Separation method of chiral medicament by applying protein functionalized magnetic nano-particles
A technology of magnetic nanoparticles and protein functions, which is applied in the field of medicine, can solve the problems of fast separation and analysis, unsuitable preparation separation, small sample loading, etc., and achieve the effects of short reaction time, improved optical purity of products, and easy operation
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Embodiment 1
[0036] A method for splitting chiral drugs using protein functionalized magnetic nanoparticles, comprising the steps of:
[0037] (1) The surface of superparamagnetic particles is modified by physical adsorption method:
[0038] Mix an aqueous solution of superparamagnetic particles with a mass concentration of 2g / L and an aqueous solution of polydiallyldimethylammonium chloride with a mass concentration of 0.1g / L in equal volumes, and adsorb for 25 minutes at 25°C to obtain surface modification The superparamagnetic particle; The superparamagnetic particle is Fe with an average particle diameter of 15nm and a saturation magnetization of 70emu / g 3 o 4 ;
[0039] (2) Loading proteins with chiral recognition:
[0040]Mixing the surface-modified superparamagnetic particle aqueous solution with a mass concentration of 5 g / L and the bovine serum albumin aqueous solution with a concentration of 1 g / L in equal volumes, and adsorbing for 3 hours to obtain protein-modified magnetic ...
Embodiment 2
[0044] A method for splitting chiral drugs using protein functionalized magnetic nanoparticles, comprising the steps of:
[0045] (1) The surface of superparamagnetic particles is modified by physical adsorption method:
[0046] Mix an aqueous solution of superparamagnetic particles with a mass concentration of 4g / L and an aqueous solution of polyethyleneimine with a mass concentration of 0.02g / L in equal volumes, and adsorb for 20 minutes at 30°C to obtain surface-modified superparamagnetic particles; The superparamagnetic particles are γ-Fe with an average particle diameter of 10nm and a saturation magnetization of 80emu / g. 2 o 3 ;
[0047] (2) Loading proteins with chiral recognition:
[0048] mixing the surface-modified superparamagnetic particle aqueous solution with a mass concentration of 2 g / L and the human serum albumin aqueous solution with a concentration of 0.8 g / L in equal volumes, and adsorbing for 2 hours to obtain protein-modified magnetic nanoparticles;
...
Embodiment 3
[0052] A method for splitting chiral drugs using protein functionalized magnetic nanoparticles, comprising the steps of:
[0053] (1) The surface of superparamagnetic particles is modified by physical adsorption method:
[0054] Mix an aqueous solution of superparamagnetic particles with a mass concentration of 6 g / L and an aqueous solution of polyallylamine with a mass concentration of 1 g / L in equal volumes, and adsorb for 30 minutes at 45° C. to obtain surface-modified superparamagnetic particles; the superparamagnetic particles The paramagnetic particles are CoFe with an average particle size of 20nm and a saturation magnetization of 50emu / g 2 o 4 ;
[0055] (2) Loading proteins with chiral recognition:
[0056] mixing the surface-modified superparamagnetic particle aqueous solution with a mass concentration of 7 g / L and the ovomucoid aqueous solution with a concentration of 5 g / L in equal volumes, and adsorbing for 3 hours to obtain protein-modified magnetic nanopartic...
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