WO1989003876A1 - Procede de production de cellules - Google Patents

Procede de production de cellules Download PDF

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Publication number
WO1989003876A1
WO1989003876A1 PCT/US1988/003737 US8803737W WO8903876A1 WO 1989003876 A1 WO1989003876 A1 WO 1989003876A1 US 8803737 W US8803737 W US 8803737W WO 8903876 A1 WO8903876 A1 WO 8903876A1
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WO
WIPO (PCT)
Prior art keywords
cells
electrically conductive
polymer
polypyrrole
group
Prior art date
Application number
PCT/US1988/003737
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English (en)
Inventor
Barbara Schneider
Original Assignee
Biosyn-R Corporation
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
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Publication of WO1989003876A1 publication Critical patent/WO1989003876A1/fr

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
    • C08G61/122—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
    • C08G61/123—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds
    • 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
    • C12M25/00—Means for supporting, enclosing or fixing the microorganisms, e.g. immunocoatings
    • C12M25/06—Plates; Walls; Drawers; Multilayer plates
    • C12M25/08—Plates; Walls; Drawers; Multilayer plates electrically charged
    • 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
    • C12M35/00—Means for application of stress for stimulating the growth of microorganisms or the generation of fermentation or metabolic products; Means for electroporation or cell fusion
    • C12M35/02—Electrical or electromagnetic means, e.g. for electroporation or for cell fusion
    • 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
    • C12N13/00—Treatment of microorganisms or enzymes with electrical or wave energy, e.g. magnetism, sonic waves

