吴俊发,谭健辉,马 鑫.超高效液相色谱法同时测定保健品中4种大豆异黄酮[J].食品安全质量检测学报,2021,12(6):2264-2269
超高效液相色谱法同时测定保健品中4种大豆异黄酮
Simultaneous determination of 4 kinds of soybean isoflavones in health products by ultra performance liquid chromatography
投稿时间:2020-11-24  修订日期:2021-04-01
DOI:
中文关键词:  超高效液相色谱法  保健品  大豆异黄酮
英文关键词:ultra performance liquid chromatography  health products  soybean isoflavones
基金项目:
作者单位
吴俊发 广州检验检测认证集团有限公司, 国家加工食品质量检验中心(广东) 
谭健辉 广州检验检测认证集团有限公司, 国家加工食品质量检验中心(广东) 
马 鑫 广州检验检测认证集团有限公司, 国家加工食品质量检验中心(广东) 
AuthorInstitution
WU Jun-Fa Guangzhou Inspection and Testing Certification Group Co., National Quality Testing Center for Processed Food (Guangdong) 
TAN Jian-Hui Guangzhou Inspection and Testing Certification Group Co., National Quality Testing Center for Processed Food (Guangdong) 
MA Xin Guangzhou Inspection and Testing Certification Group Co., National Quality Testing Center for Processed Food (Guangdong) 
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中文摘要:
      目的 建立超高效液相色谱法(ultra performance liquid chromatography, UPLC)同时测定保健品中大豆苷(daidzin)、染料木苷(genistin)、染料木素(daidzein)和大豆素(genistein)4种大豆异黄酮的分析方法。方法 样品用80%甲醇超声提取后, 以甲醇-0.1%磷酸水(V/V)作为流动相梯度洗脱分离, 使用二极管阵列检测器(photo-diode array, PDA)于260 nm波长下测定。结果 4种大豆异黄酮在1.0~50 mg/L范围内, 标准曲线线性良好, 相关系数r2均大于0.999。平均回收率为86.7%~106%, 相对标准偏差(relative standard deviation, RSD)为1.31%~6.32%。方法检出限为0.5~1.0 mg/kg, 方法定量限为1.5~3.0 mg/kg。结论 该方法回收率高, 灵敏度高, 且操作简单, 快速高效, 可应用于实际样品测定。
英文摘要:
      Objective To establish a method for the determination of 4 soybean isoflavones in health products included daidzin, genistin, daidzein and genistein by ultra performance liquid chromatography (UPLC). Method Samples were ultrasonic extracted by 80% methanol-water, then separated by methanol-0.1% phosphoric acid-water (V/V) as mobile phase with gradient elution, finally detected by photo-diode array detector under the wavelength of 260 nm. Results The standard curve of four soybean isoflavones exhibited a good linearity in the concentration range of 1.0?50 mg/L, while the correlation coefficient (r2) were both greater than 0.999. Moreover, the average recoveries were ranged from 86.7% to 106% with the relative standard deviations were ranged from 1.31% to 6.32%. The limits of detection and the limits of quantitation were 0.5?1.0 mg/kg and 1.5?3.0 mg/kg respectively. Conclusion This method has high recovery rate and high sensitivity. It is simple operation, fast and efficient that can be applied to actual determination.
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