Univ. Grenoble Alpes, CNRS, Grenoble INP, G2Elab, 38000 Grenoble, France, 21 Avenue des Martyrs, 38031 Grenoble, France and Univ. Grenoble Alpes, CNRS, Grenoble INP, Institut Néel, 38000 Grenoble, France, 25 Avenue des Martyrs, 38042, Grenoble, France.
Univ. Grenoble Alpes, CNRS, Grenoble INP, G2Elab, 38000 Grenoble, France, 21 Avenue des Martyrs, 38031 Grenoble, France and Univ. Grenoble Alpes, CNRS, INSERM, IAB, 38000 Grenoble, France, Site Santé - Allée des Alpes, 38700 La Tronche, France.
Soft Matter. 2018 Apr 4;14(14):2671-2681. doi: 10.1039/C7SM02324C.
Micro-magnets producing magnetic field gradients as high as 106 T m-1 have been used to efficiently trap nanoparticles with a magnetic core of just 12 nm in diameter. Particle capture efficiency increases with increasing particle concentration. Comparison of measured capture kinetics with numerical modelling reveals that a threshold concentration exists below which capture is diffusion-driven and above which it is convectively-driven. This comparison also shows that two-way fluid-particle coupling is responsible for the formation of convective cells, the size of which is governed by the height of the droplet. Our results indicate that for a suspension with a nanoparticle concentration suitable for bioassays (around 0.25 mg ml-1), all particles can be captured in less than 10 minutes. Since nanoparticles have a significantly higher surface-to-volume ratio than the more widely used microparticles, their efficient capture should contribute to the development of next generation digital microfluidic lab-on-chip immunoassays.
已经使用产生高达 106 T m-1 的磁场梯度的微型磁铁来有效地捕获直径仅为 12nm 的具有磁性核的纳米粒子。颗粒捕获效率随颗粒浓度的增加而增加。将测量的捕获动力学与数值模拟进行比较表明,存在一个阈值浓度,低于该浓度时捕获是扩散驱动的,高于该浓度时捕获是对流驱动的。这种比较还表明,双向流固耦合是形成对流单元的原因,其尺寸由液滴的高度决定。我们的结果表明,对于适用于生物测定的悬浮液(约 0.25mg/ml),所有颗粒都可以在不到 10 分钟内捕获。由于纳米颗粒的表面积与体积比远远高于更广泛使用的微颗粒,因此它们的有效捕获应该有助于下一代数字微流控芯片实验室免疫测定的发展。