JP2005330270A - Decalcification inhibitory composition and food and beverage containing the same - Google Patents

Decalcification inhibitory composition and food and beverage containing the same Download PDF

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JP2005330270A
JP2005330270A JP2005119747A JP2005119747A JP2005330270A JP 2005330270 A JP2005330270 A JP 2005330270A JP 2005119747 A JP2005119747 A JP 2005119747A JP 2005119747 A JP2005119747 A JP 2005119747A JP 2005330270 A JP2005330270 A JP 2005330270A
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phosphate
demineralization
decalcification
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JP4729332B2 (en
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Yoshikazu Sunada
美和 砂田
Reiichiro Sakamoto
禮一郎 阪本
Toshiyuki Kimura
敏幸 木村
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New Oji Paper Co Ltd
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Abstract

<P>PROBLEM TO BE SOLVED: To obtain an oral cavity composition exhibiting a decalcification inhibitory activity under an acidic condition, and to provide a food and beverage containing the same. <P>SOLUTION: The decalcification inhibitory composition contains at least 1 kind selected from maltodextrin phosphate, a reduced maltodextrin phosphate, an oligo-saccharide phosphate, a starch phosphate and their salts, and the food, the beverage, a seasoning, an oral cavity preparation, a medicine, a cosmetic, feed or a fertilizer containing the decalcification inhibitory composition are provided. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

本発明は、酸性条件下において歯面表層下の脱灰を抑制する脱灰抑制用組成物とそれを含有する飲食物などに関する。   The present invention relates to a composition for inhibiting demineralization that suppresses demineralization under the surface of the tooth surface under acidic conditions, food and drink containing the same, and the like.

口腔内は様々な環境に晒され、通常、脱灰(歯面表層下のヒドロキシアパタイトが溶解すること)と再石灰化(リン酸カルシウムが歯面表層下に再結晶化すること)を繰り返しているが、このバランスが崩れ、再石灰化が脱灰に追いつかなくなり、自己修復不可能な状態までになると初期う蝕(表層下脱灰)となる。う蝕の予防の第一歩はこの表層下脱灰を防ぐことである。   Although the oral cavity is exposed to various environments, it usually repeats demineralization (dissolution of hydroxyapatite under the tooth surface) and remineralization (calcium phosphate recrystallizes under the tooth surface). When this balance is lost, remineralization cannot catch up with decalcification, and when self-repair is impossible, initial caries (subsurface demineralization) occurs. The first step in preventing caries is to prevent this subsurface demineralization.

脱灰は口腔内のpHが約5.5以下に低下したときに起こるといわれており、これは(1)主に醗酵性糖質であるスクロース、グルコースなどの単糖類やオリゴ糖、又はこれらの重合体を基質に口腔内細菌が産生する酸によるpH低下、(2)酸性の飲食物が直接歯面に接触することなどが原因とされている。このような脱灰を防ぐ方法としてはキシリトールやフッ素が有効であることが知られているが、その他にも特許文献1にヘキサフルオロチタン酸塩を必須成分としたう蝕の予防及び進行抑制用組成物について、特許文献2には再石灰化に負に衝撃を与えずに脱灰を抑制する水溶性リン酸塩、特にピロリン酸塩又はトリポリリン酸塩を含むエナメル質脱灰阻害剤について記載がある。ヘキサフルオロチタン酸塩は定期的に当該組成物を歯に塗布する必要があり、使用者にとって煩わしさが残る。水溶性リン酸塩は主に歯磨き剤に適用されるものである。   Demineralization is said to occur when the oral pH drops to about 5.5 or lower. This is mainly due to (1) monosaccharides and oligosaccharides such as sucrose and glucose, which are mainly fermentable carbohydrates, or these The reason is that the pH is lowered by the acid produced by oral bacteria using the polymer of (2), and (2) the acidic food or drink is in direct contact with the tooth surface. As a method for preventing such demineralization, xylitol and fluorine are known to be effective. In addition, Patent Document 1 discloses prevention of caries and suppression of progression using hexafluorotitanate as an essential component. Regarding the composition, Patent Document 2 describes a water-soluble phosphate that suppresses demineralization without negatively impacting remineralization, particularly an enamel demineralization inhibitor containing pyrophosphate or tripolyphosphate. is there. Hexafluorotitanate needs to be periodically applied to the teeth, leaving the user bothersome. Water-soluble phosphates are mainly applied to dentifrices.

