Woolley Christine F, Hayes Mark A
Department of Chemistry and Biochemistry, Arizona State University, Tempe, AZ, USA.
Anal Methods. 2015 Oct 21;7(20):8632-8639. doi: 10.1039/C5AY01071C. Epub 2015 Aug 20.
To achieve improved sensitivity in cardiac biomarker detection, a batch incubation magnetic microbead immunoassay was developed and tested on three separate human protein targets: myoglobin, heart-type fatty acid binding protein, and cardiac troponin I. A sandwich immunoassay was performed in a simple micro-centrifuge tube allowing full dispersal of the solid capture surface during incubations. Following magnetic bead capture and wash steps, samples were analyzed in the presence of a manipulated magnetic field utilizing a modified microscope slide and fluorescent inverted microscope to collect video data files. Analysis of the video data allowed for the quantitation of myoglobin, heart-type fatty acid binding protein and cardiac troponin I to levels of 360 aM, 67 fM, and 42 fM, respectively. Compared to the previous detection limit of 50 pM for myoglobin, this offers a five-fold improvement in sensitivity. This improvement in sensitivity and incorporation of additional markers, along with the small sample volumes required, suggest the potential of this platform for incorporation as a detection method in a total sample analysis device enabling multiplexed detection for the analysis of clinical samples.
为了提高心脏生物标志物检测的灵敏度,开发了一种批量孵育磁珠免疫测定法,并在三种不同的人类蛋白质靶点上进行了测试:肌红蛋白、心脏型脂肪酸结合蛋白和心肌肌钙蛋白I。在一个简单的微量离心管中进行夹心免疫测定,使固体捕获表面在孵育过程中充分分散。经过磁珠捕获和洗涤步骤后,利用改良的显微镜载玻片和荧光倒置显微镜在可控磁场存在的情况下对样品进行分析,以收集视频数据文件。对视频数据的分析使得肌红蛋白、心脏型脂肪酸结合蛋白和心肌肌钙蛋白I的定量分别达到360 aM、67 fM和42 fM水平。与之前肌红蛋白50 pM的检测限相比,灵敏度提高了五倍。灵敏度的提高、额外标志物的加入以及所需样品体积小,表明该平台有可能作为一种检测方法纳入全样品分析装置中,实现对临床样品分析的多重检测。