http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5626861-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8381805eba6d034fc77bd230dd02e6e2
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61L2430-02
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08L85-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61L27-46
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61L27-46
filingDate 1994-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1997-05-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7780226254493224e544a2faef6149df
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1955283bdb06df7fc16d307c20c5fd91
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fc39fba725bd78e42da18bc225eadc12
publicationDate 1997-05-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5626861-A
titleOfInvention Polymeric-hydroxyapatite bone composite
abstract A method for the fabrication of three-dimensional macroporous polymer matrices for use as bone graft or implant material was developed. The composites are formed from a mixture of biodegradable, biocompatible polymer and hydroxyapatite (HA), a particulate calcium phosphate ceramic. The method leaves irregular pores in the composite between 100 and 250 microns in size. In a preferred embodiment, implants are composed of a 50:50 poly(lactide-co-glycolide) (PLGA) polymer and reinforced by hydroxyapatite. Mechanical and histological analysis showed the matrix fabricated by this method to be structurally and mechanically similar to cancellous bone. Prior to degradation, pure polymer specimens exhibited an elastic modulus of 293 MPa and specimens which were 50% HA by weight exhibited a modulus of 1459 MPa. After six weeks of degradation under physiological conditions, the reinforcing effect of ceramic loading had diminished. Modulus of polymer matrices at all HA load levels had decreased sharply to approximately 10 MPa. Mean macro- and micropore diameters of the polymer specimens were 100 μm and 20 μm respectively and remained constant throughout degradation.
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