Journal
BIOSENSORS & BIOELECTRONICS
Volume 91, Issue -, Pages 489-496Publisher
ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2016.12.071
Keywords
Microfluidics; Air-bubble mixing; Single molecule RNA detection; Point-of-care
Categories
Funding
- W.M. Keck Center for Nanoscale Optofluidics at UC Santa Cruz
- NIH [4R33AI100229, 1R21AI100229]
- NSF [CBET-1159453, CBET-1159423]
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An automated microfluidic sample preparation multiplexer (SPM) has been developed and evaluated for Ebola virus detection. Metered air bubbles controlled by microvalves are used to improve bead-solution mixing thereby enhancing the hybridization of the target Ebola virus RNA with capture probes bound to the beads. The method uses thermally stable 4-formyl benzamide functionalized (4FB) magnetic beads rather than streptavidin coated beads with a high density of capture probes to improve the target capture efficiency. Exploiting an on chip concentration protocol in the SPM and the single molecule detection capability of the antiresonant reflecting optical waveguide (ARROW) biosensor chip, a detection limit of 0.021 pfu/mL for clinical samples is achieved without target amplification. This RNA target capture efficiency is two orders of magnitude higher than previous results using streptavidin beads and the limit of detection (LOD) improves 10x. The wide dynamic range of this technique covers the whole clinically applicable concentration range. In addition, the current sample preparation time is similar to 1 h which is eight times faster than previous work. This multiplexed, miniaturized sample preparation microdevice establishes a key technology that intended to develop next generation point-of care (POC) detection system.
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