Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Cationic brush block copolymer and preparation method as well as application thereof

A block copolymer, cationic technology, applied in the field of its preparation, cationic brush-shaped block copolymer, can solve the problem of increasing the toxicity of the carrier, achieve good application value, prolong the cycle time, and improve the effect of distribution

Inactive Publication Date: 2014-09-17
SUZHOU UNIV
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the electrostatic interaction between the cationic carrier and DNA limits the dissociation and release of the gene after entering the nucleus, and excessive positive charges will increase the toxicity of the carrier

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
  • Cationic brush block copolymer and preparation method as well as application thereof
  • Cationic brush block copolymer and preparation method as well as application thereof
  • Cationic brush block copolymer and preparation method as well as application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0042] Embodiment one: ATRP macromolecular initiator polyhydroxyethyl methacrylate PHEMA 33 Synthesis of -Cl

[0043] Put the branch tube round bottom flask in an oven at 120 ℃ to dry, then plug it with a ground glass stopper, pump it to cool until it reaches room temperature, fill it with argon after three times of filling and degassing. The monomer hydroxyethyl methacrylate (HEMA) (4.1 g, 31.50 mmol) was dissolved in methanol (10 mL) and added to the vial, and the small molecule initiator methyl α-bromopropionate (119 mu L, 1.05 mmol), ligand 2,2′-bipyridine (328.0 mg, 2.1 mmol), cuprous chloride (104.0 mg, 1.05 mmol) with a purity of 99.99% were added to the above mixed system, and argon was introduced Protect. Raise the temperature to 30°C, and maintain this temperature, stir with magnetic force, and react for 10-12 hours.

[0044] Methanol was added to dilute the reaction product, and it was contacted with air while stirring to terminate the reaction. After the solut...

Embodiment 2

[0046] Example 2: Diblock copolymer PHEMA with side groups containing hydroxyl groups 33 - b -PDMAEMA 66 Synthesis

[0047] Put the branch tube round bottom flask in an oven at 120 ℃ to dry, then plug it with a ground glass stopper, pump it to cool down until it reaches room temperature, fill and discharge the argon gas three times, and then continue to fill the glass bottle with argon gas. The macroinitiator PHEMA that embodiment one prepares 33 -Cl (2.2 g, 0.5 mmol) dissolved in methanol (15 mL) was added to the vial, the ligand 2,2′-bipyridine (156.2 mg, 1.0 mmol), the monomer methacrylic acid-2-(dimethyl Amino)ethyl ester (DMAEMA) (4.6 g, 30 mmol) and cuprous chloride (49.5 mg, 0.5 mmol) with a purity of 99.99% were added to the above mixed system, and argon protection was introduced. Raise the temperature to 35°C, and maintain this temperature, stir with magnetic force, and react for 24-28 hours.

[0048] Methanol was added to dilute the reaction product, and it was ...

Embodiment 3

[0050] Example 3: Diblock copolymer PHEMA with side groups containing hydroxyl groups 33 - b -PDMAEMA 50 Synthesis

[0051] Put the branch tube round bottom flask in an oven at 120 ℃ to dry, then plug it with a ground glass stopper, pump it to cool down until it reaches room temperature, fill and discharge the argon gas three times, and then continue to fill the glass bottle with argon gas. The macroinitiator PHEMA that embodiment one prepares 33-Cl (2.2 g, 0.5 mmol) dissolved in methanol (15 mL) was added to the vial, the ligand 2,2′-bipyridine (156.2 mg, 1.0 mmol), the monomer methacrylic acid-2-(dimethyl Amino)ethyl ester (DMAEMA) (3.8 g, 25 mmol) and cuprous chloride (CuCl, 49.5 mg, 0.5 mmol) with a purity of 99.99% were added to the above mixed system, and argon gas protection was introduced. Raise the temperature to 35°C, and maintain this temperature, stir with magnetic force, and react for 24-28 hours.

[0052] Methanol was added to dilute the reaction product, an...

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 present invention disclosed a cationic brushing sync, its preparation methods and applications.For the first time, the present invention combines the atomic metastasis free radical aggregation (ATRP) and the opening polymerization (ROP) to prepare the cost -type brushing embedded cluster with the side chain containing biochemolytic polyphothexate.Methaline hydroxyl ethyl athylene performed ATRP polymerization reactions to obtain macromolecules with bromine or chlorine substituent at the end.Paragraph cluster; then use the hydroxyl groups of the two -in -segment cluster side to perform open -ring clusters on the ring -shaped phosphate monomer to obtain a cationic brushing embedded segment of the side chain.The new type of side chain developed by the present invention has good biocompatibility, biodegradability, and low toxicity for polycopic acid brushing embedded segments containing polyphothexide. It can be used as a genetic carrier. It has good application prospects in biomedicineEssence

Description

technical field [0001] The invention belongs to the field of biomedical polymer materials, and in particular relates to a cationic brush-shaped block copolymer, its preparation method and its application as a gene carrier. Background technique [0002] Today, genomics has made breakthroughs in the treatment of congenital and acquired diseases, and gene therapy has become one of the most active research fields. Gene therapy refers to the introduction of human normal genes or therapeutic genes into human target cells in a certain way to correct gene defects or exert therapeutic effects, so as to achieve the purpose of treating diseases. Constructing a vector with good biocompatibility, biodegradability, high safety, high transfection efficiency and high expression level, so that the target gene can be expressed in target cells in a safe, controllable, efficient and stable way is the research of gene therapy. an important direction. [0003] Gene carriers currently used for g...

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
Patent Type & Authority Patents(China)
IPC IPC(8): C08F293/00C08F220/28C08F220/34C08F8/40C08F6/10C08F6/12C12N15/87
Inventor 倪沛红郝莹何金林张明祖刘坚张洋
Owner SUZHOU UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com