PROPERTIES OF SILK FIBROIN/POLY(ETHYLENE GLYCOL)400 BLEND FILMS

来源 :Chinese Journal of Polymer Science | 被引量 : 0次 | 上传用户:kcb2639
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The blend film of silk fibroin (SF) and poly(ethylene glycol)400 (PEG400) with a blend ratio of 2/1 (wt/wt) wasprepared simply by dropping a little PEG400 into the SF solution and then casting the mixed aqueous solution at 50℃. Theresulting film exhibited much better mechanical properties in the dry and wet state than SF itself, owing to theconformational change of SF in the blends from the random coil to the β-sheet structure and intermolecular hydrogen bondformation between SF and PEG400. Thermogravimetric analysis showed that the initial thermal decomposition temperatureof the blend film was 170℃, which was 80℃ lower than that of SF (250℃) and 20℃ higher than that of PEG400 (150℃),and indicated a Strong interaction between two components of the blend. No crystalline peaks were observed in the X-raydiffraction curve of the blend film. Cell culture test showed that SF/PEG400 was a suitable substrate for the growth of humanumbilical vein endothelial cells (HUVEC). The blend film of silk fibroin (SF) and poly (ethylene glycol) 400 (PEG400) with a blend ratio of 2/1 (wt / wt) wasprepared simply by dropping a little PEG400 into the SF solution and then casting the mixed aqueous solution at 50 ° C. Theresulting film exhibits much better mechanical properties in the dry and wet state than SF itself, due to the formation of SF in the blends from the random coil to the β-sheet structure and intermolecular hydrogen bondformation between SF and PEG 400. Thermogravimetric analysis showed that the initial thermal decomposition temperature of the blend film was 170 ° C, which was 80 ° C lower than that of SF (250 ° C) and 20 ° C higher than that of PEG400 (150 ° C), and indicated a Strong interaction between two components of the blend. No crystalline peaks were observed in the X-raydiffraction curve of the blend film. Cell culture test showed that SF / PEG400 was a suitable substrate for the growth of humanumbilical vein endothelial cells (HUVEC).
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