol diglycidyl ether (0.96g, Fluka) was added and was stirred into the polymer mixture using a mechanical stirrer.
- the solution was then crosslinked, with stirring, in a water bath at 50°C for 8 hours.
- the gel formed was subsequently immersed in de-ionised water and allowed to swell until it reached constant weight, during which time the water was replaced 4-5 times to remove unreacted residual crosslinker.
- the water absorption capacity of the gel was 9464% and gave a final concentration of llmg/ml for both polymers.
- the sample was homogenised on the high shear mixer to enable the gel to be injected from a syringe through a 30G needle.
- the mean particle size (D4,3) was 218 ⁇ m.
- the sample had a G' elastic modulus value of 600 to 900 Pa measured in oscillatory shear over the frequency range from 0.01 - 10 Hz.
- the concentration of N-Carboxymethyl chitosan and HA was 38mg/ml and 39mg/ml respectively.
- HA (1.9g, prepared by fermentation, Hyaltech Ltd) was dissolved in water to give a solution which had a final concentration of 5% weight of polymer. The two solutions were refrigerated overnight to assist the dissolution of the polymers.
- the two polymer solutions were then mixed together on a high shear mixer and 1,4-butanediol diglycidyl ether (0.7g, Fluka) was added and was stirred into the polymer mixture using a mechanical stirrer.
- the solution was then crosslinked with stirring in a water bath at 50°C for IVi hours.
- the gel formed was subsequently immersed in de-ionised water and allowed to swell over a period of 2-3 days until it reached constant weight, during which time the water was replaced 4-5 times to remove unreacted residual crosslinker.
- the water absorption capacity of the gel was 7995% and gave a concentration of 12.5mg/ml for each polymer.
- the sample was homogenised on the high shear mixer to enable the gel to be injected from a syringe through a 30G needle.
- the mean particle size (D4,3) was 403 ⁇ m.
- the sample had a G' elastic modulus value of 500 to 800 Pa measured in oscillatory shear over the frequency range from 0.01 - 10 Hz.
- HA (O.lg) was added to the O-Hydroxy ethyl chitosan solution and stirred until the HA had dissolved.
- 1,4-Butanediol diglycidyl ether (0.2g, Sigma) was added and was stirred into the polymer mixture. The solution was then transferred to a Petri dish and was allowed to evaporate for 18 hours during which time a crosslinked film was formed. The film was subsequently immersed in de-ionised water and allowed to swell. The water absorption capacity of the film was 151% and gave a concentration of 660mg/ml for O-Hydroxy ethyl chitosan and 388mg/ml for HA. The swelling water was tested for [HA] after 48 hours and resulted in 9.38% of the HA being released. After leaving the film in the swelling water for a further 96 hours no further release of HA was detected.
- Re-acetylated chitosan (0.5g) was dissolvedhydrated— in de-ionised water at a concentration of 2%.
- HA 0.5g, produced by fermentation, Hyaltech Ltd
- BDDE 0.g, Fluka
- the WAC of the film was 258% corresponding to a concentration of 383mg/ml for HA and 387mg/ml for re-acetylated chitosan. After swelling 0.45% of HA was released from the film. After a further 4 days there was no further detectable release of HA .
