WO1997025936A1 - Buffered resorbable internal fixation devices for repair of bone fractures - Google Patents
Buffered resorbable internal fixation devices for repair of bone fractures Download PDFInfo
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- WO1997025936A1 WO1997025936A1 PCT/US1997/000215 US9700215W WO9725936A1 WO 1997025936 A1 WO1997025936 A1 WO 1997025936A1 US 9700215 W US9700215 W US 9700215W WO 9725936 A1 WO9725936 A1 WO 9725936A1
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- bioerodible
- polymer
- buffer
- implantable material
- lactide
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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
- A61L27/58—Materials at least partially resorbable by the body
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1611—Inorganic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1617—Organic compounds, e.g. phospholipids, fats
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1629—Organic macromolecular compounds
- A61K9/1641—Organic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, poloxamers
- A61K9/1647—Polyesters, e.g. poly(lactide-co-glycolide)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2009—Inorganic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/2027—Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/2031—Organic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, polyethylene oxide, poloxamers
- A61K9/204—Polyesters, e.g. poly(lactide-co-glycolide)
-
- 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
- A61L27/14—Macromolecular materials
- A61L27/18—Macromolecular materials obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2210/00—Particular material properties of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
- A61F2210/0004—Particular material properties of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof bioabsorbable
Definitions
- This invention relates to the field of implantable internal fixation devices for repair of bone fractures, and more specifically to resorbable bone implant biomaterials which contain a buffering compound.
- Biopolymers such as pol (glycolic acid) (PGA) , poly(lactide) (PLA) , and copolymers of lactic and glycolic acids, (poly(lactide-co-glycolide) or PLGA) have been used in the production of internal fixation devices, such as screws, pins, and rods to hold bone together following surgery, or to repair broken bones.
- Other polymers such as poly(dioxanone) , have also been considered for use in the manufacture of surgical internal fixation devices.
- tissue response to resorbable implants fabricated from these biopolymers is not uniformly acceptable (Bostman, J. Bone and Joint Surg. 23, 148-153 (1991)).
- the inflammatory reaction is not limited to poly(glycolide) polymers. Internal fixation devices made from poly(lactide) have also been observed to exhibit an inflammatory reaction.
- Eitenmuller et al. reports that 9 of 19 patients (47.7%) who had fractures of the ankle treated with absorbable plates and screws of poly(lactide) had an inflammatory response. (J. Eitenmuller, A. David, A. Pomoner, and G. Muhyr: "Dieretencing von Sprunggelenlzsfrakturen awake suddenly von Platten und ringen aus resorbserbarem Polymermaterial", Read attentagung der Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen Deutschen
- the bioerodible materials and methods of the invention include a bioerodible polymer that forms acidic products as it degrades.
- the bioerodible polymer undergoes hydrolysis in the body and generates acidic products that cause irritation, inflammation, and swelling (sterile abscess formation) in the treated area.
- a buffer is included in the bioerodible material to neutralize the acidic degradation products and thereby reduce the sterile abscess reaction.
- the buffer included in the bioerodible material of the invention maintains the pH surrounding the area of surgery to approximately neutrality
- the bioerodible material includes a bioerodible polymer that undergoes hydrolysis to produce acidic products when exposed to an aqueous medium.
- the PLGA polymers used according to the invention have a lactide to glycolide ratio in the range of 0:100% to 100:0%, inclusive, i.e., the PLGA polymer can consist of 100% lactide, 100% glycolide, or any combination of lactide and glycolide residues. These polymers have the property of degrading hydrolytically to form lactic and glycolic acids.
- the buffering compound included in the bioerodible material of the invention may be any base capable of reacting with the acidic products generated upon hydrolysis of the bioerodible polymer.
- Exemplary buffering materials that may be implemented according to the invention include the salts of inorganic acids, the salts of organic acids, or the salts of polymeric organic acids.
- the calcium salts of weak acids are used, such as calcium carbonate, although calcium phosphates, calcium acetates, calcium citrates and calcium succinates may also be used.
- the buffering compound has an acid dissociation constant that is smaller than the acid dissociation constant of the acidic products generated upon hydrolysis of the bioerodible polymer.
- the buffering compound preferably has a hydrolysis constant that is greater than the hydrolysis constant of the acidic products.
- the buffering compound included in the material of the invention is only partially soluble in an aqueous medium.
- buffers of lower solubility are preferred because buffer loss from the polymer by diffusion will be minimized (Gresser and Sanderson, "Basis for Design of biodegradable Polymers for Sustained Release of Biologically Active Agents" in Biopoly eric Controlled Release Systems. Ch. 8, D.L. Wise, Ed., CRC Press, 1984).
- the invention also includes methods of making a buffered bioerodible material for implantation into a surgical site.
- the method according to the invention includes the steps of dissolving a bioerodible polymer in a solvent, and mixing a buffering compound with the dissolved bioerodible polymer, the buffering compound capable of buffering the acidic products within a desired pH range.
- the resulting mixture is cast into a sheet, and the solvent is evaporated to produce a buffered bioerodible implantable material in film form.
- the resulting film may be further processed, for example, compacted under pressure, extruded through a die, injection molded, or shaped into a form useful for bone repair.
- the method according to the invention includes mixing dry, solid bioerodible polymer particles of a specific size with dry, solid buffering compound particles of a specific size, and mixing the bioerodible polymer particles and the buffering compound particles in a desired proportion. This mixture may then be processed as described above.
- the method of the invention includes providing an open celled bioerodible foam polymer of controlled density and providing a buffer dissolved in a solvent wherein the foam polymer is not soluble in the solvent, such as described in U.S. Pat. No. 5,456,917 to Wise et al., the whole of which is incorporated by reference herein.
- the buffer is loaded into the foam polymer, and the loaded foam polymer is freeze dried to remove the solvent.
- the resulting loaded bioerodible polymer may be further ground into particles of a predetermined size, extruded through a die, or shaped into useful forms.
