WO2002045830A1 - Appareil pour le traitement extracorporel du sang ou du plasma comprenant une membrane semi-permeable humide et procedes de fabrication - Google Patents
Appareil pour le traitement extracorporel du sang ou du plasma comprenant une membrane semi-permeable humide et procedes de fabricationInfo
- Publication number
- WO2002045830A1 WO2002045830A1 PCT/IB2001/002297 IB0102297W WO0245830A1 WO 2002045830 A1 WO2002045830 A1 WO 2002045830A1 IB 0102297 W IB0102297 W IB 0102297W WO 0245830 A1 WO0245830 A1 WO 0245830A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- semi
- membrane
- blood
- circulation
- aqueous
- Prior art date
Links
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
- A61L2/0005—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor for pharmaceuticals, biologicals or living parts
- A61L2/0011—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor for pharmaceuticals, biologicals or living parts using physical methods
- A61L2/0029—Radiation
- A61L2/0035—Gamma radiation
-
- 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
- B01D63/02—Hollow fibre modules
- B01D63/021—Manufacturing thereof
-
- 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
- B01D63/02—Hollow fibre modules
- B01D63/021—Manufacturing thereof
- B01D63/0233—Manufacturing thereof forming the bundle
-
- 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
- B01D63/081—Manufacturing thereof
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D65/00—Accessories or auxiliary operations, in general, for separation processes or apparatus using semi-permeable membranes
- B01D65/02—Membrane cleaning or sterilisation ; Membrane regeneration
- B01D65/022—Membrane sterilisation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D67/00—Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
- B01D67/0081—After-treatment of organic or inorganic membranes
- B01D67/0088—Physical treatment with compounds, e.g. swelling, coating or impregnation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D67/00—Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
- B01D67/0081—After-treatment of organic or inorganic membranes
- B01D67/0097—Storing or preservation
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2202/00—Aspects relating to methods or apparatus for disinfecting or sterilising materials or objects
- A61L2202/20—Targets to be treated
- A61L2202/22—Blood or products thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
- A61M1/14—Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis
- A61M1/16—Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis with membranes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2321/00—Details relating to membrane cleaning, regeneration, sterilization or to the prevention of fouling
- B01D2321/34—Details relating to membrane cleaning, regeneration, sterilization or to the prevention of fouling by radiation
- B01D2321/346—Details relating to membrane cleaning, regeneration, sterilization or to the prevention of fouling by radiation by gamma radiation
Definitions
- the present invention relates to an apparatus for the treatment of blood or plasma by extracorporeal circulation comprising a semi-permeable wet membrane and methods of manufacturing this apparatus.
- wet semi-permeable membrane is meant, throughout this text, a flat semi-permeable membrane or a bundle of hollow semi-permeable fibers, which contains at least 40% by weight of water, based on the weight of the semi-permeable membrane.
- apparatus throughout this text, an apparatus for the treatment of blood or plasma by extracorporeal circulation which generally comprises two compartments separated by a semi-permeable membrane, each provided two accesses, a first compartment being intended for the circulation of the patient's blood or plasma, and a second compartment being intended for the circulation of spent liquid.
- the two compartments of the device are also separated by the potting mass, based on an appropriate adhesive composition, intended to form, as the case may be:
- Devices for the treatment of blood or plasma by extracorporeal circulation are used in various medical or paramedical applications such as: treatment of renal failure by dialysis or hemofiltration, plasmapheresis and apheresis for therapeutic and non-therapeutic purposes, oxygenation of the blood, immuno-purification, etc.
- the present invention also relates to the use of an aqueous glycerol solution to limit the risks of leakage and the variations in the performance of structures made of polymeric material, semi-permeable and wet, in particular to limit the variations in the hydraulic permeability of semi membranes.
- -permeable raincoats within an acceptable range of values after the devices comprising these membranes have been subjected to a temperature below 0 ° C. for a period which may range from one day to more than one month. For example, this can happen during cold seasons, when transporting the devices in insufficiently or unheated means of transport. Under these conditions, various types of damage have been observed: in most cases, an undulation of the semipermeable membranes, due to their elongation, associated with:
- the aliphatic alcohols recommended in this application are methanol, ethanol, propanol and isopropanol, which have the drawback of being highly flammable.
