JPH0779712A - Formulation containing water-soluble hemicellulose - Google Patents
Formulation containing water-soluble hemicelluloseInfo
- Publication number
- JPH0779712A JPH0779712A JP5254817A JP25481793A JPH0779712A JP H0779712 A JPH0779712 A JP H0779712A JP 5254817 A JP5254817 A JP 5254817A JP 25481793 A JP25481793 A JP 25481793A JP H0779712 A JPH0779712 A JP H0779712A
- Authority
- JP
- Japan
- Prior art keywords
- oil
- flavor
- hemicellulose
- water
- product
- 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.)
- Pending
Links
Landscapes
- Coloring Foods And Improving Nutritive Qualities (AREA)
- General Preparation And Processing Of Foods (AREA)
- Jellies, Jams, And Syrups (AREA)
- Medicinal Preparation (AREA)
- Cosmetics (AREA)
- Feed For Specific Animals (AREA)
- Fodder In General (AREA)
Abstract
(57)【要約】
【目的】 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
付与する製剤を得る。
【構成】 水溶性ヘミセルロースを乳化剤もしくは粉末
化基材に用い、かつアルコール類を適宜使用して製剤を
調製する。(57) [Summary] [Purpose] To obtain a preparation that imparts desirable flavor, color tone, flavor and the like to foods, pharmaceuticals, cosmetics, pet foods, quasi drugs, etc. for a long period of time. [Structure] A formulation is prepared by using water-soluble hemicellulose as an emulsifying agent or powdering base material and appropriately using alcohols.
Description
【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
よびアルコール類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。TECHNICAL FIELD The present invention relates to a preparation containing water-soluble hemicellulose and alcohols. The formulations of the present invention refer to emulsion formulations and powder formulations, foods, pharmaceuticals,
It is used to impart a desired flavor, color tone, flavor, etc., which is stable for a long period of time, to cosmetics, pet food, 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ペクチン、ゼラ
チン、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 include oily substances such as essential oils, oil-soluble pigments, animal and vegetable oils and fats, pectin, gelatin, gum arabic and other natural vegetable gums or nonionic surfactants. What was emulsified in was used. Further, the powder formulation is prepared by mixing a formulation composition such as fats and oils or lipophilic or water-soluble flavors and pigments with natural gums such as gum arabic, dextrin and modified starch, emulsifying or dispersing them, and then spray-drying. Are known. In this case, natural gum arabic is widely used as an emulsifying agent or a powdering base material in the field of formulation because of its excellent emulsifying property, but natural gum substances are not suitable for production or production depending on the natural environment such as weather and temperature. The quality is not constant, there are problems such as high prices and variations in quality, and the film properties when powdered are not sufficiently stable.The flavor, color and flavor during spray drying and storage Was a problem. In addition, dextrin and modified starch are inferior to gum arabic in emulsifying property and film forming property, and when a nonionic surfactant is used, they are easily affected by pH and ingredients contained in foods and drinks and pharmaceuticals to be used. was there. In recent years, water-soluble hemicellulose has been investigated as a substitute for the above substances, but this is also not sufficiently stable in terms of emulsifying property and film forming property.
【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 emulsifying property in the manufacturing process but also the stability of the clathrate and the strength of the film are required. However, the present situation is not necessarily satisfactory, and the 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、アルコール類を適
当量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。製剤を製造する時、水溶性ヘミ
セルロースを乳化剤又は粉末化基剤として用い、かつ、
アルコール類を適当量添加することにより、製造時に於
ける乳化性、乳化安定性に優れ、粉末化後の包接物の安
定性、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で
きることが判明した。。[Means for Solving the Problems] In order to improve these drawbacks, the present inventors have earnestly studied a method of remarkably enhancing the emulsion stability and film strength of water-soluble hemicellulose, and as a result, the water-soluble hemicellulose was emulsified or When manufacturing a formulation used as a powdered base, by adding an appropriate amount of alcohols, the emulsifying power and film strength of the water-soluble hemicellulose can be significantly enhanced, and the heat resistance and retention of the perfume ingredient and the release of the perfume ingredient We have obtained the knowledge that a formulation with excellent delay effect can be provided. When manufacturing a formulation, using water-soluble hemicellulose as an emulsifying agent or powdering base, and
By adding an appropriate amount of alcohols, the emulsifiability at the time of production, the emulsion stability is excellent, the stability of the clathrate after pulverization, the strength of the film is enhanced, and the aroma that is stable for a long time in foods, It has been found that it is possible to provide a preparation capable of imparting color tone, flavor 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。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, oleoresin such as pepper, cinnamon and ginger, and jasmine. , Absolute such as rose, and oily flavoring agents such as synthetic perfume compounds, oily perfume compositions and any mixtures thereof, β-
Oil-soluble natural pigments such as carotene, paprika pigment, annatto pigment, and chlorophyll, and further fat-soluble vitamins such as liver oil, vitamin A, vitamin D, vitamin B2 butyrate, natural vitamin E mixture, soybean oil, rapeseed oil, corn oil , Animal and vegetable oils such as olive oil, palm oil, safflower oil, sunflower oil, rice oil, beef tallow, lard, fish oil,
Natural unsaturated fatty acids such as DHA, EPA, γ-linolenic acid, processed edible oils and fats such as sucrose diacetate hexaisobutyrate, medium chain saturated fatty acid triglyceride of C6 to C12, and any mixture of these edible oily materials. It can be illustrated.
