EP3837995A1 - Rauchfreier artikel - Google Patents

Rauchfreier artikel Download PDF

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Publication number
EP3837995A1
EP3837995A1 EP19217705.3A EP19217705A EP3837995A1 EP 3837995 A1 EP3837995 A1 EP 3837995A1 EP 19217705 A EP19217705 A EP 19217705A EP 3837995 A1 EP3837995 A1 EP 3837995A1
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EP
European Patent Office
Prior art keywords
particles
population
pouch
coating
nicotinic compound
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP19217705.3A
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English (en)
French (fr)
Inventor
Haydn HARRISON
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nerudia Ltd
Original Assignee
Nerudia Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nerudia Ltd filed Critical Nerudia Ltd
Priority to EP19217705.3A priority Critical patent/EP3837995A1/de
Publication of EP3837995A1 publication Critical patent/EP3837995A1/de
Withdrawn legal-status Critical Current

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    • A—HUMAN NECESSITIES
    • A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
    • A24B13/00—Tobacco for pipes, for cigars, e.g. cigar inserts, or for cigarettes; Chewing tobacco; Snuff
    • A—HUMAN NECESSITIES
    • A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
    • A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
    • A24B15/18—Treatment of tobacco products or tobacco substitutes
    • A24B15/28—Treatment of tobacco products or tobacco substitutes by chemical substances
    • A24B15/281—Treatment of tobacco products or tobacco substitutes by chemical substances the action of the chemical substances being delayed
    • A24B15/283—Treatment of tobacco products or tobacco substitutes by chemical substances the action of the chemical substances being delayed by encapsulation of the chemical substances

Definitions

  • the present invention relates to a smokeless article for oral consumption, and a method of manufacturing a smokeless article for oral consumption.
  • Smoking is generally considered to expose a smoker to potentially harmful substances. It is generally thought that the majority of the potentially harmful substances are formed by the heat generated during burning (combustion) of the article. There is interest in so-called heat not burn products, which heat a tobacco or similar substrate at a lower temperature than a conventional cigarette. These products are usually described as less harmful than conventional cigarettes. Both conventional cigarettes and heat not burn products are visible during use and produce smoke or vapour.
  • Smokeless articles are a suitable alternative because they do not require heating for substance delivery to the user. Instead, smokeless articles rely on saliva to extract soluble substances, typically nicotine and/or flavours, from tobacco contained within the smokeless article.
  • Conventional smokeless articles have a saliva permeable pouch housing a content.
  • the content is generally in the form of tobacco.
  • Such a product may be referred to as portion snus. It is typically provided as prepackaged (traditionally moist) powder in small teabag-like pouches. Each pouch is a single portion or unit. This moistened product may be referred to as original snus.
  • Smokeless articles are placed in the mouth where saliva extracts the soluble element from the tobacco contained within.
  • the smokeless article is placed in the oral cavity, sublingually or in the oral vestibule (between the teeth and lips/cheeks).
  • the user may assist extraction by oral manipulation, such as by chewing and/or sucking or pressing on the outside of the mouth to squeeze the pouch.
  • the resulting saliva which contains extracts, subsequently contacts a mucous membrane in the mouth, or at another point of the gastrointestinal tract, to deliver the soluble element across the membrane and into the bloodstream.
  • the soluble element is then transported by the bloodstream to the site of action. For example, nicotine is delivered to the brain where it acts upon acetylcholine receptors.
  • Snuff is smokeless tobacco made from ground or pulverised tobacco leaves. Snuff is available in dry form or wet (moist) form. Moist snuff may be referred to as snus. Two common varieties of snus are Scandinavian snus and American snus. Both varieties of snus are available in a loose form, but are often contained within a saliva permeable pouch.
  • snus is typically manufactured by grinding a blend of leaf tobaccos to specified particle sizes.
  • the ground tobacco is then mixed with water and sodium chloride in closed process blenders.
  • the mixture is subjected to a heat treatment, involving temperatures up to 80 - 100 °C, for several hours to pasteurize the snus. Thereafter, the snus is cooled and other ingredients may be added.
  • Snus is typically manufactured to meet the GothiaTek® standard, as detailed in " Swedish snus and the GothiaTek® standard” (2005), Rutqvist , et al.
  • Typical snus products release nicotine in a continuous manner following contact of the nicotine-containing material with saliva in the oral cavity with the concentrations of nicotine in the user's mouth decreasing overtime as the nicotine in the snus product is depleted.
  • content(s) is intended to refer to compounds, material and/or substances that may be enclosed within the pouch.
  • nicotine is intended to refer to nicotine, nicotine salt(s), nicotine complex(es); and/or nicotine solvate(s).
  • non-porous is intended to refer to a material that does not include any pores extending through the thickness of the wall (for instance, “through holes” or capillaries).
