WO2020047397A1 - Measurement of a dynamic system - Google Patents
Measurement of a dynamic system Download PDFInfo
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- WO2020047397A1 WO2020047397A1 PCT/US2019/049044 US2019049044W WO2020047397A1 WO 2020047397 A1 WO2020047397 A1 WO 2020047397A1 US 2019049044 W US2019049044 W US 2019049044W WO 2020047397 A1 WO2020047397 A1 WO 2020047397A1
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- lid
- receptacle
- wells
- fluid
- probe
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
- B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
- B01L3/508—Rigid containers without fluid transport within
- B01L3/5085—Rigid containers without fluid transport within for multiple samples, e.g. microtitration plates
- B01L3/50853—Rigid containers without fluid transport within for multiple samples, e.g. microtitration plates with covers or lids
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N1/00—Sampling; Preparing specimens for investigation
- G01N1/02—Devices for withdrawing samples
- G01N1/22—Devices for withdrawing samples in the gaseous state
- G01N1/2226—Sampling from a closed space, e.g. food package, head space
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
- C12M41/00—Means for regulation, monitoring, measurement or control, e.g. flow regulation
- C12M41/46—Means for regulation, monitoring, measurement or control, e.g. flow regulation of cellular or enzymatic activity or functionality, e.g. cell viability
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
- G01N21/64—Fluorescence; Phosphorescence
- G01N21/6428—Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes"
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
- G01N21/64—Fluorescence; Phosphorescence
- G01N21/645—Specially adapted constructive features of fluorimeters
- G01N21/6452—Individual samples arranged in a regular 2D-array, e.g. multiwell plates
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/483—Physical analysis of biological material
- G01N33/487—Physical analysis of biological material of liquid biological material
- G01N33/49—Blood
- G01N33/4925—Blood measuring blood gas content, e.g. O2, CO2, HCO3
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/483—Physical analysis of biological material
- G01N33/497—Physical analysis of biological material of gaseous biological material, e.g. breath
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/483—Physical analysis of biological material
- G01N33/497—Physical analysis of biological material of gaseous biological material, e.g. breath
- G01N33/4975—Physical analysis of biological material of gaseous biological material, e.g. breath other than oxygen, carbon dioxide or alcohol, e.g. organic vapours
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2200/00—Solutions for specific problems relating to chemical or physical laboratory apparatus
- B01L2200/02—Adapting objects or devices to another
- B01L2200/023—Adapting objects or devices to another adapted for different sizes of tubes, tips or container
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2300/00—Additional constructional details
- B01L2300/02—Identification, exchange or storage of information
- B01L2300/025—Displaying results or values with integrated means
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2300/00—Additional constructional details
- B01L2300/06—Auxiliary integrated devices, integrated components
- B01L2300/0627—Sensor or part of a sensor is integrated
- B01L2300/0654—Lenses; Optical fibres
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2300/00—Additional constructional details
- B01L2300/08—Geometry, shape and general structure
- B01L2300/0809—Geometry, shape and general structure rectangular shaped
- B01L2300/0829—Multi-well plates; Microtitration plates
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
- G01N21/64—Fluorescence; Phosphorescence
- G01N21/6428—Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes"
- G01N2021/6432—Quenching
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
- G01N21/64—Fluorescence; Phosphorescence
- G01N21/6428—Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes"
- G01N2021/6434—Optrodes
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/75—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated
- G01N21/77—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator
- G01N21/7703—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator using reagent-clad optical fibres or optical waveguides
- G01N2021/7706—Reagent provision
- G01N2021/772—Tip coated light guide
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/75—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated
- G01N21/77—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator
- G01N2021/7769—Measurement method of reaction-produced change in sensor
- G01N2021/7786—Fluorescence
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2201/00—Features of devices classified in G01N21/00
- G01N2201/02—Mechanical
- G01N2201/022—Casings
- G01N2201/0221—Portable; cableless; compact; hand-held
Definitions
- Various techniques are used to measure oxygen consumption by cells. Some techniques are open-air techniques that measure prepared cells (e.g., intact monolayers of cultured cells). Some techniques are able to perform measurements of cells in vivo. Some techniques are able to perform measurements of cells in a multi well plate (e.g., cells in wells of a microtiter plate). In some techniques a probe is used to take measurements between two distinct locations within a gradient in order to estimate flux (e.g., using a self-referencing microsensor).
