This application is the U.S. national stage application of International Patent Application No. PCT/EP2007/058664, filed Aug. 21, 2007, the disclosure of which is hereby incorporated by reference in its entirety, including all figures, tables and amino acid or nucleic acid sequences.
The present invention relates to an improved device for overturning containers, particularly containers intended for cell cultures.
The techniques for the large-scale higher organism cell culturing used today are divided into two large groups: those in which the cells are suspended in a stirred nutrient medium or those in which the cells adhere to a solid support bathed with the nutrient medium. Cells which adhere to a solid support are generally referred to as “anchorage dependent” cells. The nutrient medium is generally a liquid comprising a basal nutrient mixture and can also contain a biological extract e.g. serum derived from mammalian blood, in the absence of which the cells would no longer be viable and they would lose their ability to proliferate. In the past years, cell culture media have been developed, in which cells can be grown and maintained in the absence of serum. These media are generally called serum-free media.
For anchorage dependent cells one of the most frequently used methods today consists of using so-called roller bottles as the culture container, which bottles are usually arranged on roller racks which provide the bottles the corresponding rotation. In these roller bottles, the cells adhere to the inner wall of the bottle such that the continuous rotation thereof keeps the cell layer (the thickness of the cell layer is often equivalent to one of them, and in this case it is referred to as “single-layer”) in contact with the nutrient medium. When the cells are cultured in said media, they remain viable for a finite period until one or more nutrients of the medium is used up. Once this time has passed it is necessary to empty and refresh or replace the content of the nutrient medium inside the roller bottles, without entraining or damaging the aforementioned single-layer, which means that emptying movements must be extremely gentle and careful.
Based on the description provided above, emptying these bottles today, an operation, which in addition must be carried out very frequently with large-scale cultures, is carried out by hand or by means of very expensive and complex robots. Overturning the bottles by hand causes problems with tendonitis, discomfort in the hands and shoulders and the so-called carpal tunnel syndrome in the operators responsible for carrying out this operation with a high daily frequency. When the bottles are overturned using robots there is a problem due to the lack of gentleness in said movement, as well as the existence of vibrations, which results in the single-layer becoming detached or damaged on many occasions.
The present invention aims to solve the limits set forth above.
The present invention aims to solve the aforementioned problems by developing a device for overturning containers, particularly roller bottles intended for cell cultures, such that the cell culture inside the roller bottles is refreshed without entraining or damaging the cell culture layer or single-layer since the overturning is carried out with extremely gentle and careful movements. Furthermore, by means of the device of the invention the operator simply places the roller bottle with the culture medium that must be replaced in the device and the device carries out the complete overturning operation without the operator having to be involved again. Therefore, the invention provides a simple, inexpensive and effective device, which prevents discomforts for operators.
These and other features and advantages of the present invention will be inferred from the following detailed description of the illustrative and non-limiting embodiments thereof in relation to the attached figures.
a and 4b are plan and sectional views of the clamping of the casing of the device for overturning containers according to the invention.
a, 5b and 5c are views of the transmission shaft of the device for overturning containers according to the invention.
a and 7b are plan and sectional views of the cover of the rotation actuator of the device for overturning containers according to the invention.
a and 10b are plan views of the support for the rods of the device for overturning containers according to the invention.
a and 11b are plan and sectional views of the shifter of the transmission shaft of the device for overturning containers according to the invention.
As shown in
Possible vibrations of the rotation actuator 3 according to the invention are prevented by means of using the reducer 4 and the pneumatic brake 5 such that the movement that the mentioned actuator 3 causes for the containers 2 when they are overturned is gently and very precise, thus preventing possible unwanted detachments of the culture cells contained in the mentioned containers 2. As shown in
As can be inferred from
The dynamic brake 5 and the reducer 4 are joined to the rotation actuator 3 by means of a transmission shaft 13, preferably made of stainless steel, comprising, as can be inferred from
As shown in
As can be seen in
a and 11b show the shifter 16 of the transmission shaft comprising a pair of flat plates, preferably made of stainless steel, each of them comprising a pair of boreholes, one of which fixes said flat plate to the cover 15 of the actuator while the other borehole fixes the mentioned shifter 16 of the transmission shaft to the rod support 17. The shifter is intended to move the center of rotation of the rod support 17 with respect to the center of rotation of the cover 15 so as to adapt the overturning device 1 object of the invention to the work station. The cover 15 of the rotation actuator 3 comprises a pair of boreholes for its fixing to the mentioned actuator 3, preferably being made of stainless steel.