【0006】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 water-soluble substance include coffee, herbs, matcha, black tea, guarana, bonito, shrimp, crab, sea urchin, scallop and other extracts, strawberry, melon, banana, pineapple, apple, milk, cheese, butter, And the like, water-soluble pigments such as cochineal, safflower, beet, and turmeric, other synthetic flavors, synthetic colorants, and any mixture thereof.
【0007】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0.1〜90重量部、好ましく
は5〜50重量部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 (usually oils and fats such as soybean, palm, palm, corn, cottonseed, and shells excluding protein).
Alternatively, water-soluble dietary fiber made from plants such as cereals (rice, wheat and other normal starch etc.) can be exemplified, that is, arabinoxylan, arabinogalactan and other polysaccharides, or any mixture thereof. it can. Such water-soluble hemicellulose is contained in a proportion of 0.1 to 90 parts by weight, preferably 5 to 50 parts by weight.
【0008】本発明で利用することのできるアルコール
類としては例えばグリセリン、プロピレングリコール、
ソルビトール、マルチトール、澱粉分解還元物、グルコ
ース、蔗糖、マルトースその他の中から選ばれる1種又
は2種以上の混合物を例示することができる。このよう
なアルコール類を0.1〜90重量部、好ましくは1〜
80重量部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。Alcohols that can be used in the present invention include, for example, glycerin, propylene glycol,
One or a mixture of two or more selected from sorbitol, maltitol, starch degradation products, glucose, sucrose, maltose and the like can be exemplified. 0.1 to 90 parts by weight of such alcohols, preferably 1 to
The content is 80 parts by weight. The emulsification method used in the present invention may be any one of a colloid mill, a homomixer, a high pressure homogenizer, an ultrasonic emulsifier,
Further, any type of spray drying method may be used as the powdering method.
【0009】[0009]
【実施例】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。 実施例1 β−カロチン4g、天然ビタミンE0.5g、精製椰子
油5.5gの混合物を約150℃に加熱して、均一な油
性材料混合物を得た。別に水30gに大豆ヘミセルロー
ス10g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、これにグリ
セリン50gを添加混合し、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。EXAMPLES The effects of the present invention will be described more specifically below with reference to examples. Example 1 A mixture of 4 g of β-carotene, 0.5 g of natural vitamin E and 5.5 g of refined coconut oil was heated to about 150 ° C to obtain a uniform oily material mixture. Separately, a solution obtained by dissolving 10 g of soybean hemicellulose in 30 g of water was added, and the whole amount of the above-mentioned oily material mixture was added, pre-stirred and dispersed, and then 50 g of glycerin was added and mixed, and emulsified with a homogenizer to obtain a colorant. An emulsion (invention product No. 1) was obtained.
【0010】実施例2 レモンオイル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50gに大豆ヘミセルロー
ス10g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、これにプロ
ピレングリコール30gを添加混合し、ホモジナイザー
にて乳化し、レモン油乳化物(本発明品No.2)を得
た。Example 2 3 g of lemon oil, 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 in which 10 g of soybean hemicellulose was dissolved in 50 g of water was obtained, and the whole amount of the above-mentioned oily material mixture was added, pre-stirred and dispersed, and then 30 g of propylene glycol was added and mixed, and emulsified with a homogenizer to obtain a lemon. An oil emulsion (invention product No. 2) was obtained.
