AU2004202959A1 - Nebulizer Apparatus and Method - Google Patents

Description

S&F Ref: 430554D2

AUSTRALIA

PATENTS ACT 1990 COMPLETE SPECIFICATION FOR A STANDARD PATENT Name and Address of Applicant: Actual Inventor(s): Address for Service: Invention Title: Trudell Medical Limited, of 926 Leathome Street, London, Ontario, N5Z 3M5, Canada Jerry R. Grychowski George Baran Martin P. Foley Spruson Ferguson St Martins Tower Level 31 Market Street Sydney NSW 2000 (CCN 3710000177) Nebulizer Apparatus and Method The following statement is a full description of this invention, including the best method of performing it known to me/us:- 5845c 1 NEBULIZER APPARATUS AND METHOD 2 BACKGROUND OF THE INVENTION 3 The present invention relates to a method and 4 apparatus for delivering an aerosol, nebulized liquid or solid medicine or a vapor to a patient's respiratory 6 tract, and more particularly, the present invention 7 relates to an improved nebulizer that provides an 8 aerosol more efficiently and with improved particle 9 size uniformity.

Medical nebulizers for generating a fine spray or 11 nebula of a liquid medicine that can be inhaled by a 12 patient are well known devices commonly used for the 13 treatment of certain conditions and diseases.

14 Nebulizers have applications in treatments for is conscious, spontaneously-breathing patients and for 16 controlled ventilated patients.

17 In some nebulizers, a gas and a liquid are mixed 18 together and directed against a baffle. As a result, 19 the liquid is aerosolized, that is, the liquid is caused to form into small particles that are suspended 21 in the air. This aerosol of the liquid can then be 22 inhaled into a patient's respiratory tract. One way to 23 mix the gas and liquid together in a nebulizer is to 24 pass a quickly moving gas over a liquid orifice tip of a tube. The negative pressure created by the flow of 26 pressurized gas is a factor that contributes to drawing 1 1 the liquid out of the liquid orifice tip into the 2 stream of gas and nebulize it.

3 Some of the considerations in the design and 4 operation of nebulizers include regulation of dosages and maintenance of consistent aerosol particle size.

6 In conventional nebulizer design, pressurized gas may 7 entrain a liquid against a baffle on a continuous basis 8 until the liquid in a reservoir is depleted.

9 Continuous nebulization may result in a waste of aerosol during a patient's exhalation or during a delay 11 between a patient's inhalation and exhalation. This 12 effect may also complicate regulation of dosages 13 because the amount of wasted aerosol may be difficult 14 to quantify. Also, continuous nebulization may affect is particle size and/or density. In addition, there may 16 be excess medication lost to condensation on the 17 nebulizer or mouthpiece during periods of non- 18 inhalation. On the other hand, interrupted 19 nebulization may also affect particle size and density as.the nebulization is turned on and off.

21 There are several other considerations that relate '22 to the effectiveness of nebulizer therapies. For 23 example, it has been suggested that nebulization 24 therapy is more'effective when the generation of aerosol particles is relatively uniform, for example, 26 producing particles of a particular size, particles 27 within a range of sizes, and/or particles a substantial 28 percentage of which are within a range of sizes. One 29 particle size range that has been considered to be appropriate for inhalation therapy includes a particle 31 size range of approximately 0.5 to 2 microns. Other 32 particle size ranges may be suitable or preferable for 33 particular applications. Generally, large and small 34 size droplets should be minimized. It has also been considered desirable for some inhalation therapies that 36 a substantial percentage, e.g. over 75%, of the aerosol 37 particles be less than approximately 5 microns -2 depending on the desired are of particle deposition in the respiratory tract. In addition, it may be advantageous for a nebulizer to be able to generate a large amount of aerosol quickly and uniformly so that a proper dosage can be administered.

Accordingly, with these considerations taken into account, there is a need for an improved nebulizer.

It is the object of the present invention to substantially overcome or at least ameliorate one or more of the disadvantages of the prior art.

SUMMARY OF THE INVENTION There is disclosed herein a nebulizer comprising: 0to a housing having a chamber for holding an aerosol; an air outlet communicating with said chamber for permitting said aerosol to be withdrawn from said chamber; a liquid outlet located in said chamber; a pressurized gas outlet located in said chamber adjacent to said liquid outlet; a movable diverter located in said chamber and relative to said pressurized gas outlet and said liquid outlet so as to divert pressurized gas from said gas outlet across said liquid outlet to produce said aerosol in cycles in coordination with a patient's breathing; and an indicator associated with said diverter and configured to confirm operation of said nebulizer.

BRIEF DESCRIPTION OF THE DRAWINGS A preferred form of the present invention will now be described by way of example with reference to the accompanying drawings, wherein: -3- [R:\LIBLL] I 1774.doc:caa:TCW:hxa Figure 1 is a partial cross-section side view of a first embodiment of a nebulizer according to the present invention.

Figure 1A is a cross-sectional view of the nebulizer of Figure 1 shown in an inspiration cycle.

Figure 2 is a cross-sectional view of the nozzle assembly of the nebulizer of Figure 1.

Figure 3 is a cross-section top view of the nebulizer of Figure 1 taken along line 3-3' (without the baffle for clarity).

Figure 4 is perspective view of the top portion of the nebulizer of Figure 1.

to Figure 4A is perspective view of the top of the nebulizer shown in the inspiration cycle of Figure 1A.

Figure 5 is a cross sectional view of a second embodiment of the nebulizer of the present invention.

Figure 6 is a cross sectional view of the bottom of the chimney of the embodiment of Figure Figure 7 is a cross sectional view similar to Figure 6 showing an alternative embodiment the bottom of the chimney of the nebulizer shown in Figure Figure 8 is a cross-sectional view of a portion of the nebulizer of Figure showing the diverter ring.

Figure 9 is a cross sectional view similar to Figure 8 showing an alternative embodiment of the diverter ring arrangement for the embodiment of the nebulizer of Figure -4- [R:\LIBLL] 11774.doc:caa:TCW:hxa 1 Figure 10 is a cross sectional view similar to 2 Figure 8 showing anozher alternative embodiment of the 3 diverter rina arrangement.

4 Figure 11 is a cross sectional view of a third embodiment of the nebulizer of the present invention.

6 Figure 12 is a -op view of the embodiment nozzle 7 assembly of Figure 11.

8 Figure 13 is a cross sectional view of the 9 embodiment of Figure 11 taken along line 13-13'.

Figure 14 is a cross sectional view of a fourth 11 embodiment of the nebulizer of the present invention.

12 Figure 15 is a cross sectional view of a fifth 13 embodiment of the nebulizer of the present invention.

14 Figure 16 is a cross sectional view of a sixth embodiment of the nebulizer of the present invention.

16 Figures 17A and 17B shows cross sectional views of 17 a seventh embodiment of the present invention.

18 DETAILED DESCRIPTION OF THE 1-9 PRESENTLY PREFERRED EMBODIMENTS I. First Embodiment 21 A first preferred embodiment of a nebulizer 10 is 22 illustrated in Figure 1. The nebulizer 10 is a small 23 volume nebulizer and includes a housing or container 12 24 defining an internal chamber 14. The housing 12 is formed of a cylindrically-shaped side wall portion 18, 26 a top portion 20, and a bottom portion 22. The 27 component parts of the housing 12 may be formed of 28 separate, multiple pieces of material that are 29 connected together by welding, adhesives, etc., or more preferably, some of -he component parts may be formed 31 together of a single piece of material formed by an 32 injection molding process. For example, the bottom, 33 and side portions 22 and 18 may be formed of separate 34 pieces that are connected together, or preferably, these parts may be formed of one piece of molded 36 plastic. Any of a number of plastics may be suitable, 37 including polycarbonate, or polycarbonate blends. A I cover 21 is removably mounted on the upper portion of 2 the housing 12, such as by means of a snap-on cover 3 arrangement, twist-lock threads, screws or other types 4 of fasteners. The housing- 12 is approximately 6 cm (2.36 in) in height and has a diameter of approximately 6 4 cm (1.57 in).

