WO2014057637A1 - Composition for alleviating hunger sensation - Google Patents

Composition for alleviating hunger sensation Download PDF

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Publication number
WO2014057637A1
WO2014057637A1 PCT/JP2013/005922 JP2013005922W WO2014057637A1 WO 2014057637 A1 WO2014057637 A1 WO 2014057637A1 JP 2013005922 W JP2013005922 W JP 2013005922W WO 2014057637 A1 WO2014057637 A1 WO 2014057637A1
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glucomannan
composition
gum
feeling
chewing
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PCT/JP2013/005922
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French (fr)
Japanese (ja)
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匠 徳本
智晴 飯田
中村　準
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株式会社ロッテ
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Priority to CN201380052781.2A priority Critical patent/CN104703488A/en
Priority to KR1020157011728A priority patent/KR20150065851A/en
Publication of WO2014057637A1 publication Critical patent/WO2014057637A1/en

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    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
    • A23G4/00—Chewing gum
    • A23G4/06—Chewing gum characterised by the composition containing organic or inorganic compounds
    • A23G4/10—Chewing gum characterised by the composition containing organic or inorganic compounds characterised by the carbohydrates used, e.g. polysaccharides
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/20—Reducing nutritive value; Dietetic products with reduced nutritive value
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/20—Reducing nutritive value; Dietetic products with reduced nutritive value
    • A23L33/21—Addition of substantially indigestible substances, e.g. dietary fibres
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs

Definitions

  • Dietary restrictions may be required to prevent or treat metabolic syndrome, diabetes, obesity, arteriosclerosis, and the like. However, in the case of dietary restrictions, dietary restrictions may not be achieved by ingesting heat (calories) other than the prescribed amount without being able to withstand a feeling of hunger. There has been a demand for providing a composition that relieves hunger without ingesting heat or with low heat intake. In the present specification, alleviating feeling of hunger includes perception of feeling in the stomach or feeling in the stomach.
  • composition that relieves hunger without ingesting heat or with low heat intake.
  • composition comprising glucomannan and a gum base, which, when chewed, perceives a feeling of entering the stomach or a feeling of being present in the stomach and relieves hunger.
  • Example 2 The time schedule in Example 2 is shown. It is a figure explaining the subjective evaluation of Example 6.
  • the present invention includes glucomannan and a gum base, and when chewed, glucomannan is swallowed together with saliva, and as a result, it feels a feeling of entering the stomach and a feeling existing in the stomach, thereby reducing the feeling of hunger.
  • a composition is provided.
  • the present invention also provides the above composition, wherein glucomannan is contained in a proportion of 1 to 10% by weight.
  • the present invention also provides the above composition, wherein the composition is shaped so as to be 1 to 10 g per piece.
  • the present invention provides the above composition characterized in that it is molded so that the amount of glucomannan per unit is 0.01 to 1 g.
  • Glucomannan is a water-soluble polysaccharide in which glucose and mannose are ⁇ -1,4-linked. Glucomannan is abundant in the cell walls of plant cells, and is particularly known to be abundant in salmon. In the composition of the present invention, glucomannan is preferably contained in the composition in a proportion of 1 to 10% by weight, more preferably in a proportion of 2 to 3% by weight. The intake is preferably about 0.01 to 1 g, more preferably about 0.01 to 0.05 g.
  • the gum base is a base for the chewing gum and is not particularly limited as long as it has an appropriate elasticity for chewing and is harmless to the human body.
  • gum base leguminous tree arabic rubber tree (Acacia senegal), gum arabic, which is a secreted product of related plants of the same genus, sapodilla (Achras sapota), a sap of pine, a sap of pine ( Examples include ester gum produced by processing pine resin, vinyl acetate resin (polyvinyl acetate), which is a synthetic resin, and polyisobutylene.
  • an additive such as calcium carbonate may be added to the gum base, and sweeteners, flavors and the like may be added for flavoring.
  • the composition of the present invention can contain a sweetener.
  • sweeteners include monosaccharides, disaccharides, oligosaccharides, sugar alcohols, and high intensity sweeteners.
  • monosaccharides such as arabinose, galactose, xylose, glucose, fucose, sorbose, fructose, rhamnose, ribose, isomerized liquid sugar, N-acetylglucosamine; isotrehalose, sucrose, trehalulose, trehalose, neotrehalose, palatinose , Maltose, melibiose, lactulose, lactose and other disaccharides; ⁇ -cyclodextrin, ⁇ -cyclodextrin, isomaltoligosaccharides (isomaltose, isomaltotriose, panose, etc.), oligo-N-acetylglucosamine, galactosy
  • sweeteners can be used alone or in any combination of two or more.
  • monosaccharides, disaccharides, oligosaccharides, and sugar alcohols are added to the composition of the present invention, it is preferable to add 50 to 70% by weight.
  • high-intensity sweetener it is preferable to add 0 to 2% by weight in the composition of the present invention.
  • composition of the present invention can contain a fragrance.
  • flavors used include citrus essential oils such as orange oil, lemon oil, grapefruit oil, lime oil, tangerine oil, mandarin oil, mint essential oils such as peppermint oil, spearmint oil, allspice, anise seed
  • Known spice essential oils such as basil, laurel, cardamom, celery, clove, cinnamon, cumin, dill, garlic, parsley, mace, mustard, onion, paprika, parsley, rosemary, pepper, or oleoresin, limonene, Linalool, nerol, citronellol, geraniol, citral, L-menthol, eugenol, cinnamic aldehyde, anethole, perilla aldehyde, vanillin, ⁇ -undecalactone, allyl caproate, L-carvone, maltol.
  • known isolated or synthetic fragrances such as citrus essential oils, mint essential oils, spice essential oils or isolated / synthetic fragrances according to the purpose
  • the present invention is not limited to these exemplified substances.
  • the fragrance it is preferable to add 0 to 3% by weight when it is added to the chewing gum composition.
  • composition of the present invention is a sour agent such as citric acid, malic acid, fumaric acid, ascorbic acid, caramel dye, gardenia dye, anthocyanin dye, anato dye, paprika dye, safflower dye, safflower dye, flavonoid dye, cochineal Dye, Amaranth (Red No. 2), Erythrosine (Red No. 3), Allura Red AC (Red No. 40), New Coxin (Red No. 102), Phloxin (Red No. 104), Rose Bengal (Red No.
  • a sour agent such as citric acid, malic acid, fumaric acid, ascorbic acid, caramel dye, gardenia dye, anthocyanin dye, anato dye, paprika dye, safflower dye, safflower dye, flavonoid dye, cochineal Dye, Amaranth (Red No. 2), Erythrosine (Red No. 3),
  • Acid Red (Red 106), Tartrazine (Yellow 4), Sunset Yellow FCF (Yellow 5), Fast Green FCF (Green 3), Brilliant Blue FCF (Blue 1), Indigo Carmine (Blue 2), etc.
  • oil-soluble bases such as carotene, chlorophyll, and tocopher
  • Such Lumpur may contain harmless other additives to further human body.
  • the composition of the present invention is preferably formed in a single dose so that the intake amount per time is preferably 1 to 10 grams, more preferably 1.5 to 5 g, and most preferably 2 to 3 g. preferable.
  • the shape is not limited, and plate shape, granular shape, cube shape, rectangular parallelepiped shape, ball shape, and other shapes can be raised, and after forming, coating may be made with sugar coating or the like.
  • another composition such as a liquid or a solid may be contained in the inside or the like.
  • a liquid part can be included, or a candy or gummy can be included for the purpose of imparting an interesting texture or improving the flavor.
  • the weight of these other compositions is not included in the composition of the present invention.
  • the composition of the present invention is intended to assist dietary restriction, it is desirable that the calories be low, and preferably the caloric intake of the composition of the present invention is from 0 to 12 kilocalories, more Preferably it is from 0 to 3 kilocalories.
  • the amount of carbohydrate contained in one intake of the composition of the present invention is preferably 0 to 3 grams, more preferably 0 to 1 grams.
  • Example 1 Subjective evaluation of glucomannan solution (first time) A subjective evaluation of the glucomannan solution was performed on 10 panelists (all women). 10 ml of the control solution was weighed with a syringe and injected into the mouth of the panel as it was. Ten minutes later, a 0.2% or 0.4% glucomannan solution, like the control solution, was weighed in the same amount of 10 ml with a syringe and injected into the mouth of the panel to be ingested. Immediately after ingestion, the panel subjectively evaluated the items in Table 1 compared to the control solution. The results are summarized in Tables 2 and 3.
  • control solution 2.0% by weight maltitol Glucomannan solution (0.2%): maltitol 2.0 wt%, glucomannan 0.2 wt% Glucomannan solution (0.4%): 2.0% by weight maltitol, 0.4% by weight glucomannan
  • Example 2 Subjective evaluation of glucomannan solution (second time) A subjective evaluation of the glucomannan solution was performed on 12 panelists (all women). The panel was fasted for 4 hours before evaluation and the evaluation was performed on an empty stomach. In addition, there was no particular restriction on the intake of liquids even during fasting.
  • Evaluation was performed as follows. That is, 10 ml of the control solution was weighed with a syringe and injected into the mouth of the panel to ingest it. Ten minutes after that, similarly to the control solution, 10 ml of the same concentration of glucomannan solution was weighed with a syringe and injected into the mouth of the panel for ingestion. Immediately after ingestion, the panel performed a subjective evaluation on the same items as in Example 1 in comparison with the control solution. Further, the evaluation was performed by reversing the order of intake. The time schedule in the present embodiment is shown in FIG. The results are summarized in Tables 4-12.
  • control solution 2.0% by weight maltitol Glucomannan solution (0.2%): maltitol 2.0 wt%, glucomannan 0.2 wt% Glucomannan solution (0.3%): maltitol 2.0 wt%, glucomannan 0.3 wt% Glucomannan solution (0.4%): 2.0% by weight maltitol, 0.4% by weight glucomannan
  • Glucomannan Blending Gum The following glucomannan blending gum was produced as an example of the composition of the present invention. The production method was based on a normal gum production method, and a gum base, a powder raw material, and a liquid raw material were mixed at around 50 to 60 ° C. Glucomannan can be purchased as, for example, ROLEX (trademark) One (Shimizu Chemical Co., Ltd.).
  • Example 4 Measurement of the amount of saliva when chewing gum containing glucomannan The weight of saliva secreted by chewing about 2.1 g of glucomannan-containing gum produced by Example 3 by three female panels (panels A, B, C) was measured. At the timing of swallowing saliva, it was discharged into a test tube and its weight was measured. The test tube was changed every 1 minute and measured up to 8 minutes. According to the rhythm of the metronome, it was chewed at a pace of 80 times per minute. The results are shown in Table 13.
  • Example 5 Measurement of the amount of glucomannan eluted from the glucomannan-containing gum 2.1 grams of the glucomannan-containing gum produced in Example 3 is 2 minutes, 3 minutes, 4 minutes, 5 minutes, 6 minutes, 7 minutes, or 8 minutes Mastication was performed at a pace of 80 times per minute according to the rhythm of the metronome, the amount of glucomannan remaining in the glucomannan-containing gum after chewing was measured, and the amount and dissolution rate were calculated. As a control, measurements were also made on a glucomannan-containing gum that was not chewed. The measurement method is as follows.
  • Example 6 Subjective evaluation when chewing glucomannan-containing gum About 2.1 g of glucomannan-containing gum produced in Example 3 for 6 male panels (panels 1-6) and 6 female panels (panels 7-12), Alternatively, about 2.1 g of control gum was chewed for 7 minutes. The chewing method was not specified. In addition, the control gum used here is obtained by substituting 2.4% of glucomannan in the blended glucomannan of Example 3 with 2.4% of maltitol. The chewing hours were 11:00 am to 12:00 am and 4 pm to 5:00 pm, which are thought to make it easy to feel hungry.

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  • Food Science & Technology (AREA)
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  • Health & Medical Sciences (AREA)
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Abstract

A composition for alleviating hunger sensation without caloric intake or by low caloric intake is provided. Provided is a composition characterized in comprising glucomannan and a gum base, and in that saliva containing glucomannan is swallowed by chewing, whereby the sensation of entering the stomach and the sensation of being present in the stomach is strongly perceived, and hunger sensation is alleviated.

