TY - JOUR
T1 - Improvements to a surface plasmon resonance-based immunoassay for the steroid hormone progesterone
AU - Gillis, Els H.
AU - Traynor, Imelda
AU - Gosling, James P.
AU - Kane, Marian
PY - 2006
Y1 - 2006
N2 - The effects of modifications to an existing protocol for a surface plasmon resonance biosensor-based inhibition immunoassay for progesterone in cow's milk with a sensitivity of 3.5 ng/mL were examined to establish if the detection limit could be further reduced to broaden the potential applications of the assay. The mean relative standard deviation of duplicate measurements was 0.62% and the high precision resulted in very low values for the lower detection limits. Hence, the standard concentrations giving 95% maximum binding [effective dose (ED 95)] were compared instead. The ED 95 was not affected within a running temperature range of 20-37°C, or at a flow rate and a contact time above 20 μL/min and 90 s, respectively. Increasing both the absolute sample volume and the antibody dilution improved sensitivity. However, there was a simultaneous reduction in the working range when the assay was applied to milk due to nonspecific binding. Less antibody was associated with large decreases in the maximum binding, but because the high precision extended over a broad analytical range, an ED 95 of 0.4-0.6 ng/mL in milk and 35-60 pg/mL in HBS-EP buffer were achieved. Thus, simple procedural modifications with the same sensor chip can alter performance characteristics of the assay as required for different applications.
AB - The effects of modifications to an existing protocol for a surface plasmon resonance biosensor-based inhibition immunoassay for progesterone in cow's milk with a sensitivity of 3.5 ng/mL were examined to establish if the detection limit could be further reduced to broaden the potential applications of the assay. The mean relative standard deviation of duplicate measurements was 0.62% and the high precision resulted in very low values for the lower detection limits. Hence, the standard concentrations giving 95% maximum binding [effective dose (ED 95)] were compared instead. The ED 95 was not affected within a running temperature range of 20-37°C, or at a flow rate and a contact time above 20 μL/min and 90 s, respectively. Increasing both the absolute sample volume and the antibody dilution improved sensitivity. However, there was a simultaneous reduction in the working range when the assay was applied to milk due to nonspecific binding. Less antibody was associated with large decreases in the maximum binding, but because the high precision extended over a broad analytical range, an ED 95 of 0.4-0.6 ng/mL in milk and 35-60 pg/mL in HBS-EP buffer were achieved. Thus, simple procedural modifications with the same sensor chip can alter performance characteristics of the assay as required for different applications.
UR - https://www.scopus.com/pages/publications/33750740416
U2 - 10.1093/jaoac/89.3.838
DO - 10.1093/jaoac/89.3.838
M3 - Article
SN - 1060-3271
VL - 89
SP - 838
EP - 842
JO - Journal of AOAC International
JF - Journal of AOAC International
IS - 3
ER -