Song Han-Na, Kim Chong Hyeak, Lee Won-Yong, Cho Sung-Hee
Center for Chemical Analysis, Korea Research Institute of Chemical Technology (KRICT), Daejeon, 305-600, Korea.
Department of Chemistry, Yonsei University, Seoul, 120-749, Korea.
Rapid Commun Mass Spectrom. 2017 Apr 15;31(7):613-622. doi: 10.1002/rcm.7827.
Volatile organic compounds (VOCs) are ubiquitous environmental pollutants that have a high vapor pressure at room temperature. Some VOCs have been classified as carcinogenic to humans by the International Agency for Research on Cancer (IARC), because they can bind to DNA and cause cell mutations. Therefore, monitoring of VOCs in human urine is very important to evaluate the correlation between exposure to VOCs and human disease.
We have developed an improved analytical method for the simultaneous determination of VOCs with a wide range of polarities in human urine samples by headspace solid-phase microextraction (HS-SPME) coupled to gas chromatography/mass spectrometry (GC/MS). In the improved method, a bi-polar carboxen-polydimethylsiloxane (CAR/PDMS) fiber was used for the optimized extraction of 15 VOCs with a wide range of polarities, including benzene, toluene, ethylbenzene, xylenes (BTEX), alkylbenzenes, cresols, and naphthalene, in human urine samples. Extracted VOCs from the human urine were effectively separated by GC using a mid-polarity column (DB-35, 35% phenylmethylpolysiloxane) and monitored by MS using extracted ion monitoring (EIM) mode.
Under the optimized method, the linearity of the calibration curves was greater than 0.993. The limits of detection (LODs) at a signal-to-noise (S/N) ratio of 3 were 0.3-0.6 ng/mL. The coefficients of variation were in the range of 0.1-9.7% for within-day variation and 0.2-14.2% for day-to-day variation.
The method was shown to be rapid and simple for the simultaneous determination of VOCs with a wide range of polarities in human urine and it could be applied to monitoring and to biomedical investigations to check exposure to VOCs. Copyright © 2017 John Wiley & Sons, Ltd.
挥发性有机化合物(VOCs)是普遍存在的环境污染物,在室温下具有较高的蒸气压。一些VOCs已被国际癌症研究机构(IARC)归类为对人类致癌物质,因为它们可以与DNA结合并导致细胞突变。因此,监测人体尿液中的VOCs对于评估VOCs暴露与人类疾病之间的相关性非常重要。
我们开发了一种改进的分析方法,通过顶空固相微萃取(HS-SPME)结合气相色谱/质谱(GC/MS)同时测定人体尿液样品中多种极性的VOCs。在改进的方法中,使用双极性的碳分子筛-聚二甲基硅氧烷(CAR/PDMS)纤维对人体尿液样品中的15种极性范围广泛的VOCs进行优化萃取,这些VOCs包括苯、甲苯、乙苯、二甲苯(BTEX)、烷基苯、甲酚和萘。从人体尿液中萃取的VOCs通过使用中极性柱(DB-35,35%苯基甲基聚硅氧烷)的GC进行有效分离,并通过使用提取离子监测(EIM)模式的MS进行监测。
在优化方法下,校准曲线的线性大于0.993。信噪比(S/N)为3时的检测限(LOD)为0.3 - 0.6 ng/mL。日内变异的变异系数范围为0.1 - 9.7%,日间变异的变异系数范围为0.2 - 14.2%。
该方法被证明对于同时测定人体尿液中多种极性的VOCs快速且简便,可应用于监测和生物医学研究以检查VOCs暴露情况。版权所有© 2017约翰威立父子有限公司。