色谱 ›› 2022, Vol. 40 ›› Issue (7): 677-683.DOI: 10.3724/SP.J.1123.2022.01013

• 技术与应用 • 上一篇    

基于敞开式直接电离质谱技术的尿液中毒品检测

熊士领1, 洪欢欢1,2, 闻路红1,2, 胡舜迪1,2, 陈安琪1,2, 熊伟1,2, 陈腊1,2,*()   

  1. 1.宁波大学高等技术研究院, 浙江 宁波 315211
    2.宁波华仪宁创智能科技有限公司, 浙江 宁波 315100
  • 收稿日期:2022-02-04 出版日期:2022-07-08 发布日期:2022-07-06
  • 通讯作者: 陈腊
  • 基金资助:
    广东番禺区创新团队项目(2017-R01-5);宁波市2025重大专项(2020Z010);浙江省毒品防控技术研究重点实验室项目(2019003);云南省重点实验室项目(2020SKF03)

Detection of drugs in urine by ambient direct ionization mass spectrometry

XIONG Shiling1, HONG Huanhuan1,2, WEN Luhong1,2, HU Shundi1,2, CHEN Anqi1,2, XIONG Wei1,2, CHEN La1,2,*()   

  1. 1. Research Institute of Advanced Technologies, Ningbo University, Ningbo 315211, China
    2. China Innovation Instrument Co., Ltd., Ningbo 315100, China
  • Received:2022-02-04 Online:2022-07-08 Published:2022-07-06
  • Contact: CHEN La
  • Supported by:
    Innovative Team of Panyu District in Guangdong Province(2017-R01-5);Ningbo 2025 Major Special Project(2020Z010);Key Laboratory of Drug Prevention and Control Technology of Zhejiang Province(2019003);Key Laboratory in Yunnan Province(2020SKF03)

摘要:

尿液作为一种易于获取的体内毒品检材,在吸毒人员快速筛查中被广泛应用。针对传统快速筛查技术存在假阳性率高、定量能力不足以及实验室质谱技术在快速检测中存在前处理复杂、检测耗时长、使用环境苛刻等问题,该文提出了一种基于敞开式直接电离质谱技术的生物样本快速检测方法。该研究采用探针式电喷雾离子源与便携式质谱仪联用快速检测平台,优化了喷雾电压和质谱入口毛细管温度,开发了高效快速的前处理技术。基于该平台和前处理技术,5种常规毒品(甲基苯丙胺、氯胺酮、可卡因、O6-单乙酰吗啡和3,4-亚甲双氧甲基苯丙胺)的尿液加标溶液的检出限为0.5~30 ng/mL,且其中4种毒品定量检测的线性相关系数大于0.99。除此之外,5种常规毒品在3个不同水平下的加标回收率为56.1%~103.7%,多次检测结果的相对标准偏差为9.0%~27.8%,说明联用检测平台与前处理方法结合可以达到良好的准确度。为了进一步检验该联用仪器的实战能力,测试了某社区戒毒康复中心40份阳性和110份阴性实际尿液样本,总体检测的准确率接近99%,且通过一次进样在20 s内可同时检测多种毒品。该研究成果有利于推动快速检测技术的发展,促进敞开式直接电离质谱仪技术的推广应用,提升一线执法服务水平。

关键词: 敞开式直接电离, 便携式质谱仪, 毒品, 尿液, 快速检测

Abstract:

According to the Report of Drug Situation in China (2020), the growth rate of the number of drug abusers in China has decreased, but the number of drug abusers is still large. An efficient screening method is necessary for controlling drug abuse. As an important type of biological sample, urine is widely used for the rapid screening of drug addicts. However, because of the complex composition, low content, and strong interference from the body’s metabolism, the detection of drugs in urine remains a challenge. Traditional rapid screening techniques such as immunocolloidal gold analysis have a high false positive rate and insufficient quantitative capability. In addition, laboratory mass spectrometry methods require complicated time-consuming sample pre-processing and strict environmental conditions, and hence, are unsuitable for on-site rapid analysis. In recent years, various direct ionization mass spectrometry techniques such as direct analysis in real time (DART), desorption electrospray ionization (DESI), and dielectric barrier discharge ionization (DBDI) have advanced rapidly. These techniques have been applied to public safety, food safety, environmental detection, etc. In contrast to traditional ionization mass spectrometry methods, these direct ionization techniques allow for the in situ analysis of samples with simple or no pretreatment; moreover, they have the advantages of high analytical efficiency and sensitivity. In particular, pulsed electrospray ionization has the characteristics of less sample demand, compact, lightweight equipment, and no carrier gas. This paper presents a rapid method based on pulsed electrospray ionization mass spectrometry for the detection of urine samples. A rapid detection platform comprising a probe electrospray ionization source, a portable linear ion trap mass spectrometer (MS), and their coupling interface is adopted. The probe electrospray ion source includes a conducting metal wire, plastic handle, and silica glass capillary, whose tip has an inner diameter of 50 μm. The guide rail at the coupling interface is used to align the probe with the sample inlet of the portable mass spectrometer and maintain a distance of 10 mm between the probe tip and the sample inlet of the MS. The spray voltage of the probe electrospray ion source and the temperature of the MS inlet capillary are optimized at 1.8 kV and 205 ℃, respectively. In addition, rapid and efficient pretreatment techniques for urine samples have been developed. Buffer salts used for pH regulation and liquid-liquid extraction based on ethyl acetate were adopted for the pretreatment process. The linearity of the detection ability and the linear ranges of various drug-spiked solutions were also investigated. The results showed that the correlation coefficients for the quantitative detection of methamphetamine, ketamine, methylenedioxymethamphetamine (MDMA), and cocaine were greater than 0.99 at concentrations ranging from 1 to 100 ng/mL. Moreover, the limits of detection (LODs) for the five conventional drug-spiked urine were 0.5-30 ng/mL. The spiked recoveries ranged from 56.1% to 103.7%, with relative standard deviations (RSDs) of 9.0%-27.8%, implying that the combination of the instruments and the pretreatment method can lead to good accuracy. To validate the performance of the rapid detection method, 40 positive and 110 negative urine samples were tested and analyzed. The overall accuracy was over 99%, and the five conventional drugs in urine samples could be detected within 20 s. The research findings of this work could promote the development of rapid detection technology, accelerate the popularization and application of ambient direct ionization mass spectrometry, and improve the services of on-site law enforcement.

Key words: ambient direct ionization, portable mass spectrometer, drug, urine, rapid detection

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