Nebulizer apparatus

Information

  • Patent Grant
  • 6530370
  • Patent Number
    6,530,370
  • Date Filed
    Thursday, September 16, 1999
    25 years ago
  • Date Issued
    Tuesday, March 11, 2003
    21 years ago
Abstract
A nebulizer apparatus to atomize liquid solutions or suspensions. The nebulizer is typically used in conjunction with a breathing circuit to deliver atomized medicine to a patient. A housing with an opening covered by a thin mesh plate is supplied with the liquid to be nebulized on an “on-demand” basis. The mesh plate or liquid is vibrated at ultrasonic frequencies to atomize the liquid as it passes through the plate into breathing gases flowing through the breathing tube.
Description




BACKGROUND OF THE INVENTION




The present invention relates to an improved nebulizer apparatus. Nebulizers, or atomizers, are devices, which generate a fine spray or aerosol, usually of liquid. A particularly useful application for nebulizers is to provide a fine spray containing a dissolved or a suspended particulate or colloidal pharmaceutical agent for administration to a subject by inhalation. Such inhalation treatment is highly effective for conditions affecting the subject's respiratory organs. Further, since the lungs are close to the heart and the blood circulatory system of the body, drug administration by inhalation provides an effective and rapid delivery system to all organs of the body.




In many cases, the nebulizer is placed directly in the mouth or nose of the subject so that the spray can be entrained in the respiratory gases inhaled during normal, spontaneous breathing of the subject. In other cases, the subject breathes with the aid of a respiratory ventilator. A typical ventilator has a breathing circuit comprising an inhalation limb and an exhalation limb connected to two arms of a Y-connector. The third arm of the Y-connector is connected, via a patient limb, to a mouthpiece, mask or endotracheal tube for the subject. The ventilator provides a complete or partial supply of respiratory gases to the subject through the inhalation limb during inhalation. The contraction of the subject's lungs discharges gas through the exhalation limb during exhalation. When a nebulizer is employed in conjunction with a ventilator, it is typically placed in the patient limb.




Nebulizers currently in use for ventilator applications generate the spray either pneumatically or by means of ultrasonic vibrations. Pneumatic nebulizers are typically used with a liquid, such as an aqueous drug solution. High pressure driving gas is conducted through a nozzle to draw the drug from a drug supply for the nebulizer. The drug is discharged against a baffle or other means in a gas space of the nebulizer, breaking the liquid into a fine spray. The gas space is in fluid communication with the inhaled gas pathway of the breathing circuit so that the gas flow expelled from the nozzle along with the nebulized drug is conducted to the breathing circuit and ultimately to the subject.




Disadvantages in the use of pneumatic nebulizers include the following. If the nebulizer adds a significant quantity of gas, for example, up to five liters/minute, into the breathing circuit, the breathing gas composition is affected. The driving gas is most often either oxygen or air and, particularly when a ventilator is used in the treatment of a child, the gas flow from the nebulizer may form a major portion of the inhalation gas flow. Because of the gas flow from the nebulizer, control over the inhalation gas composition is lost. Also, due to passage of the driving gas through the nozzle, impingement of the drug on the baffle, etc., pneumatic nebulizers are noisy. This may contribute to the discomfort of the subject. And, as controlling the commencing and stopping of a drug agent spray is difficult and is not very accurate, pneumatic nebulizers are commonly active during both inhalation and exhalation. This obviously decreases the efficiency of drug delivery as measured by ratio of the amount of drug supplied to the nebulizer and the amount of drug actually delivered into the subject's air ways.




In an ultrasonic nebulizer, the fine spray is produced by ultrasonic vibration of the liquid, as by a piezoelectric crystal. The liquid is dropped on, or otherwise applied to, the crystal. The on-off operation of such nebulizers is easier to control than for a pneumatic nebulizer. However, prior art ultrasonic devices require a large electrical power consumption to power the crystal and may not be able to nebulize colloidal or particulate suspensions. Partly due to the high power consumption of ultrasonic nebulizers, the equipment tends to be bulky. This can cause considerable difficulties, given the crowded environment that may surround a subject, such as a critical care patient.




U.S. Pat. No. 5,443,059, shows an attempt to solve the problem of bulkiness in an ultrasonic nebulizer. In the '059 patent, a liquid source and metering component are provided in separate control unit that can be located at a distance from the subject. The control unit meters liquid through a feed line to a piezoelectric ceramic plate positioned in the patient limb of the breathing circuit. The piezoelectric ceramic plate nebulizes the liquid. In the event more liquid is delivered than can be nebulized, the device is equipped with a collection vessel for the excess liquid. In the structure disclosed in this patent, the metering line for the liquid to be nebulized is located above the vibrating crystal so that the liquid drops onto the crystal. However, this renders the ultrasonic nebulizer of this patent position sensitive. Additionally, during inhalation, the flow speed of the respiratory gases can exceed 10 m/s. Such a flow speed can draw the droplets of liquid away into the respiratory gases without the droplets being applied to the vibrating crystal for nebulization. This may render the inhalation therapy less effective, or may alter dosage rates, both of which can adversely affect the subject.




