SE2050382A1 - A cell monitoring device for use inside a humid incubator and a humid incubator system - Google Patents

A cell monitoring device for use inside a humid incubator and a humid incubator system

Info

Publication number
SE2050382A1
SE2050382A1 SE2050382A SE2050382A SE2050382A1 SE 2050382 A1 SE2050382 A1 SE 2050382A1 SE 2050382 A SE2050382 A SE 2050382A SE 2050382 A SE2050382 A SE 2050382A SE 2050382 A1 SE2050382 A1 SE 2050382A1
Authority
SE
Sweden
Prior art keywords
mass flow
monitoring device
casing
cell monitoring
incubator
Prior art date
Application number
SE2050382A
Inventor
Anton Andrén
Diana Cervantes
Erik Gatenholm
Hector Martinez
Niclas Johansson
Original Assignee
Cellink Ab
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 Cellink Ab filed Critical Cellink Ab
Priority to SE2050382A priority Critical patent/SE2050382A1/en
Priority to PCT/SE2021/050245 priority patent/WO2021201742A1/en
Publication of SE2050382A1 publication Critical patent/SE2050382A1/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
    • C12M41/00Means for regulation, monitoring, measurement or control, e.g. flow regulation
    • C12M41/48Automatic or computerized control
    • 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
    • C12M1/00Apparatus for enzymology or microbiology
    • C12M1/36Apparatus for enzymology or microbiology including condition or time responsive control, e.g. automatically controlled fermentors
    • C12M1/38Temperature-responsive control
    • 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
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F24HEATING; RANGES; VENTILATING
    • F24FAIR-CONDITIONING; AIR-HUMIDIFICATION; VENTILATION; USE OF AIR CURRENTS FOR SCREENING
    • F24F13/00Details common to, or for air-conditioning, air-humidification, ventilation or use of air currents for screening
    • F24F13/22Means for preventing condensation or evacuating condensate
    • 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
    • C12M23/00Constructional details, e.g. recesses, hinges
    • C12M23/48Holding appliances; Racks; Supports
    • 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
    • C12M3/00Tissue, human, animal or plant cell, or virus culture apparatus
    • 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
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F24HEATING; RANGES; VENTILATING
    • F24FAIR-CONDITIONING; AIR-HUMIDIFICATION; VENTILATION; USE OF AIR CURRENTS FOR SCREENING
    • F24F13/00Details common to, or for air-conditioning, air-humidification, ventilation or use of air currents for screening
    • F24F13/22Means for preventing condensation or evacuating condensate
    • F24F2013/221Means for preventing condensation or evacuating condensate to avoid the formation of condensate, e.g. dew
    • GPHYSICS
    • G06COMPUTING; CALCULATING OR COUNTING
    • G06TIMAGE DATA PROCESSING OR GENERATION, IN GENERAL
    • G06T2207/00Indexing scheme for image analysis or image enhancement
    • G06T2207/30Subject of image; Context of image processing
    • G06T2207/30004Biomedical image processing
    • G06T2207/30024Cell structures in vitro; Tissue sections in vitro
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05KPRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K7/00Constructional details common to different types of electric apparatus
    • H05K7/20Modifications to facilitate cooling, ventilating, or heating
    • H05K7/20009Modifications to facilitate cooling, ventilating, or heating using a gaseous coolant in electronic enclosures
    • H05K7/20209Thermal management, e.g. fan control

Abstract

The disclosure relates to a cell monitoring device for use inside a humid incubator, comprising: i. an outer casing, in open or closed arrangement, comprising a bottom, a top, a front part, a rear part, and a first and second side parts; ii. a sample tray adapted to receive at least one sample vessel, said sample tray being positioned within or on top of the outer casing; iii. at least one heat source, such as an imaging system, an optical unit and/or a live cell camera, arranged in fixed or movable position within the outer casing; and iv. one or more mass flow devices arranged within the outer casing; characterized in that the one or more mass flow device(s) have the capacity to cause a mass flow within the outer casing and/or the surrounding environment, such as an incubator, thereby levelling temperature differences created by heat emitted from the heat source(s) within the casing and/or the surrounding environment, thereby minimizing condensation in the at least one sample vessel(s). The disclosure further relates to a humid incubator system and a computer program.

