A monolithic silicon optoelectronic transducer as a real-time affinity biosensor

被引:78
作者
Misiakos, K [1 ]
Kakabakos, SE
Petrou, PS
Ruf, HH
机构
[1] NCSR Demokritos, Microelect Inst, Athens 15310, Greece
[2] NCSR Demokritos, Inst Radioisotopes & Radiodiagnost Prod, Athens 15310, Greece
[3] Univ Saarland, D-66386 St Ingbert, Germany
[4] Fraunhofer Inst Biomed Engn IBMT, D-66386 St Ingbert, Germany
关键词
D O I
10.1021/ac0353334
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An optical real-time affinity biosensor, which is based on a monolithic silicon optoelectronic transducer and a microfluidic module, is described. The transducer monolithically integrates silicon avalanche diodes as light sources, silicon nitride optical fibers, and p/n junction detectors and efficiently intercouples these elements through a self-alignment technique. The transducer surface is hydrophilized by oxygen plasma treatment, silanized with (3-aminopropyl)triethoxysilane and bioactivated through adsorption of the biomolecular probes. The use of a microfluidic module allows real-time monitoring of the binding reaction of the gold nanoparticle-labeled analytes with the immobilized probes. Their binding within the evanescent field at the surface of the optical fiber causes attenuated total reflection of the waveguided modes and reduction of the detector photocurrent. The biotin-streptavidin model assay was used for the evaluation of the analytical potentials of the device developed. Detection limits of 3.8 and 13 pM in terms of gold nanoparticle-labeled streptavidin were achieved for continuous- and stopped-flow assay modes, respectively. The detection sensitivity was improved by silver plating of the immolilized gold nanoparticles, and a detection limit of 20 fM was obtained after 20-min of silver plating. In addition, two different analytes, streptavidin and antimouse IgG, were simultaneously assayed on the same chip demonstrating the multianalyte potential of the sensor developed.
引用
收藏
页码:1366 / 1373
页数:8
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