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HPLC method for novel cannabinoid separation with electrochemical detection on boron-doped diamond electrode

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F25%3A73633566" target="_blank" >RIV/61989592:15310/25:73633566 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216224:14310/25:00141119

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S073170852500216X" target="_blank" >https://www.sciencedirect.com/science/article/pii/S073170852500216X</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jpba.2025.116875" target="_blank" >10.1016/j.jpba.2025.116875</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    HPLC method for novel cannabinoid separation with electrochemical detection on boron-doped diamond electrode

  • Original language description

    In this study, we developed a novel and environmentally friendly method for the determination of selected cannabinoids -cannabidiol, cannabinol, tetrahydrocannabinol, JWH 073 synthetic cannabinoid, hexahydrocannabinol (HHC), and hexahydrocannabinol-O-acetate - using high-performance liquid chromatography with electrochemical detection. The method employs a boron-doped diamond working electrode, which offers significant advantages in comparison with commonly used materials. Its main strengths include low background currents, reduced fouling, and an extended potential window, making it suitable for detecting compounds that are not readily oxidizable. The chromatographic system utilized a reversed-phase Gemini C18 column with a mobile phase consisting of acetonitrile and 25 mM phosphate buffer (pH 4.4) in step-gradient mode from 68 % to 88 % acetonitrile.The separation and determination of cannabinoids were optimized to be completed in less than 25 min. Hydrodynamic voltammetry was performed to identify the optimal potential for the amperometric detection, with a working potential of + 1400 mV (vs. Pd/H2) providing the best analytical response based on S/ N ratio. Under these optimal separation and detection conditions, the limits of detection were within the range of 6.1-666 nM (for cannabidiol and 9(R)-hexahydrocannabinol-O-acetate), while the response was linear within the concentration range measured up to 10 mu M. The method demonstrated good linearity, precision, and sensitivity, with limits of detection and quantitation reaching nanomolar levels. The developed method was successfully applied to commercial samples of HHC jelly bears and HHC distillate.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10406 - Analytical chemistry

Result continuities

  • Project

  • Continuities

    S - Specificky vyzkum na vysokych skolach

Others

  • Publication year

    2025

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS

  • ISSN

    0731-7085

  • e-ISSN

    1873-264X

  • Volume of the periodical

    262

  • Issue of the periodical within the volume

    SEP

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    6

  • Pages from-to

    "116875-1"-"116875-6"

  • UT code for WoS article

    001469844200001

  • EID of the result in the Scopus database

    2-s2.0-105002246574