WO2004105865A1 - Kit, device and method for controlled delivery of oxidizing agent into the skin - Google Patents
Kit, device and method for controlled delivery of oxidizing agent into the skin Download PDFInfo
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- WO2004105865A1 WO2004105865A1 PCT/IL2004/000468 IL2004000468W WO2004105865A1 WO 2004105865 A1 WO2004105865 A1 WO 2004105865A1 IL 2004000468 W IL2004000468 W IL 2004000468W WO 2004105865 A1 WO2004105865 A1 WO 2004105865A1
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- Prior art keywords
- oxidizing agent
- kit
- electrode
- patch
- body area
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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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0002—Galenical forms characterised by the drug release technique; Application systems commanded by energy
- A61K9/0009—Galenical forms characterised by the drug release technique; Application systems commanded by energy involving or responsive to electricity, magnetism or acoustic waves; Galenical aspects of sonophoresis, iontophoresis, electroporation or electroosmosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/70—Web, sheet or filament bases ; Films; Fibres of the matrix type containing drug
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/12—Keratolytics, e.g. wart or anti-corn preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/20—Antivirals for DNA viruses
- A61P31/22—Antivirals for DNA viruses for herpes viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B7/00—Electrophoretic production of compounds or non-metals
Definitions
- the present invention relates to kits, devices and methods for controlled delivery of agents onto and into a subject's body surface.
- Iontophoresis is an effective and painless method of delivering cosmetic and pharmaceutical agents to a localized tissue area by applying electrical current to a formulation of a medication comprising the agent or a precursor thereof.
- the two principal mechanisms by which electrical currents enhance molecular transport across the skin are: (a) Iontophoresis, in which a charged ion is repelled from an electrode of the same charge, and (b)Electroosmosis, the convective movement of solvent that occurs through a charged "pore” in response to the preferential passage of counter-ions when the electric field is applied.
- Oxidizing agents have many properties including therapeutic activity, such as antibacterial activity.
- oxidizing agents which have anti-acne properties, are well known in the art. These include, for example, benzoyl peroxide, alpha hydroxy acids and detergents. Benzoyl peroxide is a strong oxidizing agent which may be used as an antibacterial and keratolytic agent in the treatment of acne.
- Other oxidizing agents such as NaC10 2 , which is sold under the trade name Dioxychlor, are useful in treating skin infections.
- an oxidizing agent such as an iontophoresis/electroosmosis delivery system for delivering an oxidizing agent onto and into the body and a method of use thereof. It is desirable to have the benefit of treatment with an oxidizing agent, which is delivered with an iontophoretic device for increased penetration of the active oxidizing agent. Finally, it is desirable to have such a system, which has low cost. Preferably, such a system should be disposable.
- Embodiments of the present invention include kits, devices and methods for delivery of an oxidizing agent onto and into a subject's body surface.
- Embodiments of the kits of the present invention may comprise an electrically powered patch and a formulation including an oxidizing agent or an oxidizing agent precursor.
- Embodiments of the devices of the present invention may comprise first and second electrodes, a power source and an oxidizing agent or an oxidizing agent precursor.
- Embodiments of the methods of the present invention may also comprise providing a device for treatment of a disorder comprising a flexible, wearable patch conformable to the contour of a body area surface, contacting the body area with the device for a time period wherein the device promotes oxidizing agent penetration of the body area surface and underlying tissues, penetrating of the oxidizing agent into and/or onto the body area to treat the body area disorder, and removing the device from the body area.
- FIG. 1 shows a schematic view of one embodiment of a dermal patch for delivering an oxidizing agent of the present invention
- FIG. 2 shows an alternative embodiment of a dermal patch for delivering an oxidizing agent of the present invention
- FIG. 3 shows a schematic view of at least two current circuits resulting from use of one embodiment of the device of the present invention
- FIG. 4 shows an alternative embodiment of a dermal patch according to the present invention, wherein the electrodes are in a cofacial configuration
- FIG. 5 is a flowchart of a method according to one embodiment of the present invention.
- kits, device and method for delivering an oxidizing agent onto and or into the body may deliver an oxidizing agent using iontophoresis and/or electrosomosis onto and/or into the body.
- the kit and device may deliver an oxidizing agent using iontophoresis and/or electrosomosis for treatment of a body area with an oxidizing agent.
- a device for a combination of surface treatment, dermal treatment and transdermal treatment of a body area Preferably, the device is a thin and flexible dermal patch.
- the body area is skin.
- FIG. 1 shows a schematic view of a fully integrated patch device for delivery of an oxidizing agent according to one embodiment of the present invention.
- the patch device is fully integrated in the sense that an oxidizing agent or an oxidizing agent precursor is incorporated into the device.
- patch 100 may comprise first electrode 110(1), identified as "cathode,” second electrode 110(2), identified as “anode,” and electrochemical cell 130 as the power supply of patch 100.
