2021
DOI: 10.1016/j.bios.2020.112953
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Botulinum toxin as an ultrasensitive reporter for bacterial and SARS-CoV-2 nucleic acid diagnostics

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Cited by 10 publications
(12 citation statements)
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“…[63] Especially, aptamer-dependent sensors combining with QDs could reach extreme low detection limit to single cell level. [166,179] In addition, DNA could also be an indicator of the existence of bacteria. [134,157] As depicted in Figure 5C, an FRET mechanism for detecting of antibiotic resistance genes was employed.…”
Section: Electrostatic Interactions and Ros Generationmentioning
confidence: 99%
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“…[63] Especially, aptamer-dependent sensors combining with QDs could reach extreme low detection limit to single cell level. [166,179] In addition, DNA could also be an indicator of the existence of bacteria. [134,157] As depicted in Figure 5C, an FRET mechanism for detecting of antibiotic resistance genes was employed.…”
Section: Electrostatic Interactions and Ros Generationmentioning
confidence: 99%
“…FRET is defined as the process of the excited state segment transports the energy to the grand state [113,154,[164][165][166] along with fluorescence quenching. The excited state is the donor, which can act as a probe for sensing, and the grand state is the accepter.…”
Section: Formation and Operating Mechanisms Of Sensing Elementsmentioning
confidence: 99%
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“… Testing approaches Testing type Sample source Gene/region detection LOD Detection time Target analyte References Colorimetric biosensor based on gold nanoparticle (AuNP) POC Nasal swabs, RdRp and N genes Threshold cycle (Ct) = 36.5 3 min Spike protein, membrane protein, envelope proteins 142 Colorimetric biosensor based on botulinum neurotoxin receptor POC Blood, urine, Stool and Nasopharyngeal swabs N genes 1a.m. 1–2 h Recombinant plasmid 143 RT-PCR colorimetric assay Laboratory based Upper respiratory specimens ORF1ab and N genes 10 5 dilution factors Total ∼2–3 h But observable color change found within 10 min Nucleic acids template 144 Colorimetric detection using CRISPER/dCas9 Laboratory based Nasopharyngeal aspirates and sputum specimens N1, N2, and N3 genes 30 pM ∼2 h Nucleic acids 145 Colorimetric detection using DNAzyme sensor Laboratory and POC-based Swabs from nasopharyngeal and oropharyngeal N genes 10 1 to 10 7 copies Total duration ∼1 h and visual observation ∼5 min RNA 146 Paper-based colorimetric biosensor using electrochemical assay Laboratory and POC-based Not mentioned Immunoglobulins IgG and IgM ∼1 ng/mL 30 min Spike protein 136 Colorimetric biosensor using LAMP assay POC Nasal swabs N gene ∼62.5 viral copies/LAMP reaction 50–60 min Plasmids 147 Colorimetric detection using RT-LAMP …”
Section: Nanobiosensing Techniques For Sars-cov-2 Detectionmentioning
confidence: 99%
“…Therefore, the early diagnosis of infection and cutting off the transmission route are the keys to effectively controlling the epidemic. At the same time, the development of rapid, sensitive, convenient, and accurate virus detection technology is imminent [ 8 , 9 , 10 ].…”
Section: Introductionmentioning
confidence: 99%