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

Growth factor sustained release microsphere, tissue engineering cartilage composite stent and preparation method

A growth factor and slow-release microsphere technology, applied in the field of medical materials, can solve the problems of difficulty in realizing self-repair and regeneration, aggravation, and low self-repair and regeneration ability of cartilage tissue, and achieve the effect of improving the effect of regeneration and repair.

Active Publication Date: 2019-08-27
GENERAL HOSPITAL OF PLA
View PDF2 Cites 7 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

It is precisely because of the histological characteristics of cartilage, the composition of biochemical components, and the characteristics of low metabolism and low proliferation of chondrocytes that limit the proliferation response and migration of chondrocytes to the damaged area, resulting in the self-repair and regeneration of damaged cartilage tissue. The ability to regenerate is low, it is difficult to achieve self-repair and regeneration, and it will gradually increase, leading to osteoarthritis and joint dysfunction

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
  • Growth factor sustained release microsphere, tissue engineering cartilage composite stent and preparation method
  • Growth factor sustained release microsphere, tissue engineering cartilage composite stent and preparation method
  • Growth factor sustained release microsphere, tissue engineering cartilage composite stent and preparation method

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0056] The second aspect of the embodiments of the present invention provides a preparation method of growth factor sustained-release microspheres, through which the above-mentioned growth factor sustained-release microspheres can be prepared. The preparation method comprises the following steps:

[0057] S10, providing an aqueous rhTGF-β3 solution with a concentration of 1 μg / mL˜100 μg / mL.

[0058] In step S10, rhTGF-β3 may be dissolved in deionized water to prepare an aqueous solution of rhTGF-β3 with a concentration of 1 μg / mL-100 μg / mL as the internal water phase w 1 .

[0059] S20, providing a PLGA oil phase solution with a concentration of 20 mg / mL-25 mg / mL.

[0060] In step S20, PLGA may be dissolved in dichloromethane (DCM) to prepare a PLGA oil phase solution with a concentration of 20 mg / mL-25 mg / mL as the oil phase o. The oil phase o can have a higher encapsulation efficiency for rhTGF-β3.

[0061] In step S20, the molecular weight of PLGA is preferably 1×10 5 ...

Embodiment 1

[0112] use w 1 / o / w 2 The growth factor sustained-release microspheres loaded with rhTGF-β3 in PLGA were prepared by emulsification-solvent evaporation method. The specific process was as follows: 2 μg of rhTGF-β3 was dissolved in 200 μL of deionized water to prepare an aqueous solution of rhTGF-β3 with a concentration of 10 μg / mL. Water phase w 1 . Dissolve polylactic-co-glycolic acid (PLGA) with a molecular weight of 102,000 Da in dichloromethane (DCM) to prepare a PLGA solution with a concentration of 25 mg / mL as the oil phase o. Polyvinyl alcohol (PVA) with a molecular weight of 67,000 Da was dissolved in deionized water to prepare a 1% PVA aqueous solution as the external water phase w 2 ; Dispense 200 μL of the inner aqueous phase w 1 Join in 2mL oily phase o, form primary emulsion (w 1 / o); then the primary emulsion (w 1 / o) Add 20mL external aqueous phase w 2 At room temperature (20°C-25°C), stir magnetically at 500rpm for 12 hours, volatilize and remove DCM to ...

Embodiment 2

[0114] The difference from Example 1 is that 5 μg of rhTGF-β3 was dissolved in 200 μL of deionized water to prepare a rhTGF-β3 aqueous solution with a concentration of 25 μg / mL as the internal water phase w 1 .

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
Particle sizeaaaaaaaaaa
Heightaaaaaaaaaa
Widthaaaaaaaaaa
Login to View More

Abstract

The invention discloses a growth factor sustained release microsphere, a tissue engineering cartilage composite stent and a preparation method. The growth factor sustained release microsphere includesa polylactic acid-glycolic acid copolymer matrix material and recombinant human transforming growth factor beta 3 encapsulated in the matrix material, wherein the encapsulation amount of the recombinant human transforming growth factor beta 3 in the microsphere is 5 ng / mg to 200 ng / mg; the sustained release period of the microsphere is 28 days or above. The growth factor sustained release microsphere and the tissue engineering cartilage composite stent disclosed by the invention have higher regeneration and repair effects of defected cartilage tissues.

Description

technical field [0001] The invention belongs to the technical field of medical materials, and in particular relates to a growth factor slow-release microsphere, a tissue engineering cartilage composite scaffold and a preparation method. Background technique [0002] Cartilage is an important part of the skeletal system in humans or animals. Cartilage tissue is a highly specialized connective tissue, which is characterized by the lack of blood vessels, nerves and lymphatic vessels in the tissue. The extracellular matrix is ​​dense and solid. Chondrocytes are surrounded by a large number of cells. External matrix (such as collagen, fibers, proteins, polysaccharides, etc.) surrounded. It is precisely because of the histological characteristics of cartilage, the composition of biochemical components, and the characteristics of low metabolism and low proliferation of chondrocytes that limit the proliferation response and migration of chondrocytes to the damaged area, resulting in...

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
IPC IPC(8): A61K9/52A61K38/18A61K47/34A61L27/18A61L27/22A61L27/52A61L27/54A61L27/58A61P19/08
CPCA61K38/1841A61K9/5031A61P19/08A61L27/227A61L27/18A61L27/54A61L27/52A61L27/58A61L2300/414A61L2300/622A61L2300/604A61L2430/06C08L89/00C08L67/04
Inventor 郭全义杨振卢世璧刘舒云眭翔黄靖香郭维民田广招孙志强查康康周建
Owner GENERAL HOSPITAL OF PLA
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

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com