Quantum dots as optical labels for ultrasensitive detection of polyphenols
Considering the fact that polyphenols have versatile activity in-vivo, its detection and quantification is very much important for a healthy diet. Laccase enzyme can convert polyphenols to yield mono/polyquinones which can quench Quantum dots fluorescence. This phenomenon of charge transfer from qui...
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Veröffentlicht in: | Biosensors & bioelectronics 2014-07, Vol.57, p.317-323 |
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Sprache: | eng |
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Zusammenfassung: | Considering the fact that polyphenols have versatile activity in-vivo, its detection and quantification is very much important for a healthy diet. Laccase enzyme can convert polyphenols to yield mono/polyquinones which can quench Quantum dots fluorescence. This phenomenon of charge transfer from quinones to QDs was exploited as optical labels to detect polyphenols. CdTe QD may undergo dipolar interaction with quinones as a result of broad spectral absorption due to multiple excitonic states resulting from quantum confinement effects. Thus, “turn-off” fluorescence method was applied for ultrasensitive detection of polyphenols by using laccase. We observed proportionate quenching of QDs fluorescence with respect to polyphenol concentration in the range of 100µg to 1ng/mL. Also, quenching of the photoluminescence was highly efficient and stable and could detect individual and total polyphenols with high sensitivity (LOD-1ng/mL). Moreover, proposed method was highly efficient than any other reported methods in terms of sensitivity, specificity and selectivity. Therefore, a novel optical sensor was developed for the detection of polyphenols at a sensitive level based on the charge transfer mechanism.
•CdTe QDs were employed for the detection of polyphenols.•Quinone dependent charge transfer quenching was employed for the laccase enzyme assay.•Individual polyphenols were detected by a “finger print’ quenching profile.•Designed nanosensor was applied to detect individual and total polyphenols at 1ng/mL. |
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ISSN: | 0956-5663 1873-4235 |
DOI: | 10.1016/j.bios.2014.01.038 |