- the method of the invention includes providing a bioerodible polymer having a melting temperature and producing acidic products upon hydrolytic degradation, providing buffer particles comprising buffer material coated with a polymer having a melting temperature greater than the melting temperature of the bioerodible polymer.
- the bioerodible polymer is heated to a temperature between the melting temperatures of the bioerodible polymer and the coating polymer, and the heated bioerodible polymer is mixed with the coated buffer particles. The mixture is then cooled and processed into useful forms.
- bioerodible is defined as the susceptibility of a biomaterial to degradation over time, usually months.
- buffer is defined as any material which limits changes in the pH in the implant and its near environment only slightly upon exposure to acid or base.
- the term “acidic products” is defined herein as any product that has a pH less than 7.
- the invention relates to the field of internal fixation devices (IFD) used for surgical repair of orthopaedic and maxillofacial fractures.
- IFD internal fixation devices
- the invention is a bioerodible implantable material, comprising a bioerodible polymer capable of producing acidic products upon hydrolytic degradation, and a buffering compound that buffers the acidic products within a desired pH range.
- the bioerodible material of the invention includes at least one bioerodible polymer that undergoes hydrolysis to produce acidic products when exposed to an aqueous medium.
- the PLGA polymer can consist of 100% lactide, 100% glycolide, or any combination of lactide and glycolide. This polymer has the property of degrading hydrolytically to form organic acids (lactic acid and glycolic acid) which accumulate in the region surrounding the implant.
- the buffering compound included in the bioerodible material of the invention includes base capable of reacting with the acidic products generated upon hydrolysis of the bioerodible polymer.
- Exemplary buffering materials that may be implemented according to the invention include the salts of inorganic acids, organic acids, or polymeric organic acids.
- the calcium salts of weak acids are used, such as calcium carbonate, although calcium phosphates, calcium acetates, calcium citrates and calcium succinates may also be used.
- the buffering compound has an acid dissociation constant that is smaller than the acid dissociation constant of the acidic products generated upon hydrolysis of the bioerodible polymer.
- Ionic buffers will, in general, be the salts of weak acids.
- the acid, of which the buffer is a salt should have an ionization constant (acid dissociation constant, Ka) which is less than the Ka for the acid products of polymer hydrolysis.
- Ka acid dissociation constant
- the buffering compound has a hydrolysis constant that is greater than the hydrolysis constant of the acidic products.
- a preferred buffering compound is calcium carbonate.
- calcium carbonate forms a calcium salt, carbon dioxide (C0 2 ) , and water (H 2 0) according to the following equation:
- Gaseous carbon dioxide generated from the neutralization reaction is observed to be absorbed by the surrounding aqueous medium.
- the solubility of gaseous C0 2 in water at 760 mm Hg and 37°C is approximately 0.95 mg/ml (Merck Index, 1989) .
- gaseous C0 2 dissolves in and is eliminated from tissue fluids.
- free acid generation from the polymers of the invention proceeds slowly.
- degradation of the polymer component is the rate limiting step in the reaction, and even during the period of most rapid degradation, generation of acidic products occurs slowly. The slow rate of degradation and associated acid production gives carbon dioxide ample time to dissolve in the surrounding fluids.
- the amount of calcium carbonate required to be loaded into a bioerodible polymer matrix to neutralize a given quantity of lactic and glycolytic acids can be estimated by calculating the moles of monomeric acid produced at 100% hydrolysis.
- PLGA any composition (i.e., -[-0-CH(CH 3 )- C0-] x -[0-CH 2 -C0-] (1 . x) , where x and y are the fractions of lactide and glycolide respectively, the molecular weight of the lactide component is 72 g/mol and the molecular weight of the glycolide component is 58 g/mol) , the average monomer residue molecular weight is
- the fraction of calcium carbonate buffer loaded into the polymer matrix is 43.5% by weight. Similar determinations can be calculated for other polymer and buffer combinations and are within the skills of the ordinary skilled practicioner. Other calculations may also be made, for example, calculation of the amount of buffer required to neutralize a percentage of the acid groups generated upon hydrolysis.
- An appropriate buffer should have a low aqueous solubility so that it will not be rapidly lost by dissolution.
- the basic component of the buffer (the anion) should react easily with the protons of the acid products of hydrolysis.
- Letting B" represent the buffer anion and L " the lactate (or glycolic) anion, the equilibrium can be expressed as: HL + B " ⁇ L + HB
- HB must be a weaker acid than HL (or B " must be a stronger base than L”) .
- Ka ionization constants of the respective acids
- the H 2 P0 4 ' anion has an acid dissociation constant of approximately 6.31 x IO" 8 whereas the various racemates of lactic acid have dissociation constants in the range of approximately 1.38 x 10" to 1.62 x IO" 4 . Taking 1.5 x 10"* as a mean value, the equilibrium constant for the above reaction may be calculated as:
- Buffers are included in the polymer in solid form preferably should have a relatively small particle size, for example, between less than 1.0 and 250 ⁇ m. Particle size reduction can be accomplished by any standard means known in the art, such as ball milling, hammer milling, air milling, etc. If buffer and polymer are to be blended by the dry mixing method (described below) , the polymer particle size must also be considered. Polymers such as the PLGAs have relatively low glass transition temperatures and melting temperatures. Thus, polymer particle size reduction must be accompanied by cooling, for example using a Tekmar A-10 mill with a cryogenic attachment.
- the desired particle size range of the buffer and the polymer may be recovered by sieving through, for example, U.S. Standard sieves. Particles in the size ranges of ⁇ 45, 45-90, 90-125, 125-180, 180-250 ⁇ m may be conveniently isolated.
- particle size range it is sometimes desirable to combine two or more ranges, or to use a wide range of sizes, for instance all sizes less than 250 ⁇ m.
- Several methods may be used to incorporate the buffer into the polymer. These methods include solution casting coupled with solvent evaporation, dry mixing, incorporating the buffer into a polymer foam, and the polymer melt method.
