High Performance Sensing Research Division, Frontier Research Center, Canon Inc., Tokyo, Japan.
Nanomedicine. 2011 Dec;7(6):889-95. doi: 10.1016/j.nano.2011.02.002. Epub 2011 Mar 1.
The amount of antibody in blood is an important measure of health status for making critical decisions in clinical practice. Here, we demonstrated a single-step, label-free, molecular diagnostic method based on localized surface plasmon resonance (LSPR) using standard 96-well microtiter plates. We improved the LSPR biosensor so that it can measure antibodies to blood group antigens in human serum with a single-step operation. First, we employed the ampholytic polymeric surface modification technique to present an efficient molecular scaffold on the sensor surface. Second, we selected the combination of an appropriate reference molecule against the antigen and a blocking agent to significantly reduce the variability of signal due to nonspecific responses of the unknown in the sample. Finally, we overcame the analytical difficulty arising from serum and achieved a single-step "wash-free" measurement of the amount of target antibody in human serum.
In this paper, a novel, single-step, label-free, molecular diagnostic method is discussed for antibody detection based on localized surface plasmon resonance using standard 96-well microtiter plates.
血液中的抗体数量是衡量健康状况的重要指标,对于临床实践中的关键决策至关重要。在这里,我们展示了一种基于局域表面等离子体共振(LSPR)的单步、无标记、分子诊断方法,使用标准的 96 孔微量滴定板。我们改进了 LSPR 生物传感器,使其能够通过单步操作测量人血清中的血型抗原抗体。首先,我们采用两性聚合物表面修饰技术在传感器表面呈现高效的分子支架。其次,我们选择了合适的抗原参考分子与阻断剂的组合,以显著降低由于样品中未知物的非特异性反应导致的信号变化。最后,我们克服了血清带来的分析困难,实现了人血清中目标抗体量的单步“免洗”测量。
本文讨论了一种新颖的、基于局域表面等离子体共振的单步、无标记、分子诊断方法,使用标准的 96 孔微量滴定板用于抗体检测。