Carrier with active oxygen response, preparation method thereof and composite material
A composite material, active oxygen technology, applied in the direction of organic active ingredients, medical preparations with non-active ingredients, medical preparations containing active ingredients, etc. application and other issues, to achieve the effect of good medical prospects, low cost, and high efficiency of ROS
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preparation example Construction
[0042] The second aspect of the embodiment of the present application provides a method for preparing the above carrier, including the following steps:
[0043] S01: Provide mesoporous silica nanoparticles;
[0044] S02: mixing the mesoporous silica nanoparticles with the above-mentioned fluorescein to avoid light for labeling reaction to obtain fluorescein-labeled mesoporous silica nanoparticles;
[0045] S03: Mix the fluorescein-labeled mesoporous silica nanoparticles with the above-mentioned silane phenylene sulfide molecules to carry out a catalytic reaction to obtain a carrier.
[0046] The preparation method of the active oxygen-responsive carrier provided by this application is obtained by labeling mesoporous silica nanoparticles with fluorescein and silane phenylene sulfide molecules in sequence, so that the carrier is in the mesoporous silica nanoparticles Based on the combination of fluorescein and silane phenylene sulfide molecules, the preparation method has simpl...
Embodiment 1
[0058] Example 1 Carrier Construction with Active Oxygen Response
[0059] 1. Synthesis of Benzenethiol-3-Isocyanatopropyltriethoxysilane (PhSAPTES);
[0060] With 2mmol of (phenylthio) acetic acid [(Phenylthio) acetic acid], 2.2mmol of 11-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDCI) and 2mmol of N -Hydroxysuccinimide (NHS) was dissolved in 20ml of chloroform by means of ultrasonic assistance; then 2.46mmol of 3-aminopropyltriethoxysilane (APTES) (800μL) was added to the reaction system, and in React at room temperature for 24 hours. After the reaction, the obtained clear light yellow solution was concentrated to 4ml and separated by silica gel column chromatography, the mobile phase was petroleum ether: ethyl acetate = 3:2, and finally the solvent was removed by rotary evaporation to obtain a light yellow liquid The final product, namely silane phenylene sulfide with the following chemical structure, has a yield of about 68%.
[0061]
[0062] 2. Syn...
Embodiment 2
[0075] Carrying band and release of embodiment 2 procyanidins (PC)
[0076] 1. Carrier tape of procyanidin (PC)
[0077] Take 6mL of ultrapure water in a 15mL small centrifuge tube, add 4mL of methanol, and mix evenly; weigh 15mg of procyanidin (PC) in a 15mL small centrifuge tube, add 6mL of methanol-water mixed solution for ultrasonic dissolution; take 50mg of Example 1 The prepared carrier (fmMSNs-phs) was placed in a 15mL small centrifuge tube, and the supernatant was discarded by centrifugation. The obtained particles were washed once with ultrapure water, and the supernatant was discarded by centrifugation; 6 mL of 2.5 mg / mL PC was added to the obtained particles methanol aqueous solution, ultrasonically dissolved and then sonicated for 2min; the mixed solution was rotated and mixed on a rotary mixer for 24h, sealed and protected from light; after mixing, the resulting solution was centrifuged, and the supernatant and particles were separated to obtain the composite mate...
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