| Literature DB >> 24781061 |
Xiang Wu1, Maung Kyaw Khaing Oo2, Karthik Reddy3, Qiushu Chen4, Yuze Sun5, Xudong Fan4.
Abstract
Enzyme-linked immunosorbent assay (ELISA) is a powerful method for biomolecular analysis. The traditional ELISA employing light intensity as the sensing signal often encounters large background arising from non-specific bindings, material autofluorescence and leakage of excitation light, which deteriorates its detection limit and dynamic range. Here we develop the optofluidic laser-based ELISA, where ELISA occurs inside a laser cavity. The laser onset time is used as the sensing signal, which is inversely proportional to the enzyme concentration and hence the analyte concentration inside the cavity. We first elucidate the principle of the optofluidic laser-based ELISA, and then characterize the optofluidic laser performance. Finally, we present the dual-mode detection of interleukin-6 using commercial ELISA kits, where the sensing signals are simultaneously obtained by the traditional and the optofluidic laser-based ELISA, showing a detection limit of 1 fg ml(-1) (38 aM) and a dynamic range of 6 orders of magnitude.Entities:
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Year: 2014 PMID: 24781061 DOI: 10.1038/ncomms4779
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919