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Supramolecular Gelation of a Polymeric Prodrug for Its Encapsulation and Sustained Release

机译:高分子前药的超分子凝胶化及其封装和缓释作用

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摘要

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.
机译:制备了聚合前药PEG化吲哚美辛(MPEG-indo),然后在其水性混合体系中与α-环糊精(α-CD)相互作用。此过程可能导致在温和条件下形成超分子水凝胶,并同时将MPEG-indo封装在水凝胶基质中。对于形成的超分子水凝胶,通过动态和稳定的流变试验,针对MPEG-indo和α-CD量的影响,研究了其凝胶动力学,机械强度,剪切稀化行为和触变响应。同时,也探索了使用这种水凝胶基质作为可注射药物递送系统的可能性。通过体外释放和细胞活力测试,发现封装的MPEG-indo可以表现出受控和持续的释放行为,并保持其生物学活性。

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