US20170121098A1 - Non-aspirating transport gel dispenser - Google Patents
Non-aspirating transport gel dispenser Download PDFInfo
- Publication number
- US20170121098A1 US20170121098A1 US14/929,697 US201514929697A US2017121098A1 US 20170121098 A1 US20170121098 A1 US 20170121098A1 US 201514929697 A US201514929697 A US 201514929697A US 2017121098 A1 US2017121098 A1 US 2017121098A1
- Authority
- US
- United States
- Prior art keywords
- bag
- volume
- dispenser
- gel
- thixotropic gel
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D83/00—Containers or packages with special means for dispensing contents
- B65D83/14—Containers or packages with special means for dispensing contents for delivery of liquid or semi-liquid contents by internal gaseous pressure, i.e. aerosol containers comprising propellant for a product delivered by a propellant
- B65D83/60—Contents and propellant separated
- B65D83/62—Contents and propellant separated by membrane, bag, or the like
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D83/00—Containers or packages with special means for dispensing contents
- B65D83/14—Containers or packages with special means for dispensing contents for delivery of liquid or semi-liquid contents by internal gaseous pressure, i.e. aerosol containers comprising propellant for a product delivered by a propellant
- B65D83/16—Containers or packages with special means for dispensing contents for delivery of liquid or semi-liquid contents by internal gaseous pressure, i.e. aerosol containers comprising propellant for a product delivered by a propellant characterised by the actuating means
- B65D83/20—Containers or packages with special means for dispensing contents for delivery of liquid or semi-liquid contents by internal gaseous pressure, i.e. aerosol containers comprising propellant for a product delivered by a propellant characterised by the actuating means operated by manual action, e.g. button-type actuator or actuator caps
- B65D83/205—Actuator caps, or peripheral actuator skirts, attachable to the aerosol container
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D83/00—Containers or packages with special means for dispensing contents
- B65D83/14—Containers or packages with special means for dispensing contents for delivery of liquid or semi-liquid contents by internal gaseous pressure, i.e. aerosol containers comprising propellant for a product delivered by a propellant
- B65D83/44—Valves specially adapted therefor; Regulating devices
- B65D83/48—Lift valves, e.g. operated by push action
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D83/00—Containers or packages with special means for dispensing contents
- B65D83/14—Containers or packages with special means for dispensing contents for delivery of liquid or semi-liquid contents by internal gaseous pressure, i.e. aerosol containers comprising propellant for a product delivered by a propellant
- B65D83/75—Aerosol containers not provided for in groups B65D83/16 - B65D83/74
- B65D83/752—Aerosol containers not provided for in groups B65D83/16 - B65D83/74 characterised by the use of specific products or propellants
Definitions
- the present invention relates to a non-aspirating dispenser containing a gel therein for delivery to a desired surface such as a medical article. More specifically, the invention relates to a gel that is dispensed in the form of droplets that are free of air or a gas therein and with reduced drift potential.
- the dispenser comprises a container having a flexible bag therein enclosing a thixotropic gel, and comprising pressurized gas that is capable of exerting pressure on said bag and forcing said gel out of said bag in a steady stream upon pressing an actuator that is operatively connected to an ejection valve.
- the bag is free of propellants, and does not produce an aerosol.
- the gel is thixotropic and is utilized for keeping medical instruments moist in order to prevent soils present thereon from drying out, which can make reprocessing of medical instruments more difficult and less effective.
- This invention can be implemented at a point of use for transport or prior to delayed reprocessing in the reprocessing area.
- Typical spray bottles or containers dispense liquids or foams via a mechanical trigger that requires continual pumping thereof to dispense a sprayed product. Since very small amounts of product are dispensed with each pump, numerous pumps are required to adequately cover a surface. The same often exhausts the user and becomes an ergonomic issue in that in spraying numerous surfaces, articles, etc., can require a person to take a break or rest.
- dispensers such as a spray bottle, eject a fluid via aspiration such that an aerosol mist is formed.
- aerosol droplets are small and hence driftable such that they can be carried into an adjacent sterile environment and contaminate the same.
- Liquid-based instrument transport products are to be avoided as they require filled containers or basins to cover all instrument surfaces and thus increase weight and sloshing of transported items.
- dispensers contain a sprayable liquid in association with propellants such as volatile hydrocarbons, e.g. butane, propane, or fluorocarbon gases that can pose flammable or toxic problems.
- propellants such as volatile hydrocarbons, e.g. butane, propane, or fluorocarbon gases that can pose flammable or toxic problems.
- a distributor for a product under pressure has a receptacle which defines a receiving volume.
- a valve having a springy press-on valve shaft and a non-return valve part is mounted on the receptacle.
- a passage through which the valve shaft may communicate with the receiving volume is provided.
- a valve seating section is arranged such that the passage is closed off when the valve shaft is in a rest position and is open when the valve shaft is pressed on.
- a flexible bag which defines an interior space is provided within the receptacle with the valve seating section outside the bag, and the bag is connected to the valve shaft by the non-return valve part such that flow of a pressurized medium may flow through the valve shaft toward the interior space, but reverse flow is blocked. Flow of pressurized medium out of or into the receptacle through the valve shaft may be obtained without releasing pressure from the pressurized bag.
- Disclosed is a method of shaving hair by spraying a shaving preparation directly onto an area of skin to form a dispersed layer of the shaving preparation without the need for hand spreading and shaving the area with a razor.
- the shaving preparation may be an aerosol or a non-aerosol shaving preparation.
- the invention is directed to a self-foaming shaving composition in the form of a lotion.
- the shaving composition comprises water, a water dispersible surface active agent capable of forming a lather, a volatile self-foaming agent, and a water soluble thickening agent wherein the composition is in the form of a self-foaming lotion having an elastic modulus (G′) of about 100 to about 1000 Pascals, preferably about 200 to about 900 Pa, most preferably about 400 to about 800 Pa (measured with a rheometer at frequency 1 Hz, oscillatory stress range 0.01-1.0 Pa, temperature 5 DEG C., Gap 1000 microns).
- G′ elastic modulus
- the present invention is also directed to an improved shaving method in which a shaving composition of the present invention is applied to an area of skin, and then said area is shaved, preferably with a wet razor.
- U.S. Pat. No. 7,909,264 B2 issued Mar. 22, 2011.
- a discharge device and a method for evaporating a liquid to the atmosphere is proposed.
- the liquid pressurized by gas is supplied to an evaporator via a flow restriction device which restricts the flow rate of the liquid such that continuous release and evaporation of the liquid is possible.
- an evaporator is proposed.
- the evaporator comprises an evaporation surface which is designed preferably by microstructuring such that the surface area is increased and/or the liquid forms an essentially uniform film on the evaporation surface.
- a sprayable polymeric foam hemostat for both compressible and non-compressible (intracavitary) acute wounds comprises hydrophobically-modified polymers, such as hm-chitosan, or other amphiphilic polymers that anchor themselves within the membrane of cells in the vicinity of the wound.
- hydrophobically-modified polymers such as hm-chitosan, or other amphiphilic polymers that anchor themselves within the membrane of cells in the vicinity of the wound.
- a sprayable hydrogel wound dressing composed of an aqueous solution of neutralized Carbopol and silver hydrosol of silver nanoparticles electrolytically formed from silver metal without the use or inclusion of organic materials.
