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JP2633633B2 - Seasoning preparation and method for producing the same - Google Patents
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JP2633633B2 - Seasoning preparation and method for producing the same - Google Patents

Seasoning preparation and method for producing the same

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Publication number
JP2633633B2
JP2633633B2 JP63178838A JP17883888A JP2633633B2 JP 2633633 B2 JP2633633 B2 JP 2633633B2 JP 63178838 A JP63178838 A JP 63178838A JP 17883888 A JP17883888 A JP 17883888A JP 2633633 B2 JP2633633 B2 JP 2633633B2
Authority
JP
Japan
Prior art keywords
seasoning
preparation
gum
tablet
present
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
JP63178838A
Other languages
Japanese (ja)
Other versions
JPH01104138A (en
Inventor
廣治 松本
文雄 四塚
武 豊田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Takeda Pharmaceutical Co Ltd
Original Assignee
Takeda Chemical Industries Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Takeda Chemical Industries Ltd filed Critical Takeda Chemical Industries Ltd
Priority to JP63178838A priority Critical patent/JP2633633B2/en
Publication of JPH01104138A publication Critical patent/JPH01104138A/en
Application granted granted Critical
Publication of JP2633633B2 publication Critical patent/JP2633633B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Description

【発明の詳細な説明】 産業上の利用分野 本発明は即溶性でかつ澄明に溶解する調味料製剤およ
びその製造法に関するものである。
Description: FIELD OF THE INVENTION The present invention relates to a seasoning preparation which is rapidly soluble and dissolves clearly and a method for producing the same.

従来の技術 高甘味度甘味料や旨味調味料は単体では甘味や旨味が
つよすぎるためそのままで使用されることは少なく、計
量の便や粉立ちを防ぐなど、取扱いやすくするために、
顆粒やフレーム、錠剤などの製剤にすることが多い。こ
のような製剤を作る際、通常は賦形剤として糖類、糖ア
ルコール類,でん粉加水分解物(例えばデキストリン
類),多糖類,たん白,たん白質加水分解物などが使用
されるが、これらの賦形剤自体が水溶性で溶解性が大き
いため、水中で団粒化したり、表面だけが濡れて、完全
に溶解するまでにはかなりの時間を要する欠点を有し、
成型物の形状や大きさに限界があった。
Conventional technology High-intensity sweeteners and umami seasonings are rarely used as they are because the sweetness and umami are too crisp on their own.
Often, it is formulated into granules, frames, tablets, etc. In making such preparations, saccharides, sugar alcohols, starch hydrolysates (eg, dextrins), polysaccharides, proteins, protein hydrolysates, and the like are usually used as excipients. Since the excipient itself is water-soluble and highly soluble, it has the drawback that it takes a considerable amount of time to aggregate in water or wet only on the surface and completely dissolve,
There were limitations on the shape and size of the molded product.

このような問題を解決するために、錠剤には通常、崩
壊剤を添加して成形物をすみやかに崩壊させることが行
なわれている。崩壊剤としてカルボキシメチルセルロー
スのカルシウム塩およびナトリウム塩、デンプングリコ
ール酸ナトリウム,デンプンリ酸エステルナトリウム,
メチルセルロースおよびこれらの誘導体、結晶セルロー
ス,でん粉およびその熱処理物などが知られている。
In order to solve such a problem, a tablet is usually added with a disintegrant to quickly disintegrate the molded product. Calcium and sodium salts of carboxymethylcellulose as disintegrants, sodium starch glycolate, sodium starch acrylate,
Methyl cellulose and derivatives thereof, crystalline cellulose, starch and heat-treated products thereof are known.

しかし、カルボキシメチルセルロース塩類やデンプン
グリコール酸ナトリウム,デンプンリン酸エステルナト
リウム,メチルセルロースなどの食品添加物を甘味料、
調味料のような食品用の崩壊剤として効果が発揮できる
レベルまで添加することは食品衛生法上で認められてい
ないだけではなく、食品としても好ましいものではな
い。
However, food additives such as carboxymethylcellulose salts, sodium starch glycolate, sodium starch phosphate, methylcellulose,
Addition to a level that can exert an effect as a food disintegrant such as a seasoning is not only not recognized under the Food Sanitation Law, but is not preferable as a food.

