WO2011129162A1 - 医療用器具及びその製造方法 - Google Patents
医療用器具及びその製造方法 Download PDFInfo
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- WO2011129162A1 WO2011129162A1 PCT/JP2011/055202 JP2011055202W WO2011129162A1 WO 2011129162 A1 WO2011129162 A1 WO 2011129162A1 JP 2011055202 W JP2011055202 W JP 2011055202W WO 2011129162 A1 WO2011129162 A1 WO 2011129162A1
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- lubricating
- lubrication
- lubricity
- base material
- coating
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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
- A61L29/00—Materials for catheters, medical tubing, cannulae, or endoscopes or for coating catheters
- A61L29/08—Materials for coatings
- A61L29/085—Macromolecular materials
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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
- A61L2400/00—Materials characterised by their function or physical properties
- A61L2400/10—Materials for lubricating medical devices
-
- 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
- A61L2420/00—Materials or methods for coatings medical devices
- A61L2420/08—Coatings comprising two or more layers
-
- 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
- A61M25/00—Catheters; Hollow probes
- A61M25/0043—Catheters; Hollow probes characterised by structural features
- A61M25/0045—Catheters; Hollow probes characterised by structural features multi-layered, e.g. coated
- A61M2025/0046—Coatings for improving slidability
Definitions
- the present invention relates to a medical instrument and a manufacturing method thereof.
- Coating the surface of a base material of a medical device with a material having high lubricity when wet for example, various oils such as silicone oil, low friction resin such as fluororesin and silicone resin, and the like are used.
- Patent Document 1 a solution containing a hydrophilic polymer such as polyethylene oxide (PEO) or polyvinyl pyrrolidone (PVP) is applied to the surface of the plastic base layer, and then irradiated with radiation to make the surface of the plastic base layer hydrophilic. Adhering polymers is disclosed. Moreover, this patent document 1 discloses that PVP can be used as a preferred hydrophilic polymer from the viewpoint of the binding property to the substrate surface.
- PEO polyethylene oxide
- PVP polyvinyl pyrrolidone
- the present inventors for example, have a good adhesion to the base material when the surface of the base material of the medical device is coated by PVP, but on the other hand, the rise of the lubricity at the beginning of the wetting is not necessarily limited. It was not good, and the knowledge that it cannot necessarily be said that it has excellent lubricity at the beginning of wetting was obtained. In addition, if a plurality of performances required as excellent coatings are to be realized with a single material, it is considered that it is not easy because, for example, advanced techniques and processing such as construction of new materials are required.
- the present invention has been made to solve the above-mentioned problems, and it is a main object of the present invention to provide a medical instrument having excellent wettability by including a coating portion that can be constructed by a simple method and a method for producing the same. And
- the present inventors have different lubricity at the beginning of lubrication depending on each material. Specifically, the lubricity is sufficiently exhibited after the start of wetting. We paid attention to the difference in the time taken to complete. And based on this knowledge, it discovered that the said subject could be solved by employ
- the present invention is a medical device in which a coating part is formed on the surface of a base material, wherein the coating part is formed of a material different from the base material, and lubricity when wet than the base material.
- a first lubrication part having a high height and a material different from that of the base material, a part different from the first lubrication part, provided on at least a part of the outer surface of the coating part, and the first lubrication part
- a second lubricating portion having higher initial lubricity when wet than the portion.
- the second lubricating portion having higher initial lubricity when wet is exposed to the outside of the coating portion.
- this medical instrument when this medical instrument is made to contact aqueous systems, such as blood and a body fluid, for example, the lubricity outstanding with respect to the base-material surface can be provided with the 2nd lubrication part at the initial stage of wetness. Therefore, this medical device can exhibit initial lubricity on the outer surface by the second lubrication part, and can exhibit an excellent lubrication effect at the beginning of wetting. Therefore, when this instrument is introduced into the living body, it can be smoothly inserted.
- the present invention also relates to a method for manufacturing a medical device, wherein a first lubrication part having higher lubricity when wet using the first solution containing a material different from the base material is used.
- a first step formed on the surface of the base material, and after the first step, a second solution containing a material different from the base material is used, and is a portion different from the first lubricating portion.
- the medical instrument produced by the method of the present invention is brought into contact with an aqueous system such as blood or body fluid, excellent lubricity is imparted to the surface of the base material by the second lubrication part at the initial stage of wetting. That is, the medical instrument produced by the above method can exhibit an excellent lubricating effect at the beginning of wetting and can be smoothly inserted when introduced into the living body.
- the figure which shows an example of the coating part in this medical device The figure for demonstrating the apparatus used for the slipperiness test.
- the figure which shows the result of the slip test about 2 layer coating.
- the coating portion is disposed on the surface of the medical device, and has a first lubrication portion having higher lubricity when wet than the base material, and a portion different from the first lubrication portion, and an outer surface of the coating portion. And a second lubricating portion provided at least in part.
- the second lubrication part has higher initial lubricity when wet than the first lubrication part.
- the first lubrication part is disposed on the substrate side with respect to the second lubrication part, and more preferably, the coating part includes an outermost layer constituting an outer surface of the coating part, and the outermost layer.
- the outermost layer is formed by the second lubrication part
- the intermediate layer is formed by the first lubrication part.
- FIG. 1 shows an example of a coating portion in the medical instrument.
- the medical instrument 10 includes a coating portion 12 on the surface of a base material 11.
