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WO2023031041A1 - Membrane filtrante, ensemble de membrane filtrante et bioréacteur à poches souples - Google Patents

Membrane filtrante, ensemble de membrane filtrante et bioréacteur à poches souples Download PDF

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Publication number
WO2023031041A1
WO2023031041A1 PCT/EP2022/073789 EP2022073789W WO2023031041A1 WO 2023031041 A1 WO2023031041 A1 WO 2023031041A1 EP 2022073789 W EP2022073789 W EP 2022073789W WO 2023031041 A1 WO2023031041 A1 WO 2023031041A1
Authority
WO
WIPO (PCT)
Prior art keywords
membrane
filter
support
region
filter membrane
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/EP2022/073789
Other languages
English (en)
Inventor
Douglas Albagli
William A HENNESSY
Ralph Stankowski
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Cytiva Sweden AB
Global Life Sciences Solutions USA LLC
Original Assignee
Cytiva Sweden AB
Global Life Sciences Solutions USA LLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US17/464,549 external-priority patent/US20230066039A1/en
Priority claimed from US17/464,589 external-priority patent/US20230065984A1/en
Application filed by Cytiva Sweden AB, Global Life Sciences Solutions USA LLC filed Critical Cytiva Sweden AB
Priority to CN202280059050.XA priority Critical patent/CN117940548A/zh
Priority to EP22769632.5A priority patent/EP4396323A1/fr
Publication of WO2023031041A1 publication Critical patent/WO2023031041A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • 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
    • C12M23/14—Bags
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D63/00—Apparatus in general for separation processes using semi-permeable membranes
    • B01D63/08—Flat membrane modules
    • B01D63/087—Single membrane modules
    • 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
    • C12M29/00—Means for introduction, extraction or recirculation of materials, e.g. pumps
    • C12M29/04—Filters; Permeable or porous membranes or plates, e.g. dialysis
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2313/00—Details relating to membrane modules or apparatus
    • B01D2313/04—Specific sealing means
    • B01D2313/041—Gaskets or O-rings

Definitions

  • bioreactors traditionally made of stainless steel, have been replaced in many applications by disposable bags which are rocked to provide the necessary aeration and mixing necessary for cell culture.
  • disposable bags which are rocked to provide the necessary aeration and mixing necessary for cell culture.
  • These single- use bags are typically provided as sterile units and eliminate the costly and time-consuming steps of cleaning and resterilization.
  • the bags are designed to maintain a sterile environment during operation thereby minimizing the risk of contamination.
  • One of the successful disposable bioreactor systems uses a rocking table on which a bioreactor bag is placed.
  • the bioreactor bag is partially filled with liquid nutrient media and the desired cells.
  • the table rocks the bag providing constant movement of the cells in the bag and also efficient gas exchange from the turbulent air liquid surface.
  • the bag typically, has at least one gas supply tube for the introduction of air, carbon dioxide, nitrogen or oxygen, and at least one exhaust gas tube to allow for the removal of respired gases. Nutrients can be added through other tubes.
  • the cells produce waste e.g. metabolites, ammonium ions and lactate, which have an inhibitory effect on cells. This effect becomes an issue particularly in cultivation at high cell densities, which are required for cost-effective production of biopharmaceuticals such as therapeutic proteins or virus antigens.
  • One way to reduce the concentrations of inhibitory metabolites is to use perfusion cultivation where culture medium is bled off by hydraulic flow through a filter which retains the cells but lets the metabolites and proteins pass through the filter. Expressed proteins can then be recovered from the filtrate and fresh culture medium is continuously supplied to the bioreactor to compensate for the lost liquid.
  • Perfusion filters can typically be installed in the interior of a bioreactor (or outside).
  • Perfusion filters may be incorporated into a bioreactor bag in several ways.
  • One way to provide a perfusion filter to a disposable bioreactor is to provide the perfusion filter to a device comprising a screen and having a connector for attaching a tube for retrieving filtrate, often waste, and just let the device with a filter and screen float within the bioreactor.
  • Another way to provide a perfusion filter has been described in US9017997. Here it is described that the perfusion filter is attached to the bottom of the bioreactor bag.
