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JPS6327327B2 - - Google Patents

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Publication number
JPS6327327B2
JPS6327327B2 JP54054067A JP5406779A JPS6327327B2 JP S6327327 B2 JPS6327327 B2 JP S6327327B2 JP 54054067 A JP54054067 A JP 54054067A JP 5406779 A JP5406779 A JP 5406779A JP S6327327 B2 JPS6327327 B2 JP S6327327B2
Authority
JP
Japan
Prior art keywords
parts
water
acid
dry mouth
drinking
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
Application number
JP54054067A
Other languages
Japanese (ja)
Other versions
JPS55145613A (en
Inventor
Kanji Noda
Jusuke Mori
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.)
Hisamitsu Pharmaceutical Co Inc
Original Assignee
Hisamitsu Pharmaceutical Co Inc
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 Hisamitsu Pharmaceutical Co Inc filed Critical Hisamitsu Pharmaceutical Co Inc
Priority to JP5406779A priority Critical patent/JPS55145613A/en
Publication of JPS55145613A publication Critical patent/JPS55145613A/en
Publication of JPS6327327B2 publication Critical patent/JPS6327327B2/ja
Granted legal-status Critical Current

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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Non-Alcoholic Beverages (AREA)
  • Medicinal Preparation (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明はフイチン酸、無機カチオン類およびブ
ドウ糖を必須成分とする口渇回復用組成物に関す
るものである。 更に詳細には、本発明はフイチン酸0.8〜6.0
%、無機カチオン類0.8〜8.4%およびブドウ糖
78.2〜90.3%を有効成分とすることにより、カチ
オン類の吸収を著しく促進できるようにした口渇
回復用組成物に関するものである。 更に詳細には、本発明はフイチン酸によつてカ
チオン類の吸収を著じるしく促進できるようにし
た口渇回復用組成物に関するものである。 一般に、代謝並に発汗の増大する肉体的活動
時、たとえば高熱作業時、激しい運動時、発熱
時、熱傷時、日射病時、或は激しい下痢時などに
於て、軽度の場合の口渇より始り、脱力、疲労、
失神、脱水症状、或は重症の場合のシヨツク症状
に至るまでさまざまの急性症状を招くことが知ら
れ、又これらの症状の主たる原因が他液中の水分
および電解質の体外逸失、並に主としてこれに基
く体液電解質平衡の失調に帰せられることも亦よ
く知られている。 代表的な例として、激しい運動時に着目してこ
れらを更に詳細に見るに、上述の水分並に電解質
の体外逸失に加え、体液酸性化、血糖濃度低下或
は血中エネルギー源枯渇、体液高張化、組織から
のK+の逸出、組織の酸素需要増大、無気的呼吸
の需要増大、神経反射機能低下などの随伴現象が
あらわれる。 この様に複雑な生体内変化が起つていることを
考えると、前述の種々の原因によりひき起された
口渇をいやすのに単に大量の水を飲用したり、近
年まで行われていた様に食塩を併用したりする方
法は必ずしも妥当ではない。実際に空腹時に水を
大量飲用すると悪心や消化管攣縮を起したり、又
頻脈や虚脱を起すことがあるが、これらは夫々消
化管壁が急に低張環境にさらされるため、並に血
中電解質濃度が急変するために起ると考えられ
る。又、食塩併用は水の同時摂取量が少な過ぎる
と症状を逆に悪化させ、悪心、血圧低下、失神な
どを招く危険があるが、これは意図とは逆に体液
が更に高張化し、又発汗により低下している血中
K+/Na+比が更に低下することにより起るもの
と思われる。 この様な口渇時の症状を改善するためにブドウ
糖、Na+、K+、Cl′を主剤とし、用時水にとかし
て等張に近い濃度の溶液として飲用に供する口渇
回復用飲料が数種近年市販されるに至つている
が、これらは何れも配合電解質量が電解質補給の
意味をなし難い程少ないものがほとんどである。
そこでカチオン類の濃度を高めることも試みられ
るが、消化管吸収が悪く、下痢などの症状を起す
ため実施できなかつた。 発明者らは激しい運動時に汗として失われる水
分および電解質を速やかに補給し、更に同時に起
る種々の生体内変化を速やかに回復させると共
に、生理的に安全な口渇回復用飲料を開発すべく
鋭意研究した結果、フイチン酸を有効成分として
口渇回復用組成物に含有させることによつて高濃
度カチオンを吸収せしめることに成功したのであ
る。 本発明はフイチン酸、無機カチオン類およびブ
ドウ糖を必須成分としてなる口渇回復用組成物で
ある。 口渇回復用組成物中にフイチン酸が存在する
と、−12価の酸性官能基がMg++などと可溶性の
キレートを形成して吸収されるようになるため、
カチオン類を高濃度にしても吸収が早く、下痢等
の障害を起すこともなくなる。 本発明の口渇回復用組成物は、一般に用時水に
とかして飲用に供する用時溶解型固形の口渇回復
用飲料組成物に関するものであつて、好ましくは
フイチン酸を0.8〜6.0%、カリウムを0.24〜5.25
%、ナトリウムを0.14〜7.35%、マグネシウムを
0〜5.25%、ブドウ糖を78.2〜90.3%含有し、か
つ無機カチオンの配合総量が1g当り0.3〜3.7mg
当量である組成物から成る口渇回復用飲料組成物
に関するものである。 しかしながら、本発明は、液状組成物としてそ
のまま飲用できるような飲料組成物としてもよい
ことは勿論である。この場合は用時飲用固型組成
物40〜60gを1の水に溶解する割合で液状にし
たものが飲料組成物となる。 一般に、激しい筋肉運動により、組織及び体液
中の電解質平衡が著しく失調する。すなわち細胞
内のK+及びMg++が血中に漏出し、Na+、Ca++
及びCl′が細胞中に滲入し、この結果汗中に排泄
される電解質の成分濃度は下表の如く正常血漿中
の成分濃度に比しK+/Na+比及びMg++/Ca++
が大きい。
The present invention relates to a dry mouth recovery composition containing phytic acid, inorganic cations, and glucose as essential components. More specifically, the present invention relates to phytic acid 0.8 to 6.0
%, inorganic cations 0.8-8.4% and glucose
The present invention relates to a dry mouth recovery composition that can significantly promote the absorption of cations by containing 78.2 to 90.3% of the active ingredient. More specifically, the present invention relates to a composition for relieving dry mouth, which is capable of significantly promoting the absorption of cations using phytic acid. In general, dry mouth begins in mild cases during physical activities that increase metabolism and sweating, such as during high-temperature work, strenuous exercise, fever, burns, sunstroke, or severe diarrhea. fatigue, weakness, fatigue,
