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Temperature-controlled erosion of poly(N-isopropylacrylamide)-based hydrogels crosslinked by methacrylate-introduced hydrolyzable polyrotaxane

机译:引入甲基丙烯酸酯的可水解聚轮烷交联的聚(N-异丙基丙烯酰胺)基水凝胶的温度控制腐蚀

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摘要

Biodegradable hydrogels for temperature-controlled erosion were prepared by co-crosslinking N-isopropylacrylamide (NIPAAm) and methacrylate (MA)-introduced polyrotaxane (PRX) in which many α-cyclodextrins (α-CDs) are threaded onto a poly(ethylene glycol) chain capped with bulky end-groups via ester linkages. The amount of MA attached to hydroxyl group of α-CDs in PRX could be varied by the feed ratio of GMA and PRX. The prepared hydrogels were transparent below lower critical solution temperature (LCST) of PNIPAAm matrix (32℃). By elevating temperature above the LCST, water contents were slightly decreased, and the hydrogels became opaque. Elevating temperature in an aqueous condition above the LCST led to dehydration of the PNIPAAm matrix, which accompanies α-CD sliding to expose the ester linkage to the medium and enhances erosion of the hydrogels.
机译:通过将N-异丙基丙烯酰胺(NIPAAm)和甲基丙烯酸酯(MA)引入的聚轮烷(PRX)共交联制备可控温​​侵蚀的可生物降解水凝胶,其中许多α-环糊精(α-CDs)穿入到聚乙二醇中通过酯键被大端基封端的链。 PRX中α-CDs的羟基上附着的MA的量可以通过GMA和PRX的进料比来改变。所制备的水凝胶在PNIPAAm基质的较低临界溶液温度(LCST)(32℃)以下是透明的。通过将温度升高到LCST以上,水含量略有降低,水凝胶变得不透明。在LCST上方的水性条件下升高温度会导致PNIPAAm基质脱水,这伴随α-CD滑动而使酯键暴露于介质,并增强了水凝胶的侵蚀。

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