US20060137973A1 - Device and method for instrument steralization - Google Patents
Device and method for instrument steralization Download PDFInfo
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- US20060137973A1 US20060137973A1 US11/287,531 US28753105A US2006137973A1 US 20060137973 A1 US20060137973 A1 US 20060137973A1 US 28753105 A US28753105 A US 28753105A US 2006137973 A1 US2006137973 A1 US 2006137973A1
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- electrolyte
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- tank
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
- A61L2/16—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using chemical substances
- A61L2/18—Liquid substances or solutions comprising solids or dissolved gases
- A61L2/186—Peroxide solutions
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
- A61L2/02—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using physical phenomena
- A61L2/03—Electric current
- A61L2/035—Electrolysis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
- A61L2/24—Apparatus using programmed or automatic operation
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2202/00—Aspects relating to methods or apparatus for disinfecting or sterilising materials or objects
- A61L2202/20—Targets to be treated
- A61L2202/24—Medical instruments, e.g. endoscopes, catheters, sharps
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/46—Treatment of water, waste water, or sewage by electrochemical methods
- C02F1/461—Treatment of water, waste water, or sewage by electrochemical methods by electrolysis
- C02F1/467—Treatment of water, waste water, or sewage by electrochemical methods by electrolysis by electrochemical disinfection; by electrooxydation or by electroreduction
- C02F1/4672—Treatment of water, waste water, or sewage by electrochemical methods by electrolysis by electrochemical disinfection; by electrooxydation or by electroreduction by electrooxydation
- C02F1/4674—Treatment of water, waste water, or sewage by electrochemical methods by electrolysis by electrochemical disinfection; by electrooxydation or by electroreduction by electrooxydation with halogen or compound of halogens, e.g. chlorine, bromine
Definitions
- the present invention relates to an electrolytic method and apparatus for sterilizing instruments or other objects.
- Electrolytic technology utilizing dimensionally stable anodes has been used for years for the production of chlorine and other mixed-oxidant solutions.
- Dimensionally stable anodes are described in U.S. Pat. No. 3,234,110 to Beer, entitled “Electrode and Method of Making Same,” whereby a noble metal coating is applied over a titanium substrate.
- Various commercial electrolytic cells that have been used routinely for oxidant production may utilize a flow-through configuration that may or may not be under pressure that is adequate to create flow through the electrolytic device. Examples of cells of this configuration are described in U.S. Pat. No. 6,309,523 to Prasnikar, et al., entitled “Electrode and Electrolytic Cell Containing Same,” and U.S. Pat. No. 5,385,711 to Baker, et al., entitled “Electrolytic Cell for Generating Sterilization Solutions Having Increased Ozone Content,” and many other membrane-type cells.
- the oxidant is produced in an open-type cell or drawn into the cell with a syringe or pump-type device, such as described in U.S. Pat. No. 6,524,475 to Herrington, et al., entitled “Portable Water Disinfection System.”
- the pH at the surface of the anode is typically low, on the order of approximately 3.
- oxygen generated at the anode surface reacts to form hypochlorous acid and other chlor-oxygen compounds with no oxygen gas liberated.
- Typical cathodes in these electrolytic cells may be composed of titanium, noble metal coated titanium, catalyst coated titanium, nickel based allows such as Hastalloy, stainless steel, and other conductive materials impervious to high pH conditions.
- hydrogen is liberated at the cathode surface with a localized high pH value at the cathode surface.
- the metal comprising the cathode is not oxidized or otherwise damaged during electrolysis despite the production of hydrogen at the cathode surface.
- titanium hydride can form at the surface of a bare titanium cathode which may cause stress concentrations in the cathode surface.
- noble metal or catalyst coatings can be applied to the cathode surface to prevent titanium hydride from forming on the cathode surface when the cathode substrate comprises titanium.
- Sodium hydroxide with a high pH value that is produced at the cathode surface may also play a role destruction of the biofilms.
- the author presents the limitations of corrosion and oxidation of the anode and/or cathode coupon during the electrolytic process and questions the efficacy of chlorine species liberated at the anode surface as the source of destruction of biofilm at the anode.
- a medical instrument sterilizing system is described in U.S. Pat. No. 6,056,866 by Maeda, et al whereby an electrolytic solution is generated in an electrolytic cell, and a pumping device circulates the disinfectant to a separate instrument tray where the instruments are sterilized.
- the present invention is an instrument sterilization apparatus comprising at least two electrodes wherein at least one electrode comprises at least one cathode and at least one electrode comprises at least one anode, the at least one cathode comprising a tray for holding and providing electrical contact to an instrument and the at least one anode comprising a tank; at least one insulator for separating the anode and the cathode; and electrolyte disposed in the tank; wherein an electrical potential between the anode and the cathode causes an electrical charge to pass through the electrolyte, thereby generating at least one oxidant in the electrolyte.
- the instrument preferably contacts the tray, which is preferably porous.
- the apparatus preferably further comprises an electrolyte storage container which is preferably replaceable and which preferably further comprises a quick disconnect valve for allowing flow of the electrolyte to the tank only when the container is attached to the apparatus.
