Develoment and validation of HPLC-DAD methods for quantification of phenytoin and glycoprotein inhibitors (Elacridar and Tariquidar) in plasma
Descripción del Articulo
Two simple, rapid, selective and sensitive bioanalytical methods were developed and validated by HPLC-DAD, one for the determination and quantification of phenytoin, and another for inhibitors of P-glycoprotein (tariquidar and elacridar) using 0.2ml of plasma. The analytes were separated using Chrom...
Autores: | , , , , , , |
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Formato: | artículo |
Fecha de Publicación: | 2020 |
Institución: | Universidad Católica de Santa María |
Repositorio: | Revistas - Universidad Católica de Santa María |
Lenguaje: | español |
OAI Identifier: | oai:ojs.revistas.ucsm.edu.pe:article/267 |
Enlace del recurso: | https://revistas.ucsm.edu.pe/ojs/index.php/veritas/article/view/267 |
Nivel de acceso: | acceso abierto |
Materia: | HPLC-DAD Fenitoina Tariquidar Elacridar |
Sumario: | Two simple, rapid, selective and sensitive bioanalytical methods were developed and validated by HPLC-DAD, one for the determination and quantification of phenytoin, and another for inhibitors of P-glycoprotein (tariquidar and elacridar) using 0.2ml of plasma. The analytes were separated using Chromolith® Performance RP-18 100 - 4.6 mm column, with a mobile phase composed of ACN: 10mM acetate buffer pH = 5.2 (27.5: 72.5) for phenytoin and its EI, forthe determination of tariquidar , elacridar and its EI ACN: MeOH: 10mM acetate buffer pH = 5.2 (30:50:20) was used, in both methods a flow of 1mL / min, temperature of 25 ± 1 ° C, a complement of slingshot of 210nm The methods proved to be linear and sensitive, the phenytoin method in the range of 100 to 50,000 ng / mL (LC = 36.98 ng / mL, LD = 98.79 ng / mL) and inhibitors of 100 to 20,000 ng / mL (LC = 36.98 ng / mL, LD = 98.79 ng / mL), also showedto be accurate (% CV <15), reproducible and accurate. The recovery was greater than 97% (phenytoin) and 93% (inhibitors), both methods presented stability in freezing and thawing cycles, short-term stability (5h and 24h) and long-term stability for up to 3 months at -20 ° C. The bioanalytical methods developed and validated may be used to evaluate the effect on the pharmacokinetics and bioavailability of the co-administration of tariquidar and elacridar with phenytoin. |
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La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).