- patch 100 may include a plurality of cathodes 110(1), a plurality of anodes 110(2) and a plurality of power supplies 130.
- Patch 100 may also comprise conductive layer/s 120 and 140 to provide an interfacing layer between patch 100 and a body area of a subject.
- One of or both conductive layer/s 120 and 140 optionally include oxidizing agent or oxidizing agent precursor 125.
- electrodes 110(1) 110(2), conductive layers 120, 140, oxidizing agent 125, and electrochemical cell may be supported on substrate 150.
- Electrode 110(1) may be disposed in any suitable way on substrate 150 in spaced relation to electrochemical cell 130 and electrode 110(2) to define a gap between the two electrodes.
- Conductive layer 120 including oxidizing agent or oxidizing agent precursor 125 may optionally be disposed on electrode 110(2) or 110(1) or on both electrodes 110(1) and 110(2).
- patch 100 does not include conductive layer 120 (or conductive layer 140).
- oxidizing agent or oxidizing agent precursor 125 can optionally be accommodated in a holding component, such as a chamber (not shown in figure), which may be attached to electrode 110(1) or electrode 110(2).
- oxidizing agent or oxidizing agent precursor can be accommodated on electrode 110(1) or 110(2) in any other suitable way.
- the embodiment depicted in Fig. 1 is a fully integrated patch device.
- the present invention may also be practiced with a patch device that does not have an oxidizing agent or an oxidizing agent precursor incorporated into it, but which instead is part of a kit.
- a patch device is similar to the embodiment of the fully integrated patch device depicted in Fig. 1.
- the conductive layer 120 of the patch optionally (when it is part of a kit) does not include an oxidizing agent or oxidizing agent precursor 125.
- oxidizing agent or oxidizing agent precursor 125 accommodated in conductive layer 120 may be disposed in a separate holding component (not shown), which may not be integrally attached to the patch.
- separate holding component can be attached to patch just before use, such as for example when separate holding component is a chamber.
- separate holding component can be applied onto body area, such as for example when separate holding component is a sponge or other type of material absorbing device.
- oxidizing agent or oxidizing agent precursor 125 accommodated in conductive layer 120 may be applied directly onto body area or onto electrode, without use of a separate holding component.
- oxidizing agent or oxidizing agent precursor 125 can be disposed on anode or on cathode or on both anode 110(2) and cathode 110(1).
- one reactant/precursor can be disposed on the anode 110(2) and the other reactant/precursor can be disposed on the cathode 110(1).
- oxidizing agent or oxidizing agent precursor 125 is disposed on anode 110(2).
- patch 100 including patch components, is thin and flexible, to suit the contour of a body area of a subject.
- patch 100 is electrically powered.
- Patch may be any size, color and shape suitable for application to a desired body area.
- the thickness of patch 100 is preferably up to 10 mm to ensure flexibility, but may be thicker, depending on the application. The thickness of the patch may also be dependent upon the type of material used and the flexibility of that material.
- Patch 100 is preferably disposable, but may be reusable. Patch 100 is stable to a wide range of temperatures and humidity.
- power supply 130 of any size or shape, which provides an electrical potential of between about 0.2 Volt and about 100 Volt can be used according to the present invention. Yet, in a preferred embodiment, power supply 130 is an electrical battery, providing an electrical potential of between about 1.5 Volt and 12 Volt.
- power supply 130 is thin and flexible.
- power supply thickness should not exceed 4 mm and more preferably, power supply thickness should be less than 2 mm.
- power supply 130 is at least one electrochemical cell.
- the term 'electrochemical cell' as used herein includes any suitable cell in which chemical energy is converted to electric energy by a spontaneous electron transfer reaction. The term includes cells with non-spontaneous reactions, cells with spontaneous reactions, galvanic cells, electrolytic cells and a combination thereof.
- electrochemical cell includes a first layer of insoluble negative pole, a second layer of insoluble positive pole and a third layer of aqueous electrolyte, the third layer being disposed between the first and second layers and including: (a) a deliquescent material for keeping the open cell wet at all times; (b) an electroactive soluble material for obtaining required ionic conductivity; and (c) a water soluble polymer for obtaining a required viscosity for adhering the first and second layers to the third layer.
- a power source is described in U.S. Patent Nos. 5,652,043, 5,811,204 and 5,897,522, which are incorporated herein by reference in their entireties.
- any power source consistent with a flexible wearable device is within the scope of the invention.
- power supply 130 in patch 100 is a single electrochemical cell.
- power supply 100 need not be limited to one cell, but may include a plurality of connected electrochemical cells, a plurality of batteries, and/or electronics configured to increase, control, and change phase of the supplied electric current and wherein the power supply is thin and flexible.
- Electrochemical cell 130 in patch 100 preferably provides electrical potential (voltage) to the desired body area of the subject. In a preferred embodiment, the electrical potential may be adjusted to satisfy at least one of the following three criteria.
