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WO2011122567A1 - Oral tobacco material - Google Patents

Oral tobacco material Download PDF

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Publication number
WO2011122567A1
WO2011122567A1 PCT/JP2011/057656 JP2011057656W WO2011122567A1 WO 2011122567 A1 WO2011122567 A1 WO 2011122567A1 JP 2011057656 W JP2011057656 W JP 2011057656W WO 2011122567 A1 WO2011122567 A1 WO 2011122567A1
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WIPO (PCT)
Prior art keywords
tobacco material
weight
oral tobacco
oral
tobacco
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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.)
Ceased
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PCT/JP2011/057656
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French (fr)
Japanese (ja)
Inventor
岡田 拓也
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Japan Tobacco Inc
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Japan Tobacco Inc
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Application filed by Japan Tobacco Inc filed Critical Japan Tobacco Inc
Priority to DK11762791.9T priority Critical patent/DK2554059T3/en
Priority to JP2012508316A priority patent/JP5337910B2/en
Priority to EP11762791.9A priority patent/EP2554059B1/en
Publication of WO2011122567A1 publication Critical patent/WO2011122567A1/en
Priority to US13/614,752 priority patent/US20130008458A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • AHUMAN NECESSITIES
    • A24TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24BMANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
    • A24B15/00Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
    • A24B15/18Treatment of tobacco products or tobacco substitutes
    • A24B15/28Treatment of tobacco products or tobacco substitutes by chemical substances
    • A24B15/287Treatment of tobacco products or tobacco substitutes by chemical substances by inorganic substances only

