JPH04346937A - Reduction of bitterness - Google Patents
Reduction of bitternessInfo
- Publication number
- JPH04346937A JPH04346937A JP3148077A JP14807791A JPH04346937A JP H04346937 A JPH04346937 A JP H04346937A JP 3148077 A JP3148077 A JP 3148077A JP 14807791 A JP14807791 A JP 14807791A JP H04346937 A JPH04346937 A JP H04346937A
- Authority
- JP
- Japan
- Prior art keywords
- bitterness
- agar
- jelly
- agent
- carrageenan
- 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.)
- Granted
Links
- 235000019658 bitter taste Nutrition 0.000 title claims abstract description 22
- 235000015110 jellies Nutrition 0.000 claims abstract description 19
- 239000008274 jelly Substances 0.000 claims abstract description 19
- 239000000126 substance Substances 0.000 claims abstract description 18
- 229920001817 Agar Polymers 0.000 claims abstract description 13
- 239000008272 agar Substances 0.000 claims abstract description 13
- 108010010803 Gelatin Proteins 0.000 claims abstract description 11
- ZNOZWUKQPJXOIG-XSBHQQIPSA-L [(2r,3s,4r,5r,6s)-6-[[(1r,3s,4r,5r,8s)-3,4-dihydroxy-2,6-dioxabicyclo[3.2.1]octan-8-yl]oxy]-4-[[(1r,3r,4r,5r,8s)-8-[(2s,3r,4r,5r,6r)-3,4-dihydroxy-6-(hydroxymethyl)-5-sulfonatooxyoxan-2-yl]oxy-4-hydroxy-2,6-dioxabicyclo[3.2.1]octan-3-yl]oxy]-5-hydroxy-2-( Chemical compound O[C@@H]1[C@@H](O)[C@@H](OS([O-])(=O)=O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H]2OC[C@H]1O[C@H](O[C@H]1[C@H]([C@@H](CO)O[C@@H](O[C@@H]3[C@@H]4OC[C@H]3O[C@H](O)[C@@H]4O)[C@@H]1O)OS([O-])(=O)=O)[C@@H]2O ZNOZWUKQPJXOIG-XSBHQQIPSA-L 0.000 claims abstract description 11
- 239000008273 gelatin Substances 0.000 claims abstract description 11
- 229920000159 gelatin Polymers 0.000 claims abstract description 11
- 235000019322 gelatine Nutrition 0.000 claims abstract description 11
- 235000011852 gelatine desserts Nutrition 0.000 claims abstract description 11
- 235000011194 food seasoning agent Nutrition 0.000 claims abstract description 6
- 239000003349 gelling agent Substances 0.000 claims description 17
- 230000001603 reducing effect Effects 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 7
- LRBQNJMCXXYXIU-NRMVVENXSA-N tannic acid Chemical compound OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-NRMVVENXSA-N 0.000 abstract description 13
- TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 abstract description 12
- 239000001263 FEMA 3042 Substances 0.000 abstract description 12
- LRBQNJMCXXYXIU-PPKXGCFTSA-N Penta-digallate-beta-D-glucose Natural products OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-PPKXGCFTSA-N 0.000 abstract description 12
- 229940033123 tannic acid Drugs 0.000 abstract description 12
- 235000015523 tannic acid Nutrition 0.000 abstract description 12
- 229920002258 tannic acid Polymers 0.000 abstract description 12
- 244000068988 Glycine max Species 0.000 abstract description 11
- 235000010469 Glycine max Nutrition 0.000 abstract description 11
- 108090000765 processed proteins & peptides Proteins 0.000 abstract description 11
- 239000003814 drug Substances 0.000 abstract description 8
- 239000000843 powder Substances 0.000 abstract description 6
- 235000021552 granulated sugar Nutrition 0.000 abstract description 5
- 229940079593 drug Drugs 0.000 abstract description 4
- 239000007864 aqueous solution Substances 0.000 abstract description 3
- 235000013305 food Nutrition 0.000 abstract description 3
- 239000000243 solution Substances 0.000 abstract description 3
- 230000035622 drinking Effects 0.000 abstract description 2
- 239000003795 chemical substances by application Substances 0.000 abstract 3
- 235000009508 confectionery Nutrition 0.000 abstract 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 abstract 1
- 235000020278 hot chocolate Nutrition 0.000 abstract 1
- 235000013355 food flavoring agent Nutrition 0.000 description 19
- 239000000796 flavoring agent Substances 0.000 description 18
- 244000299461 Theobroma cacao Species 0.000 description 15
- 235000019219 chocolate Nutrition 0.000 description 12
- 230000001953 sensory effect Effects 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 230000000694 effects Effects 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 238000003756 stirring Methods 0.000 description 9
- 235000009470 Theobroma cacao Nutrition 0.000 description 3
- 235000013402 health food Nutrition 0.000 description 3
- 102000004196 processed proteins & peptides Human genes 0.000 description 3
- 235000020357 syrup Nutrition 0.000 description 3
- 239000006188 syrup Substances 0.000 description 3
