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[使用超高效液相色谱-串联质谱法同时测定食用油中Δ-9-四氢大麻酚、大麻二酚和大麻酚]

[Simultaneous determination of delta-9-tetrahydrocannabinol cannabidiol and cannabinol in edible oil using ultra performance liquid chromatography-tandem mass spectrometry].

作者信息

Zhang Aizhi, Wang Quanlin, Mo Shijie

机构信息

Ningbo Academy of Product Quality Supervision & Inspection, Ningbo 315041, China.

出版信息

Se Pu. 2010 Nov;28(11):1015-9.

Abstract

A method for the simultaneous determination of delta-9-tetrahydrocannabinol (THC), cannabidiol (CBD) and cannabinol (CBN) in edible oil was developed using ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). The target compounds were extracted with methanol, purified by an LC-Alumina-N solid phase extraction cartridge, separated and detected by the UPLC-MS/MS. Quantitative analysis was corrected by an isotope internal standard method using delta-9-THC-D3 as internal standard. Average recoveries for the target compounds varied from 68.0% to 101.6% with the relative standard deviations ranging from 7.0% to 20.1% at three spiked levels. The limits of detection (LOD) of the method were from 0.06-0.17 microg/kg and the limits of quantification (LOQ) were in the range of 0.20-0.52 microg/kg. The results showed that the method is able to meet the requirements for the simultaneous determination of THC, CBD and CBN in edible oil.

摘要

建立了一种采用超高效液相色谱-串联质谱法(UPLC-MS/MS)同时测定食用油中Δ⁹-四氢大麻酚(THC)、大麻二酚(CBD)和大麻酚(CBN)的方法。目标化合物用甲醇提取,通过LC-Alumina-N固相萃取柱净化,再由UPLC-MS/MS进行分离和检测。采用以Δ⁹-THC-D3为内标的同位素内标法进行定量分析。在三个加标水平下,目标化合物的平均回收率为68.0%至101.6%,相对标准偏差为7.0%至20.1%。该方法的检测限(LOD)为0.06 - 0.17μg/kg,定量限(LOQ)为0.20 - 0.52μg/kg。结果表明,该方法能够满足同时测定食用油中THC、CBD和CBN的要求。

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