Skip to main content
Top
Published in: Malaria Journal 1/2013

Open Access 01-12-2013 | Research

Gender-specific distribution of mefloquine in the blood following the administration of therapeutic doses

Authors: Walther H Wernsdorfer, Harald Noedl, Pamela Rendi-Wagner, Herwig Kollaritsch, Gerhard Wiedermann, Andrea Mikolasek, Juntra Karbwang, Kesara Na-Bangchang

Published in: Malaria Journal | Issue 1/2013

Login to get access

Abstract

Background

The objectives of the study were to elucidate the gender-specific distribution of mefloquine in cellular and fluid blood compartments when given at therapeutic dosage, to assess its correlation with the occurrence of treatment-related adverse events, and to explore the necessity of adjusting treatment guidelines for females.

Methods

The distribution of mefloquine following the administration of standard therapeutic doses (1,250 mg mefloquine in split dose) to 22 healthy Caucasian volunteers was assessed in whole blood, serum, plasma, red blood cells (RBCs), white blood cells, and platelets using high performance liquid chromatography.

Results

Plasma mefloquine concentrations after 14 hours were considerably higher in female subjects than in males (2,778 vs 1,017 ng/ml at H14), concordant with a significantly higher frequency, duration, and severity of adverse reactions. However, mean drug concentrations of RBC appeared slightly higher in male volunteers (857 vs 719 ng/ml). At H48, a similar situation prevailed, and at H168 the mefloquine concentrations in plasma continued to be higher in females compared to males (1,353 vs 666 ng/ml), while the concentrations of RBC were similar in females (389 vs 375 ng/ml). Since the observations relate to healthy individuals, they do not take into account selective uptake of mefloquine by Plasmodium-infected erythrocytes as in the case of therapeutic drug use.

