Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
7230805 | Biosensors and Bioelectronics | 2016 | 6 Pages |
Abstract
New techniques are required for the rapid and sensitive detection of Escherichia coli O157:H7 (E. coli O157:H7), a pathogenic bacterium responsible for serious and sometimes life-threatening diseases in humans. In this study, we developed a highly sensitive and efficient biosensor for the quantitative detection of E. coli O157:H7 by integrating fluorescein-releasable biolabels with a magnetism-separable probe. Hollow silica nanospheres with a diameter of approximately 350Â nm were synthesized, enriched with fluorescein, and surface-protected with macromolecule layers of poly (acrylic acid) and poly (dimethyldiallylammonium chloride). These fluorescein-enriched hollow silica nanospheres were characterized using scanning electron microscopy, transmission electron microscopy, and Fourier transform infrared spectroscopy. They were further functionalized as immune labels of E. coli O157:H7 for a sandwich-type immune reaction between this bacterium and magnetic nanoparticles (Fe3O4@SiO2). Next, the E. coli O157:H7 cells were captured, magnetically separated, and quantified based on the fluorescence intensity of the fluorescein released from the biolabels of the fluorescein-enriched hollow silica nanospheres. This analytic process can be completed within 75Â min, and the biosensor showed a linear relationship ranging from 4 to 4.0Ã108Â cfu/mL with a detection limit of 3Â cfu/mL. These results show that the developed fluorescent sensor has excellent specificity, and good reproducibility and stability. This study used real spiked samples for detection, indicating that this technique has a wide range of potential applications and may be readily adapted for detecting other pathogens.
Related Topics
Physical Sciences and Engineering
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Analytical Chemistry
Authors
Rong-Rong Hu, Zheng-Zhi Yin, Yan-Bo Zeng, Jian Zhang, Hai-Qing Liu, Yong Shao, Shi-Bin Ren, Lei Li,