  • saliva-stable is intended to refer to a material that does not substantially dissolve or disintegrate as a result of exposure to saliva in the oral cavity of the user at physiological temperature. Therefore a layer of such material is resistant to the migration of saliva (or compounds/substances dissolvable in saliva, for example nicotinic compounds) through the thickness of the material.
  • the material may also be resistant to migration of saliva (or compounds/substances dissolvable in saliva e.g. nicotinic compounds) by phase transfer mechanisms. In some cases a standard commercially available artificial saliva may be used to test saliva-stability.
  • “saliva-stable” may equate to “water-stable” and refer to a material that does not substantially dissolve or disintegrate as a result of exposure to water in the oral cavity of the user at physiological pH.
  • a layer of the material is resistant to the migration of water (or compounds/substances dissolvable in water, for example nicotinic compounds) through the thickness of the material.
  • the material may also be resistant to migration of water (or compounds/substances dissolvable in water e.g. nicotinic compounds) by phase transfer mechanisms.
  • saliva is intended to refer to the liquid substance formed in the mouth of animals, such as humans, that includes water, electrolytes and enzymes. Other components of saliva may include mucus, white blood cells, epithelial cells and/or antimicrobial agents.
  • hydrophobic is intended to refer to a material having water contact angle greater than 90°, such that the material is resistant to adsorption and/or absorption of water. In some instances such material may have a polarity lower than that of water.
  • plant material is intended to refer to a portion and/or part(s) of a plant (e.g. leaf, stem, flower or bud).
  • the plant material may be processed (for example, by shredding, grinding or drying) or it may be non-processed (that is, used whole).
  • the plant material is typically fibrous (comprising or characterised by fibres).
  • plant material is not intended to include pulp and/or paper which is derived from a plant material (typically wood) and chemically and/or mechanically processed to extract fibres before use.
  • moisture content may include water, humectants, liquid flavourants and/or other liquid compounds.
  • oral consumption is intended to refer to any oral administration route achieved by placing the smokeless article into the oral cavity. This includes, but is not limited to, buccal, sublingual, periodontal, gingival and ingestion.
  • a smokeless article for oral consumption comprising a pouch containing a first particle population comprising a plurality of particles; in the first particle population the particles comprise a core comprising a nicotinic compound, wherein the core is encapsulated by a continuous coating of a non-porous, saliva-stable material, and wherein the coating is frangible, such that in use the coating fractures on chewing.
  • the coating of a non-porous, saliva-stable material prevents saliva (or water) from contacting the core of the coated first population of particles in the pouch.
  • the non-porous, saliva-stable material also acts to prohibit migration of the nicotinic compound from the core into the user's oral cavity. Therefore, release of the nicotinic compound from the first population of particles within the pouch into the user's oral cavity is prevented.
  • the pouch further comprises a second particle population comprising a plurality of particles; in the second population the particles comprise a core comprising a nicotinic compound, wherein the nicotinic compound is releasable on exposure of the second particle population to saliva.
  • the release of the nicotinic compound from the second population of particles starts immediately on exposure of the second population to saliva in the user's mouth.
  • the frangible nature of the coating on the first population of particles enables the user to bite down or chew on the particles in the pouch to break the coating. This exposes a portion of the particulate core that was previously covered by the coating, and facilitates access of saliva (or water) from the user's oral cavity to the nicotinic compound in the core. Subsequently, the saliva extracts soluble components (in particular, the nicotinic compound) contained within the core of the first population of particles, and delivers the extracted components from the particles into the user's oral cavity. This provides a level of user control over the timing of release of the nicotinic compound after insertion of the pouch into the mouth.
  • Insertion of the pouch into the mouth may result in an initial release of nicotinic compound as saliva penetrates any second population of particles that is present or any other source of nicotinic compound in the pouch, followed by at least one further release of nicotinic compound from the first population of particles that is initiated by chewing.
  • the user has complete control over when the release of the nicotinic compound from the first population of particles is initiated. For instance, when a "hit" of nicotinic compound is desired by the user, they can simply bite down on the pouch to break the frangible coating on the first population of particles and initiate release of the nicotinic compound.
  • the provision of the coating on the plurality of particles in the first population also allows the user to obtain multiple "hits" of nicotinic compound from a single pouch.
  • a single bite on the pouch will not fracture the coating on all of the particles of the first population in the pouch.
  • a first bite on the pouch will fracture the frangible coating only on a subset of the particles with subsequent bites fracturing the coating on further subsets of the particles to provide further "hits" of nicotinic compound, thus providing the user with the ongoing ability to repeat the "hit" multiple times from a single pouch.
  • nicotinic compounds present in the smokeless article are in the cores of the plurality of particles, i.e. the release of any nicotinic compound into the oral cavity of a user would require fracture of the frangible coating on at least a subset of the plurality of particles. In these preferred cases, no nicotinic compounds are present outside the cores of the particles.