Definitions

  • the present invention relates to an oral tobacco material, and more particularly to an oral tobacco material excellent in pH stability when stored at room temperature.
  • oral tobacco products such as moist-snuff or snus have attracted attention.
  • oral tobacco materials including wet powdered tobacco are contained in a moisture-permeable pouch and inserted between the lips and gums in the oral cavity to enjoy the taste and aroma of powdered tobacco.
  • Such a wet powder tobacco generally shows weak acidity (pH of about 4.0 to 6.0), and bacteria are likely to grow. Therefore, in order to suppress the growth of bacteria and increase the storage stability, a pH adjuster is added to the powdered tobacco, and the pH is adjusted from a substantially neutral to an alkaline pH. Moreover, in order to give a desirable flavor, the pH is adjusted to one desired pH in a substantially neutral to alkaline region. From the viewpoint of maintaining the quality of the product, it is desired that the adjusted pH is substantially maintained over the entire storage period.
  • Patent Document 1 discloses using an alkali metal hydroxide, metal carbonate, or metal bicarbonate as a pH adjuster or buffer. However, any of these pH adjusting agents or buffering agents is an alkaline substance. Patent Document 1 also discloses blending an inorganic filler into powdered tobacco, and calcium phosphate is described as an example, but calcium phosphate is a substance that exhibits alkalinity.
  • Patent Document 2 discloses a tobacco product containing magnesium carbonate as a pH adjuster for making a tobacco material alkaline.
  • magnesium carbonate is a substance showing alkalinity.
  • Patent Document 2 discloses that an additional pH adjusting agent can be used in addition to magnesium carbonate, and sodium carbonate, phosphate and the like are described as examples.
  • this additional pH adjuster has been used to quickly bring the tobacco material to the desired pH value (neutral or alkaline), and therefore the described phosphate is said to be alkaline.
  • the amount of alkaline material required to bring wet powdered tobacco to the desired neutral or alkaline pH value is uniquely determined.
  • the amount of alkaline material used to bring the powdered tobacco to the desired pH value is relatively small, and thus the adjusted pH value cannot be maintained over a long period of time. Therefore, oral tobacco materials including powdered tobacco whose initial pH is adjusted using only an alkaline substance must be stored not at room temperature but at a low temperature ( ⁇ 20 ° C. to 10 ° C.).
  • the oral tobacco material including wet powder tobacco inserted into the oral cavity has a pH of 8.5 or less.
  • An object of the present invention is to provide an oral tobacco material that exhibits excellent storage stability over a long period of time at room temperature.
  • an oral tobacco material comprising powdered tobacco and a basic salt of carbonic acid and an acidic salt of phosphoric acid as a pH adjuster, and the basic salt of carbonic acid and the acidic salt of phosphoric acid in total It is included in an amount of 6% by weight or more of the dry weight of the powdered tobacco, and is formulated so that the initial pH of the oral tobacco material is 7 to 8.5, and the oral tobacco material has a moisture content of 15% by weight or more.
  • An oral tobacco material is provided.
  • the oral tobacco material of the present invention contains a relatively large amount of a pH adjusting agent, and thus exhibits excellent storage stability over a long period of time at room temperature.
  • 6 is a graph showing changes in pH over time when the oral tobacco materials of Examples 1 and 2 and Comparative Example 1 described later are stored in an atmosphere at a temperature of 25 ° C. and a relative humidity of 60%.
  • 6 is a graph showing changes in pH over time when the oral tobacco materials of Examples 1 and 2 and Comparative Example 1 described later are stored in an atmosphere at a temperature of 35 ° C. and a relative humidity of 60%. It is a graph which shows the time-dependent change of pH when the oral tobacco material of Example 3 and the comparative example 2 mentioned later is preserve
  • the oral tobacco material of the present invention contains powdered tobacco, and a basic salt of carbonic acid and an acidic salt of phosphoric acid as a pH adjuster.
  • the basic salt of carbonic acid and the acidic salt of phosphoric acid are contained in a total amount of 6% by weight or more of the dry weight of the powdered tobacco, and the initial pH of the oral tobacco material is 7 to 8.5. Blended.
  • the oral tobacco material has a moisture content of 15% by weight or more.
  • the initial pH represents the pH when adjusted with a pH adjuster.
  • the powdered tobacco contained in the oral tobacco material includes tobacco deboned leaf powder, a mixture of tobacco deboned leaf powder and tobacco middle bone powder, reconstituted tobacco powder, reconstituted tobacco powder and tobacco deboned Contains a mixture with leaf powder.
  • tobacco varieties include Burley tobacco, yellow tobacco, Orient tobacco, dark cure tobacco, and Rustica tobacco.
  • the pH adjuster contained in the oral tobacco material is a combination of a basic salt of carbonic acid and an acidic salt of phosphoric acid.
  • the basic salt of carbonic acid is preferably selected from the group consisting of sodium carbonate and potassium carbonate. Mixtures of these basic carbonate salts can also be used.
  • the acidic salt of phosphoric acid is preferably selected from the group consisting of sodium dihydrogen phosphate and potassium dihydrogen phosphate. Mixtures of these phosphoric acid salts can also be used.
  • the basic salt of carbonic acid and the acidic salt of phosphoric acid are contained in a proportion such that the initial pH of the oral tobacco material is 7 to 8.5, and in total 6% by weight or more of the dry weight of the powdered tobacco It is. If the pH value is less than 7, it is difficult to suppress the growth of bacteria. On the other hand, if the pH value exceeds 8.5, the oral mucosa may be damaged. If the total amount of the basic salt of carbonic acid and the acidic salt of phosphoric acid is less than 6% by weight, long-term storage at room temperature (15 ° C. to 35 ° C.) may be deteriorated. As described above, powdered tobacco exhibits a pH value of about 4.0 to 6.0.
  • the pH value of the oral tobacco material is adjusted to 7 to 8.5 using both an acidic substance (acidic salt of phosphoric acid) and a basic substance (basic salt of carbonic acid). Therefore, even if a large amount of basic substance (basic salt of carbonic acid) is added so that the pH of the oral tobacco material greatly exceeds 8.5, the pH can be adjusted to 7 to 8.5 by the acidic substance. Therefore, when the pH value of the oral tobacco material is adjusted to one desired value with only the alkaline substance, the amount of the alkaline substance is uniquely determined, whereas in the present invention, the pH value of the oral tobacco material is adjusted.
  • the usage amount of an acidic substance (acidic salt of phosphoric acid) and a basic substance (basic salt of carbonic acid) can be significantly changed.
  • the acid salt of phosphoric acid is preferably used in an amount of 1% by weight or more based on the dry weight of the powdered tobacco.
  • the acid salt of phosphoric acid is usually used in an amount of 10% by weight or less of the dry weight of the powdered tobacco.
  • the use amount of the basic salt of carbonic acid corresponding to the use amount of the acidic salt of phosphoric acid is determined by the initial pH value 7 to 8.5 of the oral tobacco material.
  • the moisture content of the oral tobacco material is 15% by weight or more.
  • the pH adjuster used in the present invention can have the desired effect on the oral tobacco material having a water content of 15% by weight or more.
  • the moisture content of the oral tobacco material is usually 50% by weight or less.
  • the oral tobacco material of the present invention may contain additives such as flavoring agents and wetting agents.
  • flavoring agents menthol, mint, amino acids (glycine, etc.), plant extracts (eucalyptus, rosemary, GSE), flavonoids, vitamin E, vitamin C, monosaccharides such as citric acid, salt, fructose, and disaccharides such as sucrose , Oligosaccharides, other polysaccharides, cinnamon, horseradish, pepper, salmon, cloves, ginger, turmeric, allspice, cardamom and other spices, basil, bay leaves, mabola, oregano, rosemary, sage , Tarragon, thyme, sesame, garlic, onion and other herb spices, caraway, anise lade, celery seed, coriander, cumin seed, dill seed, finnell, mace, nutmeg, poppy seed and other seed spices, chocolate, citrus And other fruit flavors, vanillin, ethyl vanillin, bergamot oil, linalool, lemon oil, and the like.
  • the flavoring agent can be used
  • wetting agent examples include polyhydric alcohols such as glycerin and propylene glycol, sugar alcohols such as erythritol, xylitol, and sorbitol, hyaluronic acid, and the like.
  • the wetting agent can be used in an amount of 1% to 5% by weight of the dry weight of the powdered tobacco.
  • the moisture content of the powdered tobacco itself as a raw material is measured.
  • the moisture content can be measured using a commercially available heat drying moisture meter (for example, MX-50 manufactured by A & D Co., Ltd.).
  • the amount of water necessary to make the moisture content of the oral tobacco material 15% by weight or more is calculated.
  • X is the weight of the raw powdered tobacco
  • a is the moisture content (%) of the raw powdered tobacco
  • Y is the total weight of additive substances such as pH adjusters and wetting agents
  • b is the target oral tobacco. It is the moisture content (%) of the material.
  • Add the specified amount of basic carbonate carbonate and acid salt of phosphoric acid, and if necessary, water-soluble additives to the amount of water calculated in this way, and add the total amount of the resulting aqueous solution to the powdered tobacco of weight X can do.
  • Other additives can be incorporated into the resulting wet powdered tobacco.
  • the oral tobacco material of the present invention typically does not contain magnesium carbonate.
  • the oral tobacco material of the present invention is contained in a water-permeable pouch known per se to provide an oral tobacco product.
  • the oral tobacco material of the present invention can substantially maintain the initial pH value adjusted with the pH adjuster of the present invention for at least 6 months even at room temperature (15 ° C. to 35 ° C.) It is excellent.
  • the water content of 5.0 g of the raw powdered tobacco was measured at 80 ° C. using a heat drying moisture meter (MX-50 manufactured by A & D Co., Ltd.). As a result, the water content was 14.0% by weight. From the moisture content of the raw powdered tobacco, the amount of water required to adjust the final moisture content of the oral tobacco material to approximately 25% by weight was calculated, and the calculated amount of water was prepared.
  • Example 1 the water prepared above corresponds to 4.8% by weight of sodium carbonate, 1.9% by weight of sodium dihydrogen phosphate, and 5.0% by weight of glycerin, respectively, of the dry weight of the raw powdered tobacco. A quantity of sodium carbonate, sodium dihydrogen phosphate and glycerin were added, and the total amount of the resulting aqueous solution was sprayed onto the raw powder tobacco. The final moisture content of the oral tobacco material thus obtained was 25.44% by weight, and the initial pH measured by the pH measurement method described later was 8.09.
  • Example 2 an amount corresponding to 8.0% by weight of sodium carbonate, 4.1% by weight of sodium dihydrogen phosphate, and 5.0% by weight of glycerin of the dry weight of the powdered tobacco was added to the prepared water.
  • An oral tobacco material was prepared in the same manner as in Example 1 except that sodium carbonate, sodium dihydrogen phosphate and glycerin were added.
  • the final moisture content of the obtained oral tobacco material was 26.39% by weight, and the initial pH measured by the pH measurement method described later was 8.08.
  • Example 1 was added except that sodium carbonate and glycerin in an amount corresponding to 2.7% by weight of sodium carbonate and 5.0% by weight of glycerin were added to the prepared water.
  • an oral tobacco material was prepared. The final moisture content of the obtained oral tobacco material was 26.53% by weight, and the initial pH measured by the pH measurement method described later was 8.11.
  • Examples 3 to 4 and Comparative Examples 2 to 3 Raw material powder cigarettes containing 35% by weight, 15% by weight, and 50% by weight of each powder of rustica, dark-cured tobacco and tobacco bone as raw materials were prepared, and the moisture content was measured by the following method. .
  • the water content of 5.0 g of the raw powdered tobacco was measured at 80 ° C. using a heat drying moisture meter (MX-50 manufactured by A & D Co., Ltd.). As a result, the water content was 12.7% by weight. From the moisture content of the raw powdered tobacco, the amount of water required to adjust the final moisture content of the oral tobacco material to approximately 15.0% or 25.0% by weight is calculated, and the calculated amount of water is calculated. Prepared.
  • Example 3 the water required to adjust the final moisture content prepared to 25.0% by weight was added to 5.8% by weight of sodium carbonate, 4.1% by weight of phosphorus, respectively, of the dry weight of the raw powdered tobacco.
  • An oral tobacco material was prepared in the same manner as in Example 1 except that sodium carbonate, sodium dihydrogen phosphate and glycerin in an amount corresponding to sodium dihydrogen acid and 5.0% by weight of glycerin were added.
  • the final moisture content of the oral tobacco material thus obtained was 26.9% by weight, and the initial pH measured by the pH measurement method described later was 7.73.
  • Example 4 5.0% by weight of sodium carbonate, 4.1% by weight of diphosphoric acid phosphate was added to the water necessary for adjusting the final moisture content prepared above to 15.0% by weight.
  • An oral tobacco material was prepared in the same manner as in Example 1 except that sodium carbonate, sodium dihydrogen phosphate and glycerin corresponding to sodium hydride and 5.0% by weight of glycerin were added.
  • the final moisture content of the obtained oral tobacco material was 18.6% by weight, and the initial pH measured by the pH measurement method described later was 7.21.
  • Comparative Example 2 the water necessary for adjusting the final moisture content prepared above to 25.0% by weight corresponds to 3.2% by weight of sodium carbonate and 5.0% by weight of glycerin of the dry weight of the powdered tobacco.
  • An oral tobacco material was prepared in the same manner as in Example 1 except that sodium carbonate and glycerin were added.
  • the final moisture content of the obtained oral tobacco material was 26.1% by weight, and the initial pH measured by the pH measurement method described later was 7.7.
  • Comparative Example 4 the water required for adjusting the final moisture content prepared above to 15.0% by weight corresponds to 3.2% by weight sodium carbonate and 5.0% by weight glycerin of the dry weight of the powdered tobacco.
  • An oral tobacco material was prepared in the same manner as in Example 1 except that sodium carbonate and glycerin were added. The final moisture content of the obtained oral tobacco material was 18.1% by weight, and the initial pH measured by the pH measurement method described later was 7.12.
  • Each of the oral tobacco materials obtained in Examples 1 and 2 and Comparative Example 1 was put in a storage pack (produced by Japan, Lamidip AL-4; moisture-proof, gas-blocking, and light-blocking container). It was stored for 6 months in an atmosphere of a temperature of 25 ° C. and a relative humidity of 60% and in an atmosphere of a temperature of 35 ° C. and a relative humidity of 60%. During the storage period, the pH was measured periodically by the pH measurement method described later. The results are shown in FIG. 1 and FIG. FIG. 1 shows the results of storage in an atmosphere at a temperature of 25 ° C. and a relative humidity of 60%, and FIG. 2 shows the results of storage in an atmosphere of a temperature of 35 ° C. and a relative humidity of 60%. In FIG.
  • a line segment a relates to Example 1
  • a line segment b relates to Example 2
  • a line segment c relates to Comparative Example 1.
  • the oral tobacco material of Comparative Example 1 has a pH of about 0.5 when stored for 6 months in an atmosphere at a temperature of 25 ° C. and a relative humidity of 60%.
  • the pH value decreases by about 1.0
  • the oral tobacco materials of Examples 1 and 2 have a pH value under any storage condition. It turns out that it hardly decreases.
  • the oral tobacco materials obtained in Examples 3 to 4 and Comparative Examples 2 to 3 were put in the above-mentioned storage packs (produced by Japan Lamidip AL-4), respectively, and the atmosphere at a temperature of 25 ° C. and a relative humidity of 60%. Stored for 6 months below. During the storage period, the pH was measured periodically by the pH measurement method described later. The results are shown in FIG. 3 and FIG. In FIG. 3, the line segment d relates to Example 3, and the line segment e relates to Comparative Example 2. In FIG. 4, the line segment f relates to Example 4, and the line segment g relates to Comparative Example 3. As is clear from the results shown in FIGS.
  • the oral tobacco material of Comparative Example 2 has a pH of about 1.2 when stored for 6 months in an atmosphere at a temperature of 25 ° C. and a relative humidity of 60%.
  • the decrease in pH value during storage under the same conditions is about 0.6, indicating that the decrease in pH during storage is suppressed.
  • the oral tobacco material of Comparative Example 3 has a pH of about 0.4 when stored for 6 months in an atmosphere at a temperature of 25 ° C. and a relative humidity of 60%.
  • the decrease in pH value during storage under conditions is about 0.25, indicating that the decrease in pH during storage is suppressed.