また、(2)の酸性の飲食物が直接歯面に接触することが原因で脱灰することを抑制するものとしては特許文献3にイソマルトオリゴ糖還元物を有効成分とする脱灰抑制剤について、特許文献4には脱灰抑制作用のあるパラチニットと特定の有機酸カルシウム塩とを含有する食品について記載がある。イソマルトオリゴ糖還元物は本発明の趣旨である酸性条件下における歯面表層下の脱灰を抑制することに近いが、十分な効果を上げるためにはイソマルトオリゴ糖還元物を飲食物に30%以上添加しなければならず、これを飲料水に適用した場合、一度に多量のイソマルトオリゴ糖還元物を摂取することになってしまう。イソマルトオリゴ糖還元物を含む多くの糖還元物(糖アルコール)類には多量に摂取すると「お腹がゆるくなる」という生理作用があり、個人差はあるが350mlの飲料をすべて飲むことは危険ですらある。特許文献4はパラチニットと特定の有機酸カルシウム塩とを含有することで再石灰化を促進することにより、脱灰を抑制するとしている。再石灰化作用は中性付近でしか効果を示さず、本発明の脱灰抑制とは異なる。   Moreover, as what suppresses demineralization by the acidic food and drink of (2) contacting a tooth surface directly, about the decalcification inhibitor which uses isomaltoligosaccharide reductant as an active ingredient in patent document 3 Patent Document 4 describes a food containing paratinite having a decalcification-inhibiting action and a specific organic acid calcium salt. Isomaltoligosaccharide reductate is close to suppressing demineralization under the surface of the tooth surface under acidic conditions, which is the gist of the present invention, but in order to increase the effect, isomaltoligosaccharide reductate is 30% in food and drink. When this is applied to drinking water, a large amount of a reduced product of isomaltoligosaccharide will be consumed at once. Many sugar reducts (sugar alcohols), including isomalttooligosaccharide reducts, have the physiological effect of “relaxing stomach” when ingested in large amounts, and it is dangerous to drink all 350 ml of beverage, although it varies depending on the individual. There is. Patent Document 4 describes that demineralization is suppressed by promoting remineralization by containing palatinit and a specific organic acid calcium salt. The remineralization action is effective only in the vicinity of neutrality, and is different from the demineralization suppression of the present invention.

特開昭55−35015号公報Japanese Patent Laid-Open No. 55-35015 特表平7−505400号公報JP 7-505400 A 特開平10−87461号公報JP-A-10-87461 特開2000−270810号公報JP 2000-270810 A

本発明は前記状況を鑑みてなされたものであり、酸性条件下において脱灰抑制作用を発現する口腔用組成物及びそれを含有する飲食物などを提供することを目的とする。   This invention is made | formed in view of the said condition, and it aims at providing the composition for oral cavity which expresses a decalcification inhibitory action on acidic conditions, food / beverage products containing it, etc.

本発明者らは、前記課題を解決するために鋭意検討した結果、リン酸マルトデキストリン、還元リン酸マルトデキストリン、リン酸オリゴ糖、還元リン酸オリゴ糖、リン酸澱粉及びそれらの塩から選ばれる少なくとも1種をことを見出し、本発明を完成した。   As a result of intensive studies to solve the above problems, the present inventors have been selected from maltodextrin phosphate, maltodextrin phosphate phosphate, oligosaccharide phosphate, reduced phosphate oligosaccharide, phosphate starch and salts thereof. At least one kind was found and the present invention was completed.

