Journal
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES
Volume 858, Issue 1-2, Pages 65-70Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.jchromb.2007.08.021
Keywords
25-OH-PPD; LC/MS/MS; pharmacokinetics
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A sensitive and specific liquid chromatography/tandem mass spectrometry (LCMS/MS) method was developed for the investigation of the pharmacokinetics of 20(R)-dammarane-3 beta,12 beta,20,25-tetrol (25-OH-PPD) in rat. Ginsenoside Rh-2 was employed as an internal standard. The plasma samples were pretreated by liquid-liquid extraction and analyzed using LC/MS/MS with an electrospray ionization interface. The mobile phase consisted of methanol-acetonitrile-10 mmol/l aqueous ammonium acetate (42.5:42.5:15, v:v:v), which was pumped at 0.4 ml/min. The analytical column (50 mm x 2.1 mm i.d.) was packed with Venusil XBP C-8 material (3.5 mu m). The standard curve was linear from 10 to 3000 ng/ml. The assay was specific, accurate (accuracy between -1.19 and 2.57% for all quality control samples), precise and reproducible (within- and between-day precisions measured as relative standard deviation were <5% and <7%, respectively). 25-OH-PPD in rat plasma was stable over three freeze-thaw cycles and at ambient temperatures for 6 h. The method had a lower limit of quantitation of 10 ng/ml, which offered a satisfactory sensitivity for the determination of (25-OH-PPD) in plasma. This quantitation method was successfully applied to pharmacokinetic studies of 25-OH-PPD after both an oral and an intravenous administration to rats and the absolute bioavailability is 64.8 +/- 14.3%. (C) 2007 Elsevier B.V. All rights reserved.
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