Microfluidic immunosensor for rapid and sensitive detection of bovine viral diarrhea virus

被引:31
作者
Heinze, Brian C. [1 ]
Song, Jae-Young [2 ]
Lee, Chang-Hee [2 ]
Najam, Anbar [1 ]
Yoon, Jeong-Yeol [1 ]
机构
[1] Univ Arizona, Dept Agr & Biosyst Engn, Tucson, AZ 85721 USA
[2] Natl Vet Res & Quarantine Serv, Anyang 430824, Gyeonggi, South Korea
基金
新加坡国家研究基金会;
关键词
Biosensor; BVDV; Static light scattering; Immunoassay; Virus detection; Lab-on-a-chip; SERUM SAMPLES; CAPTURE ELISA; ASSAY; BVDV; DEVICE;
D O I
10.1016/j.snb.2009.02.058
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We have investigated the utilization of microparticle immunoagglutination assays using forward light scattering measurements in a microfluidic chip towards detecting viral particles. The model viral target was bovine viral diarrhea Virus (BVDV). Highly carboxylated polystyrene microparticles (510 nm) were coated with anti-BVDV monoclonal antibodies. This solution Was in turn used to detect BVDV in diluted tissue culture media and fetal calf serum. The assay was first performed in a two well slide format for proof of concept and particles stability experiments, then in a simple y-channel microfluidic chip with optical fibers arranged in a close proximity setup. Microparticle immunoagglutination was detected via static forward light scattering measurements taken at 45 to incident light. In the microfluidic chip, BVDV was detected down to a concentration of 10 TCID50 mL(-1). For assay comparison purposes reverse transcriptase polymerase chain reaction (RT-PCR) was performed Oil serial dilutions of the BVDV sample used in the two well and microfluidic testing. RT-PCR was effective clown to a concentration of 10(3) TCID50 mL(-1) in detecting the identical BVDV used for microfluidic assays. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:491 / 496
页数:6
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