Continuous-Flow Separation and Efficient Concentration of Foodborne Bacteria from Large Volume Using Nickel Nanowire Bridge in Microfluidic Chip

• Published in: Micromachines (Basel) Vol. 10; no. 10; p. 644
• Main Authors: Huo, Xiaoting, Chen, Qi, Wang, Lei, Cai, Gaozhe, Qi, Wuzhen, Xia, Zengzilu, Wen, Weijia, Lin, Jianhan
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 25.09.2019; MDPI
• Subjects: 3-D printers; Antibodies; Bacteria; Binding sites; Buffer solutions; Continuous flow; Efficiency; Flow separation; Food; foodborne bacteria; immunomagnetic separation; large-volume sample; Low concentrations; Magnetic fields; Magnetism; Medical research; Methods; microfluidic chip; Microfluidics; Nanoparticles; Nanowires; Nickel; nickel nanowires bridge; Separation; United States > US; China
• ISSN: 2072-666X; 2072-666X
• DOI: 10.3390/mi10100644

Separation and concentration of target bacteria has become essential to sensitive and accurate detection of foodborne bacteria to ensure food safety. In this study, we developed a bacterial separation system for continuous-flow separation and efficient concentration of foodborne bacteria from large volume using a nickel nanowire (NiNW) bridge in the microfluidic chip. The synthesized NiNWs were first modified with the antibodies against the target bacteria and injected into the microfluidic channel to form the NiNW bridge in the presence of the external arc magnetic field. Then, the large volume of bacterial sample was continuous-flow injected to the channel, resulting in specific capture of the target bacteria by the antibodies on the NiNW bridge to form the NiNW–bacteria complexes. Finally, these complexes were flushed out of the channel and concentrated in a lower volume of buffer solution, after the magnetic field was removed. This bacterial separation system was able to separate up to 74% of target bacteria from 10 mL of bacterial sample at low concentrations of ≤102 CFU/mL in 3 h, and has the potential to separate other pathogenic bacteria from large volumes of food samples by changing the antibodies.