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Volumn 977, Issue , 2008, Pages 268-282

An overview of the biocompatibility of polymeric surfaces

Author keywords

[No Author keywords available]

Indexed keywords

BIOCOMPATIBILITY; MEDICAL APPLICATIONS;

EID: 84905583819     PISSN: 00976156     EISSN: 19475918     Source Type: Book Series    
DOI: 10.1021/bk-2008-0977.ch016     Document Type: Conference Paper
Times cited : (3)

References (104)
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    • Polymer definitions are as follows: PDMS - polydimethylsiloxane; PEU - poly(ether urethane); PEO - poly(ethylene oxide); PEG - poly(ethylene glycol); PET -poly(ethylene terephthalate); PC - polycarbonate; COC - cyclic olefin copolymer; PE - polyethylene; PMMA - poly(methyl methacrylate); PTFE - poly(tetrafluoroethylene); PSU - polysulfone; EVA - ethylene vinyl acetate copolymer; PVA - polyvinyl alcohol
    • Prasad Shastri, V. Curr. Pharm. Biotech. 2003, 4, 331-337. Polymer definitions are as follows: PDMS - polydimethylsiloxane; PEU - poly(ether urethane); PEO - poly(ethylene oxide); PEG - poly(ethylene glycol); PET -poly(ethylene terephthalate); PC - polycarbonate; COC - cyclic olefin copolymer; PE - polyethylene; PMMA - poly(methyl methacrylate); PTFE - poly(tetrafluoroethylene); PSU - polysulfone; EVA - ethylene vinyl acetate copolymer; PVA - polyvinyl alcohol).
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    • Sources: U.S. Industrial Outlook and U.S. Industry and Trade Outlook, as reported by
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    • Stryer, L.1
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    • 0004310686 scopus 로고
    • ISO 10993-1, EN 30993-1, Geneva, International Organization for Standardization (ISO), "Required Biocompatibility Training and Toxicology Profiles for Evaluation of Medical Devices, " Blue Book Memorandum G95-1, Rockville, MD, FDA, Center for Devices and Radiological Health (CDRH), Office of Device Evaluation, 1995
    • "Biological Evaluation of Medical Devices, Part 1: Guidance on Selection of Tests, " ISO 10993-1, EN 30993-1, Geneva, International Organization for Standardization (ISO), 1992; "Required Biocompatibility Training and Toxicology Profiles for Evaluation of Medical Devices, " Blue Book Memorandum G95-1, Rockville, MD, FDA, Center for Devices and Radiological Health (CDRH), Office of Device Evaluation, 1995.
    • (1992) Biological Evaluation of Medical Devices, Part 1: Guidance on Selection of Tests
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    • Wu, S.1
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    • Hin, T.S.1
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    • (2006) Polymer , vol.47 , pp. 4210-4217
    • Li, Y.1
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.