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Biology subjects

Semar, B. A.

Publications and source records attributed to Semar, B. A..

2 recordsLinked to original sources

PEDOT:PSS Microparticles for Extrudable and Bioencapsulating Conducting Granular Hydrogel Bioelectronics

Conducting hydrogels are promising materials for forming physiomimetic bioelectronic interfaces to monitor and stimulate biological activity. However, most developed materials are non-microporous and possess fixed shapes, both of which can limit the integration of cells and tissues with devices. In non-conducting biomaterials, materials fabrication strategies imparting microporosity and dynamic mechanical properties have been shown to support cell infiltration and support biointerfaces of various geometries. Specifically, granular hydrogels have enabled encapsulating, conformal, and injectable interfaces through these features. However, granular hydrogels remain largely unexplored as conducting biomaterials. We present methods for fabricating spherical, poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) hydrogel microparticles. When densely packed, these microparticles form a conducting granular hydrogel with microporosity as well as shear-thinning and self-healing dynamic mechanical properties. The PEDOT:PSS granular hydrogel can be extruded and maintain structure post-3D printing. Modulating microparticle PSS content achieves high granular hydrogel conductivity (137 S/m), and microparticles exhibit excellent cytocompatibility (>98% viability). Finally, we demonstrate utility as bioencapsulating electrodes for electrophysiological monitoring. These results highlight the functionality of our PEDOT:PSS conducting granular hydrogel, suggesting its potential as 3D printed bioencapsulating electrodes, 3D tissue engineering scaffolds for monitoring encapsulated cells, and injectable therapies for enhanced cell recruitment and tissue regeneration combined with electronic stimulation.

bioengineering↗

3D printed bioelectronic scaffolds with soft tissue-like stiffness

3D printing is a leading technique for fabricating tissue engineering scaffolds that facilitate native cellular behavior. Engineering scaffolds to possess functional properties like electronic conductivity is the first step towards integrating new technological capabilities like stimulating or monitoring cellular activity beyond the traditionally presented biophysical and biochemical cues. However, these bioelectronic scaffolds have been largely underdeveloped since the majority of electrically conducting materials possess high stiffness values outside the physiological range and that may negatively impact desired cell behavior. Here, we present methods of 3D printing poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) hydrogel scaffolds and provide techniques to achieve stiffness relevant to many soft tissues (<100 kPa). Structures were confirmed as ideal tissue scaffolds by maintaining biostability and promoting high cell viability, appropriate cell morphology, and proliferation. With these findings, we contribute a customizable 3D platform that provides favorable soft cellular microenvironments and envision it to be adaptable to several bioelectronic applications.

bioengineering↗