TY - GEN
T1 - Bioprinting induced cell damage in cellular micro-fluidic channel fabrication
AU - Yu, Yin
AU - Ozbolat, Ibrahim Tarik
PY - 2013
Y1 - 2013
N2 - Bioprinting, or layer by layer additive tissue fabrication, is a revolutionary concept recently emerged as an interdisciplinary effort to produce three-dimensional living organ for clinical application. Among many challenges, it was agreed that inclusion of vascular system is critical for maintaining the viability and functionality of relatively thick 3D bioprinted tissue constructs. Our previous research addressed the printability of novel vessel-like micro-fluidic channels with alginate hydrogel and co-axial nozzles. Here, we further investigated the influence of bioprinting parameters on cartilage progenitor cells (CPCs) survival during and post printing. The results of this study revealed that quantifiable cell death could be induced by varying dispensing pressure, co-axial nozzle geometry, biomaterial concentration. However, damaged cells were able to recover during incubation, as well as undergo proliferation to certain extend. These findings may serve as a guideline for optimizing our system as well as predict cell damage in future studies.
AB - Bioprinting, or layer by layer additive tissue fabrication, is a revolutionary concept recently emerged as an interdisciplinary effort to produce three-dimensional living organ for clinical application. Among many challenges, it was agreed that inclusion of vascular system is critical for maintaining the viability and functionality of relatively thick 3D bioprinted tissue constructs. Our previous research addressed the printability of novel vessel-like micro-fluidic channels with alginate hydrogel and co-axial nozzles. Here, we further investigated the influence of bioprinting parameters on cartilage progenitor cells (CPCs) survival during and post printing. The results of this study revealed that quantifiable cell death could be induced by varying dispensing pressure, co-axial nozzle geometry, biomaterial concentration. However, damaged cells were able to recover during incubation, as well as undergo proliferation to certain extend. These findings may serve as a guideline for optimizing our system as well as predict cell damage in future studies.
UR - http://www.scopus.com/inward/record.url?scp=84890288719&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84890288719&partnerID=8YFLogxK
U2 - 10.1115/MSEC2013-1081
DO - 10.1115/MSEC2013-1081
M3 - Conference contribution
AN - SCOPUS:84890288719
SN - 9780791855454
T3 - ASME 2013 International Manufacturing Science and Engineering Conference Collocated with the 41st North American Manufacturing Research Conference, MSEC 2013
BT - ASME 2013 International Manufacturing Science and Engineering Conference Collocated with the 41st North American Manufacturing Research Conference, MSEC 2013
T2 - ASME 2013 International Manufacturing Science and Engineering Conference Collocated with the 41st North American Manufacturing Research Conference, MSEC 2013
Y2 - 10 June 2013 through 14 June 2013
ER -