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

Preparation method of in-situ cross-linked collagen fiber

A collagen fiber and in-situ cross-linking technology, which is applied in the fields of fiber chemical characteristics, single-component protein rayon, textiles and papermaking, can solve the problems of long cross-linking time, improve mechanical strength, improve forming process conditions, The effect of shortening the time

Inactive Publication Date: 2019-02-26
TIANJIN POLYTECHNIC UNIV
View PDF0 Cites 7 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, if the collagen fibers cross-linked in the cross-linking bath want to achieve a higher degree of cross-linking, a longer cross-linking time is usually required to fully carry out the cross-linking reaction, which has certain limitations in industrial production and application.

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

[0022] EDC is mixed with NHS (EDC quality is 15% of collagen protein quality) by mass ratio 3: 1, is dissolved in 20ml, 0.5mol / L glacial acetic acid as cross-linking agent and forms the glacial acetic acid solution that contains cross-linking agent; 0.45g of collagen (collagen is bovine tendon type I collagen, its molecular weight is 300kDa, its ultraviolet absorption peak is 220-240nm, and its hydroxyproline content is not less than 9%) is dissolved in the above-mentioned glacial acetic acid solution containing cross-linking agent , use mechanical stirring to fully stir for 10 hours, the temperature of the solution during the dissolution process is between 4-6 ° C, and a collagen solution with a mass concentration of 1.5% is prepared; the collagen solution is refrigerated and centrifuged at 4 ° C for 40 minutes to obtain a collagen spinning stock solution; Wet spinning is adopted, the extrusion speed of the syringe pump is 0.5ml / min, the residence time of the primary fiber in ...

Embodiment 2

[0024] EDC is mixed with NHS (EDC quality is 15% of collagen protein quality) by mass ratio 3: 1, is dissolved in 20ml, 0.5mol / L glacial acetic acid as cross-linking agent and forms the glacial acetic acid solution that contains cross-linking agent; 0.45g of collagen (collagen is bovine tendon type I collagen, its molecular weight is 300kDa, its ultraviolet absorption peak is 220-240nm, and its hydroxyproline content is not less than 9%) is dissolved in the above-mentioned glacial acetic acid solution containing cross-linking agent , fully stirred by mechanical stirring for 11 hours, the temperature of the solution during the dissolution process was between 4-6°C, and a type I collagen solution with a mass concentration of 1.5% was prepared; the collagen solution was refrigerated and centrifuged at 4°C for 40 minutes to obtain collagen spinning Stock solution: Wet spinning is adopted, the extrusion speed of the syringe pump is 0.5ml / min, the residence time of the primary fiber ...

Embodiment 3

[0026] EDC is mixed with NHS (EDC quality is 15% of collagen protein quality) by mass ratio 3: 1, is dissolved in 20ml, 0.5mol / L glacial acetic acid as cross-linking agent and forms the glacial acetic acid solution that contains cross-linking agent; 0.45g of collagen (collagen is bovine tendon type I collagen, its molecular weight is 300kDa, its ultraviolet absorption peak is 220-240nm, and its hydroxyproline content is not less than 9%) is dissolved in the above-mentioned glacial acetic acid solution containing cross-linking agent , use mechanical stirring to fully stir for 12 hours, and the temperature of the solution during the dissolution process is between 4-6°C to prepare a collagen solution with a mass concentration of 1.5%; freeze and centrifuge the collagen solution at 4°C for 40 minutes to obtain a collagen spinning stock solution; Wet spinning is adopted, the extrusion speed of the syringe pump is 0.5ml / min, the residence time of the primary fiber in the coagulation ...

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

PropertyMeasurementUnit
diameteraaaaaaaaaa
elongation at breakaaaaaaaaaa
Login to View More

Abstract

The invention discloses a preparation method of in-situ cross-linked collagen fiber. The preparation method comprises following steps: 1, EDC and NHS are mixed at a certain mass ratio, an obtained mixture is dissolved in 0.5mol / L glacial acetic acid as a crosslinking agent (wherein the mass amount of EDC accounts for 1 to 20% of that of collagen) so as to obtain a glacial acetic acid solution containing the crosslinking agent; 2, collagen is dissolved in the glacial acetic acid solution containing the crosslinking agent, mechanical stirring is adopted for full stirring, in dissolving process,the temperature of the solution is maintained at 4 to 6 DEG C, and at last a collagen solution with a mass concentration of 1.5% is prepared; 3, the collagen solution is subjected to freezing centrifugation defoaming for 40min at 4 DEG C so as to obtain a collagen spinning stock solution, wet method spinning is adopted, syringe pump extrusion speed is controlled to be 0.5ml / min, the stay time of obtained nascent fiber in a coagulation bath is controlled to be 100 to 300s so as to obtain collagen fiber, the gel state collagen fiber discharged from coagulation bath is loaded with 5g counterweight and is subjected to suspension treatment, and after 1h of natural airing, collagen fiber is obtained. According to the preparation method, introduction of EDC / NHS is capable of improving collagen fiber crystallization degree, in-situ crosslinking is capable of shortening the crosslinking time of collagen fiber, and improving forming technical conditions. The tensile strength of the collagen fiber prepared using the preparation method ranges from 1.06 to 1.43cN / dTex.

Description

technical field [0001] The invention relates to a method for preparing collagen fibers, in particular to a method for preparing collagen fibers which are cross-linked in situ by using EDC / NHS. Background technique [0002] Collagen, as an indispensable and water-insoluble fibrin outside the cells, is a structural protein that makes up the extracellular matrix (EMC) of organisms. Its appearance is generally white and transparent, without any branched fibrils. From the appearance, collagen macromolecules are in the shape of long and thin rods, which can be dissolved in strong acid or strong alkali solution, and have excellent water retention. Collagen, which provides elasticity and tension to cells, can undergo a series of reactions in the extracellular matrix to form semi-crystalline fibers, and play a key role in cell growth and migration. From the perspective of the microscopic structure of collagen, collagen molecules are composed of three α-peptide chains. The dimer pep...

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 Applications(China)
IPC IPC(8): D01F4/00D01F1/10
CPCD01F4/00D01F1/10
Inventor 丁长坤岳程飞曹悦苗李璐张宇鑫程博闻
Owner TIANJIN POLYTECHNIC 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