発明が解決しようとする課題 従来から使用されている天然物としての崩壊剤には結
晶セルロースやでん粉、その他糊料が知られているが、
これらを甘味料や調味料の崩壊剤として用いた場合、崩
壊力が弱く、さらに崩壊後に濁りや沈澱物、浮遊物など
の不溶物が残り、使用した食品の外観を著しく損ない、
特に卓上用甘味料や卓上用調味料の場合外観上好ましい
ものではない。
Problems to be Solved by the Invention Conventionally used disintegrants as natural products include crystalline cellulose, starch, and other pastes,
When these are used as disintegrants for sweeteners and seasonings, the disintegration power is weak, and after disintegration, insolubles such as turbidity, precipitates, and suspended matter remain, significantly impairing the appearance of the food used,
Particularly, in the case of a tabletop sweetener or a tabletop seasoning, it is not preferable in appearance.

課題を解決するための手段 上記のような状況に鑑み、本発明者らは種々検討した
結果、特定の天然物質由来の高分子物質を崩壊剤とし
て、さらに特定の糖類等の中から選ばれた1種以上の賦
形剤と調味料を組み合わすことにより速やかに崩壊し、
しかも不溶物を全く生じない調味料製剤が得られること
を見出し本発明を完成した。
Means for Solving the Problems In view of the above situation, the present inventors have conducted various studies, and as a disintegrant, a polymer substance derived from a specific natural substance, further selected from among specific saccharides and the like. Disintegrate quickly by combining one or more excipients and seasonings,
In addition, they have found that a seasoning preparation which does not produce any insoluble matter can be obtained, and have completed the present invention.

すなわち本発明は、(1)調味料および、カラギーナ
ン,キサンタンガム,タラガムおよびローカストビーン
ガムのうち少なくとも1種ならびに、ブドウ糖,乳糖,
ラフィノース,パラチノース、グリシンおよびアラニン
のうち少なくとも1種を含有してなる調味料製剤、およ
び、(2)調味料および、カラギーナン,キサンタンガ
ム,タラガムおよびローカストビーンガムのうち少なく
とも1種ならびに、ブドウ糖,乳糖,ラフィノース,パ
ラチノース、グリシンおよびアラニンのうち少なくとも
1種を配合した後、成型することを特徴とする調味料製
剤の製造法に関するものである。
That is, the present invention relates to (1) a seasoning, at least one of carrageenan, xanthan gum, cod gum and locust bean gum, and glucose, lactose,
A seasoning preparation containing at least one of raffinose, palatinose, glycine and alanine, and (2) a seasoning and at least one of carrageenan, xanthan gum, tara gum and locust bean gum, and glucose, lactose, The present invention relates to a method for producing a seasoning preparation, which comprises molding at least one of raffinose, palatinose, glycine and alanine and then molding.

本発明で用いられる調味料としては、甘味料およびう
ま味調味料が好ましく、該甘味料としては、例えばアス
パルテーム,サッカリンナトリウム,アセスルファムK,
シュクラロース,アリテーム等の合成甘味料およびステ
ビオサイド,α−グリコシルステビオサイド,レバウデ
ィオサイド,グリチルリチン,ソーマチン等の天然甘味
料などの高甘味度甘味料が挙げられる。また該うま味調
味料としては、例えばL−グルタミン酸,L−アスパラギ
ン酸,5′−リボヌクレオチド,5′−イノシン酸,5′−グ
アニル酸,コハク酸等の各ナトリウム,カリウム,アン
モニウム,カルシウム,マグネシウム塩などが挙げられ
る。
As the seasonings used in the present invention, sweeteners and umami seasonings are preferable. Examples of the sweeteners include aspartame, saccharin sodium, acesulfame K,
Synthetic sweeteners such as sucralose and alitame, and high-intensity sweeteners such as natural sweeteners such as stevioside, α-glycosylstebioside, rebaudioside, glycyrrhizin, thaumatin and the like can be mentioned. Examples of the umami seasoning include sodium, potassium, ammonium, calcium, and magnesium such as L-glutamic acid, L-aspartic acid, 5'-ribonucleotide, 5'-inosinic acid, 5'-guanylic acid, and succinic acid. And the like.