【0011】実施例3 イオン交換水200gに大豆ヘミセルロース80gを溶
解し、50℃に保持しながらオレンジオイル20gを添
加混合する。これにソルビトール20gを添加混合し、
この溶液を高圧ホモジナイザーにて乳化し、乳化液を噴
霧乾燥してオレンジ香料粉末100g(本発明品No.
3)を得た。Example 3 80 g of soybean hemicellulose was dissolved in 200 g of ion-exchanged water, and 20 g of orange oil was added and mixed while maintaining the temperature at 50 ° C. Add 20 g of sorbitol to this, and mix,
This solution was emulsified with a high pressure homogenizer, and the emulsion was spray-dried to obtain 100 g of orange flavor powder (Product No.
3) was obtained.
【0012】実施例4 イオン交換水200gにコーンヘミセルロース20gと
シュークロース80gを溶解し、50℃に保持しながら
メントールを12g含んだオイル15gを添加混合す
る。これにグリセリン20gを添加し、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.4)を得た。Example 4 20 g of corn hemicellulose and 80 g of sucrose were dissolved in 200 g of ion-exchanged water, and 15 g of oil containing 12 g of menthol was added and mixed while maintaining at 50 ° C. 20 g of glycerin was added thereto, 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. 4 of the present invention).
【0013】実施例5 イオン交換水200gに大豆ヘミセルロース80gとマ
ルチトール25g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.5)を得た。Example 5 80 g of soybean hemicellulose and 25 g of maltitol were dissolved in 200 g of ion-exchanged water, and β-
20 g of oil containing 1.2 g of 30% carotene suspension is heated to 140 ° C. and mixed. This solution was emulsified with a high-pressure homogenizer and the emulsion was spray-dried to obtain 100 g of colorant powder (Product No. 5 of the present invention).
【0014】実施例6 イオン交換水200gに米ぬかヘミセルロース25gと
ラクトース50gを溶解し、50℃に保持しながらEP
A2gを含んだオイル20gを添加混合する。これにプ
ロピレングリコール15gを添加し、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粉末油脂
100g(本発明品No.6)を得た。Example 6 25 g of rice bran hemicellulose and 50 g of lactose were dissolved in 200 g of ion-exchanged water, and EP was maintained while maintaining the temperature at 50 ° C.
20 g of oil containing 2 g of A is added and mixed. 15 g of propylene glycol was added to this, this solution was emulsified by a high-pressure homogenizer, and the emulsion was spray-dried to obtain 100 g of a powdered fat and oil (invention product No. 6).
【0015】対照例1 実施例1においてグリセリンを使用せず、その重量不足
分をイオン交換水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 product No. 1) was obtained under the same conditions as in Example 1 except that glycerin was not used in Example 1 and the weight shortage was supplemented with ion-exchanged water. .
【0016】対照例2 実施例2においてプロピレングリコールを使用せず、そ
の重量不足分をイオン交換水で補った他は実施例2と同
じ条件によってレモン油乳化物(対照品No.2)を得
た。Comparative Example 2 A lemon oil emulsion (control product No. 2) was obtained under the same conditions as in Example 2, except that propylene glycol was not used in Example 2 and the weight shortage was supplemented with ion-exchanged water. It was
【0017】対照例3 実施例2において大豆ヘミセルロースのかわりにアラビ
アガム15gを使用した他は実施例2と同じ条件によっ
てレモン油乳化物(対照品No.3)を得た。Control Example 3 A lemon oil emulsion (control product No. 3) was obtained under the same conditions as in Example 2 except that 15 g of gum arabic was used instead of soybean hemicellulose in Example 2.
【0018】対照例4 実施例3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3と同じ条件によってオレ
ンジ香料粉末100g(対照品No.4)を得た。Control Example 4 100 g of orange flavor powder (control product No. 4) was obtained under the same conditions as in Example 3 except that gum arabic was used instead of soybean hemicellulose in Example 3.
【0019】対照例5 実施例3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3と同じ条件によってオレンジ
香料粉末100g(対照品No.5)を得た。Control Example 5 100 g of orange flavor powder (control product No. 5) was obtained under the same conditions as in Example 3 except that modified starch was used in place of soybean hemicellulose.
