Aperture plate and methods for its construction and use

Information

  • Patent Grant
  • 7066398
  • Patent Number
    7,066,398
  • Date Filed
    Friday, March 30, 2001
    23 years ago
  • Date Issued
    Tuesday, June 27, 2006
    18 years ago
Abstract
A method for performing an aperture plate comprises providing a mandrel that is constructed of a mandrel body having a conductive surface and a plurality of nonconductive islands disposed on the conductive surface. The mandrel is placed within a solution containing a material that is to be deposited onto the mandrel. Electrical current is applied to the mandrel to form an aperture plate on the mandrel, with the apertures having an exit angle that is in the range from about 30° to about 60°.
Description
BACKGROUND OF THE INVENTION

This invention relates generally to the field of liquid dispensing, and in particular to the aerosolizing of fine liquid droplets. More specifically, the invention relates to the formation and use of aperture plates employed to produce such fine liquid droplets.


A great need exists for the production of fine liquid droplets. For example, fine liquid droplets are used in for drug delivery, insecticide delivery, deodorization, paint applications, fuel injectors, and the like. In many applications, it may be desirable to produce liquid droplets that have an average size down to about 0.5 μl. For example, in many medical applications, such a size is needed to insure that the inhaled drug reaches the deep lung.


U.S. Pat. Nos. 5,164,740; 5,586,550; and 5,758,637, the complete disclosures of which are herein incorporated by reference, describe exemplary devices for producing fine liquid droplets. These patents describe the use of aperture plates having tapered apertures to which a liquid is supplied. The aperture plates are then vibrated so that liquid entering the larger opening of each aperture is dispensed through the small opening of each aperture to produce the liquid droplets. Such devices have proven to be tremendously successful in producing liquid droplets.


Another technique for aerosolizing liquids is described in U.S. Pat. No. 5,261,601 and utilizes a perforate membrane disposed over a chamber. The perforate membrane comprises an electroformed metal sheet using a “photographic process” that produces apertures with a cylindrical exit opening.


The invention provides for the construction and use of other aperture plates that are effective in producing fine liquid droplets at a relatively fast rate. As such, it is anticipated that the invention will find even greater use in many applications requiring the use of fine liquid droplets.


SUMMARY OF THE INVENTION

The invention provides exemplary aperture plates and methods for their construction and use in producing fine, liquid droplets at a relatively fast rate. In one embodiment, a method is provided for forming an aperture plate. The method utilizes a mandrel that comprises a mandrel body having a conductive surface and a plurality of nonconductive islands disposed on the conductive surface such that the islands extend above the conductive surface. The mandrel is placed within a solution containing a material that is to be deposited onto the mandrel. Electrical current is then applied to the mandrel to form an aperture plate on the mandrel, with the apertures having an exit angle that is in the range from about 30° to about 60°, more preferably from about 41° to about 49°, and still more preferably about 45°. Construction of the aperture plate to have such an exit angle is particularly advantageous in that it maximizes the rate of droplet production through the apertures.


In one particular aspect, the islands have a geometry that approaches a generally conical shape or a dome shape having a circular base, with the base being seated on the mandrel body. Conveniently, the islands may have a base diameter in the range from about 20 microns to about 200 microns, and a height in the range from about 4 microns to about 20 microns.


In another particular aspect, the islands are formed from a photoresistent material using a photolithography process. Conveniently, the islands may be treated following the photolithography process to alter the shape of the islands. In another aspect, the aperture plate is removed from the mandrel, and is formed into a dome shape. In still another aspect, the material in the solution that forms the aperture plate may be a material such as a palladium nickel alloy, palladium cobalt, or other palladium or gold alloys.


The invention further provides an exemplary aperture plate that comprises a plate body having a top surface, a bottom surface, and a plurality of apertures that taper in a direction from the top surface to the bottom surface. Further, the apertures have an exit angle that is in the range from about 30° to about 60°, more preferably about 41° to about 49°, and more preferably at about 45°. The apertures also have a diameter that is in the range from about 1 micron to about 10 microns at the narrowest portion of the taper. Such an aperture plate is advantageous in that it may produce liquid droplets having a size that are in the range from about 2 μm to about 10 μm, at a rate in the range from about 4 μL to about 30 μL per 1000 apertures per second. In this way, the aperture plate may be employed to aerosolize a sufficient amount of a liquid medicament so that a capture chamber that may otherwise be employed to capture the aerosolized medicament will not be needed.


The aperture plate may be constructed of a high strength and corrosion resistant material. As one example, the plate body may be constructed from a palladium nickel alloy. Such an alloy is corrosion resistant to many corrosive materials particularly solutions for treating respiratory diseases by inhalation therapy, such as an albuterol sulfate and ipratroprium solution, which is used in many medical applications. Further, the palladium nickel alloy has a low modulus of elasticity and therefore a lower stress for a given oscillation amplitude. Other materials that may be used to construct the plate body include gold, gold alloys, and the like.


In another aspect, the plate body has a portion that is dome shaped in geometry. In one particular aspect, the plate body has a thickness in the range from about 20 microns to about 70 microns.


In another embodiment, the invention provides a mandrel for forming an aperture plate. The mandrel comprises a mandrel body or plate having a conductive, generally flat top surface and a plurality of nonconductive islands disposed on the conductive surface. The islands extend above the conductive surface and have a geometry approaching a generally conical or dome shape. Such a mandrel is particularly useful in an electroforming process that may be employed to form an aperture plate on the mandrel body. The shaped nonconductive islands when used in such a process assist in producing apertures that have an exit angle in the range from about 30° to about 60°, more typically in the range from about 41° to about 49°, and still more typically at about 45°.


In one aspect, the islands have a base diameter in the range from about 20 microns to about 200 microns, and a height in the range from about 4 microns to about 20 microns. In another aspect, the islands may have an average slope in the range from about 15° to about 30° relative to the conductive surface. Conveniently, the islands may be formed from a photoresist material using a photolithography process. The islands may be treated following the photolithography process to further shape the islands.


In still another embodiment, the invention provides a method for producing a mandrel that may be employed to form an aperture plate. According to the method, an electroforming mandrel body is provided. A photoresist film is applied to the mandrel body, and a mask having a pattern of circular regions is placed over the photoresist film. The photoresist film is then developed to form an arrangement of nonconductive islands that correspond to the location of the holes in the pattern. Following this step, the mandrel body is heated to permit the islands to melt and flow into a desired shape. For example, the islands may be heated until they are generally conical or dome shaped in geometry and have a slope relative to the surface of the mandrel body. Optionally, the steps of applying the photoresist film, placing a mask having a smaller pattern of circular regions over the photoresist film, developing the photoresist film and heating the mandrel body may be repeated to form layers of a photoresist material and thereby further modify the shape of the nonconductive islands.


In one aspect, the photoresist film has a thickness in the range from about 4 microns to about 15 microns. In another aspect, the mandrel body is heated to a temperature in the range from about 50° C. to about 250° C. for about 30 minutes. Typically, the mandrel body will be heated to this temperature at a rate that is less than about 3° C. per minute.


