Ratiometric fluorescent probe and application thereof

A fluorescent probe, ratio-based technology, used in fluorescence/phosphorescence, luminescent materials, chemical instruments and methods, etc., can solve the problems of easy photobleaching, influence of the accuracy of the results, poor probe specificity, etc., to improve the specificity. High stability and good water solubility

Active Publication Date: 2011-08-10
DALIAN INST OF CHEM PHYSICS CHINESE ACAD OF SCI
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AI Technical Summary

Problems solved by technology

The method using fluorescent molecular probes in the above method is a simple, sensitive and specific analysis method, so far, several fluorescent molecular probes have been successfully used in ONOO - Determination of dichlorodihydrofluorescein (DCFH) and dihydrorhodamine (DHR) (document 8: H.Possel, H.Noack, FEBS Lett.1997, 416, 175; document 9: N.W.Kooy, J.A.Royall , Free Radic.Biol.Med.1994, 16, 149), although this method has higher sensitivity, the specificity of this type of probe is poor, and other biological oxidants such as hypochlorous acid, thiol and peroxidase can also Oxidation of DCFH and DHR to Generate Strongly Fluorescent Dichlorofluorescein and Rhodamine
In recent years, two novel ONOO based on aromatic ring nitration and ketone oxidation reactions - Fluorescent probes: NiSPYs and HKGreens have been synthesized successively (Document 10: T.Ueno, T.Nagano, J.Am.Chem.Soc.2006, 128, 10640; Document 11: D.Yang, H.Wang, J.Am.Chem.Soc.2006, 128, 600; Literature 12: Z.Sun, H.Wang, D.Yang, Org.Lett.2009, 11, 1887), these two probes can be combined with ONOO - Specific reaction leads to a significant enhancement of fluorescence intensity, but the probe has poor water solubility, is easy to be photobleached, has a small Stokes shift, and has a short retention time in the cell, which is not conducive to the long-term observation and trace of peroxynitrite anion in the cell. Quantitative determination
In addition, the existing ONOO - Fluorescent probes use fluorescence intensity as a characterization parameter. Although the operation is simple, the accuracy of the results is easily affected by factors such as changes in the external environment and instrument conditions, such as optical paths, photobleaching, scattering, and background light.

Method used

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  • Ratiometric fluorescent probe and application thereof
  • Ratiometric fluorescent probe and application thereof
  • Ratiometric fluorescent probe and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0030] Embodiment 1: Ligand [4'-(2,4-dimethoxyphenyl)-2,2':6'2"-biterpyridine-6,6"-dimethylamine]tetraacetic acid ( Synthesis of DTTA for short) and its methyl acetate (AM-DTTA for short).

[0031] 1. Synthesis of DTTA

[0032] Synthetic route such as figure 1 As shown, the basic operation process is as follows:

[0033] (1) Synthesis of 4'-(2,4-dimethoxyphenyl)-2,2':6',2"-biterpyridine (compound 1)

[0034] 3.32 grams of 2,4-dimethoxybenzaldehyde (20mmol), 4.84 grams of 2-acetylpyridine (40mmol), and 2.64 grams of KOH (85%, 40mmol) were mixed and dissolved in 100mL of absolute ethanol, and then 50mL of concentrated ammonia was added , stirred at 50°C for 10 hours, and the precipitate was collected by filtration. The crude product was recrystallized from ethanol to obtain 3.61 g of the target compound, with a yield of 48.9%. 1 H NMR (CDCl 3 ) measurement results: δ=8.71 (d, J, 4.8Hz, 2H); 8.66 (d, J, 7.6Hz, 2H); 8.62 (s, 2H); 7.86 (t, J, 7.6Hz, 2H); 7.49 (d, J, 8.4Hz, 1H...

