Aptamer-based sandwich assay for on chip detection of Ochratoxin A by an array of amorphous silicon photosensors

被引:44
作者
Costantini, Francesca [1 ,6 ]
Sberna, Cristiana [1 ,2 ]
Petrucci, Giulia [2 ]
Reverberi, Massimo [3 ]
Domenici, Fabio [4 ]
Fanelli, Corrado [3 ]
Manetti, Cesare [1 ]
de Cesare, Giampiero [2 ]
DeRosa, Maria [5 ]
Nascetti, Augusto [6 ]
Caputo, Domenico [2 ]
机构
[1] Univ Roma La Sapienza, Dept Chem, Ple A Moro 5, I-00186 Rome, Italy
[2] Univ Roma La Sapienza, Dept Informat Engn Elect & Telecommun, Via Eudossiana 18, I-00184 Rome, Italy
[3] Univ Roma La Sapienza, Dept Environm Biol, Ple A Moro 5, I-00186 Rome, Italy
[4] Univ Roma La Sapienza, Dept Phys, Ple A Moro 5, I-00186 Rome, Italy
[5] Carleton Univ, Dept Chem, 1125 Colonel By Dr, Ottawa, ON K1S 5B6, Canada
[6] Univ Roma La Sapienza, Sch Aerosp Engn, Via Salaria 851-881, I-00138 Rome, Italy
关键词
Lab-on-chip; Aptamer; Ochratoxin A; Multichannel chip; Amorphous silicon; Photosensors; Polymer brushes; FOOD SAFETY; CHEMILUMINESCENCE DETECTION; DNA APTAMERS; WINE; MICROREACTORS; IMMUNOASSAY; SENSORS; LEVEL;
D O I
10.1016/j.snb.2016.02.036
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A multichannel glass-PDMS microfluidic chip functionalized with a novel aptasensor has been developed for the detection of Ochratoxin A (OTA). The aptasensor is built on a glass substrate covered with a poly( 2hydroxyethtyl methacrylate) brush layer, which is subsequently functionalized with an aptamer having high affinity towards OTA. The assay relies on an aptamer-linked immobilized sorbent assay (ALISA) using two different OTA aptamers, which, in presence of OTA, assemble to form a sandwich-like structure generating a chemiluminescent signal. The chip is combined with an array of amorphous silicon photosensors that transduce the chemiluminescent signal into an electrical signal that can be processed to detect and quantify the OTA in the sample. The successful detection of OTA has been demonstrated in standard solutions and in beer samples spiked with OTA. The results shows that the values measured for OTA, applying the ALISA assay, are comparable to those measured by the reference methods. The sensitivity of the proposed analytical method is 0.32 pA L/mg, while the LOD and the LOQ are 0.82 and 2.5 mg/L, respectively. Taking into account both the LOD of the ALISA and the method applied for OTA extraction from beer samples, we extrapolated that 1.1 g of beer sample is sufficient to detect OTA contamination under the regulatory limits. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:31 / 39
页数:9
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