化学计量辅助紫外光谱和液相色谱法分离阿司匹林、阿托伐他汀和氯吡格雷三元混合物

M. Issa, R. M. Nejem, A. A. Shanab, Raluca-Ioana Stefan-van Staden
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引用次数: 11

摘要

提出了两种化学计量辅助紫外分光光度法在不进行化学预处理的情况下对三元混合物进行分离的方法。第一种方法是基于h点标准添加法的改进,通过同时添加三种分析物,允许同时分析来自一个独特校准集的三种物质。得到阿司匹林、阿托伐他汀和氯吡格雷的光谱商,结果表明阿司匹林、阿托伐他汀和氯吡格雷在阿司匹林2.5 ~ 20 μ mL−1、阿托伐他汀2.5 ~ 17.5 μ mL−1和氯吡格雷2.5 ~ 20 μ mL−1的线性范围内可以同时测定。第二种方法是基于一阶导数谱和克拉默矩阵规则的结合。在矩阵计算中,氯吡格雷在316.8 nm和212 nm处有零点交叉点,而阿托伐他汀在250 nm处有零点交叉点,矩阵大大简化,易于求解。线性浓度范围为阿司匹林2.5 ~ 20 μ mL−1、阿托伐他汀2.5 ~ 17.5 μ mL−1、氯吡格雷2.5 ~ 20 μ mL−1。结果表明,阿司匹林、阿托伐他汀、氯吡格雷的同时测定是可以遵守的。两种方法均适用于含三种成分的胶囊,结果与替代液相色谱法一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Resolution of Ternary Mixture of Aspirin, Atorvastatin, and Clopidogrel by Chemometric-Assisted UV Spectroscopic and Liquid Chromatography Methods
Two chemometrics-assisted UV spectrophotometric methods were proposed for the resolution of ternary mixtures without any chemical pretreatment. The first method is based on modification of H-point standard addition method which permits simultaneous analysis of three species from a unique calibration set by making the simultaneous addition of the three analytes. Quotient between the spectra of aspirin, atorvastatin, and clopidogrel was obtained and the results showed that simultaneous determination of aspirin, atorvastatin, and clopidogrel can be obeyed in the linear range 2.5–20 μg mL−1 of aspirin, 2.5–17.5 μg mL−1 of atorvastatin, and 2.5–20 μg mL−1 of clopidogrel in ternary mixture. The second method is based on the combination of the first derivative spectra and Cramer's matrix rule. In the matrix calculation, clopidogrel has zero crossing point at 316.8 and 212 nm, while for atorvastatin the zero crossing point at 250 nm where the matrix is greatly simplified and easily solved. The linear concentration ranges were 2.5–20 μg mL−1 aspirin, 2.5–17.5 μg mL−1 atorvastatin and 2.5–20 μg mL−1 clopidogrel in ternary mixtures. The results proved that the simultaneous determination of aspirin, atorvastatin, and clopidogrel could be obeyed. Both methods were applied for capsules containing the three ingredients and results were in good concordance with alternative liquid chromatography.
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