JPS5883616A - Preparation of tablet for salt supply - Google Patents

Preparation of tablet for salt supply

Info

Publication number
JPS5883616A
JPS5883616A JP56181487A JP18148781A JPS5883616A JP S5883616 A JPS5883616 A JP S5883616A JP 56181487 A JP56181487 A JP 56181487A JP 18148781 A JP18148781 A JP 18148781A JP S5883616 A JPS5883616 A JP S5883616A
Authority
JP
Japan
Prior art keywords
salt
tablet
fine
glucose
citric acid
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
Application number
JP56181487A
Other languages
Japanese (ja)
Other versions
JPS6318458B2 (en
Inventor
Yukio Hirano
平野 行雄
Yoshiyuki Kurimoto
栗本 義之
Kazunori Tokuda
徳田 一憲
Shigeomi Tamura
田村 重臣
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.)
Asahi Kogyo KK
Original Assignee
Asahi Kogyo KK
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 Asahi Kogyo KK filed Critical Asahi Kogyo KK
Priority to JP56181487A priority Critical patent/JPS5883616A/en
Publication of JPS5883616A publication Critical patent/JPS5883616A/en
Publication of JPS6318458B2 publication Critical patent/JPS6318458B2/ja
Granted legal-status Critical Current

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  • Medicinal Preparation (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)
  • Seasonings (AREA)

Abstract

PURPOSE:To obtain a tablet capable of supplying salt effectively to persons perspired much by the work at high temperatures, etc., by mixing specific fine common salt particles having the appearance of an uneven surface and porous spherical shape with glucose and citric acid with the respective specific particle diameters uniformly, and tableting the resultant mixture. CONSTITUTION:Fine common salt particles, having the appearance of an uneven surface and porous spherical shape as a whole and 50-150mu particle diameter, and prepared by binding the fine common salt particles with a gum, e.g. guar gum, or a water-soluble high polymer, e.g. tamarind seed polysaccharide, propylene glycol ester of alginic acid or carboxymethyl cellulose (CMC), are uniformly mixed with glucose having 50-150mu particle diameter and citric acid having 50-150mu particle diameter to give a fine particulate mixture, which is then tableted to afford the aimed tablet. The mixture can be tableted with a good tableting property, and the resultant tablet has improved keeping quality due to the uniform dispersion of the respective components, assumes a pickled UME-like taste having a soft salty taste and is capable of supplying the salt and nutriments at the same time.

Description

【発明の詳細な説明】 本発明は、高温労働やスポーツ等で多部に発汗する人達
が効果的に塩分補給を行なうことができる錠剤を製造す
る方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing tablets that can effectively replenish salt for people who sweat profusely due to high-temperature work or sports.

従来から、高温労働環境等で働く人達は、多量の発汗に
伴って失われる塩分を補給するために、梅干や食塩をそ
のまま嘗めたりして対応してきた。しかしながら、衛生
上問題があったり、空腹時に食塩を直接胃に入れると悪
心や嘔吐、むくみなどの症状がでたり、あるいは塩だけ
では塩辛くて摂取しにくいといった問題がある。
Traditionally, people working in high-temperature working environments have responded by eating umeboshi (pickled plums) or table salt as they are to replenish the salt lost through excessive sweating. However, there are problems with hygiene, such as nausea, vomiting, swelling, and other symptoms when salt is put directly into the stomach on an empty stomach, and salt alone is salty and difficult to ingest.

また、食塩を錠剤化したものも製造されているが、粉末
状の食塩と比べて携帯に便利であるという利点以外は、
上記のごとき問題点を同様に備えている。さらには、か
ような食塩錠剤は食塩結晶粒子と同様に潮解性を有する
ため保存性が思いという欠点も有している。
Tablets of table salt are also manufactured, but they have the advantage of being more portable than powdered table salt.
It also has the same problems as mentioned above. Furthermore, such salt tablets have a deliquescent property like salt crystal particles, and therefore have a short shelf life.

そこで本発明は、携帯に便利な錠剤型としただけでなく
、保存時に潮解しにくく、しかも摂取時には単に塩辛い
だけでなく酸味と甘味を有する柔かな塩味を呈する塩分
補給用錠剤を提供することを目的としてなされたもので
ある。
SUMMARY OF THE INVENTION Therefore, the present invention aims to provide a salt replenishment tablet that is not only in the form of a tablet that is convenient to carry, but also is resistant to deliquescence during storage and exhibits not only a salty taste but also a soft salty taste with sourness and sweetness when ingested. It was done for a purpose.