Description

空腹感を緩和する組成物Composition that relieves hunger
　メタボリックシンドローム、糖尿病、肥満、動脈硬化などの予防、治療のため、食事制限が必要な場合がある。しかしながら、食事制限の際は、空腹感に耐えられずに、規定以外の熱量（カロリー）を摂取してしまうことで、食事制限を達成できないことがある。
　熱量を摂取することなく、あるいは低い熱量の摂取で、空腹感を緩和する組成物の提供が求められてきた。なお、本明細書中、空腹感を緩和するとは、胃に入った感じ、あるいは、胃に存在する感じを知覚させることを含む。 Dietary restrictions may be required to prevent or treat metabolic syndrome, diabetes, obesity, arteriosclerosis, and the like. However, in the case of dietary restrictions, dietary restrictions may not be achieved by ingesting heat (calories) other than the prescribed amount without being able to withstand a feeling of hunger.
There has been a demand for providing a composition that relieves hunger without ingesting heat or with low heat intake. In the present specification, alleviating feeling of hunger includes perception of feeling in the stomach or feeling in the stomach.
　熱量を摂取することなく、あるいは低い熱量の摂取で、空腹感を緩和する組成物の提供。 Provide a composition that relieves hunger without ingesting heat or with low heat intake.
　グルコマンナンとガムベースを含み、咀嚼されることで、胃に入った感じや、胃に存在する感じを知覚させ、空腹感を緩和することを特徴とする組成物を提供する。 Provided is a composition comprising glucomannan and a gum base, which, when chewed, perceives a feeling of entering the stomach or a feeling of being present in the stomach and relieves hunger.
　胃に入った感じや、胃に存在する感じを知覚させ、空腹感が緩和されるため、食事制限の達成を容易にする。 Sense the feeling of entering the stomach and the feeling of being in the stomach, and the feeling of hunger is alleviated, making it easier to achieve dietary restrictions.
実施例２におけるタイムスケジュールを示す。The time schedule in Example 2 is shown. 実施例６の主観評価について説明する図である。It is a figure explaining the subjective evaluation of Example 6.
　本発明はグルコマンナンとガムベースを含み、咀嚼されることでグルコマンナンが唾液と共に飲み込まれ、その結果、胃に入った感じや、胃に存在する感じを知覚させ、空腹感を緩和することを特徴とする組成物を提供する。また、本発明はグルコマンナンが１～１０重量％の割合で含有されることを特徴とする上記組成物を提供する。また、本発明は１個あたり１～１０ｇとなるように成形されていることを特徴とする上記組成物を提供する。さらに、本発明は、１個あたりグルコマンナンの量が０．０１～１ｇとなるように成形されたことを特徴とする上記組成物を提供する。 The present invention includes glucomannan and a gum base, and when chewed, glucomannan is swallowed together with saliva, and as a result, it feels a feeling of entering the stomach and a feeling existing in the stomach, thereby reducing the feeling of hunger. A composition is provided. The present invention also provides the above composition, wherein glucomannan is contained in a proportion of 1 to 10% by weight. The present invention also provides the above composition, wherein the composition is shaped so as to be 1 to 10 g per piece. Furthermore, the present invention provides the above composition characterized in that it is molded so that the amount of glucomannan per unit is 0.01 to 1 g.
　グルコマンナン（ｇｌｕｃｏｍａｎｎａｎ）は、グルコースとマンノースがβ－１，４－結合した水溶性多糖である。グルコマンナンは植物細胞の細胞壁に多く含まれ、特に、蒟蒻芋に多く含まれることで知られる。本発明の組成物に、グルコマンナンは好ましくは１～１０重量％の割合で、より好ましくは２～３重量％の割合で、本組成物中に含まれ、重量としては、一度のグルコマンナンの摂取量が０．０１～１ｇ、より好ましくは約０．０１ｇ～０．０５ｇ程度となることが好ましい。 Glucomannan is a water-soluble polysaccharide in which glucose and mannose are β-1,4-linked. Glucomannan is abundant in the cell walls of plant cells, and is particularly known to be abundant in salmon. In the composition of the present invention, glucomannan is preferably contained in the composition in a proportion of 1 to 10% by weight, more preferably in a proportion of 2 to 3% by weight. The intake is preferably about 0.01 to 1 g, more preferably about 0.01 to 0.05 g.
　ガムベースとは、チューインガムのベースとなるもので、咀嚼にするのに適度な弾力があり、人体に無害なものであれば、特に限定されない。ガムベースの例として、マメ科の樹木アラビアゴムノキ　（Ａｃａｃｉａ　ｓｅｎｅｇａｌ）、またはその同属近縁植物の分泌物であるアラビアガム、アカテツ科の樹木であるサポジラ　（Ａｃｈｒａｓ　ｓａｐｏｔａ）から得られるチクル、マツの樹液（松脂）を加工して作るエステルガム、合成樹脂である酢酸ビニル樹脂（ポリ酢酸ビニル）、ポリイソブチレンなどをあげることができる。ガムベースには、硬さを保持するために、炭酸カルシウムなどの添加物を加えてもよく、また、風味付けのために、甘味料、香料などを加えてもよい。 The gum base is a base for the chewing gum and is not particularly limited as long as it has an appropriate elasticity for chewing and is harmless to the human body. As an example of gum base, leguminous tree arabic rubber tree (Acacia senegal), gum arabic, which is a secreted product of related plants of the same genus, sapodilla (Achras sapota), a sap of pine, a sap of pine ( Examples include ester gum produced by processing pine resin, vinyl acetate resin (polyvinyl acetate), which is a synthetic resin, and polyisobutylene. In order to maintain hardness, an additive such as calcium carbonate may be added to the gum base, and sweeteners, flavors and the like may be added for flavoring.
