WO2006005808A1 - A method and an apparatus for biological analysis - Google Patents

A method and an apparatus for biological analysis Download PDF

Info

Publication number
WO2006005808A1
WO2006005808A1 PCT/FI2005/050274 FI2005050274W WO2006005808A1 WO 2006005808 A1 WO2006005808 A1 WO 2006005808A1 FI 2005050274 W FI2005050274 W FI 2005050274W WO 2006005808 A1 WO2006005808 A1 WO 2006005808A1
Authority
WO
WIPO (PCT)
Prior art keywords
cells
cell
unit
culture
population
Prior art date
Application number
PCT/FI2005/050274
Other languages
French (fr)
Inventor
Juha Korpinen
Jussi Tarvainen
Timo Ylikomi
Hanna TÄHTI
Jouko Viitanen
Original Assignee
Chip-Man Technologies Oy
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
Application filed by Chip-Man Technologies Oy filed Critical Chip-Man Technologies Oy
Publication of WO2006005808A1 publication Critical patent/WO2006005808A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12MAPPARATUS 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
    • C12M29/00Means for introduction, extraction or recirculation of materials, e.g. pumps
    • C12M29/10Perfusion
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12MAPPARATUS 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
    • C12M41/00Means for regulation, monitoring, measurement or control, e.g. flow regulation
    • C12M41/12Means for regulation, monitoring, measurement or control, e.g. flow regulation of temperature
    • C12M41/14Incubators; Climatic chambers
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12MAPPARATUS 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
    • C12M41/00Means for regulation, monitoring, measurement or control, e.g. flow regulation
    • C12M41/30Means for regulation, monitoring, measurement or control, e.g. flow regulation of concentration
    • C12M41/36Means for regulation, monitoring, measurement or control, e.g. flow regulation of concentration of biomass, e.g. colony counters or by turbidity measurements
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12MAPPARATUS 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
    • C12M41/00Means for regulation, monitoring, measurement or control, e.g. flow regulation
    • C12M41/46Means for regulation, monitoring, measurement or control, e.g. flow regulation of cellular or enzymatic activity or functionality, e.g. cell viability

