Strong oncolytic rod-shaped nano-assembly, preparation method and application thereof
A nano-assembly, oncolytic technology, applied in the field of medical biomaterials, can solve problems such as toxic and side effects of healthy tissues, and achieve the effects of increasing tumor enrichment, enhancing cell entry efficiency and oncolytic effect, and improving the effect of membrane rupture.
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[0041] The present invention provides an oncolytic rod-shaped supramolecular assembly, such as figure 1 , and the construction method, the oncolytic rod-shaped supramolecular assembly has a multifunctional combined strong oncolytic effect, such as figure 2 shown. Preparation method, concrete steps are as follows:
[0042] (1) Preparation of oncolytic monomers of peptide dendrimers
[0043] (2) After oxidizing and breaking the single-walled carbon nanotubes to prepare short carbon nanotubes (~300nm) with a relatively uniform length, modify Arg-Gly-Asp for targeting.
[0044] Take the oncolytic monomer (10n equivalent) in step (1) and the single-walled carbon nanotubes (1n equivalent) in step (2), dissolve them in a good solvent (DMSO), drop them into deionized Water, through hydrophilic-hydrophobic self-assembly and π-π stacking, the hydrophobic anti-tumor drug at the end of the fan-shaped oncolytic monomer drives the self-assembly of the oncolytic monomer to the surface of...
Embodiment 1
[0045] Example 1: Preparation of oncolytic monomers of peptide dendrimers
[0046] Modification of residues with the function of cell membrane penetration: arginine is selected as the membrane-penetrating functional group, and is coupled to the periphery of the peptide dendrimer skeleton through a covalent bond. Accurately weigh 3.0 g of second-generation lysine, 11.62 g of Boc-protected and pdf lysine, 11.83 g of benzotriazol-1-yl-oxytripyrrolidinylphosphonium hexafluorophosphate (PyBop) and 3.04 g of 1 -Hydroxybenzotriazole (HOBT) was dissolved in a single-necked bottle with a branch tube, N,N-dimethylamide (DMF) was added under nitrogen atmosphere, and 12.14mL N,N-diisopropylethyl Amine (DIPEA). After reacting at room temperature for 24 hours, the reaction solution was washed, dried, concentrated, purified and separated by column chromatography, and hydrazine hydrate was modified at the end of lysine (coupling tert-butoxycarbonylhydrazine Boc-NHNH 2 ), the condensation re...
Embodiment 2
[0049] Example 2: Preparation of rod-shaped prodrug self-delivery system
[0050] Take 10 mg residue-shielded oncolytic monomer and 2 mg target-modified carbon nanotubes and dissolve them in 200 μL of good solvent dimethyl sulfoxide. Under ultrasonic conditions, the above solution was dropped into 1800 μL deionized water for self-assembly. Under the hydrophobic interaction and π-π stacking, the self-assembled rod-shaped supramolecular assembly was formed, and the organic solvent was removed by dialysis (MWCO 100KDa). The rod-shaped supramolecular assembly is collectively referred to as R-SAPs.
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