Resistant starch/pectin free-standing films reinforced with nanocellulose intended for colonic methotrexate release

Although resistant starch/pectin (RS/P) films have previously displayed suitable properties for colon-specific drug delivery, nanocomposite films were developed aiming to enhance physicochemical, thermal, mechanical and barrier properties, as well as the low oral bioavailability of methotrexate (MTX...

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Detalles Bibliográficos
Autores: Meneguin, Andréia B., Ferreira Cury, Beatriz Stringhetti [UNESP], dos Santos, Aline M. [UNESP], Franco, Douglas Faza [UNESP], Barud, Hernane S. [UNESP], da Silva Filho, Edson C.
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2017
País:Brasil
Institución:Universidade Estadual Paulista (UNESP)
Repositorio:Repositório Institucional da UNESP
Idioma:inglés
OAI Identifier:oai:repositorio.unesp.br:11449/173909
Acceso en línea:http://dx.doi.org/10.1016/j.carbpol.2016.10.062
http://hdl.handle.net/11449/173909
Access Level:acceso abierto
Palabra clave:Cellulose nanofiber
Free-standing films
Methotrexate
Nanocellulose
Pectin
Resistant starch
Descripción
Sumario:Although resistant starch/pectin (RS/P) films have previously displayed suitable properties for colon-specific drug delivery, nanocomposite films were developed aiming to enhance physicochemical, thermal, mechanical and barrier properties, as well as the low oral bioavailability of methotrexate (MTX). FEG-SEM micrographs of nanocomposite films showed different interaction patterns occurring among nanocellulose and RS/P. The nanofiller addition led to an increase in the thermal stability, probably due to its interaction with RS crystalline double helices. Results also displayed an improvement of the puncture strength, while barrier properties revealed a low water vapor permeability. Ex vivo bioadhesion test displayed the nanocomposites films to interact strongly with porcine gastrointestinal mucosa. In vitro drug release studies showed that the films developed enhanced the drug dissolution rates with approximately 80% of MTX release in 150 min, suggesting the potential of these materials as a poor solubility drugs carrier, which constitutes an important tool for enhancing oral bioavailability.