The invention still further provides a method for aerosolizing a liquid. According to the method, an aperture plate is provided that comprises a plate body having a top surface, a bottom surface, and a plurality of apertures that taper in a direction from the top surface to the bottom surface. The apertures have an exit angle that is in the range from about 30° to about 60°, preferably in the range from about 41° to about 49°, more preferably at about 45°. The apertures also have a diameter that is in the range from about 1 micron to about 10 microns at the narrowest portion of the taper. A liquid is supplied to the bottom surface of the aperture plate, and the aperture plate is vibrated to eject liquid droplets from the top surface.


Typically, the droplets have a size in the range from about 2 μm to about 10 μm. Conveniently, the aperture plate may be provided with at least about 1,000 apertures so that a volume of liquid in the range from about 4 μL to about 30 μL may be produced within a time of less than about one second. In this way, a sufficient dosage may be aerosolized so that a patient may inhale the aerosolized medicament without the need for a capture chamber to capture and hold the prescribed amount of medicament.


In one particular aspect, the liquid that is supplied to the bottom surface is held to the bottom surface by surface tension forces until the liquid droplets are ejected from the top surface. In another aspect, the aperture plate is vibrated at a frequency in the range from about 80 KHz to about 200 KHz.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a side view of one embodiment of an aperture plate according to the invention.



FIG. 2 is a cross-sectional side view of a portion of the aperture plate of FIG. 1.



FIG. 3 is a more detailed view of one of the apertures of the aperture plate of FIG. 2.



FIG. 4 is a graph illustrating the flow rate of liquid through an aperture as the exit angle of the aperture is varied.



FIG. 5 is a top perspective view of one embodiment of a mandrel having nonconductive islands to produce an aperture plate in an electroforming process according to the invention.



FIG. 6 is a side view of a portion of the mandrel of FIG. 5 showing one of the nonconductive islands in greater detail.



FIG. 7 is a flow chart illustrating one method for producing an electroforming mandrel according to the invention.



FIG. 8 is a cross-sectional side view of the mandrel of FIG. 5 when used to produce an aperture plate using an electroforming process according to the invention.



FIG. 9 is flow chart illustrating one method for producing an aperture plate according to the invention.



FIG. 10 is a cross-sectional side view of a portion of an alternative embodiment of an aperture plate according to the invention.



FIG. 11 is a side view of a portion of an alternative electroforming mandrel when used to form the aperture plate of FIG. 10 according to the invention.



FIG. 12 illustrates the aperture plate of FIG. 1 when used in an aerosol generator to aerosolize a liquid according to the invention.





DESCRIPTION OF THE SPECIFIC EMBODIMENTS

The invention provides exemplary aperture plates and methods for their construction and use. The aperture plates of the invention are constructed of a relatively thin plate that may be formed into a desired shape and includes a plurality of apertures that are employed to produce fine liquid droplets when the aperture plate is vibrated. Techniques for vibrating such aperture plates are described generally in U.S. Pat. Nos. 5,164,740; 5,586,550; and 5,758,637, previously incorporated herein by reference. The aperture plates are constructed to permit the production of relatively small liquid droplets at a relatively fast rate. For example, the aperture plates of the invention may be employed to produce liquid droplets having a size in the range from about 2 microns to about 10 microns, and more typically between about 2 microns to about 5 microns. In some cases, the aperture plates may be employed to produce a spray that is useful in pulmonary drug delivery procedures. As such, the sprays produced by the aperture plates may have a respirable fraction that is greater than about 70%, preferably more than about 80%, and most preferably more than about 90% as described in U.S. Pat. No. 5,758,637, previously incorporated by reference.


In some embodiments, such fine liquid droplets may be produced at a rate in the range from about 4 microliters per second to about 30 microliters per second per 1000 apertures. In this way, aperture plates may be constructed to have multiple apertures that are sufficient to produce aerosolized volumes that are in the range from about 4 microliters to about 30 microliters, within a time that is less than about one second. Such a rate of production is particularly useful for pulmonary drug delivery applications where a desired dosage is aerosolized at a rate sufficient to permit the aerosolized medicament to be directly inhaled. In this way, a capture chamber is not needed to capture the liquid droplets until the specified dosage has been produced. In this manner, the aperture plates may be included within aerosolizers, nebulizers, or inhalers that do not utilize elaborate capture chambers.


As just described, the invention may be employed to deliver a wide variety of drugs to the respiratory system. For example, the invention may be utilized to deliver drugs having potent therapeutic agents, such as hormones, peptides, and other drugs requiring precise dosing including drugs for local treatment of the respiratory system. Examples of liquid drugs that may be aerosolized include drugs in solution form, e.g., aqueous solutions, ethanol solutions, aqueous/ethanol mixture solutions, and the like, in colloidal suspension form, and the like. The invention may also find use in aerosolizing a variety of other types of liquids, such as insulin.


In one aspect, the aperture plates may be constructed of materials having a relatively high strength and that are resistant to corrosion. One particular material that provides such characteristics is a palladium nickel alloy. One particularly useful palladium nickel alloy comprises about 80% palladium and about 20% nickel. Other useful palladium nickel alloys are described generally in J. A. Abys, et al., “Annealing Behavior of Palladium-Nickel Alloy Electrodeposits,” Plating and Surface Finishing, August 1996, “PallaTech® Procedure for the Analysis of Additive IVS in PallaTech® Plating Solutions by HPLC” Technical Bulletin, Lucent Technologies, Oct. 1, 1996, and in U.S. Pat. No. 5,180,482, the complete disclosures of which are herein incorporated by reference.


Aperture plates constructed of such a palladium nickel alloy have significantly better corrosion resistance as compared to nickel aperture plates. As one example, a nickel aperture plate will typically corrode at a rate of about 1 micron per hour when an albuterol sulfate solution (PH 3.5) is flowing through the apertures. In contrast, the palladium nickel alloy of the invention does not experience any detectable corrosion after about 200 hours. Hence, the palladium nickel alloy aperture plates of the invention may be used with a variety of liquids without significantly corroding the aperture plate. Examples of liquids that may be used and which will not significantly corrode such an aperture plate include albuterol, chromatin, and other inhalation solutions that are normally delivered by jet nebulizers, and the like.


Another advantage of the palladium nickel alloy is that it has a low modulus of elasticity. As such, the stress for a given oscillation amplitude is lower as compared to a nickel aperture plate. As one example, the modulus of elasticity for such a palladium alloy is about 12×106 psi, whereas the modulus of elasticity for nickel is about 33×106 psi. Since the stress is proportional to the amount of elongation and the modulus of elasticity, by providing the aperture plate with a lower modulus of elasticity, the stress on the aperture plate is significantly reduced.


Alternative materials for constructing the aperture plates of the invention include pure palladium and gold, as well as those described in copending U.S. application Ser. No. 09/313,914, filed May 18, 1999, the complete disclosure of which is herein incorporated by reference.


