Interactions of helquats with chiral acidic aromatic analytes investigated by partial-filling affinity capillary electrophoresis
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články
PubMed
27578406
DOI
10.1016/j.chroma.2016.08.053
PII: S0021-9673(16)31130-X
Knihovny.cz E-zdroje
- Klíčová slova
- Affinity capillary electrophoresis, Binding constant, Chiral separation, Helquats, Noncovalent interactions, Partial filling,
- MeSH
- algoritmy MeSH
- aromatické uhlovodíky analýza MeSH
- barvicí látky MeSH
- celulosa analogy a deriváty MeSH
- elektroforéza kapilární metody MeSH
- indikátory a reagencie MeSH
- léčivé přípravky analýza MeSH
- ligandy MeSH
- stereoizomerie MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- aromatické uhlovodíky MeSH
- barvicí látky MeSH
- celulosa MeSH
- hydroxypropylcellulose MeSH Prohlížeč
- indikátory a reagencie MeSH
- léčivé přípravky MeSH
- ligandy MeSH
Noncovalent molecular interactions between helquats, a new class of dicationic helical extended diquats, and several chiral acidic aromatic drugs and catalysts have been investigated using partial-filling affinity capillary electrophoresis (PF-ACE). Helquats dissolved at 1mM concentration in the aqueous background electrolyte (40mM Tris, 20mM acetic acid, pH 8.1) were introduced as ligand zones of variable length (0-130mm) into the hydroxypropylcellulose coated fused silica capillary whereas 0.1mM solutions of negatively charged chiral drugs or catalysts (warfarin, ibuprofen, mandelic acid, etodolac, binaphthyl phosphate and 11 other acidic aromatic compounds) were applied as a short analyte zone at the injection capillary end. After application of electric field, analyte and ligand migrated against each other and in case of their interactions, migration time of the analyte was increasing with increasing length of the ligand zone. From the tested compounds, only isomers of those exhibiting helical chirality and/or possessing conjugated aromatic systems were enantioselectively separated through their differential interactions with helquats. Some compounds with conjugated aromatic groups interacted with helquats moderately strongly but non-enantiospecifically. Small compounds with single benzene ring exhibited no or very weak non-enantiospecific interactions. PF-ACE method allowed to determine binding constants of the analyte-helquat complexes from the changes of migration times of the analytes. Binding constants of the weakest complexes of the analytes with helquats were less than 50L/mol, whereas binding constants of the strongest complexes were in the range 1 000-1 400L/mol.
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