- 239000000679 carrageenan Substances 0.000 description 2
- 235000010418 carrageenan Nutrition 0.000 description 2
- 229920001525 carrageenan Polymers 0.000 description 2
- 229940113118 carrageenan Drugs 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- -1 granulated sugar Chemical class 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 235000019640 taste Nutrition 0.000 description 2
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 2
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- 108010011485 Aspartame Proteins 0.000 description 1
- 108010004032 Bromelains Proteins 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 229930091371 Fructose Natural products 0.000 description 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
- 239000005715 Fructose Substances 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 239000004365 Protease Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- UEDUENGHJMELGK-HYDKPPNVSA-N Stevioside Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@]12C(=C)C[C@@]3(C1)CC[C@@H]1[C@@](C)(CCC[C@]1([C@@H]3CC2)C)C(=O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O UEDUENGHJMELGK-HYDKPPNVSA-N 0.000 description 1
- 239000000605 aspartame Substances 0.000 description 1
- 235000010357 aspartame Nutrition 0.000 description 1
- IAOZJIPTCAWIRG-QWRGUYRKSA-N aspartame Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 IAOZJIPTCAWIRG-QWRGUYRKSA-N 0.000 description 1
- 229960003438 aspartame Drugs 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 235000019835 bromelain Nutrition 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 238000005538 encapsulation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000576 food coloring agent Substances 0.000 description 1
- 235000002864 food coloring agent Nutrition 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- 235000015203 fruit juice Nutrition 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 235000012907 honey Nutrition 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 229940069445 licorice extract Drugs 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 229960001855 mannitol Drugs 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 235000020124 milk-based beverage Nutrition 0.000 description 1
- 235000019204 saccharin Nutrition 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 229940081974 saccharin Drugs 0.000 description 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 229960002920 sorbitol Drugs 0.000 description 1
- 235000010356 sorbitol Nutrition 0.000 description 1
- 235000013322 soy milk Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 229940013618 stevioside Drugs 0.000 description 1
- OHHNJQXIOPOJSC-UHFFFAOYSA-N stevioside Natural products CC1(CCCC2(C)C3(C)CCC4(CC3(CCC12C)CC4=C)OC5OC(CO)C(O)C(O)C5OC6OC(CO)C(O)C(O)C6O)C(=O)OC7OC(CO)C(O)C(O)C7O OHHNJQXIOPOJSC-UHFFFAOYSA-N 0.000 description 1
- 235000019202 steviosides Nutrition 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 238000009495 sugar coating Methods 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
Landscapes
- Jellies, Jams, And Syrups (AREA)
- Medicinal Preparation (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は医薬品や健康食品等の中
に間々存在する非常に苦くて摂取しにくい物質の苦味を
低減させる方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for reducing the bitterness of very bitter substances that are often present in pharmaceuticals, health foods, etc. and are difficult to ingest.
【0002】0002
【従来の技術】「良薬は口に苦し」とはいうものの、ひ
どく苦い薬は飲みにくく、特にそれが粉末状であったり
すると幼小児や老人には「のどのつかえ」や「むせ」が
起きて服用に困難をきたすことが少なくない。これは最
近出まわっている健康食品でも同じ様に問題になってい
る。[Prior Art] Although it is said that ``good medicine tastes bitter,'' extremely bitter medicines are difficult to swallow, especially if they are in powder form, which can cause ``choking'' and ``choking'' in young children and the elderly. It is often difficult to take the medication. This is also a problem with the health foods that are on the market these days.
【0003】これらの苦味問題を出来るだけ緩和して、
苦味のある薬等の物質を摂取しやすくする工夫は従来か
ら種々とられてきた。その代表例が錠剤における糖衣や
剤型のカプセル化である。これらは確立された技術であ
って効果には問題がないが、周知のように工程が多く、
又設備にも多額の費用を要する。又、その他の代表的方
法にシロップ化があるが、シロップ化が困難な物質の場
合には採用できない。[0003] To alleviate these bitterness problems as much as possible,
Various efforts have been made to make it easier to ingest bitter-tasting substances such as medicines. Typical examples are sugar coating in tablets and encapsulation of dosage forms. These are established technologies and there are no problems with their effectiveness, but as is well known, there are many steps involved.
