自愈水凝胶
甲基丙烯酸酯
原子转移自由基聚合
共聚物
低临界溶液温度
高分子化学
材料科学
乙二醇
差示扫描量热法
傅里叶变换红外光谱
甲基丙烯酸羟乙基酯
肿胀 的
凝胶渗透色谱法
自由基聚合
化学工程
聚合物
化学
有机化学
复合材料
工程类
物理
热力学
作者
Fu‐Jian Xu,E. T. Kang,K. G. Neoh
出处
期刊:Biomaterials
[Elsevier BV]
日期:2006-01-27
卷期号:27 (14): 2787-2797
被引量:246
标识
DOI:10.1016/j.biomaterials.2006.01.003
摘要
Well-defined poly((2-dimethyl amino)ethyl methacrylate-co-2-hydroxyethyl methacrylate)-b-poly(N-isopropylacrylamide)-b-poly((2-dimethyl amino)ethyl methacrylate-co-2-hydroxyethyl methacrylate), or P(DMAEMA-co-HEMA)-b-P(NIPAAm)-b-P(DMAEMA-co-HEMA), triblock copolymers were synthesized by consecutive atom transfer radical polymerizations (ATRPs), using ethylene glycol di-2-bromoisobutyrate (Br–EG–Br) as the starting ATRP initiator. The hydroxyl groups of the incorporated HEMA units were used as crosslinking sites for the preparation of smart hydrogels. The so-prepared hydrogels exhibited both temperature- and pH-sensitive behavior derived, respectively, and independently, from the P(NIPAAm) blocks and P(DMAEMA) units, in the crosslinked matrices. The hydrogels exhibited a lower critical solution temperature (LCST) of 31–32 °C in aqueous media of pH 1–7, not unlike that of the P(NIPAAm) homopolymer. The swelling ratios and swelling/deswelling kinetics of the hydrogels depended strongly on pH and temperature of the medium. The copolymers were characterized by gel-permeation chromatography, X-ray photoelectron spectroscopy (XPS), Fourier-transform infrared (FTIR) spectroscopy, and 1H nuclear magnetic resonance (1H NMR) spectroscopy. The resultant stimuli-responsive hydrogels were characterized by differential scanning calorimetry (DSC). These stimuli-responsive hydrogels will have potential applications in biomedical areas, such as tissue engineering and drug delivery.
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