  • WO2012/158108 and WO2015/034416 describe flexible bags for cell culture provided with internal filters attached to the wall of the bag by a filter holding device, adapted to maintain a distance between the filter and the wall of the bag.
  • EP 3 356 509 Bl describes a filter holding device that can be used within a bioreactor bag.
  • Fig. 1A shows schematically a cross section side view of the filter holding device 101.
  • the filter holding device 101 is provided in a flexible bag 103.
  • the filter holding device 101 is suitably a flat or somewhat curved plate.
  • the filter holding device 101 comprises some kind of distancing means on one side of a middle part 105 of the filter holding device.
  • This distancing means could be for example ribs or a screen or some other kind of structure.
  • the distancing means is provided on the side of the filter holding device to which a filter 107 should be attached.
  • the word filter is used but it could also be a membrane or a bioprocessing separation device used to retain or refrain.
  • FIG. IB shows a schematic bottom view of the filter holding device shown in FIG. 1A.
  • the filter sealing area 109 can be seen to enclose the distancing means, here in the form of ribs 131. All the ribs are given the same numbers. The configuration and number of the ribs could vary.
  • the function of the ribs is to hold the filter and distance the filter from the other side of the filter holding device such that the fluid can be filtered through the filter and drawn out through the opening 113 and port 111.
  • the filter holding device 101 comprises further a filter sealing area 109 provided around the distancing means.
  • the filter sealing area 109 is arranged to be sealed to a periphery of the filter 107 to be held by the filter holding device.
  • the filter will then be covering the distancing means when it has been sealed to the filter sealing area 109 of the filter holding device.
  • the filter can also be sealed to one or more areas of the distancing means in order to prevent the filter from slacking.
  • the filter holding device comprises a port 111 arranged around an opening 113 in the filter holding device 101, which opening connects fluidically with the spaces between the ribs. Said port 111 is arranged to be connected to a tube 115 for retrieving filtrate, usually waste.
  • the port 111 and opening 113 are in one embodiment of the invention provided in the middle of the filter holding device 101 and centered inside the filter sealing area 109.
  • the port and opening can also be provided in another position but they still need to be provided within the filter sealing area 109.
  • the flexible bag is shown here placed in a rocker tray 117.
  • Attaching means are provided to the filter holding device for attaching the filter holding device to an inner surface of the flexible bag such that the at least one filter held by the filter holding device is provided at a distance from the inner surface of the flexible bag.
  • the attaching means are provided as four openings 119a-d (only 119a and 119b can be seen) in the filter holding device and four standoffs 121a-d to be received in the openings.
  • Each one of the stand-offs 121a-d is attached one to each opening 119a-d in the filter holding device in a suitable way for example by heat sealing or my mechanical retention.
  • the stand-offs 121a-d are then attached to the flexible bag inner surface for example by heat sealing or mechanical retention.
  • the stand-offs 121a-d are shown to be attached to the bottom wall of the flexible bag 103 but they could as well be attached to another wall.
  • the stand-offs are molded together with the filter holding device.
  • the number of openings and stand-offs and their positions could be varied.
  • the height of the attaching means which in this shown embodiment are the standoffs, should be adapted for assuring that there will be a suitable distance between the filter and the bag inner surface for letting fluid flow between the filter and the bag surface and thereby create a crossflow effect over the filter, also called tangential flow.
  • the attaching means is in the form of sealing two opposite sides of the filter holding device to the inner surface of the flexible bag. In order to provide a passage or channel for the fluid to pass between the filter and the bag surface the filter holding device needs to be bent or curved in some way.
  • the filter holding device 101 further comprises two deflector areas 123a, 123b. These deflector areas 123a, 123b are provided on opposite sides of the filter holding device and outside the filter sealing area 109.
  • the deflector areas 123a, 123b are angled in relation to the rest of the filter holding device and they are pointing away from the inner surface of the flexible bag to which the filter holding device is attached when the filter holding device is mounted to the flexible bag.
  • the deflector areas 123a, 123b affects the fluid flow in the flexible bag.
  • the rocking tray is moved in a specific pattern such that the fluid inside the flexible bag is moving back and forth in a wave like motion.
