Synthesis of ceramic-polymer-drug biocomposites at room temperature

The preparation of hard composites by the free radical polymerization at room temperature of a blend of β-tricalcium phosphate, poly(ethyl methacrylate), methyl methacrylate monomer and fosfosal ® is described. After the immersion of the composites in a buffered solution, the controlled release of a...

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Published inSolid state ionics Vol. 101; no. pt 2; pp. 887 - 892
Main Authors Vallet-Regí, M., Gordo, M., Ragel, C.V., Cabañas, M.Y., Román, J.San
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.11.1997
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Abstract The preparation of hard composites by the free radical polymerization at room temperature of a blend of β-tricalcium phosphate, poly(ethyl methacrylate), methyl methacrylate monomer and fosfosal ® is described. After the immersion of the composites in a buffered solution, the controlled release of an analgesic drug, fosfosal, is observed. The ceramic component participates actively in the control of the release of the drug by means of the formation of a bridging complex with the fosfosal, as demonstrated by FTIR studies.
AbstractList The preparation of hard composites by the free radical polymerization at room temperature of a blend of beta -tricalcium phosphate, poly(ethyl methacrylate), methyl methacrylate monomer and fosfosal is described. After the immersion of the composites in a buffered solution, the controlled release of an analgesic drug, fosfosal, is observed. The ceramic component participates actively in the control of the release of the drug by means of the formation of a bridging complex with the fosfosal, as demonstrated by FTIR studies.
The preparation of hard composites by the free radical polymerization at room temperature of a blend of β-tricalcium phosphate, poly(ethyl methacrylate), methyl methacrylate monomer and fosfosal ® is described. After the immersion of the composites in a buffered solution, the controlled release of an analgesic drug, fosfosal, is observed. The ceramic component participates actively in the control of the release of the drug by means of the formation of a bridging complex with the fosfosal, as demonstrated by FTIR studies.
Author Cabañas, M.Y.
Román, J.San
Gordo, M.
Ragel, C.V.
Vallet-Regí, M.
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Issue pt 2
Keywords Drug release
Polymerization at room temperature
Ceramic-drug complex
β-Tricalcium phosphate
Poly(ethyl methacrylate)
Methyl methacrylate
Biocomposites
Fosfosal
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Hench (BIB1) 1991; 208
Ko (BIB3) 1989; 3
Park (BIB5) 1995
Constantino, Friedman (BIB8) 1994; 27
Jarcho, Salsbury, Thomas, Doremus (BIB6) 1979; 14
Elvira, Levenfe, Vázquez, Román (BIB9) 1996; 34
Román (BIB10) 1990; 413
Nakamoto (BIB14) 1986
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Snippet The preparation of hard composites by the free radical polymerization at room temperature of a blend of β-tricalcium phosphate, poly(ethyl methacrylate),...
The preparation of hard composites by the free radical polymerization at room temperature of a blend of beta -tricalcium phosphate, poly(ethyl methacrylate),...
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StartPage 887
SubjectTerms Biocomposites
Ceramic materials
Ceramic-drug complex
Controlled drug delivery
Drug products
Drug release
Fourier transform infrared spectroscopy
Free radical polymerization
Monomers
Polymer blends
Polymerization at room temperature
Polymethyl methacrylates
Synthesis (chemical)
Title Synthesis of ceramic-polymer-drug biocomposites at room temperature
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