7 A lower portion 23 of the chamuber 14 serves as a 8 reservoir for holding a fluid 25 for nebulizing, such 9 as a solution containing a medication. Located in the lower portion 23 of the housing 12 is a nozzle assembly 11 24. Referring to Figures 1-3, the nozzle assembly 24 12 extends downward from the chamber 14 of the housing 12 13 to a f itting 28 located external of the chamber 14 on a 14 bottom side 22 of the housing 12. The fitting 28 is sized to connect to a supply 27 of pressurized gas 16 provided through conventional tubing 29. The 17 pressurized gas may be supplied by any suitable source, is such as a conventional gas supply used in hospitals, a 19 pump, compressor, cartridge, canister, etc.

The nozzle assembly 24 is comprised of an outer 21 tubular member 30 and an inner tubular member 32. The 22 inner tubular member 32 has a passageway 34 that 23 extends from an opening 36 in the bottom end of the 24 fitting 28 to a gas outlet orifice 38 located at a top end 39 of the nozzle assembly 24. The inner tubular 26 member 32 is located .in an inner passageway 40 of the 27 outer tubular member 30. The inner tubular member 32 28 is sized to slide into the inner passageway 40 of the 29 outer tubular member 30 so that it is aligned therein.

A passageway 42 is formed by grooves or slots on the 31 outer surface of the inner tubular member 32 and/or the 32 inner surface of the outer tubular member 30. The 33 passageway 42 extends from an opening 44 located at the 34 reservoir 223 of the lower portion of the chamber 14 to a liquid outlet orifice 46 located at the top end 39 of 36 the nozzle assembly 24. The passageway 42 serves to 37 convey liquid medicine from the reservoir 23 at the 6- I bottom of the chamber 14 to the liquid outlet orifice 2 46 at the top of the nozzle assembly 24. (In an 3 alternative embodiment, the passageway 42 may be formed 4 by spaces or regions between fins located on the outer surface of the inner tubular member 32 and/or the inner 6 surface of the outer tubular member 7 As shown in Figure 3, the liquid outlet orifice 46 8 has an annular shape defined by the top ends 'of the .9 outer tubular member 30 and the inner tubular member 32 of the nozzle assembly 24. The gas outlet orifice 38 11 has a ,circular shape -and is located concentrically of 12 the annular liquid orifice. In one embodiment, the gas 13 outlet orifice 38 is approximately 0.022 inches in it. diameter and the liquid outlet orifice 46 has an outer is diameter of approximately 0.11.0 to 0.125 inches and an 1.6 inner diameter of approximately 0.084 inches. These 117 dimensions are provided by way of example and the 1s nebulizer may be made in other sizes with different 19 dimensions as desired.

The top end 39 of the nozzle assembly 24 ir, formed 21 by the top ends of the outer and inner tubular members 22 30 and 32. In a present embodiment, the top end 39 is 23 a generally flat surface having a diameter of 24 approximately 0.18 inches. In alternative embodiments, the top end 39 may have an octher-than-flat shape, for 26 example, the inner tubular member 32 may be spaced 27 above the outer tubular member 30 so that the liquid orifice 46 is located below the gas orifice 38.

29 The nozzle assembly 24, or a portion thereof, may be formed as part of the housing 12 as a single piece 31 of material in an injection molding process. For 32 example, the inner tubular member 32 may be formed of 33 the same piece of injected molded plastic as the bottom 34 of the housing 12.

Referring again to Figure 1, the nebulizer 10 also 36 includes a chimney assembly 50. The chimney assembly 37 50 is located in an upper portion of the chamber 14 7- 1 above the liquid reservoir 23. The chim-ney assembly 2 includes a tubular body 51 that defines an internal 3 passageway S2 that extends from an inlet opening 56 in 4 the housing cover 21 to atn outlet opening 58 at a s bottom end of the tubular body S1. Thus, the chi mney 6 assembly 50 serves as an inlet channel for ambient air 7 to enter into the chamber 14. The inlet opening 56 8 communicates with ambient air (through ports of an 9 actuator button, as described below) and the outlet opening 58 communicates with the chamber 14.

11 Located on the lower end of the chimney assembly 12 50 is a diverter 60. The diverter 60 may be formed of 13 the same piece of molded plastic material as the 14 chimney 50 or alternatively, the diverter 60 may be formed of a separate piece of material that is attached 16 by suitable means to the rest of the chimney assembly 17 50. (The diverter may also be provided pneumatically, 38 for example by an opposing gas source located directly 19 opposite the nozzle.) The diverter 60 is located directly opposite from the gas outlet orifice 38 and 21 the liquid outlet orifice 46 located at the top end 39 22 of the nozzle assembly 24. The diverter 60 is movable 23 so that the distance between the diverter 60 and the 24 top surface 39 of the nozzle assembly 24 can be varied.

The diverter 60 has of a flat circular shape with a 26 diameter of approximately 0.18 inches so that it 27 extends over both the gas and liquid orifices 38 and 46 28 out to approximately the edge of the top surface 39 of 29 the nozzle assembly 24.

The chimney assembly 50 is connected to the 31. housing 12. Specifically, the chimney assembly So is 32 attached to the top portion 20 of the housing 12 by 33 means of a membrane or diaphragm 64. The membrane 64 34 is a ring-shaped piece of a flexible, resilient material, such as silicone rubber. kn outer rim or 36 bead of the membrane 64 is secured in a groove inl the 37 top portion 20 of the housing 12 an,:/or the cover 21.

An inner rim of the membrane 64 is secured in a slot 2 formed by two parts of the chiney assembly 5o. The 3 membrane 64 has a rolled cross-sectional profile as 4 shown in Figure i. This permits the membrane 64 to act as a rolling diaphragm. The membrane 64 permits 6 limited movement of the chimney assembly 50. The 7 chimney assembly 50 is connected to the membrane 64 so 8 that the membrane 64 biases the chimney assembly So 9 away from the nozzle assembly 24 as shown in Figure 1.

When installed in the manner shown in Figure 1, the 11 bottom of the chimney assembly 50 is approximately 0.15 12 inches away from the top surface of the nozzle assembly 13 24.

14 Located at the top end of the chimney assembly is1 is an actuator'68. The actuator 68 connects to the 16 tubular body 51 of the chimney assembly 50 and extends 17 through the opening 56 at the top of the housing 12 in 18 the cover 21. The actuator 68 includes a closed top 19 side 70 with one or more side opening ports 72.

Referring to Figure 4, located on the sideas of the 21 body of the actuator 68 are indicators 69A and 69B.

22 The indicators 69A and 69B may be formed'of colored 23 markings* or parallel rings on the sides of the actuator 24 68. In a preferred embodiment, the indicator 69A is red and is located next to the top side 21. of the 26 nebulizer body 1 2. The indicator 69B is preferably 27 green and is adjacent to and above the indicator 69A.

~28 Located in the chamber 14 at the bottom end oF the 29 chimney assembly 50 is a bell-shaped baffle 74. The baffle 74 extends from the opening 58 at the bottom o: 31 the chimney passageway 51 outward toward the inside 32 wall of the cylindrical portion 18 of he housing 12.

33 The baffle 74 includes a horizontal portion 75 and a 34 vertical portion 76 that extends downward from the horizontal portion 75 toward the top of the nozzle 36 assembly 24. The baf fle 74 has an open bottom side I providing an air passageway around the bottom side of 2 the cylindrical vertical wall 76.

3 As mentioned above, the diverter 60 is movable 4- relative to the nozzle assembly 24. The present s embodiment provides a means to limit the travel of the 6 diverter relative to the nozzle assembly 24. This may 7 be accomplished in any of several suitable ways. In a 8 present embodiment, the movement of the diverter 9 toward the nozzle assembly 24 is limited by one or more stop pins 80. The stop pins 80 extend up from the 11 bottom portion 22 of the housing. In a present 12 embodiment, there are three stop pins. The top ends of 13 the stop pins 80 are spaced away from the bottom end of 14 the vertical wall 76 of the baffle 74. Because the J is chimney assembly 50 is movable vertically due to its 16 connection to the housing 12 by means of the flexible 17 membrane 64, the stop pins 80 provide a lower limit to 18 the movement of the chimney assembly 50. In a present 19 embodiment, the stop pins 80 are spaced so that when the lower edge of the vertical wall 76 of the baffle 74 21 is brought into contact with the stop pins 80, a space 22 1h, is provided between the diverter 60 and the upper 23 surface 39 of the nozzle assembly 24. in a preferred 24 embodiment, the space is approximately between 0.025 and 0.045 inches, or more preferably 26 approximately between 0.030 and 0.040 inches, and most 27 preferably approximately 0.033 inches.

