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采用气相色谱-串联质谱法和液相色谱-串联质谱法测定毛发样本中的九种芬太尼类药物。

Determination of Nine Fentanyl Drugs in Hair Samples by GC-MS/MS and LC-MS/MS.

作者信息

Wei Qi, Su Fu Hai

机构信息

Key Laboratory of Chemical Metrology and Applications on Nutrition and Health for State Market Regulation, National Institute of Metrology, No.18 Beisanhuan Donglu, Chaoyang District, Beijing 100013, PR China.

出版信息

ACS Omega. 2022 May 31;7(23):19176-19182. doi: 10.1021/acsomega.2c00087. eCollection 2022 Jun 14.

Abstract

We established GC-MS/MS and LC-MS/MS analysis methods for nine fentanyl drugs in hair samples. Human hairs were prepared by soaking in a solution of water-dimethyl sulfoxide with target analytes. The drugs were norfentanyl, acetyl fentanyl, -fluorofentanyl, isobutyryl fentanyl, fentanyl, thiofentanyl, 4-fluoroisobutyr fentanyl, ocfentanil, and tetrahydrofuran fentanyl. For a single-factor experiment, a Box-Behnken design-response surface was used to optimize the pretreatment conditions of samples. The prepared samples were quantitatively analyzed by GC-MS/MS and LC-MS/MS. The working curve method was used for quantitative analysis with fentanyl-D5 as the internal standard. The concentrations of the nine fentanyl drugs in the samples were 1.488-6.494 ng mg, RSDs < 5.0%. For GC-MS/MS, the linear range of the nine fentanyl drugs was 0.5-5.0 ng mg, > 0.999. The detection limits were 0.02-0.05 ng mg, and the recovery rates were >86%. For LC-MS/MS, the nine fentanyl drugs had an excellent linear relationship within the concentration range of 3.0-220.0 pg mg, > 0.999. The detection limits were 0.05 pg mg and the recovery rates were >84%. The established methods were used for the detection of fentanyl drugs in human hairs, with high sensitivity, accuracy, and specificity. These two methods can be used for the certification of fentanyl certified reference substances (CRMs). In the experiment, the developed hair CRMs, which will continue to be studied in the future, are expected to be used in forensic drug abuse detection.

摘要

我们建立了毛发样本中9种芬太尼类药物的气相色谱-串联质谱(GC-MS/MS)和液相色谱-串联质谱(LC-MS/MS)分析方法。人发样本通过浸泡在含有目标分析物的水-二甲基亚砜溶液中进行制备。这些药物分别是去甲芬太尼、乙酰芬太尼、α-氟芬太尼、异丁酰芬太尼、芬太尼、硫代芬太尼、4-氟异丁酰芬太尼、奥芬太尼和四氢呋喃芬太尼。对于单因素实验,采用Box-Behnken设计-响应面法优化样本的预处理条件。制备好的样本通过GC-MS/MS和LC-MS/MS进行定量分析。采用工作曲线法,以芬太尼-D5作为内标进行定量分析。样本中9种芬太尼类药物的浓度为1.488 - 6.494 ng/mg,相对标准偏差(RSDs)<5.0%。对于GC-MS/MS,9种芬太尼类药物的线性范围为0.5 - 5.0 ng/mg,相关系数(r)>0.999。检测限为0.02 - 0.05 ng/mg,回收率>86%。对于LC-MS/MS,9种芬太尼类药物在3.0 - 220.0 pg/mg的浓度范围内具有良好的线性关系,r>0.999。检测限为0.05 pg/mg,回收率>84%。所建立的方法用于人发中芬太尼类药物的检测,具有高灵敏度、准确性和特异性。这两种方法可用于芬太尼标准物质(CRMs)的认证。在实验中,所开发的毛发标准物质未来将继续研究,有望用于法医药物滥用检测。

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