On the progress of hydrogel-based 3D printing: Correlating rheological properties with printing behaviour

3D打印 表征(材料科学) 背景(考古学) 计算机科学 自愈水凝胶 纳米技术 质量(理念) 设计质量 机械工程 材料科学 过程(计算) 生化工程 工艺工程 工程类 运营管理 古生物学 高分子化学 下游(制造业) 生物 哲学 认识论 操作系统
作者
Sara Bom,Ricardo Ribeiro,Helena Margarida Ribeiro,Catarina Santos,Joana Marto
出处
期刊:International Journal of Pharmaceutics [Elsevier BV]
卷期号:615: 121506-121506 被引量:130
标识
DOI:10.1016/j.ijpharm.2022.121506
摘要

One of the exciting future directions in the 3D printing field is the development of innovative personalized smart constructions for bio-applications, including drug delivery, namely high-throughput drug screening and customized topical/oral administration of pharmaceuticals, as well as tissue engineering. In this context, hydrogels have emerged as a promising material that, when combined with extrusion 3D printing, allow the creation of soft-material structures with defined spatial locations, that can be printed at room temperature and customized by tuning the geometric design and/or the formulation components. Thus, the efficacy and quality of such vehicles is dependent on formulation, design, and printing process parameters. However, hydrogel inks are often designed and characterized using different methods and this lack of uniformity impairs. Characterization techniques are usually arbitrary and differ among research groups, challenging the inference of possible conclusions on hydrogel behaviour and potential applications. Therefore, to properly analyse the potential of a particular hydrogel ink formulation, we review, for the first time, the most frequently employed characterization procedures, from rheological approaches to printing parameters and settings, and discuss their relevance, limitations and drawbacks, and highlight future perspectives. Overall, to accelerate the development of high-quality 3D constructs, comprehensive characterization protocols for both pre-printing and printing assays should be adopted. Furthermore, their transversal adoption could serve as a boost in terms of quality requirements and regulatory aspects.
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