JP2011235189A - Blood processing filter, blood treatment system and method of producing blood product - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a useful blood processing filter which can fully easily and surely discharge air in a collection bag for storing blood after filtration.SOLUTION: The blood processing filter includes: a sheet-like filter material; a container which is jointed to flexible sheets storing the sheet-like filter material; a first joint part for defining a blood processing region by jointing the filter material and the container; a second joint part for jointing the periphery of the container; an entrance installed in one side of the container; and an exit installed in the other side of the container. The first joint part includes: an entrance side joint part for jointing faces of the flexible sheets of the entrance side of the container and the entrance side of the filter material; and an exit side joint part for jointing faces of the flexible sheets of the exit side of the container and the exit side of the filter material. Peel strength of the exit side joint part is lower than that of the entrance side joint part so that the flexible sheets can be peelable from the face of the exit side of the filter material in the exit side joint part by pulling the flexible sheets composed of the exit side of the container.

Description

  The present invention relates to a blood processing filter for removing undesirable components such as aggregates and leukocytes from blood and a blood processing system using the same, and further relates to a method for producing a blood product using the system. The “blood” in the present invention includes not only whole blood but also blood products such as red blood cell preparations, platelet preparations and plasma preparations.

  In the field of blood transfusion, so-called leukocyte-removed blood transfusion, in which a blood product is transfused after removing contaminating leukocytes contained in the blood product, has become widespread. This includes relatively minor side effects such as headache, nausea, chills, and non-hemolytic fever reaction associated with blood transfusion, severe alloantigen sensitization, virus infection, post-transfusion GVHD, etc. This is because it has been clarified that such a side effect is mainly caused by leukocytes mixed in the blood product.

  There are several methods for removing leukocytes. Among them, the filter method is currently popular because it has advantages such as excellent leukocyte removal performance, simple operation, and low cost. For example, Patent Document 1 describes a leukocyte remover in which a housing that houses a filter member is made of a soft resin.

  The blood processing system used in the filter method is configured by connecting a bag containing blood to the upstream side of the filter and connecting a blood collection bag to the downstream side of the filter (see FIG. 4). It is common practice to place a bag containing a blood product that may contain white blood cells, etc. at a position 20 to 100 cm higher than the filter, filter the blood product by the action of gravity, and collect it in a downstream bag. ing. After filtration, the bag containing the blood components is separated from the system and stored.

  When blood is filtered in the system configured as described above, the air in the filter may be stored in the collection bag together with the blood. When blood is stored in a state where air is mixed in the collection bag, there is a problem that the blood components are likely to be altered or deteriorated. For this reason, prior to separating the collection bag from the blood processing system, an operation for removing the air in the collection bag is performed. This operation is called “burping” and is performed by pressing the collection bag directly by hand or by mechanically applying pressure using the apparatus.

  Patent Document 2 describes a filter system including a bypass circuit and a check valve for eliminating air in the collection bag. Patent Document 3 describes a filter having an air storage portion inside in order to easily and surely perform barping.

JP 2000-342680 A JP 2004-249087 A JP 2006-43297 A

  By the way, although the nonwoven fabric and porous body which make a filter material have high air permeability in the dried state, they have the property that air permeability falls remarkably in the state containing blood after filtration processing. In the leukocyte remover described in Patent Document 1, since the housing for housing the filter member is made of a soft resin, when the collection bag is pressurized, the outflow side blood chamber of the leukocyte remover housing swells, and the collection bag contains There is a possibility that the air can be discharged. However, since a large force is required to press the collection bag, there are problems that the collection bag and the tube are loaded and the operability is poor.

  The filter system described in Patent Document 2 requires a bypass circuit, a check valve, and the like for barping, requires a complicated clamping operation, and has room for improvement in terms of operability. The filter described in Patent Document 3 has a problem in that it has an air reservoir inside and thus becomes large in size and has a problem in handling, and blood tends to remain in the filter, resulting in a reduction in blood recovery.

