[脉冲直流电喷雾质谱法快速检测头发中的四种苯丙胺类药物]。

IF 1.2 4区 化学 Q4 CHEMISTRY, ANALYTICAL
Kun Mi, Wentian Zhang, Luhong Wen, Jin Wang
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引用次数: 0

摘要

苯丙胺类药物是具有苯丙胺母体结构的合成化合物。这类化合物会导致成瘾、中枢神经系统兴奋和幻觉。由于苯丙胺类药物可以用简单的人工方法合成,全球吸毒人数逐渐增加。由于毒品分析物数量大、种类多、检测时间长,目前的禁毒筛选和毒物鉴定方法受到限制。因此,开发广谱、快速、高通量的检测方法迫在眉睫。此外,传统的苯丙胺类毒品检测样本,如血液和尿液,只适用于短期毒品鉴定。毛发具有易保存、稳定性好、检测窗口期长等优点,可以弥补体液类检测材料的不足。毛发样本可以反映长期使用毒品的情况,有利于追查毒品来源,已成为法庭提供证据的重要手段。由于大多数实验室仪器无法对毛发中的苯丙胺类毒品进行现场快速检测,因此有必要建立一种高通量、定性和定量的现场快速检测方法。本研究采用脉冲直流电喷雾离子化(Pulsed-DC-ESI)结合质谱法对毛发中的四种苯丙胺类毒品(苯丙胺、甲基苯丙胺、3,4-亚甲二氧基苯丙胺和 3,4-亚甲二氧基甲基苯丙胺)进行了快速检测。提取溶剂为甲醇,提取方法为研磨法。前处理过程包括切割、研磨和离心。每个样品的预处理时间约为 10 分钟。多个样品可分批处理,大大提高了分析效率。脉冲-直流-ESI 是一种环境电离技术,可通过直接进样进行,无需色谱分离。喷射毛细管的顶端浸没在样品溶液表面下 1 厘米处,以便通过毛细管效应进行吸收。当喷射毛细管中含有 1 μL 样品溶液时,即可进行检测。脉冲直流ESI产生的电喷雾频率与质谱频率相同,从而避免了传统ESI中经常出现的样品浪费问题。用于分析的便携式质谱仪是线性离子阱质谱仪。根据苯丙胺类药物的质谱响应,优化了脉冲直流ESI的参数,如喷雾毛细管尖端内径、喷雾电压、电极与溶液之间的距离等。优化的离子源条件包括毛细管喷头内径为 25 μm,喷射电压为 2 kV,电极与溶液之间的距离为 20 mm。最佳样品溶剂为甲醇。苯丙胺、甲基苯丙胺和另外两种药物的线性范围分别为1-25、1-100和1-50 ng/mg。毛发中四种药物的检测和定量限分别为 0.1-0.2 和 1 纳克/毫克。线性相关系数均大于 0.99,平均加标回收率为 86.6%-114.7%。日内精确度为 4.14%-7.34%,日间精确度为 3.71%-8.43%。使用所建议的方法对不同检测机构提供的 2000 个样本进行了筛查。共有 5 个样本对甲基苯丙胺呈阳性反应,这与传统法医鉴定方法的结果一致。因此,所开发的方法可用于快速检测苯丙胺类毒品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Rapid detection of four amphetamine-type drugs in hair by pulsed direct current electrospray mass spectrometry].

Amphetamine-type drugs are synthetic compounds with an amphetamine parent structure. These compounds cause addiction, central nervous system excitation, and hallucinations. The number of drug users worldwide has gradually increased because amphetamine-type drugs can be synthesized in a simple and artificial manner. The current methods for anti-drug screening and toxicant identification are limited by the large quantity and variety of the drug analytes and long detection times. Thus, the development of broad-spectrum, rapid, and high-throughput detection methods is an urgent necessity. In addition, conventional amphetamine-type drug test samples, such as blood and urine, are only suitable for short-term drug identification. Hair has the advantages of easy preservation, stability, and a long detection window, which can compensate for the deficiencies of body-fluid-based test materials. Hair samples can reflect long-term drug use, which is beneficial for tracing drug sources, and has become an important means of providing evidence in court. Because most laboratory instruments are unable to perform the rapid on-site detection of amphetamine-type drugs in hair, establishing a high-throughput, qualitative and quantitative rapid on-site detection method is necessary. In this study, pulsed direct current electrospray ionization (Pulsed-DC-ESI) coupled with mass spectrometry was used for the rapid detection of four amphetamine-type drugs (amphetamine, methamphetamine, 3,4-methylenedioxyamphetamine, and 3,4-methylenedioxymethamphetamine) in hair. Methanol was used as the extraction solvent, and the grinding method was used for extraction. The pretreatment process included cutting, grinding, and centrifugation. The pretreatment time for each sample was about 10 min. Multiple samples could be processed in batches, greatly improving the efficiency of analysis. Pulsed-DC-ESI is an ambient ionization technology that can be conducted via direct injection without chromatographic separation. The tip of the spray capillary tube was immersed 1 cm below the surface of the sample solution to allow absorption via the capillary effect. When the spray capillary tube contained 1 μL of the sample solution, detection was performed. Pulsed-DC-ESI generates an electrospray at the same frequency as the mass spectrum, thereby avoiding the problem of sample wastage, which often occurs in traditional ESI. The portable mass spectrometer used for analysis is a linear ion trap mass spectrometer. The parameters of Pulsed-DC-ESI, such as the inner diameter of spray capillary tip, spray voltage, and distance between electrode and solution, were optimized based on the mass spectral responses of the amphetamine-type drugs. The optimized ion source conditions included a inner diameter of spray capillary tip of 25 μm, spray voltage of 2 kV, and the distance between electrode and solution of 20 mm. The optimal sample solvent was methanol. The optimized method can achieve simultaneous detection of the four amphetamine-type drugs within 20 s. The linear ranges of amphetamine, methamphetamine, and the two other drugs were 1-25, 1-100, and 1-50 ng/mg, respectively. The limits of detection and quantification of the four drugs in hair were 0.1-0.2 and 1 ng/mg, respectively. All linear correlation coefficients were greater than 0.99, and the average spiked recoveries were 86.6%-114.7%. The intra-day precisions were 4.14%-7.34%, and the inter-day precisions were 3.71%-8.43%. The proposed method was used to screen 2000 samples provided by various testing institutions. A total of five samples were positive for methamphetamine, which is consistent with the results of conventional forensic identification methods. Thus, the developed method can be used for the rapid detection of amphetamine-type drugs.

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来源期刊
色谱
色谱 CHEMISTRY, ANALYTICAL-
CiteScore
1.30
自引率
42.90%
发文量
7198
期刊介绍: "Chinese Journal of Chromatography" mainly reports the basic research results of chromatography, important application results of chromatography and its interdisciplinary subjects and their progress, including the application of new methods, new technologies, and new instruments in various fields, the research and development of chromatography instruments and components, instrument analysis teaching research, etc. It is suitable for researchers engaged in chromatography basic and application technology research in scientific research institutes, master and doctoral students in chromatography and related disciplines, grassroots researchers in the field of analysis and testing, and relevant personnel in chromatography instrument development and operation units. The journal has columns such as special planning, focus, perspective, research express, research paper, monograph and review, micro review, technology and application, and teaching research.
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