Literature DB >> 3814460

The disposition of amodiaquine in man after oral administration.

P Winstanley, G Edwards, M Orme, A Breckenridge.   

Abstract

A method is described for the simultaneous determination of amodiaquine (AQ) and desethylamodiaquine (AQm) in plasma, urine, whole blood and packed red cells. After oral administration of AQ (600 mg) to seven healthy subjects, absorption of AQ was rapid, reaching peak concentrations in plasma, whole blood, and packed cells at 0.5 +/- 0.03, 0.5 +/- 0.1 and 0.5 +/- 0.1 h respectively (mean +/- s.e. mean). The apparent terminal half-life of AQ was 5.2 +/- 1.7 h. AQ was detectable for no longer than 8 h. AQ underwent rapid conversion to AQm, which reached peak concentrations in plasma, whole blood and packed cells at 3.4 +/- 0.8, 2.3 +/- 0.5 and 3.6 +/- 1.1 h respectively. AQm was still detectable at the end of the sampling period (96 h) when the plasma concentration was 29 +/- 8 ng ml-1. The area under the plasma concentration vs time curve (AUC(0, infinity] for AQ was 154 +/- 38 ng ml-1 h; the corresponding value for AQm was 8037 +/- 1383 ng ml-1 h. There were no significant differences in the values for AUC of AQ between plasma, whole blood, or packed cells. The whole blood to plasma concentration ratio for AQm was 3.1 +/- 0.2, and the AUC (0.24) for AQm in whole blood (6811 +/- 752 ng ml-1 h) was significantly greater than that in plasma (2304 +/- 371 ng ml-1 h), P less than 0.001. The recovery of AQm from urine collected 0-24 h was 6.8 +/- 0.8 mg (n = 6).(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1987        PMID: 3814460      PMCID: PMC1386133          DOI: 10.1111/j.1365-2125.1987.tb03002.x

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


  15 in total

1.  Fatal agranulocytosis during treatment with a amodiaquine.

Authors:  L GLICK
Journal:  Br Med J       Date:  1957-04-20

2.  The detection of amodiaquine in blood after oral administration.

Authors:  P A Winstanley; G Edwards; M L Orme; A M Breckenridge
Journal:  Br J Clin Pharmacol       Date:  1986-05       Impact factor: 4.335

3.  Isolation, characterization and standardization of a major metabolite of amodiaquine by chromatographic and spectroscopic methods.

Authors:  F C Churchill; D L Mount; L C Patchen; A Björkman
Journal:  J Chromatogr       Date:  1986-04-25

4.  High-performance liquid chromatographic analysis of amodiaquine in human plasma.

Authors:  G W Mihaly; D D Nicholl; G Edwards; S A Ward; M L Orme; D A Warrell; A M Breckenridge
Journal:  J Chromatogr       Date:  1985-01-11

5.  Intravenous amodiaquine and oral amodiaquine/erythromycin in the treatment of chloroquine-resistant falciparum malaria.

Authors:  S Looareesuwan; R E Phillips; N J White; J Karbwang; Y Benjasurat; P Attanath; D A Warrell
Journal:  Lancet       Date:  1985-10-12       Impact factor: 79.321

6.  Agranulocytosis coincident with amodiaquine therapy.

Authors:  K Booth; K Larkin; I Maddocks
Journal:  Br Med J       Date:  1967-07-01

7.  Frequency of severe neutropenia associated with amodiaquine prophylaxis against malaria.

Authors:  C S Hatton; T E Peto; C Bunch; G Pasvol; S J Russell; C R Singer; G Edwards; P Winstanley
Journal:  Lancet       Date:  1986-02-22       Impact factor: 79.321

8.  Amodiaquine-induced agranulocytosis: toxic effect of amodiaquine in bone marrow cultures in vitro.

Authors:  D E Lind; J A Levi; P C Vincent
Journal:  Br Med J       Date:  1973-02-24

9.  Effectiveness of amodiaquine as treatment for chloroquine-resistant Plasmodium falciparum infections in Kenya.

Authors:  W M Watkins; D G Sixsmith; H C Spencer; D A Boriga; D M Kariuki; T Kipingor; D K Koech
Journal:  Lancet       Date:  1984-02-18       Impact factor: 79.321

10.  Distribution of chloroquine and its metabolite desethyl-chloroquine in human blood cells and its implication for the quantitative determination of these compounds in serum and plasma.

Authors:  Y Bergqvist; B Domeij-Nyberg
Journal:  J Chromatogr       Date:  1983-01-14
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4.  CYP2C8 polymorphism frequencies among malaria patients in Zanzibar.

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Review 5.  Antimalarial pharmacokinetics and treatment regimens.

Authors:  N J White
Journal:  Br J Clin Pharmacol       Date:  1992-07       Impact factor: 4.335

6.  Computational models to assign biopharmaceutics drug disposition classification from molecular structure.

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Journal:  Pharm Res       Date:  2007-09-11       Impact factor: 4.200

7.  A comparative study of the formation of chemically reactive drug metabolites by human liver microsomes.

Authors:  N R Kitteringham; C Lambert; J L Maggs; J Colbert; B K Park
Journal:  Br J Clin Pharmacol       Date:  1988-07       Impact factor: 4.335

8.  The disposition of oral amodiaquine in Papua New Guinean children with falciparum malaria.

Authors:  F W Hombhanje; I Hwaihwanje; T Tsukahara; J Saruwatari; M Nakagawa; H Osawa; M M Paniu; N Takahashi; J K Lum; B Aumora; A Masta; M Sapuri; T Kobayakawa; A Kaneko; T Ishizaki
Journal:  Br J Clin Pharmacol       Date:  2005-03       Impact factor: 4.335

9.  Field-adapted sampling of whole blood to determine the levels of amodiaquine and its metabolite in children with uncomplicated malaria treated with amodiaquine plus artesunate combination.

Authors:  Muhammad Ntale; Celestino Obua; Jackson Mukonzo; Margarita Mahindi; Lars L Gustafsson; Olof Beck; Jasper W Ogwal-Okeng
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Authors:  April M Bobenchik; Jae-Yeon Choi; Arunima Mishra; Iulian N Rujan; Bing Hao; Dennis R Voelker; Jeffrey C Hoch; Choukri Ben Mamoun
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