- the apparatus preferably further comprises a microprocessor circuit that identifies the electrolyte storage container with the apparatus or measures a remaining volume of the electrolyte in the storage container.
- the apparatus optionally further comprises a brine generating device.
- the apparatus preferably further comprises an oxidant residual measuring device.
- the apparatus also preferably further comprises a vent or reactor for eliminating hydrogen gas generated during sterilization.
- the apparatus preferably further comprises a tube for circulating electrolyte to the interior of an instrument.
- the present invention is also a method for sterilizing and instrument, the method comprising the steps of disposing electrolyte in a tank; placing an instrument in a tray, the tray electrically insulated from the tank; providing an electrical potential between the tank and the tray so that the tank becomes an anode in an electrolytic reaction and the tray becomes a cathode in the reaction; and generating at least one oxidant in the electrolyte.
- the method preferably comprises placing the instrument in electrical contact with the tray, in which case hydrogen gas is preferably generated at the surface of the instrument.
- the method preferably further comprises the step of measuring a value of a characteristic of the electrolyte, and optionally adjusting the electrical potential so that the value remains within a desired range.
- the method preferably further comprises the step of circulating electrolyte to an interior surface or interior component of the instrument.
- the method preferably further comprises the step of eliminating hydrogen gas generated during the reaction by venting or reacting the hydrogen gas.
- the method preferably further comprises the step of rinsing the instrument with a sterile solution.
- the method preferably further comprises the step of drying the instrument with heated air.
- An object of the present invention is to simplify sterilizing apparatuses by using sterilizing trays as the anode and cathode together in one unit.
- a further object of the present invention is to utilize on or more of hydrogen formation, chlorine or mixed oxidant formation, and sodium hydroxide formation to sterilize instruments.
- An advantage of the present invention is that the medical instruments or other devices requiring sterilization are preferably utilitzed as the anode and/or cathode in the electrolytic process, thus enhancing the sterilizing properties of the system.
- FIG. 1 is a system view of an embodiment of the present invention where the device to be sterilized is in electrical contact with a cathode tray.
- FIG. 2 is a view of the quick disconnect electrolyte cartridge of the present invention.
- FIG. 3 is a view of the present invention comprising optional heater sterile water rinse modules.
- the present invention comprises an electrolytic device and method for generation of hydrogen gas at the cathode surface and oxidants produced at both the anode and cathode, which are utilized to expel contaminants such as biofilms and to disinfect surfaces, such as for sterilizing instruments and other devices.
- the present invention preferably utilizes the features of stable anodes and cathodes, formation of hydrogen formed at the cathode surface, formation of sodium hydroxide generated at the cathode surface, and formation of chlorine and mixed-oxidant species generated in a low pH environment at the anode surface as the basis for sterilizing instruments or objects.
- to “sterilize” means to sterilize, disinfect, or otherwise clean.
- instrument means any object or device to be sterilized, including but not limited to surgical instruments, endoscopes, utensils, and the like.
- the instrument to be sterilized is preferably used as the cathode in an electrolytic process.
- Hydrogen liberated at the cathode (instrument) surface discharges all materials, including but not limited to biofilms, from the instrument surface.
- Sodium hydroxide at high pH acts as a caustic substance to disinfect the device.
- Chlorine liberated at the anode surface at low pH (acidic) disinfects microorganisms on the device surface, or creates a disinfectant in the solution to kill microorganisms on the device surface and microorganisms or organic material in the electrolyte fluid.
- the instrument is preferably at least partially electrically conductive, and more preferably at least partially metallic.
- Instruments preferably comprise titanium, Hastalloy, stainless steel, conductive plastic, or other caustic (high pH) resisting materials.
- Plastic components of the instruments are optionally impregnated with titanium, hastalloy, stainless, carbon, or other conductive filings that then make the plastic electrically conductive to facilitate hydrogen formation at the surface of the plastic.
- An oxidant solution pump is preferably utilized to pump oxidant to the internal components and surfaces of instruments such as endoscopes.
- a hydrogen vent and recombiner device preferably converts hydrogen liberated in the electrolysis process, and oxygen from the atmosphere, to water vapor to mitigate the dangers associated with hydrogen gas.
- tank 12 preferably acts as the anode and preferably comprises a catalytic coating on its interior surface, which contains electrolyte 62 .
- Inner tray 14 preferably comprises the primary cathode.
- Inner tray 14 preferably comprises a suitable cathode material, preferably titanium, and further preferably comprises perforations 50 that allow electrolyte 62 to freely flow around both the outside and the inside of inner tray 14 .
- Inner tray 14 is optionally removeable.
- the electrolyte is preferably converted to chlorine-based mixed-oxidant species within electrolysis space 26 .
- instrument 38 When instrument 38 is placed within inner tray 14 , instrument 38 preferably comes into electrical contact with inner tray 14 and thereby also acts as a cathode in the electrolysis process.
- inner tray 14 is not used, and negative DC electrical power is directly applied to instrument 38 via cathode electrical conductor 18 ; in this case, instrument 38 preferably rests in a perforated plastic mesh, perforated Teflon liner, or the like, or rests on insulating supports, within tank 12 so there is no electrical contact between tank 12 (the anode) and instrument 38 (the cathode).
