Spectrophotometric Determination Of Rifampin in the Presence of its Degradation Products in Pharmaceutical Preparations
- 1 September 1993
- journal article
- research article
- Published by Taylor & Francis in Analytical Letters
- Vol. 26 (9) , 1905-1917
- https://doi.org/10.1080/00032719308017439
Abstract
The determination of rifampin in the presence of its main degradation products, 3-formyl rifampin and rifampin quinone using two spectrophotometric methods is described. Both Glenn's method and first derivative spectrophotometry were successfully adopted. No preliminary separation steps were required in either cases. Both methods gave accurate and reproducible results for the determination of the drug in dosage forms. The percentage recoveries ranged from 99.33% ±0.63 to 100.2% ± 0.44. The proposed methods are more simple, rapid than other existing methods and can be readily adopted in control laboratory.Keywords
This publication has 8 references indexed in Scilit:
- High Performance Liquid Chromatographic Analysis of Rifampin and Related Impurities in Pharmaceutical FormulationsJournal of Liquid Chromatography, 1979
- Analysis of rifampicin and of its hydrogenated deriavites by high-performance liquid chromatographyJournal of Chromatography A, 1978
- Thin-layer chromatographic identity and purity test for rifampinJournal of Chromatography A, 1977
- High Pressure Liquid ChromatographyJournal of Pharmaceutical Sciences, 1973
- Applications of High Speed Reversed-Phase Liquid ChromatographyJournal of Chromatographic Science, 1971
- Fluorometric and Microbiological Assays for Rifampicin and the Determination of Serum Levels in the DogChemotherapy, 1971
- Rifampicin: A New Orally Active RifamycinChemotherapy, 1966
- Rifamycin XXIII. The Polarographic Behavior of Rifamycin B, Rifamycin O, Rafamycin S, and Rifamycin SV.Analytical Chemistry, 1962