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Post-bioprinting processing methods to improve cell viability and pattern fidelity in heterogeneous tissue test systems

机译:后生生物监测处理方法,以改善异构组织测试系统中的细胞活力和模式保真度

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Bioprinted tissue test systems show promise as a powerful tool for studying cell-cell interaction in heterogeneous, tissue-like co-culture. Several challenges were encountered while attempting to consistently fabricate samples with high viability and pattern fidelity. This paper evaluates four methods for processing samples after bioprinting but prior to adding media for incubation. These methods, composed of various combinations of three techniques meant to promote cell hydration, are evaluated with respect to sample viability and pattern preservation. In the best performing method, Hank's Balanced Salt Solution was applied immediately after fabrication and a collagen overlayer was applied one hour thereafter. The success of this method highlights the ability of the collagen substrate to absorb moisture, which promotes cell health without disturbing the cell's printed location. An addendum to the main study is an investigation of the limits of an HP26 print cartridge to deposit cells at a faster rate for the purpose of creating cell layers with densities that approach confluence.
机译:Bioplinted组织测试系统将承诺作为研究异质,组织状共同培养中的细胞 - 细胞相互作用的强大工具。遇到了几种挑战,同时尝试一致地制造具有高活力和模式保真度的样品。本文评估生物制品后处理样品的四种方法,但在添加培养基之前进行培养。通过三种技术的各种组合组成的这些方法是根据样品活力和模式保存的三种技术的各种组合组成。在最佳性能的方法中,在制造后立即施加Hank的平衡盐溶液,然后将胶原覆层覆盖物在此后一小时施加。该方法的成功突出了胶原基质吸收水分的能力,这促进了细胞健康而不会扰乱细胞的印刷位置。主要研究的增编对于HP26打印盒的限制,以更快的速率进行沉积电池的限制,以便创造具有接近汇合的密度的细胞层。

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