液液萃取—超高效液相色谱串联质谱法同时测定尿中11种羟基多环芳烃

    Simultaneous determination of 11 hydroxy-polycyclic aromatic hydrocarbons in urine by LLE and UPLC-MS/MS

    • 摘要:
      目的 建立可同时测定尿中11种羟基多环芳烃(hydroxy-polycyclic aromatic hydrocarbons, OH-PAHs)的超高效液相色谱串联质谱分析(ultra-high performance liquid chromatography tandem with mass spectrometry, UPLC-MS/MS)法。
      方法 尿液样品在pH=5.5条件下, 在37 ℃水浴中经β-葡萄糖苷酸酶—芳基硫酸酯酶避光水解16 h, 3.0 mL正己烷萃取、涡旋、离心, 取上层有机相, 重复萃取两次, 合并萃取液, 氮吹至近干, 再复溶于20%乙腈水溶液中。流动相为水和10%异丙醇甲醇溶液, 梯度洗脱模式洗脱, CORTECS C18色谱柱分离, ESI-模式测定尿液中11种羟基多环芳烃浓度, 内标法定量分析。
      结果 11种羟基多环芳烃线性关系良好, 相关系数(r)均大于0.997。方法的检出限为0.01~0.10 ng/mL; 日间回收率为79.8%~97.3%, 精密度为1.9%~4.7%(n=3);日内回收率为78.6%~92.3%, 精密度为3.7%~7.1%(n=3)。
      结论 该方灵敏度高, 准确可靠, 适用于人群中多种羟基多环芳烃的监测。

       

      Abstract:
      Objective To develop a method for simultaneous determination of 11 hydroxy-polycyclic aromatic hydrocarbons(OH-PAHs) in urine by ultra-high performance liquid chromatography tandem with mass spectrometry(UPLC-MS/MS).
      Methods The urine sample was hydrolyzed by β-glucuronidase/arylsulfatase in a water bath at 37℃ under the condition of pH 5.5 for 16 h away from light overnight, then extracted by 3.0 mL n-hexane. The upper organic phase was separated from urine sample by vortex and centrifugation. The extraction procedure was repeated twice and the two extracts were combined, and evaporated with nitrogen gas to almost dryness. The residues were re-dissolved in 20% acetonitrile solution, followed by gradient elution and separation by a CORTECS C18 column with 10% isopropanol methanol solution and water as mobile phases. The internal standard method was performed to measure the concentrations of 11 OH-PAHs by UPLC-MS/MS under ESI-mode.
      Results The method showed good linearity for the 11 OH-PAHs (r>0.997), with detection limits of 0.01-0.10 ng/mL. The inter-day recoveries were 79.8%-97.3%, with relative standard deviations of 1.9%-4.7% (n=3), and the intra-day recoveries were 78.6%-92.3%, with relative standard deviations of 3.7%-7.1% (n=3).
      Conclusion The proposed method is sensitive and accurate, and is suitable for the monitoring of multiple OH-PAHs in human urine samples.

       

    /

    返回文章
    返回