- Instrument 38 is preferably constructed of a conducting material, or can be produced from a plastic material with additives to make the plastic components electrically conductive.
- hydrogen is liberated at the surface of the cathode.
- Hydrogen bubbles preferably act as a physical scrubbing agent to remove material from the surface of instrument 38 .
- Such material includes but is not limited to organic materials, biological materials, biofilms, or other organic matter.
- the organic contaminants are then transferred to bulk electrolyte 62 , which is preferably concurrently converted to a chlorine-based mixed oxidant solution.
- the mixed-oxidant solution then acts as a disinfecting solution to destroy the organic contaminants within bulk electrolyte 62 .
- Tank 12 which preferably serves as the anode in the system, preferably mechanically supports and is electrically insulated from inner tray 14 , which preferably serves as the cathode, by a plurality of insulators 20 , 22 .
- one insulator may be disposed on the inside of tank 12 , for example in a ring shape, for supporting inner tray 14 .
- inner tray 14 is preferably attached to insulators 20 , 22 , it may optionally removeably rest on insulators 20 , 22 , optionally via a lip on the tray or by some other means.
- Positive DC electrical power is preferably applied to tank 12 via anode electrical conductor 16 .
- Negative DC electrical power is preferably applied to inner tray 14 via cathode electrical conductor 18 .
- Power to tank 12 and inner tray 14 is preferably regulated and controlled by controller 56 , which also preferably controls the system.
- the present system and method preferably comprise a batch process that maintains a desired residual oxidant value, preferably a residual chlorine value, within electrolyte 62 .
- the sterilizing device of the present invention preferably comprises an oxidant residual monitoring device 70 , which preferably comprises an oxidation reduction potential (ORP) sensor or a chlorine sensor, preferably mounted on an integrated circuit device (for example, a chlorine sensor-on-a-chip).
- ORP oxidation reduction potential
- the ORP value may optionally be adjusted for variations in temperature and pH of electrolyte 62 .
- Monitoring device 70 may be then used in a feedback system for controlling the electrolytic operation of the system.
- Oxidant residual monitoring device 70 monitors the chlorine residual value, preferably via controller 56 . If the chlorine residual value is below the desired value, controller 56 provides additional power to tank 12 and inner tray 14 thereby producing additional oxidant in electrolyte 62 . In this mode of operation, neither the oxidant demand nor the volume or fluid level of electrolyte 62 are important to maintaining the desired chlorine or other oxidant residual value. If the chlorine residual value is not sufficient, controller 56 continues making oxidant until the desired chlorine residual is maintained.
- Circulation of electrolyte 62 in the device may be desirable.
- internal components of endoscope 100 used for some medical procedures may become contaminated.
- pump 42 preferably transfers electrolyte 62 through passage 40 from tank 12 and through 3-way valve 52 and passage 44 into tube 46 and out of tube end 48 .
- Tube end 48 is preferably connected to a hollow passage of a medical instrument, such as endoscope 100 , so that sterilizing fluid can be flushed through the internal components of the medical instruments.
- electrolyte 62 may optionally be discarded from the sterilizing tray by switching the valve position of 3-way valve 52 and thereby discharging electrolyte through outlet 54 .
- Pump 42 and 3-way valve 52 are preferably controlled by controller 56 .
- Electrolysis typically generates hydrogen gas at the cathode electrode.
- Hydrogen gas is explosive at a wide range of pressures. Only below a concentration of approximately 4.1% hydrogen in the atmosphere, or above a concentration of about 74.2% hydrogen in the atmosphere, is the gas mixture not combustible. Thus, for proper safety, hydrogen containment or elimination is desirable.
- hydrogen gas accumulates in the upper space 64 of the sterilizing unit and is contained there by device cover 24 .
- the hydrogen gas is preferably transferred from upper space 64 via passage 28 to catalytic recombiner 34 , which is preferably utilized to burn hydrogen with oxygen to produce water vapor, which is preferably discharged out of port 36 .
- Normal atmospheric air is preferably drawn into blower 32 and transferred through passage 30 to provide the oxygen source for reacting with hydrogen within catalytic combiner 34 .
- hydrogen is destroyed and is no longer available as a fuel source for an explosive event.
- a vent pipe transfers hydrogen from upper space 64 to a ventilation duct and discharges it outside of the room or facility that houses the sterilizing device.
- Electrolyte 62 preferably comprises a sodium chloride brine solution. Other halide salts may alternatively be utilized to produce electrolyte 62 .
- a preferred source of brine solution is 0.9% saline Ringers solution.
- Pre-made electrolyte solution 60 is preferably stored within electrolyte storage container 58 for use with the present invention.
- electrolyte storage container 58 is optionally attached to the sterilizing tray via support 74 and is preferably quickly removable from the system by means of quick disconnect self-sealing valve 68 for subsequent replacement by a new electrolyte storage container.
- electrolyte storage container 58 may be refillable.
