Next Article in Journal
The Effect of Chondroitin Sulphate and Hyaluronic Acid on Chondrocytes Cultured within a Fibrin-Alginate Hydrogel
Previous Article in Journal
Silencing Bcl-2 Expression in Epithelial Cancer Cells Using “Smart” Particles
Article Menu

Export Article

Open AccessArticle
J. Funct. Biomater. 2014, 5(3), 183-196;

IPNs from Cyclodextrin:Chitosan Antioxidants: Bonding, Bio-Adhesion, Antioxidant Capacity and Drug Release

VTPCHEM PTY Ltd, Glenhuntly, Melbourne 3163, Australia
Oral and Dental Research Institute, Faculty of Dentistry, University of the Western Cape, Private Bag X1, Tygerberg 7505, Cape Town, South Africa
School of Material Science and Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China
These authors contributed equally to this work.
Author to whom correspondence should be addressed.
Received: 18 August 2014 / Revised: 1 September 2014 / Accepted: 9 September 2014 / Published: 17 September 2014
Full-Text   |   PDF [3743 KB, uploaded 17 September 2014]   |  


IPNs are unique “alloys” of cross-linked polymers in which at least one network is synthesized and/or cross-linked in the presence of the other. IPNs are also known as entanglements of polymer networks that are ideally held together only by permanent topological interactions. The objectives of this study are to evaluate novel chitosan-based functional drug delivery systems that can be successfully incorporated into “dual action bioactive tooth restorative materials”. These materials should be capable of inducing an improved wound healing prototype. The novel hydrogels will be investigated with respect to the antioxidant capacity of conventional antioxidants, such as resveratrol, b-carotene and propolis, as a designer drug delivery system, with the use of SEM imaging for the characterization of the surfaces, bio-adhesive property, antioxidant capacity, free radical defence, antioxidant, active ingredient stability and reactive features of novel materials. The additional benefit of the site-specific “functional restorative material” for use in dressings to deliver antibiotics to wound sites can provide tissue compatibility and reduced interference with wound healing. The materials were tested using an effective in vitro free radical generation model as functional additive prototypes for further development of “dual function restorative wound healing materials”. We quantified the effects of functional designer biomaterials on the dentin bond strength of a composite and evaluated the bio-adhesive capacity of the materials in the two separate “in vitro” systems. The added benefits of the chitosan/vitamin C/cyclodextrin (CD) host:guest complex-treated hydrogels involved a positive influence on the tetracycline release, increased dentin bond strength, as well as a demonstrated in vitro “built-in” free radical defence mechanism and, therefore, acting as a “proof of concept” for functional multi-dimensional restorative wound healing materials with a built-in free radical defence mechanism. Based on our results, we can conclude that the CD:chitosan-antioxidant-containing hydrogels are a suitable carrier for tetracycline to be slow-released. Within the limitations of the study design, chitosan-based hydrogels are suitable materials for functional restorative and wound healing applications in vitro. Cytotoxicity data are currently being evaluated in our laboratory. View Full-Text
Keywords: chitosan; β-cyclodextrin; antioxidants; cumulative release; free radical damage chitosan; β-cyclodextrin; antioxidants; cumulative release; free radical damage

Figure 1

This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).

Share & Cite This Article

MDPI and ACS Style

Perchyonok, V.T.; Grobler, S.R.; Zhang, S. IPNs from Cyclodextrin:Chitosan Antioxidants: Bonding, Bio-Adhesion, Antioxidant Capacity and Drug Release. J. Funct. Biomater. 2014, 5, 183-196.

Show more citation formats Show less citations formats

Related Articles

Article Metrics

Article Access Statistics



[Return to top]
J. Funct. Biomater. EISSN 2079-4983 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert
Back to Top