Definitions

  • the present invention relates to a method for stimulating and/or growing cells. More particularly, the invention is concerned with a method for culturing of cells using electrically conductive polymeric material and an electrical current or voltage.
  • fibroblasts on a collagen matrix can be stimulated to grow by passing an electric current through the media in which the fibroblast and collagen preparation is placed.
  • Other workers have shown that cells grown on evaporated gold electrodes may be used as biosensors to monitor cell growth.
  • Any molecule containing a terminal amino group including but not limited to lower alkyl diamines, may be utilized. It is further possible to couple the antibody-linking molecule to a conducting polymer by modifying the polymer to contain a carboxyl group and coupling at the amine and carboxyl groups.
  • the present invention provides a method of culturing cells and promoting cell growth through the utilization of electrical energy which is applied to the support on which the cells are cultivated, to the polymer formed on the cell surface, to the conducting polymer latexes surrounding the cell or ingested by the cell. More particularly, the process relates to the promotion of the proliferation of cells, including the germination of spores of sporulating microorganisms, through the use of electrically conductive mediums and the application of an electrical energy.
  • cells which are cultivated in a nutrient media by anchorage to a support are grown in the present invention by attachment to an electrically conductive film or gel, which is subjected to an electrical current of between about 0.5 microamps to about 1 milliamp.
  • the germination of spores is accelerated by the passage of an electrical charge through an electrically conductive gel or macromolecular material which comes into contact with the spores.
  • the growth of cells is promoted and the cells altered by the application of an electrical charge through the electrically conductive medium upon which the cells are grown or an electrical charge through the media in which the cells are cultivated.
  • the growth of cells is promoted by surrounding the cells with a latex of conducting polymers and the passage of an electrical charge through the latex and to the cell membrane.
  • latex particles of conducting polymers are ingested by the cells and an electrical current is applied so as to stimulate the cells.
  • the conducting polymers are linked to an antibody molecule either by direct polymerization or by a linking group and either oriented on the surface of the membrane or spanning the cell membrane. An electrical current or microwave stimulus is then applied to the polymer.
  • a combination of cells having ingested polymers and/or antibodies attached to the conducting polymers are used to form a battery configuration.
  • the cells which can be used in the process of the present invention may be animal, plant or microorganism.
  • the animal cells include mammalian. avian and amphibian.
  • cells which may be grown in accordance with the invention are various mammalian cells which can be cultured in vitro, particularly tumor cells and hybridomas.
  • the microorganisms include bacteria, fungi and viruses.
  • Cells of fungal origin include aspergillus and rhizopus.
  • Bacterial microorganisms include Bacillus and Clostridium genera.
  • the method of the invention is especially useful in the cultivation of E. Coli and yeast which are used in the production of chemical compounds through biotechnological procedures. That is, not only can naturally occurring microorganisms and cells be employed, but also microorganisms and cells which have been modified by genetic engineering techniques, such as transformation, DNA insertions, transduction, fusion and the like.
  • the invention is especially useful with human diploid cells.
  • the invention is adaptable to all types of animal cells including, for example, mammalian, avian and amphibian cells.
  • Primary cells taken from embryonic, adult or tumor tissues as well as of established cell lines can thus be used. Examples of typical cells are primary rhesus monkey kidney cells, baby hamster kidney cells, pig kidney cells, mouse embryo fibroblasts, normal human lung embryo fibroblasts, HeLa cells, primary and secondary chick fibroblasts, and various cells transformed with SV-40 or polyoma virus. After suitable growth of the cells, the cells can be harvested and further treated for the production of desired products by various means.
  • human diploid foreskin fibroblasts cultured by the method of this invention can be treated for the production of angiogenic factor, plasminogen activator and interferon.
  • Angiogenic factor can be isolated from the growth medium or from the cells.
  • Plas inogen activator can be harvested from a serum- free maintenance medium during a period of aging after the cells have reached their maximum density.
  • Interferon can be induced in the aged fibroblasts and its production enhanced due to the high cell density.
  • Cells can be employed in the present process in which DNA replication is substantially inhibited or terminated, but metabolism continues for relatively long periods of time.
  • the cells continue to express genes, other than the blocked genes involved with DNA replication. Where the cells have been transformed with exogenous genes, these genes will be expressed to provide the desired product.
  • DNA replication By preventing DNA replication, the nutrients are used more efficiently for the functioning of the microbiological reactor.
  • the inhibition of DNA replication can be achieved in a variety of ways, such as chemical inhibitors, temperature sensitive mutants, mutants lacking an intermediate in the biosynthetic pathway to DNA replication, or the like, and the growth facilitated by the present process.
  • the nutrient medium employed will be dependent upon the microorganism or cell involved, and the product desired.
  • the nutrient medium will be adapted to the particular microorganism or cell.
  • other substances may be included to support growth and/or cell differentiation.
  • a natural product such as an excreted protein, e.g., enzymes, hormones, lymphokines, toxins, immunoglobulins, or the like or a non-proteinaceous organic compound resulting from transformation of a substrate, such as by expoxidation, hydroxylation, esterification, e.g, acetate, phosphate, uronate, or sulfate, reduction, methylation, etherification with sugars or the like, may be added.
