WO2014050766A1 - Medical tool and medical system - Google Patents

Medical tool and medical system Download PDF

Info

Publication number
WO2014050766A1
WO2014050766A1 PCT/JP2013/075571 JP2013075571W WO2014050766A1 WO 2014050766 A1 WO2014050766 A1 WO 2014050766A1 JP 2013075571 W JP2013075571 W JP 2013075571W WO 2014050766 A1 WO2014050766 A1 WO 2014050766A1
Authority
WO
WIPO (PCT)
Prior art keywords
packaging material
lumen
long member
opening
medical device
Prior art date
Application number
PCT/JP2013/075571
Other languages
French (fr)
Japanese (ja)
Inventor
克彦 清水
周平 三枝
Original Assignee
テルモ株式会社
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by テルモ株式会社 filed Critical テルモ株式会社
Publication of WO2014050766A1 publication Critical patent/WO2014050766A1/en

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M25/00Catheters; Hollow probes
    • A61M25/0067Catheters; Hollow probes characterised by the distal end, e.g. tips
    • A61M25/0082Catheter tip comprising a tool
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M25/00Catheters; Hollow probes
    • A61M25/0067Catheters; Hollow probes characterised by the distal end, e.g. tips
    • A61M25/0068Static characteristics of the catheter tip, e.g. shape, atraumatic tip, curved tip or tip structure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M31/00Devices for introducing or retaining media, e.g. remedies, in cavities of the body