  The present invention has been made in view of the above circumstances, and an object of the present invention is to provide a blood processing filter useful for discharging the air in a collection bag for storing blood after filtration sufficiently easily and reliably. To do. It is another object of the present invention to provide a blood processing system using the filter and a method for producing a blood product using the system.

  The blood processing filter according to the present invention contains a sheet-like filter material, a filter material, a container formed by joining a flexible sheet, and a filter in the thickness direction of the filter. Provided on one surface of the container, a first joint that joins the material and the container to define a blood treatment region, a second joint that joins the peripheral edge of the container in the thickness direction of the filter, and An inlet provided on the other side of the container, and the first joint is an inlet-side joint for joining the flexible sheet forming the inlet of the container and the inlet-side surface of the filter medium And an outlet side joint that joins the flexible sheet forming the outlet side of the container and the outlet side surface of the filter medium, and the outlet side joint has a peel strength higher than that of the inlet side joint. At the outlet side joint by pulling the flexible sheet that is low and forms the outlet side of the container The flexible sheet from the surface of the outlet side of the super wood can be peeled off.

  The blood treatment filter of the present invention may have the following aspects. That is, the blood processing filter according to the present invention contains a sheet-like filter material, a container containing the filter material, and formed by joining a flexible sheet, and in the thickness direction of the filter. A first joint that joins the filter medium and the container to define a blood treatment region, a second joint that joins the peripheral edge of the container in the thickness direction of the filter, and one surface of the container The inlet side provided with the provided inlet and the outlet provided in the other side of the container, and the 1st joined part joins the flexible sheet which makes the inlet side of a container, and the surface of the inlet side of a filter material It has an outlet-side joint that joins the joint and the flexible sheet forming the outlet side of the container and the outlet-side surface of the filter medium, and the outlet-side joint is more than the second joint. Peel strength is low and the outlet side is joined by pulling the flexible sheet on the outlet side of the container The flexible sheet can be peeled off from the surface of the outlet side of the filtering material in.

  One of the points of the filter of the present invention is that the flexible sheet peels from the outlet side surface of the filter medium at the outlet side joint portion by pulling the flexible sheet forming the outlet side of the container. By peeling the flexible sheet from the outlet-side joint at the first joint, the tension of the flexible sheet is weakened, and the volume of fluid that can be accommodated on the outlet side of the container can be increased afterwards. For this reason, even if the pressing force against the collection bag is small, the air in the collection bag can be discharged to the outlet side of the filter.

  The outlet-side joint in the first joint is set to have a lower peel strength than the inlet-side joint and / or the second joint, and before the separation at the outlet-side joint occurs, The second joint is not damaged. For this reason, the flexible sheet can be peeled off from the outlet-side joint part sufficiently easily, and blood remaining in the filter after filtration can be sufficiently prevented from leaking from the second joint part.

  In the filter of the present invention, the peel strength of the outlet side joint is preferably 0.5 to 1.5 N / mm from the viewpoint of ease of peeling work and prevention of blood leakage.

  The blood processing system of the present invention includes a storage bag for storing blood to be filtered, the blood processing filter, a recovery bag for storing blood filtered by the filter, a storage bag, and an inlet of the filter And a second tube for connecting the outlet of the filter and the collection bag.

  According to the blood treatment system, after filtration, the volume of the fluid that can be accommodated on the outlet side of the filter container is increased afterwards, so that the air in the collection bag can be discharged to the filter sufficiently easily and reliably.

  In the blood processing system, it is not necessary to provide a bypass circuit for barping. That is, this system may be one that does not include a tube that communicates the first tube and the second tube and bypasses the filter. In this case, the second tube forms a flow path for transferring the blood that has passed through the filter to the collection bag, and also forms a flow path for transferring the air remaining in the collection bag after the filtration to the filter.

The present invention provides a method for producing a blood product using the blood processing system. This method
A) placing the blood to be filtered into a storage bag;
B) filtering the blood in the storage bag with a filter;
C) collecting the blood that has passed through the filter in a collection bag;
D) peeling the flexible sheet from the outlet side surface of the filter medium at the outlet side joint by pulling the flexible sheet forming the outlet side of the filter container;
E) the step of transferring air remaining in the collection bag after the step C) to the outlet side of the filter after the step D);
F) The step of sealing the collection bag after the step E),
Is provided.

