Pharmacokinetic Interactions Between Eperisone Hydrochloride and Aceclofenac: A Randomized, Open-Label, Crossover Study of Healthy Korean Men

被引:8
|
作者
Kim, Mi Jo [1 ,2 ]
Lim, Hyeong-Seok [1 ,2 ]
Noh, Yook-Hwan [1 ,2 ]
Kim, Yo Han [1 ,2 ]
Choi, Hee Youn [1 ,2 ]
Park, Kyung-Mi [3 ]
Kim, Sei-Eun [3 ]
Bae, Kyun-Seop [1 ,2 ]
机构
[1] Asan Med Ctr, Dept Clin Pharmacol & Therapeut, Seoul, South Korea
[2] Univ Ulsan Coll Med, Seoul 138736, South Korea
[3] Hanmi Pharmaceut Co Ltd, Clin Res Team, Seoul, South Korea
关键词
aceclofenac; drug-drug interaction; eperisone hydrochloride; fixed dose combination; HUMAN PLASMA; MULTICENTER; MANAGEMENT; METABOLISM; DICLOFENAC; SAFETY; AGENT; PAIN;
D O I
10.1016/j.clinthera.2013.08.012
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Eperisone hydrochloride, a centrally acting muscle relaxant, is a calcium antagonist that causes vasodilation and antispastic actions. Aceclofenac, an anti-inflammatory analgesic and antipyretic drug, has similar efficacy and improved gastrointestinal tolerance compared with other nonsteroidal anti-inflammatory drugs, such as diclofenac. Although eperisone hydrochloride and aceclofenac are frequently coadministered, no published studies have reported on the pharmacokinetic interactions between these 2 drugs. Objective: The aim of this study was to investigate any pharmacokinetic interactions between eperisone hydrochloride and aceclofenac in healthy Korean men. Methods: This was a randomized, open-label, crossover study. Each participant was randomly assigned to 1 of 6 treatment sequences and received eperisone hydrochloride (3 doses of 50 mg each), aceclofenac (2 doses of 100 mg each), or both as a single dose with a 7-day washout period between each dose. Blood samples were collected <= 24 hours after dosing, and plasma eperisone hydrochloride and aceclofenac concentrations were determined using validated LC/MS-MS. Pharmacokinetic analyses were conducted using noncompartmental methods. A safety profile was determined using the measurement of vital signs, ECG, and clinical laboratory tests. Results: A total 24 of men were enrolled, and all completed the study. The geometric mean ratios (90% CIs) of the C-max and AUC(0-infinity) values for eperisone were 1.18 (0.828-1.673) and 1.12 (0.836-1.507), respectively. The geometric mean ratios (90% CIs) of the C-max and AUC(0-infinity) for aceclofenac were 0.93 (0.847-1.022) and 1.01 (0.979-1.036), respectively. A total of 7 adverse events were reported in 7 men. All adverse events were mild, and no significant differences were found between treatment groups. Conclusion: No clinically significant pharmacokinetic differences exist between 150 mg eperisone hydrochloride and 200 mg aceclofenac when administrated as a monotherapy or in combination. (C) 2013 Elsevier HS Journals, Inc. All rights reserved.
引用
收藏
页码:1528 / 1535
页数:8
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