JP4736509B2 - Candy - Google Patents

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Publication number
JP4736509B2
JP4736509B2 JP2005105475A JP2005105475A JP4736509B2 JP 4736509 B2 JP4736509 B2 JP 4736509B2 JP 2005105475 A JP2005105475 A JP 2005105475A JP 2005105475 A JP2005105475 A JP 2005105475A JP 4736509 B2 JP4736509 B2 JP 4736509B2
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weight
sorbitol
tablet
fatty acid
silicon dioxide
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JP2006280288A (en
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宇野  明
炳▲しょう▼ 祝
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Kobayashi Pharmaceutical Co Ltd
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Kobayashi Pharmaceutical Co Ltd
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Priority to JP2005105475A priority Critical patent/JP4736509B2/en
Priority to PCT/JP2006/305444 priority patent/WO2006109429A1/en
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Classifications

    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23GCOCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
    • A23G3/00Sweetmeats; Confectionery; Marzipan; Coated or filled products
    • A23G3/34Sweetmeats, confectionery or marzipan; Processes for the preparation thereof
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23GCOCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
    • A23G3/00Sweetmeats; Confectionery; Marzipan; Coated or filled products
    • A23G3/34Sweetmeats, confectionery or marzipan; Processes for the preparation thereof
    • A23G3/36Sweetmeats, confectionery or marzipan; Processes for the preparation thereof characterised by the composition containing organic or inorganic compounds
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23GCOCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
    • A23G3/00Sweetmeats; Confectionery; Marzipan; Coated or filled products
    • A23G3/34Sweetmeats, confectionery or marzipan; Processes for the preparation thereof
    • A23G3/36Sweetmeats, confectionery or marzipan; Processes for the preparation thereof characterised by the composition containing organic or inorganic compounds
    • A23G3/362Sweetmeats, confectionery or marzipan; Processes for the preparation thereof characterised by the composition containing organic or inorganic compounds containing inorganic compounds
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23GCOCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
    • A23G3/00Sweetmeats; Confectionery; Marzipan; Coated or filled products
    • A23G3/34Sweetmeats, confectionery or marzipan; Processes for the preparation thereof
    • A23G3/36Sweetmeats, confectionery or marzipan; Processes for the preparation thereof characterised by the composition containing organic or inorganic compounds
    • A23G3/42Sweetmeats, confectionery or marzipan; Processes for the preparation thereof characterised by the composition containing organic or inorganic compounds characterised by the carbohydrates used, e.g. polysaccharides
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23GCOCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
    • A23G3/00Sweetmeats; Confectionery; Marzipan; Coated or filled products
    • A23G3/34Sweetmeats, confectionery or marzipan; Processes for the preparation thereof
    • A23G3/50Sweetmeats, confectionery or marzipan; Processes for the preparation thereof characterised by shape, structure or physical form, e.g. products with supported structure

Description

本発明は、ソルビトールを主原料として含有する錠菓に関する。   The present invention relates to a tablet confection containing sorbitol as a main raw material.

錠菓は、錠剤の形をした固体の菓子類等であり、粉末または顆粒状のショ糖などの甘味料、クエン酸、ビタミン類などを、ブドウ糖、デンプン糖等とともに混合し、この混合物を圧縮打錠することにより成型し、製品としていた。   Tablet confectionery is solid confectionery in the form of tablets. Sweeteners such as powdered or granular sucrose, citric acid, vitamins, etc. are mixed with glucose, starch sugar, etc., and this mixture is compressed. Molded by tableting and made into a product.

近年、健康志向が高まる中、低カロリーであり、且つ、抗う触性である糖アルコール類を従来の糖類に替えて用いることが注目されており、各種の糖アルコールの製法や用途の開発がなされている(例えば、特許文献1、2)。   In recent years, with increasing health consciousness, attention has been paid to using sugar alcohols that are low in calories and have anti-tactile properties in place of conventional sugars, and various sugar alcohol production methods and applications have been developed. (For example, Patent Documents 1 and 2).

