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Original Research Article | OPEN ACCESS

Studies on the toxicokinetics of intragastrically-administered paracetamol, aminophenazone, caffeine and chlorphenamine maleate tablets in rats

Wei Sun, Shenghua Gu , Xin Zhang, Jinyao Lu, Yingmin Gu, Yiwen Huang, Guifeng Xu, Jiajun Xie

Innovation Research Institute of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, China;

For correspondence:-  Shenghua Gu   Email: gnymu5@163.com

Accepted: 25 October 2019        Published: 30 November 2019

Citation: Sun W, Gu S, Zhang X, Lu J, Gu Y, Huang Y, et al. Studies on the toxicokinetics of intragastrically-administered paracetamol, aminophenazone, caffeine and chlorphenamine maleate tablets in rats. Trop J Pharm Res 2019; 18(11):2403-2409 doi: 10.4314/tjpr.v18i11.25

© 2019 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To study the toxicokinetics of paracetamol (PCT), aminophenazone (ACP), caffeine (CFN) and chlorphenamine maleate CPM) tablets after a single oral gavage, and after oral gavage for 14 consecutive days in rats.
Methods: Eighty Sprague Dawley (SD) rats (half male, half female) were randomly divided into 4 groups with 20 rats in each group. Half of the rats were used for the toxicokinetic test after a single oral gavage of PCT, ACP, CFN and CPM tablets, while rats in the other half were used for the toxicokinetic tests after oral gavage for 14 consecutive days. The doses of the four groups were set as 0, 0.5, 1 and 2 tablets/kg body weight, respectively. Blood was taken from the rats and the plasma concentration of paracetamol was determined.
Results: There was a significant difference in AUC0-∞ between male and female rats at single oral gavage of 2 tablets/kg of each of the drugs. The exposure amount of PCT (AUC0~t, AUC0-∞ and Cmax) increased with increase in dose, and showed a good linear relationship after a single intragastric administration of each drug, and after 14 consecutive days of intragastric administration at low, medium and high doses.
Conclusion: The amount of PCT to which SD rats are exposed after a single intragastric administration of PCT, ACP, CFN and CPM tablets is lower in male than in female rats. However, no significant gender difference in exposure results when these drugs are given intragastrically for 14 consecutive days.

Keywords: Oral gavage, Toxicokinetics, Paracetamol, AUC

Impact Factor
Thompson Reuters (ISI): 0.6 (2023)
H-5 index (Google Scholar): 49 (2023)

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