WO2006046703A1 - 電極及びイオントフォレーシス装置 - Google Patents
電極及びイオントフォレーシス装置 Download PDFInfo
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- WO2006046703A1 WO2006046703A1 PCT/JP2005/019909 JP2005019909W WO2006046703A1 WO 2006046703 A1 WO2006046703 A1 WO 2006046703A1 JP 2005019909 W JP2005019909 W JP 2005019909W WO 2006046703 A1 WO2006046703 A1 WO 2006046703A1
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- electrode
- conductive
- conductive sheet
- terminal member
- carbon fiber
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N1/00—Electrotherapy; Circuits therefor
- A61N1/18—Applying electric currents by contact electrodes
- A61N1/20—Applying electric currents by contact electrodes continuous direct currents
- A61N1/30—Apparatus for iontophoresis, i.e. transfer of media in ionic state by an electromotoric force into the body, or cataphoresis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N1/00—Electrotherapy; Circuits therefor
- A61N1/02—Details
- A61N1/04—Electrodes
- A61N1/0404—Electrodes for external use
- A61N1/0408—Use-related aspects
- A61N1/0428—Specially adapted for iontophoresis, e.g. AC, DC or including drug reservoirs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N1/00—Electrotherapy; Circuits therefor
- A61N1/02—Details
- A61N1/04—Electrodes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N1/00—Electrotherapy; Circuits therefor
- A61N1/02—Details
- A61N1/04—Electrodes
- A61N1/0404—Electrodes for external use
- A61N1/0472—Structure-related aspects
- A61N1/048—Electrodes characterised by a specific connection between lead and electrode
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N1/00—Electrotherapy; Circuits therefor
- A61N1/02—Details
- A61N1/04—Electrodes
- A61N1/0404—Electrodes for external use
- A61N1/0472—Structure-related aspects
- A61N1/0492—Patch electrodes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N1/00—Electrotherapy; Circuits therefor
- A61N1/02—Details
- A61N1/04—Electrodes
- A61N1/0404—Electrodes for external use
- A61N1/0408—Use-related aspects
- A61N1/0428—Specially adapted for iontophoresis, e.g. AC, DC or including drug reservoirs
- A61N1/0432—Anode and cathode
- A61N1/0436—Material of the electrode
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N1/00—Electrotherapy; Circuits therefor
- A61N1/02—Details
- A61N1/04—Electrodes
- A61N1/0404—Electrodes for external use
- A61N1/0408—Use-related aspects
- A61N1/0428—Specially adapted for iontophoresis, e.g. AC, DC or including drug reservoirs
- A61N1/0444—Membrane
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N1/00—Electrotherapy; Circuits therefor
- A61N1/02—Details
- A61N1/04—Electrodes
- A61N1/0404—Electrodes for external use
- A61N1/0408—Use-related aspects
- A61N1/0428—Specially adapted for iontophoresis, e.g. AC, DC or including drug reservoirs
- A61N1/0448—Drug reservoir
Definitions
- the present invention relates to an electrode used in an apparatus for energizing a living body, such as an iontophoresis device or a low-frequency treatment device, and more specifically, has a low surface resistance and is a metal ion living body. It is related with the electrode in which the countermeasure about transfer to was taken.
- the present invention also relates to an iontophoresis device including an electrode having a low sheet resistance and a countermeasure against the migration of metal ions to a living body.
- Devices such as iontophoresis devices and low-frequency treatment devices are designed to energize living bodies (human bodies, etc.) through the skin to administer drugs or obtain effects such as massage. It is summer.
- an electrode used for energizing a living body often includes a terminal member formed of a metal material for receiving energization from the apparatus main body, A conductive sheet having a certain area (for example, about 10 to 50 ⁇ ⁇ , or about 10 to 50 mm square) electrically connected to the terminal member, and in many cases, the conductive sheet and the living body An additional member is provided between the skin and the skin for improving the adhesion with the skin (or for holding a drug for administration to a living body).
- the conductive grease in which carbon powder is mixed in the conductive sheet is used.
- a highly flexible sheet material such as a conductive silicon rubber or a metal thin film is used.
- the conductive sheet in this type of electrode has a certain area in order to increase the drug administration efficiency or obtain an appropriate massage effect.
- the resistance value of the conductive sheet increases, the current density of the part force away from the terminal member force on the conductive sheet decreases, and the current is applied only slightly in the vicinity of the terminal member. The area power will be done.
- a conductive sheet made of a metal thin film often has a low resistance and can easily obtain sufficient flexibility by a thin film, but the conductive sheet is not suitable for energization of a living body. Metal components may ionize and migrate into the body, causing health hazards.
- Patent Document 1 JP 2002-233584 A
- the present invention is an electrode used for energization of a living body, and has a low resistance value. Therefore, when energizing, the entire conductive sheet has a more uniform current density.
- An object of the present invention is to provide an electrode that can be energized and has solved the problem of migration of metal ions to a living body, and an iontophoresis device that uses this electrode.
- An electrode having a conductive terminal member made of a nonmetallic material and a conductive sheet made of a nonmetallic material attached to the terminal member,
- the conductive sheet has an intrinsic resistance lower than that of the terminal member.
- both the terminal member for receiving power from devices such as an iontophoresis device and a low frequency treatment device and the conductive sheet for energizing the living body are made of metal. It is possible to solve the problem of migration of metal ions to the living body during energization because they are composed of materials.
- both the conductive sheet and the terminal member are also configured with non-metallic material force
- both the conductive sheet and the terminal member are also configured with non-metallic material force
- it is configured, as a conductive sheet, it is possible to ensure safety to the living body, and as long as it has a certain degree of flexibility, it is possible to select a wide range of non-metallic materials with a low specific resistance
- terminal members as long as they have strength, durability, and chemical resistance as terminals, it is possible to use even materials with high specific resistance to some extent, so the range of material selection is expanded. It becomes possible.
- the conductive sheet has a surface resistance value of 1 to 30 ⁇ , particularly 1 to 10 ⁇ , so that the entire surface force of the conductive sheet is substantially uniform. It is possible to conduct electricity at a high current density.
- the conductive sheet of the present invention is made of carbon fiber or carbon fiber paper. It is preferable to comprise.
- the carbon fiber may be a natural fiber carbon fiber or polyacrylic acid as long as it has sufficiently high conductivity to allow energization with a substantially uniform current density of the entire surface of the conductive sheet.
- Any type of carbon fiber such as tolyl-based carbon fiber, pitch-based carbon fiber, and rayon-based carbon fiber can be used.
- carbon fiber paper any carbon fiber can be matted or paper-shaped using papermaking technology. What was shape
- the conductive sheet of the present invention can also be composed of carbon fiber or carbon fiber paper, and a polymer elastomer impregnated in the carbon fiber or carbon fiber paper. Alternatively, it is possible to prevent deterioration of the electrode quality due to the dropping of the carbon fiber paper, and to improve the handleability of the electrode in the manufacturing process.
- thermoplastic polyurethane a material that does not contain a toxic substance for a living body having high flexibility, such as thermoplastic polyurethane.
- a non-metallic conductive filler is dispersed in the polymer elastomer. It is preferable to use a polymer elastomer whose conductivity is improved by,
- the terminal member according to the present invention includes a polymer matrix and a polymer matrix. It should preferably be composed of non-metallic conductive filler that is scattered.
- silicon rubber or silicone resin is particularly preferably used from the viewpoint of safety to the living body, but sufficient mechanical strength and durability sufficient to serve as a connection terminal.
