Patent Application
20240425795
The present disclosure relates to a bioreactor, for example, a bioreactor for cell culturing.
Cell and gene therapy manufacturing processes are often complex and include manual or semi-automated steps across several devices. Equipment systems used in various steps (i.e., unit operations) of cell-based therapeutic products (CTP) manufacturing may include devices for cell collection, cell isolation/selection, cell expansion, cell washing and volume reduction, cell storage and transportation. The unit operations can vary immensely based on the manufacturing model (i.e., autologous versus allogenic), cell type, intended purpose, among other factors. In addition, cells are “living” entities sensitive to even the simplest manipulations (such as differences in a cell transferring procedure). The role of cell manufacturing equipment in ensuring scalability and reproducibility is an important factor for cell and gene therapy manufacturing.
In addition, cell-based therapeutic products (CTP) have gained significant momentum thus there is a need for improved cell manufacturing equipment for various cell manufacturing procedures, for example, but not limited to stem cell enrichment, generation of chimeric antigen receptor (CAR) T cells, and various cell manufacturing processes such as collection, purification, gene modification, incubation/recovery, washing, infusion into patient and/or freezing.
The culture or processing of cells typically requires the use of a device to hold the cells, for example, in an appropriate culture medium when culturing the cells. The known devices include shaker flasks, roller bottles, T-flasks and bags.
A key limiting factor in the production of cells or gene therapies for use in medicine is the absence of compact, automated closed systems for performing unit operations without contamination. For example, during cell culture, upstream or subsequent processing of cells, there is a risk of contamination when making additions to the culture vessel, or when removing cells or removing liquid samples. The operating systems are largely manual and hence expensive to operate. Multiple pieces of equipment are typically required to cover all of the non-cell culture steps, which involves many transfers, each of which is an opportunity for operator errors and contamination to occur. Furthermore, with increasing manual operations comes increasing risk of manual errors and therefore the current labor-intensive processes lack the robustness required for the manufacture of clinical-grade therapeutics.
There is therefore a need for cell processing devices (e.g., multistep cell processors) that permit such processing that avoids the requirement for constant movement of cells into fresh devices.
According to an aspect of the present disclosure, there is provided a bioreactor for cell culturing, the bioreactor comprising:
In examples, the sensor element is disposed on the base. In other examples, the sensor element is additionally or alternatively disposed on the side wall. The container, in particular, the base or side wall, may comprise a sensor window, and the sensor element may be disposed on the sensor window. The sensor window is preferably configured to permit transmission of light between the sensor element and the sensor receiver.
In examples, the rotational axis extends through the base and the internal volume of the container.
In examples, the sensor element comprises an annulus centered on the rotational axis of the bioreactor. Accordingly, the sensor receiver is aligned with the annulus sensor element regardless of the rotational position of the bioreactor. In examples where the sensor element is on the base, the sensor element forms an annulus on the base. In examples where the sensor element is on the side wall, the sensor element extends about the circumference of the side wall.
In examples, the sensor element may comprise a plurality of discrete portions. The discrete portions may be arranged on the base, in particular, on a common circumference from the rotational axis, or on the side wall.
In examples, the sensor element or at least one of the discrete portions of the sensor element may comprise an annular sector. The annular sector may extend about the rotational axis by between about 20 degrees and about 350 degrees so that the sensor receiver is aligned with the annular sector sensor element through a portion of the rotation of the bioreactor. In examples, the annular sector may extend about the rotational axis by any amount, for example, between about 20 degrees and about 180 degrees, or between about 45 degrees and about 90degrees.
In examples, the sensor element or at least one of the discrete portions of the sensor element may comprise a dot, for example, a circular dot or square dot. The dots may be evenly distributed about the rotational axis, for example, twelve dots can be positioned at 30degree intervals, four dots can be positioned at 90 degree intervals, or three dots can be positioned at 120 degree intervals, etc.
In examples, the bioreactor may comprise a second sensor element disposed on an internal surface of the container. In examples, the second sensor element may be disposed on the sensor window, or on a second sensor window. The second sensor element may be aligned with the rotational axis of the bioreactor and arranged to align with a second sensor receiver positioned externally of the base and operable to interact with the second sensor element to detect a characteristic of the cell suspension. Accordingly, the second sensor receiver and second sensor element are aligned regardless of the rotational position of the bioreactor. In examples, the sensor element may be spaced from the second sensor element, or they may be abutting along an edge.
