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Fabrication of Cell-Laden Hydrogel Fibers with Controllable Diameters

机译:直径可控的含细胞水凝胶纤维的制备

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摘要

Cell-laden hydrogel fibers are widely used as the fundamental building blocks to fabricate more complex functional three-dimensional (3D) structures that could mimic biological tissues. The control on the diameter of the hydrogel fibers is important so as to precisely construct structures in the above 3D bio-fabrication. In this paper, a pneumatic-actuated micro-extrusion system is developed to produce hydrogel fibers based on the crosslinking behavior of sodium alginate with calcium ions. Excellent uniformity has been obtained in the diameters of the fabricated hydrogel fibers as a proportional-integral-derivative (PID) control algorithm is applied on the driving pressure control. More importantly, a linear relationship has been obtained between the diameter of hydrogel fiber and the driving pressure. With the help of the identified linear model, we can precisely control the diameter of the hydrogel fiber via the control of the driving pressure. The differences between the measured and designed diameters are within ±2.5%. Finally, the influence of the calcium ions on the viability of the encapsulated cells is also investigated by immersing the cell-laden hydrogel fibers into the CaCl2 bath for different periods of time. LIVE/DEAD assays show that there is little difference among the cell viabilities in each sample. Therefore, the calcium ions utilized in the fabrication process have no impact on the cells encapsulated in the hydrogel fiber. Experimental results also show that the cell viability is 83 ± 2% for each sample after 24 h of culturing.
机译:载有细胞的水凝胶纤维被广泛用作制造更复杂的可以模仿生物组织的功能性三维(3D)结构的基本构件。水凝胶纤维直径的控制很重要,以便在上述3D生物加工中精确构建结构。在本文中,基于藻酸钠与钙离子的交联行为,开发了一种气动微挤出系统来生产水凝胶纤维。通过将比例积分微分(PID)控制算法应用于驱动压力控制,已在制造的水凝胶纤维的直径方面获得了出色的均匀性。更重要的是,已经在水凝胶纤维的直径和驱动压力之间获得了线性关系。借助已确定的线性模型,我们可以通过控制驱动压力来精确控制水凝胶纤维的直径。测量直径与设计直径之间的差异在±2.5%之内。最后,还通过将载有细胞的水凝胶纤维浸入CaCl2浴中不同时间来研究钙离子对包封细胞活力的影响。 LIVE / DEAD分析表明,每个样品中的细胞活力之间几乎没有差异。因此,在制造过程中使用的钙离子对封装在水凝胶纤维中的细胞没有影响。实验结果还显示,培养24小时后,每个样品的细胞活力为83±2%。

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