TY - JOUR
T1 - Rapid and cytocompatible cell-laden silk hydrogel formation via riboflavin-mediated crosslinking
AU - Piluso, Susanna
AU - Flores Gomez, Daniela
AU - Dokter, Inge
AU - Moreira Texeira, Liliana
AU - Li, Yang
AU - Leijten, Jeroen
AU - van Weeren, René
AU - Vermonden, Tina
AU - Karperien, Marcel
AU - Malda, Jos
N1 - Funding Information:
The authors would like to thank Riccardo Levato and Lizette Utomo for kindly providing ACPCs and DPSCs, respectively. The authors also thank Thomas N. Ran for the support with FTIR characterization. This work was supported by the Dutch Arthritis Association (LLP12, LLP22, and LLP25); and the strategic alliance program entitled: Advanced Biomanufacturing, funded by the University of Twente, Utrecht University and University Medical Center Utrecht, project title: Bioprinting functional tissues from stem cells and enabling biomaterials.
Publisher Copyright:
© The Royal Society of Chemistry.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020/11/7
Y1 - 2020/11/7
N2 - Bioactive hydrogels based on naturally-derived polymers are of great interest for regenerative medicine applications. Among naturally-derived polymers, silk fibroin has been extensively explored as a biomaterial for tissue engineering due to its unique mechanical properties. Here, we demonstrate the rapid gelation of cell-laden silk fibroin hydrogels by visible light-induced crosslinking using riboflavin as a photo-initiator, in presence of an electron acceptor. The gelation kinetics were monitored by in situ photo-rheometry. Gelation was achieved in minutes and could be tuned owing to its direct proportionality to the electron acceptor concentration. The concentration of the electron acceptor did not affect the elastic modulus of the hydrogels, which could be altered by varying the polymer content. Further, the biocompatible riboflavin photo-initiator combined with sodium persulfate allowed for the encapsulation of cells within silk fibroin hydrogels. To confirm the cytocompatibility of the silk fibroin formulations, three cell types (articular cartilage-derived progenitor cells, mesenchymal stem cells and dental-pulp-derived stem cells) were encapsulated within the hydrogels, which associated with a viability >80% for all cell types. These results demonstrated that fast gelation of silk fibroin can be achieved by combining it with riboflavin and electron acceptors, which results in a hydrogel that can be used in tissue engineering and cell delivery applications. This journal is
AB - Bioactive hydrogels based on naturally-derived polymers are of great interest for regenerative medicine applications. Among naturally-derived polymers, silk fibroin has been extensively explored as a biomaterial for tissue engineering due to its unique mechanical properties. Here, we demonstrate the rapid gelation of cell-laden silk fibroin hydrogels by visible light-induced crosslinking using riboflavin as a photo-initiator, in presence of an electron acceptor. The gelation kinetics were monitored by in situ photo-rheometry. Gelation was achieved in minutes and could be tuned owing to its direct proportionality to the electron acceptor concentration. The concentration of the electron acceptor did not affect the elastic modulus of the hydrogels, which could be altered by varying the polymer content. Further, the biocompatible riboflavin photo-initiator combined with sodium persulfate allowed for the encapsulation of cells within silk fibroin hydrogels. To confirm the cytocompatibility of the silk fibroin formulations, three cell types (articular cartilage-derived progenitor cells, mesenchymal stem cells and dental-pulp-derived stem cells) were encapsulated within the hydrogels, which associated with a viability >80% for all cell types. These results demonstrated that fast gelation of silk fibroin can be achieved by combining it with riboflavin and electron acceptors, which results in a hydrogel that can be used in tissue engineering and cell delivery applications. This journal is
UR - http://www.scopus.com/inward/record.url?scp=85094890610&partnerID=8YFLogxK
U2 - 10.1039/d0tb01731k
DO - 10.1039/d0tb01731k
M3 - Article
C2 - 33001117
SN - 2050-750X
VL - 8
SP - 9566
EP - 9575
JO - Journal of Materials Chemistry B
JF - Journal of Materials Chemistry B
IS - 41
ER -