On-chip fabrication and in-flow 3D-printing of microgel constructs: from chip to scaffold materials in one integral process

被引:0
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作者
Reineke, Benjamin [1 ,2 ]
Paulus, Ilona [3 ,4 ]
Loeffelsend, Sophia [3 ,4 ]
Yu, Chien-Hsin [1 ,2 ]
Vinogradov, Dmitrii [1 ,2 ]
Meyer, Anna [1 ,2 ]
Hazur, Jonas [7 ]
Roeder, Jonas [7 ]
Vollmer, Madita [5 ]
Tamgueney, Gueltekin [5 ,6 ]
Hauschild, Stephan [1 ]
Boccaccini, Aldo R. [7 ]
Groll, Juergen [3 ,4 ]
Foerster, Stephan [1 ,2 ]
机构
[1] Forschungszentrum Julich, Julich Ctr Neutron Sci JCNS 1 & IBI 8, D-52425 Julich, Germany
[2] Rhein Westfal TH Aachen, Inst Phys Chem, D-52074 Aachen, Germany
[3] Univ Wurzburg, Dept Funct Mat Med & Dent FMZ, D-97070 Wurzburg, Germany
[4] Univ Wurzburg, Bavarian Polymer Inst BPI, D-97070 Wurzburg, Germany
[5] Forschungszentrum Julich, Inst Biol Informat Proc Struct Biochem IBI 7, D-52425 Julich, Germany
[6] Heinrich Heine Univ Dusseldorf, Inst Phys Biol, D-40225 Dusseldorf, Germany
[7] Friedrich Alexander Univ Erlangen Nurnberg, Dept Mat Sci & Engn, Cauerstr 6, D-91058 Erlangen, Germany
关键词
microfluidics; 3D-printing; microgels; DROP SIZE; ENCAPSULATION; PRESSURE; CELLS;
D O I
10.1088/1758-5090/ad3318
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Bioprinting has evolved into a thriving technology for the fabrication of cell-laden scaffolds. Bioinks are the most critical component for bioprinting. Recently, microgels have been introduced as a very promising bioink, enabling cell protection and the control of the cellular microenvironment. However, the fabrication of the bioinks involves the microfluidic production of the microgels, with a subsequent multistep process to obtain the bioink, which so far has limited its application potential. Here we introduce a direct coupling of microfluidics and 3D-printing for the continuous microfluidic production of microgels with direct in-flow printing into stable scaffolds. The 3D-channel design of the microfluidic chip provides access to different hydrodynamic microdroplet formation regimes to cover a broad range of droplet and microgel diameters. After exiting a microtubing the produced microgels are hydrodynamically jammed into thin microgel filaments for direct 3D-printing into two- and three-dimensional scaffolds. The methodology enables the continuous on-chip encapsulation of cells into monodisperse microdroplets with subsequent in-flow cross-linking to produce cell-laden microgels. The method is demonstrated for different cross-linking methods and cell lines. This advancement will enable a direct coupling of microfluidics and 3D-bioprinting for scaffold fabrication.
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页数:14
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