  • the deflector areas 123a, 123b will direct and force more fluid to pass between the filter and the bag surface to which the filter holding device is attached. Thereby a crossflow effect over the filter is created which will reduce clogging and fouling.
  • the present inventors have perceived a need to improve on filter membranes and filter holding assemblies in order to incorporate membrane filters made by more advanced membrane production techniques that incorporate materials having different characteristics than the typical materials utilized in filter holders used within bioreactor bags. Accordingly, the present invention seeks to improve microporous membranes and filter assemblies for holding those membranes.
  • the invention involves a filter membrane comprising a porous filter region, the porous filter region comprising a plurality of pores having a minimum dimension of less than 100 microns; and a support region, where the support region comprises at least one support structure.
  • the support structure may comprise a plurality of membrane support holes, the membrane support holes having a minimum dimension greater than the minimum dimension of the pores.
  • the filter membrane may also have a plurality of standoff holes (e.g., four standoff holes).
  • the filter membrane may include a pore free region between the support holes and the porous filter region.
  • the pore free region may surround several of the support holes.
  • each of the support holes may be surrounded by a pore free region, and the pore region surrounds each of the support holes and corresponding pore free region.
  • the filter membrane may have a thickness in the range of 5 to 25 microns.
  • the pores may have an aspect ratio ranging from 0.5: 1 to 20: 1.
  • the pores may have a minimum dimension of 20 nm.
  • the invention involves a polyimide filter membrane comprising a porous filter region, the porous filter region comprising a plurality of pores; and a support region, where the support region comprises a plurality of membrane support holes, the membrane support holes having a minimum dimension greater than the minimum dimension of the pores.
  • the invention involves a filter assembly comprising: (1) a support plate; and (2) a filter membrane, the filter membrane comprising a porous filter region, the porous filter region comprising a plurality of pores having a minimum dimension of less than 100 microns; and a support region, where the support region comprises at least one support structure; (3) an underdrain seal abutting the filter membrane; and (4) an underdrain plate adapted to engage with the support plate and secure the perfusion filter membrane and underdrain seal in the perfusion filter assembly.
  • the support structure may comprise a plurality of membrane support holes, the membrane support holes having a minimum dimension greater than the minimum dimension of the pores.
  • the filter membrane may have a membrane frame, the membrane frame comprising a plurality of frame support holes, the frame support holes being aligned with the membrane support holes.
  • the membrane frame may have a different thickness and/or material composition than the filter membrane and engaging with the support region of the filter membrane.
  • the filter membrane may comprise a membrane frame having the same material as the membrane with a different thickness.
  • the filter membrane may comprise a membrane frame having a different material than the membrane.
  • the membrane frame may have a plurality of frame support holes.
  • the underdrain plate and the support plate may be engaged with each other by a plurality of posts, and the support structure comprises a plurality of support holes that allow the plurality of support posts to pass through and engage with the plurality of support holes to secure the filter membrane within the filter assembly.
  • the underdrain plate and the support plate may be engaged with each other by bonding wherein the underdrain plate and support plate include a recessed region for engaging with the support structure of the filter membrane and securing the filter membrane within the filter assembly.
  • the filter membrane may be a polyimide filter membrane comprising a porous filter region, the porous filter region comprising a plurality of pores; and a support region, where the support region comprises a plurality of membrane support holes, the membrane support holes having a minimum dimension greater than the minimum dimension of the pores.
  • the invention may include a flexible bag bioreactor comprising: an inner surface and an outer surface; and a filter assembly, the filter assembly comprising: (1) a support plate; (2) a filter membrane, the filter membrane comprising: a porous filter region, the porous filter region comprising a plurality of pores having a minimum dimension of less than 100 microns; and a support region, where the support region comprises at least one support structure; (3) an underdrain seal abutting the filter membrane; and (4) an underdrain plate adapted to engage with the support plate and secure the perfusion filter membrane and underdrain seal in the perfusion filter assembly, wherein the filter assembly is attached to the inner surface of the flexible bag such that the filter membrane held by the filter assembly is provide at least a distance from the inner surface of the flexible bag.
