JPH07101884A - Prpearation containing water-soluble hemicellulose - Google Patents
Prpearation containing water-soluble hemicelluloseInfo
- Publication number
- JPH07101884A JPH07101884A JP5269551A JP26955193A JPH07101884A JP H07101884 A JPH07101884 A JP H07101884A JP 5269551 A JP5269551 A JP 5269551A JP 26955193 A JP26955193 A JP 26955193A JP H07101884 A JPH07101884 A JP H07101884A
- Authority
- JP
- Japan
- Prior art keywords
- water
- flavor
- hemicellulose
- oil
- soluble
- 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
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- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 235000010983 sucrose acetate isobutyrate Nutrition 0.000 description 1
- UVGUPMLLGBCFEJ-SWTLDUCYSA-N sucrose acetate isobutyrate Chemical group CC(C)C(=O)O[C@H]1[C@H](OC(=O)C(C)C)[C@@H](COC(=O)C(C)C)O[C@@]1(COC(C)=O)O[C@@H]1[C@H](OC(=O)C(C)C)[C@@H](OC(=O)C(C)C)[C@H](OC(=O)C(C)C)[C@@H](COC(C)=O)O1 UVGUPMLLGBCFEJ-SWTLDUCYSA-N 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 235000013976 turmeric Nutrition 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 235000019155 vitamin A Nutrition 0.000 description 1
- 239000011719 vitamin A Substances 0.000 description 1
- NCYCYZXNIZJOKI-UHFFFAOYSA-N vitamin A aldehyde Natural products O=CC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C NCYCYZXNIZJOKI-UHFFFAOYSA-N 0.000 description 1
- 235000019164 vitamin B2 Nutrition 0.000 description 1
- 239000011716 vitamin B2 Substances 0.000 description 1
- 235000019166 vitamin D Nutrition 0.000 description 1
- 239000011710 vitamin D Substances 0.000 description 1
- 150000003710 vitamin D derivatives Chemical class 0.000 description 1
- 229940045997 vitamin a Drugs 0.000 description 1
- 229940046008 vitamin d Drugs 0.000 description 1
- OENHQHLEOONYIE-JLTXGRSLSA-N β-Carotene Chemical compound CC=1CCCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C OENHQHLEOONYIE-JLTXGRSLSA-N 0.000 description 1
Landscapes
- General Preparation And Processing Of Foods (AREA)
- Jellies, Jams, And Syrups (AREA)
- Medicinal Preparation (AREA)
- Medicines Containing Plant Substances (AREA)
Abstract
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。FIELD OF THE INVENTION The present invention relates to a formulation containing water-soluble hemicellulose and a surfactant. The preparation of the present invention refers to an emulsified preparation and a powdered preparation, and is used for imparting a desirable flavor, color tone, flavor and the like to foods, pharmaceuticals, cosmetics, pet foods, quasi drugs and the like for a long period of time.
【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やがん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 prepared by emulsifying an oily substance 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 being used. In addition, a 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 cancer-containing components of foods and drinks and pharmaceuticals used. There was a characteristic called. 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、有機酸を適宜添加
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、
有機酸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ができる製剤を提供するこ
とにある。[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 appropriately adding an organic acid, the emulsifying power and film strength of the water-soluble hemicellulose are significantly enhanced, and the heat resistance and retention of the perfume ingredients and the release delay of the perfume ingredients are delayed. We obtained the knowledge that a highly effective preparation can be provided. The present invention uses a water-soluble hemicellulose as an emulsifying agent or a powdering base during the production of a preparation, and
By adding an appropriate amount of organic acid, the emulsifiability and emulsion stability at the time of production are excellent, the stability of the clathrate after pulverization and the strength of the base film are enhanced, and the aroma that is stable for a long time in foods, etc. ,
It is intended 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。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, 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. As a water-soluble substance,
Extracts such as coffee, herbs, matcha, black tea, guarana, bonito, shrimp, crab, sea urchin, scallop, etc.
Examples of essences such as strawberry, melon, banana, pineapple, apple, milk, cheese, butter, water-soluble pigments such as cochineal, safflower, beet, turmeric, other synthetic flavors, synthetic colorants, and any mixture 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 (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-excluded starch), that is, arabinoxylan, arabinogalactan and other polysaccharides, or any mixture thereof may be used. it can. Such water-soluble hemicellulose is contained in the formulation in an amount of 0.1 to 98% by weight, preferably 5 to 50% by weight.
