A Review on Development and validation of analytical method for estimation of Rifapentine in bulk and Pharmaceutical formulation

Asian Journal of Pharmaceutical Research 2026

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Authors: Manish Kumar Sahu, Dolly Dewangan, Jitendra Yadav, Kamraj Kamraj, Krity Gupta, Parimal Verma, Prashant Kumar Sahu, Shweta Sinha, Adeep Kujur, Sanjay J. Daharwal
DOI: 10.52711/2231-5691.2026.00014
Cited by: 0
References: 7

Abstract

A simple analytical Method is developed for identification and quantification of related impurities in the API and pharmaceutical dosage form. Rifapentine is an antibiotic from the rifamycin class that is utilized in the treatment of tuberculosis. The solvent, method, analytical procedure, reaction time, Solvent concentration used are carefully optimized with Maximum sensitivity. The developed method is Validated as per the guidelines of International Conference Harmonization (ICH.) the proposed method is precise and accurate and for the routine analysis of Rifapentine hence can be used for bulk and pharmaceutical dosage form.

Fields of Study & Subjects

Analytical Methods in Pharmaceuticals Pharmaceutical Quality and Counterfeiting Biosimilars and Bioanalytical Methods

Publication details

Journal / source
Asian Journal of Pharmaceutical Research
Volume
16
Issue
1
Pages
101–101
Publication date
22 January 2026
Language
EN