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A highly sensitive multiplex immunoassay for inflammatory cytokines in dried blood spots
Objectives Inflammatory cytokines are key regulators of inflammation, but current measurement approaches require venous blood to quantify low circulating concentrations associated with chronic, low‐grade inflammation. This article describes a highly sensitive multiplex immunoassay protocol for the m...
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Published in: | American journal of human biology 2021-11, Vol.33 (6), p.e23558-n/a |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Objectives
Inflammatory cytokines are key regulators of inflammation, but current measurement approaches require venous blood to quantify low circulating concentrations associated with chronic, low‐grade inflammation. This article describes a highly sensitive multiplex immunoassay protocol for the measurement of IL6, IL8, IL10, and TNFα in finger stick dried blood spot (DBS) samples.
Methods
The protocol uses a multiplex electrochemiluminescent immunoassay platform. The following measures of assay performance were evaluated: reliability (inter‐assay percent coefficient of variation; %CV), precision (intra‐assay %CV), lower limit of detection (LLD), linearity of dilution, and agreement with results from matched plasma samples.
Results
Analysis of three control samples across the assay range indicated an acceptable level of precision and reliability for each cytokine. Linearity of dilution returned average values that ranged from 104.1 to 127.6% of expected. Lower limits of detection for IL6, IL8, and IL10 were |
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ISSN: | 1042-0533 1520-6300 |
DOI: | 10.1002/ajhb.23558 |