すなわち、本発明は以下の発明を包含する。
(1)リン酸マルトデキストリン、還元リン酸マルトデキストリン、リン酸オリゴ糖、還元リン酸オリゴ糖、リン酸澱粉及びそれらの塩から選ばれる少なくとも1種を含有する脱灰抑制用組成物。
(2)更に、少なくとも1種の水溶性カルシウム塩を含有する前記(1)記載の脱灰抑制用組成物。
(3)脱灰抑制用組成物がpH4以下において脱灰抑制作用を有する前記(1)又は前記(2)に記載の脱灰抑制用組成物。
(4)食品、飲料、調味料、口腔剤、医薬品、化粧品、飼料又は肥料に添加するための前記(1)〜(3)のいずれかに記載の脱灰抑制用組成物。
(5)前記(1)〜(3)のいずれかに記載の脱灰抑制用組成物を含有する食品、飲料、調味料、口腔剤、医薬品、化粧品、飼料又は肥料。
That is, the present invention includes the following inventions.
(1) A composition for inhibiting demineralization comprising at least one selected from maltodextrin phosphate, reduced maltodextrin phosphate, oligosaccharide phosphate, reduced phosphate oligosaccharide, phosphate starch and salts thereof.
(2) The composition for suppressing demineralization according to (1), further comprising at least one water-soluble calcium salt.
(3) The demineralization-suppressing composition according to (1) or (2), wherein the demineralization-suppressing composition has a decalcification-suppressing action at a pH of 4 or less.
(4) The composition for suppressing demineralization according to any one of (1) to (3), which is added to foods, beverages, seasonings, oral preparations, pharmaceuticals, cosmetics, feed, or fertilizers.
(5) Foods, beverages, seasonings, oral preparations, pharmaceuticals, cosmetics, feeds or fertilizers containing the composition for suppressing demineralization according to any one of (1) to (3).

本発明によれば、脱灰が始まる口腔内のpH5.5以下という酸性条件下でも脱灰を抑制することができる。更に、従来全く知られていないpH4以下という、飲料に多い低pH領域下においても脱灰抑制できる。   According to the present invention, decalcification can be suppressed even under acidic conditions of pH 5.5 or less in the oral cavity where demineralization begins. Furthermore, deashing can be suppressed even in a low pH region, which is often unknown in beverages, of pH 4 or less, which is not known at all.

以下に本発明を詳細に説明する。
本発明におけるリン酸マルトデキストリン(以下、PMDと称す)はグルコース重合度10を越えるマルトデキストリンに少なくとも1個のリン酸基が結合しているリン酸化糖であり、還元リン酸マルトデキストリン(以下、還元PMDと称す)はグルコース重合度10を越える還元マルトデキストリンに少なくとも1個のリン酸基が結合しているリン酸化糖である。リン酸オリゴ糖(以下、POSと称す)はグルコース重合度10以下のオリゴ糖に少なくとも1個のリン酸基が結合しているリン酸化糖であり、還元リン酸オリゴ糖(以下、還元POSと称す)はグルコース重合度10以下の還元オリゴ糖に少なくとも1個のリン酸基が結合しているリン酸化糖である。リン酸澱粉は澱粉にリン酸基が結合した酸性多糖であり、食品添加物に規定されている「でんぷんリン酸エステルナトリウム」もその一つである。でんぷんリン酸エステルナトリウムは結合リン含量が3重量%以内、無機リン比率が全リンの20%以下と規定されている。なお、本発明では食品添加物の規定に含まれないリン酸澱粉も対象として含まれる。
The present invention is described in detail below.
The maltodextrin phosphate (hereinafter referred to as PMD) in the present invention is a phosphorylated saccharide in which at least one phosphate group is bonded to maltodextrin having a glucose polymerization degree exceeding 10, and a reduced maltodextrin phosphate (hereinafter referred to as PMD). (Referred to as reduced PMD) is a phosphorylated saccharide in which at least one phosphate group is bound to a reduced maltodextrin having a glucose polymerization degree exceeding 10. Phosphate oligosaccharide (hereinafter referred to as POS) is a phosphorylated saccharide in which at least one phosphate group is bonded to an oligosaccharide having a glucose polymerization degree of 10 or less, and a reduced phosphate oligosaccharide (hereinafter referred to as reduced POS). Is a phosphorylated saccharide in which at least one phosphate group is bound to a reducing oligosaccharide having a glucose polymerization degree of 10 or less. Phosphoric acid starch is an acidic polysaccharide in which phosphate groups are bonded to starch, and “starch phosphate sodium” defined in food additives is one of them. Starch phosphate sodium is specified to have a bound phosphorus content of 3% by weight or less and an inorganic phosphorus ratio of 20% or less of the total phosphorus. In addition, in this invention, the phosphate starch which is not contained in prescription | regulation of a food additive is also included as object.