- the patch voltage may be adjusted to enable an iontophoretic delivery of the oxidizing agent/s into the body area.
- the patch voltage may be adjusted to minimize the penetration of the oxidizing agent/s through the body, and to maximize the amount into the desired body area.
- the patch voltage may be adjusted to minimize body area irritation, which may result from excessive electric current, passing into and through the body.
- the power supply may optionally be located in any suitable position on the patch.
- a power supply to the patch may provide a duty cycle and pulse partition rate of between about 1% and about 99%.
- the frequency of the power supply may preferably be from about 1Hz to about 1000Hz.
- the power supply may provide voltage in a range of from about 0.2V to about 100V to the patch.
- Cathode and anode electrodes 110(1) and 110(2) are preferably composed of a conductive material.
- at least one electrode is an active electrode and at least one electrode is a counter electrode.
- the active electrode can be the cathode or anode or both the cathode and the anode. Defining which electrode is the active electrode is dependent on the charge of the formulation or oxidizing agent being used.
- Any suitable conductive material may optionally be used, such as, but not limited to silver, silver/silver chloride, graphite, zinc, copper, carbon, platinum, manganese dioxide or a combination thereof.
- at least one of the electrodes may include zinc, copper, silver and silver/silver chloride.
- Electrodes may optionally be provided in any suitable form, such as, but not limited to as thin sheets, linked to the power source, or printed onto a substrate in spaced relation to each other to define a gap therebetween.
- the electrode area can be continuous, or formed in any shape or configuration.
- cathode 110(1) and anode 110(2) may not have the same shape and/or same area.
- cathode and anode may be in any suitable conformation in relation to each other including but not limited to a coplanar and cofacial arrangement.
- patch can include a plurality of anodes and a plurality of cathodes.
- connection means 155 include, but are not limited to wiring, conductive ink, printed connection means, soldered connection means, connection means attached by UV, glued connection means and a combination thereof.
- Substrate base layer 150 is optionally any suitable material, which can accommodate the oxidizing agent delivery patch components. Suitable materials include, but are not limited to woven material, non-woven material, polymers, conducting material, non-conducting material, paper, cardboard, plastic, synthetic materials, natural materials, fabric, metals, wood, glass, Perspex, or a combination thereof. Preferably, substrate material is a non-rconductive material. More preferably, substrate is made from polyester.
- substrate base layer 150 can be made up of a plurality of substrate base layers 150, which can be stacked or connected in a co-planar way by any suitable attachment means. Preferably, substrate layer 150 is made up of one continuous piece of substrate layer 150.
- substrate base layer 150 can be any suitable size, shape or color.
- substrate base layer 150 may readily facilitate attachment of the device 100 to a desired body area.
- Attachment mechanisms may include but are not limited to conductive adhesive, adhesive strip, suction cups and/or any combinations thereof.
- patch 100 is configured to attach to the body area by conductive layer 140.
- the patch may be attached to the body area by, for example, the frame of the substrate and/or other attachment mechanisms.
- Conductive layers 120 and 140 may optionally be any suitable conductive composition, such as an aqueous gel, hydrogel or a conductive adhesive.
- anode electrode 110(2) is active.
- either anode electrode 110(2), cathode electrode 110(1), or both electrodes may be active for delivering an oxidizing agent.
- the features of the patch of the present invention described above are the same regardless of whether the patch is a fully integrated patch device, or a patch included as part of a kit.
- oxidizing agents according to the present invention may be part of a formulation, placed in the interface area between one or both of the electrodes of the device. Providing that they possess a certain degree of water solubility, they can be mobilized from the formulation towards the body surface, via the electromotive forces of iontophoresis and/or electro-osmosis.
- the term 'formulation' as used herein includes any type of suitable formulation, which can accommodate an oxidizing agent or oxidizing agent precursor.
- the term includes conductive layers, such as aqueous gel or hydrogel.
- the term further includes any pharmaceutical or cosmetic active or inactive formulation, including active ingredients, solvents, fragrance and additives.
- Additives to such formulations include but are not limited to water, surfactants, emulsifiers, diglycerides, triglycerides, stabilizing agents, thickening agents, alpha-hydroxy carboxylic acids, antioxidants, preservatives, moisturizers, petroleum, mineral oil, glycerol, ethanol, propanol, isopropanol, butanol, polymeric gelling agents, flavoring, colorant and odorant agents and other formulation components, used in the art of pharmaceutical and cosmetic formulary.
- the formulation containing the oxidizing agent can optionally be applied directly onto the skin between the two electrodes, or alternatively the oxidizing agent is disposed in a holding component, such as, but not limited to a sponge placed between the two electrodes or applied onto the substrate between the two electrodes.
- the formulation is contained in a conductive layer, such as, but not limited to, a hydrogel.
- a conductive layer such as, but not limited to, a hydrogel.