- Other rubber materials such as natural rubber and synthetic rubber, or other natural or synthetic resin materials such as thermosetting resin and thermoplastic resin can be used as long as the properties such as It is.
- carbon can be particularly preferably used. Specifically, graphite, graphite, carbon black, or glassy carbon is used. It is possible to use short fibers cut from fine powder or carbon fiber
- the amount of carbon mixed into the polymer matrix is a force that can be determined by the balance between strength and electrical conductivity required for the terminal member.
- the terminal of the present invention Since the member can have a relatively thick cross section and a short length, it is not always necessary to have a highly conductive composition.
- silicon rubber is used as a polymer matrix.
- carbon black is used as carbon, the composition can be 20 to 60 parts by weight of carbon black per 100 parts by weight of silicon rubber.
- the terminal member can be attached to the conductive sheet.
- the terminal member can be attached to the conductive sheet by integral molding, whereby the manufacturing cost of the electrode can be reduced.
- the terminal member in the present invention is a male type that fits into a female type (or male type) fitting part of a connector connected to a power source such as an iontophoresis device or a low frequency treatment device. (Or female type) It is possible to provide a fitting part, which improves the convenience of connection operation. It can be done.
- the electrode of the present invention is desired to be energized at a uniform current density with a wider area force, and to the living body of metal ions. It is particularly suitable for use in an iontophoresis device in which it is necessary to avoid this migration.
- the electrode of the present invention as at least one of the working electrode structure and the non-working electrode structure provided in the iontophoresis device.
- the electrode of the present invention in the case of an iontophoresis device that administers a dissociating drug, at least in the case of an iontophoresis device that uses the electrode of the present invention in the non-working side electrode structure and administers a drug dissociating into positive ions. If so, it is preferable to use the electrode of the present invention in at least the working electrode structure.
- the iontophoresis device of the present invention comprises:
- the working electrode structure is
- a first electrode connected to a terminal of the first conductivity type of the power source
- a first conductive medium layer disposed in front of the first electrode
- a drug layer that is disposed in front of the first ion exchange membrane and holds a drug solution containing a drug dissociated into ions of the first conductivity type;
- a second ion exchange membrane disposed on the front surface of the drug layer and selecting ions of the first conductivity type
- the non-working side electrode structure is
- a second electrode connected to the second conductivity type terminal of the power source
- a second conductive medium layer disposed on the front surface of the second electrode
- An electrode having a conductive terminal member made of a nonmetallic material and a conductive sheet made of a nonmetallic material attached to the terminal member It is particularly preferable that the conductive sheet is an electrode having a lower specific resistance than the terminal member, thereby suppressing the transfer of ions having a conductivity type opposite to that of drug ions from the living body to the working electrode. Drug ions efficiently into the living body, and H + ions, OH- ions, etc.
- the non-working side electrode structure in the iontophoresis device further selects the second conductivity type ions arranged on the front surface of the second conductive medium layer.
- a third conductive medium layer disposed on the front surface of the fourth ion exchange membrane
- the first or second conductivity type means plus or minus
- the ion exchange membrane for selecting the first or second conductivity type ion is plus ion or minus ion.
- FIG. 1 (a) is a plan view of an electrode 10a according to an embodiment of the present invention
- FIGS. 1 (b) and 1 (c) are cross-sectional views of the electrode 10a.
- the electrode 10a is a terminal formed of conductive silicon rubber having a male fitting portion 11a, a body portion ib, and a joint portion 11c. And a member 11 and a conductive sheet 12 made of carbon fiber obtained by carbonizing a woven fabric such as silk or cotton by high-temperature treatment.
- the terminal member 11 is made of 140 to 140 pounds of a compound in which 50 parts by weight of carbon black and 5 parts by weight of a sulfur-based vulcanizing agent are blended in 100 parts by weight of silicon rubber in a mold disposed on the conductive sheet 12. It is vulcanized at 160 ° C, and the silicone rubber and carbon black in the above compound are solidified in a state of being impregnated in the carbon fibers constituting the conductive sheet 12 during the vulcanization process. It is integrated with the sheet 12.
- the electrode 10a is used for protecting the upper surface of the conductive sheet 12, or when the electrode 10a is used in combination with a liquid such as a conductive medium, as will be described later.
- a cover 13 as shown in FIG. 1 (c) can be provided.
- FIGS. 2A to 2C are cross-sectional views of electrodes 10b to LOd according to another embodiment of the present invention.
- the electrodes 10b to 10d in FIGS. 2 (a) to 2 (c) are provided with a terminal member 11 and a conductive sheet 12 formed of the same material as the electrode 10a.
- the electrode 10a shown in FIG. The manner of attaching the conductive sheet 12 to the terminal member 11 is different!
- the conductive sheet 12 is engaged with a small hole provided at the center thereof. It is attached to the terminal member 11 by inserting the stop portion l ie.In the electrode 10c of FIG. 2 (b), the width of the locking portion 11e is further narrowed, and the tapered shape is formed. The conductive sheet 12 can be easily inserted into the small holes. Further, in the electrode 10d of FIG. 2 (c), a shaft hole is formed in the body portion 1 lb of the terminal member 11, and the shaft 14a of the stopper 14 made of conductive silicon rubber similar to the terminal member 11 is used as the shaft hole. The conductive sheet 12 is sandwiched between the engaging portions 14b of the stopper 14 by being inserted.
- each of the electrodes 10a to 10d a device such as an iontophoresis device or a low-frequency treatment device is used.
- the wiring from the vessel is connected to the male fitting part 11a, and the current to the living body passes through the male fitting part 11a ⁇ trunk l lb ⁇ joint l lc ⁇ conductive sheet 12 and below the conductive sheet 12 To the biological skin located in
- the size of the body portion l ib can be configured to be large and short, for example, l to 3 mm, ⁇ diameter X O. 5 to 2 mm, and the like. Even if the material constituting the material does not necessarily have high conductivity, it is easy to prevent the energization of the conductive sheet 12 by setting the shape and dimensions of the terminal member 11, Therefore, it is possible to design the terminal member 11 with priority given to characteristics such as strength, durability, and chemical resistance.
- the conductive sheet made of carbon fiber has a very low surface resistance such as 1 to 10 ⁇ well (4 probe method, JIS K71 94), the current led from the joint 11c is conducted. The entire area force of the electric sheet is also uniformly guided to the living skin.
- carbon fiber paper obtained by forming carbon fibers into a mat shape or a paper shape by using a papermaking technique can be used for the conductive sheet 12 of the electrodes 10a to: LOd. Yes, or carbon fiber or carbon fiber paper impregnated with a polymer elastomer made of thermoplastic polyurethane or silicon rubber can be used.
- the surface resistance of the conductive sheet is 1 to: It can be set to a very low value such as ⁇ ⁇ .
- a thin film member impregnated with a conductive medium is interposed between the conductive sheet 12 and the living skin, or the conductive sheet 12
- a part of the conductive medium permeates the carbon fiber of the conductive sheet 12, and the conductive sheet 12 is energized.
- a thin film member, or a conductive state between the conductive sheet and the conductive medium becomes better.
- energization from a device such as an iontophoresis device or a low-frequency treatment device may be performed by connecting a metal connector having a female fitting portion to the male fitting portion 11a.
