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A method for measuring multiple cytokines from small samples.

Kevin A O'Connor·Adelina Holguin·Michael K Hansen·Steven F Maier·Linda R Watkins
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Abstract

Commercially available enzyme-linked immunosorbent assay (ELISA) kits are commonly used to assess levels of proinflammatory cytokines in biological samples. Most of these kits require sample volumes of at least 50 microl. Thus, in order to examine multiple cytokines, volumes greater than 100 microl must be collected. However, the volume of many biological samples, especially those collected from the central nervous system (i.e., microdialysates, push-pull perfusions, or cerebrospinal fluid samples), is much less than 100 microl. Therefore, we developed a method for analyzing multiple cytokines from a single, low-volume biological sample, which involves serially assaying the samples on multiple proinflammatory cytokine ELISA kits. In many cases, assaying for one cytokine does not interfere with subsequent assay for another cytokine in the same sample. Moreover, when interference is observed, the interfering factor can be identified and its effect minimized.

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AnimalsBody FluidsEnzyme-Linked Immunosorbent AssayInterleukin-1Interleukin-6MaleRatsRats, Sprague-DawleyReproducibility of ResultsSample SizeSensitivity and SpecificityTumor Necrosis Factor-alphaComparative StudyJournal ArticleResearch Support, U.S. Gov't, P.H.S.Validation Study

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Kevin A O'Connor, Adelina Holguin, Michael K Hansen, Steven F Maier, Linda R Watkins. 2004. A method for measuring multiple cytokines from small samples.. https://doi.org/10.1016/j.bbi.2003.09.009

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