Aranda-Rodriguez Rocio, Cabecinha Ashley, Harvie Jeromy, Jin Zhiyun, Marchand Axelle, Tardif Robert, Nong Andy, Haddad Sami
Exposure and Biomonitoring Division, Environmental Health Science and Research Bureau, 50 Columbine Driveway, Tunney's Pasture, Health Canada, Ottawa, ON K1A 0K9, Canada.
Exposure and Biomonitoring Division, Environmental Health Science and Research Bureau, 50 Columbine Driveway, Tunney's Pasture, Health Canada, Ottawa, ON K1A 0K9, Canada.
J Chromatogr B Analyt Technol Biomed Life Sci. 2015 Jun 15;992:76-85. doi: 10.1016/j.jchromb.2015.04.020. Epub 2015 Apr 20.
Humans are continuously exposed to volatile organic compounds (VOCs) as these chemicals are ubiquitously present in most indoor and outdoor environments. In order to assess recent exposure to VOCs for population-based studies, VOCs are measured in the blood of participants. This work describes an improved method to detect 12 VOCs by head-space solid-phase microextraction gas chromatography coupled with isotope-dilution mass spectrometry in selected reaction monitoring mode (SPME-GC-MS/MS). This method was applied to the analysis of trihalomethanes, styrene, trichloroethylene, tetrachloroethylene and BTEX (benzene, toluene, ethylbenzene, m-xylene, p-xylene, o-xylene) in a population-based biomonitoring study (Canadian Health Measures Survey). The method showed good linearity (>0.990) in the range of 0.010-10μg/L and detection limits between 0.007 and 0.027μg/L, precision better than 25% and good accuracy (±25%) based on proficiency testing materials. Quality Control data among runs over a 7 month period showed %RSD between 14 and 25% at low levels (∼0.03μg/L) and between 9 and 23% at high levels (∼0.4μg/L). The method was modified to analyze samples from a pharmacokinetic study in which 5 healthy volunteers were exposed to single, binary and quaternary mixtures of CTEX (chloroform, ethylbenzene, toluene and m-xylene), thus the expected concentration in blood was 1 order of magnitude higher than those found in the general population. The method was modified by reducing the sample size (from 3g to 0.5g) and increasing the upper limit of the concentration range to 395μg/L. Good linearity was found in the range of 0.13-395μg/L for toluene and ethylbenzene and 0.20-609μg/L for m/p-xylene. Quality control data among runs over the period of the study (n=13) were found to vary between 7 and 25%.
人类持续暴露于挥发性有机化合物(VOCs)中,因为这些化学物质在大多数室内和室外环境中普遍存在。为了在基于人群的研究中评估近期VOCs暴露情况,需对参与者血液中的VOCs进行测量。本研究描述了一种改进方法,通过顶空固相微萃取气相色谱结合同位素稀释质谱,在选择反应监测模式(SPME-GC-MS/MS)下检测12种VOCs。该方法应用于一项基于人群的生物监测研究(加拿大健康测量调查)中的三卤甲烷、苯乙烯、三氯乙烯、四氯乙烯和BTEX(苯、甲苯、乙苯、间二甲苯、对二甲苯、邻二甲苯)分析。该方法在0.010 - 10μg/L范围内线性良好(>0.990),检测限在0.007至0.027μg/L之间,基于能力验证材料,精密度优于25%,准确度良好(±25%)。7个月期间各批次的质量控制数据显示,低浓度(约0.03μg/L)时相对标准偏差(%RSD)在14%至25%之间,高浓度(约0.4μg/L)时在9%至23%之间。该方法经修改后用于分析一项药代动力学研究的样本,其中5名健康志愿者暴露于CTEX(氯仿、乙苯、甲苯和间二甲苯)的单一、二元和四元混合物中,因此血液中的预期浓度比普通人群中发现的浓度高1个数量级。通过减小样本量(从3g减至0.5g)并将浓度范围上限提高到395μg/L对该方法进行了修改。对于甲苯和乙苯,在0.13 - 395μg/L范围内线性良好,对于间/对二甲苯,在0.20 - 609μg/L范围内线性良好。在研究期间(n = 13)各批次的质量控制数据在7%至25%之间变化。