It is known that it can lead to various acute symptoms ranging from fainting, dehydration, and even shock symptoms in severe cases, and the main cause of these symptoms is the loss of water and electrolytes from other fluids, and It is also well known that it is caused by an imbalance in body fluid electrolyte balance. As a typical example, if we look at these in more detail during intense exercise, in addition to the above-mentioned loss of water and electrolytes from the body, acidification of body fluids, decrease in blood sugar concentration or depletion of blood energy sources, and hypertonicity of body fluids. , associated phenomena such as escape of K + from tissues, increased demand for oxygen in tissues, increased demand for anaerobic respiration, and decreased neural reflex function appear. Considering that such complex biological changes occur, it is difficult to relieve dry mouth caused by the various causes mentioned above by simply drinking large amounts of water, or as was done until recently. Methods such as using salt in combination are not necessarily appropriate. In fact, drinking large amounts of water on an empty stomach can cause nausea, gastrointestinal spasm, tachycardia, and collapse, but these are caused by the sudden exposure of the gastrointestinal wall to a hypotonic environment. This is thought to be caused by a sudden change in blood electrolyte concentration. In addition, if the amount of water consumed at the same time is too small, it may actually worsen the symptoms, leading to nausea, decreased blood pressure, and syncope. Blood levels are lowered due to
This appears to be caused by a further decrease in the K + /Na + ratio. In order to improve the symptoms of dry mouth, a dry mouth recovery drink containing glucose, Na + , K + , and Cl' as main ingredients, is prepared by dissolving it in water and drinking it as a solution with a near isotonic concentration. Several types have come on the market in recent years, but most of them have a blended amount of electrolyte that is so small that it is hardly useful for electrolyte replenishment.
Therefore, attempts have been made to increase the concentration of cations, but this has not been possible due to poor gastrointestinal absorption and causing symptoms such as diarrhea. The inventors aimed to develop a dry mouth recovery drink that quickly replenishes water and electrolytes lost through sweat during intense exercise, quickly recovers from various biological changes that occur at the same time, and is physiologically safe. As a result of extensive research, they succeeded in absorbing high concentrations of cations by incorporating phytic acid as an active ingredient into a dry mouth recovery composition. The present invention is a dry mouth recovery composition comprising phytic acid, inorganic cations, and glucose as essential components. When phytic acid is present in the dry mouth recovery composition, the -12-valent acidic functional group forms a soluble chelate with Mg ++ etc. and is absorbed.
Even at high concentrations of cations, they are absorbed quickly and do not cause problems such as diarrhea. The composition for relieving dry mouth of the present invention generally relates to a solid drink composition for relieving dry mouth that is dissolved at the time of use and is dissolved in water for drinking, and preferably contains 0.8 to 6.0% of phytic acid. Potassium 0.24-5.25
%, sodium 0.14-7.35%, magnesium 0-5.25%, glucose 78.2-90.3%, and the total amount of inorganic cations is 0.3-3.7mg per gram.
The present invention relates to a dry mouth relief beverage composition comprising an equivalent amount of the composition. However, it goes without saying that the present invention may be applied to a beverage composition that can be drunk as it is as a liquid composition. In this case, the beverage composition is prepared by liquefying 40 to 60 g of the solid composition for drinking at a ratio of 1 part to 1 part water. In general, strenuous muscular exercise significantly disrupts the electrolyte balance in tissues and body fluids. In other words, intracellular K + and Mg ++ leak into the blood, and Na + and Ca ++
and Cl' seep into the cells, and as a result, the concentration of electrolyte components excreted in sweat is as shown in the table below, compared to the concentration of components in normal plasma, K + /Na + ratio and Mg ++ /Ca ++
is large.

