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Method for preparing chitosan immobilized cyclodextrin derivative from chitin

A technology of cyclodextrin and derivatives, applied in the field of polymer material preparation, can solve the problems of limited application, increase of by-products, complicated immobilization reaction, etc.

Inactive Publication Date: 2012-09-26
BEIJING INSTITUTE OF TECHNOLOGYGY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

On the one hand, the above-mentioned reaction steps make the immobilization reaction complicated, the by-products increase, and the yield decreases; Water solubility and application effect have great limitations
The above problems also further limit the application of chitosan 6-OH positioning immobilized cyclodextrin derivatives

Method used

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  • Method for preparing chitosan immobilized cyclodextrin derivative from chitin

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0066] Weigh 1 part of chitin, under nitrogen protection, add 40 parts of DMAc and 3 parts of LiCl at the same time, stir at 40°C for 30 minutes to fully swell the chitin. Afterwards, the temperature of the reaction system was lowered to 0°C under the reaction conditions, 15 parts of NaOH was added, and then 5 parts of p-toluenesulfonyl chloride was dissolved in 40 parts of chloroform, and slowly added into the chitin solution within 20 minutes using a dropping funnel. React for 10 hours. After the reaction, add ethanol to precipitate, filter with suction, wash off unreacted p-toluenesulfonyl chloride with chloroform, and dry under vacuum at 60°C to obtain chitin derivative a.

[0067] Weigh 1 part of chitin derivative a and dissolve it in 20 parts of DMAc, stir at 30°C to dissolve it. After adding 2 parts of sodium azide, the reaction was stirred at 60° C. for 10 hours. After the reaction, use ethanol to precipitate, wash the precipitate with water, and finally wash with DMA...

Embodiment 2

[0073] Chitin-loaded cyclodextrin derivative e was prepared by the click chemical reaction of chitin derivative b and β-cyclodextrin derivative d prepared in Example 1:

[0074] Weigh 1 part of chitin derivative b, disperse and swell in 12 parts of DMAc, and weigh another 0.03 part of CuSO 4 ·5H 2 O was dispersed in 6 parts of organic solvent, adding 0.03 part of sodium ascorbate and 0.08 part of water to promote dissolution, and mixed the solution; weighed 3.5 parts of β-cyclodextrin derivative d, added the above solution, and stirred at 40°C for reaction After 6 hours, stop the reaction, add precipitant acetonitrile, wash 4 times with DMF, vacuum dry the filter cake at 60°C to obtain chitin-immobilized cyclodextrin derivative e.

[0075] Soak 1 part of the obtained chitin-supported cyclodextrin derivative e in 20 parts of an aqueous solution of NaOH with a mass concentration of 20%, stir and react by heating at 80°C for 20 hours, filter, wash twice with DMF, and place in V...

Embodiment 3

[0077]Weigh 1 part of chitin, add 40 parts of hexafluoroisopropanol at the same time, stir at 40°C for 30 minutes to fully swell the chitin. Then cool down the reaction system to -10°C under the reaction conditions, add 30 parts of triethylamine, then dissolve 4 parts of p-toluenesulfonyl chloride in 40 parts of chloroform, and slowly add chitin in 15 minutes with a dropping funnel The solution was reacted for 10 hours. After the reaction was completed, tetrahydrofuran was added, filtered with suction, unreacted p-toluenesulfonyl chloride was washed away with chloroform, and the chitin derivative a was obtained by vacuum drying at 60°C.

[0078] Weigh 1 part of chitin derivative a and dissolve it in 25 parts of hexafluoroisopropanol, stir at 30°C to dissolve it. After adding 2.8 parts of sodium azide, the reaction was stirred at 60° C. for 12 hours. After the reaction is finished, use acetone to precipitate, wash the precipitate with water, and finally wash with hexafluoroiso...

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Abstract

The invention which relates to a method for preparing a chitosan immobilized cyclodextrin derivative from chitin belongs to the technical field of the preparation of high molecular materials. The method is characterized in that: an acetamido group in the chitin molecule is treated as an amino protective group, 6-OH on chitin is subjected to tosylation substitution, a click chemical reaction process is adopted to prepare the positioning immobilized cyclodextrin derivative, and chitin is subjected to deacetylation under alkali conditions to form the 6-OH high efficiency positioning immobilized cyclodextrin chitosan derivative. The method of the invention allows the positioning immobilization efficiency of cyclodextrin on the 6-OH of chitosan to be improved, the cyclodextrin immobilization efficiency of the obtained product to reach above 195mumol.g<-1>, the deacetylation degree of the prepared product to reach 95%, and the product to have good water solubility.

Description

technical field [0001] The invention relates to a method for preparing chitosan immobilized cyclodextrin derivatives by utilizing chitin, and belongs to the technical field of polymer material preparation. Background technique [0002] Chitosan has 2-NH on the pyran ring 2 With its unique structure, good modifiability and physiological activity, it is a hotspot in the research of new functional polymer materials. Cyclodextrin has a unique internal hydrophobic and external hydrophilic cavity structure. It is a kind of macrocyclic main compound that has been studied more in supramolecular chemistry. , supramolecular construction and so on played a great role. The immobilization of cyclodextrin on the chitosan molecular chain can effectively combine the excellent properties of the two, and prepare a biomacromolecule-based supramolecular host material with excellent performance. At present, there are many reports on the construction of supramolecular bodies by chitosan-immobi...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C08G81/00C08B37/08C08B37/16
Inventor 陈煜郭燕文叶彦春
Owner BEIJING INSTITUTE OF TECHNOLOGYGY