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Synthesis and properties of polyN-(2-hydroxypropyl) methacrylamideconjugates of superoxide dismutase

机译:超氧化物歧化酶聚N-(2-羟丙基)甲基丙烯酰胺偶联物的合成及性能

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摘要

The synthesis ofN-(2-hydroxypropyl)methacrylamide (HPMA) copolymers and semi-telechelic polymers (HPMA) conjugates superoxide dismutase (SOD) is described.The polymer was conjugated with SOD by means of nondergradable or degradable oligopeptide spacers randomly distributed along the polymer backbone.A second type of conjugation,to a semi-telechelic polymer,poly(HPMA),(PHPMA) containing reactive chain end groups,with the SOD amino groups formed star structures.Phyiscochemical properties of the conjugates,such as temperature stability and stability to oxidation with hydrogen peroxide,were studied and compared tonative SOD;an increase in temperature stability by the conjugates and an increase in stability towards oxidationw ith hydrogen peroxide was observed.The in vivobiological evaluation of PHPMA-SOD conjugates showed a significant decrease in innunogenicity compared to free SOD.A preliminary in vivo study of ischemic/reperfusion injury,revealed significantly more pronounced protective effects by PHPMA-SOD conjugates in comparison with the free SOD.
机译:描述了N-(2-羟丙基)甲基丙烯酰胺(HPMA)共聚物和半远程螯合聚合物(HPMA)偶联物超氧化物歧化酶(SOD)的合成。聚合物通过沿聚合物主链随机分布的不可降解或可降解寡肽间隔物与SOD偶联。第二种偶联,以半螯合聚合物,聚(HPMA),(PHPMA)含有反应性链端基,与SOD氨基形成星形结构。研究了共轭物的物理化学性质,如温度稳定性和过氧化氢氧化稳定性,并与天然SOD进行了比较;观察到共轭物的温度稳定性增加,对氧化的稳定性增加,双氧水。PHPMA-SOD偶联物的体内生物学评估显示,与游离SOD相比,INNUNOGENITY显著降低。对缺血/再灌注损伤的初步体内研究表明,与游离SOD相比,PHPMA-SOD偶联物的保护作用明显更明显。

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