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同位素稀释-超高效液相色谱-串联质谱法同时测定精油中的7种雌性激素
引用本文:黄百芬,韩铮,徐小民,蔡增轩,姜维,任一平.同位素稀释-超高效液相色谱-串联质谱法同时测定精油中的7种雌性激素[J].色谱,2011,29(1):20-25.
作者姓名:黄百芬  韩铮  徐小民  蔡增轩  姜维  任一平
作者单位:1. 浙江省疾病预防控制中心, 浙江 杭州 310051; 2. 浙江大学, 浙江 杭州 310058
基金项目:浙江省医药卫生科技计划项目(No. 2008A026).
摘    要:建立了采用同位素稀释-超高效液相色谱-串联质谱同时快速测定精油中7种雌性激素(雌三醇、雌二醇、雌酮、炔雌醇、己二烯雌酚、己烷雌酚、己烯雌酚)的方法。样品中雌性激素用乙酸乙酯-正己烷(2:98, v/v)溶液提取后,经硅胶固相萃取小柱净化,通过ACQUITY UPLCTM BEH SHELD RP18色谱柱(100 mm×2.1 mm, 1.7 μm)、以水-乙腈作流动相梯度洗脱对7种雌性激素进行分离,采用串联质谱在负离子扫描方式下通过多反应监测(MRM)模式进行定性定量分析。以雌三醇-D3、雌二醇-D3、己烯雌酚-D6为内标,有效减少了样品基质的影响。该方法对精油中7种雌激素的检出限(LOD)为0.3~7 μg/kg,定量限(LOQ)为1~20 μg/kg。待测物与内标物定量离子的峰面积比值与待测物的质量浓度在20~500 μg/L范围内呈良好的线性关系,相关系数(r2)均大于0.997;在20~500 μg/kg范围内3个水平的加标平均回收率为88.5%~114.8%,日内精密度(以相对标准偏差计)(n=6)为4.8%~18.9%。应用该方法对浙江杭州地区不同超市或美容院随机采集的12份精油样品进行测定的结果显示,有1份样品含有雌二醇和雌酮,其余11份样品均未检出雌性激素。

关 键 词:同位素稀释  超高效液相色谱-串联质谱  雌性激素  精油
收稿时间:2010-09-15

Simultaneous determination of 7 female sex hormones in essential oil by high performance liquid chromatography- tandem mass spectrometry with isotope dilution
HUANG Baifen,HAN Zheng,XU Xiaomin,CAI Zengxuan,JIANG Wei,REN Yiping.Simultaneous determination of 7 female sex hormones in essential oil by high performance liquid chromatography- tandem mass spectrometry with isotope dilution[J].Chinese Journal of Chromatography,2011,29(1):20-25.
Authors:HUANG Baifen  HAN Zheng  XU Xiaomin  CAI Zengxuan  JIANG Wei  REN Yiping
Institution:1. Zhejiang Provincial Center for Disease Prevention and Control, Hangzhou 310051, China; 2. Zhejiang University, Hangzhou 310058, China
Abstract:A reliable ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method for the simultaneous determination of 7 female sex hormones (estriol, estradiol, estrone, ethinyloestradiol, dienestrol, hexestrol, diethylstilbestrol) in essential oil was developed. The sample was extracted by ethylacetate-normal hexane solution (2:98, v/v) and the extract was purified by a silica solid phase extraction-based clean-up column. Then, the analytes were separated on an ACQUITY UPLC BEH SHELD RP18 column (100 mm×2.1 mm, 1.7 μm) in gradient elution with the mobile phases of water and acetonitrile. The separated compounds were detected with a Waters Xevo TQ MS tandem quadrupole mass spectrometer operated in negative electro-spray ionization using multiple reaction monitoring mode. Estriol-D3, estradiol-D3 and diethylstilbestrol-D6 were used as the internal standards to reduce the matrix effects. The limits of detection and quantitation for the 7 female sex hormones in essential oil were 0.3~7 μg/kg and 1~20 μg/kg, respectively. Good linear relationships and high correlation coefficients (r2≥0.997) were obtained in the mass concentration range of 20~500 μg/L. The average recoveries were 88.5%~114.8% and the intra-assay relative standard deviations were 4.8%~18.9% at the spiked levels of 20~500 μg/kg. Finally, a total of 12 samples randomly collected from different supermarkets in Zhejiang Province were screened for the 7 female sex hormones by the proposed method. The results showed that only one sample contained estradiol and estrone.
Keywords:isotope dilution  ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS)  female sex hormones  essential oil
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