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pH-Responsive Hyperbranched Copolymers from One-pot RAFT Copolymerization of Propylacrylic Acid and Poly(Ethylene Glycol Diacrylate)

机译:来自丙烯酸和聚(乙二醇二丙烯酸乙二醇酯)的单盆筏共聚的pH-响应性超接收共聚物

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pH-Responsive polymers have attracted much attention for biotechnology applications as carriers or matrix to facilitate intracellular or extracellular therapeutic drug delivery and release. In this paper, we report the development of new pH-responsive and hyperbranched copolymers with potential for such applications. These pH-responsive hyperbranched copolymers were synthesized via one pot reversible addition-fragmentation chain transfer (RAFT) copolymerization of propylacrylic acid (PAA) and a branching co-monomer poly(ethylene glycol diacrylate) (PEGDA) (Mn=258 Da) at the monomer feed molar ratios [PAA]_0/[PEGDA]_0 = 99/1, 90/10 and 80/20. The resultant poly(PAA-PEGDA) copolymers were characterized by Proton Nuclear Magnetic Resonance (~1H NMR) and Gel Permeation Chromatography (GPC) to obtain the molecular weight, copolymer composition and degree of acrylate functionality. The hydrodynamic dimensions of these copolymers at pH range between 5.0 and 7.4 were studied using Dynamic Light Scattering technique (DLS). Moreover, these hyperbranched copolymers demonstrated composition- and size-dependent membrane disruptive properties by red blood cell hemolysis assay. Poly(PAA-PEGDA) with the copolymer composition [PAA]/[PEGDA]= 68/32, obtained from the copolymerization at the monomer feed molar ratio [PAA]_0/[PEGDA]_0 = 99/1, demonstrated significant membrane disruptive activity.
机译:PH响应性聚合物吸引了生物技术应用作为载体或基质的巨大关注,以促进细胞内或细胞外治疗药物递送和释放。在本文中,我们报告了新的pH-响应性和超支化共聚物的开发,具有此类应用的潜力。通过丙烯酸(PAA)的一个罐可逆添加 - 碎片链转移(筏)共聚合成这些pH-响应的超抗原共聚物,并在该分支共聚单体聚(乙二醇二丙烯酸乙二醇酯)(PEGDA)(MN = 258Da)中单体饲料摩尔比[PAA] _0 / [PEGDA] _0 = 99/1,90 / 10和80/20。通过质子核磁共振(〜1H NMR)和凝胶渗透色谱(GPC)表征所得聚(PAA-PEGDA)共聚物,得到分子量,共聚物组成和丙烯酸酯官能度的程度。使用动态光散射技术(DLS)研究了5.0和7.4之间的pH范围内这些共聚物的流体动力学尺寸。此外,这些超支化共聚物通过红细胞溶血测定证明了组成和依赖性膜破坏性质。与共聚物组合物[PAA] / [PEGDA] = 68/32的聚(PAA-PEGDA)从单体供给摩尔比[PAA] _0 / [PEGDA] _0 = 99/1的共聚获得,证明了显着的膜破坏性活动。

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