- the hydrogel is sprayed with a physical barrier sprayer system which separates the hydrogel from the propellant.
- the hydrogel is thixotropic/shear thinning so that the viscosity of the hydrogel is sufficient reduced in the sprayer to allow spray formation and regains sufficient viscosity to resist running when deposited on a vertical surface.
- One embodiment relates to a system including a first bag-on-valve aerosol container including a first valve comprising a first valve stem, and a body having an aperture extending therethrough from a first end of the body to a second end of the body.
- the aperture is sized to accept the first valve stem at the first end of the body.
- the aperture is also sized to accept a second valve stem at the second end of the body; the body sized to accept the first valve stem and a second valve stem at the same time.
- An aqueous formulation for dispensing as a spray polymeric microcapsules containing at least one active ingredient comprising: (i) water; (ii) polymeric microcapsules having an oil-soluble core containing the at least one active ingredient; (iii) a cross linked acrylic acid co-polymer; (iv) a neutralizing amine for activating the cross linked acrylic acid copolymer to form a gel suspension for the polymeric microcapsules whereby the polymeric microcapsules are suspended in the water; (v) a chelant for protecting the aqueous formulation against destabilization by excessive metal ions; and (vi) an inhibitor for inhibiting bacterial growth in the water.
- a topical therapeutic hydrophobic breakable composition includes a carrier comprising (a) about 60% to about 99% by weight of at least one hydrophobic oil; (b) at least one viscosity-modifying agents selected from the group consisting of a fatty alcohol, a fatty acid and a wax; and (c) a tetracycline antibiotic, characterized in that at least part of the tetracycline antibiotic is suspended in the composition; the viscosity of the composition is at least about 30% higher than the viscosity of the carrier without the tetracycline antibiotic; and is higher than the viscosity of the hydrophobic oil and the tetracycline antibiotic without the viscosity modifying agents.
- the tetracycline is chemically stable in the composition for at least six months; wherein more than about 90% of the tetracycline has not broken down.
- the composition is packaged as a breakable foam that breaks easily upon application of shear force.
- a non-aspirating, non-propellant dispenser for dispensing a moisturizing thixotropic gel contained in a flexible bag in a pressurized gas container with the gel having a relatively high viscosity and the formed droplets being of a size that reduces drift potential.
- the dispenser contains a flexible bag containing the gel with the bag located in a container having a non-flammable, non-hydrocarbon-based compressed gas therein.
- a further object of the present invention is to provide non-foam gel droplets.
- the dispenser does not require priming but continuously dispenses the gel in droplet form upon pushing an actuator to provide non-priming, aerosol-free droplets for use in the medical field as for keeping instruments moist, in order to prevent soils thereon from drying out. Soil that has been allowed to dry can make reprocessing of medical instruments more difficult and less effective.
- one aspect of the invention relates to a non-aspirating dispenser for a transport gel, comprising: a thixotropic gel; said thixotropic gel having a viscosity of less than about 2,000 centipoises; said dispenser having walls forming a container and a flexible bag therein, said bag containing said thixotropic gel; a non-bag volume located between said dispenser walls and said flexible bag, said non-bag volume having a pressurized gas therein, said non-bag volume being substantially free of a propellant, a volatilizable liquid, or a foam forming gas, or any combination thereof; said dispenser having a valve, an actuator operatively connected to said valve, said actuator upon activation thereof being capable of opening said valve so that said pressurized gas will exert pressure on said bag and force said thixotropic gel out of said dispenser container in the form of non-aspirated droplets; and said droplets having a mean volume diameter that reduces drift potential.
- FIG. 1 relates to a cross-section elevation view of a non-aspirating dispenser of the present invention wherein a container contains a bag having a gel therein.
- Ergonomic friendly dispenser 10 of the present invention comprises an actuator 24 .
- Actuator 24 is connected in any conventional manner such as through disconnectable valve 30 to dispenser container 40 .
- the container contains a flexible bag 45 therein that through disconnectable valve 30 can be filled with a desired thixotropic gel of the present invention.
- Dispenser, container 40 can be in the shape of a cylinder or other suitable form and made of a pressure resistant material such as a metal, for example steel or aluminum or a plastic, such as Polyethylene terephthalate (PET).
- Bag 45 contains a thixotropic gel 50 therein.
- Non-bag or internal volume 47 located between bag 45 and dispenser container walls 40 contains a compressed eco-gas therein such as nitrogen, air, or CO 2 Suitable pressures range from about 25 to about 60 psi, and preferably from about 30 to about 50 psi.
- the compressed gas is not what would normally be considered a propellant, a volatilizable liquid, or a foam forming gas, or any combination thereof.
- propellant it is meant that the gas in contact with the product is a volatile hydrocarbon such as various alkanes, for example propane, isopropane, butane, isobutene, or other volatile alkanes including various cyclic alkanes.
- chloro-fluoro hydrocarbons as well as various fluoro-hydrocarbons are not utilized such as 1,1,1,2 tetrafluorethane (Dymel 134); 1,1,1,2,3,3,3 heptafluoropropane (Dymel 227); 1,1, difluoro ethane (Dymel 152); or 1,1,1,2,2,2 hexafluoropropane.
- Dymel 134 1,1,1,2 tetrafluorethane
- Dymel 227 1,1,1,2,3,3,3 heptafluoropropane
- Dymel 152 1,1, difluoro ethane
- 1,1,1,2,2,2 hexafluoropropane 1,1,1,2,2,2 hexafluoropropane.
- propellants can be flammable, toxic, and the like and hence the present invention is substantially free thereof.
- gases that are volatilizable liquids that are liquids under pressure, but upon being emitted from container 40 at ambient pressure volatize.
- gases include dimethyl ether, propane, isobutane, and n-butane.
- Gases that form a foam upon being emitted from dispenser 10 are also avoided by the present invention because they can obscure instruments visually, especially sharps. Also, upon breaking, the foams become liquid that readily runs off of the surface of themedical article.
- the foam can be formed either through trigger sprayers with a foaming tip or through the use of aerosols and propellants.
- gases that can form a foam include blend of propane and isobutane, A-31, P-152a, nitrous oxide, and CO 2 .
- the present invention is substantially free of the above noted propellants, volatilizable liquid; or foam forming gases.
- free thereof it is meant that any such gases contained within non-bag or internal area 47 , if used, exist in very minute amounts, for example about 5% or less, desirably about 3% or less, and preferably about 1% or less based upon the total volume of non-bag or internal volume 47 .
- a highly preferred embodiment is that non-bag or internal volume 47 contains no such gases therein.
- dispenser 10 is a non-aspirating dispenser. That is, they do not utilize suction to take up various fluids, or air, and mix the same with gel 50 of the present invention. Aspirators are avoided because when utilized as in the medical field or industry, they can draw in air that is contaminated and then dispense the same in ejected material 26 . Hence, viruses, bacteria, fungi, bodily fluids and other harmful materials can be contained in sprayer ejected material 26 that result in a harmful environment as in a sterile room, an operating room, etc. and the like.