  • the sporulating microorganisms may be cultivated in accordance with the invention utilizing standard fermentation techniques and physiological germinants together with the passage of electrical energy through the conductive support according to the present invention.
  • the physiological germinants that may be used in the practice of this invention include sugars, amino acids and nucleosides. Examples of sugars include glucose, maltose, lactose and sucrose.
  • amino acids examples include tyrosine, L-alanine, DL-valine, DL-cysteine, methionine, glutamic acid, L- arginine, L-phenylalanine, L-leucine, L-tryptophane, aspartic acid, glycine, lysine, L-isoleucine, histidine, serine, threonine and proline.
  • nucleosides include inosine, guanosine and adenosine. Glucose, L-alanine and inosine are preferred.
  • Some of these physiological germinants are more specific for germinating certain spores and, depending on the spore to be germinated, faster times for the germination phase are obtained.
  • the spores of B. subtilis and B. stearothermophilus are germinated faster employing glucose or L-alanine or a combination thereof.
  • a faster germination time is obtained employing the physiological germinant inosine.
  • the amount of the physiological germinant utilized according to this invention will depend, to some extent, upon the particular germinant and the spores to be germinated.
  • An effective concentration of the physiological germinant is at least .001 mg per 10 3 to 10 9 spores. In most instances, it was found that an amount below .001 mg does not sufficiently decrease the time required for the germination phase. Generally, the preferred range is from about 0.01 mg to about 10 mg per 10 3 to 10 9 spores.
  • the physiological germinants may be used in amounts above 10 mg, for example 25 mg, usually it is without commensurate advantage. In the case of L-alanine, for example, an amount of about 2 to about 5 milligrams/10 3 to about 10 9 is especially preferred.
  • the electrically conductive materials which may be utilized in the present invention are the natural and synthetic polymers, including gums, which are normally utilized in the cultivation of cells that are electrically conductive or have been made electrically conductive by incorporation or intercalation of other polymers or materials.
  • the aforementioned article of Qian, et al. discloses such materials and how the material can be made electrically conductive.
  • One way of preparing conductive polymers is by polymerizing in situ acetylene, pyrrole, or thiophene in a flexible matrix as described by Qian, et al.
  • Molecular composites with polyacetylene, polypyrrole, polythiophene, polystyrene, and the like may be prepared with nylon, polyvinyl chloride, polyvinyl alcohol, pplyvinyl acetate, polyvinyl butyral, polyethylene glycol, gelatin, collagen, guar gum, elastin, glycoproteins, carotenoids, hem-ins, diazobenzyloxymethyl, nitrocellulose, paper, and the like.
  • the following examples are illustrative of the present invention. It will be apparent to those skilled in the art that many modifications, both of materials and methods, can be made without departing from the spirit and scope of the invention.
  • a polysaccharide matrix, cellulose dialysis membrane, is suspended in a solution prepared by dissolving approximately 5.4 ml of pyrrole in 200 ml of 0.10 M NaCl.
  • the duration of the suspension (from seconds to days) and the temperature of the solution (from Ox to 20xC) do not significantly affect the subsequent formation of the conducting polymer film.
  • the oxidizing solution is prepared by dissolving 4.6 g of ammonium persulfate, (NH4)2S2 ⁇ g, in 200 ml of 0.10 M NaCl.
  • the oxidizing solution is then added to the solution containing the monomer and the matrix. Over a period of several seconds (less than 1 minute) , the solution changes color from clear to aqua to black.
  • the oxidizing solution is prepared by dissolving 11.5 g of ammonium persulfate, (NH4) 2 S 2 0 8 , in 200 ml of 1.0 M HC1. The oxidizing solution is then added to the solution containing the monomer and the matrix. Over a period of several seconds (less than 1 minute) , the solution changes color from clear to aqua to green.
  • the cellulose matrix is removed and washed with copious quantities of 1.0 M HC1.
  • the wash process removes excess conducting polymer from the conducting polymer film. Loosely adhering polyaniline and electrolyte are further removed by gently wiping the film. The resulting material is allowed to dry.
  • the conductivity is between- 0.1 to 1 S/cm. The stability of this material can be increased by exposure to base. This polymer has been used for growing fungal microorganisms.
  • PVA polyvinyl alcohol
  • Aldrich #18,966-a average molecular wt 88,000 was dissolved in 200 ml of 0.1 M NaCl and then heated to 65xC.
  • PVA polyvinyl alcohol
  • the solution was cooled to room temperature, after which 10.8 ml of pyrrole was added while stirring the solution.
  • the solution was left ⁇ overnight at 4xC.
  • a 200 ml portion of 0.2 M ammonium persulfate cooled to 4xC was added slowly to the PVA/pyrrole solution with stirring. The color of the solution turned from light green to dark green to dark brown and was left stirring for 15-30 minutes at room temperature.
  • the solution was then filtered through glass wool.
  • the dark filtrate contained polypyrrole polyvinyl alcohol (grafted) polymer in solution.
  • the filtrate 50 ml was then poured slowly into 1 liter of acetonitrile on a large dish (depth of solvent was 1-1.5 cm) and left undisturbed for 1-2 hours.
  • the casting of polymer on the organic solvent resulted in thin film of the polymer (black in color) .
  • the solvent was discarded and the black film was washed three times with 100 ml acetonitrile and dried.
  • Lower molecular weight PVA (mol. wt. 2000) was polymerized in the same fashion to yield similar results.
  • the resistance when measured by a two prong probe, in a polymer sample approximately one cm long, was 0.08 - 0.1 k ohms.
  • conductive polymers comprising polystyrene-pyrrole, polyvinylbutyral-pyrrole, polyethylene-pyrrole and polypropylene-pyrrole.
  • Hexachlorocyclotriphosphazene (phosphonitrillic chloride trimer) (NPC1 2 )3 obtained from Aldrich produced a high molecular weight dichlorophosphazene polymer when heated at 250xC. The uncrosslinked polymer was then dissolved in a suitable organic solvent that also dissolved polypyrrole. Upon reacting, the highly reactive dichlorophosphazene polymer generated a grafted polymer.
  • trimer is reacted with polypyrrole, or the trimer is dissolved in a solvent, to which pyrrole is added, where pyrrole will replace the chloride ion in the trimer.
