WO2011040867A1 - Methods and kits for cell release - Google Patents
Methods and kits for cell release Download PDFInfo
- Publication number
- WO2011040867A1 WO2011040867A1 PCT/SE2010/051033 SE2010051033W WO2011040867A1 WO 2011040867 A1 WO2011040867 A1 WO 2011040867A1 SE 2010051033 W SE2010051033 W SE 2010051033W WO 2011040867 A1 WO2011040867 A1 WO 2011040867A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- layer
- cells
- cell culture
- culture support
- releasing
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N5/00—Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
- C12N5/0068—General culture methods using substrates
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
- C12M23/00—Constructional details, e.g. recesses, hinges
- C12M23/20—Material Coatings
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
- C12M33/00—Means for introduction, transport, positioning, extraction, harvesting, peeling or sampling of biological material in or from the apparatus
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2533/00—Supports or coatings for cell culture, characterised by material
- C12N2533/30—Synthetic polymers
- C12N2533/32—Polylysine, polyornithine
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2539/00—Supports and/or coatings for cell culture characterised by properties
- C12N2539/10—Coating allowing for selective detachment of cells, e.g. thermoreactive coating
Definitions
- the invention relates to methods for cell release. More particularly, the invention relates to methods for cell release from a polymer-based cell culture support.
- Adherent cells have conventionally been grown on glass surfaces or on polymer substrates.
- the surfaces for cell culture are often pre-treated to enhance cell adhesion and proliferation.
- Matrices for adherent cells that allow on-demand cell detachment or cell release have long been needed in biomedical and biological applications.
- Cultured cells may be detached or released from cell culture supports by a variety of methods.
- Commonly used cell release methods comprise mechanical methods (such as scraping), treatment with proteolytic enzymes (such as trypsin), use of calcium chelators (such as EDTA), or a combination of such methods.
- proteolytic enzymes such as trypsin
- calcium chelators such as EDTA
- many of these conventional cell release methods may cause adverse effects on cultured cells, and may modify their inherent structure and function.
- treatment of cells with trypsin i.e., trypsinization
- is a harsh method and is not desirable for delicate cells such as stem cells, due to its potential effect on cell phenotype.
- trypsin is typically derived from animals, and may contain impurities like co-fractionated proteins or biological agents (such as viruses or mycoplasma). Impurities of animal origin may limit the use of released cells for critical applications such as cell therapy. Mechanical methods for releasing cells are labor intensive and are often impractical for industrial-scale cell culture applications.
- Non-enzymatic methods include physical methods that use ultrasounds or shock waves, which generate bubbles that facilitate cell detachment.
- Cultured cells from cell culture supports comprising thermoresponsive polymers like poly-N-isopropylacrylamide (PNIPAAm) may be released by cooling the cell culture support to a temperature in a range from about 4- 20°C.
- PNIPAAm poly-N-isopropylacrylamide
- Efficient cell release is particularly important for high yield in industrial-scale cell culture processes. Therefore, there is an emerging need to develop better cell release techniques for fast, efficient cell detachment without affecting cell morphology and cell viability.
- the invention generally comprises both methods and kits for releasing cells from a cell culture support.
- An example of a method for releasing cells from a cell culture support comprises providing cultured cells on a cell culture support and releasing the cultured cells from the cell culture support by adding a releasing solution.
- the releasing solution comprises dimethyl sulfoxide (DMSO).
- the cell culture support comprises a multi-layer polyelectrolyte-based coating on a substrate.
- kits for culturing cells generally comprises a cell culture support, and a releasing solution for cell release.
- the releasing solution comprises DMSO.
- the cell culture support comprises a substrate, and a multi-layer polyelectrolyte-based coating on the substrate.
- Another example of a method for releasing cells comprises the steps of providing cultured human mesenchymal stem cells on a cell culture support (comprising a multi- layer polyelectrolyte-based coating on a substrate), and releasing the cultured cells from the cell culture support at room temperature by incubating the cells with a releasing solution.
- the releasing solution comprises about 0.01% DMSO in PBS.
- FIG. 1A is an image of an uncoated glass slide after addition of a releasing solution comprising DMSO.