Description

A cell monitoring device for use inside a humid incubator and a humid incubator system Technical field The present disclosure relates to a cell monitoring device for use inside a humid incubator, ahumid incubator system and a computer program. More specifically, the disclosure relates toa cell monitoring device for use inside a humid incubator, a humid incubator system and a computer program as defined in the introductory parts of claim 1, claim 15 and claim 17.
Background art This invention relates to improved instruments and modules used inside incubators to reducecondensation. ln particular, the present application relates to cell culture imaging devices andsystems with a fan and mass flow configuration designed to reduce and/or eliminatecondensation problems in a cell culture vessel for optimal cell culture conditions and live-cell monitoring.
The present invention is a system able to decrease the temperature differences insideenclosed chambers generally used to perform experiments such as cell culture. Thesechambers or incubators have active systems to control temperature and gas concentrations.
Additionally, some are designed to promote high relative humidity conditions.
These incubators use a high humidity to reduce the evaporation of liquids contained in avessel that has a loose-fitting lid. The air above the surface of the liquid is saturated with vaporwhile the surrounding air is not and because of this difference the vapor tries to distribute bydiffusion to create an equilibrium. The gas concentration and the temperature are modifieddepending on the experiments performed in the incubator, e.g. at 37°C, 5% C02 for a mammalian cell culture. ln such instruments, condensation is an issue since the volume of liquid lost by condensationalters the volume in the experiment, introducing a difficult to track variable. Condensation isthe physical process where matter changes from gas to liquid, in the mentioned enclosedchambers condensation occurs when the temperature of a surface inside the chamber isbelow the temperature point at which the air saturated with water vapor turns into liquid, dew point. At constant temperature, the dew point is proportional to humidity i.e. at 37°C and 295% relative humidity the dew point is 36.1°C meaning that theoretically any surface belowthis point will get condensation. Since the difference in temperature needed to createcondensation in high humidity chambers is especially small, the introduction of any type ofdevice producing heat increases the probability of condensation in the surroundings of the heat source, altering the conditions inside this type of incubators.
To avoid condensation inside the mentioned incubators, different solutions have been createdtrying to keep the heat away from the liquid containing vessels as well as heating/cooling thesurfaces ofthe liquid containing vessels prone to condensation (see e.g. US2017/0037355 related to an ”INCUBATION AND DETECTION DEVICE”.
A problem with the solutions of the prior art is that heaters/coolers are expensive and requireextensive testing, since the heaters/coolers need to be able to stand high humidity and warm temperature.
There is thus a need for improved and alternative solutions within this field, minimizing theproblems of condensation in sample vessels, and to avoid disturbing the experiments performed in cell incubators.
Summary lt is an object of the present disclosure to mitigate, alleviate or eliminate one or more oftheabove-identified deficiencies and disadvantages in the prior art and solve at least the abovementioned problem(s). According to a first aspect there is provided a cell monitoring devicefor use inside a humid incubator, comprising: i. an outer casing, in open or closedarrangement, comprising a bottom, a top, a front part, a rear part, and a first and second sideparts; ii. a sample tray adapted to receive at least one sample vessel, the sample tray beingpositioned within or on top ofthe outer casing; iii. at least one heat source, such as an imagingsystem, composed of an optical unit and/or a live cell camera, arranged in fixed or movableposition within the outer casing; and iv. one or more mass flow devices arranged within theouter casing; characterized in that the one or more mass flow device have the capacity tocause a mass flow within the outer casing and/or a surrounding environment, such as a humid incubator, thereby levelling temperature differences created by heat emitted from the heat 3source within the casing and/or the surrounding environment, thereby minimizing condensation in the at least one sample vesse|(s).
Thus, the inventors have surprisingly found out that by using a mass flow device, such as a fan,for creating a mass flow, which levels out temperature differences in an incubator, theproblems ofthe prior art can be solved. Hereby, excessive costs can be avoided and thesystem can be simplified. Specifically, the inventors have been able, using mass flow devices,especially fans, to create a flow in a specific direction and with a suitable potency to be able todrag hot air away in such a way that the main function ofthe device is not disturbed. To thisend, it is important to stress that in a cell culturing or cell monitoring device, where living cellsare growing, a controllable and non-disturbing environment is very important, e.g.uncontrolled vibrations, noise, changes in temperature and atmosphere conditions should be avoided as far as possible.
According to some embodiments, the invention can be applied to bioreactors or cellmonitoring devices, such as a live-cell imaging device, and other condensation prone devices placed insude humid incubators..
Thus, the principles ofthe invention are applicable to a wide range of devices, having thecommon challenge of levelling temperature from a heat source so that condensation in sample vesselse is minimized and/or eliminated.According to some embodiments, the mass is a gas, such as air.
The principles of the invention can be applied to any mass flow that can be used for distributing heat. Gaseous flow (air) is the preferred choice for practical reasons.
According to some embodiments, the heat source, in the form of an imaging system, ismovable within the casing underneath the sample tray so that each sample vessel of the sample tray can be monitored by the imaging system. ln a cell monitoring system, the vessels containing cells should be possible to monitor withminimum disturbance for the cultured cells, and therefore the imaging system must typicallybe movable, which in practice means that the heat source moves within the device casing.Hence, the mass flow devices and the mass flow created must be able to take care of this situation. As shown in the present application, the inventors have been successful in creating a 4mass flow device coupled to a cell monitoring system, such as a live-cell imaging system,thereby levelling temperature with a movable imaging system. Especially, as proof of concept this has been shown for the CELLCYTE system.