- This method may be used with buffers which are either soluble or insoluble in the solvent.
- the polymer is dissolved in any suitable volatile solvent, such as acetone, tetrahydrofuran (THF) , or methylene chloride.
- THF tetrahydrofuran
- the buffer which may be soluble or insoluble in this solvent, is added to give the final desired ratio of polymer to buffer. If particle size reduction of the buffer is necessary, it may be accomplished by ball milling the suspension of buffer in the polymer solution. In contrast, if the buffer is soluble in the chosen solvent, particle size reduction at any stage is not necessary.
- the suspension or co-solution is cast as a film on a glass or other inert surface, and the solvent is removed by air drying.
- Residual solvent remaining in the film may be further removed by subjecting the film to vacuum drying at elevated temperatures.
- the buffer content of the composition should be 27.8%.
- to prepare 50 grams of composite 36.1 grams of PLGA-50:50 are dissolved in approximately 250 ml of tetrahydrofuran, and 13.9 grams of calcium carbonate of the desired particle size range is added to the solution mixture. After distributing the calcium carbonate homogeneously by mixing, the suspension is dried to a film as described above.
- the resulting film may be processed by compaction under high pressure, extruded through a die, injection molded, or other method known in the art. Further definition of the final shape may be accomplished at this point by any desirable machining process, such as lathing.
- a polymer of appropriate particle size range is mixed with the buffer, also of chosen particle size range, in proportions to give the desired stoichiometric buffering capacity.
- the dry mixture is thoroughly blended by rotating the mixture in a ball mill jar from which the grinding balls have been omitted, or other suitable mixing device.
- the blended mixture may then be processed by compaction, extrusion, injection molding, etc., as described above.
- An open celled polymer foam of controlled density may be formed by lyophilization of a polymer solution as described in U.S. Pat. No. 5,456,917 to Wise et al., the whole of which is incorporated by reference herein.
- open celled PLGA-85:15 foams i.e., foams with 85% lactide and 15% glycolide by weight
- the density and void volume of the foam is a function of the initial polymer solution as shown in TABLE 1.
- buffers which are soluble in a solvent which does not dissolve the polymer foam are preferred, such as water soluble buffers or low molecular weight alcohols, such as ethanol.
- the weight fraction of the buffer in the polymer/buffer composite, f will depend on both absolute density of the polymer, d p , the density of the foam, d f , and the concentration of the buffer in the solvent, C. This dependency is given by the loading equation:
- TABLE 2 shows loading of PLGA-85:15 foams prepared from acetic acid solutions with the anti-tuberculosis drug isoniazid dissolved in water. Results of these loading experiments are given in TABLE 2.
- a buffer solution comprising a chosen buffer in a suitable solvent is forced into the pores of the open celled foam by repeated cycles of evacuation (degassing) and repressurization (by emitting air at atmospheric pressure or higher) .
- excess solution is drained off and the saturated foam is subjected to a second lyophilization to remove the solvent.
- the polymer/buffer composite may be processed as described above.
- a known weight of the buffer is incorporated by mixing into a known weight of a suitable melted polymer.
- a quantity of polymer is heated to a temperature above its melting point, and a suitable buffer is blended into the melted polymer.
- the resulting polymer/buffer composite is solidified by cooling, and may be processed as described above, or ground and sieved prior to processing.
- the buffering compound may be desirable to protect the buffering compound, for example, during processing according to the melt method, or to make the buffering compound available at the later stages of polymer degradation.
- Exemplary materials used to coat the buffering compound particles include high molecular weight poly(L-lactide) or poly(e-caprolactone) .
- the particles of buffering compound may be coated with the protective material by any method that coats particles, such as spray coating with a solution of protecting polymer or microencapsulation.
- a chosen protective polymer may be made in a melted state and buffer particles are added.
- the melt is cooled and ground and milled to the desired particle size range.
- the buffering compound may be added to a solution of the protective polymer and removing the solvent by evaporation.
- the dried mass is compacted in a mold under high pressure and grinding or milling the compacted mass to the appropriate particle size range.
- PLGA polymers are used in the preceeding examples, one of ordinary skill in the art will appreciate that other polymers, such as polydioxanone, poly(e- caprolactone) ; polyanhydrides; poly(ortho esters) ; copoly(ether-esters) ; polyamides; polylactones; poly(propylene fumarates) ; and combinations thereof, may be similarly processed according to the methods of the invention.
- selection of a particular polymer is based primarily on the known properties of the polymer such as the degree of cross-linking, polymer strength, polymerization rate, rate of hydrolytic degradation, etc.
- One of ordinary skill in the art may take these and/or other properties into account in selecting a particular polymer for a particular application. Thus, such a selection of a particular polymer is within the skills of the ordinary skilled practioner.
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Abstract
A bioerodible implantable material, comprising a bioerodible poly(lactide-co-glycolide) polymer that produces acidic products upon hydrolytic degradation, and a buffering compound that buffers the acidic products and maintains the local pH within a desired range. The buffer compound acts to reduce the inflammatory foreign body response generated by the acidic products and reduces the sterile abscess condition that occurs at the site of the bioerodible implant materials of the prior art. Materials made according to the invention may be used for internal fixation devices (IFDs) for bone repair.
Description
BUFFERED RESORBABLE INTERNAL FIXATION DEVICES FOR REPAIR OF BONE FRACTURES
FIELD OF THE INVENTION This invention relates to the field of implantable internal fixation devices for repair of bone fractures, and more specifically to resorbable bone implant biomaterials which contain a buffering compound.
