WO2006022358A1 - 積層体 - Google Patents
積層体 Download PDFInfo
- Publication number
- WO2006022358A1 WO2006022358A1 PCT/JP2005/015491 JP2005015491W WO2006022358A1 WO 2006022358 A1 WO2006022358 A1 WO 2006022358A1 JP 2005015491 W JP2005015491 W JP 2005015491W WO 2006022358 A1 WO2006022358 A1 WO 2006022358A1
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- WIPO (PCT)
- Prior art keywords
- layer
- laminate
- film
- pores
- laminate according
- Prior art date
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Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B3/00—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form
- B32B3/26—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form characterised by a particular shape of the outline of the cross-section of a continuous layer; characterised by a layer with cavities or internal voids ; characterised by an apertured layer
- B32B3/30—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form characterised by a particular shape of the outline of the cross-section of a continuous layer; characterised by a layer with cavities or internal voids ; characterised by an apertured layer characterised by a layer formed with recesses or projections, e.g. hollows, grooves, protuberances, ribs
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B3/00—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form
- B32B3/10—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form characterised by a discontinuous layer, i.e. formed of separate pieces of material
- B32B3/12—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form characterised by a discontinuous layer, i.e. formed of separate pieces of material characterised by a layer of regularly- arranged cells, e.g. a honeycomb structure
Definitions
- the present invention relates to a laminate. More specifically, the present invention relates to a laminate having a plurality of pores arranged in an 82-cam shape.
- honeycomb structures are produced by casting a dope containing a polymer and an organic solvent, and by forming regularly arranged water droplets formed when the organic solvent evaporates into a bowl shape. It is called a chemical film.
- the polymer concentration, cast amount, etc. dominate the success or failure of pattern formation.
- the polymer concentration should not be too high for the water droplets to be arranged uniformly.
- the amount of dope cast per unit area exceeds a certain amount, water droplets cannot be maintained and a non-uniform pattern is formed. For this reason, the concentration of the polymer cannot be increased inevitably, and since the cast amount is limited, the thickness of the film that is substantially formed is also limited.
- Patent Document 1 Japanese Patent Application Laid-Open No. 2001-157574
- Patent Document 2 Japanese Patent Application Laid-Open No. 2003-128832
- Patent Document 3 Japanese Unexamined Patent Publication No. 2003-149096 Disclosure of the invention
- An object of the present invention is to provide a laminate having a plurality of pores arranged in an 82-cam shape, having a thickness and excellent strength, and a method for producing the same.
- the present invention relates to a laminate having an outer layer (A layer) that is a surface having a plurality of pores (S surface) arranged on one surface in a honeycomb shape, and the S surface is disposed on the outermost surface of the laminate It is a laminated body.
- a layer an outer layer
- S surface a surface having a plurality of pores
- the present invention is also a method for producing a laminate comprising laminating an outer layer (A layer), wherein the A layer is
- a method for producing a laminate characterized in that the method comprises a step of evaporating water droplets, wherein one surface (S surface) has a plurality of pores arranged in a honeycomb shape. .
- FIG. 1 is a schematic diagram showing a honeycomb arrangement.
- Fig. 2 is a schematic diagram showing an 82-cam configuration.
- Fig. 3 is a schematic cross-sectional view of the outer layer.
- FIG. 4 is a schematic diagram of a cross-sectional structure of one embodiment of the laminate of the present invention.
- FIG. 6 is a schematic diagram of a cross-sectional structure of one embodiment of the laminate of the present invention.
- FIG. 7 is a schematic diagram of a cross-sectional structure of one embodiment of the laminate of the present invention.
- FIG. 8 is a schematic diagram of a cross-sectional structure of one embodiment of the laminate of the present invention. Explanation of symbols 1 outer layer
- the laminate of the present invention has a plurality of pores arranged in a honeycomb shape, it can absorb blood and tissue fluid on the surface of the living tissue and can be attached to the surface of the living tissue.
