Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
7617843 | Journal of Chromatography B | 2014 | 5 Pages |
Abstract
Two high-performance liquid chromatography (HPLC) coupled with electrospray ionization (ESI) mass spectrometry methods were developed and validated for the simultaneous determination of asperosaponin VI (A-VI) and hederagenin (HG) in rats' various tissues. Biological samples were processed with methanol extraction, and glycyrrhetinic acid was chosen as the internal standard (IS). The analytes were separated on a C18 column with two gradient elution programs for different rat tissue samples. The MS/MS detection was carried out by monitoring the transitions of m/z [MH]â 927.5 â 603.4 for A-VI, m/z [MH]â 471.3 â 471.3 for HG and m/z [MH]â 469.4 â 425.4 for the IS, respectively. The lower limits of quantification (LLOQ) for the two analytes in different rat tissues were 2-6 ng/mL, respectively. The methods were successfully applied to a tissue distribution study of A-VI and its active metabolite HG in rats. The results of the tissue distribution study showed that the highest concentration of A-VI was in the gastrointestinal (GI) tract. Besides, A-VI was mainly distributed in lung, liver, fat and ovary. HG was almost undetectable in most tissues except for the GI tract.
Keywords
ULOQLLOQESIAsperosaponin VIMRMRSDLC–MS/MSMatrix effectinternal standardrelative standard deviationcollision energyTissue distributionupper limit of quantificationlower limit of quantificationrelative errorGastrointestinalmultiple reaction monitoringHederageninsodium carboxymethylcellulosequality controlelectrospray ionization
Related Topics
Physical Sciences and Engineering
Chemistry
Analytical Chemistry
Authors
Run Zhang, He Zhu, Li Ding, Zhonglin Yang,