Porous chitosan adhesives with L-DOPA for enhanced photochemical tissue bonding.


Journal

Acta biomaterialia
ISSN: 1878-7568
Titre abrégé: Acta Biomater
Pays: England
ID NLM: 101233144

Informations de publication

Date de publication:
01 01 2020
Historique:
received: 22 05 2019
revised: 27 09 2019
accepted: 30 10 2019
pubmed: 5 11 2019
medline: 6 1 2021
entrez: 5 11 2019
Statut: ppublish

Résumé

L-3,4-dihydroxyphenylalanine (L-DOPA) is a naturally occurring catechol that is known to increase the adhesive strength of various materials used for tissue repair. With the aim of fortifying a porous and erodible chitosan-based adhesive film, L-DOPA was incorporated in its fabrication for stronger photochemical tissue bonding (PTB), a repair technique that uses light and a photosensitiser to promote tissue adhesion. The results showed that L-DOPA did indeed increase the tissue bonding strength of the films when photoactivated by a green LED, with a maximum strength recorded of approximately 30 kPa, 1.4 times higher than in its absence. The addition of L-DOPA also did not appreciably change the swelling, mechanical and erodible properties of the film. This study showed that strong, porous and erodible adhesive films for PTB made from biocompatible materials can be obtained through a simple inclusion of a natural additive such as L-DOPA, which was simply mixed with chitosan without any chemical modifications. In vitro studies using human fibroblasts showed no negative effect on cell proliferation indicating that these films are biocompatible. The films are convenient for various surgical applications as they can provide strong tissue support and a microporous environment for cellular infusion without the use of sutures. STATEMENT OF SIGNIFICANCE: Tissue adhesives are not as strong as sutures on wounds under stress. Our group has previously demonstrated that strong sutureless tissue repair can be realised with chitosan-based adhesive films that photochemically bond to tissue when irradiated with green light. The advantage of this technique is that films are easier to handle than glues and sutures, and their crosslinking reactions can be controlled with light. However, these films are not optimal for high-tension tissue regenerative applications because of their non-porous structure, which cannot facilitate cell and nutrient exchange at the wound site. The present study resolves this issue, as we obtained a strong and porous photoactivated chitosan-based adhesive film, by simply using freeze drying and adding L-DOPA.

Identifiants

pubmed: 31683016
pii: S1742-7061(19)30734-2
doi: 10.1016/j.actbio.2019.10.046
pii:
doi:

Substances chimiques

Biocompatible Materials 0
Tissue Adhesives 0
Dihydroxyphenylalanine 63-84-3
Chitosan 9012-76-4

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

314-326

Informations de copyright

Copyright © 2019. Published by Elsevier Ltd.

Auteurs

Herleen Ruprai (H)

School of Science and Health, Western Sydney University, Locked Bag 1797, Penrith, NSW 2751, Australia. Electronic address: 17995131@student.westernsydney.edu.au.

Anu Shanu (A)

School of Medicine, Western Sydney University, Locked Bag 1797, Penrith, NSW 2751, Australia. Electronic address: a.shanu@westernsydney.edu.au.

Damia Mawad (D)

School of Materials Science and Engineering, University of New South Wales, Sydney, NSW 2052, Australia; Australian Centre for NanoMedicine, ARC Centre of Excellence in Convergent BioNano Science and Technology, and Centre for Advanced Macromolecular Design, University of New South Wales, Sydney, NSW 2052, Australia. Electronic address: damia.mawad@unsw.edu.au.

James M Hook (JM)

Mark Wainwright Analytical Centre, University of New South Wales, Sydney, NSW 2052, Australia; School of Chemistry, University of New South Wales, Sydney, NSW 2052, Australia. Electronic address: j.hook@unsw.edu.au.

Kristopher Kilian (K)

School of Materials Science and Engineering, University of New South Wales, Sydney, NSW 2052, Australia; School of Chemistry, University of New South Wales, Sydney, NSW 2052, Australia. Electronic address: k.kilian@unsw.edu.au.

Laurel George (L)

Advanced Materials Characterization Facility, Western Sydney University, Locked Bag 1797, Penrith, NSW 2751, Australia. Electronic address: l.george@westernsydney.edu.au.

Richard Wuhrer (R)

Advanced Materials Characterization Facility, Western Sydney University, Locked Bag 1797, Penrith, NSW 2751, Australia. Electronic address: richard.wuhrer@westernsydney.edu.au.

Jessica Houang (J)

Biomedical Engineering, School of Aerospace, Mechanical and Mechatronic Engineering, University of Sydney, Sydney, NSW 2006, Australia. Electronic address: jhou5747@uni.sydney.edu.au.

Simon Myers (S)

School of Science and Health, Western Sydney University, Locked Bag 1797, Penrith, NSW 2751, Australia; School of Medicine, Western Sydney University, Locked Bag 1797, Penrith, NSW 2751, Australia. Electronic address: s.myers@westernsydney.edu.au.

Antonio Lauto (A)

School of Science and Health, Western Sydney University, Locked Bag 1797, Penrith, NSW 2751, Australia; School of Medicine, Western Sydney University, Locked Bag 1797, Penrith, NSW 2751, Australia; Biomedical Engineering and Neuroscience Research Group, The MARCS Institute, Western Sydney University, Locked Bag 1797, Penrith, NSW 2751, Australia. Electronic address: a.lauto@westernsydney.edu.au.

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Classifications MeSH