Gill Biban, Jobst Karl, Britz-McKibbin Philip
Department of Chemistry and Chemical Biology, McMaster University, Hamilton, Ontario, L8S 4M1, Canada.
Department of Chemistry, Memorial University of Newfoundland, St. John's, Newfoundland and Labrador, A1B 3X7, Canada.
Anal Chem. 2020 Oct 6;92(19):13558-13564. doi: 10.1021/acs.analchem.0c03212. Epub 2020 Sep 22.
Urinary 1-hydroxypyrene (HP) is a widely used biomarker of polycyclic aromatic hydrocarbon exposure relevant for biomonitoring the deleterious health impacts from tobacco smoke and ambient air pollution, as well as the hazards of certain occupations. Conventional methods for urinary HP analysis based on liquid chromatography with native fluorescence detection or tandem mass spectrometry (MS/MS) and gas chromatography-mass spectrometry (GC-MS) are limited by low sample throughput and complicated sample workup protocols that are prone to bias. Herein, we introduce a high throughput method to directly analyze the intact glucuronide conjugate of HP (HP-G) in human urine after a simple acidified ether extraction procedure when using multisegment injection-capillary electrophoresis-tandem mass spectrometry (MSI-CE-MS/MS). Multiplexed analyses of 13 independent urine extracts are achieved in a single run (<3 min/sample) with stringent quality control while avoiding enzyme deconjugation and precolumn chemical derivatization. Method validation demonstrates good technical precision (CV = 7.7%, = 45) and accuracy with a mean recovery of (93 ± 3%) for urinary HP-G at three concentration levels with adequate detection limits (7 ng/L, = 3). An interlaboratory method comparison of urine samples collected from firefighters deployed in the 2016 Fort McMurray wildfire also confirms good mutual agreement with an acceptable negative bias (mean bias = 15%, = 55) when measuring urinary HP-G by MSI-CE-MS/MS as compared to total hydrolyzed urinary HP by GC-MS due to the low residual levels of free HP and its sulfate conjugate. This multiplexed separation platform is optimal for large-scale biomonitoring studies of air pollution relevant to global health as well as occupational smoke exposures in firefighters susceptible to dermal PAH absorption when using personal protective equipment.
尿中1-羟基芘(HP)是一种广泛应用的多环芳烃暴露生物标志物,可用于生物监测烟草烟雾和环境空气污染对健康的有害影响,以及某些职业的危害。基于液相色谱-天然荧光检测或串联质谱(MS/MS)以及气相色谱-质谱(GC-MS)的尿HP分析传统方法,受到低样品通量和复杂样品预处理方案的限制,这些方案容易产生偏差。在此,我们介绍一种高通量方法,在使用多段进样-毛细管电泳-串联质谱(MSI-CE-MS/MS)时,通过简单的酸化乙醚萃取程序,直接分析人尿中HP的完整葡萄糖醛酸共轭物(HP-G)。在一次运行中(<3分钟/样品)可对13个独立尿液提取物进行多重分析,并具有严格的质量控制,同时避免了酶解共轭和柱前化学衍生化。方法验证表明,该方法具有良好的技术精密度(CV = 7.7%,n = 45)和准确度,在三个浓度水平下尿HP-G的平均回收率为(93 ± 3%),检测限足够低(7 ng/L,n = 3)。对2016年麦克默里堡野火中部署的消防员收集的尿液样本进行的实验室间方法比较也证实,与GC-MS测定的总水解尿HP相比,MSI-CE-MS/MS测定尿HP-G时具有良好的相互一致性,且负偏差可接受(平均偏差 = 15%,n = 55),这是由于游离HP及其硫酸盐共轭物的残留水平较低。当使用个人防护设备时,这个多重分离平台对于与全球健康相关的空气污染以及易受皮肤多环芳烃吸收影响的消防员职业烟雾暴露的大规模生物监测研究而言是最佳选择。