BACKGROUND OF THE INVENTION The trend in internal fixation devices for repair of damaged bone is toward the use of resorbable, tissue compatible biopolymers. Biopolymers such as pol (glycolic acid) (PGA) , poly(lactide) (PLA) , and copolymers of lactic and glycolic acids, (poly(lactide-co-glycolide) or PLGA) have been used in the production of internal fixation devices, such as screws, pins, and rods to hold bone together following surgery, or to repair broken bones. Other polymers, such as poly(dioxanone) , have also been considered for use in the manufacture of surgical internal fixation devices. However, it has been observed that tissue response to resorbable implants fabricated from these biopolymers is not uniformly acceptable (Bostman, J. Bone and Joint Surg. 23, 148-153 (1991)).
The tissue response to biopolymer-based implants has been well documented. Late sterile inflammatory foreign body response (sterile abscess) has been reported in about 8% of fractures repaired with these polymers (Bostman, supra) . In a randomized study of 56 open reduction and internal fixation of malleolar fractures of the ankle with metal ASIF screws and plates or with rods of PLGA, two cases of sterile inflammatory wound sinus were observed 3 to 4 months after the operation in the injuries fixed with the polymer rods (Rokkanen et al., Lancet I, 1422-1425 (1985); Bostman et al., J. Bone and Joint Surg., 69-BC4.. 615-619 (1987)). Other
studies have also documented an inflammatory reaction following implantation of PGA or PLGA fixation devices. The fraction of patients suffering from this reaction ranges from 4.6 to 22.5% (Bostman et al., Clin. Orthop. 238, 195-203 (1989); Bostman et al., Intemat. Orthop. 14., 1-8 (1990); Hirvensalo et al., Acta Orthop. Scandinavica, Supplementum 227. 78-79 (1988); Hoffman et al., Unfallchirurgie 91, 430- 434 (1989); Partio et al., Acta Orthop. Scandinavica, Supplementum 237, 43-44 (1990); Bostman et al., Intemat. Orthop. 2Aι -8 (1990)). The inflammatory reaction is not limited to poly(glycolide) polymers. Internal fixation devices made from poly(lactide) have also been observed to exhibit an inflammatory reaction. Eitenmuller et al. reports that 9 of 19 patients (47.7%) who had fractures of the ankle treated with absorbable plates and screws of poly(lactide) had an inflammatory response. (J. Eitenmuller, A. David, A. Pomoner, and G. Muhyr: "Die Versorgung von Sprunggelenlzsfrakturen unter Verwendung von Platten und Schrauben aus resorbserbarem Polymermaterial", Read at Jahrestagung der Deutschen Gesellschaft fur Unfallheilkunde, Berlin, Nov. 22, 1989).
In vitro studies have been performed to monitor pH changes as well as weight loss and the appearance of lactic acid from screws fabricated from poly(lactide-co-glycolide) with a lactide:glycolide ratio of 85:15. (Vert et al., J. Controlled Release 16, 15-26 (1991)). An induction period of about ten weeks was observed before any significant change in media pH or weight loss occurred. This time period corresponds to the induction periods of seven to twenty weeks noted by clinicians. However, no attempt has been made to alleviate the source of inflammation.
SUMMARY OF THE INVENTION The invention is a bioerodible implantable material, comprising a bioerodible polymer that produces acidic products upon hydrolytic degradation, and a buffering
compound that buffers the acidic products and maintains the local pH within a desired range. The buffer compound incorporated into the material of the invention acts to neutralize the acidic degradation products which cause inflammatory foreign body response upon degradation of the bioerodible polymer. Thus, the invention reduces the sterile abscess condition that occurs in the bioerodible implant materials of the prior art. Materials made according to the invention may be used for internal fixation devices (IFDs) for bone repair.
The bioerodible materials and methods of the invention include a bioerodible polymer that forms acidic products as it degrades. The bioerodible polymer undergoes hydrolysis in the body and generates acidic products that cause irritation, inflammation, and swelling (sterile abscess formation) in the treated area. To counteract this effect, a buffer is included in the bioerodible material to neutralize the acidic degradation products and thereby reduce the sterile abscess reaction. The buffer included in the bioerodible material of the invention maintains the pH surrounding the area of surgery to approximately neutrality
(i.e., pH 7) , or any other pH chosen by the surgeon.
Preferably, the pH is maintained in the range of 6-8, and more preferably in the range of 6.8-7.4. According to the invention, the bioerodible material includes a bioerodible polymer that undergoes hydrolysis to produce acidic products when exposed to an aqueous medium. The bioerodible polymers useful in the invention include polydioxanone, poly(c-caprolactone) ; polyanhydrides; poly(ortho esters); copoly(ether-esters) ; polyamides; polylactones; poly(propylene fumarates) (H[-0-CH(CH3)-CH2-0- CH=CH-CO-]nOH) ; and combinations thereof. In a preferred embodiment, the polymer poly(lactide-co-glycolide) (H[-OCHR- CO-]„OH, R=H, CH3) (PLGA) is used. The PLGA polymers used according to the invention have a lactide to glycolide ratio in the range of 0:100% to 100:0%, inclusive, i.e., the PLGA
polymer can consist of 100% lactide, 100% glycolide, or any combination of lactide and glycolide residues. These polymers have the property of degrading hydrolytically to form lactic and glycolic acids. The buffering compound included in the bioerodible material of the invention may be any base capable of reacting with the acidic products generated upon hydrolysis of the bioerodible polymer. Exemplary buffering materials that may be implemented according to the invention include the salts of inorganic acids, the salts of organic acids, or the salts of polymeric organic acids. Preferably, the calcium salts of weak acids are used, such as calcium carbonate, although calcium phosphates, calcium acetates, calcium citrates and calcium succinates may also be used. Preferably, the buffering compound has an acid dissociation constant that is smaller than the acid dissociation constant of the acidic products generated upon hydrolysis of the bioerodible polymer. Alternatively, the buffering compound preferably has a hydrolysis constant that is greater than the hydrolysis constant of the acidic products.