- the system comprises a sterile, disposable probe lid attached beneath a durable handheld electronic array of optoelectronic sensors.
- the probe lid and electronic sensor array are positioned on top of a standard multi-well tissue culture plate.
- Optical probes integrated within and extending vertically from the disposable lid are inserted into the fluid of multiple tissue wells.
- the system is designed to avoid hindering overall transport of oxygen to the cells and to minimally disrupt oxygen concentration gradients.
- the lid is sterile, and the system can reside within an incubator.
- the system is ideally suited for continual use during a cell culture experiment, lasting up to several weeks.
- the system is also ideally suited for measuring a response of cells to a treatment (e.g., measuring a change in oxygen consummation after addition of a drug).
- an apparatus for measurement of a molecule levels (e.g., concentration, rate of consumption or production) in fluid in a receptacle.
- the apparatus including a device configured to be attached as part of a cover over a receptacle, which has a set of one or more wells each for holding a biological sample immersed in fluid.
- the device includes a plurality of optoelectronic sensors arranged to acquire optical signals from probes immersed in the fluid. These optical signals represent a molecule level in the fluid at a sensor of the probe.
- the device also includes a set of one or more actuators configurable to adjust a relative position of the device and the receptacle. Control circuitry in the device is used to control the set of actuators to vary the relative position of the device and the receptacle, and to acquire the optical signals at a plurality of relative positions.
- An advantage of the device forming part of the cover over the receptacle is that the device is portable with the receptacle (e.g., a receptacle covered with the device is“handheld” and can be easily moved from one location to another, placed on an incubator shelf, etc.).
- aspects can include one or more of the following features.
- each sensor can be kept at the same height above the well floor and/or at the same depth in the fluid as each other sensor.
- the control circuitry is configured to maintain a relative orientation of a plane defined by the sensors of the probes and a plane defined by the set of wells of the receptacle to be parallel.
- the varying of the relative position of the device and the receptacle is over range of motion. In some examples, this range of motion is between 10 micrometers and 3 millimeters.
- the apparatus further comprises the receptacle.
- each of the probes 160 includes a probe tip 162, which is immersed in the liquid 174 and which converts a property such as oxygen concentration into an optical emission, which is passed via the corresponding probe to the optoelectronic sensor 112 in the device 110 (e.g., in response to an optical signal emitted from the sensor 112 that excites the probe tip 162).
- Circuitry 118 in the device then stores and/or communicates the measurements to an external processing system.
- the device includes electrically controlled actuators 114 (only one of which is illustrated in the cross-section of FIG. 1A), which can change of separation of the device 110 and the plate 120, for example, by extending separator pins 116 that push against the top surface of the plate 120 through the lid 130, thereby control change of location of the probe tips 162 within the wells 122.
- the durable device 110 contains electronic circuitry 110 that assists to process oxygen concentration readings, monitor additional sensor inputs, run decision-making algorithms based on these inputs, provide sampling and actuation instructions, and communicate with a data hub.
- additional electronics include microcontrollers for general processing and specialized digital processing devices such as field programmable gate arrays (FPGA) for high speed control and calculations.
- the electronics also include non-volatile memory for storing device specific information, including calibration variables for the device. These calibration variables can potentially account for variances in electronics including oscillators, amplifiers, gain resistors, capacitors, etc.
- Patterns and threshold values from sensor readings can automatically trigger the initialization or termination of measurement and or actuation series. In this manner, the device can smartly anticipate user intention and eliminate the need for certain user interface mechanisms like buttons.
- the acceleration sensor can also be configured to detect movement caused by the actuation features. In this
- the acceleration sensor can be used to monitor system performance and can trigger corrective steps if the system is not performing as expected.
- vertical (i.e., z-axis) motion of the device 110 and lid 130 relative to the plate 120 is accomplished with a single actuator and linear guides such that the actuator maintains a parallel arrangement of the device and the plate, thereby causing a plane through the probe tips to remain parallel to the plate.
- vertical position of the probes within the well can be controlled by setting height at three positions in the x v- plane of the device 110 and the fixidly attached lid 130.
- the three actuation points can be operated in synchronization with each other to keep the plane of the probe tips parallel to the plate.
- the actuators may be operated to achieve different separation of the device and the plate at the different actuator points such that tilt of the lid and corresponding plane of the probe tips can be controlled. For example, in such an alternative some probes travel across a greater distance than other probes in the system.