【表】 体液電解質平衡の正常状態への回復を外因的に
促進させるためには単に汗中に失われた電解質を
補給するだけでは不充分であつて、血中より細胞
内に向う濃度勾配に於てK+及びMg++のそれを特
に高める必要があり、これらの電解質を飲料とし
て補給する場合、消化管よりの吸収動態をも考え
あわせてK+及びMg++の相対量を大きくする必要
がある。Na+及びCl′は能働輸送により吸収され、
Ca++もブドウ糖等の糖類と同時投与することに
より能働的に吸収されるのでこれら3者について
は単なる補充を考慮すればよいがK+及びMg++
吸収され難いので特別の配慮が必要である。K+
については受働輸送による吸収の様相が強く消化
管中濃度が5mM以上でないと吸収され難いので
飲料への配合濃度は希望する吸収濃度+5mMと
する必要がある。又Mg++は塩類下剤として利用
される例からも明らかな如くそのままでは甚だ吸
収され難い。このようなときにフイチン酸が共存
すればフイチン酸がこれらカチオンと水溶性のキ
レートを作り、これによつて容易に吸収されるよ
うになる。 本発明の口渇回復用組成物はその主目的の一つ
に水分の速やかな補給があり、当然水溶液として
飲用に供するものであるが、変質防止並に携帯の
便のため用時溶解型の固形組成物としたものであ
り、使用に当つては本発明品の分包された一定量
又は容易に分取される一定量を定められた適量の
飲料水に溶解して飲用に供する。 又、本発明品はフイチン酸および各種無機カチ
オンを主剤として構成されるが、賦形増量、嗜好
性改善並に疲労回復補助のため、用時の滲透圧濃
度が等張を超えない範囲内に於て下記の成分を配
合することができる。 賦形増量−ブドウ糖、果糖、蔗糖、ソルビトー
ル、マンニトール、キシローズ、キシリトー
ル、ガラクトーズ等の糖類及びペクチン、デキ
ストラン、マンナン等の多糖類及び誘導体。 嗜好性改善−クエン酸、酒石酸、フマール酸、リ
ンゴ酸、リン酸等の酸類、天然及び人工甘味料
及び香料。 疲労回復補助剤−アスコルビン酸、チアミン、リ
ボフラビン、ピリドキシン、シアノコバラミ
ン、パントテン酸、チオクト酸、アクセルフト
ール、トコフエロール等のビタミン類および誘
導体。 タウリン、アルギニン、ヒスチジン、グルタ
ミン酸、アスパラギン酸、ガンマアミノ酪酸等
のアミノ酸及び誘導体。 カフエイン、テオブロミン等の中枢興奮剤。 コリン、レシチン、次亜硫酸ナトリウム、ク
ロロフイリン、グルクロン酸、グルタチオン、
ペモリン等の解毒剤。 THAM等の酸中和剤。 以上の口渇回復用組成物はすべてを水に溶解し
て凍結乾燥したり、噴霧乾燥したり、流動乾燥し
たりして用時溶解型固形の口渇回復用組成物とさ
れる。 以上述べた如く、本発明口渇回復用組成物は、 (1) フイチン酸は1分子に12ケの酸基を有するた
め1当量当りのモル濃度がきわめて低く、溶液
の滲透圧濃度を低く設定することができるた
め、水分の吸収を防げない、 (2) 味が良く、又Na+やK+を当量配合しても鹹
味が小さいため嗜好性が高い、 (3) フイチン酸アニオンの消化管吸収はNa+
K+等の吸収よりもおくれるので、アシド−シ
スを急速に緩解し、その後予備アルカリの一つ
となる、 (4) オキシヘモグロビンの親和性を減弱させ、細
胞サイトに於ける酸素放出を促進させるので有
気的呼吸の効率を高める。この作用はL−アス
コルビン酸との協同作用により更に促進され
る、 (5) イノシトールおよびリン酸の補給源として栄
養的に意義がある、 (6) 神経機能賦活作用のあるホスフアチジルイノ
シトールの前駆体としての意義がある。 (7) 脳、肝、眼の保護並に機能賦活作用を有する
ミオイノシトールの補給源としての意義があ
る、 等のすぐれた効果を有するものである。 本発明口渇回復用組成物はたとえば次の場合に
有用である。 (a) スポーツ時の疲労防止および疲労回復促進。 (b) 高熱或は低湿度環境に於ける作業時の水分お
よび電解質補給。 (c) 熱傷、あつさまけの予防並に応急処置。 (d) 火傷時の脱水症状緩解。 (e) 低カリウム症状の緩解。 (f) 肉体的および精神的疲労の回復促進。 (g) 宿酔の緩解。 (h) 乳児下痢に於ける脱水症状の緩解。 (i) 虚血性心不全の食餌療法。 実施例 1 処方: フイチン酸(固型換算) 4.00% 水酸化カリウム(100%換算) 1.36% 酸化マグネシウム(100%換算) 0.48% L−アルギニン 0.20% 塩化ナトリウム 2.00% タウリン 0.20% 無水カフエイン 0.02% 無水ソルビトール 5.60% 無水ブドウ糖 80.00% 無水クエン酸 3.60% L−アスコルビン酸 0.40% 水 分 2.14% 調製法: 先ず50%フイチン酸液に撹拌しつつ含水酸化マ
グネシウムを加え澄明に溶けるまで撹拌し、次い
で50%水酸化カリウム液を注加する。別容器に水
20部をとり、L−アルギニン0.2部、塩化ナトリ
ウム2.0部、タウリン0.2部、無水カフエイン0.02
部、無水ソルビトール5.6部、無水クエン酸3.6
部、L−アスコルビン酸0.4部を加えてとかした
液を作り、両液を合して均一に混合し、凍結温度
−20〜−30℃、二次乾燥温度50℃で凍結乾燥し、
得たるケーキを40メツシユ篩を用いて精粒し、こ
の精粒粉末の20部を結晶無水ブドウ糖80部と均一
に混合して目的の製剤を得る。 この製剤50gを水にとかして1とし、飲用に
供する。 物性: 実施例1の試料は褐色粒と純白粒の混合物であ
り、流動性極めて良好である。この50gを水にと
かして1とする時、振盪すれば速やかにとけて
無色澄明の液となり、PHは3.60、氷点は−0.52℃
であつて、体液と略々等張である。 試験結果: 上の溶液夫々250mlと冷水夫々250mlを男子3
名、女子7名のパネルに軽作業時に試飲させ、検
定の結果95%信頼限界で次の結果が得られた。 (1) 水より飲み易く抵抗感が少い。 (2) 酸味および甘味は何れも軽く爽快で適当であ
る。鹹味および苦味はかすかに感ずる程度であ
り、特に飲用を妨げるものではない。又後味は
残らず、むしろ清爽感が残る。すなわち嗜好性
は良好と判定される。 (3) 口渇回復促進或は疲労回復促進については、
このパネルが軽作業にあつたため、効果は判然
としなかつた。 (4) 男子1名に於て略々疲労困ぱいに至る迄全力
疾走したる後試飲したる所、単に水を飲んだ場
合に比し、疲労よりの回復が自覚的に著しく早
い、との報告を得ている。 実施例 2 処方: フイチン酸(固型換算) 4.31% 水酸化カリウム(100%換算) 1.46% 酸化マグネシウム(100%換算) 0.51% L−アルギニン 0.22% 塩化ナトリウム 2.15% タウリン 0.22% 無水ブドウ糖 86.12% 無水クエン酸 3.94% L−アスコルビン酸 0.43% 水 分 0.64% 調製法: 実施例と略々同様の技法を用い、50%フイチン
酸液8.62部、水酸化カリウム1.46部、酸化マグネ
シウム0.51部、L−アルギニン0.22部、塩化ナト
リウム2.15部、タウリン0.22部、無水クエン酸
3.94部、L−アスコルビン酸0.43部および水20部
より成る混液を調製し、これを流入風温110〜130
℃の噴霧乾燥機を用いて噴霧乾燥し、得たる粉末
13.88部を結晶無水ブドウ糖86.12部と均一に混合
して目的の製剤を得る。 この製剤46.4gを水にとかして1とし、飲用
に供する。 物性: 市販類似商品と対比して示すに下表の如くであ
る。
[Table] In order to extrinsically promote the recovery of body fluid electrolyte balance to a normal state, it is insufficient to simply replenish electrolytes lost in sweat, and the concentration gradient from the blood to the inside of cells is insufficient. It is necessary to particularly increase the levels of K + and Mg ++ , and when replenishing these electrolytes in the form of drinks, the relative amounts of K + and Mg ++ should be increased, taking into consideration the absorption dynamics from the gastrointestinal tract. There is a need. Na + and Cl′ are absorbed by active transport,
