A simple and rapid process for multiscale printing of bioinks with dot widths ranging from hundreds of microns down to 0.5 mu m is presented. The process makes use of spontaneous surface charges generated pyroelectrically that are able to draw little daughter droplets directly from the free meniscus of a mother drop through jetting ("p-jet"), thus avoiding time-consuming and expensive fabrication of microstructured nozzles. Multiscale can be easily achieved by modulating the parameters of the p-jet process. Here, it is shown that the p-jet allows us to print well-defined adhesion islands where NIH-3T3 fibroblasts are constrained to live into cluster configurations ranging from 20 down to single cell level. The proposed fabrication approach can be useful for high-throughput studies on cell adhesion, cytoskeleton organization, and stem cell differentiation.
Simple and Rapid Bioink Jet Printing for Multiscale Cell Adhesion Islands / Mecozzi, L; Gennari, O; Rega, R; Battista, L; Ferraro, P; Grilli, S. - In: MACROMOLECULAR BIOSCIENCE. - ISSN 1616-5187. - 17:3(2017). [10.1002/mabi.201600307]
Simple and Rapid Bioink Jet Printing for Multiscale Cell Adhesion Islands
Mecozzi LPrimo
;
2017
Abstract
A simple and rapid process for multiscale printing of bioinks with dot widths ranging from hundreds of microns down to 0.5 mu m is presented. The process makes use of spontaneous surface charges generated pyroelectrically that are able to draw little daughter droplets directly from the free meniscus of a mother drop through jetting ("p-jet"), thus avoiding time-consuming and expensive fabrication of microstructured nozzles. Multiscale can be easily achieved by modulating the parameters of the p-jet process. Here, it is shown that the p-jet allows us to print well-defined adhesion islands where NIH-3T3 fibroblasts are constrained to live into cluster configurations ranging from 20 down to single cell level. The proposed fabrication approach can be useful for high-throughput studies on cell adhesion, cytoskeleton organization, and stem cell differentiation.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.