Flexible conductive graphene/polyurethane composite films for biomedical applications

石墨烯 聚氨酯 复合数 材料科学 导电体 复合材料 纳米技术
作者
Kaur Gagan,Raju Adhikari,Cass Peter,Bown Mark,V. Aditya,Gunatillake Pathiraja
出处
期刊:Frontiers in Bioengineering and Biotechnology [Frontiers Media]
卷期号:4 被引量:1
标识
DOI:10.3389/conf.fbioe.2016.01.01877
摘要

Event Abstract Back to Event Flexible conductive graphene/polyurethane composite films for biomedical applications Gagan Kaur1*, Raju Adhikari1, Peter Cass1, Mark Bown1, Aditya V. Vashi1 and Pathiraja Gunatillake1 1 CSIRO, Manufacturing Flagship, Australia Introduction: Electrically conductive polymeric materials have recently attracted considerable interest from researchers to explore their potential in biomedical applications such as in biosensors, biomedical implants and tissue engineering[1],[2]. Polyurethanes (PUs) composites incorporating conductive particles are of particular interest to make conductive materials because of their good biocompatibility, processability and excellent mechanical properties[3],[4]. In the present work, composites of graphene and a siloxane PU (Elast-Eon™) were prepared for the first time for potential use in biomedical applications. Elast-Eon™ was chosen because of its well established biostability and use in implant devices[5]. The composites were evaluated for their electrical conductivity, mechanical properties, thermal stability and cell viability. Materials and Methods: Elast-EonTM (E2A) and graphene were obtained from Aortech Biomaterials and ACS Materials, respectively. The composites were prepared by solution mixing method using THF and compression moulded into films of ~100 µm thickness. The electrical conductivity was determined using a two-point probe method using Ag electrodes to facilitate electrical contact. Tensile testing was carried out with an Instron 5565 Testing Machine and a Mettler Toledo TGA/SDTA 851 was used for thermogravimetric analysis (TGA). The in vitro cytotoxicity was assessed using an MTT assay and live-dead viability kit was used to examine the cell adhesion (L929 cells) on the surface of composite films Results and Discussion: The graphene/PU composites were prepared using different methods i.e. solution mixing, melt processing and in situ polymerisation. The solution mixing method was found to be best because it resulted in the composites with higher electrical conductivity. Using this method, composites were prepared with varying content of graphene and their electrical conductivity was determined (Figure 1). A conductivity of 1.1 × 10-3 S cm-1 was achieved with 5 wt% loading of graphene and a maximum conductivity of 5.9 × 10-2 S cm-1 was obtained for composites with graphene content of 15 wt%. In an attempt to improve the conductivity of composite films we examined the effect of cooling rate during compression moulding as well as annealing of composite films (Figure 1). Both of these approaches were found to significantly improve the conductivity of composites with lower graphene content (≤5 wt%). The enhanced conductivity may be attributed to the re-alignment of graphene sheets which promotes the formation of macroscopic conductive networks[6]. The tensile test results showed that composites possessed a tensile strength of about 11 MPa, 58% less compared to control PU. The modulus of the composites was found to increase to 48 MPa as expected due to graphene sheets working as fillers (Figure 2a). The TGA results showed that the film was thermally stable up to ~250 °C (Figure 2b). Furthermore, the films did not show significant cytotoxicity in indirect cytotoxicity tests. The in vitro cell viability assay tests also suggested that although the composite surface was not ideal for cell adhesion, the graphene/PU composite surface was not cytotoxic to living cells (Figure 3). Conclusions: Conductive composites of graphene and a siloxane polyurethane were prepared using solution mixing. The composites exhibited good mechanical and thermal properties with an electrical conductivity of 1.1 × 10-3 S cm-1 with 5 wt% loading of graphene. In addition, cell-based cytotoxicity tests showed that composites were not cytotoxic. The authors would like to acknowledge the financial support provided by CSIRO Office of Chief Executive Postdoctoral Program. The authors would also like to acknowledge Dr Ajay Padsalgikar of St Jude Medical for providing Elast-Eon™ Samples and Dr Gavin Collis for his advice and fruitful discussions.References:[1] J. Jagur-Grodzinski, E-Polymers, 2012, 12, 722-740.[2] G. Kaur, R. Adhikari, P. Cass, M. Bown and P. Gunatillake, RSC Adv., 2015, 5, 37553-37567.[3] S. Gogolewski, Colloid. Polym. Sci., 1989, 267, 757-785.[4] A. Silvestri, P. M. Serafini, S. Sartori, P. Ferrando, F. Boccafoschi, S. Milione, L. Conzatti and G. Ciardelli, J. Appl. Polym. Sci., 2011, 122, 3661-3671.[5] A. Simmons, J. Hyvarinen, R. A. Odell, D. J. Martin, P. A. Gunatillake, K. R. Noble and L. A. Poole-Warren, Biomaterials, 2004, 25, 4887-4900.[6] J. Yu, L. Q. Zhang, M. Rogunova, J. Summers, A. Hiltner and E. Baer, J. Appl. Polym. Sci., 2005, 98, 1799-1805. Keywords: composite, material design, biomedical application, Polymeric material Conference: 10th World Biomaterials Congress, Montréal, Canada, 17 May - 22 May, 2016. Presentation Type: Poster Topic: Composites: polymeric, ceramic and metallic Citation: Kaur G, Adhikari R, Cass P, Bown M, Vashi AV and Gunatillake P (2016). Flexible conductive graphene/polyurethane composite films for biomedical applications. Front. Bioeng. Biotechnol. Conference Abstract: 10th World Biomaterials Congress. doi: 10.3389/conf.FBIOE.2016.01.01877 Copyright: The abstracts in this collection have not been subject to any Frontiers peer review or checks, and are not endorsed by Frontiers. They are made available through the Frontiers publishing platform as a service to conference organizers and presenters. The copyright in the individual abstracts is owned by the author of each abstract or his/her employer unless otherwise stated. Each abstract, as well as the collection of abstracts, are published under a Creative Commons CC-BY 4.0 (attribution) licence (https://creativecommons.org/licenses/by/4.0/) and may thus be reproduced, translated, adapted and be the subject of derivative works provided the authors and Frontiers are attributed. For Frontiers’ terms and conditions please see https://www.frontiersin.org/legal/terms-and-conditions. Received: 27 Mar 2016; Published Online: 30 Mar 2016. * Correspondence: Dr. Gagan Kaur, CSIRO, Manufacturing Flagship, Clayton, Australia, Email1 Login Required This action requires you to be registered with Frontiers and logged in. To register or login click here. Abstract Info Abstract The Authors in Frontiers Gagan Kaur Raju Adhikari Peter Cass Mark Bown Aditya V Vashi Pathiraja Gunatillake Google Gagan Kaur Raju Adhikari Peter Cass Mark Bown Aditya V Vashi Pathiraja Gunatillake Google Scholar Gagan Kaur Raju Adhikari Peter Cass Mark Bown Aditya V Vashi Pathiraja Gunatillake PubMed Gagan Kaur Raju Adhikari Peter Cass Mark Bown Aditya V Vashi Pathiraja Gunatillake Related Article in Frontiers Google Scholar PubMed Abstract Close Back to top Javascript is disabled. Please enable Javascript in your browser settings in order to see all the content on this page.

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