![Sample our Physical Sciences journals, sign in here to start your FREE access for 14 days]({"type":"image" , "src" : "/sda/110819/TOC-Subject-Sample-2021-Physical-Sciences.jpg"})
ABSTRACT
Sofosbuvir (SOF) and ledipasvir (LED) are recently approved and coformulated as directly acting antiviral agents used for treatment of hepatitis C virus (HCV). A reversed phase high performance liquid chromatography - diode array detector (RP-HPLC/DAD) method was developed and validated for the first time for the analysis of newly formulated anti-HCV combination, in pure form, pharmaceutical formulation and in human plasma. In the developed method, separation was performed on Zorbax® Eclipse C18 column using a gradient mixture of acetonitrile–water as a mobile phase and scanning was performed at 260 nm (for SOF) and 330 nm (for LED). The two drugs were completely separated from each other and from plasma, where plasma peak appeared at 2.76 ± 0.05 min, SOF at 4.25 ± 0.05, and LED at 7.35 ± 0.05. The developed method showed high sensitivity, the drugs showed linearity in the range of 1–45 µg/mL for both pure form and spiked human plasma. Three freeze–thaw cycles were performed separately at two different temperatures, −8 and −20°C. No significant loss of the studied drugs were observed during repeated thawing and freezing. Validation parameters such as accuracy, precision, robustness, and ruggedness were tested in compliance with USP recommendations, where acceptable results were obtained. Applying to pharmaceutical formulation showed no interference from tablet excipients.
GRAPHICAL ABSTRACT
