首页> 外文期刊>Analytical and Bioanalytical Chemistry >Use of proton transfer reaction time-of-flight mass spectrometry for the analytical detection of illicit and controlled prescription drugs at room temperature via direct headspace sampling
【24h】

Use of proton transfer reaction time-of-flight mass spectrometry for the analytical detection of illicit and controlled prescription drugs at room temperature via direct headspace sampling

机译:使用质子转移反应飞行时间质谱通过直接顶空进样在室温下分析检测非法和受控处方药

获取原文
获取原文并翻译 | 示例
           

摘要

The first reported use of proton transfer reaction time-of-flight mass spectrometry (PTR-TOF-MS) for the detection of a range of illicit and prescribed drugs is presented here. We describe the capabilities of PTR-TOF-MS to detect the following commonly used narcotics—ecstasy (N-methyl-3,4-methylenedioxyamphetamine), morphine, codeine, cocaine and heroin—by the direct sampling of the headspace above small solid quantities (approximately 50 mg) of the drugs placed in glass vials at room temperature, i.e. with no heating of the sample and no pre-concentration. We demonstrate in this paper the ability to identify the drugs, both illicit and prescribed, using PTR-TOF-MS through the accurate m/z assignment of the protonated parent molecule to the second decimal place. We have also included in this study measurements with an impure sample of heroin, containing typical substances found in “street” heroin, to illustrate the use of the technology for more “real-world” samples. Therefore, in a real-world complex chemical environment, a high level of confidence can be placed on the detection of drugs. Although the protonated parent is observed for all drugs, the reactant channel leading to this species is not the only one observed and neither is it necessarily the most dominant. Details on the observed fragmentation behaviour are discussed and compared to electrospray ionisation MSn studies available in the literature.
机译:本文首次报道了质子转移反应飞行时间质谱(PTR-TOF-MS)用于检测一系列非法和处方药的用途。我们描述了PTR-TOF-MS通过以下方式直接检测顶空上的少量固体来检测以下常用的麻醉品的能力:摇头丸(N-甲基-3,4-亚甲基二氧基苯丙胺),吗啡,可待因,可卡因和海洛因(约50 mg)的药物在室温下放置在玻璃小瓶中,即不加热样品也不进行预浓缩。我们在本文中证明了通过PTR-TOF-MS通过质子化母体分子的精确m / z赋值到小数点后第二位来识别非法药物和处方药物的能力。在本研究中,我们还使用了不纯净的海洛因样品(其中包含“街头”海洛因中发现的典型物质)进行测量,以说明该技术在更多“真实世界”样品中的使用。因此,在现实世界中复杂的化学环境中,可以将高度的信心放在药物的检测上。尽管所有药物均观察到质子化的亲本,但导致该物种的反应物通道并不是唯一观察到的通道,也不一定是最主要的通道。对观察到的碎片行为的细节进行了讨论,并与文献中的电喷雾电离MS n 研究进行了比较。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号