Quantitation of trans-resveratrol and detection of its metabolites in human plasma and urine by high performance liquid chromatography

被引:167
|
作者
Boocock, David J.
Patel, Ketan R.
Faust, Guy E. S.
Normolle, Daniel P.
Marczylo, Timothy H.
Crowell, James A.
Brenner, Dean E.
Booth, Tristan D.
Gescher, Andreas
Steward, William P.
机构
[1] Leicester Royal Infirm, Canc Biomakers & Prevent Grp, Dept Canc Studies & Mol Med, Leicester LE2 7LX, Leics, England
[2] Univ Michigan, Sch Med, Dept Internal Med, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Sch Med, Dept PharmacolMed, Ann Arbor, MI 48109 USA
[4] VA Med Ctr, Ann Arbor, MI USA
[5] Univ Michigan, Sch Med, Dept Radiat Oncol, Ann Arbor, MI 48109 USA
[6] Univ Michigan, Sch Med, Comprehens Canc Ctr, Ann Arbor, MI 48109 USA
[7] Royalmount Pharma, Montreal, PQ H4P 2T4, Canada
[8] NCI, Div Canc Prevent, Bethesda, MD 20892 USA
关键词
resveratrol; conjugated metabolites; HPLC; human; plasma; urine;
D O I
10.1016/j.jchromb.2006.10.017
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We describe a reversed-phase HPLC method that uses gradient elution and UV detection (325 nm) to determine levels of resveratrol and identify six major conjugated metabolites in the plasma and urine of human volunteers after administration of a single oral dose of I g. Waters Atlantis C-18 3 mu m served as the stationary phase. The gradient was formed using ammonium acetate and methanol, containing 2% propan-2-ol. Detection is linear between 5 ng/mL and 500 ng/mL in plasma (5-1000 ng/mL in urine). The coefficient of variation for intra- and inter-day variation is <10%. The average recovery of resveratrol from plasma and urine is 58 +/- 3%. The data presented in this report demonstrate a rapid, sensitive and accurate method for the analysis of resveratrol and its metabolites in human plasma and urine for pharmacokinetic studies. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:182 / 187
页数:6
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