To enhance the rate of droplet production while maintaining the droplets within a specified size range, the apertures may be constructed to have a certain shape. More specifically, the apertures are preferably tapered such that the aperture is narrower in cross section where the droplet exits the aperture. In one embodiment, the angle of the aperture at the exit opening (or the exit angle) is in the range from about 30° to about 60°, more preferably from about 41° to about 49°, and more preferably at about 45°. Such an exit angle provides for an increased flow rate while minimizing droplet size. In this way, the aperture plate may find particular use with inhalation drug delivery applications.


The apertures of the aperture plates will typically have an exit opening having a diameter in the range from about 1 micron to about 10 microns, to produce droplets that are about 2 microns to about 10 microns in size. In another aspect, the taper at the exit angle is preferably within the desired angle range for at least about the first 15 microns of the aperture plate. Beyond this point, the shape of the aperture is less critical. For example, the angle of taper may increase toward the opposite surface of the aperture plate.


Conveniently, the aperture plates of the invention may be formed in the shape of a dome as described generally in U.S. Pat. No. 5,758,637, previously incorporated by reference. Typically, the aperture plate will be vibrated at a frequency in the range from about 45 kHz to about 200 kHz when aerosolizing a liquid. Further, when aerosolizing a liquid, the liquid may be placed onto a rear surface of the aperture plate where the liquid adheres to the rear surface by surface tension forces. Upon vibration of the aperture plate, liquid droplets are ejected from the front surface as described generally in U.S. Pat. Nos. 5,164,740, 5,586,550 and 5,758,637, previously incorporated by reference.


The aperture plates of the invention may be constructed using an electrodeposition process where a metal is deposited from a solution onto a conductive mandrel by an electrolytic process. In one particular aspect, the aperture plates are formed using an electroforming process where the metal is electroplated onto an accurately made mandrel that has the inverse contour, dimensions, and surface finish desired on the finished aperture plate. When the desired thickness of deposited metal has been attained, the aperture plate is separated from the mandrel. Electroforming techniques are described generally in E. Paul DeGarmo, “Materials and Processes in Manufacturing” McMillan Publishing Co., Inc., New York, 5th Edition, 1979, the complete disclosure of which is herein incorporated by reference.


The mandrels that may be utilized to produce the aperture plates of the invention may comprise a conductive surface having a plurality of spaced apart nonconductive islands. In this way, when the mandrel is placed into the solution and current is applied to the mandrel, the metal material in the solution is deposited onto the mandrel. Examples of metals which may be electrodeposited onto the mandrel to form the aperture plate have been described above.


One particular feature of the invention is the shape of the nonconductive islands on the aperture plate. These islands may be constructed with a certain shape to produce apertures that have exit angles in the ranges as described above. Examples of geometric configurations that may be employed include islands having a generally conical shape, a dome shape, a parabolic shape, and the like. The nonconductive islands may be defined in terms of an average angle or slope, i.e., the angle extending from the bottom of the island to the top of the island relative to the conductive surface, or using the ratio of the base and the height. The magnitude of this angle is one factor to be considered in forming the exit angle in the aperture plate. For instance, formation of the exit angle in the aperture plate may depend on the electroplating time, the solution used with the electroplating process, and the angle of taper of the nonconductive islands. These variables may be altered alone or in combination to achieve the desired exit angle in the aperture plate. Also, the size of the exit opening may also depend on the electroplating time.


As one specific example, the height and diameter of the nonconductive islands may be varied depending on the desired end dimensions of the apertures and/or on the process employed to create the aperture plates. For instance, in some cases the rear surface of the aperture plate may be formed above the islands. In other cases, the rear surface of the aperture plate may be formed adjacent to the conductive surface of the mandrel. In the latter case, the size of the exit opening may be defined by the cross-sectional dimension of the non-conductive islands at the ending thickness value of the aperture plate. For the former process, the nonconductive islands may have a height that is up to about 30 percent of the total thickness of the aperture plate.


To construct the nonconductive islands, a photolithography process may be employed. For example, a photoresist film may be applied to the mandrel body and a mask having a pattern of circular regions placed over the photoresist film. The photoresist film may then be developed to form an arrangement of nonconductive islands that correspond to the location of the holes in the pattern. The nonconductive islands may then be further treated to produce the desired shape. For example, the mandrel may be heated to allow the photoresist material to melt and flow into the desired shape. Optionally, this process may be repeated one or more additional times to build up layers of photoresist materials. During each additional step, the size of the holes in the pattern may be reduced to assist in producing the generally conical shape of the islands.


A variety of other techniques may be employed to place a pattern of nonconducted material onto the electroforming mandrel. Examples of techniques that may be employed to produce the desired pattern include exposure, silk screening, and the like. This pattern is then employed to control where plating of the material initiates and continues throughout the plating process. A variety of nonconductive materials may be employed to prevent plating on the conductive surface, such as a photoresist, plastic, and the like. As previously mentioned, once the nonconducting material is placed onto the mandrel, it may optionally be treated to obtain the desired profile. Examples of treatments that may be used include baking, curing, heat cycling, carving, cutting, molding or the like. Such processes may be employed to produce a curved or angled surface on the nonconducting pattern which may then be employed to modify the angle of the exit opening in the aperture plate.


Referring now to FIG. 1, one embodiment of an aperture plate 10 will be described. Aperture plate 10 comprises a plate body 12 into which are formed a plurality of tapered apertures 14. Plate body 12 may be constructed of a metal, such as a palladium nickel alloy or other metal as previously described. Conveniently, plate body 12 may be configured to have a dome shape as described generally in U.S. Pat. No. 5,758,637, previously incorporated by reference. Plate body 12 includes a top or front surface 16 and a bottom or rear surface 18. In operation, liquid is supplied to rear surface 18 and liquid droplets are ejected from front surface 16.


Referring now to FIG. 2, the configuration of apertures 14 will be described in greater detail. Apertures 14 are configured to taper from rear surface 18 to front surface 16. Each aperture 14 has an entrance opening 20 and an exit opening 22. With this configuration, liquid supplied to rear surface 18 proceeds through entrance opening 20 and exits through exit opening 22. As shown, plate body 12 further includes a flared portion 24 adjacent exit opening 22. As described in greater detail hereinafter, flared portion 24 is created from the manufacturing process employed to produce aperture plate 10.


As best shown in FIG. 3, the angle of taper of apertures 14 as they approach exit openings 22 may be defined by an exit angle θ. The exit angle is selected to maximize the ejection of liquid droplets through exit opening 20 while maintaining the droplets within a desired size range. Exit angle θ may be constructed to be in the range from about 30° to about 60°, more preferably from about 41° to about 49°, and most preferably around 45°. Also, exit opening 22 may have a diameter in the range from about 1 micron to about 10 microns. Further, the exit angle θ preferably extends over a vertical distance of at least about 15 microns, i.e., exit angel θ is within the above recited ranges at any point within this vertical distance. As shown, beyond this vertical distance, apertures 14 may flare outward beyond the range of the exit angle θ.


