Michael A Odeniyi, Kolawole T Jaiyeoba
Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, University of Ibadan, Ibadan, Nigeria;For correspondence:- Kolawole Jaiyeoba Email: jaiyeobakt@yahoo.co.uk
Published: 15 June 2004
Citation: Odeniyi MA, Jaiyeoba KT. Effects of interacting variables on the releasevproperties of chloroquine and aminophylline suppositories. Trop J Pharm Res 2004; 3(1):285-290 doi: 10.4314/tjpr.v3i1.4
© 2004 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..
Method: Suppositories were formulated with theobroma oil and Witepsol H15 as bases at ‘low’ and ‘high’ levels respectively. Chloroquine and aminophylline, both water-soluble drugs, were incorporated as active constituents at ‘low’ and ‘high’ levels respectively while Tween 80 was incorporated as surfactant in some of the formulations. Disintegration time and time taken for 50% of the drug to dissolve were used as assessment parameters.
Results: The inclusion of surfactant in the suppository formulation proved to be the most significant variable in the formulation. The ranking for the individual coefficient values for the formulations was S>>B>D for disintegration time DT and S>>>D>B for the dissolution parameter t50. While the ranking for the interaction effects was B-D>B-S>S-D on DT and on t50 S-D>B-S>B-D.
Conclusion: The results suggest that in formulating water-soluble drugs such as chloroquine and aminophylline as suppositories in a hydrophobic base, the presence of a surfactant is the most influential variable.
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