- FIG. 2 shows a schematic view of a fully integrated patch device for delivery of an oxidizing agent, wherein the oxidizing agent is disposed in the interface area between the two electrodes according to one embodiment of the present invention.
- patch 200 may comprise first electrode 210(1), identified as “cathode,” second electrode 210(2), identified as “anode,” and electrochemical cell 220 as the power supply of patch 200.
- patch 200 may include a plurality of cathodes 210 (1), a plurality of anodes 210 (2) and a plurality of power supplies 220.
- Patch 200 preferably comprises conductive layer 230 to accommodate oxidizing agent and/or oxidizing agent precursor.
- Conductive layer 230 provides an interfacing layer between patch 200 and a body area of a subject.
- Patch 200 preferably includes a holding component 250, which may be configured to hold a formulation including oxidizing agent 240 and/or oxidizing agent precursor.
- electrodes 210(1) 210(2), conductive layer 230, holding component 250, oxidizing agent 240, and electrochemical cell 220 are preferably supported on substrate 260.
- Electrode 210(1) may be disposed in any suitable way on substrate 260 in spaced relation to electrochemical cell 220 and electrode 210(2) to define a gap between the two electrodes.
- Conductive layer 230 may optionally be disposed on electrodes 210(1) and 210(2) or in holding component 250. In an alternative embodiment, patch 200 may not include conductive layer 230.
- holding component 250 is disposed in the interface between electrode 210(1) and 210(2).
- holding component 250 may be any suitable means for accommodating oxidizing agent, such as, but not limited to a sponge, a chamber and substrate.
- holding component 250 may be made from a non-woven and non-conductive material.
- the device of Figure 2 may facilitate a combination of both surface treatment of the skin with the oxidizing agent and iontophoretic delivery and/or electroosmosis delivery into the skin of the oxidizing agent for transdermal and dermal treatment.
- Figure 3 shows a schematic view of at least two current circuits resulting from a device for delivering an oxidizing agent, wherein the oxidizing agent is disposed between the two electrodes of patch 300.
- battery 305 supplies current to electrodes 320 and 330.
- Current circuit 310 is the current circuit resulting from current flow between electrodes 320 and 330 through the conductive composition containing oxidizing agent 340.
- Current circuit 350 is the current circuit resulting from current flow from electrode/s 320 and 330 to skin 360.
- flow of current through circuit 310 facilitates production and flow of ions from the components, such as oxidizing agent disposed in conductive composition/formulation 340. The produced ions provide surface treatment of skin 360.
- flow of current through current circuit 350 facilitates iontophoretic and/or electroosmotic delivery of the oxidizing agent and any other active agent disposed in conductive composition 340, onto and into skin 360.
- the ratio of the current flowing through current circuits 310 and 350 may be controlled by changing the space 370 between electrodes 320 and 330. The smaller the space 370, the higher the current flowing in circuit 310 and the more surface treatment is achieved. In this way, it may be possible to control the ratio of surface treatment to iontophoretic delivery of the oxidizing agent being used.
- FIG. 4 shows a schematic view of an alternative embodiment of a fully integrated patch device for delivery of an oxidizing agent, wherein the electrodes are in a cofacial conformation.
- patch 400 may comprise first electrode 410(1), identified as “cathode,” second electrode 410(2), identified as “anode,” and electrochemical cell 420 as the power supply of patch 400.
- patch 400 may include a plurality of cathodes 410 (1), a plurality of anodes 410(2) and a plurality of power supplies 420.
- Patch 400 preferably comprises conductive layer 430 to accommodate oxidizing agent and/or oxidizing agent precursor 440.
- Patch 400 preferably includes a separator, which is preferably holding component 450, which may be configured to hold a formulation/conductive layer 430 including oxidizing agent and/or oxidizing agent precursor 440.
- a separator which is preferably holding component 450, which may be configured to hold a formulation/conductive layer 430 including oxidizing agent and/or oxidizing agent precursor 440.
- electrodes 410(1) 410(2), conductive layer 430, holding component 450, oxidizing agent 440, and electrochemical cell 420 are preferably supported on substrate 460.
- Electrode 410(1) may be disposed in a cofacial arrangement on substrate 460 with relation to electrode 410(2), Holding component 450 forms a separator layer between electrode 410(1) and 410(2).
- conductive layer 430 is disposed in holding component 450.
- holding component 450 may be any suitable means for accommodating oxidizing agent, such as, but not limited to a sponge, a chamber and substrate.
- oxidizing agent and/or oxidizing agent precursor 440 can be administered into the patch through loading holes 470 in the patch.
- Patch 400 may optionally have either cathode or anode in contact with the skin.
- the electrode, which is in contact with the skin is in a porous form, such as in net form, in order to facilitate contact between oxidizing agent 440 and the skin.
- electrode 410(1) is made in a net form and is in contact with skin.