Definitions

  • the invention relates to a method for biological analysis, utilizing equip ⁇ ment comprising at least a culture unit with controllable conditions, such as a perfusion unit, an incubation unit, or the like, with a substrate arrangement for culturing cells, cell samples and/or a population.
  • the method according to the invention is primar ⁇ ily characterized in that in the method, the parameters to be monitored for the analysis are determined simultaneously for each single cell, cell sample and/or population, including for example the number of cells, the type of cells, the cell division, the time involved in the cell cycle, the death of cells (necrosis, apoptosis), the movement of cells, other mor- phological properties of cells, the cell pedigree and/or the like; and several parameters to be specified are analyzed simultaneously on the basis of the imaging data.
  • the most significant advantages of the method according to the inven ⁇ tion include the simplicity and efficiency of its principle and use, wherein a compact analyzing apparatus functioning according to the method makes it possible to work in a way which is considerably more efficient than conventional analyzing techniques. Thanks to the auto- mation and mechanization of the method, it is possible to reduce the work further to a fraction of that performed today. Furthermore, the number of materials used and chemicals required will be reduced.
  • the method according to the invention also makes it possible to monitor heterogeneous populations by analyzing cells/cell samples and or a cell population/cell populations in substrate arrange ⁇ ments, such as culture sites on a well plate, by a simultaneous analysis of, for example, six predetermined parameters and/or processes to be monitored.
  • the method according to the invention thus makes a fully automatic instrumentation possible, wherein all the functions can be controlled centrally by means of software in a data processing unit.
  • One essential advantage of the method according to the invention also lies in avoiding extra work involved in conventional manual arrange ⁇ ments, particularly in marking.
  • Another essential advantage is the fact that the parameters measured at different time points are measured from the same cells/cell samples and/or population/populations, which reduces fluctuations in the measuring results.
  • the invention also relates to an apparatus functioning according to the method, as defined in more detail in the preamble of the independent claim relating to the apparatus.
  • the primary characteristics of the appa ⁇ ratus will be presented in the characterizing part of the respective claim.
  • the most significant advantages of the apparatus according to the invention include the simplicity and reliability of its assembly and use, as well as the possibility to make the process of biological analysis considerably more efficient for a variety of uses.
  • the efficiency of the apparatus according to the invention is based, first of all, on the imag ⁇ ing arrangement by which the morphological, dynamic, kinematic and/or corresponding changes in the single cells/cell samples making up the heterogeneous population can be analyzed by mechanical imaging at regular intervals. By means of the imaging, it is also possi ⁇ ble to monitor the development of the cells/cell samples as a function of time for the several parameters to be monitored by analyzing the successive imaging data recorded of the cells/cell samples by means of software in the data processing unit of the apparatus.
  • the appa ⁇ ratus further comprises, in an advantageous embodiment, an actuator arrangement which automatically changes the culture medium at regular intervals or, if necessary, adds drugs, chemicals, markers or the like in the substrate arrangements, wherein thanks to mechanical operations, extra work is avoided when changing the culture medium.
  • the invention relates to a method for biological analysis, utilizing equip ⁇ ment comprising at least a culture unit with controllable conditions, such as a perfusion unit, an incubation unit, and/or the like, with a sub ⁇ strate arrangement for culturing cells, cell samples and/or a population.
  • a culture unit with controllable conditions such as a perfusion unit, an incubation unit, and/or the like
  • a sub ⁇ strate arrangement for culturing cells, cell samples and/or a population.
  • Cells, cell samples and/or a population/populations in a substrate arrangement are automatically imaged by means of an imaging unit in connection with the culture unit, after which they are automatically analyzed by a data processing unit in connection with the culture unit, to monitor predetermined parameters individually according to the imaging data.
  • the substrate arrangement comprises several culture sites which are imaged at regular intervals mechanically by means of an imaging arrangement belonging to the culture unit, to detect morphological, dynamic, kinematic, and/or corresponding changes and processes in cells/cell samples constituting a homogeneous or heterogeneous population.
  • the cells are analyzed by monitoring the development of single cells/cell samples in the same population by analyzing successive imaging data on them to observe the develop ⁇ ment as a function of time with respect to the parameters to be moni ⁇ tored.
  • the cells of a het ⁇ erogeneous or homogeneous population are analyzed by analyzing the type and phase of a single cell/cell sample, such as the the cell divi ⁇ sion, the time involved in the cell cycle, the death of cells (necrosis, apoptosis), the movement of cells, or the morphological properties of cells.
  • the cells are ana ⁇ lyzed without a need to select the cells/cell samples manually before- hand.
  • the cells are ana ⁇ lyzed without cell markers.
  • the cells are ana ⁇ lyzed on the basis of the morphology and/or structures of the cells. Furthermore, in another advantageous embodiment, the cell morphol ⁇ ogy and/or structures are taught to the data processing unit.
  • the analysis is con ⁇ trolled by software in a data processing unit which is at least in a data transmission connection with the culture unit and in which the parameters to be monitored simultaneously for each single cell/cell sample are determined in advance, including the number of cells, the type of cells, the cell division, the time involved in the cell cycle, the death of cells (necrosis, apoptosis), the movement of cells, other mor ⁇ phological properties of cells, the cell pedigree and/or the like.
  • the culture medium used in perfusion or incubation is also changed at predeter ⁇ mined intervals automatically by an actuator arrangement in the appa ⁇ ratus.
  • drugs, chemicals, cell markers and/or the like are advanta- geously added by the actuator arrangement into the substrate arrangement, such as the culture medium, after which the area of each cell/cell sample to be examined at a time is defined again for the imaging arrangement, if necessary.
  • the substrate arrange ⁇ ment used is one or more well plates consisting of wells including sev ⁇ eral culture sites.
  • the invention also relates to an apparatus applying the method and comprising, first of all, a culture unit with controllable conditions, such as a perfusion unit, an incubation unit, or the like, with a substrate arrangement for culturing cells, cell samples and/or a population.
  • the apparatus comprises, in connection with the culture unit, an imaging unit for imaging the cells, cell samples and/or a population/populations in the substrate arrangement at predetermined intervals by an imaging arrangement therein.
  • the apparatus comprises a data processing unit which is at least in a data transmission connection with the culture unit and in which the parameters to be monitored simulta- neously for each single cell, cell sample and/or cell population/cell populations have been determined in advance, including the number of cells, the type of cells, the cell division, the time involved in the cell cycle, the death of cells (necrosis, apoptosis), the movement of cells, other morphological properties of cells, the cell pedigree and/or the like.
  • the apparatus com ⁇ prises an actuator arrangement for changing the culture medium used for incubation and/or perfusion and/or for adding drugs, chemicals, cell markers and/or the like into the substrate in the substrate arrangement, such as one or more well plates consisting of wells comprising several culture sites, automatically at predetermined intervals.
  • the invention is not limited to the applications pre- sented or explained above, but it can be modified within the scope of the basic idea of the invention according to each use. It is thus possible to use, firstly instead of well plates as the substrate arrangement, other types of constructions from which the cells/cell samples can be imaged in an unobstructed way.
  • the machine vision of the imaging arrange- ment can also be implemented by various digital imaging/video arrangements by using a variety of techniques for generating the images as such.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Zoology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Microbiology (AREA)
  • General Engineering & Computer Science (AREA)
  • Genetics & Genomics (AREA)
  • Sustainable Development (AREA)
  • Biomedical Technology (AREA)
  • General Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • Analytical Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Cell Biology (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Apparatus Associated With Microorganisms And Enzymes (AREA)