Also, the equipment requires a large amount of cost. Another typical method is to make a syrup, but it cannot be used if the substance is difficult to make into a syrup.
【0004】0004
【発明が解決しようとする課題】本発明は従来技術に比
べ、より簡便で経済的な苦味のある物質の苦味低減方法
を提供することを課題とするものである。SUMMARY OF THE INVENTION It is an object of the present invention to provide a method for reducing the bitterness of bitter substances that is simpler and more economical than the prior art.
【0005】[0005]
【課題を解決するための手段】本発明者は種々研究の結
果、ゲル化剤を用いてゼリー化し、且つそれに適切な味
付けをすることにより上記課題を解決できることを見出
し本発明を完成した。即ち本発明は、苦味のある物質に
ゲル化剤と味付け剤を添加し味付ゼリー状にすることを
特徴とする苦味低減方法を提供するものである。[Means for Solving the Problems] As a result of various studies, the present inventors have found that the above problems can be solved by making a jelly using a gelling agent and seasoning it appropriately, and have completed the present invention. That is, the present invention provides a method for reducing bitterness, which is characterized by adding a gelling agent and a seasoning agent to a bitter substance to make it into a flavored jelly.
【0006】本発明の方法によれば、苦味低減効果があ
る上に粉末状であるが故の飲みにくさも改善される。本
発明が対象とする苦味のある物質は、医薬品の中で苦味
が問題となるものであり、又、食品、例えば健康食品の
中で苦味があって摂取しにくい物質である。実施例では
タンニン酸、小柴胡湯及び大豆ペプチドの例を示すが、
これらに限定されないことは勿論である。[0006] According to the method of the present invention, not only is there an effect of reducing bitterness, but also the difficulty of drinking due to the powder form is improved. Bitter-tasting substances targeted by the present invention are those in pharmaceuticals whose bitterness is a problem, and substances in foods such as health foods that have a bitter taste and are difficult to ingest. In the examples, examples of tannic acid, Shosaikoto and soybean peptide are shown,
Of course, it is not limited to these.
【0007】本発明で用いるゲル化剤は寒天、ゼラチン
、κ‐カラギーナン等から選ばれる。これらのゲル化剤
を入手するには市販品を購入するのが簡便である。これ
らゲル化剤の使用量については、苦味物質がタンニン酸
である場合、その0.1g(50ml水溶液)当り、ま
た小柴胡湯の場合はその2.5g(50ml水溶液)当
り、さらに大豆ペプチドの場合はその50ml当り、寒
天(粉末)は0.1〜0.5g、ゼラチン(粉末)は1
.0〜2.5g、又、κ‐カラギーナンは0.2〜1.
0g、夫々に用いられる。The gelling agent used in the present invention is selected from agar, gelatin, κ-carrageenan and the like. It is easy to obtain these gelling agents by purchasing commercially available products. The amount of gelling agent used is per 0.1 g (50 ml aqueous solution) of tannic acid when the bitter substance is tannic acid, and per 2.5 g (50 ml aqueous solution) of soybean peptide in the case of Shosaikoto. 0.1 to 0.5 g of agar (powder) and 1 g of gelatin (powder) per 50 ml.
.. 0-2.5g, and κ-carrageenan is 0.2-1.
0g, respectively.
【0008】ゲル化剤の添加量を上記の範囲よりも低減
した場合、苦味軽減効果は低くなり、また、約15分で
ゼリー化しないこともある。逆に、添加量を増加させた
場合には、ゼリー配合剤が均一に溶解せず、溶解不良が
生じたり、ゼリーがかたくなり過ぎ食感が悪くなる。従
って、苦味軽減効果を有し、且つゼリー剤の溶解性が良
く、均一で、表面が平滑で、食感の比較的良いという効
果を有する上記の範囲が好ましい。[0008] If the amount of the gelling agent added is lower than the above range, the bitterness reducing effect will be lower and the gelatinization may not be made in about 15 minutes. On the other hand, if the amount added is increased, the jelly ingredients will not be dissolved uniformly, resulting in poor dissolution, or the jelly will become too hard, resulting in poor texture. Therefore, the above-mentioned range is preferable, which has the effect of reducing bitterness, and has the effect that the jelly has good solubility, is uniform, has a smooth surface, and has a relatively good texture.
