De-agglomerator for breath-actuated dry powder inhaler

Information

  • Patent Grant
  • 6748947
  • Patent Number
    6,748,947
  • Date Filed
    Saturday, June 23, 2001
    22 years ago
  • Date Issued
    Tuesday, June 15, 2004
    19 years ago
Abstract
A de-agglomerator is provided for use with a breath-actuated dry powder inhaler for breaking up aggregates and micronizing particles of dry powder prior to inhalation of the powder by a patient using the inhaler. The de-agglomerator includes an inner wall defining a swirl chamber extending along an axis from a first end to a second end, a dry powder supply port, an inlet port, and an outlet port. The supply port is in the first end of the swirl chamber for providing fluid communication between a dry powder delivery passageway of an inhaler and the first end of the swirl chamber. The inlet port is in the inner wall of the swirl chamber adjacent to the first end of the swirl chamber and provides fluid communication between a region exterior to the de-agglomerator and the swirl chamber. The outlet port provides fluid communication between the second end of the swirl chamber and a region exterior to the de-agglomerator, whereby a breath induced low pressure at the outlet port causes air flows into the swirl chamber through the dry powder supply port and the inlet port. The air flows collide with each other and with the wall of the swirl chamber prior to exiting through the outlet port, such that any powder entrained in the air flows is broken down and micronized. The de-agglomerator further includes vanes at the first end of the swirl chamber for creating additional collisions and impacts of entrained powder.
Description




FIELD OF THE INVENTION




The invention relates to a breath-actuated dry powder inhaler for administering dry powder medicament, or a dry powder composition of medicament mixed with a suitable carrier agent, e.g., lactose, to a patient. More particularly, the present disclosure relates to a de-agglomerator for a breath-actuated dry powder inhaler and a method of de-agglomerating a dry powder medicament or a dry powder composition of medicament and a suitable carrier.




BACKGROUND OF THE INVENTION




Metered dose medicament inhalers are well known for dispensing medicament to the lungs of a patient. Some previous inhalers have comprised a pressurized aerosol dispensing container, wherein the aerosols contain gas propellants in which the powdered medicament is suspended. Upon actuation, the aerosol contents are expelled, through a metering valve, and into the lungs of the patient. However, it is now known that some aerosol propellants, including those used in metered dose inhalers, can cause depletion of the ozone layer in the atmosphere. In addition, such aerosol systems are not suitable for all patients.




Several types of non-aerosol, breath actuated dry powder inhalers have therefore been provided. For example, U.S. Pat. No. 5,503,144 to Bacon, which is assigned to the assignee of the present disclosure and incorporated herein by reference, shows a breath-actuated dry-powder inhaler. The device includes a dry powder reservoir for containing a dry powdered medicament, a metering chamber for removal of the powdered medicament from the reservoir in discrete amounts, and an air inlet for entraining the removed powdered medicament through a mouth piece upon patient inhalation.




Regardless of whether an aerosol or non-aerosol inhaler is used, it is of utmost importance that particles of the dispensed dry powder medicament be small enough to ensure the adequate penetration of the medicament into the bronchial region of a patient's lungs during inhalation. However, because the dry powder medicament is composed of very small particles, and often provided in a composition including a carrier such as lactose, non-defined agglomerates or aggregates of the medicament form at random prior to being dispensed. It has therefore been found preferably to provide breath-actuated dry powder inhalers with means for breaking down the agglomerates of medicament or medicament and carrier before inhalation of the medicament.




Accordingly, there is desired an improved dry powder inhaler and, in particular, an improved breath-actuated dry powder inhaler. There is also desired a de-agglomerator for a breath-actuated dry powder inhaler and method for breaking down agglomerates of medicament, or medicament and carrier, before inhalation of the medicament by a patient.




SUMMARY OF THE INVENTION




The present disclosure accordingly provides a de-agglomerator for use with a breath-actuated dry powder inhaler for breaking up aggregates and micronizing particles of dry powder prior to inhalation of the powder by a patient. The de-agglomerator includes an inner wall defining a swirl chamber extending along an axis from a first end to a second end, a dry powder supply port, an inlet port, and an outlet port.




