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Enantiomeric separation of bupropion by liquid chromatography on derivatized cyclofructan chiral stationary phase

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F62690094%3A18470%2F22%3A50019392" target="_blank" >RIV/62690094:18470/22:50019392 - isvavai.cz</a>

  • Result on the web

    <a href="https://onlinelibrary.wiley.com/doi/10.1002/chir.23496" target="_blank" >https://onlinelibrary.wiley.com/doi/10.1002/chir.23496</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/chir.23496" target="_blank" >10.1002/chir.23496</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Enantiomeric separation of bupropion by liquid chromatography on derivatized cyclofructan chiral stationary phase

  • Original language description

    High-performance liquid chromatography (HPLC) is an ideal tool for enantiomeric separations of different drugs. In this study, the direct enantioseparation of bupropion, an atypical antidepressant structurally related to cathinone, was explored by using five chiral columns, including three based on derivatized cyclofructans, macrocyclic glycopeptide teicoplanin, and an immobilized amylose derivative under multimodal elution conditions. Baseline enantioseparation was obtained on the LarihcShell CF6-RN column, with derivatized cyclofructan 6, in the polar organic mode. The effects of the mobile-phase composition, type and content of major components, the nature and the amount of mobile-phase additives, and the column temperature on the retention, selectivity, and resolution were investigated to optimize enantioseparation. The calibration curve was linear in the range of 10-125 mu g/ml for each enantiomer. The limits of detection and quantification were 0.1 and 0.3 mu g/ml for both enantiomers of bupropion. The chiral recognition was controlled especially by H bonds, pi-pi, dipole-dipole interactions, and steric effects. Finally, the developed method was applied to the determination of bupropion in the commercially available drug.

  • 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

    2022

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    CHIRALITY

  • ISSN

    0899-0042

  • e-ISSN

    1520-636X

  • Volume of the periodical

    34

  • Issue of the periodical within the volume

    10

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    9

  • Pages from-to

    1311-1319

  • UT code for WoS article

    000828904600001

  • EID of the result in the Scopus database

    2-s2.0-85134515767