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- W2007297553 abstract "Abstract Cytocompatible polymers are of increasing importance for tissue engineering scaffolds and implanted devices. Polyurethane (PU) membranes were modified by grafting polymerization of methacrylic acid (MAA) initiated by UV light and further covalent immobilization of gelatin or arginine‐glycine‐aspartic (RGD) peptide using 1‐ethyl‐3‐(3‐dimethylaminopropyl) carbodiimide hydrochloride as a condensing agent. The immobilization of gelatin or RGD peptide was confirmed by FTIR attenuated total reflection (ATR) spectroscopy and X‐ray photoelectron spectroscopy (XPS). The results for endothelial cells cultured in vitro proved that the PU membrane modified with gelatin or RGD peptide had better cytocompatibility than the control PU or the PMAA grafted PU membrane. ATR‐FTIR spectra of PU‐ graft ‐PMAA (a), PU‐ graft ‐PMAA‐ graft ‐RGD (b), and their subtraction result (c). The PMAA grafting degree is 21.56 × 10 −2 mg/cm 2 . magnified image ATR‐FTIR spectra of PU‐ graft ‐PMAA (a), PU‐ graft ‐PMAA‐ graft ‐RGD (b), and their subtraction result (c). The PMAA grafting degree is 21.56 × 10 −2 mg/cm 2 ." @default.
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- W2007297553 date "2003-04-01" @default.
- W2007297553 modified "2023-10-14" @default.
- W2007297553 title "Surface Immobilization of Bioactive Molecules on Polyurethane for Promotion of Cytocompatibility to Human Endothelial Cells" @default.
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- W2007297553 doi "https://doi.org/10.1002/mabi.200390020" @default.
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