糖アルコール類としては、例えば、キシリトール、ソルビトール、マンニトール、エリスリトール、ラクチノール、イソマルトール等が知られているが、中でも特にソルビトールは、他の糖アルコール類と比較して、打錠した際の錠剤硬度が高く、ソルビトールを含有する錠菓が、例えば、特許文献3に記載されている。
特開平11−113525号公報 特表2001−504342 特開2003−250450号公報
As sugar alcohols, for example, xylitol, sorbitol, mannitol, erythritol, lactinol, isomaltol, and the like are known. Among them, sorbitol has tablet hardness when compressed compared to other sugar alcohols. For example, Patent Document 3 discloses a tablet confection that is high and contains sorbitol.
JP-A-11-113525 Special table 2001-504342 JP 2003-250450 A

ソルビトールを主原料として錠菓を打錠する際、打錠が困難であるという問題がある。このような問題を解消するために、二酸化ケイ素およびショ糖脂肪酸エステルをさらに配合することが考えられるが、二酸化ケイ素及びショ糖脂肪酸エステルの配合量が高くなると、口内に入れたときに、舌にザラツキ感が生じ、食感上好ましくない。   When tableting a tablet confection using sorbitol as a main raw material, there is a problem that tableting is difficult. In order to solve such problems, it is conceivable to further add silicon dioxide and sucrose fatty acid ester. However, when the amount of silicon dioxide and sucrose fatty acid ester increases, A rough feeling is generated, which is not preferable in terms of texture.

本発明は、上記事情に鑑みてなされたものであり、打錠がし易く、かつ、舌ザラツキ感が生じない錠菓を提供することを目的とする。   The present invention has been made in view of the above circumstances, and an object of the present invention is to provide a tablet confection that is easy to be tableted and does not cause a feeling of rough tongue.

本発明者らは、糖アルコール類として、噴霧乾燥法により製造された嵩密度が0.3〜0.6g/ml、比表面積が0.7〜1.5m2/gのソルビトールを主原料とし、かつ、これに、0.5〜1.5重量%の二酸化ケイ素および0.5〜1.5重量%のショ糖脂肪酸エステルを配合することにより、打錠がし易く、かつ、舌ザラツキ感を生じないようにすることができることを見出し、本発明を完成するに至った。 The present inventors mainly use sorbitol having a bulk density of 0.3 to 0.6 g / ml and a specific surface area of 0.7 to 1.5 m 2 / g produced by spray drying as sugar alcohols. And, by blending 0.5 to 1.5% by weight of silicon dioxide and 0.5 to 1.5% by weight of sucrose fatty acid ester, it is easy to tablet and has a rough texture. As a result, the present invention has been completed.

すなわち、本発明の錠菓は、ソルビトールと、二酸化ケイ素と、ショ糖脂肪酸エステルとを含有する錠菓において、ソルビトールが噴霧乾燥法により製造された嵩密度が0.3〜0.6g/mlであり、比表面積が0.7〜1.5m2/gのものであり、二酸化ケイ素の含有量が0.5〜1.5重量%であり、ショ糖脂肪酸エステルの含有量が0.5〜1.5重量%であることを特徴とするものである。 That is, the tablet confection of the present invention is a tablet confection containing sorbitol, silicon dioxide, and sucrose fatty acid ester, and the bulk density produced by spray drying of sorbitol is 0.3 to 0.6 g / ml. The specific surface area is 0.7 to 1.5 m 2 / g, the silicon dioxide content is 0.5 to 1.5% by weight, and the sucrose fatty acid ester content is 0.5 to 1.5%. It is characterized by being 1.5% by weight.

本発明の錠菓は、噴霧乾燥法により製造された嵩密度が0.3〜0.6g/mlであり、比表面積が0.7〜1.5m2/gのソルビトールを用い、0.5〜1.5重量%の二酸化ケイ素および0.5〜1.5重量%のショ糖脂肪酸エステルを含有しているので、打錠がし易く、かつ、舌ザラツキ感を生じない。 The tablet confectionery of the present invention uses sorbitol having a bulk density of 0.3 to 0.6 g / ml produced by a spray drying method and a specific surface area of 0.7 to 1.5 m 2 / g. Since it contains ˜1.5% by weight of silicon dioxide and 0.5 to 1.5% by weight of sucrose fatty acid ester, it is easy to tablet and does not cause a rough texture.

