Please use this identifier to cite or link to this item: https://doi.org/10.1038/srep39140
Title: Hybrid microscaffold-based 3D bioprinting of multi-cellular constructs with high compressive strength: A new biofabrication strategy
Authors: Tan, Y.J 
Tan, X
Yeong, W.Y
Tor, S.B
Keywords: polyethylene glycol dimethacrylate hydrogel
animal
bioprinting
body temperature
cell line
cell proliferation
cell survival
chemistry
compressive strength
devices
human
procedures
three dimensional printing
tissue scaffold
Animals
Bioprinting
Body Temperature
Cell Line
Cell Proliferation
Cell Survival
Compressive Strength
Humans
Hydrogel, Polyethylene Glycol Dimethacrylate
Printing, Three-Dimensional
Tissue Scaffolds
Issue Date: 2016
Citation: Tan, Y.J, Tan, X, Yeong, W.Y, Tor, S.B (2016). Hybrid microscaffold-based 3D bioprinting of multi-cellular constructs with high compressive strength: A new biofabrication strategy. Scientific Reports 6 : 39140. ScholarBank@NUS Repository. https://doi.org/10.1038/srep39140
Rights: Attribution 4.0 International
Abstract: A hybrid 3D bioprinting approach using porous microscaffolds and extrusion-based printing method is presented. Bioink constitutes of cell-laden poly(D,L-lactic-co-glycolic acid) (PLGA) porous microspheres with thin encapsulation of agarose-collagen composite hydrogel (AC hydrogel). Highly porous microspheres enable cells to adhere and proliferate before printing. Meanwhile, AC hydrogel allows a smooth delivery of cell-laden microspheres (CLMs), with immediate gelation of construct upon printing on cold build platform. Collagen fibrils were formed in the AC hydrogel during culture at body temperature, improving the cell affinity and spreading compared to pure agarose hydrogel. Cells were proven to proliferate in the bioink and the bioprinted construct. High cell viability up to 14 days was observed. The compressive strength of the bioink is more than 100 times superior to those of pure AC hydrogel. A potential alternative in tissue engineering of tissue replacements and biological models is made possible by combining the advantages of the conventional solid scaffolds with the new 3D bioprinting technology. © The Author(s) 2016.
Source Title: Scientific Reports
URI: https://scholarbank.nus.edu.sg/handle/10635/178746
ISSN: 20452322
DOI: 10.1038/srep39140
Rights: Attribution 4.0 International
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