  • the presence of the continuous coating of non-porous, saliva-stable material imparts an additional benefit that the loss of moisture from the core of the first population of particles prior to use is retarded.
  • the coating retards or prevents the passage of moisture with the result that the rate of loss of moisture from the core material over time is reduced as compared to a smokeless article having no such coating or in which the coating is breached; providing a smokeless article having a longer shelf-life.
  • Provision of the coating on the first population of particles within the pouch shields the coating from premature breakage as it is provided on a surface that is within the enclosed volume of the pouch. Provision of the coating on the outer surface of the first population of particles may also have the benefit of reducing or preventing clumping of the core material which can lead to an uneven sensation when the pouch is in use, for example where the core comprises a plant material.
  • the non-porous, saliva-stable material comprises a polymer.
  • the physical properties of the non-porous, saliva-stable material can easily be tuned by selection of an appropriate material. This is advantageous from a manufacturing and processability perspective. It is also advantageous from the perspective of use of the article. For example, the degree of frangibility of the coating can be tuned be selection of an appropriate material.
  • the non-porous, saliva-stable material is selected from sorbitol, maltitol, isomalt, mannitol, starch, gelatin, gum arabic, polyvinyl acetate, carob bean gum, refined paraffin wax, shellac, locust bean gum, petroleum wax, terpene resin, tragacanth, polyethylene, xanthan gum, and combinations thereof.
  • the non-porous, saliva-stable material is hydrophobic.
  • the coating more effectively repels saliva (or water) to prevent access of saliva (or water) to the core material of the first population of particles.
  • the core material is tobacco-free.
  • the particles are tobacco-free.
  • the content of the pouch is tobacco-free.
  • the user may experience a similar or enhanced recreational/pharmaceutical effect as compared to conventional tobacco-containing products without experiencing undesirable components inherent to tobacco (e.g. tobacco flavour).
  • tobacco flavour undesirable components inherent to tobacco
  • the coating may be applied to the core material by any suitable means, for example, brushing, spraying, or immersion. It is preferred that the coating is uniform across the surface of the core material.
  • the coating is applied by spray coating.
  • the pouch contains a first and second particle population as described herein.
  • the pouch contains only two particle populations. In some cases more than two, e.g. three, four or five particle populations may be included.
  • the pouch contains no components other than the particle populations (i.e. the first particle population and any further particle populations that are present, e.g. the second particle population).
  • first and second particle populations are both present, preferably about 20 wt.%, about 25 wt.%, about 50 wt.%, about 75 wt.%, about 80 wt.% or about 90 wt.% of the total amount of nicotinic compound in the smokeless article is present as the nicotinic compound in the first particle population.
  • This control of the distribution of the nicotinic compound in the pouch allows control of the amount of nicotinic compound that can be released upon simple contact with saliva when both first and second particle populations are present in the pouch, i.e. release starts without delay on insertion of the pouch into the user's mouth, as compared to the amount of nicotinic compound that is released upon breaking of the non-porous, saliva-stable coating on the first population of particles, for example upon chewing by the user.
  • a second particle population is present in the pouch, to ensure an initial release of nicotinic compound without requiring chewing of the article, less than 100 wt.% of the total amount of the nicotinic compound in the smokeless article is present as the nicotinic compound in the first particle population.
  • the user experiences an initial period of time during which the release of nicotinic compound exhibits a similar profile to that from a traditional snus product but the user can then refresh the release of nicotinic compound as desired by chewing on the pouch.
  • the user can refresh the release of nicotinic compound multiple times by chewing the pouch on multiple different occasions during use.
  • first and second particle populations are both present, preferably at least about 10 wt.%, or at least about 25 wt.%, or at least about 50 wt.% of total amount of nicotinic compound in the smokeless article is present in the second particle population.
  • the weight ratio of the amount of the nicotinic compound in the first and second particle populations is selected from 5:95, 10:90, 20:80, 25:75, 30:70, 40:60, 50:50, 60:40, 70:30, 75:25, 80:20, 90:10, and 95:5.
  • nicotinic compound present in the smokeless article is contained in the cores of the particles, preferably all in the combination of the first and second particle populations.
  • a smokeless article for oral consumption comprising:
  • step ii) of the method described herein may comprise forming a porous pouch containing the plurality of particles and one or more additional components, such as those listed above.
  • the incorporation of the first and second populations of particles before sealing of the pouch allows a predetermined ratio of the first and second populations of particles to be achieved.
  • the predetermined ratio may be as described herein in relation to the first aspect.
  • the coating material is typically applied to the cores of the first population of particles in a spreadable or sprayable state, for example as a liquid or paste. After application, the coating material then becomes frangible overtime, for example upon curing or evaporation of solvent. In some cases the coated cores are only incorporated into the pouch after the coating becomes frangible; this may reduce the chances of particles sticking together if the coating is sticky or tacky prior to becoming frangible, e.g. if it is not fully cured or dried. In some cases, the coating may become non-sticky or non-tacky before the coating dries or cures full to become frangible.
