Development and Validation of a Stability-Indicating RP-HPLC Method for the Simultaneous Determination of Sofosbuvir, Velpatasvir, and Voxilaprevir in Tablet Formulation
Keywords:
stabilityindicating, method development, validation, RP-HPLC, sofosbuvir
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References
Sandhya Rani, J Devanna, N (2018) Development and validation of RP-HPLC method for the simultaneous estimation of Sofosbuvir, velpatasvir, and voxilaprevir in bulk and tablet dosage forms. 11(2), 452-459.
Sandhya Rani, J Devanna, N (2017) New RP-HPLC method development and validation for simultaneous estimation of sofosbuvir and velpatasvir in a pharmaceutical dosage form. 4(11), 145-152.
Geetha Susmitha, A Rajitha, G (2018) Development and validation of stability indicating UPLC method for simultaneous estimation of sofosbuvir and velpatasvir in a tablet dosage form. 9(11), 4764-4769.
Lakshmana Rao, A Pallavi, A (2019) Method Development and Validation of Stability Indicating RP-HPLC Method for Simultaneous Estimation of Sofosbuvir and Velpatasvir in Tablet Dosage Form. 2(1), 1-8.
B; Balaswami, P Ramana, ; Venkata, B Rao, P Subba; Sanjeeva (2018) A New Simple Stability-Indicating RP-HPLC-PDA Method for Simultaneous Estimation of Triplicate Mixture of Sofosbuvir, Velpatasvir, and Voxilaprevir in Tablet Dosage Form. 11(9), 4147-4156.
Memthoibi Devi, L, Dr Rama Mohan Reddy, T Dr, K Abbulu (2010) Simultaneous determination and validation of third generation antiviral drugs by RP-HPLC method. 8(1), 1-8.
K Lalitha, Raveendra Reddy, J Devanna, N (2018) Stability indicating RP-HPLC method development and validation for estimation of Sofosbuvir in a pharmaceutical dosage form. 7(5), 656-662.
Phillip Borman, David Elder (2005) Q2(R1) Validation of Analytical Procedures. 127-166.
(1996) ICH: Q2B. Harmonized Tripartite Guideline, Validation of Analytical Procedure: Methodology, IFPMA.
G Ngwa (2010) Forced degradation studies as an integral part of HPLC stability indicating method development. 10, 56-59.
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2020-04-07
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