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Quantisal口腔液采集装置对药物稳定性的影响。

Impact of Quantisal Oral Fluid Collection Device on Drug Stability.

作者信息

Riggio Michela, Dave Keyur A, Koscak Branko, Blakey Mark, Appleton Charles

机构信息

Central Laboratories, Toxicology, Biochemistry Queensland Medical Laboratory (QML) Pathology, Brisbane, QLD, Australia.

出版信息

Front Toxicol. 2021 Jul 5;3:670656. doi: 10.3389/ftox.2021.670656. eCollection 2021.

DOI:10.3389/ftox.2021.670656
PMID:35295159
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8915805/
Abstract

The stability of drugs can affect drug tests and interpretations. A comprehensive study to verify drug stability in Quantisal oral fluid (OF) collection device was undertaken in accordance with Australian standard, AS/NZS 4760:2019 (SAI-Global, 2019). The evaluation was performed for the following drugs: (±) amphetamine, (±) methylamphetamine, (±) 3,4-methylenedioxymethylamphetamine (MDMA), (-)Δ9-tetrahydrocannabinol (THC), cocaine, benzoylecgonine, morphine, codeine, and oxycodone. Stability was assessed at four different storage temperatures over seven time points at ±50% cut-off concentrations (Appendix A, Para A4-4.1, AS/NZS 4760:2019) (SAI-Global, 2019). All drugs were found to be significantly more stable at 4 and -20°C, with stability spanning at least 14 days with percentage change within ±20% from the cut-off concentrations (SAI-Global, 2019). In addition, we report a variation trend with cocaine and benzoylecgonine at elevated temperatures, suggesting hydrolytic decomposition of cocaine and a concomitant increase in benzoylecgonine quantitative values. We confirm the cross-talk by showing that the percentage change in the profile of average cocaine-benzoylecgonine measurement is within the acceptance concentration range of ±20%. This finding highlights the importance of precaution during storage and careful considerations during subsequent interpretation of liquid chromatography-mass spectrometry (LCMS) measurements.

摘要

药物的稳定性会影响药物检测及结果解读。依据澳大利亚标准AS/NZS 4760:2019(SAI - Global,2019),开展了一项全面研究以验证Quantisal口腔液(OF)采集装置中药物的稳定性。对以下药物进行了评估:(±)苯丙胺、(±)甲基苯丙胺、(±)3,4 - 亚甲基二氧甲基苯丙胺(摇头丸)、(-)Δ9 - 四氢大麻酚(THC)、可卡因、苯甲酰爱康宁、吗啡、可待因和羟考酮。在四个不同储存温度下的七个时间点,以±50%的截断浓度评估稳定性(附录A,第A4 - 4.1段,AS/NZS 4760:2019)(SAI - Global,2019)。发现所有药物在4℃和 - 20℃时稳定性显著更高,稳定性至少持续14天,与截断浓度相比变化百分比在±20%以内(SAI - Global,2019)。此外,我们报告了可卡因和苯甲酰爱康宁在高温下的变化趋势,表明可卡因发生水解分解,同时苯甲酰爱康宁定量值增加。我们通过显示平均可卡因 - 苯甲酰爱康宁测量曲线的变化百分比在±20%的可接受浓度范围内来证实这种相互影响。这一发现凸显了储存期间采取预防措施以及在随后液相色谱 - 质谱(LCMS)测量结果解读时仔细考虑的重要性。

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本文引用的文献

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J Anal Toxicol. 2020 Oct 12;44(7):697-707. doi: 10.1093/jat/bkaa089.
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Detection of Drugs in Oral Fluid Samples Using a Commercially Available Collection Device: Agreement with Urine Testing and Evaluation of A and B Samples Obtained from Employees at Different Workplace Settings with Uncontrolled Sampling Procedures.使用市售采集装置检测口腔液样本中的药物:与尿液检测的一致性,以及在无控制采样程序的不同工作场所环境下从员工处获得的 A 和 B 样本的评估。
J Anal Toxicol. 2021 Jan 21;44(9):1004-1011. doi: 10.1093/jat/bkaa024.
3
Stability and Degradation Pathways of Different Psychoactive Drugs in Neat and in Buffered Oral Fluid.
不同精神活性药物在未缓冲和缓冲口腔液中的稳定性和降解途径。
J Anal Toxicol. 2020 Jul 31;44(6):570-579. doi: 10.1093/jat/bkz114.
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Monitoring of the stability of cocaine and some metabolites in water and oral fluid by a newly developed CE method.通过一种新开发的毛细管电泳方法监测水中和口腔液中可卡因及某些代谢物的稳定性。
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Stability of cocaine and its metabolites in municipal wastewater--the case for using metabolite consolidation to monitor cocaine utilization.城市废水中可卡因及其代谢物的稳定性——利用代谢物综合监测可卡因使用情况的案例。
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