- Patch 400 preferably results in current flow between electrodes 410(2) and 410(1) through the conductive composition 430 containing oxidizing agent 440.
- flow of current facilitates production and flow of oxidizing ions from the components, such as oxidizing agent disposed in conductive composition/ formulation 440.
- the produced ions provide surface treatment of skin.
- oxidizing agents or oxidizing agent precursors may be embedded or disposed on the surface of one or both of the device electrodes (as shown in Figure 1), which readily facilitates delivery of the oxidizing agent from the electrode area towards the body surface using iontophoresis and/or electroosmosis.
- electrode can be manufactured with oxidizing agent or precursor mixed with electrode material.
- the formulation containing the oxidizing agents can be applied directly onto the skin or can be applied onto the electrode or to the interface area between one or both of the electrodes.
- Oxidizing agent' as referred to herein includes any suitable oxidizing agent including any substance, which will readily add or take on electrons.
- Oxidizing agent includes inorganic and organic oxidizing agents, such as, but not limited to quinones.
- Oxidizing agents according to the present invention also include agents, which can spontaneously exert an oxidizing effect on a body organ living cells and pathogens.
- oxidizing agents according to the present invention include, but are not limited to oxidizing agents or oxidation agents in any suitable form, such as a liquid, semi-liquid, semi-solid, solid, gaseous, semi-gaseous, pure oxidizing agent, oxidizing agent or oxidizing agent precursor as part of a formulation, mixtures of more than one oxidizing agent and any combination thereof.
- suitable oxidizing agents include, but are not limited to oxygen; peroxides, such as hydrogen peroxide and benzoyl peroxide; elemental halogen species, as well as oxygenated halogen species, such as hypochlorite ions and perchlorite species.
- the oxidizing agent may be applied to the device of the present invention.
- the oxidizing agents are produced in-situ from a precursor, upon closure of an electrical circuit. Still in another preferred embodiment, the oxidizing agent is produced by any suitable electrochemical reaction, such as a redox process, or electrolysis upon closure of an electrical circuit. Examples of such electrochemical and redox processes, yielding oxidizing agents are presented below in Table 1 :
- the electrode mass including at least one precursor in the electrode mass, or as an embedded layer on the surface of one or both of the electrodes, or in the formulation interfacing between the electrodes and a body surface or one precursor or reactant on one electrode and a second precursor or reactant on a second electrode and closing an electrical circuit, preferably in a potential higher than required to generate the respective oxidizing agent via a redox process, evolves an active oxidizing agent.
- the strength of the electrical current (i.e., current density) and the precursor concentration are preferably both positively correlated with the amount of oxidizing agent evolved.
- oxidizing agents include agents that may spontaneously exert an oxidizing effect on a body organ living cells and pathogens. Such effect may result in therapeutic affects as exemplified in the following list: Pathogen killing
- Oxidizing agents are generally capable of killing pathogens.
- Bacterial pathogens are generally classified, in a non-limiting fashion, as follows:
- Gram positive bacteria such as the aerobic cocci Staphylococcus aureus and Staphylococcus epidermidis; aerobic rods, e.g., Bacillus anthracis, Bacillus cereus, Lactobacillus sp., Listeria monocytogenes, Corynebacterium diptheriae and Propionibacterium acnes; anaerobic rods, such as Actinomyces sp. Clostridium botulinum, Clostridium difficile and Clostridium perfringens; and Anaerobic, Gram-positive cocci.
- aerobic rods e.g., Bacillus anthracis, Bacillus cereus, Lactobacillus sp., Listeria monocytogenes, Corynebacterium diptheriae and Propionibacterium acnes
- anaerobic rods such as Actinomyces sp. Clostridium botulinum, Clostridium difficile and Clostridium perfringens; and
- Gram negative bacteria include, for example, Aerobic, Gram-negative cocci, e.g., Neisseria gonorrhoeae, Neisseria meningitides and Moraxella catarrhalis; anaerobic, Gram-negative cocci; aerobic, Gram-negative rods, including Fastidious Gram-negative rods, Enterobacteriaceae (glucose- fermenting Gram-negative rods), oxidase-positive glucose-fermenting Gram- negative rods glucose-nonfermenting Gram-negative rods; and anaerobic Gram- negative rods.
- Aerobic, Gram-negative cocci e.g., Neisseria gonorrhoeae, Neisseria meningitides and Moraxella catarrhalis
- anaerobic, Gram-negative cocci e.g., Neisseria gonorrhoeae, Neisseria meningitides and Moraxella catarrhalis
- pathogens include Common, contagious types of human papillomavirus.
- kits and device of the present invention readily facilitates treatment of diseases and disorders, which are susceptible to oxidation with an oxidizing agent.
- oxidizing agents are also commonly used for accomplishing bleaching or whitening effects. This may be useful, for example in the whitening or lightening of the skin and teeth. Therefore, the device or kit of the present invention can be used for skin and teeth whitening or lightening.