Conclusion

Although plasma mefloquine concentrations in female healthy volunteers are considerably higher and the concentrations of the RBCs are initially lower compared to males, they do not seem to justify an adjustment of treatment guidelines for mefloquine in female Caucasian individuals.
Appendix
Available only for authorised users
Literature
1.
go back to reference Na-Bangchang K, Karbwang J: Current status of malaria chemotherapy and the role of pharmacology in antimalarial drug research and development. Fundam Clin Pharmacol. 2009, 23: 387-409. 10.1111/j.1472-8206.2009.00709.x.CrossRefPubMed Na-Bangchang K, Karbwang J: Current status of malaria chemotherapy and the role of pharmacology in antimalarial drug research and development. Fundam Clin Pharmacol. 2009, 23: 387-409. 10.1111/j.1472-8206.2009.00709.x.CrossRefPubMed
2.
go back to reference Palmer KJ, Holliday SM, Brogden RN: Mefloquine. A review of its antimalarial activity, pharmacokinetic properties and therapeutic efficacy. Drugs. 1993, 45: 430-475.CrossRefPubMed Palmer KJ, Holliday SM, Brogden RN: Mefloquine. A review of its antimalarial activity, pharmacokinetic properties and therapeutic efficacy. Drugs. 1993, 45: 430-475.CrossRefPubMed
3.
go back to reference Barrett PJ, Emmins PD, Clarke PD, Bradley DJ: Comparison of adverse events associated with use of mefloquine and combination of chloroquine and proguanil as antimalarial prophylaxis: postal and telephone survey of travellers. BMJ. 1996, 313: 525-528. 10.1136/bmj.313.7056.525.PubMedCentralCrossRefPubMed Barrett PJ, Emmins PD, Clarke PD, Bradley DJ: Comparison of adverse events associated with use of mefloquine and combination of chloroquine and proguanil as antimalarial prophylaxis: postal and telephone survey of travellers. BMJ. 1996, 313: 525-528. 10.1136/bmj.313.7056.525.PubMedCentralCrossRefPubMed
4.
5.
go back to reference Rendi-Wagner P, Noedl H, Wernsdorfer WH, Wiedermann G, Mikolasek A, Kollaritsch H: Unexpected frequency, duration and spectrum of adverse events after therapeutic dose of mefloquine in healthy adults. Acta Trop. 2002, 81: 167-173. 10.1016/S0001-706X(01)00210-8.CrossRefPubMed Rendi-Wagner P, Noedl H, Wernsdorfer WH, Wiedermann G, Mikolasek A, Kollaritsch H: Unexpected frequency, duration and spectrum of adverse events after therapeutic dose of mefloquine in healthy adults. Acta Trop. 2002, 81: 167-173. 10.1016/S0001-706X(01)00210-8.CrossRefPubMed
6.
go back to reference Kollaritsch H, Karbwang J, Wiedermann G, Mikolasek A, Na-Bangchang K, Wernsdorfer WH: Mefloquine concentration profiles during prophylactic dose regimens. Wien Klin Wochenschr. 2000, 112: 441-447.PubMed Kollaritsch H, Karbwang J, Wiedermann G, Mikolasek A, Na-Bangchang K, Wernsdorfer WH: Mefloquine concentration profiles during prophylactic dose regimens. Wien Klin Wochenschr. 2000, 112: 441-447.PubMed
7.
go back to reference Lim LY, Go ML: The anticholinesterase activity of mefloquine. Clin Exp Pharmacol Physiol. 1985, 12: 527-531. 10.1111/j.1440-1681.1985.tb00904.x.CrossRefPubMed Lim LY, Go ML: The anticholinesterase activity of mefloquine. Clin Exp Pharmacol Physiol. 1985, 12: 527-531. 10.1111/j.1440-1681.1985.tb00904.x.CrossRefPubMed
8.
go back to reference Na-Bangchang K, Karbwang J, Palacios PA, Ubalee R, Saengtertsilapachai S, Wernsdorfer WH: Pharmacokinetics and bioequivalence evaluation of three commercial tablet formulations of mefloquine when given in combination with dihydroartemisinin in patients with acute uncomplicated falciparum malaria. Eur J Clin Pharmacol. 2000, 55: 743-748. 10.1007/s002280050008.CrossRefPubMed Na-Bangchang K, Karbwang J, Palacios PA, Ubalee R, Saengtertsilapachai S, Wernsdorfer WH: Pharmacokinetics and bioequivalence evaluation of three commercial tablet formulations of mefloquine when given in combination with dihydroartemisinin in patients with acute uncomplicated falciparum malaria. Eur J Clin Pharmacol. 2000, 55: 743-748. 10.1007/s002280050008.CrossRefPubMed
9.
go back to reference Weidekamm E, Rusing G, Caplain H, Sorgel F, Crevoisier C: Lack of bioequivalence of a generic mefloquine tablet with the standard product. Eur J Clin Pharmacol. 1998, 54: 615-619. 10.1007/s002280050523.CrossRefPubMed Weidekamm E, Rusing G, Caplain H, Sorgel F, Crevoisier C: Lack of bioequivalence of a generic mefloquine tablet with the standard product. Eur J Clin Pharmacol. 1998, 54: 615-619. 10.1007/s002280050523.CrossRefPubMed
10.
go back to reference Karbwang J, White NJ: Clinical pharmacokinetics of mefloquine. Clin Pharmacokinet. 1990, 19: 264-279. 10.2165/00003088-199019040-00002.CrossRefPubMed Karbwang J, White NJ: Clinical pharmacokinetics of mefloquine. Clin Pharmacokinet. 1990, 19: 264-279. 10.2165/00003088-199019040-00002.CrossRefPubMed
11.
go back to reference Wernsdorfer WH: Antimalarial drugs. Health Co-operation Papers. 1997, 15: 151-198. Wernsdorfer WH: Antimalarial drugs. Health Co-operation Papers. 1997, 15: 151-198.
12.
go back to reference Looareesuwan S, White NJ, Warrell DA, Forgo I, Dubach UG, Ranalder UB, Schwartz DE: Studies of mefloquine bioavailability and kinetics using a stable isotope technique: a comparison of Thai patients with falciparum malaria and healthy Caucasian volunteers. Br J Clin Pharmacol. 1987, 24: 37-42. 10.1111/j.1365-2125.1987.tb03133.x.PubMedCentralCrossRefPubMed Looareesuwan S, White NJ, Warrell DA, Forgo I, Dubach UG, Ranalder UB, Schwartz DE: Studies of mefloquine bioavailability and kinetics using a stable isotope technique: a comparison of Thai patients with falciparum malaria and healthy Caucasian volunteers. Br J Clin Pharmacol. 1987, 24: 37-42. 10.1111/j.1365-2125.1987.tb03133.x.PubMedCentralCrossRefPubMed
13.
go back to reference Karbwang J, Molunto P, Na-Bangchang K, Bunnag D: Determination of mefloquine in biological fluids using high performance liquid chromatography. Southeast Asian J Trop Med Public Health. 1989, 20: 55-60.PubMed Karbwang J, Molunto P, Na-Bangchang K, Bunnag D: Determination of mefloquine in biological fluids using high performance liquid chromatography. Southeast Asian J Trop Med Public Health. 1989, 20: 55-60.PubMed
