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A novel and highly sensitive upconversion fluorescence and colorimetric dual readout iodate (IO) nanosensor system was constructed by using both the outstanding optical performance of NaYF:Yb, Tm upconversion nanoparticles (UCNPs) and the analyte-triggered cascade signal amplification (CSA) technique. The construction of the sensing system consisted of three processes. First, IO oxidized o-phenylenediamine (OPD) to diaminophenazine (OPDox), while IO was reduced to I. Second, the generated I can further oxidize OPD to OPDox. This mechanism has been verified by H NMR spectra titration analysis and HRMS measurement, which effectively improves the selectivity and sensitivity of the measurement of IO. Third, the generated OPDox can effectively quench the fluorescence of UCNPs via the inner filter effect (IFE), realize analyte-triggered CSA, and allow quantitative determination of IO. Under the optimized conditions, the fluorescence quenching efficiency showed a good linear relationship to IO concentration in the range of 0.06-100 μM, and the detection limit reached 0.026 μM (3RSD/slope). Moreover, this method was applied to detect IO in table salt samples, yielding satisfactory determination results with excellent recoveries (95.5-105%) and high precision (RSD <5.5%). These results suggest that the dual-readout sensing strategy with well-defined response mechanisms has promising application prospects in physiological and pathological studies.
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http://dx.doi.org/10.1016/j.talanta.2023.124661 | DOI Listing |
Talanta
August 2023
Henan Key Laboratory of Rare Earth Functional Materials; International Joint Research Laboratory for Biomedical Nanomaterials of Henan, Zhoukou Normal University, Zhoukou, 466001, China.
A novel and highly sensitive upconversion fluorescence and colorimetric dual readout iodate (IO) nanosensor system was constructed by using both the outstanding optical performance of NaYF:Yb, Tm upconversion nanoparticles (UCNPs) and the analyte-triggered cascade signal amplification (CSA) technique. The construction of the sensing system consisted of three processes. First, IO oxidized o-phenylenediamine (OPD) to diaminophenazine (OPDox), while IO was reduced to I.
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
August 2022
School of Chemistry and Chemical Engineering, Qufu Normal University, Qufu City 273165, Shandong, China. Electronic address:
A sensitive fluorescence sensing platform consisting of manganese dioxide nanosheets (MnO) and gold nanoparticles (AuNPs) as dual nanoquenchers has been constructed to detect isoniazid combined with analyte-triggered cascade reactions. The fluorescence of 2,3-diaminophenazine (DAP) is quenched simultaneously by MnO and AuNPs via inner filter effect. MnO is decomposed by isoniazid to generate Mn, which makes AuNPs aggregated.
View Article and Find Full Text PDFACS Appl Mater Interfaces
May 2021
Department of Laboratory Medicine, State Key Laboratory of Biotherapy and Cancer Center, Med+X Center for Manufacturing, West China Hospital, Sichuan University and Collaborative Innovation Center, Chengdu 610041, China.
The characterization of circulating tumor cells (CTCs) by liquid biopsy has a great potential for precision medicine in oncology. Here, a universal and tandem logic-based strategy is developed by combining multiple nanomaterials and nanopore sensing for the determination of mucin 1 protein (MUC1) and breast cancer CTCs in real samples. The strategy consists of analyte-triggered signal conversion, cascaded amplification via nanomaterials including copper sulfide nanoparticles (CuS NPs), silver nanoparticles (Ag NPs), and biomaterials including DNA hydrogel and DNAzyme, and single-molecule-level detection by nanopore sensing.
View Article and Find Full Text PDFBioorg Med Chem Lett
September 2008
Anorganisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, 69120 Heidelberg, Germany.
A two-step reaction cascade is applied to the sequence-specific detection of single-stranded DNA, including analyte-triggered re-activation of apo-aldolase by its cofactor Zn(2+) and catalytic conversion of a chromophore.
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