- the laminate of the present invention has a large thickness, it has excellent mechanical strength. Therefore, it is suitably used in applications that require mechanical strength. For example, it is suitably used as a medical material, in particular, an adhesion prevention material as a sealant.
- the laminate of the present invention is thicker than a single-layer film, it is excellent in handleability.
- the outer layer (A layer) is characterized in that one surface is a surface (S surface) having a plurality of pores arranged in a honeycomb shape.
- the double cam-like arrangement means a structure in which regular hexagons are arranged adjacent to each other as shown in FIG. Therefore, the positional relationship between the plurality of pores on the S plane corresponds to the positional relationship between the regular hexagons shown in FIG. Therefore, six pores are arranged around one pore.
- Fig. 2 shows a state in which circular pores are arranged in a non-nicky shape. It is preferable that the pores have substantially the same shape.
- the pores are preferably circular with a diameter of 0.1 to 100 rn, more preferably 1 to 20 m, more preferably 1 to 15 m, and even more preferably 1 to 10 m. preferable.
- the diameter (radius) of the pore is the S plane The diameter (radius) of the hole at. If the radius of the pore is r and the distance between the centers of adjacent pores is a, then r and a are preferably expressed as 1 and a / 2r ⁇ 2.
- Figure 3 shows a schematic diagram of the cross section of the outer layer.
- 4 is the S plane
- 5 is the R plane.
- the thickness of the outer layer is preferably 1 to 10 mm, more preferably 3 to 8 m.
- the outer layer is preferably made of a biodegradable polymer.
- Biodegradable polymers include aliphatic polyesters such as polylactic acid, polyglycolic acid, polyhydroxybutyric acid, polystrength prolactone, polyethylene adipate, polybutylene adipate, and copolymers of these that are soluble in organic solvents. It is preferable from the viewpoint.
- aliphatic polycarbonates such as polybutylene strength monoponate and polyethylene strength monoponate are preferable.
- polylactic acid, polylactic acid-polyglycolic acid copolymer, polystrength prolactone, and lactic acid-strength prolactone copolymer are desirable from the viewpoint of availability and price.
- the outer layer (A layer) preferably contains phospholipids in addition to these polymers.
- a preferred content is 0.1 to 100 parts by weight, more preferably 0.2 to 10 parts by weight of phospholipid with respect to 100 parts by weight of the polymer. More preferably, it is 0.5 to 2 parts by weight.
- Phospholipids are substances that make up biological membrane systems, and since they are inherently in vivo, they are highly biocompatible and are also used in drug delivery systems and have high safety. Are known.
- Phospholipids can be used regardless of their origin, whether they are extracted from animal tissues or artificially synthesized. It is preferable to use a phospholipid selected from the group consisting of phosphatidylethanolamine, phosphatidylcholine, phosphatidylserine, phosphatidylglycerol and derivatives thereof. More preferred is phosphatidylethanolamine, and more preferred is L-phosphatidylethanolamine oil.
- the outer layer may contain an amphiphilic polymer in addition to these polymers.
- an amphiphilic polymer is not toxic in consideration of use as an adhesion preventing material.
- a polyethylene glycol Z polypropylene glycol block copolymer an amphiphilic polymer having an acrylamide polymer as the main chain skeleton, a dodecyl group as a hydrophobic side chain, and a lactose group or a carboxyl group as a hydrophilic side chain. Is preferred.
- Heparin is a hydrophilic group of dextran sulfate, anion complexes of anionic polymers such as DNA and RNA nucleic acids and long-chain alkyl ammonium salts, and water-soluble proteins such as gelatin, collagen, and albumin. Amphiphilic polymers can be used.
- Biodegradable and amphiphilic polymers may be used.
- examples of such a polymer include a polylactic acid-polyethylene glycol block copolymer, a poly ⁇ -force prolactone-polyethylene glycol block copolymer, and a polyphosphonic acid-polymalic acid alkyl ester block copolymer. . (Manufacture of outer layers)
- the film constituting the outer layer (hereinafter sometimes referred to as film ( ⁇ )) is: (1) a step of casting a dope containing a polymer and an organic solvent on a substrate to form a liquid film;
- the dope contains a polymer and an organic solvent.
