3D Printed Chondrogenic Functionalized PGS Bioactive Scaffold for Cartilage Regeneration

被引:15
|
作者
Wang, Sinan [1 ,2 ]
Luo, Bin [3 ]
Bai, Baoshuai [2 ]
Wang, Qianyi [1 ]
Chen, Hongying [1 ]
Tan, Xiaoyan [1 ]
Tang, Zhengya [1 ]
Shen, Sisi [1 ]
Zhou, Hengxing [2 ]
You, Zhengwei [3 ]
Zhou, Guangdong [1 ]
Lei, Dong [1 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 9, Sch Med, Dept Cardiol,Dept Plast & Reconstruct Surg, Shanghai 200011, Peoples R China
[2] Shandong Univ, Qilu Hosp, Ctr Orthopaed, Adv Med Res Inst,Cheeloo Coll Med,Dept Orthopaed, Jinan 250012, Peoples R China
[3] Donghua Univ, Inst Funct Mat, Coll Mat Sci & Engn, Key Lab Modificat Chem Fibers & Polymer Mat, Shanghai 201620, Peoples R China
基金
中国国家自然科学基金; 上海市自然科学基金;
关键词
3D printing; cartilage regeneration; functionalized scaffolds; poly(glycerol sebacate); swelling absorption; TISSUE; BONE; ELASTOMER; POLYMER; REPAIR;
D O I
10.1002/adhm.202301006
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
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.
引用
收藏
页数:15
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