WO2020105044A1 - Biological fluidic system - Google Patents
Biological fluidic systemInfo
- Publication number
- WO2020105044A1 WO2020105044A1 PCT/IL2019/051264 IL2019051264W WO2020105044A1 WO 2020105044 A1 WO2020105044 A1 WO 2020105044A1 IL 2019051264 W IL2019051264 W IL 2019051264W WO 2020105044 A1 WO2020105044 A1 WO 2020105044A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- arrangement
- chamber
- fluid
- duct
- cultivation
- Prior art date
Links
Classifications
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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
- C12M37/00—Means for sterilizing, maintaining sterile conditions or avoiding chemical or biological contamination
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- 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
- C12M23/00—Constructional details, e.g. recesses, hinges
- C12M23/02—Form or structure of the vessel
- C12M23/04—Flat or tray type, drawers
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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
- C12M23/00—Constructional details, e.g. recesses, hinges
- C12M23/28—Constructional details, e.g. recesses, hinges disposable or single use
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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
- B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
- B01L3/5027—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
- B01L3/502761—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip specially adapted for handling suspended solids or molecules independently from the bulk fluid flow, e.g. for trapping or sorting beads, for physically stretching molecules
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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
- B01L3/56—Labware specially adapted for transferring fluids
- B01L3/563—Joints or fittings ; Separable fluid transfer means to transfer fluids between at least two containers, e.g. connectors
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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
- C12M23/00—Constructional details, e.g. recesses, hinges
- C12M23/02—Form or structure of the vessel
- C12M23/16—Microfluidic devices; Capillary tubes
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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
- C12M23/00—Constructional details, e.g. recesses, hinges
- C12M23/26—Constructional details, e.g. recesses, hinges flexible
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- 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
- C12M23/00—Constructional details, e.g. recesses, hinges
- C12M23/34—Internal compartments or partitions
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- 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
- C12M23/00—Constructional details, e.g. recesses, hinges
- C12M23/42—Integrated assemblies, e.g. cassettes or cartridges
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- 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
- C12M23/00—Constructional details, e.g. recesses, hinges
- C12M23/44—Multiple separable units; Modules
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
- C12M25/00—Means for supporting, enclosing or fixing the microorganisms, e.g. immunocoatings
- C12M25/02—Membranes; Filters
- C12M25/04—Membranes; Filters in combination with well or multiwell plates, i.e. culture inserts
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- 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
- C12M29/00—Means for introduction, extraction or recirculation of materials, e.g. pumps
- C12M29/10—Perfusion
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- 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
- C12M29/00—Means for introduction, extraction or recirculation of materials, e.g. pumps
- C12M29/12—Pulsatile flow
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- 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
- C12M29/00—Means for introduction, extraction or recirculation of materials, e.g. pumps
- C12M29/20—Degassing; Venting; Bubble traps
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- 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
- C12M31/00—Means for providing, directing, scattering or concentrating light
- C12M31/02—Means for providing, directing, scattering or concentrating light located outside the reactor
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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
- C12M31/00—Means for providing, directing, scattering or concentrating light
- C12M31/10—Means for providing, directing, scattering or concentrating light by light emitting elements located inside the reactor, e.g. LED or OLED
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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
- C12M33/00—Means for introduction, transport, positioning, extraction, harvesting, peeling or sampling of biological material in or from the apparatus
- C12M33/14—Means for introduction, transport, positioning, extraction, harvesting, peeling or sampling of biological material in or from the apparatus with filters, sieves or membranes
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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
- C12M41/06—Means for regulation, monitoring, measurement or control, e.g. flow regulation of illumination
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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
- C12M41/12—Means for regulation, monitoring, measurement or control, e.g. flow regulation of temperature
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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
