Designing active mats based on cellulose acetate/polycaprolactone core/shell structures with different release kinetics

Core/shell electrospun mats based on cellulose acetate (CA) and polycaprolactone (PCL) were developed as novel active materials for releasing quercetin (Quer) and curcumin (Cur). The effect of polymeric uniaxial and coaxial electrospun systems and the chemical structures of Quer and Cur on the struc...

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Bibliographic Details
Authors: Rojas, Adrián, Velásquez, Eliezer, Piña, Constanza, Galotto, María José, López de Dicastillo, Carol
Format: article
Status:Versión aceptada para publicación
Publication Date:2021
Country:España
Institution:Consejo Superior de Investigaciones Científicas (CSIC)
Repository:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/376930
Online Access:http://hdl.handle.net/10261/376930
https://api.elsevier.com/content/abstract/scopus_id/85101994631
Access Level:Open access
Keyword:Cellulose acetate
Electrospinning
Core/shell Structure
Kinetic release
cellulose acetate
Description
Summary:Core/shell electrospun mats based on cellulose acetate (CA) and polycaprolactone (PCL) were developed as novel active materials for releasing quercetin (Quer) and curcumin (Cur). The effect of polymeric uniaxial and coaxial electrospun systems and the chemical structures of Quer and Cur on the structural, thermal, and mass transfer properties of the developed mats were investigated. Release modelling indicated that the diffusion of the active agents from the uniaxial PCL fibers was highly dependent on the type of food simulant. Higher diffusion coefficients were obtained for both active agents in acid food simulant due to the higher swelling of the electrospun mats. In addition, CA/PCL coaxial structures slowed down the diffusion of both active agents into both food simulants. CA increased the retention of the active compounds in the polymer structure, resulting in partition coefficients values higher than the values obtained for uniaxial active PCL mats.