- the oxidizing agent is preferably delivered towards a body surface by an electromotive process, known as " Iontophoresis".
- Iontophoresis can be defined as a mean of enhancing the flux of ionic compounds across a membrane, by the application of an electric current across it.
- This technique has been reported useful for the enhancement of transdermal delivery of ionized drugs, including macromolecules.
- the skin is a multilayered organ delimiting the body. It is constituted of several layers and the outermost layer, stratum corneum, is the main barrier to drug transport. The application of electric current, however, is able to increase the penetration of molecules through this barrier.
- the two principal mechanisms by which iontophoresis enhances molecular transport across the skin are: (a) iontophoresis, in which a charged ion is repelled from an electrode of the same charge, and
- Electroosmosis the convective movement of solvent that occurs through a charged "pore” in response to the preferential passage of counter-ions when the electric field is applied. Electroosmosis is useful for the delivery of uncharged, yet, water soluble molecules.
- 'iontophoresis' includes, but is not limited to iontophoresis, electroosmosis or iontophoresis in combination with another mechanism and a combination thereof.
- the strength of the electrical current i.e., voltage and current density
- the oxidizing agent concentration are both positively correlated with the amount of oxidizing agent evolved. Modulation of these two parameters is useful in adjusting the amount of the oxidizing agent, available in the target body surface and the underlying body layers.
- Other parameters which may influence the rate of oxidizing agent migration and tissue availability, are pH, electrode surface area, formulation properties, viscosity, adhesiveness and conductivity of the formulation interfacing between the electrodes and the body surface.
- the therapeutic system of the present invention may further comprise any additional therapeutic agents or active agents or additives, which may contribute to the therapy of the disorder or another related or unrelated disorder.
- Non-Limiting Examples of skin disorders which can benefit from the oxidizing agent treatment are set forth in Table 2.
- the body area to be treated with the device and oxidizing agent of the present invention includes, but is not limited to skin, keratinized tissue, nails, teeth, hair, organ, non-malignant growth and tumor.
- the body area to be treated with the oxidizing agent is skin.
- the device and kit of the present invention is for use on humans.
- the device and kit of the present invention can be used on non-humans.
- the patch and kit of the present invention may be applied by the subject himself or by a third party.
- the patch and kit of the present invention readily facilitates home use in addition to use in a clinic or other supervised environment.
- treatment according to the present inventions may be beneficial in all body areas.
- Treatments of the oral cavity using oxidizing agents may be beneficial in all body areas.
- Non-limiting examples of oral disorders, suitable for treatment according to the present invention include bacterial, fungal and viral infections of the oral cavity. Teeth whitening using oxidizing agents according to the present invention is also very useful.
- the patch and kit of the present invention including any suitable oxidizing agent or oxidizing agent precursor may optionally be used to reduce dental hypersensitivity, in oral anesthesia, plaque removal, ulcer treatment and for fluoride treatment.
- treatment of any mucosal disorder which is responsive to treatment with oxidizing agents is included in the scope of the present invention.
- the preferred devices of the present invention can be designed to fit any area of the body surface and to have any desirable size, according to the area having the disorder.
- the patch of the present invention may be made using any suitable techniques.
- the patch of the present invention is a printed patch, wherein the electrodes and power supply are printed onto the substrate using any suitable printing technology.
- FIG. 5 is a flowchart of a method according to embodiments of the present invention.
- the flowchart applies to a non-limiting method using a fully integrated patch, or to a method using a kit including a patch.
- a subject may contact (510) a body area with an oxidizing agent/or oxidizing agent precursor/s (which may or may not be an integrated part of a patch).
- the subject may promote (520) penetration and/or generation of oxidizing agent onto and/or into the body area through the use of an electrically powered patch.
- the patch is removed from the body area (530) at the end of the treatment time.
- end of treatment time is determined by depletion of the active agent and/or sufficient therapeutic effect of the treatment or by a predetermined time. While the principles of the invention have been discussed in relation to exemplary embodiments discussed herein, it is understood that the principles of the invention are not limited thereto.
- hydrogen peroxide is used as an oxidizing agent with the kit/device of the present invention to treat a skin infection.
- Hydrogen peroxide is placed in a formulation containing hydrogel on the anode.
- the patch When the patch is contacted with the infected skin area of the subject, current flows and oxygen is produced in situ. The oxygen is delivered dermally to treat the infection.
- Example 2 Treatment of skin infection with an oxidizing agent
- the kit or dermal patch of the present invention is effective in the treatment of skin infections.
- the patch or kit is used with a formulation including the oxidizing agent NaC10 2 resulting in iontophoretic treatment and topical treatment of skin infections.
- any suitable formulation including the oxidizing agent NaC10 2 is envisioned for use with the dermal patch.
- the oxidizing agent NaC10 2 is preferably contained in the hydrogel to form a mixture. The mixture can optionally be applied directly to the desired area of the body.