- C12M41/30—Means for regulation, monitoring, measurement or control, e.g. flow regulation of concentration
- C12M41/36—Means for regulation, monitoring, measurement or control, e.g. flow regulation of concentration of biomass, e.g. colony counters or by turbidity measurements
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N1/00—Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
- C12N1/04—Preserving or maintaining viable microorganisms
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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
- B01L2200/06—Fluid handling related problems
- B01L2200/0684—Venting, avoiding backpressure, avoid gas bubbles
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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
- B01L2300/0681—Filter
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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
- B01L2300/12—Specific details about materials
- B01L2300/123—Flexible; Elastomeric
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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
- B01L2400/00—Moving or stopping fluids
- B01L2400/04—Moving fluids with specific forces or mechanical means
- B01L2400/0475—Moving fluids with specific forces or mechanical means specific mechanical means and fluid pressure
- B01L2400/0481—Moving fluids with specific forces or mechanical means specific mechanical means and fluid pressure squeezing of channels or chambers
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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
- B01L2400/00—Moving or stopping fluids
- B01L2400/06—Valves, specific forms thereof
- B01L2400/0677—Valves, specific forms thereof phase change valves; Meltable, freezing, dissolvable plugs; Destructible barriers
- B01L2400/0683—Valves, specific forms thereof phase change valves; Meltable, freezing, dissolvable plugs; Destructible barriers mechanically breaking a wall or membrane within a channel or chamber
Definitions
- the present disclosure concerns a biological fluidic system, in particular a cultivation system.
- the present disclosure concerns a biological fluidic system that provides a high degree of sterilization by performing the biological processing in a closed system in which the fluid is contained in chambers that are isolated from the environment in a manner that does not permit ingress of contaminants.
- the biological fluid e.g. liquid or gas
- the processing arrangement may be in some embodiments used as a cultivating arrangement for the cultivation of living matter.
- Some non-limiting examples for 'living matter' are microorganisms, cells, tissues.
- the polymeric sheets, particularly where the system is intended for cultivation of living matter e.g.
- microorganisms may be made of transparent or translucent polymeric material.
- Said arrangement includes one or more processing chambers for accommodating reaction liquids that comprise biological components and one or more ducts to permit liquid circulation within the arrangement.
- the biological arrangement is pliable and through selective pressure on various regions thereof, e.g. on regions of the one or more ducts, a fluid is driven to flow to thereby circulate through said arrangement.
- 'fluid' includes, but not limited to, liquids, gases and plasmas.
- the processing arrangement may be stretchable and contractible in some degree allowing the flow of fluids and biological components therein by applying forces, e.g. lateral forces, on the processing arrangement.
- forces e.g. lateral forces
- Application of lateral forces on the processing arrangement may stimulate the cultivation of cells or tissues, such as muscle tissues, tendons and more.
- the biological processing that is carried out within said arrangement may include, but not limited to, cultivation of microorganism, cell cultures (of animal or plant cells), soft and hard tissues, biological assays such as Isothermal PCR, immunoassays, protein based assays, chemical assays, chromatography, or other chemical and biochemical assays.
- a system for cultivation of living matter such as cells or microorganisms.
- the system comprising a cultivating arrangement formed between two polymeric sheets fixed to one another.
- the sheets may be made of a variety of polymeric materials, including single layer or multi-layer polymeric sheets.
- the polymer may, for example, be nylon including polyamide and/or polyethylene.
- the cultivating arrangement is formed with at least one chamber that is configured for cultivating microorganisms and at least one duct, each linking between two ports of the at least one chamber.
- the at least one duct has a flow-driving region that is configured for engagement with a fluid driving mechanism that, through a peristaltic action propels fluid flow through the duct between the two ports.
- first port will be used, for convenience, for one of the ports and“second port” for the other.
- the qualification of the ports as“first” or“second” has no hierarchal significance and are used only in order to streamline the description.
- the fluids can flow in both directions, namely from the first port to the second and vice versa.
- the fluid driving mechanism may be controllable either in terms of speed of action, namely the rate of fluids it propels in a time unit or in terms of predetermined operation times.
- the fluid driving mechanism may be set to operate at a predetermined cycles, e.g. once every 1 hour or several times a day at a predetermined intervals between operation times, each operation may last for a few seconds or minutes.
