Evaluation of the recently reported USP gradient HPLC method for analysis of anti-tuberculosis drugs for its ability to resolve degradation products of rifampicin

Author:

Mohan Bhavika,Sharda Nishi,Singh Saranjit

Publisher

Elsevier BV

Subject

Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry

Reference5 articles.

1. A critical review of the probable reasons for the poor variable bioavailability of rifampicin from anti-tubercular fixed-dose combination (FDC) products, and the likely solutions to the problem

2. Anonymous, Pharmacopoeial Previews, Pharmacopeial Forum 26, Sept.–Oct. 2000, pp. 1420–1422.

3. Anonymous, Interim Revision Announcement, Pharmacopeial Forum 27, Nov.–Dec. 2001, pp. 3232–3233.

4. B. Mohan, Development of a stability indicating assay method for rifampicin, isoniazid and pyrazinamide in combination, MSc (Pharm.) thesis, NIPER, S.A.S. Nagar, India, 2001.

5. The Reason for an Increase in Decomposition of Rifampicin in the Presence of Isoniazid under Acid Conditions

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