首页> 外文期刊>Journal of AOAC International >Application of derivative, derivative ratio, and multivariate spectral analysis and thin-layer chomatography-densitometry for determination of a ternary mixture containing drotaverine hydrochloride, caffeine, and paracetamol
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Application of derivative, derivative ratio, and multivariate spectral analysis and thin-layer chomatography-densitometry for determination of a ternary mixture containing drotaverine hydrochloride, caffeine, and paracetamol

机译:导数,导数比,多元光谱分析和薄层色谱-密度测定法在测定盐酸盐酸屈花碱,咖啡因和扑热息痛的三元混合物中的应用

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New selective, precise, and accurate methods are described for the determination of a ternary mixture containing drotaverine hydrochloride (I), caffeine (II), and paracetamol (III). The first method uses the first (D1) and third (D3) derivative spectrophotometry at 331 and 315 nm for the determination of (I) and (III), respectively, without interference from (II). The second method depends on the simultaneous use of the first derivative of the ratio spectra (DD1) with measurement at 312.4 nm for determination of (I) using the spectrum of 40 microg/mL (III) as a divisor or measurement at 286.4 and 304 nm after using the spectrum of 4 microg/mL (I) as a divisor for the determination of (II) and (III), respectively. In the third method, the predictive abilities of the classical least-squares, principal component regression, and partial least-squares were examined for the simultaneous determination of the ternary mixture. The last method depends on thin-layer chromatography-densitometry after separation of the mixture on silica gel plates using ethyl acetate-chloroform-methanol (16 + 3 + 1, v/v/v) as the mobile phase. The spots were scanned at 281, 272, and 248 nm for the determination of (I), (II), and (III), respectively. Regression analysis showed good correlation in the selected ranges with excellent percentage recoveries. The chemical variables affecting the analytical performance of the methodology were studied and optimized. The methods showed no significant interferences from excipients. Intraday and interday assay precision and accuracy values were within regulatory limits. The suggested procedures were checked using laboratory-prepared mixtures and were successfully applied for the analysis of their pharmaceutical preparations. The validity of the proposed methods was further assessed by applying a standard addition technique. The results obtained by applying the proposed methods were statistically analyzed and compared with those obtained by the manufacturer's method.
机译:描述了一种新的选择性,精确和准确的方法,用于测定含有盐酸屈花碱(I),咖啡因(II)和对乙酰氨基酚(III)的三元混合物。第一种方法在331和315 nm处使用一阶(D1)和三阶(D3)导数分光光度法分别测定(I)和(III),而不受(II)的干扰。第二种方法取决于同时使用比率光谱(DD1)的一阶导数与在312.4 nm处的测量值同时确定(I),使用40微克/毫升的光谱(III)作为除数或在286.4和304处进行测量分别使用4微克/毫升的光谱(I)作为除数分别测定(II)和(III)的λ。在第三种方法中,检查了古典最小二乘,主成分回归和偏最小二乘的预测能力,以便同时确定三元混合物。最后一种方法取决于在硅胶板上使用乙酸乙酯-氯仿-甲醇(16 + 3 + 1,v / v / v)作为流动相分离混合物后的薄层色谱-密度法。在281、272和248 nm处扫描斑点,分别测定(I),(II)和(III)。回归分析显示在选定范围内具有良好的相关性,回收率极佳。研究和优化了影响方法学分析性能的化学变量。该方法显示没有明显的辅料干扰。日内和日间分析的精密度和准确度值均在规定的范围内。使用实验室制备的混合物检查了建议的程序,并将这些程序成功地用于分析其药物制剂。通过应用标准添加技术进一步评估了所提出方法的有效性。对通过应用建议的方法获得的结果进行统计分析,并将其与通过制造商的方法获得的结果进行比较。

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