- the first port is located at one side of the chamber, e.g. an upper side, and the second port at another side, e.g. a lower side.
- a flow of liquids between the ports e.g. between a lower second port to an upper first port, circulates the liquid in the processing chamber.
- a flow from the second port to the first causes the circulation of liquids from a bottom portion of the chamber to a top portion thereof, while a flow from the first, top port to the second causes bubbling of air from the top portion of the chamber into the liquid.
- the system further includes an inlet duct linkning the at least one chamber that is configured for cultivating microorganisms to a medium reservoir.
- the medium reservoir includes growth medium suitable for the microorganisms that grow in the at least one chamber.
- the growth medium is driven either by a manual force application or by a medium driving mechanism that drives the growth medium from the medium reservoir towards the at least one chamber.
- the medium reservoir may be part of the cultivating arrangement or connectable thereto.
- the system further includes an outlet duct linking the at least one chamber that is configured for cultivating microorganisms to a discharge reservoir that is configured to receive discharged medium from the at least one chamber.
- the discharged medium is driven either by a manual force application or by a discharge driving mechanism that drives the discharged medium from the at least one chamber towards the discharge reservoir.
- the discharge reservoir may be part of the cultivating arrangement or connectable thereto.
- the flow-driving region of the duct may be made to trace at least a section of a circle and may be generally circular.
- the fluid driving mechanism is configured as a peristaltic pump to peristaltically propel the liquid and to permit the bi-directionality of the circulation of the fluids.
- the driving mechanism comprises at least one engaging element configured to engage the flow-driving region and to propel fluid therethrough.
- the engagement element may be physically separated from the driving mechanism and being magnetically coupled to a driving motor to be driven thereby to propel the fluid.
- the system may comprise a venting arrangement to permit gas exchange between the interior of the processing arrangement and the exterior environment.
- the venting arrangement may comprise at least one of a (i) filter for filtering particles in the introduced gas, such as a HEPA filter, paper or plastic made filter, activated carbon filter; and (ii) uni-directional valve that permits either the introduction of gas into the processing arrangement or the flow of excess gas from the processing arrangement into the environment.
- the venting arrangement is configured to permit gas exchange without passage of microorganism therethrough, for example by having a swan-necked shape.
- the processing arrangement may have an introduction region configured to hold the cells such that they are separated from the processing chamber that contains the necessary biological components for cultivation. This separation assists to control the initiation time of the cultivation process.
- the separation may be carried out by a (i) swan-necked duct linking the microorganisms and the cultivation chamber that requires application of force on the polymeric sheets to drive the microorganisms into the chamber; (ii) sealing member that separates the microorganisms region and the cultivation chamber, the sealing member being rupturable or breakable to permit the introduction of the microorganisms into the chamber; or (iii) combination of a swan necked duct and a sealing member.
- the processing arrangement may also comprise an inoculation port for introducing microorganisms into the chamber.
- the processing chamber comprises one or more regions in which opposite walls thereof are fixed to one another, e.g. laser welded, to prevent substantial expansion of the dimensions of the chamber, due to the elasticity of its walls, in the presence of liquid or the increase of the internal pressure (e.g. by gaseous products of the microorganisms).
- the processing arrangement preferably may be disposable.
- the system further comprising a base structure that comprises the driving mechanism and configured for association with the cultivating arrangement.
- the system comprising a temperature control unit that comprises at least one temperature sensor for sensing the temperature of the fluids in the processing arrangement, and specifically in the cultivation chamber.
- the sensed temperature may affect the operation of the temperature control unit to maintain a range of temperatures within the processing arrangement, or more specifically within the cultivation chamber.
- the temperature control unit maintains the range of temperatures within the cultivation between 25°C and 100°C.
- the system may further comprise at least one light source and at least one light sensor for sensing the light reflection from or light transmission through the fluid within the cultivation chamber.
- the light source may be selected from any one of a laser source of a LED light source.
