Functionalized Bioink with Optical Sensor Nanoparticles for O2 Imaging in 3D-Bioprinted Constructs

被引:69
|
作者
Trampe, Erik [1 ]
Koren, Klaus [2 ]
Akkineni, Ashwini Rahul [3 ,4 ]
Senwitz, Christian [3 ,4 ]
Krujatz, Felix [5 ]
Lode, Anja [3 ,4 ]
Gelinsky, Michael [3 ,4 ]
Kuhl, Michael [1 ]
机构
[1] Univ Copenhagen, Dept Biol, Marine Biol Sect, Strandpromenaden 5, DK-3000 Helsingor, Denmark
[2] Aarhus Univ, Dept Biosci, Microbiol Sect, Ny Munkegade 116, DK-8000 Aarhus, Denmark
[3] Tech Univ Dresden, Fac Med, Ctr Translat Bone Joint & Soft Tissue Res, Fetscherstr 74, D-01307 Dresden, Germany
[4] Tech Univ Dresden, Univ Hosp Carl Gustav Carus, Ctr Translat Bone Joint & Soft Tissue Res, Fetscherstr 74, D-01307 Dresden, Germany
[5] Tech Univ Dresden, Inst Nat Mat Technol, Bergstr 120, D-01069 Dresden, Germany
关键词
bioprinting; chemical imaging; nanoparticles; photosynthesis; respiration; OXYGEN; DYNAMICS; GROWTH; PH; CELLS; TEMPERATURE; DESIGN;
D O I
10.1002/adfm.201804411
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Research on 3D bioprinting of living cells has strong focus on printable biocompatible materials and monitoring of cell growth in printed constructs, while cell metabolism is mostly measured in media surrounding the constructs or by destructive sample analyses. Bioprinting is combined with online imaging of O-2 by functionalizing a hydrogel bioink via addition of luminescent optical sensor nanoparticles. Rheological properties of the bioink enable 3D printing of hydrogel layers with uniform response to O-2 concentration. Co-immobilization of sensor nanoparticles with green microalgae and/or mesenchymal stem cells does not affect cell viability over several days. Interference from microalgal autofluorescence on the O-2 imaging is negligible, and no leakage or photobleaching of nanoparticles is observed over 2-3 days. Oxygen dynamics due to respiration and photosynthesis of cells can be imaged online and the metabolic activity of different cell types can be discriminated in intact 3D structures. Bioinks containing chemical sensor particles enable noninvasive mapping of cell metabolism and spatiotemporal dynamics of their chemical microenvironment in 3D-printed structures. This major advance now facilitates rapid evaluation of cell activity in printed constructs as a function of structural complexity, metabolic interactions in mixed species bioprints, and in response to external incubation conditions.
引用
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页数:11
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