- the polymer is preferably the aforementioned biodegradable polymer.
- organic solvents halogen organic solvents such as chloroform, methylene chloride and the like, aromatic hydrocarbons such as benzene, toluene and xylene, esters such as ethyl acetate and butyl acetate, and water insoluble such as methyl isoptyl ketone Ketones, carbon disulfide Etc.
- organic solvents may be used alone or as a mixture of these solvents.
- the dopant contains phospholipid in addition to the polymer.
- the preferred content is 0.1 to 100 parts by weight, more preferably 0.2 to 10 parts by weight, and still more preferably 0.5 to 2 parts by weight of phospholipid per 100 parts by weight of the polymer.
- the dope may contain an amphiphilic polymer in addition to the polymer.
- the solute concentration in the dope combined with the polymer, phospholipid, and amphiphilic polymer is preferably 0.01 to 10% by weight, more preferably 0.05 to 5% by weight.
- inorganic materials examples include glass, metal, and silicon wafers.
- examples of the polymer include polypropylene, polyethylene, and polyether ketone.
- examples of the liquid include water, liquid paraffin, and liquid polyether.
- the liquid film is allowed to stand in an atmosphere with a relative humidity of 50 to 95% to evaporate the organic solvent.
- the relative humidity is preferably 50 to 85%. If the relative humidity is less than 50%, condensation on the liquid film will be insufficient, and if it exceeds 95%, it is not preferable because it is difficult to control the humidity.
- the temperature may be a temperature at which the organic solvent gradually evaporates, and is preferably 10 to 30 ° C, more preferably room temperature.
- the organic solvent evaporates and water vapor condenses on the liquid film surface to form water droplets. This takes away latent heat when the organic solvent evaporates, and the temperature of the liquid film surface This is because water vapor in the atmosphere is condensed on the liquid film surface.
- the surface tension between the condensed water vapor and the organic solvent is reduced by the action of the hydrophilic group in the polymer, and the condensed water vapor aggregates into minute water droplets.
- microscopic water droplets packed in a hexagonal arrangement are arranged on the liquid film surface.
- the water droplets sink into the liquid film, and the surface of the liquid film has a structure in which the water droplets surrounded by the polymer are regularly arranged.
- the organic solvent in the liquid film completely evaporates, Form a film.
- pores having a diameter of 0.1 to 100 m are regularly formed.
- the diameter of the pores is preferably from 0.1 to 20 im, more preferably from 1 to 15 111, and even more preferably from 1 to 10 zm.
- the back surface that was in contact with the substrate is a flat surface that does not penetrate through the pores.
- the depth of the pores is preferably 0.1 to 20 m, more preferably 1 to 15 m, and further preferably 1 to 10 m.
- the film thickness is thinner than the size of the water droplet, a film (A) having fine pores can be obtained.
- the film constituting the substrate layer may be composed of any polymer, but is preferably composed of a biodegradable polymer.
- biodegradable polymers include polylactic acid, polydaricholic acid, polyhydroxybutyric acid, polyproprolactone, polyethylene adipate, aliphatic polyesters such as polybutylene adipate, and copolymers thereof that are soluble in organic solvents. It is preferable from the viewpoint.
- aliphatic polycarbonate such as polyethylene glycol and polyethylene strength—Pone is preferred.
- polylactic acid polylactic acid-polyglycolic acid copolymer
- poly-strength prolactone poly-strength prolactone copolymer
- lactic-strength prolactone copolymer are desirable from the viewpoint of availability and price.
- the method for producing the film (B) is not particularly limited, and for example, a casting method or a melt molding method can be selected.
- the casting method is performed by casting a polymer containing the polymer (B) and a solvent containing a solvent on a substrate and evaporating the solvent.
- melt molding method examples include an extrusion molding method, a calendar method, and a T-die method.
