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

Multifunctional bioreactor system and methods for cell sorting and culturing

A bioreactor, cell culture technology, applied in the field of multifunctional bioreactors

Active Publication Date: 2013-09-11
NANJING XINNUODAN BIOTECH
View PDF4 Cites 26 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] The vast majority of bioreactors have been previously designed for culturing adherent or suspension cells, and there have been no reports of bioreactors supporting the growth of partially adherent cells

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
  • Multifunctional bioreactor system and methods for cell sorting and culturing
  • Multifunctional bioreactor system and methods for cell sorting and culturing
  • Multifunctional bioreactor system and methods for cell sorting and culturing

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0041] Example 1. Hematopoietic stem cells (HSCs) were sorted from Buffy's layer cells and then cultured. Parenchyma cells can be obtained from cord blood, bone marrow, peripheral blood or other tissues using standard Ficoll grading procedures. Use conventional methods to count parenchymal cells and resuspend them to the correct volume with the required buffer (e.g. 1% human albumin in PBS), then add the correct amount of magnetically labeled anti-CD34, mix thoroughly, and Incubate at 4°C for 10 to 30 minutes. During the cultivation period, connect the operating system of the bioreactor to the carbon dioxide incubator, connect all the wiring of the control box, and connect to the computer. Power on the bioreactor and computer, select the cell sorting and cell culture program. Depending on cell requirements, edit the program for each specific step or select a general program. After culturing, the cells are placed in a culture chamber containing magnetic beads. can use Fi...

example 2

[0043] Example 2. Expansion of CMV-specific CD8+ cytotoxic T cells. Parenchyma cells obtained from CMV antibody-positive individuals. The application can use 2 methods. The first method is roughly the same as shown in Example 1, but uses magnetically labeled anti-CD8 and CMV-specific CD8+ cytotoxic T cell expansion medium instead of magnetically labeled anti-CD34 and HSC expansion medium , to increase the removal of damaged cells at the end of the culture (see description of the second method below). When cell numbers are low, eg less than one million, the second method is preferred and CD8+ cells are isolated in the middle of the expansion procedure rather than at the beginning. On day 0, after Ficoll isolation, parenchyma cells were washed twice with CTL Medium and resuspended in CTL Medium containing IL-2 and IL-7 to 10 7 / ml, add 10ul CMV pp65 / 10 at 37°C 7 cells / ml PBMC for 5-10 minutes. Cells were then diluted to 10 with stimulation medium 6 / ml, and then placed in...

example 3

[0044] Example 3. Fibroblast culture. Fibroblasts are a typical adherent cell.

[0045] After trypsinization and washing, fibroblasts are resuspended in a suitable medium, such as 10% BSA RPMI 1640, at 10000-40000 / ml. Pour the cells into a cell culture chamber, e.g. Figure 4 The cell culture bag is shown. Connect the culture chamber port with the pipeline, and install the cassette and the culture bag into the flipping arm of the carbon dioxide incubator, as shown in Example 1. Initiate standard adherent cell culture procedures. During this procedure, the cell culture chamber is kept agitated for 24 hours to allow the cells to adhere to the magnetic beads. On the following day, the medium containing non-adherent cells was drained into a waste container or syringe, and fresh medium was added. Cell culture chambers are grown by turning the cell culture chamber slowly and intermittently, followed by programmed media changes during the turning period. Cell culture was stopp...

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 present disclosure relates to bioreactors and more particularly bioreactors for growing and separating cells. The bioreactor comprises at least one reaction chamber, an adjustable magnetic field, and a multifunctional cell supporting system, and may further comprise an optional protective perfusion system and an optional computerized control system.

Description

technical field [0001] The present invention relates to multifunctional bioreactors for cell culture and cell sorting. Background technique [0002] This application relates generally to bioreactors, and more particularly to bioreactors for culturing and sorting cells. [0003] Many types of cells, especially hematopoietic stem cells and immune cells, require their isolation from the original sample during their culture for efficient expansion and directed differentiation. This isolation procedure is also known as cell sorting, purification, or cell dissociation. In the past, cell sorting and culture were completed by special systems, that is, the target cells were freed first, and then transferred to culture vessels for culture. This traditional method involves the use of two completely different devices and systems, which is cumbersome, and there is a greater risk of cell contamination, damage, and death during the process from cell sorting to cell culture. Our current ...

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): C12M1/00B01F23/00
CPCC12M23/44C12M25/16C12M29/04C12M35/06C12M47/04C12M25/14C12M27/02B03C1/01B03C1/0332B03C1/0335B03C1/288B03C2201/18B03C2201/26C12M23/34C12M29/10C12M41/36C12M41/48B01F29/64B01F33/25B01F33/251B01F33/35B01F33/451B01F33/452C12M1/06C12M1/42
Inventor 张永新王瑛莫妮卡·张
Owner NANJING XINNUODAN BIOTECH
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