NZ747468A - Nicotine particle delivery consumable - Google Patents

Abstract

nicotine particle delivery consumable article includes a receptacle having a body extending from a receptacle first end to an opposing receptacle second end and defining a cavity. A capsule is disposed within the cavity. The capsule contains particles including nicotine. The receptacle includes a membrane sealing the receptacle first end and an air outlet extending through the receptacle second end and into the cavity. An air inlet, close to the receptacle first end, extends through a side wall of the body and into the cavity. membrane sealing the receptacle first end and an air outlet extending through the receptacle second end and into the cavity. An air inlet, close to the receptacle first end, extends through a side wall of the body and into the cavity.

Description

PCT/18201 46 NICOTINE PARTICLE DELIVERY CONSUMABLE This disclosure relates to an article that includes a receptacle containing a capsule containing nicotine particles. The e may rotate about a longitudinal axis when air flows through the receptacle.

Nicotine particle inhalers are not always suitable to provide nicotine particles to the lungs at inhalation or air flow rates that are within conventional g regime inhalation or air flow rates. Nicotine particle inhalers do not always include nicotine particle consumable which is easily replaceable once consumed.

It is desirable to provide an article that contains a capsule holding nicotine particles that may be a modular component of an inhaler and be easily replaceable once consumed. It is desirable that the e facilitates ry of nicotine particles to the consumer at tional smoking regime inhalation or air flow rates. The consumable article may alleviate one or more of the above mentioned problems.

This disclosure is directed to an e comprising a receptacle and a capsule disposed in a cavity of the receptacle. The e contains particles comprising nicotine. The receptacle includes a body extending from a receptacle first end to an opposing receptacle second end and defining a cavity. A membrane seals the acle first end. An air outlet extends through the receptacle second end into the . An air inlet extends through a side wall of the body and into the cavity. The air inlet is closer to the receptacle first end than the acle second end.

Airflow management through the receptacle preferably causes the capsule to rotate and release nicotine particles (once pierced) into the airflow. The receptacle may be sealed or air- tight prior to ption or insertion into an inhaler device.

Preferably, the article is suitable to be used in a nicotine particle r. The article may be a modular component of a multi-use nicotine particle inhaler. The article may be easily replaceable within the multi-use inhaler. Once consumed, the article may be removed from the PCT/18201 7/053546 multi-use inhaler and ded. The acle may be sealed prior to ion into the inhaler to preserve the e within the receptacle.

Advantageously, the article described herein provides a r component approach when ed with a re-usable or multi-use inhaler. The article may be sealed or air-tight prior to consumption or insertion into an inhaler device. Airflow management through the receptacle may cause the capsule to rotate during inhalation and ption. This rotation may suspend and aerosolize the nicotine particles in the inhalation air moving through the article. The capsule may also comprise flavour particles. These flavour particles may be larger than the nicotine particles and assist in transporting the nicotine particles into the lungs of the user while the flavour particles preferentially remain in the mouth or buccal cavity of the user.

The term “nicotine" refers to nicotine and nicotine derivatives such as ase nicotine, nicotine salts and the like.

The term “‘flavourant” or “flavour" refers to leptic compounds. compositions, or materials that alter and are intended to alter the taste or aroma characteristics of ne during consumption or inhalation thereof. The term “flavourant” or “flavour” preferably refers to compounds disclosed in the Flavor & Extract Manufacturers Association (FEMA) Flavor Ingredient Library and in particular in the GRAS Flavoring Substances publications 3 to 27, for example. see Hall, R.L. & Oser, B.L., Food Technology, ry 1965 pg 151-197, and in the GRAS flavoring substances 27 SM. Cohen et al.. Food Technology Aug. 2015 pg. 40-59, and intervening GRAS Flavoring Substances publications 4 to 26. For the purpose of this disclosure, nicotine is not considered as a flavourant or flavour.

The size of a le, stated herein, preferably refers to the aerodynamic diameter of the particle. The aerodynamic diameter of the particles is preferably measured with a cascade impactor.