Abstract

A method for biological analysis, utilizing equipment comprising at least a culture unit with controllable conditions, comprising a substrate arrangement for culturing cells, cell samples and/or a population. Cells, cell samples and/or a population/populations in the substrate arrangement are imaged automatically by means of an imaging unit in connection with the culture unit, after which they are analyzed automatically by a data processing unit in connection with the culture unit, to monitor predetermined parameters individually according to the imaging data. The invention also relates to an apparatus for applying the method.

Description

A method and an apparatus for biological analysis
Field of the invention
The invention relates to a method for biological analysis, utilizing equip¬ ment comprising at least a culture unit with controllable conditions, such as a perfusion unit, an incubation unit, or the like, with a substrate arrangement for culturing cells, cell samples and/or a population.
Background of the invention
At present, the monitoring of cells and possible other measures on them are always performed manually. Firstly, this has the result that a so-called individual monitoring and analysis of cells is not carried out in a larger population, unless a cell marker is used. However, the use of a cell marker involves additional steps, thereby increasing the quantity of manual work needed. On the other hand, homogeneous cell popula¬ tions are normally used, because cell markers affect not only the desired target cell but all cells in the cell population. Consequently, when heterogeneous cell populations are used, it is difficult to deter¬ mine what type of cells are marked with the cell marker. Furthermore, the cell markers used may be detrimental to the cells as such, or may cause distorted measurement results in another way.
Description of the invention
It is an aim of the method according to the present invention to provide a decisive improvement to the above-presented problems and thereby to substantially improve the state of art in the field.
To attain this purpose, the method according to the invention is primar¬ ily characterized in that in the method, the parameters to be monitored for the analysis are determined simultaneously for each single cell, cell sample and/or population, including for example the number of cells, the type of cells, the cell division, the time involved in the cell cycle, the death of cells (necrosis, apoptosis), the movement of cells, other mor- phological properties of cells, the cell pedigree and/or the like; and several parameters to be specified are analyzed simultaneously on the basis of the imaging data.
The most significant advantages of the method according to the inven¬ tion include the simplicity and efficiency of its principle and use, wherein a compact analyzing apparatus functioning according to the method makes it possible to work in a way which is considerably more efficient than conventional analyzing techniques. Thanks to the auto- mation and mechanization of the method, it is possible to reduce the work further to a fraction of that performed today. Furthermore, the number of materials used and chemicals required will be reduced. On the other hand, the method according to the invention also makes it possible to monitor heterogeneous populations by analyzing cells/cell samples and or a cell population/cell populations in substrate arrange¬ ments, such as culture sites on a well plate, by a simultaneous analysis of, for example, six predetermined parameters and/or processes to be monitored. This can be implemented by using an imaging arrangement in the culture unit, by recording the cells/cell samples and/or a cell population/cell populations in the substrate arrangements mechanically and systematically at regular intervals to detect morphological, dynamic, kinematic and/or corresponding changes and/or processes therein. The method according to the invention thus makes a fully automatic instrumentation possible, wherein all the functions can be controlled centrally by means of software in a data processing unit. One essential advantage of the method according to the invention also lies in avoiding extra work involved in conventional manual arrange¬ ments, particularly in marking. Another essential advantage is the fact that the parameters measured at different time points are measured from the same cells/cell samples and/or population/populations, which reduces fluctuations in the measuring results.
Advantageous embodiments of the method according to the invention will be presented in the respective dependent claims. The invention also relates to an apparatus functioning according to the method, as defined in more detail in the preamble of the independent claim relating to the apparatus. The primary characteristics of the appa¬ ratus will be presented in the characterizing part of the respective claim.
The most significant advantages of the apparatus according to the invention include the simplicity and reliability of its assembly and use, as well as the possibility to make the process of biological analysis considerably more efficient for a variety of uses. The efficiency of the apparatus according to the invention is based, first of all, on the imag¬ ing arrangement by which the morphological, dynamic, kinematic and/or corresponding changes in the single cells/cell samples making up the heterogeneous population can be analyzed by mechanical imaging at regular intervals. By means of the imaging, it is also possi¬ ble to monitor the development of the cells/cell samples as a function of time for the several parameters to be monitored by analyzing the successive imaging data recorded of the cells/cell samples by means of software in the data processing unit of the apparatus. Thus, by means of the apparatus according to the invention, it is possible to automatically perform all the functions relating to culturing, imaging and analysis in such a way that the risks and disadvantages related to con¬ ventional manual operations can be avoided. In this respect, the appa¬ ratus further comprises, in an advantageous embodiment, an actuator arrangement which automatically changes the culture medium at regular intervals or, if necessary, adds drugs, chemicals, markers or the like in the substrate arrangements, wherein thanks to mechanical operations, extra work is avoided when changing the culture medium.
