Validated high-performance liquid chromatographic method utilizing solid-phase extraction for the simultaneous determination of naringenin and hesperetin in human plasma

被引:39
|
作者
Kanaze, FI [1 ]
Kokkalou, E [1 ]
Georgarakis, M [1 ]
Niopas, I [1 ]
机构
[1] Aristotle Univ Thessaloniki, Sch Hlth Sci, Dept Pharm, Thessaloniki 54124, Greece
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2004年 / 801卷 / 02期
关键词
naringenin; hesperetin;
D O I
10.1016/j.jchromb.2003.11.030
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Naringenin and hesperetin, the aglycones of the flavanone glucosides naringin and hesperidin occur naturally in citrus fruits. They exert a variety of pharmacological effects such as antioxidant, blood lipid-lowering, anticarcinogenic and inhibit selected cytochrome P-450 enzymes resulting in drug interactions. A specific, sensitive, precise, and accurate solid-phase extraction high-performance liquid chromatographic (HPLC) assay for the simultaneous determination of naringenin and hesperetin in human plasma was developed and validated. After addition of 7-ethoxycoumarin as internal standard, plasma samples were incubated with beta-glucuronidase/sulphatase, and the analytes were isolated from plasma by solid-phase extraction using C-18 cartridges and separated on a C-8 reversed phase column with methanol/water/acetic acid (40:58:2, v/v/v) as the eluent at 45 degreesC. The method was linear in the 10-300 ng/ml concentration range for both naringenin and hesperetin (r > 0.999). Recovery for naringenin, hesperetin and internal standard was greater than 76.7%. Intra- and inter-day precision for naringenin ranged from 1.4 to 4.2% and from 1.9 to 5.2%, respectively, and for hesperetin ranged from 1.3 to 4.1% and from 1.7 to 5.1%, respectively. Accuracy was better than 91.5 and 91.3% for naringenin and hesperetin, respectively. (C) 2004 Elsevier B.V. All rights reserved.
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页码:363 / 367
页数:5
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