In examples, the bioreactor may comprise a third sensor element disposed on an internal surface of the container. In examples, the third sensor element may be disposed on the sensor window, on the second sensor window, or on a third sensor window. The third sensor element may be offset from the rotational axis of the bioreactor and arranged to align with a third sensor receiver positioned externally of the base and operable to interact with the third sensor element to detect a characteristic of the cell suspension. In examples, the third sensor element is arranged to align with the third sensor receiver in at least two rotational positions of the bioreactor during use. In examples, the sensor element may be spaced from the third sensor element, or they may be abutting along an edge.
In examples, the sensor element and/or second sensor element may be adhered to the internal surface of the container, for example, to an internal surface of the sensor window. In examples, the sensor element and/or the second sensor element comprises an oxygen-sensitive coating or a pH-sensitive coating. In examples, the sensor element and/or the second sensor element may comprise a substrate having an oxygen-sensitive coating or a pH-sensitive coating on one side and an adhesive on the other side for fixing to the sensor window. The sensor element and/or second sensor element, in particular, a material or coating of the sensor element and/or second sensor element, may be configured to respond to incident light that induces a fluorescent signal based on a characteristic of the cell suspension within the bioreactor, for example, an oxygen concentration or pH of the cell suspension. Accordingly, the sensor receiver can receive the fluorescent signal and a sensor meter can be used to measure the fluorescent signal to determine the characteristic of the cell suspension.
The sensor window is transparent or translucent to the wavelength of light at which the sensor element and sensor receiver operate. In examples, the sensor window comprises a transparent or translucent material, for example, a polymer such as polycarbonate, polyethylene terephthalate, or polymethyl methacrylate, or another material such as glass.
In examples, the side wall comprises a compressible side wall, for example, a bellows wall. Accordingly, the container may be a compressible or deformable container.
In examples, the bioreactor may further comprise an interface plate attached to the side wall opposite to the base. The interface plate may comprise one or more ports for adding fluid to, or extracting fluid from, the container.
According to a further aspect of the present disclosure, there is also provided a bioreactor system comprising the bioreactor described above, and a housing adapted to support the bioreactor such that the bioreactor is rotatable relative to the housing about the rotational axis.
In examples, the housing may be an incubator housing configured to control an environment of the bioreactor.
For example, the bioreactor may comprise an interface plate attached to the side wall opposite to the base, and the housing may comprise a bioreactor receiving portion adapted to support the interface plate such that the side wall and base are suspended below the interface plate.
The interface plate may comprise a plurality of connector interfaces for connecting a consumable for adding fluid to, or extracting fluid from, the bioreactor. The plurality of connector interfaces may be spaced about the interface plate at a common distance from the rotational axis of the bioreactor. The bioreactor may be rotatable to index between connector interfaces on the interface plate. For example, the bioreactor system may include a consumable attachment point for attaching a consumable to the bioreactor system such that it can engage a connector interface on the interface plate. The bioreactor can be rotated to bring different connecter interfaces into alignment with the consumable attachment point. In examples, the sensor element and the sensor receiver are arranged to be aligned with each other in each of the rotational positions of the bioreactor that correspond to alignment between a connector interface and the consumable attachment point.
In examples, the housing, in particular, the bioreactor receiving portion, may comprise an actuator operable to rotate the bioreactor.
In examples, the bioreactor system may further comprise a sensor receiver positionable externally of the base and arranged to be aligned with the sensor element in at least two rotational positions of the bioreactor relative to the housing.
In examples, the sensor receiver may comprise an optical receiver, for example, an optical fiber. The bioreactor system may further comprise a sensor meter arranged to receive an optical signal from the optical receiver. In examples, the sensor receiver includes an optical mount arranged to position the optical receiver, in particular, the optical fiber, in alignment with the sensor element. In examples, the sensor meter may be configured to transmit a sensor excitation signal to the sensor element, and to receive a sensor signal returned from the sensor element.
In examples, the sensor receiver may be movably mounted and movable to an operational position in which the sensor receiver is in contact with, or adjacent to, the container of the bioreactor proximal to the sensor element. In some examples, in the operational position the sensor receiver is in contact with, or adjacent to, a surface of the base or side wall of the container, for example, a sensor window. Specifically, in the operational position the sensor receiver may abut, or be proximal to, the sensor window. For example, the sensor receiver may be positioned within about 10 millimeters of the external surface of the container (e.g., sensor window), preferably within about 7 millimeters.