これら甘味料、うま味調味料は単独で用いてもよい
し、1種以上を組合わせてもよく該調味料の製剤中に占
める割合は調味料の種類により異なるが、甘味料の場合
は、一般に約0.02〜50重量%,好ましくは約2〜50重量
%,うま味調味料の場合は一般に約0.5〜80重量%,好
ましくは約10〜80重量%である。
These sweeteners and umami seasonings may be used alone or in combination of one or more.The proportion of the seasonings in the preparation differs depending on the type of the seasonings. It is about 0.02 to 50% by weight, preferably about 2 to 50% by weight, and in the case of umami seasonings it is generally about 0.5 to 80% by weight, preferably about 10 to 80% by weight.

前記カラギーナン,キサンタンガム,タラガムおよび
ローカストビーンガムは、本発明製剤において一般に崩
壊剤として働き、本発明製剤においては、これらのうち
少なくとも1種以上を約0.1〜10重量%、とりわけ約1
〜5重量%を配合することが好ましい。これらの成分は
冷水あるいは熱水により容易に膨潤して成形物を崩壊
し、澄明に溶解するため、煮込り、沈澱、浮遊物などの
問題は全くない。
The carrageenan, xanthan gum, cod gum and locust bean gum generally function as disintegrants in the preparation of the present invention, and in the preparation of the present invention, at least one or more of them is used in an amount of about 0.1 to 10% by weight, especially about 1%.
It is preferable to mix 〜5% by weight. Since these components easily swell with cold or hot water to disintegrate the molded product and dissolve clearly, there is no problem such as boiling, sedimentation or suspended matter.

また、ブドウ糖,乳糖,ラフィノース,パラニノー
ス,グリシンおよびアラニンは、本発明製剤において一
般に賦形剤として働き、本発明製剤においてはこれらの
うち少なくとも1種以上を用いるが、製剤中に占めるそ
の割合は、前記調味料および崩壊剤成分の量比により任
意に選択されるが一般に約10〜90重量%が好ましい。
In addition, glucose, lactose, raffinose, paraninose, glycine and alanine generally function as excipients in the preparation of the present invention, and at least one or more of these are used in the preparation of the present invention. It is arbitrarily selected depending on the ratio of the seasoning and the disintegrant component, but generally about 10 to 90% by weight is preferred.

本発明の製剤においては必要に応じてさらに滑沢剤を
配合してもよく溶解後の澄明性の点からバリン,ロイシ
ン,イソロイシン,乳酸カルシウムなどを用いるのが好
ましい。さらに他の呈味成分(例、クエン酸,酒石酸,
リンゴ酸,食塩など),風味成分(例、コーヒー,ココ
ア,ミルク,ミントの各フレーバーの他植物性各種香
料、ハーブ香辛料など)、色素(例、β−カロチン,ク
ロロフイル,モナスカスなど)等も適宜配合してもよ
い。
In the preparation of the present invention, a lubricant may be further added as necessary, and valine, leucine, isoleucine, calcium lactate and the like are preferably used from the viewpoint of clarity after dissolution. Still other taste components (eg, citric acid, tartaric acid,
Malic acid, salt, etc.), flavor components (eg, coffee, cocoa, milk, mint, other vegetable flavors, herb spices, etc.), pigments (eg, β-carotene, chlorophyll, monascus, etc.), etc. You may mix.

次に本発明の製剤の製造法について述べる。本発明の
製剤は、上記各成分を任意の順序で混合した後、常法に
従って成型することにより得られる。該成型法としては
例えば、押出造粒法,流動層造粒法,圧延造粒法(乾式
造粒法),直接打錠法,スラッグ打錠法,湿式錠剤法な
どが挙げられる。
Next, a method for producing the preparation of the present invention will be described. The preparation of the present invention can be obtained by mixing the above components in an arbitrary order and then molding the mixture according to a conventional method. Examples of the molding method include an extrusion granulation method, a fluidized bed granulation method, a roll granulation method (dry granulation method), a direct tableting method, a slug tableting method, a wet tablet method and the like.

本発明においては崩壊剤の効果を高めるために、でき
るだけ水の使用量は少ない方が好ましく、従って圧延造
粒法や直接打錠法がとりわけ望ましい。また、打錠する
ために混合する各成分の粒度は約80メッシュ以下である
ことが好ましい。
In the present invention, in order to enhance the effect of the disintegrant, it is preferable to use as little water as possible. Therefore, the rolling granulation method and the direct tableting method are particularly desirable. Further, the particle size of each component to be mixed for tableting is preferably about 80 mesh or less.