Definitions

  • the present invention relates to a medical instrument and a medical system.
  • a catheter is provided with a lumen through which a drug can flow and a discharge hole for discharging the drug from the lumen (see, for example, Patent Document 1).
  • the medicine filled in the lumen adheres to the inner wall of the lumen, there is a problem that the whole amount of the filled medicine cannot be discharged into the living body.
  • the drug is a powder
  • the amount of adhesion to the inner wall of the lumen tends to increase, and the dead volume of the drug that cannot be discharged from the catheter tends to increase.
  • the gas or physiological saline is mixed with the drug while the drug moves through the lumen, so the drug has a reduced concentration.
  • the drug has a reduced concentration.
  • the present invention has been invented in order to solve the above-mentioned problems, and prevents a biological introduction material from adhering to a long member such as a catheter when a biological introduction material such as a drug is introduced into the living body.
  • An object of the present invention is to provide a medical instrument and a medical system that can introduce a living body introduction material into a living body without waste.
  • a medical device comprising: an opening for opening the packaging material.
  • the opening portion is provided in the elongated member, and leaks the living body introduction material to at least a part of the packaging material as the packaging material passes through the lumen. It has a cutting part which forms a cut,
  • the medical instrument given in the above (1) characterized by things.
  • the opening part is provided in the long member, and has an opening part that opens the valve body by contacting a valve body that is provided in the packaging material and seals the packaging material.
  • the opening portion is connected to an opening provided in the packaging material and has a string for opening the opening in a closed state.
  • the long member further includes a holding portion for holding the opened packaging material on the long member, according to any one of the above (1) to (4), Medical instruments.
  • the holding portion includes a hook portion that holds the packaging material when the opened packaging material passes through the lumen.
  • the packaging material includes a first diameter portion having a first diameter, and a second diameter portion that is formed on the tip side of the first diameter portion and has a smaller diameter than the first diameter portion. And an intermediate portion connected to the first diameter portion and the second diameter portion, and the holding portion is held by the intermediate portion abutting when the packaging material passes through the lumen.
  • the medical device according to any one of the above (5) to (7), wherein the medical device has an abutting portion.
  • the guide member may further include a guide member that is disposed in the lumen of the elongate member and guides the movement of the packaging material so that the packaging material moves along the axial direction in the lumen.
  • a medical system comprising:
  • the living body introduction material is moved in the lumen of the long member while the living body introduction material such as a medicine is enclosed in the packaging material, and the living body introduction material enters the living body.
  • the packaging material can be opened before being introduced. For this reason, it is possible to prevent the living body introduction material from adhering to the inner wall of the lumen, and to introduce the living body introduction material into the living body without waste.
  • the packaging material can be opened by a simple operation of moving the packaging material in the lumen of the long member, the usability of the medical instrument can be improved. .
  • the packaging material can be opened without forming a cut in the packaging material, it is possible to prevent the scattering of the packaging material before it occurs. It is possible to more suitably prevent the packaging material from being introduced into the body.
  • the packaging material can be opened without forming a cut in the packaging material, it is possible to prevent the scattering of the packaging material before it occurs. It is possible to more suitably prevent the packaging material from being introduced into the body.
  • the packaging material can be prevented from being introduced into the living body.
  • a packaging material can be hold
  • the packaging material can be held in the hook portion provided in the holding portion, the packaging material can be suitably prevented from being introduced into the living body.
  • the packaging material can be held by the long member by abutting the intermediate portion of the packaging material against the abutting portion provided in the holding portion. It can prevent suitably being introduced into the body.
  • the packaging material can be prevented from being introduced into the living body by the string attached to the packaging material. Further, the packaging material can be easily collected using the string.
  • the packaging material can be moved along the axial direction of the long member, the opened packaging material can be prevented from scattering, and the packaging material. Can be suitably prevented from being introduced into the living body.
  • the packaging material can be easily opened, the living body introduction material can be reliably removed from the packaging material.
  • FIG. 2 is a diagram for explaining the configuration of the medical device according to the first embodiment.
  • FIG. 2A is a partial cross-sectional view of the distal end side of the long member provided in the medical device
  • FIG. ) Is a plan view of a holding part provided in the medical instrument
  • FIG. 2C is a plan view of a cutting part provided in the medical instrument.
  • FIG. 3 (A) is a top view of a packaging material
  • FIG.3 (B) is sectional drawing of a packaging material.
  • FIG. 5 is a diagram for explaining the operation of the medical device according to the first embodiment
  • FIG. 5A is a partial cross-sectional view showing a state before the packaging material passes through the cutting portion of the medical device.
  • FIG. 5 (B) is a partial cross-sectional view showing a state in which the packaging material is held in the holding part of the medical device.
  • FIG. 6 is a view for explaining Modification Example 1 of the medical device according to the first embodiment, and FIG. 6 (A) is a partial cross-sectional view showing a state before a cut is formed in the packaging material.
  • FIG. 5 is a diagram for explaining the operation of the medical device according to the first embodiment
  • FIG. 5A is a partial cross-sectional view showing a state before the packaging material passes through the cutting portion of the medical device.
  • FIG. 5 (B) is a partial cross-sectional view showing a state in which the packaging material is held in the holding part of the medical device.
  • FIG. 6 is a view for explaining Modification Example 1 of
  • FIG. 6B is a partial cross-sectional view showing a state in which the packaging material is held in the hook portion provided in the long member.
  • 7 is a view for explaining modified examples 2 to 4 of the medical instrument according to the first embodiment, and FIG. 7A is a partial sectional view for explaining the medical instrument according to the modified example 2.
  • FIG. 7B is a partial cross-sectional view for explaining the medical instrument according to the third modification, and
  • FIG. 7C is a partial cross-sectional view for explaining the medical instrument according to the fourth modification. It is.
  • FIG. 8 is a view for explaining a modified example 5 of the medical instrument according to the first embodiment, and FIG. 8A is a part showing a state before the packaging material passes through the cutting part of the medical instrument.
  • FIG. 8 is a view for explaining a modified example 5 of the medical instrument according to the first embodiment, and FIG. 8A is a part showing a state before the packaging material passes through the cutting part of the medical instrument.
  • FIG. 8B is a partial cross-sectional view showing a state in which the packaging material is held in the holding part of the medical device.
  • 9A and 9B are partial cross-sectional views for explaining a medical device according to the second embodiment of the present invention.
  • FIG. 10 is a view for explaining a modified example of the medical instrument according to the second embodiment, and FIG. 10 (A) is a partial sectional view showing a state before the packaging material is opened, FIG. B) is a partial cross-sectional view showing a state after the packaging material is opened.
  • FIG. 1 to 4 are diagrams for explaining each configuration of the medical instrument and the medical system according to the first embodiment of the present invention
  • FIG. 5 is an explanation of the operation of the medical instrument and the medical system according to the first embodiment.
  • FIG. In the description of the drawings, the same elements are denoted by the same reference numerals, and redundant description is omitted.
  • the dimensional ratios in the drawings are exaggerated for convenience of explanation, and may be different from the actual ratios.
  • the long member 20 includes a lumen 21 extending from the distal end side to the proximal end side, and the long member 20 is interposed therebetween.
  • the packaging material 50 enclosing the living body introduction material 60 introduced into the living body has an opening portion 30 that opens the packaging material 50 while passing through the lumen 21.
  • the unsealing part 30 is provided in the long member 20, and a cut for leaking the biological introduction material 60 to at least a part of the packaging material 50 as the packaging material 50 passes through the lumen 21. It is comprised by the cutting part to form (refer FIG. 5 (A), (B)).
  • an axial direction means the direction where the elongate member 20 was extended
  • the medical instrument 10 can be used together with a fluid supply unit 60 for supplying a fluid for moving the packaging material 50 in the lumen 21 to the elongate member 20, and the medical system includes the medical instrument 10 and the fluid supply unit 60. 100 can be built.
  • Examples of the biological introduction material 70 introduced into the living body using the medical instrument 10 include, but are not limited to, drugs, and are intended for introduction into the living body such as various cells, blood, and metabolites. It can be appropriately selected from the products to be performed.
  • the packaging material 50 is introduced into the lumen 21 of the long member 20 in a state where the living body introduction material 70 is enclosed. As will be described later, at the time of passing through the lumen 21, at least a part is cut by the long member 20, thereby leaking the biological introduction material 70 enclosed therein.
  • the long member 20 can be constituted by a catheter known in the medical field.
  • An opening 22 communicating with the lumen 21 is formed at the distal end of the long member 20, and the living body introduction material 70 can be discharged from the opening 22.
  • a connector 23 to which a tube 61 for connecting the fluid supply unit 60 and the long member 20 can be connected is provided at the base end of the long member 20.
  • a mechanical connector capable of connecting the tube 61 by fitting or screwing can be used.
  • the material constituting the long member 20 is not particularly limited.
  • the fluid supply unit 60 one capable of pumping various fluids into the lumen 21 of the long member 20 can be used.
  • a known fluid pump or the like can be used.
  • gas and liquid can be used as the fluid supplied from the fluid supply part 60, for example, air, physiological saline, etc. can be used.
  • a known resin tube having flexibility can be used for the tube 61.
  • a syringe pump known in the medical field can be used. When using a syringe pump, the connector 23 of the long member 20 and the syringe pump may be directly connected without using the tube 61.
  • the cutting portion 30 provided in the long member 20 includes, for example, a blade 31 configured to easily cut the packaging material 50 and the blade 31 attached thereto.
  • the frame member 32 may be provided.
  • the blade 31 can be made of metal or the like. Further, the blade surface can be provided by sharpening the tip of the blade 31. For example, as shown in the figure, four blades 31 can be installed at equal positions in the circumferential direction.
  • the frame member 32 is provided to fix the blade 31 to the long member 20.
  • the frame member 32 can be fixed to the long member 20 by adhesion or fusion, for example.
  • the cutting part 30 is disposed in the lumen 21 of the long member 20.
  • the long member 20 can be provided with a holding portion 40 for holding the packaging material 50 in which the cut is formed on the long member 20.
  • the holding part 40 can be constituted by, for example, a holding mesh material 41 arranged on the distal end side with respect to the cutting part 30. As shown in FIGS. 5A and 5B, after the packaging material 50 passes through the lumen 21 and a cut is formed in the packaging material 50 by the cutting portion 30, the packaging material 50 is disposed on the tip side from the cutting portion 30. The packaging material 50 is held in the holding mesh material 41.
  • the holding mesh material 41 has a mesh with a roughness that can hold the packaging material 50, and the holding mesh material 41 is provided in the same manner as the cutting portion 30.
  • a frame member 42 for fixing to the long member 20 is provided.
  • the frame member 42 can be fixed to the long member 20 by adhesion or fusion, for example.
  • the material constituting the holding mesh material 41 is not particularly limited, and a metal or a hard resin material can be used. Further, the holding mesh material is not limited to a configuration having a grid-like mesh, and for example, even if it has a configuration in which a plurality of round holes are formed as in the mesh material 43 shown in FIG. Good. In the case of using the holding mesh materials 41 and 43 having either the lattice shape or the round hole shape, the function of holding the packaging material 50 can be provided.
  • the packaging material 50 has a bag structure in which the biological introduction material 70 can be enclosed.
  • the packaging material 50 should just be provided so that the inside of the lumen
  • the material constituting the packaging material 50 include polyolefins such as polyethylene, polypropylene, and ethylene-propylene copolymers, polyesters such as polyethylene terephthalate, polyvinyl chloride, ethylene-vinyl acetate copolymers, and crosslinked ethylene-vinyl acetate.
  • resin materials such as copolymers, thermoplastic resins such as polyurethane, polyamide elastomer, silicone rubber, and latex rubber.
  • the packaging material 50 can be provided with an opening assisting portion 51 configured to be easier to open than other parts of the packaging material 50 in a part of the packaging material 50.
  • the opening assisting part 51 can be formed, for example, by using a material in which a cut is more easily formed than other parts, by making the wall thickness thinner than other parts, or by making a small cut in advance. .
  • a plurality of opening assisting portions 51 are formed by previously making small cuts at a plurality of locations of the packaging material 50.
  • the living body introduction material 70 sealed in the packaging material 50 is not particularly limited as long as it is intended for introduction into the living body, but in this embodiment, a thrombolytic drug (alteplase, monteplase, etc.) is used. It is used as the living body introduction material 70.
  • examples of drugs used as the biointroducing material 70 include anticoagulants (heparin, enoxaparin, etc.), antineoplastic drugs (sorafenib, cisplatin, etc.), drugs that act on inflammation and allergy (mometasone furanate, dexamethasone) Pesyl esters, etc.), drugs that act on the respiratory system (salmeterol, tiotropium), drugs that act on the nervous system (olanzapine, donepezil hydrochloride, etc.) can also be used, and the state when encapsulated There is also no particular limitation, and it may be granular, powdery, gelled, liquid or the like. There is no particular limitation as long as the part into which the living body introduction material 70 is introduced is in the living body, and an otoscope, a respiratory region, various body tubes and blood vessels can be selected as the application target.
  • the elongate member 20 provided in the medical device 10 enables the drug to be delivered to the inside of the nasal cavity, the drug can be directly delivered to the brain via the nervous system existing in the vicinity of the nasal cavity. Compared with the case where a drug is administered transvascularly to the brain as in the prior art, the efficacy of the drug can be made to act more effectively.
  • a packaging material 50 in which a living body introduction material 70 is sealed is filled into the lumen 21 of the long member 20.
  • the fluid supply unit 60 is operated to feed a fluid for moving the packaging material 50 into the lumen 21.
  • the packaging material 50 moves in the lumen 21 by the fluid and comes into contact with the cutting part 30 disposed in the lumen 21.
  • a cut is formed in the packaging material 50 with the contact with the cutting part 30.
  • the packaging material 50 When the fluid continues to be fed, the packaging material 50 is pressed against the holding portion 40 disposed on the front end side with respect to the cutting portion 30. At this time, the living body introduction material 70 enclosed in the packaging material 50 leaks from the packaging material 50 and is discharged from the opening 22 of the long member 20. Since the packaging material 50 is held by the holding unit 40, the packaging material 50 is prevented from being discharged from the opening 22 of the long member 20 into the living body.
  • the living body introduction material 70 is moved in the lumen 21 of the elongate member 20 while the living body introduction material 70 such as a medicine is enclosed in the packaging material 50, and
  • the packaging material 50 can be opened before the introduction material 60 is introduced into the living body.
  • the living body introduction material 70 can be prevented from adhering to the inner wall of the lumen 21 and the living body introduction material 70 can be introduced into the living body without waste.
  • the packaging material 50 is moved by a simple operation of moving the packaging material 50 in the lumen 21 of the long member 20. Therefore, the usability of the medical device 10 can be improved.
  • the packaging material 50 is replaced with the long member 20. Therefore, the packaging material 50 can be prevented from being introduced into the living body.
  • the packaging material 50 can be held by the holding mesh material 41, and thus the packaging material 50 is brought into the living body. It can prevent suitably being introduced.
  • the packaging material 50 is configured to have an opening assisting part 51 configured to be easier to form a cut in a part of the packaging material 50 than other parts of the packaging material 50,
  • the living body introduction material 60 can be reliably removed from the packaging material 50.
  • the medical system 100 is comprised by the medical instrument 10 and the fluid supply part 60, the medical system for moving the packaging material 50 smoothly in the lumen
  • FIGS. 6A and 6B show a medical instrument 110 according to the first modification.
  • the mechanism for holding the packaging material 150 in which the cuts are formed is different from the embodiment described above.
  • the holding portion is configured to have a hooking portion 127 on which the packaging material 150 is hooked and held when the packaging material 150 in which the cut is formed passes through the lumen 121 of the long member 120. Yes.
  • the long member 120 is configured to include a small-diameter portion 123 disposed on the distal end side and a large-diameter portion 125 disposed closer to the proximal end side than the small-diameter portion 123.
  • An end portion on the proximal end side of the small diameter portion 123 is disposed in the large diameter portion 125, and this end portion is configured as a hook portion 127. Further, this end portion also has a function as a cutting portion for forming a cut in the packaging material 150.
  • the packaging material 150 in which a break is formed can be held in the hook portion 127 included in the holding unit, and thus the packaging material 150 is introduced into the living body. This can be suitably prevented.
  • FIG. 7A shows a medical instrument 210 according to the second modification.
  • the mechanism for holding the packaging material 250 with cuts is different from the above-described embodiment.
  • the packaging material 250 includes a first diameter portion 251 having a first diameter, and a first diameter portion 251 formed on the distal end side of the first diameter portion 251 and having a smaller diameter than the first diameter portion 251.
  • the second diameter portion 252 and the intermediate portion 253 connected to the first diameter portion 251 and the second diameter portion 252 are configured.
  • the holding part is configured to have an abutting part 225 that abuts and holds the intermediate part 253 of the packaging material 250 when the packaging material 250 passes through the lumen 221 of the long member 220.
  • the cutting part 30 for forming a cut in the packaging material 250 is arranged in the small diameter part 223 formed in the long member 220.
  • the tip of the packaging material 250 comes into contact with the cutting part 30.
  • a cut is formed in the packaging material 250 and the in-vivo introduction material 60 is leaked.
  • the intermediate portion 253 of the packaging material 250 is abutted against the abutting portion 225 of the long member 220, whereby the packaging material 250 is held with respect to the long member 220.
  • the long member 220 holds the packaging material 250 by abutting the intermediate portion 253 of the packaging material 250 against the abutting portion 225 provided in the holding portion. Therefore, the packaging material 250 can be suitably prevented from being introduced into the living body.
  • FIG. 7B shows a medical instrument 310 according to Modification 3.
  • a predetermined string 333 is attached to the packaging material 310.
  • the string 333 has a length derived from the proximal end side of the long member 320 when the packaging material 350 is introduced into the lumen 321 of the long member 320.
  • the medical instrument 310 according to this modification by holding the string 333 outside the lumen 321 of the long member 320, the packaging material 350 in which the cut is formed is prevented from being introduced into the living body. be able to. Further, it is possible to easily collect the packaging material 350 using the string 333.
  • FIG. 7C shows a medical instrument 410 according to the fourth modification.
  • a guide member 460 for guiding the movement of the packaging material 450 within the lumen 421 of the long member 420 is provided.
  • the guide member 460 is disposed in the lumen 421 of the long member 420.
  • the guide member 460 guides the movement of the packaging material 450 so that the packaging material 450 moves along the axial direction in the lumen 421.
  • the guide member 460 is configured by a rail-structured member installed in the lumen 421 of the long member 420.
  • the packaging material 450 is provided with a string 433 for hooking the packaging material 450 to the guide member 460.
  • the cutting part 30 is arrange
  • the packaging material 450 can be moved along the axial direction of the long member 420, so that the packaging material 450 is brought into contact with the cutting portion 30. Can be prevented from being scattered and the like, and the packaging material 450 can be suitably prevented from being introduced into the living body. For example, if the packaging material 450 moves in the lumen 421 while rotating irregularly, the packaging material 450 may come into contact with the cutting portion 30 while rotating, and fragments of the packaging material 450 may be scattered. According to the medical instrument 410, such scattering of the packaging material 450 can be prevented in advance.
  • FIGS. 8A and 8B show a medical instrument 510 according to the fifth modification. 6 (A) and 6 (B), the hook member 127 functioning as a holding portion for holding the packaging material 550 is provided in the long member 120, and the hook member 127 is further attached to the packaging material 550.
  • a configuration that functions as a cutting unit for cutting was shown.
  • this modified example by sharply sharpening the tip of the hook portion 527 provided on the long member 520, it becomes easy to form a cut in the packaging material 550 by the hook portion 527, and further, the packaging material 550 in the hook portion 527. It is possible to increase the holding power.
  • the packaging material 550 moves in the lumen 521 and is abutted against the hook portion 527, a cut is formed in the packaging material 550, and the living body introduction material 70 is transferred from the packaging material 550. Leak. Further, the packaging material 550 is held by being hooked on the hook portion 527.
  • the medical instrument 510 according to the present modification, a break is easily formed in the packaging material 550 by the hook portion 527, so that the introduction property of the living body introduction material 70 into the living body can be improved. Furthermore, since the holding power of the packaging material 550 in the hook portion 527 can be increased, the packaging material 550 can be more reliably prevented from being introduced into the living body.
  • each modification can be combined as appropriate.
  • a mesh material for holding can be provided in each modification, and a packaging material in which an opening assisting part is formed in each modification can also be used.
  • the cutting part provided in a long member should just have the structure which can form a cut
  • a wire wire, a blade wire, or a projecting shape that can puncture a packaging material can be appropriately employed.
  • the cutting part is preferably arranged on the distal end side of the main body part as much as possible in consideration of adhesion of the biological introduction material to the inner wall of the lumen, but the position is not particularly limited, and the length of the long member It can be appropriately changed according to the dimensions and the like.
  • the configuration of the opening part that opens the packaging material is different from the medical instrument according to the first embodiment described above.
  • the cutting part which can open a packaging material by making a cut into a packaging material is used as an opening part.
  • an opening portion having a configuration capable of opening the packaging material without cutting the packaging material is provided. This is different from the first embodiment described above.
  • the medical device 610 includes an opening 630 that can open the packaging material 650 by opening the valve body 660 provided in the packaging material 650.
  • This opening part 630 functions as an opening part for opening the packaging material 650.
  • the packaging material 650 is provided with a valve body 660 that seals the opening 663 provided at a predetermined portion of the packaging material 650, and by opening the valve body 660, The living body introduction material 70 enclosed inside can be leaked to the outside of the packaging material 650.
  • the opening part 630 provided in the medical device 610 opens this valve body 660 by contacting the valve body 660.
  • the valve body 660 can be comprised by the one-way valve etc. which were comprised openably by the contact with another member, for example.
  • the opening part 630 provided in the long member 620 is aligned and installed in advance so as to be abutted against a predetermined part of the valve body 660 provided in the packaging material 650, for example.
  • the opening 630 can be formed in a shape that protrudes toward the valve body 660 so that it can be easily brought into contact with the valve body 660, but is not limited to such a shape.
  • the shape and structure which can open the said valve body 660 by contacting the valve body 660 should just be provided.
  • the packaging material 650 can be held in the opening portion 630. Therefore, there is no need to separately provide a holding portion for holding the packaging material 650. Can be made simpler.
  • the packaging material 650 can be opened without forming a cut in the packaging material 650 like the medical device 610 according to the present embodiment, the following advantages are obtained. If a cut is formed in the packaging material 650, the packaging material 650 may be cut finely and the fragments may be scattered and introduced into the living body. On the other hand, if it becomes possible to take out the living body introduction material 70 from the packaging material 650 without forming a cut, it is possible to prevent the packaging material 650 from being scattered and the packaging material in the living body. It is possible to more suitably prevent 650 from being introduced.
  • the outer shape of the packaging material 650 can be formed in a substantially spherical shape as exemplified in the first embodiment.
  • the contact area of the long member 620 with the inner wall of the lumen 621 is small. It is preferable to use one having a large length dimension so as to be large.
  • the packaging material 650 can easily move in the lumen 621 of the long member 620 along the axial direction. It becomes easy to make the opening part 630 provided in the member 620 contact.
  • the packaging material 650 can be moved in the lumen 621 of the long member 620.
  • the packaging material 650 can also be moved within the lumen 621 using a pusher-like member 680.
  • a pressing member 685 provided on the distal end side of the pusher 680 is introduced into the packaging material 650, and the packaging material 650 and the pusher 680 are integrally formed. It can also be set as the structure which opens the valve body 660 by operation which moves the pusher 680 by comprising by a valve.
  • the living body introduction material 70 can be taken out from the packaging material 650 by using the opening 630 and the pusher 660 together.
  • the medical device 710 according to the present modification is provided with an opening that can leak the living body introduction material from the packaging material without forming a cut in the packaging material, as in the above-described embodiment.
  • an opening 770 is provided in the packaging material 750, and the opening portion is constituted by a string 730 for opening the opening 770.
  • the packaging material 750 is introduced into the long member 720 with the opening 770 closed. Then, as shown in FIG. 10 (B), after being moved through the lumen 721 of the long member 720, the opening 770 is opened by pulling the string 730 at a predetermined position, and enclosed inside.
  • the living body introduction material 70 is leaked.
  • the string 730 is pulled by a manual operation to collect the packaging material 750, or the packaging material 750 is held by the string 730 and the packaging material 750 is introduced into the living body. Can also be prevented.
  • the living body introduction material 70 can be taken out from the packaging material 750 without forming a cut in the packaging material 750, it is possible to prevent the packaging material 750 from being scattered. It is possible to prevent the packaging material 750 from being introduced into the living body.
  • the opening part shown in each embodiment may be arranged on the front end surface of the long member, and the packaging material may be opened immediately after passing the lumen. Even in such a configuration, it is possible to suitably prevent the living body introduction material from adhering to the lumen.

