2010
DOI: 10.1016/j.bios.2010.08.060
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Detection of swine-origin influenza A (H1N1) viruses using a localized surface plasmon coupled fluorescence fiber-optic biosensor

Abstract: Swine-origin influenza A (H1N1) virus (S-OIV) was identified as a new reassortant strain of influenza A virus in April 2009 and led to an influenza pandemic. Accurate and timely diagnoses are crucial for the control of influenza disease. We developed a localized surface plasmon coupled fluorescence fiber-optic biosensor (LSPCF-FOB) which combines a sandwich immunoassay with the LSP technique using antibodies against the hemagglutinin (HA) proteins of S-OIVs. The detection limit of the LSPCF-FOB for recombinant… Show more

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Cited by 59 publications
(36 citation statements)
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References 33 publications
(15 reference statements)
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“…953 The sensitivity of these assays can be enhanced using fluorescence-labeled antibodies decorated with AuNPs, leading to the technique called localized surface plasmon resonance coupled fluorescence fiber optic sensor. 954957 …”
Section: Aunp-based Surface Plasmon Resonance Sensorsmentioning
confidence: 99%
“…953 The sensitivity of these assays can be enhanced using fluorescence-labeled antibodies decorated with AuNPs, leading to the technique called localized surface plasmon resonance coupled fluorescence fiber optic sensor. 954957 …”
Section: Aunp-based Surface Plasmon Resonance Sensorsmentioning
confidence: 99%
“…These sensors include biologically active structures that detect the target, such as bacterial cells, enzymes, antibodies and other proteins and allow the detection of proteins [132], viruses [133,134], pesticides [135], living cells [136], etc.…”
Section: Resonance-based Sensorsmentioning
confidence: 99%
“…As illustrated in Figure 7, a significant change in the current was observed after hybridization with the complementary sequence ( Figure 7B) and DNA with one base mismatch. The current value for [Fe(CN) 6 ] −3/−4 with ssDNA was 5.62 µA, which increased to 7.44 µA on complementary DNA binding, but for the single-base-mismatched sequence, the current further decreased to 6.67 µA due to improper hybridization and enhanced repulsive forces compared to perfectly paired-up DNA sequences of the p16 gene. In the presence of noncomplementary targets, no visible current changes were observed due to the lack of any hybridization event.…”
Section: Selectivity Of the Biosensormentioning
confidence: 99%
“…4,5 This limitation was the major reason for researchers to explore and identify other biomarkers such as plectin-1, macrophage inhibitory cytokine-1, IGFBP-1, haptoglobin, SAA, TIMP-1, HE4, NGAL, and particularly human UL16-binding protein 2 (ULBP2) for PC screening. [6][7][8][9] However, apart from these serum biomarkers, researchers have also focused on genetic alterations in PC to detect the early onset of PC. The major cause of all cancers is related to genetic mutations as well as the alteration in the regulatory pathways due to mutations.…”
Section: Introductionmentioning
confidence: 99%