Develoment and validation of HPLC-DAD methods for quantification of phenytoin and glycoprotein inhibitors (Elacridar and Tariquidar) in plasma

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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...

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Detalles Bibliográficos
Autores: Stefany Huaynasi Aguirre, Yemima Onque Quirita, Julitza Paredes Fuentes, José Carpio Carpio, José Villanueva Salas, Rita Nieto Montesinos, Karin Vera López
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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network_acronym_str REVUCSM
network_name_str Revistas - Universidad Católica de Santa María
repository_id_str
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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repository.name.fl_str_mv
repository.mail.fl_str_mv
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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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