将脱细胞细胞外基质微凝胶制成模块化生物墨水,用于挤压式生物打印,具有良好的打印性能和打印后细胞的高存活率。

Biomaterials Translational Pub Date : 2023-06-28 eCollection Date: 2023-01-01 DOI:10.12336/biomatertransl.2023.02.006
Hanyu Chu, Kexin Zhang, Zilong Rao, Panpan Song, Zudong Lin, Jing Zhou, Liqun Yang, Daping Quan, Ying Bai
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引用次数: 2

摘要

生物墨水的可印刷性和印刷后的细胞存活率对于基于挤压的生物打印至关重要。合适的生物墨水不仅能为结构保真提供机械支持,还能为细胞封装和保护提供合适的三维(3D)微环境。本研究开发了一种基于水凝胶的复合生物墨水,由甲基丙烯酰明胶(GelMA)作为连续相,脱细胞细胞外基质微凝胶(DMs)作为离散相。采用流动聚焦微流体系统,以高通量方式制造含有细胞的 DMs。将DMs和GelMA轻柔混合后,流变学特性和三维打印测试表明,生成的DM-GelMA水凝胶保留了GelMA的剪切稀化特性、机械性能和良好的可打印性。DM的集成不仅为细胞封装提供了类似细胞外基质的微环境,还为打印后细胞的高存活率提供了相当大的抗剪切性。三维打印机针头的 DM 大小和内径相互关联,并针对基于喷嘴的挤压进行了优化。此外,由 RSC96 许旺细胞包裹的 DM 和人脐静脉内皮细胞包裹的 GelMA 组成的概念验证生物墨水被成功地生物打印到三维构建体中,形成了一个具有独特细胞/材料分布的模块化共培养系统。总之,模块化 DM-GelMA 生物墨水为未来的精密生物制造提供了跳板,并将在组织工程和药物筛选等众多生物医学应用中发挥作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Harnessing decellularised extracellular matrix microgels into modular bioinks for extrusion-based bioprinting with good printability and high post-printing cell viability.

The printability of bioink and post-printing cell viability is crucial for extrusion-based bioprinting. A proper bioink not only provides mechanical support for structural fidelity, but also serves as suitable three-dimensional (3D) microenvironment for cell encapsulation and protection. In this study, a hydrogel-based composite bioink was developed consisting of gelatin methacryloyl (GelMA) as the continuous phase and decellularised extracellular matrix microgels (DMs) as the discrete phase. A flow-focusing microfluidic system was employed for the fabrication of cell-laden DMs in a high-throughput manner. After gentle mixing of the DMs and GelMA, both rheological characterisations and 3D printing tests showed that the resulting DM-GelMA hydrogel preserved the shear-thinning nature, mechanical properties, and good printability from GelMA. The integration of DMs not only provided an extracellular matrix-like microenvironment for cell encapsulation, but also considerable shear-resistance for high post-printing cell viability. The DM sizes and inner diameters of the 3D printer needles were correlated and optimised for nozzle-based extrusion. Furthermore, a proof-of-concept bioink composedg of RSC96 Schwann cells encapsulated DMs and human umbilical vein endothelial cell-laden GelMA was successfully bioprinted into 3D constructs, resulting in a modular co-culture system with distinct cells/materials distribution. Overall, the modular DM-GelMA bioink provides a springboard for future precision biofabrication and will serve in numerous biomedical applications such as tissue engineering and drug screening.

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CiteScore
6.70
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