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使用比率光谱导数分光光度法和多元校准技术同时分光光度法测定药物制剂中盐酸伪麻黄碱和布洛芬的含量。

Simultaneous spectrophotometric determination of pseudoephedrine hydrochloride and ibuprofen in a pharmaceutical preparation using ratio spectra derivative spectrophotometry and multivariate calibration techniques.

作者信息

Palabiyik I Murat, Dinç Erdal, Onur Feyyaz

机构信息

Department of Analytical Chemistry, Faculty of Pharmacy, University of Ankara, 06100 Tandoğan, Ankara, Turkey.

出版信息

J Pharm Biomed Anal. 2004 Feb 18;34(3):473-83. doi: 10.1016/s0731-7085(03)00578-8.

Abstract

Spectrophotometric methods are described for the simultaneous determination of pseudoephedrine hydrochloride and ibuprofen in their combination. The obtained data were evaluated by using five different methods. In the first method, ratio spectra derivative spectrophotometry, analytical signals were measured at the wavelengths corresponding to either maximums and minimums for both drugs in the first derivative spectra of the ratio spectra obtained by using each other spectra as divisor in their solution in 0.1 M HCl. In the other four spectrophotometric methods using chemometric techniques, classical least-squares, inverse least-squares, principal component regression and partial least-squares (PLS), the concentration data matrix were prepared by using the synthetic mixtures containing these drugs in methanol:0.1 M HCl (3:1). The absorbance data matrix corresponding to the concentration data matrix was obtained by the measurements of absorbances in the range 240-285 nm in the intervals with deltalambda = 2.5 nm at 18 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 pseudoephedrine hydrochloride and ibuprofen in their mixture. The procedures did not require any separation step. The linear range was found to be 300-1300 microg/ml for ibuprofen and 100-1300 microg/ml for pseudoephedrine hydrochloride in all five methods. The accuracy and the precision of the methods have been determined and they have been validated by analyzing synthetic mixtures. The five methods were successfully applied to tablets and the results were compared with each other.

摘要

描述了用于同时测定盐酸伪麻黄碱和布洛芬复方制剂中二者含量的分光光度法。采用五种不同方法对所得数据进行评估。在第一种方法即比率光谱导数分光光度法中,以0.1 M盐酸中彼此的光谱为除数,在所得比率光谱的一阶导数光谱中,于对应两种药物最大和最小吸收波长处测量分析信号。在使用化学计量学技术的其他四种分光光度法中,即经典最小二乘法、逆最小二乘法、主成分回归法和偏最小二乘法(PLS),通过使用含有这些药物的甲醇:0.1 M盐酸(3:1)的合成混合物制备浓度数据矩阵。通过在其零阶光谱中18个波长处、间隔为2.5 nm、范围为240 - 285 nm测量吸光度,获得与浓度数据矩阵对应的吸光度数据矩阵,然后,通过使用吸光度数据矩阵和浓度数据矩阵进行校准或回归,以预测混合物中盐酸伪麻黄碱和布洛芬的未知浓度。该方法无需任何分离步骤。在所有五种方法中,布洛芬的线性范围为300 - 1300 μg/ml,盐酸伪麻黄碱的线性范围为100 - 1300 μg/ml。已测定该方法的准确度和精密度,并通过分析合成混合物进行了验证。这五种方法成功应用于片剂,并对结果进行了相互比较。

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