A microfluidic colorimetric biosensor for rapid detection of Escherichia coli O157:H7 using gold nanoparticle aggregation and smart phone imaging

We intended to develop a novel biosensor using gold nanoparticles (AuNPs) for indicating different concentrations of E. coli O157:H7 and smart phone imaging APP for monitoring color change of the AuNPs. The magnetic nanoparticles (MNPs) modified with the capture antibodies and the polystyrene micros...

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Published inBiosensors & bioelectronics Vol. 124-125; pp. 143 - 149
Main Authors Zheng, Lingyan, Cai, Gaozhe, Wang, Siyuan, Liao, Ming, Li, Yanbin, Lin, Jianhan
Format Journal Article
LanguageEnglish
Published England Elsevier B.V 15.01.2019
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Abstract We intended to develop a novel biosensor using gold nanoparticles (AuNPs) for indicating different concentrations of E. coli O157:H7 and smart phone imaging APP for monitoring color change of the AuNPs. The magnetic nanoparticles (MNPs) modified with the capture antibodies and the polystyrene microspheres (PSs) modified with the detection antibodies and the catalases were simultaneously used to react with the target bacteria in the first mixing channel of the microfluidic chip, and hydrogen peroxide was injected and catalyzed by the catalases on the MNP-bacteria-PS complexes. After the mixture of the AuNPs and the crosslinking agents were injected to react with the catalysate in the second mixing channel and incubated in the detection chamber, the aggregation of the AuNPs was triggered through the crosslinking agents, resulting in the color of the AuNPs changing from blue to red. Finally, the color was measured using the smart phone imaging APP to determine the amount of the bacteria. This biosensor exhibited a good specificity and sensitivity for detection of E. coli O157:H7 in chicken samples with a lower detection limit of 50 CFU/mL. •AuNP aggregation were successfully used for signal indication.•HSL-based smart phone imaging was effective to detect color change.•Microfluidic chip was successfully developed for on-chip bioreaction.•The detection limit of this biosensor was 50 CFU/mL for E coli O157:H7.•The mean recovery of E coli O157:H7 in the spiked chicken samples was ~96.8%.
AbstractList We intended to develop a novel biosensor using gold nanoparticles (AuNPs) for indicating different concentrations of E. coli O157:H7 and smart phone imaging APP for monitoring color change of the AuNPs. The magnetic nanoparticles (MNPs) modified with the capture antibodies and the polystyrene microspheres (PSs) modified with the detection antibodies and the catalases were simultaneously used to react with the target bacteria in the first mixing channel of the microfluidic chip, and hydrogen peroxide was injected and catalyzed by the catalases on the MNP-bacteria-PS complexes. After the mixture of the AuNPs and the crosslinking agents were injected to react with the catalysate in the second mixing channel and incubated in the detection chamber, the aggregation of the AuNPs was triggered through the crosslinking agents, resulting in the color of the AuNPs changing from blue to red. Finally, the color was measured using the smart phone imaging APP to determine the amount of the bacteria. This biosensor exhibited a good specificity and sensitivity for detection of E. coli O157:H7 in chicken samples with a lower detection limit of 50 CFU/mL. •AuNP aggregation were successfully used for signal indication.•HSL-based smart phone imaging was effective to detect color change.•Microfluidic chip was successfully developed for on-chip bioreaction.•The detection limit of this biosensor was 50 CFU/mL for E coli O157:H7.•The mean recovery of E coli O157:H7 in the spiked chicken samples was ~96.8%.
We intended to develop a novel biosensor using gold nanoparticles (AuNPs) for indicating different concentrations of E. coli O157:H7 and smart phone imaging APP for monitoring color change of the AuNPs. The magnetic nanoparticles (MNPs) modified with the capture antibodies and the polystyrene microspheres (PSs) modified with the detection antibodies and the catalases were simultaneously used to react with the target bacteria in the first mixing channel of the microfluidic chip, and hydrogen peroxide was injected and catalyzed by the catalases on the MNP-bacteria-PS complexes. After the mixture of the AuNPs and the crosslinking agents were injected to react with the catalysate in the second mixing channel and incubated in the detection chamber, the aggregation of the AuNPs was triggered through the crosslinking agents, resulting in the color of the AuNPs changing from blue to red. Finally, the color was measured using the smart phone imaging APP to determine the amount of the bacteria. This biosensor exhibited a good specificity and sensitivity for detection of E. coli O157:H7 in chicken samples with a lower detection limit of 50 CFU/mL.We intended to develop a novel biosensor using gold nanoparticles (AuNPs) for indicating different concentrations of E. coli O157:H7 and smart phone imaging APP for monitoring color change of the AuNPs. The magnetic nanoparticles (MNPs) modified with the capture antibodies and the polystyrene microspheres (PSs) modified with the detection antibodies and the catalases were simultaneously used to react with the target bacteria in the first mixing channel of the microfluidic chip, and hydrogen peroxide was injected and catalyzed by the catalases on the MNP-bacteria-PS complexes. After the mixture of the AuNPs and the crosslinking agents were injected to react with the catalysate in the second mixing channel and incubated in the detection chamber, the aggregation of the AuNPs was triggered through the crosslinking agents, resulting in the color of the AuNPs changing from blue to red. Finally, the color was measured using the smart phone imaging APP to determine the amount of the bacteria. This biosensor exhibited a good specificity and sensitivity for detection of E. coli O157:H7 in chicken samples with a lower detection limit of 50 CFU/mL.