  • the next step is to polymerize the pyrrole on the phosphazene trimer by adding oxidants such as ammonium persulfate to the solution. After the pyrrole has polymerized on the trimer, the trimer can be heated to form the uncrosslinked polyphosphazene polypyrrole polymer.
  • microgranular cellulose powder (Whatman, cc41, cat #4061 - 050) was suspended in 200 ml of monomer solution (10.8 ml of pyrrole/0.1 M NaCl), overnight at 4xC. The suspension of cellulose powder was then stirred gently for 2 hours, after which 200 ml of 0.2 M ammonium persulfate in 0.1 M NaCl was added in a dropwise manner, with stirring. Stirring was continued for 1 hour, then the powder was washed three times with NaCl (0.1 M) and then several times with water, until the supernatant was free of chloride ions. The aqueous suspension of cellulose was cast in petri dishes (square and circular) and left overnight to dry. The resistance of the cast cellulose was measured by two pin probes attached to a multimeter. The average resistance of the material was between 0.1 to 0.7 k ohms when the probes were placed about 1 to 2 cm apart.
  • Acid soluble collagen (4 mg) from Sigma (type III, acid soluble. No. c-3511) was dissolved in 2 ml of acetic acid (diluted 1: 1000) at 4xC for 48 hours, then spun for 1 hour at 23,000 RPM. To the supernatant, 1/6 volume of 0.1 N NaOH was added (1 ml of supernatant mixed with 166 microliters of NaOH) . A white precipitate resulted. The mixture was centrifuged at 1500 RPM for 20 minutes. The white pellet which formed was then suspended in 1 ml of pyrrole (0.1 M pyrrole in 0.1 M NaCl) solution overnight at 4xC.
  • pyrrole 0.1 M pyrrole in 0.1 M NaCl
  • 0.1 M ammonium persulfate solution in 0.1 M NaCl was added dropwise to the collagen/pyrrole solution, vortexed and left to incubate at 4xC, for 1 hour.
  • the resulting black suspension was centrifuged for 20 minutes at 1500 RPM. The supernatant was discarded, the pellet washed three times with 0.1 M NaCl and then several times with distilled water.
  • 1 ml of (1:1000) acetic acid was added and the mixture was left overnight at 4xC. The suspension was centrifuged for 30 minutes. Unbound polypyrrole and collagen was removed in the supernatant.
  • the collagen/polypyrrole was made into a thin film by dissolving the complex in an ethanol solution then spraying onto a glass surface. The organic solvent vaporized leaving the biomolecule on the surface.
  • SBK saline-bicarbonate-potassium
  • Spreading was assayed as the percentage of cells which ceased to be rounded, and became uniform or polygonal in shape, having distinct corners. Cells which merely increased in size without becoming angular were not regarded as "spread".
  • the percent spread of cells measured in charges per 10 cm 2 square for the control was 0.6.
  • the percent spread of cells for the electrically stimulated cells was 70.
  • Fibroblasts, yeasts, hybridomas, bacteria and fungi can also be grown following this procedure.
  • Late log-phase cultures of HeLa cells growing on plastic dishes were harvested by a 5-min exposure to EGTA (2 mM) and trypsin (0.05%) in PBS, the cells collected by centrifugation at 200 g for 5 in and suspended in MEM containig 10% foetal calf serum.
  • One ml aliquots of this cell suspension were then put into 35 mm plastic tissue culture dishes containing gels of native collagen fibers as a control and the gel of Example 7 to give an initial number of 10 4 cells per dish.
  • the dishes were incubated at 37xC in a humidified C0 2 incubator for 120 minutes.
  • the dish containing the pyrrole-collagen had a current of 0.5 mA constantly delivered through platinum wires connected to conductive posts inserted in the gel.
  • the total cell number was estimated by dissolving the gel with collagenase (Sigma, C-2139, 0.2 mg/ml) in serum-free MEM and counting the cells with a Coulter electronic particle counter. Total cell number and the percentage of cells detached by exposure to trypsin were determined in parallel dishes by a 2-step procedure. First, dishes were washed 3 times with Hanks' balanced salt solution, incubated with trypsin (0.25%) in PBS for 10 min and the number of detached cells counted; the gels were then dissolved by exposure to collagenase and the number of remaining and the number of remaining attached cells determined as above. Total cell, number was estimated by this second procedure by the addition of the number of cells detached by trypsin and those remaining attached to the gel. This figure always agreed within 10% with the total cell number obtained by simple collagenase digestion of the gel. It was observed that in the electrically stimulated dishes cell adhesion was rapid and extensive. Approximately 95% of the cells attached and spread. In the control, attachment was about 70%.
  • a control slant culture of B. stearothermophilus is transferred to 100 ml of nutrient broth in a 500 ml Erlenmeyer flask. The flask is placed on a rotary shaker at 300 RPM for 24 hours. Sterile nutrient agar 100 x 15 mm plates are inoculated with 0.5-1.0 ml of the contents of the flask and held for 7 days at 55xC during which time the organisms sporulate. The spore concentration is 10 8 spores/ml of solution. Bacillus spores were prepared as above except that the 100 x 15 plates were coated with polypyrrole- polyvinyl alcohol following the procedure of Example 3. After a 2 day incubation under a constant potential of 0.8A, the spore concentration was 10 10 spores/ml of solution.
  • Dispersion polymerization reactions were carried out in 500 ml flasks. Initially 0.3 g of PVA plus 8.83 g (0.033 moles) of eCl ⁇ • 6 H 2 0 were dissolved in 100 ml of water. * To this solution was added 1 ml (0.014 moles) of purified pyrrole monomer, and the mixture was stirred magnetically at 20xC for 18-14 h. It was shown in all cases that greater than 95% conversion of monomer was achieved within this time. Within a few seconds of adding the pyrrole to the reaction mixture, the color changed from orange to brown-black, indicative of the onset of polymerization, but no precipitate was formed.
  • the dispersions formed were centrifuged at 15,000 rpm for about 1 h. This led to a black sediment and a pale green, but transparent supernatant. Indeed, it was subsequently shown by visible absorption spectroscopy that the supernatant contained no polypyrrole. The sediment could be readily redispersed by shaking in pure water. The dispersions formed in this way showed no tendency to aggregate on standing. The aqueous dispersions were freeze-dried to yield a fine, black powder.

