Literature DB >> 16870794

In vitro interactions between piperaquine, dihydroartemisinin, and other conventional and novel antimalarial drugs.

Timothy M E Davis1, Juliana Hamzah, Kenneth F Ilett, Harin A Karunajeewa, John C Reeder, Kevin T Batty, Sara Hackett, P Hugh R Barrett.   

Abstract

In an in vitro assessment of antimalarial combinations, dihydroartemisinin (DHA) showed no interaction or was mildly antagonistic when combined with piperaquine, pyronaridine, or naphthoquine. Interactions between 4-aminoquinolines and related drugs were also indifferent/antagonistic. The clinical significance of mildly antagonistic DHA combinations is uncertain but may become important if parasite drug sensitivity declines.

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Year:  2006        PMID: 16870794      PMCID: PMC1538683          DOI: 10.1128/AAC.00177-06

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  22 in total

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Journal:  Clin Infect Dis       Date:  2002-12-02       Impact factor: 9.079

4.  Synergistic antiviral and antiproliferative activities of Escherichia coli-derived human alpha, beta, and gamma interferons.

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5.  A method for testing for synergy with any number of agents.

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6.  Evaluation of the sensitivity in vitro of Plasmodium falciparum and in vivo of Plasmodium chabaudi Malaria to various drugs and their combinations.

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7.  Human malaria parasites in continuous culture.

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Authors:  Tinh Hien Tran; Christiane Dolecek; Phuong Mai Pham; Thi Dung Nguyen; Thanh Truong Nguyen; Hong Thai Le; Thi Hoai An Dong; Tan Thanh Tran; Kasia Stepniewska; Nicholas J White; Jeremy Farrar
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9.  In vitro antimalarial activity of retinoids and the influence of selective retinoic acid receptor antagonists.

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10.  Plasmodium falciparum: assessment of in vitro growth by [3H]hypoxanthine incorporation.

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  15 in total

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Journal:  Antimicrob Agents Chemother       Date:  2011-06-06       Impact factor: 5.191

2.  Absence of association between piperaquine in vitro responses and polymorphisms in the pfcrt, pfmdr1, pfmrp, and pfnhe genes in Plasmodium falciparum.

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3.  Desbutyl-lumefantrine is a metabolite of lumefantrine with potent in vitro antimalarial activity that may influence artemether-lumefantrine treatment outcome.

Authors:  Rina P M Wong; Sam Salman; Kenneth F Ilett; Peter M Siba; Ivo Mueller; Timothy M E Davis
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4.  Effects of piperaquine, chloroquine, and amodiaquine on drug uptake and of these in combination with dihydroartemisinin against drug-sensitive and -resistant Plasmodium falciparum strains.

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6.  Pharmacokinetics and pharmacodynamics of piperaquine in a murine malaria model.

Authors:  Brioni R Moore; Kevin T Batty; Christopher Andrzejewski; Jeffrey D Jago; Madhu Page-Sharp; Kenneth F Ilett
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7.  Role of known molecular markers of resistance in the antimalarial potency of piperaquine and dihydroartemisinin in vitro.

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8.  In Silico Investigation of the Decline in Clinical Efficacy of Artemisinin Combination Therapies Due to Increasing Artemisinin and Partner Drug Resistance.

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Review 9.  Naphthoquine: An Emerging Candidate for Artemisinin Combination Therapy.

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Journal:  Drugs       Date:  2016-05       Impact factor: 9.546

Review 10.  Mannich bases in medicinal chemistry and drug design.

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