Abstract
The chemical modification of polyamide66 (PA66) membrane by graft polymerization with methacrylic acid (MAA) was initiated under ultraviolet light. Subsequently, covalent immobilization of bioactive surface was obtained by coupling gelatin to the MAA graft chains with the aid of a waterβsoluble carbodiimide (WSC). The existence of carboxyl groups grafted on PA66 surface was verified quantitatively by UVβvis spectroscopy. The chemical composition, surface topography, and wettability were investigated by Fourier transform infrared (FTIR) technique, Xβray photoelectron spectroscopy, atomic force microscopy, and water contact angle (WCA) measurement. Results showed that the WCA changed from the original value of 67.5Β° to the minimum value of 30Β° after grafting with PMAA. Original PA66 displayed a smooth surface morphology [root mean square (RMS) roughness was around 16 nm]. The modified PA66 surface exhibited an increase in roughness (RMS roughness around 21 nm). Simultaneously, the original and modified PA66 membranes were cultured with MG63 cells to investigate their cytocompatibility. The in vitro biological evaluation demonstrated that the immobilization of gelatin on PA66 membrane acted as a good template for the attachment and proliferation of cells. Also, the less toxic reagents and the moderate reaction conditions involved will be very helpful for the introduction of functional groups onto polymer surface. Β© 2009 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2009