Sample-to-Answer Droplet Magnetofluidic Platform for Point-of-Care Hepatitis C Viral Load Quantitation

被引:48
|
作者
Shin, Dong Jin [1 ]
Trick, Alexander Y. [2 ]
Hsieh, Yu-Hsiang [3 ]
Thomas, David L. [4 ,5 ]
Wang, Tza-Huei [1 ,2 ,6 ]
机构
[1] Johns Hopkins Univ, Dept Mech Engn, Whiting Sch Engn, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Dept Biomed Engn, Whiting Sch Engn, Baltimore, MD 21218 USA
[3] Johns Hopkins Univ, Sch Med, Dept Emergency Med, Baltimore, MD USA
[4] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[5] Johns Hopkins Univ, Sch Med, Infect Dis Ctr Viral Hepatitis, Baltimore, MD USA
[6] Johns Hopkins Univ, Inst NanoBioTechnol, Baltimore, MD USA
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
关键词
VIRUS HCV RNA; PCR; AMPLIFICATION; MANIPULATION; INFECTION; DIAGNOSIS; ANTIBODY; RANGE;
D O I
10.1038/s41598-018-28124-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Gold standard quantitative nucleic acid tests for diagnosis of viral diseases are currently limited to implementation in laboratories outside of the clinic. An instrument for conducting nucleic acid testing at the point-of-care (POC) that is easily operable by the clinician would reduce the required number of visits to the clinic and improve patient retention for proper treatment. Here we present a droplet magnetofluidic (DM) platform, which leverages functionalized magnetic particles to miniaturize and automate laboratory assays for use in the clinic at the POC. Our novel thermoformed disposable cartridge coupled to a portable multiaxial magnetofluidic instrument enables real-time PCR assays for quantitative and sensitive detection of nucleic acids from crude biosamples. Instead of laborious benchtop sample purification techniques followed by elution and spiking into PCR buffer, the user simply injects the biosample of interest into a cartridge with magnetic particles and loads the cartridge into the instrument. We demonstrate the utility of our platform with hepatitis C virus (HCV) RNA viral load quantitation from blood serum in approximately 1 hour. Clinical serum samples (n = 18) were directly processed on cartridges with no false positives and a limit of detection of 45 IU per 10 mu l sample injection.
引用
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页数:12
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