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Abstract Electrically conductive scaffolds, mimicking the unique directional alignment of muscle fibers in the myocardium, are fabricated using the 3D printing micro-stereolithography technique. Polyethylene glycol diacrylate (photo-sensitive polymer), Irgacure 819 (photo-initiator), curcumin (dye) and polyaniline (conductive polymer) are blended to make the conductive ink that is crosslinked using free radical photo-polymerization reaction. Curcumin acts as a liquid filter and prevents light from penetrating deep into the photo-sensitive solution and plays a central role in the 3D printing process. The obtained scaffolds demonstrate well defined morphology with an average pore size of 300 ± 15 μm and semi-conducting properties with a conductivity of ~ 10–6 S/m. Cyclic voltammetry analyses detect the electroactivity and highlight how the electron transfer also involve an ionic diffusion between the polymer and the electrolyte solution. Scaffolds reach their maximum swelling extent 30 min after immersing in the PBS at 37 °C and after 4 weeks they demonstrate a slow hydrolytic degradation rate typical of polyethylene glycol network. Conductive scaffolds display tunable conductivity and provide an optimal environment to the cultured mouse cardiac progenitor cells.

Additive manufacturing (AM), or 3D printing processes, is introducing new possibilities in electronic, biomedical, sensor-designing, and wearable technologies. In this context, the present work focuses on the development of flexible 3D-printed polyethylene glycol diacrylate (PEGDA)- sulfonated polyaniline (PANIs) electrically conductive hydrogels (ECHs) for pH-monitoring applications. PEGDA platforms are 3D printed by a stereolithography (SLA) approach. Here, we report the successful realization of PEGDA–PANIs electroconductive hydrogel (ECH) composites produced by an in situ chemical oxidative co-polymerization of aniline (ANI) and aniline 2-sulfonic acid (ANIs) monomers at a 1:1 equimolar ratio in acidic medium. The morphological and functional properties of PEGDA–PANIs are compared to those of PEGDA–PANI composites by coupling SEM, swelling degree, I–V, and electro–chemo–mechanical analyses. The differences are discussed as a function of morphological, structural, and charge transfer/transport properties of the respective PANIs and PANI filler. Our investigation showed that the electrochemical activity of PANIs allows for the exploitation of the PEGDA–PANIs composite as an electrode material for pH monitoring in a linear range compatible with that of most biofluids. This feature, combined with the superior electromechanical behavior, swelling capacity, and water retention properties, makes PEGDA–PANIs hydrogel a promising active material for developing advanced biomedical, soft tissue, and biocompatible electronic applications.

Abstract This study is devoted to synthesizing and modifying conductive Ti‐doped diamond (TiD) biosubstrates with polyaniline (PANI) to provide a soft interface with high ionic conductivity and charge storage capacity for developing advanced scaffolds and implantable electrode materials. The diamond supports are prepared by an ad‐hoc chemical vapor deposition methodology allowing for the synthesis and contemporary doping of diamond lattice. An optimized potentiostatic electropolymerization method assures the growth of a homogenous PANI coating on a diamond surface. Scanning electron microscopy, atomic force microscopy, Raman, and reflectance infrared spectroscopy characterizations guarantee the production of nanostructured diamond layers with high surface electrical conductivity and good phase quality as well as of a rough polymer film in the conductive emeraldine form. Cyclic voltammetry and electrochemical impedance spectroscopy measurements point out a quasi‐reversible electron transfer among polymer chains ruled by the bulky dodecyl sulfate anion chosen as polymer dopant. This induces a cation exchange with the solution upon backbone redox reactions. The capability of the PANI‐TiD system to transduce ionic current into electronic current and vice versa via redox reaction with the surroundings can be reliably exploited to reproduce electrical stimulation processes through which to mimic the original bioelectricity functions of the human body for advanced biomedical applications.

Designing fully green materials for flexible electronics is an urgent need due to the growing awareness of an environmental crisis. With the aim of developing a sustainable, printable, and biocompatible material to be exploited in flexible electronics, the rheological, structural and charge transport properties of water-based hydroxypropyl cellulose (HPC)-detonation nanodiamond (DND) viscous dispersions are investigated. A rheological investigation disclosed that the presence of the DND affects the orientation and entanglement of cellulose chains in the aqueous medium. In line with rheological analyses, the NMR diffusion experiments pointed out that the presence of DND modifies the hydrodynamic behavior of the cellulose molecules. Despite the increased rigidity of the system, the presence of DND slightly enhances the ionic conductivity of the dispersion, suggesting a modification in the charge transport properties of the material. The electrochemical analyses, performed through Cyclic Voltammetry (CV) and Electrochemical Impedance Spectroscopy (EIS), revealed that the HPC-DND system is remarkably stable in the explored voltage range (−0.1 to +0.4 V) and characterized by a lowered bulk resistance with respect to HPC. Such features, coupled with the printability and filmability of the material, represent good requirements for the exploitation of such systems in flexible electronic applications.