The supply port is in the first end of the swirl chamber for providing fluid communication between a dry powder delivery passageway of an inhaler and the first end of the swirl chamber. The inlet port is in the inner wall of the swirl chamber adjacent to the first end of the swirl chamber and provides fluid communication between a region exterior to the de-agglomerator and the swirl chamber. The outlet port provides fluid communication between the second end of the swirl chamber and a region exterior to the de-agglomerator.




A breath induced low pressure at the outlet port causes air flows into the swirl chamber through the dry powder supply port and the inlet port. The air flows collide with each other and with the wall of the swirl chamber prior to exiting through the outlet port, such that any powder entrained in the air flows is broken down and micronized. The de-agglomerator further includes vanes at the first end of the swirl chamber for creating additional collisions and impacts of entrained powder.




The present disclosure also provides a method of de-agglomerating dry powder from a breath-actuated dry powder inhaler, prior to inhalation of the dry powder by a patient. The method includes directing a first breath-actuated air flow for entraining a dry powder from an inhaler into a first end of a chamber extending longitudinally between the first end and a second end, the first air flow directed in a longitudinal direction.




A second breath-actuated airflow is directed in a substantially transverse direction into the first end of the chamber such that the air flows collide and substantially combine. Then, a portion of the combined air flows is deflected in a substantially longitudinal direction towards a second end of the chamber, and a remaining portion of the combined air flows is directed in a spiral path towards the second end of the chamber. All the combined air flows and any dry powder entrained therein are then delivered from the second end of the chamber to a patient's mouth.




The de-agglomerator and method of de-agglomerating according to the present disclosure, therefore, ensure that particles of dry powder are small enough for adequate penetration of the powder into a bronchial region of a patient's lungs during inhalation of the dry powder by the patient.




Further features and advantages of the presently disclosed de-agglomerator and method of de-agglomerating will become more readily apparent to those having ordinary skill in the art to which the present disclosure relates from the following detailed description and attached drawings.











BRIEF DESCRIPTION OF THE DRAWINGS




So that those having ordinary skill in the art will more readily understand how to construct a de-agglomerator in accordance with the present disclosure, a preferred embodiment is described in detail below with reference to the drawing figures wherein:





FIG. 1

is an exploded isometric view of a de-agglomerator according to the present disclosure;





FIG. 2

is a side elevation view of the de-agglomerator of

FIG. 1

;





FIG. 3

is a top plan view of the de-agglomerator of

FIG. 1

;





FIG. 4

is a bottom plan view of the de-agglomerator of

FIG. 1

;





FIG. 5

is a sectional view of the de-agglomerator of

FIG. 1

taken along line


5





5


of

FIG. 2

; and





FIG. 6

is a sectional view of the de-agglomerator of

FIG. 1

taken along line


6





6


of FIG.


3


.











DESCRIPTION OF THE PREFERRED EMBODIMENT




Referring to

FIGS. 1 through 6

, the present disclosure provides a de-agglomerator


10


for breaking down agglomerates of medicament, or medicament and carrier, before inhalation of the medicament by a patient. Although not shown, the de-agglomerator


10


is for use with a breath-actuated dry powder inhaler including a dry powder delivery passageway and a dry powder reservoir for exposing a predetermined amount of dry powder to the dry powder delivery passageway. Preferably, the dry powder delivery passageway of the inhaler will include a venturi adjacent the dry powder reservoir such that an air flow passing therethrough will entrain dry powder in the reservoir. Examples of breath-actuated dry powder inhalers utilizing the presently disclosed de-agglomerator


10


are shown in co-pending provisional U.S. patent application Ser. No. 60/213,668, filed Jun. 23, 2000 (entitled “Breath-Actuated Dry Powder Inhaler”), provisional U.S. patent application Ser. No. 60/213,669, filed Jun. 23, 2000 (entitled “Pre-Metered Dose Magazine for Breath-Actuated Dry Powder Inhaler”). Both co-pending applications are assigned to the assignee of the present disclosure and have been incorporated herein by reference.




