HPLC method validation for measurement of sulforaphane level in broccoli by-products

被引:74
作者
Campas-Baypoli, O. N. [1 ]
Sanchez-Machado, D. I. [1 ]
Bueno-Solano, C. [1 ]
Ramirez-Wong, B. [2 ]
Lopez-Cervantes, J. [1 ]
机构
[1] Inst Tecnol Sonora, Dept Biotecnol & Ciencias Alimentarias, Obregon 85000, Sonora, Mexico
[2] Univ Sonora, Dept Invest & Posgrado Alimentos, Hermosillo 83000, Sonora, Mexico
关键词
sulforaphane; HPLC; broccoli; by-products; MSR; SPE; SOLID-PHASE EXTRACTION; BRASSICA; PURIFICATION; SEPARATION; NITRILE; FATE;
D O I
10.1002/bmc.1303
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A simple and specific analytical method was developed and tested for the determination of sulforaphane in broccoli by-products. The method includes the optimization of the conversion of glucoraphanin to sulforaphane, followed by purification of extracts using solid-phase extraction and high-performance liquid chromatography (HPLC) analysis. The response surface methodology was used to find optimum conditions for the preparation and purification procedure. Chromatographic conditions for reversed-phase HPLC with UV photodiode array detection were as follows: column, Exil ODS C-18, 25 x 0.46 cm, 5 mu m; column temperature, 36 degrees C; mobile phase, a 30:70 (v/v) mixture of acetonitrile:water; flow rate, 0.6 mL/min. The detection wavelength was UV 202 nm. Under these conditions, excellent linearity was obtained (r(2) = 1), and the overall recovery was 97.5 and 98.1% for fresh florets and lyophilized florets, respectively. The precision results showed that the relative standard deviation of the repeatability for florets fresh and lyophilized was 3.0 and 4.0%, respectively. Sulforaphane contents were determined in the edible portion of fresh broccoli, and broccoli crop remains. Copyright (C) 2009 John Wiley & Sons, Ltd.
引用
收藏
页码:387 / 392
页数:6
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