EP4023274B1 - Dampfinhalator ohne erwärmung - Google Patents
Dampfinhalator ohne erwärmungInfo
- Publication number
- EP4023274B1 EP4023274B1 EP20856003.7A EP20856003A EP4023274B1 EP 4023274 B1 EP4023274 B1 EP 4023274B1 EP 20856003 A EP20856003 A EP 20856003A EP 4023274 B1 EP4023274 B1 EP 4023274B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- atomization
- liquid
- flavor inhaler
- heating type
- type flavor
- 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.)
- Active
Links
Classifications
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24F—SMOKERS' REQUISITES; MATCH BOXES; SIMULATED SMOKING DEVICES
- A24F40/00—Electrically operated smoking devices; Component parts thereof; Manufacture thereof; Maintenance or testing thereof; Charging means specially adapted therefor
- A24F40/05—Devices without heating means
-
- 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
- A24B15/10—Chemical features of tobacco products or tobacco substitutes
- A24B15/16—Chemical features of tobacco products or tobacco substitutes of tobacco substitutes
- A24B15/167—Chemical features of tobacco products or tobacco substitutes of tobacco substitutes in liquid or vaporisable form, e.g. liquid compositions for electronic cigarettes
-
- 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
- A24B15/30—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances
-
- 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
- A24B15/30—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances
- A24B15/32—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances by acyclic compounds
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24F—SMOKERS' REQUISITES; MATCH BOXES; SIMULATED SMOKING DEVICES
- A24F40/00—Electrically operated smoking devices; Component parts thereof; Manufacture thereof; Maintenance or testing thereof; Charging means specially adapted therefor
- A24F40/10—Devices using liquid inhalable precursors
Definitions
- the present invention relates to a non-heating type flavor inhaler and a liquid for atomization for a non-heating type flavor inhaler.
- a non-combustion flavor inhaler uses, as an aerosol source, glycerol, propylene glycol, or water.
- Patent Literature (PTL) 1 discloses an electronic cigarette that heats a liquid material containing glycerin.
- PTL 2 discloses a non-combustion flavor inhaler including capsules that contain water, a triglyceride, and a flavor, where a user inhales the flavor inside the capsules by breaking the capsules. In this case, the triglyceride acts as a diluent for the flavor.
- PTL 3 discloses an inhibitor of peristalsis in gastrointestinal tract smooth muscle, containing water, a triglyceride, and an emulsifier but does not suggest anything about flavor inhalation.
- GB 2524856 A is concerned with a pulmonary delivery apparatus comprising: a first chamber adapted to thermally vaporize a quantity of a first liquid to form a relatively warm first vapor (B) and a second chamber adapted to atomize a quantity of a second liquid without heating of the second liquid to form a mist of a relatively cold second vapor (A).
- a pulmonary delivery apparatus comprising: a first chamber adapted to thermally vaporize a quantity of a first liquid to form a relatively warm first vapor (B) and a second chamber adapted to atomize a quantity of a second liquid without heating of the second liquid to form a mist of a relatively cold second vapor (A).
- an active ingredient such as nicotine
- an inert liquid such as a water-glycol mixture
- the carrier liquids can comprise one of more of the group comprising solubilizers, solvents and mixtures thereof such as water, alcohols such as glycerol, propylene glycol, polyethylene glycol, vegetable oils, mineral oils, lipids, and cyclodextrins.
- solubilizers such as water, alcohols such as glycerol, propylene glycol, polyethylene glycol, vegetable oils, mineral oils, lipids, and cyclodextrins.
- the excipient, carriers or substances can be water: terpenes, such as menthol; alcohols, such as ethanol, propylene glycol, glycerol and other similar alcohols; dimethylformamide; dimethylacetamide; wax; supercritical carbon dioxide; dry ice; lipids, triglycerides, acids, surfactants and mixtures or combinations thereof.
- an aerosol delivery device which includes a chamber having an upstream opening and a downstream opening which allow gas to flow through the chamber, and a heat-conductive substrate located at a position between the upstream and downstream openings. Formed on the substrate is a drug composition film.
- a heat source in the device is operable to supply heat to the substrate to produce a substrate temperature greater than 300°C, and to substantially volatilize the drug composition film from the substrate.
- US 2012/192861 A1 is concerned with formulations of pirfenidone or pyridone analog compounds for aerosolization.
- a glycerol- or propylene glycol-based aerosol source is used from a viewpoint of obtaining a stable aerosol.
