2022
DOI: 10.1016/j.bios.2022.114288
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Plasmon-modulated fluorescence nanoprobes for enzyme-free DNA detection via target signal enhancement and off-target quenching

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Cited by 8 publications
(6 citation statements)
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“…As known, the small NPs with a diameter of <30 nm can serve as excellent fluorescence quenchers because absorption is dominant, while relatively larger particles, typically >30 nm in diameter, tend to scatter, making them more suitable as a fluorescence enhancer. , On the other hand, the spectra overlap between the LSPR band of plasmonic nanoparticles and the excitation/emission band of the emitter also has a greater influence on the fluorescence of emitters . Hence, in order to obtain the PEF and the quenching of RF, respectively, Ag@SiO 2 with big core size and small Ag NPs were chosen.…”
Section: Resultsmentioning
confidence: 99%
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“…As known, the small NPs with a diameter of <30 nm can serve as excellent fluorescence quenchers because absorption is dominant, while relatively larger particles, typically >30 nm in diameter, tend to scatter, making them more suitable as a fluorescence enhancer. , On the other hand, the spectra overlap between the LSPR band of plasmonic nanoparticles and the excitation/emission band of the emitter also has a greater influence on the fluorescence of emitters . Hence, in order to obtain the PEF and the quenching of RF, respectively, Ag@SiO 2 with big core size and small Ag NPs were chosen.…”
Section: Resultsmentioning
confidence: 99%
“…In summary, the modulation of the fluorescence signals through the PEF depends on many factors, including particle size, concentration, proximity to the fluorophore, and spectral overlap. Typically, particles smaller than 30 nm quench fluorescence due to absorption, while larger particles enhance fluorescence by scattering light . Under optimal conditions, such as appropriate spectral overlaps and distances, PEF occurs due to increased excitation rates and radiative transition rates.…”
Section: Resultsmentioning
confidence: 99%
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“…Consequently, the need for a simple, rapid, and high-throughput approach to detect and monitor the dissemination of ARGs within bacterial populations has become increasingly pressing. PCR-free methods for detecting ARGs have also been developed, such as electrochemical/photoelectrochemical, , fluorescence sensors, paper-based chips, and colorimetric methods . Among these methods, fluorescence sensors are widely used for genetic testing due to their high sensitivity and ease of operation.…”
Section: Introductionmentioning
confidence: 99%