Preferably, the buffering compound included in the material of the invention is only partially soluble in an aqueous medium. In general, buffers of lower solubility are preferred because buffer loss from the polymer by diffusion will be minimized (Gresser and Sanderson, "Basis for Design of biodegradable Polymers for Sustained Release of Biologically Active Agents" in Biopoly eric Controlled Release Systems. Ch. 8, D.L. Wise, Ed., CRC Press, 1984).
The invention also includes methods of making a buffered bioerodible material for implantation into a surgical site. In one embodiment, the method according to the invention includes the steps of dissolving a bioerodible polymer in a solvent, and mixing a buffering compound with the dissolved bioerodible polymer, the buffering compound capable of buffering the acidic products within a desired pH range. The resulting mixture is cast into a sheet, and the solvent is
evaporated to produce a buffered bioerodible implantable material in film form. The resulting film may be further processed, for example, compacted under pressure, extruded through a die, injection molded, or shaped into a form useful for bone repair.
In another embodiment, the method according to the invention includes mixing dry, solid bioerodible polymer particles of a specific size with dry, solid buffering compound particles of a specific size, and mixing the bioerodible polymer particles and the buffering compound particles in a desired proportion. This mixture may then be processed as described above.
In another embodiment, the method of the invention includes providing an open celled bioerodible foam polymer of controlled density and providing a buffer dissolved in a solvent wherein the foam polymer is not soluble in the solvent, such as described in U.S. Pat. No. 5,456,917 to Wise et al., the whole of which is incorporated by reference herein. The buffer is loaded into the foam polymer, and the loaded foam polymer is freeze dried to remove the solvent. The resulting loaded bioerodible polymer may be further ground into particles of a predetermined size, extruded through a die, or shaped into useful forms.
In another embodiment, the method of the invention includes providing a bioerodible polymer having a melting temperature and producing acidic products upon hydrolytic degradation, providing buffer particles comprising buffer material coated with a polymer having a melting temperature greater than the melting temperature of the bioerodible polymer. The bioerodible polymer is heated to a temperature between the melting temperatures of the bioerodible polymer and the coating polymer, and the heated bioerodible polymer is mixed with the coated buffer particles. The mixture is then cooled and processed into useful forms. As used herein, the term "bioerodible" is defined as the susceptibility of a biomaterial to degradation over time,
usually months. The term "buffer" is defined as any material which limits changes in the pH in the implant and its near environment only slightly upon exposure to acid or base. The term "acidic products" is defined herein as any product that has a pH less than 7.
DETAILED DESCRIPTION OF THE INVENTION The invention relates to the field of internal fixation devices (IFD) used for surgical repair of orthopaedic and maxillofacial fractures. The invention is a bioerodible implantable material, comprising a bioerodible polymer capable of producing acidic products upon hydrolytic degradation, and a buffering compound that buffers the acidic products within a desired pH range. The bioerodible material of the invention includes at least one bioerodible polymer that undergoes hydrolysis to produce acidic products when exposed to an aqueous medium. The bioerodible polymers useful in the invention include, but are not limited to, polydioxanone (H[-0-CHR-CO-]nOH) ; poly(e- caprolactone) ; polyanhy-drides; poly(ortho esters); copoly(ether-esters) ; polyamides; polylactones; poly(propylene fumarates) (H[-0-CH(CH3)-CH2-0-CH=CH-CO-]nOH) ; and combinations thereof. A preferred polymer material useful in the invention is poly(lactide-co-glycolide) (H[- OCHR-CO-]nOH, R=H, CH3) with a lactide to glycolide ratio in the range of 0:100% to 100:0%. Accordingly, the PLGA polymer can consist of 100% lactide, 100% glycolide, or any combination of lactide and glycolide. This polymer has the property of degrading hydrolytically to form organic acids (lactic acid and glycolic acid) which accumulate in the region surrounding the implant.
The buffering compound included in the bioerodible material of the invention includes base capable of reacting with the acidic products generated upon hydrolysis of the bioerodible polymer. Exemplary buffering materials that may be implemented according to the invention include the salts
of inorganic acids, organic acids, or polymeric organic acids. Preferably, the calcium salts of weak acids are used, such as calcium carbonate, although calcium phosphates, calcium acetates, calcium citrates and calcium succinates may also be used.
In general, buffers of lower solubility are preferred because buffer loss from the polymer by diffusion will be slower (Gresser and Sanderson, supra) . Preferably, the buffering compound has an acid dissociation constant that is smaller than the acid dissociation constant of the acidic products generated upon hydrolysis of the bioerodible polymer. Ionic buffers will, in general, be the salts of weak acids. The acid, of which the buffer is a salt, should have an ionization constant (acid dissociation constant, Ka) which is less than the Ka for the acid products of polymer hydrolysis. Altematively, the buffering compound has a hydrolysis constant that is greater than the hydrolysis constant of the acidic products.
According to the invention, a preferred buffering compound is calcium carbonate. Upon reaction with an acid, calcium carbonate forms a calcium salt, carbon dioxide (C02) , and water (H20) according to the following equation:
2R-C02H + CaC03 ► (R-C02)2Ca + H20 + C02.
Gaseous carbon dioxide generated from the neutralization reaction is observed to be absorbed by the surrounding aqueous medium. The solubility of gaseous C02 in water at 760 mm Hg and 37°C is approximately 0.95 mg/ml (Merck Index, 1989) . Thus, upon being generated in situ , gaseous C02 dissolves in and is eliminated from tissue fluids. In addition, free acid generation from the polymers of the invention proceeds slowly. Thus, degradation of the polymer component is the rate limiting step in the reaction, and even during the period of most rapid degradation, generation of acidic products occurs slowly. The slow rate of degradation
and associated acid production gives carbon dioxide ample time to dissolve in the surrounding fluids.