U.S. Pat. No. 3,812,854 describes a nebulizer for inhalation therapy in which the spray is generated on the front surface of a vibrating, porous body. The pores of the body form a network of passages that enable the liquid to flow through the body. The liquid to be nebulized is supplied under pressure from a liquid supply through a liquid conduit to the pores, and forced through the pores to the front surface of the porous body where it is discharged as a spray.




However, the complicated flow paths in the porous body increase the flow resistance so that high liquid pressure is required to transport the liquid through the body. To resist the forces resulting from the high liquid pressure, a thick porous body is required. But, such thickness increases the weight of the nebulizer as well as the amount of electric power required to vibrate same. Also, when used with suspensions containing suspended particulate or colloidal particles, the particles may be entrapped in the complicated flow paths through the porous body.




U.S. Pat. No. 5,478,378 describes a nebulizer in which the aerosol is formed using a mesh plate instead of a porous solid body, thereby to lessen or eliminate the foregoing shortcomings. The mesh plate has a plurality of orifices for the liquid in a reservoir. The orifices are tapered outwardly toward the outlet for the liquid. The liquid or the nozzle assembly is vibrated ultrasonically by a piezoelectric element to nebulize the liquid. The liquid reservoir is preferably permanently filled with liquid and maintained at a slight negative pressure.




BRIEF SUMMARY OF THE INVENTION




An object of the present invention is to provide an improved nebulizer apparatus of the mesh plate type that can atomize both solutions and suspensions without clogging. Another object of the invention is to provide such an apparatus that has a liquid supply control means and a means for substantially equalizing pressures in the nebulizer apparatus with pressures in the breathing circuit. These means avoid pressure stressing of the mesh plate and avoid leaking of the liquid to be nebulized through the mesh plate. Yet another object of the invention is to provide such an apparatus that has a relative small size and low power consumption thereby facilitating its use. Yet another further object of the invention is to provide such an apparatus that is insensitive to the position in which it is operated. An additional object of the invention is provide such an apparatus that has fast response to activation and deactivation, enabling nebulization to be triggered in response to the subject's breathing pattern. A further object of the invention is to provide such an apparatus that efficiently transforms all the liquid into an aerosol.




Provided in accordance with one aspect of the present invention is a nebulizer apparatus for atomizing a liquid into fine droplets. The aerosol so produced may contain medication to be delivered to breathing gases for a patient. In such an environment, the nebulizer apparatus is mounted in a breathing circuit adapter through which the breathing gases pass. The nebulizer has a housing. A mesh plate spanning a cavity in the housing has one side exposed to the gases passing through the housing. The liquid to be nebulized flows into the cavity from a liquid transport line to a rear surface of the mesh plate. A vibration means vibrates the plate or liquid to cause the liquid to pass through holes in the mesh plate to be broken up into droplets and discharged as an aerosol from the front surface of the mesh plate in the flow of breathing gases. The vibrator means for vibrating the mesh plate or liquid is preferably a piezoelectric element energized by an ultrasonic frequency power service.




The mesh plate employed in the present invention is thin as compared to the ceramic bodies used in prior art nebulizers. This permits reduced operating pressures and forces, less energy to vibrate the plate, and allows the use of suspensions since particulates in a suspension can flow through the paths defined by the holes instead of the myriad of complicated flow paths found in ceramic bodies.




The pressure at the rear surface of the mesh plate and at the front surface of the mesh plate is equalized to avoid stresses in the thin mesh plate. This equalization of pressure is accomplished by the use of a pressure channel in the housing communicating between the cavity in the housing and the breathing gas passage.




The delivery of liquid to be nebulized is preferably controlled responsive to the amount of liquid at the rear surface of the mesh plate. For this purpose, a sensor, such as a pair of electrodes spaced from the rear surface of the mesh plate, may be used for sensing the presence of liquid at the rear surface of the mesh plate by changes in impedance. When the appropriate amount of liquid has been delivered, delivery of liquid is stopped or altered to prevent undue pressure in the volume and resulting stress on the plate or liquid leakage through the mesh plate. The supply of liquid is resumed when the liquid on the mesh plate has been consumed or reduced, as detected by the sensor. In an embodiment of the invention, the mesh plate may serve as one of the electrodes. Or, an optical sensor may be used as a liquid detector.




The nebulizer apparatus may include a control valve connected in a liquid transport line for the liquid to be nebulized. This valve may be opened and closed, responsive to the sensor, to control the liquid flow through the transport line to the mesh plate.




