首页> 外文会议>NATO Advanced Study Institute on Chemicals as Intentional and Accidental Global Environmental Threats; 20051116-27; Borovetz(BG) >METHOD FOR THE DETERMINATION OF SOME SELECTED STEROID HORMONES AND BISPHENOL A IN WATER AT LOW NG/L LEVEL BY ON-LINE SOLID-PHASE EXTRACTION COMBINED WITH LIQUID CHROMATOGRAPHY-TANDEM MASS SPECTROMETRY
【24h】

METHOD FOR THE DETERMINATION OF SOME SELECTED STEROID HORMONES AND BISPHENOL A IN WATER AT LOW NG/L LEVEL BY ON-LINE SOLID-PHASE EXTRACTION COMBINED WITH LIQUID CHROMATOGRAPHY-TANDEM MASS SPECTROMETRY

机译:固相萃取-液相色谱-串联质谱法测定低NG / L水平水中某些甾体激素和双酚A

获取原文
获取原文并翻译 | 示例

摘要

A sensitive analytical method based on automatic on-line Solid-Phase Extraction (SPE) combined with Liquid Chromatography-Tandem Mass Spectrometry (LC-ESI-MS-MS) has been developed for the determination of six Endocrine-Disrupting Compounds (EDC's): 17-α-estradiol, 17-α-ethynylestradiol, 17-β-estradiol, bisphenol A, Estriol and Estrone in water samples. In order to enhance the sensitivity for these analytes, post column addition of different bases such as ammonia and 1,8-diazabicyclo(5,4,0)undec-7en (DBU) was evaluated. The post column addition of base is proposed here to raise effluent pH, helping in the ionization process of the compounds. The use of ammonium hydroxide diluted in methanol-acetonitrile mixture, proved to be the most efficient post column reagent for enhancing the MS signal. This strategy permitted direct determination of the six compounds at low ng/L levels. For the application to real water samples, an extraction and preconcentration step using SPE was carried out with cross-linked styrene-divinylbenzene polymer (PLPR-s) material. The recovery for all six compounds was satisfactory percentage (80-110%). The limits of quantification are between 1.0 and 2.0 ng/L. Application of the whole method, SPE-LC-ESI-MS-MS, to nature waters permitted low nanogram-per-liter determination of all six compounds.
机译:已开发出一种基于自动在线固相萃取(SPE)结合液相色谱-串联质谱(LC-ESI-MS-MS)的灵敏分析方法,用于测定六种干扰内分泌的化合物(EDC):水样中的17-α-雌二醇,17-α-乙炔基雌二醇,17-β-雌二醇,双酚A,雌三醇和雌酮。为了提高这些分析物的灵敏度,在柱后添加了不同的碱,例如氨和1,8-二氮杂双环(5,4,0)十一烷基-7en(DBU),进行了评估。在这里建议在柱后添加碱以提高废水的pH,从而有助于化合物的电离过程。事实证明,使用稀释在甲醇-乙腈混合物中的氢氧化铵是增强MS信号的最有效的柱后试剂。该策略可以直接测定低ng / L含量的六种化合物。为了应用于实际水样品,使用SPE对交联的苯乙烯-二乙烯基苯聚合物(PLPR-s)材料进行了萃取和预浓缩步骤。所有六个化合物的回收率均令人满意(80-110%)。定量限在1.0到2.0 ng / L之间。将整个方法SPE-LC-ESI-MS-MS应用于自然水域,可以对所有六种化合物进行低纳升/升的测定。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号