【0009】本発明において用いられる味付剤はグラニ
ュー糖やココアといった呈味成分の他、必要に応じて香
料や色素も含まれる。このうち呈味成分としては、グラ
ニュー糖等の砂糖類、ブドウ糖、果糖、乳糖、麦芽糖、
水飴、蜂蜜、甘草エキス、ソルビット、マンニット、ス
テビオサイド、サッカリン、アスパルテーム等の甘味類
が主に用いられる他、ココア、コーヒー、濃縮果汁、乳
性飲料等の嗜好飲料類の添加も好ましい。これらのうち
グラニュー糖は分散剤としても有効であり、その添加に
よりゼリー配合剤の溶解性を向上せしめ、均一なゼリー
にするという優れた効果を有している。[0009] The flavoring agent used in the present invention includes flavoring ingredients such as granulated sugar and cocoa, as well as flavoring agents and pigments, if necessary. Among these, taste components include sugars such as granulated sugar, glucose, fructose, lactose, maltose,
Sweeteners such as starch syrup, honey, licorice extract, sorbitol, mannitol, stevioside, saccharin, and aspartame are mainly used, and it is also preferable to add preferred beverages such as cocoa, coffee, concentrated fruit juice, and milk drinks. Among these, granulated sugar is also effective as a dispersant, and its addition has the excellent effect of improving the solubility of the jelly formulation and making it a uniform jelly.
【0010】香料としては、パウダーチョコレートのよ
うに食品の着香料として認められているものならいずれ
も使用できる。また、色素も食品用着色料として認めら
れているものの中から選択して使用すれば良い。この味
付剤の配合の一例を示すと、グラニュー糖186.6重
量部、パウダードチョコレート8004(香料)3.0
g、SRチョコレート色NO2(色素)3.0g、ネッ
スルココアPMT16.0gの例があげられる。[0010] As the flavoring agent, any flavoring agent that is approved as a food flavoring agent, such as powdered chocolate, can be used. Furthermore, the coloring matter may be selected from among those approved as food coloring agents. An example of the blending of this flavoring agent is as follows: 186.6 parts by weight of granulated sugar, 3.0 parts by weight of powdered chocolate 8004 (flavoring)
Examples include: g, SR chocolate color NO2 (pigment) 3.0 g, and Nestl Cocoa PMT 16.0 g.
【0011】味付剤の使用量は、タンニン酸に対しては
その0.1g当り、又小柴胡湯の場合にはその2.5g
当り、さらに大豆ペプチドはその50ml当り夫々に5
.0〜14.0g、用いるのがよい。ゼリー化は、上記
したゲル化剤及び味付剤を苦味物質に混合し、水50m
l(大豆ペプチドは不要)を加えて、寒天の場合には9
0〜100℃、ゼラチンの場合には50〜60℃、カラ
ギーナンの場合には70〜80℃の湯にそれぞれ数分間
、攪拌下に温浴させて溶解した後、常温以下に冷却して
行なう。[0011] The amount of seasoning used is per 0.1 g of tannic acid, and 2.5 g of tannic acid in the case of Shosaikoto.
per 50ml of soybean peptides.
.. It is preferable to use 0 to 14.0 g. To make a jelly, mix the above-mentioned gelling agent and flavoring agent with a bitter substance and add 50ml of water.
1 (soybean peptide is unnecessary), and in the case of agar, add 9
The gelatin is dissolved in hot water at 0 to 100°C, 50 to 60°C in the case of gelatin, and 70 to 80°C in the case of carrageenan in a warm bath with stirring for several minutes, and then cooled to room temperature or below.
【0012】0012
【実施例】以下実施例で本発明を説明する。なお、実施
例中に示す官能テストはパネル人数8人(男4人、女4
人)で行い、評価は++(苦い)、+、±、−、−−(
全く苦味を感じない)で表わした。又、実施例で用いた
味付剤は表1の配合によるチョコレート味付剤である。[Examples] The present invention will be explained below with reference to Examples. In addition, the sensory test shown in the examples consisted of 8 panels (4 men, 4 women).
The evaluation was ++ (bitter), +, ±, −, −−(
No bitterness at all). Further, the flavoring agent used in the examples was a chocolate flavoring agent having the formulation shown in Table 1.
