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Effect of food components and dosing times on the oral pharmacokinetics of nifedipine in rats

Authors
Cao, Qing-RiCui, Jing-HaoPark, Jun BomHan, Hyo-KyungLee, JaehwiOh, Kyung TaekPark, InchoonLee, Beom-Jin
Issue Date
Aug-2010
Publisher
ELSEVIER SCIENCE BV
Keywords
Nifedipine; Food components; Multiple dosing; Dosing times; Oral pharmacokinetics; Double peak phenomena; Circadian zeitgeber
Citation
INTERNATIONAL JOURNAL OF PHARMACEUTICS, v.396, no.1-2, pp 39 - 44
Pages
6
Journal Title
INTERNATIONAL JOURNAL OF PHARMACEUTICS
Volume
396
Number
1-2
Start Page
39
End Page
44
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/22255
DOI
10.1016/j.ijpharm.2010.06.002
ISSN
0378-5173
1873-3476
Abstract
The present study was aimed to investigate the effect of food components and dosing time on the oral exposure of nifedipine in rats Nifedipine was given orally to rats with and without food components at 8:00 a m (morning time) or 4:00 p m (evening time) during winter periods Food components included milk, sodium chloride, oleic acid, and sodium taurocholate. Plasma concentration profiles of nifedipine showed double peak phenomena which were generally retained regardless of food components, vehicle types and the dosing time. Sodium chloride, milk and sodium taurocholate significantly increased the AUC while oleic acid did not, when drug was dosed in the morning time. After the dosing in the evening time, milk and sodium chloride significantly increased the plasma concentrations of nifedipine but oleic acid and sodium taurocholate decreased them. Overall, the systemic in vivo exposure of nifedipine was invariably lower with the evening dosing compared to the dosing in the morning, but this circadian rhythm dependency was not reversed by the multiple dosing of food components in rats Food components and dosing time significantly altered the oral pharmacokinetics of nifedipine in rats, implying that the altered bioavailability and higher plasma concentrations in the morning time may influence dosing regimens of nifedipine for hypertension patients. (C) 2010 Elsevier B.V All rights reserved
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대학원 (글로벌혁신신약학과)
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