Preparation method of ready-to-use nanometer targeted drug carrier
A targeted and drug-based technology, applied in the field of nanomaterials, can solve the problems of cumbersome steps, time-consuming, inability to meet the requirements of personalized assembly of nanoparticles and immediate use, and achieve simple synthesis steps, mild conditions, and instant assembly efficiency the effect of the appeal
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Embodiment 1
[0034] Embodiment 1: Through the strong interaction of SA and BT, the method for modifying folic acid molecules on the surface of magnetic nanocrystal clusters
[0035] 0.1g of magnetic nanocrystal clusters (MSP) with carboxyl groups on the surface, 0.1g of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC·HCl) and 0.1g of N-hydroxy Succinimide (NHS) was dispersed in 100 ml of phosphate buffer solution, and 0.2 g of streptavidin was added after activation for two hours. After stirring and reacting for 24 hours, the unreacted SA and small molecule reactants were removed by magnetic separation, and the magnetic separation was repeated 5 times, followed by vacuum drying at 40°C for 2 days to obtain SA surface-modified Magnetic nanocrystal clusters.
[0036] Put 0.1 g of folic acid into water, add 0.05 g of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC·HCl) and 0.05 g of N-hydroxysuccinimide (NHS), at 25 o Activation at C for 2h; then add 0.2g ...
Embodiment 2
[0038] Embodiment 2: Through the strong interaction of SA and BT, the method for modifying FITC molecules on the surface of magnetic nanocrystal clusters
[0039] 0.1g of magnetic nanocrystal clusters (MSP) with carboxyl groups on the surface, 0.1g of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC·HCl) and 0.1g of N-hydroxy Succinimide (NHS) was dispersed in 100 ml of phosphate buffer solution, and 0.2 g of streptavidin was added after activation for two hours. After stirring and reacting for 24 hours, the unreacted SA and small molecule reactants were removed by magnetic separation, and the magnetic separation was repeated 5 times, followed by vacuum drying at 60 °C for 1 day to obtain SA surface-modified Magnetic nanocrystal clusters.
[0040] Put 0.1g FITC into water, then add 0.2g biotin hydrazide, stir and react at 25°C for 24 h, and finally obtain FITC-modified biotin.
[0041] Finally, disperse 0.1 g of SA-grafted magnetic nanocrystal clusters obtained...
Embodiment 3
[0042] Embodiment 3: Through the strong interaction of SA and BT, the method for modifying rhodamine molecules on the surface of magnetic nanocrystal clusters
[0043] 0.1g of magnetic nanocrystal clusters (MSP) with carboxyl groups on the surface, 0.1g of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC·HCl) and 0.1g of N-hydroxy Succinimide (NHS) was dispersed in 100 ml of phosphate buffer solution, and 0.2 g of streptavidin was added after activation for two hours. After stirring and reacting for 24 hours, the unreacted SA and small molecule reactants were removed by magnetic separation, and the magnetic separation was repeated 5 times, and then dried at 50°C for 1.5 days by vacuum drying method to obtain SA surface-modified Magnetic nanocrystal clusters.
[0044] Put 0.1 g of rhodamine into water, add 0.05 g of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC·HCl) and 0.05 g of N-hydroxysuccinyl Amine (NHS), at 35 o C for 10 h, then add 0...
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