According to some embodiments, the device further comprises a gantry system arranged atleast partly within the outer casing, said gantry system comprises a framework of connectedextended members, said framework comprising: a first extended member being configured toextend in at least a latitudinal direction, and at least one second extended member beingconfigured to extend in a longitudinal direction, said longitudinal direction beingperpendicular to said latitudinal direction and a gantry frame structure extending along anorthogonal direction being perpendicular to the latitudinal direction and the longitudinaldirection, at least one movement member, the heat source, in form of an imaging systemarranged on the gantry frame structure, wherein the imaging system comprises a detectionlayer and an illumination layer, and wherein the gantry frame structure comprises an internalorifice enabling the sample tray to be positioned within said orifice, and said detection layer isarranged within the outer casing and attached to a lower portion ofthe frame structure, andunder the sample tray, such that the detection layer is movable in a planar direction in relation to the sample tray in response to actuation of said at least one movement member.
The cell monitoring device of this embodiment relates e.g. to the CELLCYTE system (providedby CELLINK AB; www.cellink.com). This device is an open cell monitoring device, to be usedinside an incubator. lt was found out by the inventors that not only the use of mass flowdevices, such as fans, was important, but also the power and position ofthe mass flow deviceswithin the casing ofthe device in order to minimize and preferably eliminate condensation. Amass flow device having too high power was efficient in creating a mass flow, but also inemitting heat, thereby causing additional heating problems in the whole incubator, resultingin undesired condensation. Therefore, using too powerful mass flow devices may result in theincubator being overheated, which is deteriorating for the cell culture and would affect anyexperiment performed in such incubator. Hence, it is important to use a mass flow devicehaving a sufficient capacity to create a mass flow so that the heat emitted from the primaryheat source(s), such as a camera, is transported away and levelled out, without creating unnecessary heat. Thus, it is a balance and task of optimizing the position, direction and 5power of the mass flow devices for any specific cell monitoring device placed inside an incubator, so that a specific mass flow is created.
According to some embodiments, a first mass flow device is arranged to create a mass flowfrom the surrounding environment, such as the incubator, into the casing, and a second massflow device is arranged to create a mass flow from the casing to the surrounding environment, such as the incubator.
Thus, by exchanging mass with the environment surrounding the device casing, e.g. with theincubator in which the device is used, mass can be moved from locations where it is hotter,such as in the proximity ofthe heat source, to locations where it is cooler, such as in thebottom of an incubator, and vice versa. ln this way, temperature differences can be levelled out to such an extent that condensation is minimized and/or eliminated in the sample vessels.
According to some embodiments, the first mass flow device is arranged at the bottom of thecasing, and the second mass flow device is arranged at the front, rear or side parts of the casing.
According to some embodiments, the first mass flow device is arranged at the bottom of thecasing, close to the front part, and the second mass flow device is arranged at the rear part of the casing.
Thus, in one workable solution it showed important to place mass flow devices at the bottomof the case to bring air of lower temperature into the casing and having a mass flow device inthe back (rear) of the casing getting air of higher temperature out of the system, equalizingtemperature differences that is causing condensation. Placing the fans for cooling down thesystem at the front and the fan to drag out the hot air at the back of the case was alsoimportant since the inventors needed to drag the hot air to one point, in this case the back (rear), and then take it out.
According to some embodiments, the casing further is equipped with vents or holes allowing mass to flow in and out of the casing to the incubator.
Hereby, when suitable, mass can be exchanged with the surroundings via holes/vents allowing a more ”passive” levelling of temperature differences. 6Thus, the invention has the capacity to level temperature differences of heat source(s) having a wide range of power and therefore heat emission.
According to some embodiments, the sample tray comprises sample vessels in the form of 96-well p|ates with 0.1 ml liquid per well, 48 well p|ates with 0.5mL per well, 24 well p|ates with 1mL per well, 12 well p|ates with 1mL per well and 6 well p|ates with 2ml per well.
Thus, the invention has the capacity to eliminate condensation in sample trays and sample vessels of a great variety.According to some embodiments, the mass flow device is a fan.
Typically, the mass flow device is a fan, which e.g. can be of radial or axial type. Typically, axial type fans are preferred, since radial fans tend to producr more heat and vibrations.According to some embodiments, each mass flow device have the following characteristics:i. a potency in the range of 1-10 W, preferably in the range of 2-3 W; and/or ii. a maximum mass flow rate capacity in the interval of 0,25 - 5 m3/min, preferably in the interval of 0,5-2,5 m3/min.
For some preferred embodiments related to the CELLCYTE device, it has been shown thatpotencies in the range of 1-10 and especially 2-3 W is a good optimization, as well as mass flow rates in the order of 0,25 - 5 m3/min, and especially 0,5-2,5 m3/min.
According to some embodiments, the cell monitoring device further comprises at least onecontrol unit and a data storage unit. For example, the mass flow devices can be controlled bythe same processor/computer controlling the monitoring device. Alternatively, another processor/computer may be used.
According to some embodiments, the cell monitoring device further comprises at least onetemperature sensor for detecting temperature variations in the device. Temperature sensor(s)that can detect temperature variations of 0.1°C and upwards can be used, and a PID(proportionaI-integral-derivative) controller can be used to regulate the mass flow. By ”temperature variations" is meant variations up and/or down in temperature, such as a higher 7temperature as a result of heat emitted from the one or more heat sources, and a lower temperature(s) as a result of mass flow from a cooler to a warmer location.
According to a second aspect there is provided a humid incubator system, comprising: a humidincubator; the cell monitoring device ofthe first aspect; and means to control temperature, gas concentration and/or humidity condition within the incubator.
Hereby, a complete system for incubating and culturing cells is provided, having the advantageof minimized and/or eliminated condensation in the sample vessels. By a ”humid incubator system” is meant any chamber with a regulated environment for cell culturing purposes.
