Literature DB >> 21556929

Distribution of mefloquine in the blood of Thai patients with acute uncomplicated falciparum malaria following administration of therapeutic doses of artesunate.

Kesara Na-Bangchang1, Ronnatrai Ruengweerayut, Walther H Wernsdorfer.   

Abstract

PURPOSE: The study objectives to investigate the distribution of the antimalarial drug mefloquine (MQ) in cellular and fluid blood compartments when given at therapeutic dosage with artesunate and to investigate an eventual association with the occurrence of treatment-related adverse events in Thai patients with acute uncomplicated falciparum malaria.
METHODS: MQ distribution following administration of standard therapeutic doses (1,250 mg MQ in split dose) with artesunate to 20 Thai patients with acute uncomplicated falciparum malaria was assessed in whole blood, serum, plasma, red blood cells (RBC), white blood cells (WBC), and platelets using high -performance liquid chromatography.
RESULTS: All patients responded to treatment without reappearance of parasitemia during the 42-day follow-up period. There was no significant gender difference in MQ levels. The chronological change in MQ levels in all blood components, including ratios of plasma to serum, whole blood, RBC, platelets or WBC were similar and parallel in both genders. MQ concentrations at 14 and 168 h, in descending order, in both male and female patients were as follow: WBC > platelets > plasma > serum > whole blood > RBC. Gender-specific whole blood, serum, and RBC concentrations were similar at all time points, with median ratios of plasma:whole blood, plasma:serum, and plasma:RBC of 0.84:1.21, 1.09:1.64, and 1.59:3.79, respectively. Plasma vs whole blood and plasma vs RBC MQ concentrations showed a highly significant correlation, with r = 0.923 and 0.867, respectively. No association between occurrence of treatment-related adverse events and MQ concentrations in various blood components/fluids was observed in either gender.
CONCLUSIONS: Based on these observations, gender-specific therapeutic MQ dose adjustment is obviously not required.

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Year:  2011        PMID: 21556929     DOI: 10.1007/s00228-011-1058-8

Source DB:  PubMed          Journal:  Eur J Clin Pharmacol        ISSN: 0031-6970            Impact factor:   2.953


  21 in total

1.  Unexpected frequency, duration and spectrum of adverse events after therapeutic dose of mefloquine in healthy adults.

Authors:  Pamela Rendi-Wagner; Harald Noedl; Walther H Wernsdorfer; Gerhard Wiedermann; Andrea Mikolasek; Herwig Kollaritsch
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2.  Comparison of adverse events associated with use of mefloquine and combination of chloroquine and proguanil as antimalarial prophylaxis: postal and telephone survey of travellers.

Authors:  P J Barrett; P D Emmins; P D Clarke; D J Bradley
Journal:  BMJ       Date:  1996-08-31

3.  Determination of mefloquine in biological fluids using high performance liquid chromatography.

Authors:  J Karbwang; P Molunto; K Na Bangchang; D Bunnag
Journal:  Southeast Asian J Trop Med Public Health       Date:  1989-03       Impact factor: 0.267

4.  Divided-dose kinetics of mefloquine in man.

Authors:  G Franssen; B Rouveix; J Lebras; J Bauchet; F Verdier; C Michon; F Bricaire
Journal:  Br J Clin Pharmacol       Date:  1989-08       Impact factor: 4.335

5.  Serious adverse events of mefloquine in relation to blood level and gender.

Authors:  E Schwartz; I Potasman; M Rotenberg; S Almog; S Sadetzki
Journal:  Am J Trop Med Hyg       Date:  2001-09       Impact factor: 2.345

6.  Mefloquine concentration profiles during prophylactic dose regimens.

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7.  A study of the uptake of chloroquine in malaria-infected erythrocytes. High and low affinity uptake and the influence of glucose and its analogues.

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Journal:  Biochem Pharmacol       Date:  1985-09-01       Impact factor: 5.858

Review 8.  Conquering the intolerable burden of malaria: what's new, what's needed: a summary.

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9.  Compliance with a three-day course of artesunate-mefloquine combination and baseline anti-malarial treatment in an area of Thailand with highly multidrug resistant falciparum malaria.

Authors:  Kanungnit Congpuong; Pongwit Bualombai; Vick Banmairuroi; Kesara Na-Bangchang
Journal:  Malar J       Date:  2010-02-04       Impact factor: 2.979

Review 10.  Current malaria status and distribution of drug resistance in East and Southeast Asia with special focus to Thailand.

Authors:  Kesara Na-Bangchang; Kanungnit Congpuong
Journal:  Tohoku J Exp Med       Date:  2007-02       Impact factor: 1.848

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  4 in total

1.  Investigation of the in vitro gender-specific partitioning of mefloquine in malarial infected red blood cells and plasma.

Authors:  Nongluk Seethorn; Walther H Wernsdorfer; Harald Noedl; Juntra Karbwang; Kesara Na-Bangchang
Journal:  Am J Trop Med Hyg       Date:  2013-09-03       Impact factor: 2.345

2.  Preliminary investigation of the contribution of CYP2A6, CYP2B6, and UGT1A9 polymorphisms on artesunate-mefloquine treatment response in Burmese patients with Plasmodium falciparum malaria.

Authors:  Papichaya Phompradit; Poonuch Muhamad; Anurak Cheoymang; Kesara Na-Bangchang
Journal:  Am J Trop Med Hyg       Date:  2014-06-02       Impact factor: 2.345

3.  Significance of higher drug concentration in erythrocytes of mice infected with Schistosoma japonicum and treated orally with mefloquine at single doses.

Authors:  Yi Tao; Jian Xue; Bin Jiang; Hao-Bing Zhang; Shu-Hua Xiao
Journal:  Parasitol Res       Date:  2015-09-04       Impact factor: 2.289

4.  Patient age does not affect mefloquine concentrations in erythrocytes and plasma during the acute phase of falciparum malaria.

Authors:  José Luiz Fernandes Vieira; Larissa Maria Guimarães Borges; Michelle Valéria Dias Ferreira; Juan Gonzalo Bardarez Rivera; Margarete do Socorro Mendonça Gomes
Journal:  Braz J Infect Dis       Date:  2016-08-16       Impact factor: 3.257

  4 in total

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