- extrusion molding method a material heated and flown in an extruder is continuously extruded from a die attached to the tip of the extruder and formed into a film.
- force render method the material is rolled while being melted by a heated rotating roller, and further rolled while being cooled by 3 to 4 or more rolls to form a film or sheet.
- T-Die method a heated and fluidized material is extruded from a horizontally long die (die) attached to an extruder to a cooling roll (casting roll), which is rapidly cooled and solidified to form a film.
- volatile solvents are substances that have a boiling point of 200 ° C. or less at normal pressure and liquid at 27 ° C.
- volatile solvents include methylene chloride, black-form, acetone, methanol, ethanol, propanol, isopropanol, toluene, tetrahydrofuran, 1, 1, 1, 3, 3, 3-hexafluoroisopropanol, water 1,4-dioxane, carbon tetrachloride, cyclohexane, cyclohexanone, N, N-dimethylformamide, and acetonitrile.
- methylene chloride, black mouth form, and acetone are particularly preferred from the viewpoint of the solubility of the aliphatic polyester.
- the laminate of the present invention preferably has the following cross-sectional structure.
- the B layer may be composed of a plurality of layers.
- the A layer, the B layer, and the A ′ layer may be the same material or different materials.
- the material of each layer By selecting the material of each layer, a laminate having desired physical properties can be obtained.
- the decomposition time of the laminate can be controlled by changing the type of polymer constituting each layer of the laminate. For example, polylactic acid in the polymer of layer A , And using a polylactic acid-polyglycolic acid copolymer for the polymer of the B layer, the degradation of the A layer can be made slower.
- a layer, B layer and A layer are arranged in this order, and the R surface of each A layer is located on the B layer side.
- Figure 5 shows the schematic.
- a layer, B layer, and A ′ layer are arranged in this order, and the R surface of the A layer and A ′ layer is located on the B layer side.
- Figure 6 shows the schematic.
- the A ′ layer is an outer layer having a plurality of pores arranged in a honeycomb shape, but having an S surface that is different from the A layer in the size of the pores.
- the thickness of the laminate is preferably 10 m or more, more preferably 15 m or more, and further preferably 30 to 300 m.
- the A layer can be laminated on the B layer by thermocompression bonding.
- the temperature for thermocompression bonding is not particularly limited, but is preferably higher than the glass transition point of the polymer constituting the A layer and the B layer.
- an elastic body such as silicon rubber together as needed during crimping.
- a method for producing a laminate comprising laminating outer layers (A layers) Where the A layer is
- the A layer is laminated on the B layer, or the A layers are laminated.
- a plurality of pores having substantially the same shape are formed on the S surface, and an A layer in which six pores are arranged around one pore is formed.
- the elastic modulus was obtained by tensile testing with a Tensilon apparatus using a 1 x 5 cm test piece as the film. Test conditions were as follows: sample width (10mm), thickness (depending on each sample: mm), gauge distance (distance between clips: 30mm), and test speed (30mmZmin).
- PE Phosphatidylethanolamine-dioleoyl oil
- the mixture was prepared at a ratio of The dope was cast on a glass substrate and allowed to stand at room temperature and 70% humidity, and the solvent was gradually evaporated to prepare a film (A).
- a plurality of pores were arranged in a honeycomb shape, and the diameter of each pore was about 5 m.
- the other surface (R surface) was smooth.
- the thickness of film (A) was 4 m and was a non-penetrating film. the film (A) was subjected to an annealing treatment at 70 ° C. for 10 minutes.
- a black mouth form solution (10% by weight) of polylactic acid (molecular weight 200,000) was cast on a glass substrate to obtain a film (B) having a film thickness of 46 m. Annealing was performed at 70 ° C for 10 minutes.
- the film (A) is stacked on the film (B) so that the R side is the film (B) side.
- Annealing is performed at 70 ° C for 10 minutes, and both films are bonded to obtain a stacked body. It was.
- the thickness of the laminate was 50.
- the elastic modulus of the laminate was 129 IMpa.