The nicotine particle delivery consumable or article described herein may be combined with an inhaler or dry powder r to deliver the nicotine particles to a consumer. A plurality of these articles may be combined with an inhaler to form a kit. The nicotine particles may be PCT/18201 46 red with the inhaler at inhalation or air flow rates that are within conventional smoking regime inhalation or airflow rates.

An inhaler article may include an inhaler body extending between a mouthpiece portion and a distal end portion. An inhaler receptacle cavity may be defined within the inhaler body between the mouthpiece portion and the distal end portion. The article (nicotine particle delivery consumable) may define an outer surface that mates with the inhaler receptacle cavity. A consumer may access the inhaler receptacle cavity to insert the article into the inhaler receptacle cavity or replace a depleted article (nicotine particles delivered to the consumer) with a full or un-used e into the inhaler receptacle cavity. 1O An air inlet may extend through a side wall of the inhaler body and into the inhaler receptacle cavity. A mouthpiece air channel is fluidly connected to the inhaler receptacle cavity and a proximal end of the mouthpiece. The air inlet or air inlets that extend h the inhaler body may mate or align with the air inlet or air inlets that extend through the sidewall of the article placed into the inhaler acle cavity. The article air outlet extending thought the receptacle second end may mate or align with the iece air channel of the inhaler body.

Once the article is placed into the inhaler receptacle cavity. air may flow through the article from the air inlet through the cavity and through the air outlet onto the mouthpiece air l.

The inhaler body may resemble a smoking article or cigarette in size and shape.

The article includes a receptacle defining a cavity. A capsule is ed within the cavity. The receptacle is configured to n the capsule within the cavity. The cavity may have a ar cross-section extending along at least a portion of the cavity length. The cavity may have a central axis or centroid longitudinal axis. Preferably the cavity has a shape r to the shape of the capsule. The cavity may have a circular cross-sectional shape and a first diameter and the capsule may have a second diameter that is less than the first diameter. The second diameter may be in a range from about 80% to about 99% of the first diameter. or the second diameter may be in a range from about 90% to about 98% of the first diameter.

The article receptacle includes a acle second end that is configured to contain the capsule and prevent the capsule from passing through the receptacle second end. The receptacle second end may be d by a lateral wall integral with the body of the receptacle.

PCT/18201 7/053546 The receptacle second end may be defined by an end cap that is fixed to the body of the receptacle. One or more air s may extend through the receptacle second end to allow air to flow from the article cavity to the exterior of the article.

A membrane may seal the receptacle first end. The capsule may be placed into the cavity of the receptacle through an open first end and then the membrane may seal the open first end to retain the capsule within the cavity of the article. The membrane may form a hermetic or airtight seal or barrier.

The membrane may be formed of a pierce-able material. The inhaler may include a ng element that passes through the membrane and puncture the capsule within the acle. The membrane may re-seal once the piercing element is retracted from the membrane. Re-sealable membranes may include a septum-like element. lable membranes may be formed of elastic material such as rubber, ne, metal foil co—laminated with a polymer, or latex and the like. Alternatively, the membrane may not re-seal once the piercing element is retracted from the membrane. The membranes may not re-seal and include metal foil, for e.

An air inlet may extend h a side wall of the receptacle body and into the cavity.

The cavity may have a length in a range from about 15 mm to about 25 mm or from about 20 mm to about 24 mm. The cavity may have an inner diameter in a range from about 5 mm to about 10 mm or from about 6 mm to about 8 mm. The cavity may have a length of about 20 mm and an inner diameter of about 6.6 mm when containing a capsule size 3 flat. The cavity may have a length of about 24 mm and an inner diameter of about 7.7 mm when ning a capsule size 1 flat.

The air inlet may be closer to the receptacle first end than the receptacle second end.

The air inlet may be located within about 30%. or about 25%, or about 20%, or about 15%, or about 10% of the total length from the receptacle first end. The air inlet may be located within about 5 mm or within about 4 mm or within about 3 mm or within about 2 mm of the receptacle first end. The air inlet may be located from about 1 mm to about 5 mm of the receptacle first end or from about 2 mm to about 4 mm of the receptacle first end.