- the actuation points can be set within the footprint of standard multi-well plates, where they can press off from a flat surface near the top of wells.
- the xy-coordinate system can be translated such that one of the actuation points resides on the origin and a second point resides on the x-axis.
- Each well center is then translated onto the new set of axes.
- the slope between the first actuation point at the origin and the second actuation point on the new x-axis is then found.
- the slope between the new x-axis and the value of the third actuation point along the ne -axis is found.
- the z position of each of the well centers is now possible to find using the slopes and coordinates of each well center along the new set of axes.
- Actuators are designed to provide approximate absolute positioning of the probes within the wells and precise positioning relative to previous positions.
- the actuation points are rods 116 that extend from the durable device 110.
- the rods can be coupled to the durable device through threaded bushings in the actuators 114. When the rods are turned around their cylindrical axis, they extend or retract relative to the device.
- a disk with an incline abuts the upper end of the pin such that at the thickest portion of the disk, the pin is extended from the device and when the thinnest portion of the disk is aligned with the pin, the pin is allowed to retract into the device.
- flexures are used to translate horizontal motion into vertical motion.
- actuators are held at a fixed height and three lead screws are used to lift or lower the durable portion of the device.
- stepper motors oriented horizontally are coupled with a gear head to increase torque and decrease step size.
- the gear heads then drive bevel gears which translate the axis of rotation from a horizontal orientation to a vertical orientation.
- Actuation pins are threaded with a fine pitch and are coupled to matching bushings housed in the durable device.
- Each step of the stepper motor translates the extension of the pin roughly 1 mih (target translation per step is between 0.01 and 10 mhi). Larger step sizes require fewer steps through the full range of travel, which is ideal for power consumption, whereas smaller step sizes allow for smoother operation and increased precision.
- Backlash occurs when the direction of movement is reversed. This backlash can be measured and accounted for during operation by adding additional steps each time the direction is reversed. Furthermore, the impact of rotational backlash can be minimized if a lead screw with a fine thread pitch is selected. In this manner, a nominal angular backlash translates to a smaller vertical backlash.
- the total mechanical advantage of the system for translating stepper steps into vertical positional changes can be maintained by balancing the mechanical advantage gained from a gear box attached to the motor, the ratio of pinion to bevel gear teeth, and the thread pitch of the lead screw. For a given angular backlash, concentrating mechanical advantage to occur at the lead screw can be advantageous in minimizing backlash.
- the lid 130 includes the array of probes 160, for example with the probes being formed as integral rods that extend from the inner surface of the lid.
- each probe is coupled to a sensor 112 in the sensor array of the device.
- the lid (or combination of the lid and device) constrains all of the probes such that they move together in a planar fashion.
- the probes 160 are configured to extend along a vector normal to the plane of the lid (i.e., the horizontal plan parallel to the top of the plate 120).
- the probes are configured in the x-y plane to align with an array of wells in the well plate 120.
- the lid resides on top of the culture plate and promotes a sterile barrier across the top of the culture wells.
- the non-sterile actuation pins should not directly contact the surface of the culture plate, but (in the case where the actuation pins are contained within the footprint of the plate) should instead contact the lid, which can in turn contact the culture plate.
- the lid can be configured to include features that enable translation of actuation initiated by circuitry in the durable device to alter the position of the probes relative to the well plates. More specifically, the lid can be configured to enable the optoelectronic sensor array to move the probes vertically within the wells.
- the magnets can be arranged or moved between positions such that the holding force can be turned on or off.
- an electromagnet can be turned on or off, or can be turned on to oppose a permanent magnet.
- An alternate configuration could allow the actuation pins to go around the sterile barrier of the lid while staying within the footprint of the plate if a feature of the lid can vertically slide up and down within the lid. When pressed by the actuation pins, these passive pins could in turn press off a horizontal surface of the culture plate.
- a flexible membrane is employed. This membrane can be folded or held loosely in place so as to minimize resistance against translation of the actuation pins.
- a potential drawback to this approach is that a thick membrane may not maintain a constant thickness when pressed by the lid and a thin membrane relative to the thickness of the lid creates a dead space through which the actuation pin can be configured to travel before any movement of the probes occurs relative to the well.
- a pin which can slide vertically within the lid.
- a planar constraint can be for example a bore hole for a cylinder.
- it can be desirable to minimize the thickness of the lid, for example to facilitate injection molding.
- the vertically sliding pin can be located in the thin vertical wall of the lid. The vertical travel limits of the pin can be constrained so that the pin remains coupled with the lid.
