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Simultaneous spectrophotometric determination of ezetimibe and simvastatin in pharmaceutical preparations using chemometric techniques

机译:化学计量法同时分光光度法测定药物制剂中的依泽替米贝和辛伐他汀

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摘要

Two spectrophotometric methods are described for the simultaneous determination of ezetimibe (EZE) and simvastatin (SIM) in pharmaceutical preparations. The obtained data was evaluated by using two different chemometric techniques, Principal Component Regression (PCR) and Partial Least-Squares (PLS-1). In these techniques, the concentration data matrix was prepared by using the mixtures containing these drugs in methanol. The absorbance data matrix corresponding to the concentration data matrix was obtained by the measurements of absorbances in the range of 240 – 300 nm in the intervals with Δλ = 1 nm at 61 wavelengths in their zero order spectra, then, calibration or regression was obtained by using the absorbance data matrix and concentration data matrix for the prediction of the unknown concentrations of EZE and SIM in their mixture. The procedure did not require any separation step. The linear range was found to be 5 – 20 µg mL-1 for EZE and SIM in both methods. The accuracy and precision of the methods were assessed. These methods were successfully applied to a pharmaceutical preparation, tablet; and the results were compared with each other.
机译:描述了两种分光光度法同时测定药物制剂中的依泽替米贝(EZE)和辛伐他汀(SIM)。通过使用两种不同的化学计量技术,主成分回归(PCR)和偏最小二乘(PLS-1)对获得的数据进行评估。在这些技术中,通过使用在甲醇中包含这些药物的混合物来制备浓度数据矩阵。通过在零阶光谱中以61个波长处的λλ= 1 nm的间隔内测量240至300 nm范围内的吸光度,获得与浓度数据矩阵相对应的吸光度数据矩阵,然后通过以下方法获得校准或回归使用吸光度数据矩阵和浓度数据矩阵预测混合物中EZE和SIM的未知浓度。该过程不需要任何分离步骤。两种方法中的EZE和SIM的线性范围均为5 – 20 µg mL-1。评估了方法的准确性和精确性。这些方法已成功地应用于药物制剂片剂;并将结果相互比较。

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