Pharmacokinetics of proguanil in malaria patients treated with proguanil plus atovaquone

Clinical studies have shown atovaquone (ATQ), a new blood schizontocidal drug, in combination with proguanil (PROG) to be very effective in the treatment of acute multidrug-resistant falciparum malaria. The multiple dose pharmacokinetics of PROG were determined in Thai patients with acute falciparum...

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Main Authors: M. D. Edstein, S. Looareesuwan, C. Viravan, D. E. Kyle
Other Authors: Australian Army Malaria Institute
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Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/17741
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spelling th-mahidol.177412018-07-04T14:29:54Z Pharmacokinetics of proguanil in malaria patients treated with proguanil plus atovaquone M. D. Edstein S. Looareesuwan C. Viravan D. E. Kyle Australian Army Malaria Institute Mahidol University Walter Reed Army Institute of Research Royal Australian Army Medical Corps Medicine Clinical studies have shown atovaquone (ATQ), a new blood schizontocidal drug, in combination with proguanil (PROG) to be very effective in the treatment of acute multidrug-resistant falciparum malaria. The multiple dose pharmacokinetics of PROG were determined in Thai patients with acute falciparum malaria given PROG alone (200 mg PROG twice a day for 3 days, n = 4) and concurrently PROG and ATQ (200 mg PROG and 500 mg ATQ twice a day for 3 days, n = 12). There were no statistical differences (p > 0.05) in the area under the plasma drug concentration-time curve (AUC), apparent oral clearance (CL/F) and elimination half-life (t12) of PROG between patients given PROG alone and PROG/ ATQ. The median (range) kinetic values of PROG in patients given PROG alone and PROG/ATQ were respectively: CL/F = 1.25 1/h/kg (0.99-1.45) and 0.95 (0.73-1.32) 1/h/kg, and t1/2 = 14.2 hours (9.3-16.8) and 13.6 hours (9.1-17.6). The CL/F and t1/2of PROG in the Thai patients treated with the 2 treatment regimens were also comparable to values reported in healthy Thai volunteers given a standard prophylactic dose (200 mg PROG). The results of this preliminary study suggest that ATQ is unlikely to affect the pharmacokinetics of PROG to a clinically important extent at an ATQ dosage of 500 mg twice a day for 3 days in malaria infected patients. 2018-07-04T07:29:54Z 2018-07-04T07:29:54Z 1996-06-01 Article Southeast Asian Journal of Tropical Medicine and Public Health. Vol.27, No.2 (1996), 216-220 01251562 2-s2.0-0030154493 https://repository.li.mahidol.ac.th/handle/123456789/17741 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0030154493&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Medicine
spellingShingle Medicine
M. D. Edstein
S. Looareesuwan
C. Viravan
D. E. Kyle
Pharmacokinetics of proguanil in malaria patients treated with proguanil plus atovaquone
description Clinical studies have shown atovaquone (ATQ), a new blood schizontocidal drug, in combination with proguanil (PROG) to be very effective in the treatment of acute multidrug-resistant falciparum malaria. The multiple dose pharmacokinetics of PROG were determined in Thai patients with acute falciparum malaria given PROG alone (200 mg PROG twice a day for 3 days, n = 4) and concurrently PROG and ATQ (200 mg PROG and 500 mg ATQ twice a day for 3 days, n = 12). There were no statistical differences (p > 0.05) in the area under the plasma drug concentration-time curve (AUC), apparent oral clearance (CL/F) and elimination half-life (t12) of PROG between patients given PROG alone and PROG/ ATQ. The median (range) kinetic values of PROG in patients given PROG alone and PROG/ATQ were respectively: CL/F = 1.25 1/h/kg (0.99-1.45) and 0.95 (0.73-1.32) 1/h/kg, and t1/2 = 14.2 hours (9.3-16.8) and 13.6 hours (9.1-17.6). The CL/F and t1/2of PROG in the Thai patients treated with the 2 treatment regimens were also comparable to values reported in healthy Thai volunteers given a standard prophylactic dose (200 mg PROG). The results of this preliminary study suggest that ATQ is unlikely to affect the pharmacokinetics of PROG to a clinically important extent at an ATQ dosage of 500 mg twice a day for 3 days in malaria infected patients.
author2 Australian Army Malaria Institute
author_facet Australian Army Malaria Institute
M. D. Edstein
S. Looareesuwan
C. Viravan
D. E. Kyle
format Article
author M. D. Edstein
S. Looareesuwan
C. Viravan
D. E. Kyle
author_sort M. D. Edstein
title Pharmacokinetics of proguanil in malaria patients treated with proguanil plus atovaquone
title_short Pharmacokinetics of proguanil in malaria patients treated with proguanil plus atovaquone
title_full Pharmacokinetics of proguanil in malaria patients treated with proguanil plus atovaquone
title_fullStr Pharmacokinetics of proguanil in malaria patients treated with proguanil plus atovaquone
title_full_unstemmed Pharmacokinetics of proguanil in malaria patients treated with proguanil plus atovaquone
title_sort pharmacokinetics of proguanil in malaria patients treated with proguanil plus atovaquone
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/17741
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