Abstract

Un procédé de production de cellules dans un milieu consiste à utiliser un matériau électroconducteur en contact avec la cellule et à faire passer une tension ou un courant électrique au travers du matériau électroconducteur en contact avec les cellules.
PCT/US1988/003737 1987-10-21 1988-10-21 Procede de production de cellules WO1989003876A1 (fr)

Applications Claiming Priority (2)

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US11136087A 1987-10-21 1987-10-21
US111,360 1987-10-21

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WO1989003876A1 true WO1989003876A1 (fr) 1989-05-05

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EP (1) EP0382784A4 (fr)
JP (1) JPH03502044A (fr)
WO (1) WO1989003876A1 (fr)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997016545A1 (fr) * 1995-11-03 1997-05-09 Massachusetts Institute Of Technology Stimulation neuronale faisant appel a des polymeres electriquement conducteurs
US5843741A (en) * 1994-08-01 1998-12-01 Massachusetts Insitute Of Technology Method for altering the differentiation of anchorage dependent cells on an electrically conducting polymer
US6190893B1 (en) 1998-09-18 2001-02-20 Massachusetts Institute Of Technology Electroactive materials for stimulation of biological activity of bone marrow stromal cells
WO2002000759A1 (fr) * 2000-06-26 2002-01-03 Agfa-Gevaert Latex redispersible a base de polyothiophene
WO2003000309A2 (fr) * 2001-05-08 2003-01-03 Fidia Advanced Biopolymers S.R.L. Biomateriaux polymeres electriquement conducteurs, procede de fabrication et utilisation de ces biomateriaux dans le domaine biomedical et le domaine des services de sante
WO2003000838A1 (fr) * 2001-06-25 2003-01-03 Hakuju Institute For Health Science Co., Ltd. Dispositif et procede de culture
WO2003038031A1 (fr) * 2001-10-31 2003-05-08 Hakuju Institute For Health Science Co., Ltd. Systeme de culture de cellules et procede de mesure dose-reponse
US6890584B2 (en) 2000-06-28 2005-05-10 Agfa-Gevaert Flexographic ink containing a polymer or copolymer of a 3,4-dialkoxythiophene
US7015034B2 (en) 1996-11-08 2006-03-21 Morphogenesis, Inc. Materials and procedures for the purification of cells
EP2710111A4 (fr) * 2011-05-17 2015-03-25 3Dtro Ab Échafaudage de fibres revêtues pour la culture cellulaire tridimensionnelle de cellules neurales

