TY - JOUR
T1 - Fabrication of scalable and structured tissue engineering scaffolds using water dissolvable sacrificial 3D printed moulds
AU - Mohanty, Soumyaranjan
AU - Larsen, Layla Bashir
AU - Trifol Guzman, Jon
AU - Szabo, Peter
AU - Burri, Harsha Vardhan Reddy
AU - Canali, Chiara
AU - Dufva, Martin
AU - Emnéus, Jenny
AU - Wolff, Anders
N1 - This is an open access article under the CC BY-NC-ND license
PY - 2015
Y1 - 2015
N2 - One of the major challenges in producing large scale engineered tissue is the lack of ability to create large highly perfused scaffolds in which cells can grow at a high cell density and viability. Here, we explore 3D printed polyvinyl alcohol (PVA) as a sacrificial mould in a polymer casting process. The PVA mould network defines the channels and is dissolved after curing the polymer casted around it. The printing parameters determined the PVA filament density in the sacrificial structure and this density resulted in different stiffness of the corresponding elastomer replica. It was possible to achieve 80% porosity corresponding to about 150 cm2/cm3 surface to volume ratio. The process is easily scalable as demonstrated by fabricating a 75 cm3 scaffold with about 16,000 interconnected channels (about 1 m2 surface area) and with a channel to channel distance of only 78 μm. To our knowledge this is the largest scaffold ever to be produced with such small feature sizes and with so many structuredchannels. The fabricated scaffoldswere applied for in-vitro culturing of hepatocytes over a 12-day culture period. Smaller scaffolds (6× 4mm) were tested for cell culturing and could support homogeneous cell growth throughoutthe scaffold. Presumably, the diffusion of oxygen and nutrient throughout the channel network is rapid enough to support cell growth. In conclusion, the described process is scalable, compatible with cell culture, rapid, and inexpensive.
AB - One of the major challenges in producing large scale engineered tissue is the lack of ability to create large highly perfused scaffolds in which cells can grow at a high cell density and viability. Here, we explore 3D printed polyvinyl alcohol (PVA) as a sacrificial mould in a polymer casting process. The PVA mould network defines the channels and is dissolved after curing the polymer casted around it. The printing parameters determined the PVA filament density in the sacrificial structure and this density resulted in different stiffness of the corresponding elastomer replica. It was possible to achieve 80% porosity corresponding to about 150 cm2/cm3 surface to volume ratio. The process is easily scalable as demonstrated by fabricating a 75 cm3 scaffold with about 16,000 interconnected channels (about 1 m2 surface area) and with a channel to channel distance of only 78 μm. To our knowledge this is the largest scaffold ever to be produced with such small feature sizes and with so many structuredchannels. The fabricated scaffoldswere applied for in-vitro culturing of hepatocytes over a 12-day culture period. Smaller scaffolds (6× 4mm) were tested for cell culturing and could support homogeneous cell growth throughoutthe scaffold. Presumably, the diffusion of oxygen and nutrient throughout the channel network is rapid enough to support cell growth. In conclusion, the described process is scalable, compatible with cell culture, rapid, and inexpensive.
KW - Tissue engineering
KW - 3D printing
KW - Scalable
KW - PVA
U2 - 10.1016/j.msec.2015.06.002
DO - 10.1016/j.msec.2015.06.002
M3 - Journal article
C2 - 26117791
SN - 1873-0191
VL - 55
SP - 569
EP - 578
JO - Materials Science and Engineering C: Materials for Biological Applications
JF - Materials Science and Engineering C: Materials for Biological Applications
ER -