  • the invention involves a filter assembly comprising: (1) a support plate; and (2) a filter membrane, the filter membrane comprising a porous filter region, the porous filter region comprising a plurality of pores having a minimum dimension of less than 100 microns; and a support region, where the support region comprises at least one support structure; (3) an underdrain seal abutting the filter membrane; and (4) an underdrain plate adapted to engage with the support plate and secure the perfusion filter membrane and underdrain seal in the perfusion filter assembly.
  • the support structure may comprise a plurality of membrane support holes, the membrane support holes having a minimum dimension greater than the minimum dimension of the pores.
  • the filter membrane may have a membrane frame, the membrane frame comprising a plurality of frame support holes, the frame support holes being aligned with the membrane support holes.
  • the membrane frame may have a different thickness and/or material composition than the filter membrane and engaging with the support region of the filter membrane.
  • the filter membrane may comprise a membrane frame having the same material as the membrane with a different thickness.
  • the filter membrane may comprise a membrane frame having a different material than the membrane.
  • the membrane frame may have a plurality of frame support holes.
  • the underdrain plate and the support plate may be engaged with each other by a plurality of posts, and the support structure comprises a plurality of support holes that allow the plurality of support posts to pass through and engage with the plurality of support holes to secure the filter membrane within the filter assembly.
  • the underdrain plate and the support plate may be engaged with each other by bonding wherein the underdrain plate and support plate include a recessed region for engaging with the support structure of the filter membrane and securing the filter membrane within the filter assembly.
  • the filter membrane may be a polyimide filter membrane comprising a porous filter region, the porous filter region comprising a plurality of pores; and a support region, where the support region comprises a plurality of membrane support holes, the membrane support holes having a minimum dimension greater than the minimum dimension of the pores.
  • the invention may include a flexible bag bioreactor comprising: an inner surface and an outer surface; and a filter assembly, the filter assembly comprising: (1) a support plate; (2) a filter membrane, the filter membrane comprising: a porous filter region, the porous filter region comprising a plurality of pores having a minimum dimension of less than 100 microns; and a support region, where the support region comprises at least one support structure; (3) an underdrain seal abutting the filter membrane; and (4) an underdrain plate adapted to engage with the support plate and secure the perfusion filter membrane and underdrain seal in the perfusion filter assembly, wherein the filter assembly is attached to the inner surface of the flexible bag such that the filter membrane held by the filter assembly is provide at least a distance from the inner surface of the flexible bag.
  • the invention involves a filter membrane comprising a porous filter region, the porous filter region comprising a plurality of pores having a minimum dimension of less than 100 microns; and a support region, where the support region comprises at least one support structure.
  • the support structure may comprise a plurality of membrane support holes, the membrane support holes having a minimum dimension greater than the minimum dimension of the pores.
  • the filter membrane may also have a plurality of standoff holes (e.g., four standoff holes).
  • the filter membrane may include a pore free region between the support holes and the porous filter region.
  • the pore free region may surround several of the support holes.
  • each of the support holes may be surrounded by a pore free region, and the pore region surrounds each of the support holes and corresponding pore free region.
  • the filter membrane may have a thickness in the range of 5 to 25 microns.
  • the pores may have an aspect ratio ranging from 0.5: 1 to 20: 1.
  • the pores may have a minimum dimension of 20 nm.
  • the invention involves a polyimide filter membrane comprising a porous filter region, the porous filter region comprising a plurality of pores; and a support region, where the support region comprises a plurality of membrane support holes, the membrane support holes having a minimum dimension greater than the minimum dimension of the pores.
  • FIG. 1A shows a prior art perfusion filter assembly.
  • Fig. IB shows a first view of a portion of the prior art filter assembly shown in Fig. 1A.
  • Fig. 2A shows a first process that can be utilized to make a perfusion filter membrane for use in a perfusion filter assembly, according to an embodiment of the invention.
  • Fig. 2B shows a second process that can be utilized to make a perfusion filter membrane for use in a perfusion filter assembly, according to an embodiment of the invention.
  • Fig. 2C shows a third process that can be utilized to make a perfusion filter membrane for use in a perfusion filter assembly, according to an embodiment of the invention.
  • FIG. 3A shows a perfusion filter assembly utilizing a support frame with membrane support holes according to an embodiment of the invention.
