Validated High-Performance Liquid Chromatographic Method Utilizing Solid-Phase Extraction for ‎the Simultaneous Determination of Naringenin And Hesperetin in Human Plasma

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Journal Title, Volume, Page: 
Journal of Chromatography B, Volume 801, Issue 2, Pages 363–367
Year of Publication: 
2004
Authors: 
Feras Imad Kanaze
Department of Pharmacy, School of Health Sciences, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece
Current Affiliation: 
Department of Pharmacy,Faculty of Medicine & Health Sciences, An-Najah National University, Nablus, Palestine
Eugene Kokkalou
Department of Pharmacy, School of Health Sciences, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece
Manolis Georgarakis
Department of Pharmacy, School of Health Sciences, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece
Ioannis Niopas
Department of Pharmacy, School of Health Sciences, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece
Preferred Abstract (Original): 

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 β-glucuronidase/sulphatase, and the analytes were isolated from plasma by solid-phase extraction using C18cartridges and separated on a C8 reversed phase column with methanol/water/acetic acid (40:58:2, v/v/v) as the eluent at 45 °C. 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.

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