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首页> 外文期刊>Bioactive Materials >3D-printable supramolecular hydrogels with shear-thinning property: fabricating strength tunable bioink via dual crosslinking
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3D-printable supramolecular hydrogels with shear-thinning property: fabricating strength tunable bioink via dual crosslinking

机译:具有剪切稀疏性的3D可印刷的超分子水凝胶:通过双交联制造强度可调性生物锁

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3-dimensional (3D) bioprinting technology provides promising strategy in the fabrication of artificial tissues and organs. As the fundamental element in bioprinting process, preparation of bioink with ideal mechanical properties without sacrifice of biocompatibility is a great challenge. In this study, a supramolecular hydrogel-based bioink is prepared by polyethylene glycol (PEG) grafted chitosan, α -cyclodextrin ( α -CD) and gelatin. It has a primary crosslinking structure through the aggregation of the pseudo-polyrotaxane-like side chains, which are formed from the host-guest interactions between α -CD and PEG side chain. Apparent viscosity measurement shows the shear-shinning property of this bioink, which might be due to the reversibility of the physical crosslinking. Moreover, with β -glycerophosphate at different concentrations as the secondary crosslinking agent, the printed constructs demonstrate different Young's modulus (p??0.001). They could also maintain the Young's modulus in cell culture condition for at least 21 days (p??0.05). By co-culturing each component with fibroblasts, CCK-8 assay demonstrate cellular viability is higher than 80%. After bioprinting and culturing, immunofluorescence staining with quantification indicate the expression of Ki-67, Paxillin, and N-cadherin is higher in day 14 than those in day 3 (p??0.05). Oil red O and Nissl body specific staining reflect strength tunable bioink may have impact on the cell fate of mesenchymal stem cells (p??0.05). This work might provide new idea for advanced bioink in the application of re-establishing complicated tissues and organs.
机译:3维(3D)生物监测技术在人工组织和器官的制造方面提供了有希望的策略。作为生物监测过程中的基本要素,具有理想的机械性能的生物链,没有生物相容性的牺牲是一个很大的挑战。在该研究中,通过聚乙二醇(PEG)接枝壳聚糖,α-环糊精(α-CD)和明胶制备了基于超分子的水凝胶的生物蛋白。它通过伪聚光甲烷的侧链的聚集具有主要交联结构,该副聚甲烷的侧链由α-CD和PEG侧链之间的宿主 - 客体相互作用形成。表观粘度测量显示了该生物链的剪切闪存性能,这可能是由于物理交联的可逆性。此外,用不同浓度的β-甘油磷酸盐作为二次交联剂,印刷构建体展示了不同的杨氏模量(P?<0.001)。它们还可以将杨氏模量保持在细胞培养条件至少21天(P?<?0.05)。通过将每个组分与成纤维细胞共同培养,CCK-8测定表明细胞活力高于80%。在生物制品和培养后,用定量的免疫荧光染色表达了KI-67,帕西林和N-钙粘蛋白的表达,在第14天比第3天(P?<0.05)。油红色O和NISSL体特异性染色反射强度可调谐生物链可能对间充质干细胞的细胞命运产生影响(P?<β05)。在重建复杂组织和器官的应用中,这项工作可能为高级生物链接提供新的想法。

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