4.8 Article

Nanoscale Functionalized Particles with Rotation-Controlled Capture in Shear Flow

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 10, Issue 34, Pages 29058-29068

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.8b05328

Keywords

microparticle capture; surface heterogeneity; hydrodynamic; flow; shear; colloid deposition; patchy particles; flow vorticity

Funding

  1. NSF [12-64855]
  2. National Institutes of Health [T32 GM008515]

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Important processes in nature and technology involve the adhesive capture of flowing particles or cells on the walls of a conduit. This paper introduces engineered spherical microparticles whose capture rates are limited by their near surface motions in flow. Specifically, these microparticles are sparsely functionalized with nanoscopic regions (patches) of adhesive functionality, without which they would be non-adhesive. Not only is particle capture on the wall of a shear chamber limited by surface chemistry as opposed to transport, but also the capture rates depend specifically on particle rotations that result from the vorticity of the shear flow field. These particle rotations continually expose new particle surface to the opposing chamber wall, sampling the particle surface for an adhesive region and controlling the capture rate. Control studies with the same patchy functionality on the chamber wall rather than the particles reveal a related signature of particle capture but substantially faster (still surface limited) particle capture rates. Thus, when the same functionality is placed on the wall rather than the particles, the capture is faster because it depends on the particle translation past a functionalized wall rather than on the particle rotations. The dependence of particle capture on functionalization of the particles versus the wall is consistent with the faster near-wall particle translation in shearing flow compared with the velocity of the rotating particle surface near the wall. These findings, in addition to providing a new class of nanoscopically patchy engineered particles, provide insight into the capture and detection of cells presenting sparse distinguishing surface features and the design of delivery packages for highly targeted pharmaceutical delivery.

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