In operation, liquid is applied to rear surface 18. Upon vibration of aperture plate 10, liquid droplets are ejected through exit opening 22. In this manner, the liquid droplets will be propelled from front surface 16. Although exit opening 22 is shown inset from front surface 16, it will be appreciated that other types of manufacturing processes may be employed to place exit opening 22 directly at front surface 16.


Shown in FIG. 4 is a graph containing aerosolization simulation data when vibrating an aperture plate similar to aperture plate 10 of FIG. 1. In the graph of FIG. 4, the aperture plate was vibrated at about 180 kHz when a volume of water was applied to the rear surface. Each aperture had a exit diameter of 5 microns. In the simulation, the exit angle was varied from about 10° to about 70° (noting that the exit angle in FIG. 4 is from the center line to the wall of the aperture). As shown, the maximum flow rate per aperture occurred at about 45°. Relatively high flow rates were also achieved in the range from about 41° to about 49°. Exit angles in the range from about 30° to about 60° also produced high flow rates. Hence, in this example, a single aperture is capable of ejecting about 0.08 microliters of water per second when ejecting water. For many medical solutions, an aperture plate containing about 1000 apertures that each have an exit angle of about 45° may be used to produce a dosage in the range from about 30 microliters to about 50 microliters within about one second. Because of such a rapid rate of production, the aerosolized medicament may be inhaled by the patient within a few inhalation maneuvers without first being captured within a capture chamber.


It will be appreciated that the invention is not intended to be limited by this specific example. Further, the rate of production of liquid droplets may be varied by varying the exit angle, the exit diameter and the type of liquid being aerosolized. Hence, depending on the particular application (including the required droplet size), these variables may be altered to produce the desired aerosol at the desired rate.


Referring now to FIG. 5, one embodiment of an electroforming mandrel 26 that may be employed to construct aperture plate 10 of FIG. 1 will be described. Mandrel 26 comprises a mandrel body 28 having a conductive surface 30. Conveniently, mandrel body 28 may be constructed of a metal, such as stainless steel. As shown, conductive surface 30 is flat in geometry. However, in some cases it will be appreciated that conductive surface 30 may be shaped depending on the desired shape of the resulting aperture plate.


Disposed on conductive surface 30 are a plurality of nonconductive islands 32. Islands 32 are configured to extend above conductive surface 30 so that they may be employed in electroforming apertures within the aperture plate as described in greater detail hereinafter. Islands 32 may be spaced apart by a distance corresponding to the desired spacing of the resulting apertures in the aperture plate. Similarly, the number of islands 32 may be varied depending on the particular need.


Referring now to FIG. 6, construction of islands 32 will be described in greater detail. As shown, island 32 is generally conical or dome shaped in geometry. Conveniently, island 32 may be defined in terms of a height h and a diameter D. As such, each island 32 may be said to include an average angle of incline or slope that is defined by the inverse tangent of ½ (D)/h. The average angle of incline may be varied to produce the desired exit angle in the aperture plate as previously described.


As shown, island 32 is constructed of a bottom layer 34 and a top layer 36. As described in greater detail hereinafter, use of such layers assists in obtaining the desired conical or domed shape. However, it will be appreciated that islands 32 may in some cases be constructed from only a single layer or multiple layers.


Referring now to FIG. 7, one method for forming nonconductive islands 32 on mandrel body 28 will be described. As shown in step 38, the process begins by providing an electroforming mandrel. As shown in step 40, a photoresist film is then applied to the mandrel. As one example, such a photoresist film may comprise a thick film photoresist having a thickness in the range from about 7 to about 9 microns. Such a thick film photoresist may comprise a Hoechst Celanese AZ P4620 positive photoresist. Conveniently, such a resist may be pre-baked in a convection oven in air or other environment for about 30 minutes at about 100° C. As shown in step 42, a mask having a pattern of circular regions is placed over the photoresist film. As shown in step 44, the photoresist film is then developed to form an arrangement of nonconductive islands. Conveniently, the resist may be developed in a basic developer, such as a Hoechst Celanese AZ 400 K developer. Although described in the context of a positive photoresist, it will be appreciated that a negative photoresist may also be used as is known in the art.


As shown in step 46, the islands are then treated to form the desired shape by heating the mandrel to permit the islands to flow and cure in the desired shape. The conditions of the heating cycle of step 46 may be controlled to determine the extent of flow (or doming) and the extent of curing that takes place, thereby affecting the durability and permanence of the pattern. In one aspect, the mandrel is slowly heated to an elevated temperature to obtain the desired amount of flow and curing. For example, the mandrel and the resist may be heated at a rate of about 2° C. per minute from room temperature to an elevated temperature of about 240° C. The mandrel and resist are then held at the elevated temperature for about 30 minutes.


In some cases, it may be desirable to add photoresist layers onto the nonconductive islands to control their slope and further enhance the shape of the islands. Hence, as shown in step 48, if the desired shape has not yet been obtained, steps 4046 may be repeated to place additional photoresist layers onto the islands. Typically, when additional layers are added, the mask will contain circular regions that are smaller in diameter so that the added layers will be smaller in diameter to assist in producing the domed shape of the islands. As shown in step 50, once the desired shape has been attained, the process ends.


Referring now to FIGS. 8 and 9, a process for producing aperture plate 10 will be described. As shown in step 52 of FIG. 9, a mandrel having a pattern of nonconductive islands is provided. Conveniently, such a mandrel may be mandrel 26 of FIG. 5 as illustrated in FIG. 8. The process then proceeds to step 54 where the mandrel is placed in a solution containing a material that is to be deposited on the mandrel. As one example, the solution may be a Pallatech PdNi plating solution, commercially available from Lucent Technologies, containing a palladium nickel that is to be deposited on mandrel 26. As shown in step 56, electric current is supplied to the mandrel to electro deposit the material onto mandrel 26 and to form aperture plate 10. As shown in step 56, once the aperture plate is formed, it may be peeled off from mandrel 26.


To obtain the desired exit angle and the desired exit opening on aperture plate 10, the time during which electric current is supplied to the mandrel may be varied. Further, the type of solution into which the mandrel is immersed may also be varied. Still further, the shape and angle of islands 32 may be varied to vary the exit angle of the apertures as previously described. Merely by way of example, one mandrel that may be used to produce exit angles of about 45° is made by depositing a first photoresist island having a diameter of 100 microns and a height of 10 microns. The second photoresist island may have a diameter of 10 microns and a thickness of 6 microns and is deposited on a center of the first island. The mandrel is then heated to a temperature of 200° C. for 2 hours.


Referring now to FIG. 10, an alternative embodiment of an aperture plate 60 will be described. Aperture plate 60 comprises a plate body 62 having a plurality of tapered apertures 64 (only one being shown for convenience of illustration). Plate body 62 has a rear surface 66 and a front surface 68. Apertures 64 are configured to taper from rear surface 66 to front surface 68. As shown, aperture 64 has a constant angle of taper. Preferably, the angle of taper is in the range from about 30° to about 60°, more preferably about 41° to about 49°, and most preferably at about 45°. Aperture 64 further includes an exit opening 70 that may have a diameter in the range from about 2 microns to about 10 microns.