- the devices thus treated cannot be sterilized by gamma irradiation because this energy sterilization leads to the transformation of the aforementioned aliphatic alcohols into products such as aldehydes, which are toxic at the concentrations reached after this transformation.
- Japanese patent application No. 6296838 teaches that a glycerol concentration of less than 20% by weight in the claimed aqueous solution does not prevent the freezing of this solution.
- the devices for the extracorporeal treatment of blood or plasma are degassed and rinsed with an aqueous solution of sodium chloride, sterile and pyrogen-free.
- an aqueous solution of sodium chloride sterile and pyrogen-free.
- Glycerol is also known for its antifreeze properties.
- high concentrations of glycerol are necessary to lower the freezing point of water by a few degrees (Celsius), as can be seen from the reading of the table below, in which the freezing temperature of an aqueous glycerol solution depending on the amount of glycerol in the solution.
- an apparatus for the extracorporeal treatment of blood or plasma comprising two compartments, a compartment intended for the circulation of the blood or plasma, and a compartment intended for the circulation of used liquid, separated by a semi-permeable wet membrane, when this device is subjected to a temperature lower than 0 ° C, for example - 18 ° C, during a period of variable time that can range from a day to more than a month, if this device has the following three technical characteristics before and after sterilization:
- the membrane is impregnated with an aqueous solution of glycerol
- the aqueous glycerol solution contains from 7 to 15% by weight of glycerol and is free from toxic chemical compounds;
- the two compartments are purged of the aqueous glycerol solution.
- the aqueous solution according to the present invention used to impregnate the semi-permeable membrane, contains a small amount of glycerol, from 7 to 15% by weight relative to the total weight of the solution, preferably from 8 to 12% by weight. weight, these quantities being considered insufficient by the aforementioned state of the art, in particular Japanese patent application No. 6296838 (KOKAI) and the aforementioned data appearing in the work entitled "Handbook of Chemistry and Physics".
- the temperatures to which a device can be subjected without the appearance of leaks between the compartments or significant variation in the hydraulic permeability can reach - 20 ° C., or even be slightly lower than - 20 ° C., when using an aqueous glycerol solution containing 10 to 15% by weight of glycerol.
- the membrane impregnated with the aqueous glycerol solution containing 7 to 15% by weight of glycerol is not damaged by very energetic sterilization, such as sterilization by gamma irradiation ;
- the implementation of the device by the user is exactly identical to that of any device of the same type, the device being, moreover, easy to handle because its two compartments are purged, and easy to rinse before use, compared to a device of the same type comprising a glycerine membrane (at least 40% by weight of glycerol based on the weight of the membrane);
- the characteristics (hemocompatibility, diffusive and convective transfer capacity, protein adsorption capacity) of the device subjected to a temperature below 0 ° C, for example equal to -10 ° C or - 18 ° C, during a variable period of time which can range from a day to more than a month, are not significantly altered if compared to the same device
- the minimum quantity of aqueous glycerol solution represents 50% by weight relative to the total weight of the semi-permeable membrane.
- the aqueous glycerol solution is free of chemical compounds which are toxic or which become toxic after energetic sterilization, of the gamma irradiation type.
- the aqueous glycerol solution is free from monohydric aliphatic alcohols, such as methanol, ethanol, propanol and isopropanol.
- the aqueous glycerol solution is free of toxic chemical compounds but known for their antifreeze properties, such as for example ethylene glycol.
- the aqueous glycerol solution can comprise one or more chemical compounds intended to treat the semi-permeable membrane in the mass or on the surface to improve its biocompatibility: by way of example, mention may be made of polyethyleneimines (PEI), polyvinylpyrrolidones (PVP) and polyethylene glycols (PEG).
- PEI polyethyleneimines
- PVP polyvinylpyrrolidones
- PEG polyethylene glycols
- the chemical nature of the semi-permeable membrane of the device according to the invention is not critical. It can be based, for example, on polyacrylonitrile, polymethyl methacrylate, polysulfone, polyethersulfone, cellulose, polyamide.