得られる製剤の大きさおよび形は特に限定されない
が、たとえば顆粒、錠剤,キューブなどの剤型が特に好
ましい。
The size and shape of the obtained preparation are not particularly limited, but dosage forms such as granules, tablets and cubes are particularly preferred.

また、該製剤の硬度は、5Kg/cm2以下であることが好
ましい。
The hardness of the preparation is preferably 5 kg / cm 2 or less.

実施例 以下に実験例、実施例を挙げて本発明をさらに詳細に
説明する。なお、以下に用いるパーセント(%)は重量
パーセントを示すものとする。
Examples Hereinafter, the present invention will be described in more detail with reference to Experimental Examples and Examples. The percentages (%) used below indicate percent by weight.

実験例1 α−無水乳糖60%,アスパルテーム30%,L−バリン8
%,崩壊剤2%の割合で第1表に示す各種崩壊剤を用い
た錠剤(直径6mm,重量60mg)を作り崩壊速度、不溶物の
有無について比較検討した。
Experimental Example 1 α-anhydrolactose 60%, aspartame 30%, L-valine 8
Tablets (diameter 6 mm, weight 60 mg) were prepared using various disintegrants shown in Table 1 at a ratio of 2% and disintegrant 2%, and the disintegration rate and the presence or absence of insolubles were compared and examined.

打錠には打錠成型機CR10型(マシーナ社製)を用いて
直打法で行ない、得られた錠剤の硬度は2.0〜4.0Kg/cm2
になるよう調整した。
The tableting was performed by a direct compression method using a tableting molding machine CR10 (manufactured by Masina), and the hardness of the obtained tablet was 2.0 to 4.0 kg / cm 2.
It was adjusted to become.

なお崩壊速度は100mlの水(25℃)又は湯(60℃)を1
00mlのビーカーに入れ錠剤1錠を投入したのち、静置
し、錠剤が細粒にまで完全に崩壊するまでの時間(秒)
を測定した。
The disintegration rate is 100 ml of water (25 ° C) or hot water (60 ° C).
After putting one tablet in a beaker of 00 ml and allowing it to stand, the time until the tablet completely disintegrates into fine granules (seconds)
Was measured.

実験例2 賦形剤60%,アスパルテーム30%,L−バリン8%,カ
ラギーナン(ミルクゲルタイプ)2%の割合で各種賦形
剤を用いた錠剤をつくり、崩壊速度について検討した。
結果を第2表に示す。なお錠剤の大きさ、製造方法およ
び崩壊速度の測定は実験例1に準じた。
Experimental Example 2 Tablets were prepared using various excipients at a ratio of excipient 60%, aspartame 30%, L-valine 8%, carrageenan (milk gel type) 2%, and the disintegration rate was examined.
The results are shown in Table 2. In addition, the measurement of the tablet size, the manufacturing method, and the disintegration rate conformed to Experimental Example 1.

実験例3 キサンタンガムの割合を第3表のように変え、アセス
ファムK30%,L−ロイシン6%,残りの成分を乳糖(結
晶)で調製した錠剤をつくり、崩壊性を検討した。
Experimental Example 3 Tablets were prepared in which the ratio of xanthan gum was changed as shown in Table 3 and Acesfam K 30%, L-leucine 6%, and the remaining components were made from lactose (crystal), and the disintegration was examined.

錠剤の大きさ、製造方法および崩壊速度の測定は実験
例1に準じた。結果を第3表に示す。
The measurement of the tablet size, the production method and the disintegration rate were in accordance with Experimental Example 1. The results are shown in Table 3.

実施例1 アスパルテーム700g,カラギーナン(水ゲルタイプ)4
0g,乳糖(結晶)1160g,L−ロイシン100gをマイクロスピ
ードミキサー(宝工機(株)製、MS 5型)にて混合し
(1500rpm,1分間)、90%エタノール溶液100mlを加え加
湿した。
Example 1 700 g of aspartame, carrageenan (water gel type) 4
0 g, lactose (crystal) 1160 g, and L-leucine 100 g were mixed using a micro speed mixer (manufactured by Takara Machine Co., Ltd., MS 5) (1500 rpm, 1 minute), and 100 ml of a 90% ethanol solution was added and humidified.

