Simple Plex: A Novel Multi‐Analyte, Automated Microfluidic Immunoassay Platform for the Detection of Human and Mouse Cytokines and Chemokines

American Journal of Reproductive Immunology - Tập 75 Số 6 - Trang 678-693 - 2016
Paulomi Aldo1, Gregory Marusov2, Danielle Svancara2, James David3, Gil Mor1
1Division of Reproductive Sciences, Department of Obstetrics, Gynecology and Reproductive Sciences, Yale University School of Medicine. New Haven, CT, USA
2ProteinSimple, San Jose, CA, USA
3R&D Systems Minneapolis MN USA

Tóm tắt

ProblemQuantitative measurement of proteins in bodily fluids or cellular preparations is critical for the evaluation of biomarkers or the study of complex cellular processes. While immunoassays are the most common quantitative approach used so far, they are not practical for the evaluation of multiple proteins. Microfluidic technology allows a fine spatial control in immobilizing proteins and biomolecules inside microchannels, eliminating cross‐reactivity between competing analytes, and allowing rapid and sensitive detection of targeted antigens for multiple applications. We report the characterization and validation of the Simple Plex platform for the detection and quantification of cytokines and chemokines from human and mouse samples.MethodCytokine and chemokine expression levels were determined using Simple Plex cartridges from ProteinSimple. Serum samples were obtained from the Yale Biorepository.ResultsOur data demonstrate an excellent correlation between the results obtained with Simple Plex and conventional immunoassays such as ELISA and Luminex.ConclusionWe describe the characterization and validation of Simple Plex, a novel multi‐analyte, automated microfluidic platform that allows the evaluation of cytokines and chemokines from human and mice biological samples. Simple Plex showed significant advantages over traditional approaches in terms of low sample volume requirements, sensitivity and dynamic range, coefficient of variation, and reproducibility.

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10.1089/aid.2012.0345

10.1158/1078-0432.CCR-07-1569

10.1186/ar3383

10.1373/clinchem.2009.127514

10.1373/clinchem.2008.120717

10.1128/CVI.05032-11

10.1158/1055-9965.EPI-08-0311

10.1016/j.bios.2006.06.005

10.1007/s00216-010-3678-8

10.1021/ac1009707

10.3184/003685012X13361524970266

10.1111/aji.12288

10.1111/j.1600-0897.2010.00908.x

10.1177/1933719114522553

10.1189/jlb.1206755

10.1084/jem.20060206