PMD、還元PMD、POS及び還元POS、リン酸澱粉の塩としては、例えばナトリウム塩、カリウム塩等のアルカリ金属塩、カルシウム塩、マグネシウム塩等のアルカリ土類金属塩、アンモニウム塩、鉄塩、亜鉛塩、アルミニウム塩などが挙げられる。   Examples of salts of PMD, reduced PMD, POS and reduced POS, and phosphate starch include alkali metal salts such as sodium salt and potassium salt, alkaline earth metal salts such as calcium salt and magnesium salt, ammonium salt, iron salt and zinc Examples include salts and aluminum salts.

本発明は、PMD、還元PMD、POS、還元POS及びそれらの塩から選ばれる少なくとも1種、好ましくは、更に前記成分に水溶性カルシウム塩を併用することで脱灰を抑制するものである。   In the present invention, decalcification is suppressed by using at least one selected from PMD, reduced PMD, POS, reduced POS and salts thereof, preferably a water-soluble calcium salt in combination with the above components.

PMD、還元PMD、POS、還元POS及びそれらの塩は少量で脱灰抑制作用を発現し、口腔内細菌によって資化されないため、口腔内pHを低下させる酸が産生することがない。また、これらの物質はリン酸イオンとカルシウムイオンが共存する系においてリン酸カルシウムが結晶となって沈殿することを防ぐCa可溶化作用と、同時に同じ系内に歯のリン酸カルシウムの結晶成分であるヒドロキシアパタイトが存在すると、結晶のヒドロキシアパタイトにリン酸カルシウムを沈着させる再石灰化作用の二つの作用を有する物質である。しかも、これらの物質は特許文献4のように再石灰化を促進し、その結果脱灰を抑制するものではなく、酸性条件下において脱灰そのものを抑制する作用も持っているのである。   PMD, reduced PMD, POS, reduced POS, and salts thereof exhibit a decalcification inhibitory action in a small amount and are not assimilated by oral bacteria, so that an acid that lowers oral pH is not produced. In addition, these substances have a Ca solubilization action that prevents calcium phosphate from precipitating as crystals in a system in which phosphate ions and calcium ions coexist, and at the same time, hydroxyapatite that is a crystal component of calcium phosphate in the teeth is contained in the same system. When present, it is a substance having two actions of remineralization that deposits calcium phosphate on crystalline hydroxyapatite. In addition, these substances promote remineralization as in Patent Document 4, and as a result do not suppress decalcification, but also have an effect of suppressing decalcification itself under acidic conditions.

脱灰抑制剤として用いる場合にはPMD、還元PMD、POS、還元POS、リン酸澱粉及びそれらの塩から選ばれる少なくとも1種を飲食物に対して0.0001〜10w/w%添加することが好ましい。   When used as a decalcification inhibitor, 0.0001-10 w / w% of at least one selected from PMD, reduced PMD, POS, reduced POS, phosphate starch and salts thereof may be added to food and drink. preferable.

本発明の脱灰抑制用組成物は、更に水溶性カルシウム塩を配合することにより、その効果が増強される。水溶性カルシウム塩としては、例えば乳酸カルシウム、グルコン酸カルシウム、パントテン酸カルシウム、クエン酸カルシウム、第一リン酸水素カルシウム、リン酸カルシウム、グリセロリン酸カルシウム、塩化カルシウムなどが挙げられ、これらは飲食物に対して0.001〜1w/w%添加することが好ましい。   The effect of the deashing suppression composition of the present invention is enhanced by further blending a water-soluble calcium salt. Examples of the water-soluble calcium salt include calcium lactate, calcium gluconate, calcium pantothenate, calcium citrate, calcium hydrogen phosphate, calcium phosphate, calcium glycerophosphate, calcium chloride, and the like. It is preferable to add 0.001 to 1 w / w%.