A reservoir for the nebulizer apparatus connected to the liquid transport line stores the liquid prior to nebulization. The reservoir may be pressurized to supply liquid to the liquid transport line. Alternatively, a pump or elevated reservoir may be used to supply the liquid.




If small amounts of liquid are to be delivered, a pre-determined amount of the liquid may be stored in a two-part reservoir prior to nebulization. One part of the reservoir comprises a chamber for receiving the liquid to be nebulized. This chamber is separated from the other part of the reservoir by a flexible wall. The other part of the reservoir is pressurized with liquid or gas to supply the liquid from the chamber to the liquid supply line.




To avoid condensation on the front surface of the mesh plate in the moist breathing circuit environment, to reduce liquid viscosity, and/or to provide comfort to the patient, a heater, such as a resistor, may be incorporated in the nebulizer apparatus or liquid transport line.




Various other features, objects, and advantages of the invention will be made apparent from the following detailed description and the drawings.











BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWING




The foregoing objects and advantages, as well as the invention itself, will be more fully understood from the attached drawing and following detailed description.




In the drawings:





FIG. 1

is a general cross sectional view of the nebulizer apparatus of the present invention, the operating environment for the nebulizer apparatus being shown in a generalized schematic form;





FIG. 2

is a cross-sectional side elevational view of the nebulizer apparatus shown generally in

FIG. 1

;





FIG. 3

shows an cross-sectional side elevation of an alternative embodiment of the nebulizer apparatus;





FIGS. 4 and 5

show alternative embodiments for the control apparatus and liquid supply for the nebulizer apparatus shown in

FIG. 1

;




FIGS.


6


(


a


) through


6


(


d


) show schematic views of alternative embodiments of the nebulizer apparatus liquid reservoir;





FIG. 7

shows use of an optical liquid sensor;





FIG. 8



a


is an exploded, partial view showing a further embodiment of the nebulizer apparatus according to the present invention; and





FIGS. 8



b


and


8




c


are schematic views showing the operation of the nebulizer apparatus of

FIG. 8



a.













DETAILED DESCRIPTION OF THE INVENTION




Nebulizer apparatus


1


of the present invention is typically used in conjunction with breathing circuit


2


, ventilator


4


and control unit


6


, as shown in FIG.


1


. The nebulizer atomizes liquid solutions or suspensions for delivery to a subject, as for example as a drug treatment for a patient. Breathing circuit


2


includes inhalation limb


8


, which is coupled to ventilator


4


at inhalation limb connector


10


. Exhalation limb


12


is connected to ventilator


4


at exhalation limb connector


14


. Inhalation limb


8


and exhalation limb


12


are connected to two arms of Y-connector


16


. A third arm of Y-connector


16


is connected to one end of patient limb


18


. The other end of patient limb


18


is directed to a mouthpiece, facemask, or endotracheal tube for the subject.




Ventilator


4


provides all or a portion of the respiratory gases for the subject by providing inhalation gases in inhalation limb


8


. The inhalation gases pass through Y-connector


16


and into patient limb


18


for supply to the subject. On exhalation, the respiratory gases pass through patient limb


18


, Y-connector


16


, and exhalation limb


12


back to ventilator


4


.




As shown in

FIG. 1

, nebulizer apparatus


1


is preferably positioned in patient breathing circuit


2


as near the patient as possible to minimize the aerosol transport path, and to minimize the deposition of the aerosol on the breathing circuit walls. To this end, nebulizer apparatus


1


may be inserted in the breathing circuit between Y-connector


16


and patient limb


18


. Y-connector


16


has socket


20


for receiving tubular projection


22


of adapter


24


for nebulizer apparatus


1


. Tubular socket


26


of adapter


24


receives patient limb


18


. The nebulizer apparatus is placed in opening


28


in adapter


24


and held in place with O-ring seal


30


. When nebulizer apparatus


1


is not needed, or when the nebulizer apparatus is removed for cleaning or maintenance, a cap (not shown) may be fitted into or over the opening


28


to allow breathing circuit


2


to function in a normal manner. Alternatively, the entire adapter


24


containing nebulizer apparatus


1


may be removed from the breathing circuit and patient limb


18


reconnected to Y-connector


16


. Control unit


6


may be located at a distance from nebulizer apparatus


1


and may be incorporated in ventilator


4


, if desired.




Nebulizer apparatus


1


is connected to a source of material to be nebulized. In the embodiment shown in

FIG. 1

, conduit


32


and transport line


32




a


supply material from reservoir


34


to apparatus


1


. Reservoir


34


can be placed at a desired location and can be proximate to, or remote from, nebulizer apparatus


1


. Control valve


40


is provided in supply conduit


32


and transport line


32




a.


