γ-羟基丁酸摄入后全血4-棕榈酰氧基丁酸作为潜在生物标志物的初步评价。

IF 2.3 3区 医学 Q3 CHEMISTRY, ANALYTICAL Journal of analytical toxicology Pub Date : 2024-12-10 DOI:10.1093/jat/bkae095
Jennifer Liut, Burkhard Madea, Dirk Meißner, Arne Lützen, Sirous Javidi, Cornelius Hess, Michael Krämer
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引用次数: 0

摘要

寻找合适的生物标志物来扩大γ-羟基丁酸(GHB)摄入的检测窗口是法医毒理学研究的一个挑战。基于先前发表的结果,本研究涉及全血中GHB脂肪酸酯(4-棕榈酰氧基丁酸酯(GHB- pal))作为潜在生物标志物的评估,以延长GHB使用的检测窗口,例如在药物性侵犯(DFSA)中。建立了全血中GHB-Pal的液相色谱-质谱(LC-MS/MS)定量方法。采集了警察路边对照(113例)和控制给药Xyrem®(氧化钠)后的发作性睡病患者(10例)的全血样本。这两组样品先前使用两种不同的方法进行了GHB检测:超高效液相色谱-串联质谱法(UPLC-MS/MS)和气相色谱-质谱法(GC-MS)。在常规警察案件样本中,在分析的113个ghb阳性样本中,有67个样本检测到GHB-Pal,平均浓度为0.8 ng/mL±0.5 ng/mL(标准差)。在两种化合物检测呈阳性的样品中,GHB和GHB- pal浓度之间没有线性相关性(r=0.508)。相比之下,在分析的患者血液样本中未检测到GHB-Pal。患者队列中GHB和GHB- pal的缺失可能归因于剂量摄入和采血之间的时间间隔(约为10分钟)。3和6 h),在此期间GHB从体内排出。此外,GHB- pal仅在GHB浓度至少为16 μ g/mL时才可检测到,这表明内源性浓度或低剂量的GHB- pal可能不足以形成。由于这两种化合物之间缺乏相关性,并且GHB- pal在给药后几小时内没有检测到,因此可以认为血液中的GHB- pal不是一个合适的生物标志物来扩大GHB的检测窗口。
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Initial evaluation of 4-palmitoyloxy butyrate in whole blood as potential biomarker after γ-hydroxybutyric acid intake.

The problem of finding a suitable biomarker to widen the detection window of γ-hydroxybutyric acid (GHB) intake remains a challenge in forensic toxicology. Based on previously published results, the present study deals with the evaluation of a fatty acid ester of GHB (4-palmitoyloxy butyrate (GHB-Pal)) in whole blood as a potential biomarker to extend the detection window of GHB use e.g. in drug-facilitated sexual assaults (DFSA). A liquid chromatography-mass spectrometry (LC-MS/MS) method for the quantification of GHB-Pal in whole blood was validated. Whole blood samples were collected from subjects involed in police roadside controls (n=113) and from narcolepsy patients (n=10) after the controlled administration of Xyrem® (sodium oxybate). Both sample collectives were previously tested for GHB using two different methods: ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) and gas chromatography-mass spectrometry (GC-MS). In samples from routine police casework, GHB-Pal was detected in 67 out of 113 analysed GHB-positive samples with a mean concentration of 0.8 ng/mL ± 0.5 ng/mL (standard deviation). Among samples that were tested positive for both compounds, no linear correlation was observed between GHB and GHB-Pal concentrations (r=0.508). In contrast, GHB-Pal was not detected in any of the blood samples analysed from the patients. The absence of GHB and GHB-Pal in the patient cohort may be attributed to the time interval between dose intake and blood collection (approx. 3 and 6 h), during which GHB was eliminated from the body. Furthermore, GHB-Pal was only detectable at a GHB concentration of at least 16 µg/mL, which indicates that endogenous concentrations or low GHB doses may not be sufficient for GHB-Pal formation. Due to missing correlation between both compounds and the lack of GHB-Pal detection several hours after GHB administration, it can be assumed that GHB-Pal in blood is not a suitable biomarker to widen the detection window of GHB.

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来源期刊
CiteScore
5.10
自引率
20.00%
发文量
92
审稿时长
6-12 weeks
期刊介绍: The Journal of Analytical Toxicology (JAT) is an international toxicology journal devoted to the timely dissemination of scientific communications concerning potentially toxic substances and drug identification, isolation, and quantitation. Since its inception in 1977, the Journal of Analytical Toxicology has striven to present state-of-the-art techniques used in toxicology labs. The peer-review process provided by the distinguished members of the Editorial Advisory Board ensures the high-quality and integrity of articles published in the Journal of Analytical Toxicology. Timely presentation of the latest toxicology developments is ensured through Technical Notes, Case Reports, and Letters to the Editor.
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