Referring to FIG. 11, one method that may be employed to construct aperture plate 62 will be described. The process employs the use of an electroforming mandrel 72 having a plurality of non-conductive islands 74. Conveniently, island 74 may be constructed to be generally conical or domed-shaped in geometry and may be constructed using any of the processes previously described herein. To form aperture plate 60, mandrel 72 is placed within a solution and electrical current is applied to mandrel 72. The electroplating time is controlled so that front surface 68 of aperture plate 60 does not extend above the top of island 74. The amount of electroplating time may be controlled to control the height of aperture plate 60. As such, the size of exit openings 72 may be controlled by varying the electroplating time. Once the desired height of aperture plate 60 is obtained, electrical current is ceased and mandrel 72 may be removed from aperture plate 60.


Referring now to FIG. 12, use of aperture plate 10 to aerosolize a volume of liquid 76 will be described. Conveniently, aperture plate 10 is coupled to a cupped shaped member 78 having a central opening 80. Aperture plate 10 is placed over opening 80, with rear surface 18 being adjacent liquid 76. A piezoelectric transducer 82 is coupled to cupped shaped member 78. An interface 84 may also be provided as a convenient way to couple the aerosol generator to other components of a device. In operation, electrical current is applied to transducer 82 to vibrate aperture plate 10. Liquid 76 may be held to rear surface 18 of aperture plate 10 by surface tension forces. As aperture plate 10 is vibrated, liquid droplets are ejected from the front surface as shown. As also shown in FIG. 12, cup shaped member 78 has a base portion 79 and a walled portion 81. The cross sectional length L1 of base portion 79 is greater than the cross sectional width W1 of base portion 79. Also, the cross sectional length L2 of piezoelectric transducer 82 is greater than the cross sectional width W2 of piezoelectric transducer 82. As further shown, length L1 is parallel to length L2.


As previously mentioned, aperture plate 10 may be constructed so that a volume of liquid in the range from about 4 microliters to about 30 microliters may be aerosolized within a time that is less than about one second per about 1000 apertures. Further, each of the droplets may be produced such that they have a respirable fraction that is greater than about 90 percent. In this way, a medicament may be aerosolized and then directly inhaled by a patient.


In some cases, the aperture plates described herein may be use in non-vibratory applications. For example, the aperture plates may be used as a non-vibrating nozzle where liquid is forced through the apertures. As one example, the aperture plates may be used with ink jet printers that use thermal or piezoelectric energy to force the liquid through the nozzles. The aperture plates of the invention may be advantageous when used as non-vibrating nozzles with ink jet printers because of their non-corrosive construction and because the apertures have a low resistance to flow due to their relatively short necked regions.


The invention has now been described in detail for purposes of clarity of understanding. However, it will be appreciated that certain changes and modifications may be practiced within the scope of the appended claims.

