Teh Shia-Yen, Khnouf Ruba, Fan Hugh, Lee Abraham P
Biomicrofluidics. 2011 Dec;5(4):44113-4411312. doi: 10.1063/1.3665221. Epub 2011 Dec 9.
In this paper, we present a microfluidic platform for the continuous generation of stable, monodisperse lipid vesicles 20-110 μm in diameter. Our approach utilizes a microfluidic flow-focusing droplet generation design to control the vesicle size by altering the system's fluid flow rates to generate vesicles with narrow size distribution. Double emulsions are first produced in consecutive flow-focusing channel geometries and lipid membranes are then formed through a controlled solvent extraction process. Since no strong solvents are used in the process, our method allows for the safe encapsulation and manipulation of an assortment of biological entities, including cells, proteins, and nucleic acids. The vesicles generated by this method are stable and have a shelf life of at least 3 months. Here, we demonstrate the cell-free in vitro synthesis of proteins within lipid vesicles as an initial step towards the development of an artificial cell.
在本文中,我们展示了一种微流控平台,用于连续生成直径为20 - 110μm的稳定、单分散脂质囊泡。我们的方法利用微流控流动聚焦液滴生成设计,通过改变系统的流体流速来控制囊泡大小,以生成具有窄尺寸分布的囊泡。首先在连续的流动聚焦通道几何结构中产生双重乳液,然后通过可控的溶剂萃取过程形成脂质膜。由于该过程中不使用强溶剂,我们的方法允许安全地封装和操作各种生物实体,包括细胞、蛋白质和核酸。通过这种方法生成的囊泡是稳定的,保质期至少为3个月。在此,我们展示了脂质囊泡内蛋白质的无细胞体外合成,作为迈向人工细胞开发的第一步。