Advantageous embodiments of the apparatus according to the inven¬ tion will be presented in the respective dependent claims.
The invention relates to a method for biological analysis, utilizing equip¬ ment comprising at least a culture unit with controllable conditions, such as a perfusion unit, an incubation unit, and/or the like, with a sub¬ strate arrangement for culturing cells, cell samples and/or a population. Cells, cell samples and/or a population/populations in a substrate arrangement are automatically imaged by means of an imaging unit in connection with the culture unit, after which they are automatically analyzed by a data processing unit in connection with the culture unit, to monitor predetermined parameters individually according to the imaging data.
The substrate arrangement comprises several culture sites which are imaged at regular intervals mechanically by means of an imaging arrangement belonging to the culture unit, to detect morphological, dynamic, kinematic, and/or corresponding changes and processes in cells/cell samples constituting a homogeneous or heterogeneous population.
In an advantageous embodiment, the cells are analyzed by monitoring the development of single cells/cell samples in the same population by analyzing successive imaging data on them to observe the develop¬ ment as a function of time with respect to the parameters to be moni¬ tored.
Furthermore, in another advantageous embodiment, the cells of a het¬ erogeneous or homogeneous population are analyzed by analyzing the type and phase of a single cell/cell sample, such as the the cell divi¬ sion, the time involved in the cell cycle, the death of cells (necrosis, apoptosis), the movement of cells, or the morphological properties of cells.
Furthermore, in another advantageous embodiment, the cells are ana¬ lyzed without a need to select the cells/cell samples manually before- hand.
Furthermore, in another advantageous embodiment, the cells are ana¬ lyzed without cell markers.
Furthermore, in another advantageous embodiment, the cells are ana¬ lyzed on the basis of the morphology and/or structures of the cells. Furthermore, in another advantageous embodiment, the cell morphol¬ ogy and/or structures are taught to the data processing unit.
Further, in another advantageous embodiment, the analysis is con¬ trolled by software in a data processing unit which is at least in a data transmission connection with the culture unit and in which the parameters to be monitored simultaneously for each single cell/cell sample are determined in advance, including the number of cells, the type of cells, the cell division, the time involved in the cell cycle, the death of cells (necrosis, apoptosis), the movement of cells, other mor¬ phological properties of cells, the cell pedigree and/or the like.
Furthermore, in an advantageous embodiment in practice, the culture medium used in perfusion or incubation is also changed at predeter¬ mined intervals automatically by an actuator arrangement in the appa¬ ratus.
Moreover, drugs, chemicals, cell markers and/or the like are advanta- geously added by the actuator arrangement into the substrate arrangement, such as the culture medium, after which the area of each cell/cell sample to be examined at a time is defined again for the imaging arrangement, if necessary.
Furthermore, in an advantageous embodiment, the substrate arrange¬ ment used is one or more well plates consisting of wells including sev¬ eral culture sites.
The invention also relates to an apparatus applying the method and comprising, first of all, a culture unit with controllable conditions, such as a perfusion unit, an incubation unit, or the like, with a substrate arrangement for culturing cells, cell samples and/or a population. The apparatus comprises, in connection with the culture unit, an imaging unit for imaging the cells, cell samples and/or a population/populations in the substrate arrangement at predetermined intervals by an imaging arrangement therein. In an advantageous embodiment, the apparatus comprises a data processing unit which is at least in a data transmission connection with the culture unit and in which the parameters to be monitored simulta- neously for each single cell, cell sample and/or cell population/cell populations have been determined in advance, including the number of cells, the type of cells, the cell division, the time involved in the cell cycle, the death of cells (necrosis, apoptosis), the movement of cells, other morphological properties of cells, the cell pedigree and/or the like.
Furthermore, in an advantageous embodiment, the apparatus com¬ prises an actuator arrangement for changing the culture medium used for incubation and/or perfusion and/or for adding drugs, chemicals, cell markers and/or the like into the substrate in the substrate arrangement, such as one or more well plates consisting of wells comprising several culture sites, automatically at predetermined intervals.
It is obvious that the invention is not limited to the applications pre- sented or explained above, but it can be modified within the scope of the basic idea of the invention according to each use. It is thus possible to use, firstly instead of well plates as the substrate arrangement, other types of constructions from which the cells/cell samples can be imaged in an unobstructed way. The machine vision of the imaging arrange- ment can also be implemented by various digital imaging/video arrangements by using a variety of techniques for generating the images as such.

