Radboud University , Institute for Molecules and Materials, Heyendaalseweg 135, 6525 AJ Nijmegen, The Netherlands.
J Am Chem Soc. 2016 Jun 22;138(24):7584-91. doi: 10.1021/jacs.6b02107. Epub 2016 Jun 9.
Liposomes are self-assembled phospholipid vesicles with great potential in fields ranging from targeted drug delivery to artificial cells. The formation of liposomes using microfluidic techniques has seen considerable progress, but the liposomes formation process itself has not been studied in great detail. As a result, high throughput, high-yielding routes to monodisperse liposomes with multiple compartments have not been demonstrated. Here, we report on a surfactant-assisted microfluidic route to uniform, single bilayer liposomes, ranging from 25 to 190 μm, and with or without multiple inner compartments. The key of our method is the precise control over the developing interfacial energies of complex W/O/W emulsion systems during liposome formation, which is achieved via an additional surfactant in the outer water phase. The liposomes consist of single bilayers, as demonstrated by nanopore formation experiments and confocal fluorescence microscopy, and they can act as compartments for cell-free gene expression. The microfluidic technique can be expanded to create liposomes with a multitude of coupled compartments, opening routes to networks of multistep microreactors.
脂质体是由磷脂自组装形成的囊泡,在靶向药物输送到人工细胞等领域具有巨大的应用潜力。使用微流控技术制备脂质体已经取得了相当大的进展,但脂质体的形成过程本身并没有被详细研究。因此,尚未证明具有高通量、高产率的方法来制备具有多个隔室的单分散脂质体。在这里,我们报告了一种表面活性剂辅助的微流控途径,用于制备均匀的、单双层脂质体,尺寸范围从 25 到 190μm,并且具有或不具有多个内部隔室。我们方法的关键是通过在外水相中添加额外的表面活性剂,精确控制复杂的 W/O/W 乳液系统在脂质体形成过程中的界面能的发展。通过纳米孔形成实验和共聚焦荧光显微镜证明了这些脂质体由单层组成,并且可以作为无细胞基因表达的隔室。微流控技术可以扩展到创建具有多种耦合隔室的脂质体,为多步微反应器网络开辟了道路。