US2012184009A1PendingUtilityA1

Continuous culture apparatus with mobile vessel, allowing selection of fitter cell variants and producing a culture in a continuous manner

Assignee: DE CRECY EUDES FRANCOIS MARIEPriority: Feb 23, 2004Filed: Mar 26, 2012Published: Jul 19, 2012
Est. expiryFeb 23, 2024(expired)· nominal 20-yr term from priority
Inventors:Eudes De Crecy
C12M 23/34C12M 23/24C12M 41/40C12N 5/0669C12M 23/06C12N 5/04C12M 1/3453C12M 23/26C12N 5/0647C12M 41/26C12M 3/06C12M 41/36C12N 5/0622C12N 1/20C12N 5/0602C12N 5/0606C12M 1/007C12N 5/0605C12M 1/02C12N 1/16C12M 3/02C12M 1/24C12N 7/00C12M 23/22C12M 3/00
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Claims

Abstract

A method and device for growing plant, animal or stem cells in a continuous manner.

Claims

exact text as granted — not AI-modified
1 . A method for growing cells, comprising:
 a) providing flexible tubing containing culture medium, and a surface in which the living cells can grow on in said tubing, and a system of clamps, each of the clamps being capable of open and closed positions, the clamps being positioned so as to be able to divide the tubing into:
 i) an upstream region containing unused culture medium; 
 ii) a downstream region containing spent culture medium; and 
 iii) a growth chamber region for growing said cells disposed between the upstream and downstream regions; and 
   b) closing selected ones of the clamps on the tubing to define the growth chamber region of the tubing between the upstream and downstream regions of the tubing, and introducing viable cells into the growth chamber region;   c) cyclically closing and opening selected ones of the clamps to redefine the growth chamber region of the tubing so that a first portion of the previously defined growth chamber region becomes a portion of the downstream region of the tubing, and a portion of the previously defined upstream region of the tubing becomes a portion of the growth chamber region of the tubing; and   d) repeating step c) until a sufficient amount of cells have been grown.   
     
     
         2 . The method according to  claim 1 , comprising the further step of withdrawing a sample of living cells from said culture medium from the downstream region. 
     
     
         3 . The method according to  claim 1 , further comprising isolating said living cells from the downstream region. 
     
     
         4 . The method according to  claim 1 , wherein the living cells are selected from the group consisting of yeast cells, animal cells, plant cells, and stem cells. 
     
     
         5 . The method according to  claim 1 , wherein the living cells are stem cells. 
     
     
         6 . The method according to  claim 5 , wherein the living cells are selected from the group consisting of hematopoietic stem cells, bone marrow stem cells, stromal cells, astrocytes, oligidendrocytes, embryonic stem cells, fetal stem cells, umbilical cord stem cells, placenta derived stem cells, and adult stem cells. 
     
     
         7 . The method according to  claim 6 , wherein the living cells are selected from the group consisting of hematopoietic stem cells, bone marrow stem cells, stromal cells, astrocytes and oligidendrocytes. 
     
     
         8 . The method according to  claim 1 , wherein the surface in which the cells are grown is the interior surface of the tubing. 
     
     
         9 . The method according to  claim 1 , wherein the surface in which the cells are grown is a continuous fiber. 
     
     
         10 . The method according to  claim 1 , further comprising growing the cells in one or more growth chambers that are present in the growth chamber region. 
     
     
         11 . The method according to  claim 1 , further comprising growing one or more types of cells in the growth chamber region. 
     
     
         12 . The method according to  claim 1 , wherein the sufficient amount of cells of step d) is defined as a pre-determined density level of the cells. 
     
     
         13 . The method according to  claim 1 , wherein the tubing is gas permeable 
     
     
         14 . The method according to  claim 1 , wherein the tubing is gas impermeable. 
     
     
         15 . The method according to  claim 1 , wherein the tubing is one of transparent and translucent, a turbidimeter being used to determine the density level of the cells. 
     
     
         16 . The method according to  claim 1 , further comprising regulating the pressure of the growth chamber portion of the tubing relative to ambient pressure. 
     
     
         17 . The method according to  claim 1 , further comprising measuring a pH of the culture medium in the growth chamber region. 
     
     
         18 . The method according to  claim 1 , further comprising regulating the temperature of the growth chamber region with a temperature regulator constructed to control the temperature of the growth chamber region of the tubing. 
     
     
         19 . The method according to  claim 1 , further comprising agitating the culture medium in the growth chamber region with an agitator. 
     
     
         20 . The method according to  claim 19 , wherein the agitator comprises at least one stirring bar. 
     
     
         21 . The method according to  claim 1 , further comprising subjecting the growth culture chamber region to at least one of radio waves, light waves, x-rays, sound waves, an electro magnetic field, and radioactive field. 
     
     
         22 . The method according to  claim 1 , further comprising subjecting the growth chamber region to a different gravitational force.

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