Isoniazid, pyrazinamide and rifampicin content variation in split fixed-dose combination tablets

• Published in: PloS one 2014-07, Vol.9 (7), p.e102047-e102047
• Main Authors: Pouplin, Thomas, Phuong, Pham Nguyen, Toi, Pham Van, Nguyen Pouplin, Julie, Farrar, Jeremy
• Format: Article
• Language: English
• Subjects: Bioavailability; Biology and Life Sciences; Chemistry, Pharmaceutical - standards; Children; Children & youth; Chromatography; Combination drug therapy; Developing countries; Dosage and administration; Drug Combinations; Drug delivery systems; Drug development; Drug dosages; Drugs; Formulations; High performance liquid chromatography; HIV; Human immunodeficiency virus; Humans; Isoniazid; Isoniazid - analysis; Isoniazid - therapeutic use; LDCs; Liquid chromatography; Medical screening; Medicine; Medicine and Health Sciences; Pediatrics; Physical Sciences; Pyrazinamide; Pyrazinamide - analysis; Pyrazinamide - therapeutic use; Quality Control; Research and Analysis Methods; Rifampin; Rifampin - analysis; Rifampin - therapeutic use; Tablets; Tuberculosis; Tuberculosis, Pulmonary - drug therapy
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0102047

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. To determine Isoniazid, Pyrazinamide and Rifampicin content uniformity in split FDC tablets used in the treatment of childhood tuberculosis. 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. 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. 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.