Abstract
Description
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Priority Applications (10)
Application Number | Priority Date | Filing Date | Title |
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US10/583,888 US20070197754A1 (en) | 2003-12-23 | 2004-12-22 | Compositions of semi-interpenetrating polymer network |
JP2006546331A JP2007516333A (en) | 2003-12-23 | 2004-12-22 | Semi-interpenetrating polymer network composition |
AU2004303599A AU2004303599B2 (en) | 2003-12-23 | 2004-12-22 | Compositions of semi-interpenetrating polymer network |
CA002550906A CA2550906A1 (en) | 2003-12-23 | 2004-12-22 | Compositions of semi-interpenetrating polymer network |
EP04806237A EP1704182A1 (en) | 2003-12-23 | 2004-12-22 | Compositions of semi-interpenetrating polymer network |
BRPI0417974-9A BRPI0417974A (en) | 2003-12-23 | 2004-12-22 | composition, method for preparation thereof, biomaterial, and use of a composition or biomaterial |
CN2004800386904A CN1898315B (en) | 2003-12-23 | 2004-12-22 | Compositions of semi-interpenetrating polymer network |
IL176285A IL176285A0 (en) | 2003-12-23 | 2006-06-13 | Compositions of semi-interpenetrating polymer network |
NO20062960A NO20062960L (en) | 2003-12-23 | 2006-06-23 | Compositions of Semi-Interpenetrating Polymer Network |
US12/947,082 US20110117198A1 (en) | 2003-12-23 | 2010-11-16 | Compositions of semi-interpenetrating polymer network |
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GBGB0329907.0A GB0329907D0 (en) | 2003-12-23 | 2003-12-23 | Compositions |
GB0329907.0 | 2003-12-23 |
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US12/947,082 Continuation US20110117198A1 (en) | 2003-12-23 | 2010-11-16 | Compositions of semi-interpenetrating polymer network |
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WO2005061611A1 true WO2005061611A1 (en) | 2005-07-07 |
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US (2) | US20070197754A1 (en) |
EP (1) | EP1704182A1 (en) |
JP (2) | JP2007516333A (en) |
CN (1) | CN1898315B (en) |
AU (1) | AU2004303599B2 (en) |
BR (1) | BRPI0417974A (en) |
CA (1) | CA2550906A1 (en) |
GB (1) | GB0329907D0 (en) |
IL (1) | IL176285A0 (en) |
NO (1) | NO20062960L (en) |
WO (1) | WO2005061611A1 (en) |
ZA (1) | ZA200605168B (en) |
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US9056316B2 (en) | 2010-06-25 | 2015-06-16 | 3M Innovative Properties Company | Semi-interpenetrating polymer network |
US9314530B2 (en) | 2012-06-13 | 2016-04-19 | Laboratoires Vivacy | Composition, in aqueous medium, that comprises at least a hyaluronic acid and at least an hydrosoluble salt of sucrose octasulfate |
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5496933A (en) | 1993-06-01 | 1996-03-05 | Chemische Fabrik Stockhausen Gmbh | Super-absorbents and a process for their preparation |
US5620706A (en) | 1995-04-10 | 1997-04-15 | Universite De Sherbrooke | Polyionic insoluble hydrogels comprising xanthan and chitosan |
US5658915A (en) | 1990-11-29 | 1997-08-19 | Iatron Laboratories, Inc. | Polyelectrolyte complex antibacterial agent and antibacterial material |
WO2000046252A1 (en) | 1999-02-05 | 2000-08-10 | Vitrolife Uk Limited | Process for cross-linking hyaluronic acid to polymers |
US6224893B1 (en) | 1997-04-11 | 2001-05-01 | Massachusetts Institute Of Technology | Semi-interpenetrating or interpenetrating polymer networks for drug delivery and tissue engineering |
Family Cites Families (36)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3778431A (en) * | 1972-10-16 | 1973-12-11 | Standard Brands Inc | Gelatinizable crosslinked cationic starch and method for its manufacture |
US4501834A (en) * | 1983-12-22 | 1985-02-26 | Colgate-Palmolive Company | Gels formed from anionic and cationic polymers |
SE452469B (en) * | 1986-06-18 | 1987-11-30 | Pharmacia Ab | MATERIALS CONSISTING OF A CROSS-BONDED CARBOXYL-GROUPED POLYSACCHARIDE AND PROCEDURE IN THE PREPARATION OF THE SAME |
US6174999B1 (en) * | 1987-09-18 | 2001-01-16 | Genzyme Corporation | Water insoluble derivatives of polyanionic polysaccharides |
GB8820332D0 (en) * | 1988-08-26 | 1988-09-28 | Allied Colloids Ltd | Graft copolymers |