- the present invention is more particularly suitable for devices comprising a semi-permeable membrane which must be kept wet, such as polyacrylonitrile membranes or polymethyl methacrylate membranes.
- the semi-permeable membrane is a flat membrane or a bundle of hollow fibers made up of at least one polymer which is a homo- or co-polymer of acrylonitrile, this polymer preferably being electronegative.
- acrylonitrile copolymer suitable for the present invention, there may be mentioned:
- the invention is particularly suitable for compounds for which the anionic or anionizable comonomer is olefinically unsaturated and which carries anionic groups chosen from sulfonate, carboxyl, phosphate, phosphonate and sulfate groups, and more particularly still, when this comonomer is the sodium methallylsulfonate: this membrane, which is manufactured by the company HOSPAL and known under the trade name AN69, must be kept in the wet state, and generally contains around 70% by weight of water.
- alkyl acrylates and, in particular, methyl acrylate.
- the present invention is also suitable for devices comprising a semi-permeable membrane treated, in the mass or on the surface, to improve its biocompatibility.
- the invention also relates to a method for limiting the risks of leakage and the variations in the hydraulic permeability of an apparatus for the extracorporeal treatment of blood or plasma which is subjected to a temperature below 0 ° C., this apparatus comprising two compartments, a compartment intended for the circulation of blood or plasma, and a compartment intended for the circulation of used liquid, separated by a semi-permeable wet membrane, the method comprising the steps of:
- the aqueous glycerol solution is brought to the contact of the semi-permeable membrane by circulating this solution:
- the aqueous glycerol solution contains 8 to 12% by weight of glycerol
- the aqueous glycerol solution contains one or more chemical compounds intended to treat the semi-permeable membrane in the mass or on the surface to improve its biocompatibility, preferably a chemical compound chosen from polyethyleneimines
- the method according to the invention can be implemented with the steps of: - prepare a solution containing one or more chemical compounds intended to improve the biocompatibility of the membrane;
- the membrane is rinsed with water or an aqueous solution, for example an aqueous solution of sodium chloride, in order to remove certain ( s) chemical compound (s) temporarily present in the membrane, which are useful for its manufacture and / or its conservation.
- an aqueous solution for example an aqueous solution of sodium chloride
- the AN69 membrane is kept in the wet state and, to do this, is glycerinated by soaking in a water / glycerol mixture, most often in corresponding weight proportions 40/60.
- the membrane must therefore be deglycerinated before being impregnated with the aqueous glycerol solution containing from 7 to 15% by weight of glycerol.
- the rinsing operation in order to deglycerinate the membrane A 69 is carried out by bringing water or an aqueous solution, for example an aqueous solution of sodium chloride in contact with the membrane A 69.
- the rinsing operation is carried out, preferably, by circulating water or an aqueous solution of sodium chloride in the compartment intended for the circulation of blood or plasma.
- FIG. 1 shows a schematic longitudinal sectional view of a hollow fiber dialyzer
- FIG. 2 shows the effect of the amount of glycerol in the aqueous solution used to impregnate the AN69 membrane on the appearance of leaks between the dialyzer compartments stored at - 10 ° C;
- FIG. 3 shows the effect of the amount of glycerol in the aqueous solution used to impregnate the AN69 membrane on the hydraulic permeability of dialyzers stored at - 10 ° C
- the type of device used in the examples is a hemodialyzer / hemofilter comprising, conventionally two compartments separated by a semi-membrane permeable.
- a first compartment is intended to be connected by means of a sampling pipe and a restitution pipe to the patient's vascular circuit, while the second compartment has an inlet possibly connected to a source of dialysis liquid (hemodialysis treatment and hemodia iltration) and an outlet connected to a waste liquid discharge (spent dialysate and / or ultrafiltrate).
- the membrane is chosen to allow diffusive and / or convective transfers of metabolic waste, from the blood compartment to the compartment for spent liquid.
- the membrane can be made in the form of a flat membrane or a bundle of hollow fibers.
