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Determination of a novel ACE inhibitor in the presence of alkaline and oxidative degradation products using smart spectrophotometric and chemometric methods

机译:使用智能分光光度法和化学计量学方法在碱性和氧化降解产物存在下测定新型ACE抑制剂

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摘要

Simple, accurate, sensitive and validated UV spectrophotometric and chemometric methods were developed for the determination of imidapril hydrochloride (IMD) in the presence of both its alkaline (AKN) and oxidative (OXI) degradation products and in its pharmaceutical formulation. Method A is the fourth derivative spectra (D4) which allows the determination of IMD in the presence of both AKN and OXD, in pure form and in tablets by measuring the peak amplitude at 243.0 nm. Methods B, C and D, manipulating ratio spectra, were also developed. Method B is the double divisor-ratio difference spectrophotometric one (DD-RD) by computing the difference between the amplitudes of IMD ratio spectra at 232 and 256.3 nm. Method C is the double divisor-first derivative of ratio spectra method (DD-DR1) at 243.2 nm, while method D is the mean centering of ratio spectra (MCR) at 288.0 nm. Methods A, B, C and D could successfully determine IMD in a concentration range of 4.0-32.0 mg/mL. Methods E and F are principal component regression (PCR) and partial least-squares (PLS), respectively, for the simultaneous determination of IMD in the presence of both AKN and OXI, in pure form and in its tablets. The developed methods have the advantage of simultaneous determination of the cited components without any pre-treatment. The accuracy, precision and linearity ranges of the developed methods were determined. The results obtained were statistically compared with those of a reported HPLC method, and there was no significant difference between the proposed methods and the reported method regarding both accuracy and precision.
机译:开发了一种简单,准确,灵敏且经过验证的紫外分光光度法和化学计量方法,用于在碱性(AKN)和氧化(OXI)降解产物同时存在及其药物制剂中测定盐酸咪达普利(IMD)。方法A是四阶导数光谱(D4),通过测量243.0 nm的峰振幅,可以在AKN和OXD存在的情况下以纯净形式和片剂形式测定IMD。方法B,C和D的操纵比谱也得到了发展。方法B是通过计算232和256.3 nm处的IMD比谱的幅值之差来实现双除数比差分光光度法(DD-RD)。方法C是比率光谱法(DD-DR1)在243.2 nm处的双除数一阶导数,而方法D是比率光谱(MCR)在288.0 nm处的平均居中。方法A,B,C和D可以成功测定4.0-32.0 mg / mL范围内的IMD。方法E和F分别是主成分回归(PCR)和偏最小二乘(PLS),用于在AKN和OXI的存在下以纯净形式及其片剂同时测定IMD。所开发的方法的优点是无需任何预处理即可同时测定所列举的组分。确定了所开发方法的准确性,精密度和线性范围。将获得的结果与报告的HPLC方法进行统计学比较,在准确性和精密度方面,建议的方法与报告的方法之间没有显着差异。

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