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Determination of 25-OH-PPD in rat plasma by high-performance liquid chromatography-mass spectrometry and its application in rat pharmacokinetic studies.

Determination of 25-OH-PPD in rat plasma by high-performance liquid chromatography-mass spectrometry and its application in rat pharmacokinetic studies. Research Abstract Details 

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  • Determination of 25-OH-PPD in rat plasma by high-performance liquid chromatography-mass spectrometry and its application in rat pharmacokinetic studies. Abstract Text:

    xiangrong zhangXiangrong Zhang,dan zhangDan Zhang,jinghua xuJinghua Xu,jingkai guJingkai Gu,yuqing zhaoYuqing Zhao,xiangrong zhangXiangrong Zhang,dan zhangDan Zhang,jinghua xuJinghua Xu,jingkai guJingkai Gu,yuqing zhaoYuqing Zhao,xiangrong zhangXiangrong Zhang,dan zhangDan Zhang,jinghua xuJinghua Xu,jingkai guJingkai Gu,yuqing zhaoYuqing Zhao,

    A sensitive and specific liquid chromatography/tandem mass spectrometry (LC/MS/MS) method was developed for the investigation of the pharmacokinetics of 20(R)-dammarane-3beta,12beta,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 C8 material (3.5 microm). 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 6h. 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%.

    Determination of 25-OH-PPD in rat plasma by high-performance liquid chromatography-mass spectrometry and its application in rat pharmacokinetic studies. Publishing Authors By Initials

    x zhangX Zhang,d zhangD Zhang,j xuJ Xu,j guJ Gu,y zhaoY Zhao,x zhangX Zhang,d zhangD Zhang,j xuJ Xu,j guJ Gu,y zhaoY Zhao,x zhangX Zhang,d zhangD Zhang,j xuJ Xu,j guJ Gu,y zhaoY Zhao,

    For similar abstracts research abstracts see: abstracts research

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    Determination of 25-OH-PPD in rat plasma by high-performance liquid chromatography-mass spectrometry and its application in rat pharmacokinetic studies. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Journal of chromatography. B, Analytical technolog

    VOLUME: 858

    Page Numbers: 65-70

    Journal Abbreviation: J. Chromatogr. B Analyt. Techn

    ISSN: 1570-0232

    DAY: 23

    MONTH: 08

    YEAR: 2007

    Determination of 25-OH-PPD in rat plasma by high-performance liquid chromatography-mass spectrometry and its application in rat pharmacokinetic studies. Information

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    LANGUAGE: eng

    NlmUniqueID: 101139554

    Determination of 25-OH-PPD in rat plasma by high-performance liquid chromatography-mass spectrometry and its application in rat pharmacokinetic studies. Keywords Mesh Terms:

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    Grant and Affiliation Information for Determination of 25-OH-PPD in rat plasma by high-performance liquid chromatography-mass spectrometry and its application in rat pharmacokinetic studies.

    AFFILIATION: Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang 110016, China.

    Country: Netherlands

    Netherlands Research PublicationNetherlands Research Publication

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    MEDLINETA: J Chromatogr B Analyt Technol

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