Claims
  • 1. An apparatus comprising: a holding member having a cross sectional length that is greater than a cross sectional width and a central opening;a vibratable member comprising a piezoelectric transducer that is configured to vibrate upon application of an electrical signal, wherein the vibratable member has a cross sectional length that is greater than a cross sectional width and is coupled to the holding member outside of the central opening with the length of the vibratable member being parallel to the length of the holding member;a plate body operably coupled to the vibratable member by the holding member such that the plate body is disposed across the central opening, the plate body having a top surface, a bottom surface, and a plurality of apertures extending from the top surface to the bottom surface, wherein each aperture is defined by a tapered portion which tapers inward from the bottom surface toward the top surface and a flared portion that extends from the top surface toward the bottom surface and that flares away from the tapered portion, and wherein the flared portion and the tapered portion share an axis of symmetry such that when a liquid is supplied to the bottom surface and the aperture plate is vibrated using the vibratable member, liquid droplets are ejected through the flared portion, wherein the plate body is electroformed to produce the apertures, and wherein the tapered portion at an intersection with the flared portion has a size in the range from about 1 micron to about 10 microns.
  • 2. An apparatus as in claim 1, wherein the plate body is constructed from materials selected from a group consisting of palladium, palladium nickel and palladium alloys.
  • 3. An apparatus as in claim 1, wherein the plate body includes a portion that is dome shaped in geometry.
  • 4. An apparatus as in claim 1, wherein the plate body has a thickness in the range from about 20 microns to about 70 microns.
  • 5. An apparatus as in claim 1, wherein the apertures have an exit angle that is in the range from about 41° to about 49°.
  • 6. An apparatus as in claim 1, wherein the flared portion has a height that is approximately one-third of the thickness of the plate body.
  • 7. An apparatus as in claim 1, wherein the plate body has a thickness of at least about 20 microns.
  • 8. An apparatus comprising: a holding member having a cross sectional length that is greater than a cross sectional width and a central opening;a vibratable member comprising a piezoelectric transducer that is configured to vibrate upon application of an electrical signal, wherein the vibratable member has cross sectional length that is greater than a cross sectional width and is coupled to the holding member outside of the central opening with the length of the vibratable member being parallel to the length of the holding member;a plate body operably coupled to the vibratable member by the holding member such that the plate body is disposed across the central opening, the plate body having a top surface, a bottom surface, and a plurality of apertures extending from the top surface to the bottom surface, wherein the apertures each include an upper portion and a lower portion, wherein the lower portion extends upwardly from the bottom surface and is generally concave in geometry, and wherein the upper portion is tapered in a direction from the top surface to the bottom surface and intersects at an intersection with the lower portion which flares outward such that when a liquid is supplied to the top surface and the aperture plate is vibrated using the vibratable member, liquid passes through the upper portion and is ejected through the lower portion as liquid droplets, wherein the plate body is electroformed to produce the apertures, and wherein the upper portion at the intersection has a size in the range from about 1 micron to about 10 microns.
  • 9. An apparatus as in claim 8, wherein the upper portion has an angle of taper that is in the range from about 30° to about 60° at the intersection with the lower portion, and a diameter that is in the range from about 1 micron to about 10 microns at the intersection with the lower portion.
  • 10. An apparatus as in claim 9, wherein the lower portion has a diameter at the lower surface that is in the range from about 20 microns to about 200 microns, and a height in the range from about 4 microns to about 20 microns.
US Referenced Citations (420)
Number Name Date Kind
550315 Allen Nov 1895 A
809159 Willis et al. Jan 1906 A
1680616 Horst Aug 1928 A
2022520 Philbrick Nov 1935 A
2101304 Wright Dec 1937 A
2158615 Wright May 1939 A
2187528 Wing Jan 1940 A
2223541 Baker Dec 1940 A
2266706 Fox et al. Dec 1941 A
2283333 Martin May 1942 A
2292381 Klagges Aug 1942 A
2360297 Wing Oct 1944 A
2375770 Dahlberg May 1945 A
2383098 Wheaton Aug 1945 A
2404063 Healy Jul 1946 A
2430023 Longmaid Nov 1947 A
2474996 Wallis Jul 1949 A
2512004 Wind Jun 1950 A
2521657 Severy Sep 1950 A
2681041 Zodtner et al. Jun 1954 A
2705007 Gerber Mar 1955 A
2735427 Sullivan Feb 1956 A
2764946 Henderson Oct 1956 A
2764979 Henderson Oct 1956 A
2779623 Eisenkraft Jan 1957 A
2935970 Morse et al. May 1960 A
3103310 Lang Sep 1963 A
3325031 Singier Jun 1967 A
3411854 Rosler et al. Nov 1968 A
3515348 Coffman, Jr. Jun 1970 A
3550864 East Dec 1970 A
3558052 Dunn Jan 1971 A
3561444 Boucher Feb 1971 A
3563415 Ogle Feb 1971 A
3680954 Frank Aug 1972 A
3719328 Hindman Mar 1973 A
3738574 Guntersdorfer et al. Jun 1973 A
3771982 Dobo Nov 1973 A
3790079 Berglund et al. Feb 1974 A
3804329 Martner Apr 1974 A
3812854 Michaels et al. May 1974 A
3838686 Szekely Oct 1974 A
3842833 Ogle Oct 1974 A
3865106 Palush Feb 1975 A
3903884 Huston et al. Sep 1975 A
3906950 Cocozza Sep 1975 A
3908654 Lhoest et al. Sep 1975 A
3950760 Rauch et al. Apr 1976 A
3951313 Coniglione Apr 1976 A
3958249 DeMaine et al. May 1976 A
3970250 Drews Jul 1976 A
3983740 Danel Oct 1976 A
3993223 Welker, III et al. Nov 1976 A
4005435 Lundquist et al. Jan 1977 A
4030492 Simburner Jun 1977 A
4052986 Scaife Oct 1977 A
4059384 Holland et al. Nov 1977 A
D246574 Meierhoefer Dec 1977 S
4076021 Thompson Feb 1978 A
4083368 Freezer Apr 1978 A
