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Multi-stimulus-response cross-linked polymer nano-hydrogel, method for preparing same and application of multi-stimulus-response cross-linked polymer nano-hydrogel

A multi-stimulus-responsive, nano-hydrogel technology, applied in the field of biomedicine, to achieve the effect of clear and concise preparation process, excellent degradable performance, and good comprehensiveness

Active Publication Date: 2017-09-12
HARBIN INST OF TECH WUXI RES INST OF NEW MATERIALS +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0005] However, there is no nano-hydrogel carrier that is responsive to multiple stimuli such as glutathione, pH, and temperature stimulation. This is also an important direction for future research and development.

Method used

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  • Multi-stimulus-response cross-linked polymer nano-hydrogel, method for preparing same and application of multi-stimulus-response cross-linked polymer nano-hydrogel
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  • Multi-stimulus-response cross-linked polymer nano-hydrogel, method for preparing same and application of multi-stimulus-response cross-linked polymer nano-hydrogel

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Embodiment 1

[0028] Add 20g of polyethylene glycol diglycidyl ether (Mn=200) and 6g of anhydrous piperazine to 60ml of ethanol, and reflux for 6 hours under magnetic stirring at 60°C; then add 3.8g of cystamine to the reactant solution and continue to reflux React for 12 hours; after the reaction, precipitate the reaction mixture in methanol, then filter, wash the product three times with methanol, and dry it in vacuum at 50° C. for 24 hours to obtain nano hydrogel particles.

Embodiment 2

[0030] Add 20g of polyethylene glycol diglycidyl ether (Mn=2000) and 0.4g of anhydrous piperazine to 206ml of ethanol, and reflux reaction under magnetic stirring at 80°C for 24 hours; then add 0.19g of cystamine to the reactant solution to continue Reflux reaction for 24 hours; after the reaction, the reaction mixture was precipitated in methanol, then filtered, the product was repeatedly washed with methanol three times, and vacuum-dried at 50° C. for 10 hours to obtain nano hydrogel particles.

Embodiment 3

[0032] Add 20g of polypropylene glycol diglycidyl ether (Mn=200) and 3g of propylamine to 60ml of ethanol, and reflux for 12 hours under magnetic stirring at 70°C; then add 2g of cystamine to the reactant solution and continue to reflux for 18 hours; the reaction is over Finally, the reaction mixture was precipitated in methanol, and then filtered, and the product was repeatedly washed with methanol three times, and dried in vacuum at 30° C. for 24 hours to obtain nano hydrogel particles.

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Abstract

The invention discloses multi-stimulus-response cross-linked polymer nano-hydrogel, a method for preparing the same and application of the multi-stimulus-response cross-linked polymer nano-hydrogel. The size of the multi-stimulus-response cross-linked polymer nano-hydrogel is 50-950 nm, and the poly-dispersity of the multi-stimulus-response cross-linked polymer nano-hydrogel is 0.04-0.16. The multi-stimulus-response cross-linked polymer nano-hydrogel, the method and the application have the advantages that the method for preparing the multi-stimulus-response cross-linked polymer nano-hydrogel is simple, and the multi-stimulus-response cross-linked polymer nano-hydrogel prepared by the aid of the method has response characteristics for glutathione, PH (potential of hydrogen) and thermal stimulus and is excellent in degradability.

Description

technical field [0001] The invention relates to the field of biomedicine, in particular to a multi-stimuli-responsive cross-linked polymer nano hydrogel, its preparation method and application. Background technique [0002] According to a large number of studies, doxorubicin is an effective anticancer drug, which can inhibit the synthesis of RNA and DNA, has the strongest inhibitory effect on RNA, has a wide antitumor spectrum, and can kill tumor cells in various growth cycles. Killing effect. However, the dose to reach the tumor tissue through body fluid circulation after direct injection is very low, and it will bring serious side effects to the human body. There have been many studies in the world to develop target-targeted drug delivery systems (drug delivery systems, DDS) to enhance drug efficacy and reduce side effects. These drug carriers include various forms of nanoparticles, micelles, microcapsules, and nanohydraulic Glue etc. [0003] Among various drug carrier...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C08G65/333C08G65/334A61K9/06A61K9/00A61K31/704A61K47/34
CPCA61K9/0002A61K9/06A61K31/704A61K47/34C08G65/33306C08G65/33317C08G65/3348
Inventor 白永平王利鹏黄磊李卫东席丹殷晓芬
Owner HARBIN INST OF TECH WUXI RES INST OF NEW MATERIALS