Cast-Molded Channelized Hydrogel Scaffolds With Stereolithography-Printed Templates

IF 3.6 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Chi Wang, Yingge Zhou
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引用次数: 0

Abstract

Creating internal vascular networks within hydrogel scaffolds is crucial for providing the encapsulated cells with the necessary nutrients, oxygen, and metabolic exchange. Current methods for hydrogel scaffold fabrication face significant hurdles, including the challenge of forming sufficient internal channels, achieving precise scaffold geometry, and maintaining high cell viability, often compromised by the fabrication process and properties of the polymer materials used. Stereolithography (SLA) emerges as a promising 3D printing technique due to its exceptional precision, efficiency, and resolution, allowing for the creation of complex geometries with fine detail. This paper explores the application of SLA as a novel strategy to fabricate hydrogel scaffolds with interconnected small diameter channels, surpassing the capabilities of fused deposition modeling method to create templates. The encapsulated fibroblasts grown in the hydrogel scaffold containing channels showed significantly elevated cell viability compared to the ones without any channels. The capability of this SLA-assisted strategy to create channel structures with encapsulated cells demonstrate significant potential for generating 3D artificial tissue composites with precisely controlled micron-scale channels.

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浇铸成型通道化水凝胶支架与立体光刻印刷模板
在水凝胶支架内建立内部血管网络对于为被包裹的细胞提供必要的营养、氧气和代谢交换至关重要。目前的水凝胶支架制造方法面临着巨大的障碍,包括形成足够的内部通道,实现精确的支架几何形状,以及保持高细胞活力的挑战,这些都经常受到制造工艺和所用聚合物材料性能的影响。立体光刻(SLA)由于其卓越的精度,效率和分辨率而成为一种有前途的3D打印技术,允许创建具有精细细节的复杂几何形状。本文探讨了SLA作为一种新策略的应用,以制造具有相互连接的小直径通道的水凝胶支架,超越了熔融沉积建模方法创建模板的能力。与没有通道的水凝胶支架相比,在含有通道的水凝胶支架中生长的包被成纤维细胞的细胞活力显著提高。这种SLA辅助策略能够用封装细胞创建通道结构,这在生成具有精确控制微米级通道的3D人工组织复合材料方面显示出巨大的潜力。
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来源期刊
Biotechnology and Bioengineering
Biotechnology and Bioengineering 工程技术-生物工程与应用微生物
CiteScore
7.90
自引率
5.30%
发文量
280
审稿时长
2.1 months
期刊介绍: Biotechnology & Bioengineering publishes Perspectives, Articles, Reviews, Mini-Reviews, and Communications to the Editor that embrace all aspects of biotechnology. These include: -Enzyme systems and their applications, including enzyme reactors, purification, and applied aspects of protein engineering -Animal-cell biotechnology, including media development -Applied aspects of cellular physiology, metabolism, and energetics -Biocatalysis and applied enzymology, including enzyme reactors, protein engineering, and nanobiotechnology -Biothermodynamics -Biofuels, including biomass and renewable resource engineering -Biomaterials, including delivery systems and materials for tissue engineering -Bioprocess engineering, including kinetics and modeling of biological systems, transport phenomena in bioreactors, bioreactor design, monitoring, and control -Biosensors and instrumentation -Computational and systems biology, including bioinformatics and genomic/proteomic studies -Environmental biotechnology, including biofilms, algal systems, and bioremediation -Metabolic and cellular engineering -Plant-cell biotechnology -Spectroscopic and other analytical techniques for biotechnological applications -Synthetic biology -Tissue engineering, stem-cell bioengineering, regenerative medicine, gene therapy and delivery systems The editors will consider papers for publication based on novelty, their immediate or future impact on biotechnological processes, and their contribution to the advancement of biochemical engineering science. Submission of papers dealing with routine aspects of bioprocessing, description of established equipment, and routine applications of established methodologies (e.g., control strategies, modeling, experimental methods) is discouraged. Theoretical papers will be judged based on the novelty of the approach and their potential impact, or on their novel capability to predict and elucidate experimental observations.
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