【0007】本発明で利用できる有機酸としては、クエ
ン酸、クエン酸三ナトリウム、グルコン酸、コハク酸、
コハク酸一ナトリウム、コハク酸二ナトリウム、酢酸ナ
トリウム、DL−酒石酸、L−酒石酸、DL−酒石酸ナ
トリウム、L−酒石酸ナトリウム、乳酸ナトリウム、乳
酸カルシウム、DL−リンゴ酸、DL−リンゴ酸ナトリ
ウム、フマル酸一ナトリウムおよびこれらの任意の混合
物等が挙げられる。このような有機酸を製剤に対して
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。Organic acids usable in the present invention include citric acid, trisodium citrate, gluconic acid, succinic acid,
Sodium succinate, disodium succinate, sodium acetate, DL-tartaric acid, L-tartaric acid, DL-sodium tartrate, sodium L-tartrate, sodium lactate, calcium lactate, DL-malic acid, DL-sodium malate, fumaric acid Monosodium and any mixture thereof and the like. Such an organic acid is contained in the formulation in an amount of 0.01 to 10% by weight, preferably 0.05 to 5% by weight. As the emulsification method used in the present invention,
A colloid mill, a homomixer, a high-pressure homogenizer, an ultrasonic emulsifier, etc. may be used, and a powdering method may be any type of spray drying method. Hereinafter, the effects of the present invention will be described more specifically with reference to examples.
【0008】[0008]
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、DL−リンゴ酸ナトリウム0.3g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 0.3 g of DL-sodium malate in 69 g of water was added, and the whole amount of the above-mentioned oily material mixture was added and pre-stirred to disperse and then emulsified with a homogenizer,
A colorant emulsion (invention product No. 1) 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、ク
エン酸三ナトリウム0.1gを溶解し、50℃に保持し
ながらコーヒーオイル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
てコーヒー香料粉末100g(本発明品No.2)を得
た。Example 2 85 g of soybean hemicellulose and 0.1 g of trisodium citrate were dissolved in 200 g of ion-exchanged water, and 20 g of coffee oil was 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 100 g of coffee flavor powder (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、L−酒石酸ナトリウム0.1g
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 3 200 g of ion-exchanged water, 70 g of corn hemicellulose, 40 g of sucrose, and 0.1 g of sodium L-tartrate.
Is dissolved and 15 g of oil containing 12 g of menthol is added and mixed while maintaining at 50 ° C. 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】対照例1 実施例1においてDL−リンゴ酸ナトリウムを使用せ
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N
o.1)を得た。Control Example 1 The same procedure as in Example 1 was carried out except that DL-sodium malate was not used and the weight shortage was supplemented with soybean hemicellulose.
o. 1) was obtained.
【0012】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 product No. 2) was obtained under the same conditions as in Example 1 except that gum arabic was used instead of soybean hemicellulose in Example 1.
【0013】対照例3 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.3)を得た。Control Example 3 Under the same conditions as in Example 2, except that gum arabic was used in place of soybean hemicellulose in Example 2, 100 g of mint flavor powder (control product No. 3) was obtained.
【0014】対照例4 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.4)を得た。Control Example 4 100 g of mint flavor powder (control product No. 4) was obtained under the same conditions as in Example 2 except that modified starch was used in place of soybean hemicellulose.
【0015】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.5)を得た。Control Example 5 A mint oil emulsion (control product No. 5) was obtained under the same conditions as in Example 2 except that dextrin was used instead of soybean hemicellulose in Example 2.
【0016】対照例6 実施例2においてクエン酸三ナトリウムを使用せず、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100g(対照品
No.6)を得た。Control Example 6 100 g of mint flavor powder (control product No. 6) was used under the same conditions as in Example 2 except that trisodium citrate was not used and the weight shortage was supplemented with soybean hemicellulose. Obtained.
【0017】対照例7 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.7)を得た。Control Example 7 100 g of menthol flavor powder (control product No. 7) was obtained under the same conditions as in Example 3 except that gum arabic was used instead of corn hemicellulose.
【0018】対照例8 実施例3においてL−酒石酸ナトリウムを使用せず、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.8)を得た。Control Example 8 100 g of menthol flavor powder was prepared under the same conditions as in Example 3, except that L-sodium tartrate was not used in Example 3 and the weight shortage was supplemented with corn hemicellulose.
(Control product No. 8) was obtained.
