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

被引:14
作者
Krausz, Alyse D. [1 ]
Korley, Frederick K. [2 ]
Burns, Mark A. [1 ,3 ]
机构
[1] Univ Michigan, Biomed Engn Dept, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Emergency Med & Michigan Medicle, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Chem Engn Dept, Ann Arbor, MI 48109 USA
来源
BIOSENSORS-BASEL | 2021年 / 11卷 / 09期
关键词
microfluidics; traumatic brain injury; multiplex; immunoassay; biomarkers; FIBRILLARY ACIDIC PROTEIN; ASSAY; ANTIBODIES; FLUID; MILD;
D O I
10.3390/bios11090320
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
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.
引用
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页数:17
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