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JP3342550B2 - Formulations containing water-soluble hemicellulose - Google Patents

Formulations containing water-soluble hemicellulose

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Publication number
JP3342550B2
JP3342550B2 JP26955093A JP26955093A JP3342550B2 JP 3342550 B2 JP3342550 B2 JP 3342550B2 JP 26955093 A JP26955093 A JP 26955093A JP 26955093 A JP26955093 A JP 26955093A JP 3342550 B2 JP3342550 B2 JP 3342550B2
Authority
JP
Japan
Prior art keywords
control
oil
flavor
hemicellulose
water
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
JP26955093A
Other languages
Japanese (ja)
Other versions
JPH07101883A (en
Inventor
英介 折越
智秋 山平
雅之 西野
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
San Ei Gen FFI Inc
Original Assignee
San Ei Gen FFI Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by San Ei Gen FFI Inc filed Critical San Ei Gen FFI Inc
Priority to JP26955093A priority Critical patent/JP3342550B2/en
Publication of JPH07101883A publication Critical patent/JPH07101883A/en
Application granted granted Critical
Publication of JP3342550B2 publication Critical patent/JP3342550B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • General Preparation And Processing Of Foods (AREA)
  • Jellies, Jams, And Syrups (AREA)
  • Medicinal Preparation (AREA)
  • Medicines Containing Plant Substances (AREA)

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は水溶性ヘミセルロースお
よび界面活性剤を含有する製剤に関する。本発明の製剤
は、乳化製剤および粉末製剤を指し、食品、医薬品、化
粧品、ペットフード、医薬部外品等に長期間安定で望ま
しい香味、色調、風味等を付与するのに使用される。
The present invention relates to a preparation containing water-soluble hemicellulose and a surfactant. The preparation of the present invention refers to an emulsion preparation and a powder preparation, and is used for imparting long-term stable and desirable flavor, color tone, flavor and the like to foods, pharmaceuticals, cosmetics, pet foods, quasi-drugs and the like.

【0002】[0002]

【従来の技術】従来の乳化製剤は精油類、油溶性色素
類、動植物性油脂類のような油性物質を、アラビアガム
などの植物性天然ガム質または非イオン系の界面活性剤
等で乳化したものが用いられていた。また、粉末製剤は
油脂や親油性または水溶性の香料および色素等の調合組
成物を、アラビアガム等の天然ガム、デキストリンおよ
び加工澱粉を配合して乳化、または分散した後、噴霧乾
燥する方法が知られている。この場合、天然のアラビア
ガムは乳化性が優れている点で広く製剤の分野で乳化剤
もしくは粉末化基材として使用されているが、天然ガム
質は天候、気温などの自然環境によってその生産量や品
質が一定せず、価格の高騰や品質のバラツキなどの問題
があり、また粉末化した場合の皮膜性については充分に
安定なものではなく、噴霧乾燥中及び保存中での香味や
色調、風味の劣化などが問題であった。また、デキスト
リンや加工澱粉は乳化性や皮膜性についてアラビアガム
に劣り、非イオン系の界面活性剤を用いた場合は、使用
する飲食品や医薬品等のpHや含有成分によって影響を
受け易いという特性があった。また近年、上記物質の代
替品として水溶性ヘミセルロースが検討されているが、
これも乳化性および皮膜性等について充分に安定なもの
ではない。
2. Description of the Related Art Conventional emulsified preparations are obtained by emulsifying oily substances such as essential oils, oil-soluble pigments, animal and vegetable oils and fats with a natural vegetable gum such as gum arabic or a nonionic surfactant. Things were used. In addition, powder formulations are prepared by emulsifying or dispersing a composition such as an oil or fat or a lipophilic or water-soluble flavor and a pigment with natural gum such as gum arabic, dextrin and modified starch, and then spray drying. Are known. In this case, natural gum arabic is widely used in the field of pharmaceutical preparations as an emulsifier or a powdered base because of its excellent emulsifiability, but natural gum is produced and produced depending on the natural environment such as weather and temperature. The quality is not constant, there are problems such as price spikes and quality variation, and the film properties when powdered are not sufficiently stable, and the flavor, color, and flavor during spray drying and storage are not sufficient. Degradation was a problem. In addition, dextrin and modified starch are inferior to gum arabic in emulsifying property and film property, and when nonionic surfactants are used, they are susceptible to pH and contained components of foods and drinks and pharmaceuticals used. was there. In recent years, water-soluble hemicellulose has been studied as a substitute for the above substances,
This is also not sufficiently stable with respect to emulsifying properties and film properties.

