Method for preparing glycoprotein imprinting fluorescent nanoparticles based on macromolecule self-assembling

A technology of fluorescent nanometer and glycoprotein, which is applied in the direction of fluorescence/phosphorescence, analytical materials, measuring devices, etc., can solve the problems of poor selectivity and achieve good selectivity, fast adsorption speed, and environmental friendliness

Active Publication Date: 2018-04-06
郎溪品旭科技发展有限公司
View PDF3 Cites 6 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the molecularly imprinted polymers prepared by these methods are only suitable for organic solvent systems. In aqueous systems, due to the influence of water polarity, the selectivity is poor, and the detect

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Method for preparing glycoprotein imprinting fluorescent nanoparticles based on macromolecule self-assembling

Examples

Experimental program
Comparison scheme
Effect test

Example Embodiment

[0019] Example 1

[0020] The first step: the monomer acrylic acid (0.3603g, 5mmol), vinyl carbazole (0.9663g, 5mmol), vinylbenzene boronic acid (0.0015g, 0.01mmol) azobisisobutyl cyanide (0.0328g, 2% mt %) into a 50ml round-bottomed flask, add 15mL solvent N,N-dimethylformamide (DMF), pass N 2 After removing the oxygen in the solution for 20 minutes, under stirring, the temperature was kept at 80°C and reacted in an oil bath for 24 hours. The monomers ethylene glycol methacrylate (0.711g, 5mmol) and triphenylphosphine (0.0262g, 0.1mmol) and hydroquinone (0.0028g, 0.025mmol) were dissolved in 5mL DMF and added dropwise to the above polymer solution through a constant pressure dropping funnel. Under stirring, the temperature was kept at 95℃. React in a bath for 12 hours, precipitate with petroleum ether three times, and dry overnight at 40°C in a vacuum oven to obtain a photocrosslinkable amphiphilic random copolymer containing phenylboronic acid;

[0021] Step 2: Dissolve 10mg of...

Example Embodiment

[0023] Example 2

[0024] The first step: the monomer acrylic acid (0.3603g, 5mmol), vinyl carbazole (0.9663g, 5mmol), vinylbenzene boronic acid (0.0015g, 0.01mmol) azobisisobutyl cyanide (0.0328g, 2% mt %) into a 50ml round-bottomed flask, add 15mL solvent N,N-dimethylformamide (DMF), pass N 2 After removing the oxygen in the solution for 20 minutes, under stirring, the temperature was kept at 80 ℃ and reacted in an oil bath for 24 hours. The monomer ethylene glycol methacrylate (0.355g, 2.5mmol), triphenylphosphine (0.0262g) , 0.1mmol) and hydroquinone (0.0028g, 0.025mmol) were dissolved in 5mL DMF, and added dropwise to the above polymer solution through a constant pressure dropping funnel. Under stirring, the temperature was kept at 95℃. React in an oil bath for 12 hours, precipitate with petroleum ether three times, and dry overnight at 40°C in a vacuum oven to obtain a photocrosslinkable amphiphilic random copolymer containing phenylboronic acid;

[0025] Step 2: Dissolve 1...

Example Embodiment

[0027] Example 3

[0028] The first step: the monomer acrylic acid (0.3603g, 5mmol), vinyl carbazole (0.9663g, 5mmol), vinylbenzene boronic acid (0.0015g, 0.01mmol) azobisisobutyl cyanide (0.0328g, 2% mt %) into a 50ml round-bottomed flask, add 15mL solvent N,N-dimethylformamide (DMF), pass N 2 After removing the oxygen in the solution for 20 minutes, under stirring, the temperature was kept at 80°C and reacted in an oil bath for 24 hours. The monomers ethylene glycol methacrylate (0.711g, 5mmol) and triphenylphosphine (0.0262g, 0.1mmol) and hydroquinone (0.0028g, 0.025mmol) were dissolved in 5mL DMF and added dropwise to the above polymer solution through a constant pressure dropping funnel. Under stirring, the temperature was kept at 95℃. React in a bath for 12 hours, precipitate with petroleum ether three times, and dry overnight at 40°C in a vacuum oven to obtain a photocrosslinkable amphiphilic random copolymer containing phenylboronic acid;

[0029] Step 2: Dissolve 8mg of ...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention discloses a method for preparing glycoprotein imprinting fluorescent nanoparticles based on macromolecule self-assembling, relating to the scientific and technical fields of high molecular material science, life health, self-assembling and the like. According to the method, photo-cross-linkable vinyl carbazole containing fluorescent units, hydrophilic monomers and a random amphophilic copolymer containing abornic acid identification unit are firstly prepared and are co-assembled with a photoinitiator and a cross-linking agent under the induction of water so as to form nanoparticles, glycoprotein is packaged in the nanoparticles through the covalent binding with boric acid in an assembling process, the structure of the glycoprotein is stabilized by virtue of a photo-crosslinking technique, the pH value is adjusted, the glycoprotein is eluted, and then the prepared nanoparticles can be used for specifically reconogizing and detecting glycoprotein in a water phase. By integrating the advantages that a nano-material is large in specific surface area, a molecular imprinting material is good in selectivity, the sensitivities of the boric acid-glycoprotein covalent binding and a fluorescence detection technique are high, and the prepared nanoparticles can be applied to high-selectivity and high-sensitivity rapid detection of low-abundance glycoprotein in an actual sampleand particularly have important significance to the trace detection of the glycoprotein in clinical diagnosis and curative effect evaluation.

Description

technical field [0001] The present invention relates to scientific and technological fields such as polymer material science, life and health, and self-assembly, and in particular to a method for preparing glycoprotein imprinted fluorescent nanoparticles based on macromolecular self-assembly Background technique [0002] Glycoproteins are macromolecules formed by the covalent bonding of peptide chains and sugar chains. They are widely present in living organisms and have a variety of biological activities. The well-documented functions include lubrication, transportation, recognition, and protection. Glycoprotein is related to the occurrence and development of many diseases such as infection, tumor, cardiovascular disease, liver disease, kidney disease, diabetes and some genetic diseases. Glycoproteins and sugar esters on the cell surface can "shed" into the surrounding environment or enter the blood circulation, and their detection can provide information for clinical diagn...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
IPC IPC(8): C08F285/00C08F212/36C08F271/02C08F222/14C08F220/06C08F226/12C08F230/06C08F2/48G01N21/64
CPCC08F2/48C08F220/06C08F226/12C08F265/02C08F271/02C08F285/00G01N21/6428G01N21/6486G01N2021/6432C08F212/36C08F230/06C08F222/102
Inventor 罗静黄婧许升刘晓亚
Owner 郎溪品旭科技发展有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products