4094317 Wasnich Jun 1978 A
4101041 Mauro, Jr. et al. Jul 1978 A
4106503 Rsenthal et al. Aug 1978 A
4109174 Hodgson Aug 1978 A
4113809 Abair et al. Sep 1978 A
D249958 Meierhoefer Oct 1978 S
4119096 Drews Oct 1978 A
4121583 Chen Oct 1978 A
4159803 Cameto et al. Jul 1979 A
4207990 Weiler et al. Jun 1980 A
4210155 Grimes Jul 1980 A
4226236 Genese Oct 1980 A
4240081 Devitt Dec 1980 A
4240417 Holever Dec 1980 A
4248227 Thomas Feb 1981 A
4261512 Zierenberg Apr 1981 A
D259213 Pagels May 1981 S
4268460 Boiarski et al. May 1981 A
4294407 Reichl et al. Oct 1981 A
4298045 Weiler et al. Nov 1981 A
4299784 Hense Nov 1981 A
4300546 Kruber Nov 1981 A
4301093 Eck Nov 1981 A
4319155 Makai et al. Mar 1982 A
4334531 Reichl et al. Jun 1982 A
4336544 Donald et al. Jun 1982 A
4338576 Takahashi et al. Jul 1982 A
4368476 Uehara et al. Jan 1983 A
4368850 Szekely Jan 1983 A
4374707 Pollack Feb 1983 A
4389071 Johnson, Jr. et al. Jun 1983 A
4408719 Last Oct 1983 A
4428802 Kanai et al. Jan 1984 A
4431136 Janner et al. Feb 1984 A
4454877 Miller et al. Jun 1984 A
4465234 Maehara et al. Aug 1984 A
4474251 Johnson, Jr. Oct 1984 A
4474326 Takahashi Oct 1984 A
4475113 Lee et al. Oct 1984 A
4479609 Maeda et al. Oct 1984 A
4512341 Lester Apr 1985 A
4530464 Yamamoto et al. Jul 1985 A
4533082 Maehara et al. Aug 1985 A
4539575 Nilsson Sep 1985 A
4544933 Heinzl Oct 1985 A
4546361 Brescia et al. Oct 1985 A
4550325 Viola Oct 1985 A
4566452 Farr Jan 1986 A
4591883 Isayama May 1986 A
4593291 Howkins Jun 1986 A
4605167 Maehara Aug 1986 A
4613326 Szwarc Sep 1986 A
4620201 Heinzl et al. Oct 1986 A
4628890 Freeman Dec 1986 A
4632311 Nakane et al. Dec 1986 A
4658269 Rezanka Apr 1987 A
4659014 Soth et al. Apr 1987 A
4677975 Edgar et al. Jul 1987 A
4678680 Abowitz Jul 1987 A
4679551 Anthony Jul 1987 A
4681264 Johnson, Jr. Jul 1987 A
4693853 Falb et al. Sep 1987 A
4702418 Carter et al. Oct 1987 A
4722906 Guire Feb 1988 A
4790479 Matsumoto et al. Dec 1988 A
4793339 Matsumoto et al. Dec 1988 A
4796807 Bendig et al. Jan 1989 A
4799622 Ishikawa et al. Jan 1989 A
4805609 Roberts et al. Feb 1989 A
4819629 Jonson Apr 1989 A
4819834 Thiel Apr 1989 A
4826080 Ganser May 1989 A
4826759 Guire et al. May 1989 A
4828886 Hieber May 1989 A
4843445 Stemme Jun 1989 A
4849303 Graham et al. Jul 1989 A
4850534 Takahashi et al. Jul 1989 A
4865006 Nogi et al. Sep 1989 A
4871489 Ketcham Oct 1989 A
4872553 Suzuki et al. Oct 1989 A
4877989 Drews et al. Oct 1989 A
4888516 Daeges et al. Dec 1989 A
4922901 Brooks et al. May 1990 A
4926915 Deussen et al. May 1990 A
4934358 Nilsson et al. Jun 1990 A
4954225 Bakewell Sep 1990 A
4957239 Tempelman Sep 1990 A
4964521 Wieland et al. Oct 1990 A
D312209 Morrow et al. Nov 1990 S
4968299 Ahlstrand et al. Nov 1990 A
4971665 Sexton Nov 1990 A
4973493 Guire Nov 1990 A
4976259 Higson et al. Dec 1990 A
4979959 Guire Dec 1990 A
4994043 Ysebaert Feb 1991 A
5002048 Makiej, Jr. Mar 1991 A
5002582 Guire et al. Mar 1991 A
5007419 Weinstein et al. Apr 1991 A
5016024 Lam et al. May 1991 A
5021701 Takahashi et al. Jun 1991 A
5022587 Hochstein Jun 1991 A
5024733 Abys et al. Jun 1991 A
5046627 Hansen Sep 1991 A
5062419 Rider Nov 1991 A
5063396 Shiokawa et al. Nov 1991 A
5073484 Swanson et al. Dec 1991 A
5076266 Babaev Dec 1991 A
5080093 Raabe et al. Jan 1992 A
5080649 Vetter Jan 1992 A
5086765 Levine Feb 1992 A
5086785 Gentile et al. Feb 1992 A
5115803 Sioutas May 1992 A
5115971 Greenspan et al. May 1992 A
D327008 Friedman Jun 1992 S
5122116 Kriesel et al. Jun 1992 A
5129579 Conte Jul 1992 A
5134993 Van Der Linden et al. Aug 1992 A
5139016 Waser Aug 1992 A
5140740 Weigelt Aug 1992 A
5147073 Cater Sep 1992 A
5152456 Ross et al. Oct 1992 A
5157372 Langford Oct 1992 A
5164740 Ivri Nov 1992 A
5169029 Behar et al. Dec 1992 A
5170782 Kocinski Dec 1992 A
5180482 Abys et al. Jan 1993 A
5186164 Raghuprasad Feb 1993 A
5186166 Riggs et al. Feb 1993 A
5198157 Bechet Mar 1993 A
5201322 Henry et al. Apr 1993 A
5213860 Laing May 1993 A
5217148 Cater Jun 1993 A
5217492 Guire et al. Jun 1993 A
5227168 Chvapil Jul 1993 A
5230496 Shillington et al. Jul 1993 A
5245995 Sullivan et al. Sep 1993 A
5248087 Dressler Sep 1993 A
5258041 Guire et al. Nov 1993 A
5261601 Ross et al. Nov 1993 A
5263992 Guire Nov 1993 A
5279568 Cater Jan 1994 A
5297734 Toda Mar 1994 A
5299739 Takahashi et al. Apr 1994 A
5303854 Cater Apr 1994 A
5309135 Langford May 1994 A
5312281 Takahashi et al. May 1994 A
5313955 Rodder May 1994 A
5319971 Osswald et al. Jun 1994 A
5320603 Vetter et al. Jun 1994 A
5322057 Raabe et al. Jun 1994 A
5342011 Short Aug 1994 A
5342504 Hirano et al. Aug 1994 A
5347998 Hodson et al. Sep 1994 A
5348189 Cater Sep 1994 A
5350116 Cater Sep 1994 A
5355872 Riggs et al. Oct 1994 A
5357946 Kee et al. Oct 1994 A
5372126 Blau Dec 1994 A
5383906 Burchett et al. Jan 1995 A
5388571 Roberts et al. Feb 1995 A
5392768 Johansson et al. Feb 1995 A
5396883 Knupp et al. Mar 1995 A
5414075 Swan et al. May 1995 A
5415161 Ryder May 1995 A
5419315 Rubsamen May 1995 A
5426458 Wenzel et al. Jun 1995 A
5431155 Marelli Jul 1995 A
5435282 Haber et al. Jul 1995 A
5435297 Klein Jul 1995 A
5437267 Weinstein et al. Aug 1995 A
5445141 Kee et al. Aug 1995 A
D362390 Weiler Sep 1995 S
5449502 Igusa et al. Sep 1995 A
5452711 Gault Sep 1995 A
5458135 Patton et al. Oct 1995 A
5458289 Cater Oct 1995 A
5474059 Cooper Dec 1995 A
5477992 Jinks et al. Dec 1995 A
5479920 Piper et al. Jan 1996 A
5487378 Robertson et al. Jan 1996 A
5489266 Grimard Feb 1996 A
5497944 Weston et al. Mar 1996 A
D369212 Snell Apr 1996 S
5511726 Greenspan et al. Apr 1996 A
5512329 Guire et al. Apr 1996 A
5515841 Robertson et al. May 1996 A
5515842 Ramseyer et al. May 1996 A
5516043 Manna et al. May 1996 A
5518179 Humberstone et al. May 1996 A
5529055 Gueret Jun 1996 A
5533497 Ryder Jul 1996 A
5542410 Goodman et al. Aug 1996 A
5549102 Lintl et al. Aug 1996 A
5560837 Trueba Oct 1996 A
5563056 Swan et al. Oct 1996 A
D375352 Bologna Nov 1996 S
5579757 McMahon et al. Dec 1996 A
5582330 Iba Dec 1996 A
5584285 Salter et al. Dec 1996 A
5586550 Ivri et al. Dec 1996 A
5588166 Burnett Dec 1996 A
5601077 Imbert Feb 1997 A
5609798 Liu et al. Mar 1997 A
5632878 Kitano May 1997 A
5635096 Singer et al. Jun 1997 A
5637460 Swan et al. Jun 1997 A