The amount of calcium carbonate required to be loaded into a bioerodible polymer matrix to neutralize a given quantity of lactic and glycolytic acids can be estimated by calculating the moles of monomeric acid produced at 100% hydrolysis. For PLGA of any composition (i.e., -[-0-CH(CH3)- C0-]x-[0-CH2-C0-](1.x), where x and y are the fractions of lactide and glycolide respectively, the molecular weight of the lactide component is 72 g/mol and the molecular weight of the glycolide component is 58 g/mol) , the average monomer residue molecular weight is
72x + 58(l-x) = 14x + 58
Thus, one gram of PLGA-50:50 (where x = 0.5) will generate approximately 0.0154 moles of monomeric acid upon hydrolysis. Referring to the neutralization reaction above, the amount of calcium carbonate buffer needed to neutralize this quantity of acid is 0.0077 moles, or 0.77 grams (mol. wt. of CaC03 = 100 g/mol) . Thus, the fraction of calcium carbonate buffer loaded into the polymer matrix is 43.5% by weight. Similar determinations can be calculated for other polymer and buffer combinations and are within the skills of the ordinary skilled practicioner. Other calculations may also be made, for example, calculation of the amount of buffer required to neutralize a percentage of the acid groups generated upon hydrolysis.
An appropriate buffer should have a low aqueous solubility so that it will not be rapidly lost by dissolution. The basic component of the buffer (the anion) should react easily with the protons of the acid products of hydrolysis. Letting B" represent the buffer anion and L" the lactate (or glycolic) anion, the equilibrium can be expressed as:
HL + B" ^ L + HB
In other words, HB must be a weaker acid than HL (or B" must be a stronger base than L") . These relationships may be expressed quantitatively by ionization constants of the respective acids (Ka) :
Ka™ < Ka"1- Thus a viable buffer would be CaHP04 (dibasic calcium phosphate) . The reaction of lactic acid with the anion, HP04 is: HL + HP04 "2 ^ L" + H2P04 "
The H2P04' anion has an acid dissociation constant of approximately 6.31 x IO"8 whereas the various racemates of lactic acid have dissociation constants in the range of approximately 1.38 x 10" to 1.62 x IO"4. Taking 1.5 x 10"* as a mean value, the equilibrium constant for the above reaction may be calculated as:
# ""e_,e„/ = = 2.4 x 103 it***0*
Thus, the equilibrium lies to the right and protons produced by ionization of lactic or glycolic acids will be removed by the buffer.
Buffers are included in the polymer in solid form preferably should have a relatively small particle size, for example, between less than 1.0 and 250 μm. Particle size reduction can be accomplished by any standard means known in the art, such as ball milling, hammer milling, air milling, etc. If buffer and polymer are to be blended by the dry mixing method (described below) , the polymer particle size must also be considered. Polymers such as the PLGAs have relatively low glass transition temperatures and melting temperatures. Thus, polymer particle size reduction must be
accompanied by cooling, for example using a Tekmar A-10 mill with a cryogenic attachment.
Following milling, the desired particle size range of the buffer and the polymer may be recovered by sieving through, for example, U.S. Standard sieves. Particles in the size ranges of <45, 45-90, 90-125, 125-180, 180-250 μm may be conveniently isolated.
In selection of particle size range, it is sometimes desirable to combine two or more ranges, or to use a wide range of sizes, for instance all sizes less than 250 μm.
Larger particles may be preferred in some applications of the invention because larger particles take longer to be eroded by the acids and will therefore extend the useful lifetime of the buffer. In some cases particle size reduction will not be necessary, such as when commercially available precipitated calcium carbonate is used (e.g.. Fisher
Scientific, Inc., Catalog No. C-63)
Several methods may be used to incorporate the buffer into the polymer. These methods include solution casting coupled with solvent evaporation, dry mixing, incorporating the buffer into a polymer foam, and the polymer melt method.
Method 1. Solution Casting - Solvent Evaporation
This method may be used with buffers which are either soluble or insoluble in the solvent. The polymer is dissolved in any suitable volatile solvent, such as acetone, tetrahydrofuran (THF) , or methylene chloride. The buffer, which may be soluble or insoluble in this solvent, is added to give the final desired ratio of polymer to buffer. If particle size reduction of the buffer is necessary, it may be accomplished by ball milling the suspension of buffer in the polymer solution. In contrast, if the buffer is soluble in the chosen solvent, particle size reduction at any stage is not necessary. The suspension or co-solution is cast as a film on a glass or other inert surface, and the solvent is removed by
air drying. Residual solvent remaining in the film may be further removed by subjecting the film to vacuum drying at elevated temperatures. As an example, if calcium carbonate is to be used as a buffering compound and it is desired to neutralize 50% of the acid formed by hydrolysis of PLGA- 50:50, the buffer content of the composition should be 27.8%. In an exemplary embodiment, to prepare 50 grams of composite, 36.1 grams of PLGA-50:50 are dissolved in approximately 250 ml of tetrahydrofuran, and 13.9 grams of calcium carbonate of the desired particle size range is added to the solution mixture. After distributing the calcium carbonate homogeneously by mixing, the suspension is dried to a film as described above.
The resulting film may be processed by compaction under high pressure, extruded through a die, injection molded, or other method known in the art. Further definition of the final shape may be accomplished at this point by any desirable machining process, such as lathing.
Method 2. Dry-Mixing
A polymer of appropriate particle size range is mixed with the buffer, also of chosen particle size range, in proportions to give the desired stoichiometric buffering capacity. The dry mixture is thoroughly blended by rotating the mixture in a ball mill jar from which the grinding balls have been omitted, or other suitable mixing device. The blended mixture may then be processed by compaction, extrusion, injection molding, etc., as described above.
Method 3. Incorporating the Buffer into a Polymer Foam
This method deposits the buffer as microcrystals within the pores of a foamed polymer. An open celled polymer foam of controlled density may be formed by lyophilization of a polymer solution as described in U.S. Pat. No. 5,456,917 to Wise et al., the whole of which is incorporated by reference herein. For example, open celled PLGA-85:15 foams (i.e.,
foams with 85% lactide and 15% glycolide by weight) with different morphologies are created by lyophilization of frozen solutions of the polymer from either benzene or glacial acetic acid. The density and void volume of the foam is a function of the initial polymer solution as shown in TABLE 1.
