He Xiaoqin, Xi Cunxian, Tang Bobin, Wang Guomin, Chen Dongdong, Peng Tao, Mu Zhaode
a College of Pharmacy , Chongqing Medical University , Yuzhong District , Chongqing , China.
Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2014;31(10):1625-38. doi: 10.1080/19440049.2014.953602. Epub 2014 Sep 4.
A novel analytical method employing solid-phase extraction (SPE) coupled with ultra-high-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) was developed for the simultaneous determination of 30 hormones in anti-ageing functional foods (capsules, powders and tablets). The analytes were extracted with acetic acid-acetonitrile (1-99 v/v), methanol and acetone, respectively. The extract was purified using a combined column, followed by analyte detection with electrospray ionisation in positive- or negative-ion modes. The results indicated that the 30 compounds had good linear correlations in the range of 1-1000 μg kg⁻¹, and the correlation coefficients were above 0.99. The limits of detection (LOD) and limits of quantification (LOQ) were 0.03-2 and 0.1-5 μg kg⁻¹, respectively. The average recovery of 30 compounds at the three spiked levels varied from 74.7% to 124.1%, and the relative standard deviation (RSD) was 2.4-15.0%. This method was applied to the analysis of hormones in 14 real samples of which seven hormones (such as estrone, dienestrol) were detected in four samples, but the remainder of the hormones were not detected. The developed method is sensitive, efficient, reliable and applicable to real samples.
建立了一种采用固相萃取(SPE)与超高效液相色谱 - 串联质谱(UPLC - MS/MS)联用的新型分析方法,用于同时测定抗衰老功能食品(胶囊、粉剂和片剂)中的30种激素。分别用乙酸 - 乙腈(1 - 99 v/v)、甲醇和丙酮提取分析物。提取物通过组合柱进行净化,然后在正离子或负离子模式下采用电喷雾电离进行分析物检测。结果表明,这30种化合物在1 - 1000 μg kg⁻¹范围内具有良好的线性相关性,相关系数均高于0.99。检测限(LOD)和定量限(LOQ)分别为0.03 - 2 μg kg⁻¹和0.1 - 5 μg kg⁻¹。30种化合物在三个加标水平下的平均回收率在74.7%至124.1%之间,相对标准偏差(RSD)为2.4 - 15.0%。该方法应用于14个实际样品的激素分析,其中在4个样品中检测到7种激素(如雌酮、己烯雌酚),但其余激素未检测到。所建立的方法灵敏、高效、可靠,适用于实际样品分析。