琼脂糖
自愈水凝胶
3D生物打印
组织工程
材料科学
生物医学工程
泊洛沙姆
生物相容性
复合材料
聚合物
化学
色谱法
高分子化学
共聚物
医学
冶金
作者
Gabriel R. López-Marcial,Anne Zeng,C. Osuna,Joseph M. Dennis,Jeannette M. Garcı́a,Grace D. O’Connell
出处
期刊:ACS Biomaterials Science & Engineering
[American Chemical Society]
日期:2018-09-14
卷期号:4 (10): 3610-3616
被引量:140
标识
DOI:10.1021/acsbiomaterials.8b00903
摘要
Hydrogels are useful materials as scaffolds for tissue engineering applications. Using hydrogels with additive manufacturing techniques has typically required the addition of techniques such as cross-linking or printing in sacrificial materials that negatively impact tissue growth to remedy inconsistencies in print fidelity. Thus, there is a need for bioinks that can directly print cell-laden constructs. In this study, agarose-based hydrogels commonly used for cartilage tissue engineering were compared to Pluronic, a hydrogel with established printing capabilities. Moreover, new material mixtures were developed for bioprinting by combining alginate and agarose. We compared mechanical and rheological properties, including yield stress, storage modulus, and shear thinning, as well as construct shape fidelity to assess their potential as a bioink for cell-based tissue engineering. The rheological properties and printability of agarose–alginate gels were statistically similar to those of Pluronic for all tests (p > 0.05). Alginate–agarose composites prepared with 5% w/v (3:2 agarose to alginate ratio) demonstrated excellent cell viability over a 28-day culture period (>∼70% cell survival at day 28) as well matrix production over the same period. Therefore, agarose–alginate mixtures showed the greatest potential as an effective bioink for additive manufacturing of biological materials for cartilage tissue engineering.
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