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3D Bioprinting of Collagen-based Microfluidics for Engineering Fully-biologic Tissue Systems

bioRxiv the preprint server for biology(2024)

Department of Biomedical Engineering | Department of Materials Science and Engineering

Cited 0|Views10
Abstract
Microfluidic and organ-on-a-chip devices have improved the physiologic and translational relevance of in vitro systems in applications ranging from disease modeling to drug discovery and pharmacology. However, current manufacturing approaches have limitations in terms of materials used, non-native mechanical properties, patterning of extracellular matrix (ECM) and cells in 3D, and remodeling by cells into more complex tissues. We present a method to 3D bioprint ECM and cells into microfluidic collagen-based high-resolution internally perfusable scaffolds (CHIPS) that address these limitations, expand design complexity, and simplify fabrication. Additionally, CHIPS enable size-dependent diffusion of molecules out of perfusable channels into the surrounding device to support cell migration and remodeling, formation of capillary-like networks, and integration of secretory cell types to form a glucose-responsive, insulin-secreting pancreatic-like microphysiological system.
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Bioprinting,Microfluidic Devices,Organ-on-a-Chip,Microfluidics,Tissue Engineering
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要点】:本文提出了一种3D生物打印技术,用以制造基于胶原的微流控支架,实现了全生物性组织系统的工程化构建,解决了现有技术在材料、机械性能、细胞外基质三维构型以及细胞重塑方面的局限。

方法】:作者通过3D生物打印技术将细胞外基质(ECM)和细胞打印成高分辨率的内部可灌注的胶原基支架(CHIPS),这些支架能够模拟生理环境,并提供细胞重塑的复杂三维结构。

实验】:研究中,作者使用自定义的3D生物打印机,以胶原为原料,打印出了内部可灌注的微流控支架,并通过实验验证了这些支架能够支持细胞迁移、重塑,形成类似毛细血管的网络,并整合分泌型细胞构建出能够响应葡萄糖、分泌胰岛素的胰腺样微生理系统。论文中未明确提及使用的数据集名称。