In examples, the bioreactor system may include a second sensor receiver for a second sensor element, as described above. In such examples, the second sensor receiver may be mounted in the same manner as the sensor receiver described above. The sensor receiver and second sensor receiver may be provided in a sensor unit that is movable to the operational position.
In examples, the bioreactor system may comprise an actuator operable to move the sensor receiver and/or the sensor unit into the operational position.
In examples, the side wall of the bioreactor may comprise a compressible side wall, for example, a bellows wall. In such examples, the bioreactor system may further comprise an agitator operable to engage the base of the bioreactor. The agitator may be operable to compress the container of the bioreactor, and/or to tilt the base of the bioreactor, in order to agitate the contents of the bioreactor.
In examples, the sensor receiver may be mounted to the agitator such that the sensor receiver and/or sensor unit is in the operational position when the agitator engages the base of the bioreactor. For example, the agitator may comprise an agitator plate operable to engage the base of the bioreactor, and the sensor receiver and/or sensor unit may be mounted to the agitator plate.
In examples, the agitator may be configured to couple to the base of the bioreactor. In particular, an agitator plate of the agitator may be configured to couple to the base, for example, by a mechanical clip or by an electromagnetic coupling.
In examples, the agitator may be configured to decouple from the base to permit rotation of the bioreactor relative to the housing. Alternatively, the agitator, in particular, the agitator plate, may include a rotatable portion that is rotatable with the bioreactor.
According to a further aspect of the present disclosure, there is also provided a method of culturing cells in the bioreactor system described above, the method comprising:
As described above, the bioreactor may be rotated in order to bring different connector interfaces of the bioreactor into alignment with a consumable attachment point on the housing.
In examples, the method may further comprise agitating the cell suspension in the container.
In examples, sensing a characteristic of the cell suspension may comprise sensing a dissolved oxygen or pH of the cell suspension.
When sensing the characteristic of the cell suspension an optical signal may pass from the sensor element to the sensor receiver.
Embodiments of the invention are further described hereinafter with reference to the accompanying drawings, in which:
The bioreactor 1 shown in
The interface plate 3 is attached to a top of the cell culture container 2, for example, acting as a lid or closure. The interface plate 3 comprises at least one connector interface 5 for connecting to an external component, for example, a consumable for delivering a fluid to, or extracting a fluid from, the cell culture container 2. Preferably, the interface plate 3 includes a plurality of connector interfaces 5 for connecting to external components. Each connector interface 5 may be used once or more for adding or removing fluid. The connector interfaces 5 may be distributed about the interface plate 3. Accordingly, the interface plate 3 provides for adding media and other fluids to the cell culture container 2 during cell processing, and/or for removing fluid from the cell culture container 2 during processing, for example, to remove a sample or waste fluid.
The cell culture container 2 may be extendable and/or compressible. In particular, the cell culture container 2 has a compressible wall element 6, for example, a bellows wall. The cell culture container 2 has a base 7 disposed opposite to the interface plate 3, and a compressible wall element 6 defining a sidewall of the cell culture container 2. A top part of the compressible wall element 6 is attached to the interface plate 3. The top part of the compressible wall element 6 may include a rigid ring 8 or similar for attaching to the interface plate 3. The compressible wall element 6 is compressible and/or extendible such that the base 7 can move toward and away from the interface plate 3, changing the internal volume of the cell culture container 2. The base 7 may be moved relative to the interface plate 3 in order to agitate or mix the fluid 4 in the cell culture container 2.
The compressible wall element 6 may be a bellows wall, having a concertina arrangement that allows the compressible wall element 6 to fold onto itself in order to compress. In particular, as illustrated the compressible wall element 6 may comprise a series of alternately arranged deformable portions 9a, 9b, specifically inwardly deformable portions 9a and outwardly deformable portions 9b. Leaf segments 10 extend between the deformable portions 9a, 9b. The leaf segments 10 are more rigid than the deformable portions 9a, 9b. The deformable portions 9a, 9b act as hinges that allow the compressible wall element 6 to collapse like a bellows or concertina, with the leaf segments 10 remaining substantially non-deformed.