  • Fig. 3B shows a bottom up view of the perfusion filter assembly of Fig. 3A with support frame.
  • Fig. 3C shows a bottom up view of the perfusion filter assembly of Fig. 3A without support frame.
  • Fig. 3D shows the support frame of Fig. 3A.
  • Fig. 4A shows a perfusion filter assembly utilizing a support frame with membrane support holes according to an embodiment of the invention.
  • Fig. 4B shows a bottom up view of the perfusion filter assembly of Fig. 4A with support frame.
  • Fig. 5A shows a bottom up view of a perfusion filter assembly according to an embodiment of the invention.
  • Fig. 5B shows a support frame according to an embodiment of the invention.
  • Fig. 5C shows a bottom up view of the perfusion filter assembly of Fig. 5A with support frame.
  • Fig. 6A shows a side view of a perfusion filter assembly and structure for securing the support frame and filter membrane according to an embodiment of the invention.
  • Fig. 6B shows a side view of a perfusion filter assembly and structure for securing the support frame and filter membrane according to an embodiment of the invention.
  • Fig. 6C shows a side view of a perfusion filter assembly and structure for securing the support frame and filter membrane according to an embodiment of the invention.
  • Fig. 6D shows a side view of a perfusion filter assembly and structure for securing the support frame and filter membrane according to an embodiment of the invention.
  • Fig. 6E shows a side view of a perfusion filter assembly and structure for securing the support frame and filter membrane according to an embodiment of the invention.
  • Fig. 7A shows a filter membrane in accordance with an embodiment of the invention.
  • Fig. 7B shows a filter membrane in accordance with an embodiment of the invention.
  • Fig. 7C shows a filter membrane in accordance with an embodiment of the invention.
  • Fig. 7D shows a filter membrane in accordance with an embodiment of the invention.
  • the present invention involves perfusion filter assemblies and filer membranes for use in those perfusion filter assemblies.
  • the perfusion filter assemblies and perfusion membranes disclosed herein are particularly adapted to membranes that are made with advanced processes, such as photolithography and etching.
  • the present inventors have found that membranes made according to these processes have material characteristics that make them unsuitable for use with traditional perfusion filter assemblies.
  • polyimide membranes can be difficult to bond to the polyethylene components used in perfusion filter assemblies, including perfusion filter bags.
  • the filter membranes and filter assemblies disclosed herein include features that overcome one or more of these obstacles.
  • the membrane layer 102 and base 100 have a similar coefficient of thermal expansion such that a glass substrate and polyimide membrane layer is utilized.
  • the first step in making the membrane from the structure of Fig. 2(a) is to provide a patterned photoresist layer 104 by exposing the surface of the photoresist to a light pattern, and developing the photoresist to leave the photoresist pattern shown in Fig. 2(b).
  • the hard mask 103 is etched in the location of the opening 101 to form the hard mask opening 106 as shown in Fig. 2(c) and photoresist 104 is then removed as shown in Fig. 2(d).
  • the hard mask layer 103 After etching the membrane layer 102 to form the membrane layer opening 107, the hard mask layer 103 should be removed as shown in Fig. 2(f). The removal of the hard mask layer 103 is desirably conducted in a manner that is selective relative to the membrane layer 102. After removal of the hard mask layer 103, the patterned membrane layer 102 is separated from the base layer 100 as shown in Fig. 2(g).
  • These membranes include a plurality of first membrane material layer strips 101, a second membrane material 104 binding to each of the plurality of first membrane material layer strips, the second membrane material comprising a plurality of windows 106 exposing each of the first membrane material strips, wherein the biocompatible polymeric filtration membrane comprises pores defined by uniform passages defined by the first membrane material layer strips 101 and the second membrane material layer 104 that fluidically connect within each window 106.
  • the uniform pore is formed by etching a sacrificial material layer (not shown) deposited on the first membrane material layer strips 101.
  • These methods allow formation of pores having a minimum pore size defined by the thickness of a sacrificial layer. In many cases, the minimum dimension of pores made using this technique may range from 20 to 1000 nm.
  • the thickness of membranes made according to these techniques preferably ranges from 2—10 microns.