  • the method may further include a step of curing or allowing solvent to evaporate from the coating material to form a frangible coating.
  • This step may occur between steps (i) and (ii) above; or between steps (ii) and (iii) above; or between steps (iii) and (iv) above; or between steps (ii) and (iv) if step (iii) is excluded; or following step (iv) above.
  • this step occurs between steps (i) and (ii) above.
  • An advantage of applying the frangible coating to the first population of particles is that the pouch material itself provides some protection to the particles. In this way, the frangible coating on the particles in the resultant smokeless article is protected from pre-mature breakage during storage and/or use.
  • the coating material is applied by spray-coating.
  • a smokeless article for oral consumption produced by a process according to the second aspect.
  • kits comprising a plurality of smokeless articles according to the first aspect and/or the third aspect and a container.
  • the smokeless article may be described as a snus article.
  • the smokeless article preferably has a mass of about 0.1 g to 5.0 g, such as about 0.5 g to about 4.0 g or about 1.0 g to about 3.0 g.
  • the smokeless article preferably has a length of about 30 mm, such as about 28 mm or 26 mm, a width of about 12 mm, such as about 10 mm or 8 mm, and a depth of about 5 mm, such as about 4 mm or 3 mm.
  • the pouch is preferably formed from a porous substrate.
  • the porous substrate may be comprised of one or more materials.
  • the porous substrate may be comprised of fiber, paper, cloth and fabric or combinations thereof.
  • the porous substrate may be comprised of one or more polymeric materials.
  • the polymeric material may be selected from one or more of hydroxypropyl cellulose (HPC), hydroxypropyl methylcellulose (HPMC), polyvinyl alcohol (PVOH), polyvinylpyrrolidone (PVP), polyethylene oxide (PEO) hydroxyethyl cellulose (HEC), polyethylene glycol (PEG), pullulan, sodium alginate, xanthan gum, tragancanth gum, guar gum, acacia gum, arabic gum, polyacrylic acid, maltodextrin, methylmethacrylate copolymer, carboxyvinyl copolymers, starch and gelatin.
  • HPC hydroxypropyl cellulose
  • HPMC hydroxypropyl methyl
  • the porous substrate is typically completely insoluble in saliva.
  • Suitable insoluble porous substrate materials include, but are not limited to, fiber, paper, water-insoluble polymers, cloth and fabric.
  • Suitable soluble porous substrate materials include, but are not limited to, water-soluble polymers such as polyethylene oxide (PEO), hydroxypropyl cellulose (HPC) and hydroxypropyl methylcellulose (HPMC).
  • the pouch may be formed by, for example, folding a single sheet of porous substrate on itself or bringing two or more sheets of a porous substrate together and sealing the edges.
  • the edges may initially be partially sealed to provide an open pouch in which the content may be placed before completely sealing the pouch closed.
  • the sheets may be the same thickness or different thicknesses.
  • At least 50% of the pores of the porous substrate have a diameter of 50 ⁇ m to 200 ⁇ m, such as 100 ⁇ m to 175 ⁇ m or 125 ⁇ m or 150 ⁇ m. At least 50% of the pores have a diameter of at least 100 ⁇ m. For example, at least 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or 100% of the pores have such diameters.
  • the pouch may be coloured or include markings, such as brand logos and text, to improve user perception.
  • the pouch may be partially or completely coloured by a colourant.
  • the content may comprise one or more substances either in addition to the particles defined herein, or as incorporated into the cores of some or all of the particles.
  • An advantage of this is that all of the components included in the cores are protected by the coating during storage leading to a longer shelf-life.
  • the additional substances are not provided in the particle cores.
  • the smokeless article behaves in a similar way to existing smokeless articles, e.g. in terms of mouthfeel and physical and tactile parameters, leading to higher consumer acceptance.
  • some additional substances may be incorporated in the cores of the first population of particles (e.g. those requiring more protection during storage) and some may be provided in the cores of any further populations of particles (e.g. the second population of particles) or addition to the particles (e.g. those contributing more to mouthfeel or physical behaviour of the smokeless article).
  • the or each substance may individually be a biologically/pharmacologically active compound, pH stabilisers or adjusters, humectants, flavourants, fillers, preservatives, aqueous/non-aqueous solvents and binders.
  • the or each substance may be provided for more than one purpose.
  • any substances included in addition to the particles defined herein in the pouch are not sources of a nicotinic compound, i.e. the only source of a nicotinic compound in the smokeless article is in the core of the particles.
  • the content of the pouch preferably occupies substantially all of the internal volume of the pouch.
  • the content may occupy 80%, 85%, 90%, 95% or 100% of the internal volume of the pouch.
