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Abstract

Aim


The aim of the present research work was to develop a sensitive, rapid and accurate, RP-UPLC method for the simultaneous estimation of voxilaprevir (VXR), sofosbuvir (SFR), and velpatasvir (VLR) in formulations.


Materials and methods


The chromatographic separation of mixture of VXR, SFR, and VLR was attained in isocratic method utilizing a  mobile phase of 0.01N potassium dihydrogen orthophosphate (pH 4.8)  and  methanol  in the proportion  of 50:50%  v/v utilizing a CHS C18 column which has dimensions of 100×2.1mm,2.0 µmparticlesizeandtheflowrateof1.0mL/min.Thedetectionsystemwasmonitoredat260nm wavelength maximum with


1.0 mL injection volume.


Results


The retaining time for VXR, SFR, and VLR was achieved at 1.468 min, 0.606 min, and 0.848 min, respectively.


Conclusion


The developed method was highly  ensitive, rapid, precise, and accurate than the earlier reported methods. The total  run time was decreased to 3.0 min;  hence, the technique  was  more precise and economical. The projected method  can be utilized for routine analysis in quality control department in pharmaceutical companies.

Keywords

RP-UPLC Sofosbuvir Velpatasvir Voxilaprevir

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