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使用不同采样设备对干血斑中磷脂酰乙醇进行实验室间比对

Interlaboratory comparison of phosphatidylethanol in dried blood spots using different sampling devices.

作者信息

Bantle Matthias, Stöth Frederike, Weinmann Wolfgang, Luginbühl Marc

机构信息

Institute of Forensic Medicine, Forensic Toxicology and Chemistry, University of Bern, Bern, Switzerland.

Department of Chemistry, Biochemistry and Pharmaceutical Sciences, University of Bern, Bern, Switzerland.

出版信息

Drug Test Anal. 2025 Jun;17(6):834-841. doi: 10.1002/dta.3784. Epub 2024 Aug 16.

Abstract

Phosphatidylethanol (PEth) has become an important marker to assess drinking behaviour and monitor abstinence. Despite its increasing use, knowledge on robustness and standardization and comparability of methods and results are still limited. In 2022, the first international consensus for the use of PEth and its interpretation was published. To establish an experience-based foundation for further harmonization, three rounds of interlaboratory comparison using microsamples were conducted. Participating laboratories sent their sampling devices to the laboratory of Forensic Toxicology at the University of Bern, where for each round, four different authentic blood samples were applied to the devices and sent back. The PEth 16:0/18:1 target concentrations covered a range between 16 and 474 ng/mL (0.023 and 0.676 μmol/L, respectively) and included sample concentrations close to the decision limits of 20 and 200 ng/mL (0.025 and 0.28 μmol/L, respectively). Evaluation of the results based on guidelines by Horwitz and the Society of Toxicological and Forensic Chemistry (GTFCh) showed that 73% of all participating laboratories quantified and reported all samples (N = 4 for each round) within the acceptable limits. More than 90% quantified and reported at least one sample within the acceptable limits.

摘要

磷脂酰乙醇(PEth)已成为评估饮酒行为和监测戒酒情况的重要标志物。尽管其使用越来越广泛,但关于方法和结果的稳健性、标准化及可比性的知识仍然有限。2022年,关于PEth使用及其解读的首个国际共识发表。为建立基于经验的进一步协调基础,进行了三轮使用微量样本的实验室间比对。参与实验室将其采样设备送至伯尔尼大学法医毒理学实验室,在每一轮中,将四种不同的真实血液样本应用于这些设备并送回。PEth 16:0/18:1的目标浓度范围在16至474 ng/mL之间(分别为0.023和0.676 μmol/L),并包括接近20和200 ng/mL(分别为0.025和0.28 μmol/L)决策限的样本浓度。根据霍维茨准则以及毒理学和法医化学协会(GTFCh)的指南对结果进行评估,结果显示,所有参与实验室中有73%在可接受限度内对所有样本(每轮N = 4)进行了定量和报告。超过90%的实验室在可接受限度内对至少一个样本进行了定量和报告。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7988/12151716/9bcd00b60d39/DTA-17-834-g002.jpg

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