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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

Active Publication Date: 2012-04-11
TIANJIN TIANDI CHUANGZHI TECH DEV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Chinese patent 200510110689.4 invented a method of carbon nanotube immobilized protein as a stationary phase filled in a PMMA chip separation channel, based on a microfluidic chip for chiral separation and analysis. This method has a fast separation and analysis speed and is suitable for drug detection and analysis, but Due to the small sample load, it is not suitable for preparative separations with large throughput
Chinese patent 200810113779.2 invented a tandem continuous multi-stage chiral separation device. Firstly, a macromolecular chiral selector (BSA, etc.) Membrane separation, this method overcomes the disadvantages of chiral membrane separation flux and low enantioselectivity, but the device is more complicated, and the separation time is 1-4h
At present, the separation of chiral drug enantiomers by loading functionalized proteins on the surface of superparamagnetic particles and magnetic separation has not been reported.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

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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Abstract

The invention discloses a separation method of a chiral medicament by applying protein functionalized magnetic nano-particles. The method comprises the following steps: (1) modifying the surfaces of superparamagnetic particles by adopting a physical adsorption method; (2) loading protein with chiral identification effect; and (3) mixing protein-modified superparamagnetic nano-particle aqueous solution and a chiral medicament racemic aqueous solution at a volume ratio of 1:1, adsorbing, and performing magnetic separation, wherein the supernatant is liquid containing the separation product of one enantiomer, and the superparamagnetic particle adsorbate is the separation product of the other enantiomer. The method is simple to operate, and has mild condition, short reaction time, and large protein immobilization capacity; the medicament identification capability of the protein is maintained; and the optical purity of the product is remarkably increased.

Description

technical field [0001] The invention belongs to the technical field of medicine, and in particular relates to a method for splitting chiral drugs by using protein functionalized magnetic nanoparticles. Background technique [0002] Enantiomers of chiral drugs often exhibit different physiological behaviors—often one stereoisomer is potent, while its mirror image is either toxic, has the opposite potency, or has no effect at all Pharmacodynamics [J.Chromat.A, 2001, 906, 3-33]. Therefore, the research and development of high-efficiency single-enantiomer chiral compound production technology has become the focus of scientific research and industry. The preparation of single-enantiomer chiral compounds relies on stereoselective synthesis and chiral resolution. Sub technology. At present, the methods for enantiomer resolution of chiral drugs mainly include crystallization, membrane resolution, chromatography, capillary electrophoresis, etc. Chromatography and capillary electro...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07B57/00C12P41/00C12P13/00C07C57/30C07C51/42C07C59/64C07D213/38C07C59/84C07D307/87
Inventor 李韡张金利付雁黄天天李灵均冯子洋刘璐李艳莉
Owner TIANJIN TIANDI CHUANGZHI TECH DEV
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