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首页> 外文期刊>Macromolecular Research >Immobilization effect of bone morphogenetic protein-2 on collagen membrane via photoreactive gelatin derivatives: Biocompatibility and preservability of osteoinductive activity
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Immobilization effect of bone morphogenetic protein-2 on collagen membrane via photoreactive gelatin derivatives: Biocompatibility and preservability of osteoinductive activity

机译:骨形态发生蛋白2通过光反应性明胶衍生物对胶原膜的固定作用:骨诱导活性的生物相容性和防腐性

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摘要

To photo-immobilize bone morphogenetic protein-2 (BMP-2), UV light-reactive gelatin (azidophenyl gelatin, Az-gel), which is introduced with an N-(4-azidobenzoyloxy) succinimide-containing an azide group, was prepared as a carrier of BMP-2. Characterization of the photo-reactivity of Az-gel was evaluated by the curing ratio and it was micropatterned using a photomask. The cross-linking ratio and an enzyme-linked immunosorbent assay, enzymelinked immunospecific assay (ELISA)-based BMP-2-release test were used to determine the optimal density of Azgel (1, 3, and 5%) and UV treatment time (10, 30, 60 s) of the BMP-2 carrier in collagen matrix. The results showed that 5% Az-gel with 60 s of UV treatment was the most efficient condition for cross-linking. Cytotoxicity assays using the C2C12 mouse myoblast cell line showed that there were no cytotoxic effects of Az-gel. Alkaline phosphatase activity and calcium ion detection assays to evaluate the osteoinductive activities were conducted in assumed optimal condition of Az-gel (5% and 60 s UV treatment) 14 days post-treatment. In our study, the osteoinductive activities were the highest in cells treated with BMP-2 and the photo-reactive Az-gel carrier compared to BMP-2 alone or untreated control cells in collagen matrix at all time points (3, 7, and 14 days).
机译:为了将骨形态发生蛋白2(BMP-2)光固定,制备了带有含叠氮基的N-(4-叠氮苯甲酰氧基)琥珀酰亚胺的紫外光反应性明胶(叠氮苯基明胶,Az-gel)。作为BMP-2的载体。通过固化率评价Az-凝胶的光反应性的表征,并使用光掩模对其进行微图案化。使用交联比和酶联免疫吸附测定,基于酶联免疫特异性测定(ELISA)的BMP-2-释放试验确定Azgel的最佳密度(1、3和5%)和UV处理时间( 10、30、60 s)的胶原蛋白基质中的BMP-2载体。结果表明,经过60 s的UV处理的5%Az-gel是最有效的交联条件。使用C2C12小鼠成肌细胞系的细胞毒性试验表明,Az-gel没有细胞毒性作用。在治疗后14天,在假定的最佳Az-gel(5%和60 s UV处理)条件下进行碱性磷酸酶活性和钙离子检测试验,以评估骨诱导活性。在我们的研究中,在所有时间点(3、7和14),与单独使用BMP-2或未处理的胶原蛋白对照细胞相比,在用BMP-2和光反应性Az-gel载体处理的细胞中骨诱导活性最高天)。

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