In general, the presently disclosed de-agglomerator


10


includes an inner wall


12


defining a swirl chamber


14


extending along an axis A from a first end


18


to a second end


20


. The swirl chamber


14


includes circular cross-sectional areas arranged transverse to the axis A, that decrease from the first end


18


to the second end


20


of the swirl chamber


14


, such that any air flow traveling from the first end of the swirl chamber to the second end will be constricted and at least in part collide with the inner wall


12


of the chamber. Preferably, the cross-sectional areas of the swirl chamber


14


decrease monotonically. In addition, the inner wall


12


is preferably convex, i.e., arches inwardly towards the axis A, as shown best in FIG.


6


.




As shown in

FIGS. 1

,


3


and


6


, the de-agglomerator


10


also includes a dry powder supply port


22


in the first end


18


of the swirl chamber


14


for providing fluid communication between a dry powder delivery passageway of an inhaler and the first end


18


of the swirl chamber


14


. Preferably, the dry powder supply port


22


faces in a direction substantially parallel with the axis A such that an air flow, illustrated by arrow


1


in

FIG. 6

, entering the chamber


14


through the supply port


22


is at least initially directed parallel with respect to the axis A of the chamber.




Referring to

FIGS. 1 through 6

, the de-agglomerator


10


additionally includes at least one inlet port


24


in the inner wall


12


of the swirl chamber


14


adjacent to or near the first end


18


of the chamber providing fluid communication between a region exterior to the de-agglomerator and the first end


18


of the swirl chamber


14


. Preferably, the at least one inlet port comprises two diametrically opposed inlet ports


24


,


25


that extend in a direction substantially transverse to the axis A and substantially tangential to the circular cross-section of the swirl chamber


14


. As a result, air flows, illustrated by arrows


2


and


3


in

FIGS. 1 and 5

, entering the chamber


14


through the inlet ports are at least initially directed transverse with respect to the axis A of the chamber and collide with the air flow


1


entering through the supply port


22


to create turbulence. The combined air flows, illustrated by arrow


4


in

FIGS. 5 and 6

, then collide with the inner wall


12


of the chamber


14


, form a vortex, and create additional turbulence as they move towards the second end


20


of the chamber.




Referring to

FIGS. 1-3

and


6


, the de-agglomerator


10


includes vanes


26


at the first end


18


of the swirl chamber


14


extending at least in part radially outwardly from the axis A of the chamber. Each of the vanes


26


has an oblique surface


28


facing at least in part in a direction transverse to the axis A of the chamber. The vanes


26


are sized such that at least a portion


4


A of the combined air flows


4


collide with the oblique surfaces


28


, as shown in FIG.


6


. Preferably, the vanes comprise four vanes


26


, each extending between a hub


30


aligned with the axis A and the wall


12


of the swirl chamber


14


.




As shown in

FIGS. 1 through 6

, the de-agglomerator


10


further includes an outlet port


32


providing fluid communication between the second end


20


of the swirl chamber


14


and a region exterior to the de-agglomerator. The outlet port


32


acts as a mouthpiece for a patient using an inhaler incorporating the de-agglomerator


10


. A breath induced low pressure at the outlet port


32


causes the air flow


1


through the supply port


22


and the air flows


2


,


3


through the inlet ports and draws the combined air flow


4


through the swirl chamber


14


. The combined air flow


4


then exits the de-agglomerator through the outlet port


32


. Preferably the outlet port


32


extends substantially transverse to the axis A, such that the air flow


4


will collide with an inner wall of the outlet port


32


and create further turbulence.




