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  Afr. J. Biotechnol.

  Vol. 7 No. 25

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  Brisibe EA
  Ferreira JFS

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Scientific Research and Essays
 

African Journal of Biotechnology Vol. 7 (25), pp. 48844896, 29 December 2008

ISSN 1684-5315  © 2008 Academic Journals  

 

 

Review

 

Building a golden triangle for the production and use of artemisinin derivatives against falciparum malaria in Africa

 

Ebiamadon Andi Brisibe1,2*, Edak A. Uyoh1, Fraideh Brisibe3, Pedro M. Magalhäes4 and Jorge F. S. Ferreira5

 

1Department of Genetics and Biotechnology, University of Calabar, Calabar, Nigeria.

2Molecular Bio/Sciences Limited, 124 MCC Road, Calabar, Nigeria.

3Department of Veterinary Public Health and Preventive Medicine, Faculty of Veterinary Medicine, University of Maiduguri, Maiduguri, Nigeria.

4Chemical, Biological and Agricultural Pluridisciplinary Research Center (CPQBA), University of Campinas, Campinas, SP, Brazil.

5USDA, ARS, Appalachian Farming System Research Center, 1224 Airport Road, Beaver, West Virginia 25813, USA

 

*Corresponding author. E-mail: brisibe2002@yahoo.co.uk.

 

Accepted 12 December, 2008

 
   Abstract
 

Use of the conventional quinoline- and sulphanamide-based drugs for the symptomatic treatment of malaria is gradually being replaced by artemisinin-based combination therapies (ACTs) due to increasing resistance by the Plasmodium parasite. This development has drastically increased artemisinin demand world-wide, and Artemisia annua L. is currently the only commercial source for the supply of this vital antimalarial drug to the international market. Recent advances, however, demonstrate that the production of isoprenoid precursors in micro-organisms is a feasible complementary strategy that would help reduce artemisinin cost in the future. The key genes encoding for enzymes regulating the biosynthesis of artemisinin in planta are fully understood to enable metabolic engineering of the pathway, and results from pilot genetic engineering studies in microbial strains thus far are very inspiring. This review, therefore, explores the current status of artemisinin derived drugs against malaria and highlights some implications of crop agronomy, biotechnology and solvent extraction strategies in enhancing the total yield of artemisinin for the production of ACTs, which are responsible for saving the lives of countless numbers of patients in malaria-stricken societies and are currently in very high demand, especially in Africa.

 

Key words: Artemisia annua, ACTs, biotechnology, malaria, Plasmodium spp.

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