　本発明の組成物は甘味料を含むことができる。甘味料の例としては、単糖類、二糖類、オリゴ糖類、糖アルコール類、高甘味度甘味料を挙げることができる。具体的には、アラビノース、ガラクトース、キシロース、グルコース、フコース、ソルボース、フルクトース、ラムノース、リボース、異性化液糖、Ｎ－アセチルグルコサミン等の単糖類；イソトレハロース、スクロース、トレハルロース、トレハロース、ネオトレハロース、パラチノース、マルトース、メリビオース、ラクチュロース、ラクトース等の二糖類；α－サイクロデキストリン、β－サイクロデキストリン、イソマルトオリゴ糖（イソマルトース、イソマルトトリオース、パノース等）、オリゴ－Ｎ－アセチルグルコサミン、ガラクトシルスクロース、ガラクトシルラクトース、ガラクトピラノシル（β１－３）ガラクトピラノシル（β１－４）　グルコピラノース、ガラクトピラノシル（β１－３）グルコピラノース、ガラクトピラノシル（β１－６）ガラクトピラノシル　（β１－４）　グルコピラノース、ガラクトピラノシル（β１－６）グルコピラノース、キシロオリゴ糖（キシロトリオース、キシロビオース等）、ゲンチオオリゴ糖（ゲンチオビオース、ゲンチオトリオース、ゲンチオテトラオース等）、スタキオース、テアンデオリゴ、ニゲロオリゴ糖（ニゲロース等）、パラチノースオリゴ糖、パラチノースシロップ、フラクトオリゴ糖（ケストース、ニストース等）、フラクトフラノシルニストース、ポリデキストロース、マルトシル－β－サイクロデキストリン、マルトオリゴ糖（マルトトリオース、テトラオース、ペンタオース、ヘキサオース、ヘプタオース等）、ラフィノース、砂糖結合水飴（カップリングシュガー）、大豆オリゴ糖、転化糖、水飴等のオリゴ糖類；イソマルチトール、エリスリトール、キシリトール、グリセロール、ソルビトール、パラチニット、マルチトール、マルトテトライトール、マルトトリイトール、マンニトール、ラクチトール、還元イソマルトオリゴ糖、還元キシロオリゴ糖、還元ゲンチオオリゴ糖、還元麦芽糖水飴、還元水飴等の糖アルコール；α－グルコシルトランスフェラーゼ処理ステビア、アスパルテーム、アセスルファムカリウム、アリテーム、カンゾウ抽出物（グリチルリチン）、グリチルリチン酸三アンモニウム、グリチルリチン酸三カリウム、グリチルリチン酸三ナトリウム、グリチルリチン酸二アンモニウム、グリチルリチン酸二カリウム、グリチルリチン酸二ナトリウム、クルクリン、サッカリン、サッカリンナトリウム、シクラメート、スクラロース、ステビア抽出物、ステビア末、ズルチン、タウマチン（ソーマチン）、テンリョウチャ抽出物、ナイゼリアベリー抽出物、ネオテーム、ネオヘスペリジンジヒドロカルコン、フラクトシルトランスフェラーゼ処理ステビア、ブラジルカンゾウ抽出物、ミラクルフルーツ抽出物、ラカンカ抽出物、酵素処理カンゾウ、酵素分解カンゾウ等の高甘味度甘味料；その他蜂蜜、果汁、果汁濃縮物等を例示することができる。これらの甘味料は１種単独で使用することも２種以上を任意に組み合わせて使用することもできる。単糖類、二糖類、オリゴ糖類及び糖アルコール類については、本発明の組成物に配合させる場合、５０～７０重量％を配合するのが好適である。また高甘味度甘味料については、本発明の組成物中、０～２重量％を配合するのが好適である。 The composition of the present invention can contain a sweetener. Examples of sweeteners include monosaccharides, disaccharides, oligosaccharides, sugar alcohols, and high intensity sweeteners. Specifically, monosaccharides such as arabinose, galactose, xylose, glucose, fucose, sorbose, fructose, rhamnose, ribose, isomerized liquid sugar, N-acetylglucosamine; isotrehalose, sucrose, trehalulose, trehalose, neotrehalose, palatinose , Maltose, melibiose, lactulose, lactose and other disaccharides; α-cyclodextrin, β-cyclodextrin, isomaltoligosaccharides (isomaltose, isomaltotriose, panose, etc.), oligo-N-acetylglucosamine, galactosylsucrose, galactosyl Lactose, galactopyranosyl (β1-3) galactopyranosyl (β1-4) glucopyranose, galactopyranosyl (β1-3) glucopyranose, galactopi Lanosyl (β1-6) galactopyranosyl (β1-4) glucopyranose, galactopyranosyl (β1-6) glucopyranose, xylo-oligosaccharide (xylotriose, xylobiose, etc.), gentio-oligosaccharide (gentiobiose, gentiotriose, Gentiotetraose, etc.), stachyose, theande oligo, nigerooligosaccharide (eg, nigerose), palatinose oligosaccharide, palatinose syrup, fructooligosaccharide (kestose, nystose, etc.), fructofuranosyl nystose, polydextrose, maltosyl-β-cyclodextrin, Malto-oligosaccharides (maltotriose, tetraose, pentaose, hexaose, heptaose, etc.), raffinose, sugar-bound starch syrup (coupling sugar), soybean oligosaccharide, invert sugar, syrup Oligosaccharides: isomalitol, erythritol, xylitol, glycerol, sorbitol, palatinit, maltitol, maltoteitol, maltotriitol, mannitol, lactitol, reduced isomaltoligosaccharide, reduced xylooligosaccharide, reduced gentiooligosaccharide, reduced maltose starch syrup Α-glucosyltransferase-treated stevia, aspartame, acesulfame potassium, alitame, licorice extract (glycyrrhizin), triammonium glycyrrhizinate, tripotassium glycyrrhizinate, trisodium glycyrrhizinate, diammonium glycyrrhizinate, glycyrrhizin Dipotassium acid, disodium glycyrrhizinate, curculin, saccharin, saccharin sodium, cyclamate Sucralose, stevia extract, stevia powder, dulcin, thaumatin (thaumatin), tenroucha extract, nigerian berry extract, neotame, neohesperidin dihydrochalcone, fructosyltransferase-treated stevia, brazilian licorice extract, miracle fruit extract, lacanka Examples include high-sweetness sweeteners such as extracts, enzyme-treated licorice, and enzyme-decomposed licorice; and other honey, fruit juice, fruit juice concentrate, and the like. These sweeteners can be used alone or in any combination of two or more. When monosaccharides, disaccharides, oligosaccharides, and sugar alcohols are added to the composition of the present invention, it is preferable to add 50 to 70% by weight. As for the high-intensity sweetener, it is preferable to add 0 to 2% by weight in the composition of the present invention.
　本発明の組成物は香料を含むことができる。使用される香料の例としては、オレンジ油、レモン油、グレープフルーツ油、ライム油、タンジェリン油、マンダリン油などの柑橘精油類、ペパーミント油、スペアミント油、のようなミント精油類、オールスパイス、アニスシード、バジル、ローレル、カルダモン、セロリー、クローブ、シンナモン、クミン、ディル、ガーリック、パセリ、メース、マスタード、オニオン、パプリカ、パセリ、ローズマリー、ペッパーのような公知のスパイス精油類またはオレオレジン類、リモネン、リナロール、ネロール、シトロネロール、ゲラニオール、シトラール、Ｌ－メントール、オイゲノール、シンナミックアルデハイド、アネトール、ペリラアルデハイド、バニリン、γ－ウンデカラクトン、カプロン酸アリル、Ｌ－カルボン、マルトールなどのような公知の単離、または合成香料、および、これら柑橘精油類、ミント精油類、スパイス精油類または単離・合成香料を目的に沿った割合で混合したシトラスミックス、ミックスミント、各種フルーツなどを表現させた調合香料が挙げられ、その他、ガム用油溶性基剤であるカロチン、クロロフィル、トコフェロールなどを含んでもよいが、本発明では、これらの例示物質に限定されるものではない。香料については、チューインガム組成物に配合させる場合、０～３重量％を配合するのが好適である。 The composition of the present invention can contain a fragrance. Examples of flavors used include citrus essential oils such as orange oil, lemon oil, grapefruit oil, lime oil, tangerine oil, mandarin oil, mint essential oils such as peppermint oil, spearmint oil, allspice, anise seed Known spice essential oils such as basil, laurel, cardamom, celery, clove, cinnamon, cumin, dill, garlic, parsley, mace, mustard, onion, paprika, parsley, rosemary, pepper, or oleoresin, limonene, Linalool, nerol, citronellol, geraniol, citral, L-menthol, eugenol, cinnamic aldehyde, anethole, perilla aldehyde, vanillin, γ-undecalactone, allyl caproate, L-carvone, maltol. Citrus mix, mix mint, various fruits, etc. mixed with known isolated or synthetic fragrances such as citrus essential oils, mint essential oils, spice essential oils or isolated / synthetic fragrances according to the purpose In addition, although it may include carotene, chlorophyll, tocopherol and the like, which are oil-soluble bases for gums, the present invention is not limited to these exemplified substances. As for the fragrance, it is preferable to add 0 to 3% by weight when it is added to the chewing gum composition.