- the coating portion 12 includes an outermost layer 12 a that constitutes the outer surface thereof, and an intermediate layer 12 b that is interposed between the outermost layer 12 a and the surface of the substrate 11.
- the intermediate layer 12 b is the 1st lubrication part.
- the second lubrication part may cover a part of the first lubrication part, but preferably the second lubrication part covers the entire first lubrication part as shown in FIG. It is a form.
- the intermediate layer 12b is formed by the first lubrication part and the outermost layer 12a is formed by the second lubrication part, another layer containing, for example, a drug is interposed between the intermediate layer 12b and the outermost layer 12a.
- the outermost layer 12a is laminated in contact with the intermediate layer 12b, or the material contained in the outermost layer 12a and the material contained in the intermediate layer 12b
- the outermost layer 12a is laminated on the intermediate layer 12b via a transition layer (not shown).
- the outermost layer 12a is not fixed to the intermediate layer 12b or the transition layer by a chemical bond, that is, the outermost layer 12a is not fixed to the surface of the substrate 11 by a chemical bond.
- the production of the coating portion 12 can be simplified.
- a process for example, introduction of a functional group
- the production of the coating portion 12 can be simplified.
- the first lubrication part as the intermediate layer 12b is arranged on the substrate 11 side of the second lubrication part as the outermost layer 12a
- the outermost layer 12a is arranged by the second lubrication part.
- the first lubricating part can maintain the lubricating effect when wet. Therefore, it is significant in that the production thereof can be simplified while securing the lubrication effect of the coating portion 12.
- the 1st lubricating part has the adhesiveness with respect to a base material higher than a 2nd lubricating part. More specifically, when comparing the lubricity at the time of wetting on the surface of the base material in each of the case where the first lubricating portion is disposed with respect to the surface of the base material and the case where the second lubricating portion is disposed, In the initial stage of wetting, it is preferable that the second lubrication part is higher and the first lubrication part is higher thereafter.
- the initial lubricity when wet is expressed by the second lubricating part, and the durability (durability) of the lubricating effect is expressed by the first lubricating part.
- the plurality of lubrication performances required as excellent coatings that is, initial lubricity and sustainability of the lubrication effect can be imparted to the substrate surface relatively easily.
- the target site When inserting into the target, it can be smoothly and reliably inserted to the target site.
- the outermost layer 12a is the second lubrication portion and the intermediate layer 12b is the first lubrication portion, high adhesion to the entire adhesion surface between the coating portion 12 and the substrate 11 is achieved. This is preferable because the lubricating effect can be continuously imparted to the surface of the substrate 11.
- the intermediate layer 12b as the first lubrication part may be bonded to the surface of the base material via a layer different from the intermediate layer 12b, but preferably, as shown in FIG.
- the layer 12 b is in a form arranged in contact with the surface of the substrate 11. In this case, a complicated process for forming another layer can be omitted, and the production of the instrument 10 can be simplified.
- the first lubrication part is preferably thicker than the second lubrication part.
- the lubrication material (first lubrication material) contained in the first lubrication part is cross-linked. It is assumed that the second lubricating part contains this first lubricating material. Then, the density of cross-linking formed by the first lubricating material is made lower in the second lubricating portion than in the first lubricating portion, or the first lubricating material has a cross-linking structure in the first lubricating portion, and In the two lubrication parts, the first lubrication material is not a crosslinked structure.
- the first lubricating portion contains a crosslinking agent and, if necessary, a radical initiator in addition to the first lubricating material.
- the second lubrication part does not contain a cross-linking agent, or the content of the cross-linking agent in the second lubrication part is less than that of the first lubrication part.
- the first lubricating part contains a first lubricating material
- the second lubricating part contains a second lubricating material different from the first lubricating material.
- the second lubricating material has a higher initial lubricating property when wet than the first lubricating material, whereby the wet initial lubricating performance of the second lubricating portion is exhibited.
- the first lubricating material has higher adhesion to the base material than the second lubricating material. By doing so, the first lubricating material exhibits the continuous performance of the lubricating effect in the first lubricating portion.
- the first lubricating portion and the second lubricating portion have better adhesion or initial property than the other. Lubricity can be expressed relatively easily.
- some lubricating materials have characteristics such as high adhesiveness to the surface of the base material and continuous lubrication performance, but low initial lubricity when wet.
- some of the initial lubricity when wet is high, but some have low adhesion to the substrate surface.
- the lubrication performance initial lubricity, durability of the lubrication effect
- the lubrication performance that is insufficient in one lubrication material is complemented by a plurality of lubrication materials, thereby maintaining the initial lubricity and the durability of the lubrication effect. It is possible to form a coating portion having both of these by a relatively simple process.
- the first lubrication part contains the first lubrication material as a main component, and further does the second lubrication material not be contained? Or even if it contains, it is preferable that it is a trace amount.
- the presence of the second lubrication material in the first lubrication part may reduce the adhesion of the first lubrication part (intermediate layer 12b) to the base material 11 and may reduce the durability of the lubrication effect. is there.
- the adhesion of the first lubricating material to the substrate is preferably expressed by being fixed to the substrate surface by a chemical bond such as a covalent bond.
- a material having a higher reactivity than at least the second lubricating material may be used as the first lubricating material.
- the method for fixing the first lubricating material is not particularly limited.
- a functional group that can be bonded to the other functional group is newly introduced to the first lubricating material or a portion (base material surface) to which the first lubricating material is adhered, and these functional groups are introduced.