Abstract

[Problem] To provide: a medical tool which makes it possible to prevent the adhesion of a biological induction material, e.g., a drug, onto a long member, e.g., a catheter, during the introduction of the biological introduction material into a living body so that the biological introduction material can be introduced into the living body laconically; and a medical system. [Solution] A medical tool (10) comprises: a long member (20) equipped with a lumen (21) that extends from a tip side toward a base end side; and a cut section (30) provided on the long member. In the cut section, a packaging material to be introduced into the lumen of the long member is notched so as to leak a biological introduction material enclosed in the packaging material.

Description

医療器具、および医療システムMedical instrument and medical system
 本発明は、医療器具、および医療システムに関する。 The present invention relates to a medical instrument and a medical system.
 生体内へ薬剤等の生体導入材を送達するための医療器具として、カテーテルのような長尺状の医療器具が広く用いられている。一般的に、カテーテルには薬剤が流通可能なルーメンおよびルーメンから薬剤を吐出させるための吐出孔が設けられている(例えば、特許文献1を参照)。 Long medical devices such as catheters are widely used as medical devices for delivering biological introduction materials such as drugs into the living body. Generally, a catheter is provided with a lumen through which a drug can flow and a discharge hole for discharging the drug from the lumen (see, for example, Patent Document 1).
 従来は、カテーテルを使用して薬剤の投与を行う場合にはカテーテルのルーメン内に所定量の薬剤を充填した後、ルーメン内へガスや生理食塩水などを流入させたり、押し子のような部材で薬剤を押し込んだりする作業が行われていた。 Conventionally, when a drug is administered using a catheter, a predetermined amount of drug is filled into the lumen of the catheter, and then a member such as a pusher is used to flow gas or physiological saline into the lumen. There was a work to push drugs.
特開2010-125229号JP 2010-125229 A
 上記のような投与方法では、ルーメン内に充填した薬剤がルーメン内壁に付着してしまうため、充填した薬剤の全量を生体内へ吐出させることができないという問題がある。特に、薬剤が紛体である場合には、ルーメン内壁への付着量が増え易く、カテーテルから吐出させることができない薬剤のデッドボリュームが増加する傾向にある。これに加えて、ガスや生理食塩水などをルーメン内へ流入させる方法を採用すると、ルーメン内を薬剤が移動する間にガスや生理食塩水が薬剤と混合されてしまうため、濃度が低下した薬剤が生体内へ導入されてしまうという問題も生じる。 In the administration method as described above, since the medicine filled in the lumen adheres to the inner wall of the lumen, there is a problem that the whole amount of the filled medicine cannot be discharged into the living body. In particular, when the drug is a powder, the amount of adhesion to the inner wall of the lumen tends to increase, and the dead volume of the drug that cannot be discharged from the catheter tends to increase. In addition to this, if a method of flowing gas or physiological saline into the lumen is employed, the gas or physiological saline is mixed with the drug while the drug moves through the lumen, so the drug has a reduced concentration. There is also a problem that is introduced into the living body.
 本発明は、上記課題を解決するために発明されたものであり、薬剤等の生体導入材を生体内へ導入する際に、カテーテルのような長尺部材に生体導入材が付着することを防止して、生体導入材を無駄なく生体内へ導入させることを可能にする医療器具、および医療システムを提供することを目的とする。 The present invention has been invented in order to solve the above-mentioned problems, and prevents a biological introduction material from adhering to a long member such as a catheter when a biological introduction material such as a drug is introduced into the living body. An object of the present invention is to provide a medical instrument and a medical system that can introduce a living body introduction material into a living body without waste.
 (1)先端側から基端側へ延伸されたルーメンを備える長尺部材と、前記長尺部材を介して生体内に導入される生体導入材を封入した包装材が前記ルーメンを通過する間に当該包装材を開封させる開封部と、を有することを特徴とする医療器具。 (1) While a packaging material enclosing a long member having a lumen extending from the distal end side to the proximal end side and a living body introduction material introduced into the living body through the long member passes through the lumen A medical device comprising: an opening for opening the packaging material.
 (2)前記開封部は、前記長尺部材に設けられており、かつ、前記包装材が前記ルーメンを通過するのに伴って当該包装材の少なくとも一部に前記生体導入材を漏洩させるための切れ目を形成する切断部を有することを特徴とする上記(1)に記載の医療器具。 (2) The opening portion is provided in the elongated member, and leaks the living body introduction material to at least a part of the packaging material as the packaging material passes through the lumen. It has a cutting part which forms a cut, The medical instrument given in the above (1) characterized by things.
 (3)前記開封部は、前記長尺部材に設けられており、かつ、前記包装材に設けられ当該包装材を封止する弁体に接触することにより当該弁体を開放する開放部を有することを特徴とする上記(1)に記載の医療器具。 (3) The opening part is provided in the long member, and has an opening part that opens the valve body by contacting a valve body that is provided in the packaging material and seals the packaging material. The medical device according to (1) above, wherein
 (4)前記開封部は、前記包装材に設けられた開口部に接続されており、かつ、閉じられた状態の当該開口部を開くための紐を有することを特徴とする上記(1)に記載の医療器具。 (4) In the above (1), the opening portion is connected to an opening provided in the packaging material and has a string for opening the opening in a closed state. The medical device described.
 (5)前記長尺部材は、開封された前記包装材を当該長尺部材に保持させるための保持部をさらに有することを特徴とする上記(1)~(4)のいずれか1つに記載の医療器具。 (5) The long member further includes a holding portion for holding the opened packaging material on the long member, according to any one of the above (1) to (4), Medical instruments.
 (6)前記保持部は、前記ルーメン内において前記包装材を保持する保持用のメッシュ材を有することを特徴とする上記(5)に記載の医療器具。 (6) The medical device according to (5), wherein the holding portion includes a mesh material for holding the packaging material in the lumen.
 (7)前記保持部は、開封された前記包装材が前記ルーメンを通過する際に当該包装材が引っ掛けて保持される引っ掛け部を有することを特徴とする上記(5)または上記(6)に記載の医療器具。 (7) In the above (5) or (6), the holding portion includes a hook portion that holds the packaging material when the opened packaging material passes through the lumen. The medical device described.
 (8)前記包装材は、第1の径を備える第1径部と、前記第1径部よりも先端側に形成され、かつ、前記第1径部よりも小さな径を備える第2径部と、前記第1径部と前記第2径部とに連なる中間部と、を有しており、前記保持部は、前記包装材が前記ルーメンを通過する際に前記中間部が突き当てて保持される突き当て部を有することを特徴とする上記(5)~(7)のいずれかに1つに記載の医療器具。 (8) The packaging material includes a first diameter portion having a first diameter, and a second diameter portion that is formed on the tip side of the first diameter portion and has a smaller diameter than the first diameter portion. And an intermediate portion connected to the first diameter portion and the second diameter portion, and the holding portion is held by the intermediate portion abutting when the packaging material passes through the lumen. The medical device according to any one of the above (5) to (7), wherein the medical device has an abutting portion.
 (9)前記包装材に取り付けられるとともに前記包装材を前記ルーメン内に導入した際に前記長尺部材の基端側から導出される紐をさらに有することを特徴とする上記(1)~(8)のいずれか1つに記載の医療器具。 (9) The above (1) to (8), further comprising a string attached to the packaging material and led out from a proximal end side of the long member when the packaging material is introduced into the lumen. ) A medical device according to any one of the above.
 (10)前記長尺部材のルーメン内に配置され、前記ルーメン内において前記包装材が軸方向に沿って移動するように前記包装材の移動をガイドするガイド部材をさらに有することを特徴とする上記(1)~(9)のいずれか1つに記載の医療器具。 (10) The guide member may further include a guide member that is disposed in the lumen of the elongate member and guides the movement of the packaging material so that the packaging material moves along the axial direction in the lumen. (1) The medical device according to any one of (9).
 (11)前記包装材は、当該包装材の一部に、当該包装材の他の部位よりも開封され易く構成された開封補助部を有することを特徴とする上記(1)~(10)のいずれか1つに記載の医療器具。 (11) The packaging material according to any one of (1) to (10) above, wherein a part of the packaging material has an opening assisting part configured to be opened more easily than other parts of the packaging material. The medical device as described in any one.
 (12)上記(1)~(11)のいずれか1つに記載の医療器具と、前記包装材を前記ルーメン内において移動させるための流体を前記長尺部材へ供給する流体供給部と、を有することを特徴とする医療システム。 (12) The medical device according to any one of (1) to (11) above, and a fluid supply unit that supplies a fluid for moving the packaging material in the lumen to the elongated member. A medical system comprising:
 上記(1)に記載の医療器具によれば、薬剤等の生体導入材を包装材に封入した状態で生体導入材を長尺部材のルーメン内において移動させ、かつ、生体導入材が生体内へ導入される前に包装材を開封させることができる。このため、ルーメンの内壁に生体導入材が付着することを防止して、生体導入材を無駄なく生体内へ導入させることができる。 According to the medical instrument described in the above (1), the living body introduction material is moved in the lumen of the long member while the living body introduction material such as a medicine is enclosed in the packaging material, and the living body introduction material enters the living body. The packaging material can be opened before being introduced. For this reason, it is possible to prevent the living body introduction material from adhering to the inner wall of the lumen, and to introduce the living body introduction material into the living body without waste.
 上記(2)に記載の医療器具によれば、長尺部材のルーメン内において包装材を移動させる簡単な作業により包装材を開封することができるため、医療器具の使用性を向上させることができる。 According to the medical instrument described in the above (2), since the packaging material can be opened by a simple operation of moving the packaging material in the lumen of the long member, the usability of the medical instrument can be improved. .
 上記(3)に記載の医療器具によれば、包装材に切れ目を形成することなく当該包装材を開封させることができるため、包装材の飛散が生じることを未然に防止することができ、生体内に包装材が導入されてしまうことをより好適に防止することができる。 According to the medical instrument described in the above (3), since the packaging material can be opened without forming a cut in the packaging material, it is possible to prevent the scattering of the packaging material before it occurs. It is possible to more suitably prevent the packaging material from being introduced into the body.
 上記(4)に記載の医療器具によれば、包装材に切れ目を形成することなく当該包装材を開封させることができるため、包装材の飛散が生じることを未然に防止することができ、生体内に包装材が導入されてしまうことをより好適に防止することができる。 According to the medical instrument described in the above (4), since the packaging material can be opened without forming a cut in the packaging material, it is possible to prevent the scattering of the packaging material before it occurs. It is possible to more suitably prevent the packaging material from being introduced into the body.
 上記(5)に記載の医療器具によれば、開封された包装材を長尺部材に保持させることができるため、包装材が生体内へ導入されることを防止できる。 According to the medical instrument described in (5) above, since the opened packaging material can be held by the long member, the packaging material can be prevented from being introduced into the living body.
 上記(6)に記載の医療器具によれば、保持部が備える保持用のメッシュ材によって包装材を保持させることができるため、包装材が生体内へ導入されることを好適に防止することができる。 According to the medical instrument as described in said (6), since a packaging material can be hold | maintained with the mesh material for a holding | maintenance with which a holding | maintenance part is equipped, it can prevent suitably that a packaging material is introduce | transduced into a biological body. it can.
 上記(7)に記載の医療器具によれば、保持部が備える引っ掛け部において包装材を保持させることができるため、包装材が生体内へ導入されることを好適に防止することができる。 According to the medical instrument described in the above (7), since the packaging material can be held in the hook portion provided in the holding portion, the packaging material can be suitably prevented from being introduced into the living body.
 上記(8)に記載の医療器具によれば、包装材の中間部を保持部が備える突き当て部に突き当てることにより、包装材を長尺部材に保持させることができるため、包装材が生体内へ導入されることを好適に防止することができる。 According to the medical instrument described in the above (8), the packaging material can be held by the long member by abutting the intermediate portion of the packaging material against the abutting portion provided in the holding portion. It can prevent suitably being introduced into the body.
 上記(9)に記載の医療器具によれば、包装材に取り付けられた紐により、包装材が生体内へ導入されることを防止できる。また、紐を使用して包装材の回収を容易に行うことができる。 According to the medical instrument described in the above (9), the packaging material can be prevented from being introduced into the living body by the string attached to the packaging material. Further, the packaging material can be easily collected using the string.
 上記(10)に記載の医療器具によれば、包装材を長尺部材の軸方向に沿って移動させることが可能になるため、開封された包装材が飛散等することを防止でき、包装材が生体内へ導入されることを好適に防止することができる。 According to the medical instrument described in the above (10), since the packaging material can be moved along the axial direction of the long member, the opened packaging material can be prevented from scattering, and the packaging material. Can be suitably prevented from being introduced into the living body.
 上記(11)に記載の医療器具によれば、包装材を開封し易くなるため、包装材から生体導入材を確実に取り出すことができる。 According to the medical instrument described in (11) above, since the packaging material can be easily opened, the living body introduction material can be reliably removed from the packaging material.
 上記(12)に記載の医療システムによれば、医療器具が備える長尺部材のルーメン内において包装材を円滑に移動させることが可能な医療システムを提供することが可能になる。 According to the medical system described in (12) above, it is possible to provide a medical system capable of smoothly moving the packaging material in the lumen of the long member provided in the medical instrument.
