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用于原位内皮化和微流体灌注的无孔隙三维生物打印

Void-free 3D Bioprinting for In-situ Endothelialization and Microfluidic Perfusion.

作者信息

Ouyang Liliang, Armstrong James P K, Chen Qu, Lin Yiyang, Stevens Molly M

机构信息

Department of Materials, Department of Bioengineering, Institute of Biomedical Engineering, Imperial College London, London, SW7 2AZ, UK.

出版信息

Adv Funct Mater. 2020 Jun;30(26):1909009. doi: 10.1002/adfm.201909009. Epub 2020 Feb 5.

Abstract

Two major challenges of 3D bioprinting are the retention of structural fidelity and efficient endothelialization for tissue vascularization. We address both of these issues by introducing a versatile 3D bioprinting strategy, in which a templating bioink is deposited layer-by-layer alongside a matrix bioink to establish void-free multimaterial structures. After crosslinking the matrix phase, the templating phase is sacrificed to create a well-defined 3D network of interconnected tubular channels. This void-free 3D printing (VF-3DP) approach circumvents the traditional concerns of structural collapse, deformation and oxygen inhibition, moreover, it can be readily used to print materials that are widely considered "unprintable". By pre-loading endothelial cells into the templating bioink, the inner surface of the channels can be efficiently cellularized with a confluent endothelial layer. This in-situ endothelialization method can be used to produce endothelium with a far greater uniformity than can be achieved using the conventional post-seeding approach. This VF-3DP approach can also be extended beyond tissue fabrication and towards customized hydrogel-based microfluidics and self-supported perfusable hydrogel constructs.

摘要

3D生物打印面临的两大挑战是保持结构保真度以及实现组织血管化的高效内皮化。我们通过引入一种通用的3D生物打印策略来解决这两个问题,即在模板生物墨水与基质生物墨水并排逐层沉积,以建立无空隙的多材料结构。在交联基质相后,牺牲模板相以创建一个定义明确的相互连接的管状通道3D网络。这种无空隙3D打印(VF-3DP)方法避免了传统的结构坍塌、变形和氧气抑制问题,此外,它可以很容易地用于打印被广泛认为“无法打印”的材料。通过将内皮细胞预加载到模板生物墨水中,通道的内表面可以有效地被汇合的内皮细胞层细胞化。这种原位内皮化方法可用于产生比传统接种后方法具有更高均匀性的内皮。这种VF-3DP方法还可以扩展到组织制造之外,用于定制的基于水凝胶的微流体和自支撑可灌注水凝胶构建体。

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