Toxic Tear Gas 2‐Chloroacetophenone (CN) Forms Adducts With Endogenous Plasma Thiols In Vitro Valuable as Biomarkers of Exposure

化学 体外 加合物 谷胱甘肽 内生 胱氨酸 硫醇 质谱法 串联质谱法 同型半胱氨酸 体外毒理学 生物化学 半胱氨酸 分子 小分子 自动氧化 致癌物 代谢物 电喷雾电离 亚硫酸 色谱法 药理学 苯乙酮 血浆
作者
P. Sieber,Dirk Steinritz,Franz Worek,Harald John
出处
期刊:Drug Testing and Analysis [Wiley]
卷期号:18 (1): 74-84
标识
DOI:10.1002/dta.3964
摘要

As the tear gas of the highest toxicity, 2-chloroacetophenone (CN) poses a potential threat for exposed individuals. Several fatality cases following exposure to CN are documented, but an unambiguous identification of CN exposure is still missing. Thus, we herein present the identification of in vitro reaction products between CN and endogenous molecules useful as biomarkers. After incubation of human plasma with CN, diverse acetophenone (AcPhen)-adducts were formed with the small molecule thiols homocysteine (HCys), glutathione (GSH), and cystine (Cys-Cys). All adducts were detected by microbore liquid chromatography-electrospray ionization high-resolution tandem mass spectrometry (μLC-ESI MS/HRMS) working in the parallel reaction monitoring (PRM) mode and were characterized as potential biomarkers of CN exposure. Time- and concentration-dependent adduct formations were investigated, and the stability of AcPhen-adducts in plasma during 4 freeze-and-thaw cycles and in the autosampler was tested. The limit of identification (LOI) of identified AcPhen-adducts in vitro was found at about 6 μM (concentration of CN in plasma) but showed quite limited in vitro stability. The AcPhen-adducts herein presented might be beneficial for future studies addressing CN exposure in vivo.
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