首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >Qualitative and quantitative analysis of THC, 11-hydroxy-THC and 11-nor-9-carboxy-THC in whole blood by ultra-performance liquid chromatography/tandem mass spectrometry
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Qualitative and quantitative analysis of THC, 11-hydroxy-THC and 11-nor-9-carboxy-THC in whole blood by ultra-performance liquid chromatography/tandem mass spectrometry

机译:超高效液相色谱/串联质谱法对全血中THC,11-羟基-THC和11-nor-9-羧基-THC进行定性和定量分析

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摘要

A qualitative and quantitative analytical method was developed for the simultaneous determination of δ~9-tetrahydrocannabinol (THC), 11-hydroxy-A9-tetrahydrocannabinol (11-OH-THC) and l1-nor-9-carboxy- δ~9-tetrahydrocannabinol (THC-COOH) in whole blood. The samples were prepared by solid-phase extraction followed by ultra-performance liquid chromatography/tandem mass spectrometry (UPLC/MS/MS) analysis using positive ion electrospray ionization and multiple reaction monitoring. The chromatographic separation was performed with an Acquity UPLC~? HSS T3 (50 × 2.1 mm i.d., 1.8 μm) reversed-phase column using a methanol/2 mM ammonium formate (formic acid 0.1%) gradient in a total run time of 9.5 min. MS/MS detection was achieved with two precursor-product ion transitions per substance. The method was fully validated, including selectivity and capacity of identification, according to the identification criteria (two transitions per substance, signal-tonoise ratio, relative retention time and ion ratio) without the presence of interferences, limit of detection (0.2 μg/L for THC and 0.5 μg/L for 11-OH-THC and THC-COOH), limit of quantitation (0.5 μg/L for all cannabinoids), recovery (53-115%), carryover, matrix effect (34-43%), linearity (0.5-100 μg/L), intra-assay precision (CV < 10% for the relative peak area ratios and <0.1% for the relative retention time), inter-assay accuracy (mean relative error <10%) and precision (CV <11%). The method has already been successfully used in proficiency tests and subsequently applied to authentic samples in routine forensic analysis.
机译:建立了同时测定δ〜9-四氢大麻酚(THC),11-羟基-A9-四氢大麻酚(11-OH-THC)和l1-nor-9-羧基-δ〜9-四氢大麻酚的定性和定量分析方法(THC-COOH)在全血中​​。通过固相萃取,然后使用正离子电喷雾电离和多反应监测进行超高效液相色谱/串联质谱分析(UPLC / MS / MS),制备样品。色谱分离用Acquity UPLC进行。 HSS T3(50×2.1 mm内径,1.8μm)反相色谱柱,使用甲醇/ 2 mM甲酸铵(甲酸0.1%)梯度洗脱,总运行时间为9.5分钟。 MS / MS检测通过每种物质的两个前体产物离子跃迁实现。根据鉴定标准(每种物质的两个过渡,信噪比,相对保留时间和离子比率),在没有干扰的情况下,对方法进行了充分验证,包括鉴定能力和检测限(0.2μg/ L)对于THC,对于11-OH-THC和THC-COOH是0.5μg/ L),定量限(所有大麻素为0.5μg/ L),回收率(53-115%),残留,基质效应(34-43%) ,线性(0.5-100μg/ L),测定内精度(相对峰面积比的CV <10%和相对保留时间<0.1%),测定间精度(平均相对误差<10%)和精度(CV <11%)。该方法已经成功地用于能力验证,并随后应用于常规法医分析中的真实样品。

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