Abstract
AbstractPolydimethylsiloxane (PDMS), commonly used in organ-on-a-chip (OoC) systems, faces limitations in replicating complex geometries, hindering its effectiveness in creating 3D OoC models. In contrast, poly(ethylene glycol)diacrylate (PEGDA-250), favored for its fabrication ease and resistance to small molecule absorption, is increasingly used for 3D printing microfluidic devices. However, its application in cell culture has been limited due to poor cell adhesion. Here, we introduce a nanoporous PEGDA ink (P-PEGDA) designed to enhance cell adhesion. P-PEGDA is formulated with a porogen, photopolymerized, followed by the removal of the porogen. Utilizing P-PEGDA, complex microstructures and membranes as thin as 27 µm were 3D-printed. Porogen concentrations from 10% to 30% were tested yielding constructs with increasing porosity, and without compromising printing resolution. Our tests across four cell lines showed over 80% cell viability, with a notable 52-fold increase in MDA-MB-231 cell coverage compared to non-porous PEGDA. Finally, we introduce an OoC model comprising a gyroid scaffold with a central opening filled with a cancer spheroid. This setup, after a 14-day co-culture, demonstrated significant endothelial sprouting and integration within the spheroid. The P-PEGDA is suitable for high-resolution 3D printing of constructs for 3D cell culture and OoC owing to its printability, biocompatibility, and cell adhesion.
Publisher
Cold Spring Harbor Laboratory
Cited by
2 articles.
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