4.7 Article

A Variable Height Microfluidic Device for Multiplexed Immunoassay Analysis of Traumatic Brain Injury Biomarkers

期刊

BIOSENSORS-BASEL
卷 11, 期 9, 页码 -

出版社

MDPI
DOI: 10.3390/bios11090320

关键词

microfluidics; traumatic brain injury; multiplex; immunoassay; biomarkers

资金

  1. Joyce and Don Massey Family Foundation through the Michigan Center for Integrative Research in Critical Care (MCIRCC) at the University of Michigan
  2. Microfluidics in Biomedical Sciences Training Program (MBSTP) [T32 EB005582]
  3. Scholars Awards grant program of Precision Health at the University of Michigan

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The study introduced a novel variable height microfluidic device for multiplexing multiple TBI biomarkers simultaneously, which can passively multiplex bead-based immunoassays by trapping beads based on their diameter matching the channel height.
Traumatic brain injury (TBI) is a leading cause of global morbidity and mortality, partially due to the lack of sensitive diagnostic methods and efficacious therapies. Panels of protein biomarkers have been proposed as a way of diagnosing and monitoring TBI. To measure multiple TBI biomarkers simultaneously, we present a variable height microfluidic device consisting of a single channel that varies in height between the inlet and outlet and can passively multiplex bead-based immunoassays by trapping assay beads at the point where their diameter matches the channel height. We developed bead-based quantum dot-linked immunosorbent assays (QLISAs) for interleukin-6 (IL-6), glial fibrillary acidic protein (GFAP), and interleukin-8 (IL-8) using Dynabeads M-450, M-270, and MyOne, respectively. The IL-6 and GFAP QLISAs were successfully multiplexed using a variable height channel that ranged in height from similar to 7.6 mu m at the inlet to similar to 2.1 mu m at the outlet. The IL-6, GFAP, and IL-8 QLISAs were also multiplexed using a channel that ranged in height from similar to 6.3 mu m at the inlet to similar to 0.9 mu m at the outlet. Our system can keep pace with TBI biomarker discovery and validation, as additional protein biomarkers can be multiplexed simply by adding in antibody-conjugated beads of different diameters.

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