以下、本発明の錠菓を詳細に説明する。   Hereinafter, the tablet confectionery of the present invention will be described in detail.

本発明の錠菓は、嵩密度が0.3〜0.6g/mlであり、比表面積が0.7〜1.5m2/gのソルビトールを含有している。このようなソルビトールとしては、例えば、メルク社製のソルビトールが挙げられる(例えば、特公平5−1247号公報参照)。当該ソルビトールは、例えば、公知の噴霧乾燥法により製造することができ、例えば、グルコースを含有する溶液に対して、170℃より低い温度でグルコースの水素添加を行うことによりソルビトール溶液を製造し、そして、得られたソルビトール溶液を、生成物の含水率が1%未満となるように140〜170℃の温度で噴霧乾燥することにより得られる。ソルビトールの含有量は、90〜99重量%であることが好ましい。ソルビトールの含有量が90重量%に満たないと、他の原料の影響を受けやすく、打錠しにくくなったり、ザラツキを生じやすくなる傾向にある。ソルビトールの含有量が99重量%を超えると、ショ糖脂肪酸エステル、二酸化ケイ素の配合量が少なくなり、錠菓として成形することができないという問題がある。 The tablet confectionery of the present invention contains sorbitol having a bulk density of 0.3 to 0.6 g / ml and a specific surface area of 0.7 to 1.5 m 2 / g. Examples of such sorbitol include sorbitol manufactured by Merck & Co., Inc. (see, for example, Japanese Patent Publication No. 5-12247). The sorbitol can be produced, for example, by a known spray drying method, for example, producing a sorbitol solution by hydrogenating glucose at a temperature lower than 170 ° C. to a solution containing glucose, and The obtained sorbitol solution is obtained by spray drying at a temperature of 140 to 170 ° C. so that the water content of the product is less than 1%. The content of sorbitol is preferably 90 to 99% by weight. If the content of sorbitol is less than 90% by weight, it tends to be affected by other raw materials, making it difficult to tablet and tend to cause roughness. When the content of sorbitol exceeds 99% by weight, there is a problem that the amount of sucrose fatty acid ester and silicon dioxide is reduced, and cannot be formed as a tablet confectionery.

また、本発明の錠菓は、二酸化ケイ素を含有している。本発明に含有の二酸化ケイ素は微粒二酸化ケイ素が望ましい。微粒二酸化ケイ素とは、平均粒子径が15μm以下のものをいう。この二酸化ケイ素の含有量は、0.5〜1.5重量%である。二酸化ケイ素の含有量が0.5重量%に満たないと、錠菓として成形することができないという問題があり、二酸化ケイ素の含有量が1.5重量%を超えると、打錠後の錠菓を口に入れた際に舌にザラツキ感が生じるという問題がある。   The tablet confectionery of the present invention contains silicon dioxide. The silicon dioxide contained in the present invention is preferably fine silicon dioxide. Fine silicon dioxide refers to those having an average particle size of 15 μm or less. The silicon dioxide content is 0.5 to 1.5% by weight. If the content of silicon dioxide is less than 0.5% by weight, there is a problem that it cannot be formed as a tablet confection. If the content of silicon dioxide exceeds 1.5% by weight, the tablet confection after tableting There is a problem that the mouth feels rough when you put it in your mouth.

また、本発明の錠菓は、ショ糖脂肪酸エステルを含有している。このショ糖脂肪酸エステルの含有量は、0.5〜1.5重量%である。ショ糖脂肪酸エステルの含有量が0.5%未満であると、ショ糖脂肪酸エステルが少なすぎて錠菓として成形することができない。また、1.5重量%を超えると、打錠後の錠菓を口に入れた際に舌にザラツキ感が生じる。ショ糖の水酸基とエステル結合してショ糖脂肪酸エステルを形成する脂肪酸は特に限定されることはないが、例えば、炭素数16〜18のものが挙げられる。また、HLBは3〜5のものが好ましい。   The tablet confectionery of the present invention contains a sucrose fatty acid ester. The content of this sucrose fatty acid ester is 0.5 to 1.5% by weight. If the content of sucrose fatty acid ester is less than 0.5%, the amount of sucrose fatty acid ester is too small to form as a tablet confectionery. On the other hand, when the content exceeds 1.5% by weight, a rough feeling is generated on the tongue when the tableted confectionery is put in the mouth. Although the fatty acid which ester-bonds with the hydroxyl group of sucrose and forms sucrose fatty acid ester is not specifically limited, For example, a C16-C18 thing is mentioned. The HLB is preferably 3-5.