- non-aspirating dispenser it is meant that flexible bag 45 is under positive pressure due to the enclosed gas in the non-bag or internal volume 47 area that dispenses the gel outward under pressure with no flow back into the dispenser container due to pressure differential between the dispenser container as compared to the environment outside the dispenser container. In other words, said pressure differential is always at least 2 psi greater than the outside environment pressure during dispensing.
- Dispenser 10 of the present invention containing non-aspirating nozzle 25 can be any conventional dispenser container known to the art and to the literature such as those manufactured by Ball, CCL Container, Crown, Exal, and actuators by such manufacturers Aptar, Coster, Lindal Group, and Precision Global.
- Actuator portion 24 can be connected to dispenser container 40 in any conventional manner as known to the literature and to the art.
- dispenser container 40 is of a BOV, i.e. bag-on-valve, bottle, or container wherein, as shown in FIG. 1 , flexible bag 45 is located within dispenser container 40 .
- Bag 45 can be any conventional flexible material such as various plastic and metalized films typically laminated together for optimal barrier and compatibility properties. Examples of suitable flexible laminate materials include LLDPE/Nylon/Aluminum/Polyester, LLDPE/Polyester, PP/Nylon/Aluminum/Polyester, and LLPE/Aluminum/Nylon.
- the volume of bag 45 is generally from about 50 to about 90%, desirably from about 60% to about 80%, and preferably from about 65% to about 75% based upon the total volume of dispenser container 40 .
- the non-bag or internal volume 47 i.e. pressurized gas volume
- the remainder or difference i.e. generally from about 10% to about 50%, desirably from about 20 to about 40%, and preferably from about 25 to about 35%.
- Gel material 50 is a thixotropic gel inasmuch as it is generally a semi-solid at room temperature, but upon the application of pressure thereto, flows like a liquid.
- the purpose of the gel is to keep various medical instruments moist in order to prevent soils from drying out, which can make reprocessing of medical instruments more difficult and less effective.
- This invention may be used at a point of use for transport or prior to delayed reprocessing in a reprocessing area.
- gels utilized are those that contain one or more thickening agents to help with dispensing and cling properties, humectants to keep soils moist, corrosion inhibitors so that extended contact with moisture does not promote corrosion of instrumentation, surfactants to penetrate soils, sequestrants to aid in anti-redeposition, and preservatives to prevent contamination of the product and water. All of these compounds are well known to the art and to the literature. Gels that can be used include “Pre-Klenz”, Instrument Transport Gel made by Steris Corporation, and OptiPro Instrument Gel made by Ecolab. Other examples of gel include cellulose, hydrophobically modified cellulose, guar gum, quaternized guar gum, alginate, or cationated alginate comprising calcium, magnesium, or sodium cations, or any combination thereof.
- the viscosity of the thixotropic gel is less than about 2,000, desirably from about 100 to about 1,700, and preferably from about 150 to about 1,500 centipoise.
- dispenser 10 The operation of dispenser 10 is generally as follows.
- a suitable amount of a particular type of gel for example Pre-Klenz, is added to flexible bag 45 .
- an eco-gas such as air, etc.
- the amount of pressure therein can generally be from about 25 to about 60 psi, and desirably from about 30 to about 50, dependent upon the type of sprayer.
- valve 30 Upon pressurizing interior area 47 , valve 30 is closed to the bag.
- Dispenser 10 can be activated as by pressing actuator 24 , or another release mechanism, that through a typical mechanical connection, opens valve 30 so that eco-gas 60 applies pressure to thixotropic gel 50 and forces the gel through the non-aspirating sprayer and is ejected through nozzle 25 in the form of ejected material 26 such as liquid droplets.
- the size of the liquid droplets is another important aspect of the present invention. If they are too small, droplets will tend to drift, i.e. remain suspended in the air and could be diverted to an undesirable area such as the sterile field within a surgical suite or operating room. Thus, reduced drift potential is desired. If too heavy, the droplets conglomerate and will not spray on the instruments in fan spray pattern that gives adequate coverage but as more of a stream. Desirably, the mean volume droplet diameter ranges from about 80 to about 500, desirably from about 100 to about 450, and preferably from about 150 to about 400 microns, with about 250 microns being highly preferred.
- This droplet size can be tested with a piece of equipment such as the Malvern Spraytec Particle Size Analyzer, as per methods published by International Standards Organization ISO 13320 (2009) Particle Size Analysis-Laser Diffraction Methods.
- An ergonomic aspect of the present invention is that once actuator 24 is pressed, it remains open until released. Thus, a steady spray of droplets 26 of the thixotropic gel are emitted from nozzle 25 in a non-aspiratable form.
- the non-aspirating dispenser of the present invention suitable for keeping instruments moist, in order to prevent soils thereon from drying out, that can make reprocessing of medical instruments more difficult and less effective.
- soils could include blood, tissue, bodily fluids, mucus, feces, adipose tissue, synovial fluid, or other soils associated with medical procedures.
- surgical instruments such as forceps, hemostats, clamps, scalpels, retractors, bone saws, chisels, cannulas, curettes, osteotomes, rongeurs
- other medical instruments such as endoscopes (both rigid and flexible), or probes can also be coated with the gel.
- the invention can be used at point of use for transport or prior to delayed reprocessing in the reprocessing area.
- the can sizes can be from 25 mm to 65 mm in diameter, the bag lengths from 50-240 mm in length, and from 79-120 mm in width prior to filling. Bags are placed into the cans in a rolled (flattened) state and as the bag fills with product bag rounds, decreasing the width.
- the can preferably can be a 7 oz. aluminum 53 ⁇ 200 mm can, bag length 104 mm, bag width 97 mm or a 13.5 oz. aluminum 66 ⁇ 220 mm can, bag length 187 mm, bag width 124 mm with a 40 psi pressure and 70% fill volume.
- the bag material can be made of polyester/aluminum/nylon/polypropylene.
- a prior art trigger sprayer will dispense about 1 gram per pull and about 1.1 grams per second average, not including priming.
- the priming can take up to an average of 16 pulls of the trigger.
- the present invention requires no priming and will dispense an average of 5.4 grams per second, and will continue dispensing until the pressure is exhausted from the actuator.
- the droplet size is 250 microns (mean diameter based on volume distribution).
Landscapes
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Containers And Packaging Bodies Having A Special Means To Remove Contents (AREA)
- Cosmetics (AREA)
- Nozzles (AREA)
Abstract
Description
- The present invention relates to a non-aspirating dispenser containing a gel therein for delivery to a desired surface such as a medical article. More specifically, the invention relates to a gel that is dispensed in the form of droplets that are free of air or a gas therein and with reduced drift potential. The dispenser comprises a container having a flexible bag therein enclosing a thixotropic gel, and comprising pressurized gas that is capable of exerting pressure on said bag and forcing said gel out of said bag in a steady stream upon pressing an actuator that is operatively connected to an ejection valve. The bag is free of propellants, and does not produce an aerosol. The gel is thixotropic and is utilized for keeping medical instruments moist in order to prevent soils present thereon from drying out, which can make reprocessing of medical instruments more difficult and less effective. This invention can be implemented at a point of use for transport or prior to delayed reprocessing in the reprocessing area.
