作者：Lei Sun, Xinge Zhang*, Chao Zheng, Zhongming Wu, Xiaoting Xia, Chaoxing Li*
关键字：microgel, drug delivery
论文来源：期刊
具体来源：RSC Advance, 2012, 2, 9904-9913.
发表时间：2012年

In this paper, a novel core–shell microgel was prepared based on poly(N-isopropylacrylamide-co-3-acrylamidophenylboronic acid-co-dextran-maleic acid) (p(NIPAM-co-AAPBA-co-Dex-Ma)) coated silica nanoparticles via radical polymerization. The core–shell microgels presented glucose- and temperature-sensitivity, and the shell thickness could be easily regulated by the molar ratio of the comonomers. The polymer shell was active in drug loading as it underwent a distinct transition from a swollen state to a collapsed state as the temperature increased. Insulin was applied as a model drug and the behaviors of insulin loading/release were investigated. The insulin loading was temperature-dependent and up to 20%. The cumulative release of insulin in vitro showed that insulin release was dependent on glucose concentration. The glucose sensitivity of the microgels could be adjusted simply by adjusting the pH. The cytotoxicity assay indicated that the core–shell microgels have good biocompatibility. These results showed that the core–shell microgels have potential for a controlled insulin release system.