  • the content may comprise a solid material to provide physical integrity, such as an organic material (e.g. plant material) or an inorganic material. Such solid materials may naturally or inherently contain one or more biologically/pharmacologically active compounds and/or additives.
  • the particle population(s) form the entire contents of the pouch, i.e. no additional materials are enclosed in the pouch.
  • the pouch contains only the first population of particles and no other materials.
  • the pouch contains only the first and second populations of particles and no other materials.
  • the Nicotinic compound is selected from nicotine, nicotine salt(s), nicotine complex(es); and/or nicotine solvate(s).
  • Nicotine salts may include a salt selected from the group consisting of nicotine hydrochloride, nicotine dihydrochloride, nicotine monotartrate, nicotine bitartrate, nicotine bitartrate dehydrate, nicotine sulfate, nicotine zinc chloride monohydrate, nicotine salicylate and mixtures thereof.
  • the nicotinic compound may be provided from a natural or synthetic source. Natural sources include plant materials containing a nicotinic compound, such as Nicotiana species (Tobacco).
  • Any type of tobacco may be used. This includes, but is not limited to, flue-cured tobacco, burley tobacco, Maryland Tobacco, dark-air cured tobacco, oriental tobacco, dark-fired tobacco, perique tobacco and rustica tobacco. This also includes blends of the above mentioned tobaccos.
  • any suitable parts of the tobacco plant may be used. This includes leaves, stems, roots, bark, seeds and flowers.
  • the tobacco may comprise one or more of leaf tobacco, stem tobacco, tobacco powder, tobacco dust, tobacco derivatives, expanded tobacco, homogenised tobacco, shredded tobacco, extruded tobacco, cut rag tobacco and/or reconstituted tobacco (e.g. slurry recon or paper recon).
  • the content may comprise a gathered sheet of homogenised (e.g. paper/slurry recon) tobacco or gathered shreds/strips formed from such a sheet.
  • homogenised e.g. paper/slurry recon
  • the sheet may have a grammage greater than or equal to 100 g/m 2 , e.g. greater than or equal to 110 g/m 2 such as greater than or equal to 120 g/m 2 .
  • the sheet may have a grammage of less than or equal to 300 g/m 2 e.g. less than or equal to 250 g/m 2 or less than or equal to 200 g/m 2 .
  • the sheet may have a grammage of between 120 and 190 g/m 2 .
  • the cores of the particles may simply comprise, or consist of, tobacco strands.
  • the first population of particles comprises tobacco strands coated with the frangible coating as described herein.
  • Any second population of particles may comprise tobacco strands that are not coated with such a frangible coating (they may have an alternative coating that does not impede release of nicotinic compounds from the tobacco or, preferably, they may be uncoated). This arrangement provides the advantage that the mouthfeel of the smokeless product may be more like a traditional snus due to the second population of particles but the added advantage of the tailored released profile is provided by inclusion of the first population of particles.
  • Biologically/pharmacologically active compounds are provided to produce a pharmacological effect in the user.
  • Suitable biologically/pharmacologically active compounds include the group consisting of: cocaine, caffeine, opiates and opioids, cathine and cathinone, kavalactones, mysticin, beta-carboline alkaloids, salvinorin A together with any combinations, functional equivalents to, and/or synthetic alternatives of the foregoing.
  • Biologically/pharmacologically active compounds may also have additive properties.
  • the biologically/pharmacologically active compounds included in addition to the nicotinic compound in the coated cores is a non-nicotinic compound.
  • pH stabilisers or adjusters may be provided to adjust the user experience and/or modify the bioavailability of a pharmacologically active compound. For instance, under acidic conditions, nicotine is protonated and does not readily cross mucous membranes.
  • suitable pH stabilisers include ammonia, ammonium carbonate, sodium carbonate and calcium carbonate.
  • the overall pH of the smokeless article is preferably pH 7 to pH 9, such as pH 7.25 to pH 8.75 or pH 7.5 to pH 8.5.
  • the overall pH of a smokeless article may be determined by, for example, (i) placing the content of the smokeless article in 10 mL of distilled water (iii) agitating the mixture for at least 5 minutes and (iv) measuring the pH of the solution with a pH probe.
  • Fillers may be provided to increase the volume of the smokeless article (e.g. by increasing the volume contained within the pouch and to strengthen the content).
  • Suitable fillers include calcium carbonate, calcium phosphate, corn starch, grains, lactose, polysaccharides (e.g. maltodextrin), polyols, sugars (e.g. dextrose, manitol, xylitol, sorbitol), natural fibres (e.g. non-tobacco fibres), microcrystalline cellulose, cellulose and cellulose derivatives (e.g. finely divided cellulose), lignocellulose fibres (e.g. wood fibres), jute fibres and combinations thereof.
  • the amount of filler is 5 to 10 wt% of the content e.g. around 6 to 9 wt%.