すなわち本発明によれば、食塩微細結晶粒子が水溶性高
分子物質により粘着し全体として表面凹凸の多孔質球状
粒子の外観をもつ粒径50〜150μの食塩微細粒子と
、粒径50〜150μのブドウ糖と、粒径50〜150
μのクエン酸とを均一に混合して微粉末混合物となし、
この微粉末混合物を打錠して錠剤とすることによって目
的とする塩分補給用錠iI+を製造することができる。
That is, according to the present invention, salt microcrystalline particles have a particle size of 50 to 150μ and have a particle size of 50 to 150μ, which are adhered by a water-soluble polymer substance and have the appearance of porous spherical particles with an uneven surface as a whole. Glucose and particle size 50-150
Mix uniformly with μ citric acid to form a fine powder mixture,
By compressing this fine powder mixture into tablets, the intended salt supplement tablets iI+ can be manufactured.

本発明で使用する食塩結晶粒子叫、従来の食塩結晶粒子
と巽なり、表面が凹凸で多孔質球状粒子の外観をもつ微
細粒子であり、微細構造的にみれば、食塩微細結晶粒子
が水溶性高分子物質、例えばグアーガム等のガム類、タ
マリンド神子多糖類、アルギン酸プ【」ピレングリコー
ル1ステル、CMC等で互いに結着しているとともに結
晶粒子表面の一部あるいは大部分が被覆され、全体とし
てポーラスな球形粒子となっているものである。
The salt crystal particles used in the present invention are fine particles with an uneven surface and the appearance of porous spherical particles, unlike conventional salt crystal particles. They are bound to each other by polymeric substances such as gums such as guar gum, tamarind miko polysaccharide, alginic acid pyrene glycol 1 ester, CMC, etc., and part or most of the surface of the crystal particles is coated, and the whole It is a porous spherical particle.

この多孔質食塩微細粒子は、通常粒径5〇−150μを
有し、嵩密度は0.4〜0.7g /’♂と比較的小さ
く、サラザラした状態で流動性がよく、固結しにくいた
め保存性に侵れ、さらkは溶解しやすく、刺激のないソ
フトな塩味を51するといった特異な性質を備えている
These porous salt fine particles usually have a particle size of 50-150μ, a relatively small bulk density of 0.4-0.7g/'♂, have good fluidity in a smooth state, and are difficult to clump. Sarak has unique properties such as being easy to dissolve and having a mild, non-irritating salty taste.

かような多孔質食塩微細粒子の製造方法については、い
くつかの方法が既に特許されており、例えば食塩に水溶
性高分子の少鰻を溶解せしめた溶液を乾燥雰囲気中に噴
霧して乾燥する方法(特公昭51−28704号)、食
塩の過飽和部分が微細粒子で懸濁して存在する過飽和食
塩水と水溶性^分子物質とからなる懸濁混溶液を均一な
分散状態を保ちつつ乾燥雰囲気中に噴霧して乾燥する方
法(特公昭52−39907号)等が知られている。
Several methods have already been patented for manufacturing such porous salt fine particles, such as spraying a solution of a small amount of a water-soluble polymer dissolved in salt into a dry atmosphere and drying it. A method (Japanese Patent Publication No. 51-28704), in which a suspended mixed solution consisting of a supersaturated saline solution in which the supersaturated portion of common salt is suspended in fine particles and a water-soluble molecular substance is kept in a dry atmosphere while maintaining a uniformly dispersed state. A method of spraying and drying (Japanese Patent Publication No. 52-39907) is known.

また、かような多孔質食塩微細粒子は、例えば商品名r
ss−8ALTJ  (佐原食品工業■製)として市販
品として入手できる。
Further, such porous salt fine particles are available under the trade name r
It is available as a commercial product as ss-8ALTJ (manufactured by Sawara Food Industry Co., Ltd.).

