Development of highly sensitive electrochemical genosensor based on multiwalled carbon nanotubes-chitosan-bismuth and lead sulfide nanoparticles for the detection of pathogenic Aeromonas
Autor: | Jiadi Sun, Byong H. Lee, Xiulan Sun, Mandour H. Abdalhai, António Maximiano Fernandes, Jian Ji, Bing-Wen Xi, Rasoamandrary Noeline, Jun Xie |
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Rok vydání: | 2014 |
Předmět: |
DNA
Bacterial Sulfide Biomedical Engineering Biophysics Analytical chemistry Nanoparticle Biosensing Techniques Sulfides chemistry.chemical_compound Limit of Detection Electrochemistry Humans Lead sulfide chemistry.chemical_classification Detection limit Chitosan biology Chemistry Oligonucleotide Nanotubes Carbon Nucleic Acid Hybridization General Medicine Electrochemical Techniques biology.organism_classification Aeromonas Lead Food Microbiology Nanoparticles Differential pulse voltammetry Biosensor Bismuth Biotechnology Nuclear chemistry |
Zdroj: | Biosensorsbioelectronics. 63 |
ISSN: | 1873-4235 |
Popis: | In this paper, we reported the construction of new high sensitive electrochemical genosensor based on multiwalled carbon nanotubes-chitosan-bismuth complex (MWCNT-Chi-Bi) and lead sulfide nanoparticles for the detection of pathogenic Aeromonas. Lead sulfide nanoparticles capped with 5'-(NH2) oligonucleotides thought amide bond was used as signalizing probe DNA (sz-DNA) and thiol-modified oligonucleotides sequence was used as fixing probe DNA (fDNA). The two probes hybridize with target Aeromonas DNA (tDNA) sequence (fDNA-tDNA-szDNA). The signal of hybridization is detected by differential pulse voltammetry (DPV) after electrodeposition of released lead nanoparticles (PbS) from sz-DNA on the surface of glass carbon electrode decorated with MWCNT-Chi-Bi, which improves the deposition and traducing electrical signal. The optimization of incubation time, hybridization temperature, deposition potential, deposition time and the specificity of the probes were investigated. Our results showed the highest sensibility to detect the target gene when compared with related biosensors and polymerase chain reaction (PCR). The detection limit for this biosensor was 1.0×10(-14) M. We could detect lower than 10(2) CFU mL(-1) of Aeromonas in spiked tap water. This method is rapid and sensitive for the detection of pathogenic bacteria and would become a potential application in biomedical diagnosis, food safety and environmental monitoring. |
Databáze: | OpenAIRE |
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