Hydrolyzable Polyrotaxanes Consisting of β-Cyclodextrins and Pluronic® for Drug Delivery

A. Ito, T. Ooya, N. Yui
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Abstract

In recent years, polyrotaxanes (PRXs) have been extensively studied as a novel supramolecular assembly that has interlocked structure between a cyclic molecule and a linear polymeric chain. Based on the interlocked structure of PRXs, one can expect excellent properties in terms of supramolecular motion of the cyclic molecules. In pharmaceutical fields, we have studied biodegradable PRXs as a drug carrier, in which many α-cyclodextrins (α-CDs) are threaded onto a poly (ethylene glycol) (PEG) capped with bulky blocking group via peptide linkages1). Drugs were immobilized α-CDs via biodegradable spacer. When the terminals of PRX were enzymatically hydrolyzed, drug-immobilized α-CDs could be released.
由β-环糊精和Pluronic®组成的可水解聚轮烷用于给药
近年来,聚轮烷(PRXs)作为一种在环状分子和线性聚合物链之间具有互锁结构的新型超分子组装体得到了广泛的研究。基于prx的互锁结构,人们可以期望在环分子的超分子运动方面具有优异的性能。在制药领域,我们已经研究了可生物降解的PRXs作为药物载体,其中许多α-环糊精(α-CDs)通过肽键连接到覆盖有大块阻断基团的聚乙二醇(PEG)上。药物通过可生物降解的间隔剂固定α-CDs。当PRX末端被酶解时,可以释放药物固定化的α-CDs。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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