Additive Manufacturing of Bioactive Glasses: Focus on Bone Tissue Engineering



Mozafari M¹ ; Kargozar S² ; Kermani F³ ; Milan PB^{4, 5, 6} ; Baino F⁷
Source: Bioceramics: Status in Tissue Engineering and Regenerative Medicine (Part 2) Published:2024

Abstract

In tissue engineering and regenerative medicine, bioactive glasses (BGs) offer many potential advantages. These inorganic substances belong to the bioceramics family and are traditionally produced in powder and granular formats via the sol-gel and melt-quenching synthesis routes. In order to mimic the native structure of human tissues, BGs should be fabricated into three-dimensional (3D) constructs (i.e., scaffolds). There are specific conventional fabrication methods for producing BG-based scaffolds (e.g., foam replication); however, they suffer from some critical limitations such as the lack of exact control on the pore dimension and distribution. In this regard, additive manufacturing (AM), also known as 3D printing, has emerged for the generation of precise and high-resolution BG-based scaffolds. Currently, 3D printing of BG-based scaffolds is performed by using a series of well-developed AM techniques, including direct 3D printing, selective laser sintering (SLS), robocasting, and stereolithography (SLA). In some methods, BGs are added to polymeric matrices and then introduced into the 3D printing machine as a raw material. In general, 3D-printed constructs exhibit important advantages over conventionally-fabricated tissue-engineering scaffolds in terms of reproducibility, scalability, architecture (e.g., controllable strut thickness, pore shape and size), and biomechanical properties. It is of significance that BGs can be simultaneously printed with mammalian cells (e.g., stem cells), known as 3D bioprinting. Still, some challenges (e.g., decreased cell viability) remain that should be addressed by conducting further research and proposing innovative solutions. © 2024 Bentham Science Publishers.