- the body portion 1 lb is separated from the male fitting portion 1 la and the conductive sheet 12 which may come into contact with such a metal member. ! /, Or in the case where a cover 13 is provided on the conductive sheet 12, in order to be further protected by the cover 13, the electric power of such a metal member Generation of metal ions by decomposition and migration of such metal ions into the conductive sheet 12 or conductive medium is prevented.
- each of the electrodes 10a to 10d has a preferable characteristic as an electrode used for energization of the living body.
- the electrode 10a is the electrode 10b to the locking portion l in the LOd.
- it is a configuration that does not have a convex protrusion on the side of the conductive sheet 12, and is particularly preferable in that the adhesion between the living body skin and the electrode can be kept better.
- the electrode of the present invention has a metal reinforcing member 15 on the terminal member 11 in addition to the above-described configuration as illustrated in 10e and 10f of FIGS. 3 (a) and 3 (b). It is also possible to install it, thereby improving the strength and durability of the terminal member 11 or improving the contact between the terminal member 11 and the connector when the electrode is energized through the connector. be able to.
- FIG. 4 is an explanatory diagram showing the configuration of an iontophoresis device using the electrode of the present invention.
- the iontophoresis device 20 a includes a working electrode structure 21, a non-working electrode structure 22, and a power source 23 as large components (members).
- Reference numeral 27 indicates living body skin (or mucous membrane).
- the working electrode structure 21 is connected to the first conductive type terminal of the power source 23 via the cord 24a and the female connector 25a, and maintains electrical connection with the electrode 30.
- a first conductive medium layer 33 disposed on the first conductive medium layer 33 and a conductive type opposite to the first conductive type disposed on the front surface of the first conductive medium layer 33 (hereinafter referred to as “second conductive type”).
- the whole is housed in a cover or container 26a.
- the non-working side electrode structure 22 is connected to the second conductivity type terminal of the power source 23 with the cord 24b, the The electrode 40 connected via the connector 25b, the second conductive medium layer 43 arranged so as to keep an electrical connection with the electrode 40, and arranged on the front surface of the second conductive medium layer 43
- the ion exchange membrane 46 for selecting ions of the above conductivity type is provided, and the whole is accommodated in a cover container 26b.
- the electrodes 30 and 40 are conductive silicon including an os-type fitting portion 1 la, a body portion l ib, and a joint portion 11c in the same manner as the electrodes 10a to LOf shown in Figs.
- a terminal member 11 made of rubber and a conductive sheet 12 made of carbon fiber obtained by carbonizing a woven fabric such as silk or cotton by high-temperature treatment are provided.
- the shapes and dimensions of the terminal member 11 and the conductive sheet 12 can be determined as appropriate in consideration of the strength and handleability of the electrodes 30 and 40, the drug administration efficiency, and the like.
- the member 11 uses a composition in which 20 to 60 parts by weight of carbon black is combined with 100 parts by weight of silicon rubber, and the male fitting part 11a is formed into a curved shape of about 2.3 mm ⁇ .
- b is formed in a cylinder shape of 2. Omm ⁇ and length of about 10 mm, and the joint is formed in a disk shape of about 4.0 mm ⁇ and thickness of about 0.5 mm
- the conductive sheet 12 is a woven cloth such as silk cloth or cotton. It can be made into a 30 mm ⁇ (thickness of about 0.5 mm) circular sheet made of carbon fiber carbonized by high-temperature treatment.
- Conductive media such as phosphate buffered saline and physiological saline are used for the conductive media layers 33, 43, and 45 in order to improve the electrical connection between the electrodes 30 and 40 and the conductive sheet 12. Is used.
- the above-mentioned conductive medium is subjected to an electrolytic reaction of water (with a positive electrode). From the viewpoints of biosafety and economy (inexpensive and easy to obtain), it is possible to add compounds.
- the conductive medium layers 33, 43, 45 may be formed of a polymer material or the like in order to hold the conductive medium as described above in a liquid state or to improve handling.
- the conductive medium as described above may be impregnated and held in the water-absorbing thin film body.
- Examples of materials that can be used as the water-absorbing thin film in this case include acrylic hydrogel films, segmented polyurethane gel films, and ion-conductive porous sheets for forming gelled solid electrolytes (for example, JP disclosed in Akira 11- two hundred seventy-three thousand four hundred fifty-two, acrylonitrile least 50 mol% (preferably 70 to 98 mole 0/0), porosity 20 to 80% acrylic - porous polymers based on tolyl co polymer)
- the impregnation rate of the conductive medium impregnated in this is 100 X (W-D) ZD [% where D is the weight when dried and W is the weight after impregnation. ]) Is preferably 30 to 40% impregnation rate.
- the drug layer 35 holds a drug solution in which the medicinal component is ionically dissociated into drug ions of the first conductivity type having the same conductivity type as the terminal to which the working electrode structure 21 is connected.
- this drug layer 35 may be a liquid that holds the drug solution in a liquid state or is made of a polymer material or the like for improved handling.
- the formed water-absorbing thin film body for example, an acrylic hydrogel film may be impregnated with the drug solution and held.
- ion exchange membranes 34, 36, 44, and 46 that select ions of the first or second conductivity type include Neocepta manufactured by Tokuma Corporation (NEOSEPTA, CM-1, CM-2, CMX).
- Cation exchange membranes such as CMS, CMB) or key-on exchange membranes such as Tokama Neoceptor (NEOSEPTA, AM-1, AM-3, AMX, AHA, ACH, ACS) can be used.
- a cation exchange membrane in which a part or all of the voids of the porous film is filled with an ion exchange resin having a cation exchange capacity, or an ion exchange resin having an anion action is used.
- a packed anion exchange membrane can be preferably used.
- the ion-exchange resin a fluorine-based resin in which an ion-exchange group is introduced into a perfluorocarbon skeleton, or a hydrocarbon-based resin having a non-fluorinated resin as a skeleton.
- hydrocarbon-based ion exchange resins are preferred because of the simplicity of the manufacturing process.
- the filling rate of the ion exchange resin is related to the porosity of the porous film, it is generally 5 to 95% by mass, particularly 10 to 90% by mass, and further 20 to 60% by mass. % Is preferable.
- the ion exchange group possessed by the ion exchange resin is not particularly limited as long as it is a functional group that generates a group having a negative or positive charge in an aqueous solution.
- Specific examples of such functional groups that can serve as ion exchange groups include sulfonic acid groups, carboxylic acid groups, and phosphonic acid groups. These acid groups may exist as a free acid or in the form of a salt.
- Examples of the counter cation in the case of a salt include alkali metal cations such as sodium ion and potassium ion, and ammonium ions. Of these cation exchange groups, sulfonic acid groups that are strongly acidic groups are generally particularly preferred.
- anion exchange group examples include primary to tertiary amino groups, quaternary ammonium groups, pyridyl groups, imidazole groups, quaternary pyridinium groups, and quaternary imidazolium groups.
- counter ions in these anion exchange groups include halogen ions such as chlorine ions and hydroxy ions.
- anion exchange groups generally, quaternary ammonium groups and quaternary pyridinium groups, which are strongly basic groups, are preferably used.
- porous film a film having a large number of pores communicating with the front and back or a sheet-like one is used without particular limitation, but in order to achieve both high strength and flexibility. It is preferably made of thermoplastic rosin.