本発明の錠菓は、さらに他の成分を含んでいてもよく、例えば、香料、色素、酸味料、甘味料、ビタミン類、機能性物質等を含んでいてもよい。   The tablet confectionery of the present invention may further contain other components, for example, a flavor, a pigment, a sour agent, a sweetener, vitamins, a functional substance, and the like.

香料としては、粉末香料製造に際して既に用いられているものであればいかなるものも用いることができるが、例えば、オレンジ、レモン、グレープフルーツ等のシトラス系香料、アップル、バナナ、グレープ、ピーチ、ストロベリー、パイナップル等のフルーツ系香料、ペパーミント、スペアミント等のミント系香料、ペッパー、シンナモン、ナツメグ、クローブ等のスパイス系香料、バニラ、コーヒー、ココア、ヘーゼルナッツ等のナッツ系香料、紅茶、緑茶等の茶系香料、ビーフ、チキン、サーモン、クラブ等の畜肉・水産系香料、ミルク、チーズ等のデイリー系香料等が挙げられる。また、香料の種類としては、調合することにより製造される調合香料、有効成分を抽出して得られる精油等を用いることができる。また、シトラール、ゲラニオール、1−メントール、バニリン等の合成系香料も使用することができる。さらに、水蒸気蒸留、超臨界流体抽出により得られたコーヒー、紅茶等、鰹節等、天然の果汁等からの香気成分も使用することができる。また、ここで挙げた香料は複数種を混合して用いることもできる。   Any fragrance can be used as long as it is already used in the production of powdered fragrances. For example, citrus fragrances such as orange, lemon, grapefruit, apple, banana, grape, peach, strawberry, pineapple Fruit flavors such as peppermint and spearmint, spice flavors such as pepper, cinnamon, nutmeg and clove, nut flavors such as vanilla, coffee, cocoa and hazelnut, tea flavors such as tea and green tea, Examples include meat and fish-based flavors such as beef, chicken, salmon and clubs, and daily flavors such as milk and cheese. Moreover, as a kind of fragrance | flavor, the blended fragrance | flavor manufactured by mixing, the essential oil obtained by extracting an active ingredient, etc. can be used. Synthetic fragrances such as citral, geraniol, 1-menthol and vanillin can also be used. Furthermore, aromatic components from natural fruit juices and the like such as coffee, tea, etc. obtained by steam distillation and supercritical fluid extraction can be used. Moreover, the fragrance | flavor mentioned here can also be used in mixture of multiple types.

色素としては、β−カロチン、パプリカ色素、アナトー色素、クロロフィル等の油溶性天然色素類、ウコン色素、カラメル色素、コチニール色素、ブドウ果皮抽出物等の天然色素類等を使用することができる。ここで挙げた色素は複数種を混合して用いることもできる。   As the pigment, oil-soluble natural pigments such as β-carotene, paprika pigment, anato pigment, chlorophyll, natural pigments such as turmeric pigment, caramel pigment, cochineal pigment, grape skin extract and the like can be used. The dyes mentioned here can also be used as a mixture of plural kinds.

酸味料としては、例えば、クエン酸、リンゴ酸、アスコルビン酸、コハク酸、フマル酸の粉末化物等、柑橘系果実等から得られた果汁の粉末化物等が挙げられる。ここで挙げた酸味料は複数種を混合して用いることもできる。   Examples of the sour agent include powdered products of fruit juice obtained from citrus fruits and the like, such as powdered products of citric acid, malic acid, ascorbic acid, succinic acid, and fumaric acid. The acidulants mentioned here can be used in combination of a plurality of types.

糖質或いは甘味料としては、例えば、アスパルテーム、パラチノース、ラフィノース、トレハロース、エリトリトール、キシリトール等が挙げられる。ここで挙げた甘味料は複数種を混合して用いることもできる。   Examples of the sugar or sweetener include aspartame, palatinose, raffinose, trehalose, erythritol, xylitol and the like. The sweeteners mentioned here can also be used as a mixture of plural kinds.