  After collecting the blood in the collection bag (after the step (C)), the volume of the fluid that can be accommodated on the outlet side of the filter container can be increased afterwards by performing the step D). Thereby, the air in the collection bag can be discharged to the filter sufficiently easily and reliably in the step E). In addition, since it is post hoc to increase the volume of fluid that can be accommodated on the outlet side of the container, the amount of blood remaining in the filter at the end of filtration increases compared to the conventional case, and the amount of blood collected decreases. There is no problem.

  In the above method, it is not necessary to use a bypass circuit for barping. That is, in step C), the blood that has passed through the filter is transferred to the collection bag through the second tube, and in step E), the air remaining in the collection bag is passed through the second tube. You may transfer to the exit side of a filter.

  According to the present invention, the air in the collection bag that stores the filtered blood can be discharged to the filter sufficiently easily and reliably.

It is a top view which shows suitable embodiment of the filter which concerns on this invention. It is sectional drawing along the II-II line of FIG. It is sectional drawing which shows the state which the flexible sheet peeled from the exit side surface of a filter medium in an exit side junction part. It is a schematic diagram which shows the structure of the blood processing system provided with the filter which concerns on this invention. It is a top view which shows the variation of the shape of the filter which concerns on this invention.

[Blood processing filter]
The filter 10 according to the present embodiment is for removing microaggregates and white blood cells that cause side effects from blood for transfusion, and has a rectangular flat shape. As shown in FIG. 1, the filter 10 includes a sheet-shaped filter medium 1, a flexible container 3 that accommodates the filter medium 1, an inner joint portion (first joint portion) 5 that defines the blood treatment region R, and And an outer joint (second joint) 6.

  The container 3 is made of a flexible sheet, and an inlet 7 is provided on one side F1, and an outlet 8 is provided on the other side F2. The inlet 7 and the outlet 8 are provided with tube connection ports 7a and 8a, respectively. In use, the filter 10 is arranged in the vertical direction so that the blood flowing in from the inlet 7 flows vertically downward and reaches the outlet 8 so that the inlet 7 is located above and the outlet 8 is located below. The Hereinafter, the configuration of the filter 10 will be described, but the positional relationship between the elements of the filter 10 will be described based on the arrangement when the filter 10 is used.

  In the filter 10, the shape of the filter medium 1 is approximately square, and the shape of the container 3 is approximately square. The inner joint portion 5 integrally joins the filter medium 1 and the container 3 to define a blood treatment region R (hereinafter referred to as “region R”) of the filter 10.

  The region R has a substantially square shape, like the inner joint 5. As shown in FIG. 1, in the region R, the inlet port 7a and the outlet port 8a are arranged on a diagonal line connecting the upper vertex C1 and the lower vertex C2. By forming the inlet port 7a and the outlet port 8a at such positions, the distance between the inlet 7 and the outlet 8 can be increased, and a sufficient distance for blood to flow through the filter medium 1 is secured. it can.

  As shown in FIG. 2, the inner joint 5 includes an inlet-side joint 5 a that joins the flexible sheet 3 a that forms the inlet of the container 3 and the inlet-side surface 1 a of the filter medium 1, and an outlet of the container 3. It has the exit side junction part 5b which joins the flexible sheet | seat 3b which makes the side, and the surface 1b of the exit side of the filter medium 1. FIG. The outlet side joint 5b is set to have a lower peel strength than the inlet side joint 5a, and is set to have a lower peel strength than the outer joint 6. Thereby, by pulling the flexible sheet 3b that forms the outlet side of the container 3, the flexible sheet 3b can be peeled from the outlet-side surface 1b of the filter medium 1 at the outlet-side joint portion 5b.

