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在可控氧分压条件下卡托普利在水溶液中的氧化动力学及机理

Kinetics and mechanism of captopril oxidation in aqueous solution under controlled oxygen partial pressure.

作者信息

Lee T Y, Notari R E

机构信息

Stuart Pharmaceuticals, Division of ICI Americas Inc., Wilmington, Delaware 19897.

出版信息

Pharm Res. 1987 Apr;4(2):98-103. doi: 10.1023/a:1016406716989.

Abstract

The stability of captopril in aqueous solution at 32 degrees C was studied in the pH range 6.6 to 8.0 under controlled oxygen partial pressure (90-760 mm Hg) with and without the addition of cupric ion. The oxidation product, captopril disulfide, was found to be the sole degradation product. A change in reaction rate from first order to zero order occurs as the captopril concentration decreases. The concentration at which this transition takes place is a function of the pH, oxygen partial pressure, and cupric ion concentration. The apparent first-order rate constants show a first-order dependency on both the oxygen partial pressure and the cupric ion concentration. However, the apparent zero-order rate constants show a first-order dependency on oxygen partial pressure and a second-order dependency on cupric ion concentration. As the pH increases from 6.6 to 8.0, the first-order process becomes more predominant. A mechanism which consists of cupric ion- and molecular oxygen-catalyzed oxidation is proposed to explain those observations.

摘要

在32摄氏度下,于6.6至8.0的pH范围内,在有和没有添加铜离子的情况下,在受控氧分压(90 - 760毫米汞柱)条件下研究了卡托普利在水溶液中的稳定性。发现氧化产物卡托普利二硫化物是唯一的降解产物。随着卡托普利浓度降低,反应速率从一级变为零级。发生这种转变的浓度是pH、氧分压和铜离子浓度的函数。表观一级速率常数对氧分压和铜离子浓度均呈一级依赖性。然而,表观零级速率常数对氧分压呈一级依赖性,对铜离子浓度呈二级依赖性。随着pH从6.6增加到8.0,一级过程变得更加占主导。提出了一种由铜离子和分子氧催化氧化组成的机制来解释这些观察结果。

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