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Microfluidic mixing and the formation of nanoscale lipid vesicles

机译:微流混合和纳米脂质囊泡的形成

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We investigate the formation of unilamellar lipid vesicles (liposomes) with diameters of tens of nanometers by controlled microfluidic mixing and nanoparticle determination (COMMAND). Our study includes liposome synthesis experiments and numerical modeling of our microfluidic implementation of the batch solvent injection method. We consider microfluidic liposome formation from the perspective of fluid interfaces and convective-diffusive mixing, as we find that bulk fluid flow parameters including hydrodynamically focused alcohol stream width, final alcohol concentration, and shear stress do not primarily determine the vesicle formation process. Microfluidic device geometry in conjunction with hydrodynamic flow focusing strongly influences vesicle size distributions, providing a coarse method to control liposome size, while total flow rate allows fine-tuning the vesicle size in certain focusing regimes. Although microfluidic liposome synthesis is relatively simple to implement experimentally, numerical simulations of the mixing process reveal a complex system of fluid flow and mass transfer determining the formation of nonequilibrium vesicles. These results expand our understanding of the microfluidic environment that controls liposome self-assembly and yield several technological advances for the on-chip synthesis of nanoscale lipid vesicles.
机译:我们通过控制微流体混合和纳米颗粒测定(COMMAND)研究了直径为数十纳米的单层脂质囊泡(脂质体)的形成。我们的研究包括脂质体合成实验和微流体实现间歇溶剂注射方法的数值模型。我们从流体界面和对流-扩散混合的角度考虑微流体脂质体的形成,因为我们发现包括流体动力学聚焦的醇流宽度,最终醇浓度和剪切应力在内的大量流体流动参数并不主要决定囊泡的形成过程。微流体装置的几何形状与流体动力流聚焦相结合会强烈影响囊泡大小分布,从而提供了一种粗略的方法来控制脂质体的大小,而总流速允许在某些聚焦方式下微调囊泡大小。尽管微流体脂质体合成相对容易地通过实验实现,但是混合过程的数值模拟显示了复杂的流体流动和传质系统,决定了非平衡囊泡的形成。这些结果扩大了我们对控制脂质体自组装的微流体环境的理解,并为纳米级脂质囊泡的片上合成带来了几项技术进步。

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