法医学杂志 ›› 2020, Vol. 36 ›› Issue (1): 45-51.DOI: 10.12116/j.issn.1004-5619.2020.01.010

• 论著 • 上一篇    下一篇

LC-MS/MS快速测定血液中13种安眠镇静类药物及其代谢产物

石银涛1, 王绘军1, 王俊伟1, 郑经1, 吴玉红2,3   

  1. 1. 重庆市公安局物证鉴定中心,重庆 400021; 2. 重庆警察学院,重庆 401331; 3. 重庆市毒物毒品分析重点实验室,重庆 401331
  • 发布日期:2020-02-25 出版日期:2020-02-28
  • 通讯作者: 王俊伟,男,主任法医师,主要从事法医毒理学和法医毒物分析;E-mail:wjwry@tom.com
  • 作者简介:石银涛(1980—),男,硕士,高级工程师,主要从事法医毒物分析;E-mail:275368290@qq.com
  • 基金资助:
    公安部技术研究计划资助项目(2016JSYJB11);重庆市公安局科技攻关计划资助项目(G2016-01,G2016-04)

Rapid Determination of 13 Sedative Substances and Their Metabolites in Blood by LC-MS/MS

SHI Yin-tao1, WANG Hui-jun1, WANG Jun-wei1, ZHENG Jing1, WU Yu-hong2,3   

  1. 1. Institute of Forensic Science, Chongqing Public Security Bureau, Chongqing 400021, China; 2. Chongqing Police College, Chongqing 401331, China; 3. Chongqing Key Laboratory of Toxicant and Drug Analysis, Chongqing 401331, China
  • Online:2020-02-25 Published:2020-02-28

摘要: 目的 采用液液提取与液相色谱-串联质谱(liquid chromatography-tandem mass spectrometry,LC-MS/MS)技术,建立同时测定血液中13种安眠镇静类药物及其代谢产物的分析方法,并将其应用于实际案例。 方法 血液加入内标后,用乙酸乙酯提取,浓缩至近干后,用甲醇溶解残渣,过0.22 μm滤膜后测定。13种安眠镇静类药物及其代谢物经C18色谱柱分离,以甲醇和20 mmol/L甲酸铵(含0.1%甲酸)水溶液进行梯度洗脱,电喷雾正离子模式检测,内标法定量。 结果 血液中13种安眠镇静类药物及其代谢物在5~200 μg/L范围内具有良好的线性关系,相关系数为0.990 3~0.999 8,检出限为0.1~1.0 μg/L;在10、50、200 μg/L 3个添加浓度水平的回收率为71.2%~93.4%,日内和日间精密度≤8.6%,准确度(偏倚)在±9.8%范围内。 结论 本方法快速、简单、高效、灵敏度高,可用于法医毒物学领域血液中13种安眠镇静类药物及其代谢产物的分析。

关键词: 法医毒理学;催眠药和镇静药;色谱法, 液相;质谱分析法;液液萃取;血液

Abstract: Objective To establish an analysis method for simultaneous determination of 13 sedative substances and their metabolites in blood by liquid-liquid extraction and liquid chromatography-tandem mass spectrometry (LC-MS/MS) technology and to apply the method to actual cases. Methods The samples were extracted with ethyl acetate after an internal standard was added. The extract was condensed until it was nearly dry and then its residues were dissolved with methanol, filtered through 0.22 μm filter and finally determined. The 13 sedative substances and their metabolites were separated through the C18 chromatographic column, then gradient elution was performed on them with methanol and 20 mmol/L ammonium formate (containing 0.1% formic acid) solution. After that, they were determined in the electrospray positive ion mode and quantified by internal standard method. Results The 13 sedative substances and their metabolites in blood showed good linearity in the range of 5-200 μg/L with correlation coefficients ranging from 0.990 3 to 0.999 8. The detection limits were 0.1-1.0 μg/L. Recovery rates of sedative substances were in the range of 71.2%-93.4% when solutions with concentrations of 10, 50 and 200 μg/L were added. The deviations of intra-day and inter-day relative standard deviations (RSD) were not more than 8.6%. Accuracies (bias) were within ±9.8%. Conclusion This method is rapid, simple, effective and sensitive, and can be applied to analysis of 13 sedative substances and their metabolites in blood in forensic toxicology.

Key words: forensic toxicology, hypnotics and sedative, chromatography, liquid, mass spectrometry, liquid-liquid extraction, blood