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Characterization of enzymatic micromachining for construction of variable cross-section microchannel topologies

机译:用于构建可变截面微通道拓扑的酶促微加工的表征

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摘要

The ability to harness enzymatic activity as an etchant to precisely machine biodegradable substrates introduces new possibilities for microfabrication. This flow-based etching is straightforward to implement, enabling patterning of microchannels with topologies that incorporate variable depth along the cross-sectional dimension. Additionally, unlike conventional small-molecule formulations, the macromolecular nature of enzymatic etchants enables features to be precisely positioned. Here, we introduce a kinetic model to characterize the enzymatic machining process and its localization by co-injection of a macromolecular inhibitor species. Our model captures the interaction between enzyme, inhibitor, and substrate under laminar flow, enabling rational prediction of etched microchannel profiles so that cross-sectional topologies incorporating complex lateral variations in depth can be constructed. We also apply this approach to achieve simultaneous widening of an entire network of microchannels produced in the biodegradable polymeric substrate poly(lactic acid), laying a foundation to construct systems incorporating a broad range of internal cross-sectional dimensions by manipulating the process conditions.
机译:利用酶活性作为蚀刻剂来精确加工可生物降解基材的能力为微细加工提供了新的可能性。这种基于流的蚀刻易于实现,从而可以对微通道进行构图,使其拓扑结构的横截面深度可变。另外,与常规的小分子制剂不同,酶促蚀刻剂的大分子性质使特征能够精确定位。在这里,我们介绍一个动力学模型来表征酶促加工过程及其通过共注入大分子抑制剂物质的定位。我们的模型捕获层流下酶,抑制剂和底物之间的相互作用,从而能够合理地预测蚀刻的微通道轮廓,从而可以构建结合深度复杂变化的横截面拓扑。我们还应用这种方法来同时拓宽可生物降解的聚合物基质聚乳酸中产生的微通道的整个网络,从而为通过操纵工艺条件来构建具有广泛内部横截面尺寸的系统奠定了基础。

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