Patent Grant
11033692
Inhaling powder nicotine has become an effective and popular way to deliver nicotine to the bloodstream while reducing the hazardous effects of smoking. Unpleasant odors and the hazardous effects of second hand smoke are just some of the effects that can be avoided by using a dry powder inhaler over a traditional cigarette. Conventional dry powder nicotine formulations may be substantially flavorless, or otherwise have a subtle or consequential flavor that may not be desired by the user. In addition, some users may prefer to introduce a particular flavor or a generally appealing that will taste pleasant during inhalation.
It is known in the art that flavored particles can be mixed into a dry powder formulation and inhalation device as a composition with the active ingredient, such that the flavored element aerosolizes with the active ingredient during inhalation for a more pleasant taste (see for example P.C.T. Publication No. WO 2013133903 to Kamler et al. and U.S. Patent Publication No. 2007/0267032 to Shan). However, once a particular flavor is pre-mixed with the active ingredient, the user cannot switch to a different flavor without replacing the entire mixture, potentially wasting the medicament. Likewise, if the user wants to switch to a flavorless taste, the same wasteful result would occur since the flavored elements cannot be later removed from the active ingredient.
Further, a typical smoker often experiences an increase in coughing. Coughing is a reflex triggered in order to clear the airways of secretions and particulates (Polverino et al., Multidiscip Respir Med. 2012; 7(1): 5). Among other causes, coughing can be triggered by mechanical or chemical stimulants on cough receptors found in various parts of the human airways such as trachea, branching points of large airways, pharynx and larynx. At a minimum, coughing can be an unpleasant side effect which the smoker may negatively associate with a nicotine formulation, or smoking cessation treatment. But at the same time, coughing may also render a treatment ineffective by expelling inhaled nicotine formulation particles outside of the airways. An effective formulation for the treatment of nicotine addiction should ideally be able to deliver to the airways of the smoker enough of a nicotine formulation in a form and concentration that will mimic the effects of cigarette smoking, while at the same time controlling and suppressing the coughing reflex.
Menthol is a known and widely used topical analgesic, decongestant and cough suppressant. Almost all cigarettes contain menthol in order to adjust flavoring and reduce coughing. When the menthol concentration in cigarettes exceeds 3%, then it is labeled as a menthol cigarette. Methods of using menthol in cigarettes include addition to the tobacco leaf. A plastic ball filled with menthol can be stored in the filter of a cigarette, and then crushed prior to smoking the cigarette. Upon lighting up the cigarette, the heated smoke acts to volatilize and carry the menthol into the airways of the smoker.
But adding menthol to dry powder formulations of nicotine raises several challenges in terms of the effectiveness of the final product. Of particular interest is the effectiveness of menthol in reaching the cough receptors of the smoker. If the menthol particles hit a lesser number of receptors than the nicotine particles, then the effectiveness of menthol in suppressing cough will be at best attenuated, or even inexistent.
Thus, there is a need in the art for improved devices and methods for optionally incorporating a flavor and/or cough suppressant component via an inhalation device, such that the user has a high level of flexibility and option as to what additional compounds are added or removed during the course of administering all or a portion of the active ingredient. The present invention satisfies this need.
A device for adding a flavor component to an inhaler is described. The device includes a housing having an interior chamber, wherein the housing includes at least one air inlet and at least one air outlet connected to the interior chamber, thereby forming an airflow pathway through the interior chamber, and at least one flavoring component positioned within the interior chamber, wherein the housing is attachable to an exterior surface of an inhaler having at least one air inlet, such that the at least one air outlet of the device aligns with the at least one air inlet of the inhaler to form an airflow path through the device and into the inhaler.
Also described is a dry powder inhaler. The inhaler includes a first housing having a proximal end, a distal end and a length therebetween, wherein the housing defines an internal passage having proximal, intermediate and distal regions along the first housing length, a proximal end opening, a distal end opening and proximal region opening each in connection with the internal passage, a dry powder medicament compartment within the distal region of the internal passage, a powder fluidization and deagglomeration apparatus within the intermediate region of the internal passage, and a second housing having an interior chamber, wherein the second housing includes at least one air inlet and at least one air outlet connected to the interior chamber, thereby forming an airflow pathway through the interior chamber, and at least one flavoring component positioned within the interior chamber, wherein the at least one air outlet of the second housing aligns with the proximal region opening of the first housing when the second housing engages the first housing.
