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首页> 外文期刊>Journal of Applied Polymer Science >Synthesis, characterization, and antitumor activity of poly(maleic anhydride-co-vinyl acetate-co-acrylic acid)
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Synthesis, characterization, and antitumor activity of poly(maleic anhydride-co-vinyl acetate-co-acrylic acid)

机译:聚(马来酸酐-乙酸乙烯酯-丙烯酸)的合成,表征和抗肿瘤活性

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The ternary copolymerization of maleic anhydride (MA), vinyl acetate (VA), and acrylic acid (AA) [P(MA-co-VA-co-AA)], which is considered to be an acceptor-donor-acceptor system, was carried out in 1,4-dioxane with benzoyl peroxide as an initiator at 70 degrees C tinder a nitrogen atmosphere. Constants of complex formation for the monomer systems in the study were determined by UV-visible (hydrogen-bonding complex) and H-1-NMR (charge transfer complex) methods, respectively. The results show that polymerization of the P(MA-co-VA-co-AA) system proceeds by an alternating terpolymerization mechanism. It is shown that the synthesized copolymers have typical polyelectrolyte behavior, ability for reversible hydrolysis-anhydrization reactions, and semicrystalline structures. In these cases, including radical polymerization, and formation of semicrystalline structures, the hydrogen-bonding effect plays a significant role. The in vitro cytotoxicities of the synthesized terpolymer and alternating copolymer were evaluated using Raji cells (human Burkitt lymphoma cell line). The antitumor activities of prepared anion-active copolymers were Studied using methyl-thiazol-tetrazolium colorimetric assay and 50% of the cytotoxic dose of each copolymer and terpolymer were calculated. Hydrolyzed P(MA-co-VA-co-AA) and P(MA-alt-AA) copolymers have sufficiently high antitumor activity, which depends on the amount of hydrogen-bonding carboxylic groups and their regular distribution in the side chain of functional macromolecules. (c) 2006 Wiley Periodicals, Inc.
机译:马来酸酐(MA),乙酸乙烯酯(VA)和丙烯酸(AA)[P(MA-co-VA-co-AA)]的三元共聚,被认为是受体-供体-受体体系,在1,4-二恶烷中,以过氧化苯甲酰为引发剂,在70℃,氮气气氛下进行。本研究中单体系统的配合物形成常数分别通过紫外可见(氢键配合物)和H-1-NMR(电荷转移配合物)方法确定。结果表明,P(MA-co-VA-co-AA)体系的聚合是通过交替的三元聚合机理进行的。结果表明,合成的共聚物具有典型的聚电解质性能,可逆的水解-脱水反应能力和半结晶结构。在这些情况下,包括自由基聚合和半结晶结构的形成,氢键效应起着重要作用。使用Raji细胞(人类Burkitt淋巴瘤细胞系)评估了合成的三元共聚物和交替共聚物的体外细胞毒性。使用甲基噻唑-四唑鎓比色法研究了制备的阴离子活性共聚物的抗肿瘤活性,并计算了每种共聚物和三元共聚物的细胞毒性剂量的50%。水解的P(MA-co-VA-co-AA)和P(MA-alt-AA)共聚物具有足够高的抗肿瘤活性,这取决于氢键合羧基的数量及其在官能团侧链中的规则分布大分子。 (c)2006年Wiley Periodicals,Inc.

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