研究目的
Investigating the development and application of a novel iminocoumarin-based red to near-infrared fluorescent turn-on probe for the detection of H2S in living cells and animals.
研究成果
The developed iminocoumarin-based fluorescent probe shows rapid and significant fluorescent turn-on signal changes for H2S with high selectivity, sensitivity, long emission wavelength in the red-to-NIR region, and a large Stokes shift. It has low cytotoxicity and can be used to image H2S in living cells and animals, making it a valuable tool for real-time detection and imaging of H2S both in vitro and in vivo.
研究不足
The probe is not effective under acidic conditions (pH <6) due to the pKa value of H2S. The probe has poor or no subcellular location specificity to mitochondria and lysosome.
1:Experimental Design and Method Selection:
The study involved the synthesis of a tetrahydroquinoxaline iminocoumarin-based NIR fluorescent probe (NIR-IC-H2S) for H2S detection. The probe's design rationale was based on the thiolysis of the 2,4-dinitrobenzenesulfoamide group mediated by H2S.
2:2S. Sample Selection and Data Sources:
2. Sample Selection and Data Sources: HeLa cells and RAW
3:7 cells were used for cell imaging experiments. Kunming mice were used as the animal model for in vivo detection. List of Experimental Equipment and Materials:
2 A Varian Mercury 600 spectrometer for NMR spectra, a Waters E2695 LC-MS system and a Bruker microTOF-Q instrument for mass spectra, an Agilent Cary 100 UV-Vis spectrophotometer for absorption spectra, an Agilent Cary Eclipse fluorescence spectrophotometer for fluorescence measurements, an inverted fluorescence microscopy (OLYPUS) for cell images, and a Bruker In Vivo-Xtreme imaging system for mice images.
4:Experimental Procedures and Operational Workflow:
The probe's response to H2S was tested in HEPES buffer. Cell imaging involved incubating cells with the probe and then with NaHS. In vivo imaging involved injecting mice with the probe and then with NaHS.
5:Data Analysis Methods:
Fluorescence intensity changes were monitored at 652 nm. The detection limit was determined using the 3σ method.
独家科研数据包,助您复现前沿成果,加速创新突破
获取完整内容-
Bruker microTOF-Q instrument
microTOF-Q
Bruker
Acquiring mass spectra
-
Agilent Cary 100 UV-Vis spectrophotometer
Cary 100
Agilent
Recording absorption spectra
-
Agilent Cary Eclipse fluorescence spectrophotometer
Cary Eclipse
Agilent
Recording fluorescence measurements
-
Bruker In Vivo-Xtreme imaging system
In Vivo-Xtreme
Bruker
Taking mice images
-
Varian Mercury 600 spectrometer
600
Varian
Recording NMR spectra
-
Waters E2695 LC-MS system
E2695
Waters
Acquiring mass spectra
-
Inverted fluorescence microscopy
OLYPUS
Taking cell images
-
登录查看剩余5件设备及参数对照表
查看全部