【0020】対照例6 実施例3において大豆ヘミセルロースのかわりにデキス
トリンを使用した他は実施例3と同じ条件によってオレ
ンジ油乳化物(対照品No.6)を得た。Control Example 6 An orange oil emulsion (control product No. 6) was obtained under the same conditions as in Example 3 except that dextrin was used instead of soybean hemicellulose in Example 3.
【0021】対照例7 実施例3においてソルビトールを使用しない他は実施例
3と同じ条件によってオレンジ香料粉末100g(対照
品No.7)を得た。Control Example 7 Under the same conditions as in Example 3 except that sorbitol was not used, 100 g of orange flavor powder (control product No. 7) was obtained.
【0022】対照例8 実施例4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4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 Under the same conditions as in Example 4, except that gum arabic was used instead of corn hemicellulose in Example 4, 100 g of menthol flavor powder (control product No. 8) was obtained.
【0023】対照例9 実施例4においてコーン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4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 flavor powder (control product No. 9) was obtained under the same conditions as in Example 4 except that modified starch was used in place of corn hemicellulose.
【0024】対照例10 実施例5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5と同じ条件によって着色
料粉末100g(対照品No.10)を得た。Control Example 10 Under the same conditions as in Example 5, except that gum arabic was used in place of soybean hemicellulose in Example 5, 100 g of a colorant powder (control product No. 10) was obtained.
【0025】対照例11 実施例5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5と同じ条件によって着色料粉
末100g(対照品No.11)を得た。Control Example 11 100 g of a colorant powder (control product No. 11) was obtained under the same conditions as in Example 5 except that modified starch was used in place of soybean hemicellulose in Example 5.
【0026】対照例12 実施例5においてマルチトールを使用しない他は実施例
5と同じ条件によって着色料粉末100g(対照品N
o.12)を得た。Control Example 12 100 g of colorant powder (control product N) was prepared in the same manner as in Example 5 except that maltitol was not used.
o. 12) was obtained.
【0027】対照例13 実施例6において米ぬか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7と同じ条件によって粉
末油脂100g(対照品No.13)を得た。Control Example 13 100 g of powdered oil and fat (control product No. 13) was obtained under the same conditions as in Example 7 except that gum arabic was used instead of rice bran hemicellulose in Example 6.
【0028】対照例14 実施例6において米ぬか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6と同じ条件によって粉末油
脂100g(対照品No.14)を得た。Control Example 14 100 g of powdered oil and fat (control product No. 14) was obtained under the same conditions as in Example 6 except that modified starch was used in place of rice bran hemicellulose in Example 6.
【0029】比較実験1 実施例1および対照例1で得た乳化組成物を同一日に調
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。そ
の結果を表1に示す。Comparative Experiment 1 The emulsion compositions obtained in Example 1 and Comparative Example 1 were prepared on the same day, and laser diffraction particle size distribution analyzer SALD-1100 was used.
(Shimadzu Corporation) was used to measure the particle size distribution. The results are shown in Table 1.
【0030】[0030]
【表1】 [Table 1]
【0031】以上の結果から明らかな通り、本発明品N
o.1は、対照品No.1に較べて大豆ヘミセルロース
の乳化力が非常に高くなり、より微細な粒子が得られ
た。As is clear from the above results, the product N of the present invention
o. No. 1 is the control product No. Compared with 1, the emulsifying power of soybean hemicellulose was much higher, and finer particles were obtained.
【0032】比較実験2 実施例2および対照例2、対照例3のレモン油乳化物を
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、同時にグラニュー糖120g、クエン酸4
g、を125gの水に溶解し、この溶液に実施例2およ
び対照例2、対照例3で得られた乳化物を1ml添加
し、炭酸水にて全体を1lとした。瓶に充填後打栓し、
炭酸飲料を得た。これを室温で静置し、経時変化を観察
した。結果を表2に示す。Comparative Experiment 2 Lemon oil emulsions of Example 2 and Comparative Examples 2 and 3 were prepared on the same day, and laser diffraction particle size distribution analyzer SALD-
The particle size distribution was measured using 1100 (Shimadzu Corporation). At the same time, 120 g of granulated sugar and 4 citric acid
g was dissolved in 125 g of water, and 1 ml of the emulsions obtained in Example 2 and Comparative Examples 2 and 3 was added to this solution, and the whole was made up to 1 liter with carbonated water. After filling the bottle, stopper it,
A carbonated drink was obtained. This was left to stand at room temperature and the change with time was observed. The results are shown in Table 2.
