Analysis of basic drugs by liquid chromatography with environmentally friendly mobile phases in pharmaceutical formulations
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Otros documentos de la autoría: Peris García, Ester; Ruiz Ángel, M. J.; Carda-Broch, Samuel; García-Álvarez Coque, M. C.
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Mostrar el registro completo del ítemcomunitat-uji-handle:10234/9
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https://doi.org/10.1016/j.microc.2017.06.009 |
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Título
Analysis of basic drugs by liquid chromatography with environmentally friendly mobile phases in pharmaceutical formulationsFecha de publicación
2017Editor
ElsevierISSN
0026-265XTipo de documento
info:eu-repo/semantics/articleVersión de la editorial
https://www.sciencedirect.com/science/article/pii/S0026265X17304952Versión
info:eu-repo/semantics/publishedVersionPalabras clave / Materias
Resumen
Basic drugs are positively charged in the usual working pH (2–8) in reversed-phase liquid chromatography. This gives rise to a strong association with the residual ionized silanols in conventional silica-based stationary ... [+]
Basic drugs are positively charged in the usual working pH (2–8) in reversed-phase liquid chromatography. This gives rise to a strong association with the residual ionized silanols in conventional silica-based stationary phases, which is translated in poor peak shape and high consumption of organic solvent to get appropriate retention times. Micellar mobile phases containing surfactants give rise to modified stationary phases, where silanols are masked, improving the peak shape. However, mobile phases containing the anionic surfactant sodium dodecyl sulfate (SDS) require a small amount of organic solvent to conveniently decrease the retention of cationic analytes. An alternative is the use of mixed micellar mobile phases prepared with SDS and the more polar non-ionic surfactant Brij-35, which modulates the retention of basic drugs to practical analysis times, eliminating the need of organic solvent. Two simple chromatographic procedures for the control of the β-adrenoceptor antagonists atenolol, celiprolol, metoprolol, oxprenolol and propranolol in pharmaceutical formulations were developed and compared, using 0.15 M SDS/15% 1-propanol and 0.15 M SDS/0.05 M Brij-35 at pH 3 with UV detection. Both methods were validated according to the ICH guideline. Satisfactory recoveries were achieved, with intra- and inter-day relative standard deviations usually below 2% for both micellar modes. Sample preparation was simple and only required solubilization and filtration previously to injection. [-]
Publicado en
Microchemical Journal 134 (2017) 202–210Proyecto de investigación
CTQ2016-75644-P ; PROMETEO/2016/128Derechos de acceso
0026-265X/© 2017 Elsevier B.V. All rights reserved.
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