128 In alternative embodiments, movement of the 29 diverter 60 toward the nozzle assembly 24 may be limited by means other than stop pins. For example, if 31 the housing were f ormed by an injection molding 32 process, steps, shoulders, fins, or other structures, 33 may he provided along the walls of the housing in order 34 to limit the downward travel of the chimney and/or diverter.

36 Also located in the chamber 14 is a diverting ring 37 82. The diverting ring 82 is located on the inner wall 10 1 of the cylindrical portion 18 of the housing 12.

2 Specifically, the diverting ring 82 is positioned 3 adjacen!t- to the baffle 74. The diverting ring 82 is 4 sized to define a gap 86 around the baffle 74. The diverting ring 82 serves to impede large droplets of 6 liquid that might form on the inner wall of the housing 7 12 and divert large droplets back down into the 8 reservoir 23 at the bottom of the housing 12. In 9 addition, the diverting ring 82 serves to provide a relatively tortuous path for the flow of aerosol 3.1 particles from the lower portion of the chamber 14 to 2.2 the upper portion. This tortuous path also serves to 13 reduce the presence of larger particles and helps to 14 make the particle size distribution more uniform.

As mentioned above, the bottom of the chamber 14 16 serves as a reservoir 23 for a liquid to be nebulized.

112 In a present embodiment, the reservoir has a funnel- 18 like shape to direct the liquid to be nebulized in a 19 downwa rd direction toward the inlet 44. The reservoir portion of the chamber 14 is formed of at least two 21 portions or stages. In a present embodiment, an upper 22 portion 88 of the reservoir is relatively wide having a 23 diameter approximately the same as that of the 24 cylindrical portion 18 of the housing 12 2.36 in) The upper portion 88 is relatively shallow (e.g.

26 0.3125-0.2S in). The upper portion 88 of the reservoir 27 tapers in a funnel-like manner toward a lower portion 28 90 (or secondary well) of the reser-vc-'r. The lower 29 portion 90 is relatively narrow, but relatively deep) 0.25 in) The lower portion 90 of the reservoir 31 is slightly wider 0.625 in) than the outer 32 diameter of the nozzle assembly 24. :-he opening 44 33 from which the liquid is drawn is located at the bottom 34 of the lower portion 90 of the reservoir. Ir a presentembodiment, the reservoir 23 also includes an 36 intermediate portion 92 located between the upper 37 portion 88 and the lower portion 90. The intermediate 11 1 portion 92 of the reservoir 23 has a height and a width 2 between that of the upper and lower portions.

3 In the embodiment of the nebulizer shown in 4 Figure i, the relative sizes and dimensions of the s upper, lower and intermediate portions of the reservoir 6 23 contribute to the generation of an aerosol wherein 7 the aerosol particle size and output is relatively 8 uniform overall. As described more below, the liquid 9 in the reservoir 23 is drawn through the opening 44 and up the liquid passageway 42 in part by the negative 11 pressure caused by the flow of gas across the liquid 12 orifice 46. The suction force provided by the gas flow 13 both draws the liquid up out of the reservoir to the 14 top of the nozzle and entrains the liquid with a certain velocity in the air flow. As the liquid is 16 nebulized, the surface level of the liquid in the 17 reservoir goes down, thereby directly increasing the 18 distance that the liquid has to be drawn up out of the 19 reservoir to the orifice at the top of the nozzle. As the distance of the top of the nozzle over the liquid 21 surface increases, more energy is required to draw the 22 liquid up to the liquid orifice at the top of the 23 nozzle assembly 24. Assuming a relatively constant gas 24 pressure, this increasing distance may have the effect of decreasing liquid flow through the liquid orifice 26 which in turn may affect the uniformity of the aerosol 27 particle size and rate.

.26 The embodiment of the nebulizer in Figure 1 29 reduces this possible adverse effect. With the embodiment of Figure 1, a relatively large portion of 31 the liquid is stored in =he upper portion 88 of the 32 reservoir and a relatively smaller portion of the 33 liquid is stored in the lower portion 90 of the 34 reservoir. Since the large portion 88 of the reservoir is wide and relatively shallow, the surface level of 36 the liquid in the reservoir changes relatively slightly 37 as the liquid in this portion of the reservoir is drawn 12 1 down. Therefore, there is little change in the energy 2 needed to draw this amount of liquid up from the 3 reservoir to the liquid orifice 46 as this portion of 4 the liquid is depleted. When all the liquid in the upper portion 88 of the reservoir is nebulized, the 6 remaining liquid in the lower portion 90 of the 7 reservoir is drawn into the liquid passageway 42 and a the height of the top surface of the liquid falls 9 rapidly. However, since the lower portion 90 of the reservoir is relatively narrow, it contains only a 11 small portion of the liquid being nebulized so there is 12 relatively little overall effect on aerosol particle 13 size and output from this portion of the liquid.

14 Another advantage provided by the funnel shape of the reservoir is that the relatively narrow size of the 16 lower portion 90 of the reservoir has less surface area 17 thereby directing the liquid toward the opening 44.

1s This causes most or all of the liquid to be directed to 19 opening 44 with little waste.

The nebulizer 10 of Figures 1-3 may also include a 21 sensor 89. The sensor 89 may be attached to the 22 housing 12 at any suitable location, such as on the 23 cover 21, as shown in Figure 1. The sensor 89 monitors 24 the operating cycles of the nebulizer 10. The sensor 89 may monitor operating cycles by monitoring the 26 movement of the chimney portion 50 relative to the 2*7 housing body 12. The sensor 89 may utilize any .28 suitable technology, such as electronic, pneumatic, or 29 mechanical. For example, the sensor may be responsive to a change in local capacitance as the chimney moves 31 closer and further from the top of the housing.

32 Alternatively, the sensor may be responsive to a 33 embedded magnet, or may measure an optical parameter, 34 etc. The sensor 89 monitors the cycles of operation and provides a count that can be observed by the user 36 or a medical care provider. This enables the user or 37 care provider to estimate how much medication has been 13 I delivered. The sensor 89 includes a display or similar 2 device for this purpose. In addition, the sensor may 3 also include appropriate programming to report on the 4 duration, frequency, speed, etc. of nebulizer operation. These parameters may also be provided to 6 inform the patient or care provider about the delivery 7 of medication. This embodiment of the nebulizer may 8 also include appropriate programming to limit the 9 amount of medication or drugs that can be administered.

For example, if the nebulizer is used to deliver drugs 11. for pain control, such as morphine, the nebulizer can 1.2 be programmed to limit the amount of such drugs that 13 can be delivered to the patient.

:14 The embodiment of the nebulizer shown in Figures -is 1-3 is adapted for use by a spontaneously breathing 16 patient, so the aerosol from the nebulizer is output to 17 a mouthpiece or mask that can be used by the 18 spontaneously breathing patient. Accordingly, located 19 in an upper portion of the chamber 14 is an adapter 99 having an outlet 98 that connects to a mouthpiece 100.

21 In alternative embodiments, as described further below, 22 the nebulizer may be used with ventilator systems and 23 instead of the mouthpiece 100, the adapter 99 would 24 connect the outlet 98 to the ventilator circuit.

To operate the nebulizer 10, a suitable amount of 26 a liquid such as a medicine or water is placed in the 27 reservoir of the chamber 14. The liquid may be placed in the reservoir by first removing the cover 21, 29 membrane 64, and chimney 50, filling an appropriate amount of liquid into the reservoir, and replacing the 31 cover 21, membrane 64, and chimney 50 onto the housing 32 12. In a preferred embodiment, the cover, membrane'and 33 chimney are assembled together and would be removable 34 together as a unit. (Alternatively, the liquid may be placed into the reservoir through che mouthpiece 100, 36 or further, the nebulizer may be provided pre-tilled 37 with ihe appropriate amount of medicine fromi the 14 I manufacturer, or in yet another alternative, the 2 nebulizer may be provided with a resealable fill port.) 3 The source of pressurized gas 27 is connected to the 4 fitting 28. The source of pressurized gas 27 may be an external source that provides gas at a rate of 4 to 6 liters per minute in a range from 35 p.s.i to 50 p.s.i, 7 although other rates and pressures could also be 8 suitable. Gas is delivered through the passageway 34 -9 and is expelled from the gas outlet orifice 38 into the chamber 14. However, at this stage, prior to 11 inhalation by the patient, the gas travels upward from 12 the gas outlet orifice 38 and nebulization does not 13 occur since the diverter 60 is in the non-nebulizing 14 position. The membrane 64 holds the chimney assembly 50, including the diverter 60, away from the nozzle 24.