ビタミン類としては、例えば、ビタミンA、ビタミンD、ビタミンK、ビタミンP等が挙げられる。ここで挙げたビタミン類は複数種を混合して用いることもできる。   Examples of vitamins include vitamin A, vitamin D, vitamin K, vitamin P, and the like. The vitamins mentioned here can be used in combination of two or more.

機能性物質としては、例えば、シソエキス、ソバ等のポリフェノール、プロポリス、ロイヤルゼリー、DHA、EPA等の魚油、リノール酸、リノレン酸等が挙げられる。ここで挙げた機能性物質は複数種を混合して用いることもできる。   Examples of the functional substance include polyphenols such as perilla extract and buckwheat, fish oil such as propolis, royal jelly, DHA, and EPA, linoleic acid, and linolenic acid. The functional substances mentioned here can be used in a mixture of plural kinds.

本発明の錠菓は、上記に挙げた噴霧乾燥法により製造された嵩密度:0.3〜0.6g/mlで、比表面積:0.7〜1.5m2/gのソルビトールと、二酸化ケイ素、とショ糖脂肪酸エステルを含有し、さらに必要に応じて、香料、酸味料、甘味料、ビタミン類、機能性物質等を含有するものであるが、このような成分を含有する本発明の錠菓の製造方法は、特に制限されるものではなく、公知の錠菓の製造方法を適用することができる。具体的には、本発明の錠菓は、上記各成分を混合した後、打錠することにより製造することができる。 The tablet confectionery of the present invention comprises sorbitol having a bulk density of 0.3 to 0.6 g / ml and a specific surface area of 0.7 to 1.5 m 2 / g produced by the spray drying method listed above, and dioxide dioxide. It contains silicon and sucrose fatty acid ester, and further contains a flavoring agent, a sour agent, a sweetener, vitamins, a functional substance, etc., if necessary. The method for producing tablet confection is not particularly limited, and a known method for producing tablet confection can be applied. Specifically, the tablet confectionery of the present invention can be produced by mixing the above components and then tableting.

以下、本発明を具体的に説明するために、本発明の実施例およびこれとの比較を示すための比較例をいくつか挙げる。ただし、本発明の錠菓は、下記実施例によって制限されるものではない。   Hereinafter, in order to specifically describe the present invention, some examples of the present invention and comparative examples for comparing with the examples will be given. However, the tablet confectionery of this invention is not restrict | limited by the following Example.

下記表1に示す成分を混合し、粉末組成物を得た。この粉末組成物を菊水製作所のバーゴ小型回転式錠剤機を用いて、9.00kNの打錠圧の条件にて打錠し、直径8mm、厚さ4.0〜4.2mm、重量200mg/錠、打錠直後の硬度10〜15kgの錠剤を製造した。   The components shown in Table 1 below were mixed to obtain a powder composition. This powder composition was tableted using a Burgo small rotary tableting machine manufactured by Kikusui Seisakusho under the conditions of a tableting pressure of 9.00 kN, and had a diameter of 8 mm, a thickness of 4.0 to 4.2 mm, and a weight of 200 mg / tablet. A tablet having a hardness of 10 to 15 kg immediately after tableting was produced.

(実施例1)
嵩密度:0.3〜0.6g/mlで、比表面積:0.7〜1.5m2/gの噴霧乾燥法により製造したソルビトール(メルク社製)が100重量%、カープレックスCS‐500(DSL.ジャパン株式会社製の二酸化ケイ素)が1重量%、DKエステルF−20W(第一工業製薬株式会社製のショ糖脂肪酸エステル)が1.2重量%、その他ミントオイル(小川香料株式会社)が2重量%で各成分を混合し、その後、この混合物を打錠することにより錠菓を製造した。
Example 1
100% by weight of sorbitol (manufactured by Merck) manufactured by spray drying with a bulk density of 0.3 to 0.6 g / ml and a specific surface area of 0.7 to 1.5 m 2 / g, Carplex CS-500 1% by weight (silicon dioxide manufactured by DSL Japan Co., Ltd.), 1.2% by weight DK ester F-20W (sucrose fatty acid ester manufactured by Daiichi Kogyo Seiyaku Co., Ltd.), and other mint oil (Ogawa Fragrance Co., Ltd.) ) Was mixed at 2% by weight, and then the mixture was tableted to produce tablet confectionery.

