DK1740945T3 - Kke-invasive, in-vitro funktionele vævspøvesystemer - Google Patents
Kke-invasive, in-vitro funktionele vævspøvesystemer Download PDFInfo
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- DK1740945T3 DK1740945T3 DK05730755.5T DK05730755T DK1740945T3 DK 1740945 T3 DK1740945 T3 DK 1740945T3 DK 05730755 T DK05730755 T DK 05730755T DK 1740945 T3 DK1740945 T3 DK 1740945T3
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- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
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- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/483—Physical analysis of biological material
- G01N33/4833—Physical analysis of biological material of solid biological material, e.g. tissue samples, cell cultures
- G01N33/4836—Physical analysis of biological material of solid biological material, e.g. tissue samples, cell cultures using multielectrode arrays
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- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
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- G01N33/5014—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics for testing toxicity
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- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
- G01N33/5008—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics
- G01N33/502—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics for testing non-proliferative effects
- G01N33/5023—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics for testing non-proliferative effects on expression patterns
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- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
- G01N33/5008—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics
- G01N33/5044—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics involving specific cell types
- G01N33/5058—Neurological cells
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
- G01N33/5008—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics
- G01N33/5044—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics involving specific cell types
- G01N33/5073—Stem cells
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
- G01N33/5008—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics
- G01N33/5082—Supracellular entities, e.g. tissue, organisms
- G01N33/5088—Supracellular entities, e.g. tissue, organisms of vertebrates
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- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/543—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals
- G01N33/54366—Apparatus specially adapted for solid-phase testing
- G01N33/54373—Apparatus specially adapted for solid-phase testing involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings
- G01N33/5438—Electrodes
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2800/00—Detection or diagnosis of diseases
- G01N2800/52—Predicting or monitoring the response to treatment, e.g. for selection of therapy based on assay results in personalised medicine; Prognosis
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- Micro-Organisms Or Cultivation Processes Thereof (AREA)
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Claims (19)
1. Funktionel in-vitro-celle- og vævsassayfremgangsmåde til at tilvejebringe og / eller at profilere en forbindelse af interesse, der omfatter: (a) at dyrke et biologisk materiale omfattende celler, et celleaggregat, væv eller et organ på et elektrodearray; (b) at underkaste det biologiske materiale for et teststof; og (c) at måle elektrisk aktivitet af det biologiske materiale gennem elek-trodearrayet og at analysere en eller alle af de følgende parametre: (i) Na+-kanaler; (ii) Ca2+-/ K+-kanaler; (iii) K+-kanaler; (iv) amplitude og / eller feltpotentialevarighed (FDP); (v) hjertecellekronotropi eller nervecellers affyringsperioder; (vi) arytmier, EAD-lignende fænomener; (vii) pH-værdi (viii) partialtryk af ilt (pO2); (ix) slagstop og / eller (x) analyse af AV-dissociationskontraktilitet, NO-virkninger og / eller morfologiske ændringer; hvor cellerne, celleaggregatet, vævet og organet tilvejebringes fra stamceller, der er genetisk forandret, til at omfatte en selekterbar markør, der er operativt forbundet til en første celletypespecifik regulatorisk sekvens, der er specifik for den første celletype og differentieret og udtømt af forholdsvis udifferentierede celler og / eller uønskede celletyper ved anvendelse af et selektionssystem, der er dødeligt for de uønskede celler og celletyper ved at udtrykke et selekterbart markørgen, der gør celler af specifik celletyper resistente over for den dødelige effekt.
2. Assay ifølge krav 1, hvor stamcellerne er embryonale stamceller (ES).
3. Assay ifølge krav 2, hvor det biologiske materiale er væv eller vævlignende strukturer tilvejebragt ved dyrkning af en ES afledt første celle- type, under tilstedeværelse af mindst en embryonisk anden celletype.
4. Assay ifølge ethvert af kravene 1 til 3, hvor den selekterbare markør giver resistens overfor puromycin, neomycin eller hygromycin.
5. Assay ifølge ethvert af kravene 3 til 4, hvor den embryonale stamcelle af den første celletype af embryonale stamceller yderligere omfatter et reportergen, der er operativt forbundet med en celletypespecifik regulatorisk sekvens, der er specifik for den første celletype.
