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Embedding Synthetic Microvascular Networks in Poly(Lactic Acid) Substrates with Rounded Cross-Sections for Cell Culture Applications

机译:将合成的微血管网络嵌入具有圆形横截面的聚乳酸基质中用于细胞培养

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摘要

Synthetic microvascular networks are essential to enable in vitro studies of cell biology, biophysics, hemodynamics, and drug discovery, as well as in applications involving tissue engineering and artificial vasculature. But current limitations make it challenging to construct networks incorporating a hierarchy of microchannel diameters that possess cell-favored circular cross-sectional topographies. We report a new approach that overcomes these limitations by employing pressure-assisted expansion of biocompatible degradable poly(lactic acid) (PLA) substrates. This single-step process is straightforward and highly controllable, making it possible to simultaneously shape the interior topology of branched 3D and pseudo-3D microchannel networks across wide range of diameters. We further demonstrate in vitro culture of confluent endothelial cell monolayers in microchannel networks treated by this process, suggesting potential as a tool to help generate bio-mimicking vascular-like environments.
机译:合成的微血管网络对于细胞生物学,生物物理学,血液动力学和药物发现的体外研究以及涉及组织工程和人工脉管系统的应用至关重要。但是当前的局限性使得构建具有微通道直径的层次结构的网络具有挑战性,该微通道直径具有细胞有利的圆形横截面形貌。我们报告了一种新的方法,通过采用压力辅助扩展生物相容性可降解聚乳酸(PLA)底物来克服这些局限性。此单步过程非常简单且可控性强,因此可以在各种直径范围内同时塑造分支3D和伪3D微通道网络的内部拓扑。我们进一步证明了融合培养的内皮细胞单层在通过该过程处理的微通道网络中的体外培养,表明其潜力可作为一种工具来帮助产生类似生物的血管样环境。

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