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首页> 外文期刊>Macromolecular Research >Preparation of Photoreactive Azidophenyl Hyaluronic Acid Derivative: Protein Immobilization for Medical Applications
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Preparation of Photoreactive Azidophenyl Hyaluronic Acid Derivative: Protein Immobilization for Medical Applications

机译:光反应性叠氮苯基透明质酸衍生物的制备:用于医学应用的蛋白质固定化

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Photoreactive azidophenyl hyaluronic acid (Az-HA) derivative was synthesized to immobilize proteins such as epidermal growth factor (EGF) and bone morphogenetic protein (BMP). The photosensitizing group, 4-azidoaniline, was introduced to the carboxyl group of hyaluronic acid by a water soluble carbodiimide, l-ethyl-3-(3-dimethylamino-propyl)carbodiimide hydrochloride (EDC). To characterize the synthesized Az-HA, Fourier transform infrared (FTTR), proton nuclear magnetic resonance ('H NMR) and ultraviolet/visible (UV/vis) absorbance spectroscopy were performed. We demonstrated protein immobilization by using fluorescein isothiocyanate conjugated albumin (FITC-BSA) on Az-HA derivative surfaces that were patterned with micro scale. Cytotoxicity and relative cell proliferation tests of the Az-HA derivative were performed on an MG-63 human osteoblast cell line for biocompatibility.
机译:合成光反应性叠氮苯基透明质酸(Az-HA)衍生物以固定表皮生长因子(EGF)和骨形态发生蛋白(BMP)等蛋白。通过水溶性碳二亚胺1-乙基-3-(3-二甲基氨基-丙基)碳二亚胺盐酸盐(EDC)将光敏基团4-叠氮基苯胺引入透明质酸的羧基中。为了表征合成的Az-HA,进行了傅里叶变换红外(FTTR),质子核磁共振('H NMR)和紫外/可见(UV / vis)吸收光谱。我们展示了通过使用微尺度图案化的Az-HA衍生物表面上使用荧光素异硫氰酸酯共轭白蛋白(FITC-BSA)来固定蛋白质。为了生物相容性,在MG-63人成骨细胞系上进行了Az-HA衍生物的细胞毒性和相对细胞增殖测试。

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