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Effect of food on systemic exposure to niflumic acid following postprandial administration of talniflumate

Authors
Kang, WonkuKim, KibumKim, Eun-YoungKwon, Kwang-ilBang, Jun SeokYoon, Young-Ran
Issue Date
Jul-2008
Publisher
SPRINGER
Citation
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, v.64, no.10, pp 1027 - 1030
Pages
4
Journal Title
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY
Volume
64
Number
10
Start Page
1027
End Page
1030
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/148158
DOI
10.1007/s00228-008-0524-4
ISSN
0031-6970
1432-1041
Abstract
Purpose Talniflumate was designed as a prodrug of niflumic acid, a potent analgesic and anti-inflammatory drug, which is widely prescribed for treating rheumatoid diseases. The prandial effect on talniflumate absorption remains unclear; therefore, this study investigated the effect of food on the systemic exposure to niflumic acid in healthy volunteers.Methods Volunteers received a single 740-mg dose of talniflumate 30 min after consuming a high-fat breakfast, a low-fat breakfast, or no food ( fasting condition). Plasma concentrations of both talniflumate and niflumic acid were measured using validated high-performance liquid chromatography coupled to tandem mass spectrometry. Results The maximum concentration of niflumic acid was 224 +/- 193 ng/ml at similar to 2.7 h in the fasted condition compared with 886 +/- 417 ng/ml (p< 0.05) at 1.8 h and 1,159 +/- 508 ng/ml (p< 0.01) at 2.2 h with the low- and high-fat meals, respectively. The mean area under the curve from zero to infinity (AUC(inf)) values after the low- and high-fat meals were four- and fivefold, respectively, the value while fasting ( p< 0.05). Conclusions It is strongly recommended that talniflumate be taken after a meal to increase systemic exposure to its active metabolite. Our results suggest a reduction in the daily dosage of talniflu
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