Simultaneous determination of flurbiprofen and its hydroxy metabolite in human plasma by liquid chromatography-tandem mass spectrometry for clinical application
- Authors
- Lee, Hye-In; Choi, Chang-Ik; Byeon, Ji-Yeong; Lee, Jung-Eun; Park, So-Young; Kim, Young-Hoon; Kim, Se-Hyung; Lee, Yun-Jeong; Jang, Choon-Gon; Lee, Seok-Yong
- Issue Date
- 15-Nov-2014
- Publisher
- ELSEVIER SCIENCE BV
- Keywords
- Flurbiprofen; 4 '-Hydroxyflurbiprofen; HPLC-MS/MS; Human plasma; Pharmacokinetics
- Citation
- JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, v.971, pp 58 - 63
- Pages
- 6
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES
- Volume
- 971
- Start Page
- 58
- End Page
- 63
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/24855
- DOI
- 10.1016/j.jchromb.2014.09.007
- ISSN
- 1570-0232
1873-376X
- Abstract
- Flurbiprofen (FLB) is one of the phenylalkanoic acid derivatives of non-steroidal anti-inflammatory drugs used for the management of pain and inflammation in patients with arthritis. We developed and validated a rapid and sensitive high-performance liquid chromatography analytical method utilizing tandem mass spectrometry (HPLC-MS/MS) for the simultaneous determination of FLB and its major metabolite, 4'-hydroxyflurbiprofen (4'-OH-FLB), in human plasma. Probenecid was used as an internal standard (IS). After liquid-liquid extraction with methyl t-butyl ether, chromatographic separation of the two analytes was achieved using a reversed-phase Luna C-18 column (2.0 mm x 50 mm, 5 mu m particles) with a mobile phase of 10 mM ammonium formate buffer (pH 3.5)-methanol (15:85, v/v) and quantified by MS/MS detection in ESI negative ion mode. The flow rate of the mobile phase was 250 mu l/min and the retention times of FLB,4'-OH-FLB, and IS were 1.1, 0.8, and 0.9 mm, respectively. The calibration curves were linear over a range of 0.01-10 mu g/ml for FLB and 0.01-1 mu g/ml for 4'-OH-FLB. The lower limit of quantifications using 100 mu l of human plasma was 0.01 mu g/ml for both analytes. The mean accuracy and precision for intra- and inter-run validation of FLB and 4'-OH-FLB were all within acceptable limits. The present HPLC-MS/MS method showed improved sensitivity for quantification of the FLB and its major metabolite in human plasma compared with previously described analytical methods. The validated method was successfully applied to a pharmacokinetic study in humans. (C) 2014 Elsevier B.V. All rights reserved.
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