Biomimetic and mechanically supportive 3D printed scaffolds for cartilage and osteochondral tissue engineering using photopolymers and digital light processing. (16th September 2021)

• Record Type: Journal Article
• Authors: Schoonraad, Sarah A; Fischenich, Kristine M; Eckstein, Kevin N; Crespo-Cuevas, Victor; Savard, Lea M; Muralidharan, Archish; Tomaschke, Andrew A; Uzcategui, Asais Camila; Randolph, Mark A; McLeod, Robert R; Ferguson, Virginia L; Bryant, Stephanie J
• Is Part Of: Biofabrication. Volume 13:Number 4(2021)
• Publication Date: 2021-09-16
• Subjects: digital light processing -- tissue engineering -- 3D printing -- hydrogel -- mesenchymal stem cell -- cartilage -- osteochondral; Biomedical engineering -- Periodicals; Tissue engineering -- Periodicals; Biomedical materials -- Microstructure -- Periodicals; Bioengineering -- Periodicals; 610.28
• DOI: 10.1088/1758-5090/ac23ab
• Languages: English
• ISSNs: 1758-5082

Abstract

Abstract: Successful 3D scaffold designs for musculoskeletal tissue engineering necessitate full consideration of the form and function of the tissues of interest. When designing structures for engineering cartilage and osteochondral tissues, one must reconcile the need to develop a mechanically robust system that maintains the health of cells embedded in the scaffold. In this work, we present an approach that decouples the mechanical and biochemical needs and allows for the independent development of the structural and cellular niches in a scaffold. Using the highly tuned capabilities of digital light processing-based stereolithography, structures with complex architectures are achieved over a range of effective porosities and moduli. The 3D printed structure is infilled with mesenchymal stem cells and soft biomimetic hydrogels, which are specifically formulated with extracellular matrix analogs and tethered growth factors to provide selected biochemical cues for the guided differentiation towards chondrogenesis and osteogenesis. We demonstrate the ability to utilize these structures to (a) infill a focal chondral defect and mitigate macroscopic and cellular level changes in the cartilage surrounding the defect, and (b) support the development of a stratified multi-tissue scaffold for osteochondral tissue engineering.