Thrombin-loaded DNA (deoxyribonucleic acid) self-assembly nano-structure, as well as preparation method and application thereof
A nanostructure, thrombin technology, which is used in medical preparations with non-active ingredients, medical preparations containing active ingredients, drug combinations, etc., can solve the problems of uncomfortable intravenous injection and short half-life of thrombin, and achieve uniform size, Good stability and good biocompatibility
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Embodiment 1
[0057] Example 1: Preparation of DNA self-assembled nanostructure loaded with thrombin in the present invention
[0058] Specific steps are as follows:
[0059] (1) Preparation of rectangular DNA origami structure
[0060] The M13 phage genomic DNA backbone and staple strands were mixed, and the final concentrations of the backbone and staple strands were 10 nM and 80 nM, respectively. The mixture was slowly annealed using a gradient PCR instrument. The annealing conditions were as follows: from 65° C. to 25° C., each 1° C. was a gradient, and the residence time of each gradient was 10 minutes. The entire annealing process was about 7 hours.
[0061] After the annealing procedure was completed, the DNA origami structure samples were taken out and centrifuged with a 100kDa spin column (MWCO) to remove excess staple strands and capture strands. The centrifugation conditions are: take 100 μL sample, add 350 μL 1×TAE-Mg buffer solution, centrifuge at 4700 rpm for 3 minutes, the ...
Embodiment 2
[0067] Example 2: Anti-tumor effect of the DNA self-assembled nanostructure loaded with thrombin in the present invention
[0068] Evaluation method of anti-tumor effect:
[0069] will be 2.0×10 6 Human MDA-MB-231 breast cancer cells were orthotopically inoculated in the mammary pad of BALB / c nude mice until the tumor volume grew to about 100mm 3 . The thrombin-loaded DNA self-assembled nanoparticle solution prepared in Example 1 was injected into the tail vein of tumor-bearing mice at a dosage of about 1.5 U unit thrombin per mouse, and the tumor volume was measured once every 2 days. After 6 injections, the changes in tumor volume were statistically analyzed. Tumor volume was calculated according to the following formula: volume = (d 2 ×D) / 2, where d is the smallest diameter of the tumor and D is the largest diameter. Inject normal saline, free thrombin, and blank DNA nanoparticles as negative controls. Experimental results such as image 3 shown.
[0070] Depend on ...
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