- FIG. IB is an image of a glass slide with a multi-layer polyelectrolyte- based coating after releasing cells using a releasing solution comprising DMSO.
- FIG. 2 represents graphical plots of a WST-1 cell assay, illustrating the change in optical density of the WST-1 reagent when mixed with released cells and measured at 450 nm. The optical density at 450 nm correlates with number of cells present in the assay system. Cells were released from uncoated or multi-layer polyelectrolyte coated glass slides using a releasing solution comprising DMSO in PBS.
- a "cell culture support”, as referred to herein, is a support for adhering and culturing cells.
- the cell culture support may comprise a substrate.
- the substrate may be coated or layered with a suitable coating material for cell adherence and proliferation.
- suitable coating materials may include, but are not limited to, polyelectrolytes.
- a “substrate”, as referred to herein, is a base or a holder, which provides support for a coating.
- the coated substrate may be used as a cell culture support.
- a "releasing solution”, as referred to herein, is a solution that helps to release or detach cells from a cell culture support.
- the releasing solution comprises one or more polar aprotic solvents, e.g. dimethyl sulfoxide (DMSO).
- DMSO dimethyl sulfoxide
- polar aprotic solvents include but are not limited to: tetrahydrofurane, acetone, N, N-dimethylformamide.
- Those solvents strongly interact with polymers such as polyelectrolytes and are capable to disturb hydrogen bonds as well as electrostatic interactions, which affect polymer aggregation and cell adhesion.
- the releasing solution comprises DMSO in phosphate buffered saline (PBS).
- PBS phosphate buffered saline
- Polyelectrolytes as referred to herein, are polymers wherein the repeating units of the polymer bear an electrolyte group. The polymers become charged while these groups are dissociated in aqueous solutions (e.g., water). Polyelectrolyte properties are thus similar to both electrolytes (salts) and polymers (high molecular weight compounds), and are sometimes called polysalts.
- the polyelectrolyte solutions are electrically conductive like salts and are often viscous like polymers. Many biological molecules are polyelectrolytes. Examples of polyelectrolytes include but not limited to polypeptides (or proteins), DNA, and polymers.
- a high yield of healthy, viable cells is required for applications such as drug screening and cell therapy.
- Industrial-scale cell manufacturing units or cell bioreactors often employ suitable cell culture supports for culturing cells. Efficient non-enzymatic methods for releasing cells from the cell culture support can be particularly useful if the cultured cells are to be used in therapeutic applications.
- the methods and kits of the invention for releasing cells from a cell culture support are useful for delicate cells, such as stem cells. Efficient release of normal cells or delicate cells may acquire using the methods and kits for cell release of the present invention.
- One example of the method for releasing cultured cells comprises the steps of:
- the cell culture support may comprise multiple layers (multi-layer) of polyelectrolyte immobilized on a substrate.
- the cells are released using a releasing solution comprising DMSO.
- concentration of DMSO (v/v) in the releasing solution may range from about 0.01% to 1.0%. In some embodiments, the concentration of DMSO in the releasing solution may range from about 0.02% to 0.5%, and 0.1% to 0.5%.
- Cell release efficiency may be enhanced by changing the concentration of DMSO in the releasing solution. The efficiency for cell release may increase with increasing concentrations of DMSO.
- the releasing solution may further comprise DMSO in a phosphate buffered saline (PBS) wherein pH of the solution is about 7.5.
- PBS phosphate buffered saline
- the release of the cultured cells may be further optimized by incubating the cell culture support with the releasing solution at room temperature or in ranges from about 15°C to 37°C, about 20°C to 35°C or about 20°C to 30°C.
- the cells may be released from the cell culture support by incubating on the cell culture support at room temperature for various periods of time, such as, for about 1 hr to 2 hrs, about 30 min to 1 hr, or about 10 min to 30 min.
- cell release efficiency may be modified, by changing incubation time for cell release after adding releasing solution. For example, cell release efficiency may be increased with increasing incubation time.
- the method for releasing cells comprises the step of providing cultured cells on a cell culture support.
- the method may include culturing the cells on the cell culture support.
