Photoresponse silicon oxide nanometer vector and preparation method thereof
A light-responsive, nano-carrier technology, applied in the field of multifunctional nano-carriers constructed by atom transfer radical polymerization and its preparation, can solve the effects of difficult to achieve cancer treatment effects, lack of precise control, and tumor heterogeneity and other issues, to achieve the effect of improving gene transfection efficiency, low price, and controllable size
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Embodiment 1
[0042] Embodiment 1: Preparation of hollow silica nanoparticles HNP
[0043] 0.2g cetyltrimethylammonium bromide (CTAB) was dissolved in 96mL H 2 O, add 0.055g perfluorooctanoic acid (PFOA), then add 0.7mL NaOH (2M), and finally add 1mL tetraethyl orthosilicate (TEOS), and stir vigorously at 80°C for 2h. The resulting reaction product was collected by centrifugation, dried at 60°C, and calcined at 550°C for 6h to remove the template.
Embodiment 2
[0044] Example 2: Preparation of photosensitive group functionalized silica nanoparticles HNP-Cou
[0045] Dissolve 1.12g of 1,3-benzenediol (10.18mmol) and 1.11g of ethyl bromoacetoacetate (8.52mmol) in 70% H 2 SO 4 , reacted at room temperature for 8 hours, added 72 mL of water, filtered, and dried in vacuo to obtain the photosensitive group 4-bromomethyl-7-hydroxy-coumarin (Cou).
[0046] Take 200 mg of silicon oxide nanoparticles obtained in Example 1 and dissolve them in 18 mL of absolute ethanol, add 2 mL of water and 300 μL of 3-aminopropyltriethoxysilane (APTES), react at room temperature for 6 hours, add 160 μL of triethylamine, and continue the reaction for 12 hours . The obtained product was centrifuged and washed three times with ethanol, dried in vacuum, and solidified at 130°C for 3 hours to obtain HNP-NH 2 .
[0047] 1 g of succinic anhydride (SA) was dissolved in 10 mL of anhydrous DMF. The above obtained HNP-NH 2 Dissolve 190 mg in 10 mL of anhydrous DMF...
Embodiment 3
[0050] Embodiment 3: the preparation of silica nanoparticle initiator HNP-Cou-Br
[0051] Get the photosensitive group functionalized silicon oxide nanoparticles HNP-Cou100mg and 105mg 2-bromoisobutyric acid (0.63mmol) obtained in Example 2 and dissolve them in 10mL of anhydrous DMF, then add 105mg of potassium carbonate (K 2 CO3 ) (0.63mmol), reacted at 37°C for 24h. The product was centrifuged three times with methanol and water, and dried in vacuum to obtain HNP-Cou-Br.
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