  When the flexible sheet 3b is peeled from the outlet side joint 5b in the inner joint 5, the tension of the flexible sheet 3b is weakened as shown in FIG. Thereby, the volume of the fluid which can be accommodated in the exit side of the container 3 increases afterwards. For this reason, it becomes possible to discharge the air in the collection bag 22 to the outlet side of the container only by applying a small pressing force to the collection bag 22 shown in FIG.

  The peel strength of the flexible sheet 3b at the inner joint 5 to the filter medium 1 (peel strength of the outlet-side joint 5b) is preferably 0.5 to 1.5 N / mm, more preferably 0.8 to 1.2 N / mm. When the strength is less than 0.5 N / mm, blood tends to enter the region between the inner joint portion 5 and the outer joint portion 6 as compared with the case where the strength is 0.5 N / mm or more. If it exceeds 1.5 N / mm, the peeling operation tends to be difficult compared to the case of 1.5 N / mm or less.

  The peel strength of the flexible sheet 3a with respect to the filtering material 1 at the inner joint portion 5 (peel strength of the inlet side joint portion 5a) is set higher than the peel strength of the outlet side joint portion 5b. When the peel strength is set in this manner, the flexible sheet 3b can be peeled from the filter medium 1 before the flexible sheet 3a at the inner joint portion 5 by pulling the flexible sheet 3b. The peel strength of the inlet side bonded portion 5a is preferably 2.0 to 6.0 N / mm, more preferably 3.0 to 5.0 N / mm.

  The outer joint portion 6 seals the container 3 in the thickness direction of the filter 10 in order to more reliably protect the filter medium 1 from the external environment. The outer joint portion 6 is provided so as to form the outer periphery of the rectangular container 3.

  The outer joint portion 6 is set to have a higher peeling strength than the outlet side joint portion 5 b in the inner joint portion 5, and the outer joint portion 6 is not damaged by the separation in the inner joint portion 5. As a result, blood remaining in the filter 10 after filtration can be sufficiently prevented from leaking from the outer joint portion 6. The peel strength between the flexible sheet 3a and the flexible sheet 3b in the outer joint portion 6 (peel strength of the outer joint portion 6) is preferably 2.0 to 6.0 N / mm, more preferably 3. 0.0 to 5.0 N / mm. When the strength is less than 2.0 N / mm, the outer joint portion 6 tends to be damaged by peeling at the inner joint portion 5 as compared with the case of 2.0 N / mm or more.

[Method for producing blood processing filter]
First, a sheet-form filter material having the ability to adsorb aggregates and leukocytes contained in blood is prepared, and this is cut into a predetermined size to obtain the filter medium 1. The filter material can be cut with a blade, an ultrasonic cutter or a laser cutter.

  As a material for a filter medium, a material having flexibility is preferable, such as a fiber structure such as a nonwoven fabric manufactured by a melt blow method, a porous body (sponge-like structure) having continuous pores, a porous film, etc. Is mentioned. As a material for a filter medium, a material composed of a fiber structure, a porous body or a porous membrane, or a material obtained by using these as a base material and chemically or physically modified on the surface thereof may be used. As the filter material, a fiber structure, a porous body, or a porous membrane may be used as a single layer, or a combination of these may be used as a plurality of layers.

Examples of the material for the fiber structure include polyester, polypropylene, polyamide, polyacrylonitrile, polytrifluoroethylene, polymethyl methacrylate, polystyrene, and the like. When a fiber structure is used as the filter medium 1 or its base material, the fiber structure may be composed of fibers having a substantially uniform fiber diameter, and is disclosed in WO 97/232266. A form in which a plurality of types of fibers having different fiber diameters are mixed may be used. In order to reduce the white blood cell count of the blood after filtration to 5 × 10 ⁶ cells / unit or less, the average fiber diameter of the fibers forming the filter medium 1 is preferably 3.0 μm or less, more preferably 0.9 μm. ~ 2.5 μm.

Examples of the material of the porous body or porous membrane include polyacrylonitrile, polysulfone, cellulose acetate, polyvinyl formal, polyester, polyacrylate, polymethacrylate, and polyurethane. In order to reduce the white blood cell count of the blood after filtration to 5 × 10 ⁶ / unit or less, the average pore diameter of the porous body or porous membrane is preferably 2 μm or more and less than 10 μm.

