A Novel Stability Indicating RP-HPLC Method for Determination of Sofosbuvir in Bulk and Tablet Dosage
Journal Title: Journal of Pharmaceutical and Medicinal Chemistry - Year 2019, Vol 5, Issue 1
Abstract
The proposed work was accurate and precise stability indicating RP-HPLC method has been developed and validation of Sofosbuvir, in tablet dosage form. The separation was achieved on a Kromasil C18 (4.6×250 mm, 5µ) column using a mixture of Methanol: water (60: 40% v/v) as the mobile phase at a flow rate of 1.0 mL/min and detected 247 nm. The retention time of sofosbuvir 3.475 minutes. The linear responses in the concentration range of 10-60 µg/mL of Sofosbuvir. The method precision for the determination of assay was less than 2.0% RSD. The method is useful in the quality control of bulk and pharmaceutical formulations.
Authors and Affiliations
G. Kumaraswamy
Keywords
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- EP ID EP649496
- DOI 10.21088/jpmc.2395.6615.5119.2
- Views 146
- Downloads 0
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