Amino acid chiral ionic liquids combined with hydroxypropyl-beta-cyclodextrin for drug enantioseparation by capillary electrophoresis

Four amino acid chiral ionic liquids were evaluated in dual systems with hydroxypropyl-beta-cyclodextrin to investigate the enantioseparation by CE of a group of seven drugs as model compounds (duloxetine, verapamil, terbutaline, econazole, sulconazole, metoprolol, and nadolol). The use of two of th...

ver descrição completa

Detalhes bibliográficos
Autores: Salido Fortuna, Sandra|||0000-0002-0792-3559, Greño Ocariz, Maider, Castro Puyana, María|||0000-0003-1412-4103, Marina Alegre, María Luisa|||0000-0002-5583-1624
Formato: artículo
Fecha de publicación:2019
País:España
Recursos:Universidad de Alcalá (UAH)
Repositorio:e_Buah Biblioteca Digital Universidad de Alcalá
Idioma:inglés
OAI Identifier:oai:ebuah.uah.es:10017/45973
Acesso em linha:http://hdl.handle.net/10017/45973
https://dx.doi.org/10.1016/j.chroma.2019.460375
Access Level:acceso abierto
Palavra-chave:Capillary electrophoresis
Chiral ionic liquids
Cyclodextrin
Drugs
Enantioseparation
Química
Chemistry
Descrição
Resumo:Four amino acid chiral ionic liquids were evaluated in dual systems with hydroxypropyl-beta-cyclodextrin to investigate the enantioseparation by CE of a group of seven drugs as model compounds (duloxetine, verapamil, terbutaline, econazole, sulconazole, metoprolol, and nadolol). The use of two of these chiral ionic liquids (tetramethylammonium L-Lysine ([TMA][L-Lys]) and tetramethylammonium L-glutamic acid ([TMA][L-Glu]) as modifiers in CE is reported for the first time in this work whereas tetrabutylammonium L-lysine [TBA][L-Lys]) and tetrabutylammonium L-glutamic acid ([TBA][L-Glu]) were employed previously in CE although very scarcely. The effect of the nature and the concentration of each ionic liquid added to the separation buffer containing the neutral cyclodextrin on the enantiomeric resolution and the migration time obtained for each drug, was investigated. A synergistic effect was observed when combining each chiral ionic liquid with hydroxypropyl-beta-cyclodextrin in the case of the five compounds for which the cyclodextrin showed enantiomeric discrimination power when used as sole chiral selector (duloxetine, verapamil, terbutaline, econazole, sulconazole). Buffer concentration and pH, temperature and separation voltage were varied in order to optimize the enantiomeric separation of these five compounds using dual systems giving rise to resolutions ranging from 1.1 to 6.6. (C) 2019 Elsevier B.V. All rights reserved.