A kind of photodynamic therapy compound and its preparation method and application
A compound and compound technology, applied in the field of photodynamic therapy compound and its preparation, can solve the problems of limiting wide application, limiting the therapeutic effect of photodynamic therapy, reducing the effect of photodynamic therapy, etc., so as to improve the production of active oxygen and solve the The effect of reducing oxygen production and avoiding normal tissue damage
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Embodiment 1
[0065] Embodiment 1, the preparation of photodynamic therapy compound
[0066] (1), preparation of nanoparticles composed of compounds shown in formula I and formula II
[0067] Dissolve 0.5 mg of the compound shown in Formula I (n is 560-960) and 0.25 mg of the compound shown in Formula II in 5 mL of tetrahydrofuran and use ultrasound to dissolve it completely, then drop the above tetrahydrofuran solution into 15 mL of ultrapure water and ultrasonic dispersion. After ultrasonic dispersion with 50W power for 5 minutes, continue to stir in a fume hood at 25°C overnight to obtain nanoparticles composed of compounds represented by formula I and formula II, and then filter through a 0.22 μm filter membrane to obtain the above target nanoparticles NPs in the filtrate.
[0068]
[0069] (2), preparation of nanoparticles modified by bovine hemoglobin
[0070] Add 0.3 mg of NHS and 0.6 mg of EDC to the filtrate obtained above, react in PBS buffer solution with pH = 7.4 at 37 ° C ...
Embodiment 2
[0076] Embodiment 2, the characterization of photodynamic therapy compound
[0077] (1) Characterization of particle size and zeta potential
[0078] The obtained nanoparticles NPs ( figure 1 ) and photodynamic therapy complex Hb-NPs@liposome ( image 3 ) structure for characterization. The above-mentioned bovine hemoglobin-modified nanoparticles Hb-NPs were characterized by a dynamic light scattering instrument for surface charge changes ( figure 2 ).
[0079] from figure 1 It can be seen that the nanoparticles NPs are uniformly distributed, spherical particles, and the hydration radius is about 20nm.
[0080] from figure 2 It can be seen from the figure that after the modification of bovine hemoglobin, the surface charge of the nanoparticles changed from -40mV to -17mV, indicating that the modification was successful.
[0081] from image 3 It can be seen that the photodynamic therapy complex Hb-NPs@liposome is uniformly spherical, and the hydration radius is about...
Embodiment 3
[0086] Example 3. The photodynamic therapy complex is used for tumor cell killing under the activation of chemical activators
[0087] (1) Determination of bioluminescent energy transfer spectroscopy between luminol and Hb-NPs
[0088] Add 20 μL of 20 mM luminol and 150 μL of 45 mg / mL Hb-NPs to 805 μL of pH9.0 sodium carbonate buffer, vortex for 5 s, add 25 μL of 20 mM hydrogen peroxide aqueous solution for 2 s and measure the luminescence spectrum immediately, the spectral range is 300 nm to 700 nm. See Figure 5 .
[0089] from Figure 5 It can be seen that efficient energy transfer can occur between luminol and Hb-NPs.
[0090] (2) Determination of active oxygen
[0091] Activation of reduced 2,7-dichlorofluorescein (DCFH): add 2mL 0.01M NaOH to 500μL 2,7-dichlorofluorescein diethyl ester (DCFH-DA), let it stand at room temperature for 30min, then add 10mL phosphate buffer solution (25mM, pH=7.4), mix well and store in dark place on ice until use.
[0092] Add 90 μL o...
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