According to some embodiments, the volume of the incubator is typically in the range of 10 to 1000 l, preferably 50-500 l, more preferably 100-250 l.Hence, a large variation of incubator sizes can be used.
According to a third aspect, there is provided a computer program for controlling theoperation of the one or more mass flow devices of the cell monitoring device of the firstaspect, comprising instructions, which when executed cause the program to control theoperation of the one or more mass flow devices. For example, this can be done as a responseto temperature variations detected by the at least one temperature sensor of the monitoring device, and/or as a response to any other input. ln this way, the mass flow devices can be controlled by a computer program. For example, themass flow devices can be controlled by the same processor/computer controlling the monitoring device. Alternatively, another processor/computer may be used.
Effects and features of the second and third aspects are to a large extent analogous to thosedescribed above in connection with the first aspect. Embodiments mentioned in relation to the first aspect are largely compatible with the second and third aspects.
The present disclosure will become apparent from the detailed description given below. Thedetailed description and specific examples disclose preferred embodiments ofthe disclosureby way of illustration only. Those skilled in the art understand from guidance in the detailed description that changes and modifications may be made within the scope of the disclosure.
Hence, it is to be understood that the herein disclosed disclosure is not limited to the particular component parts of the device described or steps of the methods described sincesuch device and method may vary. lt is also to be understood that the terminology usedherein is for purpose of describing particular embodiments only, and is not intended to belimiting. lt should be noted that, as used in the specification and the appended claim, thearticles "a", "an", "the", and "said" are intended to mean that there are one or more oftheelements unless the context explicitly dictates otherwise. Thus, for example, reference to "aunit" or "the unit" may include several devices, and the like. Furthermore, the words"comprising", "including", "containing" and similar wordings does not exclude other elements or steps.
Brief descriptions of the drawings The above objects, as well as additional objects, features and advantages of the presentdisclosure, will be more fully appreciated by reference to the following illustrative and non-limiting detailed description of example embodiments of the present disclosure, when taken in conjunction with the accompanying drawings.
Figure 1 shows the cell monitoring device 1 according to an embodiment ofthe presentdisclosure. I\/|ore in detail, Figure 1 is a diagram disclosing a cell monitoring system forautomatic cell monitoring comprising an outer casing 2, a sample tray 3 positioned within theouter casing, a gantry system 4 arranged at least partly within the outer casing, and animaging system arranged on the gantry system. The heat source (not shown) in the form of an optical unit is within the casing, as well as the mass flow device(s) (not shown).
Figure 2 is a top view showing the sample tray (inner dashed line) 3 and the casing (outerdashed line) 2, including the movable heat source 5 (the imaging device), as well as mass flow device(s) 6, 7 and 8.
Figure 3 shows various solutions (11 concepts) of fans and bottom holes that were studied according to the invention.
Figure 4 shows condensation test results for the different fan solutions (11 concepts) studied. 9Figure 5 shows a diagram of the air flow using concept 11. The arrows show the amss flow caused by the mass flow devices.
Detailed description The present disclosure will now be described with reference to the accompanying drawings, inwhich preferred example embodiments ofthe disclosure are shown. The disclosure may,however, be embodied in other forms and should not be construed as limited to the hereindisclosed embodiments. The disclosed embodiments are provided to fully convey the scope of the disclosure to the skilled person.
The first aspect of this disclosure (figure 1 and 2) shows a cell monitoring device 1 for useinside a humid incubator, comprising: i. an outer casing 2, in open or closed arrangement, forexample comprising a bottom 11, a top 12, a front part 13, a rear part (back) 14, and a firstand second side parts 15,16 (even though other configurations and designs are fully possible,as long the technical effect of the invention can be achieved), ii. a sample tray 3 adapted toreceive at least one sample vessel, the sample tray being positioned within or on top of theouter casing; iii. at least one heat source 5, such as an imaging system, an optical unit and/or alive cell camera, arranged in fixed or movable position within the outer casing; and iv. one ormore mass flow devices arranged within the outer casing; characterized in that the one ormore mass flow devices have the capacity to cause a mass flow within the outer casing and/orthe incubator thereby levelling temperature differences created by heat emitted from theheat sources within the casing and/or the surroundings, e.g. the incubator, thereby minimising condensation in at least one sample vessels.
Limiting or eliminating condensation in sample vessels is an objective according to the presentdisclosure. lt is preferred than no condensation occurs, or at least only a small amount. Somedew may be acceptable, if not accumulating over time. However, no dew at all is what is desired (condensation problem thereby solved).
The cell monitoring device can be any type of cell monitoring device, such as an incubator, abioreactor, a cell monitoring device, such as a live-cell imaging device (including the CELLCYTE device provided by CELLINK AB). Also, the cell monitoring device can be a system further comprising means for dispensing biological material, such as cells and/or single cells, to the sample vessel(s).
The casing can have be an open (have mass flow communication with the surroundings) orclosed arrangement, in which closed arrangement the casing has essentially no direct massflow communication with the surroundings. The casing may have many different shapes and sizes, and typically its size is as small as possible for practical and manufacturing reasons.
One or more sample trays including sample vessels are typically positioned within or on top ofthe casing, even though other positions are fully possible. For a live-cell imaging device, it ispractical if the sample tray is positioned so that an optical unit can monitor the sample vesselsof the sample tray. ln such embodiment, the sample tray may for example be positioned ontop ofthe casing, so that the samples can be monitored by an optical unit positioned withinthe casing, below the sample tray. ln such embodiment, the top ofthe casing is typicallytransparent or open. The sample tray may for example comprise sample vessels in the form of96-well plates with 100pL liquid per well, 48 well plates with 0.5mL per well, 24 well plates with 1mL per well, 12 well plates with 1mL per well and/or 6 well plates with 2ml per well.
