A microfluidic multiplex proteomic immunoassay device for translational research

作者:Cao Jing; Seegmiller Jesse; Hanson Naomi Q; Zaun Christopher; Li Danni*
来源:Clinical Proteomics, 2015, 12(1): 28.
DOI:10.1186/s12014-015-9101-x

摘要

Objective: Microfluidic technology has the potential to miniaturize and automate complex laboratory procedures. The objective of this study was to assess a microfluidic immunoassay device, Simple Plex, which simultaneously measured IL-1 beta, TNF-alpha, IL-6, and IL-10 in serum samples. This assessment is important to understanding the potentials of this microfluidic device as a valuable tool in translational research efforts. Methods: We studied the operational characteristics of Simple Plex, and compared to other immunoassay systems including bead-based (i.e., Bio-Plex (R) from Bio-Rad) and planar micro-spot based (i.e., Multi-Array from Meso Scale Discovery) multiplex assays. We determined imprecisions for each of the Simple Plex assays and evaluated the ability of Simple Plex to detect IL-1 beta, TNF-alpha, IL-6, and IL-10 in serum samples. Results: Simple Plex assays required 25 mu L serum, and 1.5 h to run 16 samples per cartridge per instrument. Assay imprecisions, evaluated by measurement of 6 replicates in duplicate from a serum pool using three different cartridges, were less than 10 % for all 4 cytokine protein biomarkers, comparable to the imprecisions of traditional ELISAs. The Simple Plex assays were able to detect 32, 95, 97, and 100 % [i.e., percentages of the results within the respective analytical measurement ranges (AMRs)] of IL-1 beta, TNF-alpha, IL-6, and IL-10, respectively, in 66 serum samples. Conclusions: Simple Plex is a microfluidic multiplex immunoassay device that offers miniaturized, and automated analysis of protein biomarkers. Microfluidic devices such as Simple Plex represent a promising platform to be used in translational research to measure protein biomarkers in real clinical samples.

  • 出版日期2015-12-11