3D Printed Vascular Networks Enhance Viability in High-Volume Perfusion Bioreactor

被引:31
作者
Ball, Owen [1 ]
Nguyen, Bao-Ngoc B. [1 ]
Placone, Jesse K. [1 ]
Fisher, John P. [1 ]
机构
[1] Univ Maryland, Fischell Dept Bioengn, 2330D Jeong H Kim Engn Bldg, College Pk, MD 20742 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
Vascular; Bioreactor; Perfusion; hMSCs; 3D printed; Modeling; Computer-aided design; MESENCHYMAL STEM-CELLS; GEL LAYER FORMATION; DYNAMIC CULTURE; ILIAC CREST; IN-VITRO; SCAFFOLDS; SYSTEM; OXYGEN; DIFFERENTIATION; IMPACT;
D O I
10.1007/s10439-016-1662-y
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
There is a significant clinical need for engineered bone graft substitutes that can quickly, effectively, and safely repair large segmental bone defects. One emerging field of interest involves the growth of engineered bone tissue in vitro within bioreactors, the most promising of which are perfusion bioreactors. Using bioreactor systems, tissue engineered bone constructs can be fabricated in vitro. However, these engineered constructs lack inherent vasculature and once implanted, quickly develop a necrotic core, where no nutrient exchange occurs. Here, we utilized COMSOL modeling to predict oxygen diffusion gradients throughout aggregated alginate constructs, which allowed for the computer-aided design of printable vascular networks, compatible with any large tissue engineered construct cultured in a perfusion bioreactor. We investigated the effect of 3D printed macroscale vascular networks with various porosities on the viability of human mesenchymal stem cells in vitro, using both gas-permeable, and non-gas permeable bioreactor growth chamber walls. Through the use of 3D printed vascular structures in conjunction with a tubular perfusion system bioreactor, cell viability was found to increase by as much as 50% in the core of these constructs, with in silico modeling predicting construct viability at steady state.
引用
收藏
页码:3435 / 3445
页数:11
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