Alaa El-Gindy , Samy Emara , Mostafa K. Mesbah , Ghada M. Hadad
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引用次数: 55
摘要
介绍了分光光度法和高效液相色谱法测定非诺贝特、长春西汀及其水解产物的含量。采用紫外光谱的偏最小二乘(PLS-1)和主成分回归(PCR)方法对非诺贝特和长春西汀及其水解产物进行了分离;以及图形分光光度法分别作为比值光谱(1DD)的一阶导数或长春西汀和非诺贝特的一阶(1D)和二阶(2D)导数分光光度法。此外,建立了以ODS柱为流动相的高效液相色谱法,流动相为乙腈-水(80:20,v/v, pH 4),在287 nm处检测非诺贝特;流动相为乙腈- 10 mM KH2PO4,含0.1%二乙胺(60:40,v/v, pH 4.6),在270 nm处检测长春西汀。该方法成功地应用于实验室配制的混合制剂和药物制剂中每种药物及其水解产物的测定。采用高效液相色谱法和导数分光光度法研究了各药物的酸性和碱性水解动力学。研究了各药物在布列顿-罗宾逊缓冲液中水解的ph值分布。
Spectrophotometric and liquid chromatographic determination of fenofibrate and vinpocetine and their hydrolysis products
Several spectrophotometric and HPLC methods are presented for the determination of fenofibrate, vinpocetine and their hydrolysis products. The resolution of either fenofibrate or vinpocetine and their hydrolysis products has been accomplished by using numerical spectrophotometric methods as partial least squares (PLS-1) and principal component regression (PCR) applied to UV spectra; and graphical spectrophotometric methods as first derivative of ratio spectra (1DD) or first (1D) and second (2D) derivative spectrophotometry for vinpocetine and fenofibrate, respectively. In addition HPLC methods were developed using ODS column with mobile phase consisting of acetonitrile–water (80:20, v/v, pH 4) with UV detection at 287 nm for fenofibrate and a mobile phase consisting of acetonitrile–10 mM KH2PO4, containing 0.1% diethylamine (60:40, v/v, pH 4.6) with UV detection at 270 nm for vinpocetine.
The proposed methods were successfully applied for the determination of each drug and its hydrolysis product in laboratory-prepared mixture and pharmaceutical preparation. The proposed HPLC and derivative spectrophotometric methods were used to investigate the kinetics of acidic and alkaline hydrolytic processes of each drug. The pH-rate profile of hydrolysis of each drug in Britton–Robinson buffer solutions was studied.