Also described is a method for dry powder inhalation. In certain embodiments, the method includes the steps of providing a dry powder inhaler including a proximal end having a proximal opening, a distal end, and shaft wall extending from the proximal end to the distal end, a first compartment configured to hold a dry powder, a pathway connected to the first compartment by a first opening, the pathway including the proximal opening, and a second opening in the shaft wall connected to the pathway. In certain embodiment, the method provides a housing attachable to the shaft wall and configured to at least partially cover the second opening, the housing having first and second housing openings and at least one flavoring or cough suppressant component. The method may also include the step of generating a negative pressure at the proximal opening such that a portion of the dry powder exits the first compartment and enters the pathway, a portion of the at least one flavoring or cough suppressant component exits the housing and enters the pathway through the second opening, and the portion of the dry powder and the portion of the at least one flavoring or cough suppressant mix in an airflow generated by the negative pressure.
The foregoing purposes and features, as well as other purposes and features, will become apparent with reference to the description and accompanying figures below, which are included to provide an understanding of the invention and constitute a part of the specification, in which like numerals represent like elements, and in which:
The present invention can be understood more readily by reference to the following detailed description, the examples included therein, and to the Figures and their following description. The drawings, which are not necessarily to scale, depict selected embodiments and are not intended to limit the scope of the invention. The detailed description illustrates by way of example, not by way of limitation, the principles of the invention. The skilled artisan will readily appreciate that the devices and methods described herein are merely examples and that variations can be made without departing from the spirit and scope of the invention. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting. It is to be understood that the figures and descriptions of the present invention have been simplified to illustrate elements that are relevant for a more clear comprehension of the present invention, while eliminating, for the purpose of clarity, many other elements found in systems and methods of providing flavoring and/or cough suppressant compounds for an inhalation device. Those of ordinary skill in the art may recognize that other elements and/or steps are desirable and/or required in implementing the present invention. However, because such elements and steps are well known in the art, and because they do not facilitate a better understanding of the present invention, a discussion of such elements and steps is not provided herein. The disclosure herein is directed to all such variations and modifications to such elements and methods known to those skilled in the art.
Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Although any methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, the preferred methods and materials are described.
As used herein, each of the following terms has the meaning associated with it in this section.
The articles “a” and “an” are used herein to refer to one or to more than one (i.e., to at least one) of the grammatical object of the article. By way of example, “an element” means one element or more than one element.
“About” as used herein when referring to a measurable value such as an amount, a temporal duration, and the like, is meant to encompass variations of ±20%, ±10%, ±5%, ±1%, and ±0.1% from the specified value, as such variations are appropriate.
As used herein, the term “dry powder” refers to a fine particulate composition that is not suspended or dissolved in a propellant, carrier, or other liquid, and it is not meant to necessarily imply a complete absence of all water molecules.
Unless stated otherwise, the described size or size range of a particle should be considered as the mass median aerodynamic diameter (MMAD) of the particle or set of particles. Such values are based on the distribution of the aerodynamic particle diameters defined as the diameter of a sphere with a density of 1 gm/cm3 that has the same aerodynamic behavior as the particle which is being characterized. Because the particles described herein may be in a variety of densities and shapes, the size of the particles is expressed as the MMAD and not the actual diameter of the particles.
Ranges: throughout this disclosure, various aspects of the invention can be presented in a range format. It should be understood that the description in range format is merely for convenience and brevity and should not be construed as an inflexible limitation on the scope of the invention. Where appropriate, the description of a range should be considered to have specifically disclosed all the possible subranges as well as individual numerical values within that range. For example, description of a range such as from 1 to 6 should be considered to have specifically disclosed subranges such as from 1 to 3, from 1 to 4, from 1 to 5, from 2 to 4, from 2 to 6, from 3 to 6 etc., as well as individual numbers within that range, for example, 1, 2, 2.7, 3, 4, 5, 5.3, and 6. This applies regardless of the breadth of the range.
Referring now in detail to the drawings, in which like reference numerals indicate like parts or elements throughout the several views, in various embodiments, presented herein is a flavoring and/or cough suppressant compartment suitable for use in conjunction with an inhalation device, such as may be used for inhalation of nicotine based formulations.
