Fluorophore Derivatives and Applications for Determination of Superoxide Anion and Hydrogen Polysulfide
A technology of superoxide anion and hydrogen polysulfide, applied in the field of fluorescent probes, to reduce interference and improve detection accuracy
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Embodiment 1
[0051] Embodiment 1. Preparation of cyanine compound:
specific Embodiment
[0052] The cyanine-based fluorophore shown in the general formula I comes from commercially available products, and then different positioning groups are respectively modified on the corresponding positions of the fluorophore. Finally, the corresponding cyanine compound is obtained by reacting the fluorophore modifying the positioning group and the substituted benzoic acid in dichloromethane solvent. Specific examples are as follows:
[0053] Preparation of a compound of formula:
[0054] Dissolve m-nitrophenol (0.696g, 5.00mmol) in a 30ml anhydrous DMF round-bottomed flask, add 0.208g (60% in oil) NaH at room temperature, and stir for 15min under argon protection. Heptacyanine fluorophore (0.5 g, 0.83 mmol) was added to the above solution as described above, stirred at room temperature for 24 h, washed with saturated potassium iodide solution, extracted with dichloromethane, and rotary evaporated. The crude product was purified by column chromatography using ethyl acetate a...
Embodiment 2
[0064] The prepared formula one compound is used as a probe in water system, simulated physiological environment and intracellular detection of superoxide anion and hydrogen polysulfide, simulated physiological conditions, the following experiments are all carried out under the condition of pH=7.4 (HEPES buffer solution, the concentration is 40 mM), and the probe concentration is 10 μM.
[0065] The response of the above-mentioned prepared compound formula to superoxide anion:
[0066] pH was controlled with HEPES buffer solution. Add 10μM compound of formula 1 to a 10ml colorimetric tube, then add 40mM HEPES, then add 10μM superoxide anion, dilute the volume to 10ml with ultrapure water, shake the solution well, and after equilibrating for 2 minutes, add the above working solution into a fluorescent dish to measure the fluorescence spectrum . The changes of the fluorescence spectrum before and after the detection of superoxide anion are as follows: figure 1 shown. In orde...
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