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海他西林在水溶液中的水解和差向异构化动力学

Hydrolysis and epimerization kinetics of hetacillin in aqueous solution.

作者信息

Tsuji A, Itatani Y, Yamana T

出版信息

J Pharm Sci. 1977 Jul;66(7):1004-9. doi: 10.1002/jps.2600660727.

Abstract

Methods were developed for quantitating epimerization to epihetacillin and hydrolysis to ampicillin in the alkaline degradation of hetacillin, and both rates in deuterium oxide at 35 degrees and in water at various temperatures were determined. In each case, plots of log k for the epimerization against pH or pD yielded straight lines with a positive slope, which verified the first-order dependence on the hydroxide ion or deuteroxide ion. The activation energy of the epimerization process was 21.2 kcal/mole. In aqueous solution at high pH, epimerization rather than conversion to ampicillin represents a major pathway of hetacillin degradation, although the beta-lactam ring of the hetacillin molecule is highly resistant to attack by the hydroxide ion.

摘要

已开发出定量测定海他西林在碱性降解过程中差向异构化为表他西林以及水解为氨苄西林的方法,并测定了在35℃重水中和不同温度下水中的两种反应速率。在每种情况下,差向异构化的log k对pH或pD作图均得到具有正斜率的直线,这证实了对氢氧根离子或氘氧根离子的一级依赖性。差向异构化过程的活化能为21.2千卡/摩尔。在高pH的水溶液中,尽管海他西林分子的β-内酰胺环对氢氧根离子的攻击具有高度抗性,但差向异构化而非转化为氨苄西林是海他西林降解的主要途径。

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