ついでローラーコンパクター(フロイント産業(株)
製、モデルMINI)で圧延した(ロール回転数5rpm,処理
量2Kg/Hr,ロール圧800〜1500Kg/cm2)のち、パワーミル
(昭和化学機械工作所製)を用いて整粒し、16メッシュ
ないし8メッシュの顆粒品(A)1300gを得た。
Roller compactor (Freund Sangyo Co., Ltd.)
(Model: MINI), rolled (roll rotation speed 5 rpm, processing amount 2 kg / hr, roll pressure 800-1500 kg / cm 2 ), and then sized using a power mill (manufactured by Showa Chemical Machinery Co., Ltd.). 1300 g of an 8-mesh granule (A) was obtained.

対照としてアスパルテーム700g,乳糖(結晶)1200g,L
−ロイシン100gを同様に処理して顆粒品(B)を1350g
得た。
Aspartame 700g, lactose (crystal) 1200g, L
-Treat 100 g of leucine in the same way to obtain 1350 g of granule (B)
Obtained.

上記で得られた顆粒2gを25℃の水100mlを入れたビー
カーに入れ、崩壊時間を測定した結果、(A)は16秒で
崩壊分散して澄明な溶液になったが、(B)は水中で塊
りになり、表面した溶解せず、顆粒全体が溶解するには
撹拌を必要とし、本発明の顆粒の方が明らかにすぐれて
いた。
2 g of the granules obtained above was placed in a beaker containing 100 ml of water at 25 ° C., and the disintegration time was measured. As a result, (A) was disintegrated and dispersed in 16 seconds to give a clear solution, but (B) was The granules of the present invention were agglomerated in water, did not dissolve on the surface, required stirring to dissolve the whole granules, and the granules of the present invention were clearly superior.

実施例2 α−グルコシルステビオサイド250g,ブドウ糖690g,L
−ロイシン40g,ローカストビーンガム20gを用いて実験
例1の方法に準じて錠剤(直径6mm,重量60mg)を製造し
た。
Example 2 250 g of α-glucosyl stevioside, 690 g of glucose, L
Tablets (diameter 6 mm, weight 60 mg) were produced according to the method of Experimental Example 1 using 40 g of leucine and 20 g of locust bean gum.

本錠剤を25℃の水100mlに投入し、実験例1の方法に
従って崩壊速度を測定した結果、12秒で崩壊分散し澄明
に溶解した。
This tablet was put into 100 ml of water at 25 ° C., and the disintegration rate was measured in accordance with the method of Experimental Example 1. As a result, the tablet was disintegrated and dispersed in 12 seconds and dissolved completely.

実施例3 リボタイド(5′−リボヌクレオチドナトリウム,武
田薬品工業製)50g,L−グルタミン酸ナトリウム200g,L
−ロイシン50g,カラギーナン(水ゲルタイプ)30g,DL−
アラニン670gを用いて実験例1の方法に準じて、直径10
mm,重さ100mgの錠剤を得た。
Example 3 50 g of ribotide (sodium 5'-ribonucleotide, manufactured by Takeda Pharmaceutical Co., Ltd.), 200 g of sodium L-glutamate, L
−Leucine 50g, Carrageenan (water gel type) 30g, DL−
Using 670 g of alanine, a diameter of 10
A tablet weighing 100 mm in mm was obtained.

本錠剤を60℃の湯200mlに投入し、実験例1の方法に
従って崩壊速度を測定した結果5秒で崩壊し、30秒で完
全に溶解した。
The tablet was poured into 200 ml of hot water at 60 ° C., and the disintegration rate was measured according to the method of Experimental Example 1. As a result, the tablet disintegrated in 5 seconds and completely dissolved in 30 seconds.

実施例4 アスパルテーム240g,結晶乳糖685g,L−バリン60g,カ
ラギーナン10g,キサンタンガン(「オルノー X−1」
武田薬品工業製)5gを用いて実験例1の方法に準じて大
きさ4.0mm×4.0mm×4.0mm,重量75mgのキューブ型錠剤を
得た。本錠剤を60℃で紅茶150mlに投入したところ、ス
プーンで軽くかきまぜただけで30秒で完全溶解した。
Example 4 240 g of aspartame, 685 g of crystalline lactose, 60 g of L-valine,
Laginan 10g, xanthan ("Ornaut X-1 "
Using Takeda Pharmaceutical Co., Ltd.) 5 g and large according to the method of Experimental Example 1.
Cube tablets with a size of 4.0 mm × 4.0 mm × 4.0 mm and a weight of 75 mg
Obtained. This tablet was added to 150 ml of black tea at 60 ° C.
The mixture was completely dissolved in 30 seconds by gently stirring with a poon.