PCT/18201 7/053546 The air inlet may be off-set from the id longitudinal (central) axis of the acle cavity or capsule contained within the cavity. The off-set air inlet s the capsule to rotate or spin within the receptacle during inhalation by the consumer. The air inlet may be off-set from the longitudinal (central) axis of the capsule or receptacle cavity by about 1 mm or about 2 mm or about 3 mm or about 4 mm where the cavity may have an inner diameter of about 5 mm to about 10 mm or from about 6 mm to about 8 mm. The one or more air inlets may have a diameter from about 0.5 to about 1.5 mm or about 0.7 mm to about 0.9 mm. Preferably, the air inlet directs air tangentially to the outer diameter of the capsule contained within the receptacle.

The article receptacle preferably has a circular cross-sectional shape extending (a length 1O distance) along its central axis and forming a cylindrical acle. Preferably the receptacle defines a right ar cylinder with a radius and having a length extending along a central axis.

The air inlet may enter the receptacle tially to the cylindrical receptacle. Two or more air inlets enter the acle cavity tangentially to the cylindrical receptacle. Preferably these air inlets oppose each other and a first air inlet directs air tangentially to the cylindrical receptacle in a first direction and the second air inlet directs air tangentially to the cylindrical receptacle in a second direction that opposes or is in the opposite direction as the first direction. These opposing air inlets may direct inhalation air at ng sides of the capsule contained within the receptacle promoting the on of the capsule contained within the receptacle.

The capsule may be sealed within the article prior to ption or placement into an inhaler. The article may be contained within a sealed or airtight ner or bag. The article may include one or more peelable seal layers to cover the one or more air inlets or one or more air outlets on the article. An air outlet seal layer may be disposed on the air outlet. This seal layer may be configured to be punctured or be peelable to expose the air outlet. An air inlet seal layer may be disposed on the air inlet. This seal layer may be configured to be punctured or be peelable to expose the air inlet. The inhaler may e air inlet piercing element or an air outlet piercing element that are configured to puncture one or both of these seal layers upon insertion of the article into the r or upon activation of the inhaler.

The capsule is configured to rotate about its' longitudinal or central axis when air flows through the article (from the air inlet through the receptacle to the air outlet). The capsule may be formed of an airtight material that may be pierced or punctured by a piercing element that PCT/18201 7/053546 may form part of the inhaler. The capsule may formed of a metallic or polymeric material that serves to keep contaminates out of the capsule but may be pierced or punctured by a piercing element prior to consumption of the nicotine particles within the capsule. Preferably, the capsule is formed of a polymer material. The polymer al may be hydroxypropylmethylcellulose (HPMC). Preferably, the capsule is a size 1 to size 4 or a size 3 capsule.

The e contains the solid ne particles (also referred to as “nicotine powder” or cles comprising nicotine”) and optional flavour les. The capsule may contain a predetermined amount of nicotine particles and optional flavour particles. The capsule may contain enough nicotine particles to provide at least 2 inhalations or “puffs", or at least about 5 inhalations or “puffs", or at least about 10 inhalations or "puffs". Preferably. the capsule may contain enough ne particles to provide from about 5 to 50 inhalations or ”puffs”, or from about 10 to 30 inhalations or "puffs“. Each tion or "puff’ may deliver from about 0.1 mg to about 3 mg of nicotine les to the lungs of the user or from about 0.2 mg to about 2 mg of nicotine particles to the lungs of the user or about 1 mg of nicotine particles to the lungs of the user.

The nicotine particles may have any useful concentration of nicotine based on the particular formulation employed. The nicotine particles may have at least about 5%wt nicotine up to about 30%wt, or from about 5%wt to about 25%wt. or from about 5%wt to about 20%wt, or from about 5%wt to aboUt 15%wt, or from about 7%wt to about 13%wt, nicotine. Preferably, about 50 to about 150 micrograms of nicotine is delivered to the lungs of the user with each "puff”.

The capsule may hold or contain at least about 5 mg of ne particles or at least about 10 mg of nicotine particles. Preferably, the capsule holds or contains less than about 900 mg of nicotine particles, or less than about 300 mg of nicotine particles. or less than 150 mg of nicotine particles. The capsule may hold or contain from about 5 mg to about 300 mg of nicotine particles or from about 10 mg to about 200 mg of nicotine particles.