- a dope was prepared. The dope was cast on a glass substrate and allowed to stand at room temperature and humidity of 70%, and the solvent was gradually evaporated to prepare a film (A).
- a chloroform solution (10% by weight) of polylactic acid-polypolyprolactone copolymer (molecular weight 163,000) was cast on a glass substrate to obtain a film (B) having a film thickness of 34 m.
- Film (B) was annealed at 70 ° C for 10 minutes.
- the film (B) was laminated on the film (B) so that the R side was on the film (B) side, and the film was annealed at 60 for 10 minutes, and both films were adhered to obtain a laminated body. .
- the thickness of the laminate was 40 m.
- the elastic modulus of the laminate was 325 MPa.
- the dope was cast on a glass substrate and allowed to stand at room temperature and 70% humidity, and the solvent was gradually evaporated to prepare a film (A) having a honeycomb structure.
- the film (A) On one surface (S surface) of the film (A), a plurality of pores are arranged in a honeycomb shape.
- the diameter of the bush was about 5 m.
- the other surface (surface) was smooth.
- the film thickness was 5 zm and was a non-penetrating film.
- the film (A) was subjected to an annealing treatment at 70 ° (:, 10 minutes).
- a black mouth form solution (10% by weight) of polylactic acid (molecular weight 200,000) was cast on a glass substrate to obtain a film (B) having a film thickness of 20 1! 1.
- Film (B) was annealed at 70 ° C. for 10 minutes.
- Film (B) Laminate the film (A) on both the top and bottom surfaces so that the R side is on the film (B) side, and 70 ° (:, 10 minutes annealing treatment to adhere each film and laminate (AZBZA) was obtained
- the thickness of the laminate was 30.
- the elastic modulus of the laminate was 1118 MPa.
- Two films (A) are laminated so that one R-side and the other R-side are bonded together, and annealed at 70 ° C for 10 minutes to bond the two films to form a laminate (AZA). Obtained.
- the thickness of the laminate was 10 m.
- the elastic modulus of the laminate was 556 Mpa.
- the film was cast on a glass substrate and allowed to stand at room temperature and 70% humidity, and the solvent was gradually evaporated to prepare a film (A) having a ⁇ two-cam structure.
- the film (A) On one surface (S surface) of the film (A), a plurality of pores were arranged in a honeycomb shape, and the diameter of each pore was about 5 m. The other surface (surface) was smooth. The film thickness was 4 m and it was a non-penetrating film.
- the film (A) was annealed at 70 ° (:, 10 minutes. The film (A) had a viscosity of 286 MPa.
- the dope was cast on a glass substrate and allowed to stand at room temperature and humidity of 70%, and the solvent was gradually evaporated to prepare a film (A).
- a plurality of pores were arranged in a honeycomb shape, and the diameter of each pore was about 5 m.
- the other surface (R surface) was smooth.
- the film thickness was 6 m and it was a non-penetrating film.
- Film (A) was annealed at 60 ° C. for 10 minutes. As a result of measuring the tensile strength of the film (A), the elastic modulus was 17 IMpa.
- the laminate of the present invention has a plurality of pores arranged in a honeycomb shape in the A layer, it can be easily attached to the surface of a living tissue.
- it has a structure in which a plurality of layers are laminated and has a large thickness, so that the flow of fluid from one surface of the laminate to the other surface can be blocked. This effect is particularly great when a substrate layer is provided. Therefore, when used as an anti-adhesion material, the distribution of fiber can be suppressed.
- the laminate of the present invention is suitably used particularly for preventing adhesion during surgery.
- laparotomy for diseases such as liver, spleen, spleen, kidney, uterus, ovary, 1
- adhesion may occur at the organ incision and ventral abdominal wall incision. Adhesion can be prevented by applying a honeycomb structure film to the pressure ulcer after surgery.
- Adhesion can be prevented by applying the laminate of the present invention to the pressure ulcer after surgery.
