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Coding Cell Micropatterns Through Peptide Inkjet Printing for Arbitrary Biomineralized Architectures

机译:通过肽喷墨印刷为任意生物矿化的体系结构编码细胞微模式。

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摘要

Well-designed micropatterns present in native tissues and organs involve changes in extracellular matrix compositions, cell types and mechanical properties to reflect complex biological functions. However, the design and fabrication of these micropatterns in vitro to meet task-specific biomedical applications remains a challenge. A de novo design strategy to code and synthesize functional micropatterns is presented to engineer cell alignment through the integration of aqueous-peptide inkjet printing and site-specific biomineralization. The inkjet printing provides direct writing of macroscopic biosilica selective peptide-R5 patterns with micrometer-scale resolution on the surface of a biopolymer (silk) hydrogel. This is combined with in situ biomineralization of the R5 peptide for site-specific growth of silica nanoparticles on the micropatterns, avoiding the use of harsh chemicals or complex processing. The functional micropatterned systems are used to align human mesenchymal stem cells and bovine serum albumin. This combination of peptide printing and site-specific biomineralization provides a new route for developing cost-effective micropatterns, with implications for broader materials designs.
机译:存在于天然组织和器官中的精心设计的微模式涉及细胞外基质组成,细胞类型和机械特性的变化,以反映复杂的生物学功能。然而,体外设计和制造这些微图案以满足特定任务的生物医学应用仍然是一个挑战。提出了一种从头设计策略,用于编码和合成功能性微模式,以通过水肽喷墨印刷和特定于位置的生物矿化的整合来设计细胞比对。喷墨印刷可在生物聚合物(丝绸)水凝胶的表面上以微米级分辨率直接书写宏观的生物二氧化硅选择性肽R5模式。这与R5肽的原位生物矿化相结合,可在微图案上进行二氧化硅纳米颗粒的定点生长,从而避免使用刺激性化学物质或进行复杂的处理。功能性微模式系统用于对齐人间充质干细胞和牛血清白蛋白。肽印刷与特定位置的生物矿化的结合为开发具有成本效益的微图案提供了一条新途径,对更广泛的材料设计产生了影响。

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