Chiral separation of benzothiazole derivatives of amino acids using capillary zone electrophoresis
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články
PubMed
27888567
DOI
10.1002/jssc.201600689
Knihovny.cz E-zdroje
- Klíčová slova
- amino acids, benzothiazole derivatives, capillary zone electrophoresis, dual cyclodextrin systems, polydimethylacrylamide-coated capillaries,
- MeSH
- aminokyseliny chemie metabolismus MeSH
- benzothiazoly izolace a purifikace MeSH
- chemické techniky analytické metody MeSH
- cyklodextriny chemie MeSH
- elektroforéza kapilární * MeSH
- stereoizomerie MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- aminokyseliny MeSH
- benzothiazoly MeSH
- cyklodextriny MeSH
A method for the separation of enantiomers of leucine and phenylalanine benzothiazole derivatives as potential antimicrobial agents was developed using capillary zone electrophoresis with a dual cyclodextrin (CD) system. The best resolution of enantiomers was achieved in 100 mmol/L phosphate background electrolyte (pH 3.5) with the dual CD system consisting of 10 mmol/L of β-CD with 10 mmol/L of 2-hydroxypropyl-β-cyclodextrin for leucine derivative and 10 mmol/L of 2-hydroxypropyl-γ-cyclodextrin for phenylalanine derivative, respectively. Under the optimal conditions, the highest enantioresolution of 1.25 was achieved in a noncoated-fused silica capillary at 17°C and 24 kV applied voltage.
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