Liver-cancer-targeted doxorubicin-supporting silica-gold composite material, and preparation method and application thereof
A technology of loading doxorubicin and silicon dioxide, which is applied in the nano-biomedicine field of biomedical materials science, can solve the problems of centralized heating in untreated areas, poor therapeutic effect, and large toxic and side effects, so as to reduce toxic and side effects, Low immunogenicity and high biocompatibility
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Embodiment 1
[0062] Embodiment 1: Preparation of nano-silica-gold core-shell particles
[0063] Synthesis of seeded core nanoparticles on the surface of silica nanomaterials by first using 3-aminopropyltriethoxysilane to ammonia the surface of silica nanoparticles, followed by reduction of synthesized gold nanoparticles using tetrakishydroxymethylphosphonium chloride , and finally the chloroauric acid solution is reduced by formaldehyde, a large number of gold nanocrystals are generated in the solution, and then these crystals grow with the gold nanoparticles on the seed core as nucleation sites, and finally form a complete core-shell structure of nano-silica- Gold core-shell particles. For the specific process of synthesizing silica-gold nano-core-shell particles in this example, refer to Chinese patent document 200710040691.8 "A nanocomposite silica-metal core-shell particle and its preparation".
Embodiment 2
[0064] Embodiment 2: polyethylene glycol diamine (NH 2 -PEG-NH 2 )Synthesis
[0065] PEG→NPC-PEG-NPC
[0066] PEG2000 (10.0g, 10mmol) and freshly distilled pyridine (3.955g, 50mmol) were added to 70mL of dry dichloromethane (DCM) solution, under nitrogen protection, the p-NPC (8.07 g, 40mmol) was added dropwise to the reaction system, after the dropwise addition was completed, the reaction solution was raised to normal temperature and continued to react for 24 hours. After the reaction, the p-NPC-activated PEG2000 was reprecipitated with pre-cooled glacial ether, and dried in vacuum before use.
Embodiment 3
[0067] Embodiment 3: Synthesis of Cys-PEG-Dox
[0068] Cystamine hydrochloride (Cys, 0.612g, 2.72mmol) and TEA (0.568g, 5.61mmol) were dissolved in 5mL of DMF, and PEG-NPC (2.787g, 0.540mmol) in DMF was The solution (10 mL) was added dropwise into the flask and reacted overnight. The reaction solution was reprecipitated twice with pre-cooled ice ether and dried in vacuo to obtain the crude Cys-PEG-NPC product. Then Cys-PEG-NPC (0.2g, 0.08mmol) was dissolved in 10mL DMSO, then 50mg of doxorubicin hydrochloride (0.08mmol) and 57 μL TEA were added, and the reaction was carried out under nitrogen protection at room temperature for 48 hours. After the reaction, the reaction liquid Add 30 mL of aqueous solution to the solution, and then use a dialysis bag with a molecular weight cut-off of 1000 to dialyze for 3 days to remove unreacted cystamine and Dox. After dialysis, freeze-dry to obtain purple Cys-PEG-Dox dry powder. The absorption peak intensity of Cys-PEG-Dox at 488nm was de...
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