| Literature DB >> 27341312 |
Oier Aizpurua-Olaizola1, Iratxe Zarandona1, Laura Ortiz1, Patricia Navarro1, Nestor Etxebarria1, Aresatz Usobiaga1.
Abstract
A high performance liquid chromatography coupled to tandem mass spectrometry (HPLC-MS/MS) method for simultaneous quantification of Δ9-tetrahydrocannabinol (THC), its two metabolites 11-hydroxy-Δ9-tetrahydrocannabinol (11-OH-THC) and 11-nor-9-carboxy-Δ9-tetrahydrocannabinol (THC-COOH), and four additional cannabinoids (cannabidiol (CBD), cannabigerol (CBG), tetrahydrocannabivarin (THCV), and cannabinol (CBN)) in 1 mL of human urine and plasma was developed and validated. The hydrolysis process was studied to ensure complete hydrolysis of glucuronide conjugates and the extraction of a total amount of analytes. Initially, urine and plasma blank samples were spiked with THC-COOH-glucuronide and THC-glucuronide, and four different pretreatment methods were compared: hydrolysis-free method, enzymatic hydrolysis with Escherichia Coli β-glucuronidase, alkaline hydrolysis with 10 M NaOH, and enzyme-alkaline tandem hydrolysis. The last approach assured the maximum efficiencies (close to 100%) for both urine and plasma matrices. Regarding the figures of merit, the limits of detection were below 1 ng/mL for all analytes, the accuracy ranged from 84% to 115%, and both within-day and between-day precision were lower than 12%. Finally, the method was successfully applied to real urine and plasma samples from cannabis users.Entities:
Keywords: cannabinoids and metabolites; enzymatic-alkaline glucuronide hydrolysis; high performance liquid chromatography-mass spectrometry; plasma and urine analysis; solid-phase extraction
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Year: 2016 PMID: 27341312 DOI: 10.1002/dta.1998
Source DB: PubMed Journal: Drug Test Anal ISSN: 1942-7603 Impact factor: 3.345