Ca ++ is also actively absorbed when co-administered with sugars such as glucose, so simple supplementation can be considered for these three, but K + and Mg ++ are difficult to absorb and require special consideration. is necessary. K +
Since it is strongly absorbed by passive transport and is difficult to absorb unless the concentration in the gastrointestinal tract is 5mM or more, the concentration added to the drink needs to be the desired absorption concentration + 5mM. Furthermore, as is clear from the example of its use as a saline laxative, Mg ++ is extremely difficult to absorb as it is. If phytic acid coexists in such a case, phytic acid forms a water-soluble chelate with these cations, which allows for easy absorption. One of the main purposes of the dry mouth recovery composition of the present invention is to quickly replenish water, and it is naturally intended for drinking as an aqueous solution. It is a solid composition, and when used, a predetermined amount of the product of the present invention is dissolved in a predetermined appropriate amount of drinking water and made available for drinking. In addition, the product of the present invention is composed of phytic acid and various inorganic cations as main ingredients, but in order to increase excipient volume, improve palatability, and assist in recovery from fatigue, the osmotic pressure concentration during use must be within a range that does not exceed isotonicity. The following ingredients can be blended. Excipient bulking - sugars such as glucose, fructose, sucrose, sorbitol, mannitol, xyrose, xylitol, galactose, and polysaccharides and derivatives such as pectin, dextran, mannan. Improved palatability - acids such as citric acid, tartaric acid, fumaric acid, malic acid, phosphoric acid, natural and artificial sweeteners and flavors. Fatigue recovery aids - vitamins and derivatives such as ascorbic acid, thiamine, riboflavin, pyridoxine, cyanocobalamin, pantothenic acid, thioctic acid, axelftol, tocopherol. Amino acids and derivatives such as taurine, arginine, histidine, glutamic acid, aspartic acid, gamma-aminobutyric acid. Central stimulants such as caffeine and theobromine. Choline, lecithin, sodium hyposulfite, chlorophyllin, glucuronic acid, glutathione,
Antidotes such as pemoline. Acid neutralizer such as THAM. The above composition for relieving dry mouth is dissolved in water and freeze-dried, spray-dried, or fluidized to obtain a solid composition for relieving dry mouth that can be dissolved at the time of use. As mentioned above, the dry mouth recovery composition of the present invention has the following features: (1) Since phytic acid has 12 acid groups in one molecule, the molar concentration per equivalent is extremely low, and the osmotic pressure concentration of the solution is set low. (2) It tastes good, and even if an equivalent amount of Na + or K + is added, it has a small salty taste, making it highly palatable. (3) The gastrointestinal tract of phytate anion Absorption is Na + ,
Since it lags behind the absorption of K + etc., it rapidly relieves acidosis and then becomes one of the reserve alkalis. (4) Attenuates the affinity of oxyhemoglobin and promotes oxygen release at cell sites. So it increases the efficiency of aerobic respiration. This action is further promoted by the synergistic action with L-ascorbic acid. (5) It is nutritionally significant as a source of inositol and phosphate. (6) It is a precursor of phosphatidylinositol, which has a neurostimulatory effect. It has a meaning as a body. (7) It has excellent effects such as being significant as a source of myo-inositol, which protects the brain, liver, and eyes and has function-activating effects. The dry mouth recovery composition of the present invention is useful, for example, in the following cases. (a) Preventing fatigue during sports and promoting recovery from fatigue. (b) Hydration and electrolyte replenishment during work in high heat or low humidity