The heat source(s) may be any type of device emitting heat, such as an optical unit, a live-cellcamera (such as acA2440-35um - Basler ace; httpsz//tvyvvt/.basleryvellcom/'en/products/cameras/a rea-scan-cameras/ace/acaZÅMO- ššumfätalfispecs) (power 2,5 W), a microscope or the like, or any other type of devicetypically used in a cell monitoring device. Depending on the power of and the heat emittedfrom the heat source(s), the arrangements of mass flow devices may differ. According to someembodiments, the monitoring device may comprise more than one heat source, and the heatsources may be positioned in different locations ofthe device, such as an optical unit withinthe casing, and means for dispensing biological material to the sample vessels above thesample tray. For such embodiments, the choice and positioning of the mass flow devices mayneed to be optimised for each individual heat source, and/or for the entire monitoring device, so that condensation in the sample vessels is minimized or, preferably, eliminated.
For example, using the CELLCYTE cell monitoring device, the heat source is a camera that has a typical power of 2,5 W, and a temperature that typically is in the range of 42-55 °C.
Typically, one could expect that the heat source(s) used in cell monitoring devices are opticalunits having a power value of about 0,5-10 W, for example in the interval of 1-5 W, or in theinterval of 2-3 W. Such optical units will emit heat so that the optical unit, during operation ofthe device, exhibits an outer temperature of e.g. about 37- 60 °C, such as about 40-55 °C.Hence, the arrangement of mass flow device must be configured so that the heat emittedfrom the heat source is redistributed from the air in close proximity ofthe heat source to other places ofthe device and/or its surrounding environment.
The mass flow devices, typically in the form of axial or radial fans having a suitable potency,may be arranged in different ways depending on the size, shape and details of the casing, heatsource and other components ofthe device. Typically, the fans may be covered by a metallicmesh to protect users from being hurt (by accidentally putting their fingers into the fans). Theexact solution for each specific cell monitoring device may need to be optimized. For theCELLCYTE device, the fans were attached by screws, and a metallic tray was placed betweenthe fans and the case. The fans may e.g. have a potency in the range of 1-10 W, preferably inthe range of 2-3 W. A skilled person would know where to get such fans. For example, the fan (e.g. as the back (rear) fan used in concept 11) can be ”httpsy//wwwxíigikeycom/prcsriuct- detaii/en/deita--electronics/EFB0612HHA/ESGB--ïßåß--ND/1014357". This fan has a mass flow rate of 0,594 m3/min (CFM (cubic feet per minute) of 21,2), and a maximum speed of 4800rpm. Maximum power is about 2-3 W, such as 2,16 W or 3,0 W. Further, for example, the fan(e.g. as the bottom fans of concept 11) can be ”EK-Vardar EVO 120ER White BB (500-2200rpm)". This fan has a max air flow of 77 CFM = 131 m3/h (2,18 m3/min), and speed 500- 2200 rpm. Maximum power is about 2,16 W.
The mass flow rate caused by each mass flow device should be on a level suitable forefficiently distributing the heat emitted by the heat source, without emitting unnecessaryadditional heat. Thus, a balance between power and mass flow rate capacity must be chosen.This level may be different for different devices, depending on heat source, it position, thedesign of the casing and the entiree cell monitoring device, as well as the characteristics ofthesurrounding environment. For the CELLCYTE system, which device has been used as a proof ofconcept for the invention, a maximum mass flow rate (per fan) in the interval of about 0,25 - 5 m3/min is suitable, preferably in the interval of 0,5-2,5 m3/min. ln order to obtain a mass flow that allows a suitable and sufficient distribution of heat inaccordance with the invention, it is preferable if the mass flow is configured so that cooler airis distributed to the location of the heat source, and that heat emitted from the heat source isdistributed to a location of the monitoring device and/or the surrounding environment whereit can be easily ”absorbed” by the surrounding air, without any direct impact on thecondensation in the sample vessels. This can be obtained for example by placing a first massflow device so that it can distribute air from the environment surrounding the casing of themonitoring device (typically cooler air) into the casing, and placing a second mass flow deviceso that it can distribute air close to the heat source (typically warmer air) out of the casing tothe surrounding environment. Especially, it is advantageous if the first and second mass flowdevice can cooperate to create a continuous mass flow from the surrounding environmentinto the casing in close proximity of the heat source, and out again from the casing to thesurrounding environment. Hereby, any heat emitted by the heat source is continuouslydistributed to other locations ofthe monitoring device and especially the environmentsurrounding the casing of the monitoring device, such as an incubator, in which themonitoring device is placed. A solution in accordance with this principle can be seen inconcept 11 of figure 3 and 4, and is further disclosed in figure 5. lf a movable heat source isused, it is important that the mass flow created by the mass flow devices will allowredistribution of air within the entire volume ofthe casing, in which the movable heat source Cafl mOVe.
Especially, in accordance with the embodiment disclosed in figure 2, 3, 4 and 5, it has shownto be preferable that two mass flow devices are positioned at the bottom ofthe casing,allowing cooler air from underneath the bottom of the casing of the monitoring device intothe casing to cool down the heat source, and that one mass flow device is positioned at theback (rear part) ofthe casing, thereby allowing heat emitted from the heat source to bedistributed out from the casing. ln this way a continuous flow of mass is created, having theoverall effect that temperature differences in the monitoring device and in the surroundingenvironment is levelled out, thereby minimizing condensation in the sample vessels. Otherconfigurations are are also fully possible, such as 1, 2, 3 or 4 mass flow device at the bottom ofthe casing, and 1, 2, 3 or 4 mass flow device at the back ofthe casing, as long as the mass flow created is sufficient, and heat emitted from the mass flow devices is minimized. Generally, it 13appears important to provide a slightly stronger mass flow of cool air into the casing,compared to the mass flow of warm air out from the casing at the back, acccording to this embodiment. Air can also escape e.g. via the top of the casing, which typically is open.
For condensation to occur, heat is typically transferred to the sample vessels from the heat source via the air in the incubator, or via heating of the top layer ofthe casing, or both.
The mass may be a gas or a liquid, such as air or water. Typically, the mass is air. Inside anincubator, the temperature for mammalian cell culture applications may e.g. vary betweenabout 20-40 °C, and often a temperature around 37 °C is used. The humidity is typically above 90% relative humidity for mammalian cell culture applications.