実施例5 アセスファムK80g,グリシン320g,DL−アラニン500g,L
−ロイシン80g,カラギーナン20gを用いて、実験例1の
方法に準じて大きさ13.0mm×13.0mm×1.0mm,200mgの錠
剤を得た。本品を4℃の水200mlに投入し、溶解時間を
測定したところ、投入直後に錠剤は完全に崩壊し、45秒
で完全溶解した。
Example 5 Acesfam K80g, glycine 320g, DL-alanine 500g, L
Using 80 g of leucine and 20 g of carrageenan, tablets of size 13.0 mm × 13.0 mm × 1.0 mm, 200 mg were obtained according to the method of Experimental Example 1. The product was put into 200 ml of water at 4 ° C., and the dissolution time was measured. As a result, the tablet completely disintegrated immediately after the addition, and was completely dissolved in 45 seconds.

発明の効果 本発明の調味料製剤は、即溶性でしかも澄明に溶解す
るので卓上用の調味料として有利に用いられる。
Effect of the Invention The seasoning preparation of the present invention is readily soluble and dissolves clearly, so that it is advantageously used as a tabletop seasoning.

Claims (4)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】調味料および、カラギーナン,キサンタン
ガム,タラガムおよびローカストビーンガムのうち少な
くとも1種ならびに、ブドウ糖,乳糖,ラフィノース,
パラチノース、グリシンおよびアラニンのうち少なくと
も1種を含有してなる調味料製剤。
1. A seasoning and at least one of carrageenan, xanthan gum, tara gum and locust bean gum, and glucose, lactose, raffinose,
A seasoning preparation comprising at least one of palatinose, glycine and alanine.
【請求項2】該調味料が甘味料である特許請求の範囲第
1項記載の調味料製剤。
2. The seasoning preparation according to claim 1, wherein said seasoning is a sweetener.
【請求項3】該調味料がうま味調味料である特許請求の
範囲第1項記載の調味料製剤。
3. The seasoning preparation according to claim 1, wherein the seasoning is an umami seasoning.
【請求項4】調味料および、カラギーナン,キサンタン
ガム,タラガムおよびローカストビーンガムのうち少な
くとも1種ならびに、ブドウ糖,乳糖,ラフィノース,
パラチノース、グリシンおよびアラニンのうち少なくと
も1種を配合した後、成型することを特徴とする調味料
製剤の製造法。
4. A seasoning and at least one of carrageenan, xanthan gum, cod gum and locust bean gum, and glucose, lactose, raffinose,
A method for producing a seasoning preparation, comprising mixing at least one of palatinose, glycine and alanine and then molding.
JP63178838A 1987-07-21 1988-07-18 Seasoning preparation and method for producing the same Expired - Fee Related JP2633633B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63178838A JP2633633B2 (en) 1987-07-21 1988-07-18 Seasoning preparation and method for producing the same

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP18139487 1987-07-21
JP62-181394 1987-07-21
JP63178838A JP2633633B2 (en) 1987-07-21 1988-07-18 Seasoning preparation and method for producing the same

Publications (2)

Publication Number Publication Date
JPH01104138A JPH01104138A (en) 1989-04-21
JP2633633B2 true JP2633633B2 (en) 1997-07-23

Family

ID=26498894

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP2633633B2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100404883B1 (en) * 1999-12-13 2003-11-10 주식회사 엘지화학 Polymer electrolytes for electrochemical device
JP4328490B2 (en) * 2002-03-01 2009-09-09 天野エンザイム株式会社 Flavor improving agent for food and drink, food to which this is added, and method for improving flavor of food and drink
JP2006232680A (en) * 2005-02-22 2006-09-07 Kyoto Pharmaceutical Industries Ltd Disintegrator for tablet and tablet using the same
JP4361597B2 (en) * 2006-11-13 2009-11-11 伊那食品工業株式会社 Disintegrant and tablets and granules containing the same

Also Published As

Publication number Publication date
JPH01104138A (en) 1989-04-21

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