environments. (c) Prevention and first aid for burns and burns. (d) Alleviation of dehydration symptoms during burns. (e) Remission of hypokalemia symptoms. (f) Promote recovery from physical and mental fatigue. (g) Remission of hangover. (h) Remission of dehydration symptoms in infant diarrhea. (i) Dietary therapy for ischemic heart failure. Example 1 Formulation: Phytic acid (solid equivalent) 4.00% Potassium hydroxide (100% equivalent) 1.36% Magnesium oxide (100% equivalent) 0.48% L-arginine 0.20% Sodium chloride 2.00% Taurine 0.20% Anhydrous caffeine 0.02% Anhydrous Sorbitol 5.60% Anhydrous glucose 80.00% Anhydrous citric acid 3.60% L-ascorbic acid 0.40% Water 2.14% Preparation method: First, add hydrated magnesium oxide to a 50% phytic acid solution with stirring until it dissolves clearly, then 50% Add potassium hydroxide solution. water in a separate container
Take 20 parts, add 0.2 parts of L-arginine, 2.0 parts of sodium chloride, 0.2 parts of taurine, and 0.02 parts of anhydrous caffeine.
part, anhydrous sorbitol 5.6 parts, anhydrous citric acid 3.6 parts
1 part and 0.4 parts of L-ascorbic acid to make a dissolved solution, combine both solutions, mix uniformly, and freeze-dry at a freezing temperature of -20 to -30°C and a secondary drying temperature of 50°C.
The resulting cake is granulated using a 40 mesh sieve, and 20 parts of this granulated powder is uniformly mixed with 80 parts of crystalline anhydrous glucose to obtain the desired formulation. Dissolve 50 g of this preparation in water to make 1 and use it for drinking. Physical properties: The sample of Example 1 is a mixture of brown grains and pure white grains, and has extremely good fluidity. When 50g of this is dissolved in water to make 1, it quickly dissolves when shaken to form a clear, colorless liquid with a pH of 3.60 and a freezing point of -0.52℃.
It is approximately isotonic with body fluids. Test results: 250ml each of the above solutions and 250ml each of cold water for boy 3.
A panel of 7 women and women sampled the product during light work, and the following results were obtained with a 95% confidence limit. (1) It is easier to drink than water and causes less resistance. (2) Both sourness and sweetness are light, refreshing, and appropriate. The salty and bitter tastes are only slightly perceptible and do not particularly interfere with drinking. There is no aftertaste, but rather a refreshing feeling. In other words, the taste is determined to be good. (3) Regarding promotion of dry mouth recovery or fatigue recovery,
Since this panel was subjected to light work, its effectiveness was unclear. (4) One male sampled the product after running at full speed until he was nearly exhausted, and reported that his recovery from fatigue was significantly faster than when he simply drank water. I am getting . Example 2 Formulation: Phytic acid (solid equivalent) 4.31% Potassium hydroxide (100% equivalent) 1.46% Magnesium oxide (100% equivalent) 0.51% L-arginine 0.22% Sodium chloride 2.15% Taurine 0.22% Anhydrous glucose 86.12% Anhydrous Citric acid 3.94% L-ascorbic acid 0.43% Water 0.64% Preparation method: Using almost the same technique as in the example, 8.62 parts of 50% phytic acid solution, 1.46 parts of potassium hydroxide, 0.51 part of magnesium oxide, L-arginine 0.22 parts, sodium chloride 2.15 parts, taurine 0.22 parts, citric acid anhydride
A mixture of 3.94 parts of L-ascorbic acid, 0.43 parts of L-ascorbic acid, and 20 parts of water was prepared, and this was heated to an inflow air temperature of 110 to 130 parts.
Spray dry the obtained powder using a spray dryer at ℃
Uniformly mix 13.88 parts with 86.12 parts of crystalline anhydrous glucose to obtain the desired formulation. Dissolve 46.4 g of this preparation in water to make 1 and use it for drinking. Physical properties: Comparison with commercially available similar products is shown in the table below.