  • FIG. 2C Another advanced method for making porous membrane is described in U.S. Patent Application No. 17/219,428, entitled “MICROPORE MEMBRANES AND METHODS OF FABRICATION THEREOF USING PILLAR TEMPLATES,” and filed March 31, 2021, which describes such polymeric membranes and techniques.
  • a filter membrane made according to this process is shown in Fig. 2C.
  • the porous membrane 101 is produced using a pillar template which allows for formation of a well-defined and reproducible exit dimension defined by the second region 108 when used in conjunction with photolithographic techniques performed on the polymeric layer 102 of the porous membrane 101.
  • the polymer layer 102 of the membrane 101 has a bottom surface 103 and top surface 104.
  • the plurality of pores 105 extend through the polymer layer 102.
  • Each pore has a first region 106 with a tapered profile 107 that opens wider at the intersection of the top surface of the membrane 104, and a second region 108 with a substantially vertical profile 109 that intersects the bottom surface of the membrane 103.
  • the tapered profile 107 may be a conical profile.
  • the first region 106 intersects the second region 108 at an intermediate surface 110 exposed through the opening created by the first region 106.
  • the intermediate surface 110 provides a buffer that allows for nonuniformity in the etching and formation of the first region among different pores in the same membrane, and between separate manufacturing runs of different membranes.
  • Figs. 3A— D show a perfusion filter membrane utilizing membrane support holes according to an embodiment of the invention.
  • a bioreactor bag 303 includes a filter holding device 301 placed at the bottom of the bioreactor bag 303 where the filter membrane 307 faces the bottom of the bioreactor bag 303.
  • a port 311 allows filtered fluid to exit the bioreactor bag through opening 313 and out of the tube 315.
  • the filter holding device includes openings 319a-d which are used for attaching to standoffs 321a-d (only 321a and 321b are shown).
  • the filter holding device 301 includes deflector areas 323 that improve the flow under the filter holding device 301 within the bioreactor bag 305.
  • the bioreactor bag 305 may be placed on a rocker tray 317.
  • the filter holding device 301 may be attached to the bottom of the bioreactor bag 303 using standoffs 321a-d (only 321a and 321b are shown) which correspond to holes 319a-d as seen in Fig. 3B.
  • the filter membrane 307 may be attached to the filter holding device 301 using the support structure, such as support frame 332 of Fig. 3D, and a seal 309.
  • the seal 309 can be an O-ring made from a resilient material such as rubber as shown in Fig. 3C.
  • the seal 309 is adapted to prevent liquid from leaking from the bioreactor bag past the filter membrane 307.
  • the seal may be seated in a groove in the shape of the seal.
  • the support frame 332 may include support holes 330 where a pin or other structure may be used to further secure the support frame 332 a membrane 307 in place.
  • the number of support holes 330 may depend on the materials and the use case. In the case where higher pressures are utilized, more support holes may be used.
  • the support pins 330 may be threaded such that they may be screwed into the periphery of the filter membrane support. Although not necessary to seal the filter membrane 307 due to the seal 309, the support pins may be provided with seals or washers depending on the thickness of the membrane 307 and seal 309 and the need for compression.
  • Figs. 4A— B show a perfusion filter assembly utilizing a support frame with membrane support holes according to an embodiment of the invention.
  • a bioreactor bag 403 includes a filter holding device 401 placed at the bottom of the bioreactor bag 403 where the filter membrane 407 faces the bottom of the bioreactor bag 403.
  • a port 411 allows filtered fluid to exit the bioreactor bag through opening 413 and out of the tube 415.
  • the filter holding device includes openings 419a-d which are used for attaching to standoffs 42 la-d (only 42 la and 42 lb are shown).
  • the filter holding device 401 includes deflector areas 423 that improve the flow under the filter holding device 401 within the bioreactor bag 405.
  • the bioreactor bag 405 may be placed on a rocker tray 417.
  • the filter holding device 401 may be attached to the bottom of the bioreactor bag 403 using standoffs 42 la-d (only 421a and 421b are shown) which correspond to holes 419a-d as seen in Fig. 4B.
  • the filter membrane 407 may be attached to the filter holding device 401 using the support structure, such as support frame 432, and a seal 409 as shown in Fig. 4B.