- Typical spray bottles or containers dispense liquids or foams via a mechanical trigger that requires continual pumping thereof to dispense a sprayed product. Since very small amounts of product are dispensed with each pump, numerous pumps are required to adequately cover a surface. The same often exhausts the user and becomes an ergonomic issue in that in spraying numerous surfaces, articles, etc., can require a person to take a break or rest.
- Moreover, various dispensers, such as a spray bottle, eject a fluid via aspiration such that an aerosol mist is formed. These dispensers are undesirable in sterile situations since the air pulled in by the aspirator can be from a contaminated environment. Moreover, the aerosol droplets are small and hence driftable such that they can be carried into an adjacent sterile environment and contaminate the same. Liquid-based instrument transport products are to be avoided as they require filled containers or basins to cover all instrument surfaces and thus increase weight and sloshing of transported items.
- Various other dispensers contain a sprayable liquid in association with propellants such as volatile hydrocarbons, e.g. butane, propane, or fluorocarbon gases that can pose flammable or toxic problems.
- Examples of specific dispensers include the following:
- U.S. Pat. No. 6,085,945, issued Jul. 11, 2000. A distributor for a product under pressure has a receptacle which defines a receiving volume. A valve having a springy press-on valve shaft and a non-return valve part is mounted on the receptacle. A passage through which the valve shaft may communicate with the receiving volume is provided. A valve seating section is arranged such that the passage is closed off when the valve shaft is in a rest position and is open when the valve shaft is pressed on. A flexible bag which defines an interior space is provided within the receptacle with the valve seating section outside the bag, and the bag is connected to the valve shaft by the non-return valve part such that flow of a pressurized medium may flow through the valve shaft toward the interior space, but reverse flow is blocked. Flow of pressurized medium out of or into the receptacle through the valve shaft may be obtained without releasing pressure from the pressurized bag.
- U.S. Pat. No. 6,622,943 B2, issued Sep. 23, 2003. Disclosed is a method of shaving hair by spraying a shaving preparation directly onto an area of skin to form a dispersed layer of the shaving preparation without the need for hand spreading and shaving the area with a razor. Also disclosed is a dispensing apparatus for spraying a shaving preparation directly onto an area of skin to be shaved. The shaving preparation may be an aerosol or a non-aerosol shaving preparation.
- U.S. Pat. No. 6,682,726 B2, issued Jan. 27, 2004. The invention is directed to a self-foaming shaving composition in the form of a lotion. The shaving composition comprises water, a water dispersible surface active agent capable of forming a lather, a volatile self-foaming agent, and a water soluble thickening agent wherein the composition is in the form of a self-foaming lotion having an elastic modulus (G′) of about 100 to about 1000 Pascals, preferably about 200 to about 900 Pa, most preferably about 400 to about 800 Pa (measured with a rheometer at frequency 1 Hz, oscillatory stress range 0.01-1.0 Pa, temperature 5 DEG C., Gap 1000 microns). The present invention is also directed to an improved shaving method in which a shaving composition of the present invention is applied to an area of skin, and then said area is shaved, preferably with a wet razor.
- U.S. Pat. No. 7,909,264 B2, issued Mar. 22, 2011. A discharge device and a method for evaporating a liquid to the atmosphere is proposed. The liquid pressurized by gas is supplied to an evaporator via a flow restriction device which restricts the flow rate of the liquid such that continuous release and evaporation of the liquid is possible. Further, an evaporator is proposed. The evaporator comprises an evaporation surface which is designed preferably by microstructuring such that the surface area is increased and/or the liquid forms an essentially uniform film on the evaporation surface.
- U.S. Pat. No. 8,668,899 B2, issued Mar. 11, 2014. A sprayable polymeric foam hemostat for both compressible and non-compressible (intracavitary) acute wounds is disclosed. The foam comprises hydrophobically-modified polymers, such as hm-chitosan, or other amphiphilic polymers that anchor themselves within the membrane of cells in the vicinity of the wound. By rapidly expanding upon being released from a canister pressurized with liquefied gas propellant, the foam is able to enter injured body cavities and staunch bleeding. The seal created is strong enough to substantially prevent the loss of blood from these cavities. Hydrophobically-modified polymers supposedly prevent microbial infections and are suitable for oxygen transfer required during normal wound metabolism. The amphiphilic polymers form solid gel networks with blood cells to create a physical clotting mechanism that prevent loss of blood.
- U.S. Pat. No. 8,876,020 B2, issued Nov. 4, 2014. A sprayable hydrogel wound dressing composed of an aqueous solution of neutralized Carbopol and silver hydrosol of silver nanoparticles electrolytically formed from silver metal without the use or inclusion of organic materials. The hydrogel is sprayed with a physical barrier sprayer system which separates the hydrogel from the propellant. The hydrogel is thixotropic/shear thinning so that the viscosity of the hydrogel is sufficient reduced in the sprayer to allow spray formation and regains sufficient viscosity to resist running when deposited on a vertical surface.
- U.S. Patent Application Publication 2010/0218845 A1, published Sep. 2, 2010. One embodiment relates to a system including a first bag-on-valve aerosol container including a first valve comprising a first valve stem, and a body having an aperture extending therethrough from a first end of the body to a second end of the body. The aperture is sized to accept the first valve stem at the first end of the body. The aperture is also sized to accept a second valve stem at the second end of the body; the body sized to accept the first valve stem and a second valve stem at the same time.
- U.S. Patent Application Publication 2012/0071581 A1, published Mar. 22, 2012. Additive combinations for various products allow the product to be dispensed from a BOV aerosol dispensing arrangement.
- U.S. Patent Application Publication 2013/0345647 A1, published Dec. 26, 2013. Devices and methods for dispensing a fluidly dispensable material under pressure but without using a gas propellant are presented. In some embodiments an elastic sleeve is utilized to impart pressure to a bag of dispensable material positioned within the sleeve. Pressure so created pressurizes contents of the bag, which can then be dispensed through a valve. Methods for manufacturing various embodiments are presented.
- U.S. Patent Application Publication 2014/0187469 A1, published Jul. 3, 2014. An aqueous formulation for dispensing as a spray polymeric microcapsules containing at least one active ingredient, the aqueous formulation comprising: (i) water; (ii) polymeric microcapsules having an oil-soluble core containing the at least one active ingredient; (iii) a cross linked acrylic acid co-polymer; (iv) a neutralizing amine for activating the cross linked acrylic acid copolymer to form a gel suspension for the polymeric microcapsules whereby the polymeric microcapsules are suspended in the water; (v) a chelant for protecting the aqueous formulation against destabilization by excessive metal ions; and (vi) an inhibitor for inhibiting bacterial growth in the water.
- U.S. Patent Application Publication 2015/0056149 A1, published Feb. 26, 2015. A topical therapeutic hydrophobic breakable composition includes a carrier comprising (a) about 60% to about 99% by weight of at least one hydrophobic oil; (b) at least one viscosity-modifying agents selected from the group consisting of a fatty alcohol, a fatty acid and a wax; and (c) a tetracycline antibiotic, characterized in that at least part of the tetracycline antibiotic is suspended in the composition; the viscosity of the composition is at least about 30% higher than the viscosity of the carrier without the tetracycline antibiotic; and is higher than the viscosity of the hydrophobic oil and the tetracycline antibiotic without the viscosity modifying agents. The tetracycline is chemically stable in the composition for at least six months; wherein more than about 90% of the tetracycline has not broken down. The composition is packaged as a breakable foam that breaks easily upon application of shear force.
