Novel targeting nanoparticle as well as preparation method and application thereof
A nanoparticle and targeting technology, applied in the field of biomedicine, can solve problems such as incompleteness, and achieve the effects of prolonging survival time, improving radiosensitivity, and high stability
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[0038] The preparation method of the novel targeting nanoparticles comprises the following steps:
[0039] (1) Dissolve the positron polymer carrier PEI-CyD-FA (H1) in double-distilled water to obtain solution 1, and let it stand at room temperature for 5 minutes in the dark;
[0040] (2) Take the double-stranded DNA molecule Dbait with a hairpin-like structure of a small fragment and dissolve it in double-distilled water to obtain solution 2, and let it stand at room temperature for 5 minutes;
[0041] (3) Drop solution 1 into solution 2 in the dark and vortex, continue to vortex for 15 seconds, fully mix solution 1 and solution 2, keep in the dark and stand at room temperature for 20 minutes to obtain the new targeting nanoparticles H1 / Dbait can be used for subsequent related experiments.
[0042] The application of the novel targeted nanoparticle for tumor radiotherapy.
[0043] Further, the tumor is prostate cancer, colorectal cancer, liver cancer, lung cancer, melanoma...
Embodiment 1
[0047] Example 1. The particle size and Zeta potential detection of novel targeted nanoparticles
[0048] Take freshly prepared H1 / Dbait mixtures with different N / P ratios (1:1, 6:1, 12:1, 18:1, 24:1), and use a particle size / Zeta potential measuring instrument to measure the H1 / Dbait The light scattering particle size and Zeta potential value of the nanoparticles were measured.
Embodiment 2
[0049] Example 2. Stability and encapsulation rate detection of novel targeted nanoparticles
[0050] Take freshly prepared H1 / Dbait mixtures with different N / P ratios (1:1, 6:1, 12:1, 18:1, 24:1), and use agarose gel electrophoresis to analyze the new targeting nanoparticles H1 / Dbait's stability and package rate are tested. The specific steps of agarose gel electrophoresis are as follows:
[0051] (1) Weigh 0.5g of agarose and place it in a conical flask, add 50ml of 1×TAE solution, turn the mouth of the bottle upside down into a small beaker, heat in a microwave oven until the agarose is completely melted, and boil 3 times;
[0052] (2) When the agarose gel liquid is cooled to 60°C, add 5ul of nucleic acid dye, shake well and pour it into the spare gel-making tank of the device, so that the gel liquid is evenly spread on the bottom of the gel-making tank. Stand at room temperature until the gel is completely solidified, pull out the toothed comb in the gel-making tank ver...
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