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EDTA enhances high‐throughput two‐dimensional bioprinting by inhibiting salt scaling and cell aggregation at the nozzle surface
Author(s) -
Parzel Cheryl A.,
Pepper Matthew E.,
Burg Timothy,
Groff Richard E.,
Burg Karen J. L.
Publication year - 2009
Publication title -
journal of tissue engineering and regenerative medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.835
H-Index - 72
eISSN - 1932-7005
pISSN - 1932-6254
DOI - 10.1002/term.162
Subject(s) - nozzle , chemistry , throughput , scaling , cell , nanotechnology , biophysics , materials science , computer science , engineering , biology , biochemistry , mathematics , mechanical engineering , telecommunications , geometry , wireless
Tissue‐engineering strategies may be employed in the development of in vitro breast tissue models for use in testing regimens of drug therapies and vaccines. The physical and chemical interactions that occur among cells and extracellular matrix components can also be elucidated with these models to gain an understanding of the progression of transformed epithelial cells into tumours and the ultimate metastases of tumour cells. The modified inkjet printer may be a useful tool for creating three‐dimensional (3D) in vitro models, because it offers an inexpensive and high‐throughput solution to microfabrication, and because the printer can be easily manipulated to produce varying tissue attributes. We hypothesized, however, that when ink is replaced with a biologically based fluid (i.e. a ‘bio‐ink’), specifically a serum‐free cell culture medium, printer nozzle failure can result from salt scale build‐up as fluid evaporates on the printhead surface. In this study, ethylene diamine tetra‐acetic acid (EDTA) was used as a culture medium additive to prevent salt scaling and cell aggregation during the bioprinting process. The results showed that EDTA, at a concentration typically found in commercially available trypsin solutions (0.53 m M ), prevented nozzle failure when a serum‐free culture medium was printed from a nozzle at 1000 drops/s. Furthermore, increasing concentrations of EDTA appeared to mildly decrease aggregation of 4T07 cells. Cell viability studies were performed to demonstrate that addition of EDTA did not result in significant cell death. In conclusion, it is recommended that EDTA be incorporated into bio‐ink solutions containing salts that could lead to nozzle failure. Copyright © 2009 John Wiley & Sons, Ltd.