MMN, Gulliver, ESPCI 10 rue Vauquelin, 75005 Paris, France.
Langmuir. 2010 Feb 16;26(4):2369-73. doi: 10.1021/la9028047.
Limitations in the methods employed to generate micrometric colloidal droplets hinder the emergence of key applications in the fields of material science and drug delivery. Through the use of dedicated nanofluidic devices and by taking advantage of an original physical effect called capillary focusing, we could circumvent some of these limitations. The nanofluidic (i.e., submicrometric) devices introduced herein are made of soft materials, and their fabrication relies upon rapid technologies. The objects that we have generated are simple droplets, multiple droplets, particles, and Janus particles whose sizes lie between 900 nm and 3 microm (i.e., within the colloidal range). Colloidal droplets have been assembled on-chip into clusters and crystals, yielding discrete diffraction patterns. We illustrate potential applications in the field of drug delivery by demonstrating the ability of multiple droplets to be phagocytosed by murine macrophage-type cells.
所采用的生成微尺度胶体液滴的方法存在局限性,这限制了其在材料科学和药物输送等领域的关键应用的发展。通过使用专用的纳流控装置,并利用一种称为毛细聚焦的原始物理效应,我们可以规避其中的一些限制。本文所介绍的纳流控(即亚微尺度)装置由软材料制成,其制造依赖于快速技术。我们生成的物体是尺寸在 900nm 到 3 微米之间(即胶体范围内)的简单液滴、多液滴、颗粒和双节粒子。胶体液滴已在芯片上组装成簇和晶体,产生离散的衍射图案。我们通过展示多液滴被鼠源巨噬细胞样细胞吞噬的能力,说明了在药物输送领域的潜在应用。