Simultaneous Determination of First-Line 4-FDC Antituberculosis Drugs by UHPLC-UV and HPLC-UV: A Comparative Study.

J AOAC Int

Universidade Federal de Minas Gerais, Faculdade de Farmácia, Departamento de Produtos Farmacêuticos, Avenida Presidente Antônio Carlos 6627, 31270-901 Belo Horizonte, MG, Brazil.

Published: July 2017

AI Article Synopsis

  • Tuberculosis is a leading infectious disease, causing over 1 billion deaths in 200 years, with approximately 9.6 million infections and 1.5 million deaths reported in 2014.
  • First-choice treatment involves a fixed-dose combination of four antibiotics, but existing testing methods for these drugs are time-consuming and complex.
  • A new ultra-high-performance liquid chromatography (UHPLC) method was developed to greatly reduce analysis time from 17 to 4 minutes while maintaining accuracy and significantly lowering costs and resource usage.

Article Abstract

Tuberculosis is the second most deadly infectious disease, surpassed only by HIV/AIDS, and has resulted in over 1 billion deaths in the last 200 years. The World Health Organization estimates that in 2014, 9.6 million people were infected by this disease and 1.5 million had died. First-choice treatment consists of fixed-dose combination tablets containing rifampicin, isoniazid, pyrazinamide, and ethambutol hydrochloride (4-FDC). There are pharmacopeial protocols available to test 4-FDC, but they are prolonged, two-step methods. One single-step method in the literature performs the simultaneous determination by HPLC, but requires a long acquisition time. In this context, an ultra-HPLC (UHPLC) method was developed based on the HPLC method with the objective of reducing analysis time. A C18 column (1.9 µm particle size) was used with UV-diode-array detection at 238 and 282 nm. The method was found to be selective, linear, exact, precise, and robust. Samples from two batches were analyzed and the results compared with those obtained by the HPLC method, with no statistically significant differences observed (P > 0.05). This UHPLC method reduced the analysis time from 17 to 4 min, with a more than 90% reduction in sample and reagent consumption and a financial economy of almost 50-fold.

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Source
http://dx.doi.org/10.5740/jaoacint.16-0200DOI Listing

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