Stability and toxicity studies for duloxetine and econazole on Spirodela polyrhiza using chiral capillary electrophoresis

Stability and toxicity studies for duloxetine and econazole were achieved using individual solutions and their mixtures. Stability of drugs racemates and enantiomers was investigated under abiotic and biotic conditions. Toxicity was evaluated for the first time on Spirodela polyrhiza. EC50 values we...

ver descrição completa

Detalhes bibliográficos
Autores: Marina Alegre, María Luisa|||0000-0002-5583-1624, Valimaña Traverso, Jesús Manuel, Amariei, Georgiana|||0000-0002-5412-6325, Boltes Espínola, Ana Karina|||0000-0001-9686-7730, García González, María Ángeles|||0000-0001-6292-8232
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:10017/41566
Acesso em linha:http://hdl.handle.net/10017/41566
https://dx.doi.org/10.1016/j.jhazmat.2019.04.027
Access Level:acceso abierto
Palavra-chave:Aquatic plant
Chiral capillary electrophoresis
Duloxetine
Econazole
Mixture toxicity and stability
Química
Chemistry
Descrição
Resumo:Stability and toxicity studies for duloxetine and econazole were achieved using individual solutions and their mixtures. Stability of drugs racemates and enantiomers was investigated under abiotic and biotic conditions. Toxicity was evaluated for the first time on Spirodela polyrhiza. EC50 values were calculated for each individual drug and for their binary mixture. Real (not nominal) concentrations determined by Capillary Electrophoresis were employed in the calculations of toxicity parameters. The use of a 25 mM phosphate buffer (pH 3.0) with 1.5% S-beta-CD as chiral selector at a temperature of 30 degrees C and a separation voltage of - 20 kV enabled the simultaneous enantiomeric separation of duloxetine and econazole in 7.5 min with enantiomeric resolutions of 7.9 and 6.5, respectively. For individual solutions, decay percentages under abiotic conditions were higher for duloxetine (80%) than for econazole (60%), while in presence of Spirodela polyrhiza they increased for duloxetine but not for econazole. Econazole showed the highest decay percentages under abiotic or biotic conditions (100%) in binary mixtures. EC50 values for duloxetine and econazole enabled to include both drugs within the group of very toxic compounds although econazole showed a higher toxicity than duloxetine and the binary mixture.