Event Abstract Back to Event Covalent incorporation of biomolecules for improving functional properties of freestanding conductive hydrogels Alexander Patton1, Rylie A. Green1 and Laura A. Poole-Warren1 1 University of New South Wales, Graduate School of Biomedical Engineering, Australia Introduction: Soft conductive materials have great potential for biomedical applications, in particular those dependent on electrical stimulation of neural and cardiac tissues. Previous research has demonstrated the feasibility of growth of the conducting polymer (CP), poly(3,4-ethylenedioxythiophene) (PEDOT) through a hydrogel with chemically synthesised dispersions of coupled CP:dopant for nucleation[1]. Despite proof-of-concept that such soft electroactive materials can be formed without a metal substrate, the electrodeposition is lengthy and the resulting electrical properties of the conducting hydrogels (CH) are significantly lower than CPs alone[1]. The aim of this study was to investigate the impact of biological molecule incorporation on the properties of freestanding conductive hydrogels. Two aspects were investigated: (i) the use of the anionic glycosaminoglycan (GAG), heparin, as a doping molecule and (ii) the addition of the non-doping cell attachment protein, gelatin. Previous studies evidence the incorporation of gelatin into hydrogels as a support for the adherence of neural cells[2]. Methods: Methacrylate modified poly(vinyl alcohol) (PVA-MA) control hydrogels (20 wt%) with 0.5 wt% chemically synthesised PEDOT:poly(styrene sulfonate) (PEDOT:PSS)[3] were formed by photo-initiated crosslinking[1],[4]. As reported previously the PEDOT:PSS is added to enable secondary nucleation sites within the gels. Test hydrogels were formed in the same way but with the addition of 18 wt% PVA-MA and 2 wt% methacrylated heparin[1],[4]. Electrodeposition of CP in control and test hydrogels was conducted at 1mA/cm2 for 0 to 160 minutes in 0.03 M EDOT monomer solution. Electrical properties were analysed using electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). Hydrogel stiffness was measured by compression tests (50 N load cell, 0.5 mm/min, loaded to failure). PC12 cells were used as a neuron-like cell model to assess adhesion and neurite viability at 96 hours. This was examined on 4 different gels: with and without gelatin loading; and with and without 40 minutes of electrodeposited PEDOT. Results and Discussion: As shown in Table 1, no differences to the modulus of elasticity were seen when undertaking electrodeposition of CP through the gels, likely caused by the fact that the mass of the PVA is much greater relative to the PEDOT component. The incorporation of heparin as a bound dopant significantly improved the electroactivity of the standalone hydrogels as shown in Table 2. This is hypothesised to be due to the presence of bound heparin which has been shown to act as an effective dopant in CPs[4]. Gelatin was observed to promote cellular adherence across gels both with and without PEDOT grown through them, with greater viability observed in these cases. Table 1: Characteristics of non-heparin loaded PEDOT:PSS hydrogels Table 2: Electroactivity differences produced with addition of heparin to PEDOT:PSS gels Conclusions: The incorporation of heparin into these gels significantly improves the ability of electrodeposited conducting polymer to form and develop conductive pathways. The incorporation of gelatin significantly promotes cell adhesion and viability. It was also seen here that the formation of PEDOT through the gels does not significantly impact the mechanics, making them a conductive system with soft, tailorable mechanics.
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