- Electrolyte storage container 58 preferably comprises vent valve 66 that allows the introduction of air into electrolyte storage container 58 as pre-made electrolyte solution 60 is drawn out of container 58 thereby avoiding negative pressure in container 58 .
- Container 58 optionally comprises microchip device 72 that identifies container 58 with the total system, and preferably provides for electronic monitoring of the volume of the contents of container 58 based on the number of cycles of the system or another property.
- Electrolyte storage container 58 is optionally replaced with a brine generating device.
- Such brine generating device is preferably filled with salt, preferably a halogen salt, and mixes water with the halogen salt to produce a liquid brine solution.
- the liquid brine solution performs as electrolyte 62 .
- the sterilizing system optionally comprises heater/dryer module 80 and sterile water purge module 82 .
- the initial sterilizing cycle is preferably followed by draining of electrolyte via 3-way valve 52 through outlet 54 and subsequent closure of 3-way valve 52 .
- 3-way purge valve 86 is opened to allow transfer of sterile water, or another sterile solution, from sterile water purge module 82 for rinsing tank 12 ; 3-way purge valve 86 preferably prevents the sterile water from exiting via outlet 54 .
- 3-way purge valve 86 is preferably opened to drain sterile water via outlet 54 .
- 3-way valve 84 is preferably opened to allow heated dry air from heater/dryer module 80 to dry the instruments within tank 12 .
- the present invention optionally comprises one or more oxidant storage containers and at least one port for injecting one or more oxidants into an instrument, including but not limited to a closed fluid body, an open fluid body, a pipe with fluid flowing therein, a sump, a basin, a trough, or a plenum.
- the present invention is particularly applicable to medical instrument sterilization. However, it will be obvious to those versed in the art that this invention can be utilized in a variety of applications where other objects or devices need to be sterilized or otherwise cleaned, including but not limited to dishwashing machines, cabinets, or other configurations.
Abstract
Description
- The present invention relates to an electrolytic method and apparatus for sterilizing instruments or other objects.
- Note that the following discussion refers to a number of publications and references. Discussion of such publications herein is given for more complete background of the scientific principles and is not to be construed as an admission that such publications are prior art for patentability determination purposes.
- Electrolytic technology utilizing dimensionally stable anodes (DSA) has been used for years for the production of chlorine and other mixed-oxidant solutions. Dimensionally stable anodes are described in U.S. Pat. No. 3,234,110 to Beer, entitled “Electrode and Method of Making Same,” whereby a noble metal coating is applied over a titanium substrate.
- An example of an electrolytic cell with membranes is described in U.S. Pat. RE 32,077 to deNora, et al., entitled “Electrode Cell with Membrane and Method for Making Same,” whereby a circular dimensionally stable anode is utilized with a membrane wrapped around the anode, and a cathode concentrically located around the anode/membrane assembly.
- An electrolytic cell with dimensionally stable anodes without membranes is described in U.S. Pat. No. 4,761,208 to Gram, et al., entitled “Electrolytic Method and Cell for Sterilizing Water.”
- Various commercial electrolytic cells that have been used routinely for oxidant production may utilize a flow-through configuration that may or may not be under pressure that is adequate to create flow through the electrolytic device. Examples of cells of this configuration are described in U.S. Pat. No. 6,309,523 to Prasnikar, et al., entitled “Electrode and Electrolytic Cell Containing Same,” and U.S. Pat. No. 5,385,711 to Baker, et al., entitled “Electrolytic Cell for Generating Sterilization Solutions Having Increased Ozone Content,” and many other membrane-type cells.
- In other configurations, the oxidant is produced in an open-type cell or drawn into the cell with a syringe or pump-type device, such as described in U.S. Pat. No. 6,524,475 to Herrington, et al., entitled “Portable Water Disinfection System.”
- U.S. Pat. No. 6,736,966 to Herrington, et al., entitled “Portable Water Disinfection System”, the specification and claims of which is incorporated herein by reference, describes disinfection devices that utilize, in one instance, a cell chamber whereby hydrogen gas is generated during electrolysis of an electrolyte, and provides the driving force to expel oxidant from the cell chamber through restrictive check valve type devices. In this configuration, unconverted electrolyte is also expelled from the body of the cell as hydrogen gas is generated. In an alternate configuration in the same application, hydrogen gas pressure is contained in a cell chamber during electrolysis, but the pressure within the cell chamber is limited by the action of a spring loaded piston that continues to increase the volume of the cell chamber as gas volume increases. Ultimately, a valve mechanism opens, and the spring-loaded piston fills the complete volume of the cell chamber forcing the oxidant out of the cell chamber.