【0003】[0003]

【発明が解決しようとする課題】上述の様に、製剤に於
いては、製造過程に於ける乳化性はもとより、その包接
物の安定性及び皮膜の強度に優れることが求められてい
るが、現状では必ずしも満足されている訳ではなく、更
に改善された製剤の創出は当業界の課題であった。
As described above, in the preparation, not only the emulsifiability in the production process but also the stability of the inclusion and the strength of the film are required to be excellent. However, the present situation is not always satisfactory, and creation of a further improved formulation has been a problem in the art.

【0004】[0004]

【課題を解決するための手段】本発明者らは、これらの
欠点を改善するため、水溶性ヘミセルロースの乳化安定
性および皮膜強度を著しく増強させる方法を鋭意研究し
た結果、水溶性ヘミセルロースを乳化剤あるいは粉末化
基剤として用いた製剤を製造する時、界面活性剤を適宜
添加することにより、水溶性ヘミセルロースの乳化力お
よび皮膜強度を著しく増強させ、香料成分の耐熱性、保
留性及び香料成分の放出遅延効果に優れた製剤を提供で
きる知見を得た。本発明は、製剤の製造時に、水溶性ヘ
ミセルロースを乳化剤または粉末化基剤として用い、か
つ、界面活性剤を適宜添加することにより、製造時に於
ける乳化性、乳化安定性が優れ、粉末化後の包接物の安
定性、基剤皮膜の強度を増強させ、食品等に長期間安定
な香気、色調、風味等を付与することのできる製剤を提
供することにある。
Means for Solving the Problems In order to remedy these drawbacks, the present inventors have intensively studied a method for remarkably enhancing the emulsion stability and film strength of water-soluble hemicellulose. When manufacturing a formulation used as a powdered base, by adding a surfactant as appropriate, the emulsifying power and film strength of water-soluble hemicellulose are remarkably enhanced, and the heat resistance, retention and release of the flavor component of the flavor component are released. The knowledge which can provide the preparation excellent in the delay effect was obtained. The present invention uses a water-soluble hemicellulose as an emulsifier or a powdered base during the production of a preparation, and by appropriately adding a surfactant, has excellent emulsifiability and emulsion stability during the production, and after pulverization. It is an object of the present invention to provide a preparation which can enhance the stability of the clathrate, the strength of the base film, and impart long-term stable aroma, color tone, flavor and the like to foods and the like.

