Enantiomeric separation of panthenol by Capillary Electrophoresis. Analysis of commercial formulations and toxicity evaluation on non-target organisms

The first CE methodology enabling the enantiomeric separation of panthenol was developed in this work. Electrokinetic chromatography with cyclodextrins (CD-EKC) was the CE mode employed for this purpose. The effect of different experimental variables such as the nature and concentration of the cyclo...

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Detalles Bibliográficos
Autores: Jiménez Jiménez, Sara|||0000-0002-4096-6235, Amariei, Georgiana|||0000-0002-5412-6325, Boltes Espínola, Ana Karina|||0000-0001-9686-7730, García González, María Ángeles|||0000-0001-6292-8232, Marina Alegre, María Luisa|||0000-0002-5583-1624
Tipo de recurso: artículo
Fecha de publicación:2021
País:España
Institución:Universidad de Alcalá (UAH)
Repositorio:e_Buah Biblioteca Digital Universidad de Alcalá
Idioma:inglés
OAI Identifier:oai:ebuah.uah.es:10017/59847
Acceso en línea:http://hdl.handle.net/10017/59847
https://dx.doi.org/10.1016/j.chroma.2021.461919
Access Level:acceso abierto
Palabra clave:capillary electrophoresis
cyclodextrin
chiral separation
panthenol
toxicity
Spirodela polyrhiza
Química
Chemistry
Descripción
Sumario:The first CE methodology enabling the enantiomeric separation of panthenol was developed in this work. Electrokinetic chromatography with cyclodextrins (CD-EKC) was the CE mode employed for this purpose. The effect of different experimental variables such as the nature and concentration of the cyclodextrin, the temperature and the separation voltage was investigated. The best enantiomeric separation was obtained with 25 mM (2-carboxyethyl)-?-CD (CE-?-CD) in 100 mM borate buffer (pH 9.0), with a separation voltage of 30 kV and a temperature of 30?C. Under these conditions, an enantiomeric resolution of 2.0 in an analysis time of 4.2 min was obtained, being the biologically active enantiomer D-panthenol (dexpanthenol) the second-migrating enantiomer. The analytical characteristics of the method were evaluated in terms of precision, accuracy, selectivity, linearity, LOD, and LOQ, showing a good performance for the quantitation of dexpanthenol in cosmetic and pharmaceutical formulations. The enantiomeric impurity (L-panthenol) could be detected at a 0.1 % level with respect to the majority enantiomer, allowing to accomplish the requirements of the ICH guidelines. The method was also successfully applied to study the stability of panthenol under abiotic and biotic conditions and its toxicity on non-target organisms (the aquatic plant Spirodela polyrhiza).