  • Flavourants may be provided in solid or liquid form. Suitable flavourants include coffee, eucalyptus, menthol, liquorice, peppermint, spearmint, chocolate, fruit flavour (including e.g. citrus, cherry etc.), vanilla, spice (e.g. ginger, cinnamon) and tobacco flavour.
  • the flavourant may be evenly dispersed throughout the content or may be provided in isolated locations and/or varying concentrations throughout the content.
  • the term "flavourant” denotes a compound having a desirable taste, aroma or both.
  • Humectants may be provided to control moisture content thereby preventing the smokeless article from drying out during storage and reducing the amount of saliva wetting required before the user experience begins.
  • Suitable humectants include polyhydric alcohols (e.g. propylene glycol (PG), triethylene glycol, 1,2-butane diol and vegetable glycerine (VG)) and their esters (e.g. glycerol mono-, di- or tri-acetate).
  • the humectant may have a lower limit of at least 1 % by weight of the content such as at least 2 wt%, such as at least 5 wt%, such as at least 10 wt%, such as at least 20 wt%, such as at least 30 wt%, or such as least 40 wt%.
  • the humectant may have an upper limit of at most 50% by weight of the contents, such as at most 40 wt%, such as at most 30 wt%, or such as at most 20 wt%, such as at most 10 wt %, such as at most 5 wt %, such as at most 2 wt%.
  • the amount of humectant is 1 to 40 wt% of the content, such as 2 to 20 wt% or 5 to 10 wt%.
  • Smokeless articles having a total moisture content of 10% or less are generally considered to be 'dry'.
  • Smokeless articles having a total moisture content of 40% or more are generally considered to be 'wet'.
  • Sweeteners may be provided to modify the user taste perception and, in particular, overcome bitter flavours that result from other substances.
  • Suitable sweeteners include honey, sugar, brown sugar, glucose, fructose, sucrose, aspartame, xylitol, maltitol, saccharin sodium, glycyrrhizin tripotassium liquorice, jujube or a mixture thereof.
  • the amount of sweetener is in some cases 1 to 20 % by weight of the content, such as 2 to 15 wt% or 5 to 10 wt%.
  • Stabilisers are provided to prevent decomposition or degradation over time during storage by, for example, retarding oxidation or unwanted biological activity.
  • Stabilisers may be selected from the group consisting of antioxidants including vitamin E, such as tocopherole, ascorbic acid, sodium pyrosulfite, butylhydroxytoluene, butylated hydroxyanisole, edetic acid and salts thereof; and preservatives including citric acid, tartaric acid, lactic acid, malic acid, acetic acid, benzoic acid, sorbic acid and salts thereof.
  • vitamin E such as tocopherole, ascorbic acid, sodium pyrosulfite, butylhydroxytoluene, butylated hydroxyanisole, edetic acid and salts thereof
  • preservatives including citric acid, tartaric acid, lactic acid, malic acid, acetic acid, benzoic acid, sorbic acid and salts thereof.
  • Binders may be provided. Suitable binders include starches and/or cellulosic binders such as methyl cellulose, ethyl cellulose, hydroxypropyl cellulose, hydroxyethyl cellulose and carboxymethyl cellulose, gums such as xanthan, guar, arabic and/or locust bean gum, organic acids and their salts such as alginic acid (sodium alginate), agar and pectins. In some embodiments the amount of binder is 5 to 10 wt% of the content e.g. around 6 to 9 wt% or 7 to 8 wt%.
  • Colourants may be provided to modify the user impression of the smokeless article. Colourants include whitening agents. Colourants may be selected from one or more of common colourants such as curcumin (E100), turmeric (E100(ii)), riboflavin (E101), riboflavin-5'-phosphate (E101 (ii)), tartrazine (E102), quinoline yellow (E104), riboflavin-5-sodium phosphate (E106), yellow 2G (E107), sunset yellow FCF (E110), carmine, cochineal (E120), azorubine (E122), amaranth (E123), ponceau 4R (E124), erythrosine (E127), red 2G (E128), allura red AC (E129), patent blue V (E131), indigotine (E132), brilliant blue FCF (E133), chlorophylls (E140), copper complexes of chlorophyll (E141), green S (E142), caramel (E150a-d), brilliant black BN (E
  • Plant material may be provided for physical integrity and may function as a natural source of substances such as, for example, biologically/pharmacologically active compounds, flavourants, pH stabilisers etc.
  • the plant material may comprise least one plant material selected from the list including Amaranthus dubius, Arctostaphylos uva-ursi (Bearberry), Argemone mexicana, Amica, Artemisia vulgaris, Yellow Tees, Galea zacatechichi, Canavalia maritima (Baybean), Cecropia mexicana (Guamura), Cestrum noctumum, Cynoglossum virginianum (wild comfrey), Cytisus scoparius, Damiana, Entada rheedii, Eschscholzia califomica (California Poppy), Fittonia albivenis, Hippobroma longiflora, Humulus japonica (Japanese Hops), Humulus lup
  • any plant material included in addition to the first, and the second (where included), population of particles is not a source of a nicotinic compound; for example it is not a Nicotiana species (Tobacco).
