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Highly Uniform Gold Nanobipyramids for Ultrasensitive Colorimetric Detection of Influenza Virus

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  • Highly Uniform Gold Nanobipyramids for Ultrasensitive Colorimetric Detection of Influenza Virus

    Anal Chem. 2017 Feb 7;89(3):1617-1623. doi: 10.1021/acs.analchem.6b03711. Epub 2017 Jan 10.
    Highly Uniform Gold Nanobipyramids for Ultrasensitive Colorimetric Detection of Influenza Virus.

    Xu S1, Ouyang W1, Xie P1, Lin Y1, Qiu B1, Lin Z1, Chen G1, Guo L1.
    Author information

    Abstract

    Gold nanoparticles (AuNPs) have been frequently utilized for the construction of diverse colorimetric biosensors. Normally, AuNPs with sharp edges could have better sensitivity. However, the poor monodipersity of AuNPs with sharp edges seriously confines their utility for colorimetric biosensing. Herein, we demonstrate the utility of highly uniform gold nanobipyramids (Au NBPs) for ultrasensitive colorimetric detection of H5N1 virus. The proposed method is based on the fact that alkaline phosphatase (ALP) could catalyze the decomposition of 4-aminophenyl phosphate (4-APP) to generate 4-aminophenol (4-AP), which would then reduce silver nitrate to metal silver and then deposited on Au NBPs. The metal silver shell coated on the Au NBPs changed the refractive index of gold and thus resulted in a blue shift of longitudinal localized surface plasmon resonance (LSPR) and accompanied a vivid color change. This method exhibited a higher sensitivity than that of other Au NPs such as gold nanorods due to the high-index-faceted on the tips of the Au NBPs. This method was used to detect the activity of ALP. It exhibited a linear range of 0.1-5 mU/mL with a limit of detection (LOD) of 0.086 mU/mL. Finally, the proposed method was used in immunoassay to detect H5N1 virus. The results showed that the corresponding linear range for the detection of H5N1 virus antigen was 0.001-2.5 ng/mL, and the LOD was determined to be 1 pg/mL, which is more sensitive than those in most of the colorimetric biosensors reported previously.


    PMID: 28208287 DOI: 10.1021/acs.analchem.6b03711
    [PubMed - in process]
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