Hydrogel controlled by double switch of hydrogen bond and π-π stacking and its preparation and application

A hydrogel, π stacking technology, applied in the field of drug controlled release system research, can solve the problem of inability to match drug metabolism

Active Publication Date: 2011-12-14
江苏先进无机材料研究院
View PDF0 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the current synthetic drug controlled release system cannot match the drug release with the metabolism of the human metabolic system.

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
  • Hydrogel controlled by double switch of hydrogen bond and π-π stacking and its preparation and application
  • Hydrogel controlled by double switch of hydrogen bond and π-π stacking and its preparation and application
  • Hydrogel controlled by double switch of hydrogen bond and π-π stacking and its preparation and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0023] 1. Preparation of functional monomers

[0024] (1) p-nitrophenol methacrylate

[0025] Dissolve methacryloyl chloride, p-nitrophenol and triethanolamine (1:1:1 molar ratio) in chloroform, stir and react for 5-60 hours at a low temperature of -10-5°C (such as an ice-water bath), and wash with saturated NH 4 Cl ends the reaction, and the reaction product is recrystallized from ethanol to obtain white crystals. The resulting product is dried below 100°C for future use.

[0026] (2) p-nitrophenol acrylate

[0027] Dissolve acryloyl chloride, p-nitrophenol and triethanolamine (1:1:1 molar ratio) in chloroform, stir and react at a low temperature of -10 to 5°C (such as an ice-water bath) for 5 to 60 hours, and wash with saturated NH 4 Cl ends the reaction, and the reaction product is recrystallized from ethanol to obtain white crystals. The resulting product is dried below 100°C for future use.

[0028] The proton magnetic resonance spectrum of the product that the synth...

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 relates to a PMAA and PAA-based hydrogel, which has an ordered lamellar structure and is made of aryl monomers with π-π stacking effect and carboxyl monomers with hydrogen bond effect. The hydrogel of the present invention controls the drug release system through hydrogen bonds and π-π stacking dual switches to realize continuous regulation of drug release; gel swelling performance test shows that the hydrogel of the present invention has excellent pH responsiveness; The drug release experiment simulating the human metabolic system shows that the drug controlled release system prepared by the hydrogel of the present invention can match the drug release with the metabolism of the human metabolic system, effectively reducing the waste of drugs and the side effects of excessive drugs on the human body .

Description

technical field [0001] The invention relates to the research field of drug controlled release systems, in particular to hydrogel materials, and more specifically to hydrogels controlled by double switches of hydrogen bonds and π-π stacking, and their preparation and application. Background technique [0002] Controlled-release local drug delivery and targeted drug delivery technology can solve the problems of sudden release, short drug release time, cytotoxicity and non-selective release of drugs in traditional drug delivery methods, and has become an important development of drug therapy. one of the directions. Polymer hydrogels with environmental responsive properties are a hotspot in the field of controlled drug release. [0003] Both polyacrylic acid (PAA) and polymethacrylic acid (PMAA) hydrogels are important pH-responsive hydrogels due to their good physicochemical stability, controllable mechanical Due to the sharp phase transition phenomenon, it is widely used as ...

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): A61K47/32A61K9/00A61K31/192A61P29/00
Inventor 祝迎春李芳
Owner 江苏先进无机材料研究院
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