- the sensed data may be communicated by a communication module to an external unit for either storing or processing the data.
- the arrangement comprises (i) a cultivation chamber, (ii) a duct between two ports of the chamber to permit flow of fluid between the two ports through the duct, and (iii) a flow-driving region defined within the duct that is configured for engagement with a fluid driving mechanism to thereby propel fluid flow between the two ports.
- a biological fluidic system comprising a fluid driving mechanism and a biological arrangement formed between two polymeric sheets.
- the arrangement comprises (i) at least one chamber, (ii) at least one duct to permit flow of fluid between two ports of a chamber and/or between two chambers, and (iii) a flow-driving region defined within the at least one duct that is configured for engagement with the fluid driving mechanism to thereby propel fluid flow between the two ports.
- Yet another aspect of the present disclosure provides a cultivating arrangement formed between two polymeric sheets and having a pre-cultivating, storage compartment, for storing living matter, that is separated from a cultivation chamber by a rupturable or breakable sealing.
- the sealing may be broken or ruptured by an external force, e.g. a finger pressing or an actuation arrangement configured to rupture the sealing and drive the living matter into the cultivation chamber via an inoculation port the cultivation chamber comprises nutrients suitable for allowing cultivation of the living matter.
- the cultivation arrangement may further comprise a duct between two ports of the chamber to permit flow of fluid between the two ports through the duct, and having a flow-driving region defined within the duct that is configured for engagement with a fluid driving mechanism to thereby propel fluid flow between the two ports.
- Yet another aspect of the present disclosure makes use of the structure of the fluidic system described above for performing chemical reactions in a sterilized closed system.
- the system comprising a reacting arrangement formed between two polymeric sheets fixed to one another.
- the reacting arrangement is formed with a first and second chambers, each configured for holding a chemical component, and at least one duct linking between the first and the second chambers.
- each of the first and second chambers may be linked to one or more additional chambers holding additional chemical components via linking ducts.
- the first and the second chambers are separated by rupturable or breakable sealing.
- the sealing may be broken or ruptured by an external force, e.g. a finger pressing or an actuation arrangement configured to rupture the sealing and drive the chemical components from one chamber to the other.
- the reacting arrangement comprises one or more uni directional valves permitting the introduction or removal of gas to or from one of the chambers.
- the reacting arrangement comprising a flow-driving duct linking between two ports of one of the first and second chambers and comprises a flow-driving region that is configured for engagement with a fluid driving mechanism that, through a peristaltic action propels fluid flow through the duct between the two ports.
- FIGs. 1A-1C are perspective views of schematic illustrations of examples of the macro-fluidic system of the present disclosure.
- Fig. 1A shows separately the cultivation arrangement and the base structure of the macro-fluidic system;
- Fig. IB shows the cultivation arrangement associated with the base structure, together with the engaging elements engaging the flow-driving region;
- Fig. 1C shows the working scheme of a stretching mechanism macro-fluidic system of the present disclosure.
- Fig. 2A-2B are top views of schematic illustrations of examples of the fluidic system of the present disclosure for carrying out chemical reactions.
- Fig. 2A shows a two chambers structure of the system;
- Fig. 2B shows a three chambers structure of the system.
- Fig. 1A is a perspective view of a schematic illustration of the macro-fluidic system configured for cultivating microorganisms.
- the system 100 includes a cultivating arrangement 102 formed between two polymeric sheets 104 and 106 welded to one another by laser welding. The two sheets are welded to one another to form a structure of internal spaces confined between the two sheets that are not welded to one another. This spaces form, among other structures, a cultivation chamber 108 configured for accommodating microorganisms and biological components such as bacterial cells, growth media, antibiotics, viral particles, nucleic acids, enzymes, etc. to thereby serve as a basis for cultivation.
- the cultivation chamber 108 has two ports 110A and HOB, at a top and a bottom portion of the chamber 108 respectively.
- the two ports 110A and HOB are linked one to the other by a duct 112 that is configured to permit the flow of fluids therethrough, such as liquid and gases.
