Literature DB >> 15047998

Developing artemisinin based drug combinations for the treatment of drug resistant falciparum malaria: A review.

P L Olliaro1, W R Taylor.   

Abstract

The emergence and spread of drug resistant malaria represents a considerable challenge to controlling malaria. To date, malaria control has relied heavily on a comparatively small number of chemically related drugs, belonging to either the quinoline or the antifolate groups. Only recently have the artemisinin derivatives been used but mostly in south east Asia. Experience has shown that resistance eventually curtails the life-span of antimalarial drugs. Controlling resistance is key to ensuring that the investment put into developing new antimalarial drugs is not wasted. Current efforts focus on research into new compounds with novel mechanisms of action, and on measures to prevent or delay resistance when drugs are introduced. Drug discovery and development are long, risky and costly ventures. Antimalarial drug development has traditionally been slow but now various private and public institutions are at work to discover and develop new compounds. Today, the antimalarial development pipeline is looking reasonably healthy. Most development relies on the quinoline, antifolate and artemisinin compounds. There is a pressing need to have effective, easy to use, affordable drugs that will last a long time. Drug combinations that have independent modes of action are seen as a way of enhancing efficacy while ensuring mutual protection against resistance. Most research work has focused on the use of artesunate combined with currently used standard drugs, namely, mefloquine, amodiaquine, sulfadoxine/pyrimethamine, and chloroquine. There is clear evidence that combinations improve efficacy without increasing toxicity. However, the absolute cure rates that are achieved by combinations vary widely and depend on the level of resistance of the standard drug. From these studies, further work is underway to produce fixed dose combinations that will be packaged in blister packs. This review will summarise current antimalarial drug developments and outline recent clinical research that aims to bring artemisinin based combinations to those that need them most.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15047998

Source DB:  PubMed          Journal:  J Postgrad Med        ISSN: 0022-3859            Impact factor:   1.476


  27 in total

1.  Prevalence of UGT1A9 and UGT2B7 nonsynonymous single nucleotide polymorphisms in West African, Papua New Guinean, and North American populations.

Authors:  Rajeev K Mehlotra; Moses J Bockarie; Peter A Zimmerman
Journal:  Eur J Clin Pharmacol       Date:  2006-11-09       Impact factor: 2.953

2.  Classification of Plasmodium falciparum glucose-6-phosphate dehydrogenase inhibitors by support vector machine.

Authors:  Xiaoli Hou; Aixia Yan
Journal:  Mol Divers       Date:  2013-05-09       Impact factor: 2.943

Review 3.  Malaria in the post-genomics era: light at the end of the tunnel or just another train?

Authors:  D L Gardiner; J S McCarthy; K R Trenholme
Journal:  Postgrad Med J       Date:  2005-08       Impact factor: 2.401

4.  Amodiaquine and artemether-lumefantrine select distinct alleles of the Plasmodium falciparum mdr1 gene in Tanzanian children treated for uncomplicated malaria.

Authors:  G S Humphreys; I Merinopoulos; J Ahmed; C J M Whitty; T K Mutabingwa; C J Sutherland; R L Hallett
Journal:  Antimicrob Agents Chemother       Date:  2006-12-28       Impact factor: 5.191

5.  Prevalence of CYP2B6 alleles in malaria-endemic populations of West Africa and Papua New Guinea.

Authors:  Rajeev K Mehlotra; Mark N Ziats; Moses J Bockarie; Peter A Zimmerman
Journal:  Eur J Clin Pharmacol       Date:  2006-02-28       Impact factor: 2.953

6.  Utility of alkylaminoquinolinyl methanols as new antimalarial drugs.

Authors:  G S Dow; T N Heady; A K Bhattacharjee; D Caridha; L Gerena; M Gettayacamin; C A Lanteri; N Obaldia; N Roncal; T Shearer; P L Smith; A Tungtaeng; L Wolf; M Cabezas; D Yourick; K S Smith
Journal:  Antimicrob Agents Chemother       Date:  2006-09-11       Impact factor: 5.191

7.  Artemisinin resistance in Plasmodium falciparum: A process linked to dormancy?

Authors:  Qin Cheng; Dennis E Kyle; Michelle L Gatton
Journal:  Int J Parasitol Drugs Drug Resist       Date:  2012-01-27       Impact factor: 4.077

8.  Prophylactic and therapeutic effects of a novel granulated formulation of Artemisia extract on broiler coccidiosis.

Authors:  Jahangir Kaboutari; Hossien Ali Arab; Kambiz Ebrahimi; Sadegh Rahbari
Journal:  Trop Anim Health Prod       Date:  2013-07-19       Impact factor: 1.559

9.  In vitro activity of mirincamycin (U24729A) against Plasmodium falciparum isolates from Gabon.

Authors:  Jana Held; Richard Westerman; Peter G Kremsner; Benjamin Mordmüller
Journal:  Antimicrob Agents Chemother       Date:  2009-10-19       Impact factor: 5.191

Review 10.  Pumping iron: a potential target for novel therapeutics against schistosomes.

Authors:  Amber Glanfield; Donald P McManus; Greg J Anderson; Malcolm K Jones
Journal:  Trends Parasitol       Date:  2007-10-24
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.