本発明の第1実施形態に係る医療器具および医療システムを簡略化して示す図である。It is a figure which simplifies and shows the medical instrument and medical system which concern on 1st Embodiment of this invention. 図2は、第1実施形態に係る医療器具の構成を説明するための図であって、図2(A)は、医療器具が備える長尺部材の先端側の部分断面図、図2(B)は、医療器具が備える保持部の平面図、図2(C)は、医療器具が備える切断部の平面図である。FIG. 2 is a diagram for explaining the configuration of the medical device according to the first embodiment. FIG. 2A is a partial cross-sectional view of the distal end side of the long member provided in the medical device, and FIG. ) Is a plan view of a holding part provided in the medical instrument, and FIG. 2C is a plan view of a cutting part provided in the medical instrument. 実施形態に係る包装材を説明するための図であって、図3(A)は、包装材の平面図、図3(B)は、包装材の断面図である。It is a figure for demonstrating the packaging material which concerns on embodiment, Comprising: FIG. 3 (A) is a top view of a packaging material, FIG.3 (B) is sectional drawing of a packaging material. 医療器具が備える保持用のメッシュ材の改変例を示す平面図である。It is a top view which shows the modification of the mesh material for holding | maintenance with which a medical device is equipped. 図5は、第1実施形態に係る医療器具の作用を説明するための図であって、図5(A)は、包装材が医療器具の切断部を通過する前の状態を示す部分断面図であり、図5(B)は、包装材が医療器具の保持部において保持された状態を示す部分断面図である。FIG. 5 is a diagram for explaining the operation of the medical device according to the first embodiment, and FIG. 5A is a partial cross-sectional view showing a state before the packaging material passes through the cutting portion of the medical device. FIG. 5 (B) is a partial cross-sectional view showing a state in which the packaging material is held in the holding part of the medical device. 図6は、第1実施形態に係る医療器具の変形例1を説明するための図であって、図6(A)は、包装材に切れ目が形成される前の状態を示す部分断面図であり、図6(B)は、長尺部材に設けられた引っ掛け部において包装材が保持された状態を示す部分断面図である。FIG. 6 is a view for explaining Modification Example 1 of the medical device according to the first embodiment, and FIG. 6 (A) is a partial cross-sectional view showing a state before a cut is formed in the packaging material. FIG. 6B is a partial cross-sectional view showing a state in which the packaging material is held in the hook portion provided in the long member. 図7は、第1実施形態に係る医療器具の変形例2~4を説明するための図であって、図7(A)は、変形例2に係る医療器具を説明するための部分断面図であり、図7(B)は、変形例3に係る医療器具を説明するための部分断面図であり、図7(C)は、変形例4に係る医療器具を説明するための部分断面図である。7 is a view for explaining modified examples 2 to 4 of the medical instrument according to the first embodiment, and FIG. 7A is a partial sectional view for explaining the medical instrument according to the modified example 2. FIG. 7B is a partial cross-sectional view for explaining the medical instrument according to the third modification, and FIG. 7C is a partial cross-sectional view for explaining the medical instrument according to the fourth modification. It is. 図8は、第1実施形態に係る医療器具の変形例5を説明するための図であって、図8(A)は、包装材が医療器具の切断部を通過する前の状態を示す部分断面図であり、図8(B)は、包装材が医療器具の保持部において保持された状態を示す部分断面図である。FIG. 8 is a view for explaining a modified example 5 of the medical instrument according to the first embodiment, and FIG. 8A is a part showing a state before the packaging material passes through the cutting part of the medical instrument. FIG. 8B is a partial cross-sectional view showing a state in which the packaging material is held in the holding part of the medical device. 図9(A)、(B)はそれぞれ、本発明の第2実施形態に係る医療器具を説明するための部分断面図である。9A and 9B are partial cross-sectional views for explaining a medical device according to the second embodiment of the present invention. 図10は、第2実施形態に係る医療器具の変形例を説明するための図であって、図10(A)は、包装材が開封される前の状態を示す部分断面図、図10(B)は、包装材が開封された後の状態を示す部分断面図である。FIG. 10 is a view for explaining a modified example of the medical instrument according to the second embodiment, and FIG. 10 (A) is a partial sectional view showing a state before the packaging material is opened, FIG. B) is a partial cross-sectional view showing a state after the packaging material is opened.
 以下、図面を参照しつつ、本発明を実施形態に基づいて説明する。 Hereinafter, the present invention will be described based on embodiments with reference to the drawings.
 <第1実施形態>
 図1~図4は本発明の第1実施形態に係る医療器具および医療システムの各構成を説明するための図であり、図5は第1実施形態に係る医療器具および医療システムの作用の説明に供する図である。なお、図面の説明において同一の要素には同一の符号を付し、重複する説明を省略する。また、図面の寸法比率は、説明の都合上誇張されており、実際の比率とは異なる場合がある。
<First Embodiment>
1 to 4 are diagrams for explaining each configuration of the medical instrument and the medical system according to the first embodiment of the present invention, and FIG. 5 is an explanation of the operation of the medical instrument and the medical system according to the first embodiment. FIG. In the description of the drawings, the same elements are denoted by the same reference numerals, and redundant description is omitted. In addition, the dimensional ratios in the drawings are exaggerated for convenience of explanation, and may be different from the actual ratios.
 図1~図3を参照して、本実施形態に係る医療器具10は、概説すれば、先端側から基端側へ延伸されたルーメン21を備える長尺部材20と、長尺部材20を介して生体内に導入される生体導入材60を封入した包装材50がルーメン21を通過する間に当該包装材50を開封させる開封部30と、を有している。開封部30は、長尺部材20に設けられており、かつ、包装材50がルーメン21を通過するのに伴って当該包装材50の少なくとも一部に生体導入材60を漏洩させるための切れ目を形成する切断部によって構成している(図5(A)、(B)を参照)。 With reference to FIGS. 1 to 3, the medical device 10 according to the present embodiment will be briefly described. The long member 20 includes a lumen 21 extending from the distal end side to the proximal end side, and the long member 20 is interposed therebetween. The packaging material 50 enclosing the living body introduction material 60 introduced into the living body has an opening portion 30 that opens the packaging material 50 while passing through the lumen 21. The unsealing part 30 is provided in the long member 20, and a cut for leaking the biological introduction material 60 to at least a part of the packaging material 50 as the packaging material 50 passes through the lumen 21. It is comprised by the cutting part to form (refer FIG. 5 (A), (B)).
 明細書の説明において、長尺部材20が延伸された先端側(図1の左側)を医療器具10の先端側と称し、その逆側を医療器具10の基端側(図1の右側)と称する。また、軸方向とは、長尺部材20が延伸された方向、すなわち図1の左右方向を意味する。 In the description, the distal end side (left side in FIG. 1) from which the long member 20 is extended is referred to as the distal end side of the medical device 10, and the opposite side is referred to as the proximal end side (right side in FIG. 1). Called. Moreover, an axial direction means the direction where the elongate member 20 was extended | stretched, ie, the left-right direction of FIG.
 医療器具10は、包装材50をルーメン21内において移動させるための流体を長尺部材20へ供給するための流体供給部60とともに用いることができ、医療器具10および流体供給部60とによって医療システム100を構築することができる。 The medical instrument 10 can be used together with a fluid supply unit 60 for supplying a fluid for moving the packaging material 50 in the lumen 21 to the elongate member 20, and the medical system includes the medical instrument 10 and the fluid supply unit 60. 100 can be built.
 医療器具10を使用して生体内へ導入される生体導入材70としては、例えば、薬剤が挙げられるがこれに限定されず、各種の細胞や血液、代謝物など生体内への導入を目的とする物の中から適宜選択することができる。包装材50は、この生体導入材70を封入した状態で長尺部材20のルーメン21内に導入される。後述するように、ルーメン21内を通過する際に、長尺部材20によって少なくとも一部が切断されることにより、内部に封入した生体導入材70を漏洩させる。 Examples of the biological introduction material 70 introduced into the living body using the medical instrument 10 include, but are not limited to, drugs, and are intended for introduction into the living body such as various cells, blood, and metabolites. It can be appropriately selected from the products to be performed. The packaging material 50 is introduced into the lumen 21 of the long member 20 in a state where the living body introduction material 70 is enclosed. As will be described later, at the time of passing through the lumen 21, at least a part is cut by the long member 20, thereby leaking the biological introduction material 70 enclosed therein.
 長尺部材20は、医療の分野において公知であるカテーテルによって構成することができる。長尺部材20の先端には、ルーメン21に連通する開口部22が形成されており、この開口部22から生体導入材70を吐出させることが可能である。また、長尺部材20の基端には、流体供給部60と長尺部材20とを連結させるチューブ61が連結可能なコネクタ23が設けられている。このコネクタ23には、例えば、嵌合やネジ込みによってチューブ61を連結させることが可能な機械式のコネクタを使用することができる。 The long member 20 can be constituted by a catheter known in the medical field. An opening 22 communicating with the lumen 21 is formed at the distal end of the long member 20, and the living body introduction material 70 can be discharged from the opening 22. A connector 23 to which a tube 61 for connecting the fluid supply unit 60 and the long member 20 can be connected is provided at the base end of the long member 20. For this connector 23, for example, a mechanical connector capable of connecting the tube 61 by fitting or screwing can be used.
 長尺部材20を構成する材料としては、特に制限はないが、例えば、ポリ塩化ビニル、ポリエチレン、ポリプロピレン、環状ポリオレフィン、ポリスチレン、ポリ(4-メチルペンテン-1)、ポリカーボネート、アクリル樹脂、ポリエチレンテレフタレート、ポリエチレンナフタレート等のポリエステル、ブタジエン-スチレン共重合体、ポリアミド(例えば、ナイロン6、ナイロン6・6、ナイロン6・10、ナイロン12)のような各種の軟質または硬質樹脂を用いることができる。 The material constituting the long member 20 is not particularly limited. For example, polyvinyl chloride, polyethylene, polypropylene, cyclic polyolefin, polystyrene, poly (4-methylpentene-1), polycarbonate, acrylic resin, polyethylene terephthalate, Various soft or hard resins such as polyester such as polyethylene naphthalate, butadiene-styrene copolymer, polyamide (for example, nylon 6, nylon 6,6, nylon 6,10, nylon 12) can be used.
 流体供給部60としては、各種の流体を長尺部材20のルーメン21内へ圧送することができるものを使用することができ、例えば、公知の流体ポンプ等を使用することができる。また、流体供給部60から供給する流体としては、気体や液体を使用することができ、例えば、空気や生理食塩水等を使用することができる。 As the fluid supply unit 60, one capable of pumping various fluids into the lumen 21 of the long member 20 can be used. For example, a known fluid pump or the like can be used. Moreover, gas and liquid can be used as the fluid supplied from the fluid supply part 60, for example, air, physiological saline, etc. can be used.
 長尺部材20と流体供給部60とを連結するチューブ61としては、流体が流通可能であり、かつ、流体供給部60と長尺部材20とを液密・気密に接続することができるものを使用できる。例えば、可撓性を備える公知の樹脂製のチューブをチューブ61に使用することができる。なお、流体供給部60として、例えば、医療の分野において公知であるシリンジポンプなどを使用することもできる。シリンジポンプを使用する場合には、チューブ61を使用せずに長尺部材20のコネクタ23とシリンジポンプとを直接連結させてもよい。 As the tube 61 that connects the long member 20 and the fluid supply unit 60, a tube that can circulate fluid and can connect the fluid supply unit 60 and the long member 20 in a liquid-tight and air-tight manner. Can be used. For example, a known resin tube having flexibility can be used for the tube 61. As the fluid supply unit 60, for example, a syringe pump known in the medical field can be used. When using a syringe pump, the connector 23 of the long member 20 and the syringe pump may be directly connected without using the tube 61.
 図2(A)、(B)を参照して、長尺部材20に設けられた切断部30は、例えば、包装材50に切れ目を入れやすく構成されたブレード31と、ブレード31が取り付けられた枠材32とを備えるように構成することができる。ブレード31は、金属などによって構成することができる。また、ブレード31の先端を鋭利に尖らせることにより刃面を備えさせることもできる。例えば、図示するように周方向の均等な位置に4つのブレード31を設置することができる。 Referring to FIGS. 2A and 2B, the cutting portion 30 provided in the long member 20 includes, for example, a blade 31 configured to easily cut the packaging material 50 and the blade 31 attached thereto. The frame member 32 may be provided. The blade 31 can be made of metal or the like. Further, the blade surface can be provided by sharpening the tip of the blade 31. For example, as shown in the figure, four blades 31 can be installed at equal positions in the circumferential direction.
 枠材32は、ブレード31を長尺部材20に固定するために設けられる。枠材32は、例えば、接着や融着によって長尺部材20に固定することができる。医療器具10にあっては、長尺部材20のルーメン21内に切断部30を配置している。 The frame member 32 is provided to fix the blade 31 to the long member 20. The frame member 32 can be fixed to the long member 20 by adhesion or fusion, for example. In the medical instrument 10, the cutting part 30 is disposed in the lumen 21 of the long member 20.
 図2(A)、(C)を参照して、長尺部材20には、切れ目が形成された包装材50を当該長尺部材20に保持させるための保持部40を備えさせることができる。この保持部40は、例えば、切断部30よりも先端側に配置された保持用のメッシュ材41によって構成することができる。図5(A)、(B)に示すように、包装材50がルーメン21を通過して切断部30によって包装材50に切れ目が形成された後、切断部30よりも先端側に配置された保持用のメッシュ材41において包装材50が保持される。 2 (A) and 2 (C), the long member 20 can be provided with a holding portion 40 for holding the packaging material 50 in which the cut is formed on the long member 20. The holding part 40 can be constituted by, for example, a holding mesh material 41 arranged on the distal end side with respect to the cutting part 30. As shown in FIGS. 5A and 5B, after the packaging material 50 passes through the lumen 21 and a cut is formed in the packaging material 50 by the cutting portion 30, the packaging material 50 is disposed on the tip side from the cutting portion 30. The packaging material 50 is held in the holding mesh material 41.
 図2(C)に示すように、保持用のメッシュ材41は包装材50を保持し得る粗さの網目を有しており、また、切断部30と同様に当該保持用のメッシュ材41を長尺部材20に固定するための枠材42が設けられる。枠材42は、例えば、接着や融着によって長尺部材20に固定することができる。 As shown in FIG. 2C, the holding mesh material 41 has a mesh with a roughness that can hold the packaging material 50, and the holding mesh material 41 is provided in the same manner as the cutting portion 30. A frame member 42 for fixing to the long member 20 is provided. The frame member 42 can be fixed to the long member 20 by adhesion or fusion, for example.
 保持用のメッシュ材41を構成する材料は、特に限定されず、金属や硬質の樹脂材料を使用することができる。また、保持用のメッシュ材は、格子状の網目を有する構成のみに限定されず、例えば、図4に示すメッシュ材43のように、複数の丸孔が形成された構成を有していてもよい。格子状、丸孔状のいずれの構成の保持用のメッシュ材41、43を使用する場合においても、包装材50を保持する機能を備えさせることができる。 The material constituting the holding mesh material 41 is not particularly limited, and a metal or a hard resin material can be used. Further, the holding mesh material is not limited to a configuration having a grid-like mesh, and for example, even if it has a configuration in which a plurality of round holes are formed as in the mesh material 43 shown in FIG. Good. In the case of using the holding mesh materials 41 and 43 having either the lattice shape or the round hole shape, the function of holding the packaging material 50 can be provided.
 図3(A)、(B)を参照して、包装材50は、内部に生体導入材70を封入可能な袋構造を有している。包装材50は、長尺部材20のルーメン21内を通過可能に設けられていればよく、その外形形状や容積は特に限定されない。包装材50を構成する材料としては、例えば、ポリエチレン、ポリプロピレン、エチレン-プロピレン共重合体等のポリオレフィン、ポリエチレンテレフタレート等のポリエステル、ポリ塩化ビニル、エチレン-酢酸ビニル共重合体、架橋型エチレン-酢酸ビニル共重合体、ポリウレタン等の熱可塑性樹脂、ポリアミドエラストマー、シリコーンゴム、ラテックスゴム等の樹脂材料が挙げられる。 3A and 3B, the packaging material 50 has a bag structure in which the biological introduction material 70 can be enclosed. The packaging material 50 should just be provided so that the inside of the lumen | rumen 21 of the elongate member 20 can be passed, and the external shape and volume are not specifically limited. Examples of the material constituting the packaging material 50 include polyolefins such as polyethylene, polypropylene, and ethylene-propylene copolymers, polyesters such as polyethylene terephthalate, polyvinyl chloride, ethylene-vinyl acetate copolymers, and crosslinked ethylene-vinyl acetate. Examples thereof include resin materials such as copolymers, thermoplastic resins such as polyurethane, polyamide elastomer, silicone rubber, and latex rubber.
 包装材50には、当該包装材50の一部に、当該包装材50の他の部位よりも開封され易く構成された開封補助部51を備えさせることができる。開封補助部51は、例えば、他の部位よりも切れ目が形成され易い材質を使用したり、他の部位よりも肉厚を薄くしたり、予め小さな切れ目を入れておくことにより形成することができる。図示する包装材50では、包装材50の複数の箇所に予め小さな切れ目を入れることにより、複数の開封補助部51を形成している。 The packaging material 50 can be provided with an opening assisting portion 51 configured to be easier to open than other parts of the packaging material 50 in a part of the packaging material 50. The opening assisting part 51 can be formed, for example, by using a material in which a cut is more easily formed than other parts, by making the wall thickness thinner than other parts, or by making a small cut in advance. . In the illustrated packaging material 50, a plurality of opening assisting portions 51 are formed by previously making small cuts at a plurality of locations of the packaging material 50.