16 When in the non-nebulizing position, the distance 17 between the diverter 60 and the top of the nozzle is 18 approximately 0.15 inches. At this distance, the gap 19 between the diverter 60 and the nozzle 24 is such that the flow of gas does not create sufficient negative 21 pressure over the liquid orifice 46 to draw out the 22 liquid.

23 To generate an aerosol with the nebulizer, the 24 patient places the mouthpiece i00 to his/her mouth.

When the patient inhales, air is withdrawn from the 26 chamber 14 reducing the pressure inside the housing 12.

27 The lower pressure in the chamber 14 causes the -!28 membrane 64 to flex drawing the chimney 50 down. The 29 lower position of the chimney 50 is shown in Figure 1A.

Downward movement of the chimney 50 is limited by the 31 stop pins 80. When the stop pins 80 limit the downward 32 movement of the chimney So, the diverter 60 is spaced a 33 predetermined distance from the top surface 39 of 34 the nozzle assembly 24. In a present embodiment, the gap is approximately 0.033 inches.

36 The pressurized gas, which may be continuously 37 injected into the nebulizer through the fitting 38, is I 1 diverted sideways approximately 900 by the diverter 6O.

2 Since the gas outlet orifice 38, diverter 60 and nozzle 3 top 39 are generally circular, gas exiting the orifice 4 38 is dispersed evenly in an approximately 3600 or radial pattern. The liquid medicine in the reservoir 6 is then drawn up the passageway 42 and out of the 7 liquid outlet orifice 46 in part by the negative 8 pressure caused by the moving gas passing over the 9 liquid outlet orifice. The liquid drawn into the diverted gas stream is aerosolized at least by the time 11 it reaches the larger volume space of the chamber. In 12 a present embodiment, the liquid medicine drawn out of 13 the liquid orifice 46 has little or no impaction 14 against the diverter 60. However, in an alternative embodiment, the liquid drawn into the gas stream may be 16 directed against the diverter :17 As the liquid is nebulized it travels into the 1.8 chamber 14 along a path around the lower edge of the 19 baffle 74. As the patient inhales, the nebulized liquid travels upward through the gap 86 between the 21 baffle 74 and the diverting ring 82, and out through* 22 the mouthpiece 100 to the patient's respiratory tract.

23 When the patient ceases to inhale, the pressure in 24 the chamber 14 rises. The biasing of the membrane 64 is again sufficient to move the chimney 50 upward, 26 increasing the distance between the diverter 60 and the* 27 top surface 39 of the nozzle assembly 24, and causing t28 nebulization of the liquid to cease. in alternative 29 embodiments, a spring, pneumatic valve, or other biasing device may be utilized, alone or in comibination 31 with each other and the membrane, to move the diverter 32 60 into a non-nebulizing position. Thus, the nebulizer 33 automatically cycles aerosol generation in time with 34 the breathing cycle of the patien:.

If the patient exhales into the nebulizer, no 36 nebulization occurs since the diverter 60 is in the 37 non-nebulizing position due to the biasing cf the 16 1 membrane 64. Upward travel of the chimney 50 is 2 limited by the cover 21.

3 During inhalation, some air flow may be provided 4 through the nebulizer in a path through the chimney This air flow into the chamber 14 may be provided from 6 ambient in a path provided through the ports 72, the 7 chimney inlet 56, the chimney passageway 52, and the 8 chimney outlet 58. This air flow may continue during 9 both inhalation when the chimney 50 is in the lower position and exhalation when the chimney is in the 11 higher position. Alternatively, the air flow through 12 the chimney 50 may be stopped or reduced during 13 inhalation when the chimney 50 is in the lower 14 position. Control of the airflow through the nebulizer Sis during inhalation or exhalation may be effected by 16 suitable selections of the dimensions of the chimney 17 inlet 56, the chimney outlet 58, the actuator ports 72, 18 the diverter ring 82, and other components that affect 19 airflow through the chamber, such as any filters.

In the embodiment described above, the membrane 64 21 provides an elastic triggering threshold that permits 22 cyclical nebulization to occur that coincides with the 23 breathing of the patient. This threshold is set to 24 fall within normal human breathing parameters so that the diverter moves into and out of proximity with the 26 nozzle top as a result of the patient's normal 27 breathing. In one embodiment, this level may be -28 approximately less than or equal :o 3.0 cm of water.

29 It can be appreciated that the threshold may be established at different levels to account for 31 different classes of patients. For example, if the 32 nebulizer is designed to be used with infants or neo- 33 natals, the elastic threshold of the membrane may be 34 lower than the threshold used for adults. Similarly, a different threshold may be used for geriatric patients.

36 The nebulizer may be used also for veterinary 37 applications, such as equine or canine. In veterinary 17 1 applications, there may be a relatively wide range of 2 thresholds related to the various sizes of animals.

3 Nebulizers having suitably chosen operating thresholds 4 can be designed for veterinary uses. It is also s recognized that the openings into the chamber, such as 6 the opening 56, may affect the operating threshold for 7 nebulization. Thus, the operating threshold of the a nebulizer may be made readily adjustable by making the 9 actuator 68 adjustable. Alternatively, the operating threshold may be adjusted by selection of the size of 11 the openings 56 and 72 into the chamber which would 12 also control air entrainment. This would permit the 13 user to adjust the thresholds, if desired. By 14 appropriate adjustment of the operating thresholds, Is flow control through the nebulizer can be provided.

16 For example, it may be desirable that the patient not 17 inhale or exhale too quickly or too deeply. For s1 adults, a suitable flow rate may be approximately 30-60 19 liters/minute. The openings into and out of the chamber may be suitably adjusted to provide for these 21 rates.

22 The nebulizer may be operated manually instead of 23 relying on the breath-actuated feature. To operate the 24 nebulizer manually, the actuator 70 is pressed down toward the cover 21. As mentioned above, the actuator 26 70 is connected to the chimney 50. Pressing the 27 actuator 70 brings the diverter 60 down into the 28 nebulizing position close to the nozzle 24. Release of 29 the actuator 70 causes the chimney 50 to rise due to the biasing of the membrane 64 thereby causing 31 nebulization to cease.

32 Referring to Figures 4 and 4A, the indicators 69A 33 and 69B provide a convenient way to confirm the 34 operation of the nebulizer. As mentioned above, when the diverter 60 is spaced away from the top of the 36 nozzle 24, no aerosol is being generated. When the 37 diverter 60 is spaced away the actuator 68, the 18 1 actuator 68, which is connected to the diverter 2 through the chimney 50, is in an upper position and :he 3 red indicator 69A on the side of the actuator 68 is 4 visible along the top side 21 of the nebulizer 10, as shown in Figure 4. When the patient inhales 6 sufficiently to bring the diverter 60 into a lower 7 position, the red indicator 69A on the side of the 8 actuator 68 is withdrawn through the opening 56 in the 9 top side 21 of the nebulizer 10. The red indicator 69A is no longer visible, however, the green indicator 69B, 11 which is located above the red indicator 69A, remains 12 visible at the top 21 of the nebulizer. Thus, a 13 patient or medical attendant can readily determine 14 whether the nebulizer is operating. In embodiments of -/is the nebulizer for children, the actuator and/or 16 indicators can be designed with comic figures.

17 The breath actuation of the nebulizer is is convenient and efficient. By cycling the nebulization *19 of the liquid, the nebulizer can be more efficient thereby reducing the cost of the therapy.

21 An important advantage follows from the feature of 22 this nebulizer that nebulization can be cycled so as to 23 occur in coordination with a physiological cycle of the 24 patient. Specifically, by nebulizing only during an inhalation, for example, the dosage of medication 26 delivered to the patient can be more accurately 27 delivered and monitored. This enables this embodiment 28 of the nebulizer to provide for dosimetric medication 29 delivery to an extent that has been otherwise unavailable. By limiting the medication delivery to 31 the inhalation cycle of the patient, a dosime:ric 32 portion of the medication can be provided.

