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High-throughput particle manipulation by hydrodynamic electrokinetic and dielectrophoretic effects in an integrated microfluidic chip

机译:通过集成的微流控芯片中的流体动力学电动和介电泳效应进行高通量颗粒操纵

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摘要

Integrating different steps on a chip for cell manipulations and sample preparation is of foremost importance to fully take advantage of microfluidic possibilities, and therefore make tests faster, cheaper and more accurate. We demonstrated particle manipulation in an integrated microfluidic device by applying hydrodynamic, electroosmotic (EO), electrophoretic (EP), and dielectrophoretic (DEP) forces. The process involves generation of fluid flow by pressure difference, particle trapping by DEP force, and particle redirect by EO and EP forces. Both DC and AC signals were applied, taking advantages of DC EP, EO and AC DEP for on-chip particle manipulation. Since different types of particles respond differently to these signals, variations of DC and AC signals are capable to handle complex and highly variable colloidal and biological samples. The proposed technique can operate in a high-throughput manner with thirteen independent channels in radial directions for enrichment and separation in microfluidic chip. We evaluated our approach by collecting Polystyrene particles, yeast cells, and E. coli bacteria, which respond differently to electric field gradient. Live and dead yeast cells were separated successfully, validating the capability of our device to separate highly similar cells. Our results showed that this technique could achieve fast pre-concentration of colloidal particles and cells and separation of cells depending on their vitality. Hydrodynamic, DC electrophoretic and DC electroosmotic forces were used together instead of syringe pump to achieve sufficient fluid flow and particle mobility for particle trapping and sorting. By eliminating bulky mechanical pumps, this new technique has wide applications for in situ detection and analysis.
机译:为了充分利用微流体的可能性,将不同步骤集成到芯片上进行细胞处理和样品制备至关重要,因此可以使测试更快,更便宜,更准确。我们通过应用流体动力,电渗(EO),电泳(EP)和介电电泳(DEP)力证明了集成微流控设备中的粒子操纵。该过程涉及通过压差产生流体流,通过DEP力捕获颗粒,并通过EO和EP力进行颗粒重定向。施加了DC和AC信号,利用了DC EP,EO和AC DEP进行芯片上颗粒处理的优势。由于不同类型的粒子对这些信号的响应不同,因此DC和AC信号的变化能够处理复杂且高度可变的胶体和生物样品。所提出的技术可以以高通量的方式在径向上具有13个独立通道,以富集和分离微流体芯片。我们通过收集对电场梯度有不同响应的聚苯乙烯颗粒,酵母细胞和大肠杆菌细菌来评估我们的方法。成功分离了活酵母和死酵母细胞,验证了我们设备分离高度相似细胞的能力。我们的结果表明,这项技术可以实现胶体颗粒和细胞的快速预浓缩以及细胞的活力,这取决于它们的生命力。流体动力,直流电泳和直流电渗透力一起使用,而不是使用注射泵,以实现足够的流体流动和粒子迁移率,从而进行粒子捕集和分选。通过消除笨重的机械泵,这项新技术在现场检测和分析方面具有广泛的应用。

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