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首页> 外文期刊>Journal of mass spectrometry: JMS >Rapid and robust confirmation and quantification of 11-nor-Δ9- tetrahydrocannabinol-9-carboxylic acid (THC-COOH) in urine by column switching LC-MS-MS analysis
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Rapid and robust confirmation and quantification of 11-nor-Δ9- tetrahydrocannabinol-9-carboxylic acid (THC-COOH) in urine by column switching LC-MS-MS analysis

机译:通过色谱柱切换LC-MS-MS分析快速可靠地确认和定量尿液中11-nor-Δ9-四氢大麻酚9-羧酸(THC-COOH)

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摘要

A method for the rapid and robust confirmation of 11-nor-9- tetrahydrocannabinol-9-carboxylic acid (THCA) in urine involving basic hydrolysis with NaOH and direct injection of the hydrolysate in a column-switching LC-MS-MS system was developed and validated. THCA-d3 was used as internal standard. Detection was performed in negative-ion mode by monitoring the transitions from the [M-CO 2]- ion m/z 299.2→245.2 and and m/z 299.2→191.1 that were found to provide a better signal-to-noise ratio than the transition from the pseudomolecular ion at m/z 343. The high sensitivity of detection enabled the injection of a small volume (10 μl) of the NaOH hydrolysate which, together with the applied column switching system, proved to confer ruggedness to the method and to avoid the deterioration of the instrumental apparatus despite the large amount of inorganic ions in the hydrolysate. The LLOQ was established at 5 ng/ml, and the LLOD was calculated as 0.2 ng/ml (S/N =3). The method was submitted to thorough validation including evaluation of the calibration range (5-500 ng/ml), accuracy and precision, matrix effects, overall process efficiency, autosampler stability, carryover and cross-talk, and 10-times reduction of sample volume (0.1 ml). Proof of applicability was obtained by direct comparison with the reference GC-MS method in use in the lab (the R 2 between the two methods was 0.9951).
机译:开发了一种快速可靠地确定尿液中11-nor-9-四氢大麻酚9-羧酸(THCA)的方法,该方法涉及用NaOH进行碱性水解并在色谱柱切换LC-MS-MS系统中直接注入水解产物并验证。 THCA-d3用作内标。通过监测从[M-CO 2]-离子的m / z 299.2→245.2和m / z 299.2→191.1的跃迁,以负离子模式进行检测,发现这些跃迁提供的信噪比比从假分子离子在m / z 343处的跃迁。高检测灵敏度使得能够注入少量(10μl)的NaOH水解产物,并与应用的色谱柱切换系统一起证明了该方法和方法的坚固性为了避免仪器设备的损坏,尽管水解产物中有大量的无机离子。 LLOQ确定为5 ng / ml,LLOD计算为0.2 ng / ml(S / N = 3)。该方法已经过全面验证,包括评估校准范围(5-500 ng / ml),准确性和精密度,基质效应,总体处理效率,自动进样器稳定性,残留和串扰以及减少10倍的样品量(0.1毫升)。通过与实验室中使用的参考GC-MS方法直接比较获得适用性证明(两种方法之间的R 2为0.9951)。

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