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由可生物降解的三元 COS-g-PCL-b-MPEG 共聚物与α-环糊精形成的超分子水凝胶及其药物释放。

Supramolecular hydrogels formed from biodegradable ternary COS-g-PCL-b-MPEG copolymer with alpha-cyclodextrin and their drug release.

机构信息

Key Laboratory of Green Processing and Functional Textiles of New Textile Materials of Ministry of Education, Wuhan University of Science and Engineering, Wuhan 430073, PR China.

出版信息

Carbohydr Res. 2009 Nov 2;344(16):2201-8. doi: 10.1016/j.carres.2009.08.017. Epub 2009 Aug 19.

Abstract

On the basis of the synthesis of novel biodegradable amphiphilic MPEG-b-PCL-grafted chitooligosaccharide (COS-g-PCL-b-MPEG) copolymers, supramolecular hydrogels were fabricated rapidly via their inclusion complexation with alpha-cyclodextrin (alpha-CD) in aqueous solutions. The graft copolymers were characterized by (1)H NMR spectroscopy, gel permeation chromatography (GPC), and fluorescence measurement, and the supramolecular structure of the resultant hydrogels was confirmed by X-ray diffraction measurements. Rheological studies of as-obtained hydrogels indicate that the physical properties could be modulated by controlling the concentration and the graft content of the graft copolymers as well as the molar feed ratio of the graft to alpha-CD. The in vitro release kinetics studies of bovine serum albumin (BSA) entrapped in the hydrogels show that the drug release profiles are dependent on the supramolecular hydrogel compositions.

摘要

基于新型可生物降解两亲性 MPEG-b-PCL-接枝壳寡糖(COS-g-PCL-b-MPEG)共聚物的合成,通过其在水溶液中与α-环糊精(α-CD)的包合作用,快速制备超分子水凝胶。通过(1)H NMR 光谱、凝胶渗透色谱(GPC)和荧光测量对接枝共聚物进行了表征,并通过 X 射线衍射测量证实了所得水凝胶的超分子结构。所得水凝胶的流变学研究表明,通过控制接枝共聚物的浓度和接枝含量以及接枝与α-CD 的摩尔进料比,可以调节物理性质。包封在水凝胶中的牛血清白蛋白(BSA)的体外释放动力学研究表明,药物释放曲线取决于超分子水凝胶的组成。

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