 包装材50に封入する生体導入材70は、上述したように、生体内への導入を目的とするものであれば特に制限はないが、本実施形態では血栓溶解薬(アルテプラーゼ、モンテプラーゼ等)を生体導入材70として用いている。この他、生体導入材70として用いられる薬剤としては、抗凝固薬(ヘパリン、エノキサパリン等)、抗悪性腫瘍薬(ソラフェニブ、シスプラチン等)、炎症・アレルギーに作用する薬剤(フランカルボン酸モメタゾン、デキサメタゾンシペシル酸エステル等)、呼吸器系に作用する薬剤(サルメテロール、チオトロピウム)、神経系に作用する薬剤(オランザピン、塩酸ドネペジル等)なども用いることができ、また、その封入される際の状態についても特に制限はなく、粒状、粉状、ゲル状、液状などであってもよい。生体導入材70を導入させる対象となる部位も生体内であれば特に制限はなく、耳鼻や呼吸領域、各種の体管や血管などをその適用対象として選択することができる。 As described above, the living body introduction material 70 sealed in the packaging material 50 is not particularly limited as long as it is intended for introduction into the living body, but in this embodiment, a thrombolytic drug (alteplase, monteplase, etc.) is used. It is used as the living body introduction material 70. In addition, examples of drugs used as the biointroducing material 70 include anticoagulants (heparin, enoxaparin, etc.), antineoplastic drugs (sorafenib, cisplatin, etc.), drugs that act on inflammation and allergy (mometasone furanate, dexamethasone) Pesyl esters, etc.), drugs that act on the respiratory system (salmeterol, tiotropium), drugs that act on the nervous system (olanzapine, donepezil hydrochloride, etc.) can also be used, and the state when encapsulated There is also no particular limitation, and it may be granular, powdery, gelled, liquid or the like. There is no particular limitation as long as the part into which the living body introduction material 70 is introduced is in the living body, and an otoscope, a respiratory region, various body tubes and blood vessels can be selected as the application target.
 例えば、医療器具10を使用して外鼻を介して脳へ薬剤を供給することも可能である。医療器具10が備える長尺部材20により鼻腔の内部へ薬剤を送達させることが可能になるため、鼻腔の近傍に存在する神経系を経由させて直接的に脳へ薬剤を送達させることができる。従来のように経血管的に脳へ薬剤を投与する場合と比較して、薬剤の効能をより効果的に作用させることができる。 For example, it is possible to supply a medicine to the brain through the outer nose using the medical device 10. Since the elongate member 20 provided in the medical device 10 enables the drug to be delivered to the inside of the nasal cavity, the drug can be directly delivered to the brain via the nervous system existing in the vicinity of the nasal cavity. Compared with the case where a drug is administered transvascularly to the brain as in the prior art, the efficacy of the drug can be made to act more effectively.
 次に、本実施形態に係る医療器具10の作用を説明する。 Next, the operation of the medical instrument 10 according to this embodiment will be described.
 図5(A)に示すように、長尺部材20のルーメン21内へ生体導入材70を封入した包装材50を充填する。次に、流体供給部60を作動させて、包装材50を移動させるための流体をルーメン21内へ送り込む。流体によって包装材50がルーメン21内を移動してルーメン21内に配置された切断部30と接触する。切断部30との接触に伴って包装材50には切れ目が形成される。 As shown in FIG. 5A, a packaging material 50 in which a living body introduction material 70 is sealed is filled into the lumen 21 of the long member 20. Next, the fluid supply unit 60 is operated to feed a fluid for moving the packaging material 50 into the lumen 21. The packaging material 50 moves in the lumen 21 by the fluid and comes into contact with the cutting part 30 disposed in the lumen 21. A cut is formed in the packaging material 50 with the contact with the cutting part 30.
 さらに流体を送り続けると、包装材50は切断部30よりも先端側に配置された保持部40に押し付けられる。この際、包装材50の内部に封入されていた生体導入材70が包装材50から漏洩して長尺部材20の開口部22から吐出される。包装材50は、保持部40において保持されるため、包装材50が長尺部材20の開口部22から生体内へ吐出されることが防止される。 When the fluid continues to be fed, the packaging material 50 is pressed against the holding portion 40 disposed on the front end side with respect to the cutting portion 30. At this time, the living body introduction material 70 enclosed in the packaging material 50 leaks from the packaging material 50 and is discharged from the opening 22 of the long member 20. Since the packaging material 50 is held by the holding unit 40, the packaging material 50 is prevented from being discharged from the opening 22 of the long member 20 into the living body.
 以上、本実施形態に係る医療器具10によれば、薬剤等の生体導入材70を包装材50に封入した状態で生体導入材70を長尺部材20のルーメン21内において移動させ、かつ、生体導入材60が生体内へ導入される前に包装材50を開封させることができる。このため、ルーメン21の内壁に生体導入材70が付着することを防止して、生体導入材70を無駄なく生体内へ導入させることができる。 As described above, according to the medical instrument 10 according to the present embodiment, the living body introduction material 70 is moved in the lumen 21 of the elongate member 20 while the living body introduction material 70 such as a medicine is enclosed in the packaging material 50, and The packaging material 50 can be opened before the introduction material 60 is introduced into the living body. For this reason, the living body introduction material 70 can be prevented from adhering to the inner wall of the lumen 21 and the living body introduction material 70 can be introduced into the living body without waste.
 また、開封部30が包装材50に切れ目を形成する切断部を有するように構成されている場合には、長尺部材20のルーメン21内において包装材50を移動させる簡単な作業により包装材50を開封することができるため、医療器具10の使用性を向上させることができる。 Further, in the case where the opening part 30 is configured to have a cutting part that forms a cut in the packaging material 50, the packaging material 50 is moved by a simple operation of moving the packaging material 50 in the lumen 21 of the long member 20. Therefore, the usability of the medical device 10 can be improved.
 また、長尺部材20が、切れ目が形成された包装材50を当該長尺部材20に保持させるための保持部40を有するように構成されている場合には、包装材50を長尺部材20に保持させることができるため、包装材50が生体内へ導入されることを防止することができる。 In addition, when the long member 20 is configured to have the holding portion 40 for holding the packaging material 50 in which the cut is formed on the long member 20, the packaging material 50 is replaced with the long member 20. Therefore, the packaging material 50 can be prevented from being introduced into the living body.
 また、保持部40が、保持用のメッシュ材41を有するように構成されている場合には、包装材50を保持用のメッシュ材41により保持させることができるため、包装材50が生体内へ導入されることを好適に防止することができる。 Further, when the holding unit 40 is configured to have the holding mesh material 41, the packaging material 50 can be held by the holding mesh material 41, and thus the packaging material 50 is brought into the living body. It can prevent suitably being introduced.
 また、包装材50が、当該包装材50の一部に、当該包装材50の他の部位よりも切れ目が形成され易く構成された開封補助部51を有するように構成されている場合には、包装材50から生体導入材60を確実に取り出すことができる。 In addition, when the packaging material 50 is configured to have an opening assisting part 51 configured to be easier to form a cut in a part of the packaging material 50 than other parts of the packaging material 50, The living body introduction material 60 can be reliably removed from the packaging material 50.
 また、医療器具10と流体供給部60とによって医療システム100が構成される場合には、医療器具10が備える長尺部材20のルーメン21内において包装材50を円滑に移動させるための医療システムを提供することが可能になる。 Moreover, when the medical system 100 is comprised by the medical instrument 10 and the fluid supply part 60, the medical system for moving the packaging material 50 smoothly in the lumen | rumen 21 of the elongate member 20 with which the medical instrument 10 is provided. It becomes possible to provide.
 <変形例>
 次に、上述した実施形態の変形例を説明する。なお、上述した実施形態において説明した部材と同一の部材についてはその説明を省略する。
<Modification>
Next, a modified example of the above-described embodiment will be described. In addition, the description is abbreviate | omitted about the member same as the member demonstrated in embodiment mentioned above.
 図6(A)、(B)には、変形例1に係る医療器具110が示される。この変形例では、切れ目が形成された包装材150を保持する機構が前述した実施形態と異なる。具体的には、保持部は、切れ目が形成された包装材150が長尺部材120のルーメン121を通過する際に当該包装材150が引っ掛けて保持される引っ掛け部127を有するように構成されている。 6A and 6B show a medical instrument 110 according to the first modification. In this modification, the mechanism for holding the packaging material 150 in which the cuts are formed is different from the embodiment described above. Specifically, the holding portion is configured to have a hooking portion 127 on which the packaging material 150 is hooked and held when the packaging material 150 in which the cut is formed passes through the lumen 121 of the long member 120. Yes.
 長尺部材120は、先端側に配置された小径部123と、小径部123よりも基端側に配置された大径部125とを備えるように構成されている。小径部123の基端側の端部が大径部125内に配置されており、この端部が引っ掛け部127として構成されている。また、この端部は、包装材150に切れ目を形成する切断部としての機能も備えている。 The long member 120 is configured to include a small-diameter portion 123 disposed on the distal end side and a large-diameter portion 125 disposed closer to the proximal end side than the small-diameter portion 123. An end portion on the proximal end side of the small diameter portion 123 is disposed in the large diameter portion 125, and this end portion is configured as a hook portion 127. Further, this end portion also has a function as a cutting portion for forming a cut in the packaging material 150.
 図6(B)に示すように、包装材が引っ掛け部127に対して突き当てられると、包装材150に切れ目が形成されて包装材150から生体導入材70が漏洩する。また、包装材150は、引っ掛け部127に引っ掛けられることにより保持される。 As shown in FIG. 6B, when the packaging material is abutted against the hook portion 127, a cut is formed in the packaging material 150, and the living body introduction material 70 leaks from the packaging material 150. Further, the packaging material 150 is held by being hooked on the hook portion 127.
 このように、本変形例に示す医療器具110によれば、保持部が備える引っ掛け部127において切れ目が形成された包装材150を保持させることができるため、包装材150が生体内へ導入されることを好適に防止できる。 As described above, according to the medical instrument 110 shown in the present modification, the packaging material 150 in which a break is formed can be held in the hook portion 127 included in the holding unit, and thus the packaging material 150 is introduced into the living body. This can be suitably prevented.
 図7Aには、変形例2に係る医療器具210が示される。この変形例においても、切れ目が形成された包装材250を保持する機構が前述した実施形態と異なる。具体的には、包装材250は、第1の径を備える第1径部251と、第1径部251よりも先端側に形成され、かつ、第1径部251よりも小さな径を備える第2径部252と、第1径部251と第2径部252とに連なる中間部253とを有するように構成されている。また、保持部は、包装材250が長尺部材220のルーメン221を通過する際に、包装材250の中間部253が突き当てて保持される突き当て部225を有するように構成されている。 FIG. 7A shows a medical instrument 210 according to the second modification. Also in this modified example, the mechanism for holding the packaging material 250 with cuts is different from the above-described embodiment. Specifically, the packaging material 250 includes a first diameter portion 251 having a first diameter, and a first diameter portion 251 formed on the distal end side of the first diameter portion 251 and having a smaller diameter than the first diameter portion 251. The second diameter portion 252 and the intermediate portion 253 connected to the first diameter portion 251 and the second diameter portion 252 are configured. Further, the holding part is configured to have an abutting part 225 that abuts and holds the intermediate part 253 of the packaging material 250 when the packaging material 250 passes through the lumen 221 of the long member 220.
 包装材250に切れ目を形成するための切断部30は、長尺部材220に形成された小径部223に配置されている。包装材250がルーメン221内を移動すると、包装材250の先端部が切断部30に接触する。これにより、包装材250に切れ目が形成されて生体内導入材60が漏洩される。この際、包装材250の中間部253が長尺部材220の突き当て部225に突き当てられることにより、長尺部材220に対して包装材250が保持される。 The cutting part 30 for forming a cut in the packaging material 250 is arranged in the small diameter part 223 formed in the long member 220. When the packaging material 250 moves in the lumen 221, the tip of the packaging material 250 comes into contact with the cutting part 30. Thereby, a cut is formed in the packaging material 250 and the in-vivo introduction material 60 is leaked. At this time, the intermediate portion 253 of the packaging material 250 is abutted against the abutting portion 225 of the long member 220, whereby the packaging material 250 is held with respect to the long member 220.
 このように、本変形例に示す医療器具210によれば、包装材250の中間部253を保持部が備える突き当て部225に突き当てることにより、包装材250を長尺部材220に保持させることができるため、包装材250が生体内へ導入されることを好適に防止できる。 Thus, according to the medical instrument 210 shown in this modification, the long member 220 holds the packaging material 250 by abutting the intermediate portion 253 of the packaging material 250 against the abutting portion 225 provided in the holding portion. Therefore, the packaging material 250 can be suitably prevented from being introduced into the living body.
 図7Bには、変形例3に係る医療器具310が示される。この変形例では、包装材310に所定の紐333が取り付けられている。紐333は、包装材350を長尺部材320のルーメン321内に導入した際に長尺部材320の基端側から導出される長さを有している。この変形例に係る医療器具310によれば、長尺部材320のルーメン321の外で紐333を把持等することにより、切れ目が形成された包装材350が生体内へ導入されることを防止することができる。また、紐333を使用して包装材350の回収を容易に行うこともできる。なお、紐333の径や材質、設置数については特に制限はない。 FIG. 7B shows a medical instrument 310 according to Modification 3. In this modification, a predetermined string 333 is attached to the packaging material 310. The string 333 has a length derived from the proximal end side of the long member 320 when the packaging material 350 is introduced into the lumen 321 of the long member 320. According to the medical instrument 310 according to this modification, by holding the string 333 outside the lumen 321 of the long member 320, the packaging material 350 in which the cut is formed is prevented from being introduced into the living body. be able to. Further, it is possible to easily collect the packaging material 350 using the string 333. In addition, there is no restriction | limiting in particular about the diameter of the string 333, material, and the number of installation.
 図7Cには、変形例4に係る医療器具410が示される。この変形例では、長尺部材420のルーメン421内での包装材450の移動をガイドするガイド部材460が設けられる。ガイド部材460は、長尺部材420のルーメン421内に配置される。そして、このガイド部材460は、ルーメン421内において包装材450が軸方向に沿って移動するように包装材450の移動をガイドする。図示する変形例では、ガイド部材460は、長尺部材420のルーメン421内に設置されたレール構造の部材により構成されている。 FIG. 7C shows a medical instrument 410 according to the fourth modification. In this modification, a guide member 460 for guiding the movement of the packaging material 450 within the lumen 421 of the long member 420 is provided. The guide member 460 is disposed in the lumen 421 of the long member 420. The guide member 460 guides the movement of the packaging material 450 so that the packaging material 450 moves along the axial direction in the lumen 421. In the illustrated modification, the guide member 460 is configured by a rail-structured member installed in the lumen 421 of the long member 420.
 包装材450には、当該包装材450をガイド部材460に引っ掛けるための紐433が設けられる。なお、切断部30は、包装材450がガイド部材460に沿って移動した際に接触するように、ガイド部材460上に配置されている。 The packaging material 450 is provided with a string 433 for hooking the packaging material 450 to the guide member 460. In addition, the cutting part 30 is arrange | positioned on the guide member 460 so that it may contact, when the packaging material 450 moves along the guide member 460. FIG.
 この変形例に係る医療器具410によれば、包装材450を長尺部材420の軸方向に沿って移動させることが可能になるため、包装材450が切断部30に接触する際に包装材450が飛散等することを防止でき、包装材450が生体内へ導入されることを好適に防止することができる。例えば、包装材450が不規則に回転しながらルーメン421内を移動すると、切断部30に包装材450が回転しながら接触して包装材450の破片が飛散する虞がある。医療器具410によれば、このような包装材450の飛散を未然に防止することができる。 According to the medical instrument 410 according to this modification, the packaging material 450 can be moved along the axial direction of the long member 420, so that the packaging material 450 is brought into contact with the cutting portion 30. Can be prevented from being scattered and the like, and the packaging material 450 can be suitably prevented from being introduced into the living body. For example, if the packaging material 450 moves in the lumen 421 while rotating irregularly, the packaging material 450 may come into contact with the cutting portion 30 while rotating, and fragments of the packaging material 450 may be scattered. According to the medical instrument 410, such scattering of the packaging material 450 can be prevented in advance.
