| Literature DB >> 27012657 |
Jane Ru Choi1,2,3, Zhi Liu3,4, Jie Hu1,3, Ruihua Tang1,3,5,6, Yan Gong1,3, Shangsheng Feng3,7,8, Hui Ren3,9, Ting Wen10, Hui Yang5,6, Zhiguo Qu4, Belinda Pingguan-Murphy2, Feng Xu1,3.
Abstract
In nucleic acid testing (NAT), gold nanoparticle (AuNP)-based lateral flow assays (LFAs) have received significant attention due to their cost-effectiveness, rapidity, and the ability to produce a simple colorimetric readout. However, the poor sensitivity of AuNP-based LFAs limits its widespread applications. Even though various efforts have been made to improve the assay sensitivity, most methods are inappropriate for integration into LFA for sample-to-answer NAT at the point-of-care (POC), usually due to the complicated fabrication processes or incompatible chemicals used. To address this, we propose a novel strategy of integrating a simple fluidic control strategy into LFA. The strategy involves incorporating a piece of paper-based shunt and a polydimethylsiloxane (PDMS) barrier to the strip to achieve optimum fluidic delays for LFA signal enhancement, resulting in 10-fold signal enhancement over unmodified LFA. The phenomena of fluidic delay were also evaluated by mathematical simulation, through which we found the movement of fluid throughout the shunt and the tortuosity effects in the presence of PDMS barrier, which significantly affect the detection sensitivity. To demonstrate the potential of integrating this strategy into a LFA with sample-in-answer-out capability, we further applied this strategy into our prototype sample-to-answer LFA to sensitively detect the Hepatitis B virus (HBV) in clinical blood samples. The proposed strategy offers great potential for highly sensitive detection of various targets for wide application in the near future.Entities:
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Year: 2016 PMID: 27012657 DOI: 10.1021/acs.analchem.6b00195
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986