TY - JOUR
T1 - Machine learning-generated compression modulus database for 3D printing of gelatin methacryloyl
AU - Chen, Shiue Luen
AU - Senadeera, Manisha
AU - Ruberu, Kalani
AU - Chung, Johnson
AU - Rana, Santu
AU - Venkatesh, Svetha
AU - Chen, Chong You
AU - Chen, Guan Yu
AU - Wallace, Gordon
N1 - Publisher Copyright:
© 2024 Author(s). This is an Open Access article distributed under the terms of the Creative Commons Attribution License, permitting distribution, and reproduction in any medium, provided the original work is properly cited.
PY - 2024
Y1 - 2024
N2 - 3D bioprinting enables the fabrication of printable tissues, including those for neural, cartilage, and skin repair. The mechanical properties, especially stiffness, of 3D-bioprinted scaffolds are crucial for modulating cell adhesion, growth, migration, and differentiation. The stiffness of a scaffold can be adjusted post-printing by modifying the hydrogel concentration, crosslinker concentration, light intensity during photocrosslinking, and duration of crosslinking. The optimization of these conditions to produce the desired scaffold stiffness for a particular cell type or application is a time-consuming and rigorous process. This study developed an innovative approach to predict the compression modulus of 3D-printed gelatin methacryloyl (GelMA) scaffolds using the Bayesian optimization (BO) algorithm. Through just 10 iterations (75 experimental data points), the model was able to predict > 13, 000 possible compression modulus values in a search space comprising four independent variables (GelMA concentration, crosslinker concentration, ultraviolet light [UV] distance, and UV exposure time). This approach can be utilized in other photocrosslinkable bioinks for 3D printing that have a myriad of pre- or post-printing parameters that can affect scaffold stiffness.
AB - 3D bioprinting enables the fabrication of printable tissues, including those for neural, cartilage, and skin repair. The mechanical properties, especially stiffness, of 3D-bioprinted scaffolds are crucial for modulating cell adhesion, growth, migration, and differentiation. The stiffness of a scaffold can be adjusted post-printing by modifying the hydrogel concentration, crosslinker concentration, light intensity during photocrosslinking, and duration of crosslinking. The optimization of these conditions to produce the desired scaffold stiffness for a particular cell type or application is a time-consuming and rigorous process. This study developed an innovative approach to predict the compression modulus of 3D-printed gelatin methacryloyl (GelMA) scaffolds using the Bayesian optimization (BO) algorithm. Through just 10 iterations (75 experimental data points), the model was able to predict > 13, 000 possible compression modulus values in a search space comprising four independent variables (GelMA concentration, crosslinker concentration, ultraviolet light [UV] distance, and UV exposure time). This approach can be utilized in other photocrosslinkable bioinks for 3D printing that have a myriad of pre- or post-printing parameters that can affect scaffold stiffness.
KW - 3D bioprinting
KW - Bayesian optimization
KW - Compression modulus
KW - Gelatin methacryloyl
KW - Scaffold stiffness
UR - http://www.scopus.com/inward/record.url?scp=85207330410&partnerID=8YFLogxK
U2 - 10.36922/ijb.3814
DO - 10.36922/ijb.3814
M3 - Article
AN - SCOPUS:85207330410
SN - 2424-8002
VL - 10
SP - 560
EP - 573
JO - International Journal of Bioprinting
JF - International Journal of Bioprinting
IS - 5
M1 - 3814
ER -