Efficient Capture of Cannabis Terpenes in Olive Oil during Microwave-Assisted Cannabinoid Decarboxylation - PubMed
- ️Mon Jan 01 2024
Efficient Capture of Cannabis Terpenes in Olive Oil during Microwave-Assisted Cannabinoid Decarboxylation
Luisa Boffa et al. Molecules. 2024.
Abstract
The development of selective extraction protocols for Cannabis-inflorescence constituents is still a significant challenge. The characteristic Cannabis fragrance can be mainly ascribed to monoterpenes, sesquiterpenes and oxygenated terpenoids. This work investigates the entrapment of Cannabis terpenes in olive oil from inflorescences via stripping under mild vacuum during the rapid microwave-assisted decarboxylation of cannabinoids (MW, 120 °C, 30 min) and after subsequent extraction of cannabinoids (60 and 100 °C). The profiles of the volatiles collected in the oil samples before and after the extraction step were evaluated using static headspace solid-phase microextraction (HS-SPME), followed by gas chromatography coupled to mass spectrometry (GC-MS). Between the three fractions obtained, the first shows the highest volatile content (~37,400 mg/kg oil), with α-pinene, β-pinene, β-myrcene, limonene and trans-β-caryophyllene as the main components. The MW-assisted extraction at 60 and 100 °C of inflorescences using the collected oil fractions allowed an increase of 70% and 86% of total terpene content, respectively. Considering the initial terpene amount of 91,324.7 ± 2774.4 mg/kg dry inflorescences, the percentage of recovery after decarboxylation was close to 58% (mainly monoterpenes), while it reached nearly 100% (including sesquiterpenes) after extraction. The selective and efficient extraction of volatile compounds, while avoiding direct contact between the matrix and extraction solvents, paves the way for specific applications in various aromatic plants. In this context, aromatized extracts can be employed to create innovative Cannabis-based products within the hemp processing industry, as well as in perfumery, cosmetics, dietary supplements, food, and the pharmaceutical industry.
Keywords: Cannabis inflorescences; HS-SPME GC-MS analysis; flavored olive oil; microwave-assisted decarboxylation; selective extraction; terpene capture.
Conflict of interest statement
The authors declare no conflicts of interest.
Figures

Ethos LEAN MW oven configuration for the capture of Cannabis terpenes in olive oil (Milestone Srl).

Chromatogram obtained from the SPME/GC-MS of Cannabis inflorescences with 2-undecanol as IS (14.93 min).

Hundred-percent stacked column representation of the average ppm data from Table 2, obtained from SPME/GC-MS analyses.

Stacked column representation of the terpene composition of the three oil fractions (F1, F2 and F3) (expressed as mg/kg oil, average ± S.D., data in Table 2), obtained from SPME/GC-MS analyses.

Overlapped chromatograms obtained from the SPME/GC-MS of mixed and diluted (Mix F1 ÷ 3 dil.) oil fractions and oil samples from MAE at 60 °C and 100 °C (Ext. 60, Ext. 100).

Parallel column representation of the terpene composition of oil obtained after extraction at 60 and 100 °C, compared to the starting sample (Mix F1 ÷ 3 dil.), expressed as mg/kg oil (mean ± standard deviation). Data were obtained from SPME/GC-MS analyses and are shown in Table 3.

Comparison of the main terpene amounts (mg/kg oil) present in the oily samples obtained during decarboxylation (F1, F2 and F3) and after extraction of decarboxylated inflorescences at 60 and 100 °C (Ext. 60 and Ext. 100), using Mix F1 ÷ 3 dil. as solvent.
Similar articles
-
Ternelli M, Brighenti V, Anceschi L, Poto M, Bertelli D, Licata M, Pellati F. Ternelli M, et al. J Pharm Biomed Anal. 2020 Jul 15;186:113296. doi: 10.1016/j.jpba.2020.113296. Epub 2020 Apr 6. J Pharm Biomed Anal. 2020. PMID: 32334134
-
Lee S, Kim EJ, Kwon E, Oh SJ, Cho M, Kim CM, Lee W, Hong J. Lee S, et al. Molecules. 2023 Dec 14;28(24):8082. doi: 10.3390/molecules28248082. Molecules. 2023. PMID: 38138572 Free PMC article.
-
Iseppi R, Brighenti V, Licata M, Lambertini A, Sabia C, Messi P, Pellati F, Benvenuti S. Iseppi R, et al. Molecules. 2019 Jun 21;24(12):2302. doi: 10.3390/molecules24122302. Molecules. 2019. PMID: 31234360 Free PMC article.
-
Gouvêa-Silva JG, Costa-Oliveira CD, Ramos YJ, Mantovanelli DF, Cardoso MS, Viana-Oliveira LD, Costa JL, Moreira DL, Maciel-Magalhães M. Gouvêa-Silva JG, et al. Cannabis Cannabinoid Res. 2023 Jun;8(3):476-486. doi: 10.1089/can.2022.0076. Epub 2022 Jun 28. Cannabis Cannabinoid Res. 2023. PMID: 35763833 Review.
-
Micalizzi G, Vento F, Alibrando F, Donnarumma D, Dugo P, Mondello L. Micalizzi G, et al. J Chromatogr A. 2021 Jan 25;1637:461864. doi: 10.1016/j.chroma.2020.461864. Epub 2020 Dec 30. J Chromatogr A. 2021. PMID: 33422797 Review.
References
-
- Elzinga S., Fischedick J., Podkolinski R., Raber J.C. Cannabinoids and terpenes as chemotaxonomic markers in cannabis. Nat. Prod. Chem. Res. 2015;3:181. doi: 10.4172/2329-6836.1000181. - DOI
-
- Flores-Sanchez I.J., Verpoorte R. Secondary metabolism in cannabis. Phytochem. Rev. 2008;7:615–639. doi: 10.1007/s11101-008-9094-4. - DOI
-
- Veress T., Szanto J.I., Leisztner L. Determination of cannabinoid acids by high-performance liquid-chromatography of their neutral derivatives formed by thermal decarboxylation. 1. Study of the decarboxylation process in open reactors. J. Chromatogr. 1990;520:339–347. doi: 10.1016/0021-9673(90)85118-F. - DOI
MeSH terms
Substances
Grants and funding
This research received no external funding.
LinkOut - more resources
Full Text Sources
Miscellaneous