With reference to
When a negative pressure is applied to the proximal passage 22 of the MP, air is pulled from the external environment 5 through opening 17 at the distal end 16 of device 10 and past the capsule 50 or other powder reservoir into internal chamber 26 of device 10. This air is then further pulled through an opening 32 within wall 30 of the PFD housing and into internal chamber 24 of the PFD. A portion of the air entering the chamber 24 via chamber opening 32 flows directly towards the proximal opening 11, forming a primary airflow. Additionally, the low pressure area at the distal end of internal chamber 24 creates a secondary airflow directed towards this distal end region of internal chamber 24. The decreasing cross-sectional area of chamber 24 in the distal direction causes a burst of secondary airflow which enters the pierced capsule and scours the surface of powder in the capsule, entraining a small portion of powder before rejoining the primary airflow traveling proximally towards opening 11 for inhalation by the user. Alternatively, instead of (or in addition to) opening 32, PFD housing wall 30 may include any shape or geometry suitable for generating an air passage or hole within the capsule wall when punctured, such that air may flow directly from chamber 26 into the capsule. Device 10 can be used to inhale a dry powder formulation that is positioned directly into a powder reservoir chamber, or that is contained within a capsule or other separate packaging that can be placed within device 10.
An opening 40 in the housing wall 20 of the MP opens into passage 22 provides a passageway between the proximal passage 22 and the external environment 5. Accordingly, in one embodiment, the opening 40 (or CA) can serve as a chase airflow pathway, such that the velocity of the airborne powder particles drawn into the MP by the PFD can be increased and delivered deep into the lungs, instead of settling in the MP and user's mouth.
In certain embodiments, the inhalation devices described herein may be used to deliver a medicament, such as dry powder formulations of nicotine, and optionally other selected materials contained within a storage chamber, such as a capsule. For example, in one embodiment, the formulation includes nicotine particles (also referred to herein as the nicotine-based component) sized substantially between 1-10 microns, based on the MMD of the particles.
Further included is a detachable compartment 60 suitable for containing at least one flavoring and/or cough suppressant component therein, as shown in isolation in
Flavoring and/or cough suppressant component 70 may be a loose composition, such as a powder, or it may be a liquid composition within a pad or wick, such that at least a portion of the liquid composition may go through a phase transition to form a vapor within chamber 68. It should be appreciated that there is no limitation to the type of flavoring and/or cough suppressant component, to the containment mechanism of the flavoring and/or cough suppressant component, or to the release of any portion of the flavoring and/or cough suppressant component within chamber 68.
In another embodiment, component 70 may be or include a flavor component. In one embodiment, the flavor component is menthol. In another embodiment, the flavor component is vanilla. In other embodiments, the flavor component may include tobacco, fruit flavors, or food grade flavorings used in candy or baking. It should be appreciated that the flavor compound may be any flavoring compound known in the art, preferably a regulatory-approved flavoring compound. This flavor component may impact the subject in the oral cavity during use of the devices described herein to produce a desired flavor, as the flavor component particles may be limited in their ability to enter into the subject's lungs.
In one embodiment, component 70 may be or include a cough suppressant component. In one embodiment, the cough suppressant component is menthol. In another embodiment, the cough suppressant component may include benzocaine. It should be appreciated that the cough suppressant component can include any compound approved for suppressing cough. In embodiments where the component is menthol, cough may be reduced by soothing irritation in the subject's upper airways via menthol particles contacting the upper airways of the subject when inhaled via the devices described herein. In another embodiment, the cough suppressant component may also reduce a cough caused by irritation of the oro-pharynx, the glottis vocal cords and other anatomic regions more proximal or closer to the mouth that contain receptors that can trigger cough or trigger other unwanted sensations. As contemplated herein, the cough suppressant component may be formulated such that it is substantially prohibited from entering the sub-glottic airways. It should be appreciated that the cough suppressant component may act to dilute the medicament component and decrease cough caused by nicotine irritating the oro-pharynx, vocal cords and other anatomic regions proximal to the trachea.
Accordingly, the devices and methods presented herein represent a novel product and approach to delivery of dry powder nicotine-based formulations with optional or customized flavoring and/or cough suppressant components. Unlike existing technologies which do not separate or segregate material components according to size, composition or other parameter, the present invention selectively controls the combination of components delivered to the subject at the time of use according to user selection. Accordingly, a unique and superior product is presented that delivers respirable nicotine to the alveoli and small airways while optionally delivering a cough suppressant to the larger airways and/or the oro-pharynx, as well as optionally delivering flavor particles to the oral cavity.
