Hosokawa Kazuo, Omata Masaki, Maeda Mizuo
Bioengineering Laboratory, RIKEN, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan.
Anal Chem. 2007 Aug 1;79(15):6000-4. doi: 10.1021/ac070659o. Epub 2007 Jul 6.
We demonstrate a rapid (<30 min) and ultrasensitive (sub-picomolar) immunoassay on a microchip which needs no external power sources for fluid transport. We previously reported a rapid immunoassay of human C-reactive protein (CRP) on the power-free microchip with moderate sensitivity, i.e., a limit of detection (LOD) in sub-nanomolar range, due to the lack of signal amplification. In the current work, we have improved the LOD by 3 orders of magnitude by employing dendritic amplification (DA) methods. Specifically, a sandwich immunocomplex with a biotinylated secondary antibody was constructed on the inner surface of the microchannel as described in the previous report. Onto the immunocomplex, solutions of FITC-labeled streptavidin (F-SA) and biotinylated anti-streptavidin (B-anti-SA) were supplied to grow a dendritic structure. First, we alternately supplied the two solutions for layer-by-layer growth up to three layers. As a result, we obtained an LOD of 0.21 pM with a CRP sample volume of 1.0 microL and assay time of approximately 30 min under an ordinary fluorescence microscope. Second, to reduce the number of incubation steps, we have devised a new DA method: laminar flow-assisted dendritic amplification (LFDA). In this method, F-SA and B-anti-SA were simultaneously and continuously supplied from two laminar streams formed by a Y-shaped microchannel. The immunoassay with the LFDA for 10 min (total assay time of approximately 23 min) with a CRP sample volume of 0.5 microL yielded an LOD of 0.15 pM, which is equivalent to 75 zmol. The combination of the power-free microchip and the LFDA will provide a new opportunity for ultrasensitive point-of-care testing.
我们展示了一种在微芯片上进行的快速(<30分钟)且超灵敏(亚皮摩尔)的免疫测定方法,该方法在流体传输过程中无需外部电源。我们之前报道过在无电源微芯片上对人C反应蛋白(CRP)进行快速免疫测定,其灵敏度适中,即由于缺乏信号放大,检测限(LOD)在亚纳摩尔范围内。在当前工作中,我们通过采用树枝状放大(DA)方法将检测限提高了3个数量级。具体而言,如先前报道所述,在微通道内表面构建了带有生物素化二抗的夹心免疫复合物。在该免疫复合物上,供应异硫氰酸荧光素标记的链霉亲和素(F-SA)和生物素化抗链霉亲和素(B-抗-SA)溶液以生长树枝状结构。首先,我们交替供应这两种溶液进行逐层生长,直至三层。结果,在普通荧光显微镜下,使用1.0微升的CRP样品体积和大约30分钟的测定时间,我们获得了0.21皮摩尔的检测限。其次,为了减少孵育步骤的数量,我们设计了一种新的DA方法:层流辅助树枝状放大(LFDA)。在这种方法中,F-SA和B-抗-SA从由Y形微通道形成的两个层流中同时连续供应。使用LFDA进行10分钟(总测定时间约23分钟)的免疫测定,使用0.5微升的CRP样品体积,检测限为0.15皮摩尔,相当于75仄摩尔。无电源微芯片和LFDA的结合将为超灵敏即时检测提供新的机会。