Electrical control signals are supplied to control valve


40


via cable


42


from control unit


6


. As noted above, the material can comprise an aqueous solution, or a particulate or colloidal suspension, of a pharmaceutical agent. For purposes of explanation, the material undergoing nebulization is hereinafter generally described as a liquid. Reservoir


34


is pressurized by pump


36


in control unit


6


. In the embodiment shown in

FIG. 1

, pump


36


supplies a pressurizing gas to reservoir


34


through pressure line


38


.




Nebulizer apparatus


1


is shown, in detail, in FIG.


2


. The apparatus comprises housing


50


which mounts apparatus


1


in opening


28


of adapter


24


via O-ring seal


30


. Housing


50


may be formed of plastic. Housing


50


has a cavity


52


. Panel


54


spans cavity


52


. Panel


54


is hinged at one edge by hinge


56


, and contains a clip


58


at an opposite edge engaging cut-out


60


in housing


50


. Panel


54


may be opened by disengaging clip


58


from cut-out


60


, to allow the portions of apparatus


1


carrying out the nebulizing of the liquid and positioned in cavity


52


to be removed at the end of therapy for replacement, or for cleaning when a different drug is to administered to the subject. Panel


54


has an opening


61


in the central portion thereof.




Mesh plate frame


62


is received in cavity


52


. Frame


62


may be formed of, for example, aluminum or brass. Mesh plate frame


62


has a centrally located aperture defined by surface


64


. Mesh plate


66


spans the aperture with peripheral edge


68


embedded into frame


62


at surface


64


. Frame


62


has an ultrasonic vibration generator in the form of piezoelectric element


70


embedded therein to vibrate frame


62


, as well as mesh plate


66


. Mesh plate frame


62


, when placed in cavity


52


, contacts terminal


72


in housing


50


and terminal


74


in panel


54


. Terminal


72


and


74


are thus connected to piezoelectric element


70


. They are also connected, via cable


42


to an electrical power source


75


in control unit


6


having a desired frequency in the ultrasonic range. Typically frequencies range from 50 to 200 kHz. The connections may be carried out by conductors


71


and


73


in frame


62


.




Housing


50


, frame


62


, and mesh plate


66


and cavity


52


may be generally circular in form. When fitted into housing cavity, the rear surface


76


of mesh plate


66


, mesh plate frame surface


64


and housing surface


78


define an internal volume


80


. Transport line


32




a


extends through housing


50


to open into volume


80


at surface


78


.




Mesh plate


66


is a relatively thin plate having a plurality of holes


82


. Mesh plate


12


may be about 0.02 mm thick. The diameter of the holes at front surface


84


is preferably approximately 2-15 μm in diameter. Such holes may be formed in the plate by an electroforming process, which process produces holes of increasing diameter toward rear surface


76


shown in

FIGS. 2 and 3

of the drawing. However, the straight holes, shown in

FIGS. 7 and 8

will work equally well, the primary criterion being that the exit diameter in front surface


84


be such as to form droplets of the desired size.




The thinness of mesh plate


66


limits its ability to resist excessive forces generated by liquid pressures in volume


80


. Liquid pressure in volume


80


may also cause leaks through holes


82


. To insure the proper supply of liquid from transport line


32




a,


sensing elements, such as a pair of spaced electrodes


86


, are fitted in housing


50


to sense the presence or absence of the liquid in volume


80


. As shown in

FIG. 2

, electrodes


86


may be mounted in surface


78


of housing


50


adjacent the outlet of transport line


32




a.






Front surface


84


of mesh plate


66


is exposed to the pressure of the breathing gases in breathing circuit


2


. These pressures will vary during inhalation and exhalation conditions in breathing circuit


2


. For example, with artificial ventilation, breathing circuit pressures may increase up to 100 mbar during inspiration and thereafter decrease during expiration. Housing


50


is provided with pressure balancing channel


88


shown in

FIG. 2

that connects volume


80


with breathing circuit


2


for equalizing the prevailing pressure at both sides of mesh plate


66


to avoid pressure stressing mesh plate


66


and causing leaks to occur through the mesh plate.




In operation, valve


40


is opened responsive to a signal from cable


42


and liquid flows through conduit


32


and transport line


32




a


due to the pressurizing gas in reservoir


34


. The liquid flows out the end of transport line


32




a


into contact with the upper surface of mesh plate


66


. The cohesive forces in the liquid form the liquid into a column of liquid extending between the end of transport line


32




a


and mesh plate


66


, generally as shown in FIG.


2


. Piezoelectric element


70


is energized from a high frequency source


75


in control


6


through cable


42


and terminals


72


and


74


in housing


50


to vibrate mesh plate


66


. The positioning and energization of piezoelectric element


70


may be such as to cause mesh plate


84


to move toward and away from the end of transport line


32




a


and the liquid being discharged therefrom. The vibrations cause the liquid in volume


80


to pass through holes


82


in mesh plate


66


.




