Fluorescent probe for detecting peroxynitrite anions, and synthesis method and applications thereof
A peroxynitroso, fluorescent probe technology, applied in the field of applied biology, can solve the problems of interference, low selectivity, small Stoke shift, etc., and achieve the effects of accurate detection, high selectivity, and simple synthesis
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Embodiment 1
[0033] About the synthetic method of fluorescent probe, comprise following experimental steps:
[0034] (1) 2-Hydroxybenzaldehyde (122mg, 1mmol) and triethylamine (200mg, 2mmol) were dissolved in dry 10mL tetrahydrofuran, and diphenylphosphinic chloride (236.5mg, 1mmol) was added dropwise under stirring, at room temperature Down reaction 12 hours;
[0035] (2) After the reaction is completed, evaporate under reduced pressure to obtain the crude product, and then use silica gel column chromatography, wherein the volume ratio of ethyl acetate and sherwood oil in the silica gel column chromatography is 1:4 to obtain a white intermediate product (232mg, Productive rate 72%), the synthetic reaction equation of this intermediate product is as figure 1 shown;
[0036] (3) Dissolve the white intermediate product (322mg, 1mmol) and hydrazine hydrate (50mg, 1mmol) in 10mL ethanol, the reaction mixture is heated, stirred, and refluxed for 2 hours. After the reaction solution is cooled...
Embodiment 2
[0041] About testing fluorescent probe detection ONOO - effect, the experimental steps are:
[0042](1) Dissolving the fluorescent probe in N,N-dimethylformamide (DMF) to prepare a 1mmol / L probe solution;
[0043] (2) Take the probe solution and add DMF and PBS (pH = 7.4) buffer solution to form a 10 μM solution (organic phase: PBS aqueous phase = 1:99, V / V), and test the changes in the ultraviolet absorption spectrum and fluorescence emission spectrum Condition.
[0044] The changes in the UV absorption spectrum are as follows: Figure 5 As shown, where the fluorescent probe was added to ONOO - The UV-Vis absorption spectrum curve is (a), without ONOO - The UV-visible absorption spectrum curve is (b). From Figure 5 It can be seen from the figure that when ONOO is not added - In the case of , the probe has no absorption peak at 400nm, while adding ONOO - Afterwards, the probe has an obvious absorption peak at 400nm, indicating that this fluorescent probe has a strong ...
Embodiment 3
[0047] In order to test the Stoke shift value of the fluorescent probe of the present invention, the following experiment is now done.
[0048] (1) Synthesis of ONOO by autoxidation of hydroxylamine in alkaline medium - : Vigorously stir the mixed solution containing 0.01mol / L hydroxylamine, 0.5mol / LNaOH and 0.001mol / L EDTA under aerobic conditions for about 3 hours, then use MnO 2 Powder filtration mixture to remove H 2 o 2 , The filtered mixture can be used for experiments immediately or stored at -18°C. Among them, ONOO can be detected at 302nm by UV-Vis spectrophotometer - concentration.
[0049] (2) Dissolve the fluorescent probe in N,N-dimethylformamide (DMF) to prepare a 1mmol / L probe solution, add the probe solution to DMF and PBS (pH=7.4) buffer, and prepare into a 10uM (organic phase: PBS aqueous phase = 1:99, V / V) solution; then add 45uM ONOO - The reaction solution was delayed for 10 seconds, and its luminous intensity was continuously measured for 10 seconds...
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