　その他、本発明の組成物はクエン酸、リンゴ酸、フマル酸、アスコルビン酸などの酸味料、カラメル色素、クチナシ色素、アントシアニン色素、アナトー色素、パプリカ色素、紅花色素、紅麹色素、フラボノイド色素、コチニール色素、アマランス（赤色２号）、エリスロシン（赤色３号）、アルラレッドＡＣ（赤色４０号）、ニューコクシン（赤色１０２号）、フロキシン（赤色１０４号）、ローズベンガル（赤色１０５号）、アシッドレッド（赤色１０６号）、タートラジン（黄色４号）、サンセットイエローＦＣＦ（黄色５号）、ファストグリーンＦＣＦ（緑色３号）、ブリリアントブルーＦＣＦ（青色１号）、インジゴカルミン（青色２号）等の色素を含むことができ、また、油溶性基剤であるカロチン、クロロフィル、トコフェロールなど、さらに人体に無害の他の添加物を含んでもよい。 In addition, the composition of the present invention is a sour agent such as citric acid, malic acid, fumaric acid, ascorbic acid, caramel dye, gardenia dye, anthocyanin dye, anato dye, paprika dye, safflower dye, safflower dye, flavonoid dye, cochineal Dye, Amaranth (Red No. 2), Erythrosine (Red No. 3), Allura Red AC (Red No. 40), New Coxin (Red No. 102), Phloxin (Red No. 104), Rose Bengal (Red No. 105), Acid Red (Red 106), Tartrazine (Yellow 4), Sunset Yellow FCF (Yellow 5), Fast Green FCF (Green 3), Brilliant Blue FCF (Blue 1), Indigo Carmine (Blue 2), etc. Can contain pigments, and oil-soluble bases such as carotene, chlorophyll, and tocopher Such Lumpur may contain harmless other additives to further human body.
　本発明の組成物は、１回当たりの摂取量が好ましくは１～１０グラム、より好ましくは１．５～５ｇ、最も好ましくは２～３ｇとなるように、１回分が成形されていることが好ましい。形状は限定されず、板状、粒状、立方体、直方体、ボール状、その他の形状を上げることができ、成形された後に糖衣などでコーティングがなされてもよい。また、内部等に液体や固体の、別の組成物を含んでもよい。例えば、食感の面白さを付与する目的や風味を向上させる目的で、液体部分を含ませたり、キャンディやグミを含ませたりすることなどができる。なお、これらの別の組成物の重量は、本発明の組成物には含まない。 The composition of the present invention is preferably formed in a single dose so that the intake amount per time is preferably 1 to 10 grams, more preferably 1.5 to 5 g, and most preferably 2 to 3 g. preferable. The shape is not limited, and plate shape, granular shape, cube shape, rectangular parallelepiped shape, ball shape, and other shapes can be raised, and after forming, coating may be made with sugar coating or the like. Further, another composition such as a liquid or a solid may be contained in the inside or the like. For example, a liquid part can be included, or a candy or gummy can be included for the purpose of imparting an interesting texture or improving the flavor. The weight of these other compositions is not included in the composition of the present invention.
　本発明の組成物は、食事制限を補助することが目的であるので、そのカロリーは低いことが望ましく、好ましくは本発明の組成物の１回の摂取量の熱量は０キロカロリーから１２キロカロリー、より好ましくは０キロカロリーから３キロカロリーである。また、同様の理由により、本発明の組成物の１回の摂取量に含まれる糖質の量は０グラムから３グラムが好ましく、より好ましくは０グラムから１グラムである。 Since the composition of the present invention is intended to assist dietary restriction, it is desirable that the calories be low, and preferably the caloric intake of the composition of the present invention is from 0 to 12 kilocalories, more Preferably it is from 0 to 3 kilocalories. For the same reason, the amount of carbohydrate contained in one intake of the composition of the present invention is preferably 0 to 3 grams, more preferably 0 to 1 grams.
［実施例１］
グルコマンナン溶液の主観評価（１回目）
　パネル１０名（全員女性）に対し、グルコマンナン溶液の主観評価を実施した。対照溶液をシリンジで１０ｍｌ量り、そのままパネルの口に注入し、摂取させた。その１０分後に０．２％または０．４％のグルコマンナン溶液を対照溶液と同様に、同量である１０ｍｌをシリンジで量り、パネルの口へ注入し、摂取させた。摂取直後、パネルは表１の項目について、対照溶液と比較して主観評価した。結果を表２および３にまとめた。 [Example 1]
Subjective evaluation of glucomannan solution (first time)
A subjective evaluation of the glucomannan solution was performed on 10 panelists (all women). 10 ml of the control solution was weighed with a syringe and injected into the mouth of the panel as it was. Ten minutes later, a 0.2% or 0.4% glucomannan solution, like the control solution, was weighed in the same amount of 10 ml with a syringe and injected into the mouth of the panel to be ingested. Immediately after ingestion, the panel subjectively evaluated the items in Table 1 compared to the control solution. The results are summarized in Tables 2 and 3.
　なお、対照溶液と、グルコマンナン溶液はグルコマンナンと／あるいはマルチトールを水に溶解して調製した。組成は以下のとおりであった。
対照溶液：マルチトール２．０重量％
グルコマンナン溶液（０．２％）：マルチトール２．０重量％、グルコマンナン０．２重量％
グルコマンナン溶液（０．４％）：マルチトール２．０重量％、グルコマンナン０．４重量％ The control solution and the glucomannan solution were prepared by dissolving glucomannan and / or maltitol in water. The composition was as follows:
Control solution: 2.0% by weight maltitol
Glucomannan solution (0.2%): maltitol 2.0 wt%, glucomannan 0.2 wt%
Glucomannan solution (0.4%): 2.0% by weight maltitol, 0.4% by weight glucomannan
Figure JPOXMLDOC01-appb-T000001
  