【表】【table】

【表】 試飲結果: (1) 22〜50才のラグビー選手10名に壁押し運動を
疲労困ぱいするまで行わせ、持続回数のよく似
たペアを作り、その一方に実施例2の飲用溶液
500mlを、もう一方に水500mlをのませ、2分間
休憩の後壁押運動を再開させ、再び疲労困ぱい
するまでの持続回数をはかり、第二回目の持続
回数×100/第一回目持続回数を以て疲労回復
率(%)とする時、次のように実施例2を飲用
した群の方が回復率が大きかつた。
[Table] Tasting results: (1) 10 rugby players between the ages of 22 and 50 were asked to perform a wall push exercise until exhaustion, creating pairs with similar durations, and one of them was given the drinking solution of Example 2.
Pour 500ml of water into the other hand, rest for 2 minutes, then resume the wall pushing exercise. Measure the number of times you can continue until you are exhausted again. When expressed as fatigue recovery rate (%), the group that drank Example 2 had a higher recovery rate as shown below.

【表】 (2) 50才の男性被験者につき、12時間絶食後排尿
させ、実施例2の飲用溶液又は水を夫々300ml
のませ、安静に保つて15分毎に採尿し尿量をは
かつた所下表の如くであつた。すなわち水の吸
収は本品飲用時の方がはるかに速いということ
がうかがわれる。
[Table] (2) A 50-year-old male subject was made to urinate after fasting for 12 hours, and administered 300 ml each of the drinking solution of Example 2 or water.
The patient was kept at rest, and urine was collected every 15 minutes and the amount of urine was measured as shown in the table below. This suggests that water absorption is much faster when drinking this product.