When flavour particles are d or ed with the nicotine particles within the capsule, the flavour les are present in an amount that provides the desired flavour to each inhalation or "puff’ delivered to the user.

PCT/18201 7/053546 The nicotine les may have any useful size distribution for inhalation delivery preferentially into the lungs of a user. The capsule may include other particles than the nicotine les. The ne particles and the other particles form a powder system.

The capsule may hold or contain at least about 5 mg of a powder system or at least about 10 mg of a powder system. Preferably, the capsule holds or contains less than about 900 mg of a powder system, or less than about 300 mg of a powder system, or less than 150 mg of a powder system. The capsule may hold or contain from about 5 mg to about 300 mg of a powder system or from about 10 mg to about 200 mg of a powder system.

The powder system may have at least about 40% or at least about 60%, or at least about 80%, by weight of the powder system comprised in nicotine particles having a particle size of about 10 etres or less, or 5 micrometers or less, or in a range from about 1 micrometer to about 3 micrometres. ne in the powder system or nicotine particles is preferably a pharrnaceutically acceptable free-base nicotine, or nicotine salt or nicotine salt hydrate. Useful nicotine salts or nicotine salt hydrates include nicotine pyruvate, ne citrate, nicotine aspartate, nicotine lactate, nicotine bitartrate, nicotine salicylate, nicotine fumarate, nicotine mono-pyruvate, nicotine glutamate or nicotine hydrochloride, for example. The compound combining with nicotine to form the salt or salt hydrate may be chosen based on its expected pharmacological effect. For example: nicotine late may be stered for fever relief, as an anti- inflammatory or painkiller; ne fumarate may be administered to treat multiple sclerosis; and nicotine mono-pyruvate may be administered for treating chronic obstructive pulmonary disease (COPD) or for weight loss.

The nicotine particles preferably e an amino acid. Preferably the amino acid is leucine such as, ine. Providing an amino acid such as L-leucine with the les comprising nicotine, may reduce adhesion forces of the particles comprising nicotine and may reduce attraction between nicotine particles and thus reduce agglomeration of nicotine particles.

Similarly, adhesion forces to particles comprising flavour is also reduced thus agglomeration of nicotine particles with flavour particles is also reduced. The powder system PCT/18201 7/053546 described herein thus may be a free flowing material and possess a stable relative particle size of each powder ent even when the nicotine particles and the flavour particles are combined.

Preferably, the nicotine is a surface modified nicotine salt where the nicotine salt particle is a coated or composite particle. A preferred coating or composite material is L-leucine. One particularly useful nicotine particle is ne bitartrate with L-leucine.

The powder system may include flavour particles. The flavour les may have any useful size distribution for inhalation delivery selectively into the mouth or buccal cavity of a user.

The powder system may have at least about 40%, or at least about 60%, or at least about 80%, by weight of the flavour of the powder system comprised in particles having a particle size of about 20 micrometres or greater. The powder system may have at least about 40% or at least about 60%, or at least about 80%. by weight of the flavour of the powder system comprised in particles having a particle size of about 50 micrometres or greater. The powder system may have at least about 40% or at least about 60%, or at least about 80%, by weight of the flavour of the powder system comprised in particles having a particle size in a range from about 50 micrometer to about 150 etres.

Flavourants or flavours may be provided as a solid flavour (at room ature of about 22 degrees centigrade and one atmosphere pressure) and may include flavour formulations. flavour-containing materials and flavour precursors. The ant may include one or more l flavourants. one or more synthetic flavourants. or a combination of natural and synthetic flavourants. Flavourants as described herein are organoleptic compounds, compositions, or materials that are selected and utilized to alter or are intended to alter the taste or aroma characteristics of the nicotine component during consumption or inhalation thereof.

Flavourants or flavours refer to a y of flavour materials of natural or synthetic origin.

They include single compounds and mixtures. Preferably the flavour or flavourant has flavour properties that enhance the experience of the nicotine component during consumption.