- In view of the above, there is a need for a non-aspirating, non-propellant dispenser for dispensing a moisturizing thixotropic gel contained in a flexible bag in a pressurized gas container with the gel having a relatively high viscosity and the formed droplets being of a size that reduces drift potential.
- It is an aspect of the present invention to provide a non-aspirating dispenser for ejecting a thixotropic gel.
- It is another aspect of the present invention wherein the dispenser contains a flexible bag containing the gel with the bag located in a container having a non-flammable, non-hydrocarbon-based compressed gas therein.
- A further object of the present invention is to provide non-foam gel droplets.
- It is yet another aspect of the present invention that the dispenser does not require priming but continuously dispenses the gel in droplet form upon pushing an actuator to provide non-priming, aerosol-free droplets for use in the medical field as for keeping instruments moist, in order to prevent soils thereon from drying out. Soil that has been allowed to dry can make reprocessing of medical instruments more difficult and less effective.
- Accordingly, one aspect of the invention relates to a non-aspirating dispenser for a transport gel, comprising: a thixotropic gel; said thixotropic gel having a viscosity of less than about 2,000 centipoises; said dispenser having walls forming a container and a flexible bag therein, said bag containing said thixotropic gel; a non-bag volume located between said dispenser walls and said flexible bag, said non-bag volume having a pressurized gas therein, said non-bag volume being substantially free of a propellant, a volatilizable liquid, or a foam forming gas, or any combination thereof; said dispenser having a valve, an actuator operatively connected to said valve, said actuator upon activation thereof being capable of opening said valve so that said pressurized gas will exert pressure on said bag and force said thixotropic gel out of said dispenser container in the form of non-aspirated droplets; and said droplets having a mean volume diameter that reduces drift potential.
-
FIG. 1 relates to a cross-section elevation view of a non-aspirating dispenser of the present invention wherein a container contains a bag having a gel therein. - Ergonomic
friendly dispenser 10 of the present invention comprises anactuator 24.Actuator 24 is connected in any conventional manner such as throughdisconnectable valve 30 todispenser container 40. The container contains aflexible bag 45 therein that throughdisconnectable valve 30 can be filled with a desired thixotropic gel of the present invention. Dispenser,container 40 can be in the shape of a cylinder or other suitable form and made of a pressure resistant material such as a metal, for example steel or aluminum or a plastic, such as Polyethylene terephthalate (PET).Bag 45 contains athixotropic gel 50 therein. Non-bag orinternal volume 47 located betweenbag 45 anddispenser container walls 40 contains a compressed eco-gas therein such as nitrogen, air, or CO2 Suitable pressures range from about 25 to about 60 psi, and preferably from about 30 to about 50 psi. - It is an important aspect of the present invention that the compressed gas is not what would normally be considered a propellant, a volatilizable liquid, or a foam forming gas, or any combination thereof. By the term “propellant”, it is meant that the gas in contact with the product is a volatile hydrocarbon such as various alkanes, for example propane, isopropane, butane, isobutene, or other volatile alkanes including various cyclic alkanes. Moreover, chloro-fluoro hydrocarbons as well as various fluoro-hydrocarbons are not utilized such as 1,1,1,2 tetrafluorethane (Dymel 134); 1,1,1,2,3,3,3 heptafluoropropane (Dymel 227); 1,1, difluoro ethane (Dymel 152); or 1,1,1,2,2,2 hexafluoropropane. Such compounds are avoided because they are generally in contact with the product and volatilized to the air. Moreover, propellants can be flammable, toxic, and the like and hence the present invention is substantially free thereof. Other compounds that are avoided are volatilizable liquids that are liquids under pressure, but upon being emitted from
container 40 at ambient pressure volatize. Examples of such gases include dimethyl ether, propane, isobutane, and n-butane. Gases that form a foam upon being emitted fromdispenser 10 are also avoided by the present invention because they can obscure instruments visually, especially sharps. Also, upon breaking, the foams become liquid that readily runs off of the surface of themedical article. The foam can be formed either through trigger sprayers with a foaming tip or through the use of aerosols and propellants. Examples of gases that can form a foam include blend of propane and isobutane, A-31, P-152a, nitrous oxide, and CO2. - The present invention is substantially free of the above noted propellants, volatilizable liquid; or foam forming gases. By the term “free thereof”, it is meant that any such gases contained within non-bag or
internal area 47, if used, exist in very minute amounts, for example about 5% or less, desirably about 3% or less, and preferably about 1% or less based upon the total volume of non-bag orinternal volume 47. A highly preferred embodiment is that non-bag orinternal volume 47 contains no such gases therein. - Another important aspect of the present invention is that
dispenser 10 is a non-aspirating dispenser. That is, they do not utilize suction to take up various fluids, or air, and mix the same withgel 50 of the present invention. Aspirators are avoided because when utilized as in the medical field or industry, they can draw in air that is contaminated and then dispense the same in ejectedmaterial 26. Hence, viruses, bacteria, fungi, bodily fluids and other harmful materials can be contained in sprayer ejectedmaterial 26 that result in a harmful environment as in a sterile room, an operating room, etc. and the like. Moreover, such contaminated ejected material are generally in the form of small droplets that are driftable in the air and can thus readily enter adjacent rooms, areas, and the like and also contaminate the same. By the term “non-aspirating dispenser”, it is meant thatflexible bag 45 is under positive pressure due to the enclosed gas in the non-bag orinternal volume 47 area that dispenses the gel outward under pressure with no flow back into the dispenser container due to pressure differential between the dispenser container as compared to the environment outside the dispenser container. In other words, said pressure differential is always at least 2 psi greater than the outside environment pressure during dispensing. -
Dispenser 10 of the present invention containingnon-aspirating nozzle 25 can be any conventional dispenser container known to the art and to the literature such as those manufactured by Ball, CCL Container, Crown, Exal, and actuators by such manufacturers Aptar, Coster, Lindal Group, and Precision Global. -
Actuator portion 24 can be connected todispenser container 40 in any conventional manner as known to the literature and to the art. In the embodiment of the present invention,dispenser container 40 is of a BOV, i.e. bag-on-valve, bottle, or container wherein, as shown inFIG. 1 ,flexible bag 45 is located withindispenser container 40.Bag 45 can be any conventional flexible material such as various plastic and metalized films typically laminated together for optimal barrier and compatibility properties. Examples of suitable flexible laminate materials include LLDPE/Nylon/Aluminum/Polyester, LLDPE/Polyester, PP/Nylon/Aluminum/Polyester, and LLPE/Aluminum/Nylon. The volume ofbag 45 is generally from about 50 to about 90%, desirably from about 60% to about 80%, and preferably from about 65% to about 75% based upon the total volume ofdispenser container 40. Thus, the non-bag or internal volume 47 (i.e. pressurized gas volume) is the remainder or difference, i.e. generally from about 10% to about 50%, desirably from about 20 to about 40%, and preferably from about 25 to about 35%. -
Gel material 50 is a thixotropic gel inasmuch as it is generally a semi-solid at room temperature, but upon the application of pressure thereto, flows like a liquid. The purpose of the gel is to keep various medical instruments moist in order to prevent soils from drying out, which can make reprocessing of medical instruments more difficult and less effective. This invention may be used at a point of use for transport or prior to delayed reprocessing in a reprocessing area. - The type of gels utilized are those that contain one or more thickening agents to help with dispensing and cling properties, humectants to keep soils moist, corrosion inhibitors so that extended contact with moisture does not promote corrosion of instrumentation, surfactants to penetrate soils, sequestrants to aid in anti-redeposition, and preservatives to prevent contamination of the product and water. All of these compounds are well known to the art and to the literature. Gels that can be used include “Pre-Klenz”, Instrument Transport Gel made by Steris Corporation, and OptiPro Instrument Gel made by Ecolab. Other examples of gel include cellulose, hydrophobically modified cellulose, guar gum, quaternized guar gum, alginate, or cationated alginate comprising calcium, magnesium, or sodium cations, or any combination thereof.