【表】 実施例 3 処方: フイチン酸(固型換算) 2.10% 水酸化カリウム(100%換算) 0.92% 水酸化ナトリウム(100%換算) 1.22% L−アルギニン−L−グルタメート 0.21% 無水ブドウ糖 83.86% 無水クエン酸 7.67% L−アスコルビン酸 0.21% 香料末 1.26% 水 分 2.55% 調製法: 実施例1と略々同様の技法を用い、50%フイチ
ン酸液4.20部、水酸化カリウム0.92部、水酸化ナ
トリウム1.22部、L−アルギニン−L−グルタメ
ート0.21部、無水クエン酸7.67部、L−アスコル
ビン酸0.21部および水25部より成る混液を作り、
この液を流入風温70〜80℃で無水ブドウ糖83.86
部の上に造粒的に噴霧し、得たる乾燥粉末に香料
末1.26部を均一に混合して目的の製剤を得る。 この製剤53gを水にとかして1とし、飲用に
供する。 物性: 実施例3の試料は純白の顆粒状粉末であり、流
動性極めて良好、カサ密度は流動時0.554、タツ
ピング時0.622である。この53gを水に溶かして
1とする時、速やかに溶けて無色澄明の液とな
り、そのPHは3.35、氷点は−0.53℃である。 実施例 4 処方: フイチン酸(固型換算) 4.19% 無水炭酸カリウム 1.59% 水酸化ナトリウム(100%換算) 1.30% L−アルギニン−L−グルタメート 0.21% 無水ブドウ糖 83.86% 無水クエン酸 4.19% L−アスコルビン酸 0.21% 香料末 1.26% 水 分 3.19% 調製法: 実施例1と略々同様の技法を用い、50%フイチ
ン酸4.19部、水酸化ナトリウム1.30部、L−アル
ギニン−L−グルタメート0.21部、無水クエン酸
4.19部、L−アスコルビン酸0.21部および水5部
より成る混液を作り、この液を熱板温度60〜70℃
の真空乾燥機を用いて減圧乾涸し、得たる乾燥塊
を40メツシユ篩を用いて精粒し、この精粒粉末の
13.29部を無水炭酸カリウム1.59部、結晶無水ブ
ドウ糖83.86部および香料末1.26部と均一に混合
して目的の製剤を得る。 この製剤53gを水にとかして1とし、飲用に
供する。 物性: 実施例4の試料は褐色粒と純白粒の混合物であ
り、流動性極めて良好、カサ密度は流動時0.682、
タツピング時0.723である。この53gを水に溶か
して1とする時、振盪すれば速やかに溶けて微
黄色澄明の液となり、PHは3.48、氷点は−0.53℃
である。又この液の成分濃度は下の如くである。 フイチン酸-12 40.40meq アスコルビン酸-1 0.63meq クエン酸-3 10.58meq CO3 -2 12.22meq K+ 12.22meq Na+ 17.21meq ブドウ糖 246.69mM L−アルギニン−L−グルタメート 0.35mM。
[Table] Example 3 Prescription: Phytic acid (solid equivalent) 2.10% Potassium hydroxide (100% equivalent) 0.92% Sodium hydroxide (100% equivalent) 1.22% L-arginine-L-glutamate 0.21% Anhydrous glucose 83.86% Anhydrous citric acid 7.67% L-ascorbic acid 0.21% Flavor powder 1.26% Water 2.55% Preparation method: Using almost the same technique as in Example 1, 4.20 parts of 50% phytic acid solution, 0.92 parts of potassium hydroxide, hydroxide A mixed solution consisting of 1.22 parts of sodium, 0.21 parts of L-arginine-L-glutamate, 7.67 parts of anhydrous citric acid, 0.21 parts of L-ascorbic acid and 25 parts of water was prepared,
Anhydrous glucose 83.86 with an inflow air temperature of 70 to 80℃.
1.26 parts of perfume powder is uniformly mixed with the resulting dry powder to obtain the desired formulation. Dissolve 53 g of this preparation in water to make 1 and use it for drinking. Physical properties: The sample of Example 3 is a pure white granular powder with extremely good flowability, and the bulk density is 0.554 when flowing and 0.622 when tapping. When 53g of this is dissolved in water to make 1, it quickly dissolves to form a clear, colorless liquid with a pH of 3.35 and a freezing point of -0.53°C. Example 4 Formulation: Phytic acid (solid equivalent) 4.19% Anhydrous potassium carbonate 1.59% Sodium hydroxide (100% equivalent) 1.30% L-Arginine-L-Glutamate 0.21% Anhydrous glucose 83.86% Anhydrous citric acid 4.19% L-Ascorbine Acid 0.21% Flavor powder 1.26% Water 3.19% Preparation method: Using almost the same technique as in Example 1, 4.19 parts of 50% phytic acid, 1.30 parts of sodium hydroxide, 0.21 part of L-arginine-L-glutamate, anhydrous citric acid
Make a mixture of 4.19 parts of L-ascorbic acid, 0.21 parts of L-ascorbic acid, and 5 parts of water, and heat this solution on a hot plate at a temperature of 60 to 70℃.
Dry under reduced pressure using a vacuum dryer, and refine the resulting dry mass using a 40-mesh sieve.
The desired formulation is obtained by uniformly mixing 13.29 parts with 1.59 parts of anhydrous potassium carbonate, 83.86 parts of crystalline anhydrous glucose, and 1.26 parts of flavor powder. Dissolve 53 g of this preparation in water to make 1 and use it for drinking. Physical properties: The sample of Example 4 is a mixture of brown grains and pure white grains, has extremely good fluidity, and has a bulk density of 0.682 when fluidized.
It is 0.723 when tapping. When 53g of this is dissolved in water to make 1, if you shake it, it will quickly dissolve and become a clear, pale yellow liquid, with a pH of 3.48 and a freezing point of -0.53℃.
It is. The component concentrations of this liquid are as shown below. Phytic acid -12 40.40meq Ascorbic acid -1 0.63meq Citric acid -3 10.58meq CO 3 -2 12.22meq K + 12.22meq Na + 17.21meq Glucose 246.69mM L-Arginine-L-Glutamate 0.35mM.