本発明の脱灰抑制用組成物を使用した飲食物のpHは、好ましくは3〜7、更に好ましくは3〜6である。pHの調整には、例えば、クエン酸、リンゴ酸、酒石酸、グルコン酸フマル酸、コハク酸、酢酸、乳酸、アジピン酸、イタコン酸、フィチン酸、グルコノデルタラクトン及びそれら一部の塩が用いられる。   The pH of the food or drink using the deashing suppression composition of the present invention is preferably 3 to 7, more preferably 3 to 6. For adjusting the pH, for example, citric acid, malic acid, tartaric acid, fumaric acid gluconate, succinic acid, acetic acid, lactic acid, adipic acid, itaconic acid, phytic acid, glucono delta lactone, and some salts thereof are used. .

本発明の脱灰抑制用組成物は食品、飲料、調味料、口腔剤、医薬品、化粧品、飼料、肥料などに利用することができる。   The composition for inhibiting demineralization of the present invention can be used for foods, beverages, seasonings, oral preparations, pharmaceuticals, cosmetics, feeds, fertilizers and the like.

以下、実験例及び実施例により本発明を具体的に説明するが、本発明は下記実施例により、その技術的範囲が限定されるものではない。試験に使用したPMD、POS、還元PMD、(及び)還元POS及びリン酸澱粉は以下の方法で調製し、その結合リン量と平均重合度を表1に示した。   EXAMPLES Hereinafter, although an Example and an Example demonstrate this invention concretely, the technical scope of this invention is not limited by the following Example. PMD, POS, reduced PMD, (and) reduced POS and phosphate starch used in the test were prepared by the following method. The amount of bound phosphorus and the average degree of polymerization are shown in Table 1.

(試験材料の調製)
<リン酸澱粉>
コーンスターチ(王子コーンスターチ株式会社製、水分13重量%)1200kgを一定の流速でタービュライザに導入し、同時に第一リン酸ナトリウム・2水塩176kgと無水第二リン酸ナトリウム 32kgを水に溶解して全量655kgのリン酸溶液(溶液中のリン含量6.4重量%、pH6.0)を一定の流速で添加して均一に混合した。このリン酸混合澱粉をフラッシュ・ドライヤーで水分6重量%となるまで乾燥し、得られたリン酸含浸澱粉(リン含量3.5重量%、pH5.6)750kgを流動層加熱機(王子コーンスターチ株式会社製)に投入した。加熱した熱風を供給して流動加熱し、排気される熱風は流動層の系外に排出した。加熱開始後、30分で175℃まで昇温し、熱風の排気はそのまま系外に排出し続けて、175℃で120分加熱反応した。加熱反応終了後、送風を冷風に切り替え、更に熱風の排気を系外に排出し続けて、品温を100℃以下にまで冷却した。回収されたリン酸エステル澱粉は700kgであり、その結合リン含量は2.8重量%、リン酸化率は81%であった。
(Preparation of test materials)
<Phosphate starch>
Introduce 1200 kg of cornstarch (manufactured by Oji Cornstarch Co., Ltd., 13 wt% water) into the turbulator at a constant flow rate, and simultaneously dissolve 176 kg of monobasic sodium phosphate dihydrate and 32 kg of anhydrous dibasic sodium phosphate in water. 655 kg of phosphoric acid solution (phosphorus content in the solution 6.4% by weight, pH 6.0) was added at a constant flow rate and mixed uniformly. This phosphoric acid mixed starch was dried with a flash dryer until the water content became 6% by weight, and 750 kg of the resulting phosphoric acid-impregnated starch (phosphorus content 3.5% by weight, pH 5.6) was added to a fluidized bed heater (Oji Cornstarch Co., Ltd.). (Made by company). The heated hot air was supplied and fluidized and heated, and the exhausted hot air was discharged out of the fluidized bed. The temperature was raised to 175 ° C. in 30 minutes after the start of heating, and the hot air exhaust continued to be discharged out of the system as it was, and the reaction was performed at 175 ° C. for 120 minutes. After completion of the heating reaction, the air flow was switched to cold air, and the hot air exhaust was continuously discharged out of the system to cool the product temperature to 100 ° C. or lower. The recovered phosphate starch was 700 kg, the bound phosphorus content was 2.8% by weight, and the phosphorylation rate was 81%.