【0005】本発明で用いる油性物質の例としては、例
えばオレンジ、ライム、レモン、グレープフルーツなど
の柑橘類精油、ペパーミントオイル、シソオイル、など
のスパイス類の精油、ペパー、シンナモン、ジンジャー
などのオレオレジン、ジャスミン、ローズなどのアブソ
リュート、および合成香料化合物、油性調合香料組成物
およびこれらの任意の混合物の如き油性の着香料、β−
カロチン、パプリカ色素、アナトー色素、およびクロロ
フィルなどの油溶性天然色素類、更に肝油、ビタミン
A、ビタミンD、ビタミンB2酪酸エステル、天然ビタ
ミンE混合物などの脂溶性ビタミン類、大豆油、菜種
油、コーン油、オリーブ油、椰子油、サフラワー油、ひ
まわり油、米油、牛脂、豚脂、魚油などの動植物油脂、
DHA、EPA、γ−リノレン酸などの天然不飽和脂肪
酸類、シュクロースジアセテートヘキサイソブチレー
ト、C6〜C12の中鎖飽和脂肪酸トリグリセライドな
どの加工食用油脂およびこれら可食性油性材料の任意の
混合物を例示することができる。水溶性物質としては、
例えばコーヒー、ハーブ、抹茶、紅茶、ガラナ、カツ
オ、エビ、カニ、ウニ、ホタテなどのエキストラクト、
ストロベリー、メロン、バナナ、パイナップル、アップ
ル、ミルク、チーズ、バター、などのエッセンス、コチ
ニール、ベニバナ、ビート、ウコン等の水溶性色素、そ
の他合成着香料、合成着色料、およびこれらの任意の混
合物を例示することができる。
Examples of the oily substance used in the present invention include essential oils of citrus fruits such as orange, lime, lemon and grapefruit, essential oils of spices such as peppermint oil and perilla oil, oleoresins such as pepper, cinnamon and ginger, and jasmine. , An oily flavoring such as an absolute flavoring compound, such as rose, and synthetic flavoring compounds, oily blended flavoring compositions and any mixtures thereof, β-
Oil-soluble natural pigments such as carotene, paprika pigment, annatto pigment, and chlorophyll, and fat-soluble vitamins such as liver oil, vitamin A, vitamin D, vitamin B2 butyrate, and natural vitamin E mixture, soybean oil, rapeseed oil, and corn oil , Olive oil, coconut oil, safflower oil, sunflower oil, rice oil, tallow, lard, fish and other animal and vegetable oils,
DHA, EPA, natural unsaturated fatty acids such as γ-linolenic acid, processed edible fats and oils such as sucrose diacetate hexaisobutyrate, medium-chain saturated fatty acid triglyceride of C6 to C12, and any mixture of these edible oily materials. Examples can be given. As a water-soluble substance,
For example, coffee, herbs, matcha, black tea, guarana, skipjack, shrimp, crab, sea urchin, scallop and other extracts,
Essences such as strawberry, melon, banana, pineapple, apple, milk, cheese, butter, etc., water-soluble dyes such as cochineal, safflower, beet, turmeric, other synthetic flavors, synthetic colorings, and any mixtures thereof. can do.

【0006】本発明に利用することのできる水溶性ヘミ
セルロースとしては例えば油糧種子(大豆、パーム、ヤ
シ、コーン、綿実などの通常油脂や蛋白質を除いた殻)
または穀類(米、小麦など通常澱粉等を除いた粕)等の
植物を原料とした水溶性の食物繊維、すなわちアラビノ
キシラン、アラビノガラクタン等の多糖類、またはこれ
らの任意の混合物を例示することができる。このような
水溶性ヘミセルロースを製剤に対して0.1〜98重量
%、好ましくは5〜50重量%の割合で含有させる。
Examples of the water-soluble hemicellulose that can be used in the present invention include oil seeds (shells excluding ordinary fats and proteins such as soybean, palm, palm, corn, and cottonseed).
Alternatively, water-soluble dietary fiber derived from plants such as cereal grains (rice, wheat, etc., usually excluding starch and the like), that is, polysaccharides such as arabinoxylan and arabinogalactan, or any mixture thereof can be exemplified. it can. Such a water-soluble hemicellulose is contained in the preparation at a ratio of 0.1 to 98% by weight, preferably 5 to 50% by weight.

