Bioprinted chitosan-gelatin thermosensitive hydrogels using an inexpensive 3D printer

• Published in: Biofabrication Vol. 10; no. 1; pp. 015002 - 15015
• Main Authors: Roehm, Kevin D, Madihally, Sundararajan V
• Format: Journal Article
• Language: English
• Published: England IOP Publishing 01.01.2018
• Subjects: 3D printer; Animals; Bioprinting; Cell Line, Tumor; Cell Shape; Cell Survival; cells; chitosan; Chitosan - chemistry; gelatin; Gelatin - chemistry; Humans; hydrogel; Hydrogels - chemistry; Printing, Three-Dimensional - instrumentation; Rheology; Solutions; sterile printing; Sus scrofa; Temperature
• ISSN: 1758-5090; 1758-5090
• DOI: 10.1088/1758-5090/aa96dd

The primary bottleneck in bioprinting cell-laden structures with carefully controlled spatial relation is a lack of biocompatible inks and printing conditions. In this regard, we explored using thermogelling chitosan-gelatin (CG) hydrogel as a novel bioprinting ink; CG hydrogels are unique in that it undergoes a spontaneous phase change at physiological temperature, and does not need post-processing. In addition, we used a low cost (<$800) compact 3D printer, and modified with a new extruder to print using disposable syringes and hypodermic needles. We investigated (i) the effect of concentration of CG on gelation characteristics, (ii) solution preparation steps (centrifugation, mixing, and degassing) on printability and fiber formation, (iii) the print bed temperature profiles via IR imaging and grid-based assessment using thermocouples, (iv) the effect of feed rate (10-480 cm min−1), flow rate (15-60 l min−1) and needle height (70-280 m) on fiber size and characteristics, and (v) the distribution of neuroblastoma cells in printed fibers, and the viability after five days in culture. We used agarose gel to create uniform print surfaces to maintain a constant gap with the needle tip. These results showed that degassing the solution, and precooling the solution was necessary for obtaining continuous fibers. Fiber size decreased from 760, to 243 m as the feed rate increased from 10 to 100 cm min−1. Bed temperature played the greatest role in fiber size, followed by feed rate. Increased needle height initially decreased fiber size but then increased showing an optimum. Cells were well distributed within the fibers and exhibited excellent viability and no contamination after 5 d. Overall we printed 3D, sterile, cell-laden structures with an inexpensive bioprinter and a novel ink, without post-processing. The bioprinter described here and the novel CG hydrogels have significant potential as an ink for bioprinitng various cell-laden structures.