研究目的
Design and synthesis of a selective fluorescent chemosensor for Cd2+ detection in environmental and biological samples, addressing challenges such as interference from other metal ions and pH sensitivity.
研究成果
The HQ-BT conjugate serves as an effective, selective, and sensitive fluorescent chemosensor for Cd2+ in aqueous solutions with a broad pH range. It operates via a chelation-enhanced fluorescence mechanism and has been successfully applied for imaging Cd2+ in living cells, demonstrating potential for biological and environmental monitoring.
研究不足
The sensor exhibits serious fluorescence quenching at higher water contents beyond 30%, limiting its use in purely aqueous environments. Interferences from other metal ions like Zn2+ are minimized but not entirely eliminated in all conditions. The synthesis, while facile, still requires specific reaction conditions and times.
1:Experimental Design and Method Selection:
The study involved synthesizing a novel 8-hydroxylquinoline-benzothiazole conjugate (HQ-BT) and evaluating its fluorescence response to metal ions, particularly Cd2+, in aqueous methanol solutions. Theoretical calculations (DFT) and mass spectral analysis were used to understand the sensing mechanism.
2:Sample Selection and Data Sources:
Metal cation solutions were prepared from perchlorate, chloride, sulfate, or nitrate salts. The sensor HQ-BT was synthesized and dissolved in methanol for experiments. Living Hela cells were used for imaging studies.
3:List of Experimental Equipment and Materials:
Instruments included Edinburgh FS5 spectrofluorometer, SHIMADZU UV-1800 spectrophotometer, Bruker AVANCE III 400 MHz NMR spectrometer, AB Sciex 4700 MALDI TOF/TOF mass spectrometer, Mettler Toledo pH Meter, and Carl Zeiss LSM 700 microscope. Materials included 8-hydroxylquinoline, 2-aminobenzenethiol, hexamethylenetetramine, trifluoroacetic acid, hydrochloric acid, and various metal salts.
4:Experimental Procedures and Operational Workflow:
HQ-BT was synthesized via Duff reaction and condensation. Fluorescence spectra were measured with excitation at 313 nm. Titration experiments with Cd2+ were performed, and competition studies with other metal ions were conducted. pH effects and binding reversibility were tested. Confocal fluorescence imaging was done on Hela cells incubated with HQ-BT and Cd2+.
5:2+. Data Analysis Methods:
5. Data Analysis Methods: Fluorescence intensity changes were analyzed, linear relationships were established, detection limits were calculated (S/N=3), stoichiometry was determined using Job's plot, and DFT calculations were performed for structural optimization.
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spectrofluorometer
FS5
Edinburgh
Measuring fluorescence spectra
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spectrophotometer
UV-1800
SHIMADZU
Recording absorption spectra
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NMR spectrometer
AVANCE III 400 MHz
Bruker
Measuring 1H NMR and 13C NMR spectra
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microscope
LSM 700
Carl Zeiss
Conducting confocal fluorescence imaging experiments
ZEISS LSM 990 Spectral Multiplex
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mass spectrometer
4700 MALDI TOF/TOF
AB Sciex
Obtaining MALDI-TOF-MS spectra
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pH Meter
Mettler Toledo
Adjusting and measuring pH
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