(実施例2)
嵩密度:0.3〜0.6 g/mlで、比表面積:0.7〜1.5m2/gの噴霧乾燥法により製造したソルビトール(メルク社製)が97重量%、カープレックスCS‐500(DSL.ジャパン株式会社)が0.5重量%、DKエステルF−20W(第一工業製薬株式会社)が0.5重量%、その他ミントオイル(小川香料株式会社)が2重量%で各成分を混合し、その後、この混合物を打錠することにより錠菓を製造した。
(Example 2)
97% by weight of sorbitol (manufactured by Merck) produced by spray drying with a bulk density of 0.3 to 0.6 g / ml and a specific surface area of 0.7 to 1.5 m 2 / g, Carplex CS- 500 (DSL Japan Co., Ltd.) is 0.5% by weight, DK Ester F-20W (Daiichi Kogyo Seiyaku Co., Ltd.) is 0.5% by weight, and other mint oil (Ogawa Fragrance Co., Ltd.) is 2% by weight. Tablets were manufactured by mixing the ingredients and then tableting the mixture.

(実施例3)
嵩密度:0.3〜0.6g/mlで、比表面積:0.7〜1.5m2/gの噴霧乾燥法により製造したソルビトール(メルク社製)が95重量%、カープレックスCS‐500(DSL.ジャパン株式会社)が1.5重量%、DKエステルF−20W(第一工業製薬株式会社)が1.5重量%、その他ミントオイル(小川香料株式会社)が2重量%で各成分を混合し、その後、この混合物を打錠することにより錠菓を製造した。
(Example 3)
95% by weight of sorbitol (manufactured by Merck) manufactured by spray drying with a bulk density of 0.3 to 0.6 g / ml and a specific surface area of 0.7 to 1.5 m 2 / g, Carplex CS-500 (DSL. Japan Co., Ltd.) is 1.5% by weight, DK ester F-20W (Daiichi Kogyo Seiyaku Co., Ltd.) is 1.5% by weight, and other mint oil (Ogawa Fragrance Co., Ltd.) is 2% by weight. After that, tablet confectionery was produced by tableting this mixture.

(比較例1)
DKエステルF−20Wを加えず、嵩密度:0.3〜0.6g/mlで、比表面積:0.7〜1.5m2/gの噴霧乾燥法により製造したソルビトール(メルク社製)が97重量%、カープレックスCS‐500(DSL.ジャパン株式会社)が1.0重量%、その他ミントオイル(小川香料株式会社)が2重量%で各成分を混合し、その後、この混合物を打錠することにより錠菓を製造した。
(Comparative Example 1)
Sorbitol (made by Merck & Co., Inc.) manufactured by the spray drying method without adding DK ester F-20W, bulk density: 0.3-0.6 g / ml, and specific surface area: 0.7-1.5 m 2 / g 97% by weight, Carplex CS-500 (DSL Japan Co., Ltd.) is 1.0% by weight, and other mint oil (Ogawa Fragrance Co., Ltd.) is 2% by weight, and then the mixture is tableted. The tablet confection was manufactured by doing.

(比較例2)
カープレックスCS−500を加えず、嵩密度:0.3〜0.6g/mlで、比表面積:0.7〜1.5m2/gの噴霧乾燥法により製造したソルビトール(メルク社製)が96.8重量%、DKエステルF−20W(第一工業製薬株式会社)が1.2重量%、その他ミントオイル(小川香料株式会社)が2重量%で各成分を混合し、その後、この混合物を打錠することにより錠菓を製造した。
(Comparative Example 2)
Sorbitol (manufactured by Merck & Co., Inc.) produced by spray drying method without adding Carplex CS-500, bulk density: 0.3-0.6 g / ml, specific surface area: 0.7-1.5 m 2 / g 96.8% by weight, DK Ester F-20W (Daiichi Kogyo Seiyaku Co., Ltd.) 1.2% by weight, and other mint oil (Ogawa Fragrance Co., Ltd.) 2% by weight. Tablets were produced by tableting.