【0033】[0033]
【表2】 [Table 2]
【0034】但し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。 +++R ネックリングが層状となる程激しくなる。 表2の結果から明らかな通り、本発明品No.2は、対
照品No.2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No.3(アラビアガム)と同
程度の乳化力を示した。また、対照品No.2では炭酸
飲料静置後約10日で著しいネックリングの発生を認
め、商品価値を失うのに対し、本発明品および対照品N
o.3ではネックリングの発生は認められず安定であっ
た。However, each symbol in the table has the following meaning. -R Neck ring is not observed. ± R Neck ring is slightly visible. + R A clear neck ring is recognized. ++ R Remarkable neck ring is recognized. +++ R It becomes more intense as the neck ring becomes layered. As is clear from the results of Table 2, the product No. of the present invention. 2 is a control product No. The emulsifying power of the water-soluble hemicellulose was much higher than that of Comparative Example No. 2. It showed an emulsifying power similar to that of 3 (gum arabic). The reference product No. In No. 2, in about 10 days after the carbonated beverage was allowed to stand, marked necking was observed and the commercial value was lost.
o. In No. 3, no neck ring was observed and it was stable.
【0035】比較実験3 実施例3および対照例4〜7で得たオレンジ香料粉末
を、40℃にて保存し、経時変化を観察した。また、オ
レンジ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3に示す。Comparative Experiment 3 The orange flavor powders obtained in Example 3 and Comparative Examples 4 to 7 were stored at 40 ° C., and the change with time was observed. In addition, the emulsifying property when the orange oil was emulsified was also evaluated. The results are shown in Table 3.
【0036】[0036]
【表3】 [Table 3]
【0037】但し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 表3の結果から明らかなとおり、本発明品No.3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、基剤皮膜の強度及び香
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。However, each symbol in the table has the following meaning. ◎: Very good ○: Good △: Somewhat bad ×:
Poor −: Not Evaluable As is clear from the results of Table 3, the product No. of the present invention. No. 3 had a good emulsifying property, the strength of the base film was excellent even after 6 months of storage, and the flavor was not lost. In No. 4, the emulsifiability was slightly inferior, and the strength and flavor of the base film decreased over time. The tendency is that the reference product No. 7, control product No. It becomes remarkable in the order of 5. The reference product No. No. 6 could not emulsify.
【0038】比較実験4 実施例4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。その結果を表
4に示す。Comparative Experiment 4 The menthol flavor powders of Example 4 and Comparative Examples 8 to 9 were placed in a hermetically sealed container, stored at 40 ° C. and then opened, and the menthol content was measured by gas chromatography. The results are shown in Table 4.
【0039】[0039]
【表4】 [Table 4]
【0040】・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顔料に対する残存率を%で
示している。 表4の結果から明らかな通り、本発明品No.4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。The value in the table indicates the menthol content of the sample.・ The numerical value in parentheses indicates the residual rate with respect to the pigment at the time of adjustment in%. As is clear from the results of Table 4, the product No. of the present invention. The menthol content of No. 4 did not decrease even after storage for 6 months, whereas the control product No. 8 and the control product No. In No. 9, the content of menthol decreased with time, and the loss of clathrate was observed.
【0041】比較実験5 下記に示すチューインガム基材に実施例3で得られたオ
レンジ粉末香料(本発明品3及び4)と対照例4、5、
7で得られたオレンジ粉末香料(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
のチューインガムを得た。チューインガム基材組成を表
5に示す。Comparative Experiment 5 On the chewing gum bases shown below, the orange powder flavors obtained in Example 3 (Products 3 and 4 of the present invention) and Control Examples 4 and 5,
Orange powder fragrance obtained in No. 7 (control products No. 4, 5,
7) is added, kneaded and pressure-formed, and 3 g per sheet
Got chewing gum. The chewing gum base composition is shown in Table 5.