- a solution containing the first lubricating material is applied to the substrate surface or the like, and then the substrate surface is functionalized by irradiation with radiation, plasma, ultraviolet rays or the like.
- the functional group of the lubricating material is bonded to the functional group. According to this immobilization method, chemical bonding between the first lubricating material and the substrate surface can be performed relatively easily.
- the second lubricating material may be fixed to the substrate surface or the first lubricating material, or may not be fixed. This is because even if the second lubricating material is not fixed to the substrate surface or the first lubricating material, the lubricating effect of the substrate surface is maintained by the first lubricating material. Further, it is not necessary to use a material having high adhesion to the base material as the second lubricating material, and the range of selection of the material is expanded.
- the second lubrication part is composed of the first lubrication material and other lubrication materials. May be included.
- the second lubrication portion does not include a lubrication material other than the second lubrication material or includes the first lubrication material
- the second lubrication material with respect to the first lubrication material The weight ratio is 1 or more.
- the density of the crosslink is higher in the first lubrication portion than in the second lubrication portion. More preferably, the first lubricious material is crosslinked and the second lubricious material is in a substantially uncrosslinked form.
- first lubricating material and the second lubricating material As the first lubricating material and the second lubricating material, a material different from the base material and having higher lubricity when wet than the base material can be used. It can be preferably used.
- hydrophilic polymer intermolecular crosslinks are formed by heat or light irradiation. This cross-linked hydrophilic polymer absorbs water and swells (wets) when contacted with an aqueous system such as a body fluid or physiological saline, and becomes a hydrogel having lubricity.
- the water uptake rate (water absorption rate) at the time of contact with an aqueous system differs between materials, and the difference in the water absorption rate is likely to cause superiority or inferiority in initial lubricity when wet.
- a hydrophilic polymer having a high water uptake rate upon contact with an aqueous system swells quickly and immediately exhibits lubricity, and conversely, a hydrophilic polymer having a low water uptake rate exhibits sufficient lubricity. It takes time to swell so that it can be expressed, and it takes time to develop good lubricity.
- a hydrophilic polymer (second lubricating material) having a higher water uptake rate is disposed on the outer surface of the coating portion.
- the first lubricating material is a poly-N-vinyl lactam such as polyvinyl pyrrolidone (PVP), a vinyl ethyl ether maleic anhydride copolymer system, or the like.
- PVP polyvinyl pyrrolidone
- a polymer, a polyacrylamide polymer mainly containing acrylamide or a derivative thereof, and the like are preferable, and PVP is more preferable. Since PVP has a pyrrolidone ring, when there is a functional group with relatively high reactivity on the substrate surface, it can be easily bonded to the functional group on the substrate surface by activation by irradiation with ultraviolet rays or the like. Can be done.
- the second lubricating material is preferably one or more of polyethylene oxide (PEO), hydroxyethyl cellulose, carboxymethyl cellulose, starch, dextran, gelatin and the like, more preferably PEO.
- the first lubricating material is a combination of PVP and the second lubricating material is a combination of PEO.
- the lubricity on the substrate surface is better when PEO is placed in the initial stage of wetting.
- the lubricity on the surface of the base material is improved.
- PVP has a characteristic that, when comparing the lubricity between the early stage of sliding (wet initial stage) and the latter stage of sliding (late wet stage), the later stage of sliding has higher lubricity. Therefore, as shown in FIG. 1, while adhering PVP to the substrate surface and arranging PEO excellent in initial lubricity on the outer surface of the coating part, while taking advantage of the excellent adhesiveness of PVP, The initial lubricity lacking in PVP is complemented by PEO.
- the persistence of the lubrication effect in PEO is inferior to that of PVP.
- PEO is less reactive than PVP.
- the base material surface and PEO are not fixed by chemical bonds. It is thought to be caused by Considering this point, it is conceivable that PEO cannot be fixed to PVP or has a low fixing ability even if it can be fixed.
- the configuration of FIG. 1 since the state where the PVP is adhered to the surface of the base material is maintained, even if the durability of the lubricating effect of the second lubricating portion including PEO decreases with time, the basic On the surface of the material, the lubricating effect is continuously expressed by PVP.
- PEO and PVP are general-purpose materials and are easily available.
- PEO and PVP are not biological materials, and are already used for medical purposes, and are excellent in biosafety and biocompatibility.
- This coating part is produced by a relatively simple method without using advanced techniques such as construction of a new material by using plural kinds of general-purpose materials excellent in biosafety and biocompatibility.
- it is preferable in that it has excellent lubrication performance when wet.
- PEO has less stickiness when touched by an operator and has better touch comfort than PVP. Therefore, by arranging PEO on the outer surface of the coating portion, it is possible to improve the handling of the device.
- the first lubricating material When a hydrophilic polymer is used as the first lubricating material, it is preferable that a cross-linking agent is contained in the first lubricating portion in order to improve the adhesion between the first lubricating material and the substrate surface.
- the second lubricating part may or may not contain a crosslinking agent.
- the crosslinking agent is just to determine suitably content of the crosslinking agent in a 1st lubrication part and a 2nd lubrication part, However, Since wettability will fall at the time of wet, it is unpreferable if an excessive amount of crosslinking agent contains.
- (1) Monomer which has several vinyl group in 1 molecule, (2) What has two or more glycidyl groups, (3) Isocyanate compounds, such as diisocyanate and triisocyanate, (4 ) Use at least one of radical initiators and the like.