- In the electrolytic cells utilizing titanium substrates with noble metal coatings as the anode, the pH at the surface of the anode is typically low, on the order of approximately 3. With sufficiently high brine concentration in the electrolyte, and sufficiently low voltage potential at the anode surface, oxygen generated at the anode surface reacts to form hypochlorous acid and other chlor-oxygen compounds with no oxygen gas liberated. Typical cathodes in these electrolytic cells may be composed of titanium, noble metal coated titanium, catalyst coated titanium, nickel based allows such as Hastalloy, stainless steel, and other conductive materials impervious to high pH conditions. As the cathode, hydrogen is liberated at the cathode surface with a localized high pH value at the cathode surface. During electrolysis, the metal comprising the cathode is not oxidized or otherwise damaged during electrolysis despite the production of hydrogen at the cathode surface. Over time, titanium hydride can form at the surface of a bare titanium cathode which may cause stress concentrations in the cathode surface. To preclude this hydride formation, noble metal or catalyst coatings can be applied to the cathode surface to prevent titanium hydride from forming on the cathode surface when the cathode substrate comprises titanium.
- In a paper by Christine Rabinovitch, entitled “Electrochemical Control of Staphylococcus epidermidis Biofilms”, published in the Proceedings of the Winter 2004 CBE Technical Advisory Conference, Feb. 5-6, 2004 (Montana State University, Center for Biofilm Engineering), an electrolytic method is described whereby a metallic coupon with a biofilm media grown on the surface of the metallic coupon is utilized as the anode and/or cathode in an electrolytic reaction. When the metallic coupon is utilized as the cathode, hydrogen liberated at the surface of the cathode forces partial or complete discharge and removal of the biofilm from the metallic cathode surface. Sodium hydroxide with a high pH value that is produced at the cathode surface may also play a role destruction of the biofilms. The author presents the limitations of corrosion and oxidation of the anode and/or cathode coupon during the electrolytic process and questions the efficacy of chlorine species liberated at the anode surface as the source of destruction of biofilm at the anode.
- An anti-biofouling system is described in U.S. Pat. No. 6,514,401 by Chyou, et al whereby a graphite powder with binder is formed on an underwater structure immersed in seawater. The conductive surface acts as an anode or cathode when electrical power is applied to form an electrolytic surface whereby organisms are prohibited from forming on the structure.
- A medical instrument sterilizing system is described in U.S. Pat. No. 6,056,866 by Maeda, et al whereby an electrolytic solution is generated in an electrolytic cell, and a pumping device circulates the disinfectant to a separate instrument tray where the instruments are sterilized.
- The present invention is an instrument sterilization apparatus comprising at least two electrodes wherein at least one electrode comprises at least one cathode and at least one electrode comprises at least one anode, the at least one cathode comprising a tray for holding and providing electrical contact to an instrument and the at least one anode comprising a tank; at least one insulator for separating the anode and the cathode; and electrolyte disposed in the tank; wherein an electrical potential between the anode and the cathode causes an electrical charge to pass through the electrolyte, thereby generating at least one oxidant in the electrolyte. The instrument preferably contacts the tray, which is preferably porous.
- The apparatus preferably further comprises an electrolyte storage container which is preferably replaceable and which preferably further comprises a quick disconnect valve for allowing flow of the electrolyte to the tank only when the container is attached to the apparatus. The apparatus preferably further comprises a microprocessor circuit that identifies the electrolyte storage container with the apparatus or measures a remaining volume of the electrolyte in the storage container. The apparatus optionally further comprises a brine generating device. The apparatus preferably further comprises an oxidant residual measuring device. The apparatus also preferably further comprises a vent or reactor for eliminating hydrogen gas generated during sterilization. The apparatus preferably further comprises a tube for circulating electrolyte to the interior of an instrument.
- The present invention is also a method for sterilizing and instrument, the method comprising the steps of disposing electrolyte in a tank; placing an instrument in a tray, the tray electrically insulated from the tank; providing an electrical potential between the tank and the tray so that the tank becomes an anode in an electrolytic reaction and the tray becomes a cathode in the reaction; and generating at least one oxidant in the electrolyte. The method preferably comprises placing the instrument in electrical contact with the tray, in which case hydrogen gas is preferably generated at the surface of the instrument.
- The method preferably further comprises the step of measuring a value of a characteristic of the electrolyte, and optionally adjusting the electrical potential so that the value remains within a desired range. The method preferably further comprises the step of circulating electrolyte to an interior surface or interior component of the instrument. The method preferably further comprises the step of eliminating hydrogen gas generated during the reaction by venting or reacting the hydrogen gas. The method preferably further comprises the step of rinsing the instrument with a sterile solution. The method preferably further comprises the step of drying the instrument with heated air.
- An object of the present invention is to simplify sterilizing apparatuses by using sterilizing trays as the anode and cathode together in one unit.
- A further object of the present invention is to utilize on or more of hydrogen formation, chlorine or mixed oxidant formation, and sodium hydroxide formation to sterilize instruments.
- An advantage of the present invention is that the medical instruments or other devices requiring sterilization are preferably utilitzed as the anode and/or cathode in the electrolytic process, thus enhancing the sterilizing properties of the system.
- Other objects, advantages and novel features, and further scope of applicability of the present invention will be set forth in part in the detailed description to follow, taken in conjunction with the accompanying drawings, and in part will become apparent to those skilled in the art upon examination of the following, or may be learned by practice of the invention. The objects and advantages of the invention may be realized and attained by means of the instrumentalities and combinations particularly pointed out in the appended claims.