【0007】本発明における界面活性剤とは、主にデカ
グリセリルモノステアレートを指すが、場合によっては
デカグリセリルモノオレート、デカグリセリルモノパル
ミテート、デカグリセリルモノラウレート、ショ糖脂肪
酸エステルなどとの混合物でもよい。このような界面活
性剤を製剤に対して0.01〜10重量%、好ましくは
0.05〜5重量%の割合で含有させる。本発明で用い
る乳化方法としては、コロイドミル、ホモミキサー、高
圧ホモジナイザー、超音波乳化機等どのようなものでも
良く、又、粉末化方法としてもどのようなタイプの噴霧
乾燥法でも良い。以下、本発明の効果を実施例を示して
更に具体的に説明する。
[0007] The surfactant in the present invention mainly refers to decaglyceryl monostearate. In some cases, the surfactant includes decaglyceryl monooleate, decaglyceryl monopalmitate, decaglyceryl monolaurate, sucrose fatty acid ester and the like. It may be a mixture. Such a surfactant is contained in the preparation at a ratio of 0.01 to 10% by weight, preferably 0.05 to 5% by weight. The emulsification method used in the present invention may be any method such as a colloid mill, a homomixer, a high-pressure homogenizer, and an ultrasonic emulsifier, and may be any type of powder drying method such as a spray drying method. Hereinafter, the effects of the present invention will be described more specifically with reference to examples.

【0008】[0008]

【実施例】【Example】

実施例1 β−カロチン3g、天然ビタミンE0.1g、中鎖飽和
脂肪酸トリグリセライド8.5gを溶解して、均一な油
性材料混合物を得た。別に水69gに大豆ヘミセルロー
ス20g、デカグリセリルモノステアレート1gを溶解
した溶液を得、前述の油性材料混合物の全量を加えて予
備撹拌させ、分散させた後、ホモジナイザーにて乳化
し、着色剤乳化物(本発明品No.1)を得た。
Example 1 3 g of β-carotene, 0.1 g of natural vitamin E, and 8.5 g of medium-chain saturated fatty acid triglyceride were dissolved to obtain a uniform oily material mixture. Separately, a solution obtained by dissolving 20 g of soybean hemicellulose and 1 g of decaglyceryl monostearate in 69 g of water was added, and the whole amount of the oily material mixture was added, and the mixture was preliminarily stirred and dispersed. (Product No. 1 of the present invention) was obtained.

【0009】実施例2 イオン交換水200gに大豆ヘミセルロース85g、デ
カグリセリルモノステアレート2gを溶解し、50℃に
保持しながらミントオイル20gを添加混合する。この
溶液を高圧ホモジナイザーにて乳化し、乳化液を噴霧乾
燥してミント香料粉末100g(本発明品No.2)を
得た。
Example 2 85 g of soybean hemicellulose and 2 g of decaglyceryl monostearate are dissolved in 200 g of ion-exchanged water, and 20 g of mint oil is added and mixed while maintaining the temperature at 50 ° C. This solution was emulsified with a high-pressure homogenizer, and the emulsion was spray-dried to obtain mint flavor powder 100 g (product No. 2 of the present invention).

【0010】実施例3 イオン交換水200gにコーンヘミセルロース70gと
シュークロース40g、デカグリセリルモノステアレー
ト3gを溶解し、50℃に保持しながらメントールを1
2g含んだオイル15gを添加混合する。この溶液を高
圧ホモジナイザーにて乳化し、乳化液を噴霧乾燥してメ
ントール香料粉末100g(本発明品No.3)を得
た。
Example 3 70 g of corn hemicellulose, 40 g of sucrose, and 3 g of decaglyceryl monostearate were dissolved in 200 g of ion-exchanged water.
15 g of oil containing 2 g is added and mixed. This solution was emulsified with a high-pressure homogenizer, and the emulsion was spray-dried to obtain 100 g of menthol flavor powder (Product No. 3 of the present invention).

【0011】実施例4 イオン交換水200gに大豆ヘミセルロース80g、デ
カグリセリルモノステアレート2gを溶解し、50℃に
保持しながらβ−カロチン30%懸濁液1.2gを含ん
だオイル20gを140℃に加熱して添加混合する。こ
の溶液を高圧ホモジナイザーで乳化し、乳化液を噴霧乾
燥して着色料粉末100g(本発明品No.4)を得
た。
Example 4 80 g of soybean hemicellulose and 2 g of decaglyceryl monostearate were dissolved in 200 g of ion-exchanged water, and 20 g of oil containing 1.2 g of a 30% β-carotene suspension was added at 140 ° C. while maintaining the temperature at 50 ° C. And heat to mix. This solution was emulsified with a high-pressure homogenizer, and the emulsion was spray-dried to obtain 100 g of a colorant powder (product No. 4 of the present invention).

