Microfluidic devices with templated regular macroporous structures for HIV viral capture

Analyst. 2016 Mar 7;141(5):1669-77. doi: 10.1039/c5an02282g.

Abstract

There is a need to develop inexpensive, portable and easy-to-use devices for viral sample processing for resource-limited settings. Here we offer a solution to efficient virus capture by incorporating macroporous materials with regular structures into microfluidic devices for affinity chromatography. Two-dimensional simulations were first conducted to investigate the effects of two structures, a nanopost array and a spherical pore network, on nanoparticle capture. Then, the two structures were created in polymers by templating anodic aluminum oxide films and 3D close-packed silica particles, respectively. When the microdevices containing functionalized porous materials were tested for human immunodeficiency virus (HIV) isolation, capture efficiencies of 80-99% were achieved under a continuous flow. Comparatively, functionalized flatbed microchannels captured around 10% of HIV particles. As the characteristic dimensions of the nanostructures are tunable, such devices can be adapted for the capture of different submicron bioparticles. The high capture efficiency and easy-to-operate nature suit the needs of resource-limited settings and may find applications in point-of-care diagnostics.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • HEK293 Cells
  • HIV / isolation & purification*
  • Humans
  • Lab-On-A-Chip Devices*
  • Nanoparticles / chemistry
  • Nanotechnology / instrumentation*
  • Polymethyl Methacrylate / chemistry
  • Polystyrenes / chemistry
  • Porosity
  • Virion / isolation & purification

Substances

  • Polystyrenes
  • Polymethyl Methacrylate