TABLE 1
FOAM DENSITY AS A FUNCTION OF SOLUTION CONCENTRATION
Concentration of Density of Foam, mg/cm3 solution, mg/ml
30.0 43.0
40.0 60.1
45.0 65.0
50.0 70.1±0.9
66.7 87.5
In this method, buffers which are soluble in a solvent which does not dissolve the polymer foam are preferred, such as water soluble buffers or low molecular weight alcohols, such as ethanol. The weight fraction of the buffer in the polymer/buffer composite, f, will depend on both absolute density of the polymer, dp, the density of the foam, df, and the concentration of the buffer in the solvent, C. This dependency is given by the loading equation:
f = [1 + dfd„/C(dp-df)]-'
TABLE 2 shows loading of PLGA-85:15 foams prepared from acetic acid solutions with the anti-tuberculosis drug isoniazid dissolved in water. Results of these loading experiments are given in TABLE 2.
TABLE 2
INH CONTENT (WEIGHT PERCENT. IN FOAMS AS A FUNCTION OF INH SOLUTION CONCENTRATION AND FOAM DENSITY
INH Soln. Foam Density, mg/cm3 Cone. , 43.0 70.1 87.5 mg/ml
13.0 20.0'(22.8b) 21.5 26.5 (32.8) 29.4 35.0 (44.0) 5.1 6.0 (6.5) 11.5 12.0 (13.6) 25.0 24.7 (25.5) 10.0 9.0 (9.8) 21.5 18.4 (18.9) 39.5 28.0 (30.0)
a) Measured values of loading. b) Loadings as predicted by the loading equation.
A buffer solution comprising a chosen buffer in a suitable solvent is forced into the pores of the open celled foam by repeated cycles of evacuation (degassing) and repressurization (by emitting air at atmospheric pressure or higher) . After the foam has been impregnated with the buffer solution, excess solution is drained off and the saturated foam is subjected to a second lyophilization to remove the solvent. Following this loading process, the polymer/buffer composite may be processed as described above.
Method 4. Polyroer Melt
A known weight of the buffer is incorporated by mixing into a known weight of a suitable melted polymer. A quantity of polymer is heated to a temperature above its melting point, and a suitable buffer is blended into the melted polymer. The resulting polymer/buffer composite is
solidified by cooling, and may be processed as described above, or ground and sieved prior to processing.
In some applications, it may be desirable to protect the buffering compound, for example, during processing according to the melt method, or to make the buffering compound available at the later stages of polymer degradation. In such cases, it is desirable to coat the buffering compound particles with a material that degrades at a slower rate than the material chosen for the fixation devices. Thus, the buffering compound is exposed only after the body of the device and the coating material have partially degraded. Exemplary materials used to coat the buffering compound particles include high molecular weight poly(L-lactide) or poly(e-caprolactone) . The particles of buffering compound may be coated with the protective material by any method that coats particles, such as spray coating with a solution of protecting polymer or microencapsulation. Alternatively, a chosen protective polymer may be made in a melted state and buffer particles are added. The melt is cooled and ground and milled to the desired particle size range. Altematively, the buffering compound may be added to a solution of the protective polymer and removing the solvent by evaporation. The dried mass is compacted in a mold under high pressure and grinding or milling the compacted mass to the appropriate particle size range.
Although PLGA polymers are used in the preceeding examples, one of ordinary skill in the art will appreciate that other polymers, such as polydioxanone, poly(e- caprolactone) ; polyanhydrides; poly(ortho esters) ; copoly(ether-esters) ; polyamides; polylactones; poly(propylene fumarates) ; and combinations thereof, may be similarly processed according to the methods of the invention. Moreover, selection of a particular polymer is based primarily on the known properties of the polymer such as the degree of cross-linking, polymer strength,
polymerization rate, rate of hydrolytic degradation, etc. One of ordinary skill in the art may take these and/or other properties into account in selecting a particular polymer for a particular application. Thus, such a selection of a particular polymer is within the skills of the ordinary skilled practioner.
Having showed the preferred embodiments, those skilled in the art will realize many variations are possible which will still be within the spirit and scope of the claimed invention. Therefore, it is the intention to limit the invention only as indicated by the scope of the claims.
Claims
1. A bioerodible implantable material, comprising: a bioerodible polymer, said bioerodible polymer producing acidic products upon hydrolytic degradation; and a buffering compound which buffers said acidic products within a desired pH range.
2. The bioerodible implantable material of claim 1, wherein said bioerodible polymer is selected from the group consisting of polydioxanone, poly(e-caprolactone) , polyanhydride, poly(ortho ester), copoly(ether-ester) , polyamide, polylactone, poly(propylene fumarate) , and combinations thereof.
3. The bioerodible implantable material of claim 1, wherein said bioerodible polymer comprises poly(lactide-co-glycolide) with a lactide to glycolide ratio in the range of 0:100% to 100:0% inclusive.
4. The bioerodible implantable material of claim 1, wherein said buffering compound is the salt of an inorganic acid.
5. The bioerodible implantable material of claim 1, wherein said buffering compound is the salt of an organic acid.
6. The bioerodible implantable material of claim 5, wherein said organic acid is polymeric.
7. The bioerodible implantable material of claim 1, wherein said buffering compound is selected from the group consisting of carbonates, phosphates, acetates, succinates, and citrates.
8. The bioerodible, implantable material of claim 1, wherein said buffering compound is a calcium salt.
9. The bioerodible, implantable material of claim 1, wherein said buffering compound is calcium carbonate.
10. The bioerodible implantable material of claim 1, wherein the parent acid of said buffering compound has an acid dissociation constant that is smaller than the acid dissociation constant of said acidic products.
