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 |
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Revistas - Universidad Católica de Santa María |
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dc.title.none.fl_str_mv |
Develoment and validation of HPLC-DAD methods for quantification of phenytoin and glycoprotein inhibitors (Elacridar and Tariquidar) in plasma Desenvolvimiento y validación de métodos bioanalíticos por HPLC- DAD para la cuantificación de fenitoína e inhibidores de la Glicoproteína- P (elacridar y tariquidar) en plasma |
title |
Develoment and validation of HPLC-DAD methods for quantification of phenytoin and glycoprotein inhibitors (Elacridar and Tariquidar) in plasma |
spellingShingle |
Develoment and validation of HPLC-DAD methods for quantification of phenytoin and glycoprotein inhibitors (Elacridar and Tariquidar) in plasma Stefany Huaynasi Aguirre HPLC-DAD Fenitoina Tariquidar Elacridar |
title_short |
Develoment and validation of HPLC-DAD methods for quantification of phenytoin and glycoprotein inhibitors (Elacridar and Tariquidar) in plasma |
title_full |
Develoment and validation of HPLC-DAD methods for quantification of phenytoin and glycoprotein inhibitors (Elacridar and Tariquidar) in plasma |
title_fullStr |
Develoment and validation of HPLC-DAD methods for quantification of phenytoin and glycoprotein inhibitors (Elacridar and Tariquidar) in plasma |
title_full_unstemmed |
Develoment and validation of HPLC-DAD methods for quantification of phenytoin and glycoprotein inhibitors (Elacridar and Tariquidar) in plasma |
title_sort |
Develoment and validation of HPLC-DAD methods for quantification of phenytoin and glycoprotein inhibitors (Elacridar and Tariquidar) in plasma |
dc.creator.none.fl_str_mv |
Stefany Huaynasi Aguirre Yemima Onque Quirita Julitza Paredes Fuentes José Carpio Carpio José Villanueva Salas Rita Nieto Montesinos Karin Vera López |
author |
Stefany Huaynasi Aguirre |
author_facet |
Stefany Huaynasi Aguirre Yemima Onque Quirita Julitza Paredes Fuentes José Carpio Carpio José Villanueva Salas Rita Nieto Montesinos Karin Vera López |
author_role |
author |
author2 |
Yemima Onque Quirita Julitza Paredes Fuentes José Carpio Carpio José Villanueva Salas Rita Nieto Montesinos Karin Vera López |
author2_role |
author author author author author author |
dc.subject.none.fl_str_mv |
HPLC-DAD Fenitoina Tariquidar Elacridar |
topic |
HPLC-DAD Fenitoina Tariquidar Elacridar |
description |
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. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-01-20 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
https://revistas.ucsm.edu.pe/ojs/index.php/veritas/article/view/267 10.35286/veritas.v21i1.267 |
url |
https://revistas.ucsm.edu.pe/ojs/index.php/veritas/article/view/267 |
identifier_str_mv |
10.35286/veritas.v21i1.267 |
dc.language.none.fl_str_mv |
spa |
language |
spa |
dc.relation.none.fl_str_mv |
https://revistas.ucsm.edu.pe/ojs/index.php/veritas/article/view/267/188 |
dc.rights.none.fl_str_mv |
Derechos de autor 2020 Veritas info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Derechos de autor 2020 Veritas |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Universidad Católica de Santa María |
publisher.none.fl_str_mv |
Universidad Católica de Santa María |
dc.source.none.fl_str_mv |
Veritas; Vol. 21 Núm. 1 (2020): VÉRITAS: Investigación, Innovación y Desarrollo; 105-111 Veritas; Vol. 21 Núm. 1 (2020): VÉRITAS: Investigación, Innovación y Desarrollo; 105-111 Veritas; Vol. 21 Núm. 1 (2020): VÉRITAS: Investigación, Innovación y Desarrollo; 105-111 1684-7822 1684-7822 10.35286/veritas.v21i1 reponame:Revistas - Universidad Católica de Santa María instname:Universidad Católica de Santa María instacron:UCSM |
instname_str |
Universidad Católica de Santa María |
instacron_str |
UCSM |
institution |
UCSM |
reponame_str |
Revistas - Universidad Católica de Santa María |
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Revistas - Universidad Católica de Santa María |
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repository.mail.fl_str_mv |
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1842259369526296576 |
spelling |
Develoment and validation of HPLC-DAD methods for quantification of phenytoin and glycoprotein inhibitors (Elacridar and Tariquidar) in plasma Desenvolvimiento y validación de métodos bioanalíticos por HPLC- DAD para la cuantificación de fenitoína e inhibidores de la Glicoproteína- P (elacridar y tariquidar) en plasmaStefany Huaynasi AguirreYemima Onque QuiritaJulitza Paredes FuentesJosé Carpio CarpioJosé Villanueva SalasRita Nieto MontesinosKarin Vera LópezHPLC-DADFenitoinaTariquidarElacridarTwo 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.Se desarrollaron y validaron dos métodos bioanalíticos simples, rápidos, selectivos y sensibles por HPLC-DAD, uno para la determinación y cuantificación de fenitoina, y otro para inhibidores de la Glicoproteina-P (tariquidar y elacridar) usando 0.2ml de plasma. La separación de los analitos se realizó usando columna Chromolith® Performance RP-18 100 - 4.6 mm, con una fase móvil compuesta de ACN:Buffer acetato 10mM pH=5.2 (27.5:72.5) para fenitoina y suEI, para la determinación de tariquidar, elacridar y su EI se usó ACN:MeOH:Buffer acetato 10mM pH=5.2 (30:50:20), en ambos métodos se usó un flujo de 1mL/min, temperatura de 25±1°C, un complemento de honda de 210nm. Los métodos mostraron ser lineales y sensibles, el método fenitoina en el rango de 100 a 50 000 ng/mL (LC = 36.98 ng/mL, LD = 98.79 ng/ mL) e inhibidores de 100 a 20 000 ng/mL (LC = 36.98 ng/mL, LD = 98.79 ng/mL), también mostraron ser precisos (% CV <15), reproducibles y exactos. La recuperación fue superior al 97% (fenitoina) y 93% (inhibidores) ambos métodos presentaron estabilidad en ciclos de congelamiento y descongelamiento, estabilidad a corto (5h y 24h) y a largo plazo hasta por 3 meses a -20 °C. Los métodos bioanalíticos desarrollados y validados podrán servir para evaluar el efecto sobre la farmacocinética y biodisponibilidad de la coadministración de tariquidar y elacridar con fenitoina.Universidad Católica de Santa María2020-01-20info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://revistas.ucsm.edu.pe/ojs/index.php/veritas/article/view/26710.35286/veritas.v21i1.267Veritas; Vol. 21 Núm. 1 (2020): VÉRITAS: Investigación, Innovación y Desarrollo; 105-111Veritas; Vol. 21 Núm. 1 (2020): VÉRITAS: Investigación, Innovación y Desarrollo; 105-111Veritas; Vol. 21 Núm. 1 (2020): VÉRITAS: Investigación, Innovación y Desarrollo; 105-1111684-78221684-782210.35286/veritas.v21i1reponame:Revistas - Universidad Católica de Santa Maríainstname:Universidad Católica de Santa Maríainstacron:UCSMspahttps://revistas.ucsm.edu.pe/ojs/index.php/veritas/article/view/267/188Derechos de autor 2020 Veritasinfo:eu-repo/semantics/openAccessoai:ojs.revistas.ucsm.edu.pe:article/2672021-07-13T05:25:08Z |
score |
13.10263 |
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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).