- the mixture is preapplied, such as, but not limited to, during manufacture of the patch, onto the electrode/s of the patch and therefore the patch is ready for use.
- the aqueous hydrogel can be contained in a separator, which is integrally formed with the patch or in a holding component disposed between the two electrodes.
- the mixture . can be contained in a separate, non-integral holding component, such as a retainer. The retainer is then optionally connected to the patch before use.
- a typical method of treatment includes the following steps of adhering the patch of the present invention to the desired area of the body, such as, but not limited to the face and back.
- One area or more than one area of the body can be treated at the same time using a plurality of patches or the same patch with a plurality of electrodes.
- the kit of the present invention which includes a separate retainer is being used, the retainer which preferably contains NaC10 2 mixture is first attached to the patch before adhering to the skin.
- the aqueous hydrogel can be applied directly to the place of treatment on the body of the subject. In the case that the hydrogel is contained in the patch, the patch is ready to use.
- the duration of treatment is determined according to severity of condition and other skin factors. A typical treatment session lasts between about 10 to about 20 minutes. Treatment is terminated by removal of the patch. Alternatively, treatment is terminated by depletion of the battery, at least one of the electrodes or depletion of the oxidizing agent.
- the treatment is repeated in selected time intervals. At the beginning, the treatment is usually repeated more frequently, such as a few times a week and then for maintenance of the resulting effect, the treatment is repeated less frequently.
Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP04735790A EP1633431B1 (en) | 2003-06-02 | 2004-06-02 | Kit, device and method for controlled delivery of oxidizing agent into the skin |
DE602004017720T DE602004017720D1 (en) | 2003-06-02 | 2004-06-02 | KIT, DEVICE AND METHOD FOR THE TAXED DELIVERY OF AN OXIDIZING AGENT IN THE SKIN |
JP2006508485A JP2006526454A (en) | 2003-06-02 | 2004-06-02 | Kit, apparatus and method for controlled delivery of oxidant into skin |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US47459603P | 2003-06-02 | 2003-06-02 | |
US60/474,596 | 2003-06-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2004105865A1 true WO2004105865A1 (en) | 2004-12-09 |
Family
ID=33490723
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IL2004/000468 WO2004105865A1 (en) | 2003-06-02 | 2004-06-02 | Kit, device and method for controlled delivery of oxidizing agent into the skin |
Country Status (9)
Country | Link |
---|---|
US (1) | US7340297B2 (en) |
EP (1) | EP1633431B1 (en) |
JP (1) | JP2006526454A (en) |
KR (1) | KR20050121277A (en) |
CN (1) | CN1832777A (en) |
AT (1) | ATE413860T1 (en) |
DE (1) | DE602004017720D1 (en) |
ES (1) | ES2316987T3 (en) |
WO (1) | WO2004105865A1 (en) |
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US20080096074A1 (en) * | 2006-10-23 | 2008-04-24 | Eveready Battery Company, Inc. | Electrochemical air cell batteries with air flow channels |
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0318776A1 (en) * | 1987-12-04 | 1989-06-07 | Robert Tapper | Method and apparatus for minimizing skin injury with electrode use |
US5652043A (en) | 1995-12-20 | 1997-07-29 | Baruch Levanon | Flexible thin layer open electrochemical cell |
EP0900576A1 (en) * | 1996-03-17 | 1999-03-10 | Hisamitsu Pharmaceutical Co., Inc. | Electrode device for iontophoresis |
US5897522A (en) | 1995-12-20 | 1999-04-27 | Power Paper Ltd. | Flexible thin layer open electrochemical cell and applications of same |
US5911223A (en) * | 1996-08-09 | 1999-06-15 | Massachusetts Institute Of Technology | Introduction of modifying agents into skin by electroporation |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4744787A (en) * | 1984-10-29 | 1988-05-17 | Medtronic, Inc. | Iontophoresis apparatus and methods of producing same |
US4979938A (en) * | 1989-05-11 | 1990-12-25 | Iomed, Inc. | Method of iontophoretically treating acne, furuncles and like skin disorders |
JP3267291B2 (en) * | 1990-03-20 | 2002-03-18 | 株式会社きもと | Iontophoresis film |
EP0804155B1 (en) * | 1994-07-13 | 2000-11-08 | Alza Corporation | Composition and method for enhancing transdermal electrotransport agent delivery |