<PMD>
70℃の水71Lに塩化カルシウム二水和物34gを溶解した後、攪拌しながら前述のリン酸澱粉8kgを徐々に添加しながら溶解した。水酸化ナトリウムでpH6.0とした後、超耐熱性α−アミラーゼ(ターマミル クラッシック、ノボザイムズ社製)を対澱粉0.05重量%添加し、5分間保持した。粘度が下がり始めるとリン酸澱粉45kgを徐々に追加添加した。水酸化ナトリウムでpH6.0に再調整後、追加した澱粉に対してターマミル クラッシックを0.05重量%添加して10分保持した。次に、調製したリン酸澱粉分散液をジェットクッカーにて入口温度110℃、滞留時間5分の条件で処理した。ジェットクッカー処理した液をタンクに集め、ターマミル クラッシックを対澱粉0.05重量%追加添加し、60℃、3時間反応させた。酵素反応は塩酸でpH3.5に調整し、終了とした。
<PMD>
After dissolving 34 g of calcium chloride dihydrate in 71 L of water at 70 ° C., 8 kg of the above phosphate starch was gradually added and dissolved while stirring. After adjusting the pH to 6.0 with sodium hydroxide, 0.05% by weight of starch was added to the super thermostable α-amylase (Termamyl Classic, manufactured by Novozymes) and held for 5 minutes. When the viscosity began to drop, 45 kg of phosphate starch was gradually added. After re-adjusting to pH 6.0 with sodium hydroxide, 0.05% by weight of Termamyl Classic was added to the added starch and held for 10 minutes. Next, the prepared phosphate starch dispersion was treated with a jet cooker under conditions of an inlet temperature of 110 ° C. and a residence time of 5 minutes. The liquid subjected to the jet cooker treatment was collected in a tank, and 0.05% by weight of Termamyl classic was added to the starch and reacted at 60 ° C. for 3 hours. The enzymatic reaction was adjusted to pH 3.5 with hydrochloric acid and completed.

酵素処理液の精製は比較例と同様に行い、セラミック濾過に8時間を要した。その後、比較例と同様にしてスプレードライで粉末化し、36.2kgのPMDを得た。   The enzyme treatment solution was purified in the same manner as in the comparative example, and 8 hours were required for ceramic filtration. Then, it powdered by spray-drying like the comparative example, and obtained 36.2 kg PMD.

<還元PMD>
還元デキストリン100kg(東和化成(株)製PO−10)とリン酸ナトリウム溶液(リン酸1ナトリウム・2水塩15kgとリン酸2ナトリウム2.7kgを水400kgに溶解したものをスプレードライヤーで乾燥粉末化した。これを流動層に投入し、170℃まで昇温後2時間焙焼し、得られた試料を20%水溶液とし粉末活性炭を対固形分10重量%添加し、60℃、2時間攪拌保持した。その後、セラミック濾過機で残渣と活性炭を除去した。濾過供給液が減少したら純水を添加して透過液のBrixが1以下になるまで濾過を行った。NF膜で脱塩・濃縮処理を行い、さらに10重量%の水酸化ナトリウムでpH6.2に調整した。0.45μmのポリスルフォンのメンブレンフィルターで濾過後、スプレードライヤーで乾燥粉末化し還元PMDを得た。
<Reduced PMD>
Reduced dextrin 100kg (PO-10, manufactured by Towa Kasei Co., Ltd.) and sodium phosphate solution (15kg monosodium phosphate dihydrate and 2.7kg disodium phosphate dissolved in 400kg water dried powder with a spray dryer This was put into a fluidized bed, heated to 170 ° C. and then roasted for 2 hours, and the resulting sample was made into a 20% aqueous solution and 10% by weight of powdered activated carbon was added to the solid, and stirred at 60 ° C. for 2 hours. After that, the residue and activated carbon were removed with a ceramic filter.When the filtration feed liquid decreased, pure water was added and filtration was performed until the Brix of the permeate was 1 or less. Then, the solution was adjusted to pH 6.2 with 10% by weight sodium hydroxide, filtered through a 0.45 μm polysulfone membrane filter, and dried with a spray dryer. Sueka to obtain a reducing PMD.

<POS>
特開2002−325556号公報の実施例1の方法に準じてPOSを得た。
<POS>
POS was obtained according to the method of Example 1 of JP-A-2002-325556.