- the thermoplastic resin constituting this porous film includes ethylene, propylene, 1-butene, 1-pentene, 1-hexene, 3-methyl 1-butene, 4-methyl 1-pentene, 5- Polyolefin resins such as homo- or copolymers of olefins such as methyl-1-heptene; polysalt-bulle, salt-butyl acetate butyl copolymer, salt-vinyl-vinylidene chloride copolymer Polymer, vinyl chloride resin such as vinyl chloride copolymer; polytetrafluoroethylene, polytrifluoroethylene, polyvinylidene fluoride, tetrafluoroethylene monohexafluoropropylene Fluororesin such as copolymer, tetrafluoroethylene perfluoroalkyl butyl ether copolymer, tetrafluoroethylene ethylene copolymer; nylon 6, nylon Polyamide resin, such as 66; Polyimide resin
- the properties of the porous film made of the above-described thermoplastic resin are not particularly limited! However, the average pore size of the pores is thin and excellent in strength, and also has a low electrical resistance and the point of shielding. 1S is preferably 0.25 to 5.0 m, more preferably 0.10 to 2.0 m, and most preferably 0.02 to 0.2 m. In addition, the said average hole diameter means the average flow hole diameter measured based on the bubble point method (JIS K3 832-1990). Similarly, the porosity of the porous film is preferably 20 to 95%, more preferably 30 to 90%, and most preferably 30 to 60%.
- the thickness of the porous film is preferably 5 to 140 m, more preferably 10 to 120 m, and most preferably 15 to 55 m so that the ion exchange membrane has a thickness as described later. Is good.
- the ion exchange membrane and the cation exchange membrane using such a porous film have a thickness of the porous film + about 0 to 20 m.
- the drug ions in the drug layer 35 dissociated into the first conductivity type ions by the voltage applied from the power source 23 pass through the ion exchange membrane 36 and the skin 27. It is administered in vivo.
- the action of the ion exchange membranes 34, 36, 44, 46 prevents ions having a conductivity type opposite to that of the drug ions from moving to the drug layer 35 side from the living body side.
- the movement of H + and OH ⁇ generated in the above to the skin 27 side is suppressed, and it is possible to stably administer drug ions efficiently for a long time while suppressing the pH change on the skin 27.
- the conductive sheets of the electrodes 30 and 40 are formed of 12-force low-resistance carbon fibers, so that the conductive medium layer 33Z ion-exchange membrane 34Z drug layer 35Z ion-exchange membrane 36, or the conductive medium layer 43Z ion-exchange membrane 44Z conductive medium layer 45Z
- the ion-exchange membrane 46 is energized so that the entire force of the conductive sheet 12 has a very uniform current density.
- the iontophoresis device of the present invention can further increase the administration efficiency of the drug to the living body.
- the iontophoresis device of the present invention has a working electrode structure 21 and a non-working electrode.
- the necessity of using a metal material inside the structure 22 is eliminated, and therefore migration of metal ions caused by electrolysis or the like to the living body is prevented.
- the conductive medium layers 33 and 43 hold the conductive medium in a liquid state, or alternatively, the water-absorbing thin film formed of a polymer material or the like as the conductive medium. Even when impregnated and held in the body, depending on the amount of impregnation, a part of the conductive medium will permeate the carbon fibers constituting the conductive sheet 12 of the electrodes 30 and 40, and the conductive sheet 12 and the conductive sheet 12 will become conductive. The conductive state with the conductive medium layers 33 and 43 is kept better.
- the conductive sheet 12 and the female connectors 25a and 25b are separated by at least the body part ib, even if the female connectors 25a and 25b are made of metal, Further, even when the conductive medium of the conductive medium layers 33 and 43 penetrates into the conductive sheet 12, the metal components of the female connectors 25a and 25b are ionized and migrate to the conductive sheet 12, or ! I have no concerns about moving to a living body.
- FIGs. 5 and 6 are explanatory diagrams showing configurations of iontophoresis devices 20b and 20c according to other embodiments.
- the non-working side electrode structure 22 does not have the ion exchange membrane 44 and the third conductive medium layer 45, and the iontophoresis device 20c is inactive.
- the side electrode structure 22 does not have the ion exchange membrane 44, the third conductive medium layer 45, and the ion exchange membrane 46, and is the same as the iontophoresis device 20a shown in FIG.
- FIG. 7 is an explanatory diagram showing how the electrode of the present invention is used in the low frequency treatment device 50.
- the low frequency treatment device 50 is energized through the low frequency treatment device main body 51, the cords 52 and 52, and the female connectors 53 and 53 from the low frequency treatment device main body 51.
- a pair of electrodes 54, 54 is provided.
- the electrode 54 is made of conductive silicon rubber having a male fitting portion lla, a monthly part 1 lb, and a joint 1 lc, similar to the electrodes 10a to LOF shown in FIGS.
- the terminal member 11 is formed, and a conductive sheet 12 made of carbon fiber obtained by carbonizing a woven fabric such as silk or cotton by high-temperature treatment.
- a conductive adhesive layer 55 made of a gel body such as polyhydroxymetatalylate impregnated with a conductive medium such as an aqueous potassium chloride solution is disposed below the conductive sheet 12. The skin is energized through the conductive adhesive layer 55.
- reference numeral 56 in the figure denotes a cover for protecting the upper surface of the conductive sheet 12.
- the entire surface force of the conductive sheet 12 can be energized with a very uniform current density. Therefore, an action such as massage can be applied to a living body without causing discomfort due to the concentration of current in a narrow range.
- thermoplastic resins such as polyethylene, polystyrene, polychlorinated butyl, polyester and polycarbonate, phenol resin, epoxy resin, polyurethane resin, silicon resin, etc.
- the thermosetting resin can be used.
- the carbon used for the terminal member various carbon materials such as graphite, graphite, carbon black, glassy carbon fine powder, or short fibers cut from carbon fibers may be used. it can.
- the blending ratio of carbon to the polymer matrix is appropriately determined in consideration of necessary mechanical characteristics, electrical characteristics, durability, etc., depending on the polymer matrix used and the type of carbon. Is possible.
- the conductive sheet it is also possible to use carbon fiber paper obtained by forming carbon fiber into a mat shape or a paper shape using a papermaking technique.
- carbon fiber or carbon fiber paper is impregnated with a polymer such as silicon rubber or thermoplastic polyurethane, and this is used as the conductive sheet. It is also possible to use it.
- the conductive sheet may have any shape such as a square or a polygon. Can do.
- the terminal member and the conductive sheet in the electrode of the present invention are appropriately fixed to such an extent that the terminal member and the conductive sheet do not cause a problem in use, and necessary conduction between the two is ensured.
- the method is not limited to the method described in the above embodiment, and can be performed by any method.
- the terminal member is attached near the center of the conductive sheet.
- the terminal member is attached at an arbitrary position including the end portion of the conductive sheet. Can be attached.
- the electrode force iontophoresis device or the low-frequency treatment device of the present invention is used has been described.
- the electrode of the present invention may be an electrocardiograph or a facial device. It can be used as an electrode for any other device that is energized to a living body.
- FIG. 1 (a) is a plan view of an electrode according to an embodiment of the present invention, and (b) and (c) are cross-sectional views of the electrode.
- FIG. 2] (a) to (c) are cross-sectional views of an electrode according to another embodiment of the present invention.
- FIG. 3 (a) and (b) are cross-sectional views of an electrode according to another embodiment of the present invention.
- FIG. 4 is an explanatory view showing a configuration of an iontophoresis device using an electrode of the present invention, which is an iontophoresis device according to an embodiment of the present invention.
- FIG. 5 is an explanatory diagram showing a configuration of an iontophoresis device according to another embodiment of the present invention.