- The accompanying drawings, which are incorporated into and form a part of the specification, illustrate several embodiments of the present invention and, together with the description, serve to explain the principles of the invention. The drawings are only for the purpose of illustrating a preferred embodiment of the invention and are not to be construed as limiting the invention. In the drawings:
-
FIG. 1 is a system view of an embodiment of the present invention where the device to be sterilized is in electrical contact with a cathode tray. -
FIG. 2 is a view of the quick disconnect electrolyte cartridge of the present invention. -
FIG. 3 is a view of the present invention comprising optional heater sterile water rinse modules. - The present invention comprises an electrolytic device and method for generation of hydrogen gas at the cathode surface and oxidants produced at both the anode and cathode, which are utilized to expel contaminants such as biofilms and to disinfect surfaces, such as for sterilizing instruments and other devices. The present invention preferably utilizes the features of stable anodes and cathodes, formation of hydrogen formed at the cathode surface, formation of sodium hydroxide generated at the cathode surface, and formation of chlorine and mixed-oxidant species generated in a low pH environment at the anode surface as the basis for sterilizing instruments or objects. As used throughout the specification and claims, to “sterilize” means to sterilize, disinfect, or otherwise clean. As used throughout the specification and claims, “instrument” means any object or device to be sterilized, including but not limited to surgical instruments, endoscopes, utensils, and the like.
- In the present invention the instrument to be sterilized is preferably used as the cathode in an electrolytic process. Hydrogen liberated at the cathode (instrument) surface discharges all materials, including but not limited to biofilms, from the instrument surface. Sodium hydroxide at high pH acts as a caustic substance to disinfect the device. Chlorine liberated at the anode surface at low pH (acidic) disinfects microorganisms on the device surface, or creates a disinfectant in the solution to kill microorganisms on the device surface and microorganisms or organic material in the electrolyte fluid. The instrument is preferably at least partially electrically conductive, and more preferably at least partially metallic. Instruments preferably comprise titanium, Hastalloy, stainless steel, conductive plastic, or other caustic (high pH) resisting materials. Plastic components of the instruments are optionally impregnated with titanium, hastalloy, stainless, carbon, or other conductive filings that then make the plastic electrically conductive to facilitate hydrogen formation at the surface of the plastic. An oxidant solution pump is preferably utilized to pump oxidant to the internal components and surfaces of instruments such as endoscopes. A hydrogen vent and recombiner device preferably converts hydrogen liberated in the electrolysis process, and oxygen from the atmosphere, to water vapor to mitigate the dangers associated with hydrogen gas.
- Referring to
FIG. 1 ,tank 12 preferably acts as the anode and preferably comprises a catalytic coating on its interior surface, which contains electrolyte 62.Inner tray 14 preferably comprises the primary cathode.Inner tray 14 preferably comprises a suitable cathode material, preferably titanium, and further preferably comprises perforations 50 that allow electrolyte 62 to freely flow around both the outside and the inside ofinner tray 14.Inner tray 14 is optionally removeable. By application of the appropriate positive (preferably direct current) voltage and current density totank 12 and negative (preferably direct current) voltage and current density toinner tray 14, the electrolyte is preferably converted to chlorine-based mixed-oxidant species withinelectrolysis space 26. - When
instrument 38 is placed withininner tray 14,instrument 38 preferably comes into electrical contact withinner tray 14 and thereby also acts as a cathode in the electrolysis process. Alternatively,inner tray 14 is not used, and negative DC electrical power is directly applied toinstrument 38 via cathodeelectrical conductor 18; in this case,instrument 38 preferably rests in a perforated plastic mesh, perforated Teflon liner, or the like, or rests on insulating supports, withintank 12 so there is no electrical contact between tank 12 (the anode) and instrument 38 (the cathode). -
Instrument 38 is preferably constructed of a conducting material, or can be produced from a plastic material with additives to make the plastic components electrically conductive. In the electrolysis process of the present invention, hydrogen is liberated at the surface of the cathode. Hydrogen bubbles preferably act as a physical scrubbing agent to remove material from the surface ofinstrument 38. Such material includes but is not limited to organic materials, biological materials, biofilms, or other organic matter. The organic contaminants are then transferred to bulk electrolyte 62, which is preferably concurrently converted to a chlorine-based mixed oxidant solution. The mixed-oxidant solution then acts as a disinfecting solution to destroy the organic contaminants within bulk electrolyte 62. -
Tank 12, which preferably serves as the anode in the system, preferably mechanically supports and is electrically insulated frominner tray 14, which preferably serves as the cathode, by a plurality ofinsulators 20, 22. Alternatively one insulator may be disposed on the inside oftank 12, for example in a ring shape, for supportinginner tray 14. Althoughinner tray 14 is preferably attached toinsulators 20, 22, it may optionally removeably rest oninsulators 20, 22, optionally via a lip on the tray or by some other means. Positive DC electrical power is preferably applied totank 12 via anodeelectrical conductor 16. Negative DC electrical power is preferably applied toinner tray 14 via cathodeelectrical conductor 18. Power totank 12 andinner tray 14 is preferably regulated and controlled bycontroller 56, which also preferably controls the system. - The present system and method preferably comprise a batch process that maintains a desired residual oxidant value, preferably a residual chlorine value, within electrolyte 62. The sterilizing device of the present invention preferably comprises an oxidant