At the front surface


84


of the vibrating mesh plate


66


, the atomized liquid will grow into drops at each hole


82


due to the liquid surface tension. The drops will increase in size until the expelling forces arising from the movement of mesh plate


66


and the mass of each drop, exceeds the holding force determined by the size of the holes


82


in mesh plate


66


, and the surface tension of the liquid. The drops expelled from plate


66


pass through opening


61


in panel


54


into the patient limb


42


, and to the subject during inhalation.




To control the transport of liquid from reservoir


34


into the of nebulizing apparatus


1


, electrodes


86


, positioned in surface


78


of housing


50


, detect the presence of liquid between the end of transport line


32




a


and the rear surface


76


of mesh plate


66


by alteration of the impedance between the electrodes. That is, with the continued supply of liquid, the column will start to bulge and the impedance measured between the electrodes will be significantly altered. A signal from electrodes


86


is inputted to impedance sensor


87


and control unit


6


via conductors


85


and


89


and cable


42


and used to control valve


40


in liquid supply conduit


32


to close the valve. When the impedance changes, due to the liquid receding away from electrodes


86


, the control valve


40


opens to again allow flow of liquid from the end of transport line


32




a.


The supply of liquid in the nebulizer of the present invention may thus be characterized as being of the “on demand” type. The delivery of nebulized liquid can be controlled by continuously vibrating mesh plate


66


and regulating the liquid transport control or by regulating the activation of mesh plate vibration and intermittently supplying liquid when the amount of liquid in volume


80


is reduced.




Alternatively, the presence of liquid in volume


80


could be measured by an optical sensor, as shown in

FIG. 7

, that senses changes in light transmission or reflection caused by the liquid in volume


80


. When there is no liquid on mesh plate


66


, light from light source


86




a


is reflected off the mesh plate to detector


86




b.


The presence of liquid alters the light path.




The proper supply of liquid through the on-demand delivery from transport line


32




a,


as controlled by electrodes


86


, provides the following advantages. If too much liquid were to be delivered to volume


80


, liquid would pressurize mesh plate


66


and might leak through mesh plate


66


. And, if too much liquid were to be delivered to volume


80


, pressure balancing channel


88


could be occluded. This could also result in undesired pressures being applied to mesh plate


66


.




If too little liquid is delivered to volume


80


, the liquid from transport line


32




a


may not cover all the holes


82


in mesh plate


66


. However, the pressure balancing provided by channel


88


avoids breathing gas flow through the holes in mesh plate


66


in opposition to the liquid being nebulized which might otherwise degrade the operation of nebulizer apparatus


1


.




Position insensitivity for nebulizer apparatus


1


is obtained by locating the end of transport line


32




a


sufficiently close to rear surface


76


of mesh plate


66


that the surface tension in the column of liquid will maintain the column between the end of transport line


32




a


and rear surface


76


of mesh plate


66


. Since liquid is incompressible, should nebulizer apparatus be inverted from the position shown in

FIG. 2

, the liquid in transport line


32




a


will support the liquid column in volume


80


so that operation of the nebulizer apparatus is maintained.




In some applications, it may be desirable to heat the liquid to be nebulized, the mesh plate, the mesh plate frame, the housing and/or liquid supply conduit/transport line. For example, the liquid may be heated to body temperature to improve administration of the agent or to prevent discomfort to the patient. Mesh plate


66


or mesh plate frame


62


or housing


50


could be heated for these purposes and to prevent condensation of the liquid or spray on these or other elements. For these purposes, an appropriate heater, for example, a resistor


91


, may be employed and controlled through cable


42


.




An alternative embodiment of the nebulizer apparatus is shown in FIG.


3


. In the nebulizer apparatus


1




a


of

FIG. 3

, mesh plate


66




a


is formed using a conductive material such as nickel, which enables it to function as an electrode for liquid level measurement in volume


80




a.


Mesh plate


66




a


rests on annular disc


90


having an opening


92


. Annular disc


90


is made of a conductive material that is inert with respect to the liquid to be nebulized and to the breathing gases. Disc


90


forms the base of housing


50




a.


Housing


50




a


is completed with a non-conductive tubular sidewall


94


and a non-conductive top plate


96


. Top plate


96


may be removable to allow cleaning of the interior components of nebulizer apparatus


1




a.


Mesh plate


66




a


is electrically connected to disc


90


and to conductor


97


.




Sidewall


94


has an aperture that accommodates transport line


32




b.


Unlike the embodiment of

FIG. 1

, the cavity or volume


80




a


in

FIG. 3

is filled with liquid from the side of apparatus


1




a,


rather than from the top.




Conductive plate


98


is mounted in sidewall


94


as by the upright flange around its perimeter which is directed away from the mesh plate


66




a.


Plate


98


has several purposes. First, plate


98


mounts ultrasonic vibration generator


100


, preferably a piezoelectric element. Ultrasonic vibration generator


100


is affixed to plate


98


. Second, plate


98


functions as a liquid level detector in space


80




a


by serving as an electrode for measurement in conjunction with conductive mesh plate


66




a.