- a flat membrane dialyzer comprises a strip of flat membrane folded in accordion fashion, an intermediate plate being introduced into all the folds opening on the same side.
- a hollow fiber dialyzer comprises a bundle of hollow fibers 1, which is arranged in a tubular housing 2 where it is secured at its two ends by a disc of glue 3, 4. Besides bond the fibers to each other, the adhesive discs 3, 4 have the function of delimiting in the tubular housing 2 a sealed compartment to which two pipes 5, 6, perpendicular to the axis of the housing 2, provide access.
- a nozzle 7, 8 comprising an axial access tube 9, 10.
- the two tubes 9, 10 are symmetrical.
- the blood compartment of this device is constituted by the interior space delimited between each glue disc 3, 4 and the nozzle 8, 9 closing the corresponding end of the tubular housing 2, and by the interior of the hollow fibers.
- the semi-permeable membrane of the dialyzers exemplified is an AN69 membrane in the form of a bundle of hollow fibers.
- a mix of poly era is prepared, containing 35% by weight of a copolymer of acrylonitrile and sodium methallyl sulfonate, 52% by weight of dimethylformamide (DMF) and 13% by weight of glycerol.
- the polymer mixture is heated to 130 ° C and is extruded in a die - having two concentric nozzles, nitrogen being injected into the internal nozzle to form the lumen of the hollow fiber - In contact with ambient air ( about 20-25 ° C), the thermoreversible gel fiber leaving the die is the site of a thermal phase inversion.
- the fiber is then received in a water bath "wherein the solvent (DMF) in the fiber is replaced by water.
- the fiber is then immersed in hot water at 95 ° C where it is stretched on the order of four times. There follows a stabilization phase in hot water at 95 ° C.
- the fiber is glycerinated with a water / glycerol mixture, according to the 40/60 weight proportions.
- dialyzers tested are dialyzers (trade name NEPHRAL 300, manufactured by HOSPAL INDUSTRIE, France), equipped with a bundle of AN69 hollow fibers with a useful surface of 1.3 m 2 .
- the semi-permeable membrane is impregnated by circulating the aqueous glycerol solution in the blood compartment: to do this, connect one of the tubes 9 (10) of the blood circuit to a container containing the aqueous glycerol solution. , connect the other access tube 10 (9) to an empty collection container, and cause the circulation of the aqueous glycerol solution in the blood compartment, if necessary
- the aqueous glycerol solution represents approximately 70% by weight of the membrane.
- the percentage by weight of glycerol in each membrane of the dialyzers of Examples 3, 4 and 5 is respectively of the order of 3.5%, 7% and 10.5%.
- the hydraulic permeability of the dialyzers of Examples 1 to 5 was measured after 7 days, 14 days and 28 days of storage, as the case may be, at -10 ° C. or at ambient temperature of the order of 20 ° C. (Example 1: witness n ° 1).
- the hydraulic permeability describes the quantity of water which can be ultrafiltered through a semi-permeable membrane of determined active surface, with a determined transmembrane pressure in a determined period of time.
- the conditions for measuring the hydraulic permeability in the examples are as follows:
- the average of the hydraulic permeability values measured in each group of dialyzers was normalized using 100% of the average of the initial hydraulic permeability values of each group as a basis.
- the dialyzers of Example 5 (treatment with an aqueous solution containing 15% by weight of glycerol) are remarkably stable: no decrease in hydraulic permeability after 28 days at -10 ° C.
- the dialyzers of Example 4 (treatment with an aqueous solution containing 10% by weight of glycerol) have very good behavior: the decrease in hydraulic permeability after 28 days at -10 ° C is only 15%, and is very close to the decrease in hydraulic permeability of deglycerine dialyzers, stored at room temperature (example 1).
- the dialyzers of Example 3 (treatment with an aqueous solution containing 5% by weight of glycerol) are not stable: the decrease in hydraulic permeability is 20% after 15 days at -10 ° C and about 25% after 28 days at ' - 10 ° C.
- the dialyzers of Example 2 (deglycerinated and stored at - 10 ° C) all show leaks after 7 days at - 10 ° C: macroscopic and microscopic observations of these dialyzers have made it possible to demonstrate an elongation of the hollow fibers, cracks in the potting glue, fiber / glue detachments and holes in the fibers.
