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서지반출
Liquid Chromatography-Tandem Mass Spectrometry of a New $PPAR{alpha}/{gamma}$ Dual Agonist PAR-5359 in Rat Plasma
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  • Liquid Chromatography-Tandem Mass Spectrometry of a New $PPAR{alpha}/{gamma}$ Dual Agonist PAR-5359 in Rat Plasma
  • Liquid Chromatography-Tandem Mass Spectrometry of a New $PPAR{alpha}/{gamma}$ Dual Agonist PAR-5359 in Rat Plasma
저자명
Kim. Dong-Kyun,Park. Eun-Jeong,Jeong. Ji-Hyun,Jeon. Sun-Ho,Kim. Eun-Jung,Shim. Hyun-Joo,Lim. Joong-In,Lee. Hye-Suk
간행물명
Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea
권/호정보
2009년|32권 12호|pp.1743-1748 (6 pages)
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대한약학회
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정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
서지반출

기타언어초록

PAR-5359, 3-(4-{2-[4-(4-Chloro-phenyl)-3,6-dihydro-2H-pyridin-1-yl]-ethoxy}-phenyl)-2-ethoxypropionic acid, is a well-balanced $PPAR{alpha}/{gamma}$ dual agonist with the excellent antihyperglycemic and hypolipidemic activities. A reliable, selective and sensitive high-performance liquid chromatography with electrospray ionization tandem mass spectrometry was developed for the determination of PAR-5359 in rat plasma. PAR-5359 was twice extracted from rat plasma using methyl tert-butyl ether at neutral pH. The analytes were separated on an Allure Biphenyl column with the mobile phase of 78% methanol in 10 mM ammonium formate (pH 3.0) and detected by tandem mass spectrometry in the selective reaction monitoring mode. The calibration curve was linear (r = 0.9993) over the concentration range of 2.00-1000.0 ng/mL and the lower limit of quantification was 2.00 ng/mL using $50;{mu}L$ plasma sample. The coefficient of variation and relative error at four QC levels were 1.2 to 12.3% and -2.5 to 6.3%, respectively. The present method was successfully applied to the pharmacokinetic study of PAR- 5359 after oral dose of PAR-5359 at a dose of 1 mg/kg to male SD rats.