Figure JPOXMLDOC01-appb-T000001
  
Figure JPOXMLDOC01-appb-T000002
Figure JPOXMLDOC01-appb-T000002
Figure JPOXMLDOC01-appb-T000003
Figure JPOXMLDOC01-appb-T000003
［実施例２］
グルコマンナン溶液の主観評価（２回目）
　パネル１２名（全員女性）に対し、グルコマンナン溶液の主観評価を実施した。パネルは評価前４時間の固形物の絶食をし、評価は空腹の状態で行った。なお、絶食時においても液体物の摂取については特に制限を行わなかった。 [Example 2]
Subjective evaluation of glucomannan solution (second time)
A subjective evaluation of the glucomannan solution was performed on 12 panelists (all women). The panel was fasted for 4 hours before evaluation and the evaluation was performed on an empty stomach. In addition, there was no particular restriction on the intake of liquids even during fasting.
　評価は次のように行った。すなわち、対照溶液をシリンジで１０ｍｌ量り、パネルの口へ注入し、摂取させた。その１０分後に所定の濃度のグルコマンナン溶液を対照溶液と同様に、同量である１０ｍｌをシリンジで量り、パネルの口へ注入し、摂取させた。摂取直後にパネルは実施例１と同じ項目について、対照溶液と比較して主観評価を行った。また、さらに、摂取の順序を逆転して評価を行った。本実施例におけるタイムスケジュールを図１に示す。結果を表４～１２にまとめた。 Evaluation was performed as follows. That is, 10 ml of the control solution was weighed with a syringe and injected into the mouth of the panel to ingest it. Ten minutes after that, similarly to the control solution, 10 ml of the same concentration of glucomannan solution was weighed with a syringe and injected into the mouth of the panel for ingestion. Immediately after ingestion, the panel performed a subjective evaluation on the same items as in Example 1 in comparison with the control solution. Further, the evaluation was performed by reversing the order of intake. The time schedule in the present embodiment is shown in FIG. The results are summarized in Tables 4-12.
　なお、対照溶液と、グルコマンナン溶液はグルコマンナンと／あるいはマルチトールを水に溶解して調製した。組成は以下のとおりであった。
対照溶液：マルチトール２．０重量％
グルコマンナン溶液（０．２％）：マルチトール２．０重量％、グルコマンナン０．２重量％
グルコマンナン溶液（０．３％）：マルチトール２．０重量％、グルコマンナン０．３重量％
グルコマンナン溶液（０．４％）：マルチトール２．０重量％、グルコマンナン０．４重量％ The control solution and the glucomannan solution were prepared by dissolving glucomannan and / or maltitol in water. The composition was as follows:
Control solution: 2.0% by weight maltitol
Glucomannan solution (0.2%): maltitol 2.0 wt%, glucomannan 0.2 wt%
Glucomannan solution (0.3%): maltitol 2.0 wt%, glucomannan 0.3 wt%
Glucomannan solution (0.4%): 2.0% by weight maltitol, 0.4% by weight glucomannan
Figure JPOXMLDOC01-appb-T000004
Figure JPOXMLDOC01-appb-T000004
Figure JPOXMLDOC01-appb-T000005
Figure JPOXMLDOC01-appb-T000005
Figure JPOXMLDOC01-appb-T000006
Figure JPOXMLDOC01-appb-T000006
Figure JPOXMLDOC01-appb-T000007
Figure JPOXMLDOC01-appb-T000007
Figure JPOXMLDOC01-appb-T000008
Figure JPOXMLDOC01-appb-T000008
Figure JPOXMLDOC01-appb-T000009
Figure JPOXMLDOC01-appb-T000009
Figure JPOXMLDOC01-appb-T000010
Figure JPOXMLDOC01-appb-T000010
Figure JPOXMLDOC01-appb-T000011
Figure JPOXMLDOC01-appb-T000011
Figure JPOXMLDOC01-appb-T000012
Figure JPOXMLDOC01-appb-T000012
　実施例１、２の結果より、グルコマンナン溶液を摂取した場合、グルコマンナンの濃度依存的に、「テクスチャー」「喉ごし」「胃に入った感じ」「胃に存在する感じ」の各評価項目で対照溶液を摂取した場合と比較して、パネルが違いを感じやすくなっている傾向にあった。また、対照溶液とグルコマンナン溶液の摂取順序による差は見られなかった。
　グルコマンナン溶液は、対照溶液に比べ「胃に入った感じ」並びに「胃に存在する感じ」を強く感じさせることが分かった。その効果は濃度依存的と考えられる。 From the results of Examples 1 and 2, when the glucomannan solution was ingested, each evaluation of “texture”, “sore throat”, “feeling in the stomach”, and “feeling in the stomach” depending on the concentration of glucomannan. The panel tended to feel the difference more easily than when the control solution was ingested. Moreover, the difference by the intake order of a control solution and a glucomannan solution was not seen.
It was found that the glucomannan solution strongly felt “feeling in the stomach” and “feeling in the stomach” compared to the control solution. The effect is considered to be concentration dependent.
［実施例３］
グルコマンナン配合ガムの作製
　本発明の組成物の例として、以下のグルコマンナン配合ガムを作製した。製造方法は、通常のガムの製造方法に準じ、ガムベースと粉末原料、液体原料を５０～６０℃前後で混合した。グルコマンナンは、例えばレオレックス（商標）Ｏｎｅ（清水化学株式会社）などとして購入することができる。 [Example 3]
Production of Glucomannan Blending Gum The following glucomannan blending gum was produced as an example of the composition of the present invention. The production method was based on a normal gum production method, and a gum base, a powder raw material, and a liquid raw material were mixed at around 50 to 60 ° C. Glucomannan can be purchased as, for example, ROLEX (trademark) One (Shimizu Chemical Co., Ltd.).
ガムベース　　　　　　　　　　３０．９　％
マンニトール　　　　　　　　　　３．２　％
エリスリトール　　　　　　　　２０．６　％
マルチトール　　　　　　　　　３０．９　％
還元パラチノース　　　　　　　　３．４　％
グルコマンナン　　　　　　　　　２．４　％
還元麦芽糖水飴　　　　　　　　　１．７　％
３３．３％アラビアガム水溶液　　０．６　％
高甘味度甘味料　　　　　　　　　１．４　％
（アスパルテーム、アセスルファムカリウム）
酸味料　　　　　　　　　　　　　１．９　％
（クエン酸、リンゴ酸、フマル酸、アスコルビン酸）
色素　　　　　　　　　　　　　　０．３　％
香料　　　　　　　　　　　　　　２．８　％　　　　　　
　　　　　　　　　　　　　　　　１００　％
（組成は重量％で示す） Gum base 30.9%
Mannitol 3.2%
Erythritol 20.6%
Maltitol 30.9%
