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Processing variables of direct-write, near-field electrospinning impact size and morphology of gelatin fibers

机译:直接写入的处理变量,明胶纤维的近场静电纺丝影响和形态

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Several biofabrication methods are being investigated to produce scaffolds that can replicate the structure of the extracellular matrix. Direct-write, near-field electrospinning of polymer solutions and electrowriting of polymer melts are methods which combine fine fiber formation with computer-guided control. Research with such systems has focused primarily on synthetic polymers. To better understand the behavior of biopolymers used for direct-writing, this project investigated changes in fiber morphology, size, and variability caused by varying gelatin and acetic acid concentration, as well as process parameters such as needle gauge and height, stage speed, and interfiber spacing. Increasing gelatin concentration at a constant acetic acid concentration improved fiber morphology from large, planar structures to small, linear fibers with a median of 2.3 mu m. Further varying the acetic acid concentration at a constant gelatin concentration did not alter fiber morphology and diameter throughout the range tested. Varying needle gauge and height further improved the median fiber diameter to below 2 mu m and variability of the first and third quartiles to within +/- 1 mu m of the median. Additional adjustment of stage speed did not impact the fiber morphology or diameter. Repeatable interfiber spacings down to 250 mu m were shown to be capable with the system. In summary, this study illustrates the optimization of processing parameters for direct-writing of gelatin to produce fibers on the scale of collagen fibers. This system is thus capable of replicating the fibrous structure of musculoskeletal tissues with biologically relevant materials which will provide a durable platform for the analysis of single cell-fiber interactions to help better understand the impact scaffold materials and dimensions have on cell behavior.
机译:正在研究几种生物制备方法以产生可以复制细胞外基质结构的支架。聚合物溶液的直接写入,聚合物熔体的近场静电纺丝是将细纤维形成与计算机引导控制相结合的方法。使用这种系统的研究主要集中在合成聚合物上。为了更好地了解用于直接写入的生物聚合物的行为,该项目调查了通过不同明胶和乙酸浓度引起的纤维形态,尺寸和可变性的变化,以及针仪和高度,阶段速度等工艺参数互相间隔。在恒定的乙酸浓度下增加明胶浓度改善了从大型平面结构到小,线性纤维的纤维形态,中值为2.3μm。进一步改变恒定明胶浓度下的乙酸浓度在测试的范围内没有改变纤维形态和直径。不同针脚测量仪和高度进一步改善了中位数的纤维直径至低于2μm的纤维直径,并在中位数的+/-1μm内的第一和第三个四分位数的可变性。额外调整阶段速度不会影响纤维形态或直径。将可重复的互补间距下降至250μmm,并能够具有该系统。总之,该研究说明了用于在胶原纤维的等级上产生纤维的直接写入的处理参数的优化。因此,该系统能够通过生物相关材料复制肌肉骨骼组织的纤维结构,该组织将提供一种用于分析单细胞纤维相互作用的耐用平台,以帮助更好地理解撞击支架材料和尺寸对细胞行为的影响。

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