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离子迁移谱法对复杂多组分非法药物样品进行定性分析的可靠性。

Reliability of ion mobility spectrometry for qualitative analysis of complex, multicomponent illicit drug samples.

机构信息

Surface and Microanalysis Division, National Institute of Standards and Technology, Gaithersburg, MD 20899, United States.

出版信息

Forensic Sci Int. 2011 Mar 20;206(1-3):190-6. doi: 10.1016/j.forsciint.2010.08.005. Epub 2010 Sep 15.

Abstract

Ion mobility spectrometry (IMS) has been used for trace analysis of illicit drugs, but it can also provide reliable qualitative analysis of bulk forensic drug items, despite the complexity of these samples. The drug/drug and drug/excipient combinations representing over 80% of the samples reported by state and federal forensic laboratories over the past 7 years were compiled from reports of the National Forensic Laboratory Information System (NFLIS). From this set of materials, IMS detection windows were set for eight controlled substances, including methamphetamine, 3,4-methylenedioxymethamphetamine hydrochloride (MDMA), cocaine, heroin, fentanyl, hydrocodone, oxycodone, and alprazolam. The reduced mobilities of the eight controlled substances were measured over an extended period of time to determine variability with respect to the size of the detection windows. Uncertainties in reduced mobilities smaller than 0.001 cm(2)V(-1)s(-1) were obtained, and detection windows were set to between ±0.003 and ±0.005 cm(2)V(-1)s(-1). Reduced mobilities are instrument and operating condition dependent, and must be determined for each instrument. Peak overlaps are observed in the drug/drug combinations, but at least one controlled substance can be detected in each mixture. Excipient concentrations must be quite high (>75 wt%) in binary mixtures to interfere with the detection of the controlled substance. IMS can be used to identify many of the excipients, and can detect multiple (for these samples, as many as 4) substances in complex samples. Over-the-counter (OTC) tablet medications for cold, flu, and allergy relief can be distinguished from tablets containing controlled substances. Bulk materials, including tablets, are sampled simply by using a fine probe to restrict the amount of material transferred to the IMS substrate. IMS represents a distinct advantage over color tests for field analysis of illicit drugs, except in the case of cannabis/THC samples.

摘要

离子迁移谱(IMS)已被用于痕量分析非法药物,但即使是这些复杂的样本,它也可以提供可靠的批量法医药物项目的定性分析。在过去 7 年中,州和联邦法医实验室报告的超过 80%的样本中,药物/药物和药物/赋形剂组合代表了超过 80%的样本,这些组合是从国家法医实验室信息系统(NFLIS)的报告中汇编而来的。从这组材料中,我们为八种管制药物设置了 IMS 检测窗口,包括甲基苯丙胺、3,4-亚甲二氧基甲基苯丙胺盐酸盐(MDMA)、可卡因、海洛因、芬太尼、氢可酮、羟考酮和阿普唑仑。在较长时间内测量了这八种管制药物的迁移率降低值,以确定其与检测窗口大小有关的变化。获得了迁移率降低值小于 0.001 cm2V-1s-1 的不确定度,并将检测窗口设置为 ±0.003 到 ±0.005 cm2V-1s-1。迁移率降低值取决于仪器和操作条件,必须针对每台仪器进行确定。在药物/药物组合中观察到峰重叠,但在每种混合物中至少可以检测到一种管制药物。赋形剂浓度必须非常高(>75wt%),才能在二元混合物中干扰管制药物的检测。IMS 可用于识别许多赋形剂,并可以在复杂的样品中检测到多种(对于这些样品,多达 4 种)物质。非处方(OTC)感冒药、流感药和过敏药可以与含有管制药物的片剂区分开来。可以通过使用细探针简单地对块状材料(包括片剂)进行取样,以限制转移到 IMS 基底上的材料量。IMS 与非法药物的现场分析的颜色测试相比具有明显的优势,除了大麻/THC 样本的情况。

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