Preferably. the flavour is chosen to e an experience similar to that ing from smoking 201 7/053546 a combustible smoking article. For example, the flavour or rant may enhance flavour properties such as mouth fullness and complexity. xity is lly known as the overall balance of the flavour being richer without dominating single sensory attributes. Mouth fullness is described as perception of richness and volume in the mouth and throat of the consumer.

Suitable flavours include, but are not limited to, any natural or synthetic flavour, such as tobacco, smoke, l, mint (such as peppermint and speannint), ate, licorice, citrus and other fruit flavours, gamma octalactone, vanillin, ethyl vanillin, breath freshener flavours, spice flavours such as on, methyl salicylate, ol, bergamot oil, geranium oil, lemon oil, and ginger oil, and the like.

Other suitable flavours may include flavour compounds selected from the group consisting of an acid, an alcohol, an ester, an aldehyde, a ketone, a pyrazine, combinations or blends thereof and the like. Suitable flavour compounds may be selected, for example, from the group consisting of phenylacetic acid, solanone, megastigmatrienone, 2-heptanone, benzylalcohol, cishexenyl acetate, valeric acid, valeric aldehyde, ester, terpene, sesquiterpene, nootkatone. maltol, damascenone, pyrazine, lactone, anethole, iso-s valeric acid, combinations f, and the like.

Further specific examples of flavours may be found in the current literature, and are well— known to the person skilled in the art of flavouring, i.e. of imparting an odor or taste to a product.

The flavourant may be a high potency flavourant, and may be used and detected at levels that would result in less than 200 parts per million in inhalation air flow. Examples of such flavourants are key tobacco aroma compounds such as beta-damascenone, 2-ethyl-3,5- dimethylpyrazine, phenylacetaldehyde, guaiacol, and furaneol. Other flavourants may only be sensed by humans at higher concentration levels. These ants, which are referred to herein as the lower potency flavourants, are typically used at levels that results in orders of magnitude higher amounts of flavourant released into the inhalation air. le lower potency ants include, but are not limited to, natural or synthetic menthol, mint, Spearmint, coffee, tea, spices (such as on, clove and ginger), cocoa, vanilla, fruit flavours, chocolate, eucalyptus, geranium, eugenol and linalool.

PCT/18201 7/053546 The particles sing flavour may include a compound to reduce adhesion forces or surface energy and resulting agglomeration. The flavour particle may be surface modified with an on reducing compound to form a coated r particle. One preferred adhesion reducing compound is magnesium te. Providing an adhesion reducing compound such as magnesium stearate with the flavour particle. especially g the flavour particle, s adhesion forces of the particles comprising flavour and may reduce attraction between flavour particles and thus reduce agglomeration of flavour particles. Thus agglomeration of flavour particles with nicotine particles is also reduced. The powder system described herein thus may possess a stable relative particle size of the particles sing nicotine and the particles comprising flavour even when the nicotine les and the flavour particles are combined. The powder system preferably is free flowing.

Conventional formulations for dry powder inhalation typically contain carrier particles that serve to increase the fluidization of the active particles since the active particles may be too small to be influenced by simple w though the inhaler. The powder system may comprise r les. These carrier particles may be a saccharide such as lactose or mannitol that have a particle size greater than about 50 micrometres. The carrier particles may be utilized to improve dose uniformity by acting as a diluent or bulking agent in a formulation.

The powder system utilized with the nicotine powder delivery system described herein may be carrier-free or substantially free of a saccharide such as lactose or mannitol. Being carrier-free or substantially free of a saccharide such as lactose or ol may allow the nicotine and to be inhaled and delivered to the user's lungs at inhalation or airflow rates that are similar to typical smoking regime inhalation or airflow rates. In addition, since the ne is carrier-free or substantially free of a saccharide such as lactose or mannitol, the airflow path of the inhaler may have simple geometry or a simple ration.

The nicotine particles and a flavour may be combined in a single capsule. As described above, the ne particles and a flavour may each have d adhesion forces that result in a stable particle formulation where the particle size of each component does not substantially change when combined. Alternatively, the powder system includes nicotine particles contained within a single capsule and the flavour particles contained within a second capsule.