14.
go back to reference Schwartz E, Potasman I, Rotenberg M, Almog S, Sadetzki S: Serious adverse events of mefloquine in relation to blood level and gender. Am J Trop Med Hyg. 2001, 65: 189-192.PubMed Schwartz E, Potasman I, Rotenberg M, Almog S, Sadetzki S: Serious adverse events of mefloquine in relation to blood level and gender. Am J Trop Med Hyg. 2001, 65: 189-192.PubMed
15.
go back to reference Schlagenhauf P, Tschopp A, Johnson R, Nothdurft HD, Beck B, Schwartz E, Herold M, Krebs B, Veit O, Allwinn R, Steffen R: Tolerability of malaria chemoprophylaxis in non-immune travellers to sub-Saharan Africa: multicentre, randomised, double blind, four arm study. BMJ. 2003, 327: 1078-10.1136/bmj.327.7423.1078.PubMedCentralCrossRefPubMed Schlagenhauf P, Tschopp A, Johnson R, Nothdurft HD, Beck B, Schwartz E, Herold M, Krebs B, Veit O, Allwinn R, Steffen R: Tolerability of malaria chemoprophylaxis in non-immune travellers to sub-Saharan Africa: multicentre, randomised, double blind, four arm study. BMJ. 2003, 327: 1078-10.1136/bmj.327.7423.1078.PubMedCentralCrossRefPubMed
16.
go back to reference Schlagenhauf P, Steffen R, Lobel H, Johnson R, Letz R, Tschopp A, Vranjes N, Bergqvist Y, Ericsson O, Hellgren U, Rombo L, Mannino S, Handschin J, Sturchler D: Mefloquine tolerability during chemoprophylaxis: focus on adverse event assessments, stereochemistry and compliance. Trop Med Int Health. 1996, 1: 485-494. 10.1046/j.1365-3156.1996.d01-85.x.CrossRefPubMed Schlagenhauf P, Steffen R, Lobel H, Johnson R, Letz R, Tschopp A, Vranjes N, Bergqvist Y, Ericsson O, Hellgren U, Rombo L, Mannino S, Handschin J, Sturchler D: Mefloquine tolerability during chemoprophylaxis: focus on adverse event assessments, stereochemistry and compliance. Trop Med Int Health. 1996, 1: 485-494. 10.1046/j.1365-3156.1996.d01-85.x.CrossRefPubMed
17.
go back to reference Seethorn N, Wernsdorfer WH, Noedl H, Karbwang J, Na-Bangchang K: Investigation of the in vitro gender-specific partitioning of mefloquine in malarial infected red blood cells and plasma. Am J Trop Med Hyg. 2013, Sep 3. [Epub ahead of print] Seethorn N, Wernsdorfer WH, Noedl H, Karbwang J, Na-Bangchang K: Investigation of the in vitro gender-specific partitioning of mefloquine in malarial infected red blood cells and plasma. Am J Trop Med Hyg. 2013, Sep 3. [Epub ahead of print]
18.
go back to reference Diribe CO, Warhurst DC: A study of the uptake of chloroquine in malaria-infected erythrocytes. High and low affinity uptake and the influence of glucose and its analogues. Biochem Pharmacol. 1985, 34: 3019-3027. 10.1016/0006-2952(85)90143-1.CrossRefPubMed Diribe CO, Warhurst DC: A study of the uptake of chloroquine in malaria-infected erythrocytes. High and low affinity uptake and the influence of glucose and its analogues. Biochem Pharmacol. 1985, 34: 3019-3027. 10.1016/0006-2952(85)90143-1.CrossRefPubMed
19.
go back to reference Ginsburg H, Stein WD: Kinetic modelling of chloroquine uptake by malaria-infected erythrocytes. Assessment of the factors that may determine drug resistance. Biochem Pharmacol. 1991, 41: 1463-1470. 10.1016/0006-2952(91)90562-J.CrossRefPubMed Ginsburg H, Stein WD: Kinetic modelling of chloroquine uptake by malaria-infected erythrocytes. Assessment of the factors that may determine drug resistance. Biochem Pharmacol. 1991, 41: 1463-1470. 10.1016/0006-2952(91)90562-J.CrossRefPubMed
20.
go back to reference Schwartz E, Paul F, Pener H, Almog S, Rotenberg M, Golenser J: Malaria antibodies and mefloquine levels among United Nations troops in Angola. J Travel Med. 2001, 8: 113-116.CrossRefPubMed Schwartz E, Paul F, Pener H, Almog S, Rotenberg M, Golenser J: Malaria antibodies and mefloquine levels among United Nations troops in Angola. J Travel Med. 2001, 8: 113-116.CrossRefPubMed
21.
go back to reference Lobel HO, Miani M, Eng T, Bernard KW, Hightower AW, Campbell CC: Long-term malaria prophylaxis with mefloquine. Lancet. 1993, 341: 848-851. 10.1016/0140-6736(93)93058-9.CrossRefPubMed Lobel HO, Miani M, Eng T, Bernard KW, Hightower AW, Campbell CC: Long-term malaria prophylaxis with mefloquine. Lancet. 1993, 341: 848-851. 10.1016/0140-6736(93)93058-9.CrossRefPubMed
22.
go back to reference World Health Organization: Advances in malaria chemotherapy. Report of a WHO Scientific Group. WHO Tech Rep Ser no. 711. 1984, WHO: Geneva World Health Organization: Advances in malaria chemotherapy. Report of a WHO Scientific Group. WHO Tech Rep Ser no. 711. 1984, WHO: Geneva
23.
go back to reference Phillips MA, Kass RB: User acceptability patterns for mefloquine and doxycycline malaria chemoprophylaxis. J Travel Med. 1996, 3: 40-45.24. 10.1111/j.1708-8305.1996.tb00695.x.CrossRefPubMed Phillips MA, Kass RB: User acceptability patterns for mefloquine and doxycycline malaria chemoprophylaxis. J Travel Med. 1996, 3: 40-45.24. 10.1111/j.1708-8305.1996.tb00695.x.CrossRefPubMed
24.
go back to reference Todd GD, Hopperus Buma AP, Green MD, Jaspers CA, Lobel HO: Comparison of whole blood and serum levels of mefloquine and its carboxylic acid metabolite. Am J Trop Med Hyg. 1997, 57: 399-402.PubMed Todd GD, Hopperus Buma AP, Green MD, Jaspers CA, Lobel HO: Comparison of whole blood and serum levels of mefloquine and its carboxylic acid metabolite. Am J Trop Med Hyg. 1997, 57: 399-402.PubMed
Metadata
Title
Gender-specific distribution of mefloquine in the blood following the administration of therapeutic doses
Authors
Walther H Wernsdorfer
Harald Noedl
Pamela Rendi-Wagner
Herwig Kollaritsch
Gerhard Wiedermann
Andrea Mikolasek
Juntra Karbwang
Kesara Na-Bangchang
Publication date
01-12-2013
Publisher
BioMed Central
Published in
Malaria Journal / Issue 1/2013
Electronic ISSN: 1475-2875
DOI
https://doi.org/10.1186/1475-2875-12-443

