GN Thoithi
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Nairobi, P. O. Box 19676, Nairobi. Kenya
IO Kibwage
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Nairobi, P. O. Box 19676, Nairobi. Kenya
O King’ondu
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Nairobi, P. O. Box 19676, Nairobi. Kenya.
J Hoogmartens
Laboratorium voor Farmaceutische Chemie en Analyse van Geneesmiddelen, Faculteit Farmaceutische Wetenschappen, Katholieke Universiteit Leuven. E. Van Evenstraat 4, 3000 Leuven. Belgium.
Abstract
A gradient liquid chromatographic method which can separate isoniazid, pyrazinamide and rifampicin is described. A Hypersil C18, 5 mm, 250 mm x 4.6 mm internal diameter column was maintained at 40°C. The method was developed by systematic evaluation of the influence of the buffer concentration, column temperature and the mobile phase pH. The method proposed uses isocratic elution with potassium phosphate buffer (pH 6.0; 0.05 M) for 10 min, followed by linear gradient to potassium phosphate buffer (pH 6.0; 0.05 M)-methanol (40:60, v/v) in 5 min, isocratic elution at the same composition for a further 15 min and then linear gradient back to potassium phosphate buffer (pH 6.0; 0.05 M) in 5 min. The flow-rate was 1 ml/min and UV detection was at 254 nm. The method was validated and it has been used for routine analysis of tablets containing isoniazid, pyrazinamide and rifampicin. Analysis time is 35 minutes.
(E & C Afr Jnl Pharm Sci: 2002 5(1): 8-14)