Reduction responsiveness nanoscale graphene oxide coated medicine carrying mesoporous silicon dioxide nano particle and preparation method thereof
A technology of mesoporous silica and nano-graphite oxide, which can be used in pharmaceutical formulations, drug combinations, anti-tumor drugs, etc., can solve problems such as the preparation of reduction-responsive drug controlled release systems, and achieve rapid reduction-responsive release, The effect of strong biocompatibility and simple operation
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[0035] The preparation method of the reduction-responsive nano-graphene oxide-coated drug-loaded mesoporous silica nanoparticles comprises the following steps:
[0036] A. Reacting mesoporous silica capable of loading drugs with a silane coupling agent, and grafting amino groups on its surface to prepare aminated mesoporous silica;
[0037] B. reacting the aminated mesoporous silica obtained in step A with a compound containing disulfide bonds, amino groups and carboxyl groups at the same time, and grafting disulfide bonds on the surface to prepare mesoporous silica containing disulfide bonds;
[0038] C. The mesoporous silica containing disulfide bonds obtained in step B is physically impregnated to form drug-loaded mesoporous silica;
[0039] D. The amino group on the drug-loaded mesoporous silica obtained in step C is amide-reacted with the carboxyl group on the surface of nano-graphene oxide to obtain reduction-responsive nano-graphene oxide-coated drug-loaded mesoporous s...
Embodiment 1
[0041] a. Ultrasonic disperse 0.1 g of mesoporous silica nanoparticles (MSNs) with a particle size of 100 nm and a mesoporous diameter of 3 nm into 10 ml of distilled water, then add 100 μl of acetic acid and 25 μl of γ-aminopropyl triethoxy base silane, stirred at room temperature for 24 hours, centrifuged and washed to obtain aminated mesoporous silica nanoparticles (MSNs-NH 2 );
[0042] b. Disperse 0.01 g of oxidized glutathione in 10 ml of PBS buffer solution (pH=5.0), then add 50 mg of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide Aqueous solution of hydrochloride, stirred at room temperature for 1 hour so as to activate the carboxyl group on the oxidized glutathione; 0.04g MSNs-NH 2 Added into the above solution, stirred at room temperature for 24 hours, centrifuged and washed to obtain mesoporous silica nanoparticles containing disulfide bonds (MSNs-SS-NH 2 );
[0043] c. Diffusion of camptothecin molecules into MSNs-SS-NH by a simple physical impregnation method 2...
Embodiment 2
[0046] a. Ultrasonic disperse 0.1 g of mesoporous silica nanoparticles (MSNs) with a particle size of 150 nm and a mesoporous diameter of 5 nm into 10 ml of distilled water, then add 100 μl of acetic acid and 25 μl of γ-aminopropyltrimethoxy Silane, stirred at room temperature for 24 hours, centrifuged and washed to obtain aminated mesoporous silica nanoparticles (MSNs-NH 2 );
[0047] b. disperse 0.01g of cystine in 10ml of PBS buffer solution (pH=5.0), then add 50mg of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride Aqueous solution, stirred at room temperature for 1 hour in order to activate the carboxyl group on cystine; 0.04g MSNs-NH 2 Added into the above solution, stirred at room temperature for 24 hours, centrifuged and washed to obtain mesoporous silica nanoparticles containing disulfide bonds (MSNs-SS-NH 2 );
[0048] c. Diffusion of doxorubicin molecules into MSNs-SS-NH by a simple physical impregnation method 2 mesoporous channels; then MSNs-SS-NH ...
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