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Development and Validation of an LC/MS/MS Method for Determination of Valproic Acid and Its Metabolite 2-Propyl-4-pentenoic Acid in Monkey Plasma
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  • Development and Validation of an LC/MS/MS Method for Determination of Valproic Acid and Its Metabolite 2-Propyl-4-pentenoic Acid in Monkey Plasma
  • Development and Validation of an LC/MS/MS Method for Determination of Valproic Acid and Its Metabolite 2-Propyl-4-pentenoic Acid in Monkey Plasma
저자명
Hwang. Kyung-Hwa,Song. Sun-Sook,Lee. Ju-Hee,Shin. Min-Chul,Seo. Jong-Su
간행물명
Journal of the Korean Society for Applied Biological Chemistry
권/호정보
2012년|55권 1호|pp.13-17 (5 pages)
발행정보
한국응용생명화학회
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정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

A rapid, accurate, and sensitive liquid chromatography/mass spectrometry (MS)/MS method for the quantitative determination of valproic acid (VPA) and its metabolite, 2-propyl-4-pentenoic acid (4-ene VPA), in monkey plasma was developed and validated. The sample extraction was performed using hydrophilic-lipophilic balance cartridge. The analytes were separated on a Kinetex C18 ($2.1mm{ imes}100mm$, 2.6 ${mu}m$) analytical column under a mobile phase consisting of 10 mM ammonium formate (pH 8.0)/methanol (20/80, v/v) and isocratic flow at 0.15 mL/min. The tandem mass spectrometer was operated in negative electrospray ionization with selected ion monitoring conditions, 143.0, 141.0, and 121.0 for VPA, 4-ene VPA, and benzoic acid (internal standard), respectively. The linearity of calibration curve ranging from 0.1 to 20 ${mu}g/mL$ was at least 0.9996 (coefficient of correlation, r) for both analytes. Intra- and inter-day precisions for both analytes were lower than 15%, resulting from quality control (QC) samples at concentration of 0.2 (low QC), 1.6 (middle QC), and 16 (high QC) ${mu}g/mL$ except at the lower limit of quantification (LLOQ) (0.1 ${mu}g/mL$) level, which was less than 20%. The intraand inter-day accuracies were within ${pm}15%$. The recoveries were 84.4-90.8% for VPA and 88.2-100.6% for 4-ene VPA. Both analytes were stable throughout short-term temperature, post preparation for 24 h, and three freeze/thaw cycles, validating that this method could be applied to toxicokinetic and pharmacokinetic studies.