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Separation-free spectrophotometric platforms for rapid assessment of combined antiplatelet therapy in complex matrices

机译:分离的分光光度平台,用于快速评估复杂矩阵中的组合抗血小板治疗

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摘要

Aim: To develop simple and rapid UV-spectrophotometric platforms for the simultaneous quantification of a binary mixture containing clopidogrel bisulphate (CPS) and aspirin (ASP) in complex matrices without prior separation. Experimental: Five mathematical models namely ratio-difference method, mean centering of the ratio spectra, dual wavelength, induced dual wavelength and H-Point Standard Addition method, were utilized for resolving spectral overlap by mathematical processing of ratio and zero-order absorption spectra. Analytes were extracted from tested matrices (whole blood, pharmaceutical formulations and dissolution media buffer) and quantified using the proposed methods. The methods were validated according to ICH guidelines. Results: The developed methods demonstrated limits of detection ranging from 0.67 to 1.09 mu g/ml(-1) for CPS and 0.49 to 0.71 mu g.ml(-1) for ASP. All proposed methods allowed for reliable determination of CPS and ASP in complex matrices within reported reference ranges, indicating their potential application for therapeutic drug monitoring and quality control testing.
机译:目的:开发简单且快速的紫外光光度法平台,用于同时定量含有氯吡格雷硫酸盐(CPS)和阿司匹林(ASP)的二元混合物,而无需先前分离。实验:五种数学模型即比率差异方法,使用比率谱,双波长,诱导的双波长和H点标准添加方法的平均定心,用于通过比率和零阶吸收光谱的数学处理来解决光谱重叠。从测试基质(全血,药物制剂和溶解介质缓冲液)中提取分析物并使用所提出的方法进行定量。根据ICH指南验证这些方法。结果:开发的方法显示了用于CPS的0.67至1.09μg/ ml(-1)的检测限值,为ASP的0.49至0.71μg(-1)。所有所提出的方法允许在报告的参考范围内可靠地测定复杂矩阵中的CPS和ASP,表明它们潜在的治疗药物监测和质量控制测试。

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