(比較例3)
結晶化法により製造したD−ソルビットDパウダー(東和化成社製)が95.8重量%、カープレックスCS−500が1重量%、DKエステルF−20Wが1.2量%で各成分を混合し、その後、この混合物を打錠することにより錠菓を製造した。
(Comparative Example 3)
D-Sorbit D powder (manufactured by Towa Kasei Co., Ltd.) manufactured by crystallization method is 95.8% by weight, Carplex CS-500 is 1% by weight, and DK ester F-20W is 1.2% by weight. Thereafter, the mixture was tableted to produce tablet confectionery.

(比較例4)
嵩密度:0.3〜0.6g/mlで、比表面積:0.7〜1.5m2/gの噴霧乾燥法により製造したソルビトール(メルク社製)が94.4重量%、カープレックスCS500が1.8重量%、DKエステルF−20Wが1.8量%で各成分を混合し、その後、この混合物を打錠することにより錠菓を製造した。
(Comparative Example 4)
94.4% by weight of sorbitol (manufactured by Merck & Co., Inc.) produced by spray drying with a bulk density of 0.3 to 0.6 g / ml and a specific surface area of 0.7 to 1.5 m 2 / g, Carplex CS500 Was 1.8% by weight and DK ester F-20W was 1.8% by weight, and the ingredients were mixed, and then the mixture was tableted to produce tablet confectionery.

(比較例5)
嵩密度:0.3〜0.5g/mlで、比表面積:0.7〜1.5m2/gの噴霧乾燥法により製造したソルビトール(メルク社製)が97.6重量%、カープレックスCS−500が0.2重量%、DKエステルF−20Wが0.2量%で各成分を混合し、その後、この混合物を打錠することにより錠菓を製造した。
(Comparative Example 5)
97.6% by weight of sorbitol (manufactured by Merck & Co., Inc.) produced by spray drying with a bulk density of 0.3 to 0.5 g / ml and a specific surface area of 0.7 to 1.5 m 2 / g, Carplex CS Each component was mixed at −500 by 0.2 wt% and DK ester F-20W by 0.2 wt%, and then the mixture was tableted to produce a tablet confectionery.

上記実施例1〜3および比較例1〜5の各成分量および評価を下記表1に示す。   Table 1 below shows the amounts of components and evaluations of Examples 1 to 3 and Comparative Examples 1 to 5.

ザラザラ感の評価基準は下記表2に示す通りである。打錠性の評価基準は、◎は非常に良好、○は良好、×は不良を示す。

Figure 0004736509
The evaluation criteria for the rough feeling are as shown in Table 2 below. The evaluation criteria for tabletability are as follows: ◎ is very good, ◯ is good, and x is poor.
Figure 0004736509

Figure 0004736509
Figure 0004736509

表1を参照して明らかなように、実施例1〜3では、打錠性およびザラツキ感のいずれについても良好な結果が得られた。これに対して、カープレックスCS500(二酸化ケイ素)またはDKエステルF−20W(ショ糖脂肪酸エステル)のいずれかを含んでいない比較例1、2では良好な打錠性は得られなかった。また、結晶化法により製造されたソルビトールを用いた比較例3においても良好な打錠性は得られなかった。他方、カープレックスCS500、DKエステルF−20Wの含量が1.5重量%を超える比較例4では打錠性およびザラツキ感のいずれも不良であった。また、カープレックスCS500、DKエステルF−20Wの含量が0.5重量%に満たない比較例5では、良好な打錠性は得られなかった。   As is clear with reference to Table 1, in Examples 1 to 3, good results were obtained for both tableting properties and rough feeling. On the other hand, good tabletability was not obtained in Comparative Examples 1 and 2 that did not contain either Carplex CS500 (silicon dioxide) or DK ester F-20W (sucrose fatty acid ester). Also, good tabletability was not obtained in Comparative Example 3 using sorbitol produced by the crystallization method. On the other hand, in Comparative Example 4 in which the contents of Carplex CS500 and DK ester F-20W exceed 1.5% by weight, both the tableting property and the rough feeling were poor. In Comparative Example 5 in which the contents of Carplex CS500 and DK ester F-20W were less than 0.5% by weight, good tabletability was not obtained.

