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Bioprinting of a Cell-Laden Conductive Hydrogel Composite

自愈水凝胶 材料科学 光致聚合物 3D生物打印 佩多:嘘 明胶 曙红 组织工程 纳米技术 生物相容性材料 生物医学工程 聚合物 高分子化学 复合材料 聚合 染色 化学 病理 医学 生物化学 图层(电子)
作者
Andrew Spencer,Ehsan Shirzaei Sani,Jonathan R. Soucy,Carolyn C. Corbet,Asel Primbetova,Ryan A. Koppes,Nasim Annabi
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:11 (34): 30518-30533 被引量:163
标识
DOI:10.1021/acsami.9b07353
摘要

Bioprinting has gained significant attention for creating biomimetic tissue constructs with potential to be used in biomedical applications such as drug screening or regenerative medicine. Ideally, biomaterials used for three-dimensional (3D) bioprinting should match the mechanical, hydrostatic, bioelectric, and physicochemical properties of the native tissues. However, many materials with these tissue-like properties are not compatible with printing techniques without modifying their compositions. In addition, integration of cell-laden biomaterials with bioprinting methodologies that preserve their physicochemical properties remains a challenge. In this work, a biocompatible conductive hydrogel composed of gelatin methacryloyl (GelMA) and poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) was synthesized and bioprinted to form complex, 3D cell-laden structures. The biofabricated conductive hydrogels were formed by an initial cross-linking step of the PEDOT:PSS with bivalent calcium ions and a secondary photopolymerization step with visible light to cross-link the GelMA component. These modifications enabled tuning the mechanical properties of the hydrogels, with Young's moduli ranging from ∼40-150 kPa, as well as tunable conductivity by varying the concentration of PEDOT:PSS. In addition, the hydrogels degraded in vivo with no substantial inflammatory responses as demonstrated by haematoxylin and eosin (H&E) and immunofluorescent staining of subcutaneously implanted samples in Wistar rats. The parameters for forming a slurry of microgel particles to support 3D bioprinting of the engineered cell-laden hydrogel were optimized to form constructs with improved resolution. High cytocompatibility and cell spreading were demonstrated in both wet-spinning and 3D bioprinting of cell-laden hydrogels with the new conductive hydrogel-based bioink and printing methodology. The synergy of an advanced fabrication method and conductive hydrogel presented here is promising for engineering complex conductive and cell-laden structures.
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