【0019】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1および対照例1、対照例2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 Coloring agent emulsions of Example 1 and Comparative Examples 1 and 2 were prepared on the same day, and 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 10% lactic acid aqueous solution, and 1 g of the colorant emulsion obtained in Example 1 and Control Example 1 and Control Example 2 were uniformly added to the solution. Mixed in. After filling the bottle, the bottle was stoppered and sterilized at 85 ° C. for 20 minutes to obtain a colored acidic milk drink.
This was left to stand at room temperature and the change with time was observed. The results are shown in Table 1.
Shown in.
【0020】[0020]
【表1】 [Table 1]
【0021】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 neck ring is observed. ± R: Neck ring is slightly recognized. + R: A clear neck ring is recognized. R: Remarkable neck ring is recognized. -P: No precipitation is observed. ± P: Slight precipitation is observed. + P: A clear precipitate is observed. P: Remarkable precipitation is recognized.
【0022】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.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.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 shown in Table 1, the product N of the present invention
o. No. 1 is the control product No. 1 and the control product No. The emulsifying power of the water-soluble hemicellulose was much higher than that of Comparative Example No. 2. It showed a slightly higher emulsifying power than 2 (gum arabic). Moreover, when the colored acidic milk drink was allowed to stand at room temperature for about 30 days, the control product No. No precipitation occurred in No. 1, but
Acknowledged the occurrence of neck ring and lost the commercial value. Control product No. In No. 2, no neck ring was observed, but significant precipitation occurred. On the other hand, the product No. of the present invention.
In No. 1, neither coloring nor precipitation was observed, and the colored acidic milk drink was stable.
【0023】比較実験2 実施例2および対照例3〜6で得たコーヒー香料粉末
を、40℃にて保存し、経時変化を観察した。また、コ
ーヒー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 coffee flavor powders obtained in Example 2 and Comparative Examples 3 to 6 were stored at 40 ° C., and changes with time were observed. In addition, the emulsifying property when the coffee oil was emulsified was also evaluated. The results are shown in Table 2.
【0024】[0024]
【表2】 [Table 2]
【0025】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.3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.6、
対照品No.4の順で顕著になる。また対照品No.5
では乳化が行えなかった。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 2, the product No. of the present invention. No. 2 had good emulsifiability, the strength of the base film was excellent even after 6 months of storage, and there was no loss of flavor, while the control product No. In No. 3, the emulsifiability was slightly inferior, and the strength and flavor of the base film decreased with time. The tendency is that the reference product No. 6,
Control product No. It becomes remarkable in the order of 4. The reference product No. 5
I couldn't emulsify.
【0026】比較実験3 実施例3および対照例7〜8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 Comparative Examples 7 to 8 were placed in a sealed container, stored at 40 ° C. and then opened, and the menthol content was measured by gas chromatography.
【0027】[0027]
【表3】 [Table 3]
【0028】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.7および対照品No.8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 of Table 3, the product N of the present invention
o. The menthol content of the sample No. 3 did not decrease even after storage for 6 months, whereas the control sample No. 3 did not. 7 and the control product No. In No. 8, the content of menthol decreased with time and the loss of clathrate was observed.
【0029】比較実験4 下記に示すチューインガム基材に実施例2で得られたコ
ーヒー粉末香料(本発明品No.2)と対照例3、4、
6で得られたコーヒー粉末香料(対照品No.3、4、
6)をそれぞれ添加し、混練して圧展成型し、1枚3g
のコーヒー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 coffee powder flavor (obtained from the present invention No. 2) obtained in Example 2 and the control examples 3 and 4 were added to the chewing gum base material shown below.
Coffee powder flavor obtained in 6 (control products No. 3, 4,
6) is added, kneaded and pressure-formed, and 3 g per sheet
To obtain a coffee-flavored chewing gum. The chewing gum base composition is shown in Table 4.
【0030】[0030]
【表4】 [Table 4]
【0031】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。The chewing gums were subjected to a sensory evaluation by 10 expert panelists. As a result, the product of the present invention showed no significant difference in flavor intensity as compared with the control example, but was remarkably excellent in persistence and persistence. It was determined that
【0032】[0032]
【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 according to the present invention have extremely good emulsification properties and emulsion stability in the manufacturing process, and even when powdered, the formulation after powderization The stability of the adherend and the strength of the film are particularly excellent, and it has a long-lasting and desirable flavor for various foods, pharmaceuticals, etc.
Since it is possible to impart color tone, flavor, etc., its industrial significance is extremely great.