本発明においては、上記したような食塩微細粒子をブド
ウ糖微粉末とクエン酸微粉末とともに混合し、この混合
物を打錠機で直接打錠することによって、食塩微細粒子
がブドウ糖とクエン酸の中に均一に分散した状態になり
、吸湿による結晶の浮上りを防止し、保存性を有する錠
剤が得られるのであ□る。多孔質食塩微細粒子はそれ自
体で刺激のない塩味を呈するが、これがブドウ糖やクエ
ン酸の微粉末中に均一に分散されているため、より一層
柔かな塩味となる。
In the present invention, the salt fine particles as described above are mixed with the glucose fine powder and the citric acid fine powder, and this mixture is directly compressed into tablets using a tablet machine, so that the salt fine particles are mixed into the glucose and citric acid. This results in a uniformly dispersed state, which prevents the crystals from floating due to moisture absorption, and provides a tablet with shelf life. The porous salt fine particles have a mild salty taste by themselves, but because they are uniformly dispersed in the fine powder of glucose and citric acid, the salty taste becomes even softer.

食塩微細粒子をブドウ糖とクエン酸の中に均一に分散せ
しめるためには、これら各成分のすべてを粒径の揃った
微粉末として配合することが必要であり1、このため本
発明においては、食塩微細粒子の粒径を50〜150μ
、ブドウ糖およびクエン酸の粒径を50〜150μの微
粉末として用いる必要がある。
In order to uniformly disperse the fine salt particles in glucose and citric acid, it is necessary to blend all of these components as fine powder with uniform particle sizes1.For this reason, in the present invention, the salt The particle size of fine particles is 50~150μ
, glucose and citric acid must be used as fine powders with a particle size of 50 to 150μ.

本発明で使用する多孔質食塩微細粒子に代えて、食塩結
晶粒子を50〜150μ程度の粒径に微粉砕した微細結
晶粒子を使用し、これを粒径50〜150μのブドウ糖
およびクエン酸微粉末と混合して打錠した場合には、錠
剤化はできるが保存中に食塩結晶微細粒子が吸湿して比
較的大きい塊状となって錠剤表面に斑点状に浮き出てく
る坦象がみられ、こ−れを食したところ刺激のつよい塩
辛さを感じた。このことから、保存性がよく、かつ食塩
微細粒子を均一に分散せしめて刺激のない塩味をもたせ
るためには、多孔質食塩微細粒子の使用が不可欠である
ことが理解できよう。
Instead of the porous salt fine particles used in the present invention, fine crystal particles obtained by pulverizing common salt crystal particles to a particle size of about 50 to 150 μm are used, and these are used as glucose and citric acid fine powders with a particle size of 50 to 150 μm. If tablets are made by mixing with chlorine and tablets, the fine salt crystal particles absorb moisture during storage and form relatively large lumps, which appear as spots on the tablet surface. - When I ate it, I felt a strong salty taste. From this, it can be understood that the use of porous salt fine particles is essential in order to have good storage stability, uniformly disperse the salt fine particles, and provide a non-irritating salty taste.

また本発明においては、食塩とともにブドウ糖とクエン
酸とを配合したため、甘味と酸味とを有する柔かな塩味
を与えることができる。特に食塩15〜35重量部、ブ
ドウ糖40〜70重量部、クエン酸5〜25重量部の配
合割合とすることによって、梅干に類似した好ましい呈
味を与えることができる。
Furthermore, in the present invention, since glucose and citric acid are blended together with common salt, a soft salty taste with sweetness and sourness can be imparted. In particular, by mixing 15 to 35 parts by weight of salt, 40 to 70 parts by weight of glucose, and 5 to 25 parts by weight of citric acid, a desirable taste similar to that of pickled plums can be imparted.

さらにまた、ブドウ糖は体内で分解されてエネルギー源
となる物質であり、クエン酸は細胞内物質代謝に際して
重要な物質であるため、食塩とともにこれらの物質を摂
取することによって塩分の補給と同時に栄養源補給効果
も期待できる。
Furthermore, glucose is a substance that is broken down in the body and becomes an energy source, and citric acid is an important substance in intracellular substance metabolism, so by ingesting these substances together with table salt, you can replenish salt and become a nutritional source. A replenishing effect can also be expected.