- Examples of (1) include neopentyl glycol diacrylate (NPGDA), polyalkylene glycol diacrylate (methacrylate) [(poly) ethylene glycol diacrylate (methacrylate), (poly) propylene glycol diacrylate (methacrylate)]. And alkanediol diacrylate (methacrylate).
- Examples of (2) include polyalkylene glycol diglycidyl ether, neopentyl glycol diglycidyl ether, and epoxidized soybean oil.
- Examples of (3) include diisocyanates such as diphenylmethane diisocyanate, tolylene diisocyanate, and hexamethylene diisocyanate, and modified products such as adducts, allophanates, biurets, and isocyanurates.
- Examples of (4) include azo-based initiators such as azobisisobutyronitrile (AIBN), peroxide-based initiators, and the like, preferably an initiator that generates a plurality of radicals in one molecule. .
- AIBN azobisisobutyronitrile
- a combination of neopentyl glycol diacrylate (NPGDA) and a radical initiator (for example, AIBN) can be more preferably used.
- the medical device may be any device that is used in contact with a living tissue, for example, various catheters, guide wires, stents, and the like that are inserted into a body tube or a body cavity such as a blood vessel, a digestive tract, a ureter, or a trachea. Examples include, but are not limited to, endoscopes, contact lenses, artificial blood vessels, and artificial joints.
- the base material examples include polyether polyamide block copolymers such as Pebax (registered trademark), polyolefins such as polyethylene and polypropylene, polyether ether ketone, nylon, polyester, polyester elastomer, polyimide, polyurethane and other resins, metals, etc. Consists of. Preferably, it is a resin having a polar group such as a polyether polyamide block copolymer, nylon, polyester, polyester elastomer, polyimide, polyurethane, vinyl chloride or the like.
- polyolefins such as polyethylene and polypropylene, polyetheretherketone, metals, and the like can be used by performing an appropriate surface treatment for fixing the first lubricating material.
- the method for producing a medical device of the present invention uses a first solution containing a material different from a base material, and a first lubricating portion having higher lubricity when wet than the base material is provided on the surface of the base material. After the first step, and after the first step, the second solution containing a material different from the base material is used to form a portion different from the first lubrication portion and on the outer surface of the medical device. And a second step of forming a second lubrication part having higher initial lubricity when wet than the first lubrication part.
- the first lubrication portion as the intermediate layer 12 b is formed on the surface of the base material, and the second lubrication portion as the outermost layer 12 a is formed on the outer surface of the coating portion 12.
- the manufacturing procedure of the coating part 12 will be described with reference to FIG.
- First step In the first step, first, a first solution containing a first lubricating material as a material different from the base material is prepared.
- the solvent for preparing the first solution is not particularly limited as long as it can dissolve the first lubricating material.
- an alcohol such as isopropyl alcohol, distilled water, a mixed solution thereof, or the like is used.
- the first solution is brought into contact with the surface of the substrate 11.
- the form of contact is not particularly limited, and various methods such as coating, dipping, and spraying can be used.
- a surface treatment for enhancing the adhesion between the base material surface and the first lubricating material specifically, for example, corona discharge treatment or plasma.
- a process such as a process or an ultraviolet irradiation process may be performed.
- the first lubricating material is adhered to the surface of the substrate 11 by, for example, ultraviolet irradiation.
- the cross-linking agent and the radical initiator are contained in the first solution.
- the first solution contains the crosslinking agent and the radical initiator.
- the second step is subsequently performed.
- a first lubricating material or a second lubricating material preferably a second solution containing the second lubricating material is prepared.
- the solvent of the second solution may be different from the solvent used for the preparation of the first solution, but is preferably the same solvent.
- the second solution is brought into contact with the outer surface of the device 10, that is, the outer surface of the intermediate layer 12 b (first lubricating portion), and then the lubricating material in the second solution is irradiated by ultraviolet irradiation or the like. Perform immobilization.
- the lubricating material in the second solution may be crosslinked to the same extent as the first lubricating material in the first lubricating part by irradiation with ultraviolet rays or the like, but preferably, the first lubricating part It is in a state where the density of cross-linking is lower than that of the first lubricating material in the inside or is not cross-linked.
- a crosslinking agent and a radical initiator may or may not be contained.
- the second lubrication part as the outermost layer 12a is formed on the outer surface of the first lubrication part.
- the first lubricating material and the second lubricating material a combination of polyvinyl pyrrolidone (PVP) and polyethylene oxide (PEO) is preferable.
- PVP polyvinyl pyrrolidone
- PEO polyethylene oxide
- the concentration of the second lubricating material, particularly the PEO concentration in the second solution in the combination of PVP and PEO is 0.
- the content is preferably 1% by weight or more and 1.0% by weight or less. By setting the content to 0.1% by weight or more, the amount of the second lubricating material contained in the outermost layer 12a can be set to an amount sufficient to exert an excellent lubricating effect in the initial stage of wetness.
- the quantity of the 2nd lubricity material contained in the outermost layer 12a does not become excessive too much, and when the 2nd lubricity material is wet, it swells moderately. More preferably, it is 0.1 weight% or more and 0.82 weight% or less, More preferably, it is 0.2 weight% or more and 0.55 weight% or less. In particular, when the content is 0.25 wt% or more and 0.5 wt% or less, excellent lubricity can be imparted to the substrate surface.
