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一滴血液中全氟化合物的生物监测。

Biomonitoring of perfluorinated compounds in a drop of blood.

作者信息

Mao Pan, Wang Daojing

机构信息

Newomics Inc., 5980 Horton Street, Suite 525, Emeryville, California 94608, United States.

出版信息

Environ Sci Technol. 2015 Jun 2;49(11):6808-14. doi: 10.1021/acs.est.5b01442. Epub 2015 May 22.

DOI:10.1021/acs.est.5b01442
PMID:25997583
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4456762/
Abstract

Biomonitoring of pollutants and their metabolites and derivatives using biofluids provides new opportunities for spatiotemporal assessment of human risks to environmental exposures. Perfluorinated compounds (PFCs) have been used widely in industry and pose significant environmental concerns due to their stability and bioaccumulation in humans and animals. However, current methods for extraction and measurement of PFCs require relatively large volumes (over one hundred microliters) of blood samples, and therefore, are not suitable for frequent blood sampling and longitudinal biomonitoring of PFCs. We have developed a new microassay, enabled by our silicon microfluidic chip platform, for analyzing PFCs in small volumes (less than five microliters) of blood. Our assay integrates on-chip solid-phase extraction (SPE) with online nanoflow liquid chromatography-electrospray ionization-mass spectrometry (nanoLC-ESI-MS) detection. We demonstrated high sample recovery, excellent interday and intraday accuracy and precision, and a limit of detection down to 50 femtogram of PFCs, in one microliter of human plasma. We validated our assay performance using pooled human plasma and NIST SRM 1950 samples. Our microfluidic chip-based assay may enable frequent longitudinal biomonitoring of PFCs and other environmental toxins using a finger prick of blood, thereby providing new insights into their bioaccumulation, bioavailability, and toxicity.

摘要

利用生物流体对污染物及其代谢物和衍生物进行生物监测,为时空评估人类因环境暴露而面临的风险提供了新机遇。全氟化合物(PFCs)在工业中被广泛使用,因其稳定性以及在人类和动物体内的生物累积性而引发了重大环境问题。然而,目前用于提取和测量全氟化合物的方法需要相对大量(超过一百微升)的血液样本,因此,不适用于频繁的血液采样和全氟化合物的纵向生物监测。我们开发了一种新的微量分析方法,借助我们的硅微流控芯片平台,用于分析少量(少于五微升)血液中的全氟化合物。我们的分析方法将芯片上的固相萃取(SPE)与在线纳流液相色谱 - 电喷雾电离 - 质谱(nanoLC - ESI - MS)检测相结合。我们证明了该方法具有高样品回收率、出色的日间和日内准确性与精密度,以及在一微升人血浆中低至50飞克全氟化合物的检测限。我们使用混合人血浆和NIST SRM 1950样品验证了我们的分析性能。我们基于微流控芯片的分析方法或许能够通过手指采血实现对全氟化合物和其他环境毒素的频繁纵向生物监测,从而为它们的生物累积、生物可利用性和毒性提供新的见解。

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