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

3D model constructed in vitro by means of serum-free culture medium as well as construction method of 3D model

A serum-free culture, serum-free culture medium technology, applied in the field of 3D model and its construction, can solve the problems of long construction time and affect the stability of the model, achieve good repeatability, simplify the gas-liquid surface culture stage, and inhibit cell apoptosis. the effect of death

Active Publication Date: 2017-11-07
GUANGDONG BOXI BIO TECH CO LTD
View PDF9 Cites 11 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In addition, the current corneal model constructed using corneal cells takes a long time to construct. It takes up to one month to construct a batch of models in vitro. Too long construction time will increase the uncontrollable factors in the process and affect the stability of the model.

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
  • 3D model constructed in vitro by means of serum-free culture medium as well as construction method of 3D model
  • 3D model constructed in vitro by means of serum-free culture medium as well as construction method of 3D model
  • 3D model constructed in vitro by means of serum-free culture medium as well as construction method of 3D model

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0047] This example focuses on the steps of the in vitro construction method of a 3D model constructed in vitro using primary corneal epithelial cells:

[0048] Step 1: cell preparation

[0049] Take primary corneal epithelial cells, resuscitate and expand, use P7 generation cells, trypsinize them to make a single cell suspension, adjust the cell density to 5.0×10 4 Cells / mL, inoculate in a culture flask, add culture medium I to culture, gently shake the culture flask to disperse the cells evenly, and place at 37℃, 5% CO 2 Culture under conditions;

[0050] The culture solution I is DMEM, which contains a glucose content of 1.0 g / L and a glutamine content of 0.2 g / L.

[0051] Step 2: Submerged inoculation and culture of 3D model

[0052] Take the logarithmic growth phase cells and prepare a single cell suspension with culture medium II, adjust the cell density to 5.0×10 4 Pcs / mL, 200μL / chamber volume, inoculate into the small room, place the small room in the model petri dish, add appro...

Embodiment 2

[0059] This example focuses on the steps of the in vitro construction method of a 3D model constructed in vitro using immortalized corneal epithelial cells:

[0060] Step 1: cell preparation

[0061] Take immortalized corneal epithelial cells, recover and expand, use P20 generation cells, trypsinize them to make a single cell suspension, adjust the cell density to 5.0×10 5 Cells / mL, inoculate in a culture flask, add culture medium I to culture, gently shake the culture flask to disperse the cells evenly, and place at 37℃, 5% CO 2 Culture under conditions;

[0062] The culture solution I is DMEM, which contains a glucose content of 1.0 g / L and a glutamine content of 0.2 g / L.

[0063] Step 2: Submerged inoculation and culture of 3D model

[0064] Take the logarithmic growth phase cells and prepare a single cell suspension with culture medium II, adjust the cell density to 5.0×10 5 Pcs / mL, 200μL / chamber volume, inoculate into the small room, place the small room in the model petri dish, ad...

Embodiment 3

[0071] This example focuses on the in vitro construction method steps of a 3D model constructed in vitro using the oral mucosal squamous carcinoma cell line TR146:

[0072] Step 1: cell preparation

[0073] Take the oral mucosal squamous carcinoma cell line TR146, after resuscitation and expansion, use P14 generation cells, trypsinize to make a single cell suspension, adjust the cell density to 5.0×10 6 Cells / mL, inoculate in a culture flask, add culture medium I to culture, gently shake the culture flask to disperse the cells evenly, and place at 37℃, 5% CO 2 Culture under conditions;

[0074] The culture solution I is DMEM, which contains a glucose content of 1.0 g / L and a glutamine content of 0.2 g / L.

[0075] Step 2: Submerged inoculation and culture of 3D model

[0076] Take the logarithmic growth phase cells and prepare a single cell suspension with culture medium II, adjust the cell density to 5.0×10 6 Pcs / mL, 200μL / chamber volume, inoculate into the small room, place the small r...

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 3D model constructed in vitro by means of a serum-free culture medium as well as a construction method of the 3D model and relates to the technical field of biological materials in tissue engineering. Due to selection variety of seed cells and good in-vitro construction repeatability, industrial preparation of the 3D model can be realized. The model is an in-vitro model formed by primary corneal epithelial cells subjected to tissue isolation, limbal stem cells, immortalized corneal epithelial cells, primary oral epithelial cells or oral mucosa squamous cancer cell lines TR146 subjected to in-vitro amplification and stratified through the serum-free culture medium with an undersurface-gas-liquid surface staged culture method.

Description

Technical field [0001] The invention belongs to the technical field of tissue engineering biomaterials, and specifically relates to a 3D model constructed in vitro using a serum-free culture system and a construction method thereof. Background technique [0002] The 3D model in the present invention is constructed by applying the principles of cell biology and engineering to a small number of seed cells after in vitro amplification. Its structure is highly similar to that of normal human corneal epithelium. The bottom-up structure is the basal layer, The spinous layer, granular layer, and spinous layer all have no stratum corneum, have a complete epithelial structure, and express corneal-associated keratin. The 3D model constructed in vitro is mainly used to detect eye irritation in vitro to evaluate the safety of small molecule compounds, active proteins, medical devices, chemicals, cosmetics and other products. [0003] Direct contact with chemicals or exposure to the eyes can c...

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): C12N5/071C12N5/09
CPCC12N5/0621C12N5/0625C12N5/0693C12N2500/24C12N2500/32C12N2500/34C12N2500/84C12N2500/90C12N2501/11C12N2501/33C12N2513/00
Inventor 何欣李潇卢永波
Owner GUANGDONG BOXI BIO TECH CO LTD
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