Targeting light-operated nitric oxide release nanometer composite material medicine system and preparation method thereof
A nanocomposite material and drug technology, applied in the field of multifunctional nanocomposite drug system and its preparation
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[0096] The present invention also provides a preparation method of the pharmaceutical system of the present invention, which generally includes the following steps:
[0097] (1) Provide exogenous NO donors, targeting groups and carrier nanoparticles;
[0098] (2) Covalently loading the exogenous NO donor, the targeting group and the carrier nanoparticles to form the NO nanocomposite drug system.
[0099] In another preferred example, in step (1), the exogenous NO donor includes a metal nitrosyl compound [(tpy')M(R 1 )(NO)](PF 6 ) 3 , tpy' is 4'-formic acid-2,2':6',2"-terpyridine, M is metal ruthenium (Ru) or metal manganese (Mn), R 1 For DAMBO (boron dipyrrole methyl derivatives) or o-phenylenediamine.
[0100] In another preferred example, the carrier nanoparticles are surface aminated nanoparticles.
[0101] In another preferred example, the targeting group is selected from: folic acid molecule, galactose molecule, biotin, or a combination thereof.
[0102] In another ...
Embodiment 1
[0109] The nitrosyl compound of embodiment 1 metal Ru [(tpy COOH )Ru(DAMBO)(NO)](PF 6 ) 3 Synthesis
[0110] (1)[(tpy COOH )Ru(DAMBO)(Cl)](PF 6 ) synthesis (tpy COOH for 4'-formic acid-2,2':6',2"-terpyridine):
[0111] Add Ru(tpy COOH ) Cl 3 (150mg, 0.31mmol), DAMBO (117mg, 0.33mmol), LiCl (5mg, 2.0mmol) and Et 3 N0.4mL, vacuumize and nitrogen three times respectively, add 40mL of EtOH / H 2 O(3:1, v / v), in N 2 Reflux in the atmosphere for 8 hours, suction filter while hot, and concentrate the dark red filtrate to several milliliters. After cooling to room temperature, add excess saturated NH 4 PF 6 solution, and the mixture was placed in a refrigerator at 5°C overnight. The reddish-brown precipitate was filtered out and washed with H 2 O and Et 2 O were washed three times, respectively, and dried in vacuo. 182.3 mg of the target product was obtained with a yield of 64%.
[0112] (2)[(tpy COOH )Ru(DAMBO)(NO 2 )](PF 6 )Synthesis:
[0113] Will [(tpy COOH )Ru(...
Embodiment 2
[0117] Embodiment 2 nanoparticle composite drug system {Ru-NOTiO 2}Synthesis
[0118] (1) NH 2 TiO 2 (surface aminated TiO 2 Nanoparticles) Preparation
[0119] In a 50mL round bottom flask, add 9.3mg (4-NH 2 )-C 6 h 4 -PO 3 After H, add 2 mL of pH9 aqueous solution, and after the solid dissolves, add 18 mL of TiO 2 The dispersed aqueous solution of the above solution was added to the above solution, and the mixed solution was stirred overnight at room temperature, and the obtained dispersion was centrifuged at 1000 rpm for 10 minutes, the supernatant was removed, and the nanoparticles were washed twice with water to obtain the surface aminated TiO 2 Nanoparticles, redispersed in aqueous solution, ready to use.
[0120] (2) Nanoparticle composite drug system {Ru-NOTiO 2} preparation
[0121] Will [(tpy COOH )Ru(DAMBO)(NO)](PF 6 ) 3 (100mg, 0.08mmol) and FA (folic acid) (5.0mg, 0.01mmol) were dissolved in 5mL of DMF, added EDC / NHS activation for 30 minutes, after ...
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