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评估芬太尼暴露对丁酰胆碱酯酶活性的影响,作为未来现场检测方法的一种手段。

Evaluation of Fentanyl Exposure Effects on Butyrylcholinesterase Activity as a Tool for Future On-Site Detection Methods.

作者信息

Rania Vrunda, Newland Ashley, Halámková Lenka, Trojan Václav, Hřib Radovan, Halámek Jan

机构信息

Department of Environmental Toxicology, The Institute for Forensic Science, Texas Tech University, 1207 Gilbert Drive, Lubbock, Texas 79416, United States.

Cannabis Facility, International Clinical Research Centre, St. Anne's University Hospital, Brno 60200, Czech Republic.

出版信息

ACS Omega. 2024 Sep 14;9(38):40234-40241. doi: 10.1021/acsomega.4c06655. eCollection 2024 Sep 24.

Abstract

The prominence of fentanyl and fentanyl analogues or Fentanyl Related Substances (FRS) has driven a nationwide crisis of opioid overdoses, which significantly presents an issue for public health and safety. Originally developed for medical purposes, fentanyl and FRS have become critical contributors to opioid overdose deaths due to their distribution, availability, and potency. This study examined toxicodynamic properties between butyrylcholinesterase (BChE) and fentanyl analogues via Ellman's assay. The enzymatic function of BChE was significantly inhibited by each of the 5 fentanyl analogues tested, which indicates the potential for utilization of this interaction. This reaction can be immobilized for a portable, single-use kit to detect FRS directly from any surface on-site. This would immensely benefit society by reducing the frequency of exposure and overdoses by providing additional safety measures to law enforcement and first responders.

摘要

芬太尼及其类似物或芬太尼相关物质(FRS)的突出问题引发了一场全国范围的阿片类药物过量危机,这对公众健康和安全构成了重大问题。芬太尼和FRS最初是为医疗目的而开发的,但由于其流通、可得性和效力,已成为阿片类药物过量死亡的关键因素。本研究通过埃尔曼测定法研究了丁酰胆碱酯酶(BChE)与芬太尼类似物之间的毒理学特性。所测试的5种芬太尼类似物均显著抑制了BChE的酶功能,这表明利用这种相互作用的可能性。这种反应可以固定在一个便携式一次性试剂盒中,直接在现场从任何表面检测FRS。通过为执法人员和急救人员提供额外的安全措施,减少接触和过量用药的频率,这将极大地造福社会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a264/11425806/6dc132cb867f/ao4c06655_0001.jpg

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