本発明を実施するに際しては、所定の粒径範囲になるよ
うに微粉末とした多孔質食塩粒子とブドウ糖とクエン酸
とを所望割合で均一に混合し、この混合物を通常の打錠
機で直接打錠すればよい。なお、打錠に先立って、各成
分を減圧乾燥して水分含量をできるだけ低くすることが
望ましい。
In carrying out the present invention, finely powdered porous salt particles having a predetermined particle size range, glucose, and citric acid are uniformly mixed in a desired ratio, and this mixture is directly processed using an ordinary tableting machine. All you have to do is press it into tablets. Note that, prior to tabletting, it is desirable to dry each component under reduced pressure to reduce the water content as much as possible.

各成分は所定の粒径範囲内の粒瓜とづることが不可欠で
あるが、各成分の粒度をできるだけ等しく揃えることが
望ましく、例えば、いずれの成分とも約50μ程度に揃
えたり、あるいは100μ程度に揃えることが、各成分
を均一に分散せしめるために好ましい。
It is essential that each component be made into melon grains within a predetermined particle size range, but it is desirable to make the particle sizes of each component as equal as possible. It is preferable to uniformly distribute each component.

なお、打錠に際して慣用されている滑沢剤を添加するこ
とも勿論でき、さらには必要に応じてビタミン類、ミネ
ラル類等の成分を適宜添加してもよい。
In addition, it is of course possible to add a lubricant commonly used in tabletting, and further components such as vitamins and minerals may be added as appropriate.

以下に実施例を挙げて本発明をさらに説明する。The present invention will be further explained below with reference to Examples.

実施例 多孔質球状の食塩微細粒子(商品名rss−8ALTJ
 、粒径50〜′150μ、嵩密度的o、eg/cw’
)15重量部、ブドウ糖微粉末(粒径的50μ)65重
量部、クエン酸微粉末(粒径的50μ)15重量部、お
よび滑沢剤(商品名「ラブリーワックス」70インド産
業■製)5φ1部を均一に混合して微粉末混合物とした
。この混合物はそのままの状態で6重量%程度の水分を
含むため、減圧乾燥機で90℃、3時間乾燥し、水分を
0.38重量%とした。この乾燥混合物を、試作用打錠
機(TK2型)を用1)、温度21〜22℃、湿度45
〜50%の雰囲気で打錠して、0.48a/ 1錠、硬
度27.4kg/cI2の錠剤を調製した。
Example Porous spherical salt fine particles (trade name rss-8ALTJ
, particle size 50~'150μ, bulk density o, eg/cw'
) 15 parts by weight, 65 parts by weight of glucose fine powder (particle size 50 μ), 15 parts by weight citric acid fine powder (particle size 50 μ), and lubricant (trade name “Lovely Wax” 70 manufactured by India Sangyo ■) 5φ1 These parts were uniformly mixed to form a fine powder mixture. Since this mixture contained about 6% by weight of water as it was, it was dried in a vacuum dryer at 90°C for 3 hours to reduce the water content to 0.38% by weight. This dry mixture was processed using a prototype tabletting machine (TK2 type)1) at a temperature of 21 to 22°C and a humidity of 45°C.
Tablets with a hardness of 0.48a/1 tablet and a hardness of 27.4kg/cI2 were prepared by compressing in an atmosphere of ~50%.

得られた錠剤の外観は、個々の微粉末粒子が肉眼で識別
できない均質の白色光沢表面を有し、刺激のないマイル
ドな塩味をもつ梅干様の味を呈した。また、この錠剤を
簡易包装にして温度30℃、湿度80%の環境中で30
日間保存後も、外観、味ともに変化は認められなかった
The resulting tablets had a homogeneous white glossy surface in which the individual fine powder particles could not be discerned with the naked eye, and had a non-irritating, mildly salty, pickled plum-like taste. In addition, the tablets were packaged in simple packaging for 30 minutes in an environment with a temperature of 30°C and humidity of 80%.
No change in appearance or taste was observed even after storage for several days.

なお比較のために、上記実施例中の多孔質食塩微細粒子
に代えて食塩結晶微細粒子(粒径5゜〜150μ、嵩密
度的1.15!II/CI’)を用いた以外は、実施例
と同様の処方で同様の操作により錠剤を調製した。得ら
れた錠剤の外観は、食塩結晶微細粒子が白色の中に輝い
てみえるような表面を有し、この錠剤を上記横施例と同
様の環境中で保存したところ、7日経過した頃から錠剤
表面に食塩結晶粒子の塊り様の斑点が生じてきた。かよ
うな斑点のある錠剤は上記実施例の錠剤に比べて塩辛さ
が強かった。
For comparison, the same example was carried out except that salt crystalline fine particles (particle size 5° to 150μ, bulk density 1.15!II/CI') were used in place of the porous salt fine particles in the above examples. Tablets were prepared using the same recipe and procedure as in the example. The appearance of the obtained tablets was such that the fine salt crystal particles appeared to be shining in the white color, and when the tablets were stored in the same environment as in the above-mentioned horizontal example, after 7 days had passed. Spots resembling agglomerates of salt crystal particles appeared on the tablet surface. The tablets with such spots were more salty than the tablets of the above examples.

