In situ handheld three-dimensional bioprinting for cartilage regeneration

被引:242
作者
Di Bella, Claudia [1 ,2 ]
Duchi, Serena [1 ]
O'Connell, Cathal D. [3 ]
Blanchard, Romane [1 ]
Augustine, Cheryl [1 ]
Yue, Zhilian [3 ]
Thompson, Fletcher [3 ]
Richards, Christopher [3 ]
Beirne, Stephen [3 ]
Onofrillo, Carmine [1 ,3 ]
Bauquier, Sebastien H. [4 ]
Ryan, Stewart D. [4 ]
Pivonka, Peter [1 ]
Wallace, Gordon G. [3 ]
Choong, Peter F. [1 ,2 ]
机构
[1] Univ Melbourne, Dept Surg, Melbourne, Vic, Australia
[2] St Vincents Hosp, Orthopaed Dept, Melbourne, Vic, Australia
[3] Univ Wollongong, Intelligent Polymer Res Inst, ARC Ctr Excellence Electromat Sci, Wollongong, NSW, Australia
[4] Univ Melbourne, Fac Vet & Agr Sci, Translat Res & Anim Clin Trial Study Grp TRACTS, Melbourne, Vic, Australia
基金
澳大利亚研究理事会;
关键词
3D bioprinting; bioscaffold; cartilage regeneration; in vivo large animal study; surgical 3D printer; tissue engineering; ARTICULAR-CARTILAGE; BASIC SCIENCE; TREATMENT OPTIONS; TISSUE; REPAIR; BIOFABRICATION; INTEGRATION; INJURIES;
D O I
10.1002/term.2476
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Articular cartilage injuries experienced at an early age can lead to the development of osteoarthritis later in life. In situ three-dimensional (3D) printing is an exciting and innovative biofabrication technology that enables the surgeon to deliver tissue-engineering techniques at the time and location of need. We have created a hand-held 3D printing device (biopen) that allows the simultaneous coaxial extrusion of bioscaffold and cultured cells directly into the cartilage defect in vivo in a single-session surgery. This pilot study assessed the ability of the biopen to repair a full-thickness chondral defect and the early outcomes in cartilage regeneration, and compared these results with other treatments in a large animal model. A standardized critical-sized full-thickness chondral defect was created in the weight-bearing surface of the lateral and medial condyles of both femurs of six sheep. Each defect was treated with one of the following treatments: (i) hand-held in situ 3D printed bioscaffold using the biopen (HH group), (ii) preconstructed bench-based printed bioscaffolds (BB group), (iii) microfractures (MF group) or (iv) untreated (control, C group). At 8 weeks after surgery, macroscopic, microscopic and biomechanical tests were performed. Surgical 3D bioprinting was performed in all animals without any intra- or postoperative complication. The HH biopen allowed early cartilage regeneration. The results of this study show that real-time, in vivo bioprinting with cells and scaffold is a feasible means of delivering a regenerative medicine strategy in a large animal model to regenerate articular cartilage.
引用
收藏
页码:611 / 621
页数:11
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