Claims

Claims:
1. A method for biological analysis, utilizing equipment comprising at least a culture unit with controllable conditions, such as a perfusion unit, an incubation unit, and/or the like, with a substrate arrangement for culturing cells, cell samples and/or a population, comprising the steps of
- imaging cells, cell samples and/or a population/populations in the substrate arrangement by means of an imaging unit connected to the culture unit,
- analyzing the cells, cell samples and/or population/populations automatically by a data processing unit connected to the culture unit, characterized in - determining, for the analysis, the parameters to be monitored simultaneously for each single cell, cell sample and/or population, such as, for example, the number of cells, the type of cells, the cell division, the time involved in the cell cycle, the death of cells (necrosis, apoptosis), the movement of cells, other morphological properties of cells, the cell pedigree and/or the like,
- analyzing several parameters to be specified simultaneously on the basis of the imaging data.
2. The method according to claim 1 , characterized in that the sub¬ strate arrangement comprises several culture sites which are imaged at regular intervals mechanically by means of an imaging unit belong¬ ing to the culture unit, to detect morphological, dynamic, kinematic, and/or corresponding changes in the cells/cell samples constituting a homogeneous or heterogeneous population.
3. The method according to claim 1 or 2, characterized in that the cells are analyzed by monitoring the development of single cells/cell samples of the same population by analyzing successive imaging data on them, to observe the development as a function of time with respect to the parameters to be monitored.
4. The method according to any of the preceding claims 1 to 3, charac¬ terized in that the analysis is carried out by using software in a data processing unit which is at least in a data transmission connection with the culture unit and in which software the parameters to be monitored simultaneously for each single cell/cell sample are determined in advance, including the number of cells, the type of cells, the cell divi¬ sion, the time involved in the cell cycle, the death of cells (necrosis, apoptosis), the movement of cells, the morphological properties of cells, the cell pedigree and/or the like.
5. The method according to any of the preceding claims 1 to 4, charac¬ terized in that the analysis is made of cells of a heterogeneous or homogeneous population by analyzing the type and phase of a single cell/cell sample, such as the the cell division, the time involved in the cell cycle, the death of cells (necrosis, apoptosis), the movement of cells, or the morphological properties of cells.
6. The method according to any of the preceding claims 1 to 5, charac- terized in that the analysis is carried out without needing to select the cells/cell samples manually in advance.
7. The method according to any of the preceding claims 1 to 6, charac¬ terized in that the analysis is made without cell markers.
8. The method according to any of the preceding claims 1 to 7, charac¬ terized in that the analysis is made on the basis of the morphology and/or structures of the cells.
9. The method according to any of the preceding claims 1 to 8, charac¬ terized in that the morphology and/or structures of the cells/cell sam¬ ples are taught to a data processing unit.
10. The method according to any of the preceding claims 1 to 9, char- acterized in that the culture medium used in incubation or perfusion is automatically changed at predetermined intervals by an actuator arrangement in the apparatus.
11. The method according to claim 10, characterized in that drugs, chemicals, cell markers, and/or the like are added by an actuator arrangement into the substrate arrangement, such as the culture medium, after which the area of each cell/cell sample to be examined at each time is defined again for the imaging arrangement, if neces¬ sary.
12. The method according to any of the preceding claims 1 to 11 , char¬ acterized in that the substrate arrangement used is one or more well plates consisting of wells comprising several culture sites.
13. An apparatus for biological analysis, comprising at least
- a culture unit with controllable conditions, such as a perfusion unit, an incubation unit or the like, with a substrate arrangement for the culture of cells, cell samples and/or a population, - an imaging unit in connection with the culture unit, for imaging the cells, cell samples and/or a population/populations in the substrate arrangement at predetermined intervals auto¬ matically by an imaging arrangement therein, characterized in that the apparatus also comprises a data processing unit which is at least in a data transmission connection with the imaging unit and which comprises a software to be run therein, the software comprising computer executable instructions adapted to define and analyze, on the basis of the imaging data, the parameters to be moni¬ tored simultaneously for each single cell, cell sample and/or cell popu- lation/cell populations, such as, for example, the number of cells, the type of cells, the cell division, the time involved in the cell cycle, the death of cells (necrosis, apoptosis), the movement of cells, other mor¬ phological properties of cells, the cell pedigree and/or the like.
14. The apparatus according to claim 13, characterized in that the software also comprises the parameters to be monitored simultane¬ ously for each single cell/cell sample.
15. The apparatus according to claim 14 or 15, characterized in that the apparatus comprises an actuator arrangement for changing the culture medium used for incubation and/or perfusion and/or for adding drugs, chemicals, cell markers and/or the like into the substrate in the substrate arrangement, such as one or more well plates consisting of wells comprising several culture sites, automatically at predetermined intervals.
PCT/FI2005/050274 2004-07-09 2005-07-08 A method and an apparatus for biological analysis WO2006005808A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FI20040958A FI20040958A (en) 2004-07-09 2004-07-09 Method and apparatus for biological analysis
FI20040958 2004-07-09