- the cells may be cultured at a various temperature ranges from about 20°C to 37°C, about 30°C to 37°C and about 35°C to 37.5°C, depending on, for example, cell type.
- the cells may be grown in a culture flask and may be added to the cell culture support for further growth. Cells may be grown on the cell culture support after extraction from a biological source such as, but not limited to, blood, bone marrow, or tissue section.
- the cell culture support may be introduced in a spinner flask, a stacked culture flask, a stirred tank reactor, or any other in- vitro cell culture system.
- the methods may also be used to release fragile cells once they are cultured on the cell culture support.
- the fragile cells may include, but are not limited to, embryonic stem cells, adult stem cells, induced pluripotent stem cells, dendritic cells, hematopoietic cells,
- mesenchymal stromal cells mesenchymal stromal cells, neural cells, reprogrammed cells, or de-differentiated cells.
- cultured stem cells are released from the cell culture support by incubating the cell culture support with a releasing solution comprising 0.01% (v/v) of DMSO for a period of about 10 min.
- Efficient methods for stem cell culture are critical to generate stem cells having high purity in good yield for use in clinical or research applications.
- Culture of stem cells often require specialized techniques since the stem cells may lose their multipotency or pluripotency or may differentiate during cell culture.
- conventional methods of releasing cells such as mechanical scraping or trypsinization, may not be suitable for releasing the cultured stem cells.
- mesenchymal stromal cells may be successfully cultured and released using the non-enzymatic, DMSO-based cell release method described herein without any detrimental effects on the cultured mesenchymal stromal cells.
- the cell culture support may be configured as a cell culture bed, a cell carrier bead, disk or scaffold comprising one or more polymeric layers.
- substrates include a microcarrier, a membrane, a fiber, a hollow fiber, a capillary, a vessel, a flask, a disc, a bead, a Petri dish, a plate, a woven or non-woven fabric or mesh, a nano-fiber mat, a particle, a scaffold or a foam.
- substrate materials include, but are not limited to, glass, polymer, metal, ceramic and combinations thereof.
- the cell culture support may comprise a multi-layer polyelectrolyte-based coating.
- the multi-layer polyelectrolyte-based coating may comprise at least one copolymer layer or at least one homopolymer layer. In other embodiments, the multi-layer polyelectrolyte-based coating may comprise at least one copolymer layer and at least one homopolymer layer.
- the copolymer layers and the homopolymer layers may also be stacked in the coating in an alternating arrangement.
- the cell culture support may comprise alternate blocks of a copolymer layer and/or a homopolymer layer.
- the multiple layers of polyelectrolyte-based coating may be fabricated by utilizing a layer-by- layer (LBL) technique. One or more polymer layers may be arranged one over another by using the LBL technique.
- LBL layer-by- layer
- the multi-layer polyelectrolyte-based coating may comprise a copolymer wherein the copolymer may be a block copolymer.
- the coating may comprise multiple layers of identical or different block copolymers.
- a non-limiting example of a block copolymer is a
- thermoresponsive amphiphilic block copolymer may comprise poly (di (ethylene glycol) methylether mefhacrylate)-co-poly(acrylic acid).
- the multi-layer coating may further comprise one or more additional polymer layers (e.g. homopolymer or copolymer).
- homopolymers include poly (L-lysine), poly (allylamine), poly (ethylene imine) and poly (vinylpyrrolidone).
- the homopolymer or copolymer in the multi-layer polyelectrolyte coating may be responsive to one or more external stimuli such as temperature, pH, or ionic strength.
- the homopolymer may be responsive to ionic strength or pH or both.
- the copolymer may be responsive to temperature or pH or both.
- the multi-layer polyelectrolyte-based coating may be adhered to a substrate via non- covalent interaction. Attaching the polymer coating non-covalently to the substrate offers significant advantages, such as, the flexibility to use the substrate in complex substrate geometries (e.g., flat sheets, beads, cubes, porous foams, fibers and nonwovens).
- complex substrate geometries e.g., flat sheets, beads, cubes, porous foams, fibers and nonwovens.
- kits of the invention for culturing and releasing cells, may comprise a cell culture support having a substrate with multi-layer polymer-based coating on the substrate, and a releasing solution.
