Metadata
Title
Functionalisation of PLLA with polymer brushes to trigger the assembly of fibronectin into nanonetworks
Category
general
UUID
1bcf033bed76409b99ff0f31142717b7
Source URL
https://eprints.gla.ac.uk/176060/
Parent URL
https://eprints.gla.ac.uk/view/project_code/303613.html
Crawl Time
2026-03-11T05:50:46+00:00
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Functionalisation of PLLA with polymer brushes to trigger the assembly of fibronectin into nanonetworks

Source: https://eprints.gla.ac.uk/176060/ Parent: https://eprints.gla.ac.uk/view/project_code/303613.html

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Functionalisation of PLLA with polymer brushes to trigger the assembly of fibronectin into nanonetworks

Sprott, Mark Robert ORCID: https://orcid.org/0000-0002-1990-9498, Gallego-Ferrer, Gloria, Dalby, Matthew J. ORCID: https://orcid.org/0000-0002-0528-3359, Salmeron-Sanchez, Manuel ORCID: https://orcid.org/0000-0002-8112-2100 and Cantini, Marco ORCID: https://orcid.org/0000-0003-0326-1508 (2019) Functionalisation of PLLA with polymer brushes to trigger the assembly of fibronectin into nanonetworks. Advanced Healthcare Materials, 8(3), 1801469. (doi: 10.1002/adhm.201801469) (PMID:30609243)

Preview Text 176060.pdf - Published Version Available under License Creative Commons Attribution. 2MB

Abstract

Poly‐l‐lactic acid (PLLA) has been used as a biodegradable polymer for many years; the key characteristics of this polymer make it a versatile and useful resource for regenerative medicine. However, it is not inherently bioactive. Thus, here, a novel process is presented to functionalize PLLA surfaces with poly(ethyl acrylate) (PEA) brushes to provide biological functionality through PEA's ability to induce spontaneous organization of the extracellular matrix component fibronectin (FN) into physiological‐like nanofibrils. This process allows control of surface biofunctionality while maintaining PLLA bulk properties (i.e., degradation profile, mechanical strength). The new approach is based on surface‐initiated atomic transfer radical polymerization, which achieves a molecularly thin coating of PEA on top of the underlying PLLA. Beside surface characterization via atomic force microscopy, X‐ray photoelectron spectroscopy and water contact angle to measure PEA grafting, the biological activity of this surface modification is investigated. PEA brushes trigger FN organization into nanofibrils, which retain their ability to enhance adhesion and differentiation of C2C12 cells. The results demonstrate the potential of this technology to engineer controlled microenvironments to tune cell fate via biologically active surface modification of an otherwise bioinert biodegradable polymer, gaining wide use in tissue engineering applications.

Item Type: Articles
Status: Published
Refereed: Yes
Glasgow Author(s) Enlighten ID: Sprott, Dr Mark and Dalby, Professor Matthew and Salmeron-Sanchez, Professor Manuel and Cantini, Dr Marco
Authors: Sprott, M. R., Gallego-Ferrer, G., Dalby, M. J., Salmeron-Sanchez, M., and Cantini, M.
College/School: College of Medical Veterinary and Life Sciences > School of Molecular Biosciences College of Science and Engineering > School of Engineering > Biomedical Engineering
Journal Name: Advanced Healthcare Materials
Publisher: Wiley
ISSN: 2192-2640
ISSN (Online): 2192-2659
Published Online: 04 January 2019
Copyright Holders: Copyright © 2019 The Authors
First Published: First published in Advanced Healthcare Materials 8(3):1801469
Publisher Policy: Reproduced under a Creative Commons License
Data DOI: 10.5525/gla.researchdata.715

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Funder and Project Information

Funder and Project Information

Funder and Project Information

Project Code

Award No

Project Name

Principal Investigator

Funder's Name

Funder Ref

Lead Dept

72206

1

Engineering growth factor microenvironments- a new therapeutic paradigm for regenerative medicine

Manuel Salmeron-Sanchez

Engineering and Physical Sciences Research Council (EPSRC)

EP/P001114/1

ENG - BIOMEDICAL ENGINEERING

303613

0

Engineered microenvironments to harvest stem cell response to viscosity for cartilage repair

Marco Cantini

Medical Research Council (MRC)

MR/S005412/1

ENG - Biomedical Engineering

47056

3

DTC in cell and proteomic technologies (continuation)

Jonathan Cooper

Engineering and Physical Sciences Research Council (EPSRC)

EP/F500424/1

ENG - BIOMEDICAL ENGINEERING

Deposit and Record Details

Deposit and Record Details

Deposit and Record Details

ID Code: 176060
Depositing User: Ms Jacqui Brannan
Datestamp: 19 Dec 2018 10:49
Last Modified: 02 May 2025 20:13
Date of acceptance: 18 December 2018
Date of first online publication: 4 January 2019
Date Deposited: 19 December 2018
Data Availability Statement: Yes

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