  • the content may comprise at least 50 wt% plant material based on the weight of the content, e.g. at least 60 wt% plant material e.g. around 65 wt% plant material.
  • the content may comprise 80 wt% or less plant material e.g. 75 or 70 wt% or less plant material.
  • a smokeless article 10 having a pouch 12, the pouch being a porous substrate.
  • the pouch 12 contains a content 14 including particles 18 that are formed of a core 19 having a coating 11 of a non-porous, saliva-stable material surrounding the core.
  • the coating 11 is frangible.
  • the pouch 12 is substantially rectangular.
  • the pouch 12 is formed from a single sheet of a porous substrate and is substantially filled by the content 14.
  • the pouch 12 has a seal 16 along each of the three edges where the inner surface of the single sheet of porous substrate meets itself to seal the contents 14 in the pouch 12.
  • the smokeless article 10 is placed into the oral cavity of the user. Due to the coating 11, saliva present in the user's oral cavity is prohibited from contacting the cores 19 of the particles 18 contained within the pouch. Nor can the nicotinic compound in the cores 19 migrate through the coating 11. When the user desires a "hit” of nicotinic compound they bite down or chew on the smokeless article to break the coating 11. This exposes a portion of the core 19, such that saliva can contact the core material. A nicotinic compound within the core 19 is then extracted into the saliva and may enter the user's blood stream by oral consumption to provide a "hit" of nicotinic compound.
  • a smokeless article 10 having a pouch 12, the pouch being a porous substrate.
  • the pouch 12 contains a content 14 including a first population of particles 18 that are formed of a core 19 having a coating 11 of a non-porous, saliva-stable material surrounding the core. The coating 11 is frangible.
  • the pouch 12 also contains a second population of particles 13 that are formed of a core 15 but without the coating of non-porous, saliva-stable material.
  • the pouch 12 is substantially rectangular.
  • the pouch 12 is formed from a single sheet of a porous substrate and is substantially filled by the content 14.
  • the pouch 12 has a seal 16 along each of the three edges where the inner surface of the single sheet of porous substrate meets itself to seal the contents 14 in the pouch 12.
  • the smokeless article 10 is placed into the oral cavity of the user. Due to the coating 11, saliva present in the user's oral cavity is prohibited from contacting the cores 19 of the first population of particles 18 contained within the pouch. Nor can the nicotinic compound in the cores 19 migrate through the coating 11. However the saliva can contact the cores 15 of the second population of particles 13 due to the absence of the coating 11. This means that the nicotinic compound contained in the cores 15 of the second population of particles 13 can start to solubilise and pass into the oral cavity of the user. When the user desires an additional "hit" of nicotinic compound they bite down or chew on the smokeless article to break the coating 11 of the first population of particles.
  • nicotinic compound within the core 19 is then extracted into the saliva and may enter the user's blood stream by oral consumption to provide a "hit" of nicotinic compound.
  • Figure 3 shows a third embodiment of a smokeless article 10' having a pouch 12, the pouch being a porous substrate.
  • the pouch 12 contains a content 14 including particles 18 that are formed of a core 19 having a coating 11 of a non-porous, saliva-stable material surrounding the core. The coating 11 is frangible.
  • the pouch 12 also contains a second population of particles 13 that are formed of a core 15 but without the coating of non-porous, saliva-stable material. In some embodiments the second population of particles 13 is absent.
  • the pouch 12 is substantially circular.
  • the pouch 12 is formed from two opposing sheets of a porous substrate and is substantially filled by the content 14.
  • the pouch 12 has a circumferential seal 16 along the edges where the two opposing sheets of a porous substrate meet to seal the contents 14 in the pouch 12.
  • Figure 4 shows a fourth embodiment of a smokeless article 10" that, like the second embodiment, has a pouch 12 made from a single sheet of a porous substrate. However, one of the three seals 16' is formed by an overlap of the inner surface and the outer surface of the single sheet of porous substrate to seal the contents 14 in the pouch 12. The remaining two seals at opposing ends of the pouch are formed where the inner surface of the single sheet of porous substrate meets itself.
  • the pouch 12 contains a content 14 including particles 18 that are formed of a core 19 having a coating 11 of a non-porous, saliva-stable material surrounding the core. The coating 11 is frangible.
  • the pouch 12 also contains a second population of particles 13 that are formed of a core 15 but without the coating of non-porous, saliva-stable material. In some embodiments the second population of particles 13 is absent.
  • Figure 5 shows a release profile of two embodiments of the present smokeless article which contain only the first population of particles as described herein, i.e. those coated with a non-porous, saliva-stable material, and one smokeless article shown for comparison.