- the kit may further comprise cells (e.g., in a frozen condition) and/or medium for culturing cells.
- the kit may further comprise a protocol for handling, culturing and/or releasing cells from the cell culture support.
- the kit may be packaged along with a manual describing the method of using the kit. EXAMPLE 1.
- poly(di(ethyleneglycol)methylether methacrylate)-co-poly( acrylic acid) PDEGMEMA-co- PAA
- PDEGMEMA-co- PAA poly(di(ethyleneglycol)methylether methacrylate)-co-poly( acrylic acid)
- the slides were then washed with DI water and were incubated with 0.1 % solution (w/v) of Poly-L-Lysine (Aldrich) for 60 minutes at 37°C.
- the 0.1% solution of poly-L-Lysine (PLL) contained a small amount (about 0.1mol%) of poly-L- lysine functionalized with fluorescein 5-isothiocyanate (FITC-PLL) (FITC from Sigma) fluorescent probe.
- FITC-PLL fluorescein 5-isothiocyanate
- a fluorescent probe enables the measurement of the fluorescence intensity of polymer layers to determine proper formation of multi-layer coatings.
- the slides were washed with warm (37°C) DI water and were then incubated with 0.1 % solution (w/v) of poly(di(ethyleneglycol)methylether methacrylate)-co-poly(acrylic acid) for 60 min at 37 °C. Slides were washed with DI water and air-dried. The amount of deposited PLL was determined by measuring the intensity of FITC florescence on a Typhoon fluorescence imager.
- PLL/PDEGMEMA-co-PAA coating on the substrate was additionally confirmed by time of flight secondary ion mass spectrometry (ToF SIMS) analysis (data not shown).
- the ToF SIMS spectra showed a gradual decrease in the peak height and peak position for the observed negative Si0 2 ions.
- the LBL coating of samples having five PLL/PDEGMEMA-co-PAA layers was thick enough that Si0 2 ions were almost undetectable (data not shown) with respect to an uncoated glass slide.
- the cell culture support was used to culture human mesenchymal stem cells (hMSC, ATCC). These cells were first cultured on polystyrene surfaces using the Mesenchymal Stem Cell Growth Medium (PT-3001, Lonza). To culture cells, about 10 5 human mesenchymal stem cells (primary culture) were seeded on the surface of the cell culture support (uncoated and/or coated glass slides) and incubated at 37°C, in a humidified atmosphere of 5% C0 2 .
- hMSC human mesenchymal stem cells
- ATCC Mesenchymal Stem Cell Growth Medium
- FIG. 1 A shows an image of an uncoated cell culture support (2) after the attempt of releasing cultured human
- FIG IB shows an image of multi layer PLL/PDEGMEMA-co-PAA (five layers) coated cell culture support (4) after the release of human mesenchymal stem cells (6) by using a releasing solution comprising 0.01% (v/v) DMSO.
- the quantitative measurement of cell release is presented in FIG.2 by measuring the optical density of the cell proliferation assay solution at 450 nm using WST-1 assay reagent. Released cells were pelleted down by centrifuging the cell suspension at 500g for 5 min. The pelleted cells were re-suspended in 200 ⁇ 1 growth medium and were transferred in 96 well plate. The plate was spun down at 500g for 5min. 150 ⁇ 1 fresh growth medium and 15 ⁇ 1 of WST-1 cell assay reagent were added to each well. Cells with assay reagent were incubated at 37°C for 2.5hr. This experiment was performed in replicates of 3 different sets.
- FIG. 2 Cell release from uncoated glass slides (bar 8), and five layers of PLL/PDEGMEMA-co-PAA coated glass slides (bar 10) are shown in FIG. 2.
- the data shows efficient cell release for the five layers of PLL/PDEGMEMA-co-PAA coated glass slides (10) compared to uncoated surface of the glass slide (8).
- An uncoated glass slide served as a control.