33 In addition, the nebulizer 10 provides for high 34 output and uniform nebulization due to the arranaement of the gas and liquid orifices 38 and 46 relative to 36 the diverter 60. The annular configuration of the 37 liquid orifice 46 relative to the gas orifice provides 19 I for aerosol generation in a approximately 3600 2 direction. This enables a relatively high and uniform 3 rate of nebulization. The uniformity it enhanced 4 because the nebulization is formed with little or no s impaction of liquid against the diverter.

6 In alternative embodiments of the nebulizer, the 7 cover 12 may include an air filter that covers the air 8 inlet 56. The filter would serve to keep contaminants 9 out of the chamber and deter the escape of nebulized liquid. Such a filter may be removable to permit 11 simple, inexpensive replacement.

12 In a still further embodiment, the nebulizer may 13 be used in conjunction with an aerosolization spacer, 14 such as an Aerochamber® sold by Trudell Medical Partnership of London, Ontario. The Aerochamber spacer 16 is described in U.S. Pat. No. 4,470,412, the entire 17 disclosure of which is incorporated by reference 18 herein. In this alternative embodiment, the output of 19 the nebulizer would be directed into the inlet of the Aerochamber from which the patient inhales the aerosol 21 through an outlet of the Aerochamber.

22 Another advantage provided by this embodiment of 23 the nebulizer is that less aerosol is likely to escape 24 to the surrounding environment. This potentially benefits attending care providers who would otherwise 26 be exposed to aerosol medication that is released from 27 nebulizers that generate on a continuous basis.

28 In a present embodiment, the membrane 64 is biased 29 to keep the chimney in an upper, non-nebulizing position except during inhalation. Thus, in the 31 periods of time between inhalations and exhalations, or 32 if the patient pauses and removes the mouthpiece, 33 nebulizing does not take place. In alternative 34 embodiments, the membrane 64 may bias the chimney downward so that the nebulizer generates an aerosol or 36 nebula except during exhalation. This alternative may 37 not be as efficient as the prior alternative, but may 20 1 still provide significant advantages over nebulizers 2 that generate aerosol continuously.

3 In further alternative embodiments of the 4 nebulizer, the gas orifice 38, the gas passageway 34, or a portion thereof, may have a shape that modifies 6 the force of the pressurized gas against the diverter 7 60. For example, the gas orifice 38 may have a conical 8 shape that facilitates the change of direction of the 9 gas when it is directed against the diverter, so that the force of the gas would not move the diverter away 11 during inhalation thereby helping to direct the gas out 12 into the chamber. In other embodiments, the conical 13 geometry may be varied to tailor gas force and flow.

14 As mentioned above, the membrane 62 serves as a is biasing member that moves the diverter. Preferably, 16 the membrane is constructed of a silicone rubber 17 material. Other materials capable of repetitive 18 flexing, compression or expansion in response to the 19 force of inhaled or exhaled air, such as a spring, or elastic bellows, may also be used. The biasing member 21 is constructed so that it will move the diverter a 22 predetermined distance away from or toward the nozzle 23 during the course of a patient's spontaneous or 24 ventilated breathing.

In a present embodiment, the diverter moves up and 26 down in response to the patient's breathing. However, 27 in alternative embodiments, the nozzle 24 can move 28 instead of the diverter, or alternatively, both the 29 nozzle and the diverter can move. Also, in a present embodiment, the diverter movement is up and down, but 31 in alternative embodiments, the movement can be side to 32 side, rotating, or pivoting. Alternatively, instead of 33 moving diverter into proximity with a gas outlet, in 34 alternative embodiments, the liquid jet or orifice car be moved toward the gas jet or orifice, or is otherwise 36 directed toward the gas jet or orifice, or vice versa.

37 In effect, alternative embodiments contemplate various 21 1 means of bringing or diverting the gas and liquid 2 streams into proximity in a cyclical basis.

3 in alternative embodiments of the nebulizer, the 4 liquid orifice may have shapes other than annular. For s example, the liquid orifice may be located adjacent to 6 the gas orifice. Alternatively, the liquid orifice may 7 be formed of a series of orifices positioned adjacent 8 or annularly around the gas orifice.

9 The nebulizer 10 may also be provided with a plurality of support legs (not shown) that are 11 connected around the exterior of the housing 12 and 12 provide support theref or.

13 In this embodiment, the diverter 50 moves into 14 proximity with the nozzle 24 due to a negative pressure in the chamber 14. However, the pressure variance may 16 also be created by a variance in positive pressure, or 17 a combination of positive and negative pressures.

1s 11. Second Embodiment 19 A second embcodiment of a nebulizer is shown in Figure 5. According to this embodiment, a nebulizer 21 110 has a housing 112 that def ines a chamber 114. A 22 lower portion of the chamber 114 serves as a reservoir 23 123 for holding a liquid to be nebulized. Located in a 24 lower portion of the housing 112 is a nozzle assembly 124- The nozzle assembly 124 may be similar or 26 identical to the nozzle assembly of the first ,27 embodiment, described above. Like the first 28 embodiment, a bottom of the nozzle 29 assembly 124 has a fitting 128 that can be connected to a supply' of pressured gas 127 by means of conventional 31 tubing 129. Located in the nozzle assembly 124 are 32 inner and outer tubular members that define gas and 33 liquid passageways that exit at gas and liquid orifices 34 at the top of the nozzle assembly 124, as in the first embodiment. Like the first embodiment, the gas and 36 liquid orifices prfrbyhave a concentric 22 1 arrangement with the liquid or:fice having an annular 2 shape encircling the gas outlet orifice. Also, like 3 the first embodiment, in the embodiment of Figure 5 the 4 reservoir 123 includes a relatively wide, but shallow, s primary or upper portion 188 and a relatively narrow, 6 but deep, lower or secondary portion 190.

7 Although this embodiment is shown without a bell- 8 shaped baffle similar to baffle 74 of the first 9 embodiment, a baffle may be provided in this embodiment. If a baffle were provided in this 11 embodiment, it would have a construction similar to 12 that of the baffle 74 of Figure 1.

13 In the embodiment of Figure 5, a chimney 150 is 14 located in an upper portion of the housing 112. The chimney includes a first internal passageway 152. In 16 this embodiment, the internal passageway 152 of the 17 chimney assembly 150 serves as an outlet 198 from the 18 chamber 114. The outlet connects to a mouthpiece 199, 19 or other suitable means of delivering an aerosol to a patient, such as a mask. A diverter 160 is located at 21 and connected to a lower end of the chimney 150. The 22 diverter 160 is located a predetermined distance from 23 the top of the nozzle assembly 124. In this 24 embodiment, this distance is approximately 0.033 inches. Unlike the first embodiment, the chimney 26 assembly 150 in this embodiment 110 is not movable 27 between upper and lower positions. Instead, the 28 chimney assembly 150 is fixed in position so that the 29 diverter 160 is maintained a suitable distance from the top of the nozzle assembly 124 to generate an aerosol.

31 In this embodiment, a- least one second air 32 passageway 153 is provided. The second air passageway 33 153 is located adjacent to the first air passageway 152 34 in the chimney assembly 15C. The second air passageway 153 communicates with an inlet opening 161 and a 36 suction chamber 163. The suction chamber 163 is 37 located around a lower end of :he chimney assembly 150 23 1 and specif ically, around the perimeter of the diverter 2 160. An opening 158 communicates between the suction 3 chamber 163 and the chamber 114. As pressurized gas 4 and nebulized liquid flow past the perimeter of the S diverter 160, a pressure variance is created that. draws G air from ambient through the inlet opening 161 through 7 the second passage way 153 into the suction chamber a 163. In one embodiment, the pressure variance is a 9 negative pressure, however, the pressure variance may also be created by a variance in positive pressure, or 11 a combination of positive and negative pressures. The 12 suction provided at the opening 158 serves to enhance 13 generation of the aerosol.

14 A nebulizing enhancement feature provided by the i nebulizer 110 relates to the shape of wall 171 around 1.6 the opening 158. As shown in Figures 5 and 6, the .17 shape of the wall 171 includes a first region 173 and a 1s second region 175. The first region 173 is separated 19 f rom the second region 175 by a step or shoulder 177.

