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首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Evaluation of in silico and in lab sample enrichment techniques for the assessment of challengeable quaternary combination in critical ratio
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Evaluation of in silico and in lab sample enrichment techniques for the assessment of challengeable quaternary combination in critical ratio

机译:在硅和实验室样品中评价评估临界比率的竞争季度组合的评估

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CAF, respectively. The specificity of suggested methods was studied via A comparative study of successive spectrophotometric resolution technique for the simultaneous determination of a challengeable quaternary mixture of Chlorpheniramine maleate (CPM), Pseudoephedrine hydrochloride (PSE), Ibuprofen (IBU) and Caffeine (CAF) is presented, without preliminary physical separation steps. Several successive steps were applied on built-in spectrophotometer software utilizing zero and/or derivative and/or ratio spectra of the studied components. These methods, namely, Dual amplitude difference (DAD) as a novel method, Constant multiplication coupled with spectrum subtraction method (CM-SS), Factorized first derivative coupled with derivative transformation method (FD1 -DT) and Derivative ratio method (DD1). The calibration graphs are linear over the concentration range of 10.0-80.0 lg/mL,150.0-900.0 lg/mL, 200.0-1400.0 lg/mL and 3.0-30.0 lg/mL for CPM, PSE, IBU andlaboratory prepared (diverse ratios) mixtures and were successfully applied for Antiflu (R) capsules' analysis. Moreover, sample enrichment via In Silico (via software of spectrophotometer) and In Lab (via spiking with pure sample) techniques was elected for a pharmaceutical dosage form analysis comprising CPM and PSE as minor components. Accuracy, precision and specificity were between the valid limits. Validation steps were done in accordance with the ICH guidelines. Moreover, statistical comparison was carried out between the obtained and reported results for pure powder form and no significant difference appeared. (C) 2021 Elsevier B.V. All rights reserved.
机译:分别是咖啡馆。通过连续分光光度拆分技术的对比研究,研究了建议方法的特异性,该技术用于同时测定马来酸氯苯那敏(CPM)、盐酸伪麻黄碱(PSE)、布洛芬(IBU)和咖啡因(CAF)的具有挑战性的四元混合物,无需初步的物理分离步骤。利用所研究组分的零和/或导数和/或比值光谱,在内置分光光度计软件上应用了几个连续步骤。这些方法包括:双振幅差分法(DAD)作为一种新方法,常数乘法与谱减法(CM-SS)相结合,因子化一阶导数与导数变换相结合(FD1-DT)和导数比法(DD1)。CPM、PSE、IBU和实验室制备的(不同比例)混合物的校准曲线在10.0-80.0 lg/mL、150.0-900.0 lg/mL、200.0-1400.0 lg/mL和3.0-30.0 lg/mL浓度范围内呈线性,并成功应用于抗Lu(R)胶囊的分析。此外,在药物剂型分析中,选择了通过硅片(通过分光光度计软件)和实验室(通过纯样品加标)技术进行样品富集,包括CPM和PSE作为次要成分。准确度、精密度和特异性在有效限值之间。验证步骤按照ICH指南进行。此外,对纯粉末形式的所得结果和报告结果进行了统计比较,没有出现显著差异。(c)2021爱思唯尔B.V.保留所有权利。

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