JPH0352912A (en) * | 1989-07-19 | 1991-03-07 | Nippon Paint Co Ltd | Composite resin particle and production thereof |
US5260002A (en) * | 1991-12-23 | 1993-11-09 | Vanderbilt University | Method and apparatus for producing uniform polymeric spheres |
US5708152A (en) * | 1992-03-27 | 1998-01-13 | Ciba Specialty Chemicals Corporation | N-substituted chitosan derivatives in a process for their preparation |
US5334640A (en) * | 1992-04-08 | 1994-08-02 | Clover Consolidated, Ltd. | Ionically covalently crosslinked and crosslinkable biocompatible encapsulation compositions and methods |
IT1260154B (en) * | 1992-07-03 | 1996-03-28 | Lanfranco Callegaro | HYALURONIC ACID AND ITS DERIVATIVES IN INTERPENETRATING POLYMERS (IPN) |
US6129761A (en) * | 1995-06-07 | 2000-10-10 | Reprogenesis, Inc. | Injectable hydrogel compositions |
US7351421B2 (en) * | 1996-11-05 | 2008-04-01 | Hsing-Wen Sung | Drug-eluting stent having collagen drug carrier chemically treated with genipin |
JPH10139889A (en) * | 1996-11-12 | 1998-05-26 | Jsr Corp | Conjugate |
US5904927A (en) * | 1997-03-14 | 1999-05-18 | Northeastern University | Drug delivery using pH-sensitive semi-interpenetrating network hydrogels |
US6271278B1 (en) * | 1997-05-13 | 2001-08-07 | Purdue Research Foundation | Hydrogel composites and superporous hydrogel composites having fast swelling, high mechanical strength, and superabsorbent properties |
US6018033A (en) * | 1997-05-13 | 2000-01-25 | Purdue Research Foundation | Hydrophilic, hydrophobic, and thermoreversible saccharide gels and forms, and methods for producing same |
US5837752A (en) * | 1997-07-17 | 1998-11-17 | Massachusetts Institute Of Technology | Semi-interpenetrating polymer networks |
PL342996A1 (en) * | 1998-02-23 | 2001-07-16 | Mnemoscience Gmbh | Shape memory polymers |
US6331578B1 (en) * | 1998-11-18 | 2001-12-18 | Josephine Turner | Process for preparing interpenetrating polymer networks of controlled morphology |
GB9902412D0 (en) * | 1999-02-03 | 1999-03-24 | Fermentech Med Ltd | Process |
KR100698559B1 (en) * | 1999-06-11 | 2007-03-21 | 넥타르 테라퓨틱스 에이엘, 코포레이션 | Hydrogels derived from chitosan and polyethylene glycol or related polymers |
DE60026357T2 (en) * | 1999-11-12 | 2006-10-19 | MacroMed, Inc., Sandy | ADDING AND WEIGHING POLYMER MIXTURES |
US20030206958A1 (en) * | 2000-12-22 | 2003-11-06 | Cattaneo Maurizio V. | Chitosan biopolymer for the topical delivery of active agents |
JP3455510B2 (en) * | 2000-10-30 | 2003-10-14 | 紳一郎 西村 | Hybrid fibers and membranes and methods for producing them |
US7625580B1 (en) * | 2000-11-28 | 2009-12-01 | Massachusetts Institute Of Technology | Semi-interpenetrating or interpenetrating polymer networks for drug delivery and tissue engineering |
US6586493B1 (en) * | 2001-03-07 | 2003-07-01 | Arizona Board Of Regents Arizona State University | Polysaccharide-based hydrogels and pre-gel blends for the same |
US20030034304A1 (en) * | 2001-08-17 | 2003-02-20 | Huang Robert Y.M. | N-acetylated chitosan membranes |
CN1210335C (en) * | 2001-09-26 | 2005-07-13 | 天津大学 | Process for preparing dual-layer combined chitosan-gelatin-mucinase scaffold material |
KR100451399B1 (en) * | 2001-11-02 | 2004-10-06 | 주식회사 건풍바이오 | The acetylation method of chitosan |
DK1448607T3 (en) * | 2001-11-15 | 2011-04-26 | Piramal Healthcare Canada Ltd | Composition and method for homogeneous modification or cross-linking of chitosan under neutral conditions |
US7208314B2 (en) * | 2002-02-26 | 2007-04-24 | Mirus Bio Corporation | Compositions and methods for drug delivery using pH sensitive molecules |
WO2003089506A1 (en) * | 2002-04-22 | 2003-10-30 | Purdue Research Foundation | Hydrogels having enhanced elasticity and mechanical strength properties |
US6923961B2 (en) * | 2002-04-30 | 2005-08-02 | Fziomed, Inc. | Chemically activated carboxypolysaccharides and methods for use to inhibit adhesion formation and promote hemostasis |
US7090745B2 (en) * | 2002-09-13 | 2006-08-15 | University Of Pittsburgh | Method for increasing the strength of a cellulosic product |
US7524514B2 (en) * | 2003-12-01 | 2009-04-28 | Tissue Engineering Consultants, Inc. | Biomimetic composition reinforced by a polyelectrolytic complex of hyaluronic acid and chitosan |