- An important aspect of the present invention, in order to form proper size droplets of the gel once emitted from
dispenser 10, is the viscosity thereof. Generally, the viscosity of the thixotropic gel is less than about 2,000, desirably from about 100 to about 1,700, and preferably from about 150 to about 1,500 centipoise. - The operation of
dispenser 10 is generally as follows. A suitable amount of a particular type of gel, for example Pre-Klenz, is added toflexible bag 45. Throughvalve 30, an eco-gas such as air, etc., is added todispenser container 40 with the eco-gas generally being located in non-bag orinterior area 47. As noted, the amount of pressure therein can generally be from about 25 to about 60 psi, and desirably from about 30 to about 50, dependent upon the type of sprayer. Upon pressurizinginterior area 47,valve 30 is closed to the bag.Dispenser 10 can be activated as by pressingactuator 24, or another release mechanism, that through a typical mechanical connection, opensvalve 30 so that eco-gas 60 applies pressure tothixotropic gel 50 and forces the gel through the non-aspirating sprayer and is ejected throughnozzle 25 in the form of ejectedmaterial 26 such as liquid droplets. - The size of the liquid droplets is another important aspect of the present invention. If they are too small, droplets will tend to drift, i.e. remain suspended in the air and could be diverted to an undesirable area such as the sterile field within a surgical suite or operating room. Thus, reduced drift potential is desired. If too heavy, the droplets conglomerate and will not spray on the instruments in fan spray pattern that gives adequate coverage but as more of a stream. Desirably, the mean volume droplet diameter ranges from about 80 to about 500, desirably from about 100 to about 450, and preferably from about 150 to about 400 microns, with about 250 microns being highly preferred. This droplet size can be tested with a piece of equipment such as the Malvern Spraytec Particle Size Analyzer, as per methods published by International Standards Organization ISO 13320 (2009) Particle Size Analysis-Laser Diffraction Methods. An ergonomic aspect of the present invention is that once actuator 24 is pressed, it remains open until released. Thus, a steady spray of
droplets 26 of the thixotropic gel are emitted fromnozzle 25 in a non-aspiratable form. - The non-aspirating dispenser of the present invention suitable for keeping instruments moist, in order to prevent soils thereon from drying out, that can make reprocessing of medical instruments more difficult and less effective. These soils could include blood, tissue, bodily fluids, mucus, feces, adipose tissue, synovial fluid, or other soils associated with medical procedures. In addition to surgical instruments such as forceps, hemostats, clamps, scalpels, retractors, bone saws, chisels, cannulas, curettes, osteotomes, rongeurs, other medical instruments such as endoscopes (both rigid and flexible), or probes can also be coated with the gel. The invention can be used at point of use for transport or prior to delayed reprocessing in the reprocessing area.
- The following examples serve to explain the present invention, while not limiting the scope thereof.
- The can sizes can be from 25 mm to 65 mm in diameter, the bag lengths from 50-240 mm in length, and from 79-120 mm in width prior to filling. Bags are placed into the cans in a rolled (flattened) state and as the bag fills with product bag rounds, decreasing the width.
- The can preferably can be a 7 oz. aluminum 53×200 mm can, bag length 104 mm, bag width 97 mm or a 13.5 oz. aluminum 66×220 mm can, bag length 187 mm, bag width 124 mm with a 40 psi pressure and 70% fill volume. The bag material can be made of polyester/aluminum/nylon/polypropylene.
- A prior art trigger sprayer will dispense about 1 gram per pull and about 1.1 grams per second average, not including priming. The priming can take up to an average of 16 pulls of the trigger. The present invention requires no priming and will dispense an average of 5.4 grams per second, and will continue dispensing until the pressure is exhausted from the actuator. In addition the droplet size is 250 microns (mean diameter based on volume distribution).
- While in accordance with the Patent Statutes, the best mode and preferred embodiments have been set forth, the scope of the invention is not limited thereto, but rather, by the scope of the attached claims.
Claims (20)
Priority Applications (12)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US14/929,697 US20170121098A1 (en) | 2015-11-02 | 2015-11-02 | Non-aspirating transport gel dispenser |
MX2018005370A MX2018005370A (en) | 2015-11-02 | 2016-08-26 | Non-aspirating transport gel dispenser. |
EP16862642.2A EP3371074A4 (en) | 2015-11-02 | 2016-08-26 | Non-aspirating transport gel dispenser |
JP2018517436A JP2018535150A (en) | 2015-11-02 | 2016-08-26 | Non-suction transport gel dispenser |
CA3001721A CA3001721C (en) | 2015-11-02 | 2016-08-26 | Non-aspirating transport gel dispenser |
PCT/US2016/048984 WO2017078834A1 (en) | 2015-11-02 | 2016-08-26 | Non-aspirating transport gel dispenser |
CN201680063200.9A CN108349643B (en) | 2015-11-02 | 2016-08-26 | Non-aspirating transport gel dispenser |
BR112018008919-2A BR112018008919B1 (en) | 2015-11-02 | 2016-08-26 | WITHOUT ASPIRATION DISPENSER FOR A TRANSPORT GEL, MEDICAL INSTRUMENTS HAVING A THIXOTROPIC GEL APPLIED BY SAID DISPENSER AND PROCESS FOR DISPENSE A NON-Aspirated GEL |
AU2016350608A AU2016350608B2 (en) | 2015-11-02 | 2016-08-26 | Non-aspirating transport gel dispenser |
US16/664,261 US20200055662A1 (en) | 2015-11-02 | 2019-10-25 | Non-aspirating transport gel dispenser |
JP2021091948A JP2021155124A (en) | 2015-11-02 | 2021-05-31 | Non-suction-type transportgel dispenser |
US17/752,948 US11926467B2 (en) | 2015-11-02 | 2022-05-25 | Non-aspirating transport gel dispenser |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US14/929,697 US20170121098A1 (en) | 2015-11-02 | 2015-11-02 | Non-aspirating transport gel dispenser |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US16/664,261 Continuation US20200055662A1 (en) | 2015-11-02 | 2019-10-25 | Non-aspirating transport gel dispenser |
Publications (1)