- the thicknesses of the first lubrication part and the second lubrication part can be adjusted by the number of times of application of the first solution and the second solution and the concentration of the lubricating material in the solution. Therefore, in order to make the first lubricating part thicker than the second lubricating part, the concentration of the first lubricating material in the first solution is set to be higher than the concentration of the second lubricating material in the second solution.
- the number of times of application of the first solution may be higher than the number of times of application of the second solution.
- a coating solution for applying a coating to the substrate surface of a medical device was prepared.
- two types of PVP coating solution and PEO coating solution were prepared.
- As the PVP coating solution a mixed solvent in which isopropyl alcohol and distilled water are mixed at a ratio of 4: 1 (weight ratio) is used.
- Neo It was prepared by adding pentyl glycol diacrylate (NPGDA, ALDRICH) azobisisobutyronitrile (AIBN, Kishida Chemical) and stirring. Concentrations in the PVP coating solution were 0.82% by weight for PVP and 15% by weight for NPGDA with respect to the amount of PVP. A small amount of AIBN was added.
- the PEO coating solution was prepared by adding polyethylene oxide (PEO, manufactured by SIGMA-ALDRICH) to the same mixed solvent as the PVP coating solution and stirring.
- PEO polyethylene oxide
- the concentration of PEO in the PEO coating solution was 0.25% by weight.
- the PEO coating solution prepared in (1) above was further applied to the outer surface of the catheter by dip coating, and UV irradiation was performed for 30 seconds.
- the catheter (refer FIG. 1) by which the PVP layer was formed in the base-material surface and the PEO layer was formed in the further outer side of this PVP layer was obtained. Further, when the surface of the obtained catheter was touched with a hand, there was not much stickiness and the touch was good.
- a core material made of metal
- the specimen 24 is passed through the notch 23 of the rubber plate 22, which is filled with water. It was set in the water tank 21.
- the rubber plate 22 was fixed at a predetermined position in the water tank 21 by the support shaft.
- the specimen 24 was reciprocated in the vertical direction with the position of the rubber plate 22 fixed, and the frictional resistance between the rubber plate 22 and the specimen 24 at that time was measured by a frictional resistance measuring instrument (digital force gauge) 25.
- the measured value was defined as the frictional resistance value [gf].
- the measurement was performed with a stroke length of 10 cm and a stroke speed of 13 reciprocations / minute.
- a specimen coated with a single layer by applying one type of coating solution to the surface of the substrate by dip coating and irradiating with UV was prepared.
- one using 0.82 wt% PVP coating solution (Sample No. 7) 0.50 wt% PEO and 0.50 wt%
- Three specimens using a coating solution containing% PVP (Sample No. 8) were prepared.
- NPGDA was added to the coating solution used for the preparation of these specimen numbers 6 to 8.
- the NPGDA concentration was 37.5% by weight with respect to the PEO concentration for Sample No. 6, 15% by weight with respect to the PVP concentration for Sample No. 7, and the total concentration of PEO and PVP for Sample No. 8 37.5% by weight.
- AIBN was added little by little to each liquid.
- a summary of the composition of the eight specimens is shown in Table 1 below.
- FIG. 3 shows the results of a sliding test performed on specimen numbers 1 to 4 subjected to two-layer coating with PEO and PVP.
- the resistance values [gf] after 1 to 5 reciprocations are 11 to 16 for sample number 1 and 7.5 to 3 for sample number 2. It was 9.0 to 12 for 9.5, specimen number 3, and 15 to 19 for specimen number 4. Further, in any specimen, the change in the resistance value toward the increase side with the increase in the number of reciprocations is small, and the resistance value after 50 reciprocations is about 1.3 to 2.3 times the resistance value after 1 reciprocation. there were. From this, it was found that Sample Nos. 1 to 4 were able to continue to maintain the initial lubricity when wet, and the durability (durability) of the lubrication effect was good.
- each specimen was further subjected to an accelerated deterioration test by heating (60 ° C., 1 month), and then the above-described slip property test was performed.
- the resistance value after one reciprocation was almost the same as before the accelerated deterioration test, and the resistance value after 50 reciprocations was less than 1.5 times the resistance value after one reciprocation. . From this, it can be said that the product life of the samples 1 to 4 is good.
- the sample number 6 of the PEO alone and the sample number 8 of the mixed system were not so different from the sample number 2 in the resistance value after 1 round trip to 3 round trips.
- the resistance value increased with an increase in the number of reciprocations, and after 50 reciprocations, in Sample No. 2, the resistance value was about 1.3 times the resistance value after 1 reciprocation.
- the resistance value after one reciprocation was about 4 times. From this, PEO or mixed single layer coating (Sample Nos. 6 and 8) can provide initial lubricity to medical devices, but the initial lubricity is not as good as Sample No. 2 and is durable. It can be said that it is inferior to the sample number 2 in terms of sex.
- the resistance value [gf] at the initial stage of wetting was 18 after one reciprocation, which was larger than any of Sample Nos. 2, 6 and 8. In comparison with Sample No. 2, this value was more than twice that of Sample No. 2.
- the resistance value decreased as the number of reciprocations increased, and thereafter became substantially constant from 12 to 13. From this, it was found that in the single layer coating of PVP, the lubricity at the initial stage of wetness was not so good when wet, and it took time until the lubricity was developed. Note that the initial lubricity of PVP is low.
- the resistance value was smaller than the sample numbers 6 and 8, but larger than the sample number 2.
