首页> 外文期刊>Journal of Macromolecular Science, Part A: Pure and Applied Chemistry >Synthesis of Amphiphilic Azobenzene Functionalized Branched-Type Copolymer Based on Branched Poly(2-(Dimethylamino) ethyl methacrylate) and Investigation of Its Drug Release Properties
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Synthesis of Amphiphilic Azobenzene Functionalized Branched-Type Copolymer Based on Branched Poly(2-(Dimethylamino) ethyl methacrylate) and Investigation of Its Drug Release Properties

机译:基于支化聚(2-(二甲基氨基)乙基甲基丙烯酸酯)的两亲性偶氮苯官能化支化共聚物的合成及其药物释放性能的研究

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Here, we reported the synthesis of branched poly(2-(dimethylamino) ethyl methacrylate) (PDMAEMA) via a combination of activator generated by electron transfer atom transfer radical polymerization (AGET ATRP) and self-condensing vinyl polymerization (SCVP) techniques. The typical linear kinetics of the AGET ATRP of DMAEMA with the initiation of 2-(2-bromoisobutyryloxy) ethyl methacrylate (BIEM) was observed. The molecular weight (Mn ) of the branched PDMAEMA increased with the monomer conversion. The GPC traces of these polymers were unimodal and the molecular weight distributions (Mw/Mn ) were in the range of 1.30-2.10. The degree of branching (DB) determined by NMR spectra agreed with theoretical value. The branched amphiphilic copolymer functionalized with azobenzene was then prepared via AGET ATRP chain-extension of branched PDMAEMA with azobenzene monomer, 6-[4-(4-methoxyphenylazo)phenoxy]hexyl(meth)acrylate as the second monomer. The GPC traces of these branched copolymers showed the mono-peaks, which proved the successful preparation of copolymers. The properties of this branched copolymer in controlling drug release were also investigated. It was found that the drug release rate of chlorambucil can be controlled by various factors, such as polymer structure, light, temperature and pH values.View full textDownload full textKeywordsSelf-condensing vinyl copolymerization (SCVCP), multiple stimuli, drug release rate, activator generated by electron transfer atom transfer radical polymerization (AGET ATRP)Related var addthis_config = { ui_cobrand: "Taylor & Francis Online", services_compact: "citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,more", pubid: "ra-4dff56cd6bb1830b" }; Add to shortlist Link Permalink http://dx.doi.org/10.1080/10601325.2012.714675
机译:在这里,我们报道了通过电子转移原子转移自由基聚合(AGET ATRP)和自缩合乙烯基聚合(SCVP)技术产生的活化剂的组合,合成支化的聚(2-(二甲氨基)乙基甲基丙烯酸甲酯(PDMAEMA)。观察到随着甲基丙烯酸2-(2-溴异丁氧基)乙酯(BIEM)的引发,DMAEMA的AGET ATRP具有典型的线性动力学。支链PDMAEMA的分子量(M n )随单体转化率的增加而增加。这些聚合物的GPC痕迹是单峰的,分子量分布(M w / M n )在1.30-2.10范围内。通过NMR谱测定的支化度(DB)与理论值一致。然后通过支链PDMAEMA的AGET ATRP扩链制备用偶氮苯官能化的支链两亲共聚物,其中偶氮苯单体,6- [4-(4-甲氧基苯基偶氮)苯氧基]己基(甲基)丙烯酸酯为第二单体。这些支化共聚物的GPC痕迹显示了单峰,证明了共聚物的成功制备。还研究了该支链共聚物在控制药物释放中的性能。发现苯丁酸氮芥的药物释放速率可以通过多种因素控制,例如聚合物结构,光,温度和pH值。查看全文下载全文关键词自缩合乙烯基共聚(SCVCP),多种刺激,药物释放速率,活化剂由电子转移原子转移自由基聚合(AGET ATRP)生成。相关的var addthis_config = {ui_cobrand:“泰勒和弗朗西斯在线”,servicescompact:“ citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,更多“,pubid:” ra-4dff56cd6bb1830b“};添加到候选列表链接永久链接http://dx.doi.org/10.1080/10601325.2012.714675

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