【0042】[0042]
【表5】 [Table 5]
【0043】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 sensory evaluation of these chewing gums by 10 expert panelists, the product of the present invention showed no significant difference in the strength of the flavor as compared with the control example, but it was remarkably excellent in the persistence and the persistence. It was determined that
【0044】比較実験6 実施例5および対照例10〜12で得た着色料粉末のβ
−カロチン含量を液体クロマトグラフィーで測定した。
その結果を表6に示す。Comparative Experiment 6 β of the colorant powders obtained in Example 5 and Comparative Examples 10 to 12
-Carotene content was measured by liquid chromatography.
The results are shown in Table 6.
【0045】[0045]
【表6】 [Table 6]
【0046】・表中の値は試料中に含まれるβ−カロチ
ンの含量を%で示す。 ・( )内の数値は調整時の顔料に対する残存率を%で
示している。 表6の結果から明らかな通り、本発明品No.5は、粉
末化に際し殆どβ−カロチンの損失が認められず、対照
品10、11、12と比較して、優れた包接物安定性を
示した。The values in the table indicate the content of β-carotene contained in the sample in%.・ The numerical value in parentheses indicates the residual rate with respect to the pigment at the time of adjustment in%. As is apparent from the results of Table 6, the product No. of the present invention. No. 5 showed almost no loss of β-carotene during pulverization, and showed excellent inclusion inclusion stability as compared with the control products 10, 11, and 12.
【0047】比較実験7 実施例6および対照例13〜14で得た粉末油脂を40
℃にて2週間保存し、油脂の酸化度合い(POV)を測
定した。また、保存後の粉末油脂をイオン交換水にて1
000倍に希釈して、これらの希釈液を10名の専門パ
ネラーに対し、風味について官能試験を実施した。その
結果を表7に示す。Comparative Experiment 7 The powdered fats and oils obtained in Example 6 and Comparative Examples 13 to 40 were mixed with 40
It was stored at 0 ° C. for 2 weeks, and the degree of oxidation (POV) of oil and fat was measured. In addition, the powdered fat and oil after storage is deionized with 1
After diluting 000 times, these diluted solutions were subjected to a sensory test for flavor with 10 expert panelists. The results are shown in Table 7.
【0048】[0048]
【表7】 [Table 7]
【0049】・POVの単位はmeq/kg ・官能評価基準:保存前のものを標準とし、これとどの
程度の風味差があるかを以下の基準でパネラーに点数付
けさせた。 5点:全く差なし 4点:殆ど同じ 3点:僅かに酸化臭あり 2点:かなり酸化臭あり 1点:酸化臭強い 表7の結果から明らかな通り、本発明品No.6は40
℃2週間の保存後も包接物中の油脂の酸化がほとんど認
められず、風味の劣化が殆ど無いのに対し、対照品N
o.13および対照品No.14では包接物中の油脂が
明きらかに酸化しており、風味がかなり損なわれてい
た。The unit of POV is meq / kg. Sensory evaluation standard: The standard before storage was used as a standard, and the degree of flavor difference from this was evaluated by the panelists according to the following standards. 5 points: No difference 4 points: Almost the same 3 points: Slightly oxidative odor 2 points: Very oxidative odor 1 point: Strong oxidative odor 6 is 40
Even after storage at 2 ° C for 2 weeks, almost no oxidation of fats and oils in the inclusions was observed, and there was almost no deterioration in flavor, whereas the control product N
o. 13 and the control product No. In No. 14, the oil and fat in the clathrate was clearly oxidized, and the flavor was considerably impaired.
【0050】[0050]
【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
化安定性が優れ、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
品や医薬品、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 according to the present invention have excellent emulsifiability and emulsion stability in the production process, and even when powdered, the clathrate after pulverization Stability, the strength of the film is particularly excellent, since it is possible to impart a desired long-term stable and desirable flavor, color tone, flavor, etc. to various foods, pharmaceuticals, pet foods, quasi-drugs, etc. It is extremely large.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 A61K 47/10 H 47/36 H ─────────────────────────────────────────────────── ───Continued from the front page (51) Int.Cl. 6 Identification code Internal reference number FI technical display area A61K 47/10 H 47/36 H
Claims (3)
類を含有することを特徴とする製剤。1. A preparation comprising a water-soluble hemicellulose and alcohols.
こし、米ぬかを原料とする多糖類である特許請求の範囲
第1項記載の製剤。2. The preparation according to claim 1, wherein the water-soluble hemicellulose is a polysaccharide derived from soybean, corn and rice bran.