Reduced palatinose 3.4%
Glucomannan 2.4%
Reduced maltose starch syrup 1.7%
33.3% gum arabic aqueous solution 0.6%
High intensity sweetener 1.4%
(Aspartame, acesulfame potassium)
Acidulant 1.9%
(Citric acid, malic acid, fumaric acid, ascorbic acid)
Dye 0.3%
Fragrance 2.8%
100%
(Composition is given in% by weight)
［実施例４］
グルコマンナン配合ガムを咀嚼した際の唾液量の測定
　女性パネル３名（パネルＡ，Ｂ，Ｃ）が実施例３で製造したグルコマンナン配合ガム約２．１ｇを咀嚼し、分泌された唾液の重量を測定した。唾液を飲み込むタイミングで、試験管に吐出させ、その重量を測定した。試験管は１分おきに交換し、８分まで測定した。メトロノームのリズムに合わせて、１分間に８０回のペースで咀嚼させた。結果を表１３に示す。 [Example 4]
Measurement of the amount of saliva when chewing gum containing glucomannan The weight of saliva secreted by chewing about 2.1 g of glucomannan-containing gum produced by Example 3 by three female panels (panels A, B, C) Was measured. At the timing of swallowing saliva, it was discharged into a test tube and its weight was measured. The test tube was changed every 1 minute and measured up to 8 minutes. According to the rhythm of the metronome, it was chewed at a pace of 80 times per minute. The results are shown in Table 13.
Figure JPOXMLDOC01-appb-T000013
 　唾液はグルコマンナン配合ガムの咀嚼開始から３分までで、もっとも活発に分泌され、その後も一定量分泌されることが分かった。
Figure JPOXMLDOC01-appb-T000013
 It was found that saliva was secreted most actively after 3 minutes from the start of chewing of the glucomannan-containing gum, and then a certain amount was also secreted.
［実施例５］
グルコマンナン配合ガムから溶出するグルコマンナン量の測定
　実施例３で製造したグルコマンナン配合ガム２．１グラムをパネルが２分、３分、４分、５分、６分、７分、または８分メトロノームのリズムにあわせて１分間８０回のペースで咀嚼し、咀嚼後のグルコマンナン配合ガムに残存するグルコマンナン量を測定し、配合量および、溶出率を算出した。対照として、咀嚼されないグルコマンナン配合ガムについても測定を行った。
　測定方法は以下のとおりである。すなわち、咀嚼後あるいは対照のグルコマンナン配合ガムにトルエンを加え、分散させた後、水を加え沸騰状態で９０分間加熱還流抽出し、水層を集めマンナン抽出液とした。マンナン抽出液に硫酸濃度が１．８７５　Ｎになるように濃硫酸を加え９５℃５時間酸分解後、冷却し、中和（ｐＨ５～７）した。この溶液中のマンノースの定量を高速液体クロマトグラフィーにより行った。グルコマンナンを構成するグルコース：マンノースの比率は１：１．６であることから、得られたマンノース値に（１＋１．６）／１．６を乗じてグルコマンナン量を求めた。 [Example 5]
Measurement of the amount of glucomannan eluted from the glucomannan-containing gum 2.1 grams of the glucomannan-containing gum produced in Example 3 is 2 minutes, 3 minutes, 4 minutes, 5 minutes, 6 minutes, 7 minutes, or 8 minutes Mastication was performed at a pace of 80 times per minute according to the rhythm of the metronome, the amount of glucomannan remaining in the glucomannan-containing gum after chewing was measured, and the amount and dissolution rate were calculated. As a control, measurements were also made on a glucomannan-containing gum that was not chewed.
The measurement method is as follows. That is, after chewing or after adding toluene to the control glucomannan-containing gum and dispersing, water was added and the mixture was heated to reflux for 90 minutes in a boiling state, and the aqueous layer was collected to obtain a mannan extract. Concentrated sulfuric acid was added to the mannan extract so that the sulfuric acid concentration was 1.875 N, and the mixture was acid-decomposed at 95 ° C. for 5 hours, cooled, and neutralized (pH 5 to 7). The mannose in this solution was quantified by high performance liquid chromatography. Since the ratio of glucose: mannose constituting glucomannan was 1: 1.6, the amount of glucomannan was determined by multiplying the obtained mannose value by (1 + 1.6) /1.6.
　なお、高速液体クロマトグラフィーの条件は以下の通りである。
装置：ダイオネクス社　液体クロマトグラフィー　ＩＣＳ－３０００　カラム：ＣａｒｂｏＰａｃ　ＰＡ－１（４×２５０ｍｍ）
ガードカラム：　ＣａｒｂｏＰａｃ　ＰＡ－１（４×５０ｍｍ）　溶離液：水酸化ナトリウム１５０ｍＭ　検出：電気化学検出器
溶液流速：１．０ｍｌ　／　ｍｉｎ The conditions for high performance liquid chromatography are as follows.
Equipment: Liquid chromatography ICS-3000 Column: CarboPac PA-1 (4 × 250 mm)
Guard column: CarboPac PA-1 (4 × 50 mm) Eluent: Sodium hydroxide 150 mM Detection: Electrochemical detector Solution flow rate: 1.0 ml / min
　結果は表１４のとおりであった。なお、表に示される数値は、それぞれの時間の咀嚼後のグルコマンナン配合ガムにおけるグルコマンナンの溶出率である。
　なお、グルコマンナン配合ガムのグルコマンナンの配合量は、本方法の分析によると２．１９％と求められた。 The results are shown in Table 14. In addition, the numerical value shown by a table | surface is the elution rate of the glucomannan in the glucomannan combination gum after chewing of each time.
In addition, according to the analysis of this method, the blending amount of glucomannan in the glucomannan blended gum was determined to be 2.19%.
Figure JPOXMLDOC01-appb-T000014
Figure JPOXMLDOC01-appb-T000014
　咀嚼に伴い、グルコマンナン配合ガム中のグルコマンナンが徐々に減少したことがわかる。 It can be seen that glucomannan in the glucomannan-containing gum gradually decreased with chewing.
