Heyries Kevin A, Loughran Michael G, Hoffmann Daniel, Homsy Alexandra, Blum Loïc J, Marquette Christophe A
Laboratoire de Génie Enzymatique et Biomoléculaire, Université Lyon 1, CNRS 5246 ICBMS, Bât CPE, Villeurbanne Cedex, France.
Biosens Bioelectron. 2008 Jul 15;23(12):1812-8. doi: 10.1016/j.bios.2008.02.025. Epub 2008 Mar 7.
Protein microarrays for allergen-specific antibodies detection were integrated in microfluidic chips, with imaging chemiluminescence as the analytical technique. This paper demonstrates the feasibility of miniaturized chemiluminescent ELISA by presenting rapid, reproducible and sensitive detection of protein antibodies using microfluidics. Three different proteins, beta-lactoglobulin, peanut lectin and human IgG were immobilized via a "macromolecules to polydimethylsiloxane elastomer (PDMS) transfer" protocol and used as capturing agent for the detection of specific antibodies. A convenient and reversible procedure was used to bond the PDMS microarray substrate to complimentary SU-8/glass microfluidic reaction chambers. The hydrodynamic behaviours of the three proteins interactions within the micro-chambers were investigated to select the most efficient flowing parameters (come to terms with the assay time and performances). The use of optimized conditions led to the concomitant detection of three specific antibodies at pM level in 300 microL and using 6 min sample incubation time. Finally, sera from allergic patients were assayed using the microfluidic device modified with apple hazelnut and pollen allergen. The results obtained compared favourably with those obtained with the classical Pharmacia CAP system.
用于检测过敏原特异性抗体的蛋白质微阵列被集成到微流控芯片中,采用成像化学发光作为分析技术。本文通过展示使用微流控技术对蛋白质抗体进行快速、可重复且灵敏的检测,证明了小型化化学发光酶联免疫吸附测定法的可行性。通过“大分子到聚二甲基硅氧烷弹性体(PDMS)转移”方案固定了三种不同的蛋白质,即β-乳球蛋白、花生凝集素和人免疫球蛋白,并将其用作捕获剂来检测特异性抗体。采用了一种方便且可逆的程序将PDMS微阵列基板与互补的SU-8/玻璃微流控反应室进行键合。研究了微室内三种蛋白质相互作用的流体动力学行为,以选择最有效的流动参数(兼顾检测时间和性能)。使用优化条件可在300微升中于6分钟样品孵育时间内同时检测到皮摩尔水平的三种特异性抗体。最后,使用用苹果榛子和花粉过敏原修饰的微流控装置对过敏患者的血清进行检测。获得的结果与使用经典法玛西亚CAP系统获得的结果相比具有优势。