Loading…

Controlled drug release from electrospun PCL non-woven scaffolds via multi-layering and e-beam treatment

[Display omitted] •Pure polymer barrier layers decrease drug release rate from drug-loaded scaffolds.•E-beam irradiation increases the amount of drug released from scaffolds.•Burst release from electrospun fibers is not prevented by e-beam irradiation.•E-beam treatment does not impair PCL scaffolds’...

Full description

Saved in:
Bibliographic Details
Published in:Materials today communications 2021-03, Vol.26, p.102134, Article 102134
Main Authors: Volokhova, Apollinariya A., Kudryavtseva, Valeriya L., Spiridonova, Tatiana I., Kolesnik, Ilya, Goreninskii, Semen I., Sazonov, Roman V., Remnev, Gennady E., Tverdokhlebov, Sergei I.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:[Display omitted] •Pure polymer barrier layers decrease drug release rate from drug-loaded scaffolds.•E-beam irradiation increases the amount of drug released from scaffolds.•Burst release from electrospun fibers is not prevented by e-beam irradiation.•E-beam treatment does not impair PCL scaffolds’ thermal or mechanical properties. Currently, electrospun synthetic bioresorbable polymer scaffolds are applied in regenerative medicine and tissue engineering as targeted drug delivery devices because of their mechanical and physico-chemical properties. To control the rate of polymer degradation and drug release from polymer scaffolds, surface modification techniques are widely used. In this study, paracetamol-loaded poly (ε-caprolactone) electrospun fibrous scaffolds were treated by the pulsed electron beam irradiation. Pure control PCL scaffold, as well as scaffolds with four paracetamol concentrations (2 wt./wt. %, 8 wt./wt. %, 16 wt./wt. %, and 32 wt./wt.%) were modified. The mechanical and chemical properties and morphology of modified materials were examined. The sustained release of the model drug over a period of one hour for both non-treated and treated samples was demonstrated. It was shown that treatment leads to an increase in drug release rate and does not change surface morphology of scaffolds and fibers diameter distribution.
ISSN:2352-4928
2352-4928
DOI:10.1016/j.mtcomm.2021.102134