The compressible wall element 6 may comprise at least one inwardly deformable portion 9a and at least one outwardly deformable portion 9b, for example, at least two inwardly deformable portions 9a and at least two outwardly deformable portions 9b. The compressible wall element 6 may comprise three, four, or more inwardly deformable portions 9a and three, four or more outwardly deformable portions 9b.
The inwardly deformable portion(s) 9a and outwardly deformable portion(s) 9b may be formed by thinned sections in the compressible wall element 6. The inwardly deformable portion(s) 9a may comprise a thinned section arranged on the outer surface of the compressible wall element 6 such that it is deformable in an inwards direction. The outwardly deformable portion(s) 9b may comprise a thinned section arranged on the inner surface of the compressible wall element 6 such that it is deformable in an outwards direction.
In examples, the compressible wall element 6 comprises a silicone, in particular, a liquid silicone rubber. In other examples, the compressible wall element 6 comprises a low density polyethylene (LDPE). In other examples, the compressible wall element 6 comprises a thermoplastic elastomer (TPE). In examples, as described further hereinafter, the compressible wall element 6 may be coated, laminated, or otherwise treated to reduce the gas permeability of the compressible wall element 6 or to render the compressible wall element 6 impermeable to gases, particularly oxygen. In some examples, the compressible wall element 6 comprises a layer and an outer sheath, jacket, or coating. For example, the compressible wall element 6 may comprise an inner portion and a jacket over-molded onto the LDPE inner portion. The inner portion may comprise LDPE and the jacket may comprise a TPE. In another example, the compressible wall element 6 may comprise an elastomer outer, for example, a TPE outer, and a liner. For example, an LDPE liner may be blow-mounted onto the internal surface of the elastomer outer to form the liner. In another example, the liner may be an insert, for example, an LDPE insert, received within the elastomer outer but not co-molded with the elastomer outer. In such an example, it may be preferable that the liner comprises a base sheet and defines a sealed container (except for the top) to hold the cell culture.
The cell culture container 2 can therefore expand and contract, or be expanded and contracted, according to the material held in the cell culture container 2. In particular, the cell culture container 2 may expand as the volume of fluid 4 within the cell culture container 2 grows, and/or as additional materials are added.
As illustrated, the interface plate 3 also includes an expansion container 11, otherwise called a breathing container. The expansion container 11 allows for the cell culture container 2 to expand and contract without greatly changing the pressure in the cell culture container 2. Alternatively or additionally, the expansion container 11 may be operable, for example, by being mechanically or manually compressed or expanded, to expand or retract the compressible wall 6 of the cell culture container 2 and thereby change a volume of the cell culture container 2. Alternatively or additionally, the expansion container 11 may be operable, for example, by being mechanically or manually compressed or expanded, to alter the pressure within the cell culture container 2.
In various examples, the base 7 comprises a rigid base plate 40. The rigid base plate 40 is generally planar, i.e., flat. The rigid base plate 40 is attached to, or molded with, the compressible wall element 6.
The rigid base plate 40 is substantially planar and thereby defines a rigid, substantially flat bottom of the cell culture container 2. A flat bottom of the cell culture container 2 may provide for improved cell culturing, in particular, mixing and control over cell culturing. The flat bottom of the cell culture container 2 helps to ensure that cells are substantially evenly spread over the cross-section of the cell culture container 2 as the cells will sink to the bottom of the cell culture container and if the base 7 were not flat the cells would therefore be concentrated in a smaller volume, which may be detrimental to cell culturing. The flat bottom of the cell culture container 2 also helps to prevent fluid 4 being trapped in the cell culture container 2 when the cells are harvested or extracted at the end of the cell culturing process.
In various examples, the rigid base plate 40 comprises a thermoplastic, for example, a high density polyethylene (HDPE), or a polycarbonate (PC), or another rigid polymer. As described further hereinafter, the rigid base plate 40 may be opaque, transparent, or translucent.
In various examples, described in more detail hereinafter, the base 7, in particular, the rigid base plate 40, has a sensor window. The sensor window is transparent or translucent and provides an optical path into the cell culture container. Accordingly, a sensor can be arranged at least partially outside of the cell culture container and light can be transmitted through the sensor window in order to sense a characteristic of the cell culture within the cell culture container.