【0012】対照例1 実施例1においてデカグリセリルモノステアレートを使
用せず、その重量不足分を大豆ヘミセルロースで補った
他は実施例1と同じ条件によって着色剤乳化物(対照品
No.1)を得た。
Control Example 1 A colorant emulsion (Control No. 1) was prepared in the same manner as in Example 1 except that decaglyceryl monostearate was not used and the weight shortage was supplemented with soybean hemicellulose. I got

【0013】対照例2 実施例1において大豆ヘミセルロースの代わりにアラビ
アガムを使用した他は実施例1同じ条件によって着色剤
乳化物(対照品No.2)を得た。
Control Example 2 A colorant emulsion (Control No. 2) was obtained under the same conditions as in Example 1 except that gum arabic was used instead of soybean hemicellulose.

【0014】対照例3 実施例1においてデカグリセリルモノステアレートの代
わりにデカグリセリルモノラウレートを使用した他は実
施例1と同じ条件によって着色剤乳化物(対照品No.
3)を得た。
Control Example 3 A colorant emulsion (Control No. 1) was prepared under the same conditions as in Example 1 except that decaglyceryl monostearate was replaced with decaglyceryl monolaurate.
3) was obtained.

【0015】対照品4 実施例2において大豆ヘミセルロースの代わりにアラビ
アガムを使用した他は実施例2と同じ条件によってミン
ト香料粉末100g(対照品No.4)を得た。
Control 4 A mint flavor powder 100 g (Control No. 4) was obtained under the same conditions as in Example 2 except that gum arabic was used instead of soybean hemicellulose.

【0016】対照例5 実施例2において大豆ヘミセルロースの代わりに加工澱
粉を使用した他は実施例2と同じ条件によってミント香
料粉末100g(対照品No.5)を得た。
Control Example 5 100 g of mint flavor powder (Control No. 5) was obtained under the same conditions as in Example 2 except that modified starch was used instead of soybean hemicellulose.

【0017】対照例6 実施例2において大豆ヘミセルロースの代わりにデキス
トリンを使用した他は実施例2と同じ条件によってミン
ト油乳化物(対照品No.6)を得た。
Control Example 6 A mint oil emulsion (Control No. 6) was obtained under the same conditions as in Example 2 except that dextrin was used instead of soybean hemicellulose.

【0018】対照例7 実施例2においてデカグリセリルモノステアレートを使
用せず、その重量不足分を大豆ヘミセルロースで補った
他は実施例2と同じ条件によってミント香料粉末100
g(対照品No.7)を得た。
COMPARATIVE EXAMPLE 7 Mint flavor powder 100 was prepared in the same manner as in Example 2 except that decaglyceryl monostearate was not used and the weight shortage was supplemented with soybean hemicellulose.
g (control product No. 7) was obtained.

【0019】対照例8 実施例3においてコーンヘミセルロースの代わりにアラ
ビアガムを使用した他は実施例3と同じ条件によってメ
ントール香料粉末100g(対照品No.8)を得た。
Control Example 8 100 g of menthol flavoring powder (Control No. 8) was obtained under the same conditions as in Example 3 except that gum arabic was used instead of corn hemicellulose.