As can be seen in
Therefore the design of the support 17 and its support rods 7 for supporting the containers 2 is simple and easy to use for operators. The overturning device 1 according to the invention is likewise preferably located in an aseptic area so during operation thereof, no detachment of particles whatsoever that may contaminate said aseptic area has to occur. Therefore the outer parts of the mentioned device 1 according to the invention are preferably made of stainless steel, thus aiding in the cleaning of said outer parts with agents that do not cause corrosive effects on the aforementioned.
The invention further relates to a process for operating the overturning device 1 comprising the steps of:
The invention further relates to the use of the overturning device (1) of the invention for changing a cell culture medium in a roller bottle comprising a cell culture of anchorage dependent cells.
Examples of anchorage dependent cells that can be cultured in roller bottles include mammalian cells such as 3T3 cells, COS cells, human osteosarcoma cells, MRC-5 cells, BHK cells, VERO cells, CHO cells, rCHO-tPA cells, rCHO-Hep B Surface Antigen cells, NS0 cells, HEK 293 cells, rHEK 293 cells, C127 cells, normal human fibroblast cells, stroma cells, hepatocytes or PER.C6 cells.
In a preferred embodiment, the cell culture medium is a serum-free cell culture medium.
Examples for commercially available serum-free cell culture media known in the art include, e.g., SFM 90 (JRH, 67350), SFM 90.1 (JRH, 67350), Supmed300 or Supmed300 modified (JRH, 67350), DMEM (Gibco, 7490571), DMEM/F12 (Gibco, 99.5043), SFM CHO 3a (BioWhittaker), CHO PFM (Sigma, C6970), ProCHO 5, EX-CELL media such as EX-CELL 302 (JRH, Catalogue No. 14312-1000M) or EX-CELL 325 (JRH, Catalogue No. 14335-1000M), CHO-CD3 (Sigma, Catalogue No. C-1490), CHO III PFM (Gibco, Catalogue No. 96-0334SA), CHO-S-SFM II (Gibco, Catalogue No. 12052-098), CHO-DHFR (Sigma, Catalogue No. C-8862), ProCHO 5 (Cambrex, Catalogue No. BE12-766Q), SFM4CHO (HyClone, Catalogue No. SH30549.01), Ultra CHO (Cambrex, Catalogue No. 12-724Q), HyQ PF CHO (HyClone, Catalogue No. SH30220.01), HyQ SFX CHO (HyClone, Catalogue No. SH30187.01), HyQ CDM4CHO (HyClone, Catalogue No. SH30558.01), IS CHO-CD (Irvine Scientific, Catalogue No. #91119), IS CHO-V (Irvine Scientific, Catalogue No. #9197) and derivatives thereof.
In a further preferred embodiment, the anchorage dependent cells express a recombinant protein.
Such recombinant proteins include e.g. chorionic gonadotropin, follicle-stimulating hormone, lutropin-choriogonadotropic hormone, thyroid stimulating hormone, growth hormone, in particular human growth hormone, interferons (IFN), such as IFN-α, IFN-β or IFN-γ, interferon receptors (e.g., interferon gamma receptor), TNF receptors p55 and p75, TACI-Fc fusion proteins, interleukins (e.g., interleukin-2, interleukin-11), interleukin binding proteins (e.g., interleukin-18 binding protein), erythropoietin, granulocyte colony stimulating factor, granulocyte-macrophage colony-stimulating factor, pituitary peptide hormones, menopausal gonadotropin, insulin-like growth factors (e.g., somatomedin-C), keratinocyte growth factor, glial cell line-derived neurotrophic factor, thrombomodulin, basic fibroblast growth factor, insulin, Factor VIII, somatropin, bone morphogenetic protein-2, platelet-derived growth factor, hirudin, epoietin, recombinant LFA-3/IgG1 fusion protein, glucocerebrosidase, and muteins, fragments, soluble forms, functional derivatives, fusion proteins thereof. Furthermore, recombinant proteins that can be expressed by anchorage dependent cells can be antibodies, such as Abciximab, Rituximab, Basiliximab, Daclizumab, Palivizumab, Infliximab, Trastuzumab, Alemtuzumab, Adalimumab, Cetuximab, Efalizumab, Ibritumomab, Bevacizumab, or Omalizumab.
Even though the present invention has been described completely in relation to preferred embodiments, these embodiments are not considered to be limiting and any modifications comprised within the scope defined by the following claims can be introduced.
Number | Date | Country | Kind |
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200602238 | Aug 2006 | ES | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/EP2007/058664 | 8/21/2007 | WO | 00 | 2/5/2009 |
Publishing Document | Publishing Date | Country | Kind |
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WO2008/023010 | 2/28/2008 | WO | A |
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Number | Date | Country | |
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20090196726 A1 | Aug 2009 | US |