PCT/18201 7/053546 The nicotine particles and flavour particles may be combined in any useful relative amount so that the flavour particles are detected by the user when consumed with the nicotine particles. Preferably the nicotine particles and a flavour les form at least about 90%wt or at least about 95%wt or at least about 99%wt or 100%wt of the total weight of the powder system.

The nicotine particle delivery consumable (article) and inhaler are less complex and have a simplified storage and airflow path as compared to conventional dry powder inhalers.

Advantageously, rotation of the e within the inhaler aerosolizes the nicotine particles or powder system and may assist in maintaining a free flowing powder. Thus, the inhaler does not e the typical high inhalation rates of conventional inhalers to deliver the nicotine particles described above deep into the lungs.

The inhaler may use a flow rate of less than about 5 Umin or less than about 3 L/min or less than about 2 Umin or about 1.6 L/min. Preferably, the flow rate is in a range from about 1 L/min to about 3 Umin or from about 1.5 Umin to about 2.5 L/min. Preferably, the inhalation rate or flow rate is similar to that of Health Canada smoking , that is, about 1.6 Umin.

The inhaler may be used by a consumer like smoking a conventional cigarette or vaping an electronic cigarette. Such smoking or vaping is characterized by two steps: a first step during which a small volume containing the full amount of ne desired by the consumer is drawn into the mouth cavity, followed by a second step during which this small volume comprising the aerosol comprising the desired amount of ne is further diluted by fresh air and drawn deeper into the lungs. Both steps are controlled by the consumer. During the first tion step the consumer may determine the amount of nicotine to be inhaled. During the second step, the consumer may determine the volume for diluting the first volume to be drawn deeper into the lungs, maximizing the tration of active agent delivered to the aiwvay epithelial surface. This g mechanism is sometimes called "puff»inhale-exhale".

A piercing element, such as a metal or rigid needle, may form a single aperture h the capsule received in the acle. The piercing element may pass through the membrane sealing the receptacle first end.

PCT/18201 7/053546 All ific and technical terms used herein have meanings commonly used in the art unless ise specified. The definitions provided herein are to facilitate understanding of certain terms used frequently herein.

The terms eam” and “downstream" refer to relative positions of elements of the inhaler described in on to the direction of inhalation air flow as it is drawn through the body of the inhaler from a distal end portion to the mouthpiece portion.

As used herein, the singular forms “a , an", and "the" encompass embodiments having plural referents, unless the content clearly dictates othen/vise.

As used herein, “or“ is generally employed in its sense including “and/or” unless the content clearly dictates ise. The term “and/or“ means one or all of the listed elements or a combination of any two or more of the listed elements.

As used herein, “have”, “havingI) u' u , include”, “includingn , comprise", "comprising” or the like are used in their open ended sense, and generally mean “including, but not limited to”. It will be understood that “consisting essentially of", “consisting of“. and the like are subsumed in "comprising,” and the like.

The words rred” and “preferably” refer to embodiments of the invention that may afford certain benefits, under certain circumstances. However, other embodiments may also be preferred. under the same or other circumstances. Furthermore, the recitation of one or more preferred embodiments does not imply that other embodiments are not useful, and is not intended to e other embodiments from the scope of the disclosure, including the claims.

FlG.s 1-2 are perspective schematic diagrams of illustrative nicotine particle delivery ables or articles 100. is a cross-sectional tic diagram of an illustrative nicotine particle delivery consumable or article 100. is a sectional schematic diagram of an illustrative inhaler 200 with a modular article or nicotine particle delivery consumable 100 disposed n.

The schematic drawings are not necessarily to scale and are presented for purposes of illustration and not tion. The drawings depict one or more aspects described in this WO 07887 PCT/l82017/053546 disclosure. r. it will be tood that other s not depicted in the drawing fall within the scope and spirit of this disclosure.

