Novel approach to urinary 11-nor-9-carboxy-delta-9-tetrahydrocannabinol analysis in forensic applications using
Kesara Ar-Sanork1, Wichayaporn Kamsong2, Rawisara Woensanthia3
1School of Chemistry, Institute of Science, Suranaree University of Technology, 111 University Avenue, Muang District, Nakhon Ratchasima, 30000, Thailand; Institute of Pharmaceutical Analysis, College of Pharmacy/State Key Laboratory of Bioactive Molecules and Druggability Assessment/International Cooperative Laboratory of Traditional Chinese Medicine Modernization and Innovative Drug Development of Ministry of Education (MOE) of China, Jinan University, Guangzhou, 510632, China.
Background:
The escalating global use of cannabis as a narcotic demands the development of a rapid, cost-effective, and portable method for assessing cannabis intake in forensic contexts. A major cannabis metabolite, 11-nor-9-carboxy-Δ9-tetrahydrocannabinol (THC-COOH), is commonly targeted for cannabis drug testing. However, the quantification of urinary THC-COOH typically relies on chromatographic methods, which require bulky, expensive instruments and skilled expertise. This study presents a novel approach for the simple, selective, and sensitive detection of THC-COOH in human urine samples by integrating monolithic pipette-tip solid-phase extraction (monolithic PT-SPE) with an electrochemical sensor based on disposable screen-printed graphene electrodes (SPGEs).
Results:
A C18-functionalised monolithic backbone, poly(stearyl methacrylate-co-ethylene dimethacrylate), is in situ synthesised within micro-pipette tips for effective urine sample cleanup and pre-concentration of THC-COOH before quantification using the SPGE-based sensor in a few minutes. Critical parameters for PT-SPE and electrochemical detection are systematically optimised. The method exhibits a wide linear range of 50-1000 ng mL-1 (R2 = 0.9980), with both a low limit of detection (5.2 ng mL-1) and a low limit of quantification (17.5 ng mL-1). Under optimal conditions, THC-COOH is effectively isolated from complex urine matrices, achieving a 14-fold signal enhancement and good recovery (80 %-110 %), with intra- and inter-day precisions of 5.9 % and 7.1 %, respectively. Both for authentic urine specimens and spiked samples, analysis results obtained using the method developed demonstrate strong correlation with liquid chromatography with tandem mass spectrometry (LC-MS/MS) results.
Significance:
We successfully employed an electrochemical sensor for the determination of THC-COOH in human urine specimens for the first time. By coupling it with the developed monolithic PT-SPE, we achieved direct detection of THC-COOH without requiring additional electrode surface modifications. The method is environmentally friendly, requiring only a minimal volume of reagents for both extraction and detection. Furthermore, it is efficient, simple and cost-effective.
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