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Solazzo, M.

Publications and source records attributed to Solazzo, M..

2 recordsLinked to original sources

A guide to the manufacture of sustainable, ready to use in vitro platforms for the electric-field pacing of cellularised 3D porous scaffolds

Electrical activity is a key feature of most native tissues, with the most notable examples being the nervous and the cardiac systems. Modern medicine has moved towards the mimicking and regenerations of such systems both with in vitro models and therapies. Although researchers have now an increased repertoire of cell types and bio-physical cues to generate increasingly complex in vitro models, the inclusion of novel biomaterials in such systems has been negligible, with most approaches relying on scaffold-free self-assembling strategies. However, the rapid development of functional biomaterials and fabrication technologies - such as electroconductive scaffolds - warrants consideration and inclusion of materials, with recent evidence supporting the benefit of incorporating electrically active materials and their influence on the maturation of cardiac cells and tissues. In order to be manipulated in bioreactor systems, scaffold-based in vitro models require bespoke rig and bioreactors that vary from those commonly used for scaffold-free systems. In this work, we detail methods to rapid prototype an electrical pacing bioreactor and R3S - a Rig for Stimulation of Sponge-like Scaffolds. As a proof of concept and validation we demonstrate that these systems are compatible with isotropic and anisotropic porous scaffolds composed of collagen or poly(3,4-ethylene dioxythiophene):polystyrene sulfonate (PEDOT:PSS). External pacing of C3H10 cells on anisotropic porous scaffolds led to a metabolic increase and enhanced cell alignment. This setup has been designed for pacing and simultaneously live tracking of in vitro models. This platform has wide suitability for the study of electrical pacing of cellularized scaffolds in 3D in vitro cultures.

bioengineering↗

Shell Microelectrode Arrays (MEAs) for brain organoids

Brain organoids are important models for mimicking some three-dimensional (3D) cytoarchitectural and functional aspects of the brain. Multielectrode arrays (MEAs) that enable recording and stimulation of activity from electrogenic cells are widely utilized in biomedical engineering. However, conventional MEAs, initially designed for monolayer cultures, offer limited recording contact area restricted to the bottom of the 3D organoids. Inspired by the shape of electroencephalography (EEG) caps, we developed miniaturized chip-integrated MEA caps for organoids. The optically transparent shells are composed of self-folding polymer leaflets with conductive polymer-coated metal electrodes. Tunable folding of the minicaps polymer leaflets guided by mechanics simulations enables versatile recording from organoids of different sizes and we validate the feasibility of electrophysiology recording from 400-600 {micro}m sized organoids for up to four weeks and in response to glutamate stimulation. Our studies suggest that 3D shell MEAs offer significant potential for high signal-to-noise and 3D spatiotemporal brain organoid recording.

bioengineering↗