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JP2005270036A (ja) * 2004-03-25 2005-10-06 Japan Science & Technology Agency 生物活性化方法及び生物活性化組成物
JP7269594B2 (ja) * 2018-09-27 2023-05-09 株式会社村田製作所 細胞分離フィルター及び細胞分離方法

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Cited By (19)

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Publication number Priority date Publication date Assignee Title
US5843741A (en) * 1994-08-01 1998-12-01 Massachusetts Insitute Of Technology Method for altering the differentiation of anchorage dependent cells on an electrically conducting polymer
US6095148A (en) * 1995-11-03 2000-08-01 Children's Medical Center Corporation Neuronal stimulation using electrically conducting polymers
WO1997016545A1 (fr) * 1995-11-03 1997-05-09 Massachusetts Institute Of Technology Stimulation neuronale faisant appel a des polymeres electriquement conducteurs
US7015034B2 (en) 1996-11-08 2006-03-21 Morphogenesis, Inc. Materials and procedures for the purification of cells
US8030069B2 (en) 1996-11-08 2011-10-04 Morphogenesis, Inc. Materials and procedures for the purification of cells
US7598081B2 (en) 1996-11-08 2009-10-06 Morphogenesis, Inc. Materials and procedures for the purification of cells
US6190893B1 (en) 1998-09-18 2001-02-20 Massachusetts Institute Of Technology Electroactive materials for stimulation of biological activity of bone marrow stromal cells
EP1780233A1 (fr) * 2000-06-26 2007-05-02 Agfa-Gevaert Latex rédispergeable comprenant un polythiophène
EP1801143A1 (fr) * 2000-06-26 2007-06-27 Agfa-Gevaert Solutions ou dispersions de revêtement, et encres d'impression comprenant un latex redispersable avec un polythiophène
KR100847904B1 (ko) * 2000-06-26 2008-07-23 아그파-게바에르트 폴리티오펜을 포함하는 재분산성 라텍스
WO2002000759A1 (fr) * 2000-06-26 2002-01-03 Agfa-Gevaert Latex redispersible a base de polyothiophene
US6890584B2 (en) 2000-06-28 2005-05-10 Agfa-Gevaert Flexographic ink containing a polymer or copolymer of a 3,4-dialkoxythiophene
WO2003000309A3 (fr) * 2001-05-08 2003-05-01 Fidia Advanced Biopolymers Srl Biomateriaux polymeres electriquement conducteurs, procede de fabrication et utilisation de ces biomateriaux dans le domaine biomedical et le domaine des services de sante
US7253152B2 (en) 2001-05-08 2007-08-07 Fidia Advanced Biopolymers S.R.L. Electrically conductive polymeric biomaterials, the process for their preparation and the use thereof in the biomedical and healthcare field
WO2003000309A2 (fr) * 2001-05-08 2003-01-03 Fidia Advanced Biopolymers S.R.L. Biomateriaux polymeres electriquement conducteurs, procede de fabrication et utilisation de ces biomateriaux dans le domaine biomedical et le domaine des services de sante
US7081362B2 (en) 2001-06-25 2006-07-25 Hakuju Institute For Health Science Co., Ltd. Device and method for cultivation
WO2003000838A1 (fr) * 2001-06-25 2003-01-03 Hakuju Institute For Health Science Co., Ltd. Dispositif et procede de culture
WO2003038031A1 (fr) * 2001-10-31 2003-05-08 Hakuju Institute For Health Science Co., Ltd. Systeme de culture de cellules et procede de mesure dose-reponse
EP2710111A4 (fr) * 2011-05-17 2015-03-25 3Dtro Ab Échafaudage de fibres revêtues pour la culture cellulaire tridimensionnelle de cellules neurales

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EP0382784A1 (fr) 1990-08-22
EP0382784A4 (en) 1991-01-16
JPH03502044A (ja) 1991-05-16

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