A Sensitive Ultrahigh-Performance Liquid Chromatography/Tandem Mass Spectrometry Method for the Simultaneous Analysis of Phytocannabinoids and Endocannabinoids in Plasma and Brain

被引:9
作者
Ahmed, Faizy [1 ]
Torrens, Alexa [1 ]
Mahler, Stephen V. V. [2 ]
Ferlenghi, Francesca [3 ]
Huestis, Marilyn A. A. [4 ]
Piomelli, Daniele [1 ,5 ,6 ]
机构
[1] Univ Calif Irvine, Dept Anat & Neurobiol, 37 Hlth Sci Rd, Room 3107, Irvine, CA 92967 USA
[2] Univ Calif Irvine, Dept Neurobiol & Behav, Irvine, CA USA
[3] Univ Parma, Dipartimento Sci Alimenti & Farmaco, Parma, Italy
[4] Thomas Jefferson Univ, Inst Emerging Hlth Profess, Philadelphia, PA USA
[5] Univ Calif Irvine, Dept Biol Chem, Irvine, CA USA
[6] Univ Calif Irvine, Dept Pharmaceut Sci, Irvine, CA USA
关键词
???????(9)-tetrahydrocannabinol; 2-arachidonoyl-sn-glycerol; anandamide; cannabidiol; endocannabinoid; shape selectivity; ultrahigh-performance liquid chromatography/tandem mass spectrometry; SHAPE SELECTIVITY; UNITED-STATES; CANNABIS USE; PPAR-ALPHA; OLEOYLETHANOLAMIDE; RETENTION; DELTA(9)-TETRAHYDROCANNABINOL; PALMITOYLETHANOLAMIDE; QUANTIFICATION; ACTIVATION;
D O I
10.1089/can.2022.0216
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: delta(9)-tetrahydrocannabinol (THC) and cannabidiol (CBD) are major chemical constituents of cannabis, which may interact either directly or indirectly with the endocannabinoid and endocannabinoid-like ( "paracannabinoid ") systems, two lipid-based signaling complexes that play important roles in physiology. Legislative changes emphasize the need to understand how THC and CBD might impact endocannabinoid and paracannabinoid signaling, and to develop analytical approaches to study such impact. In this study, we describe a sensitive and accurate method for the simultaneous quantification of THC, its main oxidative metabolites [11-hydroxy-delta(9)-THC (11-OH-THC) and 11-nor-9-carboxy-delta(9)-THC (11-COOH-THC)], CBD, and a representative set of endocannabinoid [anandamide and 2-arachidonoyl-sn-glycerol (2-AG)] and paracannabinoid [palmitoylethanolamide (PEA) and oleoylethanolamide (OEA)] compounds. Analyte separation relies on the temperature-dependent shape selectivity properties of polymerically bonded C18 stationary phases. Materials and Methods: Analytes are extracted from tissues using acetonitrile precipitation followed by phospholipid removal. The ultrahigh-performance liquid chromatography/tandem mass spectrometry protocol utilizes a commercially available C18 polymeric-bonded phase column and a simple gradient elution system. Results: Ten-point calibration curves show excellent linearity (R-2 > 0.99) over a wide range of analyte concentrations (0.02-500 ng/mL). Lowest limits of quantification are 0.05 ng/mL for anandamide, 0.1 ng/mL for 11-OH-THC and OEA, 0.2 ng/mL for THC and CBD, 0.5 ng/mL for 11-COOH-THC, 1.0 ng/mL for 2-AG, and 2.0 ng/mL for PEA. The lowest limits of detection are 0.02 ng/mL for anandamide, 0.05 ng/mL for 11-OH-THC and OEA, 0.1 ng/mL for THC and CBD, 0.2 ng/mL for 11-COOH-THC, 0.5 ng/mL for 2-AG, and 1.0 ng/mL for PEA. Conclusions: An application of the method is presented, which showed that phytocannabinoid administration elevates endocannabinoid levels in plasma and brain of adolescent male and female mice.
引用
收藏
页码:371 / 385
页数:15
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