【0020】対照例9 実施例3においてデカグリセリルモノステアレートを使
用せず、その重量不足分をコーンヘミセルロースで補っ
た他は実施例3と同じ条件によってメントール香料粉末
100g(対照品No.9)を得た。
Control Example 9 100 g of menthol flavoring powder (Control No. 9) under the same conditions as in Example 3 except that decaglyceryl monostearate was not used in Example 3 and the insufficient weight was supplemented with corn hemicellulose. I got

【0021】比較実験1 実施例1および対照例1、対照例2の着色剤乳化物を同
一日に調製し、レーザー回折式粒度分布計 SALD−
1100((株)島津製作所)を用いて粒度分布を測定
した。また、同時に10gの脱脂粉乳を水844gに溶
解し、これにグラニュー糖140g、10%乳酸水溶液
5g、実施例2および対照例2、対照例3で得られた着
色剤乳化物を1g添加し均一に混合した。瓶に充填後打
栓し、85℃で20分殺菌し、着色酸性乳飲料を得た。
これを室温で静置し、経時変化を観察した。結果を表1
に示す。
Comparative Experiment 1 The colorant emulsions of Example 1 and Control Examples 1 and 2 were prepared on the same day, and were subjected to laser diffraction particle size distribution analyzer SALD-.
The particle size distribution was measured using 1100 (Shimadzu Corporation). Simultaneously, 10 g of skim milk powder was dissolved in 844 g of water, and 140 g of granulated sugar, 5 g of a 10% lactic acid aqueous solution, and 1 g of the colorant emulsion obtained in Example 2 and Comparative Examples 2 and 3 were added thereto. Was mixed. After filling the bottle, it was stoppered and sterilized at 85 ° C. for 20 minutes to obtain a colored acidic milk beverage.
This was allowed to stand at room temperature, and changes over time were observed. Table 1 shows the results
Shown in

【0022】[0022]

【表1】 [Table 1]

【0023】表中の各記号は下記の意味を表す。 −R ネックリングの発生は認められない。 ±R ネックリングを僅かに認める。 +R 明瞭なネックリングを認める。 R 著しいネックリングを認める。 −P 沈澱は認められない。 ±P 沈澱を僅かに認める。 +P 明瞭な沈澱を認める。 P 著しい沈澱を認める。Each symbol in the table has the following meaning. -R No occurrence of neck ring is observed. ± R Neck ring is slightly recognized. + R A clear neck ring is observed. R A remarkable neck ring is recognized. -P No precipitation is observed. ± P Precipitation is slightly observed. + P A clear precipitate is observed. P Significant precipitation is observed.

【0024】表1の結果から明らかな通り、本発明品N
o.1は、対照品No.1及び対照品No.3に較べて
水溶性ヘミセルロースの乳化力が非常に高くなり、対照
品2(アラビアガム)よりもやや高い乳化力を示した。
また、着色酸性乳飲料を室温で約30日静置したとこ
ろ、対照品No.1、対照品No.3では沈澱は発生し
なかったが、ネックリングの発生を認め、商品価値を失
った。対照品No.2ではネックリングの発生は認めら
れなかったが、著しい沈澱を生じた。これに対し、本発
明品No.1ではネックリングの発生、沈澱ともに認め
られず安定な着色酸性乳飲料であった。
As is clear from the results in Table 1, the product N of the present invention
o. No. 1 is a control product No. 1 and the control product No. 1 The emulsifying power of the water-soluble hemicellulose was much higher than that of Comparative Example 3 and slightly higher than that of Control Product 2 (gum arabic).
When the colored acidic milk beverage was allowed to stand at room temperature for about 30 days, the control product No. 1, control product No. In No. 3, no precipitation occurred, but the occurrence of neck ring was recognized and the commercial value was lost. Control product No. In No. 2, no generation of neck ring was observed, but significant precipitation occurred. On the other hand, the product No. of the present invention. In No. 1, neither generation of a neck ring nor precipitation was observed, and the colored acidic milk beverage was stable.

【0025】比較実験2 実施例2および対照例4〜7で得たミント香料粉末を、
40℃にて保存し、経時変化を観察した。また、ミント
オイルを乳化した際の乳化性についても併せて評価し
た。その結果を表2に示す。
Comparative Experiment 2 The mint flavor powders obtained in Example 2 and Control Examples 4 to 7 were
It was stored at 40 ° C. and observed over time. In addition, emulsifying properties when mint oil was emulsified were also evaluated. Table 2 shows the results.