6. Assay ifølge krav 5, hvor den celletypespecifikke regulatoriske sekvens af reportergenet er i det væsentlige den samme som den første celletypespecifikke regulatoriske sekvens af markørgenet.
7. Assay ifølge ethvert af kravene 1 til 6, hvor det biologiske materiale omfatter kardiomyocytter.
8. Assay ifølge ethvert af kravene 1 til 7, hvor celleaggregaterne er embryoide legemer (EB’er).
9. Assay ifølge ethvert af kravene 1 til 8, hvor elektrodearrayet er et multi- eller mikroelektrodearray (MEA).
10. Assay ifølge ethvert af kravene 1 til 9, hvor elektrodearrayet er overtrukket med fibronectin.
11. Assay ifølge ethvert af kravene 1 til 10, hvor mindst kronotropi af hjerteceller eller AV-dissociationskontraktilitet analyseres.
12. Assay ifølge ethvert af kravene 1 til 11, hvor det biologiske materiale omfatter embryoide legemer (EB’er), hvor EB'erne består af funktionelt hjertevæv, der bevæger sig autonomt og dækker elektrofysiologiske egenskaber af atrielle og / eller ventrikulære kardiomyocytter, såvel som af pacemakerceller.
13. Assay ifølge ethvert af kravene 1 til 12, hvor det biologiske materiale helt eller delvist er afledt af en murin ES-cellelinie.
14. Assay ifølge ethvert af kravene 1 til 13, hvor det biologiske materiale omfatter en eller flere celler, der er genetisk manipuleret til at (over)udtrykke eller inhibere udtryk af et målgen.
15. Assay ifølge ethvert af kravene 1 til 14, hvor en forbindelse kendt for at aktivere eller inhibere fremgangsmåde til differentiering og / eller vævs strukturdannelse er tilsat til dyrkningsmediet.
16. Anvendelse af et kit til at udføre en assay ifølge ethvert af kravene 1 til 15, hvor kittet indeholder en vektor eller en sammensætning af vektorer, en multi- eller pluripotent celle; og kulturmedium, rekombinante nukleinsy-remolekyler, array og / eller standardforbindelser.
17. Anvendelse af en chip omfattende et elektrodearray og celler som defineret i ethvert af kravene 1 til 15 til at udføre en assay ifølge ethvert af kravene 1 til 15.
18. Anvendelse af et apparat til analyse af elektrodearrayet i assayen ifølge ethvert af kravene 1 til 15.
19. Anvendelse af stamceller, celleaggregater, et væv, vektor eller sammensætning af vektorer, et array, et apparat eller en chip i en assay ifølge ethvert af kravene 1 til 15.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP04008497 | 2004-04-07 | ||
PCT/EP2005/003662 WO2005098425A1 (en) | 2004-04-07 | 2005-04-07 | Non-invasive, in vitro functional tissue assay systems |
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DK1740945T3 true DK1740945T3 (da) | 2019-01-21 |
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DK05730755.5T DK1740945T3 (da) | 2004-04-07 | 2005-04-07 | Kke-invasive, in-vitro funktionele vævspøvesystemer |
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US (3) | US9945840B2 (da) |
EP (1) | EP1740945B1 (da) |
JP (1) | JP5074921B2 (da) |
CA (1) | CA2560334A1 (da) |
DK (1) | DK1740945T3 (da) |
ES (1) | ES2701704T3 (da) |
WO (1) | WO2005098425A1 (da) |
Families Citing this family (19)
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ES2770067T3 (es) | 2004-05-11 | 2020-06-30 | Ncardia Ag | Descubrimiento de fármacos basado en células diferenciadas in vitro |
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2005
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EP1740945A1 (en) | 2007-01-10 |
US9945840B2 (en) | 2018-04-17 |
US20180299426A1 (en) | 2018-10-18 |
US20080132422A1 (en) | 2008-06-05 |
WO2005098425A1 (en) | 2005-10-20 |
ES2701704T3 (es) | 2019-02-25 |
US11835433B2 (en) | 2023-12-05 |
JP5074921B2 (ja) | 2012-11-14 |
CA2560334A1 (en) | 2005-10-20 |
JP2007532103A (ja) | 2007-11-15 |
US20210025869A1 (en) | 2021-01-28 |
EP1740945B1 (en) | 2018-09-19 |
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