In the illustrated examples, the cell culture container 2 is generally cylindrical, with a generally circular base 7 and a generally cylindrical compressible wall element 6. Accordingly, an axial direction is defined between the base 7 and the end of the compressible wall element 6 where the interface plate 3 is mounted. However, it will be appreciated that the cell culture container 2 may take an alternative form, such as having a generally triangular or square cross-sectional form.
As shown in
As described above, the interface plate 3 of the bioreactor includes a number of connector interfaces 5 for accessing the cell culture container in a sterile manner. In examples, the connector interfaces 5 are distributed about the interface plate 3 in a circle, so that each connector interface 5 is equally radially spaced from a central axis of the bioreactor 1. In examples, bioreactor system 32 includes a consumable attachment point 16, as illustrated in
In examples, the consumable 17 may be used to add material to, or extract material from, the bioreactor via the connector interface 5. The material may be a fluid, for example, a cell suspension, a cell culturing media, a virus suspension, or the like.
Referring to
In use, the bioreactor 1 is rotatable to align different connector interfaces 5 with the consumable attachment point 16. Accordingly, different connector interfaces 5 can be brought into alignment with the consumable attachment point 16 by rotation of the bioreactor 1 within the incubator housing 12. In this way, a single consumable attachment point 16 can be provided, and different connector interfaces 5 are selected by rotation of the bioreactor 1. In examples, each connector interface 5 on the interface plate 3 is used only once. To add to or remove a fluid from the bioreactor 1 the bioreactor 1 is rotated to bring a connector interface 5 into alignment with the consumable attachment point 16, the consumable 17 is attached, operated, and then detached, and then the bioreactor 1 can be rotated to bring a further connector interface 5 into alignment with the consumable attachment point 16 for a further fluid addition or removal operation.
As shown in
As shown in
In examples, the agitator plate 27 may couple to the base 7 by a clip, or the agitator plate 27 may include an electromagnet and the base 7 may include a ferromagnetic portion so that the electromagnet is operable to couple the agitator plate 27 to the base 7.
In examples where the agitator plate 27 couples to the base 7 of the bioreactor 1, the coupling may permit rotation of the bioreactor 1 relative to the agitator 18. For example, a part of the agitator plate 27 may be rotatable with the base 7. In other examples, the agitator plate 27 may be decoupled from the base 7 to permit rotation of the bioreactor 1 relative to the agitator 18.
The agitator 18 comprises an actuator to move the agitator plate 27 relative to the bioreactor 1 within the incubator housing 12. The actuator moves the agitator plate 27 in an agitative movement.
In the illustrated example, the actuators 29 are motors arranged to rotate articulated crank arms 33 that are rotatably connected to the base plate 28 and to the agitator plate 27 such that rotation of the articulated crank arms 33 moves the agitator plate 27. In other examples, the linear actuators may be provided to act directly between the base plate 28 and the agitator plate 27.
Supports and guides may guide the movement of the agitator plate 27.
The actuator mechanism may further include a pivotable rod 30 such that the agitator plate 27 can pivot about the pivotable rod 30 to tilt the base of the bioreactor 1. Pivoting can be provided by raising one linear actuator 29 by a different amount to the other. Accordingly, the agitator plate 27 can be moved relative to the base plate 28 in order to engage the base of the bioreactor 1 and agitate the contents of the bioreactor 1.
Referring to
As shown in
The sensor window 21 is transparent or translucent to a wavelength of light at which the sensor unit 19 operates. That is, the sensor window 21 permits transmission of light from within the bioreactor 1 to the sensor unit 19 on the exterior of the bioreactor 1. In some examples, the base 7 is formed of a transparent or translucent material (e.g., polycarbonate), in which example the sensor window 21 is a portion of the base 7. In other examples, the sensor window 21 is a transparent or translucent insert provided in a portion of the base 7.
In examples, the sensor unit 19 is provided within the incubator housing 12. In examples, the sensor unit 19 comprises an actuator that moves the sensor unit 19 into its operational position adjacent to, or in contact with, the base 7. The actuator may move the sensor unit 19 toward and away from the bioreactor 1 (in the direction of the rotational axis of the bioreactor 1), and may optionally tilt the sensor unit 19 to match the base 7 if the base 7 is also tilted. The actuator may be similar to the actuator mechanism of the agitator 18 as described with reference to
In some examples, the sensor unit 19 may be mounted to the agitator 18, in particular, the agitator plate 27. In these examples, the sensor unit 19 will be in the operational position relative to the base 7 when the agitator plate 27 is engaged with the base 7 of the bioreactor 1. In particular, the sensor unit 19 may be mounted to the agitator plate 27 such that when the agitator plate 27 is engaged with the base 7 of the bioreactor 1 the sensor unit 19 is in contact with the base 7 or adjacent to the base 7, for example, within about 10 millimeters.