Claims (1)

【特許請求の範囲】 1 フイチン酸0.8〜6.0%、無機カチオン類0.8〜
8.4%およびブドウ糖78.2〜90.3%を必須成分とす
ることを特徴とする口渇回復用組成物。 2 無機カチオン類がカリウム(K+)、ナトリウ
ム(Na+)およびマグネシウム(Mg++)である
特許請求の範囲第1項記載の口渇回復用組成物。 3 無機カチオン類の配合比、K+:Na+:Mg++
が1.0:0.6〜1.4:0〜1.0である特許請求の範囲
第1項又は第2項記載の口渇回復用組成物。 4 無機カチオンの配合総量が1g当り0.3〜3.7
mg当量である特許請求の範囲第1項、第2項又は
第3項記載の口渇回復用組成物。
[Claims] 1. Phytic acid 0.8-6.0%, inorganic cations 0.8-6.0%
A dry mouth recovery composition comprising 8.4% and 78.2 to 90.3% glucose as essential ingredients. 2. The dry mouth recovery composition according to claim 1, wherein the inorganic cations are potassium (K + ), sodium (Na + ), and magnesium (Mg ++ ). 3 Blending ratio of inorganic cations, K + :Na + :Mg ++
The dry mouth recovery composition according to claim 1 or 2, wherein the ratio is 1.0:0.6 to 1.4:0 to 1.0. 4 The total amount of inorganic cations is 0.3 to 3.7 per gram.
The dry mouth recovery composition according to claim 1, 2 or 3, which is mg equivalent.
JP5406779A 1979-05-04 1979-05-04 Thirst-relieving composition Granted JPS55145613A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5406779A JPS55145613A (en) 1979-05-04 1979-05-04 Thirst-relieving composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5406779A JPS55145613A (en) 1979-05-04 1979-05-04 Thirst-relieving composition

Publications (2)

Publication Number Publication Date
JPS55145613A JPS55145613A (en) 1980-11-13
JPS6327327B2 true JPS6327327B2 (en) 1988-06-02

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ID=12960266

Family Applications (1)

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Country Status (1)

Country Link
JP (1) JPS55145613A (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01294631A (en) * 1988-05-19 1989-11-28 Sanwa Kagaku Kenkyusho Co Ltd Remedy and preventive for diabetic disease, food and drink and table luxury
JPH01294630A (en) * 1988-05-19 1989-11-28 Sanwa Kagaku Kenkyusho Co Ltd Remedy for improving for hyperlipemia
JP4780907B2 (en) * 2003-09-30 2011-09-28 小林製薬株式会社 Hypnotic composition
CN103156243A (en) * 2013-02-22 2013-06-19 慕知君 Electrolyte functionality sports beverage and preparation method thereof
JP6300154B2 (en) * 2014-03-14 2018-03-28 ハウスウェルネスフーズ株式会社 Beverage containing star anise extract

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5486666A (en) * 1977-12-22 1979-07-10 Ajinomoto Kk Cola beverage

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