- 10 deglycerinated NEPHRAL 300 dialyzers are treated by circulation inside the fibers of each 2 liter dialyzer of a solution containing 10% glycerol by mass (flow rate of 250 ml / min).
- the liquid in the internal fiber channel is purged by air circulation.
- the dialyzers are sealed and sterilized by gamma irradiation.
- the dialyzers are placed in an enclosure regulated at a temperature of -18 ° C. After one week of storage, the dialyzers are removed from the enclosure.
- the dialyzer is rinsed with 2 liters of physiological saline;
- a dialysis bath is circulated in the compartment for spent liquid at a flow rate of 500 ml / min in open circuit.
- the dialysis bath is an aqueous solution containing (in mmol / 1): sodium: 135, potassium: 1.5, magnesium: 0.75, calcium: 1.75, chloride: 106.5, acetate: 35;
- a dialysis bath containing 1 g / 1 of urea and 100 mg / 1 of vitamin B12 is circulated in the blood compartment, in a closed circuit.
- the volume of dialysis bath is equal to 2 1 liters and is kept constant by adding a solution at a flow rate of 10 ml / min, in order to compensate for the ultrafiltration.
- the flow rate of the dialysis bath is equal to 200 ml / min;
- the ultrafiltration is fixed at the flow rate of 10 ml / min;
- the urea and vitamin B12 concentrations are determined at the entry and exit of the blood compartment.
- the permeability of the dialyzers of example 6 must be greater than 35.4 ml / hm 2 mmHg, the initial urea clearance values of the dialyzers of example 6 vary from 210 to 256 ml / min, the initial clearance values in vitamin B12 of the dialyzers of Example 6 vary from 90 to 134 ml / min,
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Inorganic Chemistry (AREA)
- Molecular Biology (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
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- External Artificial Organs (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
Abstract
Description
Claims
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/203,106 US7077961B2 (en) | 2000-12-08 | 2001-12-03 | Apparatus for extracorporeal blood or plasma treatment comprising a wet semi-permeable membrane and methods for making the same |
AT01999421T ATE460221T1 (de) | 2000-12-08 | 2001-12-03 | Verwendung einer wässrigen glyzerol lösung zur beibehaltung der leistungen von teildurchlässigen feuchten membranen für die behandlung von blut und plasma |
CA002398568A CA2398568C (fr) | 2000-12-08 | 2001-12-03 | Appareil pour le traitement extracorporel du sang ou du plasma comprenant une membrane semi-permeable humide et procedes de fabrication |
DE60141531T DE60141531D1 (de) | 2000-12-08 | 2001-12-03 | Verwendung einer wässrigen Glyzerol Lösung zur Beibehaltung der Leistungen von teildurchlässigen feuchten Membranen für die Behandlung von Blut und Plasma |
EP01999421A EP1339481B1 (fr) | 2000-12-08 | 2001-12-03 | Utilisation d'une solution aqueuse de glycérol pour préserver les performances de membranes semi-perméhables humides destinées au traitement du sang ou du plasma |
JP2002547603A JP4129393B2 (ja) | 2000-12-08 | 2001-12-03 | 湿潤半透膜を含む血液または血漿の体外処理装置およびその製造方法 |
AU20954/02A AU781447B2 (en) | 2000-12-08 | 2001-12-03 | Apparatus for extracorporeal blood or plasma treatment comprising a wet semipermeable membrane and methods for making same |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0016007A FR2817769B1 (fr) | 2000-12-08 | 2000-12-08 | Appareil pour le traitement extracorporel du sang ou du plasma comprenant une membrane semi-permeable humide et procedes de fabrication |