We intended to develop a novel biosensor using gold nanoparticles (AuNPs) for indicating different concentrations of E. coli O157:H7 and smart phone imaging APP for monitoring color change of the AuNPs. The magnetic nanoparticles (MNPs) modified with the capture antibodies and the polystyrene microspheres (PSs) modified with the detection antibodies and the catalases were simultaneously used to react with the target bacteria in the first mixing channel of the microfluidic chip, and hydrogen peroxide was injected and catalyzed by the catalases on the MNP-bacteria-PS complexes. After the mixture of the AuNPs and the crosslinking agents were injected to react with the catalysate in the second mixing channel and incubated in the detection chamber, the aggregation of the AuNPs was triggered through the crosslinking agents, resulting in the color of the AuNPs changing from blue to red. Finally, the color was measured using the smart phone imaging APP to determine the amount of the bacteria. This biosensor exhibited a good specificity and sensitivity for detection of E. coli O157:H7 in chicken samples with a lower detection limit of 50 CFU/mL.
Author Li, Yanbin
Lin, Jianhan
Zheng, Lingyan
Liao, Ming
Wang, Siyuan
Cai, Gaozhe
Author_xml – sequence: 1
  givenname: Lingyan
  surname: Zheng
  fullname: Zheng, Lingyan
  organization: Key Laboratory of Agricultural Information Acquisition Technology, Ministry of Agriculture, China Agricultural University, Beijing 100083, China
– sequence: 2
  givenname: Gaozhe
  surname: Cai
  fullname: Cai, Gaozhe
  organization: Key Laboratory of Modern Precision Agriculture System Integration Research, Ministry of Education, China Agricultural University, Beijing 100083, China
– sequence: 3
  givenname: Siyuan
  surname: Wang
  fullname: Wang, Siyuan
  organization: Key Laboratory of Agricultural Information Acquisition Technology, Ministry of Agriculture, China Agricultural University, Beijing 100083, China
– sequence: 4
  givenname: Ming
  surname: Liao
  fullname: Liao, Ming
  organization: College of Veterinary Medicine, South China Agricultural University, Guangzhou 510642, China
– sequence: 5
  givenname: Yanbin
  surname: Li
  fullname: Li, Yanbin
  organization: Department of Biological and Agricultural Engineering, University of Arkansas, Fayetteville, AR 72701, United States
– sequence: 6
  givenname: Jianhan
  surname: Lin
  fullname: Lin, Jianhan
  email: jianhan@cau.edu.cn
  organization: Key Laboratory of Agricultural Information Acquisition Technology, Ministry of Agriculture, China Agricultural University, Beijing 100083, China
BackLink https://www.ncbi.nlm.nih.gov/pubmed/30366259$$D View this record in MEDLINE/PubMed
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Keywords Gold nanoparticle aggregation
Microfluidic chip
E. coli O157:H7
Smart phone imaging APP
Colorimetric biosensor
Language English
License Copyright © 2018 Elsevier B.V. All rights reserved.
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Snippet We intended to develop a novel biosensor using gold nanoparticles (AuNPs) for indicating different concentrations of E. coli O157:H7 and smart phone imaging...
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SubjectTerms antibodies
Antibodies, Immobilized - chemistry
bacteria
Biosensing Techniques
biosensors
catalase
chickens
color
Colorimetric biosensor
Colorimetry
cross-linking reagents
detection limit
E. coli O157:H7
Escherichia coli Infections - diagnosis
Escherichia coli Infections - microbiology
Escherichia coli O157
Escherichia coli O157 - isolation & purification
Escherichia coli O157 - pathogenicity
Food Microbiology
Gold - chemistry
Gold nanoparticle aggregation
Humans
hydrogen peroxide
image analysis
magnetism
Metal Nanoparticles - chemistry
Microfluidic chip
Microfluidics - instrumentation
microparticles
mixing
mobile telephones
monitoring
nanogold
nanoparticles
organ-on-a-chip
polystyrenes
rapid methods
Smart phone imaging APP
Smartphone
Title A microfluidic colorimetric biosensor for rapid detection of Escherichia coli O157:H7 using gold nanoparticle aggregation and smart phone imaging
URI https://dx.doi.org/10.1016/j.bios.2018.10.006
https://www.ncbi.nlm.nih.gov/pubmed/30366259
https://www.proquest.com/docview/2126906403
https://www.proquest.com/docview/2176342289
Volume 124-125
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