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Microfluidic devices for multiplexed detection of foodborne pathogens
被引:48
作者:
Han, Xiaoying
[1
,2
]
Liu, Yuanhui
[1
,2
]
Yin, Juxin
[1
]
Yue, Min
[3
,4
,5
,6
]
Mu, Ying
[1
]
机构:
[1] Zhejiang Univ, State Key Lab Ind Control Technol, Inst Cyber Syst & Control, Res Ctr Analyt Instrumentat, Hangzhou 310023, Peoples R China
[2] Zhejiang Univ, Coll Life Sci, Hangzhou 310058, Peoples R China
[3] Zhejiang Univ, Coll Anim Sci, Dept Vet Med, Hangzhou 310058, Peoples R China
[4] Zhejiang Univ, Coll Anim Sci, Inst Prevent Vet Sci, Hangzhou 310058, Peoples R China
[5] Zhejiang Univ, Coll Med, Affiliated Hosp 1,State Key Lab Diag & Treatment, Natl Med Ctr Infect Dis,Natl Clin Res Ctr Infect, Hangzhou 310003, Peoples R China
[6] Zhejiang Univ, Hainan Inst, Sanya 572025, Peoples R China
关键词:
Microfluidics;
Multiplexed detection;
Foodborne pathogens;
Food safety;
MEDIATED ISOTHERMAL AMPLIFICATION;
LATERAL FLOW ASSAY;
HIGH-THROUGHPUT;
IMPEDANCE DETECTION;
DNA EXTRACTION;
DIELECTROPHORESIS ENRICHMENT;
ELECTROCHEMICAL DETECTION;
BACTERIAL PATHOGENS;
SENSITIVE DETECTION;
RAPID DETECTION;
D O I:
10.1016/j.foodres.2021.110246
中图分类号:
TS2 [食品工业];
学科分类号:
0832 ;
摘要:
The global burden of foodborne diseases is substantial and foodborne pathogens are the major cause for human illnesses. In order to prevent the spread of foodborne pathogens, detection methods are constantly being updated towards rapid, portable, inexpensive, and multiplexed on-site detection. Due to the nature of the small size and low volume, microfluidics has been applied to rapid, time-saving, sensitive, and portable devices to meet the requirements of on-site detection. Simultaneous detection of multiple pathogens is another key parameter to ensure food safety. Multiplexed detection technology, including microfluidic chip design, offers a new opportunity to achieve this goal. In this review, we introduced several sample preparation and corresponding detection methods on microfluidic devices for multiplexed detection of foodborne pathogens. In the sample preparation section, methods of cell capture and enrichment, as well as nucleic acid sample preparation, were described in detail, and in the section of detection methods, amplification, immunoassay, surface plasmon resonance and impedance spectroscopy were exhaustively illustrated. The limitations and advantages of all available experimental options were also summarized and discussed in order to form a comprehensive understanding of cuttingedge technologies and provide a comparative assessment for future investigation and in-field application.
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页数:14
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