A PDMS/paper/glass hybrid microfluidic biochip integrated with aptamer-functionalized graphene oxide nano-biosensors for one-step multiplexed pathogen detection

被引:225
作者
Zuo, Peng [1 ]
Li, XiuJun [1 ,2 ]
Dominguez, Delfina C. [3 ]
Ye, Bang-Ce [2 ]
机构
[1] Univ Texas El Paso, Dept Chem, El Paso, TX 79968 USA
[2] E China Univ Sci & Technol, State Key Lab Bioreactor Engn, Shanghai 200237, Peoples R China
[3] Univ Texas El Paso, Coll Hlth Sci, El Paso, TX 79968 USA
基金
美国国家卫生研究院;
关键词
ESCHERICHIA-COLI O157-H7; TOTAL ANALYSIS SYSTEMS; REAL-TIME PCR; STAPHYLOCOCCUS-AUREUS; SALMONELLA-ENTERICA; DNA EXTRACTION; RAPID DETECTION; CELL; SELECTION; ASSAY;
D O I
10.1039/c3lc50654a
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Infectious pathogens often cause serious public health concerns throughout the world. There is an increasing demand for simple, rapid and sensitive approaches for multiplexed pathogen detection. In this paper we have developed a polydimethylsiloxane (PDMS)/paper/glass hybrid microfluidic system integrated with aptamer-functionalized graphene oxide (GO) nano-biosensors for simple, one-step, multiplexed pathogen detection. The paper substrate used in this hybrid microfluidic system facilitated the integration of aptamer biosensors on the microfluidic biochip, and avoided complicated surface treatment and aptamer probe immobilization in a PDMS or glass-only microfluidic system. Lactobacillus acidophilus was used as a bacterium model to develop the microfluidic platform with a detection limit of 11.0 cfu mL(-1). We have also successfully extended this method to the simultaneous detection of two infectious pathogens - Staphylococcus aureus and Salmonella enterica. This method is simple and fast. The one-step 'turn on' pathogen assay in a ready-to-use microfluidic device only takes similar to 10 min to complete on the biochip. Furthermore, this microfluidic device has great potential in rapid detection of a wide variety of different other bacterial and viral pathogens.
引用
收藏
页码:3921 / 3928
页数:8
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