【0013】[0013]
【表1】[Table 1]
【0014】実施例1(タンニン酸の苦味低減)(1)
タンニン酸(岩井化学薬品製、以下同じ)0.05gを
水25mlに溶解する。これを官能テストの対照例とし
た。Example 1 (Reduction of bitterness of tannic acid) (1)
0.05 g of tannic acid (manufactured by Iwai Chemicals, same hereinafter) is dissolved in 25 ml of water. This was used as a control example for the sensory test.
【0015】(2)ゲル化剤を寒天にした場合タンニン
酸0.05gに粉末寒天(イナ寒天製、以下同じ)0.
25gとチョコレート味付剤(表1の場合のもの、以下
同じ)5.22gを加え、よく混合した後、水25ml
を加える。これを90〜100℃の温浴中、攪拌しなが
ら溶解せしめた後、冷蔵庫中で冷却しゼリー化した。こ
のものの官能テストの結果を表2に示す。(2) When using agar as the gelling agent, add 0.05 g of tannic acid to 0.05 g of powdered agar (manufactured by Ina Agar, the same applies hereinafter).
Add 25g and 5.22g of chocolate flavoring agent (from Table 1, the same applies below), mix well, and then add 25ml of water.
Add. This was dissolved in a hot bath at 90 to 100°C with stirring, and then cooled in a refrigerator to form a jelly. Table 2 shows the results of the sensory test for this product.
【0016】(3)ゲル化剤をゼラチンにした場合タン
ニン酸0.05gに粉末ゼラチン(ニッピ製、以下同じ
)1.25gとチョコレート味付剤5.22gを加え、
よく混合した後、水25mlを加える。これを50〜6
0℃の温浴中、攪拌しながら溶解せしめた後、冷蔵庫中
で冷却しゼリー化した。このものの官能テストの結果を
表2に示す。(3) When using gelatin as the gelling agent Add 1.25 g of powdered gelatin (manufactured by Nippi, the same applies hereinafter) and 5.22 g of chocolate flavoring agent to 0.05 g of tannic acid.
After mixing well, add 25 ml of water. This is 50-6
The mixture was dissolved in a 0°C hot bath with stirring, and then cooled in a refrigerator to form a jelly. Table 2 shows the results of the sensory test for this product.
【0017】(4)ゲル化剤をκ‐カラギーナンにした
場合
タンニン酸0.05gにκ‐カラギーナン(中央化成製
、以下同じ)0.38gとチョコレート味付剤5.22
gを加え、よく混合した後、水25mlを加える。これ
を70〜80℃の温浴中、攪拌しながら溶解せしめた後
、冷蔵庫中で冷却しゼリー化した。このものの官能テス
トの結果を表2に示す。(4) When using κ-carrageenan as the gelling agent: 0.05 g of tannic acid, 0.38 g of κ-carrageenan (manufactured by Chuo Kasei, the same applies hereinafter), and 5.22 g of chocolate flavoring agent.
g and mix well, then add 25 ml of water. This was dissolved in a hot bath at 70 to 80°C with stirring, and then cooled in a refrigerator to form a jelly. Table 2 shows the results of the sensory test for this product.
【0018】[0018]
【表2】[Table 2]
【0019】実施例2(小柴胡湯の苦味低減)(1)小
柴胡湯(ツムラ製、以下同じ)1.25gを水25ml
に溶解する。これを官能テストの対照例とした。Example 2 (reduction of bitterness of Shosaikoto) (1) 1.25g of Shosaikoto (manufactured by Tsumura, same hereinafter) in 25ml of water
dissolve in This was used as a control example for the sensory test.
【0020】(2)ゲル化剤を寒天にした場合小柴胡湯
1.25gに粉末寒天0.25gとチョコレート味付剤
5.22gを加え、よく混合した後、水25mlを加え
る。これを90〜100℃の温浴中、攪拌しながら溶解
せしめた後、冷蔵庫中で冷却しゼリー化した。
このものの官能テストの結果を表3に示す。(2) When agar is used as the gelling agent 0.25 g of powdered agar and 5.22 g of chocolate flavoring agent are added to 1.25 g of Shosaikoto, mixed well, and then 25 ml of water is added. This was dissolved in a hot bath at 90 to 100°C with stirring, and then cooled in a refrigerator to form a jelly. Table 3 shows the results of the sensory test for this product.