- the flexures are distributed in vicinity of the periphery of the lid (e.g. as illustrated in FIG. 1B).
- the flexure When a flexure is used for translating motion through the plate, the flexure can be configured such that the relaxed state of the flexure, the neutral position, falls anywhere inside or outside the limits of travel. Specifically, the neutral position of the flexure can be selected near or beyond the maximum extent of the actuation pin such that the spring action in the flexure does not tend to separate the lid from the durable sensor array.
- the flexure portion 132 in general has greater flexibility than other portions of the lid 130 (e.g. due to material composition or due the geometry of a cut-out of the lind forming the flexure) such that in movement of the device relative to the receptacle, at least a first portion of the lid remains in contact with the receptable and at least a second portion of the lid (e.g., the pad 133 of the flexure), separated from the first portion by the flexure portion, remains in contact with the device. 2.2.4 Flexure Integrated into Lid with Stand-Alone Cover
- the lid 130 features which allow translation may require gaps in the plane of the lid surface, but these gaps may reduce the sterile barrier formed by the lid.
- FIG 5 A shows an example gap 510.
- a separate cover, 520 shown in FIG 5B, can be inserted over the flexure such that a tortuous path 512 is created and the sterile barrier is maintained. Use of a separate cover eases the fabrication of the lid.
- the tortuous path features are directly incorporated in the lid, and the flexure is a stand-alone part that is attached to the lid during assembly.
- the cover 520 may be permanently attached to the lid 130 through gluing, solvent bonding, press fitting, ultrasonic welding, or any other technique.
- the cover is a membrane which maintains the complete sterile barrier.
- the lid is, in some embodiments, colorless and translucent so that light can pass through the lid for imaging (e.g., to illuminate the sample via the lid for viewing through a transparent bottom of the receptacle).
- the lid is formed from a translucent or transparent acrylic or a polystyrene.
- the electronics contained in the device are opaque, the device and the contained electronics are easily separated from the lid without hindering the sterile barrier formed by the lid.
- the lid in some embodiments, contains light focusing features that capture light from a large area and focus that light onto a small probe material.
- the focusing features also collimate or focus light emitted from the sensing material onto the light collection device (e.g., a photodiode).
- the light focusing and travel feature might include an optical fiber, and the optical fiber might be sheathed in a rigid material, such as a rigid plastic or a stainless steel tube.
- the end of the light focusing feature that resides in the cell culture well has a minimal diameter, typically between 250 and 800 mih diameter cross section.
- FIG. 6 shows the amount of disruption to oxygen concentration levels depending on the diameter of a probe held in place at a fixed height within the well. This figure assumes that oxygen consumption by the cells follows a zero order oxygen reaction (i.e., is not substrate limited).
- the cross section is minimized so as not to disrupt transport of oxygen to the cells in the well and to minimize disruption of fluid as the probe moves within the well.
- the shape of the light focusing feature might be cylindrical, or conical, having a larger area for light collection on the top side of the plate, with up to 4 mm or even 6 mm diameter.
- the probe can optionally be manufactured as a stand alone component then integrated with the lid for example using those techniques mentioned in Section 2.2.4
- the lid can contain receptacles for holding a small volume of fluid, such as a drug to be applied to the cells in the wells.
- a small volume of fluid such as a drug to be applied to the cells in the wells.
- the fluid can be applied to the samples, and a change in oxygen consumption measured to assess the impact of the fluid on the sample.
- An array of receptacles can align with the wells of the plate.
- methods for dispensing the fluid including pneumatic methods for example US 8318479, or mechanical methods among others.
- the design of the receptacle can include multiple flexures that are naturally closed.
- the number of flexures can be a large number, 4 up to 8 or 16, such that when they are separated, there is a minimal surface area for holding a droplet of fluid.
- the small volume of fluid can be for example less than a microliter up to 20 or 100 or more microliters.
- the maximum surface area of any single flexure can be set such that the force of gravity on the drop of fluid is larger than the force from surface tension between the flexure surface and the droplet.
- the surface tension between the droplet and multiple flexures in the closed position can be larger than the force of gravity on the droplet.
- the flexures can also include a tab at the top of the receptacle such that, when a pin is inserted into the top of the receptacle, the flexures open allowing any fluid contained in the receptacle to fall into the well below.
- the tab is, in some embodiments, positioned such that the pin will never contact fluid held in the receptacle.