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  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Toxicology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Manufacture Of Tobacco Products (AREA)

Abstract

The disclosed oral tobacco material contains: powdered tobacco; and an acid salt of phosphoric acid and a basic salt of carbonic acid as pH adjustors. The acid salt of phosphoric acid and the basic salt of carbonic acid are contained in quantities that total at least 6 wt.% of the dry weight of the powdered tobacco, and are formulated in a manner so that the initial pH of the oral tobacco material becomes 7-8.5; the aforementioned oral tobacco material contains at least 15 wt.% moisture content.

Description

オーラルタバコ材料Oral tobacco material

 本発明は、オーラルタバコ材料に係り、特に室温で保存した際のpH安定性に優れたオーラルタバコ材料に関する。 The present invention relates to an oral tobacco material, and more particularly to an oral tobacco material excellent in pH stability when stored at room temperature.

 近年、moist-snuffもしくはスヌース等のオーラルタバコ製品が注目されてきている。これらオーラルタバコ製品は、湿った粉末タバコを含むオーラルタバコ材料を、水分透過性のポーチに収容したもので、口腔内で唇と歯茎の間に挿入し、粉末タバコの味・香りを楽しむものである。 In recent years, oral tobacco products such as moist-snuff or snus have attracted attention. In these oral tobacco products, oral tobacco materials including wet powdered tobacco are contained in a moisture-permeable pouch and inserted between the lips and gums in the oral cavity to enjoy the taste and aroma of powdered tobacco.

 このような湿った粉末タバコは、それ自体、一般的に弱酸性(pH約4.0~6.0)を示し、細菌が増殖しやすい。そこで、細菌の増殖を抑制して保存安定性を高めるために、粉末タバコにpH調整剤を添加して、そのpHをほぼ中性からアルカリ性のpHに調整されている。また、望ましい風味を与えるために、pHはほぼ中性からアルカリ性の領域で1つの所望のpHに調整されている。そして、製品の品質維持の点から、全保存期間にわたって、調整されたpHが実質的に維持されることが望まれている。 Such a wet powder tobacco generally shows weak acidity (pH of about 4.0 to 6.0), and bacteria are likely to grow. Therefore, in order to suppress the growth of bacteria and increase the storage stability, a pH adjuster is added to the powdered tobacco, and the pH is adjusted from a substantially neutral to an alkaline pH. Moreover, in order to give a desirable flavor, the pH is adjusted to one desired pH in a substantially neutral to alkaline region. From the viewpoint of maintaining the quality of the product, it is desired that the adjusted pH is substantially maintained over the entire storage period.

 特許文献1は、pH調整剤または緩衝剤として、アルカリ金属水酸化物、金属炭酸塩、金属重炭酸塩を用いることを開示している。しかしながら、これらpH調整剤または緩衝剤は、いずれも、アルカリ性を示す物質である。特許文献1は、粉末タバコに無機充填材を配合することも開示し、その例としてリン酸カルシウムが記載されているが、リン酸カルシウムはアルカリ性を示す物質である。 Patent Document 1 discloses using an alkali metal hydroxide, metal carbonate, or metal bicarbonate as a pH adjuster or buffer. However, any of these pH adjusting agents or buffering agents is an alkaline substance. Patent Document 1 also discloses blending an inorganic filler into powdered tobacco, and calcium phosphate is described as an example, but calcium phosphate is a substance that exhibits alkalinity.

 特許文献2は、タバコ材料をアルカリ性にするためのpH調整剤として炭酸マグネシウムを含むタバコ製品を開示する。しかしながら、炭酸マグネシウムは、アルカリ性を示す物質である。さらに、特許文献2は、炭酸マグネシウムに加えて、追加のpH調整剤を用い得ることを開示し、その例として、炭酸ナトリウム、リン酸塩等が記載されている。しかしながら、この追加のpH調整剤は、タバコ材料を迅速に所望のpH値(中性ないしアルカリ性)にもたらすために使用されており、従って記載されたリン酸塩はアルカリ性を示すものといえる。 Patent Document 2 discloses a tobacco product containing magnesium carbonate as a pH adjuster for making a tobacco material alkaline. However, magnesium carbonate is a substance showing alkalinity. Further, Patent Document 2 discloses that an additional pH adjusting agent can be used in addition to magnesium carbonate, and sodium carbonate, phosphate and the like are described as examples. However, this additional pH adjuster has been used to quickly bring the tobacco material to the desired pH value (neutral or alkaline), and therefore the described phosphate is said to be alkaline.

 アルカリ性の物質は、湿った粉末タバコを所望の中性ないしアルカリ性のpH値にもたらすために必要な量は一義的に決定されてしまう。加えて、粉末タバコを所望のpH値にもたらすためのアルカリ性物質の使用量は、比較的少ないため、調整されたpH値を長期にわたって維持することができない。そこで、アルカリ性物質のみを用いて初期pHが調整された粉末タバコを含むオーラルタバコ材料は、室温ではなく、低温(-20℃~10℃)で保存せざるを得ない。 The amount of alkaline material required to bring wet powdered tobacco to the desired neutral or alkaline pH value is uniquely determined. In addition, the amount of alkaline material used to bring the powdered tobacco to the desired pH value is relatively small, and thus the adjusted pH value cannot be maintained over a long period of time. Therefore, oral tobacco materials including powdered tobacco whose initial pH is adjusted using only an alkaline substance must be stored not at room temperature but at a low temperature (−20 ° C. to 10 ° C.).

 なお、保存安定性を長期にわたって維持するために、多量のアルカリ性物質をオーラルタバコ材料に添加すると、pH値が大きく上昇してしまい、口腔内に挿入すると粘膜を害するおそれがある。口腔内に挿入される湿った粉末タバコを含むオーラルタバコ材料は、pH8.5以下であることが望ましい。 In addition, when a large amount of an alkaline substance is added to the oral tobacco material in order to maintain the storage stability for a long period of time, the pH value is greatly increased, and the mucous membrane may be damaged if inserted into the oral cavity. It is desirable that the oral tobacco material including wet powder tobacco inserted into the oral cavity has a pH of 8.5 or less.

特表2009-508523号公報Special table 2009-508523 国際公開WO2009/082331International Publication WO2009 / 082331

 本発明は、室温で長期にわたって優れた保存安定性を示すオーラルタバコ材料を提供することを目的とする。 An object of the present invention is to provide an oral tobacco material that exhibits excellent storage stability over a long period of time at room temperature.

 本発明によれば、粉末タバコ、およびpH調整剤として炭酸の塩基性塩とリン酸の酸性塩を含むオーラルタバコ材料であり、前記炭酸の塩基性塩とリン酸の酸性塩とは、合計で前記粉末タバコの乾燥重量の6重量%以上の量で含まれ、かつオーラルタバコ材料の初期pHが7~8.5となるように配合され、前記オーラルタバコ材料は15重量%以上の含水率を有するオーラルタバコ材料が提供される。 According to the present invention, there is provided an oral tobacco material comprising powdered tobacco and a basic salt of carbonic acid and an acidic salt of phosphoric acid as a pH adjuster, and the basic salt of carbonic acid and the acidic salt of phosphoric acid in total It is included in an amount of 6% by weight or more of the dry weight of the powdered tobacco, and is formulated so that the initial pH of the oral tobacco material is 7 to 8.5, and the oral tobacco material has a moisture content of 15% by weight or more. An oral tobacco material is provided.

 本発明のオーラルタバコ材料は、比較的多量のpH調整剤を含み、従って室温で長期にわたって、優れた保存安定性を示す。 The oral tobacco material of the present invention contains a relatively large amount of a pH adjusting agent, and thus exhibits excellent storage stability over a long period of time at room temperature.

後述する実施例1~2、比較例1のオーラルタバコ材料を、温度25℃、相対湿度60%の雰囲気下で保存したときのpHの経時変化を示すグラフである。6 is a graph showing changes in pH over time when the oral tobacco materials of Examples 1 and 2 and Comparative Example 1 described later are stored in an atmosphere at a temperature of 25 ° C. and a relative humidity of 60%. 後述する実施例1~2、比較例1のオーラルタバコ材料を、温度35℃、相対湿度60%の雰囲気下で保存したときのpHの経時変化を示すグラフである。6 is a graph showing changes in pH over time when the oral tobacco materials of Examples 1 and 2 and Comparative Example 1 described later are stored in an atmosphere at a temperature of 35 ° C. and a relative humidity of 60%. 後述する実施例3と比較例2のオーラルタバコ材料を、温度25℃、相対湿度60%の雰囲気下で保存したときのpHの経時変化を示すグラフである。It is a graph which shows the time-dependent change of pH when the oral tobacco material of Example 3 and the comparative example 2 mentioned later is preserve | saved in the atmosphere of temperature 25 degreeC and 60% of relative humidity. 後述する実施例4と比較例3のオーラルタバコ材料を、温度25℃、相対湿度60%の雰囲気下で保存したときのpHの経時変化を示すグラフである。It is a graph which shows the time-dependent change of pH when the oral tobacco material of Example 4 and the comparative example 3 mentioned later is preserve | saved in the atmosphere of temperature 25 degreeC and relative humidity 60%.

 以下、本発明の種々の態様を詳しく説明する。 Hereinafter, various aspects of the present invention will be described in detail.

 本発明のオーラルタバコ材料は、粉末タバコ、およびpH調整剤として炭酸の塩基性塩とリン酸の酸性塩を含む。炭酸の塩基性塩とリン酸の酸性塩とは、合計で粉末タバコの乾燥重量の6重量%以上の量で含まれ、かつ前記オーラルタバコ材料の初期pHが7~8.5となるように配合される。オーラルタバコ材料は、15重量%以上の含水率を有する。初期pHは、pH調整剤により調整されたときのpHを表す。 The oral tobacco material of the present invention contains powdered tobacco, and a basic salt of carbonic acid and an acidic salt of phosphoric acid as a pH adjuster. The basic salt of carbonic acid and the acidic salt of phosphoric acid are contained in a total amount of 6% by weight or more of the dry weight of the powdered tobacco, and the initial pH of the oral tobacco material is 7 to 8.5. Blended. The oral tobacco material has a moisture content of 15% by weight or more. The initial pH represents the pH when adjusted with a pH adjuster.

 上記オーラルタバコ材料に含まれる粉末タバコには、タバコ除骨葉の粉末、タバコ除骨葉の粉末とタバコ中骨との粉末の混合物、再構成タバコの粉末、再構成タバコの粉末とタバコ除骨葉の粉末との混合物が含まれる。タバコの品種としては、バーレー種タバコ、黄色種タバコ、オリエント種タバコ、ダークキュアタバコ、ルスチカ(Rustica)タバコを例示することができる。 The powdered tobacco contained in the oral tobacco material includes tobacco deboned leaf powder, a mixture of tobacco deboned leaf powder and tobacco middle bone powder, reconstituted tobacco powder, reconstituted tobacco powder and tobacco deboned Contains a mixture with leaf powder. Examples of tobacco varieties include Burley tobacco, yellow tobacco, Orient tobacco, dark cure tobacco, and Rustica tobacco.

 上記オーラルタバコ材料に含まれるpH調整剤は、炭酸の塩基性塩とリン酸の酸性塩との組み合わせからなる。炭酸の塩基性塩は、好ましくは、炭酸ナトリウムおよび炭酸カリウムからなる群の中から選ばれる。これら炭酸の塩基性塩の混合物も用いることができる。リン酸の酸性塩は、好ましくは、リン酸二水素ナトリウムおよびリン酸二水素カリウムからなる群の中から選ばれる。これらリン酸の酸性塩の混合物も用いることができる。 The pH adjuster contained in the oral tobacco material is a combination of a basic salt of carbonic acid and an acidic salt of phosphoric acid. The basic salt of carbonic acid is preferably selected from the group consisting of sodium carbonate and potassium carbonate. Mixtures of these basic carbonate salts can also be used. The acidic salt of phosphoric acid is preferably selected from the group consisting of sodium dihydrogen phosphate and potassium dihydrogen phosphate. Mixtures of these phosphoric acid salts can also be used.

 炭酸の塩基性塩とリン酸の酸性塩とは、オーラルタバコ材料の初期pHが7~8.5となるような割合で、かつ合計で粉末タバコの乾燥重量の6重量%以上の量で含まれる。pH値が7未満であると、細菌の増殖を抑制することが困難であり、他方pH値が8.5を越えると、口腔粘膜を害するおそれがある。また、炭酸の塩基性塩とリン酸の酸性塩との合計量が6重量%未満であると、室温(15℃~35℃)下での長期保存性が悪化するおそれがある。既述のように、粉末タバコは、4.0~6.0程度のpH値を示す。そして、本発明においては、酸性物質(リン酸の酸性塩)と塩基性の物質(炭酸の塩基性塩)の両方を使用して、オーラルタバコ材料のpH値を7~8.5に調整するので、塩基性物質(炭酸の塩基性塩)を、オーラルタバコ材料のpHが8.5を大幅に超えるほど多量に加えても、酸性物質により、pHを7~8.5に調整できる。従って、オーラルタバコ材料のpH値をアルカリ性物質だけで1つの所望の値に調整する場合は、アルカリ性物質の量は一義的に決定されるのに対し、本発明では、オーラルタバコ材料のpH値を1つの所望のpH値に調整するに際し、酸性物質(リン酸の酸性塩)と塩基性の物質(炭酸の塩基性塩)の使用量は、大幅に変更することができる。リン酸の酸性塩は、好ましくは粉末タバコの乾燥重量の1重量%以上の量で用いることが好ましい。リン酸の酸性塩の量は、通常、粉末タバコの乾燥重量の10重量%以下の量で用いられる。このリン酸の酸性塩の使用量に対応する炭酸の塩基性塩の使用量は、オーラルタバコ材料の初期pH値7~8.5により決まる。 The basic salt of carbonic acid and the acidic salt of phosphoric acid are contained in a proportion such that the initial pH of the oral tobacco material is 7 to 8.5, and in total 6% by weight or more of the dry weight of the powdered tobacco It is. If the pH value is less than 7, it is difficult to suppress the growth of bacteria. On the other hand, if the pH value exceeds 8.5, the oral mucosa may be damaged. If the total amount of the basic salt of carbonic acid and the acidic salt of phosphoric acid is less than 6% by weight, long-term storage at room temperature (15 ° C. to 35 ° C.) may be deteriorated. As described above, powdered tobacco exhibits a pH value of about 4.0 to 6.0. In the present invention, the pH value of the oral tobacco material is adjusted to 7 to 8.5 using both an acidic substance (acidic salt of phosphoric acid) and a basic substance (basic salt of carbonic acid). Therefore, even if a large amount of basic substance (basic salt of carbonic acid) is added so that the pH of the oral tobacco material greatly exceeds 8.5, the pH can be adjusted to 7 to 8.5 by the acidic substance. Therefore, when the pH value of the oral tobacco material is adjusted to one desired value with only the alkaline substance, the amount of the alkaline substance is uniquely determined, whereas in the present invention, the pH value of the oral tobacco material is adjusted. When adjusting to one desired pH value, the usage amount of an acidic substance (acidic salt of phosphoric acid) and a basic substance (basic salt of carbonic acid) can be significantly changed. The acid salt of phosphoric acid is preferably used in an amount of 1% by weight or more based on the dry weight of the powdered tobacco. The acid salt of phosphoric acid is usually used in an amount of 10% by weight or less of the dry weight of the powdered tobacco. The use amount of the basic salt of carbonic acid corresponding to the use amount of the acidic salt of phosphoric acid is determined by the initial pH value 7 to 8.5 of the oral tobacco material.

 本発明では、オーラルタバコ材料の含水率は、15重量%以上である。本発明で使用されるpH調整剤は、15重量%以上の含水率を有するオーラルタバコ材料に対して、所期の効果を奏することができる。オーラルタバコ材料の含水率は、通常、50重量%以下である。 In the present invention, the moisture content of the oral tobacco material is 15% by weight or more. The pH adjuster used in the present invention can have the desired effect on the oral tobacco material having a water content of 15% by weight or more. The moisture content of the oral tobacco material is usually 50% by weight or less.

 本発明のオーラルタバコ材料は、香味剤、湿潤剤等の添加剤を含有し得る。 The oral tobacco material of the present invention may contain additives such as flavoring agents and wetting agents.

 香味剤としては、メントール、ミント、アミノ酸(グリシン等)、植物エキス(ユーカリ、ローズマリー、GSE)、フラボノイド、ビタミンE、ビタミンC、クエン酸、食塩、フルクトース等の単糖類、スクロース等の二糖類、オリゴ糖、その他多糖類、シナモン、ホースラディッシュ(ワサビ)、トウガラシ、サンショウ、クローブ、ジンジャー、ターメリック、オールスパイス、カルダモン等の香辛系香辛料、バジル、ベイリーブス、マビョラ、オレガノ、ローズマリー、セージ、タラゴン、タイム、ゴマ、ガーリック、オニオン等の香草系香辛料、キャラウェイ、アニスレード、セロリシード、コリアンダー、クミンシード、ディルシード、フィンネル、メース、ナツメグ、ポピーシード等の種子系香辛料、チョコレート、柑橘類およびその他果実香味、バニリン、エチルバニリン、ベルガモット油、リナロール、レモン油等が挙げられる。香味剤は、粉末タバコの乾燥重量の1重量%~5重量%の量で用いることができる。 As flavoring agents, menthol, mint, amino acids (glycine, etc.), plant extracts (eucalyptus, rosemary, GSE), flavonoids, vitamin E, vitamin C, monosaccharides such as citric acid, salt, fructose, and disaccharides such as sucrose , Oligosaccharides, other polysaccharides, cinnamon, horseradish, pepper, salmon, cloves, ginger, turmeric, allspice, cardamom and other spices, basil, bay leaves, mabola, oregano, rosemary, sage , Tarragon, thyme, sesame, garlic, onion and other herb spices, caraway, anise lade, celery seed, coriander, cumin seed, dill seed, finnell, mace, nutmeg, poppy seed and other seed spices, chocolate, citrus And other fruit flavors, vanillin, ethyl vanillin, bergamot oil, linalool, lemon oil, and the like. The flavoring agent can be used in an amount of 1% to 5% by weight of the dry weight of the powdered tobacco.

 湿潤剤としては、グリセリン、プロピレングリコールなどの多価アルコール、エリスリトール、キシリトール、ソルビトールなどの糖アルコール、ヒアルロン酸等を挙げることができる。湿潤剤は、粉末タバコの乾燥重量の1重量%~5重量%の量で用いることができる。 Examples of the wetting agent include polyhydric alcohols such as glycerin and propylene glycol, sugar alcohols such as erythritol, xylitol, and sorbitol, hyaluronic acid, and the like. The wetting agent can be used in an amount of 1% to 5% by weight of the dry weight of the powdered tobacco.

 本発明のオーラルタバコ材料を調製するためには、まず、原料としての粉末タバコ自体の含水率を測定する。含水率の測定は、市販の加熱乾燥式水分計(例えば、(株)エー・アンド・デイ製MX-50)を用いて行うことができる。次に、オーラルタバコ材料の含水率を15重量%以上とするために必要な水の量を算出する。必要量の水の量Zは、式:Z={X×(1-a/100)+Y}÷(1-b/100)-(X+Y)によって計算することができる。ここで、Xは、原料粉末タバコの重量、aは、原料粉末タバコの含水率(%)、Yは、pH調整剤や湿潤剤等の添加物質の総重量、bは、目的とするオーラルタバコ材料の含水率(%)である。こうして計算された量の水に、所定量の炭酸の塩基性塩とリン酸の酸性塩、さらには必要により水溶性の添加剤を加え、得られた水溶液の全量を重量Xの粉末タバコに添加することができる。他の添加剤は、得られた湿った粉末タバコに配合することができる。本発明のオーラルタバコ材料は、通常、炭酸マグネシウムを含まない。 In order to prepare the oral tobacco material of the present invention, first, the moisture content of the powdered tobacco itself as a raw material is measured. The moisture content can be measured using a commercially available heat drying moisture meter (for example, MX-50 manufactured by A & D Co., Ltd.). Next, the amount of water necessary to make the moisture content of the oral tobacco material 15% by weight or more is calculated. The required amount of water Z can be calculated by the formula: Z = {X × (1−a / 100) + Y} ÷ (1−b / 100) − (X + Y). Here, X is the weight of the raw powdered tobacco, a is the moisture content (%) of the raw powdered tobacco, Y is the total weight of additive substances such as pH adjusters and wetting agents, and b is the target oral tobacco. It is the moisture content (%) of the material. Add the specified amount of basic carbonate carbonate and acid salt of phosphoric acid, and if necessary, water-soluble additives to the amount of water calculated in this way, and add the total amount of the resulting aqueous solution to the powdered tobacco of weight X can do. Other additives can be incorporated into the resulting wet powdered tobacco. The oral tobacco material of the present invention typically does not contain magnesium carbonate.

 本発明のオーラルタバコ材料は、それ自体既知の水透過性のポーチに収容されてオーラルタバコ製品を提供する。 The oral tobacco material of the present invention is contained in a water-permeable pouch known per se to provide an oral tobacco product.

 本発明のオーラルタバコ材料は、本発明のpH調整剤により調整された初期pH値を、室温(15℃~35℃)においても、少なくとも6ヶ月間実質的に維持し得、室温保存安定性に優れたものである。 The oral tobacco material of the present invention can substantially maintain the initial pH value adjusted with the pH adjuster of the present invention for at least 6 months even at room temperature (15 ° C. to 35 ° C.) It is excellent.

 次に、本発明を実施例により説明するが、本発明はそれら実施例により限定されるものではない。 Next, the present invention will be described with reference to examples, but the present invention is not limited to these examples.

 実施例1~2、比較例1
 原料としてルスチカ、ダークキュアタバコおよびタバコ中骨の各粉末をそれぞれ25重量%、25重量%、および50重量%の割合で配合した原料粉末タバコを準備し、その含水率を以下の手法により測定した。
Examples 1 and 2, Comparative Example 1
Raw material powder cigarettes containing 25% by weight, 25% by weight, and 50% by weight of each powder of rustica, dark-cured tobacco and tobacco bone as raw materials were prepared, and the moisture content was measured by the following method. .

 原料粉末タバコ5.0gの含水率を、加熱乾燥式水分計((株)エー・アンド・デイ製MX-50)を用いて、80℃で測定した。その結果、含水率は、14.0重量%であった。この原料粉末タバコの含水率から、オーラルタバコ材料の最終含水率をおよそ25重量%に調整するために必要な量の水の量を計算し、その計算量の水を用意した。 The water content of 5.0 g of the raw powdered tobacco was measured at 80 ° C. using a heat drying moisture meter (MX-50 manufactured by A & D Co., Ltd.). As a result, the water content was 14.0% by weight. From the moisture content of the raw powdered tobacco, the amount of water required to adjust the final moisture content of the oral tobacco material to approximately 25% by weight was calculated, and the calculated amount of water was prepared.

 実施例1では、上記用意した水に、それぞれ原料粉末タバコの乾燥重量の4.8重量%の炭酸ナトリウム、1.9重量%のリン酸二水素ナトリウムおよび5.0重量%のグリセリンに相当する量の炭酸ナトリウム、リン酸二水素ナトリウムおよびグリセリンを添加し、得られた水溶液の全量を上記原料粉末タバコに噴霧した。こうして得られたオーラルタバコ材料の最終含水率は25.44重量%であり、後述するpH測定法により測定した初期pHは、8.09であった。 In Example 1, the water prepared above corresponds to 4.8% by weight of sodium carbonate, 1.9% by weight of sodium dihydrogen phosphate, and 5.0% by weight of glycerin, respectively, of the dry weight of the raw powdered tobacco. A quantity of sodium carbonate, sodium dihydrogen phosphate and glycerin were added, and the total amount of the resulting aqueous solution was sprayed onto the raw powder tobacco. The final moisture content of the oral tobacco material thus obtained was 25.44% by weight, and the initial pH measured by the pH measurement method described later was 8.09.

 実施例2では、上記用意した水に、粉末タバコの乾燥重量の8.0重量%の炭酸ナトリウム、4.1重量%のリン酸二水素ナトリウムおよび5.0重量%のグリセリンに相当する量の炭酸ナトリウム、リン酸二水素ナトリウムおよびグリセリンを添加した以外は、実施例1と同様にしてオーラルタバコ材料を調製した。得られたオーラルタバコ材料の最終含水率は26.39重量%であり、後述するpH測定法により測定した初期pHは、8.08であった。 In Example 2, an amount corresponding to 8.0% by weight of sodium carbonate, 4.1% by weight of sodium dihydrogen phosphate, and 5.0% by weight of glycerin of the dry weight of the powdered tobacco was added to the prepared water. An oral tobacco material was prepared in the same manner as in Example 1 except that sodium carbonate, sodium dihydrogen phosphate and glycerin were added. The final moisture content of the obtained oral tobacco material was 26.39% by weight, and the initial pH measured by the pH measurement method described later was 8.08.

 比較例1では、上記用意した水に、粉末タバコの乾燥重量の2.7重量%の炭酸ナトリウムおよび5.0重量%のグリセリンに相当する量の炭酸ナトリウムおよびグリセリンを添加した以外は、実施例1と同様にしてオーラルタバコ材料を調製した。得られたオーラルタバコ材料の最終含水率は26.53重量%であり、後述するpH測定法により測定した初期pHは、8.11であった。 In Comparative Example 1, Example 1 was added except that sodium carbonate and glycerin in an amount corresponding to 2.7% by weight of sodium carbonate and 5.0% by weight of glycerin were added to the prepared water. In the same manner as in No. 1, an oral tobacco material was prepared. The final moisture content of the obtained oral tobacco material was 26.53% by weight, and the initial pH measured by the pH measurement method described later was 8.11.

 実施例3~4、比較例2~3
 原料としてルスチカ、ダークキュアタバコおよびタバコ中骨の各粉末をそれぞれ35重量%、15重量%、および50重量%の割合で配合した原料粉末タバコを準備し、その含水率を以下の手法により測定した。
Examples 3 to 4 and Comparative Examples 2 to 3
Raw material powder cigarettes containing 35% by weight, 15% by weight, and 50% by weight of each powder of rustica, dark-cured tobacco and tobacco bone as raw materials were prepared, and the moisture content was measured by the following method. .

 原料粉末タバコ5.0gの含水率を、加熱乾燥式水分計((株)エー・アンド・デイ製MX-50)を用いて、80℃で測定した。その結果、含水率は、12.7重量%であった。この原料粉末タバコの含水率から、オーラルタバコ材料の最終含水率をおよそ15.0重量%または25.0重量%に調整するために必要な量の水の量を計算し、その計算量の水を用意した。 The water content of 5.0 g of the raw powdered tobacco was measured at 80 ° C. using a heat drying moisture meter (MX-50 manufactured by A & D Co., Ltd.). As a result, the water content was 12.7% by weight. From the moisture content of the raw powdered tobacco, the amount of water required to adjust the final moisture content of the oral tobacco material to approximately 15.0% or 25.0% by weight is calculated, and the calculated amount of water is calculated. Prepared.

 実施例3では、上記用意した最終含水率25.0重量%に調整するために必要な水に、それぞれ原料粉末タバコの乾燥重量の5.8重量%の炭酸ナトリウム、4.1重量%のリン酸二水素ナトリウムおよび5.0重量%のグリセリンに相当する量の炭酸ナトリウム、リン酸二水素ナトリウムおよびグリセリンを添加した以外は、実施例1と同様にしてオーラルタバコ材料を調製した。こうして得られたオーラルタバコ材料の最終含水率は26.9重量%であり、後述するpH測定法により測定した初期pHは、7.73であった。 In Example 3, the water required to adjust the final moisture content prepared to 25.0% by weight was added to 5.8% by weight of sodium carbonate, 4.1% by weight of phosphorus, respectively, of the dry weight of the raw powdered tobacco. An oral tobacco material was prepared in the same manner as in Example 1 except that sodium carbonate, sodium dihydrogen phosphate and glycerin in an amount corresponding to sodium dihydrogen acid and 5.0% by weight of glycerin were added. The final moisture content of the oral tobacco material thus obtained was 26.9% by weight, and the initial pH measured by the pH measurement method described later was 7.73.

 実施例4では、上記用意した最終含水率15.0重量%に調整するために必要な水に、粉末タバコの乾燥重量の5.0重量%の炭酸ナトリウム、4.1重量%のリン酸二水素ナトリウムおよび5.0重量%のグリセリンに相当する量の炭酸ナトリウム、リン酸二水素ナトリウムおよびグリセリンを添加した以外は、実施例1と同様にしてオーラルタバコ材料を調製した。得られたオーラルタバコ材料の最終含水率は18.6重量%であり、後述するpH測定法により測定した初期pHは、7.21であった。 In Example 4, 5.0% by weight of sodium carbonate, 4.1% by weight of diphosphoric acid phosphate was added to the water necessary for adjusting the final moisture content prepared above to 15.0% by weight. An oral tobacco material was prepared in the same manner as in Example 1 except that sodium carbonate, sodium dihydrogen phosphate and glycerin corresponding to sodium hydride and 5.0% by weight of glycerin were added. The final moisture content of the obtained oral tobacco material was 18.6% by weight, and the initial pH measured by the pH measurement method described later was 7.21.

 比較例2では、上記用意した最終含水率25.0重量%に調整するために必要な水に、粉末タバコの乾燥重量の3.2重量%の炭酸ナトリウムおよび5.0重量%のグリセリンに相当する量の炭酸ナトリウムおよびグリセリンを添加した以外は、実施例1と同様にしてオーラルタバコ材料を調製した。得られたオーラルタバコ材料の最終含水率は26.1重量%であり、後述するpH測定法により測定した初期pHは、7.7であった。 In Comparative Example 2, the water necessary for adjusting the final moisture content prepared above to 25.0% by weight corresponds to 3.2% by weight of sodium carbonate and 5.0% by weight of glycerin of the dry weight of the powdered tobacco. An oral tobacco material was prepared in the same manner as in Example 1 except that sodium carbonate and glycerin were added. The final moisture content of the obtained oral tobacco material was 26.1% by weight, and the initial pH measured by the pH measurement method described later was 7.7.

 比較例4では、上記用意した最終含水率15.0重量%に調整するために必要な水に、粉末タバコの乾燥重量の3.2重量%の炭酸ナトリウムおよび5.0重量%のグリセリンに相当する量の炭酸ナトリウムおよびグリセリンを添加した以外は、実施例1と同様にしてオーラルタバコ材料を調製した。得られたオーラルタバコ材料の最終含水率は18.1重量%であり、後述するpH測定法により測定した初期pHは、7.12であった。 In Comparative Example 4, the water required for adjusting the final moisture content prepared above to 15.0% by weight corresponds to 3.2% by weight sodium carbonate and 5.0% by weight glycerin of the dry weight of the powdered tobacco. An oral tobacco material was prepared in the same manner as in Example 1 except that sodium carbonate and glycerin were added. The final moisture content of the obtained oral tobacco material was 18.1% by weight, and the initial pH measured by the pH measurement method described later was 7.12.

 上記実施例1~4および比較例1~3のオーラルタバコ材料についてのいくつかの情報を下記表1に掲げる。

Figure JPOXMLDOC01-appb-T000001
Some information on the oral tobacco materials of Examples 1-4 and Comparative Examples 1-3 above is listed in Table 1 below.
Figure JPOXMLDOC01-appb-T000001

 実施例1~2、比較例1で得られたオーラルタバコ材料を、それぞれ保存用パック((株)生産日本製ラミジップAL-4;防湿性、ガス遮断性、光遮断性の入れ物)に入れ、温度25℃、相対湿度60%の雰囲気下、および温度35℃、相対湿度60%の雰囲気下で6ヶ月間保存した。保存期間中、後述するpH測定法により、定期的にpHを測定した。結果を図1および図2に示す。図1は、温度25℃、相対湿度60%の雰囲気下で保存した結果を示し、図2は、温度35℃、相対湿度60%の雰囲気下で保存した結果を示す。図1および図2において、線分aは、実施例1に関し、線分bは、実施例2に関し、線分cは、比較例1に関する。図1および図2に示す結果から明らかなように、比較例1のオーラルタバコ材料は、温度25℃、相対湿度60%の雰囲気下で6ヶ月間保存するとpHが約0.5低下し、温度35℃、相対湿度60%の雰囲気下で6ヶ月間保存すると、pH値が約1.0低下するのに対し、実施例1および2のオーラルタバコ材料は、いずれの保存条件でも、pH値がほとんど低下しないことが分かる。 Each of the oral tobacco materials obtained in Examples 1 and 2 and Comparative Example 1 was put in a storage pack (produced by Japan, Lamidip AL-4; moisture-proof, gas-blocking, and light-blocking container). It was stored for 6 months in an atmosphere of a temperature of 25 ° C. and a relative humidity of 60% and in an atmosphere of a temperature of 35 ° C. and a relative humidity of 60%. During the storage period, the pH was measured periodically by the pH measurement method described later. The results are shown in FIG. 1 and FIG. FIG. 1 shows the results of storage in an atmosphere at a temperature of 25 ° C. and a relative humidity of 60%, and FIG. 2 shows the results of storage in an atmosphere of a temperature of 35 ° C. and a relative humidity of 60%. In FIG. 1 and FIG. 2, a line segment a relates to Example 1, a line segment b relates to Example 2, and a line segment c relates to Comparative Example 1. As is clear from the results shown in FIGS. 1 and 2, the oral tobacco material of Comparative Example 1 has a pH of about 0.5 when stored for 6 months in an atmosphere at a temperature of 25 ° C. and a relative humidity of 60%. When stored for 6 months in an atmosphere of 35 ° C. and a relative humidity of 60%, the pH value decreases by about 1.0, whereas the oral tobacco materials of Examples 1 and 2 have a pH value under any storage condition. It turns out that it hardly decreases.

 実施例3~4および比較例2~3で得られたオーラルタバコ材料を、それぞれ上記保存用パック((株)生産日本製ラミジップAL-4)に入れ、温度25℃、相対湿度60%の雰囲気下で6ヶ月間保存した。保存期間中、後述するpH測定法により、定期的にpHを測定した。結果を図3および図4に示す。図3において線分dは、実施例3に関し、線分eは、比較例2に関する。図4において、線分fは、実施例4に関し、線分gは、比較例3に関する。図3および図4に示す結果から明らかなように、比較例2のオーラルタバコ材料は、温度25℃、相対湿度60%の雰囲気下で6ヶ月間保存するとpHが約1.2低下するのに対し、実施例3のオーラルタバコ材料は、同条件下での保存中のpH値の低下は、約0.6であり、保存中のpH低下が抑制されていることが分かる。また、比較例3のオーラルタバコ材料は、温度25℃、相対湿度60%の雰囲気下で6ヶ月間保存するとpHが約0.4低下するのに対し、実施例4のオーラルタバコ材料は、同条件下での保存中のpH値の低下は、約0.25であり、保存中のpH低下が抑制されていることが分かる。 The oral tobacco materials obtained in Examples 3 to 4 and Comparative Examples 2 to 3 were put in the above-mentioned storage packs (produced by Japan Lamidip AL-4), respectively, and the atmosphere at a temperature of 25 ° C. and a relative humidity of 60%. Stored for 6 months below. During the storage period, the pH was measured periodically by the pH measurement method described later. The results are shown in FIG. 3 and FIG. In FIG. 3, the line segment d relates to Example 3, and the line segment e relates to Comparative Example 2. In FIG. 4, the line segment f relates to Example 4, and the line segment g relates to Comparative Example 3. As is clear from the results shown in FIGS. 3 and 4, the oral tobacco material of Comparative Example 2 has a pH of about 1.2 when stored for 6 months in an atmosphere at a temperature of 25 ° C. and a relative humidity of 60%. On the other hand, in the oral tobacco material of Example 3, the decrease in pH value during storage under the same conditions is about 0.6, indicating that the decrease in pH during storage is suppressed. The oral tobacco material of Comparative Example 3 has a pH of about 0.4 when stored for 6 months in an atmosphere at a temperature of 25 ° C. and a relative humidity of 60%. The decrease in pH value during storage under conditions is about 0.25, indicating that the decrease in pH during storage is suppressed.

 <pHの測定方法>
 オーラルタバコ材料2.0gをバイアルに量り入れ、20mLの蒸留水を加えて、その混合物を200rpmで10分間振盪する抽出処理に供した。5分間静置した後、抽出液のpHをpHメータ(IQ Scientific Instruments, Inc.製IQ240)を用いて測定した。
<Measurement method of pH>
2.0 g of oral tobacco material was weighed into a vial, 20 mL of distilled water was added, and the mixture was subjected to an extraction process that was shaken at 200 rpm for 10 minutes. After leaving for 5 minutes, the pH of the extract was measured using a pH meter (IQ Scientific Instruments, Inc. IQ240).

Claims (5)

 粉末タバコ、およびpH調整剤として炭酸の塩基性塩とリン酸の酸性塩を含むオーラルタバコ材料であり、前記炭酸の塩基性塩とリン酸の酸性塩とは、合計で前記粉末タバコの乾燥重量の6重量%以上の量で含まれ、かつオーラルタバコ材料の初期pHが7~8.5となるように配合され、前記オーラルタバコ材料は15重量%以上の含水率を有するオーラルタバコ材料。 A powder tobacco, and an oral tobacco material containing a basic salt of carbonic acid and an acidic salt of phosphoric acid as a pH adjuster, wherein the basic salt of carbonic acid and the acidic salt of phosphoric acid are the total dry weight of the powdered tobacco The oral tobacco material is contained so that the initial pH of the oral tobacco material is 7 to 8.5, and the oral tobacco material has a moisture content of 15% by weight or more.  前記炭酸の塩基性塩が、炭酸ナトリウムおよび炭酸カリウムからなる群の中から選ばれることを特徴とする請求項1に記載のオーラルタバコ材料。 The oral tobacco material according to claim 1, wherein the basic salt of carbonic acid is selected from the group consisting of sodium carbonate and potassium carbonate.  前記リン酸の酸性塩が、リン酸二水素ナトリウムおよびリン酸二水素カリウムからなる群の中から選ばれることを特徴とする請求項1または2に記載のオーラルタバコ材料。 The oral tobacco material according to claim 1 or 2, wherein the acidic salt of phosphoric acid is selected from the group consisting of sodium dihydrogen phosphate and potassium dihydrogen phosphate.  前記オーラルタバコ材料が、前記リン酸の酸性塩を、前記粉末タバコの乾燥重量の少なくとも1重量%の量で含む請求項1~3のいずれか1項に記載のオーラルタバコ材料。 The oral tobacco material according to any one of claims 1 to 3, wherein the oral tobacco material contains the acid salt of phosphoric acid in an amount of at least 1% by weight of the dry weight of the powdered tobacco.  前記オーラルタバコ材料が炭酸マグネシウムを含まないことを特徴とする請求項1~4のいずれか1項に記載のオーラルタバコ材料。 The oral tobacco material according to any one of claims 1 to 4, wherein the oral tobacco material does not contain magnesium carbonate.
PCT/JP2011/057656 2010-03-29 2011-03-28 Oral tobacco material Ceased WO2011122567A1 (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103005670A (en) * 2013-01-15 2013-04-03 济南鼻烟研究所 Holy basil flavored snuff
EP2653042A1 (en) 2012-04-20 2013-10-23 JT International SA pH-stabilized oral tobacco composition
WO2014196033A1 (en) * 2013-06-05 2014-12-11 日本たばこ産業株式会社 Method for producing tobacco material
WO2018154759A1 (en) * 2017-02-27 2018-08-30 日本たばこ産業株式会社 Oral tobacco product

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB201302485D0 (en) 2013-02-13 2013-03-27 British American Tobacco Co Tobacco Treatment
GB201314917D0 (en) 2013-08-21 2013-10-02 British American Tobacco Co Treated Tobacco and processes for preparing the same, Devices including the same and uses thereof
SI3280278T1 (en) * 2015-04-08 2019-09-30 Swedish Match North Europe Ab Method for producing a pouched smokeless tobacco product comprising heat treatment
US12213510B2 (en) 2019-09-11 2025-02-04 Nicoventures Trading Limited Pouched products with enhanced flavor stability
US20220071984A1 (en) * 2019-09-11 2022-03-10 Nicoventures Trading Limited Oral product with nicotine and ion pairing agent

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009508523A (en) 2005-09-22 2009-03-05 アール・ジエイ・レイノルズ・タバコ・カンパニー Smokeless tobacco composition
WO2009048522A1 (en) * 2007-10-11 2009-04-16 Richard Fuisz Smokeless tobacco product
WO2009082331A1 (en) 2007-12-21 2009-07-02 Swedish Match North Europe Ab A tobacco or non-tobacco product comprising magnesium carbonate

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5525351A (en) * 1989-11-07 1996-06-11 Dam; Anders Nicotine containing stimulant unit
AU2003288868A1 (en) * 2002-12-19 2004-07-14 Swedish Match North Europe Ab A non-chewable tobacco composition
US7861728B2 (en) * 2006-02-10 2011-01-04 R.J. Reynolds Tobacco Company Smokeless tobacco composition having an outer and inner pouch
SE0800058L (en) * 2008-01-10 2009-07-11 British American Tobacco Co Tobacco product for oral use

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009508523A (en) 2005-09-22 2009-03-05 アール・ジエイ・レイノルズ・タバコ・カンパニー Smokeless tobacco composition
WO2009048522A1 (en) * 2007-10-11 2009-04-16 Richard Fuisz Smokeless tobacco product
WO2009082331A1 (en) 2007-12-21 2009-07-02 Swedish Match North Europe Ab A tobacco or non-tobacco product comprising magnesium carbonate

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP2554059A4

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2653042A1 (en) 2012-04-20 2013-10-23 JT International SA pH-stabilized oral tobacco composition
WO2013156544A1 (en) 2012-04-20 2013-10-24 Jt International S.A. Ph-stabilized oral tobacco composition
CN103005670A (en) * 2013-01-15 2013-04-03 济南鼻烟研究所 Holy basil flavored snuff
WO2014196033A1 (en) * 2013-06-05 2014-12-11 日本たばこ産業株式会社 Method for producing tobacco material
WO2018154759A1 (en) * 2017-02-27 2018-08-30 日本たばこ産業株式会社 Oral tobacco product

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