【0026】[0026]

【表2】 [Table 2]

【0027】表中の各記号は下記の意味を示す。 ◎:極めて良好 ○:良好 △:やや悪い ×:
悪い −:評価不能
Each symbol in the table has the following meaning. :: extremely good ○: good △: slightly bad ×:
Poor-: Unable to evaluate

【0028】表2の結果から明らかなとおり、本発明品
No.2は乳化性が良く、保存後6ケ月を経過しても基
剤皮膜の強度が優れており、香味の損失も無かったのに
対し、対照品No.4ではやや乳化性が劣り、基剤皮膜
の強度および香味は経時的に低下した。その傾向は対照
品No.7、対照品No.5の順で顕著になる。また対
照品No.6では乳化が行えなかった。
As is clear from the results in Table 2, the product No. of the present invention. No. 2 had good emulsifiability and the strength of the base film was excellent even after 6 months from storage, and there was no loss of flavor. In No. 4, the emulsifiability was slightly inferior, and the strength and flavor of the base film decreased with time. The tendency is shown by the control product No. 7, control product No. It becomes significant in the order of 5. In addition, the control product No. No. 6 could not be emulsified.

【0029】比較実験3 実施例3および対照例8〜9のメントール香料粉末を密
封容器に入れ、40℃にて保存後開封し、メントール含
量をガスクロマトグラフィーで測定した。
Comparative Experiment 3 The menthol flavor powders of Example 3 and Control Examples 8 to 9 were placed in a sealed container, stored at 40 ° C., opened, and the menthol content was measured by gas chromatography.

【0030】[0030]

【表3】 [Table 3]

【0031】・表中の値は試料のメントール含量を示
す。 ・( )内の数値は調整時の含量に対する残存率を%で
示している。
The values in the table indicate the menthol content of the sample.・ The values in parentheses indicate the percentage of residual content relative to the content at the time of adjustment.

【0032】表3の結果から明らかな通り、本発明品N
o.3は6ケ月の保存後もメントール含量が低下しない
のに対し、対照品No.8および対照品No.9では経
時的にメントール含量が低下し、包接物の損失が認めら
れた。
As is clear from the results in Table 3, the product N of the present invention
o. The menthol content of Sample No. 3 did not decrease even after storage for 6 months, whereas the control product No. 3 did not. 8 and Control No. In No. 9, the menthol content decreased with time, and loss of the clathrate was observed.

【0033】比較実験4 下記に示すチューインガム基材に実施例2で得られたミ
ント粉末香料(本発明品2)と対照例4、5、7で得ら
れたミント粉末香料(対照品No.4、5、7)をそれ
ぞれ添加し、混練して圧展成型し、1枚3gのミント風
味のチューインガムを得た。チューインガム基材組成を
表4に示す。
Comparative Experiment 4 The mint powder flavors obtained in Example 2 (Product 2 of the present invention) and the mint powder flavors obtained in Comparative Examples 4, 5 and 7 (Control Product No. 4) were applied to the following chewing gum base material. , 5 and 7) were added, kneaded, and pressure-molded to obtain 3 g of mint-flavored chewing gum per sheet. Table 4 shows the chewing gum base composition.

【0034】[0034]

【表4】 [Table 4]

【0035】これらのチューインガムについて10名の
専門パネラーによって官能評価した結果、本発明品は対
照例と比較してフレーバーの強さには大きな差がないが
持続性、残留性の点で顕著に優れていると判定した。
As a result of a sensory evaluation of these chewing gums by ten expert panelists, the product of the present invention has no significant difference in flavor strength as compared with the control, but is remarkably excellent in persistence and persistence. It was determined that it was.