【0021】(3)ゲル化剤をゼラチンにした場合小柴
胡湯1.25gに粉末ゼラチン1.25gとチョコレー
ト味付剤5.22gを加え、よく混合した後、水25m
lを加える。これを50〜60℃の温浴中、攪拌しなが
ら溶解せしめた後、冷蔵庫中で冷却しゼリー化した。こ
のものの官能テストの結果を表3に示す。(3) When using gelatin as the gelling agent Add 1.25 g of powdered gelatin and 5.22 g of chocolate flavoring agent to 1.25 g of Shosaikoto, mix well, and add 25 ml of water.
Add l. This was dissolved in a hot bath at 50 to 60°C with stirring, and then cooled in a refrigerator to form a jelly. Table 3 shows the results of the sensory test for this product.
【0022】(4)ゲル化剤をκ‐カラギーナンにした
場合
小柴胡湯1.25gにκ‐カラギーナン0.38gとチ
ョコレート味付剤5.22gを加え、よく混合した後、
水25mlを加える。これを70〜80℃の温浴中、攪
拌しながら溶解せしめた後、冷蔵庫中で冷却しゼリー化
した。このものの官能テストの結果を表3に示す。(4) When using κ-carrageenan as the gelling agent Add 0.38 g of κ-carrageenan and 5.22 g of chocolate flavoring agent to 1.25 g of Shosaikoto and mix well.
Add 25ml of water. This was dissolved in a hot bath at 70 to 80°C with stirring, and then cooled in a refrigerator to form a jelly. Table 3 shows the results of the sensory test for this product.
【0023】[0023]
【表3】[Table 3]
【0024】実施例3(大豆ペプチドの苦味低減)大豆
ペプチドは、豆乳500mlを55℃、30分間インキ
ュベートし、それに0.25gの酵素液(半井化学製、
ブロメライン0.05%溶液)を加え、さらに55℃で
90分間インキュベートして調製した。
(1)この大豆ペプチド25mlを対照例とする。Example 3 (Reduction of Bitterness of Soybean Peptides) Soybean peptides were prepared by incubating 500ml of soymilk at 55°C for 30 minutes, and adding 0.25g of enzyme solution (manufactured by Hanui Chemical Co., Ltd.,
Bromelain 0.05% solution) was added thereto, and further incubated at 55°C for 90 minutes. (1) 25 ml of this soybean peptide is used as a control example.
【0025】(2)ゲル化剤を寒天にした場合大豆ペプ
チド25mlに粉末寒天0.25gとチョコレート味付
剤5.22gを加え、よく混合した寒天及び味付剤を9
0〜100℃の温浴中、攪拌しながら溶解せしめた後、
冷蔵庫中で冷却しゼリー化した。このものの官能テスト
の結果を表4に示す。(2) When using agar as the gelling agent Add 0.25 g of powdered agar and 5.22 g of chocolate flavoring agent to 25 ml of soybean peptide, and add 9 g of the well-mixed agar and flavoring agent.
After dissolving in a hot bath at 0 to 100°C with stirring,
It was cooled in a refrigerator and turned into jelly. Table 4 shows the results of the sensory test for this product.
【0026】(3)ゲル化剤をκ‐カラギーナンにした
場合
大豆ペプチド25mlにκ‐カラギーナン0.38gと
チョコレート味付剤5.22gを加え、よく混合したカ
ラギーナン及び味付剤を70〜80℃の温浴中、攪拌し
ながら溶解せしめた後、冷蔵庫中で冷却しゼリー化した
。このものの官能テストの結果を表4に示す。(3) When using κ-carrageenan as the gelling agent Add 0.38 g of κ-carrageenan and 5.22 g of chocolate flavoring agent to 25 ml of soybean peptide, and heat the well-mixed carrageenan and flavoring agent at 70 to 80°C. The mixture was dissolved in a hot bath with stirring, and then cooled in a refrigerator to form a jelly. Table 4 shows the results of the sensory test for this product.
【0027】[0027]
【表4】[Table 4]
【0027】表2〜表4の官能テストの結果にみるよう
に、全員苦味を感じていた苦味物質が本発明の味付ゼリ
ーにすることによって、ほとんど苦味を感じないように
なることがわかる。このように効果のあがった理由は確
認されていないが、苦味物質が口中に広まることなく摂
取が可能となったこととマスキング効果が相乗されたこ
とによるものと考えている。As can be seen from the results of the sensory tests in Tables 2 to 4, it can be seen that the bitter substances that all of the subjects felt were bitter tasted almost no longer when made into the flavored jelly of the present invention. Although the reason for this increased effect has not been confirmed, it is believed that this is due to the synergistic effect of the masking effect and the ability to ingest the bitter substance without it spreading into the mouth.
