Madbouly Eman A, El-Shanawani Abdalla A, El-Adl Sobhy M, Abdelkhalek Ahmed S
Department of Medicinal Chemistry, Faculty of Pharmacy, Zagazig University, Zagazig, Egypt.
Sci Rep. 2025 Jan 11;15(1):1721. doi: 10.1038/s41598-024-83049-4.
Remdesivir and moxifloxacin hydrochloride are among the most frequently co-administered drugs used for COVID-19 treatment. The current work aims to evaluate green spectrophotometric methodologies for estimating remdesivir and moxifloxacin hydrochloride in different matrices for the first time. The proposed approaches were absorbance subtraction, extended ratio subtraction and amplitude modulation methods. In order to determine the absorbance of the investigated medications in combination at the isoabsorptive point, the pure moxifloxacin hydrochloride absorbance factor is applied using the absorbance subtraction method, which modifies the zero absorption spectra of the drugs under investigation at the isoabsorptive point (229 nm). The spectrum of moxifloxacin hydrochloride is more extended in the plateau area between 340 and 400 nm, where remdesivir exhibits no absorption. So, also, the ratio spectra were successfully manipulated for quantification of the two drugs. Regarding the pharmacokinetic profile of remdesivir (Cmax 4420 ng/mL) and moxifloxacin hydrochloride (Cmax 3.56 µg/mL), the proposed methods were effectively used to spectrophotometrically determine remdesivir and moxifloxacin hydrochloride in plasma matrix. The new approach was validated using the ICH guidelines for specificity, linearity, precision, and accuracy. The greenness of the reported methodologies was evaluated using two metrics: the analytical eco-scale and the green analytical procedure index.
瑞德西韦和盐酸莫西沙星是治疗新冠肺炎最常用的联合用药。目前的工作旨在首次评估绿色分光光度法,用于估算不同基质中的瑞德西韦和盐酸莫西沙星。所提出的方法有吸光度减法、扩展比率减法和振幅调制法。为了在等吸收点测定所研究药物组合的吸光度,使用吸光度减法应用纯盐酸莫西沙星吸光度因子,该方法在等吸收点(229nm)修改所研究药物的零吸收光谱。盐酸莫西沙星的光谱在340至400nm的高原区域更宽,而瑞德西韦在该区域无吸收。因此,比率光谱也成功用于两种药物的定量分析。关于瑞德西韦(Cmax 4420 ng/mL)和盐酸莫西沙星(Cmax 3.56 µg/mL)的药代动力学特征,所提出的方法有效地用于分光光度法测定血浆基质中的瑞德西韦和盐酸莫西沙星。使用国际人用药品注册技术协调会(ICH)的特异性、线性、精密度和准确度指南对新方法进行了验证。使用两个指标评估所报告方法的绿色度:分析生态规模和绿色分析程序指数。