Microchip-based amperometric immunoassays using redox tracers Export

@article{citeulike:3734477, abstract = {A new chip-based electrochemical immunoassay protocol, based on the use of a ferrocene redox label, is described. Two reaction formats, based on direct (noncompetitive) and competitive modes of operation, were employed for illustrating the use of redox tracers in chip-based electrochemical immunoassays. The direct assay consisted of mixing the ferrocene-tagged antibody and the antigen analyte, a rapid electrophoretic separation of labeled free antibody and the labeled antigen/antibody complex, and a downstream anodic detection of the ferrocene tracer at gold-plated carbon screen-printed electrode detector. The competitive assay integrates precolumn reactions of the labeled antigen and the target antigen with the antibody with electrophoretic separation of the free and bound labeled antigens, along with amperometric detection of the redox tag. An internal standard has been used to normalize the peak area for the construction of calibration plots. Fundamental operating variables are examined and optimized. The use of a redox tracer offers the advantages of simplified protocol, wider linear range, higher stability, and higher separation efficiency compared to an analogous use of enzyme tags. The direct mouse-immunoglobulin G (IgG) assay and the competitive 3,3',5-triiodo-L-thyronine (T3) one were accomplished within less than 150 and 130 s (with field strengths of 256 and 192 V/cm), and offer minimum detectable concentrations of 2.5×10-12 and 1×10-6 g/mL, respectively. Such use of redox labels for chip-based amperometric immunoassay protocols offers considerable promise for decentralized clinical or environmental testing.}, address = {Department of Chemistry and Biochemistry, New Mexico State University, Las Cruces, NM, USA}, author = {Wang, Joseph and Ib\'{a}\~{n}ez, Alfredo and Chatrathi, Madhu P.}, citeulike-article-id = {3734477}, citeulike-linkout-0 = {http://dx.doi.org/10.1002/1522-2683(200211)23:21%3C3744::AID-ELPS3744%3E3.0.CO;2-B}, citeulike-linkout-1 = {http://www3.interscience.wiley.com/cgi-bin/abstract/100019643/ABSTRACT}, doi = {10.1002/1522-2683(200211)23:21%3C3744::AID-ELPS3744%3E3.0.CO;2-B}, journal = {ELECTROPHORESIS}, keywords = {ag\_detection, amperometry, competition, electrochemistry, ferrocene, heterogeneous, immunoassay, immunosensor}, number = {21}, pages = {3744--3749}, posted-at = {2008-12-02 09:02:30}, priority = {2}, title = {Microchip-based amperometric immunoassays using redox tracers}, url = {http://dx.doi.org/10.1002/1522-2683(200211)23:21%3C3744::AID-ELPS3744%3E3.0.CO;2-B}, volume = {23}, year = {2002} }

TY - JOUR ID - citeulike:3734477 L3 - citeulike-article-id:3734477 N2 - A new chip-based electrochemical immunoassay protocol, based on the use of a ferrocene redox label, is described. Two reaction formats, based on direct (noncompetitive) and competitive modes of operation, were employed for illustrating the use of redox tracers in chip-based electrochemical immunoassays. The direct assay consisted of mixing the ferrocene-tagged antibody and the antigen analyte, a rapid electrophoretic separation of labeled free antibody and the labeled antigen/antibody complex, and a downstream anodic detection of the ferrocene tracer at gold-plated carbon screen-printed electrode detector. The competitive assay integrates precolumn reactions of the labeled antigen and the target antigen with the antibody with electrophoretic separation of the free and bound labeled antigens, along with amperometric detection of the redox tag. An internal standard has been used to normalize the peak area for the construction of calibration plots. Fundamental operating variables are examined and optimized. The use of a redox tracer offers the advantages of simplified protocol, wider linear range, higher stability, and higher separation efficiency compared to an analogous use of enzyme tags. The direct mouse-immunoglobulin G (IgG) assay and the competitive 3,3',5-triiodo-L-thyronine (T3) one were accomplished within less than 150 and 130 s (with field strengths of 256 and 192 V/cm), and offer minimum detectable concentrations of 2.5×10-12 and 1×10-6 g/mL, respectively. Such use of redox labels for chip-based amperometric immunoassay protocols offers considerable promise for decentralized clinical or environmental testing. IS - 21 JF - ELECTROPHORESIS AD - Department of Chemistry and Biochemistry, New Mexico State University, Las Cruces, NM, USA EP - 3749 TI - Microchip-based amperometric immunoassays using redox tracers VL - 23 SP - 3744 KW - ag_detection KW - amperometry KW - competition KW - electrochemistry KW - ferrocene KW - heterogeneous KW - immunoassay KW - immunosensor AU - Wang, Joseph AU - Ibáñez, Alfredo AU - Chatrathi, Madhu PY - 2002/// UR - http://dx.doi.org/10.1002/1522-2683(200211)23:21%3C3744::AID-ELPS3744%3E3.0.CO;2-B ER -