residual monitoring device 70, which preferably comprises an oxidation reduction potential (ORP) sensor or a chlorine sensor, preferably mounted on an integrated circuit device (for example, a chlorine sensor-on-a-chip). The ORP value may optionally be adjusted for variations in temperature and pH of electrolyte 62. -
Monitoring device 70 may be then used in a feedback system for controlling the electrolytic operation of the system. Oxidantresidual monitoring device 70 monitors the chlorine residual value, preferably viacontroller 56. If the chlorine residual value is below the desired value,controller 56 provides additional power totank 12 andinner tray 14 thereby producing additional oxidant in electrolyte 62. In this mode of operation, neither the oxidant demand nor the volume or fluid level of electrolyte 62 are important to maintaining the desired chlorine or other oxidant residual value. If the chlorine residual value is not sufficient,controller 56 continues making oxidant until the desired chlorine residual is maintained. - Circulation of electrolyte 62 in the device may be desirable. For example, internal components of
endoscope 100 used for some medical procedures may become contaminated. By circulating electrolyte 62 to the internal surface ofendoscope 100, the internal components ofendoscope 100 are cleaned in the same manner as the exterior surface ofendoscope 100. To facilitate circulation of electrolyte 62, pump 42 preferably transfers electrolyte 62 throughpassage 40 fromtank 12 and through 3-way valve 52 andpassage 44 intotube 46 and out oftube end 48.Tube end 48 is preferably connected to a hollow passage of a medical instrument, such asendoscope 100, so that sterilizing fluid can be flushed through the internal components of the medical instruments. When the flushing cycle is complete, electrolyte 62 may optionally be discarded from the sterilizing tray by switching the valve position of 3-way valve 52 and thereby discharging electrolyte throughoutlet 54.Pump 42 and 3-way valve 52 are preferably controlled bycontroller 56. - Electrolysis typically generates hydrogen gas at the cathode electrode. Hydrogen gas is explosive at a wide range of pressures. Only below a concentration of approximately 4.1% hydrogen in the atmosphere, or above a concentration of about 74.2% hydrogen in the atmosphere, is the gas mixture not combustible. Thus, for proper safety, hydrogen containment or elimination is desirable. In the present invention, hydrogen gas accumulates in the
upper space 64 of the sterilizing unit and is contained there bydevice cover 24. The hydrogen gas is preferably transferred fromupper space 64 viapassage 28 tocatalytic recombiner 34, which is preferably utilized to burn hydrogen with oxygen to produce water vapor, which is preferably discharged out ofport 36. Normal atmospheric air is preferably drawn intoblower 32 and transferred throughpassage 30 to provide the oxygen source for reacting with hydrogen withincatalytic combiner 34. In this manner, hydrogen is destroyed and is no longer available as a fuel source for an explosive event. Alternatively, a vent pipe transfers hydrogen fromupper space 64 to a ventilation duct and discharges it outside of the room or facility that houses the sterilizing device. - Electrolyte 62 preferably comprises a sodium chloride brine solution. Other halide salts may alternatively be utilized to produce electrolyte 62. For medical applications, a preferred source of brine solution is 0.9% saline Ringers solution.
Pre-made electrolyte solution 60 is preferably stored withinelectrolyte storage container 58 for use with the present invention. Referring toFIG. 2 ,electrolyte storage container 58 is optionally attached to the sterilizing tray via support 74 and is preferably quickly removable from the system by means of quick disconnect self-sealingvalve 68 for subsequent replacement by a new electrolyte storage container. Alternatively,electrolyte storage container 58 may be refillable.Electrolyte storage container 58 preferably comprisesvent valve 66 that allows the introduction of air intoelectrolyte storage container 58 aspre-made electrolyte solution 60 is drawn out ofcontainer 58 thereby avoiding negative pressure incontainer 58. -
Container 58 optionally comprisesmicrochip device 72 that identifiescontainer 58 with the total system, and preferably provides for electronic monitoring of the volume of the contents ofcontainer 58 based on the number of cycles of the system or another property.Electrolyte storage container 58 is optionally replaced with a brine generating device. Such brine generating device is preferably filled with salt, preferably a halogen salt, and mixes water with the halogen salt to produce a liquid brine solution. The liquid brine solution performs as electrolyte 62. - As shown in
FIG. 3 , the sterilizing system optionally comprises heater/dryer module 80 and sterile water purge module 82. In this embodiment, the initial sterilizing cycle is preferably followed by draining of electrolyte via 3-way valve 52 throughoutlet 54 and subsequent closure of 3-way valve 52. In the second step, 3-way purge valve 86 is opened to allow transfer of sterile water, or another sterile solution, from sterile water purge module 82 for rinsingtank 12; 3-way purge valve 86 preferably prevents the sterile water from exiting viaoutlet 54. After purging, 3-way purge valve 86 is preferably opened to drain sterile water viaoutlet 54. In the final step, 3-way valve 84 is preferably opened to allow heated dry air from heater/dryer module 80 to dry the instruments withintank 12. - The present invention optionally comprises one or more oxidant storage containers and at least one port for injecting one or more oxidants into an instrument, including but not limited to a closed fluid body, an open fluid body, a pipe with fluid flowing therein, a sump, a basin, a trough, or a plenum.