- the specimen No. 7 which is a single-layer coating of PVP, is inferior to the specimen Nos. 6 and 8 in which a layer containing PEO is formed on the outer surface, but the initial lubricity when wet is inferior. It was found that sex can be expressed. On the other hand, it was found that Sample No. 2 and Sample No. 2 were better in Sample No. 2 in both initial lubricity and durability (durability) of the lubrication effect.
- the two-layer coating of the PVP layer and the PEO layer was superior in initial lubricity and durability to the single-layer coating by at least one of PVP and PEO.
- the feel of the surface of the catheter obtained was less than that of PVP monolayer coating or a mixed monolayer coating of PVP and PEO, and the feel was good.
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Abstract
Description
コーティング部における第1潤滑部及び第2潤滑部の配置の形態について、まず一つは、第1潤滑部と第2潤滑部とによってコーティング部の外表面の少なくとも一部が形成される形態がある。このとき、第1潤滑部及び第2潤滑部を基材表面に設けることにより、第1潤滑部及び第2潤滑部からなる単層のコーティング部が形成される。
第1潤滑部及び第2潤滑部の基材に対する接着性について、第1潤滑部の方が、第2潤滑部よりも基材に対する接着性が高いのが好ましい。より具体的には、基材の表面に対して第1潤滑部を配置したものと第2潤滑部を配置したものとのそれぞれの場合の基材表面における湿潤時の潤滑性を比較したとき、湿潤初期においては、第2潤滑部の場合の方が高く、その後において第1潤滑部の場合の方が高い構成とするとよい。つまり、本コーティング部では、第2潤滑部により湿潤時における初期の潤滑性を発現させ、第1潤滑部により潤滑効果の持続性(耐久性)を発現させる。こうすることにより、優れたコーティングとして求められる複数の潤滑性能、すなわち初期潤滑性及び潤滑効果の持続性を、基材表面に対し比較的容易に付与することができ、ひいては、本器具を生体内に挿入する際に、目的部位まで滑らかにかつ確実に挿入することができる。特に、図1のように、最外層12aが第2潤滑部であり中間層12bが第1潤滑部である構成では、コーティング部12と基材11との接着面全体に対して高い接着性を発揮させることができ、基材11の表面に対して潤滑効果を持続して付与することができ好ましい。
第1の潤滑性材料及び第2の潤滑性材料としては、基材とは異なる材料であって、基材よりも湿潤時における潤滑性が高い材料を用いることができ、そのうち、親水性ポリマーを好ましく用いることができる。親水性ポリマーでは、熱や光照射等により分子間架橋が形成される。この架橋された親水性ポリマーは、体液や生理食塩水等の水系に接触されることにより吸水して膨潤し(湿潤し)、潤滑性を有するヒドロゲルとなる。このようなヒドロゲルでは、水系との接触時における水の取り込み速度(吸水速度)が材料間で相違し、その吸水速度の相違により、湿潤時における初期の潤滑性に優劣が生じやすいと考えられる。すなわち、水系との接触時において、水の取り込み速度が速い親水性ポリマーは、速やかに膨潤して潤滑性を直ちに発現し、逆に水の取り込み速度が遅い親水性ポリマーは、十分な潤滑性を発現可能に膨潤するまでに時間がかかり、良好な潤滑性を発現するまでに時間を要する。これに鑑み、本コーティング部では、水の取り込み速度がより速い親水性ポリマー(第2の潤滑性材料)をコーティング部の外表面に配置する。これにより、水系との接触時において、コーティング部の外表面が速やかに膨潤され、その結果、本器具の外表面において速やかに潤滑性が発現される。
医療用器具としては、生体組織と接触して用いる器具であればよく、例えば、血管や消化管、尿管、気管等といった生体内の管や体腔に挿入される各種カテーテル、ガイドワイヤー、ステント、内視鏡、コンタクトレンズ、人工血管、人工関節等が挙げられるが、これらに限定するものではない。
本発明の医療用器具の製造方法は、基材とは異なる材料を含有する第1の溶液を用いて、該基材よりも湿潤時における潤滑性が高い第1潤滑部を前記基材の表面に形成する第1工程と、第1工程の後、基材とは異なる材料を含有する第2の溶液を用いて、第1潤滑部とは異なる部分であって同医療用器具の外表面の少なくとも一部において、第1潤滑部よりも湿潤時における初期の潤滑性が高い第2潤滑部を形成する第2工程とを備える。以下、図1に示すコーティング部12、詳しくは、基材表面に中間層12bとしての第1潤滑部が形成され、かつコーティング部12の外表面に最外層12aとしての第2潤滑部が形成されるコーティング部12の作製手順について、図1を適宜用いて説明する。
第1工程では、まず、基材とは異なる材料として第1の潤滑性材料を含む第1の溶液を準備する。第1の溶液を調製するための溶媒は、第1の潤滑性材料を溶解可能であればよく、例えばイソプロピルアルコールなどのアルコール系や蒸留水、それらの混合溶液などを使用する。続いて、第1の溶液を基材11の表面に接触させる。接触の形態は特に限定せず、例えば塗布、浸漬、噴霧等の種々の方法を使用可能である。なお、第1の溶液と基材11の表面との接触前に、基材表面と第1の潤滑性材料との接着性を高めるための表面処理、具体的には、例えばコロナ放電処理やプラズマ処理、紫外線照射処理等といった処理を実施してもよい。