上述したところかられかるように本発明においては、多
孔質球状の食塩微細粒子と、微粉末のブドウ糖とクエン
酸を用いたことによって、打錠性よく錠剤化することが
でき、また得られた錠剤は各成分が均一に分散した保存
性のよいものであり、柔かな塩味をもつ梅干様の味を!
し、塩分補給と同時に栄養補給もできるといった多(の
利点を備えている。
As can be seen from the above, in the present invention, by using porous spherical salt fine particles, fine powdered glucose and citric acid, it is possible to form tablets with good compressibility, and the obtained The tablets have a long shelf life with each ingredient evenly dispersed, and have a mild salty taste similar to pickled plums!
However, it has many advantages such as being able to supply both salt and nutrition at the same time.

特許出願人   西武化学工業株式会社代  理  人
       尾  股  行  翅目       
   茂  見     種間      荒 木 友
之助 手続補正書(方式) 1、 事件の表示 昭和rど年特 許 願オ/、P/ぐy7号2、発明の名
称 塩i゛酎好つ製8遺 3、補正をする者 ゝ   事件との関係 特許出願人 4、代理人〒104 別紙の通り
Patent Applicant Seibu Chemical Co., Ltd. Representative Person Omata Yuki Ptera
Tomonosuke Shigemi Tanema Araki procedural amendment (method) 1. Indication of the case Showa r. Relationship to the case Patent applicant 4, agent 〒104 As shown in the attached sheet

Claims (1)

【特許請求の範囲】[Claims] 1、食塩微細結晶粒子が水溶性^分子物質により結着し
全体として表面凹凸の多孔質球状粒子の外観をもつ粒径
50〜150μの食塩微細粒子と、粒径50〜150μ
のブドウ糖と、粒径50〜150μのクエン酸とを均一
に混合して微粉末混合物となし、この微粉末混合物を打
錠して錠剤とすることを特徴とする塩分補給用錠剤の製
造方法。
1. Salt microcrystalline particles are bound together by water-soluble molecular substances and have the appearance of porous spherical particles with an uneven surface as a whole.
A method for producing a tablet for salt supplementation, which comprises uniformly mixing glucose of 10% and citric acid having a particle size of 50 to 150μ to form a fine powder mixture, and compressing the fine powder mixture into tablets.
JP56181487A 1981-11-12 1981-11-12 Preparation of tablet for salt supply Granted JPS5883616A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56181487A JPS5883616A (en) 1981-11-12 1981-11-12 Preparation of tablet for salt supply

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56181487A JPS5883616A (en) 1981-11-12 1981-11-12 Preparation of tablet for salt supply

Publications (2)

Publication Number Publication Date
JPS5883616A true JPS5883616A (en) 1983-05-19
JPS6318458B2 JPS6318458B2 (en) 1988-04-19

Family

ID=16101614

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56181487A Granted JPS5883616A (en) 1981-11-12 1981-11-12 Preparation of tablet for salt supply

Country Status (1)

Country Link
JP (1) JPS5883616A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011015639A (en) * 2009-07-09 2011-01-27 Ezaki Glico Co Ltd Fizzing candy and method for producing the same
JP2018102274A (en) * 2016-12-28 2018-07-05 日清オイリオグループ株式会社 Tablet type thickening composition
JPWO2021132072A1 (en) * 2019-12-23 2021-07-01

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011015639A (en) * 2009-07-09 2011-01-27 Ezaki Glico Co Ltd Fizzing candy and method for producing the same
JP2018102274A (en) * 2016-12-28 2018-07-05 日清オイリオグループ株式会社 Tablet type thickening composition
JPWO2021132072A1 (en) * 2019-12-23 2021-07-01

Also Published As

Publication number Publication date
JPS6318458B2 (en) 1988-04-19

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