As can be seen from figure 1 and 2, the heat source, in the form of an imaging system, may bemovable within the casing underneath the sample tray so that each sample vessel of the sample tray can be monitored by the imaging system. ln one specific embodiment (see figure 2), the device further comprises a gantry system 4arranged at least partly within the outer casing 2, said gantry system comprises a frameworkof connected extended members, said framework comprising: a first extended member beingconfigured to extend in at least a latitudinal direction, and at least one second extendedmember being configured to extend in a longitudinal direction, said longitudinal directionbeing perpendicular to said latitudinal direction and a gantry frame structure extending alongan orthogonal direction being perpendicular to the latitudinal direction and the longitudinaldirection, at least one movement member, the heat source, in form of an imaging system 5arranged on the gantry frame structure, wherein the imaging system comprises a detectionlayer and an illumination layer and wherein the gantry frame structure comprises an internalorifice enabling the sample tray 3 to be positioned within said orifice, and said detection layeris arranged within the outer casing 2 and attached to a lower portion of the frame structure,and under the sample tray 3, such that the detection layer is movable in a planar direction inrelation to the sample tray 3 in response to actuation of said at least one movement member.This embodiment refers e.g. to the CELLCYTE system. Two mass flow devices 6, 7 arepositioned at the bottom, to the front, of the device, and one mass flow device 8 is positioned at the back of the device.
The principle mass flow generated by these mass flow devices can e.g be as shown in figure 5,where the two mass flow devices at the bottom causes a mass flow into the casing, and themass flow device to the back causes a mass flow out of the casing. Hereby, as a result of themass flow redistributing air, the higher temperature (T2) inside the casing, as a result of heatemitted from the heat source (not shown), is levelled with the lower temperature outside the casing.
The casing may be equipped with holes or vents in order to ventilate air to the surroundings.Especially, the bottom of the casing may be equipped with holes in order allow mass to flow inand out ofthe casing to the surroundings, e.g. the incubator. Such holes may have the size of approximately 1 cm, even though other sizes may also be used.
The second aspect ofthis disclosure shows a humid incubator system, comprising: the cellmonitoring device ofthe first aspect; and means to control temperature, gas concentrationsand/or humidity conditions within the incubator. The volume ofthe incubator may be of anysuitable size, e.g. depending on the cell monitoring device used. The volume may e.g. be in therange of 10 to 1000 l, preferably 50-500 l, more preferably 100-250 l. Examples of humidincubator systems to be used are Heracell VIOS 160i, ThermoFisher, Forma Series ll water jacketed C02, ThermoFisher. Galaxy 170R/S co2 incubators and eppendorf vials.
The third aspect of this disclosure provides a computer program for controlling the operationof the one or more mass flow devices of the cell monitoring device of the first aspect, comprising instructions, which when executed cause the program to control the operation ofthe one or more mass flow devices, as a response to temperature variations detected by the at least one temperature sensor of the monitoring device. ln this way, the mass flow devices can be controlled by a computer program. For example, themass flow devices can be controlled by the same processor/computer controlling the monitoring device. Alternatively, another processor/computer may be used.
According to some embodiments, temperature sensors that can detect temperature variationsof 0.1°C and upwards can be used, and a PID (proportionaI-integral-derivative) controller can be used to regulate the mass flow.
The person skilled in the art realizes that the present disclosure is not limited to the preferredembodiments described above. The person skilled in the art further realizes that modificationsand variations are possible within the scope of the appended claims. Additionally, variations tothe disclosed embodiments can be understood and effected by the skilled person in practicing the claimed disclosure, from a study of the drawings, the disclosure, and the appended claims.
EXAMPLES ln the present invention, the inventors have created a mass flow specifically designed toreduce the temperature differences surrounding the heat source, such as an optical unit, of acell culturing or cell monitoring device, such as a live cell imaging device, inside a humid incubator, therefore avoiding condensation in the sample vessels. ln the specific examples, the cell culturing/monitoring device used was the CELLCYTE device.The incubator used were Heracell VIOS 160i, ThermoFisher and 2 different incubators from Forma Series ll waterjacketed C02, ThermoFisher.
To develop the temperature differential reducing system, the inventors studied the differentavailable options and chose to use mass flow, especially air flow, to distribute the heat, sincethis method offers a wider solution compatible with live cell imaging systems. To determinethe correct air flow system, different possibilities were tried regarding the air flow directionand the device used to create the flow. The tests were performed using a live-cell imagingsystem where the camera was in constant movement to test for broader and advancedscenarios in this type of instruments. About the devices creating the air flow, different types offans were evaluated (Table 1) for potency of the air flow and heat created, measured as temperature in the source and the incubator, respectively.
Mass flow device (fan) information Observations Radial fan 5,5 A Produces high temperatures Axial fan 0,18 A Produces small amount of heat, low potency Axial fan 0,3 A Produces small amount of heat, low potency Axial fan 0,1 A Low potency Axial fan 0,25A Produces small amount of heat, low potency Table 1.
To determine the best air flow direction, the fans were placed at different positions in the caseof the live-cell imaging system and in different combinations (Figure 3). The main test was theevaluation of condensation/dew formation on the |id of liquid containing vessels (Figure 4).After extended tests and analysis of the results, the inventors concluded that the fan solutionthat eliminates traceable condensation (as documented by taking images) is the onepresented in Figure 4 (concept 11). This solution consists of two axial fans located at the frontand under the heat source case, the fans create an air current sucking air from the exterior ofthe case, the lower part of the incubator generally contains the colder air since heat tends tomigrate from lower to higher points, the current encounters the heat source cooling it bydragging the hot air away at the same time it keeps constant temperature under and above the liquid containing vessels (Figure 5).