FR0016007 | 2000-12-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2002045830A1 true WO2002045830A1 (fr) | 2002-06-13 |
Family
ID=8857429
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IB2001/002297 WO2002045830A1 (fr) | 2000-12-08 | 2001-12-03 | Appareil pour le traitement extracorporel du sang ou du plasma comprenant une membrane semi-permeable humide et procedes de fabrication |
Country Status (10)
Country | Link |
---|---|
US (1) | US7077961B2 (fr) |
EP (1) | EP1339481B1 (fr) |
JP (1) | JP4129393B2 (fr) |
AT (1) | ATE460221T1 (fr) |
AU (1) | AU781447B2 (fr) |
CA (1) | CA2398568C (fr) |
DE (1) | DE60141531D1 (fr) |
ES (1) | ES2342151T3 (fr) |
FR (1) | FR2817769B1 (fr) |
WO (1) | WO2002045830A1 (fr) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2311508A1 (fr) * | 2008-07-17 | 2011-04-20 | Nikkiso Company Limited | Procédé de fabrication de purificateur de sang et purificateur de sang |
US8137562B2 (en) | 2006-06-22 | 2012-03-20 | Gambro Lundia Ab | Use of a colloidal suspension of a cationic polymer to treat a support for medical use |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050045554A1 (en) | 2003-08-28 | 2005-03-03 | Gambro Lundia Ab | Membrane unit element, semipermeable membrane, filtration device, and processes for manufacturing the same |
KR20140099752A (ko) * | 2013-02-04 | 2014-08-13 | 코오롱인더스트리 주식회사 | 중공사막 및 이를 포함하는 중공사막 모듈 |
CN109689188A (zh) * | 2016-11-29 | 2019-04-26 | 甘布罗伦迪亚股份公司 | 用于吸附细菌的膜 |
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ATE210954T1 (de) * | 1997-08-18 | 2002-01-15 | Neubourg Stephanie | Schaum-hautschutzcreme |
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- 2000-12-08 FR FR0016007A patent/FR2817769B1/fr not_active Expired - Fee Related
-
2001
- 2001-12-03 DE DE60141531T patent/DE60141531D1/de not_active Expired - Lifetime
- 2001-12-03 US US10/203,106 patent/US7077961B2/en not_active Expired - Fee Related
- 2001-12-03 EP EP01999421A patent/EP1339481B1/fr not_active Expired - Lifetime
- 2001-12-03 ES ES01999421T patent/ES2342151T3/es not_active Expired - Lifetime
- 2001-12-03 CA CA002398568A patent/CA2398568C/fr not_active Expired - Fee Related
- 2001-12-03 AU AU20954/02A patent/AU781447B2/en not_active Ceased
- 2001-12-03 WO PCT/IB2001/002297 patent/WO2002045830A1/fr active IP Right Grant
- 2001-12-03 AT AT01999421T patent/ATE460221T1/de not_active IP Right Cessation
- 2001-12-03 JP JP2002547603A patent/JP4129393B2/ja not_active Expired - Fee Related
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8137562B2 (en) | 2006-06-22 | 2012-03-20 | Gambro Lundia Ab | Use of a colloidal suspension of a cationic polymer to treat a support for medical use |
EP2311508A1 (fr) * | 2008-07-17 | 2011-04-20 | Nikkiso Company Limited | Procédé de fabrication de purificateur de sang et purificateur de sang |
EP2311508A4 (fr) * | 2008-07-17 | 2012-07-25 | Nikkiso Co Ltd | Procédé de fabrication de purificateur de sang et purificateur de sang |
Also Published As
Publication number | Publication date |
---|---|
ES2342151T3 (es) | 2010-07-02 |
EP1339481A1 (fr) | 2003-09-03 |
JP4129393B2 (ja) | 2008-08-06 |
US7077961B2 (en) | 2006-07-18 |
CA2398568C (fr) | 2009-09-22 |
ATE460221T1 (de) | 2010-03-15 |
AU781447B2 (en) | 2005-05-26 |
FR2817769A1 (fr) | 2002-06-14 |
JP2004515282A (ja) | 2004-05-27 |
CA2398568A1 (fr) | 2002-06-13 |
EP1339481B1 (fr) | 2010-03-10 |
FR2817769B1 (fr) | 2003-09-12 |
DE60141531D1 (de) | 2010-04-22 |
US20030102262A1 (en) | 2003-06-05 |
AU2095402A (en) | 2002-06-18 |
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