In the exemplary embodiment shown in
During inhalation, airflow along flow path 80 passes across the flavoring and/or cough suppressant component 70, such that at least a portion of the flavoring and/or cough suppressant component (either as a vapor or other particle) is released into chamber 68 and pulled into proximal passage 22 during inhalation at the mouthpiece opening 11. Accordingly, when device 10 also has a capsule 50 engaged by the PFD, the medicament within capsule 50 is drawn into proximal passage 22, admixed with the flavoring and/or cough suppressant component 70 drawn from compartment 60, and delivered to the patient as a mix of medicament and flavoring and/or cough suppressant component. It should be appreciated that the flavoring and/or cough suppressant component may be delivered in this manner either as a mix with the medicament, as described above, or it may be delivered separately from the medicament, such as shortly before medicament delivery or shortly after medicament delivery, as desired by the subject.
In certain embodiments, a single flavoring and/or cough suppressant component 70 is shaped to form a position distally, proximally, adjacent, or above opening 40 or device 10. In alternative embodiments, multiple flavoring and/or cough suppressant components 70 can be utilized for placement at various positions near opening 40. In the exemplary embodiment of
In still other embodiments, the compartment 60 may take the form of an insertable column, as shown in
In further embodiments, the flavoring and/or cough suppressant compartment may be engaged with the distal opening 17 of device 10. Accordingly, the flavoring and/or cough suppressant component 70 may be drawn into the same flow of air prior to entrainment of the medicament powder within capsule 50.
As would be appreciated by those having ordinary skill in the art, embodiments of the invention have applications that may extend beyond dry powder inhalers. For instance, vapor-type cigarettes and diagnostic inhalation systems such as bronchial provocation devices can also benefit from the invention as described throughout the embodiments.
An exemplary method for dry powder inhalation is as follows. In certain embodiments, the method includes the steps of providing a dry powder inhaler including a proximal end having a proximal opening, a distal end, and shaft wall extending from the proximal end to the distal end, a first compartment configured to hold a dry powder, a pathway connected to the first compartment by a first opening, the pathway including the proximal opening, and a second opening in the shaft wall connected to the pathway. In certain embodiment, the method provides a housing attachable to the shaft wall and configured to at least partially cover the second opening, the housing having first and second housing openings and at least one flavoring or cough suppressant component. The method may also include the step of generating a negative pressure at the proximal opening such that a portion of the dry powder exits the first compartment and enters the pathway, a portion of the at least one flavoring or cough suppressant component exits the housing and enters the pathway through the second opening, and the portion of the dry powder and the portion of the at least one flavoring or cough suppressant mix in an airflow generated by the negative pressure. In certain embodiments the dry powder comprises nicotine. Other medicaments could also be utilized. In certain embodiments, the negative pressure is generated by a user inhalation, although it could also be generated by a machine, such as in a diagnostic device. The housing is attachable and detachable to the shaft wall, thus, in certain embodiments, the method includes the step of detaching the housing from the shaft wall, and generating a second user inhalation generating an airflow comprising the dry powder. The user could optionally reattach the housing and generate a third user inhalation, or alternatively generate a third inhalation without reattaching the housing, depending on their preference for the flavor or cough suppressant. In certain embodiments, the portion of the dry powder and the portion of the at least one flavoring or cough suppressant mix at least partially within the pathway. In certain embodiments, the portion of the dry powder and the portion of the at least one flavoring or cough suppressant mix at least partially after exiting the proximal opening. In certain embodiments, they mix both before and after leaving the proximal opening, as part of a general mixing process in the airstream. In certain embodiment, the flavoring or cough suppressant component is a liquid contained within a wick positioned within the housing, either partially or fully. In certain embodiments, the flavoring or cough suppressant component comprises menthol.
The disclosures of each and every patent, patent application, and publication cited herein are hereby incorporated herein by reference in their entirety. While this invention has been disclosed with reference to specific embodiments, it is apparent that other embodiments and variations of this invention may be devised by others skilled in the art without departing from the true spirit and scope of the invention.
This application is a national stage entry of PCT/US16/27255 filed on Apr. 13, 2016, which claims priority to U.S. provisional application No. 62/148,030 filed on Apr. 15, 2015 both of which are incorporated herein by reference in their entireties.
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