Publication Number | Publication Date |
---|---|
US20170121098A1 true US20170121098A1 (en) | 2017-05-04 |
Family
ID=58634358
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US14/929,697 Abandoned US20170121098A1 (en) | 2015-11-02 | 2015-11-02 | Non-aspirating transport gel dispenser |
US16/664,261 Abandoned US20200055662A1 (en) | 2015-11-02 | 2019-10-25 | Non-aspirating transport gel dispenser |
US17/752,948 Active US11926467B2 (en) | 2015-11-02 | 2022-05-25 | Non-aspirating transport gel dispenser |
Family Applications After (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US16/664,261 Abandoned US20200055662A1 (en) | 2015-11-02 | 2019-10-25 | Non-aspirating transport gel dispenser |
US17/752,948 Active US11926467B2 (en) | 2015-11-02 | 2022-05-25 | Non-aspirating transport gel dispenser |
Country Status (9)
Country | Link |
---|---|
US (3) | US20170121098A1 (en) |
EP (1) | EP3371074A4 (en) |
JP (2) | JP2018535150A (en) |
CN (1) | CN108349643B (en) |
AU (1) | AU2016350608B2 (en) |
BR (1) | BR112018008919B1 (en) |
CA (1) | CA3001721C (en) |
MX (1) | MX2018005370A (en) |
WO (1) | WO2017078834A1 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10960129B2 (en) | 2017-08-25 | 2021-03-30 | AZ Solutions LLC | System and method for patient skin treatment and irrigation |
US11918549B2 (en) | 2017-08-25 | 2024-03-05 | AZ Solutions LLC | System and method for wound treatment and irrigation |
US11992638B2 (en) | 2021-02-26 | 2024-05-28 | AZ Solutions LLC | System and method for patient skin treatment and irrigation |
Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5711484A (en) * | 1993-09-14 | 1998-01-27 | Minnesota Mining And Manufacturing Company | Dispensing tube for directing the dispensing of fluids |
US5976573A (en) * | 1996-07-03 | 1999-11-02 | Rorer Pharmaceutical Products Inc. | Aqueous-based pharmaceutical composition |
US6547770B2 (en) * | 2000-04-14 | 2003-04-15 | Aiolos Systems Aktiebolag (Ab) | Ophthalmic dispensing device |
US6588628B2 (en) * | 2001-11-30 | 2003-07-08 | Robert Henry Abplanalp | Aerosol valve assembly |
US6695227B1 (en) * | 1999-01-18 | 2004-02-24 | Earth Chemical Co., Ltd. | Aerosol spraying apparatus |
US20040102562A1 (en) * | 2002-11-19 | 2004-05-27 | Butuc Steluta Gina | Shear thinning hydrocarbon gel compositions and uses thereof |
US7025234B2 (en) * | 2001-10-20 | 2006-04-11 | Advanced Technology Materials, Inc. | Apparatus and method for dispensing high-viscosity liquid |
US20090324521A1 (en) * | 2007-07-27 | 2009-12-31 | Jonathan Robert Cetti | Personal Care Article For Sequentially Dispensing Compositions With Variable Concentrations Of Hydrophobic Benefit Materials |
US8857741B2 (en) * | 2012-04-27 | 2014-10-14 | Conopco, Inc. | Topical spray composition and system for delivering the same |
US8978936B2 (en) * | 2010-07-12 | 2015-03-17 | Foamix Pharmaceuticals Ltd. | Apparatus and method for releasing a unit dose of content from a container |
US20180272367A1 (en) * | 2015-07-15 | 2018-09-27 | Gary Rayner | Systems and methods for producing a foamable and/or flowable material for consumption |
Family Cites Families (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61273369A (en) * | 1985-05-22 | 1986-12-03 | 北海製罐株式会社 | Aerosol product and manufacture thereof |
FR2709131B1 (en) * | 1993-08-18 | 1995-11-10 | Cilag Laboratoire | Device for dispensing a therapeutic or cosmetic substance, the inert vehicle of which is a volatile polydiorganosiloxane, and composition intended for use in the device. |
DE4427175A1 (en) * | 1994-08-01 | 1996-02-08 | Coster Tecnologie Speciali Spa | Unit |
BE1009381A3 (en) | 1995-05-09 | 1997-03-04 | Ecopack Naamloze Vennootschap | Distributor for a product under pressure and suitable valve. |
US5915595A (en) * | 1996-08-21 | 1999-06-29 | U.S. Can Company | Aerosol dispensing container and method for assembling same |
JPH1060477A (en) * | 1996-08-23 | 1998-03-03 | Matsushita Electric Ind Co Ltd | Surface treating agent and production and usage thereof |
JP2005281315A (en) * | 1997-07-02 | 2005-10-13 | Aventis Pharmaceuticals Holdings Inc | Aqueous pharmacological composition |
US6415800B2 (en) | 2000-01-14 | 2002-07-09 | The Gillette Company | Method of shaving and a dispensing apparatus therefor |
US6387858B1 (en) * | 2000-03-31 | 2002-05-14 | Steris Inc. | Safe transport gel for treating medical instruments |
US6682726B2 (en) | 2001-04-30 | 2004-01-27 | The Gillette Company | Self-foaming shaving lotion |
JP4178293B2 (en) * | 2003-01-15 | 2008-11-12 | 株式会社ダイゾー | Aerosol products |
JP2005008204A (en) * | 2003-06-18 | 2005-01-13 | Osaka Gas Co Ltd | Double structure aerosol container |
GB0423243D0 (en) | 2004-10-20 | 2004-11-24 | Dunne Stephen T | Liquid dispensing means |
US20090148342A1 (en) * | 2007-10-29 | 2009-06-11 | Bromberg Steven E | Hypochlorite Technology |
JP5369307B2 (en) * | 2007-12-28 | 2013-12-18 | アース製薬株式会社 | Gel pest spray products |
JP5612818B2 (en) * | 2008-11-13 | 2014-10-22 | 花王株式会社 | Aerosol deodorant article |
US20100218845A1 (en) | 2009-02-27 | 2010-09-02 | Yoram Fishman | Refillable bag-on-valve system |
AU2010202421B2 (en) * | 2009-06-15 | 2014-05-08 | Gojo Industries, Inc. | Method and compositions for use with gel dispensers |
JP5469417B2 (en) * | 2009-09-07 | 2014-04-16 | 第一工業製薬株式会社 | Gel fragrance / deodorant composition and gel fragrance / deodorant using the same |
CA2776366C (en) | 2009-10-02 | 2017-07-18 | Foamix Ltd. | Surfactant-free water-free foamable compositions, breakable foams and gels and their uses |
US8668899B2 (en) | 2009-11-13 | 2014-03-11 | University Of Maryland, College Park | Advanced functional biocompatible foam used as a hemostatic agent for compressible and non-compressible acute wounds |
GB2475393B (en) * | 2009-11-17 | 2012-10-24 | Univ Salford | Aerosol spray device |
CN201686155U (en) * | 2010-01-25 | 2010-12-29 | 美格福谷公司 | Distributor for liquid stored in bag in box |
US20120071581A1 (en) | 2010-08-30 | 2012-03-22 | Sklar Ross J | Bag-on-valve aerosol dispensing arrangement and chemical formulations |
EP2681128B1 (en) | 2011-03-02 | 2020-10-07 | Greenspense Ltd. | Propellant-free pressurized material dispenser and method |
US8876020B2 (en) * | 2011-05-25 | 2014-11-04 | American Silver Llc | Sprayable gel wound dressing |