Claims (17)

1. A cell monitoring device (1) for use inside a humid incubator, comprising: i. an outer casing (2), in open or closed arrangement, comprising a bottom (11), a top (12), a front part (13), a rear part (14), and a first and second side parts (15, 16); ii. a sample tray (3) adapted to receive at least one sample vessel, said sample tray being positioned within or on top ofthe outer casing; iii. at least one heat source (5), such as an imaging system, comprising an optical unit, arranged in fixed or movable position within the outer casing; andiv. one or more mass flow devices (6, 7, 8) arranged within the outer casing; characterized in that the one or more mass flow device(s) (6, 7, 8) have thecapacity to cause a mass flow within the outer casing and/or a surrounding environment, suchas the incubator, thereby levelling temperature differences created by heat emitted from theheat source(s) within the casing and/or in the surrounding environment, such as in the incubator, thereby minimizing condensation in the at least one sample vessel(s).
2. The cell monitoring device according to claim 1, wherein the device is a bioreactor or a cell monitoring device, such as a live-cell imaging device.
3. The cell monitoring device according to claim 1 or 2, wherein the mass is a gas, such as air.
4. The cell monitoring device according to any ofthe preceding claims, wherein theheat source, in the form of an imaging system, is movable within the casing underneath thesample tray so that each sample vessel ofthe sample tray can be monitored by the imaging system.
5. The cell monitoring device according to any one of the preceding claims, wherein thedevice further comprises a gantry system arranged at least partly within the outer casing, saidgantry system comprising a framework of connected extended members, said framework comprising: a first extended member being configured to extend in at least a latitudinal direction, and at least one second extended member being configured to extend in alongitudinal direction, said longitudinal direction being perpendicular to said latitudinaldirection and a gantry frame structure extending along an orthogonal direction beingperpendicular to the latitudinal direction and the longitudinal direction, at least onemovement member, the heat source, in form of an imaging system arranged on the gantryframe structure, wherein the imaging system comprises a detection layer and an illuminationlayer, and wherein the gantry frame structure comprises an internal orifice enabling thesample tray to be positioned within said orifice, and said detection layer is arranged within theouter casing and attached to a lower portion of the frame structure, and under the sampletray, such that the detection layer is movable in a planar direction in relation to the sample tray in response to actuation of said at least one movement member.
6. The cell monitoring device according to any one of the preceding claims, wherein afirst mass flow device is arranged to create a mass flow from the surrounding environment,such as the incubator, into the casing, and a second mass flow device is arranged to create a mass flow from the casing to the surrounding environment, such as the incubator.
7. The cell monitoring device according to claim 6, wherein the first mass flow device isarranged at the bottom of the casing, and the second mass flow device is arranged at the front, rear or side parts of the casing.
8. The cell monitoring device according to claim 7, wherein the first mass flow device isarranged at the bottom ofthe casing, close to the front part, and the second mass flow device is arranged at the rear part of the casing.
9. The cell monitoring device according to any one of the preceding claims, wherein thecasing further is equipped with vents or holes allowing mass to flow in and out ofthe casing to the incubator.
10. The cell monitoring device according to any one ofthe preceding claims, whereinthe sample tray comprises sample vessels in the form of 96-well plates with 100uL liquid perwell, 48 well plates with 0.5mL per well, 24 well plates with 1mL per well, 12 well plates with 1mL per well and 6 well plates with 2ml per well.
11. The cell monitoring device according to any ofthe preceding claims, wherein the mass flow device is a fan.
12. The cell monitoring device according to any one ofthe preceding claims, wherein each mass flow device have the following characteristics:5 i. a potency in the range of 1-10 W, preferably in the range of 2-3 W; and/or ii. a maximum mass flow rate capacity in the interval of 0,25 - 5 m3/min, preferably in the interval of 0,5-2,5 m3/min.
13. The cell monitoring device according to any one of the preceding claims, further comprising at least one control unit and a data storage unit.
14. The cell monitoring device according to any one of the preceding claims, further comprising at least one temperature sensor for detecting temperature variations in the device.
15. A humid incubator system, comprising:a humid incubator;15 the cell monitoring device of claims 1-14; and means to control temperature, gas concentration(s) and/or humidity condition(s) within the incubator.
16. The humid incubator system according to claim 15, wherein the volume of the incubator is in the range of 10 to 1000 l, preferably 50-500 l, more preferably 100-250 l.
17. Computer program for controlling the operation of the one or more mass flowdevices ofthe cell monitoring device of claims 1-14, comprising instructions, which whenexecuted cause the program to control the operation of the one or more mass flow devices, asa response to temperature variations detected by the at least one temperature sensor of the monitoring device.
SE2050382A 2020-04-03 2020-04-03 A cell monitoring device for use inside a humid incubator and a humid incubator system SE2050382A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
SE2050382A SE2050382A1 (en) 2020-04-03 2020-04-03 A cell monitoring device for use inside a humid incubator and a humid incubator system
PCT/SE2021/050245 WO2021201742A1 (en) 2020-04-03 2021-03-19 A cell monitoring device for use inside a humid incubator and a humid incubator system