Publications (1)

Publication Number Publication Date
WO2006005808A1 true WO2006005808A1 (en) 2006-01-19

Family

ID=32749178

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/FI2005/050274 WO2006005808A1 (en) 2004-07-09 2005-07-08 A method and an apparatus for biological analysis

Country Status (2)

Country Link
FI (1) FI20040958A (en)
WO (1) WO2006005808A1 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006119860A1 (en) * 2005-05-06 2006-11-16 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Cell culture system and method of cultivating a cell culture
EP2202291A1 (en) * 2007-09-03 2010-06-30 Nikon Corporation Culture apparatus, culture information management method, and program
US9550970B2 (en) 2010-02-17 2017-01-24 Inq Biosciences Corporation Culture systems, apparatus, and related methods and articles
US10074199B2 (en) 2013-06-27 2018-09-11 Tractus Corporation Systems and methods for tissue mapping

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20010041347A1 (en) * 1999-12-09 2001-11-15 Paul Sammak System for cell-based screening
WO2001094528A2 (en) * 2000-06-08 2001-12-13 The Regents Of The University Of California Visual-servoing optical microscopy
US20030082818A1 (en) * 2001-07-12 2003-05-01 Automated Cell, Inc. Method and apparatus for monitoring of proteins and cells
US20030103662A1 (en) * 2001-12-05 2003-06-05 Finkbeiner Steven M. Robotic microscopy systems
US20030228565A1 (en) * 2000-04-26 2003-12-11 Cytokinetics, Inc. Method and apparatus for predictive cellular bioinformatics
WO2004088574A1 (en) * 2003-04-02 2004-10-14 Amersham Biosciences Uk Limited Method of, and computer software for, classification of cells into subpopulations
WO2005009126A1 (en) * 2003-07-23 2005-02-03 Essen Instruments, Inc. Examination systems for biological samples

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20010041347A1 (en) * 1999-12-09 2001-11-15 Paul Sammak System for cell-based screening
US20030228565A1 (en) * 2000-04-26 2003-12-11 Cytokinetics, Inc. Method and apparatus for predictive cellular bioinformatics
WO2001094528A2 (en) * 2000-06-08 2001-12-13 The Regents Of The University Of California Visual-servoing optical microscopy
US20030082818A1 (en) * 2001-07-12 2003-05-01 Automated Cell, Inc. Method and apparatus for monitoring of proteins and cells
US20030103662A1 (en) * 2001-12-05 2003-06-05 Finkbeiner Steven M. Robotic microscopy systems
WO2004088574A1 (en) * 2003-04-02 2004-10-14 Amersham Biosciences Uk Limited Method of, and computer software for, classification of cells into subpopulations
WO2005009126A1 (en) * 2003-07-23 2005-02-03 Essen Instruments, Inc. Examination systems for biological samples