【0036】[0036]

【発明の効果】本発明によって得られた製剤は、実施例
の結果から明らかなように製造工程に於ける乳化性や乳
化安定性が極めて良好で、粉末化する場合についても粉
末化後の包接物の安定性、皮膜の強度が特に優れてお
り、各種食品、医薬品等に長期間安定で望ましい香味、
色調、風味等を付与することができるため、工業的意義
は極めて大である。
As is clear from the results of the examples, the preparations obtained by the present invention have extremely good emulsifiability and emulsification stability in the production process. The stability of the clathrate and the strength of the film are particularly excellent, and it is a long-term stable and desirable flavor for various foods and pharmaceuticals.
Since the color tone, flavor and the like can be imparted, the industrial significance is extremely large.

フロントページの続き (51)Int.Cl.7 識別記号 FI A61K 47/14 A23L 1/04 (58)調査した分野(Int.Cl.7,DB名) A61K 9/00 - 9/72 A61K 47/00 - 47/48 A23L 1/00 - 1/0534 Continuation of the front page (51) Int.Cl. 7 identification code FI A61K 47/14 A23L 1/04 (58) Investigated field (Int.Cl. 7 , DB name) A61K 9/00-9/72 A61K 47 / 00-47/48 A23L 1/00-1/0534

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】水溶性ヘミセルロースおよびデカグリセリ
ルモノステアレートを含有することを特徴とする乳化製
剤。
1. An emulsified preparation comprising water-soluble hemicellulose and decaglyceryl monostearate.
【請求項2】水溶性ヘミセルロースが大豆、またはとう
もろこしを原料とする多糖類である請求項1記載の乳化
製剤。
2. The emulsified preparation according to claim 1, wherein the water-soluble hemicellulose is a polysaccharide derived from soybean or corn.
JP26955093A 1993-10-01 1993-10-01 Formulations containing water-soluble hemicellulose Expired - Fee Related JP3342550B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP26955093A JP3342550B2 (en) 1993-10-01 1993-10-01 Formulations containing water-soluble hemicellulose

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP26955093A JP3342550B2 (en) 1993-10-01 1993-10-01 Formulations containing water-soluble hemicellulose

Publications (2)

Publication Number Publication Date
JPH07101883A JPH07101883A (en) 1995-04-18
JP3342550B2 true JP3342550B2 (en) 2002-11-11

Family

ID=17473944

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Country Status (1)

Country Link
JP (1) JP3342550B2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH1160980A (en) * 1997-08-13 1999-03-05 Kagome Co Ltd Water-dispersible carotenoid pigment preparation
JP3957932B2 (en) * 1999-10-19 2007-08-15 フロイント産業株式会社 Water-soluble coating composition for food
EP1605978B1 (en) 2003-03-07 2010-09-01 Alnylam Pharmaceuticals Inc. Therapeutic compositions
CA2522349A1 (en) 2003-04-17 2004-11-04 Alnylam Pharmaceuticals, Inc. Protected monomers
EP2669377A3 (en) 2003-04-17 2015-10-14 Alnylam Pharmaceuticals Inc. Modified iRNA agents
JP2007222844A (en) * 2006-02-27 2007-09-06 Chikuno Shokuhin Kogyo Kk Emulsification composition
TW200815046A (en) * 2006-06-22 2008-04-01 Kaneka Corp Composition containing reduced coenzyme Q10 and production method thereof
US20090247608A1 (en) 2007-12-04 2009-10-01 Alnylam Pharmaceuticals, Inc. Targeting Lipids
JP2009149584A (en) * 2007-12-21 2009-07-09 Kaneka Corp Reduced coenzyme q10-containing particulate composition and its manufacturing method
US9808030B2 (en) 2011-02-11 2017-11-07 Grain Processing Corporation Salt composition
US20170304459A1 (en) 2014-10-10 2017-10-26 Alnylam Pharmaceuticals, Inc. Methods and compositions for inhalation delivery of conjugated oligonucleotide

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Publication number Publication date
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