首页> 美国卫生研究院文献>other >Simultaneous quantification of Δ9-tetrahydrocannabinol 11-hydroxy-Δ9-tetrahydrocannabinol and 11-nor-Δ9-tetrahydrocannabinol-9-carboxylic acid in human plasma using two-dimensional gas chromatography cryofocusing and electron impact-mass spectrometry
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Simultaneous quantification of Δ9-tetrahydrocannabinol 11-hydroxy-Δ9-tetrahydrocannabinol and 11-nor-Δ9-tetrahydrocannabinol-9-carboxylic acid in human plasma using two-dimensional gas chromatography cryofocusing and electron impact-mass spectrometry

机译:使用二维气相色谱低温聚焦和电子冲击质谱法同时定量测定人血浆中的Δ9-四氢大麻酚11-羟基-Δ9-四氢大麻酚和11-去-Δ9-四氢大麻酚-9-羧酸

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摘要

A two-dimensional (2D) gas chromatography/electron impact-mass spectrometry (GC/EI-MS) method for simultaneous quantification of Δ9-tetrahydrocannabinol (THC), 11-hydroxy-Δ9-tetrahydrocannabinol (11-OH-THC), and 11-nor-Δ9-tetrahydrocannabinol-9-carboxylic acid (THCCOOH) in human plasma was developed and validated. The method employs 2D capillary GC and cryofocusing for enhanced resolution and sensitivity. THC, 11-OH-THC, and THCCOOH were extracted by precipitation with acetonitrile followed by solid-phase extraction. GC separation of trimethylsilyl derivatives of analytes was accomplished with two capillary columns in series coupled via a pneumatic Deans switch system. Detection and quantification were accomplished with a bench-top single quadrupole mass spectrometer operated in electron impact-selected ion monitoring mode. Limits of quantification (LOQ) were 0.125, 0.25 and 0.125 ng/mL for THC, 11-OH-THC, and THCCOOH, respectively. Accuracy ranged from 86.0 to 113.0% for all analytes. Intra- and inter-assay precision, as percent relative standard deviation, was less than 14.1% for THC, 11-OH-THC, and THCCOOH. The method was successfully applied to quantification of THC and its 11-OH-THC and THCCOOH metabolites in plasma specimens following controlled administration of THC.
机译:用于同时定量Δ 9 -四氢大麻酚(THC),11-羟基-Δ的二维(2D)气相色谱/电子冲击质谱(GC / EI-MS)方法开发并验证了人体血浆中的9 -四氢大麻酚(11-OH-THC)和11-nor-Δ 9 -四氢大麻酚-9-羧酸(THCCOOH)。该方法采用了二维毛细管气相色谱和低温聚焦技术,以提高分离度和灵敏度。通过用乙腈沉淀来萃取THC,11-OH-THC和THCCOOH,然后进行固相萃取。 GC分离分析物的三甲基甲硅烷基衍生物是通过两个毛细管柱通过气动Deans切换系统串联完成的。检测和定量使用台式单四极杆质谱仪在电子碰撞选择离子监测模式下完成。 THC,11-OH-THC和THCCOOH的定量限(LOQ)分别为0.125、0.25和0.125 ng / mL。所有分析物的准确度范围为86.0%至113.0%。对于THC,11-OH-THC和THCCOOH,测定内和测定间精密度(相对标准偏差百分比)小于14.1%。该方法已成功应用于定量控制THC后血浆样品中THC及其11-OH-THC和THCCOOH代谢产物的定量。

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