In operation, liquid flows into volume


80




a


from transport line


32




b.


A control valve, such as valve


40


, shown in

FIG. 1

is used to control the liquid transported into volume


80




a.


When the liquid makes contact with mesh plate


66




a


and with plate


98


serving as sensing electrodes, the impedance measurement between plate


98


and mesh plate


66




a


changes. The control valve is closed, to be thereafter opened when the liquid level recedes to the point where contact with plate


98


is lost.




Piezoelectric element


100


vibrates the liquid by inducing pressure waves from plate


98


. The piezoelectric element is energized by electrical power source


75


in control unit


6


through cable


42


. The vibrating liquid is atomized as it passes through holes


82


and discharged into the breathing gases.




Thus, while in nebulizer apparatus of

FIG. 1

, mesh plate


66


is vibrated by the piezoelectric element, in nebulizer apparatus


1




a


shown in

FIG. 3

, the liquid in volume


80




a


is vibrated by the piezoelectric element.




The embodiment of the invention shown in

FIG. 4

differs from that shown in

FIG. 1

in that pump


36




a


in control unit


6


supplies liquid directly to transport line


32




c


from a liquid source (not shown). The control provided by valve


40


, shown in

FIG. 1

, can be achieved by turning pump


36


on and off. Cable


42


obtains electrical signals from the liquid level sensors in nebulizer apparatus


1


for use by control unit


6


in controlling pump


36




a.


The pump is turned off when the impedance detected by the liquid level sensors indicates that the appropriate amount of liquid has been provided to nebulizer apparatus


1


. Use of the pump


36




a


shown in

FIG. 4

has advantages over the pressurizing gas shown in

FIG. 1

in that some liquid medications cannot be exposed to the pressurizing gas without deleterious effects.




In the embodiment of

FIG. 5

, the force used to transport the liquid to the nebulizer apparatus is obtained hydrostatically. The liquid source, such as liquid reservoir


34




a,


can be arranged at an elevated position with respect to nebulizer apparatus


1


,


1




a


to generate a pressure head to supply liquid to the apparatus. Liquid supply


34




a


may comprise a flexible pouch or bag mounted on stand


102


to create a hydrostatic pressure for causing liquid to flow through transport line


32




d


when control valve


40


is opened. The arrangement shown in

FIG. 5

is especially suitable for nebulizing the large amounts of liquid often required in continuous long term treatment of a subject. The embodiment of

FIG. 5

has the advantage in that it will use less energy, and be less noisy, than embodiments using gas or liquid pumps.





FIGS. 6



a-d


show, in schematic form, various other techniques by which amounts of liquid to be nebulized may be provided to transport line


32


. In the alternatives schematically depicted in

FIG. 6

, the reservoir for the liquid to be nebulized has a flexible wall


110


which keeps the liquid in reservoir chamber


112


separate from a pressurizing agent in chamber


114


which is used to supply the liquid through transport line


32


. This avoids contamination of the liquid to be nebulized by the pressurizing agent, and/or insures sterility of the liquid to be nebulized.




In the embodiment of the invention shown in FIG.


6


(


a


), syringe


116


is used to pressurize pressure chamber


114


of reservoir


34




b


through line


117


and automatically opening and closing valve


118


. Syringe supplies a pressurizing agent, such as a gas, to chamber


114


to pressurize the liquid to be nebulized contained in reservoir chamber


112


of reservoir


34




b.


Syringe


116


may be removed once the pressurization is completed. Liquid reservoir


112


may be loaded with the required dosage of a pharmaceutical agent through conduit


119


, sealed with valve


120


or through transport line


32


, and pressure chamber


114


pressurized prior to connection of reservoir


34




b


to apparatus


1


. Valve


120


, which opens when reservoir


34




a


is connected to nebulizing apparatus


1


, is provided in conduit


32


.

FIG. 6



b


shows a reservoir


34




c


which has been filled through transport line


32


. The reservoir is shown in a condition in which most of the liquid to be nebulized has been discharged from reservoir chamber


112


.




In the embodiment of the invention shown in FIG.


6


(


c


), pressure chamber


114


is pressurized by gravitationally supplying a liquid to chamber


114


. The liquid is stored in a container


122


, elevated above reservoir


34




d


to obtain an adequate head pressure. Container


122


may be kept at the appropriate level using an adjustable stand


102


.




In the embodiment of the invention shown in FIG.


6


(


d


) the pressure chamber


114


is pressurized by pump


15




a.


The pump may be located, for example, in control unit


6


(shown in

FIGS. 1 and 2

) and connected to reservoir


34




c


by supply line


124


. Pump


15




a


may be either a liquid or gas pump. In operation, pump


15




a


is regulated by control unit


6


.