The f irst region 173 iand the second region 175 are 21 preferably horizontal, flat surfaces and the shoulder' 22 177 is preferably a vertical surface. The wall 171 23 also includes a third region 179. The third region 179 24 is located around the second region 175. The third region 179 i-*s a sloped or angled surface that extends 26 from the second region 175 to a gap 186 formed adjacent 27 to a diverting ring 182.

t28 The shapes of the first, second and third regions 29 173, 175 and 177 affect the air flow in the chamber from the diverter. The relative sizes and shapes may 31 be varied to enhance particle size generation and 32 uniformity. An alternative embodiment of the wall 171 33 and regions 173, 175, and 177 is shown in Figure 7. In 34 the embodiment of the wall 171A shown in Figure 7, the relative sizes of the first region 173A, second region 36 175A, and third region 177A are modified relative to 37 those in the embodiment of Figure 6. These sizes are 24 I varied to affect the size and uniformity of the 2 particle distribution of the nebula or aerosol.

3 Referring again to Figure 5, located in a wall of 4 Ithe chimney 150 is at least one, and preferably a plurality of openings 185. Openings 185 communicate 6 between the chamber 114 and the first air passageway 7 152 of the chimney assembly 150.

8 Referring to Figures 5 and 8, a diverting ring 182 9 may be provided in the chamber 114 to reduce the presence of large droplets and help make the aerosol 11 delivered to the patient more uniform. As mentioned 12 above in connectiohn with 'the first embodiment, the 13 diverting ring provides this function, in part, by 14 limiting the migration of droplets on the inside wall 'is11 of the nebulizer housing. In addition, by forming a 16 barrier on the inside wall of the housing, the 17 diverting ring forces the nebulized aerosol to travel 18 along a relatively non-linear path to move from the 19 lower part to the upper part of the chamber and out the mouthpiece.

21 Referring t:o Figure 5, to operate the nebulizer 22 110, a suitable amount of liquid medicine is placed in 23 reservoir of the chamber 114. The outlet 198 is 24 connected t-o the mouthpiece 199 in a suitable manner.

The source of p~ressurized gas 127 is connected to the 26 fitting 12B. T-he flow of gas f rom the top of the 27 nozzle assembly 124 is directed by the diverter 160 128 across the annular liquid orifice surrounding the gas 29 orifice causing the generation of an aerosol from the liquid in the reservoir. The aerosol is generated in a 31 3600 direction into the chamber 114 around the nozzle 32 124 and diverter 160.

33 An air flow path is established into the chamber 34 114 from the inlet 161. The gas provided by the source 127 also supplements the air supply into the chamber 36 114. Air flows into the chamber through the second 37 passageway 153 through the suction chamber 163 and 25 I opening 158. Air flow laden with aerosoli;zed liquid 2 from the chamber 114 travels past the gap 186, through 3 the opening 183, into the first air passageway 152, and 4 out from the outlet opening 198 to the mouthpiece 199 or face mask. In this embodiment, nebulization may 6 proceed continuously, or may be cycled by other means, 7 such as cycling of the gas supply.

a Alternative embodiments of the diverting ring -9 arrangement are shown in Figures 9 and 10. In Figure 9, the diverting ring 182A extends further toward the 11 chimney 150 almost overlapping an edge 183A at the .12 bottom 150A of the chimney 150. This arrangement :13 provides an even more tortuous pathway for the aerosol 14 than the embodiment shown in Figure 8. The embodiment is of Figure 8 may provide an even more uniform particle 16 distribution. In Figure 10, the passageway between the 17 diverting ring 182B and the bottom 150B of the chimney 18 is extended thereby providing a longer pathway of a 19 narrow dimension. The embodiment of Figure 10 may provide an even more uniform particle distribution than 21 the embodiments of Figures 8 or 9.

22 1I1. Third Embodiment 23A A nebulizer 210 according to another embodiment of 24 the invention is shown in Figures 11-13. The nebulizer 210 is similar to the previous embodiments of the 26 nebulizers discussed above. The nebulizer 210 includes -27 a housing 212 defining a chamber 214. In the 28 embodiment of Figure 11, the housing 212 is relatively 29 larger than the housings of the previous embodiments.

For example, the housing 212 may have a heigh: of 31 approximately 11 cm (4.33 in.) and a dianmezer of 32 a pproximately 9 crr (3.54 inj.' This enab-les :he 33 nebulizer 210 to hold a correspondingly larger Volume 34 of liquid and aerosol. A large size nebu-lizer, such as shown in Figure 11, may be suitable for certain 36 veterinary applications such as for horses, cattle, 26 1 dogs, etc. A larger size nebulizer may also be used 2 with humans for uses such as sputum induction.

3 A fitting 238 connects to a pressurized gas supply 4 -(not shown) and an outlet 298 provides nebulized s medicine from the chamber 214 to the patient. The 6 outlet 298 may connect to a mouthpiece, mask, or 7 ventilator, as appropriate. Like the first described 8 embodiment, the nebulizer 210 has a movable chimney 9 250. In the chamber 214 of the nebulizer 210, there are a plurality of nozzle assemblies 224A, 224B, and 11 224C. Each of these nozzle assemblies may be similar 12 to the nozzle assembly 24 of the first embodiment.

13 Each of the nozzle assemblies includes a gas supply 14 passageway, such as 234A, and an annular liquid supply passageway, such as 242A. At the top ends of each of ;16 the nozzles 224A, 224B, and 224C, the gas passageways 17 of each communicate with gas outlet orifices 238A, 18 238B, and 238C, respectively and the liquid passageways 19 of each communicate with liquid outlet orifices 246A, 246B, and 246C. The liquid inlets 244 into each of the 21 nozzles assemblies communicate in common with a 22 reservoir 223 formed at the bottom of the chamber 214.

23 Located at the bottom of chimney is a diverter 24 260. The diverter 260 may be formed of a single face or surface, or may be formed of multiple faces or 26 surfaces that are aligned with the multiple nozzle 27 assemblies 224A-224C, or alternatively, the diverter 28 may be formed as a ring. Further, there may be 29 provided multiple diverters. In a preferred embodiment, there is a space or gap 261 formed 31 centrally in the bcrtom of the diverter 260 to permit 32 aerosol generation in 3600 around each of the nozzles.

33 A membrane 264 may be located at the top of the 34 chimney 250 to provide a biasing function as in the embodiment of Figure 1. Due to the larger size and 36 weight of the chimr.ey assembly 250 in the embodiment of 37 Figure 11 relative to the embodiment of Figure i, a 27 1 biasing member 265 such as a spring may be provided in 2 substitution for or in addition to the membrane 264.

3 The spring or other biasing member 265 may be connected 4 to the top of the chimney assembly 250.

The nebulizer 210 is operated in a manner similar 6 to the nebulizer shown in Figure 1. Like the nebulizer 7 shown in Figure 1, the nebulizer 210 in Figure 11 is 8 breath- or pressure-actuated. After a suitable liquid 9 is stored in the housing 212, the generation of a nebula or aerosol will cycle with the cyclic decrease 11 of pressure in the chamber 214. The decrease of 12 pressure may be caused by inhalation by the patient, or 1.3 by action of ventilator. As in the first embodiment, 14 nebulization will cease upon exhalation or in the is1 absence of inhalation.

16 Because the nebulizer 210 has multiple nozzles 17 224A-C, a large amount of liquid can be nebulized 18 quickly. Since the single diverter or connected 19 multiple diverters move in unison toward the multiple nozzles with the patient's inhalation, the cycling of 21 nebulization is coordinated among all the nozzles.

22 As in the previous embodiments, the annular shape 23 of each of the liquid orifices provides for a high 24 nebulization generation rate. Although the embodiment of Figures 11-13 shows three nozzles, there can be arm' 26 number of multiple nozzles, such as two, four, five, 27 etc.

*28 In an alternative embodiment, the diverter 2E0 is 29 rotatable relative to the body 252 of the chimtney 150.

The diverter 260 may include appropriate vanes, 31 channels-or a propeller, that captures some of the 32 pressurized gas flow and causes the diverter 260 o -33 rotate inside the housing 212. Rotation of tnle 34 diverter 260 may be used to improve mixing of the aerosol inside the chamber.

