Effects of artemether on the pharmacokinetic parameters of quinine in wistar rats.

Main Article Content

L. S. Kasim
A. A. Akinlolu
C. R. Obidike
T. O. Fajemirokun
O. E. Adejumo
P. Aziba

Abstract

The effect of artemether on the pharmacokinetic parameters of Quinine(QN) was carried out in this study. The parameters were investigated using adult Wistar rats. The rats were divided into three groups; A, B and C. Group A served as the control which was administered intramuscularly (i.m) 0.9w/v normal saline while group B was administered QN and artemether (i.m) at a dose of 5.14mg/kgbody weight(b..w). and (0.5mg/kgb.w respectively while Group C was administered QN alone (i.m) at a dose of 5.14mg/kgb.w .Blood samples were collected from each group of animals at 30 min. interval for 8 hr after the injection. The investigation was based on a one-compartment model with first order absorption. Using HPLC method with a limit of detection of 0.5?g/mL, the plasma concentration of quinine was monitored and quantified. The area under the blood concentration –time curve (AUC?) of QN was not significantly different (P ? 0.05) when compared QN alone with QN in the presence of artemether being 124 ?g/mlhr and 136 ?g/mlhr for groups B and C, respectively. The half life (t1/2) and Tmax of QN in the groups B and C were the same being 8hr and 2hr respectively for both while Cmax showed a significant difference (P?0.05) being 54.63?g/ml and 90.55?g/ml in the presence and absence of QN, respectively. This work justifies the fact that these drugs can be concomitantly administered since pharmacokinetic parameters like Tmax and the (AUC?) of quinine were not significantly affected by artemether.

Downloads

Download data is not yet available.

Article Details

How to Cite
Kasim, L. S., Akinlolu , A. A., Obidike, C. R., Fajemirokun, T. O., Adejumo, O. E., & Aziba, P. (2011). Effects of artemether on the pharmacokinetic parameters of quinine in wistar rats. Nigerian Journal of Pharmaceutical and Applied Science Research, 1(1). Retrieved from https://nijophasr.net/index.php/nijophasr/article/view/38
Section
Articles
Author Biographies

L. S. Kasim

Faculty of Pharmacy, Olabisi Onabanjo University, Sagamu, Ogun State, Nigeria.

A. A. Akinlolu

Faculty of Basic Medical Sciences, Olabisi Onabanjo University, Sagamu, Ogun State, Nigeria.

C. R. Obidike

Faculty of Pharmacy, Olabisi Onabanjo University, Sagamu, Ogun State, Nigeria

T. O. Fajemirokun

Faculty of Pharmacy, Olabisi Onabanjo University, Sagamu, Ogun State, Nigeria

O. E. Adejumo

Faculty of Pharmacy, Olabisi Onabanjo University, Sagamu, Ogun State, Nigeria

P. Aziba

Faculty of Basic Medical Sciences, Olabisi Onabanjo University, Sagamu, Ogun State, Nigeria.

References

Ajibola A .Olaniyi (1998), Essentials of medicinal chemistry; Antimalarias. Published by Shaneson C.I Ltd. Ibadan ,pp. 145.

Ajibola A .Olaniyi(2000), Principles of drug quality assurance and pharmaceutical analysis. Published by Mosuro Ltd. Ibadan . pp. 150-317

Bertam G. Katzung, (2001). Basic and Clinical Pharmacology: pharmacokinetics and pharmacodynamics, 8th edition. Lange Medical/ Mc Graw Hill. London , pp.35-44

Babalola C.P , Adebayo A.S , Omosoto A., Oyeyinka A.(2004). Tropical Journal of pharmaceutical research; comparative bioavailability study of a new quinine suppository and oral quinine in healthy volunteers. 3 (1) 291-297.

Luo XD, Yeh HJC, Brossi A, Flippen-Anderson JL, Gillardi R (1984). The chemistry of drugs part IV. Configurations of antimalarials derived from qinghaosu: 16 Dihydroqingyhaosu, artemether, and artesunic acid. Helv Chim Acta; 67:1515-22.

Meshnick SR (2002). Artemisinin: mechanisms of action, resistance and toxicity. Int J Parasitol ; 32:1655-60

Martin LJ, Taniguchi H, Robert NM, Simard J, Tremblay JJ, Viger RS.(2005) GATA factors and the nuclearreceptors, steroidogenic factor 1/liver receptor homolog 1, are key mutual partners in the regulation of the human 3beta-hydroxysteroid dehydrogenase type 2 promoter. Mol Endocrinol;19:2358- 2370.

Nicholas H.G, Holford M.B,(1993) Rational dosing and the time course of drug action. Clinical Pharmacokinetics. 25;495.

Na-Bangchang K, Karbwang J, Ubalee R, Thanavibul A, Saenglertsilapachai S (2000).. Absence of significant pharmacokinetic and pharmacodynamic interactions between artemether and quinoline antimalarials. Eur. J.Drug Metab. Pharmacokinetic. 25(3-4),171-3

Oliver Burk, Katja A. Arnold (2005). Molecular Pharmacology; antimalarial artemisinnin drugs. Erlangen , Germany, pp. 116—117

Pukrittayakamee S, Supanaranond W, Looareesuwan S, Vanijanonta, White N. (1994). Quinine in severe falciparum malaria: evidence of declining efficacy in Thailand . Trans R Soc Med Hyg; 88:324-7.

Rang. I. H.P, Dale, M.M, Ritter J.M, Moore P.K,(2003). Pharmacology; how drugs act, drug elimination and pharmacokinetics. 5th edition. Published by Livingstone Ltd. England, pp. 43-47,115-116.

Schild,(1980), Applied Pharmacology, twelth edition, Longman Group Limited, Singapore . pp. 442

Tripathi K.D,(2001). Essentials of medical pharmacology.. Fifth edition. Jaypee brothers Ltd, New Dehli. pp 12-32

World Health Organization(2003). Assessment of the safety of artemisinin compounds in Pregnancy.WHO/RBM/TDR/Artemisinin/03.1. WHO/CDS/MAL.1094

William Charles Evans(1998); Trease and Evans pharmacognosy. Quinine and its alkaloids Saunders Company Ltd. U.K. pp 399