<還元POS>
上記で得たPOSを出発物質として特開2002−325556号公報の実施例10の方法に準じて還元POSを得た。
<Reduced POS>
Reduced POS was obtained according to the method of Example 10 of JP-A No. 2002-325556 using the POS obtained above as a starting material.

Figure 2005330270
Figure 2005330270

(実験例)
以下のような脱灰抑制試験を行い、脱灰抑制率を求め評価した。
(Experimental example)
The following deashing suppression test was conducted to determine and evaluate the deashing suppression rate.

(脱灰抑制試験)
表2に示すpH4.5の試験液を作成し、この対照液及び試験液10mlにヒドロキシアパタイト(SIGMA社)を5mg添加、攪拌した後、36℃で1時間脱灰反応させた。反応終了後、12000rpmで3分遠心分離を行い、その上澄み液の可溶性カルシウム濃度をカルシウム測定キット(和光純薬製カルシウムCテストワコー)で測定し、下記の式により脱灰抑制率を計算した。なお、特別の表記がない限り%の表示はw/v%である。
脱灰率=(試験液又は対照液のカルシウム濃度*/添加したヒドロキシアパタイトが全量溶解した時のカルシウム濃度)×100
*水溶性カルシウム塩を添加している試験では添加したカルシウム塩のカルシウム分を引いた濃度を使用
脱灰抑制率=(1−(試験液の脱灰率/対照液の脱灰率))×100
結果を表3に示す。
(Decalcification suppression test)
A test solution having a pH of 4.5 shown in Table 2 was prepared, and 5 mg of hydroxyapatite (SIGMA) was added to 10 ml of the control solution and the test solution and stirred, followed by decalcification at 36 ° C. for 1 hour. After completion of the reaction, the mixture was centrifuged at 12,000 rpm for 3 minutes, the soluble calcium concentration of the supernatant was measured with a calcium measurement kit (Calcium C Test Wako manufactured by Wako Pure Chemical Industries), and the decalcification inhibition rate was calculated by the following formula. Unless otherwise indicated,% is w / v%.
Decalcification rate = (calcium concentration of test solution or control solution * / calcium concentration when all of the added hydroxyapatite is dissolved) × 100
* In the test in which water-soluble calcium salt is added, the concentration obtained by subtracting the calcium content of the added calcium salt is used. Demineralization inhibition rate = (1− (decalcification rate of test solution / decalcification rate of control solution)) × 100
The results are shown in Table 3.

Figure 2005330270
Figure 2005330270

Figure 2005330270
Figure 2005330270

実験例の結果から分かるようにPMD、還元PMD、POS、還元POS、リン酸澱粉を添加することにより脱灰がかなり抑えられ、これらの物質が強い脱灰抑制作用を持っていることが確認できた。また水溶性カルシウム塩を併用することでその作用が増強されることも確認できた。
次に、本発明組成物を飲食物に利用した例を示す。
As can be seen from the results of the experimental examples, the addition of PMD, reduced PMD, POS, reduced POS, and phosphate starch can significantly suppress decalcification and confirm that these substances have a strong demineralization inhibitory effect. It was. It was also confirmed that the action was enhanced by using a water-soluble calcium salt in combination.
Next, the example which utilized this invention composition for food and drink is shown.

(実施例1)
飲食物(酸性飲料水:レモンティー)
酸性飲料水であるレモンティー(pH3.9)10mlにPMDを0.1g溶解したものを試験液、何も添加していないものを対照液とし両液にヒドロキシアパタイト(SIGMA社)を5mg添加、攪拌した後、36℃で1時間脱灰反応させた。反応終了後、12000rpmで3分遠心分離を行い、その上澄み液の可溶性カルシウム濃度を測定した。前述の脱灰抑制試験の計算式より脱灰抑制率を求めた。脱灰抑制率は40%であった。
(Example 1)
Food and drink (acidic water: lemon tea)
5 mg of hydroxyapatite (SIGMA) was added to both solutions as a test solution in which 0.1 g of PMD was dissolved in 10 ml of lemon tea (pH 3.9) which is an acidic drinking water, After stirring, the reaction was decalcified at 36 ° C. for 1 hour. After completion of the reaction, the mixture was centrifuged at 12000 rpm for 3 minutes, and the soluble calcium concentration of the supernatant was measured. The demineralization inhibition rate was calculated from the formula for the demineralization inhibition test described above. The decalcification inhibition rate was 40%.