 図8(A)、(B)には、変形例5に係る医療器具510が示される。図6(A)、(B)において示した変形例1では、包装材550を保持する保持部として機能する引っ掛け部127を長尺部材120に設け、さらに、この引っ掛け部127を包装材550を切断するための切断部として機能させる構成を示した。本変形例では、長尺部材520に設けられた引っ掛け部527の先端を鋭利に尖らせることにより、引っ掛け部527により包装材550に切れ目を形成し易くし、さらに、引っ掛け部527における包装材550の保持力を高めることを可能にしている。 8A and 8B show a medical instrument 510 according to the fifth modification. 6 (A) and 6 (B), the hook member 127 functioning as a holding portion for holding the packaging material 550 is provided in the long member 120, and the hook member 127 is further attached to the packaging material 550. A configuration that functions as a cutting unit for cutting was shown. In this modified example, by sharply sharpening the tip of the hook portion 527 provided on the long member 520, it becomes easy to form a cut in the packaging material 550 by the hook portion 527, and further, the packaging material 550 in the hook portion 527. It is possible to increase the holding power.
 図8(B)に示すように、包装材550がルーメン521内を移動して引っ掛け部527に対して突き当てられると、包装材550に切れ目が形成されて包装材550から生体導入材70が漏洩する。また、包装材550は、引っ掛け部527に引っ掛けられることにより保持される。 As shown in FIG. 8B, when the packaging material 550 moves in the lumen 521 and is abutted against the hook portion 527, a cut is formed in the packaging material 550, and the living body introduction material 70 is transferred from the packaging material 550. Leak. Further, the packaging material 550 is held by being hooked on the hook portion 527.
 このように、本変形例に係る医療器具510によれば、引っ掛け部527により包装材550に切れ目が形成され易くなるため、生体内への生体導入材70の導入性を高めることができる。さらに、引っ掛け部527における包装材550の保持力を高めることができるため、包装材550が生体内へ導入されることをより確実に防止することができる。 As described above, according to the medical instrument 510 according to the present modification, a break is easily formed in the packaging material 550 by the hook portion 527, so that the introduction property of the living body introduction material 70 into the living body can be improved. Furthermore, since the holding power of the packaging material 550 in the hook portion 527 can be increased, the packaging material 550 can be more reliably prevented from being introduced into the living body.
 上述した実施形態および各変形例は適宜に組み合わせることが可能である。例えば、各変形例において保持用のメッシュ材を備えさせることもできるし、各変形例において開封補助部が形成された包装材を使用することもできる。 The above-described embodiment and each modification can be combined as appropriate. For example, a mesh material for holding can be provided in each modification, and a packaging material in which an opening assisting part is formed in each modification can also be used.
 また、長尺部材に設けられる切断部は、包装材が長尺部材のルーメンを通過するのに伴って包装材の少なくとも一部に切れ目を形成することが可能な構成を有していればよく、例えば、ワイヤ線やブレード線、包装材に穿刺可能な突出形状などの構成のものを適宜採用することができる。また、切断部は、ルーメンの内壁への生体導入材の付着を考慮して可能な限り本体部の先端側に配置されることが好ましいがその位置は特に限定されず、長尺部材の長さ寸法等に応じて適宜変更することができる。 Moreover, the cutting part provided in a long member should just have the structure which can form a cut | interruption in at least one part of a packaging material as a packaging material passes the lumen | rumen of a long member. For example, a wire wire, a blade wire, or a projecting shape that can puncture a packaging material can be appropriately employed. In addition, the cutting part is preferably arranged on the distal end side of the main body part as much as possible in consideration of adhesion of the biological introduction material to the inner wall of the lumen, but the position is not particularly limited, and the length of the long member It can be appropriately changed according to the dimensions and the like.
 <第2実施形態>
 次に、本発明の第2実施形態に係る医療器具を説明する。なお、上述した第1実施形態において説明した部材と同一の部材についてはその説明を省略する。
Second Embodiment
Next, a medical instrument according to a second embodiment of the present invention will be described. In addition, the description is abbreviate | omitted about the member same as the member demonstrated in 1st Embodiment mentioned above.
 本実施形態に係る医療器具では、包装材を開封する開封部の構成が前述した第1実施形態に係る医療器具とは異なる。第1実施形態に係る各医療器具においては、包装材に切れ目を入れることにより包装材を開封することが可能な切断部を開封部として用いている。一方、本実施形態に係る医療器具610では、包装材に切れ目を入れることなく当該包装材を開封することが可能な構成の開封部が備えられる。このような点において上述した第1実施形態と相違する。 In the medical instrument according to the present embodiment, the configuration of the opening part that opens the packaging material is different from the medical instrument according to the first embodiment described above. In each medical instrument which concerns on 1st Embodiment, the cutting part which can open a packaging material by making a cut into a packaging material is used as an opening part. On the other hand, in the medical instrument 610 according to the present embodiment, an opening portion having a configuration capable of opening the packaging material without cutting the packaging material is provided. This is different from the first embodiment described above.
 図9(A)に示すように、医療器具610には、包装材650に設けられた弁体660を開放することにより、包装材650を開封することが可能な開放部630が備えられている。この開放部630が包装材650を開封させるための開封部として機能する。より詳細に説明すると、包装材650には、当該包装材650の所定の部位に設けられた開口部663を封止する弁体660が設けられており、当該弁体660を開放することにより、内部に封入した生体導入材70を包装材650の外部へ漏洩させることが可能な構成を有している。そして、医療器具610に設けられた開放部630は、弁体660に接触することにより、この弁体660を開放させる。なお、弁体660は、例えば、他部材との接触によって開放自在に構成された一方弁などによって構成することができる。 As shown in FIG. 9A, the medical device 610 includes an opening 630 that can open the packaging material 650 by opening the valve body 660 provided in the packaging material 650. . This opening part 630 functions as an opening part for opening the packaging material 650. More specifically, the packaging material 650 is provided with a valve body 660 that seals the opening 663 provided at a predetermined portion of the packaging material 650, and by opening the valve body 660, The living body introduction material 70 enclosed inside can be leaked to the outside of the packaging material 650. And the opening part 630 provided in the medical device 610 opens this valve body 660 by contacting the valve body 660. In addition, the valve body 660 can be comprised by the one-way valve etc. which were comprised openably by the contact with another member, for example.
 長尺部材620に設けられた開放部630は、例えば、包装材650に設けられた弁体660の所定の部位に突き当てられるように、予め位置合わせして設置される。また、この開放部630は、弁体660と容易に接触させることができるように、弁体660に向けて突出するような形状に形成することができるが、このような形状に限定されず、弁体660に接触することにより、当該弁体660を開放し得る形状および構造を備えていればよい。ただし、図示するような形状で構成する場合には、開放部630において包装材650を保持することが可能になるため、包装材650を保持するための保持部を別途に設ける必要がなく、構成をより簡素なものとすることができる。 The opening part 630 provided in the long member 620 is aligned and installed in advance so as to be abutted against a predetermined part of the valve body 660 provided in the packaging material 650, for example. Further, the opening 630 can be formed in a shape that protrudes toward the valve body 660 so that it can be easily brought into contact with the valve body 660, but is not limited to such a shape. The shape and structure which can open the said valve body 660 by contacting the valve body 660 should just be provided. However, in the case of the configuration shown in the figure, the packaging material 650 can be held in the opening portion 630. Therefore, there is no need to separately provide a holding portion for holding the packaging material 650. Can be made simpler.
 本実施形態に係る医療器具610のように、包装材650に切れ目を形成することなく当該包装材650を開封させることができると次のような利点がある。包装材650に切れ目を形成させると、包装材650が細かく切れて、その破片が飛散して生体内へ導入されてしまう虞がある。これに対して、切れ目を形成せずに生体導入材70を包装材650から取り出すことが可能になれば、包装材650の飛散が生じることを未然に防止することができ、生体内に包装材650が導入されてしまうことをより好適に防止することができる。 If the packaging material 650 can be opened without forming a cut in the packaging material 650 like the medical device 610 according to the present embodiment, the following advantages are obtained. If a cut is formed in the packaging material 650, the packaging material 650 may be cut finely and the fragments may be scattered and introduced into the living body. On the other hand, if it becomes possible to take out the living body introduction material 70 from the packaging material 650 without forming a cut, it is possible to prevent the packaging material 650 from being scattered and the packaging material in the living body. It is possible to more suitably prevent 650 from being introduced.
 包装材650の外形形状は、第1実施形態において例示したような略球形の形状に形成することもできるが、例えば、図示するように、長尺部材620のルーメン621の内壁との接触面積が大きくなるように、長さ寸法が大きく形成されたものを使用することが好ましい。包装材650がこのような外形形状に形成されていると、包装材650が長尺部材620のルーメン621内を軸方向に沿って移動し易くなるため、包装材650の弁体660と長尺部材620に設けられた開放部630とを接触させ易くなる。 The outer shape of the packaging material 650 can be formed in a substantially spherical shape as exemplified in the first embodiment. For example, as shown in the figure, the contact area of the long member 620 with the inner wall of the lumen 621 is small. It is preferable to use one having a large length dimension so as to be large. When the packaging material 650 is formed in such an outer shape, the packaging material 650 can easily move in the lumen 621 of the long member 620 along the axial direction. It becomes easy to make the opening part 630 provided in the member 620 contact.
 図9(A)に示すように、長尺部材620へ流体を供給することにより当該長尺部材620のルーメン621内において包装材650を移動させることが可能であるが、例えば、図9(B)に示すように、押し子のような部材680を使用して包装材650をルーメン621内において移動させることもできる。また、例えば、この押し子680の先端側に設けられた押し部材685を包装材650内に導入して、包装材650と押し子680とを一体的に構成し、さらに、弁体660を一方弁などにより構成することにより、押し子680を移動させる操作で弁体660を開放させる構成とすることもできる。また、このような形態において、長尺部材620に開放部630を設けることにより、開放部630と押し子660とを併用して生体導入材70を包装材650から取り出す構成とすることもできる。 As shown in FIG. 9A, by supplying a fluid to the long member 620, the packaging material 650 can be moved in the lumen 621 of the long member 620. For example, FIG. ), The packaging material 650 can also be moved within the lumen 621 using a pusher-like member 680. In addition, for example, a pressing member 685 provided on the distal end side of the pusher 680 is introduced into the packaging material 650, and the packaging material 650 and the pusher 680 are integrally formed. It can also be set as the structure which opens the valve body 660 by operation which moves the pusher 680 by comprising by a valve. Moreover, in such a form, by providing the elongate member 620 with the opening 630, the living body introduction material 70 can be taken out from the packaging material 650 by using the opening 630 and the pusher 660 together.
 <変形例>
 次に、図10(A)、(B)を参照して、第2実施形態に係る医療器具の変形例について説明する。
<Modification>
Next, with reference to FIG. 10 (A) and (B), the modification of the medical device which concerns on 2nd Embodiment is demonstrated.
 本変形例に係る医療器具710には、上述した実施形態と同様に、包装材に切れ目を形成することなく当該包装材から生体導入材を漏洩させることが可能な開封部が設けられる。具体的には、包装材750に開口部770を設け、開封部を、この開口部770を開くための紐730によって構成している。 The medical device 710 according to the present modification is provided with an opening that can leak the living body introduction material from the packaging material without forming a cut in the packaging material, as in the above-described embodiment. Specifically, an opening 770 is provided in the packaging material 750, and the opening portion is constituted by a string 730 for opening the opening 770.
 図10(A)に示すように、包装材750は、開口部770が閉じられた状態で長尺部材720内に導入される。そして、図10(B)に示すように、長尺部材720のルーメン721内を移動させられた後、所定の位置で紐730を引っ張ることにより開口部770を開口して、内部に封入された生体導入材70を漏洩させる。なお、生体導入材70を漏洩させた後は、手元の操作により紐730を手繰り寄せて包装材750を回収したり、紐730により包装材750を保持して包装材750が生体内へ導入されることを防止したりすることもできる。 As shown in FIG. 10A, the packaging material 750 is introduced into the long member 720 with the opening 770 closed. Then, as shown in FIG. 10 (B), after being moved through the lumen 721 of the long member 720, the opening 770 is opened by pulling the string 730 at a predetermined position, and enclosed inside. The living body introduction material 70 is leaked. In addition, after leaking the living body introduction material 70, the string 730 is pulled by a manual operation to collect the packaging material 750, or the packaging material 750 is held by the string 730 and the packaging material 750 is introduced into the living body. Can also be prevented.
 本変形例に係る医療器具710においても、包装材750に切れ目を形成せずに生体導入材70を包装材750から取り出すことが可能になるため、包装材750の飛散が生じることを未然に防止することができ、生体内に包装材750が導入されてしまうことをより好適に防止することができる。 Also in the medical device 710 according to this modification, since the living body introduction material 70 can be taken out from the packaging material 750 without forming a cut in the packaging material 750, it is possible to prevent the packaging material 750 from being scattered. It is possible to prevent the packaging material 750 from being introduced into the living body.
 以上、本発明に係る医療器具および医療システムを複数の実施形態および複数の変形例に基づいて説明したが、本発明は、これらの実施形態および変形例のみに限定されるものではなく、特許請求の範囲の記載に基づいて適宜変更することが可能である。例えば、各実施形態において示した開封部を、長尺部材の先端面等に配置し、ルーメンの通過直後に包装材が開封されるように構成してもよい。このような構成においても、ルーメン内に生体導入材が付着等することを好適に防止することが可能になる。 As mentioned above, although the medical instrument and medical system which concern on this invention were demonstrated based on several embodiment and several modification, this invention is not limited only to these embodiment and modification, and is a claim. It is possible to change appropriately based on the description of the range. For example, the opening part shown in each embodiment may be arranged on the front end surface of the long member, and the packaging material may be opened immediately after passing the lumen. Even in such a configuration, it is possible to suitably prevent the living body introduction material from adhering to the lumen.
 本出願は、2012年9月28日に出願された日本国特許出願第2012-215399号に基づいており、その開示内容は、参照により全体として引用されている。 This application is based on Japanese Patent Application No. 2012-215399 filed on September 28, 2012, the disclosure of which is incorporated by reference in its entirety.
10、110、210、310、410、510、610、710 医療器具、
20 長尺部材、
21 ルーメン、
30 切断部(開封部)、
40 保持部、
41、43 保持用のメッシュ材、
50 包装材、
51 開封補助部、
60 流体供給部、
70 生体導入材、
100 医療システム、
127 引っ掛け部、
225 突き当て部、
251 包装材の第1径部、
253 包装材の第2径部、
255 包装材の中間部、
333 紐、
460 ガイド部材、
527 引っ掛け部、
630 開放部、
660 弁体、
730 紐、
770 包装材の開口部。
10, 110, 210, 310, 410, 510, 610, 710 medical device,
20 long member,
21 lumens,
30 cutting part (opening part),
40 holding part,
41, 43 mesh material for holding,
50 packaging materials,
51 opening assistance part,
60 fluid supply section,
70 living body introduction material,
100 medical system,
127 hook part,
225 butting part,
251 First diameter portion of the packaging material,
253 second diameter portion of the packaging material,
255 middle part of the packaging material,
333 string,
460 guide member,
527 hook,
630 opening,
660 disc,
730 string,
770 Opening of packaging material.