During use of the de-agglomerator


10


in combination with a breath-actuated dry powder inhaler including a dry powder delivery passageway and a dry powder reservoir for exposing a predetermined amount of dry powder to the delivery passageway, patient inhalation at the outlet port


32


causes air flows


1


,


2


,


3


to enter through, respectively, the dry powder supply port


22


and the inlet ports. Although not shown, the air flow


1


through the supply port


22


entrains the dry powder into the swirl chamber


14


. The air flow


1


and entrained dry powder are directed by the supply port


22


into the chamber in a longitudinal direction, while the air flows


2


,


3


from the inlet ports are directed in a transverse direction, such that the air flows collide and substantially combine.




A portion of the combined air flow


4


and the entrained dry powder then collide with the oblique surfaces


28


of the vanes


26


causing particles and any agglomerates of the dry powder to impact against the oblique surfaces and collide with each other. The geometry of the swirl chamber


14


causes the combined air flow


4


and the entrained dry powder to follow a turbulent, spiral path, or vortex, through the chamber. As will be appreciated, the decreasing cross-sections of the swirl chamber


14


continuously changes the direction and increases the velocity of the spiraling combined air flow


4


and entrained dry powder. Thus, particles and any agglomerates of the dry powder constantly impact against the wall


12


of the swirl chamber


14


and collide with each other, resulting in a mutual grinding or shattering action between the particles and agglomerates. In addition, particles and agglomerates deflected off the oblique surfaces


28


of the vanes


26


cause further impacts and collisions. The constant impacts and collisions cause any agglomerates to break into additional particles, and cause the particles to be substantially micronized.




Upon exiting the swirl chamber


14


, the direction of the combined air flow


4


and the entrained dry powder is again changed to a transverse direction with respect to the axis A, through the outlet port


32


. The combined air flow


4


and the entrained dry powder retain a swirl component of the flow, such that the air flow


4


and the entrained dry powder spirally swirls through the outlet port


32


. Since the micronized powder and any remaining agglomerates maintain the swirl imparted from swirl chamber


14


, the swirling flow causes additional impacts in the outlet port


32


so as to result in further breaking up of any remaining agglomerates prior to being inhaled by a patient.




The de-agglomerator according to the present disclosure, therefore, ensures that particles of the dry powder are small enough for adequate penetration of the powder into a bronchial region of a patient's lungs during inhalation.




As shown in

FIGS. 1 through 6

, the de-agglomerator is preferably assembly from two pieces: a cup-like base


40


and a cover


42


. The base


40


and the cover


42


are connected to form the swirl chamber


14


. The cup-like base


40


includes the wall


12


and the second end


20


of the chamber and defines the outlet port


32


. The base


40


also includes the inlet ports of the swirl chamber


14


. The cover


42


forms the vanes


26


and defines the supply port


22


.




The base


40


and the cover


42


of the de-agglomerator are preferably manufactured from a plastic such as polypropylene, acetal or moulded polystyrene, but may be manufactured from metal or another suitable material. Preferably, the cover


42


includes an anti-static additive, so that dry powder will not cling to the vanes


26


. The base


40


and the cover


42


are then connected in a manner that provides an air tight seal between the parts. For this purpose heat or cold sealing, laser welding or ultra sonic welding could be used, for example.




It should be understood that the foregoing detailed description and preferred embodiment is only illustrative of de-agglomerator according to the present disclosure. Various alternatives and modifications to the presently disclosed de-agglomerator can be devised by those skilled in the art without departing from the spirit and scope of the present disclosure. For example, the de-agglomerator can be provided as a single piece through blow molding. In addition, the de-aggregator can be modified to be used with any inhaler and, in particular, any breath-actuated dry powder inhaler. Accordingly, the present disclosure is intended to embrace all such alternatives and modifications that fall within the spirit and scope of a de-agglomerator and a method of de-agglomerating as recited in the appended claims.



