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Synthesis of fenoprofen and gemfibrozil styrene-maleic acid copolymer conjugates.

机译:非诺洛芬和吉非贝齐苯乙烯-马来酸共聚物共轭物的合成。

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摘要

Two types of polymer-drug conjugates were synthesized starting from styrene-maleic acid anhydride copolymer (SMA). Fenoprofen and gemfibrozil were chosen as model drugs because of their short plasma half lives. Both drugs were first converted to their 2-aminoethylamides, which possess free amino groups capable of reacting with SMA anhydride rings. By modifying the degree and type of substitution, lipophilic and hydrophilic conjugates were obtained. Drug loading in the conjugates was between 17 and 47%.
机译:从苯乙烯-马来酸酐共聚物(SMA)开始合成了两种类型的聚合物-药物共轭物。非诺洛芬和吉非贝齐因血浆半衰期短而被选作模型药物。两种药物首先被转化为其2-氨基乙基酰胺,其具有能够与SMA酸酐环反应的游离氨基。通过改变取代的程度和类型,获得了亲脂性和亲水性缀合物。缀合物中的载药量为17%至47%。

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