したがって、打錠性およびザラツキ感の両方で良好な結果を得るためには、実施例1〜3のように、嵩密度が0.3〜0.6g/mlであり、比表面積が0.7〜1.5m2/gでああるソルビトールを用い、二酸化ケイ素の含有量を0.5〜1.5重量%、ショ糖脂肪酸エステルの含有量を0.5〜1.5重量%にすることが必要であることが分かった。 Therefore, in order to obtain good results in both tabletability and roughness, as in Examples 1 to 3, the bulk density is 0.3 to 0.6 g / ml, and the specific surface area is 0.7. Use sorbitol which is ˜1.5 m 2 / g, make silicon dioxide content 0.5-1.5 wt% and sucrose fatty acid ester content 0.5-1.5 wt% It turns out that is necessary.

Claims (2)

ソルビトールと、二酸化ケイ素と、ショ糖脂肪酸エステルとを含有する錠菓において、
ソルビトールの嵩密度が0.3〜0.6g/mlであり、比表面積が0.7〜1.5m2/gであり、二酸化ケイ素の含有量が0.5〜1.5重量%であり、ショ糖脂肪酸エステルの含有量が0.5〜1.5重量%であることを特徴とする錠菓。
In tablet confections containing sorbitol, silicon dioxide, and sucrose fatty acid ester,
Sorbitol has a bulk density of 0.3 to 0.6 g / ml, a specific surface area of 0.7 to 1.5 m 2 / g, and a silicon dioxide content of 0.5 to 1.5% by weight. A tablet confectionery characterized in that the content of sucrose fatty acid ester is 0.5 to 1.5% by weight.
前記ソルビトールは、噴霧乾燥法により製造されたものである、請求項1に記載の錠菓。   The tablet confection according to claim 1, wherein the sorbitol is produced by a spray drying method.
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JPH0386839A (en) * 1989-01-24 1991-04-11 Ici Americas Inc Sorbitol crystal globule
JPH1017496A (en) * 1996-07-03 1998-01-20 Riken Vitamin Co Ltd Lubricant for tablet and tablet candy
JP2000264835A (en) * 1999-03-18 2000-09-26 Mitsubishi-Kagaku Foods Corp Tablet composition containing sugar alcohol
JP2003095982A (en) * 2001-09-27 2003-04-03 Mitsubishi-Kagaku Foods Corp Improver for feeling on tongue of sorbitol tablet molding
JP2003250450A (en) * 2002-03-01 2003-09-09 Takasago Internatl Corp Powder composition for tablet confectionery, method for producing the same, tablet confectionery and method for producing the tablet confectionery

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JPS5314611B2 (en) * 1972-05-13 1978-05-18
JPS55360A (en) * 1979-03-12 1980-01-05 Dai Ichi Kogyo Seiyaku Co Ltd Lubricant composition for tableted drugs and confection
DE3245170A1 (en) * 1982-12-07 1984-06-07 Merck Patent Gmbh, 6100 Darmstadt IMPROVED SORBITE, METHOD FOR THE PRODUCTION AND USE
US5284659A (en) * 1990-03-30 1994-02-08 Cherukuri Subraman R Encapsulated flavor with bioadhesive character in pressed mints and confections
JP3807565B2 (en) * 1996-11-05 2006-08-09 第一工業製薬株式会社 Lubricant for tablets and tablet confectionery

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0386839A (en) * 1989-01-24 1991-04-11 Ici Americas Inc Sorbitol crystal globule
JPH1017496A (en) * 1996-07-03 1998-01-20 Riken Vitamin Co Ltd Lubricant for tablet and tablet candy
JP2000264835A (en) * 1999-03-18 2000-09-26 Mitsubishi-Kagaku Foods Corp Tablet composition containing sugar alcohol
JP2003095982A (en) * 2001-09-27 2003-04-03 Mitsubishi-Kagaku Foods Corp Improver for feeling on tongue of sorbitol tablet molding
JP2003250450A (en) * 2002-03-01 2003-09-09 Takasago Internatl Corp Powder composition for tablet confectionery, method for producing the same, tablet confectionery and method for producing the tablet confectionery

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