首页> 外文期刊>Journal of Polymer Research >Free radical synthesis of cross-linking gelatin base poly NVP/acrylic acid hydrogel and nanoclay hydrogel as cephalexin drug deliver
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Free radical synthesis of cross-linking gelatin base poly NVP/acrylic acid hydrogel and nanoclay hydrogel as cephalexin drug deliver

机译:交联明胶碱聚NVP /丙烯酸水凝胶和纳米山水凝胶的自由基合成作为头孢蛋蛋白药物递送

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In this research, we presented the synthesis of cross-linking poly N-vinyl pyrrolidone /acrylic acid hydrogel and nanoclay hydrogel based on gelatin which named gelatin-g-NVP-AA, gelatin-g-NVP-AA/MMT and used them as cephalexin drug delivery. These hydrogels were fully characterized by FTIR, SEM, TEM, XRD, TGA, DSC, Also, the effect of difference saline solution, temperature, the percentage of nanoclay and time were investigated. In addition, because of pH sensitivity of hydrogels, the swelling, drug loading and drug releasing were studied in different pHs, distilled water and buffers to determine the best condition for each situation which resulted illustrated the universal buffer in pH 8 was the least interaction with hydrogels and had maximum drug loading and releasing in this condition. Antibacterial activities of hydrogels were examined against the S. aureus and the E. coli and showed an interesting result for the loaded drug on gelatin-g-NVP-AA/MMT.
机译:在该研究中,我们介绍了基于明胶的交联聚烯基吡咯烷酮/丙烯酸水凝胶和纳米粘土水凝胶的合成,所述明胶被称为Gelatin-G-NVP-AA,Gelatin-G-NVP-AA / MMT并使用它们 头孢菌素药物递送。 这些水凝胶通过FTIR,SEM,TEM,XRD,TGA,DSC也完全表征了差异盐水溶液,温度,纳米粘土的百分比和时间的效果。 另外,由于水凝胶的pH敏感性,在不同的pHS,蒸馏水和缓冲剂中研究了肿胀,药物载荷和药物释放,以确定导致PH 8中的通用缓冲液的每种情况的最佳条件是与之最少的相互作用 水凝胶并在这种情况下具有最大的药物载荷和释放。 检查水凝胶的抗菌活性对抗金黄色葡萄球菌和大肠杆菌,对Gelatin-G-NVP-AA / MMT的负载药物显示出有趣的结果。

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