Complex 3D-Printed Microchannels within Cell-Degradable Hydrogels

被引:192
作者
Song, Kwang Hoon [1 ]
Highley, Christopher B. [1 ]
Rouff, Andrew [1 ]
Burdick, Jason A. [1 ]
机构
[1] Univ Penn, Dept Bioengn, 210 South 33rd St, Philadelphia, PA 19104 USA
基金
美国国家科学基金会;
关键词
3D printing; angiogenesis; cell-degradable materials; hydrogels; microchannels; MICROFLUIDIC NETWORKS; ENDOTHELIAL-CELLS; 3D; ANGIOGENESIS; FABRICATION; CONSTRUCTS; CULTURE; DESIGN;
D O I
10.1002/adfm.201801331
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
3D-printing is emerging as a technology to introduce microchannels into hydrogels, for the perfusion of engineered constructs. Although numerous techniques have been developed, new techniques are still needed to obtain the complex geometries of blood vessels and with materials that permit desired cellular responses. Here, a printing process where a shear-thinning and self-healing hydrogel "ink" is injected directly into a "support" hydrogel with similar properties is reported. The support hydrogel is further engineered to undergo stabilization through a thiol-ene reaction, permitting (i) the washing of the ink to produce microchannels and (ii) tunable properties depending on the crosslinker design. When adhesive peptides are included in the support hydrogel, endothelial cells form confluent monolayers within the channels, across a range of printed configurations (e.g., straight, stenosis, spiral). When protease-degradable crosslinkers are used for the support hydrogel and gradients of angiogenic factors are introduced, endothelial cells sprout into the support hydrogel in the direction of the gradient. This printing approach is used to investigate the influence of channel curvature on angiogenic sprouting and increased sprouting is observed at curved locations. Ultimately, this technique can be used for a range of biomedical applications, from engineering vascularized tissue constructs to modeling in vitro cultures.
引用
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页数:10
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