5647349 Ohki et al. Jul 1997 A
5653227 Barnes et al. Aug 1997 A
5654007 Johnson et al. Aug 1997 A
5654162 Guire et al. Aug 1997 A
5654460 Rong Aug 1997 A
5657926 Toda Aug 1997 A
5660166 Lloyd Aug 1997 A
5664557 Makiej, Jr. Sep 1997 A
5664706 Cater Sep 1997 A
5665068 Takamura Sep 1997 A
5666946 Langenback Sep 1997 A
5670999 Takeuchi et al. Sep 1997 A
5685491 Marks et al. Nov 1997 A
5692644 Gueret Dec 1997 A
5707818 Chudzik et al. Jan 1998 A
5709202 Lloyd et al. Jan 1998 A
5714360 Swan et al. Feb 1998 A
5714551 Bezwada et al. Feb 1998 A
5718222 Lloyd et al. Feb 1998 A
D392184 Weiler Mar 1998 S
5724957 Rubsamen et al. Mar 1998 A
5744515 Clapper Apr 1998 A
5752502 King May 1998 A
5755218 Johansson et al. May 1998 A
5758637 Ivri et al. Jun 1998 A
5775506 Grabenkort Jul 1998 A
5788665 Sekins Aug 1998 A
5788819 Onishi et al. Aug 1998 A
5790151 Mills Aug 1998 A
5810004 Ohkl et al. Sep 1998 A
5819730 Stone et al. Oct 1998 A
5823179 Grychowski et al. Oct 1998 A
5823428 Humberstone et al. Oct 1998 A
5829723 Brunner et al. Nov 1998 A
5836515 Fonzes Nov 1998 A
5839617 Cater et al. Nov 1998 A
5842468 Denyer et al. Dec 1998 A
5862802 Bird Jan 1999 A
5865171 Cinquin Feb 1999 A
5878900 Hansen Mar 1999 A
5893515 Hahn et al. Apr 1999 A
5894841 Voges Apr 1999 A
5897008 Hansen Apr 1999 A
5910698 Yagi Jun 1999 A
5915377 Coffee Jun 1999 A
5918637 Fleischman Jul 1999 A
5925019 Ljungquist Jul 1999 A
5950619 Van Der Linden et al. Sep 1999 A
5954268 Joshi et al. Sep 1999 A
5960792 Lloyd et al. Oct 1999 A
5964417 Amann et al. Oct 1999 A
5970974 Van Der Linden et al. Oct 1999 A
5976344 Abys et al. Nov 1999 A
5993805 Sutton et al. Nov 1999 A
6000396 Melker et al. Dec 1999 A
6007518 Kriesel et al. Dec 1999 A
6012450 Rubsamen Jan 2000 A
6014970 Ivri et al. Jan 2000 A
6026809 Abrams et al. Feb 2000 A
6029666 Aloy et al. Feb 2000 A
6032665 Psaros Mar 2000 A
6037587 Dowell et al. Mar 2000 A
6045215 Coulman Apr 2000 A
6045874 Himes Apr 2000 A
6047818 Warby et al. Apr 2000 A
6055869 Stemme et al. May 2000 A
6060128 Kim et al. May 2000 A
6062212 Davison et al. May 2000 A
6068148 Weiler May 2000 A
6085740 Ivri et al. Jul 2000 A
6096011 Trombley, III et al. Aug 2000 A
6105877 Coffee Aug 2000 A
6106504 Urrutia Aug 2000 A
6116234 Genova et al. Sep 2000 A
6123413 Agarwal et al. Sep 2000 A
6139674 Markham et al. Oct 2000 A
6142146 Abrams et al. Nov 2000 A
6145963 Pidwerbecki et al. Nov 2000 A
6146915 Pidwerbecki et al. Nov 2000 A
6152130 Abrams et al. Nov 2000 A
6155676 Etheridge et al. Dec 2000 A
6158431 Poole Dec 2000 A
6161536 Redmon et al. Dec 2000 A
6163588 Matsumoto et al. Dec 2000 A
6182662 McGhee Feb 2001 B1
6186141 Pike et al. Feb 2001 B1
6196218 Voges Mar 2001 B1
6196219 Hess et al. Mar 2001 B1
6205999 Ivri et al. Mar 2001 B1
6216916 Maddox et al. Apr 2001 B1
6223746 Jewett et al. May 2001 B1
6235177 Borland et al. May 2001 B1
6254219 Agarwal et al. Jul 2001 B1
6269810 Brooker et al. Aug 2001 B1
6270473 Schwebel Aug 2001 B1
6273342 Terada et al. Aug 2001 B1
6318640 Coffee Nov 2001 B1
6328030 Kidwell et al. Dec 2001 B1
6328033 Avrahami Dec 2001 B1
6341732 Martin et al. Jan 2002 B1
6358058 Strupat et al. Mar 2002 B1
6394363 Arnott et al. May 2002 B1
6402046 Loser Jun 2002 B1
6405934 Hess et al. Jun 2002 B1
6427682 Klimowicz et al. Aug 2002 B1
6443146 Voges Sep 2002 B1
6443366 Hirota et al. Sep 2002 B1
6467476 Ivri et al. Oct 2002 B1
6530370 Heinonen Mar 2003 B1
6540153 Ivri Apr 2003 B1
6540154 Ivri et al. Apr 2003 B1
6543443 Klimowicz et al. Apr 2003 B1
6546927 Litherland et al. Apr 2003 B1
6550472 Litherland et al. Apr 2003 B1
6554201 Klimowicz et al. Apr 2003 B1
6581595 Murdock et al. Jun 2003 B1
6615824 Power Sep 2003 B1
6629646 Ivri Oct 2003 B1
6640804 Ivri Nov 2003 B1
6651650 Yamamoto et al. Nov 2003 B1
6732944 Litherland et al. May 2004 B1
6755189 Ivri et al. Jun 2004 B1
6769626 Haveri Aug 2004 B1
6782886 Narayan et al. Aug 2004 B1
6814071 Klimowicz et al. Nov 2004 B1
6845770 Klimowicz et al. Jan 2005 B1
6851626 Patel et al. Feb 2005 B1
6860268 Bohn et al. Mar 2005 B1
20010013554 Borland et al. Aug 2001 A1
20010015737 Truninger et al. Aug 2001 A1
20020011247 Ivri et al. Jan 2002 A1
20020078958 Stenzler Jun 2002 A1
20020104530 Ivri et al. Aug 2002 A1
20020121274 Borland et al. Sep 2002 A1
20020134372 Loeffler et al. Sep 2002 A1
20020134374 Loeffler et al. Sep 2002 A1
20020134375 Loeffler et al. Sep 2002 A1
20020134377 Loeffler et al. Sep 2002 A1
20020162551 Litherland Nov 2002 A1
20030140921 Smith et al. Jul 2003 A1
20030150445 Power et al. Aug 2003 A1
20030150446 Patel et al. Aug 2003 A1
20030226906 Ivri Dec 2003 A1
20040000598 Ivri Jan 2004 A1
20040004133 Ivri et al. Jan 2004 A1
20040011358 Smaldone et al. Jan 2004 A1
20040035413 Smaldone et al. Feb 2004 A1
20040035490 Power Feb 2004 A1
20040050947 Power et al. Mar 2004 A1
20040139963 Ivri et al. Jul 2004 A1
20040139968 Loeffler et al. Jul 2004 A1
20040188534 Litherland et al. Sep 2004 A1
20040256488 Loeffler et al. Dec 2004 A1
20050011514 Power et al. Jan 2005 A1
Foreign Referenced Citations (45)
Number Date Country
477 855 Sep 1969 CH
555 681 Nov 1974 CH
0 049 636 Apr 1982 EP
0 103 161 Mar 1984 EP
0 134 847 Mar 1985 EP
0 178 925 Apr 1986 EP
0 387 222 Sep 1990 EP
0 432 992 Jun 1991 EP
0 476 991 Mar 1992 EP
0 480 615 Apr 1992 EP
0 510 648 Oct 1992 EP
0 516 565 Dec 1992 EP
0 542 723 May 1993 EP
0 933 138 Apr 1999 EP
0 923 957 Jun 1999 EP
1 142 600 Oct 2001 EP
2 692 569 Dec 1993 FR
973 458 Oct 1964 GB
1 454 597 Nov 1976 GB
2 073 616 Oct 1981 GB
2 101 500 Jan 1983 GB
2 177 623 Jan 1987 GB
2 240 494 Jul 1991 GB
2 272 389 May 1994 GB
2 279 571 Jan 1995 GB
57-023852 Feb 1982 JP
57-105608 Jul 1982 JP
58-061857 Apr 1983 JP
58-139757 Aug 1983 JP
59-142163 Aug 1984 JP
60-004714 Jan 1985 JP
61-008357 Jan 1986 JP
61-215059 Sep 1986 JP
02-135169 May 1990 JP
02-189161 Jul 1990 JP
60-07721 Jan 1994 JP
WO 9207600 May 1992 WO
WO 9211050 Sep 1992 WO
WO 9217231 Oct 1992 WO
WO 9301404 Jan 1993 WO
WO 93010910 Jun 1993 WO
WO 9409912 May 1994 WO
WO 9609229 Mar 1996 WO
WO 9917888 Apr 1999 WO
WO 0037132 Jun 2000 WO
Related Publications (1)
Number Date Country
20010013554 A1 Aug 2001 US
Divisions (1)
Number Date Country
Parent 09392180 Sep 1999 US
Child 09822573 US