11. The bioerodible implantable material of claim 1, wherein said buffering compound has a hydrolysis constant that is greater than the hydrolysis constant of said acidic products.
12. A method of making a buffered bioerodible, implantable material, comprising the steps of: dissolving a bioerodible polymer in a solvent, said bioerodible polymer producing acidic products upon hydrolytic degradation; mixing a buffer compound with said dissolved bioerodible polymer, said buffer capable of buffering said acidic products within a desired pH range; casting said mixture; and evaporating said solvent of said mixture to produce a buffered bioerodible implantable material.
13. The method of claim 12, wherein said bioerodible polymer is selected from the group consisting of polydioxanone, poly(e-caprolactone) , polyanhydride, poly(ortho ester), copoly(ether-ester) , polyamide, polylactone, poly(propylene fumarate), and combinations thereof.
14. The bioerodible implantable material of claim 12, wherein said bioerodible polymer comprises poly(lactide-co- glycolide) with a lactide to glycolide ratio in the range of 0:100% to 100:0% inclusive.
15. The method of claim 12, further comprising the step of milling said buffer compound in said polymer solution.
16. The method of claim 12, further comprising the step of processing said buffered bioerodible implantable material into a desired form.
17. The method of claim 12, further comprising the step of coating said buffer compound with a polymeric material that degrades at a slower rate than PLGA.
18. A method for making a buffered bioerodible implantable
PLGA material, comprising the steps of: providing bioerodible polymer particles having a specific size, said bioerodible polymer producing acidic products upon hydrolytic degradation; providing buffer particles having a specific size, said buffer particles comprising a buffer capable of buffering said acidic products; and mixing said bioerodible polymer particles and said buffer particles in a predetermined proportion.
19. The bioerodible implantable material of claim 18, wherein said bioerodible polymer particles comprise poly(lactide-co-glycolide) with a lactide to glycolide ratio in the range of 0:100% to 100:0% inclusive.
20. The method of claim 18, further comprising the step of processing said buffered bioerodible implantable material into a desired form.
21. The method of claim 18, further comprising the step of coating said buffer particles with a polymeric material that degrades at a slower rate than PLGA.
22. A method for making a buffered bioerodible implantable material, comprising the steps of: providing an open celled bioerodible foam polymer of controlled density, said bioerodible foam polymer producing acidic products upon hydrolytic degradation; providing a buffer compound dissolved in a solvent, said foam polymer not soluble in said solvent, said buffer compound capable of buffering said acidic products; loading said buffer compound dissolved in said solvent into said PLGA foam polymer; and freeze drying said buffer loaded foam polymer to remove said solvent.
23. The method of claim 22, further comprising the step of processing said buffered bioerodible implantable material into a desired form.
24. The method of claim 22, further comprising the step of coating said buffer particles with a polymeric material that degrades at a slower rate than PLGA.
25. The method of claim 22, wherein said bioerodible polymer comprises poly(lactide-co-glycolide) with a lactide to glycolide ratio in the range of 100:0 to 0:100 inclusive.
26. A method for making a buffered bioerodible implantable material, comprising the steps of: providing a bioerodible polymer having a first melting temperature, said bioerodible polymer producing acidic products upon hydrolytic degradation; providing buffer particles comprising buffer material coated with a protective polymer, said protective polymer having a second melting temperature, said second melting temperature greater than said first melting temperature, said buffer particles comprising a buffer capable of buffering said acidic products; heating said bioerodible polymer to a temperature between said first melting temperature and said second melting temperature; mixing said heated bioerodible polymer and said coated buffer particles; and cooling said mixture.
27. The method of claim 26, further comprising the step of processing said buffered bioerodible implantable material into a desired form.
28. The method of claim 26, wherein said bioerodible polymer comprises poly(lactide-co-glycolide) with a lactide to glycolide ratio in the range of 100:0 to 0:100 inclusive.
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WO2008118782A3 (en) * | 2007-03-23 | 2009-04-30 | Smith & Nephew Inc | Fixation devices and method of repair |
US9000066B2 (en) | 2007-04-19 | 2015-04-07 | Smith & Nephew, Inc. | Multi-modal shape memory polymers |
US9120919B2 (en) | 2003-12-23 | 2015-09-01 | Smith & Nephew, Inc. | Tunable segmented polyacetal |
US9770534B2 (en) | 2007-04-19 | 2017-09-26 | Smith & Nephew, Inc. | Graft fixation |
US9815240B2 (en) | 2007-04-18 | 2017-11-14 | Smith & Nephew, Inc. | Expansion moulding of shape memory polymers |
CN112587506A (en) * | 2020-12-09 | 2021-04-02 | 南京森博医药研发有限公司 | Method for preparing mesalazine enteric sustained-release capsule |
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US5397572A (en) * | 1990-03-05 | 1995-03-14 | Board Of Regents, The University Of Texas System | Resorbable materials based on independently gelling polymers of a single enantiomeric lactide |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9120919B2 (en) | 2003-12-23 | 2015-09-01 | Smith & Nephew, Inc. | Tunable segmented polyacetal |
WO2008118782A3 (en) * | 2007-03-23 | 2009-04-30 | Smith & Nephew Inc | Fixation devices and method of repair |
US9815240B2 (en) | 2007-04-18 | 2017-11-14 | Smith & Nephew, Inc. | Expansion moulding of shape memory polymers |
US9000066B2 (en) | 2007-04-19 | 2015-04-07 | Smith & Nephew, Inc. | Multi-modal shape memory polymers |
US9308293B2 (en) | 2007-04-19 | 2016-04-12 | Smith & Nephew, Inc. | Multi-modal shape memory polymers |
US9770534B2 (en) | 2007-04-19 | 2017-09-26 | Smith & Nephew, Inc. | Graft fixation |
CN112587506A (en) * | 2020-12-09 | 2021-04-02 | 南京森博医药研发有限公司 | Method for preparing mesalazine enteric sustained-release capsule |
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