Biofabrication of customized bone grafts by combination of additive manufacturing and bioreactor knowhow

被引:40
作者
Costa, Pedro F. [1 ,2 ]
Vaquette, Cedryck [3 ]
Baldwin, Jeremy [3 ]
Chhaya, Mohit [3 ]
Gomes, Manuela E. [1 ,2 ]
Reis, Rui L. [1 ,2 ]
Theodoropoulos, Christina [3 ]
Hutmacher, Dietmar W. [3 ,4 ]
机构
[1] Univ Minho, Headquarters European Inst Excellence Tissue Engn, Res Grp Biomat Biodegradables & Biomimet 3Bs, Guimaraes, Portugal
[2] ICVS 3Bs PT Govt Associate Lab, Braga, Portugal
[3] Queensland Univ Technol, Inst Hlth & Biomed Innovat, Brisbane, Qld 4001, Australia
[4] Tech Univ Munich, Inst Adv Studies, D-80290 Munich, Germany
基金
澳大利亚国家健康与医学研究理事会; 澳大利亚研究理事会;
关键词
additive manufacturing; bioreactor; tissue engineering; biofabrication; custom-made scaffolds; MINERALIZED MATRIX DEPOSITION; 3D PERFUSION CULTURE; SEEDING DENSITY; TISSUE; SCAFFOLDS; FLOW; SYSTEM; INCREASES; DESIGN; CONSTRUCTS;
D O I
10.1088/1758-5082/6/3/035006
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
This study reports on an original concept of additive manufacturing for the fabrication of tissue engineered constructs (TEC), offering the possibility of concomitantly manufacturing a customized scaffold and a bioreactor chamber to any size and shape. As a proof of concept towards the development of anatomically relevant TECs, this concept was utilized for the design and fabrication of a highly porous sheep tibia scaffold around which a bioreactor chamber of similar shape was simultaneously built. The morphology of the bioreactor/scaffold device was investigated by micro-computed tomography and scanning electron microscopy confirming the porous architecture of the sheep tibiae as opposed to the non-porous nature of the bioreactor chamber. Additionally, this study demonstrates that both the shape, as well as the inner architecture of the device can significantly impact the perfusion of fluid within the scaffold architecture. Indeed, fluid flow modelling revealed that this was of significant importance for controlling the nutrition flow pattern within the scaffold and the bioreactor chamber, avoiding the formation of stagnant flow regions detrimental for in vitro tissue development. The bioreactor/scaffold device was dynamically seeded with human primary osteoblasts and cultured under bi-directional perfusion for two and six weeks. Primary human osteoblasts were observed homogenously distributed throughout the scaffold, and were viable for the six week culture period. This work demonstrates a novel application for additive manufacturing in the development of scaffolds and bioreactors. Given the intrinsic flexibility of the additive manufacturing technology platform developed, more complex culture systems can be fabricated which would contribute to the advances in customized and patient-specific tissue engineering strategies for a wide range of applications.
引用
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页数:11
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