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高分子前药的超分子凝胶化用于其包封和缓释。

Supramolecular gelation of a polymeric prodrug for its encapsulation and sustained release.

机构信息

DSAPM Lab and PCFM Lab, Institute of Polymer Science, School of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, China.

出版信息

Biomacromolecules. 2011 Sep 12;12(9):3124-30. doi: 10.1021/bm101566r. Epub 2011 Aug 1.

Abstract

A polymeric prodrug, PEGylated indomethacin (MPEG-indo), was prepared and then used to interact with α-cyclodextrin (α-CD) in their aqueous mixed system. This process could lead to the formation of supramolecular hydrogel under mild conditions and simultaneous encapsulation of MPEG-indo in the hydrogel matrix. For the formed supramolecular hydrogel, its gelation kinetics, mechanical strength, shear-thinning behavior and thixotropic response were investigated with respect to the effects of MPEG-indo and α-CD amounts by dynamic and steady rheological tests. Meanwhile, the possibility of using this hydrogel matrix as injectable drug delivery system was also explored. By in vitro release and cell viability tests, it was found that the encapsulated MPEG-indo could exhibit a controlled and sustained release behavior as well as maintain its biological activity.

摘要

一种聚合物前药,聚乙二醇化吲哚美辛(MPEG-吲哚),被制备并用于在其水混合体系中与α-环糊精(α-CD)相互作用。在温和条件下,这个过程会导致超分子水凝胶的形成,同时将 MPEG-吲哚封装在水凝胶基质中。对于形成的超分子水凝胶,通过动态和稳态流变学测试,研究了其凝胶动力学、机械强度、剪切变稀行为和触变响应,以及 MPEG-吲哚和α-CD 用量的影响。同时,还探索了将这种水凝胶基质用作可注射药物传递系统的可能性。通过体外释放和细胞活力测试,发现封装的 MPEG-吲哚可以表现出控制和持续释放的行为,并保持其生物活性。

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