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Challenges of cannabidiol determination in emulsified cosmetics and application of solid‑phase extraction followed by HPLC‑UV‑MS/MS

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22330%2F25%3A43930219" target="_blank" >RIV/60461373:22330/25:43930219 - isvavai.cz</a>

  • Alternative codes found

    RIV/60461373:22340/25:43930219

  • Result on the web

    <a href="https://link.springer.com/article/10.1007/s00216-024-05716-9" target="_blank" >https://link.springer.com/article/10.1007/s00216-024-05716-9</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s00216-024-05716-9" target="_blank" >10.1007/s00216-024-05716-9</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Challenges of cannabidiol determination in emulsified cosmetics and application of solid‑phase extraction followed by HPLC‑UV‑MS/MS

  • Original language description

    The recent surge in popularity of cannabidiol-infused products extends beyond food and supplements to the cosmetic industry. Accurate labeling remains a significant concern, as many products fail to meet advertised cannabidiol content and/or contain psychoactive tetrahydrocannabinol above the permissible levels. In this work, we present the use of an HPLC-UV-MS/MS method for the quantification of five major cannabinoids (cannabidiol, cannabidiolic acid, tetrahydrocannabinol, tetrahydrocannabinolic acid, and cannabigerol) in oil-in-water cosmetic emulsions. The sample extraction is based on dispersing the sample in isopropanol, followed by solid-phase extraction using Bond Elut Plexa PAX cartridge. The viability of this method is demonstrated by comparing matrix effects in samples subjected to solid-phase extraction (0‒11% suppression of cannabidiol ionization) to samples extracted without additional purification steps (0‒84% ionization suppression of cannabidiol ionization). The limit of quantification is determined at 0.1 mg/g and the calibration is employed in the range of 0.1‒50 mg/g for cannabidiol and 0.1‒10 mg/g for all other analytes. Finally, 36 real cosmetic samples from the Czech market were analyzed. Of these, 14 indicated the amount of CBD on the label but only five (36%) were accurate, i.e., within 90‒110% of the labeled amount, and a considerable amount of THC (0.16 ± 0.01 mg/g) was found in one sample. These findings contribute to the cumulating evidence that cannabidiol-based consumer products are often mislabeled and highlight the importance of better regulatory compliance.

  • 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

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

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

    ANALYTICAL AND BIOANALYTICAL CHEMISTRY

  • ISSN

    1618-2642

  • e-ISSN

    1618-2650

  • Volume of the periodical

    417

  • Issue of the periodical within the volume

    6

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    11

  • Pages from-to

    1153-1163

  • UT code for WoS article

    001390273900001

  • EID of the result in the Scopus database

    2-s2.0-85214120934