- the difference between the signal for released cells from uncoated glass slide and signal for released cells from five layer PLL/PDEGMEMA-co-PAA coated glass slide gives a measure of the release efficiency, which as indicated by FIG. 2 is clearly efficient for multi-layer polymer coated cell culture support.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical & Material Sciences (AREA)
- Zoology (AREA)
- Biomedical Technology (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Microbiology (AREA)
- Sustainable Development (AREA)
- Cell Biology (AREA)
- Molecular Biology (AREA)
- Immunology (AREA)
- Clinical Laboratory Science (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Apparatus Associated With Microorganisms And Enzymes (AREA)
- Immobilizing And Processing Of Enzymes And Microorganisms (AREA)
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA2772248A CA2772248A1 (en) | 2009-09-30 | 2010-09-27 | Methods and kits for cell release |
CN2010800450145A CN102575226A (en) | 2009-09-30 | 2010-09-27 | Methods and kits for cell release |
EP10820906.5A EP2483391A4 (en) | 2009-09-30 | 2010-09-27 | Methods and kits for cell release |
IN1891DEN2012 IN2012DN01891A (en) | 2009-09-30 | 2010-09-27 | |
JP2012532045A JP2013506416A (en) | 2009-09-30 | 2010-09-27 | Methods and kits for cell release |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12/570,032 | 2009-09-30 | ||
US12/570,032 US8399252B2 (en) | 2009-09-30 | 2009-09-30 | Methods and kits for cell release |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2011040867A1 true WO2011040867A1 (en) | 2011-04-07 |
Family
ID=43780827
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/SE2010/051033 WO2011040867A1 (en) | 2009-09-30 | 2010-09-27 | Methods and kits for cell release |
Country Status (7)
Country | Link |
---|---|
US (2) | US8399252B2 (en) |
EP (1) | EP2483391A4 (en) |
JP (1) | JP2013506416A (en) |
CN (1) | CN102575226A (en) |
CA (1) | CA2772248A1 (en) |
IN (1) | IN2012DN01891A (en) |
WO (1) | WO2011040867A1 (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9926523B2 (en) | 2010-12-16 | 2018-03-27 | General Electric Company | Cell carriers and methods for culturing cells |
US9534206B2 (en) | 2010-12-16 | 2017-01-03 | General Electric Company | Cell carrier, associated methods for making cell carrier and culturing cells using the same |
US9453196B2 (en) | 2010-12-16 | 2016-09-27 | General Electric Company | Cell carrier, methods of making and use |
US9453197B2 (en) | 2010-12-16 | 2016-09-27 | General Electric Company | Methods of making cell carrier |
US9518249B2 (en) | 2010-12-16 | 2016-12-13 | General Electric Company | Cell carrier, associated methods for making cell carrier and culturing cells using the same |
KR102186676B1 (en) | 2013-09-27 | 2020-12-07 | 쓰리엠 이노베이티브 프로퍼티즈 캄파니 | Dual-sided structured film articles |
US20240110139A1 (en) * | 2020-12-31 | 2024-04-04 | Academia Sinica | Cell culture systems, methods and uses thereof |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20080241926A1 (en) * | 2007-03-02 | 2008-10-02 | Ilsoon Lee | Cell adhesion on surfaces of varying topographies |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7022522B2 (en) | 1998-11-13 | 2006-04-04 | Limin Guan | Macroporous polymer scaffold containing calcium phosphate particles |
JP4161106B2 (en) | 2004-09-30 | 2008-10-08 | 独立行政法人科学技術振興機構 | Cell peeling agent and cell sheet peeling method |
ITRM20060020A1 (en) | 2006-01-18 | 2007-07-19 | Andrea Masotti | METHOD FOR CELL CULTURE |
GB2425074A (en) * | 2006-03-23 | 2006-10-18 | Ilika Technologies Ltd | Selective cellular adhesion on polymer microarrays |
-
2009
- 2009-09-30 US US12/570,032 patent/US8399252B2/en active Active
-
2010
- 2010-09-27 EP EP10820906.5A patent/EP2483391A4/en not_active Withdrawn
- 2010-09-27 JP JP2012532045A patent/JP2013506416A/en not_active Ceased
- 2010-09-27 IN IN1891DEN2012 patent/IN2012DN01891A/en unknown
- 2010-09-27 CN CN2010800450145A patent/CN102575226A/en active Pending
- 2010-09-27 WO PCT/SE2010/051033 patent/WO2011040867A1/en active Application Filing
- 2010-09-27 CA CA2772248A patent/CA2772248A1/en not_active Abandoned
-
2013
