High Throughput,Polymeric Aqueous Two‐Phase Printing of Tumor Spheroids |
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| Authors: | Ehsan Atefi Stephanie Lemmo Darcy Fyffe Gary D. Luker Hossein Tavana |
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| Affiliation: | 1. Department of Biomedical Engineering, The University of Akron, Akron, OH, USA;2. Department of Radiology, University of Michigan, Ann Arbor, MI, USA;3. Department of Microbiology and Immunology, University of Michigan, Ann Arbor, MI, USA;4. Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA |
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| Abstract: | This paper presents a new 3D culture microtechnology for high throughput production of tumor spheroids and validates its utility for screening anti‐cancer drugs. Two immiscible polymeric aqueous solutions are used and a submicroliter drop of the “patterning” phase containing cells is microprinted into a bath of the “immersion” phase. Selecting proper formulations of biphasic systems using a panel of biocompatible polymers results in the formation of a round drop that confines cells to facilitate spontaneous formation of a spheroid without any external stimuli. Adapting this approach to robotic tools enables straightforward generation and maintenance of spheroids of well‐defined size in standard microwell plates and biochemical analysis of spheroids in situ, which is not possible with existing techniques for spheroid culture. To enable high throughput screening, a phase diagram is established to identify minimum cell densities within specific volumes of the patterning drop to result in a single spheroid. Spheroids show normal growth over long‐term incubation and dose‐dependent decrease in cellular viability when treated with drug compounds, but present significant resistance compared to monolayer cultures. The unprecedented ease of implementing this microtechnology and its robust performance will benefit high throughput studies of drug screening against cancer cells with physiologically relevant 3D tumor models. |
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| Keywords: | aqueous two‐phase system 3D cultures tumor spheroid high throughput drug screening |
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