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用于在尿液和口腔液中使用液相色谱-串联质谱法选择性测定Δ9-四氢大麻酚和11-去甲-Δ9-四氢大麻酚羧酸的分子印迹聚合物

Molecularly imprinted polymer for selective determination of Δ9-tetrahydrocannabinol and 11-nor-Δ9-tetrahydrocannabinol carboxylic acid using LC-MS/MS in urine and oral fluid.

作者信息

Lendoiro E, de Castro A, Fernández-Vega H, Cela-Pérez M C, López-Vilariño J M, González-Rodríguez M V, Cruz A, López-Rivadulla M

机构信息

Servicio de Toxicología, Instituto de Ciencias Forenses, Universidad de Santiago de Compostela, San Francisco s/n, 15782, Santiago de Compostela, Spain,

出版信息

Anal Bioanal Chem. 2014 Jun;406(15):3589-97. doi: 10.1007/s00216-013-7599-1. Epub 2014 Jan 16.

Abstract

The use of molecularly imprinted polymers (MIPs) for solid phase extraction (MISPE) allows a rapid and selective extraction compared with traditional methods. Determination of Δ(9)-tetrahydrocannabinol (THC) and 11-nor-Δ(9)-tetrahydrocannabinol carboxylic acid (THC-COOH) in oral fluid (OF) and urine was performed using homemade MISPEs for sample clean-up and liquid chromatography tandem mass spectrometry (LC-MS/MS). Cylindrical MISPE shaped pills were synthesized using catechin as a mimic template. MISPEs were added to 0.5 mL OF or urine sample and sonicated 30 min for adsorption of analytes. For desorption, the MISPE was transfered to a clean tube, and sonicated for 15 min with 2 mL acetone:acetonitrile (3:1, v/v). The elution solvent was evaporated and reconstituted in mobile phase. Chromatographic separation was performed using a SunFire C18 (2.5 μm; 2.1 × 20 mm) column, and formic acid 0.1% and acetonitrile as mobile phase, with a total run time of 5 min. The method was fully validated including selectivity (no endogenous or exogenous interferences), linearity (1-500 ng/mL in OF, and 2.5-500 ng/mL in urine), limit of detection (0.75 and 1 ng/mL in OF and urine, respectively), imprecision (%CV <12.3%), accuracy (98.2-107.0% of target), extraction recovery (15.9-53.5%), process efficiency (10.1-46.2%), and matrix effect (<-55%). Analytes were stable for 72 h in the autosampler. Dilution 1:10 was assured in OF, and Quantisal™ matrix effect showed ion suppression (<-80.4%). The method was applied to the analysis of 20 OF and 11 urine specimens. This is the first method for determination of THC and THC-COOH in OF using MISPE technology.

摘要

与传统方法相比,使用分子印迹聚合物(MIP)进行固相萃取(MISPE)能够实现快速且选择性的萃取。采用自制的MISPE进行样品净化,并结合液相色谱串联质谱法(LC-MS/MS)测定口腔液(OF)和尿液中的Δ⁹-四氢大麻酚(THC)及11-去甲-Δ⁹-四氢大麻酚羧酸(THC-COOH)。以儿茶素为模拟模板合成了圆柱形MISPE成型药丸。将MISPE加入0.5 mL的OF或尿液样品中,超声处理30分钟以吸附分析物。为进行解吸,将MISPE转移至干净的试管中,加入2 mL丙酮:乙腈(3:1,v/v)超声处理15分钟。将洗脱溶剂蒸发并重新溶解于流动相中。使用SunFire C18(2.5μm;2.1×20 mm)色谱柱进行色谱分离,流动相为0.1%甲酸和乙腈,总运行时间为5分钟。该方法经过全面验证,包括选择性(无内源性或外源性干扰)、线性(OF中为1 - 500 ng/mL,尿液中为2.5 - 500 ng/mL)、检测限(OF和尿液中分别为0.75和1 ng/mL)、不精密度(%CV <12.3%)、准确度(目标值的98.2 - 107.0%)、萃取回收率(15.9 - 53.5%)、过程效率(10.1 - 46.2%)以及基质效应(<-55%)。分析物在自动进样器中72小时内稳定。在OF中确保1:10稀释,并且Quantisal™基质效应显示离子抑制(<-80.4%)。该方法应用于20份OF和11份尿液标本的分析。这是首次使用MISPE技术测定OF中THC和THC-COOH的方法。

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