Publication: Isoniazid, pyrazinamide and rifampicin content variation in split fixed-dose combination tablets
Issued Date
2014-07-08
Resource Type
ISSN
19326203
Other identifier(s)
2-s2.0-84903881870
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Mahidol University
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SCOPUS
Bibliographic Citation
PLoS ONE. Vol.9, No.7 (2014)
Suggested Citation
Thomas Pouplin, Pham Nguyen Phuong, Pham Van Toi, Julie Nguyen Pouplin, Jeremy Farrar Isoniazid, pyrazinamide and rifampicin content variation in split fixed-dose combination tablets. PLoS ONE. Vol.9, No.7 (2014). doi:10.1371/journal.pone.0102047 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/33006
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Title
Isoniazid, pyrazinamide and rifampicin content variation in split fixed-dose combination tablets
Abstract
Setting: In most developing countries, paediatric tuberculosis is treated with split tablets leading to potential inaccuracy in the dose delivery and drug exposure. There is no data on the quality of first-line drugs content in split fixed-dose combination tablets. Objective: To determine Isoniazid, Pyrazinamide and Rifampicin content uniformity in split FDC tablets used in the treatment of childhood tuberculosis. Design: Drug contents of 15 whole tablets, 30 half tablets and 36 third tablets were analysed by high performance liquid chromatography. The content uniformity was assessed by comparing drug content measured in split portions with their expected amounts and the quality of split portions was assessed applying qualitative specifications for whole tablets. Results: All whole tablets measurements fell into the USP proxy for the three drugs. But a significant number of half and third portions was found outside the tolerated variation range and the split formulation failed the requirements for content uniformity. To correct for the inaccuracy of splitting the tablets into equal portions, a weight-adjustment strategy was used but this did not improve the findings. Conclusion: In split tablets the content of the three drugs is non-uniform and exceeded the USP recommendations. There is an absolute need to make child-friendly formulations available for the treatment of childhood tuberculosis. © 2014 Pouplin et al.