Simon Bystryak1, Rasa Santockyte. 1. Allied Innovative Systems, Hillsborough, NJ (Santockyte is now with Bristol-Myers Squibb, Princeton, NJ).
Abstract
BACKGROUND: In this study we describe a photochemical signal amplification method (PSAM) for increasing of the sensitivity of enzyme-linked immunosorbent assay (ELISA) for determination of HIV-1 p24 antigen. The photochemical signal amplification method is based on an autocatalytic photochemical reaction of a horseradish peroxidase (HRP) substrate, orthophenylenediamine (OPD). METHODS: To compare the performance of PSAM-boosted ELISA with a conventional colorimetric ELISA for determination of HIV-1 p24 antigen we employed a PerkinElmer HIV-1 p24 ELISA kit, using conventional ELISA alongside ELISA + PSAM. RESULTS: In the present study, we show that PSAM technology allows one to increase the analytical sensitivity and dynamic range of a commercial HIV-1 p24 ELISA kit, with and without immune-complex disruption, by a factor of approximately 40-fold. CONCLUSIONS: ELISA + PSAM is compatible with commercially available microtiter plate readers, requires only an inexpensive illumination device, and the PSAM amplification step takes no longer than 15 min. This method can be used for both commercially available and in-house ELISA tests, and has the advantage of being considerably simpler and less costly than alternative signal amplification methods. This method can be used for both commercially available and in-house ELISA tests, and has the advantage of being considerably simpler and less costly than alternative signal amplification methods.
BACKGROUND: In this study we describe a photochemical signal amplification method (PSAM) for increasing of the sensitivity of enzyme-linked immunosorbent assay (ELISA) for determination of HIV-1p24 antigen. The photochemical signal amplification method is based on an autocatalytic photochemical reaction of a horseradish peroxidase (HRP) substrate, orthophenylenediamine (OPD). METHODS: To compare the performance of PSAM-boosted ELISA with a conventional colorimetric ELISA for determination of HIV-1p24 antigen we employed a PerkinElmer HIV-1p24 ELISA kit, using conventional ELISA alongside ELISA + PSAM. RESULTS: In the present study, we show that PSAM technology allows one to increase the analytical sensitivity and dynamic range of a commercial HIV-1p24 ELISA kit, with and without immune-complex disruption, by a factor of approximately 40-fold. CONCLUSIONS: ELISA + PSAM is compatible with commercially available microtiter plate readers, requires only an inexpensive illumination device, and the PSAM amplification step takes no longer than 15 min. This method can be used for both commercially available and in-house ELISA tests, and has the advantage of being considerably simpler and less costly than alternative signal amplification methods. This method can be used for both commercially available and in-house ELISA tests, and has the advantage of being considerably simpler and less costly than alternative signal amplification methods.
Authors: Eun-Young Kim; Jennifer Stanton; Bette T M Korber; Kendall Krebs; Derek Bogdan; Kevin Kunstman; Samuel Wu; John P Phair; Chad A Mirkin; Steven M Wolinsky Journal: Nanomedicine (Lond) Date: 2008-06 Impact factor: 5.307