36 This embodiment may also include a bell-shaped 37 baffle as shown in the first embodiment.

2B 1 IV. Fourth Embodiment 2 Figure 14 shows a fourth embodiment of a nebul~zer 3 of the present invention. This embodiment 310 of the .4 nebulizer is adapted for use with a ventilator circuit 301. The ventilator circuit 301 includes an 6 inspiratory airflow passageway 302 that delivers air 7 from the ventilator to the patient. This embodiment of 8 the nebulizer 310 is located in the inspiratory airflow 9 passageway 302 connected between a first length cf inspirator-y tubing 303 that delivers air from the 11 ventilator circuit 301 and a second length 304 that 12 delivers air to the patient. The second-length of 13 inspiratory tubing 304 may connect to the patient by 14 means of a mask, endotracheal tube, etc.

is' Like the embodiment of Figure 1, the embodiment of 16 the nebulizer in Figure 14 is pressure- or breath- 17 actuated. Accordingly, the nebulizer 310 produces an 18 aerosol in a cyclical manner in coordination with the 19 breathing or ventilation of the patient. The nebulizer 310 has a housing 312 defining a chamber 314. A nozzle 21 assembly 324 extends up from the bottom of the chamber 22 314. Pressurized gas is delivered from a gas orifice 23 at the top end of the nozzle assembly 324 and liquid 24 from a reservoir 323 at the bottom of the chamber 314 is drawn up to a liquid orifice also located at the top 26 end of the nozzle assembly 324 as in the f irst 27 embodiment. A chimney assembly 350 extends down from a 28 top of the housing 312. The chimney 350 connects to 29 the housing by means of a flexible, resilient membrane 364. A diverter- 36C is located at the bottom of the 31 chimney assembly 350 directly opposite from the gas and 32 liquid orifices at the top of the nozzle assembly 324.

33 An inlet 356 of the chimney 350 connects to the length 34 of inspiration tubing 303 from the ventilator circuit 301. The inlet 356 communicates with an internal 36 passageway 352 of t:he chimney assembly 350.

37 Inspiratory gas from the ventilator 301 enters the 29 i nebulizer 310 via the chimney inlet 356, passes through 2 the passageway 352 of the chimney assembly 350, and -3 passes into the nebulizer chamber 314 through the 4 openings 385 located in the wall of the chimney 350.

The inspired gas exits the nebulizer chamber 314 via an 6 outlet 398. The outlet 398 connects to the second 7 length of inspiratory tubing 304 which in turn connects 8 to an endotracheal tube, a mask, or other means (not 9 shown). This embodiment may also include a bell-shaped baffle as shown in the first embodiment.

11 In the embodiment of Figure 14, the normal 12 operation of the ventilator circuit 301 causes a 13 sufficient change in the pressure in the nebulizer 310 14 to induce the chimney assembly 350 to move into and out is of proximity with the nozzle assembly 324.

16 Accordingly, during an inspiration cycle, the chimney 17 assembly 350, including the diverter 360, will be 18 brought into proximity with the top of the nozzle 19 assembly 324 causing nebulization of the liquid (as described above in connection with the first 21 embodiment). During an expiratory phase of the 22 ventilator 301, the diverter 350 is positioned away 23 from the nozzle assembly 324 thereby causing 24 nebulization to stop. Nebulization cycles automatically in synchronism with the operation of the 26 ventilator. No extra connection is required beyond 27 that necessary to withdraw the aerosol from the chamber 28 314 of the nebulizer 310 into the inspiratory tubing of 29 the ventilator circuit.

V. Fifth embodiment.

31 Figure 15 shows a fifth embodimen- 410 of the 32 nebulizer of the present invention. Like the previous 33 embodiment, the nebulizer 410 in Figure 15 is adapted 34 for use in a ventilator circuit and produces an aerosol in a cyclical manner in coordination with operation of 36 the ventilator and/or the breathing of the patient.

30 1 A ventilator circuit 401 has an inspiratory 2 passageway 402 that is formed of a first length of 3 tubing 403 that connects to the ventilator 401 and a 4 second length of tubing 404 that connects to a mask s 405, or endotracheal tube, and so on, associated with 6 the patient. The ventilator circuit 401 also includes 7 an exhalation valve pressure line 406. This exhalation 8 valve pressure line 406 connects to an exhalation valve 9 407 associated with an expiratory passageway 408.

During ventilation of the patient, pressured gas is 11 delivered in the exhalation valve pressure line 406 to 12 the exhalation valve 407 to assist in the cycling of .13 ventilation of the patient.

14 The nebulizer 410 has a housing 412 defining a chamber 414, and includes a nozzle assembly 424, a 16 flexible, resilient membrane 462, and a diverter 460, 17 arranged generally as in the previously described 18 embodiment. Instead of a chimney, the nebulizer 410 19 has a post 450 to which the diverter 460 is connected.

Unlike a chimney, the post 450 does not include air 21 openings or an internal air passageway. The diverter 22 460 is connected to a bottom side of the post directly 23 adjacent from the top of the nozzle assembly 424. The 24 embodiment of Figure 15 also differs from the previous embodiment in the manner that the ventilator circuit 26 401 is connected to the nebulizer 410 and the manner 27 that the ventilator circuit 401 causes the nebulizer 28 410 to cycle nebulization. This embodiment may also 29 include a bell-shaped baffle as shown in the first embodiment.

31 In Figure 15, the nebulizer housing 412 includes 32 an inlet 456 into the chamber 414. The inlet 456 33 connects to the first section 403 of inspiratory tubing 34 402 from the ventilator circuit 401. The nebulizer housing 412 also includes an outlet 498 from the 36 chamber 414. The outlet 498 connects to the second 37 section 404 of inspiratory tubing that leads to a 31 I conventional device 405, e.g. an endotracheal tube or 2 mask, from which the patient receives the inspiratory 3 flow from the ventilator 401 including the aerosol from 4 the nebulizer 410.

Located across the membrane 462 from the 6 nebulization chamber 414 is a passageway 483. The passageway 483 connects to the exhalation valve s pressure line 406 of the ventilator circuit 401 by a 9 suitable means, such as a tee 487. Because the ventilator 401 cycles air to and from the patient, air 11 flows in the exhalation valve pressure line 406 in a 12 cyclic manner to operate the exhalation valve 407.

13 This air flow in the exhalation valve pressure line 406 14 causes a pressure differences with the air in the chamber 414. The membrane 462 is positioned across the 16 inspiratory flow passageway 402 and the exhalation 17 valve pressure line 406 and therefore senses the 18 pressure differential across these two passageways. As 19 in the previous embodiment, the diverter 460 is brought into proximity with the top of the nozzle assembly 424 21 during the inspiratory phase of the ventilator and 22 brought out of proximity with the top of the nozzle 23 assembly 424 during the expiratory phase of the 24 ventilator. Accordingly, nebulization occurs during the inspiratory phase and not during the expiratory 26 phase.

27 VI. Sixth embodiment.

28 Figure 16 shows a sixth embodiment 510 of the 29 nebulizer of the present invention. This embodiment is similar to the embodiment of the nebulizer 110 in 31 Figure 15. The nebulizer 510 includes a housing 512 32 defining a chamber 51.4. The chamber 514 has an inlet 33 528 connected to a source of pressurized gas 527 and an 34 outlet 598 connected to a tubing 599, or similar structure, such as a mouthpiece, etc., that leads to 36 the patient 596 and from which the patient can inhale 32 1 air and aerosol. Like the embodiment of Figure 5, the 2 nebulizer 510 of Figure 16 may also include an inlet 3 for air entrainment 562. As in the other embodiment, 4 liquid and gas outlets (not shown) located at the top of a nozzle 524 directly adjacent a diverter 560 6 dispense an aerosol into the chamber 514.

7 The embodiment of the nebulizer 510 includes a s breath-actuation feature that enables the nebulizer to 9 generate a nebula in cyclic manner in coordination with a physiological cycle of the patient. In the 11 embodiment of Figure 15, the breath-actuation feature 12 is external of the nebulizer housing 512. The breath- 13 actuation feature includes a valve 569 or other 14 metering device located in-line with the inlet tubing 15 529 that provides the pressurized gas from the source 16 527 to the nebulizer inlet 528. A tubing 567 connects 17 from the outlet tubing 599 to the inlet tubing 529.