- the lowest end of the receptacle flexure can be designed with a point so as to minimize surface tension available for holding fluid suspended.
- Another option for integrating fluid dispensing ports is to provide a sloped well that has a shallow slope, where depending on the position of the actuators the slope become steeper dropping the fluid in to mix with the fluid in the receptacle below.
- a fluid dispensing method that utilizes the movement of the existing system can be used.
- the disposable lid can contain a unique identification code (e.g., embedded in a read-only memory 139 as illustrated in FIGS. 1A-B), which can be read by the durable electronic device 110 either electronically (e.g., with a reader 138 making electrical contact with the memory 139 as shown in FIGS. 1A-B), optically or otherwise.
- This identification code or process can be used to validate authenticity of the lid.
- the lid can also contain electronics for storing calibration and usage information, and for validating lid authenticity.
- the calibration information can potentially include Stem-Volmer constants relating light decay rates to oxygen concentrations, calibration can include information for performing temperature compensation, information for accounting for the useful lifetime of a sensor, and calibration information relating to the response time of the probe and or related diffusion constants.
- the lid can contain electronics (for example, an EEPROM) for storing data such as probe calibration constants, identification codes, date of manufacture, and authentication signature. This data can be read by the optoelectronic sensor array through a communication interface.
- the lid electronics can also contain features for detection of lid attachment and detachment.
- an example of a measurement process 700 that can be used when operating the measurement system includes three different types of procedures, some aspects of which may be performed concurrently: controlling (702) a probe movement pattern, acquiring (704) sensor readings, and executing (706) an algorithm for estimating parameters of the well environment - namely, cellular oxygen consumption.
- the measurement system moves a set of probes vertically according to a movement pattern.
- the described pattern is distinct from a pattern configured for taking series of measurements at various fixed heights where the measurements can then be processed such that they correspond one to one with the heights at which they were measured (a step pattern).
- a step pattern movement is configured to pause such that a measurement at a certain height is not correlated with previous heights of the probe (or the more general pattern).
- the movement pattern can be viewed as an input waveform that is transformed by the measurement environment to produce an output signal. When viewed this way, techniques used in signals analysis and processing can be used in characterization and estimation of the measurement environment in order to optimize the measurement process.
- a key aspect of some embodiments of the measurement process 700 performed using the described measurement system is that it can operate using movement patterns without the distinct pauses that some other systems may have required in order for the gradient to reestablish and/or the sensor readings to stabilize. Furthermore, while movement speed is variable, it is typically slow enough so as not to exceed a speed limit set by a dimensionless number threshold determined by Stokes flow, and possibly not to exceed a speed limit set by the diffusion constants.
- the system time constant can be based on the diameter of the probe (for example when concerning movement velocity), in other instances the system time constant can be based on the travel distance of the probe (for example when waiting for stabilization relative to a disruption of the gradient by the probe), in other instances the time constant can be based on the distance between the probes and the sample, and in other instances the time constant can be based on the distance between the sample and the air-liquid interface.
- Such continuous movement can provide continual precise disturbance of the concentration gradient, in a manner that can be modeled without requiring delays for the disturbance to dissipate.
- the system can be configured so the user is instructed to select the desired performance from a subset of options or through a short survey, and actual movement patterns are determined based on input from the user. Additionally, ideal movement patterns can be determined automatically as described below. 3.1.2 Dynamic Movement Patterns
- the system can automatically update movement based on real external events. These different pattern modes can be triggered automatically based on the environmental state as determined by the system's sensors or external sensors. For example, if a low oxygen gradient is detected across most or all wells, the optimal movement pattern may be a deeper one closer to the cells. If steep oxygen gradients are detected across most or all wells, then a movement pattern optimized for higher resolution at steeper gradients could be used. The movement pattern can also be automatically determined based at least in part on determining a direction most in need of additional information (e.g., by using the state of the Kalman filter uncertainties for the wells). Furthermore, the movement pattern can be set independently for each of the actuation points, such that not all probes move along the same vertical pattern. Any number of the following features can be used to implement dynamic movement patterns in some embodiments of the measurement system.
- the lid contains features, either electrical, active or passive, or non-electrical (eg optical, magnetic), so that the electronics can know when the lid is attached.
- the electronics have onboard sensors including possibly acceleration,
- Initiation or termination of movement series can be triggered by lid attachment (detachment) or other sensor readings.
