Potency Analysis of Semi-Synthetic Cannabinoids in Vaping Oils Using Liquid Chromatography Diode Array Detector with Electrospray Ionization Time-of-Flight Mass Spectrometry for Confirmation of Analyte Identity

• NCJ Number: 310618
• Journal: Molecules Volume: 30 Issue: 2597 Dated: June 2025
• Author(s): Shaozhong Zhang; Md Mahmud Alam; Brent D. Chandler; Jocelyn P. Lanorio; Caitlin Deskins; Liguo Song
• Date Published: June 2025
• Grant Number(s): 15PNIJ-23-GG-04234-RESS
• Sponsoring Agency: National Institute of Justice (NIJ)
• Corporate Author: Western Illinois University
• Publication Format: Article
• Publication Type: Research (Applied/Empirical)
• Country: United States of America

Abstract

Since the 2018 Farm Bill legalized hemp, semi-synthetic cannabinoids, typically derived from hemp-extracted CBD, have been marketed as offering a “legal high”, raising concerns about consumer safety, labeling, and regulation. Consequently, the potency analysis of these compounds has become increasingly important. To address this need, an LC-DAD method was developed for the quantification of seventeen cannabinoids, selected based on the synthetic pathways of semi-synthetic cannabinoids. These included naturally occurring compounds, semi-synthetic derivatives, and byproducts (CBC, CBD, CBDV, CBG, CBN, CBN-O-acetate, CBT, 9(R)-HHC, 9(S)-HHC, 9(R)-HHC-O-acetate, 9(S)-HHC-O-acetate, Δ⁸-THC, Δ⁹-THC, Δ^9,11-THC, Δ⁸-THC-O-acetate, Δ⁹-THC-O-acetate, and Δ⁹-THCV), using abnormal CBD as an internal standard. The method was validated according to ISO 17025 guidelines, demonstrating a linear calibration range from 0.1 to 50 µg/mL. The method was further applied to the potency analysis of one Δ⁸-THC, two THC-O-acetate, two HHC, and one HHC-O-acetate vaping oil sample. Using an innovative method to recover the contents of vaping cartridges, cannabinoids were extracted using methanol, diluted to a concentration of 50 µg/mL, and analyzed using the validated LC-DAD method, which provided a quantifiable range of 0.1 to 100% (w/w). Method specificity was evaluated using ESI/TOFMS and showed minimal interference, despite the presence of other isomers of the semi-synthetic cannabinoids in the samples. (Publisher abstract provided.)