  A flexible resin sheet or film for forming the container 3 is prepared. Examples of the material of the container 3 include soft polyvinyl chloride; polyurethane; ethylene-vinyl acetate copolymer; polyolefin such as polyethylene and polypropylene; hydrogenated product of styrene-butadiene-styrene copolymer; styrene-isoprene-styrene copolymer And a thermoplastic elastomer such as a polymer or a hydrogenated product thereof; and a mixture of a thermoplastic elastomer and a softening agent such as polyolefin or ethylene-ethyl acrylate. From the viewpoint of good permeability of high-pressure steam and electron beam for sterilization, and toughness that can withstand the load during centrifugation, soft vinyl chloride, polyurethane, polyolefin, and these A thermoplastic elastomer containing as a main component is particularly suitable.

  By forming the inner joint 5, the filter medium 1 and the container 3 are joined together to define the region R of the filter 10. The inner joint portion 5 can be formed by, for example, high frequency welding. Similarly to the inner joint 5, the outer joint 6 can be formed by high frequency welding.

  In the inner joint portion 5, in order to make the peel strength of the outlet side joint portion 5 b lower than the peel strength of the inlet side joint portion 5 a, the temperature at the time of forming the outlet side joint portion 5 b can be lowered or the time of the joining process Can be shortened. Further, the peel strength can be adjusted by changing the material and amount of the molten material of the filter at the inlet side joint 5a and the outlet side joint 5b.

  The inlet port 7a and the outlet port 8a may be provided at predetermined positions of the container 3 by welding, for example, and the region R may be communicated with the outside through the inlet 7 and the outlet 8. The filter 10 is manufactured through the above process.

[Blood treatment system]
As shown in FIG. 4, the blood processing system 50 according to the present embodiment is connected such that a bag 21 containing blood, a filter 10, and a blood collection bag 22 are arranged in this order from top to bottom. . The filter 10 is connected to the backs 21 and 22 by tubes 25 and 26, and a Robert clamp 27 and a chamber 28 are disposed in the middle of the tube 25.

  According to the blood processing system 50, after filtration, the volume of the fluid that can be accommodated on the outlet side of the container 3 of the filter 10 is increased afterwards, so that the air in the collection bag 22 is discharged to the filter 10 sufficiently easily and reliably. it can.

  In the blood processing system 50, the tube 25 and the tube 26 are communicated with each other, and there is no need to provide a tube (bypass circuit) that bypasses the filter 10. In the blood processing system 50, the tube 26 forms a flow path for transferring blood that has passed through the filter 10 to the collection bag 22, and air remaining in the collection bag 22 is transferred to the filter 10 after filtration is completed. Make a flow path. The blood processing system 50 does not necessarily require a bypass circuit for barping, and may be provided with a bypass circuit for some purpose.

[Production method of blood product]
The blood product manufacturing method according to the present embodiment is performed using the blood processing system 50. This method
A) putting the blood to be filtered into the storage bag 21;
B) filtering the blood in the storage bag 21 with the filter 10;
C) collecting the blood that has passed through the filter 10 in the collection bag 22;
D) peeling the flexible sheet 3b from the outlet-side surface 1b of the filter medium 1 at the outlet-side joint portion 5b by pulling the flexible sheet 3b forming the outlet side of the container 3 of the filter 10;
E) a step of transferring air remaining in the collection bag 22 after the step C) to the outlet side of the filter 10 after the step D);
F) The step of sealing the collection bag 22 after the step E),
Is provided.

  After collecting the blood in the collection bag 22 through the step C), the volume of the fluid that can be accommodated on the outlet side of the container 3 of the filter 10 can be increased afterwards by performing the step D). Thereby, the air in the collection bag 22 can be discharged to the filter 10 easily and reliably in the step E). In addition, since the operation of increasing the volume of the fluid that can be accommodated on the outlet side of the container 3 is performed after filtration, the amount of blood remaining in the filter 10 at the end of filtration increases compared to the conventional case, and the blood recovery amount decreases. There is no problem.