- Movement pattern contains a zeroing step that utilizes limit switches, potentially triggered by accelerometer / lid attachment.
- State of the movement pattern (determination of next action) is set not only by the current state of the system (dumb, pre-programmed pattern), but also is adjusted by the state of the environment (system under test) as measured by one or more of the onboard sensors.
- sensor readings can include any number of the following:
- stability of the gradient can shift the probes to move lower in the wells, can slow the actuation speed, or can increase amplitude
- a material whose optical properties are sensitive to the surrounding oxygen environment can be used. This material can be excited by light from a LED and the material can return to the ground state through emission of a photon or by transfer of energy to molecular oxygen (quenching). The amount of light emitted and decay rate of light emission are inversely related to oxygen partial pressure through the Stem Volmer relationship.
- the excitation light source intensity can be modulated between two levels (typically on and off) in an irregular pattern.
- the irregular pattern can be generated through a pseudo random code, which can be low pass filtered then discretized to two levels.
- the read time for the sensor can be set arbitrarily.
- each sensor reading might have lower precision relative to longer readings (100 to 600 ms). That is, a longer duration sensor read can be performed for better sensitivity and/or resolution in measurement or a shorter duration sensor read can be performed at the cost of measurement sensitivity and/or resolution.
- shorter readings are made, the previous reading for a given sensor can be used to initialize the recursive pattern such that algorithm startup errors are minimized. Multiple short duration readings can be further processed together, forming a single, high precision reading for downstream processing.
- This sensor method property can be used to maximize the overall performance of this system.
- the sensor read time can be changed in coordination with the movement pattern, measurement mode, or experiment type. For example, a movement pattern tuned for better temporal resolution could coincide with use of a shorter sensor read time to yield even better temporal resolution.
- a longer sensor read time could be used in concert with a movement pattern tuned for higher resolution.
- An alternative configuration could also be to use a longer sensor read time in concert with a smaller range movement pattern in order to satisfy some other system constraint such as cost, size, or power. Similar to the dynamically chosen movement patterns, this tradeoff choice can occur dynamically based on detected environment conditions.
- the configurable read time vs resolution tradeoff provided by the sensor reading method provides greater flexibility for the system design and operation.
- an example of steps in the algorithm for estimation of parameters of the well environment is as follows:
- a sensor reading is taken at a timepoint t along the movement cycle.
- the reading is converted to an oxygen concentration measurement c(t) using calibration data and temperature data.
- the sensor probes have a response delay that can be accounted for to provide accurate measurement data.
- One way of accounting for response delay is to pause at a given depth and discard readings until the sensor has had sufficient time to stabilize. This strategy may not be desirable in some embodiments because the consumption rates of cells may be variable, and long fixed pauses reduce transient responsiveness.
- the sensor readings do not necessarily stabilize at a value corresponding to the concentration at the depth where the probes are currently positioned.
- One approach is to use a movement pattern slow enough relative to the sensor delay such that the readings at a given point within the movement pattern do correspond to the actual concentration at the given depth within some threshold.
- a non-linear spatio temporal model for example a non linear autoregressive moving average model with exogenous inputs or NARMAX model
- NARMAX model for example a non linear autoregressive moving average model with exogenous inputs or NARMAX model
- both current probe position and concentration readings are fed into a non-linear model as inputs, and the model is used to estimate parameters of the underlying system including transport of the molecule of interest through the region of interest.
- FIGS. 11A and 11B show an example of concentration measurements (FIG.
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| KR1020217009424A KR20210054545A (en) | 2018-08-31 | 2019-08-30 | Measurement of dynamic systems |
| EP19770222.8A EP3843898A1 (en) | 2018-08-31 | 2019-08-30 | Measurement of a dynamic system |
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| WO2023016834A1 (en) * | 2021-08-08 | 2023-02-16 | Cytena Bioprocess Solutions Co., Ltd | Image acquisition system for acquiring an image of a liquid sample |
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| EP3843898A1 (en) | 2018-08-31 | 2021-07-07 | Lucid Scientific, Inc. | Measurement of a dynamic system |
| WO2022265970A1 (en) | 2021-06-15 | 2022-12-22 | Lucid Scientific, Inc. | Lid with variable interlayer gap |
| WO2026019867A1 (en) | 2024-07-16 | 2026-01-22 | Lucid Scientific, Inc. | Multimodal sensing of biological samples |
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| JP2021536572A (en) | 2021-12-27 |
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