探针电喷雾离子化串联质谱法用于检测和定量苯并二氮杂卓。

IF 2.8 4区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY
Therapeutic Drug Monitoring Pub Date : 2024-08-01 Epub Date: 2024-03-18 DOI:10.1097/FTD.0000000000001189
Pauline Griffeuille, Souleiman El Balkhi, Sylvain Dulaurent, Franck Saint-Marcoux
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引用次数: 0

摘要

背景:合法处方的苯并二氮杂卓(BZDs)和特制 BZDs 被广泛滥用,必须在多种情况下(如用药过量、借助药物的性侵犯或在药物影响下驾驶)进行测定。本研究旨在开发一种使用探针电喷雾离子化质谱和同位素稀释法测定血清中 BZD 水平的方法:方法:使用配备探针电喷雾离子源的串联质谱仪,采用多反应监测模式。对阿普唑仑、溴西泮、地西泮、诺地西泮、奥沙西泮、替马西泮、唑吡坦和佐匹克隆使用固定浓度的氚代内标进行同位素稀释定量。该方法包括设计的 BZDs:氯硝西泮、去氯乙唑仑、地氯西泮、依替唑仑、氟哌唑仑、氟溴西泮、氟溴唑仑、甲氯西泮、硝福西泮和吡唑仑。样品制备方法是将 10 µL 血清与 500 µL 0.01 mol/L 的乙醇/甲酸铵缓冲液混合。通过分析 40 份真实样本,对该方法进行了全面验证,并与液相色谱-质谱联用(LC-MS/MS)和免疫测定(IC)进行了比较:结果:鉴定和定量 18 种分子的分析时间为 2.5 分钟。该方法经过充分验证,根据分子的不同,定量限在 5 至 50 微克/升之间。在 40 份真实样品中,LC-MS/MS 和 PESI-MS/MS 均能检测到 100% 的分子(n = 89),回归分析表明这两种方法的一致性极佳(r2 = 0.98)。在 IC 中,分别有 2 例和 1 例未检出溴西泮和唑吡坦:结论:PESI-MS/MS 可以检测和测量血清中的 BZD。结论:PESI-MS/MS 可以检测和测量血清中的 BZD,由于采用了同位素稀释方法,因此无需校准曲线,其性能与 LC-MS/MS 相似,特异性高于 IC。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Probe Electrospray Ionization Tandem Mass Spectrometry for the Detection and Quantification of Benzodiazepines.

Background: Legally prescribed benzodiazepines (BZDs) and designer BZDs are widely misused and must be determined in multiple contexts (eg, overdose, drug-facilitated sexual assaults, or driving under the influence of drugs). This study aimed to develop a method for measuring serum BZD levels using probe electrospray ionization (PESI) mass spectrometry and an isotope dilution approach.

Methods: A tandem mass spectrometer equipped with a probe electrospray ionization source in multiple reaction monitoring mode was used. Isotope dilution was applied for quantification using a deuterated internal standard at a fixed concentration for alprazolam, bromazepam, diazepam, nordiazepam, oxazepam, temazepam, zolpidem, and zopiclone. This method included designer BZDs: clonazolam, deschloroetizolam, diclazepam, etizolam, flualprazolam, flubromazepam, flubromazolam, meclonazepam, nifoxipam, and pyrazolam. Sample preparation was done by mixing 10 µL of serum with 500 µL of an ethanol/ammonium formate 0.01 mol/L buffer. Complete validation was performed, and the method was compared with liquid chromatography coupled with mass spectrometry (LC-MS/MS) and immunoassays (IC) by analyzing 40 real samples.

Results: The analysis time for identification and quantification of the 18 molecules was 2.5 minutes. This method was fully validated, and the limits of quantification varied from 5 to 50 mcg/L depending on the molecule. In the 40 real samples, 100% of molecules (n = 89) were detected by both LC-MS/MS and PESI-MS/MS, and regression analysis showed excellent agreement between the 2 methods (r 2 = 0.98). On IC, bromazepam and zolpidem were not detected in 2 and 1 cases, respectively.

Conclusions: PESI-MS/MS allows serum BZD detection and measurement. Given the isotope dilution approach, a calibration curve was not required, and its performance was similar to that of LC-MS/MS, and its specificity was higher than that of IC.

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来源期刊
Therapeutic Drug Monitoring
Therapeutic Drug Monitoring 医学-毒理学
CiteScore
5.00
自引率
8.00%
发文量
213
审稿时长
4-8 weeks
期刊介绍: Therapeutic Drug Monitoring is a peer-reviewed, multidisciplinary journal directed to an audience of pharmacologists, clinical chemists, laboratorians, pharmacists, drug researchers and toxicologists. It fosters the exchange of knowledge among the various disciplines–clinical pharmacology, pathology, toxicology, analytical chemistry–that share a common interest in Therapeutic Drug Monitoring. The journal presents studies detailing the various factors that affect the rate and extent drugs are absorbed, metabolized, and excreted. Regular features include review articles on specific classes of drugs, original articles, case reports, technical notes, and continuing education articles.
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