GB201115660D0 (en) | 2011-09-09 | 2011-10-26 | Celesscence Internat Ltd | An aqueous formulation for dispensing as a spray polymeric microcapsules containing at least one active ingredient |
MX366656B (en) * | 2012-02-24 | 2019-07-18 | Crown Packaging Technology Inc | Aerosol container. |
JP5798220B2 (en) * | 2013-12-12 | 2015-10-21 | 株式会社ヒロマイト | Manufacturing method of double structure container |
-
2015
- 2015-11-02 US US14/929,697 patent/US20170121098A1/en not_active Abandoned
-
2016
- 2016-08-26 AU AU2016350608A patent/AU2016350608B2/en active Active
- 2016-08-26 JP JP2018517436A patent/JP2018535150A/en active Pending
- 2016-08-26 CN CN201680063200.9A patent/CN108349643B/en active Active
- 2016-08-26 MX MX2018005370A patent/MX2018005370A/en unknown
- 2016-08-26 BR BR112018008919-2A patent/BR112018008919B1/en active IP Right Grant
- 2016-08-26 WO PCT/US2016/048984 patent/WO2017078834A1/en active Application Filing
- 2016-08-26 EP EP16862642.2A patent/EP3371074A4/en not_active Ceased
- 2016-08-26 CA CA3001721A patent/CA3001721C/en active Active
-
2019
- 2019-10-25 US US16/664,261 patent/US20200055662A1/en not_active Abandoned
-
2021
- 2021-05-31 JP JP2021091948A patent/JP2021155124A/en active Pending
-
2022
- 2022-05-25 US US17/752,948 patent/US11926467B2/en active Active
Patent Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5711484A (en) * | 1993-09-14 | 1998-01-27 | Minnesota Mining And Manufacturing Company | Dispensing tube for directing the dispensing of fluids |
US5976573A (en) * | 1996-07-03 | 1999-11-02 | Rorer Pharmaceutical Products Inc. | Aqueous-based pharmaceutical composition |
US6695227B1 (en) * | 1999-01-18 | 2004-02-24 | Earth Chemical Co., Ltd. | Aerosol spraying apparatus |
US6547770B2 (en) * | 2000-04-14 | 2003-04-15 | Aiolos Systems Aktiebolag (Ab) | Ophthalmic dispensing device |
US7025234B2 (en) * | 2001-10-20 | 2006-04-11 | Advanced Technology Materials, Inc. | Apparatus and method for dispensing high-viscosity liquid |
US6588628B2 (en) * | 2001-11-30 | 2003-07-08 | Robert Henry Abplanalp | Aerosol valve assembly |
US20040102562A1 (en) * | 2002-11-19 | 2004-05-27 | Butuc Steluta Gina | Shear thinning hydrocarbon gel compositions and uses thereof |
US20090324521A1 (en) * | 2007-07-27 | 2009-12-31 | Jonathan Robert Cetti | Personal Care Article For Sequentially Dispensing Compositions With Variable Concentrations Of Hydrophobic Benefit Materials |
US8978936B2 (en) * | 2010-07-12 | 2015-03-17 | Foamix Pharmaceuticals Ltd. | Apparatus and method for releasing a unit dose of content from a container |
US8857741B2 (en) * | 2012-04-27 | 2014-10-14 | Conopco, Inc. | Topical spray composition and system for delivering the same |
US20180272367A1 (en) * | 2015-07-15 | 2018-09-27 | Gary Rayner | Systems and methods for producing a foamable and/or flowable material for consumption |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10960129B2 (en) | 2017-08-25 | 2021-03-30 | AZ Solutions LLC | System and method for patient skin treatment and irrigation |
US11918549B2 (en) | 2017-08-25 | 2024-03-05 | AZ Solutions LLC | System and method for wound treatment and irrigation |
US11992638B2 (en) | 2021-02-26 | 2024-05-28 | AZ Solutions LLC | System and method for patient skin treatment and irrigation |
Also Published As
Publication number | Publication date |
---|---|
EP3371074A4 (en) | 2019-06-26 |
JP2018535150A (en) | 2018-11-29 |
WO2017078834A1 (en) | 2017-05-11 |
CA3001721C (en) | 2020-03-31 |
BR112018008919A8 (en) | 2019-02-26 |
US20200055662A1 (en) | 2020-02-20 |
CA3001721A1 (en) | 2017-05-11 |
BR112018008919A2 (en) | 2018-11-21 |
AU2016350608B2 (en) | 2019-05-09 |
JP2021155124A (en) | 2021-10-07 |
BR112018008919B1 (en) | 2022-10-04 |
EP3371074A1 (en) | 2018-09-12 |
AU2016350608A1 (en) | 2018-05-31 |
CN108349643B (en) | 2020-02-14 |
US20220281675A1 (en) | 2022-09-08 |
US11926467B2 (en) | 2024-03-12 |
MX2018005370A (en) | 2018-11-09 |
CN108349643A (en) | 2018-07-31 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US11926467B2 (en) | Non-aspirating transport gel dispenser | |
WO2015006408A1 (en) | Consumer packaged product for viscous personal care compositions with dual propellant delivery system | |
JP2018518310A (en) | Hemostasis powder delivery device and method | |
WO2018075864A1 (en) | Devices for dispensing a hydrofluoroolefin vapocoolant composition as an aerosol | |
EP2211954A2 (en) | Spray devices and methods | |
US20070108228A1 (en) | Method and apparatus for flushing eyes and skin | |
KR20070098755A (en) | Composition for a foam pretreatment for medical instruments | |
US20240174432A1 (en) | Non-aspirating transport gel dispenser | |
EP3830002B1 (en) | Bag on valve technology | |
JP2012219034A (en) | Aerosol composition and aerosol product obtained using the aerosol composition | |
AU2015235905B2 (en) | Pump concentrated air freshener | |
JP2007145350A (en) | Cap unit and aerosol atomizer | |
JP5952544B2 (en) | Discharge composition and discharge product using the discharge composition | |
US11154874B2 (en) | Flow modulation device for dispensing pressurized fluids | |
EP4212106A1 (en) | Handheld device for applying a cyanoacrylate adhesive composition | |
US20240158596A1 (en) | Systems and methods relating to medical applications of inverse thermosensitive polymer foam formulations | |
WO2023156930A1 (en) | Bag on valve technology | |
EA046297B1 (en) | "VALVE WITH BAG" TECHNOLOGY | |
CN115040283A (en) | Pet wound atomizer | |
KR20070098757A (en) | Hydrogen peroxide foam treatment | |
PL205247B1 (en) | Method of obtaining a three-phase pressure-discharge system | |
MXPA97007837A (en) | Medium dosage aerosol valve |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: AMERICAN STERILIZER COMPANY, OHIO Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:KAISER, NANCY-HOPE E.;ROCHETTE, DANIEL;BAAN, BRADLEY A.;SIGNING DATES FROM 20151030 TO 20151102;REEL/FRAME:036935/0126 |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: NON FINAL ACTION MAILED |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: FINAL REJECTION MAILED |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: DOCKETED NEW CASE - READY FOR EXAMINATION |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: FINAL REJECTION MAILED |
|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |