Colorimetric aptasensing of ochratoxin A using Au@Fe3O4 nanoparticles as signal indicator and magnetic separator

Gold nanoparticles (Au NPs) doped Fe3O4 (Au@Fe3O4) NPs have been synthesized by a facile one-step solvothermal method. The peroxidase-like activity of Au@Fe3O4 NPs was effectively enhanced due to the synergistic effect between the Fe3O4 NPs and Au NPs. On this basis, an efficient colorimetric aptase...

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Veröffentlicht in:Biosensors & bioelectronics 2016-03, Vol.77, p.1183-1191
Hauptverfasser: Wang, Chengquan, Qian, Jing, Wang, Kun, Yang, Xingwang, Liu, Qian, Hao, Nan, Wang, Chengke, Dong, Xiaoya, Huang, Xingyi
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container_start_page 1183
container_title Biosensors & bioelectronics
container_volume 77
creator Wang, Chengquan
Qian, Jing
Wang, Kun
Yang, Xingwang
Liu, Qian
Hao, Nan
Wang, Chengke
Dong, Xiaoya
Huang, Xingyi
description Gold nanoparticles (Au NPs) doped Fe3O4 (Au@Fe3O4) NPs have been synthesized by a facile one-step solvothermal method. The peroxidase-like activity of Au@Fe3O4 NPs was effectively enhanced due to the synergistic effect between the Fe3O4 NPs and Au NPs. On this basis, an efficient colorimetric aptasensor has been developed using the intrinsic dual functionality of the Au@Fe3O4 NPs as signal indicator and magnetic separator. Initially, the amino-modified aptamer specific for a typical mycotoxin, ochratoxin A (OTA), was surface confined on the amino-terminated glass beads surafce using glutaraldehyde as a linker. Subsequently, the amino-modified capture DNA (cDNA) was labeled with the amino-functionalized Au@Fe3O4 NPs and the aptasensor was thus fabricated through the hybridization reaction between cDNA and the aptamers. While upon OTA addition, aptamers preferred to form the OTA-aptamer complex and the Au@Fe3O4 NPs linked on the cDNA were released into the bulk solution. Through a simple magnetic separation, the collected Au@Fe3O4 NPs can produce a blue colored solution in the presence of 3,3′,5,5′-tetramethylbenzidine and H2O2. When the reaction was terminated by addition of H+ ions, the blue product could be changed into a yellow one with higher absorption intensity. This colorimetric aptasensor can detect as low as 30pgmL−1 OTA with high specificity. To the best of our knowledge, the present colorimetric aptasensor is the first attempt to use the peroxidase-like activity of nanomaterial for OTA detection, which may provide an acttractive path toward routine quality control of food safety. •Au@Fe3O4 NPs have been synthesized by a facile one-step solvothermal method.•Au@Fe3O4 NPs possess high peroxidase-like activity due to the synergistic effect.•The rich -OH groups on the Au@Fe3O4 NPs facilitate their modification with aptamer.•An efficient colorimetric aptasensor for OTA was developed based on the Au@Fe3O4 NPs.•Au@Fe3O4 NPs were used as both signal indicator and magnetic separator.
doi_str_mv 10.1016/j.bios.2015.11.004
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Through a simple magnetic separation, the collected Au@Fe3O4 NPs can produce a blue colored solution in the presence of 3,3′,5,5′-tetramethylbenzidine and H2O2. When the reaction was terminated by addition of H+ ions, the blue product could be changed into a yellow one with higher absorption intensity. This colorimetric aptasensor can detect as low as 30pgmL−1 OTA with high specificity. 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bioelectronics</jtitle><addtitle>Biosens Bioelectron</addtitle><date>2016-03-15</date><risdate>2016</risdate><volume>77</volume><spage>1183</spage><epage>1191</epage><pages>1183-1191</pages><issn>0956-5663</issn><eissn>1873-4235</eissn><abstract>Gold nanoparticles (Au NPs) doped Fe3O4 (Au@Fe3O4) NPs have been synthesized by a facile one-step solvothermal method. The peroxidase-like activity of Au@Fe3O4 NPs was effectively enhanced due to the synergistic effect between the Fe3O4 NPs and Au NPs. On this basis, an efficient colorimetric aptasensor has been developed using the intrinsic dual functionality of the Au@Fe3O4 NPs as signal indicator and magnetic separator. Initially, the amino-modified aptamer specific for a typical mycotoxin, ochratoxin A (OTA), was surface confined on the amino-terminated glass beads surafce using glutaraldehyde as a linker. Subsequently, the amino-modified capture DNA (cDNA) was labeled with the amino-functionalized Au@Fe3O4 NPs and the aptasensor was thus fabricated through the hybridization reaction between cDNA and the aptamers. While upon OTA addition, aptamers preferred to form the OTA-aptamer complex and the Au@Fe3O4 NPs linked on the cDNA were released into the bulk solution. Through a simple magnetic separation, the collected Au@Fe3O4 NPs can produce a blue colored solution in the presence of 3,3′,5,5′-tetramethylbenzidine and H2O2. When the reaction was terminated by addition of H+ ions, the blue product could be changed into a yellow one with higher absorption intensity. This colorimetric aptasensor can detect as low as 30pgmL−1 OTA with high specificity. 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subjects Aptamers, Nucleotide - chemistry
Au@Fe3O4 nanoparticles
Biosensing Techniques - instrumentation
Colorimetric aptasensor
Colorimetry - instrumentation
Equipment Design
Equipment Failure Analysis
Food Analysis - instrumentation
Food Contamination - analysis
Gold - chemistry
Immunomagnetic Separation - instrumentation
Magnetic separation
Magnetics - instrumentation
Magnetite Nanoparticles - chemistry
Magnetite Nanoparticles - ultrastructure
Ochratoxin A
Ochratoxins - analysis
Ochratoxins - chemistry
Ochratoxins - isolation & purification
Peroxidase-like activity
title Colorimetric aptasensing of ochratoxin A using Au@Fe3O4 nanoparticles as signal indicator and magnetic separator
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