第1工程の終了後、続いて第2工程を実施する。第2工程では、まず、基材とは異なる材料として、第1の潤滑性材料又は第2の潤滑性材料、好ましくは上記の第2の潤滑性材料を含む第2の溶液を準備する。第2の溶液の溶媒は、第1の溶液の調製に用いた溶媒と異なっていてもよいが、同じ溶媒とするとよい。続いて、第2の溶液を、本器具10の外表面、すなわち中間層12b(第1潤滑部)の外表面に接触させ、その後、紫外線照射等により、第2の溶液中における潤滑性材料の固定化を行う。このとき、第2の溶液中における潤滑性材料が、紫外線等の照射によって、第1潤滑部中における第1の潤滑性材料と同程度に架橋されてもよいが、好ましくは、第1潤滑部中における第1の潤滑性材料よりも架橋の密度が低い状態であるか、又は架橋されていない状態である。なお、第2の溶液中には、架橋剤及びラジカル開始剤が含有されていてもよいし、含有されていなくてもよい。以上により、第1潤滑部の外表面に最外層12aとしての第2潤滑部が形成される。
医療用器具の基材表面にコーティングを施すためのコーティング溶液を調製した。ここでは、PVPコーティング溶液及びPEOコーティング溶液の2種類を準備した。PVPコーティング溶液は、イソプロピルアルコールと蒸留水とを4:1(重量比)で混合した混合溶媒を用い、これにポリビニルピロリドン(PVP、グレードK-90、分子量36万、和光純薬製)、ネオペンチルグリコールジアクリレート(NPGDA、ALDRICH社製)アゾビスイソブチロニトリル(AIBN、キシダ化学)を加えて撹拌することにより調製した。PVPコーティング溶液中における濃度は、PVPが0.82重量%、NPGDAがPVP量に対して15重量%とした。なお、AIBNは少量を加えた。
医療用器具として、Pebax(登録商標)によって基材が形成されたカテーテルを用い、その基材の表面に対し、上記の2種類のコーティング溶液(PVPコーティング溶液、PEOコーティング溶液)を用いてコーティングを施した。コーティング手順として、まず、基材表面にコロナ放電を行うことにより基材の表面処理を行った。続いて、上記(1)で調製したPVPコーティング溶液をディップコーティング法により基材表面に塗布し、その後、UV照射を90秒行った。ここでは、PVPコーティング溶液によるディップコーティング及びその後のUV照射の一連の処理を2回行った。その後、更に、上記(1)で調製したPEOコーティング溶液をディップコーティング法によりカテーテルの外表面に塗布し、UV照射を30秒行った。これにより、基材表面にPVP層が形成され、このPVP層の更に外側にPEO層が形成されたカテーテル(図1参照)が得られた。また、得られたカテーテルの表面を手で触ったところ、ベタつき感がさほどなく、手触りが良好であった。
(3-1)滑り性試験
コーティング後のカテーテルについて、湿潤時における潤滑性を評価するための滑り性試験として、図2に示す装置20を用いて摩擦抵抗値を測定した。装置20としては、図2に示すように、水槽21の中空部にゴム板22を配置したものを用いた。なお、ゴム板22は、支持軸(図示略)によって所定位置に固定した状態に支持可能になっている。ゴム板22は天然ゴム製、厚さ3mmのものを使用した。このゴム板22には、針(18G)を垂直に穿刺することでゴム板22の表裏面を貫通する切り込み23が設けられている。摩擦抵抗値の測定については、まず、準備した検体24(カテーテル)の内部に芯材(金属製)を挿入し、その検体24をゴム板22の切り込み23に通し、これを水が充填された水槽21中にセットした。このとき、ゴム板22を支持軸によって水槽21中の所定位置に固定した。その後、ゴム板22の位置を固定したまま検体24を上下方向に往復動させ、そのときのゴム板22と検体24との摩擦抵抗を摩擦抵抗測定器(デジタルフォースゲージ)25により測定した。その測定値を摩擦抵抗値[gf]とした。このとき、ストローク長を10cm、ストローク速度を13往復/分として測定を行った。
滑り性試験の検体としては、PEOコーティング溶液におけるPEO濃度が異なる4つの検体(PEO濃度:0.1重量%,0.25重量%,0.5重量%,0.82重量%)を上記(2)と同様のコーティング方法により準備した(それぞれ検体番号1~4)。また、PEO濃度に対してNPGDAを37.5重量%含む上記(1)のPEOコーティング溶液を調製し、この調製液を用いて上記(2)と同様の方法によりコーティング処理した検体を準備した(検体番号5)。なお、検体番号1~5については、基材表面にPVP層が形成され、更にその外側にPEO層が形成された2層コーティングである。
各検体について上記(3-1)の滑り性試験を行った。滑り性試験は、エチレンオキサイドガス滅菌(EOG滅菌)の実施後に行った。なお、滑り性試験に際し、検体を往復動させるときのストローク長及びストローク速度については各検体間で同じにした。
PEOとPVPとによる2層コーティングを施した検体番号1~4について滑り試験を行った結果を図3に示す。
2層コーティングの検体番号1~4のうち、湿潤時における表面潤滑性が特に良好であった検体番号2について、単層コーティングの検体番号6(PEO単独)、検体番号7(PVP単独)、検体番号8(PEOとPVPとの混合系)との比較を行った。その結果を図4に示す。なお、図4中、実線は検体番号2、点線は検体番号6、一点鎖線は検体番号7、二点鎖線は検体番号8における抵抗値の推移を示す。また、図4は、加熱滅菌後であって加速劣化試験の実施前の試験結果である。
Claims (13)
- 基材の表面にコーティング部が形成された医療用器具であって、
前記コーティング部は、
前記基材とは異なる材料により形成され、該基材よりも湿潤時における潤滑性が高い第1潤滑部と、
前記基材とは異なる材料により形成され、前記第1潤滑部とは異なる部分であって同コーティング部の外表面の少なくとも一部に設けられ、かつ前記第1潤滑部よりも湿潤時における初期の潤滑性が高い第2潤滑部と、
