Microfluidic Mixing and the Formation of Nanoscale Lipid Vesicles

被引:329
作者
Jahn, Andreas [1 ,3 ]
Stavis, Samuel M. [1 ]
Hong, Jennifer S. [1 ]
Vreeland, Wyatt N. [2 ]
Devoe, Don L. [3 ]
Gaitan, Michael [1 ]
机构
[1] Natl Inst Stand & Technol, Div Semicond Elect, Gaithersburg, MD 20899 USA
[2] Natl Inst Stand & Technol, Div Biochem Sci, Gaithersburg, MD 20899 USA
[3] Univ Maryland, Dept Mech Engn, College Pk, MD 20742 USA
关键词
liposome; lipid vesicle; nanoparticle; microfluidic mixing; hydrodynamic focusing; microfluidic injection; simulation; MUTUAL DIFFUSION-COEFFICIENT; SINGLE BILAYER LIPOSOMES; INJECTION METHOD; DIRECTED GROWTH; BINARY-MIXTURES; WATER; FLOW; MICROCHANNELS; EXTRUSION; CHIP;
D O I
10.1021/nn901676x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 locusing 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.
引用
收藏
页码:2077 / 2087
页数:11
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