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Liquid Chromatography-Tandem Mass Spectrometry for the Determination of Lithospermic Acid B in Rat Serum  

Kim, Hui-Hyun (College of Pharmacy and Phytofermentation Research Center, Wonkwang University)
Ji, Hye-Young (College of Pharmacy and Phytofermentation Research Center, Wonkwang University)
Lee, Hye-Won (College of Pharmacy and Phytofermentation Research Center, Wonkwang University)
Kim, Youn-Chul (College of Pharmacy and Phytofermentation Research Center, Wonkwang University)
Sohn, Dong-Hwan (College of Pharmacy and Phytofermentation Research Center, Wonkwang University)
Lee , Hye-Suk (College of Pharmacy and Phytofermentation Research Center, Wonkwang University)
Publication Information
Archives of Pharmacal Research / v.27, no.12, 2004 , pp. 1202-1206 More about this Journal
Abstract
A rapid, sensitive and selective liquid chromatography-tandem mass spectrometric (LC-MS/ MS) method for the determination of lithospermic acid B (LSB) in rat serum was developed. LSB and internal standard, 7-hydroxy-3-phenyl-chromen-4-one (HPC) were extracted from rat serum with methyl-tert-butyl ether at acidic pH and analyzed on a Luna $C_8$ column with the mobile phase of acetonitrile-ammonium formate (10 mM, pH 6.5) (50:50, v/v). The analytes were detected using a negative electrospray ionization tandem mass spectrometry in the multiple- reaction-monitoring mode. The standard curve was linear $(r^2 = 0.997)$ over the concentration range of 10.0-500 ng/mL. The coefficient of variation and relative error for intra- and interassay at three QC levels were 1.1~6.2% and -10.3~-2.7%, respectively. The recovery of LSB from serum sample ranged from 73.2 to 79.5%, with that of HPC (internal standard) being 75.1 %. The lower limit of quantification for LSB was 10 ng/mL using 50 ${\mu}L$ of serum sample.
Keywords
Lithospermic acid B; Rat serum; LC-MS/MS;
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