- the Achilles tendon, flexor tendon, and nerves will not move their hands, feet, and fingers due to their cutting. If an adhesion occurs during reconstruction by a suture operation, it may not move despite the suture, and an adhesion resection is required. Adhesion can be prevented by applying the laminate of the present invention to the wound after surgery.
- a laminated film having a thick and high elastic modulus it can be used particularly effectively as a sealant for the pericardium, pleura, spine and brain dura mater, knee, elbow joint and anti-adhesion materials.
- adhesion formation around the heart, lungs, trachea and esophagus can be prevented, thereby facilitating reoperation.
- it can prevent lung air leakage as a sealant.
- adhesion can be prevented by installing the laminate of the present invention to isolate the spinal cord from the surrounding spine.
- the artificial dura mater PTFE already used has the disadvantage that cerebrospinal fluid leaks between surrounding tissues and from the needle holes during suturing.
- tissue adhesiveness is improved, and a more excellent sealant effect and adhesion preventing effect can be exhibited.
- the laminate of the present invention having the A layer is installed on both sides between the skull side and the arachnoid membrane, the sealant effect and the adhesion preventing effect can be exerted on the skull side and the arachnoid membrane, respectively. At this time, it is also possible to select an appropriate pore diameter for each surface.
- the orthopedic field it can be used, for example, to prevent the formation of adhesions such as joint replacements, knees after joint revision surgery, and elbow joints.
- a layer is present on both sides
- it can be used particularly effectively, for example, in GTR (Guided Tissue Regenerat ion) to regenerate lost periodontal support tissue. That is, by installing the laminate of the present invention having the A layer on both sides between the gingival connective tissue side and the alveolar bone, the sealant effect and the anti-adhesion effect on the gingival connective tissue side and the alveolar bone side, respectively. Can be demonstrated. At this time, it is also possible to select an appropriate pore diameter for each surface.
- a space for bone acquisition is provided below the periosteum by a membrane to the bone defect portion, and the bone tissue is guided by filling with a blood clot.
- a honeycomb structure film it can be used as a GT R film with high adhesion to the applicable site and controlled absorption time.
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- Materials For Medical Uses (AREA)
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Abstract
Description
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Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2006532603A JP4393519B2 (ja) | 2004-08-24 | 2005-08-19 | 積層体 |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2004-243318 | 2004-08-24 | ||
| JP2004243318 | 2004-08-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2006022358A1 true WO2006022358A1 (ja) | 2006-03-02 |
Family
ID=35967563
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2005/015491 Ceased WO2006022358A1 (ja) | 2004-08-24 | 2005-08-19 | 積層体 |
Country Status (3)
| Country | Link |
|---|---|
| JP (1) | JP4393519B2 (ja) |
| TW (1) | TW200615144A (ja) |
| WO (1) | WO2006022358A1 (ja) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007252680A (ja) * | 2006-03-24 | 2007-10-04 | Teijin Ltd | 止血材 |