Referring now to and the rative nicotine particle delivery consumable 100 or article and the cross-section of The nicotine particle delivery consumable or article 100 includes a receptacle 110 having a body or sidewall 112 extending from a receptacle first end 111 to an opposing receptacle second end 113 and defining a cavity 116. A capsule 120 is disposed within the cavity 116. The e 120 contains particles comprising nicotine. illustrates the e 120 exploded away from the receptacle 110. The nicotine particle delivery consumable or article 100 may be formed by inserting the capsule 120 into the 1O receptacle 110 and applying the membrane 115 on the receptacle first end 111 to seal the acle first end 111 and retain the capsule 120 within the receptacle 110.

The receptacle 110 includes a lateral wall 114 fixed to or integral with the receptacle body or sidewall 112 and an air outlet 118 extending through the lateral wall 114 and into the cavity 116. A membrane 115 seals the receptacle first end 111. An air inlet 117 extends through the ll 112 or body 112 and into the cavity 116. The air inlet 117 is proximate the receptacle first end 111 or closer to the receptacle first end 111 than the receptacle second end 113. The cavity 116 has a length value L and a diameter value D. The air inlet 117 is proximate the receptacle proximal end 111 a distance L1.

The nicotine particle delivery consumable or article 100 may be a modular or a replaceable component of a re-usable inhaler 200. is a cross-sectional schematic diagram of an illustrative inhaler 200 with a modular illustrative ne particle delivery consumable or article 100 disposed therein.

The illustrative inhaler 200 es a mouthpiece portion 210 and a detachable distal portion 220. The mouthpiece portion 210 includes a receptacle cavity 212 in air flow communication with a mouthpiece air l 214. The mouthpiece portion 210 includes one or more iece air outlets 216 that mate or align with the air outlet 118 of the nicotine particle delivery consumable or article 100. One or more Inlet air flow channels mate with the one or more air inlets 117 of the nicotine particle delivery consumable or article 100.

PCT/lBZOl7/053546 The acle cavity 212 is configured to mate with the nicotine particle delivery consumable or article 100. The detachable distal portion 220 may be removed from the mouthpiece portion 210 to expose the receptacle cavity 212 to replace the modular and used or depleted nicotine particle delivery consumable or article 100 with an un-used or full particle delivery consumable or article 100.

The distal portion 220 es a piercing element 225 that may be a plunger type element with a resilient element 228 such as a spring element. The piercing element 225 includes a piercing needle 221. Depressing the piercing element 225 allows the piercing needle 221 to pass through the membrane 115 and puncture the capsule 120. Air flow ment through the nicotine particle delivery consumable or e 100 causes the capsule 120 to rotate about its longitudinal axis. Nicotine and optional flavour particles are then entrained into the air flow through the r article 200.

Once the nicotine le delivery consumable or article 100 is consumed, the depleted nicotine particle delivery consumable or article 100 may then be removed from the receptacle cavity 212 and replaced with a fresh nicotine particle delivery able or article 100. One or more seal layers (not shown) may be peeled away or punctured by elements of the receptacle cavity 212 to e air flow through the nicotine particle delivery consumable or article 100. rpaaiéds isfoSié'cfi'é‘: c'Eiifs'EAiubf PCT/'3 2017/0” 5461322>i78§a§2618 REPLACEMENT SHEET FTR1774/WO MRG 44201200201 .15.

Claims (5)

CLAIMS 1.:

1. An article for use In a ne inhaler. comprising: a acle comprising: a body comprising a sidewall extending from a receptacle first end to an ng receptacle second end and defining a cavity; a -able membrane sealing the acle first end; an air outlet extending through the receptacle second end into the cavity: an air inlet extending through the body ll and into the . the air inlet being closer to the receptacle first end than the receptacle second end; and a pierce-able capsule disposed within the cavity, the capsule containing particles comprising nicotine sized for inhalation delivery into the lungs of a user.

2. The article according to claim 1. wherein the -able membrane is an elastic material that is configured to reseal alter being punctured.

3. The article according to claim 1. wherein the pierce-able membrane is a metal foil.

4. The article according to any one of the preceding claims. wherein the air inlet is off- set from a centroid longitudinal axis of the cavity. and air flowing from the air inlet to the air outlet causes the capsule to rotate about the capsule longitudinal axis.

5. The article according to any one of the preceding claims. wherein the cavity has a circular cross-sectional shape and the air inlet ls tangential to the cavity. AMENDED SHEET