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生物玻璃复合甲基丙烯酸化胶原蛋白生物活性墨水用于骨组织的3D打印。

Bioglass incorporated methacrylated collagen bioactive ink for 3D printing of bone tissue.

作者信息

Kajave Nilabh S, Schmitt Trevor, Nguyen Thuy-Uyen, Gaharwar Akhilesh K, Kishore Vipuil

机构信息

Department of Biomedical and Chemical Engineering and Sciences, Florida Institute of Technology, Melbourne, FL 32901, United States of America.

Department of Biomedical Engineering, Texas A&M University, College Station, TX 77843, United States of America.

出版信息

Biomed Mater. 2021 Feb 26;16(3). doi: 10.1088/1748-605X/abc744.

Abstract

Bioactive three-dimensional (3D) printed scaffolds are promising candidates for bone tissue engineering (BTE) applications. Here, we introduce a bioactive ink composed of Bioglass 45S5 (BG) and methacrylated collagen (CMA) for 3D printing of biomimetic constructs that resemble the organic and inorganic composition of native bone tissue. A uniform dispersion of BG particles within the collagen network improved stability and reduced swelling of collagen hydrogels. Rheological testing showed significant improvement in the yield stress and percent recovery of 3D printed constructs upon BG incorporation. Further, addition of BG improved the bone bioactivity of 3D printed constructs in stimulated body fluid. BG incorporated CMA (BG-CMA) constructs maintained high cell viability and enhanced alkaline phosphatase activity of human mesenchymal stem cells. In addition, cell-mediated calcium deposition was significantly higher on BG-CMA constructs, compared to CMA alone. In conclusion, 3D printed BG-CMA constructs have significant potential for use in BTE applications.

摘要

生物活性三维(3D)打印支架是骨组织工程(BTE)应用中很有前景的候选材料。在此,我们介绍一种由生物玻璃45S5(BG)和甲基丙烯酸化胶原蛋白(CMA)组成的生物活性墨水,用于3D打印类似于天然骨组织有机和无机组成的仿生构建体。BG颗粒在胶原蛋白网络中的均匀分散提高了稳定性并减少了胶原蛋白水凝胶的肿胀。流变学测试表明,加入BG后,3D打印构建体的屈服应力和恢复百分比有显著改善。此外,BG的加入提高了3D打印构建体在模拟体液中的骨生物活性。含有BG的CMA(BG-CMA)构建体保持了高细胞活力,并增强了人间充质干细胞的碱性磷酸酶活性。此外,与单独的CMA相比,BG-CMA构建体上细胞介导的钙沉积明显更高。总之,3D打印的BG-CMA构建体在BTE应用中具有巨大的应用潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0c0/8326306/47a6b878e39a/nihms-1726426-f0001.jpg

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