Fabrication of hierarchically porous trabecular bone replicas via 3D printing with high internal phase emulsions (HIPEs)

材料科学 制作 多孔性 3D打印 生物医学工程 相(物质) 复合材料 工程类 医学 化学 病理 有机化学 替代医学
作者
Nihan Sengokmen-Ozsoz,Mina Aleemardani,Marco Palanca,Alice Jane Hann,Gwendolen C. Reilly,Enrico Dall’Ara,Frederik Claeyssens
出处
期刊:Biofabrication [IOP Publishing]
标识
DOI:10.1088/1758-5090/ad8b70
摘要

Combining emulsion templating with additive manufacturing enables the production of inherently porous scaffolds with multiscale porosity. This approach incorporates interconnected porous materials, providing a structure that supports cell ingrowth. However, 3D printing hierarchical porous structures that combine semi-micropores and micropores remains a challenging task. Previous studies have demonstrated that using a carefully adjusted combination of light absorbers and photoinitiators in the resin can produce open surface porosity, sponge-like internal structures, and a printing resolution of about 150 µm. In this study, we explored how varying concentrations of tartrazine (0, 0.02, 0.04, and 0.08 wt%) as a light absorber affect the porous structure of acrylate-based polymerized Medium Internal Phase Emulsions (polyMIPEs) fabricated via vat photopolymerization. Given the importance of a porous and interconnected structure for tissue engineering and regenerative medicine, we tested cell behavior on these 3D-printed disk samples using MG-63 cells, examining metabolic activity, adhesion, and morphology. The 0.08 wt% tartrazine-containing 3D-printed sample (008T) demonstrated the best cell proliferation and adhesion. To show that this HIPE resin can be used to create complex structures for biomedical applications, we 3D-printed trabecular bone structures based on microCT imaging. These structures were further evaluated for cell behaviour and migration, followed by microCT analysis after 60 days of cell culture. This research demonstrates that HIPEs can be used as a resin to print trabecular bone mimics using additive manufacturing, which could be further developed for lab-on-a-chip models of healthy and diseased bone.

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