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
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10406 - Analytical chemistry
Result continuities
Project
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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