Potential use of 3D-printed graphene oxide scaffold for construction of the cartilage layer

• Published in: Journal of nanobiotechnology 2020-07, Vol.18 (1), p.97-97, Article 97
• Main Authors: Cheng, Zhong, Xigong, Li, Weiyi, Diao, Jingen, Hu, Shuo, Wang, Xiangjin, Lin, Junsong, Wu
• Format: Article
• Language: English
• Subjects: 3-D printers; 3D printing; Aggrecan; Analysis; Animals; Apoptosis; Biocompatibility; Biological activity; Biomedical materials; Cartilage; Cartilage - cytology; Cell culture; Cell Line; Chondrocytes; Chondrocytes - cytology; Chondrocytes - metabolism; Collagen; Collagen (type I); Construction; Experiments; Fourier transforms; Graphene; Graphene oxide; Graphite; Graphite - chemistry; Immunofluorescence; Immunohistochemistry; Medical research; Morphology; Organic chemicals; Printing, Three-Dimensional; Proteins; Qualitative analysis; Rats; Rats, Sprague-Dawley; Researchers; Scaffolds; Scanning electron microscopy; Spectrum analysis; Three dimensional printing; Tissue Engineering - methods; Tissue Scaffolds - chemistry; Tissues; Transplants & implants; Transport vehicles
• ISSN: 1477-3155; 1477-3155
• DOI: 10.1186/s12951-020-00655-w

Three-dimensional (3D) printing involves the layering of seed cells, biologically compatible scaffolds, and biological activity factors to precisely recapitulate a biological tissue. Graphene oxide (GO), a type of micro material, has been utilized as a small molecule-transport vehicle. With the proliferation of GO, the biocompatibility of chondrocytes in a microenvironment constructed by 3D printed scaffolds and GO is innovative. Accordingly, we speculate that, as a type of micro material, GO can be used with 3D scaffolds for a uniform distribution in the cartilage layer. A qualitative analysis of the chondrocyte-proliferation potential revealed that the culture of 3D printing with a 10% GO scaffold was higher than that of the other groups. Meanwhile, the progress of cell apoptosis was activated. Through scanning electron microscopy, immunofluorescence, and in vivo research, we observed that the newborn cartilage matrix extended along the border of the cartilage and scaffold and matured. After an analysis with immunohistochemical staining with aggrecan and collagen I, the cartilage following the 3D-printed scaffold was thinner than that of the 3D-printed GO scaffold. Furthermore, the collagen I of the cartilage expression in treatment with the GO scaffold was significant from week 2 to 6. The findings indicate that a 3D-printed GO scaffold can potentially be utilized for the construction of a cartilage matrix. However, the optimum concentration of GO requires further research and discussion.