It will be appreciated that the reservoir for the liquid to be nebulized can comprise a pre-filled reservoir containing a desired dosage of a pharmaceutical or other agent to be dispensed by nebulizer apparatus


1


in reservoir chamber


112


.





FIGS. 8



a,




8




b,


and


8




c


show a further embodiment of the nebulizer apparatus of the present invention and in which elements similar or analogous to the embodiments of

FIGS. 1 and 3

are indicated with similar reference numerals. Nebulizer apparatus


150


shown in the cross sectional, exploded view of

FIG. 8



a


has annular housing


50




b


which mounts the apparatus in adapter


24


. Housing


50




b


is formed of plastic or similar material. Lip


152


is formed on the lower edge of housing


50




b


and contains O-ring


154


.




Disc-like plate


156


, shown with enlarged thickness in

FIG. 8



a


and comprised of a conductive material such as brass, is sealed to lip


152


by O-ring


154


. Plate


156


contains a central opening


158


. The surface of plate


156


which is the lower surface when the nebulizer apparatus is oriented as shown in

FIG. 8



a


mounts mesh plate


66




b


containing holes


82


. Mesh plate


66




b


may be mounted to plate


156


by gluing, brazing, welding, or other suitable technique.




Piezoelectric element


70




b


is mounted on the upper surface of plate


156


. Specifically, piezoelectric element


70




b


is spaced from plate


156


by a small gap


160


and secured to plate


156


about its periphery by a conductive glue, brazing, welding, or other suitable technique, shown as


162


in FIG.


8


. Piezoelectric element


70




b


has a central opening corresponding to that of plate


156


.




Plug member


164


formed of a non-conductive material, such as plastic, is placed in cavity


52




b


of housing


50




b.


Plug member


164


has depending lip


166


containing O-ring


168


. Plug member


164


is placed on top of plate


156


so that the plate is between O-rings


154


and


168


.




A central liquid transport line


32




c


extends through plug member


164


to approximately the upper surface of plate


156


. A small domed cavity


170


may be formed in the lower surface of plug member


164


to surround transport line


32




c.


Transport line


32




c


may be formed of a conductive material to allow its use in impedance measurement of the presence of liquid in nebulizer apparatus


150


.




An electric power terminal


74




b


extends through plug member


164


. The lower end of terminal


74




b,


which terminal may be in the form of a spring loaded pin, contacts piezoelectric element


70




b.


The upper end of terminal


74




b


is connected to cable


42


. A second electrical power terminal


72




b


also extends through plug member


164


. The lower end of terminal


72




b


contacts conductive plate


156


. The upper end of terminal


72




b


is connected to cable


42


. Terminal


72




b


may be electrically grounded for purposes of applying a voltage to piezoelectric element


70




b


in conjunction with terminal


74




b,


as well as for impedance measurement in conjunction with conductive liquid transport line


32




c.






In operation, alternating voltage is supplied from power source


75


through cable


42


and terminals


72




b


and


74




b


to piezoelectric element


70




b


which vibrates the element. The vibrations cause the element to contract from the normal condition, shown in

FIG. 8



b


to a radially decreased condition shown in

FIG. 8



c


and return to the normal condition. Due to the joinder of piezoelectric element


70




b


to plate


156


about the periphery of the element, the radial size reduction of piezoelectric element


70




b


causes plate


156


to bow, as shown in

FIG. 8



c,


and then return to the flat condition, shown in

FIG. 8



b,


when piezoelectric element


70




b


returns to the normal state. The action of plate


156


shown in

FIGS. 8



b


and


8




c


discharges nebulized liquid from holes


82


in mesh plate


66




b.






It is recognized that other equivalents, alternatives, and modifications aside from those expressly stated, are possible and within the scope of the appended claims.