　実施例４、５の結果より、２．１ｇのグルコマンナン配合ガムを５分間咀嚼すると、１０ｇの唾液にグルコマンナンが９０％程度（２．１ｇ×２．１９％×９０％＝約０．０４ｇ）溶出し、飲み込まれることで胃に入ることが分かった。つまり、２．１ｇのグルコマンナン配合ガムを５分間咀嚼すると、０．４％グルコマンナンを含む唾液を１０ｇ飲み込むこととなり、実施例１、２で最も効果が認められたグルコマンナン摂取量と同じとなる。すなわち、２．１ｇのグルコマンナン配合ガムを５分間咀嚼すると、グルコマンナンを含む唾液を飲み込むことによって、胃に入った感じ、並びに胃に存在する感じを強く知覚できる、ということが示唆される。 From the results of Examples 4 and 5, 2.1 g of glucomannan-containing gum was chewed for 5 minutes, and 10 g of saliva was about 90% glucomannan (2.1 g × 2.19% × 90% = about 0.04 g). ) Elution and swallowing was found to enter the stomach. That is, when chewing 2.1 g of glucomannan-containing gum for 5 minutes, 10 g of saliva containing 0.4% glucomannan is swallowed, which is the same as the amount of glucomannan intake most effective in Examples 1 and 2. Become. That is, when chewing 2.1 g of glucomannan-containing gum for 5 minutes, it is suggested that the feeling of entering the stomach and the feeling of existing in the stomach can be strongly perceived by swallowing saliva containing glucomannan.
［実施例６］
グルコマンナン配合ガムを咀嚼した際の主観評価
　男性パネル６名（パネル１～６）および女性パネル６名（パネル７～１２）に対し、実施例３で製造したグルコマンナン配合ガム約２．１ｇ、もしくは対照ガム約２．１gを７分間咀嚼させた。咀嚼方法については、特に指定しなかった。なお、ここで使用する対照ガムは、実施例３のグルコマンナン配合ガムにおいて、配合中のグルコマンナン２．４％をマルチトール２．４％に置換したものである。
　咀嚼させた時間帯は、空腹感を感じやすいと考えられる午前１１時～１２時および午後４時～５時とした。すなわち、グルコマンナン配合ガムもしくは対照ガムのうちどちらか一方を午前１１時～１２時に咀嚼させて評価を行い、午後４時～５時にもう一方を咀嚼させて評価を行った。評価については、図２に示す評価軸を用い、「コバラが紛れた」感じの強さ、について１０段階で主観評価を行った。なお、「コバラが紛れた」とは、「空腹感が緩和した」状況のことを指す。結果を表１５から表１７に示す。 [Example 6]
Subjective evaluation when chewing glucomannan-containing gum About 2.1 g of glucomannan-containing gum produced in Example 3 for 6 male panels (panels 1-6) and 6 female panels (panels 7-12), Alternatively, about 2.1 g of control gum was chewed for 7 minutes. The chewing method was not specified. In addition, the control gum used here is obtained by substituting 2.4% of glucomannan in the blended glucomannan of Example 3 with 2.4% of maltitol.
The chewing hours were 11:00 am to 12:00 am and 4 pm to 5:00 pm, which are thought to make it easy to feel hungry. That is, one of the glucomannan-containing gum and the control gum was chewed for evaluation from 11:00 to 12:00, and the other was chewed for evaluation from 4 to 5 pm. For the evaluation, the evaluation axis shown in FIG. 2 was used, and the subjective evaluation was carried out in 10 stages with respect to the strength of the feeling of “cobala was lost”. “Cobala was lost” refers to a situation where “feeling of hunger has eased”. The results are shown in Table 15 to Table 17.
Figure JPOXMLDOC01-appb-T000015
Figure JPOXMLDOC01-appb-T000015
Figure JPOXMLDOC01-appb-T000016
Figure JPOXMLDOC01-appb-T000016
Figure JPOXMLDOC01-appb-T000017
Figure JPOXMLDOC01-appb-T000017
　表１５から表１７より、パネル１および３を除き、対照ガム咀嚼時よりもグルコマンナン配合ガム咀嚼時の方が、コバラが紛れたとの主観評価点が高い傾向が見られた。主観評価点の平均を見ても、対照ガム咀嚼時よりもグルコマンナン配合ガム咀嚼時の方が高かった。主観評価点の平均について、対応のあるｔ検定による有意差判定を行った結果、ｐ＝０．０００５１８＜０．０５（有意水準）との結果であった。
　従って、グルコマンナンを配合したガムを咀嚼することで、グルコマンナンを配合しないガムを咀嚼した場合よりも有意に「コバラが紛れた」感じ、すなわち空腹感が緩和した感じが高くなることが示された。 From Table 15 to Table 17, except for panels 1 and 3, a tendency was found that the subjective evaluation score that Kobara was lost was higher when chewing gum with glucomannan was chewing than when chewing gum. Looking at the average subjective evaluation score, it was higher when chewing gum with glucomannan than when chewing gum. As a result of carrying out a significant difference determination by the corresponding t-test with respect to the average of the subjective evaluation points, the result was p = 0.000518 <0.05 (significance level).
Therefore, chewing gum containing glucomannan shows that the feeling of “cobala is lost” significantly, that is, the feeling of hunger is relaxed, is higher than when chewing gum without glucomannan. It was.
　この出願は２０１２年１０月９日に出願された日本国特許出願第２０１２－２２４１４５号からの優先権を主張するものであり、その内容を引用してこの出願の一部とするものである。 This application claims priority from Japanese Patent Application No. 2012-224145 filed on Oct. 9, 2012, the contents of which are incorporated herein by reference.

Claims (4)

  1. 　グルコマンナンとガムベースを含み、咀嚼されることで空腹感を緩和することを特徴とする組成物。 A composition comprising glucomannan and a gum base, which is chewed to relieve hunger.
  2. 　グルコマンナンが１～１０重量％の割合で含有されることを特徴とする請求項１に記載の組成物。 2. The composition according to claim 1, wherein glucomannan is contained in an amount of 1 to 10% by weight.
  3. 　１個あたり１～１０ｇに成形されていることを特徴とする請求項１または２に記載の組成物。 3. The composition according to claim 1, wherein the composition is molded to 1 to 10 g per piece.
  4. 　１個あたりグルコマンナンの量が０．０１～１ｇとなるように成形されたことを特徴とする請求項１から３のいずれかに記載の組成物。
     
     

          4. The composition according to claim 1, wherein the composition is molded so that the amount of glucomannan per unit is 0.01 to 1 g.



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USD796775S1 (en) 2015-09-09 2017-09-12 Intercontinental Great Brands Llc Confection
USD822333S1 (en) 2015-09-09 2018-07-10 Intercontinental Great Brands Llc Confection
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