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Macromolecular Drug Conjugates, Metronidazole-Cyclodextrin Prodrugs

机译:高分子药物结合物,甲硝唑-环糊精前药

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The antimicrobial drug metronidazole was covalently attached to e-cyclodextrin by --CH2-CO-bridges. The preliminary release behavior of metronidazole in the cecal fluids of rats was studied at 37 °C. Metronidazole was nearly released 60% from the macromolecular conjugates after 24 h in the cecal fluids of rats, probably via the biodegradation by glycosidases and hydrolases.
机译:抗菌药物甲硝唑通过-CH2-CO-桥与e-环糊精共价连接。在37℃下研究了甲硝唑在大鼠盲肠中的初步释放行为。在大鼠的盲肠液中24小时后,甲硝唑几乎从大分子结合物中释放了60%,这可能是由于糖苷酶和水解酶的生物降解所致。

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