Detection of heart-type fatty acid-binding protein (h-FABP) using piezoresistive polymer microcantilevers functionalized by a dry method

被引:19
作者
Agarwal, Dilip Kumar [1 ,2 ]
Prasad, Abhinav [1 ]
Vinchurkar, Madhuri [1 ]
Gandhi, Sahir [1 ]
Prabhakar, Deepika [1 ]
Mukherji, Soumyo [1 ,2 ,3 ]
Rao, V. Ramgopal [1 ,2 ]
机构
[1] Indian Inst Technol, Dept Elect Engn, Ctr Excellence Nanoelect, Bombay, Maharashtra, India
[2] Indian Inst Technol, Ctr Res Nanotechnol & Sci, Bombay, Maharashtra, India
[3] Indian Inst Technol, Dept Biosci & Bioengn, Bombay, Maharashtra, India
关键词
Microcantilevers; Piezoresistive; h-FABP; Sensing; Cardiac marker; ANTIBODY IMMOBILIZATION; SURFACE MODIFICATION; CANTILEVER; MICROCAPSULES; SILANIZATION; BIOSENSOR; PLATFORM; RELEASE; SENSORS;
D O I
10.1007/s13204-018-0723-y
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Piezoresistive microcantilever-based sensor platform is being used for the last two decades due to their low cost, rapid response and label-free detection system. In this work, we are reporting a microfabricated piezoresistive SU-8/carbon black (polymer cantilever)-based sensor platform for the detection of a clinically important early-stage cardiac marker, i.e., fatty acid-binding protein. It is a most preferred cardiac marker for the diagnosis of acute myocardial infarction. The embodiment of the sensor is a SU-8 microcantilever chip with an integrated nanoparticle composite (carbon black) as a piezoresistor for on-chip electrical transduction. Prior to improving the sensing and susceptibility towards the specific target biomolecule (i.e., h-FABP), the fabricated SU-8 polymer cantilevers were subjected to tailored functionalization. This includes the use of an in-house dry method of hot wire chemical vapour deposition technique to graft amine groups onto the SU-8 surface. The surface-modified microcantilevers were further integrated with a polydimethylsiloxane liquid flow cell and connected externally with an electrical read-out system. Immobilization of the antibody corresponding to the marker protein on the microcantilever surface and subsequent recording of the signal generated upon the antibody-antigen interaction were carried out inside the liquid flow cell. Using our optimized immobilization protocol with this experimental set-up, we were successfully able to detect h-FABP concentration as low as 100 ng/ml.
引用
收藏
页码:1031 / 1042
页数:12
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