Unlock instant, AI-driven research and patent intelligence for your innovation.

A kind of method that polypropylene glycol and polytrimethylene carbonate improve the flexibility of polypeptide film

A technology of methyl carbonate and polypropylene glycol, applied in the field of polymer film preparation, achieves the effects of simple operation, improved flexibility and easy to master

Inactive Publication Date: 2016-03-23
SHANDONG UNIV OF TECH
View PDF1 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

So far, no reports have been reported on the improvement of the flexibility of polypeptide membranes with polypropylene glycol and polytrimethylene carbonate.

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

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0017] 1) Synthesis of Polypeptide Homopolymers Containing Terminal-NCO Groups:

[0018] Add 20 grams of poly(γ-benzyl-L-glutamate) with a molecular weight of 60,000, 0.9 grams of 2,4-toluene diisocyanate and 286 mL of 1,2-dichloroethane solvent into the dry reactor, and add Dibutyltin dilaurate with a total weight of 3‰ of the above-mentioned reactants, under an inert atmosphere, stirred and reacted at 40°C for 40 minutes, terminated the reaction, and used dialysis to remove excess diisocyanate to obtain the target product;

[0019] 2) Synthesis of Polypeptide-Polypropylene Glycol Diblock Copolymer:

[0020] Add 15 g of poly(γ-benzyl-L-glutamate) containing terminal -NCO groups, 11.8 g of polypropylene glycol monobutyl ether with a molecular weight of 3000, and 420 mL of 1,2-dichloroethylene in a dry reactor. an alkane solvent, and then add dibutyltin dilaurate with a total weight of 3‰ of the above-mentioned reactants, under an inert atmosphere, stir and react at 40°C for 5...

Embodiment 2

[0025] 1) Synthesis of Polypeptide Homopolymers Containing Terminal-NCO Groups:

[0026] Add 20 grams of poly(γ-ethyl-L-glutamate) with a molecular weight of 70,000, 1.02 grams of 2,4-toluene diisocyanate and 215 mL of 1,1,2-trichloroethane solvent into the dry reactor, and Add dibutyltin dilaurate with a total weight of 4‰ of the above-mentioned reactants, under an inert atmosphere, stir and react at 45°C for 45 minutes, terminate the reaction, and remove excess diisocyanate by dialysis to obtain the target product;

[0027] 2) Synthesis of Polypeptide-Polypropylene Glycol Diblock Copolymer:

[0028] Add 15 g of poly(γ-ethyl-L-glutamate) containing terminal -NCO groups, 17.1 g of polypropylene glycol monobutyl ether with a molecular weight of 4000, and 410 mL of 1,1,2-trichloro Ethane solvent, and then add dibutyltin dilaurate with a total weight of 4‰ of the above-mentioned reactants, under an inert atmosphere, stir and react at 45°C for 55 minutes, terminate the reaction, ...

Embodiment 3

[0033] 1) Synthesis of Polypeptide Homopolymers Containing Terminal-NCO Groups:

[0034] Add 20 grams of poly(γ-methyl-L-glutamate) with a molecular weight of 80,000, 0.96 grams of 2,4-toluene diisocyanate and 155 mL of 1,2-dichloroethane solvent into the dry reactor, and add the above Dibutyltin dilaurate with a total weight of 5‰ of reactants, under an inert atmosphere, stirred and reacted at 50°C for 50 minutes, terminated the reaction, and used dialysis to remove excess diisocyanate to obtain the target product;

[0035] 2) Synthesis of Polypeptide-Polypropylene Glycol Diblock Copolymer:

[0036] Add 15 g of poly(γ-methyl-L-glutamate) containing terminal -NCO groups, 20.1 g of polypropylene glycol monobutyl ether with a molecular weight of 5000, and 352 mL of 1,2-dichloroethane into a dry reactor Solvent, then add dibutyltin dilaurate with a total weight of 5‰ of the above-mentioned reactants, under an inert atmosphere, stir and react at 50°C for 60 minutes, terminate the...

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 improving the flexibility of a polypeptide film with polypropylene glycol and polytrimethylene carbonate. After stirring and reacting at 50°C for 40 to 50 minutes, a homopolymer of polypeptide containing NCO groups was obtained; Polypropylene glycol monobutyl ether, stirred and reacted at 40-50°C for 50-60 minutes to obtain a polypeptide-polypropylene glycol diblock copolymer; Trimethylene carbonate and a solvent are stirred and mixed at 40-50° C. for 60-70 minutes, and then cast into a film and dried to obtain the object of the present invention. The preparation process of the invention is simple, and the flexibility of the obtained modified membrane is greatly improved.

Description

technical field [0001] The invention relates to a method for improving the flexibility of a polypeptide film, belonging to the technical field of polymer film preparation. Background technique [0002] Polypeptide is a biomaterial with good biocompatibility and biodegradability. Polypeptide film can be used as artificial skin, etc., but the polypeptide is relatively stiff and lacks good flexibility, so to a certain extent limits its application. Polypropylene glycol and polytrimethylene carbonate have better biocompatibility and biodegradability, are relatively soft and have better blendability with each other. First, the polypropylene glycol segment is introduced into the polypeptide segment to form a polypeptide-polypropylene glycol diblock copolymer to improve the blendability of the polypeptide, and then the polytrimethylene carbonate segment is added to the polypeptide-polypropylene glycol diblock copolymer. The block copolymer forms a blend to prepare a modified poly...

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): C08L87/00C08L69/00C08G81/00C08J5/18
Inventor 朱国全王发刚柳玉英
Owner SHANDONG UNIV OF TECH