Hosokawa Kazuo, Omata Masaki, Sato Kae, Maeda Mizuo
Bioengineering Laboratory, RIKEN, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan.
Lab Chip. 2006 Feb;6(2):236-41. doi: 10.1039/b513424b. Epub 2005 Dec 12.
This paper presents a simple fluid handling technique for microchip immunoassay. Necessary solutions were sequentially injected into a microchannel by air-evacuated poly(dimethylsiloxane), and were passively regulated by capillary force at the inlet opening. For heterogeneous immunoassay, microchips are potentially useful for reduction of sample consumption and assay time. However, most of the previously reported microchips have limitations in their use because of the needs for external power sources for fluid handling. In this paper, an on-chip heterogeneous immunofluorescence assay without such an external power source is demonstrated. The microchip consisting of poly(dimethylsiloxane) (PDMS) and glass has a simple structure, and therefore is suitable for single-use applications. Necessary solutions were sequentially injected into a microchannel in an autonomous fashion with the power-free pumping technique, which exploits the high solubility and the rapid diffusion of air in PDMS. For deionized water, this method yielded flow rates of 3-5 nL s-1 with reproducibility of 4-10%. The inlet opening of the microchannel functioned as a passive valve to hold the solution when the flow was finished. Rabbit immunoglobulin G (rIgG) and human C-reactive protein (CRP) were detected using the microchannel walls as reaction sites. With the sample consumption of 1 microL and the assay time of approximately 20 min including the antibody immobilization step, the sandwich immunoassay methods for rIgG and CRP exhibited the limits of detection of 0.21 nM (0.21 fmol) and 0.42 nM (0.42 fmol), respectively.
本文介绍了一种用于微芯片免疫测定的简单流体处理技术。通过抽气的聚二甲基硅氧烷将所需溶液依次注入微通道,并在入口处通过毛细作用力进行被动调节。对于非均相免疫测定,微芯片在减少样品消耗和测定时间方面具有潜在用途。然而,由于流体处理需要外部电源,大多数先前报道的微芯片在使用上存在局限性。本文展示了一种无需此类外部电源的芯片上非均相免疫荧光测定方法。由聚二甲基硅氧烷(PDMS)和玻璃组成的微芯片结构简单,因此适用于一次性应用。利用无外力泵技术,以自主方式将所需溶液依次注入微通道,该技术利用了空气在PDMS中的高溶解性和快速扩散性。对于去离子水,该方法产生的流速为3 - 5 nL s-1,重现性为4 - 10%。微通道的入口在流动结束时起到被动阀的作用以保持溶液。使用微通道壁作为反应位点检测兔免疫球蛋白G(rIgG)和人C反应蛋白(CRP)。在样品消耗为1 μL且测定时间约为20分钟(包括抗体固定步骤)的情况下,rIgG和CRP的夹心免疫测定方法分别表现出0.21 nM(0.21 fmol)和0.42 nM(0.42 fmol)的检测限。