18 The tubing 567 enables the valve 569 to sense the 19 pressure in the outlet tubing 599. In one embodiment, the tubing 567 may be conventional tubing and the valve 21 569 senses the pressure through the tubing 567. The 22 valve 569 is adapted to open and close the delivery of 23 pressurized gas to the nebulizer 510 in coordination 24 with the changes in the pressure in the outlet 599 as sensed via the tubing 567. Specifically, upon 26 inhalation, the pressure in the inlet 599 and the 27 connecting tubing 567 will be lower, and the valve 569 28 will open to allow pressurized gas to be delivered to 29 the nebulizer 510 thereby causing nebulization to occur. After inhalation, the pressure in the patient 31 outlet 599 and the connecting tubing 567 rises, and the 32 valve closes thereby causing nebulization to cease. In 33 this manner, the embodiment of Figure 16 can provide 34 similar breath-actuation features as the other embodiments discussed above. The tubing 567 and valve 36 569 may be either re-usable or disposable and may be 37 used with a nebulizer 510 as shown in Figure 16, or may 33 I be used with other types of nebulizers. The tubing 567 2 and valve 569 could also be used with vaporizers that 3 are used for providing humidification for ventilated 4 patients. Such vaporizers are used with prefilled bags of sterilized water, and the tubing 567 and valve 569 6 would provide adjustable air entrainment of vapor.

7 VII. Seventh embodiment.

8 Figures 17A and 17B show a seventh embodiment 610 9 of the nebulizer of the present invention. This embodiment is similar to the previous embodiments 3.1 wherein a housing 612 defines a chamber 614 for holding 1.2 and aerosolizing a liquid 625 by means of a pressured 13 gas supply 627. In this embodiment, a top end of a -~14 diverter assembly post 650 is connected to the top side is of the housing so that the bottom surface 660 of the 16 diverter post 650 is located at a fixed distance, e.g.

17 0.033 inches, from a top 639 of a nozzle assembly 624.

18 As in the previous embodiments, a gas orifice and a 19 liquid orifice (not shown) are located at the top of the nozzle assembly 624. The liquid orifice may be 21 ring-shaped and concentric with the gas orifice, or 22 alternatively, the orifices may be side by side. A 23 mouthpiece 700 permits the withdrawal of aerosol and 24 air from the chamber 614. A flexible diaphragm 664 is located in an upper region of the nebulizer chamber 614 26 and forms a boundary between the inside of the chamber 27 and the ambient outside. One or more air inlet ports 26 656 are located on a top side of the housing 612. A 29 filter 639 is located at the top of the diverter post 650.

31 A cylindrical shield or collecting surface 633 is 32 connected to the flexible diaphragm 664 and extends 33 downward into the chamber 614 over the lower portion of 34 the diverter post 650 and the upper portion of the nozzle assembly 624. The shield 633 has an inside 36 di:ameter larger than the outside diameters off the 34 1 diverter post 650 and the nozzle assembly 624 so that 2 it can readily shift relative to these parts. One or 3 more windows 637 are located in the wall of the shield 4 633. -The windows 637 are located in the wall of the s cylindrical shield 633 such that when the diaphragm 664 6 is in an upper position (as shown in Figure 17B) the 7 window 637 is not aligned with the gap between nozzle 8 624 and the diverter 660. When the shield 633 is in 9 this upper position, aerosol particles generated by the flow of pressured gas across the liquid orifice impact 11 upon the inside wall of the cylindrical shield 633 and 12 tend to form into droplets that fall back into the 13 reservoir. In addition or alternatively, depending on 14 the specific dimensions, the shield 633 may impede the flow of gas from the pressurized gas orifice across the 16 liquid orifice to the extent that there is insufficient 17 vacuum to draw the liquid out of the liquid orifice.

18 In any event, the production of aerosol particles into 19 the chamber 614 is reduced. However, when air is withdrawn from the chamber 614, such as when a patient 21 inhales through the mouthpiece 700, a decrease in 22 pressure inside the chamber 614 causes the diaphragm 23 664 to flex downward (as shown in Figure 17A). This 24 causes the cylindrical shield 633 to shift into a lower position. When the shield 633 is in a lower position, 26 the window 637 is aligned with the gap between the 27 nozzle 624 and the diverter 660 thereby permitting 28 aerosol generated from the liquid orifice to escape 29 into the chamber 614 from which it can be inhaled by the patient.

31 The above embodiments of the nebulizer have been 32 described for use in medical or therapeutic 33 applications. It is noted that the principles of the 34 invention disclosed herein may have applicability to other usages, such as industrial, manufacturing, or 36 automotive carburetors) 35 1 I: is intended that the foregoing detailed 2 descripticn be regarded as illustrative rather than 3 limiting, and that it be understood that the following 4 claims, including all equivalents, are intended to s define the scope of this invention.

36

Claims (23)

1. A nebulizer comprising: a housing having a chamber for holding an aerosol; an air outlet communicating with said chamber for permitting said aerosol to be withdrawn from said chamber; a liquid outlet located in said chamber; a pressurized gas outlet located in said chamber adjacent to said liquid outlet; a movable diverter located in said chamber and relative to said pressurized gas outlet and said liquid outlet so as to divert pressurized gas from said gas outlet across said liquid outlet to produce said aerosol in cycles in coordination with a patient's breathing; and an indicator associated with said diverter and configured to confirm operation of said nebulizer.

2. The nebulizer of claim 1, wherein said indicator is a visual indicator.

3. The nebulizer of claim 2, wherein said indicator is comprised of colored markings.

4. The nebulizer of claim 3, wherein said colored markings are comprised of red and green markings.

The nebulizer of any of claims 2 to 4, wherein said indicator is visible at a top portion of the nebulizer.

6. The nebulizer of any of claims 1 to 5, wherein said diverter discontinues nebulization during patient exhalation.

7. A nebulizer comprising: a housing having a chamber for holding an aerosol; an air outlet communicating with said chamber for permitting said aerosol to be withdrawn from said chamber; a liquid outlet located in said chamber; a pressurized gas outlet located in said chamber adjacent to said liquid outlet; a movable diverter located in said chamber and relative to said pressurized gas outlet and said liquid outlet so as to divert pressurized gas from said gas outlet across said liquid outlet to produce said aerosol in cycles in coordination with a patient's breathing; a biasing member connected to said diverter; and 37 [R:\LIBTT]03720.doc:HXA an indicator associated with said diverter and configured to confirm operation of said nebulizer.

8. The nebulizer of claim 7, wherein said indicator is a visual indicator.

9. The nebulizer of claim 8, wherein said indicator is comprised of colored markings.

The nebulizer of claim 9, wherein said colored markings are comprised of red and green markings.

11. The nebulizer of any of claims 8 to 10, wherein said indicator is visible at a top portion of the nebulizer.

12. The nebulizer of claim 7, wherein said biasing member comprises a flexible membrane.

13. The nebulizer of claim 7, wherein said biasing member comprises a spring.

14. The nebulizer of any of claims 1 to 13 further comprising: an air inlet communication with ambient air connected to an air outlet located in said chamber.

The nebulizer of any of claims 1 to 13 comprising a suction chamber communicating with said chamber.

16. The nebulizer of any of claims 1 to 15 further comprising: a means for limiting movement of said diverter.

17. A nebulizer comprising: a housing having a chamber for holding an aerosol; an air outlet communicating with said chamber for permitting said aerosol to be withdrawn from said chamber; a liquid outlet located in said chamber; a pressurized gas outlet located in said chamber adjacent to said liquid outlet; a movable diverter located in said chamber and relative to said pressurized gas outlet and said liquid outlet so as to divert pressurized gas from said gas outlet across said liquid outlet to produce said aerosol in cycles in coordination with a patient's breathing, wherein during an inhalation, said diverter is moved towards said gas outlet and forms a gap therewith such that said pressurized gas is directed in a radial direction away from 38 [R:\LIBTT]03720.doc:HXA TV 0 said gas outlet into said chamber said pressurized gas drawing liquid from said liquid outlet; and an indicator associated with said diverter and configured to confirm operation of said nebulizer.

18. The nebulizer of claim 1, wherein said diverter is movable into a non- nebulizing position away from said gas outlet.

19. The nebulizer of claim 1, wherein said liquid outlet has an annular shape surrounding said gas outlet.

The nebulizer of any of claims 1 to 19 further comprising: 0o a ventilator circuit; and wherein said chamber connects to said ventilator circuit to deliver said aerosol thereto.

21. The nebulizer of any of claims 1 to 19 further comprising: a sensor for monitoring operating cycles of the nebulizer.

22. The nebulizer of claim 21, wherein said sensor is adapted for providing a count of how much aerosol has been produced.

23. The nebulizer of claims 21 or 22, wherein said sensor comprises a display. Dated 30 June, 2004 Trudell Medical Limited Patent Attorneys for the Applicant/Nominated Person SPRUSON FERGUSON 39 [R:\LIBTT]03720.doc:HXA