A Microfluidic Biosensor Based on Magnetic Nanoparticle Separation, Quantum Dots Labeling and MnO 2 Nanoflower Amplification for Rapid and Sensitive Detection of Salmonella Typhimurium
Li Hao, Li Xue, Fengchun Huang and 6 more
Micromachines · 2020
doi:10.3390/mi11030281 (opens in a new tab)
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Abstract
Screening of foodborne pathogens is an effective way to prevent microbial food poisoning. A microfluidic biosensor was developed for rapid and sensitive detection of <i>Salmonella</i> Typhimurium using quantum dots (QDs) as fluorescent probes for sensor readout and manganese dioxide nanoflowers (MnO<sub>2 </sub>NFs) and as QDs nanocarriers for signal amplification. Prior to testing, amino-modified MnO<sub>2</sub> nanoflowers (MnO<sub>2</sub>-NH<sub>2</sub> NFs) were conjugated with carboxyl-modified QDs through EDC/NHSS method to form MnO<sub>2</sub>-QD NFs, and MnO<sub>2</sub>-QD NFs were functionalized with polyclonal antibodies (pAbs) to form MnO<sub>2</sub>-QD-pAb NFs. First, the mixture of target <i>Salmonella</i> Typhimurium cells and magnetic nanoparticles (MNPs) modified with monoclonal antibodies (mAbs) was injected with MnO<sub>2</sub>-QD-pAb NFs into a microfluidic chip to form MNP-bacteria-QD-MnO<sub>2</sub> complexes. Then, glutathione (GSH) was injected to dissolve MnO<sub>2</sub> on the complexes into Mn<sup>2+</sup>, resulting in the release of QDs. Finally, fluorescent intensity of the released QDs was measured using the fluorescent detector to determine the amount of <i>Salmonella</i>. A linear relationship between fluorescent intensity and bacterial concentration from 1.0 × 10<sup>2</sup> to 1.0 × 10<sup>7</sup> CFU/mL was found with a low detection limit of 43 CFU/mL and mean recovery of 99.7% for <i>Salmonella</i> in spiked chicken meats, indicating the feasibility of this biosensor for practical applications.
Abstract licence: CC BY
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