A fully automated microfluidic-based electrochemical sensor for real-time bacteria detection
A fully automated microfluidic-based electrochemical biosensor was designed and manufactured for pathogen detection. The quantification of Escherichia coli was investigated with standard and nanomaterial amplified immunoassays in the concentration ranges of 0.99 × 1043.98 × 109 cfu mL−1 and 103.97 ×...
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Veröffentlicht in: | Biosensors & bioelectronics 2018-02, Vol.100, p.541-548 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A fully automated microfluidic-based electrochemical biosensor was designed and manufactured for pathogen detection. The quantification of Escherichia coli was investigated with standard and nanomaterial amplified immunoassays in the concentration ranges of 0.99 × 1043.98 × 109 cfu mL−1 and 103.97 × 107 cfu mL−1 which resulted in detection limits of 1.99 × 104 cfu mL−1 and 50 cfu mL−1, respectively. The developed methodology was then applied for E. coli quantification in water samples using nanomaterial modified assay. Same detection limit for E. coli was achieved for real sample analysis with a little decrease on the sensor signal. Cross-reactivity studies were conducted by testing Shigella, Salmonella spp., Salmonella typhimurium and Staphylococcus aureus on E. coli specific antibody surface that confirmed the high specificity of the developed immunoassays. The sensor surface could be regenerated multiple times which significantly reduces the cost of the system. Our custom-designed biosensor is capable of detecting bacteria with high sensitivity and specificity, and can serve as a promising tool for pathogen detection.
•A novel custom-designed biosensor for pathogen detection was manufactured.•A real-time electrochemical sensing platform with continuous microfluidic flow was demonstrated.•Sensitive E. coli quantification was achieved in water samples with 50 cfu mL−1 LOD.•The fully automated sensor can play a major role for the diagnosis of waterborne pathogens. |
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ISSN: | 0956-5663 1873-4235 |
DOI: | 10.1016/j.bios.2017.09.046 |