Nitroreductase-responsive diagnosis and treatment integrated probe and preparation method and application thereof
A reductase and probe technology, applied in the field of biomedicine, can solve the problems of lack of effective treatment methods and difficulties in tumor diagnosis, and achieve the effects of easy promotion and application, good biological safety, and avoiding fluorescence interference
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Embodiment 1
[0045] Example 1. Preparation of integrated probe for diagnosis and treatment of nitroreductase response
[0046] The integrated diagnosis and treatment probe is synthesized according to the following route:
[0047]
[0048] Specific steps: put H 2 o 2 (62 μL, 0.6 mmol) and dichloromethane (2 mL) were mixed uniformly, trifluoroacetic anhydride (126 μL, 0.8 mmol) was added dropwise thereto, stirred at 0° C. for 30 min and then warmed to room temperature. Then the near-infrared fluorescent dye (41mg, 0.1mmol) was dissolved in dichloromethane (2mL) and added to the above solution to continue the reaction for 2h. The reaction solution was extracted with dichloromethane and water, and the organic phase was evaporated to dryness under reduced pressure to obtain the crude product. Chloromethane / methanol (20:1, V / V) was used as the eluent and separated by column chromatography on silica gel to obtain the integrated probe for diagnosis and treatment as a purple powder.
[0049]T...
Embodiment 2
[0050] Example 2. The optical response of the integrated diagnosis and treatment probe to nitroreductase
[0051] Weigh 4.4 mg of the integrated diagnosis and treatment probe, dissolve it in 10 mL of dimethyl sulfoxide, and prepare the probe stock solution (also known as mother solution, with a concentration of 1 mM), and make NADH stock solution with a concentration of 50 mM; mix 50 μL of the above probe The mother solution was added to a certain amount of phosphate buffered saline solution (PBS, 0.01M), then 25 μL of NADH mother solution and different amounts of nitroreductase solutions were added, and then the volume was adjusted to 5 mL with PBS. After reacting at 37°C for 10 minutes, test its ultraviolet-visible absorption spectrum and fluorescence emission spectrum. The excitation and emission slit widths were 20nm and 10nm, respectively, when the fluorescence emission spectrum was measured with excitation at 660nm.
[0052] Figure 4 Shown is the ultraviolet-visible a...
Embodiment 3
[0053] Example 3. The integrated probe for diagnosis and treatment is used for imaging of hypoxic tumor cells
[0054] (1) At 37°C and 5% CO 2 Under these conditions, human lung cancer cell A549 was cultured with DMEM medium containing 10% (v / v) fetal bovine serum (FBS), 100 U / mL penicillin, and 100 μg / mL streptomycin.
[0055] (2) Inoculate the A549 cells in the logarithmic growth phase in a laser confocal dish, discard the culture medium after culturing for 24 hours and wash with PBS (pH 7.4) three times, and then culture the cells with a medium containing 100 μM cobalt chloride to induce After hypoxia, the culture medium was removed after 12, 24, 36 and 48 hours respectively, and the cells were washed three times with PBS, and then co-incubated with the integrated diagnosis and treatment probe (10 μM) prepared by the present invention for 30 minutes, and then placed in a laser confocal microscope for imaging. The imaging excitation wavelength is 635nm, and the collection r...
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