Skip to main content

Research Repository

Advanced Search

Mixed polymer and bioconjugate core/shell electrospun fibres for biphasic protein release

Adala, Inchirah; Ramis, Jopeth; Ntone Moussinga, Cynthia; Janowski, Isabella; Amer, Mahetab H.; Bennett, Andrew J.; Alexander, Cameron; Rose, Felicity R.A.J.

Mixed polymer and bioconjugate core/shell electrospun fibres for biphasic protein release Thumbnail


Authors

Inchirah Adala

Jopeth Ramis

Cynthia Ntone Moussinga

Isabella Janowski

Mahetab H. Amer

Profile Image

FELICITY ROSE FELICITY.ROSE@NOTTINGHAM.AC.UK
Professor of Biomaterials and Tissue Engineering



Abstract

Effective regenerative medicine requires delivery systems which can release multiple components at appropriate levels and at different phases of tissue growth and repair. However, there are few biomaterials and encapsulation techniques that are fully suitable for the loading and controlled release of multiple proteins. In this study we describe how proteins were physically and chemically loaded into a single coaxial electrospun fibre scaffold to obtain bi-phasic release profiles. Cyto-compatible polymers were used to construct the scaffold, using polyethylene oxide (PEO) for the core and polycaprolactone (PCL) reacted or mixed with (bis-aminopropyl)polyether (Jeffamine ED2003; JFA) for the shell. Horseradish peroxidase (HRP), a model protein, was loaded in the core and functionalised onto the scaffold surface by coupling of protein carboxyl groups to the available polymer amine groups. Fibre morphologies were evaluated by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) and functional group content was determined using X-ray photoelectron spectroscopy (XPS) and time-of-flight secondary ion mass spectrometry (TOF SIMS). Hydrophobicity profiles of the fibres before and after protein loading were evaluated by water contact angle (WCA) and the mechanical properties of the electrospun scaffolds were determined by performing tensile tests. The electrospun fibre scaffolds generated by reacting PEO/PCL with 1,6-diaminohexane and those from mixing PEO/PCL with JFA were further characterised for protein conjugation and release. Fibres prepared by the mixed PEO/PCL/JFA system were found to be the most appropriate for the simultaneous release of protein from the core and the immobilisation of another protein on the shell of the same scaffold. Moreover, JFA enhanced scaffold properties in terms of porosity and elasticity. Finally, we successfully demonstrated the cytocompatibility and cell response to protein-loaded and -conjugated scaffolds using HepG2 cells. Enhanced cell attachment (2.5 fold) was demonstrated using bovine serum albumin (BSA)-conjugated scaffolds, and increased metabolic activity observed with retinoic acid (RA)-loaded scaffolds (2.7 fold).

Citation

Adala, I., Ramis, J., Ntone Moussinga, C., Janowski, I., Amer, M. H., Bennett, A. J., …Rose, F. R. (2021). Mixed polymer and bioconjugate core/shell electrospun fibres for biphasic protein release. Journal of Materials Chemistry B, 9(20), 4120-4133. https://doi.org/10.1039/d1tb00129a

Journal Article Type Article
Acceptance Date May 3, 2021
Online Publication Date May 13, 2021
Publication Date May 28, 2021
Deposit Date May 14, 2021
Publicly Available Date May 14, 2021
Journal Journal of Materials Chemistry B
Print ISSN 2050-750X
Electronic ISSN 2050-7518
Publisher Royal Society of Chemistry
Peer Reviewed Peer Reviewed
Volume 9
Issue 20
Pages 4120-4133
DOI https://doi.org/10.1039/d1tb00129a
Keywords General Materials Science; General Chemistry; Biomedical Engineering; General Medicine
Public URL https://nottingham-repository.worktribe.com/output/5529995
Publisher URL https://pubs.rsc.org/en/Content/ArticleLanding/2021/TB/D1TB00129A

Files





You might also like



Downloadable Citations