Quantitative analysis of tiropramide in human plasma by gas chromatography coupled to mass spectrometry for application to a bioequivalence test
- Authors
- Jhee, Ok Hwa; Jeon, Yong Cheol; Choi, Ho Sun; Lee, Min Ho; Om, Ae Son; Lee, Joo-Won; Hong, Jung Wook; Kim, Yong Seok; Kang, Ju Chan; Lee, Yun Sik; Shaw, Leslie M.; Kang, Ju Seop
- Issue Date
- Apr-2006
- Publisher
- Elsevier BV
- Keywords
- GC/MS; tiropramide; bioequivalence test
- Citation
- Clinica Chimica Acta, v.366, no.1-2, pp 179 - 184
- Pages
- 6
- Indexed
- SCIE
SCOPUS
- Journal Title
- Clinica Chimica Acta
- Volume
- 366
- Number
- 1-2
- Start Page
- 179
- End Page
- 184
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/181595
- DOI
- 10.1016/j.cca.2005.09.029
- ISSN
- 0009-8981
1873-3492
- Abstract
- Background: Tiropramide spectrometry (GUMS) was developed for quantification of tiropramide in human plasma using internal standard (ISD, (+/-) alpha-benzoylamino4-[2-(dimethylamino) ethoxy]-N,N-dipropylbenzenepropanamide). Methods: Tiropramide and ISD were extracted from plasma by solid-liquid extraction and analyzed on a HP-5MS column with mass selective detector. Results: The retention times of tiropramide and ISD were approximately 9.8 and 10.2 min, respectively. The calibration curve showed good linearity in the concentration range 5-500 ng/ml (r(2) = 0.998) for tiropramide in human plasma and showed good precision with CVs between 0.24% and 7.69%, respectively. The method was showed good accuracy with all intra-day (n = 5) and inter-day (n = 5) mean concentrations within 87.9-114.1% from nominal. The recovery of tiropramide and ISD were about 75.1% and 71.0% on the average, respectively. This method was successfully applied for the bioequivalence test of 2 formulations of tiropramide in 18 healthy mate volunteers who received a single 100 mg dose of each formulation.
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