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SE2050382A SE2050382A1 (en) 2020-04-03 2020-04-03 A cell monitoring device for use inside a humid incubator and a humid incubator system

Publications (1)

Publication Number Publication Date
SE2050382A1 true SE2050382A1 (en) 2021-10-04

Family

ID=78287387

Family Applications (1)

Application Number Title Priority Date Filing Date
SE2050382A SE2050382A1 (en) 2020-04-03 2020-04-03 A cell monitoring device for use inside a humid incubator and a humid incubator system

Country Status (1)

Country Link
SE (1) SE2050382A1 (en)

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050051723A1 (en) * 2003-07-23 2005-03-10 Neagle Bradley D. Examination systems for biological samples
US20050105172A1 (en) * 2003-10-24 2005-05-19 Olympus Corporation Culture microscope apparatus
WO2007145198A1 (en) * 2006-06-16 2007-12-21 Sanyo Electric Co., Ltd. Culture monitoring system
EP1916296A1 (en) * 2005-07-05 2008-04-30 Nikon Corporation Culture apparatus
US20100157423A1 (en) * 2008-12-19 2010-06-24 Sanyo Electric Co., Ltd. Observation unit
WO2016161022A2 (en) * 2015-03-30 2016-10-06 Accerlate Diagnostics, Inc. Instrument and system for rapid microorganism identification and antimicrobial agent susceptibility testing
US20170037355A1 (en) * 2014-04-07 2017-02-09 Advencis Incubation and detection device
EP3312268A1 (en) * 2015-06-22 2018-04-25 Toyo Seikan Group Holdings, Ltd. Cell culture method, jig for cell culture, and cell culture device
EP3392332A1 (en) * 2015-12-15 2018-10-24 Olympus Corporation Cell culture device and cell culture system
EP3604494A1 (en) * 2017-03-28 2020-02-05 Hitachi High-Technologies Corporation Inspection device

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050051723A1 (en) * 2003-07-23 2005-03-10 Neagle Bradley D. Examination systems for biological samples
US20050105172A1 (en) * 2003-10-24 2005-05-19 Olympus Corporation Culture microscope apparatus
EP1916296A1 (en) * 2005-07-05 2008-04-30 Nikon Corporation Culture apparatus
WO2007145198A1 (en) * 2006-06-16 2007-12-21 Sanyo Electric Co., Ltd. Culture monitoring system
US20100157423A1 (en) * 2008-12-19 2010-06-24 Sanyo Electric Co., Ltd. Observation unit
US20170037355A1 (en) * 2014-04-07 2017-02-09 Advencis Incubation and detection device
WO2016161022A2 (en) * 2015-03-30 2016-10-06 Accerlate Diagnostics, Inc. Instrument and system for rapid microorganism identification and antimicrobial agent susceptibility testing
EP3312268A1 (en) * 2015-06-22 2018-04-25 Toyo Seikan Group Holdings, Ltd. Cell culture method, jig for cell culture, and cell culture device
EP3392332A1 (en) * 2015-12-15 2018-10-24 Olympus Corporation Cell culture device and cell culture system
EP3604494A1 (en) * 2017-03-28 2020-02-05 Hitachi High-Technologies Corporation Inspection device

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
CELLINK CELLCYTE X. YouTube [Online]. CELLINK, June 28 2019 [retrieved on October 26 2020]. Retrieved from the internet *
Introducing CELLINK CELLCYTE X. YouTube [Online]. CELLINK, Feb 3 2019 [retrieved on October 26 2020]. Retrieved from the internet *

Similar Documents

Publication Publication Date Title
CN105602846B (en) One kind miniaturization Space Experiments cell culture apparatus
US8393234B2 (en) Apparatus, device and method for arranging at least one sample container
JP2012501676A (en) Cultivation system in cryogenic enclosure
US20060275896A1 (en) Apparatus and method for incubating cell cultures
US10407659B2 (en) Mini-incubator carrier box “Mini-incubator”
JP7411750B2 (en) Culture vessel rack and analysis equipment
CN106190835A (en) A kind of filling type cell culture system and method
JP2020061979A (en) Cell incubator
SE2050382A1 (en) A cell monitoring device for use inside a humid incubator and a humid incubator system
KR20180096947A (en) Autometic and Asepsis Cell Culture Apparatus
JP3712990B2 (en) Incubator equipment
WO2021201742A1 (en) A cell monitoring device for use inside a humid incubator and a humid incubator system
WO2014060360A1 (en) Embryo incubator incorporating gas control
GB2250581A (en) Temperature control for sample incubator
US7634330B2 (en) Temperature controlling method and temperature controller
CN109022265A (en) A kind of microbiological incubator
Buhler et al. Automated multichamber time-lapse videography for long-term in vivo observation of migrating cells
CN209555392U (en) Constant temperature electrophoresis control device
JP2005323509A (en) Cell culture-observing device for measuring gene expression
WO2024057426A1 (en) Specimen analysis device
CN206457492U (en) A kind of biochemical cultivation case based on image collecting device
CN107058099B (en) Embryo culture and transportation device
JP2019017340A (en) Cell culture observation device and cell observation unit
JP2019532658A (en) Bioreactor tray
CN108795743A (en) A kind of biotechnology microculture insulating box