As mentioned above, the sensor window 21 is transparent or translucent, and in particular, transparent or translucent to the wavelength of light at which the sensor receivers 22, 23 and sensor elements 24, 25 operate. Accordingly, optical sensor signals can pass between the sensor receivers 22, 23 and sensor elements 24, 25, through the sensor window 21.
The sensor elements 24, 25 comprise a characteristic-sensitive material, for example, an oxygen-sensitive or pH-sensitive material, possibly as a coating. The optical properties of the sensor elements 24, 25 thereby change according to the corresponding characteristic of the cell suspension within the bioreactor 1.
The sensor receivers 22, 23 may include optical receivers, in particular, optical fibers 34, 39, configured to transmit light from an external sensor meter 31 through the sensor window 21 to the sensor elements 24, 25, and to transmit light from the sensor elements 24, 25 through the sensor window 21 to the external sensor meter 31. The optical fibers 34, 39 may be mounted to the sensor unit 19 at optical mounts 35, 36 that position the optical fibers 34, 39 toward the corresponding sensor elements 24, 25 so that light can be directed from the optical fibers 34, 39 onto the sensor elements 24, 25, and light can be received by the optical fibers 34, 39 from the sensor elements 24, 25.
Accordingly, the sensor meter 31 and sensor receivers 22, 23 are operable to direct light onto the sensor elements 24, 25 and to detect light from the sensor elements 24, 25. The detected light is indicative of the corresponding characteristic of the cell suspension in the bioreactor 1, in particular, dissolved oxygen and/or pH according to the configuration of the sensor elements 24, 25.
As shown in
In the example of
In
In
In
In the example of
It will be appreciated that the bioreactor may include a third sensor element, and the bioreactor system may include a third sensor receiver to detect a third characteristic of the cell suspension. In such examples, the third sensor element and the third sensor receiver may be spaced from the rotational axis 26 of the bioreactor by a different amount than the other sensor elements and sensor receivers. The third sensor element may be arranged in a corresponding arrangement to the first sensor elements. Accordingly, when the bioreactor is in a rotational position where the first sensor receiver 22 is aligned with the first sensor element 24, the third sensor receiver will also be aligned with the third sensor element. The first, second and third sensor receivers may be provided in a linear arrangement. Accordingly, the bioreactor could include additional sensor elements and the sensor unit could include additional sensor receivers.
Referring to
Throughout the description and claims of this specification, the words “comprise” and “contain” and variations of them mean “including but not limited to,” and they are not intended to (and do not) exclude other components, integers or steps. Throughout the description and claims of this specification, the singular encompasses the plural unless the context otherwise requires. In particular, where the indefinite article is used, the specification is to be understood as contemplating plurality as well as singularity, unless the context requires otherwise.
Features, integers, characteristics or groups described in conjunction with a particular aspect, embodiment or example of the invention are to be understood to be applicable to any other aspect, embodiment or example described herein unless incompatible therewith. All of the features disclosed in this specification (including any accompanying claims, abstract and drawings), and/or all of the steps of any method or process so disclosed, may be combined in any combination, except combinations where at least some of such features and/or steps are mutually exclusive. The invention is not restricted to the details of any foregoing embodiments. The invention extends to any novel one, or any novel combination, of the features disclosed in this specification (including any accompanying claims, abstract and drawings), or to any novel one, or any novel combination, of the steps of any method or process so disclosed.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2113675.9 | Sep 2021 | GB | national |
This application is a national phase entry under 35 U.S.C. § 371 of International Patent Application PCT/GB2022/052402, filed Sep. 22, 2022, designating the United States of America and published as International Patent Publication WO 2023/047115 A1 on Mar. 30, 2023, which claims the benefit under Article 8 of the Patent Cooperation Treaty to Great Britain Patent Application Serial No. 2113675.9, filed Sep. 24, 2021.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/GB2022/052402 | 9/22/2022 | WO |
