Moustafa Azza A, Hegazy Maha A, Mohamed Dalia, Ali Omnia
Analytical Chemistry Department, Faculty of Pharmacy, Cairo University, Kasr-El Aini Street, 11562 Cairo, Egypt.
Analytical Chemistry Department, Faculty of Pharmacy, October University for Modern Sciences and Arts (MSA), 11787 6th October City, Egypt; Analytical Chemistry Department, Faculty of Pharmacy, Helwan University, Ein Helwan, 11795, Cairo, Egypt.
Spectrochim Acta A Mol Biomol Spectrosc. 2016 Feb 5;154:76-83. doi: 10.1016/j.saa.2015.10.010. Epub 2015 Oct 22.
A novel approach for the resolution and quantitation of severely overlapped quaternary mixture of carbinoxamine maleate (CAR), pholcodine (PHL), ephedrine hydrochloride (EPH) and sunset yellow (SUN) in syrup was demonstrated utilizing different spectrophotometric assisted multivariate calibration methods. The applied methods have used different processing and pre-processing algorithms. The proposed methods were partial least squares (PLS), concentration residuals augmented classical least squares (CRACLS), and a novel method; continuous wavelet transforms coupled with partial least squares (CWT-PLS). These methods were applied to a training set in the concentration ranges of 40-100 μg/mL, 40-160 μg/mL, 100-500 μg/mL and 8-24 μg/mL for the four components, respectively. The utilized methods have not required any preliminary separation step or chemical pretreatment. The validity of the methods was evaluated by an external validation set. The selectivity of the developed methods was demonstrated by analyzing the drugs in their combined pharmaceutical formulation without any interference from additives. The obtained results were statistically compared with the official and reported methods where no significant difference was observed regarding both accuracy and precision.
利用不同的分光光度辅助多元校准方法,展示了一种用于拆分和定量糖浆中严重重叠的马来酸氯苯那敏(CAR)、福尔可定(PHL)、盐酸麻黄碱(EPH)和日落黄(SUN)四元混合物的新方法。所应用的方法使用了不同的处理和预处理算法。所提出的方法有偏最小二乘法(PLS)、浓度残差增强经典最小二乘法(CRACLS)以及一种新方法;连续小波变换结合偏最小二乘法(CWT-PLS)。这些方法分别应用于四个组分浓度范围为40 - 100μg/mL、40 - 160μg/mL、100 - 500μg/mL和8 - 24μg/mL的训练集。所使用的方法不需要任何初步分离步骤或化学预处理。通过外部验证集评估了这些方法的有效性。通过分析药物在其复方制剂中的情况,证明了所开发方法的选择性,且不受添加剂的任何干扰。将所得结果与官方和已报道的方法进行统计学比较,在准确度和精密度方面均未观察到显著差异。