PRMSS Anuradha College of Pharmacy, Chikhli, India.
International Journal of Science and Research Archive, 2025, 15(01), 1618-1646
Article DOI: 10.30574/ijsra.2025.15.1.1253
Received on 18 March 2025; revised on 26 April 2025; accepted on 28 April 2025
This comprehensive overview takes into account a crucial function within the development and testing of analytical techniques that guarantee the effects, safety, and exceptional of antiviral tablets used for HIV treatment. In this evaluation, standards, technical, normative frameworks, and problems are systematically taken into consideration, and the drug is quantitatively determined and characterized. The main pastimes are to be very effective inside the mass evaluation of the mass evaluation and different advanced techniques of the liquid chromatography (VEGH), the liquid chromatography (LC-MS/MS), the discussion of worldwide hints, the consideration of stability, and innovation remark. Thanks to the mixing of cutting-edge literature and problem studies, this evaluation gives a roadmap for researchers and regulators who focus on the complexity of drug analysis on HIV.
Analytical Method Development; Antiretroviral Drugs; HIV Treatment; HPLC Validation; LC-MS/MS; ICH Guidelines; Drug Stability
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Shrutika Sanjay Awachat, Snehal Vijay Kalbande, Srushti Rajiv Raut, Trupti Raju Changade, Snehashish Sharadrao Sarnaik, Kishore Rodge and R. H. Kale. Analytical method development and validation of antiviral drugs for HIV. International Journal of Science and Research Archive, 2025, 15(01), 1618-1646. Article DOI: https://doi.org/10.30574/ijsra.2025.15.1.1253.