US8293890B2 (en) * | 2004-04-30 | 2012-10-23 | Advanced Cardiovascular Systems, Inc. | Hyaluronic acid based copolymers |
-
2003
- 2003-12-23 GB GBGB0329907.0A patent/GB0329907D0/en not_active Ceased
-
2004
- 2004-12-22 CN CN2004800386904A patent/CN1898315B/en not_active Expired - Fee Related
- 2004-12-22 WO PCT/GB2004/005443 patent/WO2005061611A1/en active Application Filing
- 2004-12-22 EP EP04806237A patent/EP1704182A1/en not_active Withdrawn
- 2004-12-22 US US10/583,888 patent/US20070197754A1/en not_active Abandoned
- 2004-12-22 CA CA002550906A patent/CA2550906A1/en not_active Abandoned
- 2004-12-22 BR BRPI0417974-9A patent/BRPI0417974A/en not_active IP Right Cessation
- 2004-12-22 AU AU2004303599A patent/AU2004303599B2/en not_active Ceased
- 2004-12-22 JP JP2006546331A patent/JP2007516333A/en not_active Ceased
-
2006
- 2006-06-13 IL IL176285A patent/IL176285A0/en unknown
- 2006-06-22 ZA ZA200605168A patent/ZA200605168B/en unknown
- 2006-06-23 NO NO20062960A patent/NO20062960L/en not_active Application Discontinuation
-
2010
- 2010-11-16 US US12/947,082 patent/US20110117198A1/en not_active Abandoned
-
2011
- 2011-12-02 JP JP2011264297A patent/JP2012082428A/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5658915A (en) | 1990-11-29 | 1997-08-19 | Iatron Laboratories, Inc. | Polyelectrolyte complex antibacterial agent and antibacterial material |
US5496933A (en) | 1993-06-01 | 1996-03-05 | Chemische Fabrik Stockhausen Gmbh | Super-absorbents and a process for their preparation |
US5620706A (en) | 1995-04-10 | 1997-04-15 | Universite De Sherbrooke | Polyionic insoluble hydrogels comprising xanthan and chitosan |
US6224893B1 (en) | 1997-04-11 | 2001-05-01 | Massachusetts Institute Of Technology | Semi-interpenetrating or interpenetrating polymer networks for drug delivery and tissue engineering |
WO2000046252A1 (en) | 1999-02-05 | 2000-08-10 | Vitrolife Uk Limited | Process for cross-linking hyaluronic acid to polymers |
Non-Patent Citations (1)
Title |
---|
BERGER ET AL., EUROPEAN JOURNAL OF PHANNACEUTICS AND BIOPHARMACEUTICS, vol. 57, 2004, pages 19 - 34 |
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2010511454A (en) * | 2006-12-06 | 2010-04-15 | ピエール、ファブレ、デルモ‐コスメティーク | Hyaluronic acid gel for intradermal injection |
AU2008320877B2 (en) * | 2007-10-30 | 2013-03-14 | Viscogel Ab | Chitosan composition |
WO2009056602A1 (en) * | 2007-10-30 | 2009-05-07 | Viscogel Ab | Chitosan composition |
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US9919076B2 (en) | 2007-12-07 | 2018-03-20 | Laboratoires Vivacy | Biodegradable single-phase cohesive hydrogels |
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US8563066B2 (en) | 2007-12-17 | 2013-10-22 | New World Pharmaceuticals, Llc | Sustained release of nutrients in vivo |
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WO2010080557A1 (en) | 2008-12-17 | 2010-07-15 | New World Pharmaceuticals, Llc | Sustained release of nutrients in vivo |
US9056316B2 (en) | 2010-06-25 | 2015-06-16 | 3M Innovative Properties Company | Semi-interpenetrating polymer network |
US9314530B2 (en) | 2012-06-13 | 2016-04-19 | Laboratoires Vivacy | Composition, in aqueous medium, that comprises at least a hyaluronic acid and at least an hydrosoluble salt of sucrose octasulfate |
EP3508564A4 (en) * | 2016-08-31 | 2020-04-29 | Osaka University | Cell culture carrier, cell culture carrier preparation kit, and method for producing gel/cell hybrid tissue using cell culture carrier and cell culture carrier preparation kit |
Also Published As
Publication number | Publication date |
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US20070197754A1 (en) | 2007-08-23 |
AU2004303599A1 (en) | 2005-07-07 |
NO20062960L (en) | 2006-09-11 |
AU2004303599B2 (en) | 2011-06-23 |
CN1898315A (en) | 2007-01-17 |
EP1704182A1 (en) | 2006-09-27 |
GB0329907D0 (en) | 2004-01-28 |
CN1898315B (en) | 2010-10-20 |
US20110117198A1 (en) | 2011-05-19 |
CA2550906A1 (en) | 2005-07-07 |
IL176285A0 (en) | 2006-10-05 |
JP2012082428A (en) | 2012-04-26 |
ZA200605168B (en) | 2007-10-31 |
JP2007516333A (en) | 2007-06-21 |
BRPI0417974A (en) | 2007-04-17 |
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