Claims (2)
有することを特徴とする製剤。1. A formulation comprising water-soluble hemicellulose and an organic acid.
こし、または米ぬかを原料とする多糖類である請求項1
記載の製剤。2. The water-soluble hemicellulose is a polysaccharide derived from soybean, corn or rice bran.
The described formulation.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5269551A JPH07101884A (en) | 1993-10-01 | 1993-10-01 | Prpearation containing water-soluble hemicellulose |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5269551A JPH07101884A (en) | 1993-10-01 | 1993-10-01 | Prpearation containing water-soluble hemicellulose |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH07101884A true JPH07101884A (en) | 1995-04-18 |
Family
ID=17473958
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5269551A Pending JPH07101884A (en) | 1993-10-01 | 1993-10-01 | Prpearation containing water-soluble hemicellulose |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH07101884A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6261622B1 (en) * | 1997-08-13 | 2001-07-17 | Kagome Co., Ltd. | Water-dispersible carotenoid pigment preparation |
| WO2003101374A3 (en) * | 2002-05-30 | 2004-02-26 | Akzo Nobel Nv | Use of new etonogestrel esters |
| WO2004094595A2 (en) | 2003-04-17 | 2004-11-04 | Alnylam Pharmaceuticals Inc. | MODIFIED iRNA AGENTS |
| WO2004094345A2 (en) | 2003-04-17 | 2004-11-04 | Alnylam Pharmaceuticals Inc. | Protected monomers |
| US7323454B2 (en) | 2002-05-30 | 2008-01-29 | N.V. Organon | Etonogestrel esters |
| EP2216407A2 (en) | 2003-03-07 | 2010-08-11 | Alnylam Pharmaceuticals, Inc. | Therapeutic Compositions |
| WO2016057693A1 (en) | 2014-10-10 | 2016-04-14 | Alnylam Pharmaceuticals, Inc. | Methods and compositions for inhalation delivery of conjugated oligonucleotide |
| EP3141265A1 (en) | 2007-12-04 | 2017-03-15 | Alnylam Pharmaceuticals, Inc. | Carbohydrate conjugates as delivery agents for oligonucleotides |
-
1993
- 1993-10-01 JP JP5269551A patent/JPH07101884A/en active Pending
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6261622B1 (en) * | 1997-08-13 | 2001-07-17 | Kagome Co., Ltd. | Water-dispersible carotenoid pigment preparation |
| WO2003101374A3 (en) * | 2002-05-30 | 2004-02-26 | Akzo Nobel Nv | Use of new etonogestrel esters |
| US7323454B2 (en) | 2002-05-30 | 2008-01-29 | N.V. Organon | Etonogestrel esters |
| EP2239329A1 (en) | 2003-03-07 | 2010-10-13 | Alnylam Pharmaceuticals, Inc. | Therapeutic compositions |
| EP3450559A1 (en) | 2003-03-07 | 2019-03-06 | Alnylam Pharmaceuticals, Inc. | Therapeutic compositions |
| EP2216407A2 (en) | 2003-03-07 | 2010-08-11 | Alnylam Pharmaceuticals, Inc. | Therapeutic Compositions |
| WO2004094345A2 (en) | 2003-04-17 | 2004-11-04 | Alnylam Pharmaceuticals Inc. | Protected monomers |
| EP2660322A2 (en) | 2003-04-17 | 2013-11-06 | Alnylam Pharmaceuticals Inc. | Modified iRNA agents |
| EP2664672A1 (en) | 2003-04-17 | 2013-11-20 | Alnylam Pharmaceuticals Inc. | Modified iRNA agents |
| EP2666858A1 (en) | 2003-04-17 | 2013-11-27 | Alnylam Pharmaceuticals Inc. | Modified iRNA agents |
| EP2669377A2 (en) | 2003-04-17 | 2013-12-04 | Alnylam Pharmaceuticals Inc. | Modified iRNA agents |
| WO2004094595A2 (en) | 2003-04-17 | 2004-11-04 | Alnylam Pharmaceuticals Inc. | MODIFIED iRNA AGENTS |
| EP3141265A1 (en) | 2007-12-04 | 2017-03-15 | Alnylam Pharmaceuticals, Inc. | Carbohydrate conjugates as delivery agents for oligonucleotides |
| WO2016057693A1 (en) | 2014-10-10 | 2016-04-14 | Alnylam Pharmaceuticals, Inc. | Methods and compositions for inhalation delivery of conjugated oligonucleotide |
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