3D mesoporous bioactive glass/silk/chitosan scaffolds and their compatibility with human adipose‐derived stromal cells. Issue 6 (29th August 2020)

• Record Type: Journal Article
• Authors: Phetnin, Ratiya Buapa; Suksaweang, Sanong; Giannasi, Chiara; Brini, Anna Teresa; Niada, Stefania; Srisuwan, Sawitri; Rattanachan, Sirirat Tubsungnoen
• Is Part Of: International journal of applied ceramic technology. Volume 17:Issue 6(2020)
• Page Start: 2779
• Page End: 2791
• Publication Date: 2020-08-29
• Subjects: bioactive glass -- chitosan -- composite scaffold -- human adipose‐derived stem/stromal cells -- silk fibroin -- tissue engineering; Ceramics -- Periodicals; Ceramics -- Technological innovations -- Periodicals; 620.1405
• DOI: 10.1111/ijac.13607
• Languages: English
• ISSNs: 1546-542X

Abstract

Abstract: Human adipose‐derived stem/stromal cells (hASCs) have been popularly studied as cell‐based therapy in the field of regenerative medicine due to their ability to differentiate into several cell types. In this study, in order to improve the mechanical strength and bioactivity of scaffolds for bone tissue engineering, three types of mesoporous bioactive glasses with different shapes and compositions were dispersed in the silk fibroin/chitosan (SF/CS)‐based scaffolds, which were fabricated with a combination of freezing and lyophilization. The characteristic and physical properties of these composite scaffolds were evaluated. The biocompatibility was also assessed through hASCs in vitro tests. Both Alamar Blue® and Live/Dead assay® revealed that the spherical mesoporous bioactive glass doped scaffolds enhanced cell viability and proliferation. Furthermore, the addition of spherical mesoporous bioactive glass into SF/CS scaffolds encouraged hASC osteogenic differentiation as well. These results suggested that this composite scaffold can be applicable material for bone regeneration. Abstract : Fabrication of 3D mesoporous bioactive glass/silk/chitosan scaffolds and their compatibility with Human Adipose‐derived Stromal Cells.