グリコール、ソルビトール、マルチトールである特許請
求の範囲第1項記載の製剤。3. The preparation according to claim 1, wherein the alcohol is glycerin, propylene glycol, sorbitol or maltitol.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5254817A JPH0779712A (en) | 1993-09-17 | 1993-09-17 | Formulation containing water-soluble hemicellulose |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5254817A JPH0779712A (en) | 1993-09-17 | 1993-09-17 | Formulation containing water-soluble hemicellulose |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0779712A true JPH0779712A (en) | 1995-03-28 |
Family
ID=17270294
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5254817A Pending JPH0779712A (en) | 1993-09-17 | 1993-09-17 | Formulation containing water-soluble hemicellulose |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0779712A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH07107927A (en) * | 1993-10-13 | 1995-04-25 | T Hasegawa Co Ltd | Emulsified composition |
| WO2000044375A1 (en) * | 1999-01-29 | 2000-08-03 | Mars Uk Limited | Antioxidant compositions and methods for companion animals |
| JP2000279104A (en) * | 1999-01-26 | 2000-10-10 | Sanei Gen Ffi Inc | Pharmaceutical composition having good physical properties |
| JP2001112421A (en) * | 1999-10-19 | 2001-04-24 | Freunt Ind Co Ltd | Water soluble coating composition for food |
| US6261622B1 (en) * | 1997-08-13 | 2001-07-17 | Kagome Co., Ltd. | Water-dispersible carotenoid pigment preparation |
| JP2007053935A (en) * | 2005-08-23 | 2007-03-08 | Sanei Gen Ffi Inc | Liquid composition in which precipitation of amino acids is suppressed |
| US7405070B2 (en) | 2003-11-26 | 2008-07-29 | Sk Corporation | Method for preparing (s)-indoline-2-carboxylic acid and (s)-indoline-2-carboxylic acid methyl ester using hydrolytic enzyme |
| WO2022124268A1 (en) * | 2020-12-07 | 2022-06-16 | 味の素株式会社 | Powdered food composition and method for producing same |
-
1993
- 1993-09-17 JP JP5254817A patent/JPH0779712A/en active Pending
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH07107927A (en) * | 1993-10-13 | 1995-04-25 | T Hasegawa Co Ltd | Emulsified composition |
| US6261622B1 (en) * | 1997-08-13 | 2001-07-17 | Kagome Co., Ltd. | Water-dispersible carotenoid pigment preparation |
| JP2000279104A (en) * | 1999-01-26 | 2000-10-10 | Sanei Gen Ffi Inc | Pharmaceutical composition having good physical properties |
| JP4966450B2 (en) * | 1999-01-29 | 2012-07-04 | マーズ ユー ケー リミテッド | Antioxidant composition for pet animals and method of use thereof |
| WO2000044375A1 (en) * | 1999-01-29 | 2000-08-03 | Mars Uk Limited | Antioxidant compositions and methods for companion animals |
| GB2366179A (en) * | 1999-01-29 | 2002-03-06 | Mars Uk Ltd | Antioxidant compositions and methods for companion animals |
| JP2002535364A (en) * | 1999-01-29 | 2002-10-22 | マーズ ユー ケー リミテッド | Antioxidant composition for pet animals and use thereof |
| GB2366179B (en) * | 1999-01-29 | 2003-04-16 | Mars Uk Ltd | Antioxidant compositions and methods for companion animals |
| JP2001112421A (en) * | 1999-10-19 | 2001-04-24 | Freunt Ind Co Ltd | Water soluble coating composition for food |
| US7405070B2 (en) | 2003-11-26 | 2008-07-29 | Sk Corporation | Method for preparing (s)-indoline-2-carboxylic acid and (s)-indoline-2-carboxylic acid methyl ester using hydrolytic enzyme |
| JP2007053935A (en) * | 2005-08-23 | 2007-03-08 | Sanei Gen Ffi Inc | Liquid composition in which precipitation of amino acids is suppressed |
| WO2022124268A1 (en) * | 2020-12-07 | 2022-06-16 | 味の素株式会社 | Powdered food composition and method for producing same |
| JPWO2022124268A1 (en) * | 2020-12-07 | 2022-06-16 |
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