4.5 Article

Validation and implementation of a liquid chromatography/tandem mass spectrometry assay to quantitate ON 01910.Na, a mitotic progression modulator, in human plasma

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jchromb.2007.05.047

关键词

ON 01910.Na; high performance liquid chromatography (HPLC); mass spectrometry (MS); LC-MS/MS; pharmacokinetics

资金

  1. NATIONAL CANCER INSTITUTE [P30CA006973] Funding Source: NIH RePORTER
  2. NCI NIH HHS [P30 CA006973-45] Funding Source: Medline

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A reverse-phase high performance liquid chromatographic method with tandem mass spectrometry (LC-MS/MS) was developed and validated for the quantitation of ON 01910.Na, a novel synthetic benzyl styryl sulfone, in human plasma. The assay involved a simple sample preparation with acetonitrile protein precipitation. ON 01910.Na and the internal standard temazepam were separated on a Waters X-Terra (TM) MS C-18 column with mobile phase of acetonitrile containing 0.1% formic acid/10 mM ammonium acetate (55:45, v/v) using isocratic flow at 0.2 mL/min for 5 min. The analytes were monitored by tandem-mass spectrometry with electrospray positive ionization. Two calibration curves were generated over the range of 10-2000 ng/mL and 100-20000 ng/mL. The lower limit of quantitation (LLOQ) was 10 ng/mL for ON 01910.Na in human plasma. The accuracy and within- and between-day precisions were within the acceptance criteria for bioanalytical assays. ON 01910.Na was found stable in plasma at -70 degrees C for at least 1 year. The method was successfully applied to characterize the plasma concentration-time profiles of ON 01910.Na in the cancer patients in the Phase I study. (C) 2007 Elsevier B.V. All rights reserved.

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