HPLC method with UV detection for the determination of trans-resveratrol in plasma

被引:20
作者
Katsagonis, A [1 ]
Atta-Politou, J [1 ]
Koupparis, MA [1 ]
机构
[1] Univ Athens, Dept Chem, Analyt Chem Lab, GR-15771 Athens, Greece
关键词
trans-resveratrol; HPLC; plasma; carbamazepine;
D O I
10.1081/JLC-200054884
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The main representative of phytoalexins (biologically active substances produced by the plant as an immediate immunological response to infections or abiotic stresses) in wine grapes (Vitis vinifera) is the stilbene trans-resveratrol. The proposed method for the determination of trans-resveratrol in blood plasma is based on reversed phase HPLC utilizing UV detection (310nm), under isocratic conditions (1.0mL/min), with mobile phase consisting of acetonitrile-phosphate buffer pH 4.8 (30 mM) 25:75 v/v, a C 18 Novapack 150 x 4.0 mm column (4 mu m particle size), and carbamazepine as internal standard (5 mu g/mL). Plasma samples (I mL) are buffered with phosphate buffer (0.4 mL) pH 6.0 and extracted with 3 x 3 mL of ethyl acetate. trans-resveratrol is eluted at around 4.6 min, whereas carbamazepine at approximately 9.6 min, yielding a resolution of 4.4. The method appears to be linear within a range of 0. 15 -4.0 mu g/mL (r = 0.9998), with good repeatability (%RSD = 0.86) and reproducibility (%RSD = 2.2). Detection and quantification limits were found equal to 0.10 and 0.33 mu g/mL, respectively. Accuracy, expressed as recovery determined at two concentrations of 0.3 and 3.0 mu g/mL (6-replicates) were found to be 88.3 +/- 7.5% and 100.7 +/- 0.7%, respectively. The reported method is simple, rapid, accurate, and intended for use to further bioavailability studies, aiming to the development of pharmaceutical dosage formulations of resveratrol for oral administration.
引用
收藏
页码:1393 / 1405
页数:13
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