| Literature DB >> 25444540 |
Hiroaki Yamaguchi1, Kazuaki Miyamori2, Toshihiro Sato2, Jiro Ogura2, Masaki Kobayashi2, Takehiro Yamada3, Nariyasu Mano4, Ken Iseki5.
Abstract
A liquid chromatography/tandem mass spectrometry method for the determination of intracellular accumulation in addition to transcellular transport of digoxin and ouabain in renal epithelial HK-2 cells was developed. The solid-phase extraction Bond Elut(®) C18 (100mg/1mL) cartridge was used for the extraction of digoxin and ouabain from extracellular (medium) and intracellular (cell lysate) matrices. Chromatographic separation was performed on a CAPCELL PAK C18 MGII column (2.0mm×150mm, 5μm). This method covered a linear range of 0.5-1000ng/mL of concentrations in medium and 0.5-1000ng of concentrations in cell lysate for digoxin and ouabain. The intra-day precision and inter-day precision of analysis were less than 11.9%, and the accuracy was within ±11.6%. The total run time was 16min. Our method was successfully applied to the transport experiments of digoxin and ouabain by HK-2 cell monolayers.Entities:
Keywords: Digoxin; Extracellular measurement; HK-2 cells; Intracellular measurement; LC/MS/MS; Ouabain
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Year: 2014 PMID: 25444540 DOI: 10.1016/j.jchromb.2014.09.043
Source DB: PubMed Journal: J Chromatogr B Analyt Technol Biomed Life Sci ISSN: 1570-0232 Impact factor: 3.205