2016
DOI: 10.1016/j.microc.2015.07.007
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Fluorescence energy transfer inhibition bioassay for cholera toxin based on galactose-stabilized gold nanoparticles and amine-terminated quantum dots

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Cited by 24 publications
(10 citation statements)
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“…In the intestines, the bacteria colonize the mucosa and begin to secrete cholera toxin (CT), which initiates the disease symptoms [ 127 ]. Nanosensors have been fabricated to detect both Vibrio cholerae [ 128 , 129 ] and CT, but the majority of the literature has focused on detection of CT subunit B (CT-B) [ 130 134 ] because the subunit induces cellular uptake of the toxin and not all V. cholerae isolates are toxigenic [ 135 ]. Label-based detection of CT can be achieved using antibodies, ganglioside GM1 (the binding site of CT), or β-galactose, a sugar with strong affinity towards CT. Ahn et al [ 130 ] provide a nice summary of CT-B detection and reported a fluorescence resonance energy transfer (FRET) based method with a theoretical detection limit of 280 pM.…”
Section: Analytesmentioning
confidence: 99%
“…In the intestines, the bacteria colonize the mucosa and begin to secrete cholera toxin (CT), which initiates the disease symptoms [ 127 ]. Nanosensors have been fabricated to detect both Vibrio cholerae [ 128 , 129 ] and CT, but the majority of the literature has focused on detection of CT subunit B (CT-B) [ 130 134 ] because the subunit induces cellular uptake of the toxin and not all V. cholerae isolates are toxigenic [ 135 ]. Label-based detection of CT can be achieved using antibodies, ganglioside GM1 (the binding site of CT), or β-galactose, a sugar with strong affinity towards CT. Ahn et al [ 130 ] provide a nice summary of CT-B detection and reported a fluorescence resonance energy transfer (FRET) based method with a theoretical detection limit of 280 pM.…”
Section: Analytesmentioning
confidence: 99%
“…A simple and fast bioassay has been developed by Lee et al [83] to recognize cholera toxin (CT), a protein secreted by the Vibrio cholerae bacterium which is responsible for cholera disease. A thiol-modified β-galactose derivative was used to coat 10 nm AuNPs and mixed with amino-terminated quantum dots (CdTe, QD).…”
Section: Reviewmentioning
confidence: 99%
“…In the FRET system, AuNPs are able to quench the fluorescence of fluorescent materials when a spectral overlap between the absorption spectrum of AuNPs and the emission spectrum of fluorescent materials exists [11,12,13]. Thus, the construction of fluorescent materials for L-Cys sensing is designed to be “off-on” [10,14,15,16,17]. However, the fluorescence spectrum band of traditional fluorescent materials including rhodamine B, gold nanoclusters (AuNCs) or silica nanoparticles is relatively broad and asymmetric [18,19,20], and the effective overlap of the absorbance spectrum of AuNPs or the fluorescence spectrum band of traditional fluorophores is narrow, which affects the detection sensitivity of the immunosensor.…”
Section: Introductionmentioning
confidence: 99%
“…There is a wide overlap of the absorbance spectrum of AuNPs and the fluorescence emission wavelength of fluorescent quantum dots (QDs), but the method is limited by a need for well-trained professionals and the high cost of QDs. Furthermore, some disadvantages are still retained such as cytotoxicity as a result of the release of heavy metal ions, strong dependence of the photoluminescence (PL) on the surface states, as well as chemical and colloidal instabilities of the QDs in harsh environments [14,21,22]. Silicon nanoparticles (SiNPs) are recognized as one type of important semiconductor nanomaterial to overcome these drawbacks.…”
Section: Introductionmentioning
confidence: 99%