Department of Chemistry, Molecular Science Research Hub, Imperial College London, 82 Wood Lane, London, W12 0BZ, UK and Department of Chemical Engineering, Exhibition Road, Imperial College London, London, SW7 2AZ, UK.
Department of Chemistry, Molecular Science Research Hub, Imperial College London, 82 Wood Lane, London, W12 0BZ, UK.
Phys Chem Chem Phys. 2021 Feb 19;23(6):3693-3706. doi: 10.1039/d0cp06226j.
Microfluidics has been proposed as an attractive alternative to conventional bulk methods used in the generation of self-assembled biomimetic structures, particularly where there is a desire for more scalable production. The approach also allows for greater control over the self-assembly process, and parameters such as particle architecture, size, and composition can be finely tuned. Microfluidic techniques used in the generation of microscale assemblies (giant vesicles and higher-order multi-compartment assemblies) are fairly well established. These tend to rely on microdroplet templation, and the resulting structures have found use as comparmentalised motifs in artificial cells. Challenges in generating sub-micron droplets have meant that reconfiguring this approach to form nano-scale structures is not straightforward. This is beginning to change however, and recent technological advances have instigated the manufacture and manipulation of an increasingly diverse repertoire of biomimetic nano-assemblies, including liposomes, polymersomes, hybrid particles, multi-lamellar structures, cubosomes, hexosomes, nanodiscs, and virus-like particles. The following review will discuss these higher-order self-assembled nanostructures, including their biochemical and industrial applications, and techniques used in their production and analysis. We suggest ways in which existing technologies could be repurposed for the enhanced design, manufacture, and exploitation of these structures and discuss potential challenges and future research directions. By compiling recent advances in this area, it is hoped we will inspire future efforts toward establishing scalable microfluidic platforms for the generation of biomimetic nanoparticles of enhanced architectural and functional complexity.
微流控技术已被提议作为传统批量方法的替代方法,用于生成自组装仿生结构,特别是在需要更具可扩展性的生产时。该方法还允许对自组装过程进行更好的控制,并且可以精细调整颗粒结构、大小和组成等参数。用于生成微尺度组件(巨型囊泡和更高阶多腔组件)的微流控技术已经相当成熟。这些方法往往依赖于微滴模板,并且所得到的结构已被用作人工细胞中的分区基序。生成亚微米液滴的挑战意味着,要将这种方法重新配置为形成纳米级结构并不容易。然而,这种情况正在开始改变,最近的技术进步已经引发了越来越多样化的仿生纳米组件的制造和操纵,包括脂质体、聚合物体、混合颗粒、多层结构、立方体、六面体、纳米盘和病毒样颗粒。以下综述将讨论这些高阶自组装纳米结构,包括它们的生化和工业应用,以及用于生产和分析它们的技术。我们提出了如何重新利用现有技术来增强这些结构的设计、制造和利用,并讨论了潜在的挑战和未来的研究方向。通过整理该领域的最新进展,我们希望能够激发未来的努力,建立用于生成具有增强结构和功能复杂性的仿生纳米粒子的可扩展微流控平台。