Claims (12)

  1.  先端側から基端側へ延伸されたルーメンを備える長尺部材と、
     前記長尺部材を介して生体内に導入される生体導入材を封入した包装材が前記ルーメンを通過する間に当該包装材を開封させる開封部と、を有することを特徴とする医療器具。
    A long member including a lumen extending from the distal end side to the proximal end side;
    A medical device comprising: a packaging material enclosing a living body introduction material introduced into the living body through the long member, and an opening portion for opening the packaging material while passing through the lumen.
  2.  前記開封部は、前記長尺部材に設けられており、かつ、前記包装材が前記ルーメンを通過するのに伴って当該包装材の少なくとも一部に前記生体導入材を漏洩させるための切れ目を形成する切断部を有することを特徴とする請求項1に記載の医療器具。 The opening portion is provided in the elongate member, and forms a cut for leaking the living body introduction material into at least a part of the packaging material as the packaging material passes through the lumen. The medical device according to claim 1, further comprising a cutting portion that performs cutting.
  3.  前記開封部は、前記長尺部材に設けられており、かつ、前記包装材に設けられ当該包装材を封止する弁体に接触することにより当該弁体を開放する開放部を有することを特徴とする請求項1に記載の医療器具。 The opening part is provided on the long member, and has an opening part that opens the valve body by contacting a valve body that is provided on the packaging material and seals the packaging material. The medical device according to claim 1.
  4.  前記開封部は、前記包装材に設けられた開口部に接続されており、かつ、閉じられた状態の当該開口部を開くための紐を有することを特徴とする請求項1に記載の医療器具。 The medical device according to claim 1, wherein the opening portion is connected to an opening portion provided in the packaging material and has a string for opening the opening portion in a closed state. .
  5.  前記長尺部材は、開封された前記包装材を当該長尺部材に保持させるための保持部をさらに有することを特徴とする請求項1~4のいずれか1項に記載の医療器具。 The medical device according to any one of claims 1 to 4, wherein the long member further includes a holding portion for holding the opened packaging material on the long member.
  6.  前記保持部は、前記ルーメン内において前記包装材を保持する保持用のメッシュ材を有することを特徴とする請求項5に記載の医療器具。 6. The medical instrument according to claim 5, wherein the holding part has a mesh material for holding the packaging material in the lumen.
  7.  前記保持部は、開封された前記包装材が前記ルーメンを通過する際に当該包装材が引っ掛けて保持される引っ掛け部を有することを特徴とする請求項5または請求項6に記載の医療器具。 The medical device according to claim 5 or 6, wherein the holding portion includes a hook portion that is hooked and held when the opened packaging material passes through the lumen.
  8.  前記包装材は、第1の径を備える第1径部と、前記第1径部よりも先端側に形成され、かつ、前記第1径部よりも小さな径を備える第2径部と、前記第1径部と前記第2径部とに連なる中間部と、を有しており、
     前記保持部は、前記包装材が前記ルーメンを通過する際に前記中間部が突き当てて保持される突き当て部を有することを特徴とする請求項5~7のいずれか1項に記載の医療器具。
    The packaging material includes a first diameter portion having a first diameter, a second diameter portion formed on a distal end side than the first diameter portion, and having a diameter smaller than the first diameter portion, An intermediate portion connected to the first diameter portion and the second diameter portion;
    The medical device according to any one of claims 5 to 7, wherein the holding portion has an abutting portion that is held against the intermediate portion when the packaging material passes through the lumen. Instruments.
  9.  前記包装材に取り付けられるとともに前記包装材を前記ルーメン内に導入した際に前記長尺部材の基端側から導出される紐をさらに有することを特徴とする請求項1~8のいずれか1項に記載の医療器具。 9. The apparatus according to claim 1, further comprising a string attached to the packaging material and led out from a proximal end side of the long member when the packaging material is introduced into the lumen. Medical device as described in.
  10.  前記長尺部材のルーメン内に配置され、前記ルーメン内において前記包装材が軸方向に沿って移動するように前記包装材の移動をガイドするガイド部材をさらに有することを特徴とする請求項1~9のいずれか1項に記載の医療器具。 The guide member further includes a guide member that is disposed in the lumen of the elongate member and guides the movement of the packaging material so that the packaging material moves along the axial direction in the lumen. 10. The medical instrument according to any one of 9 above.
  11.  前記包装材は、当該包装材の一部に、当該包装材の他の部位よりも開封され易く構成された開封補助部を有することを特徴とする請求項1~10のいずれか1項に記載の医療器具。 The packaging material according to any one of claims 1 to 10, wherein the packaging material has an opening assisting part configured to be easier to be opened than other parts of the packaging material, in a part of the packaging material. Medical instruments.
  12.  請求項1~11のいずれか1項に記載の医療器具と、
     前記包装材を前記ルーメン内において移動させるための流体を前記長尺部材へ供給する流体供給部と、を有することを特徴とする医療システム。
    A medical device according to any one of claims 1 to 11,
    And a fluid supply unit that supplies a fluid for moving the packaging material in the lumen to the elongated member.
PCT/JP2013/075571 2012-09-28 2013-09-20 Medical tool and medical system WO2014050766A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2012215399A JP2015231397A (en) 2012-09-28 2012-09-28 Medical device, and medical system
JP2012-215399 2012-09-28

