Rapid Concentration and Detection of Bacteria in Milk Using a Microfluidic Surface Acoustic Wave Activated Nanosieve

被引:5
作者
Ang, Bryan [1 ,2 ]
Jirapanjawat, Thanavit [3 ]
Tay, Khai Ping [1 ]
Ashtiani, Dariush [4 ]
Greening, Chris [2 ,3 ]
Tuck, Kellie L. [5 ]
Neild, Adrian [1 ]
Cadarso, Victor J. [1 ,2 ]
机构
[1] Monash Univ, Dept Mech & Aerosp Engn, Clayton, Vic 3168, Australia
[2] Monash Univ, Ctr Impact Antimicrobial Resistance, Clayton, Vic 3800, Australia
[3] Monash Univ, Dept Microbiol, Biomed Discovery Inst, Clayton, Vic 3168, Australia
[4] CryoSol World, NL-6002 EA Weert, Netherlands
[5] Monash Univ, Sch Chem, Clayton, Vic 3800, Australia
关键词
surface acoustic waves; microfluidics; bacterialdetection; ultrasonics; acoustic radiation force; concentration; PATHOGENIC BACTERIA; FLUORESCENCE; TECHNOLOGIES; PARTICLES; CELLS;
D O I
10.1021/acssensors.4c00291
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Rapid detection of microbes is a key feature for monitoring food quality. Unfortunately, current detection systems rely on labor-intensive and time-consuming lab-based processes that are not suitable for point-of-interest applications and typically require several days before results are available. Here, we demonstrate a microfluidic system capable of rapidly concentrating, fluorescent staining, and detecting bacteria in unprocessed complex biological media such as milk. This concentration is done using a surface acoustic wave-driven microfluidic device which operates based on the Bjerknes force, a force generated on one particle by another in its close proximity. We exploit this effect by exciting a tightly packed bed of 50 mu m polystyrene microparticles temporarily with surface acoustic waves within a microfluidic device to capture and release bacterial cells on demand. The bacterial cells are fluorescently stained during capture and then detected using fluorescence microscopy upon release. This device offers a high capturing efficiency (>80%) and a 34 Colony Forming Units (CFU)/mL limit of detection, which is 1 order of magnitude below that of plate counting at 30 CFU per standard 100 mu L plate (or 300 CFU/mL). This can be attained in just 1 h of processing at 10 mu L/min. With this system, we demonstrate that bacterial detection from extremely low concentration samples down to the order of similar to 10 CFU/mL is possible without requiring any additional external pre- or postprocessing.
引用
收藏
页码:3105 / 3114
页数:10
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