- the duct 112 has a generally circular region that is configured to serve as a flow-driving region 114.
- the cultivation arrangement 102 comprises four through-holes 116 in its four corners to permit hanging of the cultivation arrangement 102 on four hanging members 118 on a base structure 120 for being in a close association therewith.
- the base structure 120 comprises a driving mechanism (not shown) that is configured to be coupled magnetically with engaging members 122A and 122B, which are detachable from the base structure.
- the engaging members 122A and 122B are configured to engage the flow-driving region 114 and driven by the driving mechanism, while the cultivation arrangement 102 and the base structure are associated, to thereby propel fluids within the cultivation arrangement 102.
- the cultivation chamber 108 includes a plurality of regions in which opposite walls thereof, namely the two polymeric sheets, are welded to one another. These welded regions 124 prevents swelling of the chamber 108 due to increase of pressure of the fluids therein and the elasticity/flexibility of the walls.
- the cultivation chamber may be manufactured at first with the microorganisms separated from the cultivation chamber.
- the microorganisms may be stored in a microorganisms chamber 126 separated from the cultivation chamber 108 by a swan necked region 128 linked to an inoculation port 130, and/or a rupturable or breakable sealing member 132 that upon rupturing or breaking thereof permits the introduction of the microorganisms into the chamber 108.
- the base structure 120 is associated with a heat source 134 that is configured to be in a close association with the cultivation chamber 108 when the cultivation arrangement 102 and the base structure 120 are associated therewith.
- the heat source 134 is configured to maintain the cultivation chamber at a predetermined range of temperatures such as 32°C-42°C.
- the heat source 134 may be in data communication with a temperature control (not shown) unit configured to control the operation of the heat source 134 to maintain the desired range of temperatures.
- the control unit may comprise one or more temperature sensors for sensing the ambient temperature and/or one or more temperatures of the cultivation arrangement, e.g. the cultivation chamber or the flow-driving region.
- the base structure 120 formed with a slit 136, that upon association of the cultivation arrangement and the base structure, configured to face at least one of the duct 112 and the cultivation chamber 108.
- a spectrophotometer is comprised within the base structure 120 and configured to measure the spectral profile of the fluids within the cultivation arrangement 104 to obtain data indicative of microorganism growth or density.
- the spectrophotometer may be configured to illuminate with a wavelength in the range of 500-700 nm. In some embodiments, the spectrophotometer is configured to measure the fluid in the cultivation arrangement of at least 5 different wavelengths.
- the base structure 120 may also comprise a light source configured to illuminate at least portions of the cultivation arrangement.
- the light source may illuminate through the slit 136 or an additional slit 138 with a wavelength in the range of 425-450 nm and/or 600-700 nm for the cultivation of photosynthetic cells.
- Fig. IB exemplifies the system of the present disclosure, wherein the base structure 120 is associated with the cultivation arrangement 102 by the insertion of the hanging members 118 into the through-holes 116.
- the two engaging elements 122A and 122B are magnetically attracted to the driving mechanism, causing the attachment of the engaging elements to the flow-driving region 112.
- the engaging elements 122A and 122B are driven by the driving mechanism to rotate along the flow- driving region 112 in the direction of the arrow A, that causes a flow of gas from a top portion of the cultivation chamber 108 into a bottom portion thereof, and the bubbling of the gas into the liquid.
- the driving mechanism drives the engaging elements in an opposite direction of the arrow A, liquid from a bottom portion of the cultivation chamber 108 flow through duct 112 to the top portion of the chamber 108. Therefore the driving mechanism and the engagement elements 122A and 122B are configured together as a bi-directional peristaltic pump.
- the heat source 134 is in thermal contact with the cultivation chamber 108 and configured to heat the chamber 108 to maintain a certain range of desired temperatures suitable for the biological processing, e.g. cultivation of cells.
- the slit 136 faces the duct 112 to allow measurements of the spectrophotometer, or any other optical measurement device that may be accommodated within the base structure 120.
