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MELT ELECTROSPINNING WRITING AND THE BIOFABRICATION OF VOLUMNOUS TISSUES AND ORGANS

机译:熔体静电纺丝技术和大体积组织和器官的生物制造

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Considering the complexity of natural tissues, a major challenge in tissue engineering applications is to produce three- dimensional (3D) structures that are anatomically accurate. This requires the manufacture of high resolution scaffolds in large volume (mL) dimensions, that can be effectively vascularized. Furthermore, the structural heterogeneity that occurs in living tissue needs to be replicated, at least in part. Multimodal constructs contain features across different length scales, and are a method to manufacture a high surface area scaffold with milliliter volumes. For example, electrospinning has been used in conjunction with fused deposition modelling (FDM) to create a "bimodal" scaffold that contained both small diameter and large diameter elements. In this instance, the ordered scaffold structure is provided by the FDM component, while the electrospun fibers fill up the pores between each FDM layer. While there has been a significant effort in developing similar techniques to manufacture multimodal substrates with a defined organization, the resolutions remain limited. In general, highly resolved scaffolds with micron-scale control are difficult to build in the centimeter scale-range. Additive manufacturing is poised to achieve complex, highly resolved and vascularized tissue constructs, through advances in both printing resolution and computer-directed fabrication based on customization. One additive manufacturing approach that could address this existing situation is melt electrospinning writing. This technique electrostatically stabilizes a falling molten thread, placing it accurately onto a collector without any jet break-up. It can generate organized 3D scaffolds with a precise and predictable layer-by-layer deposition with finely resolved fibers. This solvent-free approach provides a pathway to clinical products while addressing the need for 3D architecture requirements for a variety of tissue engineering applications. Examples of MEW scaffolds are shown in Figure 1.
机译:考虑到天然组织的复杂性,在组织工程应用中的主要挑战是产生解剖学上精确的三维(3D)结构。这需要制造大体积(mL)尺寸的高分辨率支架,该支架可以有效地血管化。此外,活体组织中发生的结构异质性需要至少部分复制。多峰构造包含跨越不同长度尺度的特征,并且是制造具有毫升体积的高表面积支架的方法。例如,静电纺丝已与熔融沉积建模(FDM)结合使用,以创建包含小直径和大直径元素的“双峰”支架。在这种情况下,有序的支架结构是由FDM组件提供的,而电纺纤维则填充了每个FDM层之间的孔。尽管在开发具有相似组织的类似技术以制造多峰基材方面已付出了巨大的努力,但分辨率仍然有限。通常,具有微米级控制的高度分解的支架难以在厘米级范围内构建。通过提高打印分辨率和基于定制的计算机控制制造,增材制造有望实现复杂,高度分解和血管化的组织构造。可以解决这种现有情况的一种增材制造方法是熔融电纺丝书写。该技术可静电稳定掉落的熔融线,将其准确地放置在集热器上,而不会破坏喷嘴。它可以生成具有精细且可解析的纤维的精确且可预测的逐层沉积的组织化3D支架。这种无溶剂方法为临床产品提供了途径,同时满足了各种组织工程应用对3D架构要求的需求。 MEW支架的示例如图1所示。

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