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A Gelatin-Based Hydrogel with p-Cyclodextrin Crosslinker for Controlled Drug Release

机译:具有对-环糊精交联剂的明胶基水凝胶,可控制药物释放

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摘要

A novel gelatin hydrogel was prepared by using 1, 1'-carbonyldiimidazole (CDI) activated β-cyclodextrin (P-CD) as crosslinker. The hydrogel was characterized by 'H NMR spectroscopy, in vitro degradation, MTT assay, drug loading/release study with anticancer drug of methotrexate (MTX). Degradation and drug loading/release properties of the hydrogel can be controlled by changing the crosslinker content. In vitro cytotoxicity test indicated nontoxicity of this material to L929 cells (mouse connective tissue fibroblast), showing that this new crosslinked gelatin hydrogel is biocompatible and can be used as a potential drug carrier in human body.
机译:以1,1'-羰基二咪唑(CDI)活化的β-环糊精(P-CD)作为交联剂,制备了新型明胶水凝胶。通过1 H NMR光谱,体外降解,MTT分析,甲氨蝶呤(MTX)的抗癌药物进行药物负载/释放研究,对水凝胶进行了表征。水凝胶的降解和药物负载/释放性质可以通过改变交联剂含量来控制。体外细胞毒性试验表明该物质对L929细胞(小鼠结缔组织成纤维细胞)无毒,表明这种新的交联明胶水凝胶具有生物相容性,可用作人体中潜在的药物载体。

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