聚乙二醇甲硝唑缀合物:合成、体外和体内性质

Cinzia Bersani, Manuela Berna, Gianfranco Pasut, Francesco Maria Veronese
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引用次数: 18

摘要

甲硝唑(MTZ)是一种用于治疗由原生动物和厌氧微生物引起的原生动物感染的药物,它与5000、10000和20000 Da的线性或支链聚乙二醇偶联。聚合物和药物之间的酯键在偶联中产生聚合物前药。该修饰允许克服已知的MTZ溶解度问题,从而使我们获得更适合亲代给药的生物偶联物。不同分子量聚合物的缀合物在体外对化学降解和消化酶进行了测试。结果表明,聚乙二醇的分子量和形状对前体药物的稳定性至关重要。在胃酸介质中发现了良好的耐药性,并且可以在大肠液中缓慢释放药物。在小鼠体内进行的静脉注射或s.c.c给药研究表明,结合后的药代动力学特性得到改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PEG-metronidazole conjugates: synthesis, in vitro and in vivo properties

Metronidazole (MTZ), a drug used for the treatment of protozoal infections caused by protozoa and anaerobic microorganisms, was conjugated to linear or branched poly(ethylene glycol) of 5,000, 10,000 and 20,000 Da. An ester linkage between polymer and drug was used in the coupling to yield a polymeric prodrug. The modification allowed overcoming the known MTZ solubility problem leading us to obtain a bioconjugate more suitable for parental administration. The conjugates of various molecular weight polymers have been tested in vitro toward chemical degradation and digestive enzymes. It was found that molecular weight and shape of PEG is critical for the prodrugs stability. Good resistance in the stomach acidic media was found and a slow release of the drug in the large intestinal fluid may take place. In vivo studies carried out following i.v. or s.c. administration to mice revealed improved pharmacokinetics properties upon conjugation.

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