- a light isolating member 137 is configured to attach to the region of the slit 136 such that it is substantially isolating the measured portion of the duct 112 from ambient light while allowing the flow therein. The member 137 induces repetitive conditions between measurements, increasing the credibility of the measurements.
- Fig. 1C is a schematic illustration of an example of an embodiment of the system of the present disclosure.
- Four members 140 of a stretching mechanism (not shown) are inserted into the through-holes 116 at the four corners of the cultivation arrangement 102, and configured to move in the direction of at least one of the arrows A1-A4 to apply forces on the cultivating arrangement 102 and stretch thereof, due to its pliable characteristics.
- This mechanism may enhance the cultivation of some types of cell cultures or tissues, such as muscle tissue or tendon.
- Figs. 2A-2B are schematic illustrations of two embodiments a system for performing a chemical reaction according to the present disclosure.
- Figs. 2A-2B show a reacting arrangement 202 formed between two polymeric sheets.
- the reacting arrangement 202 has a first and a second chamber 242 and 244, each comprises a chemical component.
- the chemical component may be a fluid, e.g. in a liquid or gas form or can be made of solid particles.
- a duct 246 links between ports 248, 250 of the first and second chambers 242 and 244 respectively.
- chamber 242 is linked with an additional chamber 252 holding an additional chemical component.
- the introduction of the additional chemical component to the chamber 242 is prevented a rupturable sealing member 232 and upon rupturing thereof, the chemical component stored in chamber 252 is free to be introduced into chamber 242.
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Abstract
Description
Claims
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2021527118A JP7399501B2 (en) | 2018-11-19 | 2019-11-19 | biological fluid system |
CN201980076203.XA CN113166705B (en) | 2018-11-19 | 2019-11-19 | Biological fluid system |
KR1020217017391A KR20210093935A (en) | 2018-11-19 | 2019-11-19 | biological fluid system |
AU2019383080A AU2019383080A1 (en) | 2018-11-19 | 2019-11-19 | Biological fluidic system |
EP19886207.0A EP3884035A4 (en) | 2018-11-19 | 2019-11-19 | Biological fluidic system |
US17/294,467 US20220010259A1 (en) | 2018-11-19 | 2019-11-19 | Biological fluidic system |
CA3120243A CA3120243A1 (en) | 2018-11-19 | 2019-11-19 | Biological fluidic system |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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IL263127A IL263127B (en) | 2018-11-19 | 2018-11-19 | Biological fluidic system |
IL263127 | 2018-11-19 |
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WO2020105044A1 true WO2020105044A1 (en) | 2020-05-28 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/IL2019/051264 WO2020105044A1 (en) | 2018-11-19 | 2019-11-19 | Biological fluidic system |
Country Status (9)
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US (1) | US20220010259A1 (en) |
EP (1) | EP3884035A4 (en) |
JP (1) | JP7399501B2 (en) |
KR (1) | KR20210093935A (en) |
CN (1) | CN113166705B (en) |
AU (1) | AU2019383080A1 (en) |
CA (1) | CA3120243A1 (en) |
IL (1) | IL263127B (en) |
WO (1) | WO2020105044A1 (en) |
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- 2019-11-19 US US17/294,467 patent/US20220010259A1/en active Pending
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Also Published As
Publication number | Publication date |
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KR20210093935A (en) | 2021-07-28 |
JP7399501B2 (en) | 2023-12-18 |
EP3884035A4 (en) | 2022-08-24 |
CA3120243A1 (en) | 2020-05-28 |
JP2022509949A (en) | 2022-01-25 |
IL263127A (en) | 2020-05-31 |
CN113166705B (en) | 2024-06-07 |
CN113166705A (en) | 2021-07-23 |
US20220010259A1 (en) | 2022-01-13 |
IL263127B (en) | 2022-07-01 |
AU2019383080A1 (en) | 2021-06-03 |
EP3884035A1 (en) | 2021-09-29 |
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