Publications (1)

Publication Number Publication Date
WO2014050766A1 true WO2014050766A1 (en) 2014-04-03

Family

ID=50388169

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2013/075571 WO2014050766A1 (en) 2012-09-28 2013-09-20 Medical tool and medical system

Country Status (2)

Country Link
JP (1) JP2015231397A (en)
WO (1) WO2014050766A1 (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009500130A (en) * 2005-07-08 2009-01-08 シー・アール・バード・インコーポレイテツド Drug delivery system
JP4582391B2 (en) * 2003-12-26 2010-11-17 株式会社ウエットトラストジャパン Portable injection injector

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4582391B2 (en) * 2003-12-26 2010-11-17 株式会社ウエットトラストジャパン Portable injection injector
JP2009500130A (en) * 2005-07-08 2009-01-08 シー・アール・バード・インコーポレイテツド Drug delivery system

Also Published As

Publication number Publication date
JP2015231397A (en) 2015-12-24

Similar Documents

Publication Publication Date Title
KR101996709B1 (en) Single-use disposable set connector
ES2928322T3 (en) Apparatus and method of vial transfer and injection
JP5023121B2 (en) Fluid control device for drug supply
CN102905751B (en) The conduit dressing of sealed, sterile
JP2011504771A (en) Assembly for wetting a medical device
JP2021515676A (en) Injection or infusion device with improved release liner
CN104689467A (en) Medicament device
EP2853210B1 (en) Bone treatment system
JP5963744B2 (en) Pharmaceutical composition application device
US9233227B2 (en) Operating member
EP2673026B1 (en) Coupling devices and kits thereof
JP2012010930A (en) Medicine administration appliance
WO2014050766A1 (en) Medical tool and medical system
JP6417007B2 (en) Connections and medical kits
WO2022138740A1 (en) Medical device, and medical device set
KR101939858B1 (en) Integrated puncture needle adapter
JP4608462B2 (en) Catheter assembly
BR112013024198B1 (en) METHOD OF PRODUCTION OF A BAG TO RECEIVE MEDICAL FLUIDS, BAG AND METHOD OF REMOVAL OF A MEDICAL FLUID
JP6719546B2 (en) Drug infusion catheter and drug infusion system
WO2019189434A1 (en) Medicating appliance and liquid medicine administering system
TW202039015A (en) Syringe for drug mixing kit, drug mixing kit and method for manufacturing the same
WO2014002733A1 (en) Medical instrument
CN105555203A (en) Fluid delivery device
JP2008161240A (en) Medicine application tube
WO2021177217A1 (en) Hemostatic agent injection device

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 13840689

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 13840689

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: JP