  • the seal 409 can be an O-ring made from a resilient material such as rubber.
  • the seal 409 is adapted to prevent liquid from leaking from the bioreactor bag past the filter membrane 407.
  • the seal may be seated in a groove in the shape of the seal.
  • the support frame 432 may include support holes 430 where a pin or other structure may be used to further secure the support frame 432 a membrane 407 in place.
  • the number of support holes 430 may depend on the materials and the use case. In the case where higher pressures are utilized, more support holes may be used.
  • the support pins 430 may be threaded such that they may be screwed into the periphery of the filter membrane support. Although not necessary to seal the filter membrane 407 due to the seal 409, the support pins may be provided with seals or washers depending on the thickness of the membrane 407 and seal 409 and the need for compression.
  • the support frame 432 also include central support pins 434 that secure internal portions 433 of the frame 432 to the ribs 431 of the middle part 405 of the filter holding device.
  • Each pin 434 preferably includes a seal 410 which can be an O- ring.
  • Fig. 5A shows a bottom up view of a perfusion filter assembly according to an embodiment of the invention.
  • Ribs 531 are provided to support the filter membrane (not shown).
  • Holes 519 are used to support a standoff for supporting the device in place within the bioreactor bag as shown with previous images.
  • the holes may further secure the filter membrane within the frame 532, which is shown in Fig. 5B.
  • Additional holes 530 are provided for posts to further anchor the membrane within the filter assembly.
  • Seal 509 is further provided to prevent leakage around the filter membrane.
  • the assembled filter assembly is shown in Fig. 5C.
  • Fig. 6A— E show a side views of a perfusion filter assembly and various structures for securing the support frame and filter membrane according to an embodiment of the invention.
  • the filter membrane 607 is positioned below a support plate 611 which may have ribs or other structures supporting the filter membrane 607.
  • a frame 632 may be used to support the bottom of the filter membrane 607.
  • Holders 623 may be used with standoffs 621 to hold the filter assembly in place and position it relative to a filter bag as previously described.
  • a seal 609 is used to surround the filter membrane 607.
  • a post 650 is used to secure the support plate 611 and filter 607 within the assembly.
  • the post 650 may be a compression fit or screw.
  • Fig. 6B shows a side view of a perfusion filter assembly and bolt 660 structure for securing the support frame and filter membrane according to an embodiment of the invention.
  • the bolt may be threaded and secured by a hole with matching threads in the holder 623.
  • Fig. 6C shows a side view of a perfusion filter assembly and pins 660 for securing the support frame and filter membrane according to an embodiment of the invention.
  • the pins 660 may be integral with the support 611.
  • the pins 660 may be adapted to interface with a bottom part of the holder 623 or the frame 632. This interface may be a compression fit.
  • Fig. 6D shows a side view of a perfusion filter assembly and bolt 670 for securing the holder 623 frame, filter membrane607, and support 611 according to an embodiment of the invention.
  • the bolt 670 may be threaded, or may form a compression fit with the support 611.
  • the bolt 670 can be put into place from the lower side which can be advantageous during assembly since the filter membrane 607 would typically be placed onto the support 611 followed by the frame 632 and holder 623.
  • Fig. 6E shows a side view of a perfusion filter assembly and tapered pin 680 for securing the support frame and filter membrane according to an embodiment of the invention.
  • the tapered pin may be threaded into the support 611 for securing the membrane 607.
  • Figs. 7A— D shows a filter membranes in accordance with an embodiment of the invention.
  • the filter membrane 700 includes a pore region 702 and holes 704 for attaching to standoffs of the filter assembly.
  • Support holes 703 may be found in the non-porous region 701 of the filter membrane 700.
  • a seal such as an O-ring may be placed in region 705 when the filter membrane is placed within the filter assembly.
  • Fig. 7B shows another filter membrane 720 having support regions 721 within the porous region 702.
  • the support regions 721 have holes 723.
  • the support regions 721 allow for placement of seals, such as an O-ring, within region 722.
  • Fig. 7C shows a filter membrane 740 with several holes 742 provided within a single seal region 741. Each hole may include a seal, such as an O-ring, within region 741.