| JP2008136770A (ja) * | 2006-12-05 | 2008-06-19 | Teijin Ltd | 緑内障治療材 |
| JP2009242546A (ja) * | 2008-03-31 | 2009-10-22 | Fujifilm Corp | 多孔フィルムの製造方法 |
| JP2016063948A (ja) * | 2014-09-24 | 2016-04-28 | 富士フイルム株式会社 | フィルム |
| WO2019004381A1 (ja) * | 2017-06-29 | 2019-01-03 | 富士フイルム株式会社 | 移植用チャンバー、移植用チャンバーの製造方法、移植用デバイス、および多孔質膜の融着方法 |
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| JPH06292716A (ja) * | 1993-04-09 | 1994-10-21 | Shimizu Yoshihiko | 医用材料 |
| JPH07275344A (ja) * | 1994-04-05 | 1995-10-24 | Nippon Zeon Co Ltd | 軟組織用医療用材料 |
| JPH09140785A (ja) * | 1995-11-22 | 1997-06-03 | Jms Co Ltd | 生体分解性医療用フィルムおよびその製造方法 |
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| JP2001157574A (ja) * | 1999-11-30 | 2001-06-12 | Terumo Corp | ハニカム構造体およびその調製方法、ならびにその構造体を用いたフィルムおよび細胞培養基材 |
| WO2002102276A2 (en) * | 2001-06-14 | 2002-12-27 | Providence Health System-Oregon | Wound dressing and method for controlling severe, life-threatening bleeding |
| JP2003149096A (ja) * | 2001-11-07 | 2003-05-21 | Fuji Photo Film Co Ltd | 血液濾過膜および方法 |
| WO2003062506A1 (fr) * | 2002-01-25 | 2003-07-31 | Showa Denko K.K. | Materiau metallique composite et son procede de production, materiau metallique grave et son procede de production, et condensateur electrolytique |
| JP2005128475A (ja) * | 2003-09-30 | 2005-05-19 | Tomoegawa Paper Co Ltd | 光反射板および反射型液晶表示装置 |
-
2005
- 2005-08-19 WO PCT/JP2005/015491 patent/WO2006022358A1/ja not_active Ceased
- 2005-08-19 JP JP2006532603A patent/JP4393519B2/ja not_active Expired - Lifetime
- 2005-08-23 TW TW094128804A patent/TW200615144A/zh unknown
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH06292716A (ja) * | 1993-04-09 | 1994-10-21 | Shimizu Yoshihiko | 医用材料 |
| JPH07275344A (ja) * | 1994-04-05 | 1995-10-24 | Nippon Zeon Co Ltd | 軟組織用医療用材料 |
| JPH09140785A (ja) * | 1995-11-22 | 1997-06-03 | Jms Co Ltd | 生体分解性医療用フィルムおよびその製造方法 |
| JP2000197693A (ja) * | 1998-10-19 | 2000-07-18 | Jms Co Ltd | 多孔性癒着防止材 |
| JP2001157574A (ja) * | 1999-11-30 | 2001-06-12 | Terumo Corp | ハニカム構造体およびその調製方法、ならびにその構造体を用いたフィルムおよび細胞培養基材 |
| WO2002102276A2 (en) * | 2001-06-14 | 2002-12-27 | Providence Health System-Oregon | Wound dressing and method for controlling severe, life-threatening bleeding |
| JP2003149096A (ja) * | 2001-11-07 | 2003-05-21 | Fuji Photo Film Co Ltd | 血液濾過膜および方法 |
| WO2003062506A1 (fr) * | 2002-01-25 | 2003-07-31 | Showa Denko K.K. | Materiau metallique composite et son procede de production, materiau metallique grave et son procede de production, et condensateur electrolytique |
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007252680A (ja) * | 2006-03-24 | 2007-10-04 | Teijin Ltd | 止血材 |
| JP2008136770A (ja) * | 2006-12-05 | 2008-06-19 | Teijin Ltd | 緑内障治療材 |
| JP2009242546A (ja) * | 2008-03-31 | 2009-10-22 | Fujifilm Corp | 多孔フィルムの製造方法 |
| JP2016063948A (ja) * | 2014-09-24 | 2016-04-28 | 富士フイルム株式会社 | フィルム |
| WO2019004381A1 (ja) * | 2017-06-29 | 2019-01-03 | 富士フイルム株式会社 | 移植用チャンバー、移植用チャンバーの製造方法、移植用デバイス、および多孔質膜の融着方法 |
| CN110831636A (zh) * | 2017-06-29 | 2020-02-21 | 富士胶片株式会社 | 移植用室、移植用室的制造方法、移植用器件及多孔膜的熔接方法 |
| US11576370B2 (en) | 2017-06-29 | 2023-02-14 | Fujifilm Corporation | Chamber for transplantation, method for manufacturing chamber for transplantation, device for transplantation, and method for fusion welding porous membranes |
Also Published As
| Publication number | Publication date |
|---|---|
| JP4393519B2 (ja) | 2010-01-06 |
| JPWO2006022358A1 (ja) | 2008-05-08 |
| TW200615144A (en) | 2006-05-16 |
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