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006119860A1 (en) * 2005-05-06 2006-11-16 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Cell culture system and method of cultivating a cell culture
EP2202291A1 (en) * 2007-09-03 2010-06-30 Nikon Corporation Culture apparatus, culture information management method, and program
JPWO2009031283A1 (en) * 2007-09-03 2010-12-09 株式会社ニコン CULTURE DEVICE, CULTURE INFORMATION MANAGEMENT METHOD, AND PROGRAM
EP2202291A4 (en) * 2007-09-03 2012-03-07 Nikon Corp Culture apparatus, culture information management method, and program
US8478008B2 (en) 2007-09-03 2013-07-02 Nikon Corporation Culture apparatus, culture information management method, and computer readable medium storing program of same
US9550970B2 (en) 2010-02-17 2017-01-24 Inq Biosciences Corporation Culture systems, apparatus, and related methods and articles
US10074199B2 (en) 2013-06-27 2018-09-11 Tractus Corporation Systems and methods for tissue mapping

Also Published As

Publication number Publication date
FI20040958A (en) 2006-01-10
FI20040958A0 (en) 2004-07-09

Similar Documents

Publication Publication Date Title
Feng et al. Multi-parameter phenotypic profiling: using cellular effects to characterize small-molecule compounds
DE69733663T2 (en) ANALYTICAL SYSTEM AND METHOD
Maecker et al. A model for harmonizing flow cytometry in clinical trials
Sukardi et al. Zebrafish for drug toxicity screening: bridging the in vitro cell-based models and in vivo mammalian models
WO2006005808A1 (en) A method and an apparatus for biological analysis
CN101408862A (en) Embedded system test method
BR0212125A (en) Methods for diagnosing disease, diagnosing malignancy, screening for malignancy, and monitoring malignancy in an individual under test and kit for examining a biological specimen for the presence of malignant cells, malignant cell-derived cell debris or malignant cell-derived cell debris
DE19654135A1 (en) LED printhead and driver circuit for use therewith, with a structure for carrying out "boundary scan test"
EP1229334A3 (en) Quality control mechanism and process for a biofluid multi-ejector system
WO2005031313A1 (en) Device and method for automatically carrying out laboratory procedure steps
Carson et al. A method for automated detection of gene expression required for the establishment of a digital transcriptome‐wide gene expression atlas
Kolesnik et al. Image analysis system for quantitative immunofluorescence measurement
Pargett et al. Live‐Cell Imaging and Analysis with Multiple Genetically Encoded Reporters
Trumbull et al. High throughput electrophysiology using a fully automated, multiplexed recording system
US20190185805A1 (en) Automated electroporation of single cells in micro-well plates
DE60317330T2 (en) SYSTEMS AND METHOD FOR DETECTING THE FUNCTION OF NUCLEAR RECEPTORS USING REPORTER CYMMUTANTS COMPLEMENTATIONS
Francois et al. DNA microarrays for detecting endocrine-disrupting compounds
CN102175281B (en) Method and system for testing multi-mode apparatus
EP1148330A3 (en) Organism-specimen morphological-change detecting apparatus, and organism-specimen morphological-change detecting method
Kardos The FocalPoint system: FocalPoint slide profiler and FocalPoint GS
CN110334729A (en) Testing instruments automatic alarm notifies system
Shieh et al. Automated Parallel Oocyte Electrophysiology Test station (POETs™): a screening platform for identification of ligand-gated ion channel modulators
US20080206855A1 (en) Automated Compound Screening Using Gel-Permeation Matrix and Pin-Based Sample Transfer
US20140329716A1 (en) Devices having a calibration control region, systems and methods for immunohistochemical analyses
JP5301234B2 (en) Large-scale collection of protein samples

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KM KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NG NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SM SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): BW GH GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LT LU LV MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

DPEN Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed from 20040101)
121 Ep: the epo has been informed by wipo that ep was designated in this application
NENP Non-entry into the national phase

Ref country code: DE

WWW Wipo information: withdrawn in national office

Country of ref document: DE

122 Ep: pct application non-entry in european phase