  • Fig. 7D shows another examples of a membrane filter 760 which shows that a single seal may be provided within seal region 744 and surround several holes 7

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  • Biomedical Technology (AREA)
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  • Apparatus Associated With Microorganisms And Enzymes (AREA)

Abstract

La présente invention concerne des porte-filtres (301, 401) et des membranes (307, 407, 720) pouvant être inclus dans un système de poches pour bioréacteur (303, 305, 403, 405). Les porte-filtres et les membranes (307, 407, 720) comprennent des caractéristiques (332, 432) permettant l'incorporation de matériaux de membrane avancés possédant des caractéristiques matérielles différentes de celles des membranes traditionnelles correspondant plus étroitement aux caractéristiques du porte-filtre (301, 401).
PCT/EP2022/073789 2021-09-01 2022-08-26 Membrane filtrante, ensemble de membrane filtrante et bioréacteur à poches souples Ceased WO2023031041A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
CN202280059050.XA CN117940548A (zh) 2021-09-01 2022-08-26 过滤器膜、过滤器膜组件和柔性袋生物反应器
EP22769632.5A EP4396323A1 (fr) 2021-09-01 2022-08-26 Membrane filtrante, ensemble de membrane filtrante et bioréacteur à poches souples

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US17/464,549 US20230066039A1 (en) 2021-09-01 2021-09-01 Perfusion filter membrane and method of use
US17/464,589 2021-09-01
US17/464,549 2021-09-01
US17/464,589 US20230065984A1 (en) 2021-09-01 2021-09-01 Perfusion filter membrane assembly

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WO2023031041A1 true WO2023031041A1 (fr) 2023-03-09

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Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5139946A (en) * 1988-11-02 1992-08-18 Du Pont Merck Pharmaceutical Company Dot matrix membrane cell expansion
WO2001041905A1 (fr) * 1999-12-08 2001-06-14 Baxter International Inc. Membrane filtrante microporeuse, procede de fabrication et separateur utilisant de telles membranes
KR20060019241A (ko) * 2004-08-27 2006-03-03 주식회사 퓨어엔비텍 평막 모듈
WO2012158108A1 (fr) 2011-05-16 2012-11-22 Ge Healthcare Bio-Sciences Ab Procédé de culture de cellules sur des microsupports dans un sac
WO2015034416A1 (fr) 2013-09-06 2015-03-12 Ge Healthcare Bio-Sciences Ab Poche pour culture cellulaire à membrane de dialyse interne
US9017997B2 (en) 2008-03-20 2015-04-28 Sartorius Stedim Biotech Gmbh Bioreactor
EP3356509A1 (fr) 2015-10-01 2018-08-08 GE Healthcare Bio-Sciences AB Dispositif de fixation d'un filtre
US20190105609A1 (en) * 2017-10-05 2019-04-11 General Electric Company Systems and methods for utilizing crossflow filtration for cell enrichment

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5139946A (en) * 1988-11-02 1992-08-18 Du Pont Merck Pharmaceutical Company Dot matrix membrane cell expansion
WO2001041905A1 (fr) * 1999-12-08 2001-06-14 Baxter International Inc. Membrane filtrante microporeuse, procede de fabrication et separateur utilisant de telles membranes
KR20060019241A (ko) * 2004-08-27 2006-03-03 주식회사 퓨어엔비텍 평막 모듈
US9017997B2 (en) 2008-03-20 2015-04-28 Sartorius Stedim Biotech Gmbh Bioreactor
WO2012158108A1 (fr) 2011-05-16 2012-11-22 Ge Healthcare Bio-Sciences Ab Procédé de culture de cellules sur des microsupports dans un sac
WO2015034416A1 (fr) 2013-09-06 2015-03-12 Ge Healthcare Bio-Sciences Ab Poche pour culture cellulaire à membrane de dialyse interne
EP3356509A1 (fr) 2015-10-01 2018-08-08 GE Healthcare Bio-Sciences AB Dispositif de fixation d'un filtre
US20190105609A1 (en) * 2017-10-05 2019-04-11 General Electric Company Systems and methods for utilizing crossflow filtration for cell enrichment

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