US5624415A (en) * | 1995-04-24 | 1997-04-29 | Alza Corporation | Reduction of skin irritation and resistance during electrotransport |
US5792097A (en) * | 1996-09-27 | 1998-08-11 | Becton Dickinson And Company | Iontophoretic electrodes and surface active agents |
US6078842A (en) * | 1997-04-08 | 2000-06-20 | Elan Corporation, Plc | Electrode and iontophoretic device and method |
US6667052B2 (en) | 1997-05-29 | 2003-12-23 | Ben Gurion University Of The Negev Research And Development Authority | Transdermal delivery system |
US5882677A (en) * | 1997-09-30 | 1999-03-16 | Becton Dickinson And Company | Iontophoretic patch with hydrogel reservoir |
US6275728B1 (en) * | 1998-12-22 | 2001-08-14 | Alza Corporation | Thin polymer film drug reservoirs |
JP4162813B2 (en) * | 1999-10-28 | 2008-10-08 | 久光製薬株式会社 | Iontophoresis device |
US7643874B2 (en) * | 2001-10-24 | 2010-01-05 | Power Paper Ltd. | Dermal patch |
US6801804B2 (en) * | 2002-05-03 | 2004-10-05 | Aciont, Inc. | Device and method for monitoring and controlling electrical resistance at a tissue site undergoing iontophoresis |
-
2004
- 2004-06-02 EP EP04735790A patent/EP1633431B1/en not_active Not-in-force
- 2004-06-02 US US10/858,045 patent/US7340297B2/en not_active Expired - Fee Related
- 2004-06-02 WO PCT/IL2004/000468 patent/WO2004105865A1/en active Application Filing
- 2004-06-02 KR KR1020057023154A patent/KR20050121277A/en not_active Application Discontinuation
- 2004-06-02 JP JP2006508485A patent/JP2006526454A/en active Pending
- 2004-06-02 ES ES04735790T patent/ES2316987T3/en active Active
- 2004-06-02 AT AT04735790T patent/ATE413860T1/en not_active IP Right Cessation
- 2004-06-02 CN CNA2004800224399A patent/CN1832777A/en active Pending
- 2004-06-02 DE DE602004017720T patent/DE602004017720D1/en not_active Expired - Fee Related
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0318776A1 (en) * | 1987-12-04 | 1989-06-07 | Robert Tapper | Method and apparatus for minimizing skin injury with electrode use |
US5652043A (en) | 1995-12-20 | 1997-07-29 | Baruch Levanon | Flexible thin layer open electrochemical cell |
US5811204A (en) | 1995-12-20 | 1998-09-22 | Baruch Levanon | Flexible thin layer open electrochemical cell |
US5897522A (en) | 1995-12-20 | 1999-04-27 | Power Paper Ltd. | Flexible thin layer open electrochemical cell and applications of same |
EP0900576A1 (en) * | 1996-03-17 | 1999-03-10 | Hisamitsu Pharmaceutical Co., Inc. | Electrode device for iontophoresis |
US5911223A (en) * | 1996-08-09 | 1999-06-15 | Massachusetts Institute Of Technology | Introduction of modifying agents into skin by electroporation |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1638644A1 (en) * | 2003-06-30 | 2006-03-29 | JOHNSON & JOHNSON CONSUMER PRODUCTS, INC. | Device for treatment of human or animal barrier membranes |
EP1641524A1 (en) * | 2003-06-30 | 2006-04-05 | Johnson & Johnson Consumer Companies, Inc. | Methods of treating pores on the skin with electricity |
EP2357018A3 (en) * | 2003-06-30 | 2014-02-19 | Johnson & Johnson Consumer Products, Inc. | Device for treatment of human or animal barrier membranes |
EP2357019A3 (en) * | 2003-06-30 | 2014-02-26 | Johnson and Johnson Consumer Companies, Inc. | Methods and devices for treating pores on the skin with electricity |
US9050452B2 (en) | 2003-06-30 | 2015-06-09 | Johnson & Johnson Consumer Companies, Inc. | Device for treatment of a barrier membrane |
US9044397B2 (en) | 2009-03-27 | 2015-06-02 | Ethicon, Inc. | Medical devices with galvanic particulates |
WO2011111962A2 (en) * | 2010-03-09 | 2011-09-15 | 아이큐어㈜ | Iontophoresis patch |
WO2011111962A3 (en) * | 2010-03-09 | 2012-03-15 | 아이큐어㈜ | Iontophoresis patch |
US9717891B2 (en) | 2012-03-23 | 2017-08-01 | Microarray Limited | Skin dressing with electrodes and physiologically active precursor substance |
CN108379734A (en) * | 2018-05-14 | 2018-08-10 | 邱骅轩 | A kind of compartmentalization transdermal iontophoretic drug delivery system |
Also Published As
Publication number | Publication date |
---|---|
US20040267190A1 (en) | 2004-12-30 |
KR20050121277A (en) | 2005-12-26 |
ATE413860T1 (en) | 2008-11-15 |
DE602004017720D1 (en) | 2008-12-24 |
EP1633431B1 (en) | 2008-11-12 |
ES2316987T3 (en) | 2009-04-16 |
EP1633431A1 (en) | 2006-03-15 |
US7340297B2 (en) | 2008-03-04 |
JP2006526454A (en) | 2006-11-24 |
CN1832777A (en) | 2006-09-13 |
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