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Potentiometric Immunoassay with Quantum Dot Labels
Author(s) -
Reto Thürer,
Tamás Vigassy,
Martina Hirayama,
Joseph Wang,
Eric Bakker,
Ernö Pretsch
Publication year - 2007
Publication title -
analytical chemistry
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.117
H-Index - 332
eISSN - 1520-6882
pISSN - 0003-2700
DOI - 10.1021/ac070932m
Subject(s) - chemistry , potentiometric titration , detection limit , immunoassay , quantum dot , analytical chemistry (journal) , electrode , chromatography , hydrogen peroxide , electrochemistry , nanotechnology , organic chemistry , materials science , antibody , immunology , biology
Potentiometric sensors based on polymer membrane electrodes, if properly optimized, are useful for measurements at trace levels. The expected independence of the electrochemical signal of the sample size makes them extremely attractive for measurements in small volumes. Here, we report on electrodes for the potentiometric detection of cadmium ions that reach a detection limit of 6 nM and utilize a Na(+)-selective electrode as pseudoreference in order to facilitate measurements in 150-microL samples. A potentiometric immunoassay of mouse IgG is performed via CdSe quantum dot labels on a secondary antibody according to a sandwich immunoassay protocol in a microtiter plate format. The CdSe quantum dots are found to be easily dissolved/oxidized in a matter of minutes with hydrogen peroxide, allowing us to maintain the pH at a near-neutral value. The potentiometric protein immunoassay exhibits a log-linear response ranging from 0.15 to 4.0 pmol of IgG, with a detection limit of <10 fmol in 150-microL sample wells.

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