Claims
  • 1. A de-agglomerator for use with a breath-actuated dry powder inhaler including a dry powder delivery passageway and a dry powder reservoir for exposing a predetermined amount of dry powder to the dry powder delivery passageway, the de-agglomerator comprising:an inner wall defining a swirl chamber extending along a longitudinal axis from a first end to a second end; a dry powder supply port in the first end of the swirl chamber for providing fluid communication between a dry powder delivery passageway of an inhaler and the first end of the swirl chamber; at least one inlet port in the inner wall of the swirl chamber adjacent to the first end of the swirl chamber providing fluid communication between a region exterior to the de-agglomerator and the first end of the swirl chamber, wherein the at least one inlet port extends in a direction substantially transverse to the axis, an outlet port providing fluid communication between the second end of the swirl chamber and a region exterior to the de-agglomerator; and vanes non-rotationally fixedly attached to at the first end of the swirl chamber extending at least in part radially outwardly from the axis of the chamber, each of the vanes having an oblique surface facing at least in part in a direction transverse to the axis; whereby a breath induced low pressure at the outlet port causes air flows into the swirl chamber through the dry powder supply port and the inlet port.
  • 2. A de-agglomerator according to claim 1, wherein the vanes comprise four vanes extending from a hub aligned with the axis to the wall of the swirl chamber.
  • 3. A de-agglomerator according to claim 1, wherein the swirl chamber includes cross-sectional areas arranged transverse to the axis, the cross-sectional areas decreasing from the first end to the second end of the swirl chamber.
  • 4. A de-agglomerator according to claim 3, wherein the cross-sectional areas of the swirl chamber decrease monotonically.
  • 5. A de-agglomerator according to claim 1, wherein the inner wall of the swirl chamber is convex.
  • 6. A de-agglomerator according to claim 1, wherein the dry powder supply port faces in a direction substantially parallel to the axis.
  • 7. A de-agglomerator according to claim 1, wherein the outlet port extends substantially transverse to the axis.
  • 8. A de-agglomerator according to claim 1, wherein the swirl chamber includes generally circular cross-sectional areas coaxially arranged about the axis, and the at least one inlet port extends substantially tangential to the circular cross-sectional areas.
  • 9. A de-agglomerator according to claim 8, wherein the at least one inlet port comprises two diametrically opposed inlet ports.
  • 10. A de-agglomerator according to claim 1, wherein the vanes include an anti-static additive.
  • 11. A de-agglomerator according to claim 1, assembled from a cup-like base closed with a cover, wherein the base defines the inner wall, the second end of the chamber and the outlet port, the cover defines the first end of the chamber, the vanes and the supply port, and the inlet port is defined by both the base and the cover.
  • 12. A breath-actuated dry powder inhaler including a de-agglomerator according to claim 1, and further comprising:a dry powder delivery passageway providing fluid communication between a region exterior to the inhaler and the dry powder supply port of the de-agglomerator; and a dry powder reservoir for exposing a predetermined amount of dry powder to the dry powder delivery passageway; whereby an air flow through the dry powder delivery passageway and the dry powder supply port will entrain dry powder from the dry powder reservoir into the swirl chamber.
  • 13. An inhaler according to claim 12, wherein the dry powder delivery passageway includes a venturi adjacent the dry powder reservoir.
  • 14. An inhaler according to claim 12, further including dry powder in the dry powder reservoir.
  • 15. An inhaler according to claim 12, wherein the dry powder comprises a medicament composition having at least one active agent medicament adhered to a particulate carrier.
CROSS-REFERENCE TO RELATED APPLICATIONS

The present application claims priority to co-pending provisional U.S. patent application Ser. No. 60/213,668, filed Jun. 23, 2000 (entitled “Breath-Actuated Dry Powder Inhaler”), provisional U.S. patent application Ser. No. 60/213,667, filed Jun. 23, 2000 (entitled “Pre-Metered Dose Magazine for Breath-Actuated Dry Powder Inhaler”), and co-pending provisional U.S. patent application Ser. No. 60/213,382, filed Jun. 23, 2000 (entitled “De-Agglomerator for Breath-Actuated Dry Powder Inhaler”). Each of these co-pending applications is assigned to the assignee of the present disclosure and incorporated herein by reference.

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Provisional Applications (3)
Number Date Country
60/213668 Jun 2000 US
60/213667 Jun 2000 US
60/213382 Jun 2000 US