- FIG. 6 is an explanatory diagram showing a configuration of an iontophoresis device according to another embodiment of the present invention.
- FIG. 7 is an explanatory diagram showing how the electrode of the present invention is used in a low-frequency treatment device.
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Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP05805338A EP1808197A4 (en) | 2004-10-29 | 2005-10-28 | ELECTRODE AND IONTOPHORESIS DEVICE |
CA002585355A CA2585355A1 (en) | 2004-10-29 | 2005-10-28 | Electrode and iontophoresis apparatus |
JP2006542346A JPWO2006046703A1 (ja) | 2004-10-29 | 2005-10-28 | 電極及びイオントフォレーシス装置 |
BRPI0518072-4A BRPI0518072A (pt) | 2004-10-29 | 2005-10-28 | eletrodo e dispositivo de iontoforese |
AU2005297817A AU2005297817A1 (en) | 2004-10-29 | 2005-10-28 | Electrode and iontophoresis apparatus |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004317317 | 2004-10-29 | ||
JP2004-317317 | 2004-10-29 | ||
US11/171,953 | 2005-06-30 | ||
US11/171,953 US20060095001A1 (en) | 2004-10-29 | 2005-06-30 | Electrode and iontophoresis device |
Publications (1)
Publication Number | Publication Date |
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WO2006046703A1 true WO2006046703A1 (ja) | 2006-05-04 |
Family
ID=36263019
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/JP2005/019909 WO2006046703A1 (ja) | 2004-10-29 | 2005-10-28 | 電極及びイオントフォレーシス装置 |
Country Status (11)
Country | Link |
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US (1) | US20060095001A1 (ja) |
EP (1) | EP1808197A4 (ja) |
JP (1) | JPWO2006046703A1 (ja) |
KR (1) | KR20070084592A (ja) |
CN (1) | CN101048192A (ja) |
AU (1) | AU2005297817A1 (ja) |
BR (1) | BRPI0518072A (ja) |
CA (1) | CA2585355A1 (ja) |
RU (1) | RU2387466C2 (ja) |
SG (1) | SG142331A1 (ja) |
WO (1) | WO2006046703A1 (ja) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7890164B2 (en) | 2005-09-15 | 2011-02-15 | Tti Ellebeau, Inc. | Iontophoresis device |
US8062783B2 (en) | 2006-12-01 | 2011-11-22 | Tti Ellebeau, Inc. | Systems, devices, and methods for powering and/or controlling devices, for instance transdermal delivery devices |
US8295922B2 (en) | 2005-08-08 | 2012-10-23 | Tti Ellebeau, Inc. | Iontophoresis device |
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Families Citing this family (44)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10205373B4 (de) * | 2002-02-09 | 2007-07-19 | Aloys Wobben | Brandschutz |
WO2006055729A1 (en) * | 2004-11-16 | 2006-05-26 | Transcutaneous Technologies Inc. | Iontophoretic device and method for administering immune response-enhancing agents and compositions |
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US8386030B2 (en) | 2005-08-08 | 2013-02-26 | Tti Ellebeau, Inc. | Iontophoresis device |
US20070088332A1 (en) * | 2005-08-22 | 2007-04-19 | Transcutaneous Technologies Inc. | Iontophoresis device |
US20090254018A1 (en) * | 2005-08-24 | 2009-10-08 | Mizuo Nakayama | Electrode assembly for freezing-type iontophoresis device |
WO2007026672A1 (ja) * | 2005-08-29 | 2007-03-08 | Transcu Ltd. | イオントフォレーシス用汎用性電解液組成物 |
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US20070112294A1 (en) * | 2005-09-14 | 2007-05-17 | Transcutaneous Technologies Inc. | Iontophoresis device |
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WO2007037476A1 (ja) * | 2005-09-30 | 2007-04-05 | Tti Ellebeau, Inc. | 睡眠導入剤と興奮剤の投与量および投与時期を制御するイオントフォレーシス装置 |
JP4902543B2 (ja) * | 2005-09-30 | 2012-03-21 | Tti・エルビュー株式会社 | 形状記憶セパレータを有するイオントフォレーシス用電極構造体およびそれを用いたイオントフォレーシス装置 |
JP2009509659A (ja) * | 2005-09-30 | 2009-03-12 | Tti・エルビュー株式会社 | 生体界面への活性物質の送達のイオントフォレーシス装置及び方法 |
JP2009509657A (ja) * | 2005-09-30 | 2009-03-12 | Tti・エルビュー株式会社 | 生体界面への活性物質の送達のイオントフォレーシス装置及び方法 |
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US20070232983A1 (en) * | 2005-09-30 | 2007-10-04 | Smith Gregory A | Handheld apparatus to deliver active agents to biological interfaces |
US20070078445A1 (en) * | 2005-09-30 | 2007-04-05 | Curt Malloy | Synchronization apparatus and method for iontophoresis device to deliver active agents to biological interfaces |
JP2009509656A (ja) * | 2005-09-30 | 2009-03-12 | Tti・エルビュー株式会社 | 生体界面に活性物質を送達するイオントフォレーシス装置における動作不良を検出するための方法及びシステム |
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US20080058701A1 (en) * | 2006-07-05 | 2008-03-06 | Transcutaneous Technologies Inc. | Delivery device having self-assembling dendritic polymers and method of use thereof |
WO2008027440A2 (en) * | 2006-08-29 | 2008-03-06 | Tti Ellebeau, Inc. | An iontophoresis device and method for operation with a usb (universal serial bus) power source |
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US20080193514A1 (en) * | 2006-11-02 | 2008-08-14 | Transcu Ltd. | Compostions and methods for iontophoresis delivery of active ingredients through hair follicles |
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KR100839863B1 (ko) | 2007-03-27 | 2008-06-19 | 염현직 | 습포제용 저주파 발진기 |
MX2009012273A (es) * | 2007-05-18 | 2010-04-09 | Tti Ellebeau Inc | Dispositivos de suministro transd?rmico que aseguran la liberaci?n mejorada de un principio activo a trav?s de una interfaz biol?gica. |
JP2010187707A (ja) * | 2007-06-12 | 2010-09-02 | Hokkaido Univ | インスリンを封入したイオントフォレーシス用リポソーム製剤 |
US20100125238A1 (en) * | 2008-11-14 | 2010-05-20 | Therawire, Inc. | Iontophoretic Therapeutic Agent Delivery System |
AT507855A1 (de) * | 2009-01-20 | 2010-08-15 | Lang Leonh | Bioelektrode |
ES2655714T3 (es) | 2009-02-26 | 2018-02-21 | The University Of North Carolina At Chapel Hill | Sistema intervencionista de administración de fármacos |
FR3000897B1 (fr) * | 2013-01-14 | 2016-10-28 | Feeligreen | Dispositif autoregule d'electrostimulation et/ou iontophorese |
TWI566803B (zh) * | 2014-08-26 | 2017-01-21 | H & H-T Co Ltd | Infrared ray source generating device and manufacturing method thereof |
