Skip to Main Content
It looks like you're using Internet Explorer 11 or older. This website works best with modern browsers such as the latest versions of Chrome, Firefox, Safari, and Edge. If you continue with this browser, you may see unexpected results.
Article in Journal: Journal of Clinical Pharmacy and Therapeutics (Library Catalog Search: antimalarial pharmacology AND developing countries)
Antimalarial drug quality in Africa
Antimalarial drug quality in Africa
- Publication year:
- Journal of Clinical Pharmacy and Therapeutics v32 n5 (October 2007): 429-440
- Held by:
- Saint Leo University Cannon Memorial Library
- More Author / Title Information:
- A. A. Amin and G. O. Kokwaro
- Unique Identifier:
- <b>Background and objective: </b> There are several reports of sub-standard and counterfeit antimalarial drugs circulating in the markets of developing countries; we aimed to review the literature for the African continent.<br><b>Methods: </b> A search was conducted in PubMed in English using the medical subject headings (MeSH) terms: ‘Antimalarials/analysis’[MeSH] OR ‘Antimalarials/standards’[MeSH] AND ‘Africa’[MeSH]’ to include articles published up to and including 26 February 2007. Data were augmented with reports on the quality of antimalarial drugs in Africa obtained from colleagues in the World Health Organization. We summarized the data under the following themes: content and dissolution; relative bioavailability of antimalarial products; antimalarial stability and shelf life; general tests on pharmaceutical dosage forms; and the presence of degradation or unidentifiable impurities in formulations.<br><b>Results and discussion: </b> The search yielded 21 relevant peer-reviewed articles and three reports on the quality of antimalarial drugs in Africa. The literature was varied in the quality and breadth of data presented, with most bioavailability studies poorly designed and executed. The review highlights the common finding in drug quality studies that (i) most antimalarial products pass the basic tests for pharmaceutical dosage forms, such as the uniformity of weight for tablets, (ii) most antimalarial drugs pass the content test and (iii) <i>in vitro</i> product dissolution is the main problem area where most drugs fail to meet required pharmacopoeial specifications, especially with regard to sulfadoxine-pyrimethamine products. In addition, there are worryingly high quality failure rates for artemisinin monotherapies such as dihydroartemisinin (DHA); for instance all five DHA sampled products in one study in Nairobi, Kenya, were reported to have failed the requisite tests.<br><b>Conclusions: </b> There is an urgent need to strengthen pharmaceutical management systems such as post-marketing surveillance and the broader health systems in Africa to ensure populations in the continent have access to antimalarial drugs that are safe, of the highest quality standards and that retain their integrity throughout the distribution chain through adequate enforcement of existing legislation and enactment of new ones if necessary, and provision of the necessary resources for drug quality assurance.
- A. A. Amin, Malaria Public Health & Epidemiology Group, Centre for Geographic Medicine Research-Coast, Kenya Medical Research Institute/Wellcome Trust Research Programme, PO Box 43640-00100 GPO, Nairobi, Kenya. Tel.: +254 20 2720163; fax: +254 20 2711673; e-mail: email@example.com
- Received 30 March 2007, Accepted 15 June 2007
- Number of Figures: 2