- 2013-02-25 US US13/776,053 patent/US8993322B2/en active Active
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20080241926A1 (en) * | 2007-03-02 | 2008-10-02 | Ilsoon Lee | Cell adhesion on surfaces of varying topographies |
Non-Patent Citations (3)
Title |
---|
LIANG J.F. ET AL: "Dimethyl sulfoxide induces multilayer aggregates and prolongs survival of primary cultured hepatocytes", BIOTECHNOLOGY TECHNIQUES, vol. 11, no. 12, December 1997 (1997-12-01), pages 869 - 872, XP008159447 * |
See also references of EP2483391A4 * |
VODOUHE C. ET AL: "Control of drug accessibility on functional polyelectrolyte multilayer films", BIOMATERIALS, vol. 27, 2006, pages 4149 - 4156, XP027951321 * |
Also Published As
Publication number | Publication date |
---|---|
IN2012DN01891A (en) | 2015-07-24 |
EP2483391A1 (en) | 2012-08-08 |
CA2772248A1 (en) | 2011-04-07 |
US8399252B2 (en) | 2013-03-19 |
US20130171729A1 (en) | 2013-07-04 |
CN102575226A (en) | 2012-07-11 |
JP2013506416A (en) | 2013-02-28 |
US20110076764A1 (en) | 2011-03-31 |
US8993322B2 (en) | 2015-03-31 |
EP2483391A4 (en) | 2013-04-10 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US8993322B2 (en) | Methods and kits for cell release | |
US9469839B2 (en) | Cell culture support and associated method for cell growth and release | |
JP6492106B2 (en) | Method for preparing cells for 3D tissue culture | |
Lakard et al. | Culture of neural cells on polymers coated surfaces for biosensor applications | |
US20210355424A1 (en) | Cell culture substrate, method for producing cell culture substrate, and method for producing spheroids | |
WO2014178670A1 (en) | Method for screening surface structure suitable for culturing stem cell using culture vessel including nano gradient pattern | |
KR102554582B1 (en) | Cell culture substrate, manufacturing method and use thereof | |
LINDSTROeM et al. | Nanoporous titania coating of microwell chips for stem cell culture and analysis | |
WO2019035436A1 (en) | Culture substrate for pluripotent stem cell and method for producing pluripotent stem cell | |
US8252549B2 (en) | Multi-purpose substrates useful for cell culture and methods for making | |
WO2017034316A1 (en) | Cell patterning material, preparation method therefor, and use thereof | |
EP3712243A1 (en) | Liquid set for droplet discharging apparatus | |
JP2019033742A (en) | Culture base for pluripotent stem cells and method for producing pluripotent stem cells | |
Carangelo | Reproducing cardiac fibrosis: from state of the art analysis to the design of bioartificial electrospun fibers for in vitro pathological cardiac tissue modelling | |
EP3933034A1 (en) | Cellular spheroid production method | |
GB2425074A (en) | Selective cellular adhesion on polymer microarrays | |
Lee et al. | Nanoscale level gelatin-based scaffolds enhance colony formation of porcine testicular germ cells | |
KR20230156412A (en) | Cell culture substrate and method for manufacturing the same, method for inducing differentiation of pluripotent stem cells, and cell culture kit | |
Li et al. | Improving three-dimensional human pluripotent cell culture efficiency via surface molecule coating | |
US20090061517A1 (en) | Cell culture apparatus and methods of making and using same | |
JP2023019942A (en) | Cell culture substrate and cell culture method | |
Qian | Defining the mechanism by which synthetic polymer surfaces support human pluripotent stem cell self-renewal | |
Brafman | High-content array based screening technology for the identification of factors that regulate cell fate | |
Bigdeli | To my grandfather |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 201080045014.5 Country of ref document: CN |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 10820906 Country of ref document: EP Kind code of ref document: A1 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2772248 Country of ref document: CA |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1891/DELNP/2012 Country of ref document: IN |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2012532045 Country of ref document: JP |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2010820906 Country of ref document: EP |