CN108471971B (zh) | 2015-12-22 | 2021-09-03 | 3M创新有限公司 | 用于生物医学电极的金属圈及其制备方法 |
CN108471972A (zh) | 2015-12-22 | 2018-08-31 | 3M创新有限公司 | 电极传感器及其生产工艺 |
EP3393746B1 (en) | 2015-12-22 | 2020-08-26 | 3M Innovative Properties Company | One-piece sensor for a bioelectrode and processes for production |
DK179927B1 (en) | 2017-12-18 | 2019-10-09 | Innocon Medical Aps | SYSTEM FOR ELECTRICAL STIMULATION OF NERVES |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0097436A1 (en) | 1982-06-16 | 1984-01-04 | Minnesota Mining And Manufacturing Company | Bioelectrode |
JPH10146392A (ja) * | 1996-08-14 | 1998-06-02 | Robert Tapper | 除毛方式 |
JP2000229129A (ja) * | 1999-02-12 | 2000-08-22 | R & R Ventures Kk | イオントフォレーゼによるイオン性薬剤の投与法 |
JP2002541934A (ja) * | 1999-04-16 | 2002-12-10 | ジョンソン・アンド・ジョンソン・コンシューマー・カンパニーズ・インコーポレイテッド | 二重チャンバー式貯蔵器を備えている薬物供給装置 |
WO2003061758A1 (fr) * | 2002-01-24 | 2003-07-31 | Hisamitsu Pharmaceutical Co., Inc. | Structure d'electrode |
Family Cites Families (106)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3076727A (en) * | 1959-12-24 | 1963-02-05 | Libbey Owens Ford Glass Co | Article having electrically conductive coating and process of making |
US3998215A (en) * | 1968-12-18 | 1976-12-21 | Minnesota Mining And Manufacturing Company | Bio-medical electrode conductive gel pads |
US3645884A (en) * | 1969-07-10 | 1972-02-29 | Edwin R Gilliland | Electrolytic ion exchange apparatus |
US3891786A (en) * | 1973-10-05 | 1975-06-24 | Herculite Protective Fab | Electrically conductive sheeting |
DE2626294C3 (de) * | 1976-06-11 | 1980-01-10 | Siemens Ag, 1000 Berlin Und 8000 Muenchen | Implantierbare Dosiereinrichtung |
US4208696A (en) * | 1977-09-06 | 1980-06-17 | Minnesota Mining And Manufacturing Company | Electrically conductive web |
US4250878A (en) * | 1978-11-22 | 1981-02-17 | Motion Control, Inc. | Non-invasive chemical species delivery apparatus and method |
US4369104A (en) * | 1979-10-22 | 1983-01-18 | Hitco | Continuous filament graphite composite electrodes |
JPS5810066A (ja) * | 1981-07-10 | 1983-01-20 | 株式会社アドバンス | イオントフオレ−ゼ用プラスタ−構造体 |
EP0126064A4 (en) * | 1982-11-17 | 1985-07-01 | Chevron Res | ELECTROACTIVE POLYMERS. |
US5605536A (en) * | 1983-08-18 | 1997-02-25 | Drug Delivery Systems Inc. | Transdermal drug applicator and electrodes therefor |
US4640689A (en) * | 1983-08-18 | 1987-02-03 | Drug Delivery Systems Inc. | Transdermal drug applicator and electrodes therefor |
US4727881A (en) * | 1983-11-14 | 1988-03-01 | Minnesota Mining And Manufacturing Company | Biomedical electrode |
US4747819A (en) * | 1984-10-29 | 1988-05-31 | Medtronic, Inc. | Iontophoretic drug delivery |
US5135477A (en) * | 1984-10-29 | 1992-08-04 | Medtronic, Inc. | Iontophoretic drug delivery |
US4744787A (en) * | 1984-10-29 | 1988-05-17 | Medtronic, Inc. | Iontophoresis apparatus and methods of producing same |
US4585652A (en) * | 1984-11-19 | 1986-04-29 | Regents Of The University Of Minnesota | Electrochemical controlled release drug delivery system |
US4722726A (en) * | 1986-02-12 | 1988-02-02 | Key Pharmaceuticals, Inc. | Method and apparatus for iontophoretic drug delivery |
US4915685A (en) * | 1986-03-19 | 1990-04-10 | Petelenz Tomasz J | Methods and apparatus for iontophoresis application of medicaments at a controlled ph through ion exchange |
US4725263A (en) * | 1986-07-31 | 1988-02-16 | Medtronic, Inc. | Programmable constant current source transdermal drug delivery system |
US4731049A (en) * | 1987-01-30 | 1988-03-15 | Ionics, Incorporated | Cell for electrically controlled transdermal drug delivery |
US5080646A (en) * | 1988-10-03 | 1992-01-14 | Alza Corporation | Membrane for electrotransport transdermal drug delivery |
US5205297A (en) * | 1988-03-25 | 1993-04-27 | Lectec Corporation | Multipurpose medical stimulation electrode |
US5496266A (en) * | 1990-04-30 | 1996-03-05 | Alza Corporation | Device and method of iontophoretic drug delivery |
US4927408A (en) * | 1988-10-03 | 1990-05-22 | Alza Corporation | Electrotransport transdermal system |
CA2001444C (en) * | 1988-10-28 | 2000-07-25 | Darrel F. Untereker | Iontophoresis electrode |
US5006108A (en) * | 1988-11-16 | 1991-04-09 | Noven Pharmaceuticals, Inc. | Apparatus for iontophoretic drug delivery |
GB8928748D0 (en) * | 1989-12-20 | 1990-02-28 | Ici Plc | Solid state electrochromic devices |
US5084008A (en) * | 1989-12-22 | 1992-01-28 | Medtronic, Inc. | Iontophoresis electrode |
US5084006A (en) * | 1990-03-30 | 1992-01-28 | Alza Corporation | Iontopheretic delivery device |
MX9101782A (es) * | 1990-10-29 | 1992-06-05 | Alza Corp | Dispositivo de suministro iontoforetico y metodo para hidratar el mismo |
US5224927A (en) * | 1990-11-01 | 1993-07-06 | Robert Tapper | Iontophoretic treatment system |
US5218973A (en) * | 1991-03-22 | 1993-06-15 | Staodyn, Inc. | Disposable wound treatment electrode |
US5405317A (en) * | 1991-05-03 | 1995-04-11 | Alza Corporation | Iontophoretic delivery device |
US5203768A (en) * | 1991-07-24 | 1993-04-20 | Alza Corporation | Transdermal delivery device |
US5310404A (en) * | 1992-06-01 | 1994-05-10 | Alza Corporation | Iontophoretic delivery device and method of hydrating same |
US6317629B1 (en) * | 1992-06-02 | 2001-11-13 | Alza Corporation | Iontophoretic drug delivery apparatus |
US5380271A (en) * | 1992-09-24 | 1995-01-10 | Alza Corporation | Electrotransport agent delivery device and method |
US5322520A (en) * | 1992-11-12 | 1994-06-21 | Implemed, Inc. | Iontophoretic structure for medical devices |
US5776594A (en) * | 1992-12-04 | 1998-07-07 | Photran Corporation | Transparent electrodes for liquid cells and liquid crystal displays |
EP0600470A3 (en) * | 1992-12-04 | 1995-01-04 | Asahi Glass Co Ltd | Bipolar membrane. |
JP3587537B2 (ja) * | 1992-12-09 | 2004-11-10 | 株式会社半導体エネルギー研究所 | 半導体装置 |
