Journal
ADVANCED HEALTHCARE MATERIALS
Volume -, Issue -, Pages -Publisher
WILEY
DOI: 10.1002/adhm.202301006
Keywords
3D printing; cartilage regeneration; functionalized scaffolds; poly(glycerol sebacate); swelling absorption
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Tissue engineering is a promising approach for cartilage regeneration, and the modification and drug loading of poly(glycerol sebacate) (PGS) scaffolds pose a key challenge. In this study, a new strategy of super swelling-absorption and cross-linked networks locking was used to create a 3D printed PGS-CS/Gel scaffold based on FDA-approved PGS, gelatin, and chondroitin sulfate. The PGS-CS/Gel scaffold exhibited desirable properties and successfully repaired cartilage in a rabbit model.
Tissue engineering is emerging as a promising approach for cartilage regeneration and repair. Endowing scaffolds with cartilaginous bioactivity to obtain bionic microenvironment and regulating the matching of scaffold degradation and regeneration play a crucial role in cartilage regeneration. Poly(glycerol sebacate) (PGS) is a representative thermosetting bioelastomer known for its elasticity, biodegradability, and biocompatibility and is widely used in tissue engineering. However, the modification and drug loading of the PGS scaffold is still a key challenge due to its high temperature curing conditions and limited reactive groups, which seriously hinders its further functional application. Here, a simple versatile new strategy of super swelling-absorption and cross-linked networks locking is presented to successfully create the 3D printed PGS-CS/Gel scaffold for the first time based on FDA-approved PGS, gelatin (Gel) and chondroitin sulfate (CS). The PGS-CS/Gel scaffold exhibits the desirable synergistic properties of well-organized hierarchical structures, excellent elasticity, improved hydrophilicity, and cartilaginous bioactivity, which can promote the adhesion, proliferation, and migration of chondrocytes. Importantly, the rate of cartilage regeneration can be well-matched with degradation of PGS-CS/Gel scaffold, and achieve uniform and mature cartilage tissue without scaffold residual. The bioactive scaffold can successfully repair cartilage in a rabbit trochlear groove defect model indicating a promising prospect of clinical transformation.
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