Claims
  • 1. A nebulizer apparatus for atomizing a liquid into an aerosol of fine droplets, said nebulizer apparatus comprising:a housing having a cavity with an opening; a thin mesh plate positioned across the opening of the cavity, said mesh plate having an exposed front surface and a rear surface facing into said cavity, said mesh plate having holes extending through said mesh plate from the front surface to the rear surface; a liquid transport line opening into said cavity for supplying a volume of liquid to the rear surface of said mesh plate; a vibration generator energizable to establish vibrations in one of the mesh plate or liquid to cause the liquid to pass through the holes in the mesh plate and to be discharged from the front surface of the plate as an aerosol of fine droplets; a sensor located in said cavity, said sensor measuring the extent of a physical dimension of the volume of liquid supplied to the rear surface of said mesh plate; and means for controlling a supply of liquid from said liquid transport line to said cavity, responsive to said sensor, to maintain a desired volume of liquid on the rear surface of said mesh plate.
  • 2. The apparatus of claim 1 wherein the holes have diameters and wherein the diameters of the holes are larger at the rear surface of the mesh plate and decrease along extensions of the holes through the mesh plate to smaller diameters at the front surface of the plate.
  • 3. The apparatus of claim 1 wherein said holes are straight holes.
  • 4. The apparatus of claim 1 wherein the vibration generator comprises a piezoelectric element.
  • 5. The apparatus of claim 4 wherein said vibrator means is coupled to said mesh plate to vibrate the plate.
  • 6. The apparatus of claim 5 wherein said holes are in a central portion of said mesh plate and wherein said vibration generator is peripherally joined to said mesh plate to surround said central portion, energization of said vibration generator causing a bowing action in said mesh plate.
  • 7. The apparatus of claim 4 wherein said vibration generator contacts the liquid to induce pressure waves in the liquid.
  • 8. The apparatus of claim 1 wherein the liquid transport line is further defined as supplying liquid to form a column of liquid on the rear surface of said mesh plate.
  • 9. The apparatus of claim 1 wherein said sensor comprises spaced elements establishing an impedance therebetween and wherein said sensor measures the extent of a physical dimension of the volume of liquid supplied to the rear surface of said mesh plate by changes in impedance between said spaced elements produced by the liquid.
  • 10. The apparatus of claim 9 wherein said spaced elements comprise a pair of spaced electrodes in said cavity.
  • 11. The apparatus of claim 10 wherein said liquid transport line has an opening in said cavity on a surface opposite said rear surface of said mesh plate and wherein said electrodes are adjacent the opening of said liquid transport line.
  • 12. The apparatus of claim 9 wherein said mesh plate forms one of said spaced elements.
  • 13. The apparatus of claim 12 wherein a portion of said liquid transport line adjacent the opening of said liquid transport line forms the other of said spaced elements.
  • 14. The apparatus of claim 9 wherein a portion of said liquid transport line adjacent the opening of said liquid transport line forms one of said spaced elements.
  • 15. The apparatus of claim 1 wherein said sensor comprises an optical sensor.
  • 16. The apparatus of claim 1 including means for equalizing pressure at the rear surface of the mesh plate and pressure at the front surface of the mesh plate.
  • 17. The apparatus of claim 16 further including a pressure balance channel in said housing between said front and rear surfaces of said mesh plate, whereby the pressures at the front surface and the rear surface are equalized.
  • 18. The apparatus of claim 1 wherein the means for controlling a supply of liquid comprises a valve in said liquid transport line.
  • 19. The apparatus of claim 18 further including means for pressurizing the liquid in said liquid transport line.
  • 20. The apparatus of claim 19 wherein the liquid is contained in a reservoir connected to the liquid transport line and wherein said means for pressurizing is a gas pump for pressurizing the reservoir.
  • 21. The apparatus of claim 19 wherein the liquid is contained in a reservoir elevated with respect to said nebulizer apparatus for pressurizing the liquid with a hydrostatic head.
  • 22. The apparatus of claim 1 wherein the means for controlling a supply of liquid comprises a pump coupled to said liquid transport line.
  • 23. The apparatus of claim 1 further including a reservoir for storage of the liquid prior to atomization, wherein the reservoir is connected to said liquid transport line for delivery of the liquid to the rear surface of the mesh plate.
  • 24. The apparatus of claim 23 wherein said reservoir comprises a two-part container having a deformable liquid reservoir within a part of the container which can be pressurized for pressurizing said liquid reservoir.
  • 25. The apparatus of claim 24 further including a gas pump for pressurizing the part of the container.
  • 26. The apparatus of claim 24 further including an elevated liquid reservoir connected to said part of said container to provide a hydrostatic force for pressurizing said liquid reservoir.
  • 27. The apparatus of claim 1 further defined as a nebulizer apparatus for delivering an aerosol to the breathing gas of a subject passing in a breathing circuit, said apparatus including an adapter for coupling said housing to the breathing circuit.
  • 28. The apparatus of claim 27 including a reservoir connected to said liquid transport line for storing the liquid to be atomized.
  • 29. The apparatus of claim 1 further including a heater.
US Referenced Citations (13)
Number Name Date Kind
3812854 Michaels et al. May 1974 A
5152456 Ross et al. Oct 1992 A
5261601 Ross et al. Nov 1993 A
5443059 Koch et al. Aug 1995 A
5487378 Robertson et al. Jan 1996 A
5515841 Robertson et al. May 1996 A
5586550 Ivri et al. Dec 1996 A
5758637 Ivri et al. Jun 1998 A
6076519 Johnson Jun 2000 A
6085740 Ivri et al. Jul 2000 A
6158431 Poole Dec 2000 A
6192882 Gonda Feb 2001 B1
6196219 Hess et al. Mar 2001 B1
Foreign Referenced Citations (5)
Number Date Country
37 10 141 Oct 1988 DE
798007 Oct 1997 EP
2099710 Dec 1982 GB
2272389 May 1994 GB
9211050 Jul 1992 WO