- an aerosol source needs to have low viscosity in view of efficient aerosol generation, and thus, a water-based aerosol source is used.
- the present inventors found that when a water-based aerosol source is used, visible smoke exhibits low visibility and a short duration time compared with cases in which a glycerol- or propylene glycol-based aerosol source is used, and as a result, a user might not be fully satisfied.
- an object of the present invention is to provide a non-heating type flavor inhaler that can form visible smoke exhibiting high visibility and a long persistent state of high visibility.
- the present inventors found that the object is attained by using a liquid for atomization containing a water-based aerosol source, a triglyceride, and an emulsifier.
- the object is attained by a non-heating type flavor inhaler and a liquid for atomization for a non-heating type flavor inhaler as defined in the appended claims.
- the present invention relates to: A non-heating type flavor inhaler including
- a liquid for atomization for a non-heating type flavor inhaler containing a triglyceride, an emulsifier and a water-based aerosol source, the aerosol source containing 70 weight% or more of water, and wherein the triglyceride has an aliphatic group that is derived from a fatty acid and that has a carbon number of 6 or more.
- a triglyceride is a compound in which three hydroxy groups of glycerol are esterified with fatty acids and is represented by the following formula.
- R 1 to R 3 are aliphatic groups derived from fatty acids, and the carbon numbers are not limited as long as at least one of R 1 to R 3 is a group having the carbon number of 6 or more. However, at least two of R 1 to R 3 are preferably groups having the carbon number of 6 or more, and all of R 1 to R 3 are more preferably groups having the carbon number of 6 or more.
- the upper limit of the carbon number is not limited but is preferably 12 or less. When the carbon number is excessively large, dispersion stability in a liquid decreases. In light of this, three aliphatic groups of a triglyceride preferably have the carbon number within the above-mentioned range.
- a triglyceride in which all of R 1 to R 3 are groups having the carbon number of 6 or more is also called a medium-chain triglyceride.
- Such a medium-chain triglyceride has a feature that a user does not feel the taste or flavor during smoking.
- the concentration of a triglyceride in a liquid for atomization is not limited. However, when the concentration of a triglyceride is excessively high, the viscosity of the liquid increases. This causes a problem in which the amount to be atomized decreases in a non-heating type flavor inhaler that utilizes vibrations, such as ultrasonic vibrations.
- the upper limit of the concentration in a liquid for atomization is preferably 10 weight% or less and more preferably 5 weight% or less. Meanwhile, the lower limit of the concentration is not limited but is preferably 1 weight% or more and more preferably 2 weight% or more.
- An emulsifier has an affinity with water in a liquid for atomization and a triglyceride as a hydrophobic substance.
- any publicly known emulsifier can be used, and examples include anionic surfactants (sodium lauryl sulfate and alkyl ether carboxylates, for example), cationic surfactants (benzalkonium chloride, for example), amphoteric surfactants (lecithin, for example), and nonionic surfactants (polyglycerol fatty acid esters, sucrose fatty acid esters, calcium stearoyl lactylate, sorbitan fatty acid esters, propylene glycol fatty acid esters, polyoxyethylene alkyl ethers, polyoxyethylene sorbitan fatty acid esters, and saponins, for example).
- anionic surfactants sodium lauryl sulfate and alkyl ether carboxylates, for example
- cationic surfactants benzalkonium chloride,
- the concentration of an emulsifier in a liquid for atomization is not limited but is preferably 2 weight% or less and more preferably 1 weight% or less.
- the lower limit of the concentration is not limited but is preferably 0.1 weight% or more and more preferably 0.2 weight% or more.
- a water-based aerosol source is used.
- the expression of "water-based” herein means that 70 weight% or more of water is contained in an aerosol source. Water preferably accounts for 80 weight% or more relative to the entire aerosol source. Exemplary aerosol sources other than water include glycerol and propylene glycol. The amount of these is preferably 30 weight% or less and more preferably 20 weight% or less in an aerosol source. Alternatively, an aerosol source may solely consist of water. Moreover, water preferably accounts for 70 weight% or more in a liquid for atomization. Since water preferably contains no impurity, deionized water or the like may be used.
- a liquid for atomization used in the present invention may contain any flavor publicly known in the field concerned. Such a flavor is not limited, and examples include menthol.
- the amount may be a publicly known amount but is preferably 8 weight% or less and more preferably 5 weight% or less in a liquid for atomization.
- the lower limit of the concentration is not limited, and other components (flavor) need not be contained.
- a liquid for atomization used in the present invention does not contain nicotine in an embodiment.
- a liquid for atomization 1 originally has a structure in which an oil droplet 4 of a hydrophobic substance (triglyceride) having a low vapor pressure is finely dispersed in a water-based aerosol source 2. Such oil droplets exist in a stable manner by means of an emulsifier 6. The liquid for atomization is then atomized to form an atomized product of aggregated particles 1'.
- a hydrophobic substance triglyceride
- the diameter of the particles 1' is 0.1 to 10 ⁇ m, and the diameter of oil droplets 4 present within each particle 1' is 0.01 to 1 ⁇ m.
- oil droplets 4 act as nuclei and suppress vaporization of the surrounding aerosol source 2. Further, due to the low vapor pressure, oil droplets 4 alone remain there without vaporization even after the aerosol source 2 is vaporized. Consequently, it is presumed that the visibility of visible smoke is enhanced and the duration time of such a high visibility state increases.
- a non-heating type flavor inhaler is an apparatus that makes a flavor component contained in a liquid for atomization inhalable and that includes at least a liquid storage section for storing the liquid for atomization and an atomization section for atomizing the liquid for atomization.
- the flavor inhaler is thus used in the state in which the liquid storage section is filled with the liquid for atomization.
- the non-heating type flavor inhaler includes a mouthpiece for facilitating inhalation.
- the atomization section may have a vibration generating mechanism that can apply vibration to the liquid for atomization. Such an atomization section having a vibration generating mechanism is preferable since atomization efficiency is high.
- the atomization section preferably does not have a heating mechanism.
- a heating mechanism herein means a mechanism that can alone atomize a liquid for atomization. For example, the temperature of a liquid rises in some cases when vibration is applied by a vibration generating mechanism. In this case, however, such a vibration generating mechanism is not regarded as a heating mechanism.
- auxiliary heating mechanism herein means a heating mechanism that can heat a liquid for atomization but cannot alone atomize the liquid for atomization.
- exemplary auxiliary heating mechanisms include a heating mechanism that does not heat a liquid for atomization to its boiling point.
- Fig. 2 illustrates an embodiment of a non-heating type flavor inhaler.
- 1000 is a non-heating type flavor inhaler
- 1001D is a mouthpiece
- 1100 is an atomization section
- 1200A and 1200B are each a liquid storage section
- 1202 is a housing
- 1102 and 1104 are each an opening
- 1106 is a top surface cover of the atomization section
- 1107 is a bottom surface cover of the atomization section
- 1004 is a screw.
- the liquid storage sections 1200A and 1200B are placed in holding sections provided in the housing 1202, and to the top surfaces thereof, the atomization section 1100 and the mouthpiece 1001D are connected in this order using screws 1004.
- the atomization section 1100 is shielded with the top surface cover 1106 of the atomization section and the bottom surface cover 1107 of the atomization section.
- Fig. 3 illustrates, in the atomization section 1100, components disposed between the top surface cover 1106 of the atomization section and the bottom surface cover 1107 of the atomization section.
- the atomization section 1100 includes a PCB 1109, a piezoelectric element substrate 1031 equipped with an interdigital electrode 1033, and a pair of guide walls 1711A and 1711B.
- a top cover and a base component or the like may be disposed above and below these components, respectively.
- a sensor and/or a seal may be disposed, as necessary, between these components and the top cover.
- Fig. 4 illustrates the connection between the atomization section and the liquid storage section.
- the figure illustrates only the liquid storage section 1200A, but in fact, the liquid storage section 1200B is also connected with the atomization section 1100.
- the liquid storage section 1200A is connected with the atomization section 1100 such that a liquid discharge section provided on the top surface of the liquid storage section 1200A is in communication with a penetrating hole 1713A.
- Fig. 5 is an enlarged view of a portion of the atomization section 1100 illustrated in Fig. 3 . Specifically, Fig.
- FIG. 5 illustrates, from the atomization section 1100 illustrated in Fig. 3 , the PCB 1109, the piezoelectric element substrate 1031 equipped with the interdigital electrode 1033, the guide wall 1711A, a seal 1111, and a sensor 1070.
- the atomization section 1100 includes the piezoelectric element substrate 1031 equipped with the interdigital electrode 1033 and is configured to atomize a liquid by surface acoustic waves (SAWs) generated under application of voltage at a high frequency to the interdigital electrode 1033.
- SAWs surface acoustic waves
- a liquid for atomization inside the liquid storage sections 1200A and 1200B is atomized by surface acoustic waves, and the atomized product reaches the mouthpiece.
- the piezoelectric element substrate 1031 is configured to atomize a liquid by SAWs generated under application of voltage at a high frequency (resonance frequency) to the interdigital electrode 1033.
- the piezoelectric element substrate 1031 includes a piezoelectric body that expands and contracts by voltage application.
- a piezoelectric body any known piezoelectric body formed of, for example, ceramic, such as quartz, barium titanate, or lithium niobate, can be used.
- the interdigital electrode 1033 is electrically connected with a power source (not illustrated) provided inside the housing 1202 and is supplied with power.
- a power source not illustrated
- the interdigital electrode 1033 is formed of a gold-plated metal or the like.
- the piezoelectric element substrate 1031 has a pair of edges 1031A and 1031B that face each other.
- the guide wall 1711A is provided on the edge 1031A side of the piezoelectric element substrate 1031, and the guide wall 1711B is provided on the edge 1031B side.
- the guide walls 1711A and 1711B respectively have penetrating holes 1713A and 1713B that extend between the upper and lower surfaces.
- the guide walls 1711A and 1711B respectively have recesses 1714A and 1714B in communication with the respective penetrating holes 1713A and 1713B.
- the liquid storage sections 1200A and 1200B are respectively connected to the lower surfaces of the guide walls 1711A and 1711B.
- a liquid for atomization supplied from the liquid storage sections 1200A and 1200B by a syringe pump (not illustrated) passes through each penetrating hole 1713A or 1713B upward and reaches the recess 1714A or 1714B.
- the liquid that has reached the recess 1714A or 1714B then reaches the edge 1031A or 1031B of the piezoelectric element substrate 1031 and is atomized by the energy of the interdigital electrode 1033.
- the syringe pump is configured to supply the liquid for atomization to the edges 1031A and 1031B of the piezoelectric element substrate 1031.
- a non-heating type flavor inhaler like this is disclosed in PCT/JP 2019/015377 , for example.
- the figures illustrate an embodiment including two liquid storage sections, one liquid storage section may be included.
- a non-heating type flavor inhaler including an atomization section having a vibration generating mechanism that utilizes ultrasonic vibrations, for example, may be used as well.
- Such an atomization section is used in an ultrasonic nebulizer (for example, NE-U17 and NE-U22 from Omron Corporation) and so forth.
- a non-heating type flavor inhaler including an atomization section that uses a nozzle may also be used.
- Such an atomization section includes a liquid storage section, a nozzle for ejecting compressed air, and a suction tube that is provided adjacent to the nozzle and is in communication with the liquid for atomization holding section; and atomizes the liquid for atomization by pressure differences generated between the nozzle section and the suction tube when compressed air is ejected from the nozzle.
- Such an atomization section is used in a compressor nebulizer and so forth.
- the non-heating type flavor inhaler of the present invention may include a heating mechanism in portions excluding the atomization section.
- the flavor inhaler of Fig. 2 may be provided, around the liquid storage sections 1200A and 1200B, with a heating mechanism for heating a liquid or may be provided with a heating mechanism in the flow channel of the mouthpiece 1001D.
- a medium-chain triglyceride 5 g of Coconad ® MT (C 8 /C 10 triglyceride) from Kao Corporation, 5 g of an emulsifier (Emasol S-120V from Kao Corporation), and 490 g of water were mixed and emulsified with a homogenizer (Dostormix B DMM from Etekku Japan). The obtained liquid was further emulsified with a high pressure homogenizer (Panda Plus 2000 from GEA Niro Soavi) at a pressure of 50 MPa to yield a liquid for atomization.
- a homogenizer Dostormix B DMM from Etekku Japan
- FIG. 6 An apparatus as illustrated in Fig. 6 was prepared.
- 200 is a nebulizer (NE-U22 mesh nebulizer from Omron Corporation)
- 202 is a laser source
- 204 is a light receiving section
- 206 is a transparent chamber (5 cm ⁇ 5 cm ⁇ 24 cm)
- 208 is a tube.
- a liquid filling section of the nebulizer 200 was filled with the liquid for atomization, and smoke was generated through atomization. The smoke was sucked for 2 seconds at a rate of 55 mL/2 sec from the upper side of the chamber.
- the position 8.5 cm from the chamber bottom surface was irradiated with a laser from the start of sucking (0 second later) to measure light transmittance 5 seconds later in the center of the chamber 206.
- the light transmittance was assessed using Spraytec from Malvern Panalytical, which includes a laser source 202 and a light receiving section 204.
- the light transmittance of the chamber in the absence of smoke was set to 100%.
- the result is shown in Table 1.
- a lower light transmittance indicates higher visibility of visible smoke.
- light transmittance was continuously measured from the start of sucking (0 second later) to 30 seconds later to record the total time (T) for the light transmittance being 85% or less until 30 seconds later. The result is shown in Table 1.
- Example 2 An assessment was made in the same manner as Example 1 except for changing the concentration of a medium-chain triglyceride as shown in Table 1.
- Example 2 An assessment was made in the same manner as Example 2 except for using Coconad ® RK (Cs triglyceride) from Kao Corporation as a medium-chain triglyceride.
- Coconad ® RK Coconad ® RK (Cs triglyceride) from Kao Corporation as a medium-chain triglyceride.
- Example 2 An assessment was made in the same manner as Example 2 except for using MT-N (C 8 /C 10 triglyceride) from Kao Corporation as a medium-chain triglyceride.
- MT-N C 8 /C 10 triglyceride
- Example 2 An assessment was made in the same manner as Example 2 except for using Coconad ® ML (C 8 /C 10 /C 12 triglyceride) from Kao Corporation as a medium-chain triglyceride.
- Coconad ® ML C 8 /C 10 /C 12 triglyceride
- Example 2 An assessment was made in the same manner as Example 1 except for changing the composition of a liquid for atomization as shown in Table 1 without using a triglyceride.
- a liquid for atomization having the composition shown in Table 1 was prepared. Moreover, a commercial refillable heating-type electronic cigarette was prepared. A flavor liquid of this product was replaced by the liquid for atomization prepared in the present example, and the heating-type electronic cigarette for comparison was disposed in place of the nebulizer 200 in the apparatus illustrated in Fig. 6 . Visible smoke was generated through heating under conditions of 5 W and assessed in the same manner as Example 1. The results are shown in Table 1.
- Example Comparative Example 1 1) 2 1) 3 2) 4 3) 5 4) 1 2 Triglyceride (weight%) 1 5 5 5 5 0 0 Emulsifier (weight%) 1 1 1 1 1 1 1 1 1 1 Water (weight%) 98 94 94 94 99 0 Propylene glycol (weight%) 0 0 0 0 0 0 99 Light transmittance (%) 5 seconds later from the start of sucking 80.34 74.02 62.74 71.57 58.47 89.99 62.86 Total time (T) for light transmittance being 85% or less (sec) 4.57 12.18 18.81 14.24 20.55 3.92 28.72 1) Coconad ® MT 2) Coconad ® RK 3) MT-N 4) Coconad ® ML
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Medicinal Preparation (AREA)
- Manufacture Of Tobacco Products (AREA)
- Fats And Perfumes (AREA)
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
Claims (7)
- Nichtwärmender Aromainhalator, umfassend:eine Flüssigkeit zur Zerstäubung, enthaltend ein Triglycerid, einen Emulgator und eine wasserbasierte Aerosolquelle, wobei die Aerosolquelle 70 Gew.-% oder mehr Wasser enthält, und wobei das Triglycerid eine aliphatische Gruppe aufweist, die von einer Fettsäure abgeleitet ist und eine Kohlenstoffzahl von 6 oder mehr aufweist;einen Flüssigkeitsspeicherabschnitt zum Speichern der Flüssigkeit zur Zerstäubung; undeinen Zerstäubungsabschnitt zum Zerstäuben der Flüssigkeit zur Zerstäubung.
- Nichtwärmender Aromainhalator gemäß Anspruch 1, wobei die Konzentration des Triglycerids in der Flüssigkeit zur Zerstäubung 10 Gew.-% oder weniger beträgt.
- Nichtwärmender Aromainhalator gemäß Anspruch 1 oder 2, wobei die Aerosolquelle 80 Gew.-% oder mehr Wasser in der Aerosolquelle enthält.
- Nichtwärmender Aromainhalator gemäß einem der Ansprüche 1 bis 3, wobei die Flüssigkeit zur Zerstäubung 70 Gew.-% oder mehr Wasser in der Flüssigkeit enthält.
- Nichtwärmender Aromainhalator gemäß einem der Ansprüche 1 bis 4, wobei die Flüssigkeit zur Zerstäubung zusätzlich ein Aroma enthält.
- Nichtwärmender Aromainhalator gemäß einem der Ansprüche 1 bis 5, wobei der Zerstäubungsabschnitt einen Zerstäubungsmechanismus durch Vibrationen aufweist.
- Flüssigkeit zur Zerstäubung für einen nichtwärmenden Aromainhalator, umfassend ein Triglycerid, einen Emulgator und eine wasserbasierte Aerosolquelle, wobei die Aerosolquelle 70 Gew.-% oder mehr Wasser enthält, und wobei das Triglycerid eine aliphatische Gruppe aufweist, die von einer Fettsäure abgeleitet ist und eine Kohlenstoffzahl von 6 oder mehr aufweist.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2019158166 | 2019-08-30 | ||
| PCT/JP2020/030155 WO2021039343A1 (ja) | 2019-08-30 | 2020-08-06 | 非加熱型香味吸引器 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| EP4023274A1 EP4023274A1 (de) | 2022-07-06 |
| EP4023274A4 EP4023274A4 (de) | 2023-09-06 |
| EP4023274B1 true EP4023274B1 (de) | 2025-11-26 |
Family
ID=74683824
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP20856003.7A Active EP4023274B1 (de) | 2019-08-30 | 2020-08-06 | Dampfinhalator ohne erwärmung |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP4023274B1 (de) |
| JP (1) | JP7274586B2 (de) |
| CN (1) | CN114269174B (de) |
| TW (1) | TW202121995A (de) |
| WO (1) | WO2021039343A1 (de) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2024034126A1 (ja) * | 2022-08-12 | 2024-02-15 | 日本たばこ産業株式会社 | 吸引器 |
| WO2024138377A1 (zh) * | 2022-12-27 | 2024-07-04 | 思摩尔国际控股有限公司 | 一种雾化液、雾化器及电子雾化装置 |
| CN117223882B (zh) * | 2023-10-16 | 2025-07-25 | 江苏中烟工业有限责任公司 | 一种超低温雾化剂及其制备方法和应用 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK174559B1 (da) | 2000-02-11 | 2003-06-02 | Danfoss As | System til udmåling af portioner af fluid |
| US20080038363A1 (en) * | 2001-05-24 | 2008-02-14 | Zaffaroni Alejandro C | Aerosol delivery system and uses thereof |
| JP4526120B2 (ja) | 2002-05-22 | 2010-08-18 | 日本製薬株式会社 | L−メントール水中油型乳剤 |
| ES2913095T3 (es) * | 2011-01-31 | 2022-05-31 | Avalyn Pharma Inc | Compuestos de pirfenidona y análogos de piridona en aerosol y usos de los mismos |
| US9854839B2 (en) * | 2012-01-31 | 2018-01-02 | Altria Client Services Llc | Electronic vaping device and method |
| GB2524856B (en) * | 2014-04-02 | 2021-04-07 | Twenty Sixteen 2016 Pharma Ltd | Pulmonary delivery devices |
| US20150216237A1 (en) * | 2014-01-22 | 2015-08-06 | E-Nicotine Technology, Inc. | Methods and devices for smoking urge relief |
| US20160213866A1 (en) * | 2015-01-23 | 2016-07-28 | William Tan | Ultrasonic vaporizing element |
-
2020
- 2020-08-06 EP EP20856003.7A patent/EP4023274B1/de active Active
- 2020-08-06 CN CN202080059696.9A patent/CN114269174B/zh active Active
- 2020-08-06 TW TW109126709A patent/TW202121995A/zh unknown
- 2020-08-06 WO PCT/JP2020/030155 patent/WO2021039343A1/ja not_active Ceased
- 2020-08-06 JP JP2021542698A patent/JP7274586B2/ja active Active
Also Published As
| Publication number | Publication date |
|---|---|
| JPWO2021039343A1 (de) | 2021-03-04 |
| CN114269174A (zh) | 2022-04-01 |
| WO2021039343A1 (ja) | 2021-03-04 |
| JP7274586B2 (ja) | 2023-05-16 |
| TW202121995A (zh) | 2021-06-16 |
| CN114269174B (zh) | 2025-01-03 |
| EP4023274A4 (de) | 2023-09-06 |
| EP4023274A1 (de) | 2022-07-06 |
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