【0028】[0028]
【発明の効果】本発明には、苦くて服用或いは摂取がし
にくかった物質の苦味が大巾に軽減されるという効果と
ともに、それが粉末状である場合「のどのつかえ」や「
むせ」が起きて、幼小児、老人等にとって摂取が極めて
困難であったものを容易にするという優れた効果がある
。また、味付を工夫すれば嗜好品化することも可能であ
る。[Effects of the Invention] The present invention has the effect of greatly reducing the bitterness of substances that are bitter and difficult to take or ingest, and also has the effect of greatly reducing the bitterness of substances that are bitter and difficult to take or ingest.
It has the excellent effect of making it easier for young children, the elderly, etc. to ingest foods that would otherwise cause choking. In addition, it is possible to make it a luxury item by adjusting the seasoning.
Claims (2)
を添加し味付ゼリー状にすることを特徴とする苦味低減
方法。1. A method for reducing bitterness, which comprises adding a gelling agent and a seasoning agent to a bitter substance to make it into a flavored jelly.
ギーナンから選ばれたものである請求項1記載の苦味低
減方法。2. The method for reducing bitterness according to claim 1, wherein the gelling agent is selected from agar, gelatin, and κ-carrageenan.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3148077A JP2508555B2 (en) | 1991-05-24 | 1991-05-24 | Bitterness reduction method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3148077A JP2508555B2 (en) | 1991-05-24 | 1991-05-24 | Bitterness reduction method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04346937A true JPH04346937A (en) | 1992-12-02 |
JP2508555B2 JP2508555B2 (en) | 1996-06-19 |
Family
ID=15444710
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3148077A Expired - Lifetime JP2508555B2 (en) | 1991-05-24 | 1991-05-24 | Bitterness reduction method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2508555B2 (en) |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998043675A1 (en) * | 1997-03-28 | 1998-10-08 | Eisai Co., Ltd. | Oral pharmaceutical preparations decreased in bitterness by masking |
JPH11322624A (en) * | 1998-05-06 | 1999-11-24 | Ina Food Ind Co Ltd | Chinese medicine/crude medicine preparation to be prepared in time of use |
JP2001226293A (en) * | 2000-02-17 | 2001-08-21 | Kotaro Kanpo Seiyaku Kk | Taking assisting agent |
JP2004059503A (en) * | 2002-07-29 | 2004-02-26 | Teikoku Kanpo Seiyaku Kk | Chinese medicine-based jellylike pharmaceutical composition |
WO2006001344A1 (en) * | 2004-06-24 | 2006-01-05 | Sanwa Kagaku Kenkyusho Co., Ltd. | Isosorbide-containing jelly preparation |
JP2008007470A (en) * | 2006-06-30 | 2008-01-17 | Nippon Zoki Pharmaceut Co Ltd | Method for masking iron smell and taste |
JP2008044870A (en) * | 2006-08-11 | 2008-02-28 | Elmed Eisai Kk | Pharmaceutical composition and its production method |
WO2008084533A1 (en) * | 2007-01-10 | 2008-07-17 | Kowa Co., Ltd. | Therapeutic agent for meniere’s disease |
WO2009047859A1 (en) * | 2007-10-12 | 2009-04-16 | Ryukakusan Co. Ltd. | Granular jelly beverage for medication and process for producing the same |
JP2010042021A (en) * | 1998-10-28 | 2010-02-25 | Sanei Gen Ffi Inc | Compositions containing sucralose and application thereof |
US7727548B2 (en) | 2000-03-01 | 2010-06-01 | Eisai R&D Management Co., Ltd. | Rapidly disintegrable tablet containing polyvinyl alcohol |
JP2013021948A (en) * | 2011-07-19 | 2013-02-04 | Ina Food Industry Co Ltd | Polyphenol agar conjugate |
JP2013199439A (en) * | 2012-03-23 | 2013-10-03 | Kyorin Pharmaceutical Co Ltd | Taste masking method |
CN109965018A (en) * | 2017-12-28 | 2019-07-05 | 长沙理工大学 | Production method of bitter-free red bean and coix seed beverage |
CN111712139A (en) * | 2018-02-09 | 2020-09-25 | 三得利控股株式会社 | Liquid oral composition containing collagen peptide and method for improving flavor of liquid oral composition containing collagen peptide |