- The present invention is particularly applicable to medical instrument sterilization. However, it will be obvious to those versed in the art that this invention can be utilized in a variety of applications where other objects or devices need to be sterilized or otherwise cleaned, including but not limited to dishwashing machines, cabinets, or other configurations.
- Although the invention has been described in detail with particular reference to these preferred embodiments, other embodiments can achieve the same results. Variations and modifications of the present invention will be obvious to those skilled in the art and it is intended to cover in the appended claims all such modifications and equivalents. The entire disclosures of all references, applications, patents, and publications cited above are hereby incorporated by reference.
Claims (20)
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/287,531 US20060137973A1 (en) | 2004-11-24 | 2005-11-22 | Device and method for instrument steralization |
JP2007543565A JP2008521507A (en) | 2004-11-24 | 2005-11-23 | Device and method for sterilization of instruments |
EP05852261A EP1833515B1 (en) | 2004-11-24 | 2005-11-23 | Device and method for instrument sterilization |
AT05852261T ATE446773T1 (en) | 2004-11-24 | 2005-11-23 | DEVICE AND METHOD FOR STERILIZING INSTRUMENTS |
PCT/US2005/042893 WO2006058282A2 (en) | 2004-11-24 | 2005-11-23 | Device and method for instrument sterilization |
DE602005017426T DE602005017426D1 (en) | 2004-11-24 | 2005-11-23 | DEVICE AND METHOD FOR STERILIZING INSTRUMENTS |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US63087704P | 2004-11-24 | 2004-11-24 | |
US11/287,531 US20060137973A1 (en) | 2004-11-24 | 2005-11-22 | Device and method for instrument steralization |
Publications (1)
Publication Number | Publication Date |
---|---|
US20060137973A1 true US20060137973A1 (en) | 2006-06-29 |
Family
ID=36498594
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US11/287,531 Abandoned US20060137973A1 (en) | 2004-11-24 | 2005-11-22 | Device and method for instrument steralization |
Country Status (6)
Country | Link |
---|---|
US (1) | US20060137973A1 (en) |
EP (1) | EP1833515B1 (en) |
JP (1) | JP2008521507A (en) |
AT (1) | ATE446773T1 (en) |
DE (1) | DE602005017426D1 (en) |
WO (1) | WO2006058282A2 (en) |
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US20090229992A1 (en) * | 2006-11-28 | 2009-09-17 | Miox Corporation | Reverse Polarity Cleaning and Electronic Flow Control Systems for Low Intervention Electrolytic Chemical Generators |
US20110011736A1 (en) * | 2009-04-28 | 2011-01-20 | Electrolytic Ozone Inc. | Disposable Cartridge for an Electrolytic Cell |
US8455010B1 (en) | 2007-10-31 | 2013-06-04 | Reoxcyn Discoveries Group, Inc | Product and method for producing an immune system supplement and performance enhancer |
US8663705B2 (en) | 2007-10-30 | 2014-03-04 | Reoxcyn Discoveries Group, Inc. | Method and apparatus for producing a stabilized antimicrobial non-toxic electrolyzed saline solution exhibiting potential as a therapeutic |
US20140094773A1 (en) * | 2012-10-01 | 2014-04-03 | Merit Medical Systems, Inc. | Adjustable length catheter and method of use |
US9255336B2 (en) | 2007-10-31 | 2016-02-09 | Reoxcyn Discoveries Group, Inc. | Method and apparatus for producing a stabilized antimicrobial non-toxic electrolyzed saline solution exhibiting potential as a therapeutic |
US10143222B2 (en) * | 2013-07-05 | 2018-12-04 | Charles Adriano Duvoisin | Compact device for electrolytic sterilization of food and utensils |
US10400349B2 (en) | 2006-11-28 | 2019-09-03 | De Nora Holdings Us, Inc. | Electrolytic on-site generator |
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US11717319B2 (en) | 2019-05-10 | 2023-08-08 | Merit Medical Systems, Inc. | Drainage catheter exchange system and associated methods |
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US20090229992A1 (en) * | 2006-11-28 | 2009-09-17 | Miox Corporation | Reverse Polarity Cleaning and Electronic Flow Control Systems for Low Intervention Electrolytic Chemical Generators |
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Also Published As
Publication number | Publication date |
---|---|
EP1833515B1 (en) | 2009-10-28 |
JP2008521507A (en) | 2008-06-26 |
WO2006058282A3 (en) | 2006-10-26 |
EP1833515A4 (en) | 2008-12-31 |
WO2006058282A2 (en) | 2006-06-01 |
ATE446773T1 (en) | 2009-11-15 |
EP1833515A2 (en) | 2007-09-19 |
DE602005017426D1 (en) | 2009-12-10 |
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