Embodiment 2

[0050] Example 2: Two rare earth complexes DTTA-Eu 3+ and DTTA-Tb 3+ Determination of properties

[0051] 1. Spectral properties

[0052] DTTA-Eu was determined using 0.05mol / L boric acid buffer solution with pH value 9.1 as solvent 3+ and DTTA-Tb 3+ (The molar ratio of ligand and metal ion in the two complexes is 1:1) UV-Vis absorption spectrum, fluorescence spectrum, molar extinction coefficient (ε), fluorescence quantum yield (φ) and fluorescence lifetime (τ). The instrument used for the determination of ultraviolet-visible absorption spectrum is a Perkin Elmer Lambda 35 spectrophotometer. The fluorescence measurement instrument is a Perkin Elmer LS 50B fluorescence spectrophotometer. Fluorescence quantum yield measurement using 4’-phenyl-2,2’:6’,2”-tripyr-6,6”-dimethylaminetetraacetic acid and Eu 3+ and Tb 3+ The complex is measured as a standard according to the literature method (document 14: M.Latva, H.Takalo, J.Kankare, J.Lumin.1997, 75, 149), and the calculatio...

Embodiment 3

[0058] Example 3: with DTTA-Eu 3+ / Tb 3+ As a fluorescent probe for the determination of ONOO in aqueous solution - concentration

[0059] 1. ONOO - to DTTA-Eu 3+ with DTTA-Tb 3+ Effect of Fluorescent Properties

[0060] Add DTTA-Ln to a series of 0.05mol / L Tris-HCl buffer solutions with a pH value of 7.4 3+ (Ln 3+ =Eu 3+ or Tb 3+ , 2.0μmol / L) and different concentrations of ONOO - , After stirring and reacting for 15 minutes, the fluorescence intensity and fluorescence lifetime of each solution were measured. The measuring instrument is a PerkinElmer LS 50B fluorescence spectrophotometer.

[0061] Such as Figure 4 As shown, with ONOO - Concentration increases, DTTA-Eu 3+ The fluorescence intensity and fluorescence lifetime basically do not change; but DTTA-Tb 3+ The fluorescence intensity gradually decreases, the fluorescence lifetime is significantly shortened, and the time-resolved fluorescence intensity is significantly weakened. Figure 5 DTTA-Eu is given...

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Abstract

The invention relates to a novel rare-earth complex ratiometric fluorescent probe which can be used for measuring peroxynitrite in a biosystem. The probe is complexes formed by two trivalent rare-earth ions Eu<3+> and Tb<3+> and an organic ligand [4'-(2,4-dimethoxyphenyl)-2,2':6'2''-terpyridine-6,6''-dimethylamino]tetraacethyl (DTTA for short), wherein the structural formula of the ligand is disclosed in the specification. The probe can specifically act with the peroxynitrite, so that the two rare-earth complexes are changed at the ratio (F612 / F541) of the fluorescence intensity of 612nm and 541nm, thereby implementing the selective fluorescent measurement of the peroxynitrite in a biosystem.

Description

technical field [0001] The present invention relates to the determination technology of peroxynitrite anion, specifically a rare earth complex-based peroxynitrite anion ratio-type fluorescent probe and its application, which can be used in the selection of peroxynitrite anion in biological systems. Ratio-type rare-earth fluorescent probes for sexual fluorescence assays. Background technique [0002] Peroxynitrite anion (ONOO) in biological systems - ) is composed of nitric oxide (NO) and superoxide anion radicals (O 2 - ) is rapidly combined to form an important nitrogen-oxygen reactive compound. It is generally believed that ONOO - is compared to NO and O 2 - A potent cytotoxic substance with stronger oxidation and wider effects (Document 1: J.S.Beckman, T.W.Beckman, Proc.Natl.Acad.Sci.USA.1990, 87, 1620; Document 2: G.Ferrer- Sueta, R. Radi, ACS Chem. Biol. 2009, 4, 161). As a strong oxidizing agent, ONOO - Can produce oxidative damage to cells and tissues, so it ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C09K11/06G01N21/64
Inventor 关亚风袁景利宋翠红
Owner DALIAN INST OF CHEM PHYSICS CHINESE ACAD OF SCI
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