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用于测定他扎罗汀的化学计量学稳定性指示方法。

Stability-indicating chemometric methods for the determination of tazarotene.

机构信息

Cairo University, Faculty of Pharmacy, Department of Analytical Chemistry, Kaser El-Aini Street, ET 11562, Cairo, Egypt.

出版信息

Drug Test Anal. 2010 Jul;2(7):357-61. doi: 10.1002/dta.138.

Abstract

Two multivariate calibration methods-principal component regression (PCR) and partial least square (PLS)-have been used to determine tazarotene in the presence of its degradation products. Both methods are useful in spectral analysis because of the simultaneous inclusion of many spectral wavelengths instead of the single wavelength used in derivative spectrophotometry. A great improvement in the precision and predictive abilities of these multivariate calibrations was observed. A calibration set was constructed for the mixture and the best model was used to predict the concentration of the selected drug. The proposed methods were applied successfully in the determination of tazarotene in laboratory-prepared mixtures and in commercial preparations. Tazarotene was analyzed with mean accuracies of 100.006 ± 0.695 and 100.007 ± 0.690 using the PCR and PLS methods, respectively. The validity of the proposed methods was assessed using the standard addition technique. The proposed methods were found to be rapid, simple and required no preliminary separation. They can therefore be used for the routine analysis of tazarotene in quality-control laboratories.

摘要

已经使用两种多元校正方法 - 主成分回归(PCR)和偏最小二乘法(PLS) - 来确定维甲酸酯在其降解产物存在下的含量。由于同时包含许多光谱波长而不是导数分光光度法中使用的单个波长,因此这两种方法在光谱分析中都很有用。这些多元校正的精度和预测能力有了很大的提高。为混合物构建了一个校准集,并使用最佳模型来预测选定药物的浓度。该方法成功地应用于实验室制备的混合物和商业制剂中维甲酸酯的测定。使用 PCR 和 PLS 方法分别分析维甲酸酯的平均准确度为 100.006 ± 0.695 和 100.007 ± 0.690。使用标准添加技术评估了所提出方法的有效性。所提出的方法快速、简单,无需初步分离。因此,它们可用于质量控制实验室中维甲酸酯的常规分析。

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