US5298017A (en) * | 1992-12-29 | 1994-03-29 | Alza Corporation | Layered electrotransport drug delivery system |
EP0676973B1 (en) * | 1992-12-31 | 1998-01-28 | Alza Corporation | Electrotransport system having flexible means |
US5380272A (en) * | 1993-01-28 | 1995-01-10 | Scientific Innovations Ltd. | Transcutaneous drug delivery applicator |
US5406945A (en) * | 1993-05-24 | 1995-04-18 | Ndm Acquisition Corp. | Biomedical electrode having a secured one-piece conductive terminal |
ATE196737T1 (de) * | 1993-05-25 | 2000-10-15 | American Cyanamid Co | Adjuvantien für impfstoffe gegen das respiratorische synzitialvirus |
US6377847B1 (en) * | 1993-09-30 | 2002-04-23 | Vyteris, Inc. | Iontophoretic drug delivery device and reservoir and method of making same |
US20050159698A1 (en) * | 1993-09-30 | 2005-07-21 | Vyteris, Inc. | Iontophoretic drug delivery device and reservoir and method of making same |
US5871460A (en) * | 1994-04-08 | 1999-02-16 | Alza Corporation | Electrotransport system with ion exchange material providing enhanced drug delivery |
AU2286995A (en) * | 1994-04-08 | 1995-10-30 | Alza Corporation | Electrotransport system with ion exchange competitive ion capture |
US5503632A (en) * | 1994-04-08 | 1996-04-02 | Alza Corporation | Electrotransport device having improved cathodic electrode assembly |
JPH09511671A (ja) * | 1994-08-22 | 1997-11-25 | イオメド インコーポレイテッド | 水和水段を組み込んだイオントフォレティック(iontophoretic)デリバリー装置 |
WO1996010439A1 (fr) * | 1994-09-30 | 1996-04-11 | Kabushiki Kaisya Advance | Interface pour administration iontophoretique transcutanee, et agent et methode de traitement de la peau a cette fin |
AU701737B2 (en) * | 1995-04-07 | 1999-02-04 | Novartis Ag | Iontophoretic transdermal system for the administration of at least two substances |
US6425892B2 (en) * | 1995-06-05 | 2002-07-30 | Alza Corporation | Device for transdermal electrotransport delivery of fentanyl and sufentanil |
US6167301A (en) * | 1995-08-29 | 2000-12-26 | Flower; Ronald J. | Iontophoretic drug delivery device having high-efficiency DC-to-DC energy conversion circuit |
US5738647A (en) * | 1996-09-27 | 1998-04-14 | Becton Dickinson And Company | User activated iontophoretic device and method for activating same |
US6350259B1 (en) * | 1996-09-30 | 2002-02-26 | Vyteris, Inc. | Selected drug delivery profiles using competing ions |
US6047208A (en) * | 1997-08-27 | 2000-04-04 | Becton, Dickinson And Company | Iontophoretic controller |
JP3998765B2 (ja) * | 1997-09-04 | 2007-10-31 | シャープ株式会社 | 多結晶半導体層の製造方法及び半導体装置の評価方法 |
DK1051220T3 (da) * | 1998-01-28 | 2005-02-14 | Alza Corp | Elektrotransportelektrodesamling med lavere begyndelsesmodstand |
WO1999038564A1 (en) * | 1998-01-28 | 1999-08-05 | Alza Corporation | Electrochemically reactive cathodes for an electrotransport device |
EP0970719A3 (en) * | 1998-07-08 | 2000-08-23 | Nitto Denko Corporation | Electrode structure |
WO2000012173A1 (en) * | 1998-08-31 | 2000-03-09 | Johnson & Johnson Consumer Companies, Inc. | Electrotransport device comprising blades |
JP3620703B2 (ja) * | 1998-09-18 | 2005-02-16 | キヤノン株式会社 | 二次電池用負極電極材、電極構造体、二次電池、及びこれらの製造方法 |
US6858018B1 (en) * | 1998-09-28 | 2005-02-22 | Vyteris, Inc. | Iontophoretic devices |
US6477410B1 (en) * | 2000-05-31 | 2002-11-05 | Biophoretic Therapeutic Systems, Llc | Electrokinetic delivery of medicaments |
AU4239300A (en) * | 1999-04-16 | 2000-11-02 | Johnson & Johnson Consumer Companies, Inc. | Electrotransport delivery system comprising internal sensors |
US6385488B1 (en) * | 1999-05-20 | 2002-05-07 | Vyteris, Inc. | Circuits for increasing the reliability of an iontophoretic system |
PT1189660E (pt) * | 1999-06-08 | 2006-09-29 | Altea Therapeutics Corp | Equipamento para a formacao de microporos em membranas biologicas utilizando dispositivos de interface para o tecido de pelicula fina e processo para o mesmo |
US6377848B1 (en) * | 1999-08-25 | 2002-04-23 | Vyteris, Inc. | Devices activating an iontophoretic delivery device |
JP4414517B2 (ja) * | 1999-09-01 | 2010-02-10 | 久光製薬株式会社 | イオントフォレーシス用デバイス構造体 |
AU2001283357A1 (en) * | 2000-08-14 | 2002-02-25 | Pharmacia Corporation | Drug delivery system with bilayer electrodes |
US6553255B1 (en) * | 2000-10-27 | 2003-04-22 | Aciont Inc. | Use of background electrolytes to minimize flux variability during iontophoresis |
EP1409119B1 (en) * | 2001-07-20 | 2006-06-21 | McMaster University | Asymmetric gel-filled microporous membranes |
US20030065285A1 (en) * | 2001-07-23 | 2003-04-03 | Higuchi William I. | Method and apparatus for increasing flux during reverse iontophoresis |
DE10140666C2 (de) * | 2001-08-24 | 2003-08-21 | Univ Braunschweig Tech | Verfahren zur Herstellung eines leitfähigen strukturierten Polymerfilms und Verwendung des Verfahrens |
PL205827B1 (pl) * | 2001-10-31 | 2010-05-31 | Tti Ellebeau | Urządzenie do jontoforezy |
US6708050B2 (en) * | 2002-03-28 | 2004-03-16 | 3M Innovative Properties Company | Wireless electrode having activatable power cell |
US20060009730A2 (en) * | 2002-07-29 | 2006-01-12 | Eemso, Inc. | Iontophoretic Transdermal Delivery of One or More Therapeutic Agents |
ES2320892T3 (es) * | 2003-03-31 | 2009-05-29 | Alza Corporation | Dispositivo de electrotransporte que tiene una cubierta de deposito con un elemento conductor flexible. |
US8734421B2 (en) * | 2003-06-30 | 2014-05-27 | Johnson & Johnson Consumer Companies, Inc. | Methods of treating pores on the skin with electricity |
AU2004291040A1 (en) * | 2003-11-13 | 2005-06-02 | Alza Corporation | System and method for transdermal delivery |
US20060083962A1 (en) * | 2004-10-20 | 2006-04-20 | Nissan Motor Co., Ltd. | Proton-conductive composite electrolyte membrane and producing method thereof |
JP2006116086A (ja) * | 2004-10-21 | 2006-05-11 | Tokuyama Corp | イオントフォレーシス装置用作用極構造体及びイオントフォレーシス装置 |
