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Numerical Investigation of Cell Encapsulation for Multiplexing Diagnostic Assays Using Novel Centrifugal Microfluidic Emulsification and Separation Platform

机译:新型离心微流控乳化分离平台用于多细胞诊断分析的细胞包裹的数值研究

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In the present paper, we report a novel centrifugal microfluidic platform for emulsification and separation. Our design enables encapsulation and incubation of multiple types of cells by droplets, which can be generated at controlled high rotation speed modifying the transition between dripping-to-jetting regimes. The droplets can be separated from continuous phase using facile bifurcated junction design. A three dimensional (3D) model was established to investigate the formation and sedimentation of droplets using the centrifugal microfluidic platform by computational fluid dynamics (CFD). The simulation results were compared to the reported experiments in terms of droplet shape and size to validate the accuracy of the model. The influence of the grid resolution was investigated and quantified. The physics associated with droplet formation and sedimentation is governed by the Bond number and Rossby number, respectively. Our investigation provides insight into the design criteria that can be used to establish centrifugal microfluidic platforms tailored to potential applications, such as multiplexing diagnostic assays, due to the unique capabilities of the device in handling multiple types of cells and biosamples with high throughput. This work can inspire new development of cell encapsulation and separation applications by centrifugal microfluidic technology.
机译:在本文中,我们报告了一种用于乳化和分离的新型离心微流控平台。我们的设计可通过液滴封装和孵育多种类型的细胞,这些液滴可在受控的高转速下产生,从而改变了滴液至喷射方式之间的过渡。可以使用便捷的分叉连接设计将液滴与连续相分离。建立了三维(3D)模型,以通过计算流体力学(CFD)使用离心微流平台研究液滴的形成和沉降。将模拟结果与报告的实验进行了液滴形状和大小的比较,以验证模型的准确性。研究并量化了网格分辨率的影响。与液滴形成和沉降有关的物理场分别由邦德数和罗斯比数控制。我们的研究提供了对可用于建立针对潜在应用(如多重诊断分析)量身定制的离心微流控平台的设计标准的见解,这归因于该设备以高通量处理多种类型的细胞和生物样品的独特功能。这项工作可以通过离心微流技术激发细胞封装和分离应用的新发展。

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