を備えることを特徴とする医療用器具。 - 前記第1潤滑部は、前記基材よりも湿潤時における潤滑性が高い潤滑性材料として第1の潤滑性材料を含有し、
前記第2潤滑部は、前記第1の潤滑性材料とは異なる第2の潤滑性材料を含有する請求項1に記載の医療用器具。 - 前記第1の潤滑性材料及び前記第2の潤滑性材料が親水性ポリマーである請求項2に記載の医療用器具。
- 前記第1の潤滑性材料がポリビニルピロリドンであり、前記第2の潤滑性材料がポリエチレンオキシドである請求項3に記載の医療用器具。
- 前記第1の潤滑性材料は前記基材に対して化学結合による固定がなされ、前記第2の潤滑性材料は前記基材に対して化学結合による固定がなされていない請求項2乃至4のいずれか一項に記載の医療用器具。
- 前記第1潤滑部は、前記第2潤滑部よりも前記基材に対する接着性が高い請求項1乃至5のいずれか一項に記載の医療用器具。
- 前記基材の表面に対し、前記第1潤滑部を配置した場合と前記第2潤滑部を配置した場合との湿潤時における潤滑性を比較したとき、湿潤初期において前記第2潤滑部の場合の方が潤滑性が高く、その後において前記第1潤滑部の場合の方が潤滑性が高い請求項1乃至6のいずれか一項に記載の医療用器具。
- 前記コーティング部は、該コーティング部の外表面を構成する最外層と、同最外層と前記基材の表面との間に介在する中間層とを備え、
前記第2潤滑部により前記最外層が形成され、前記第1潤滑部により前記中間層が形成されている請求項1乃至7のいずれか一項に記載の医療用器具。 - 前記最外層は、前記中間層に接した状態で同中間層に積層されているか、又は前記最外層に含有される材料と前記中間層に含有される材料とを含む遷移層を介して前記中間層に積層されている請求項8に記載の医療用器具。
- 医療用器具の製造方法であって、
基材とは異なる材料を含有する第1の溶液を用いて、該基材よりも湿潤時における潤滑性が高い第1潤滑部を前記基材の表面に形成する第1工程と、
前記第1工程の後、前記基材とは異なる材料を含有する第2の溶液を用いて、前記第1潤滑部とは異なる部分であって同医療用器具の外表面の少なくとも一部に、前記第1潤滑部よりも湿潤時における初期の潤滑性が高い第2潤滑部を形成する第2工程と、を備えることを特徴とする医療用器具の製造方法。 - 前記第1の溶液に、前記基材よりも湿潤時における潤滑性が高い潤滑性材料として第1の潤滑性材料を含有し、
前記第2の溶液に、前記第1の潤滑性材料とは異なる第2の潤滑性材料を含有する請求項10に記載の医療用器具の製造方法。 - 前記第1の潤滑性材料がポリビニルピロリドンであり、前記第2の潤滑性材料がポリエチレンオキシドである請求項11に記載の医療用器具の製造方法。
- 前記第2の溶液中における前記第2の潤滑性材料の濃度が0.2質量%以上0.55質量%以下である請求項11又は12に記載の医療用器具の製造方法。
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Patent Citations (3)
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JP2006519039A (ja) * | 2003-02-26 | 2006-08-24 | コロプラスト アクティーゼルスカブ | 過酸化水素を含むコーティングを有する医療器具の製造用アセンブリー |
JP2007505704A (ja) * | 2003-09-16 | 2007-03-15 | アンジオテック バイオコーティングズ コーポレイション | 複数層ポリマーコーティングを有する薬物添加ステント |
JP2009526563A (ja) * | 2006-02-13 | 2009-07-23 | マーリン エムディー ピーティーイー リミテッド | 膜を有する血管内器具 |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
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US10799621B2 (en) | 2012-12-20 | 2020-10-13 | Becton, Dickinson And Company | Device and method for inhibiting movement of a medical device in a patient |
EP2934632B1 (en) * | 2012-12-20 | 2022-05-25 | Becton, Dickinson and Company | Device and method for inhibiting movement of a medical device in a patient |
JP2018008031A (ja) * | 2016-05-25 | 2018-01-18 | テレフレックス、ライフ、サイエンシーズ、アンリミテッド、カンパニーTeleflex Life Sciences Unlimited Company | すぐに使える(ready to use)カテーテル・アセンブリの製造方法およびすぐに使えるカテーテル・アセンブリ |
WO2022130631A1 (ja) * | 2020-12-18 | 2022-06-23 | 朝日インテック株式会社 | 長尺医療器具 |
JP7561876B2 (ja) | 2020-12-18 | 2024-10-04 | 朝日インテック株式会社 | 長尺医療器具 |
Also Published As
Publication number | Publication date |
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JPWO2011129162A1 (ja) | 2013-07-11 |
JP5805627B2 (ja) | 2015-11-04 |
CN102791317B (zh) | 2015-04-15 |
CN102791317A (zh) | 2012-11-21 |
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