Other articles of this Issue 1/2013

Malaria Journal 1/2013 Go to the issue
Live Webinar | 27-06-2024 | 18:00 (CEST)

Keynote webinar | Spotlight on medication adherence

Live: Thursday 27th June 2024, 18:00-19:30 (CEST)

WHO estimates that half of all patients worldwide are non-adherent to their prescribed medication. The consequences of poor adherence can be catastrophic, on both the individual and population level.

Join our expert panel to discover why you need to understand the drivers of non-adherence in your patients, and how you can optimize medication adherence in your clinics to drastically improve patient outcomes.

Prof. Kevin Dolgin
Prof. Florian Limbourg
Prof. Anoop Chauhan
Developed by: Springer Medicine
Obesity Clinical Trial Summary

At a glance: The STEP trials

A round-up of the STEP phase 3 clinical trials evaluating semaglutide for weight loss in people with overweight or obesity.

Developed by: Springer Medicine

Highlights from the ACC 2024 Congress

Year in Review: Pediatric cardiology

Watch Dr. Anne Marie Valente present the last year's highlights in pediatric and congenital heart disease in the official ACC.24 Year in Review session.

Year in Review: Pulmonary vascular disease

The last year's highlights in pulmonary vascular disease are presented by Dr. Jane Leopold in this official video from ACC.24.

Year in Review: Valvular heart disease

Watch Prof. William Zoghbi present the last year's highlights in valvular heart disease from the official ACC.24 Year in Review session.

Year in Review: Heart failure and cardiomyopathies

Watch this official video from ACC.24. Dr. Biykem Bozkurt discusses last year's major advances in heart failure and cardiomyopathies.