Fluoroimmunoassay of influenza virus using sulfur-doped graphitic carbon nitride quantum dots coupled with Ag2S nanocrystals

被引:14
作者
Achadu, Ojodomo J. [1 ]
Lioe, De Xing [2 ]
Kagawa, Keiichiro [2 ]
Kawahito, Shoji [2 ]
Park, Enoch Y. [1 ,3 ]
机构
[1] Shizuoka Univ, Res Inst Green Sci & Technol, Suruga Ku, 836 Ohya, Shizuoka 4228529, Japan
[2] Shizuoka Univ, Elect Res Inst, Naka Ku, 3-5-1 Johoku, Hamamatsu, Shizuoka 4328011, Japan
[3] Shizuoka Univ, Grad Sch Sci & Technol, Dept Biosci, Lab Biotechnol,Suruga Ku, 836 Ohya, Shizuoka 4228529, Japan
基金
日本学术振兴会;
关键词
Sulfur-doped graphitic carbon nitride QDs; Silver disulfide nanocrystals; Influenza A virus; Fluoroimmunoassay; Virus immunoassay; Localized surface plasmonic resonance; Nanosandwich complex; FLUORESCENCE; GRAPHENE; NANOPARTICLES; NANOSHEETS;
D O I
10.1007/s00604-020-04433-1
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Novel sulfur-doped graphitic carbon nitride quantum dots (S-gCNQDs) are synthesized using a single-source precursor in a one-step solvothermal process. The S-gCNQDs with a size of similar to 5-nm displayed a strong green intrinsic fluorescence at 512 nm when excited at 400 nm, with a quantum yield of similar to 33% in aqueous solution. The prepared S-gCNQDs and Ag2S nanocrystals were applied as innovative functional materials to fabricate a biosensor for virus detection based on the conjugation of specific anti-human influenza A monoclonal antibody to the S-gCNQDs and Ag2S NCs, respectively. In the presence of the influenza A virus, an interaction between the S-gCNQDs/Ag2S-labeled antibody resulted in the formation of a nanosandwich structure, which is accompanied by the fluorescence enhancement of the S-gCNQDs. The change in fluorescence intensity linearly correlats with the concentration of the influenza A virus (H1N1) in the 10 fg/mL to 1.0 ng/mL range, with a limit of detection of 5.5 fg/mL. The assay was applied to the assay of clinically isolated influenza A virus (H3N2/Yokohama) mixed with human serum. The obtained limit of detection was 100 PFU/mL within the detection range of 10(2)- 5 x 10(4)PFU/mL for the H3N2 virus.
引用
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页数:11
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