JP2006346368A (ja) * | 2005-06-20 | 2006-12-28 | Transcutaneous Technologies Inc | イオントフォレーシス装置及びその製造方法 |
JP2007000342A (ja) * | 2005-06-23 | 2007-01-11 | Transcutaneous Technologies Inc | 複数薬剤の投与量および投与時期を制御するイオントフォレーシス装置 |
US20070027426A1 (en) * | 2005-06-24 | 2007-02-01 | Transcutaneous Technologies Inc. | Iontophoresis device to deliver active agents to biological interfaces |
US8386030B2 (en) * | 2005-08-08 | 2013-02-26 | Tti Ellebeau, Inc. | Iontophoresis device |
US8295922B2 (en) * | 2005-08-08 | 2012-10-23 | Tti Ellebeau, Inc. | Iontophoresis device |
US20070060860A1 (en) * | 2005-08-18 | 2007-03-15 | Transcutaneous Technologies Inc. | Iontophoresis device |
US20070088332A1 (en) * | 2005-08-22 | 2007-04-19 | Transcutaneous Technologies Inc. | Iontophoresis device |
WO2007026672A1 (ja) * | 2005-08-29 | 2007-03-08 | Transcu Ltd. | イオントフォレーシス用汎用性電解液組成物 |
CA2619665A1 (en) * | 2005-09-15 | 2007-03-22 | Tti Ellebeau, Inc. | Rod type iontophoresis device |
WO2007038028A1 (en) * | 2005-09-28 | 2007-04-05 | Tti Ellebeau, Inc. | Iontophoresis apparatus and method to deliver active agents to biological interfaces |
US20070071807A1 (en) * | 2005-09-28 | 2007-03-29 | Hidero Akiyama | Capsule-type drug-releasing device and capsule-type drug-releasing device system |
US20070078376A1 (en) * | 2005-09-30 | 2007-04-05 | Smith Gregory A | Functionalized microneedles transdermal drug delivery systems, devices, and methods |
JP2009509656A (ja) * | 2005-09-30 | 2009-03-12 | Tti・エルビュー株式会社 | 生体界面に活性物質を送達するイオントフォレーシス装置における動作不良を検出するための方法及びシステム |
WO2007041322A2 (en) * | 2005-09-30 | 2007-04-12 | Tti Ellebeau, Inc. | Iontophoretic delivery of active agents conjugated to nanoparticles |
RU2008117153A (ru) * | 2005-09-30 | 2009-11-10 | ТиТиАй ЭЛЛЕБО, ИНК. (JP) | Аппарат для ионтофореза, доставляющий множество активных агентов к биологическим барьерам |
EP1931417A2 (en) * | 2005-09-30 | 2008-06-18 | Transcutaneous Technologies Inc. | Transdermal drug delivery systems, devices, and methods employing novel pharmaceutical vehicles |
WO2007041323A1 (en) * | 2005-09-30 | 2007-04-12 | Tti Ellebeau, Inc. | Iontophoretic delivery of vesicle-encapsulated active agents |
WO2007041526A2 (en) * | 2005-09-30 | 2007-04-12 | Transcutaneous Technologies Inc. | Iontophoresis apparatus and method to deliver antibiotics to biological interfaces |
WO2007079116A1 (en) * | 2005-12-28 | 2007-07-12 | Tti Ellebeau, Inc. | Electroosmotic pump apparatus and method to deliver active agents to biological interfaces |
WO2007079190A2 (en) * | 2005-12-29 | 2007-07-12 | Tti Ellebeau, Inc. | Device and method for enhancing immune response by electrical stimulation |
-
2005
- 2005-06-30 US US11/171,953 patent/US20060095001A1/en not_active Abandoned
- 2005-10-28 KR KR1020077011950A patent/KR20070084592A/ko not_active Application Discontinuation
- 2005-10-28 BR BRPI0518072-4A patent/BRPI0518072A/pt not_active IP Right Cessation
- 2005-10-28 CN CNA2005800372709A patent/CN101048192A/zh active Pending
- 2005-10-28 WO PCT/JP2005/019909 patent/WO2006046703A1/ja active Application Filing
- 2005-10-28 RU RU2007119711/14A patent/RU2387466C2/ru not_active IP Right Cessation
- 2005-10-28 SG SG200803304-5A patent/SG142331A1/en unknown
- 2005-10-28 CA CA002585355A patent/CA2585355A1/en not_active Abandoned
- 2005-10-28 JP JP2006542346A patent/JPWO2006046703A1/ja active Pending
- 2005-10-28 AU AU2005297817A patent/AU2005297817A1/en not_active Abandoned
- 2005-10-28 EP EP05805338A patent/EP1808197A4/en not_active Ceased
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0097436A1 (en) | 1982-06-16 | 1984-01-04 | Minnesota Mining And Manufacturing Company | Bioelectrode |
JPH10146392A (ja) * | 1996-08-14 | 1998-06-02 | Robert Tapper | 除毛方式 |
JP2000229129A (ja) * | 1999-02-12 | 2000-08-22 | R & R Ventures Kk | イオントフォレーゼによるイオン性薬剤の投与法 |
JP2002541934A (ja) * | 1999-04-16 | 2002-12-10 | ジョンソン・アンド・ジョンソン・コンシューマー・カンパニーズ・インコーポレイテッド | 二重チャンバー式貯蔵器を備えている薬物供給装置 |
WO2003061758A1 (fr) * | 2002-01-24 | 2003-07-31 | Hisamitsu Pharmaceutical Co., Inc. | Structure d'electrode |
Non-Patent Citations (1)
Title |
---|
See also references of EP1808197A4 |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8295922B2 (en) | 2005-08-08 | 2012-10-23 | Tti Ellebeau, Inc. | Iontophoresis device |
US7890164B2 (en) | 2005-09-15 | 2011-02-15 | Tti Ellebeau, Inc. | Iontophoresis device |
US8062783B2 (en) | 2006-12-01 | 2011-11-22 | Tti Ellebeau, Inc. | Systems, devices, and methods for powering and/or controlling devices, for instance transdermal delivery devices |
JP2014500077A (ja) * | 2010-11-17 | 2014-01-09 | スマート ソリュションズ テクノロジーズ, エス.エル. | 生理学的信号を取得するためのセンサー |
US10238336B2 (en) | 2010-11-17 | 2019-03-26 | Smart Solutions Technologies, S.L. | Sensors |
US10542935B2 (en) | 2010-11-17 | 2020-01-28 | Smart Solutions Technologies, S.L. | Sensors |
US10987052B2 (en) | 2010-11-17 | 2021-04-27 | Smart Solutions Technologies, S.L. | Sensor for acquiring physiological signals |
US11744516B2 (en) | 2010-11-17 | 2023-09-05 | Smart Solutions Technologies, S.L. | Sensor for acquiring physiological signals |
WO2014142624A1 (ja) * | 2013-03-15 | 2014-09-18 | 株式会社ライフリング | タッチパネル操作用シール |
JP5863141B2 (ja) * | 2013-03-15 | 2016-02-16 | 株式会社ライフリング | タッチパネル操作用シール |
TWI594149B (zh) * | 2013-03-15 | 2017-08-01 | 萊芙霖股份有限公司 | 觸控面板操作用貼片 |
Also Published As
Publication number | Publication date |
---|---|
CA2585355A1 (en) | 2006-05-04 |
RU2007119711A (ru) | 2008-12-10 |
US20060095001A1 (en) | 2006-05-04 |
SG142331A1 (en) | 2008-05-28 |
BRPI0518072A (pt) | 2008-11-04 |
EP1808197A4 (en) | 2008-04-23 |
JPWO2006046703A1 (ja) | 2008-05-22 |
AU2005297817A1 (en) | 2006-05-04 |
KR20070084592A (ko) | 2007-08-24 |
CN101048192A (zh) | 2007-10-03 |
RU2387466C2 (ru) | 2010-04-27 |
EP1808197A1 (en) | 2007-07-18 |
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