  In step C), the blood that has passed through the filter 10 is transferred to the collection bag 22 through the tube 26. In step E), air remaining in the collection bag 22 is transferred to the filter 10 through the tube 26. It can be transferred to the outlet side.

  The preferred embodiment of the present invention has been described in detail above, but the present invention is not limited to the above embodiment. For example, in the above embodiment, the filter 10 is exemplified as having a substantially square shape, but the shape is not limited to this, and may be a circle or a rectangle as shown in FIG. May be elliptical or polygonal (eg, hexagonal, octagonal).

  Moreover, in the said embodiment, although illustrated about the case where the blood processing system 50 is arrange | positioned to a perpendicular direction, when using a pump etc. instead of gravity for the transfer of blood, for example, the blood processing system 50 is set to a horizontal direction. You may arrange.

(Example)
The first filter element is a polyester nonwoven fabric having a fiber diameter of 12 μm, a basis weight of 30 g / m ² , and a thickness of 0.189 mm; and a fiber diameter of 1.2 μm, a basis weight of 40 g / m ² , and a polyester nonwoven fabric having a thickness of 0.235 mm A second filter element was prepared for each. 4 sheets of first filter elements on the blood inlet side, 26 sheets of second filter elements on the blood outlet side, and 4 sheets of first filter elements on the blood outlet side. A filter medium material was obtained. This filter medium material was cut to obtain a square filter medium of 87 mm × 87 mm.

  A flexible resin sheet is disposed on both surfaces of the filter medium, and an inner joint portion and an outer joint portion are formed by a high-frequency welding method so that the blood treatment region is a square having a side of 70 mm, and this embodiment is concerned. A filter was obtained. In addition, in the position which should form an inner side junction part, the resin sheet and filter material of an inlet side were joined by the primary welding by a high frequency, and the inlet side junction part was formed. Thereafter, the outlet side resin sheet and the filter medium were joined by high frequency secondary welding to form an outlet side joint, and the inlet side joint was heated again. Thereby, the inner side junction part whose peeling strength of an exit side junction part is lower than an entrance side junction part was formed.

  The peel strength of the outlet side joint portion of the filter obtained as described above was 1.1 N / mm, and the peel strength of the inlet side joint portion was 2.6 N / mm. In addition, the peeling strength of the outlet side joint part and the inlet side joint part in the inner joint part was measured as follows.

[Measurement method of peel strength]
(1) Preparation of test piece A cut was made in two places with a cutter so as to cross the welded joint. The interval between the cuts was about 25 mm, and the length of the cuts was about 40 mm on both sides of the joint. Next, a test piece was cut out on both sides of the joint part, at a location approximately 30 mm away from the joint part, in parallel with the joint part. The surface of the cut surface was smoothed by shaving the unevenness of the cut surface of the joint using a razor blade. One test piece was used as a peel test sample, the length of the joint was measured with three calipers, and the average value was taken as the length of the joint. Another remaining test piece was used as a sample for measuring the boundary line length.
(2) Peel test method The sample for peel test having a width of about 25 mm produced by the method of (1) was fixed to a gripping tool at a position 10 mm away from the joint, and then at a speed of 10 mm / min with a tensile tester. The tensile fracture strength of the test piece was measured by applying a force that pulled and peeled off the joint (23 ° C.). The value obtained by dividing the measured tensile fracture strength by the length of the joint was taken as the peel fracture strength.

(Comparative example)
A filter was produced in the same manner as in the example except that the inlet side joint and the outlet side joint were simultaneously formed by high frequency welding, and an inner joint having substantially the same peel strength was formed. The peel strength of the outlet side joint of the obtained filter was 2.8 N / mm, and the peel strength of the inlet side joint was 2.7 N / mm.

  A peel test was performed on the filters according to Examples and Comparative Examples. By pulling the flexible sheet by hand with the filter of the example, the outlet side flexible sheet could be easily peeled from the filter medium before the inlet side flexible sheet at the inner joint portion. However, the filter of the comparative example could not separate the inlet side flexible sheet and the outlet side flexible sheet from the inner joint portion even when the flexible sheet was pulled by hand.