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JPS5697220A (en) * | 1979-12-28 | 1981-08-05 | Shinichi Hoshino | Preliminarily dosed medicine preparation |
JPS6049751A (en) * | 1983-08-29 | 1985-03-19 | Ajinomoto Co Inc | Food composition |
JPH0262831A (en) * | 1988-08-26 | 1990-03-02 | Fuji Kapuseru Kk | Soft gel |
-
1991
- 1991-05-24 JP JP3148077A patent/JP2508555B2/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
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JPS5697220A (en) * | 1979-12-28 | 1981-08-05 | Shinichi Hoshino | Preliminarily dosed medicine preparation |
JPS6049751A (en) * | 1983-08-29 | 1985-03-19 | Ajinomoto Co Inc | Food composition |
JPH0262831A (en) * | 1988-08-26 | 1990-03-02 | Fuji Kapuseru Kk | Soft gel |
Cited By (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998043675A1 (en) * | 1997-03-28 | 1998-10-08 | Eisai Co., Ltd. | Oral pharmaceutical preparations decreased in bitterness by masking |
US7727552B1 (en) | 1997-03-28 | 2010-06-01 | Eisai R&D Management Co., Ltd. | Oral pharmaceutical preparations decreased in bitterness by masking |
JPH11322624A (en) * | 1998-05-06 | 1999-11-24 | Ina Food Ind Co Ltd | Chinese medicine/crude medicine preparation to be prepared in time of use |
JP2010042021A (en) * | 1998-10-28 | 2010-02-25 | Sanei Gen Ffi Inc | Compositions containing sucralose and application thereof |
JP2001226293A (en) * | 2000-02-17 | 2001-08-21 | Kotaro Kanpo Seiyaku Kk | Taking assisting agent |
US8263123B2 (en) | 2000-03-01 | 2012-09-11 | Eisai R&D Management Co., Ltd. | Rapidly disintegrating tablet containing polyvinyl alcohol |
US7727548B2 (en) | 2000-03-01 | 2010-06-01 | Eisai R&D Management Co., Ltd. | Rapidly disintegrable tablet containing polyvinyl alcohol |
EP1541130A4 (en) * | 2002-07-29 | 2009-01-07 | Teikoku Kanpo Seiyaku Co Ltd | Chinese herbal medical composition in the form of jelly |
US9364428B2 (en) | 2002-07-29 | 2016-06-14 | Teikoku Seiyaku Co., Ltd. | Herb medicine composition in the form of jelly |
EP1541130A1 (en) * | 2002-07-29 | 2005-06-15 | Teikoku Kanpo Seiyaku Co., Ltd. | Chinese herb medicine composition in the form of jelly |
JP2004059503A (en) * | 2002-07-29 | 2004-02-26 | Teikoku Kanpo Seiyaku Kk | Chinese medicine-based jellylike pharmaceutical composition |
WO2006001344A1 (en) * | 2004-06-24 | 2006-01-05 | Sanwa Kagaku Kenkyusho Co., Ltd. | Isosorbide-containing jelly preparation |
JP2008007470A (en) * | 2006-06-30 | 2008-01-17 | Nippon Zoki Pharmaceut Co Ltd | Method for masking iron smell and taste |
JP2008044870A (en) * | 2006-08-11 | 2008-02-28 | Elmed Eisai Kk | Pharmaceutical composition and its production method |
WO2008084533A1 (en) * | 2007-01-10 | 2008-07-17 | Kowa Co., Ltd. | Therapeutic agent for meniere’s disease |
WO2009047859A1 (en) * | 2007-10-12 | 2009-04-16 | Ryukakusan Co. Ltd. | Granular jelly beverage for medication and process for producing the same |
US9084741B2 (en) | 2007-10-12 | 2015-07-21 | Ryukakusan Co., Ltd. | Granular jelly beverage for medication and process for producing the same |
JP2013021948A (en) * | 2011-07-19 | 2013-02-04 | Ina Food Industry Co Ltd | Polyphenol agar conjugate |
JP2013199439A (en) * | 2012-03-23 | 2013-10-03 | Kyorin Pharmaceutical Co Ltd | Taste masking method |
CN109965018A (en) * | 2017-12-28 | 2019-07-05 | 长沙理工大学 | Production method of bitter-free red bean and coix seed beverage |
CN109965018B (en) * | 2017-12-28 | 2022-03-18 | 长沙理工大学 | Production method of bitter-free red bean and coix seed beverage |
CN111712139A (en) * | 2018-02-09 | 2020-09-25 | 三得利控股株式会社 | Liquid oral composition containing collagen peptide and method for improving flavor of liquid oral composition containing collagen peptide |
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