El-Gamal Rania M, Abdel-Gawad Sherif A, Belal Fathalla F, Moustapha Moustapha E
Pharmaceutical Chemistry Department, College of Pharmacy, Prince Sattam Bin-Abdul Aziz University P. O. Box 173 Al-Kharj 11942 Kingdom of Saudi Arabia
Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Mansoura University Mansoura Egypt.
RSC Adv. 2018 Sep 24;8(57):32909-32915. doi: 10.1039/c8ra06588h. eCollection 2018 Sep 18.
A new sensitive, rapid and simple spectrofluorimetric method was utilized for the assessment of velpatasvir (VPS) in its bulk form as well as in its combined tablet with sofosbovir (SFV). The technique relies on measuring the native fluorescence of VPS in methanol at 385 nm and 400 nm after excitation at 295 nm. The fluorescence-concentration plots were rectilinear through the range of 2.0-20.0 ng mL at both emission maxima with lower detection limits of 0.146 ng mL and 0.378 ng mL, and lower quantification limits of 0.444 ng mL and 1.147 ng mL at 385 nm and 400 nm, respectively. The proposed method was appropriately used for the analysis of VPS in its commercial tablet formulation and the results were in good agreement with those achieved with the applied comparison method.
一种新型灵敏、快速且简便的荧光分光光度法被用于评估维帕他韦(VPS)原料药及其与索磷布韦(SFV)的复方片剂。该技术基于在295 nm激发后,测量VPS在甲醇中于385 nm和400 nm处的固有荧光。在两个发射最大值处,荧光-浓度曲线在2.0 - 20.0 ng/mL范围内呈线性,在385 nm和400 nm处的检测下限分别为0.146 ng/mL和0.378 ng/mL,定量下限分别为0.444 ng/mL和1.147 ng/mL。所提出的方法适用于分析VPS的市售片剂制剂,结果与采用的对照方法所得结果高度一致。