  • the smokeless article In the profile for "Embodiment 1" the smokeless article is inserted into the mouth at time 0 and then chewed once 15 minutes later. The nicotine is then released from the cores of the particles over the following 40 minutes (up to 55 minutes after the article was inserted into the mouth).
  • the smokeless article is inserted into the mouth at time 0 and then chewed three times at 5 minutes, 25 minutes, and 40 minutes. The nicotine is released from a different subset of the particles after each chew.
  • the release profile of a standard uncoated tobacco snus is shown for comparison.
  • Figure 6 shows a release profile of two embodiments of the present smokeless article each containing both a first and second population of particles as described herein, and one smokeless article shown for comparison.
  • the first embodiment (“25% coated") 25 wt.% of the nicotinic compound in the article is present in a first population of particles as described herein and 75 wt.% of the nicotinic compound in the article is present in a second population of particles as described herein.
  • the release profile shows an initial nicotine release from the second population of particles followed by a user chewing the article at 9 minutes after insertion into the mouth which initiates a further release of nicotine from the first population of particles.
  • 50 wt.% of the nicotinic compound in the article is present in a first population of particles as described herein and 50 wt.% of the nicotinic compound in the article is present in a second population of particles as described herein.
  • the release profile shows an initial nicotine release from the second population of particles followed by a user chewing the article at 9 minutes after insertion into the mouth which initiates a further release of nicotine from the first population of particles.
  • a second chew at 25 minutes after insertion into the mouth initiates another release of nicotine from particles in the first population for which the first chew by the user did not fracture the coating.
  • the comparison release profile (“100% coated") shows no initial nicotine release due to all of the available nicotine being contained in particles having a non-porous, saliva-stable coating.
  • the chew by the user at 9 minutes after insertion into the mouth then initiates release of the nicotine in a similar way to that of the first embodiment.

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  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Toxicology (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Preparation (AREA)
EP19217705.3A 2019-12-18 2019-12-18 Rauchfreier artikel Withdrawn EP3837995A1 (de)

Priority Applications (1)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023112150A1 (ja) * 2021-12-14 2023-06-22 日本たばこ産業株式会社 低分子量アルギン酸化合物を含有するオーラル製品および当該製品用の組成物

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005046363A2 (en) * 2003-11-07 2005-05-26 U.S. Smokeless Tobacco Company Tobacco compositions
WO2009010875A2 (en) * 2007-07-16 2009-01-22 Philip Morris Products S.A. Oral delivery pouch product with coated seam
US20110061666A1 (en) * 2006-02-10 2011-03-17 R. J. Reynolds Tobacco Company Smokeless Tobacco Composition
US7946295B2 (en) * 2007-07-23 2011-05-24 R. J. Reynolds Tobacco Company Smokeless tobacco composition
US8061362B2 (en) * 2007-07-23 2011-11-22 R. J. Reynolds Tobacco Company Smokeless tobacco composition
US20170064995A1 (en) * 2015-09-09 2017-03-09 R.J. Reynolds Tobacco Company Flavor delivery article
WO2017093941A1 (en) * 2015-12-03 2017-06-08 Niconovum Usa, Inc. Multi-phase delivery compositions and products incorporating such compositions
US20170360078A1 (en) * 2016-06-16 2017-12-21 Altria Client Services Llc Breakable capsules and methods of forming thereof

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005046363A2 (en) * 2003-11-07 2005-05-26 U.S. Smokeless Tobacco Company Tobacco compositions
US20110061666A1 (en) * 2006-02-10 2011-03-17 R. J. Reynolds Tobacco Company Smokeless Tobacco Composition
WO2009010875A2 (en) * 2007-07-16 2009-01-22 Philip Morris Products S.A. Oral delivery pouch product with coated seam
US7946295B2 (en) * 2007-07-23 2011-05-24 R. J. Reynolds Tobacco Company Smokeless tobacco composition
US8061362B2 (en) * 2007-07-23 2011-11-22 R. J. Reynolds Tobacco Company Smokeless tobacco composition
US20170064995A1 (en) * 2015-09-09 2017-03-09 R.J. Reynolds Tobacco Company Flavor delivery article
WO2017093941A1 (en) * 2015-12-03 2017-06-08 Niconovum Usa, Inc. Multi-phase delivery compositions and products incorporating such compositions
US20170360078A1 (en) * 2016-06-16 2017-12-21 Altria Client Services Llc Breakable capsules and methods of forming thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
RUTQVIST, SWEDISH SNUS AND THE GOTHIATEK@ STANDARD, 2005

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023112150A1 (ja) * 2021-12-14 2023-06-22 日本たばこ産業株式会社 低分子量アルギン酸化合物を含有するオーラル製品および当該製品用の組成物

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