  According to the present invention, the air in the collection bag that stores the filtered blood can be discharged to the filter sufficiently easily and reliably.

DESCRIPTION OF SYMBOLS 1 ... Filter material, 3 ... Container, 3a, 3b ... Flexible sheet, 5 ... Inner side junction part, 5a ... Inlet side junction part, 5b ... Outlet side junction part, 6 ... Outer side junction part, 7 ... Inlet, 8 ... Outlet, 10 ... filter, 21, 22 ... back, 25, 26 ... tube, 50 ... blood processing system, F1 ... one side, F2 ... other side, R ... blood processing region.

Claims (8)

A blood treatment filter,
A sheet-like filter medium;
A container that contains the filtering material and is formed by joining flexible sheets;
In the thickness direction of the filter, a first joint that joins the filter medium and the container to define a blood treatment region;
A second joint that joins the peripheral edge of the container in the thickness direction of the filter;
An inlet provided on one side of the container;
An outlet provided on the other side of the container;
With
The first joint includes an inlet-side joint that joins the flexible sheet forming the inlet side of the container and the inlet-side surface of the filter medium, and a flexible sheet forming the outlet side of the container And an outlet side joint portion for joining the outlet side surface of the filter medium,
The outlet side joint portion has a lower peel strength than the inlet side joint portion, and pulls the flexible sheet forming the outlet side of the container to pull the flexible sheet from the surface on the outlet side of the filter medium at the outlet side joint portion. A filter from which a flexible sheet can be peeled. A blood treatment filter,
A sheet-like filter medium;
A container that contains the filtering material and is formed by joining flexible sheets;
In the thickness direction of the filter, a first joint that joins the filter medium and the container to define a blood treatment region;
A second joint that joins the peripheral edge of the container in the thickness direction of the filter;
An inlet provided on one side of the container;
An outlet provided on the other side of the container;
With
The first joint includes an inlet-side joint that joins the flexible sheet forming the inlet side of the container and the inlet-side surface of the filter medium, and a flexible sheet forming the outlet side of the container And an outlet side joint portion for joining the outlet side surface of the filter medium,
The outlet side joint portion has a lower peel strength than the second joint portion, and pulls a flexible sheet that forms the outlet side of the container to pull the flexible sheet from the outlet side surface of the filter medium at the outlet side joint portion. A filter from which the flexible sheet is peelable.   The filter according to claim 1 or 2, wherein the outlet-side joint has a peel strength of 0.5 to 1.5 N / mm. A storage bag for containing the blood to be filtered;
The blood processing filter according to any one of claims 1 to 3,
A collection bag for containing the blood filtered by the filter;
A first tube connecting the storage bag and the inlet of the filter;
A second tube connecting the outlet of the filter and the collection bag;
A blood processing system comprising:   The second tube forms a flow path for transferring the blood that has passed through the filter to the collection bag, and also forms a flow path for transferring air remaining in the collection bag to the filter after completion of filtration. The system of claim 4, wherein   The system according to claim 4 or 5, wherein the first tube and the second tube are communicated with each other, and the tube that bypasses the filter is not provided. A method for producing a blood product using the blood processing system according to any one of claims 4 to 6,
A) placing the blood to be filtered into the storage bag;
B) filtering the blood in the storage bag with the filter;
C) collecting the blood that has passed through the filter into the collection bag;
D) peeling the flexible sheet from the outlet side surface of the filter medium at the outlet side joint by pulling the flexible sheet forming the outlet side of the container of the filter;
E) transferring the air remaining in the collection bag after the step C) to the outlet side of the filter after the step D);
F) sealing the collection bag after step E);
A method comprising: In step C), blood that has passed through the filter is transferred to the collection bag through the second tube, and in step E), air remaining in the collection bag is transferred to the second bag. The method according to claim 7, wherein the method is transferred to the outlet side of the filter through a tube.

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