(実施例2)
飲食物(酸性飲料水:レモンティー)
酸性飲料水であるレモンティー(pH3.9)10mlにPMDを0.1g、乳酸カルシウムを0.01g溶解したものを試験液とした以外は実施例1と同様の操作を行った。脱灰抑制率は52%であった。
(Example 2)
Food and drink (acidic water: lemon tea)
The same operation as in Example 1 was performed except that 0.1 g of PMD and 0.01 g of calcium lactate were dissolved in 10 ml of lemon tea (pH 3.9) which is acidic drinking water. The decalcification inhibition rate was 52%.

(比較例1:PMD無添加例)
PMDの代わりに砂糖を0.1g溶解した以外は実施例1と同様の操作を行った。脱灰抑制率は0%であった。
(Comparative Example 1: PMD-free example)
The same operation as in Example 1 was performed except that 0.1 g of sugar was dissolved instead of PMD. The demineralization inhibition rate was 0%.

(実施例3)
飲食物(酸性飲料水:砂糖入りブラックタイプコーヒー)
酸性飲料水である砂糖入りブラックタイプコーヒー(pH5.3)10mlにPMDを0.01g溶解したものを試験液、何も添加していないものを対照液とし両液にヒドロキシアパタイト(SIGMA社)を5mg添加、攪拌した後、36℃で1時間脱灰反応させた。反応終了後、12000rpmで3分遠心分離を行い、その上澄み液の可溶性カルシウム濃度を測定した。脱灰抑制率は93%であった。
(Example 3)
Food and drink (acidic drinking water: black coffee with sugar)
Hydroxyapatite (SIGMA) was used as a test solution in which 0.01 g of PMD was dissolved in 10 ml of sugar-containing black type coffee (pH 5.3), which is acidic drinking water, and in which nothing was added as a control solution. After 5 mg was added and stirred, the reaction was decalcified at 36 ° C. for 1 hour. After completion of the reaction, the mixture was centrifuged at 12000 rpm for 3 minutes, and the soluble calcium concentration of the supernatant was measured. The decalcification inhibition rate was 93%.

(比較例2:PMD無添加例)
PMDの代わりにブドウ糖を0.01g溶解した以外は実施例3と同様の操作を行った。脱灰抑制率は0%であった。
(Comparative example 2: PMD additive-free example)
The same operation as in Example 3 was performed except that 0.01 g of glucose was dissolved instead of PMD. The demineralization inhibition rate was 0%.

(実施例4)
飲食物(酸性飲料水:フルーツジュース)
酸性飲料水であるフルーツジュース(pH3.7)10mlにPMDを0.1g溶解したものを試験液、何も添加していないものを対照液とし両液にヒドロキシアパタイト(SIGMA社)を5mg添加、攪拌した後、36℃で1時間脱灰反応させた。反応終了後、12000rpmで3分遠心分離を行い、その上澄み液の可溶性カルシウム濃度を測定した。脱灰抑制率は21%であった。
Example 4
Food and drink (acidic drinking water: fruit juice)
5 mg of hydroxyapatite (SIGMA) was added to both solutions as a test solution in which 0.1 g of PMD was dissolved in 10 ml of fruit juice (pH 3.7) which is acidic drinking water, and nothing added. After stirring, the reaction was decalcified at 36 ° C. for 1 hour. After completion of the reaction, the mixture was centrifuged at 12000 rpm for 3 minutes, and the soluble calcium concentration of the supernatant was measured. The demineralization inhibition rate was 21%.

(実施例5)
飲食物(酸性飲料水:フルーツジュース)
酸性飲料水であるフルーツジュース(pH3.7)10mlにPMD0.1gとともに乳酸カルシウムを0.01g溶解したものを試験液とした以外は実施例4と同様の操作を行った。脱灰抑制率は35%であった。
(Example 5)
Food and drink (acidic drinking water: fruit juice)
The same operation as in Example 4 was performed except that 0.01 g of calcium lactate and 0.1 g of PMD were dissolved in 10 ml of fruit juice (pH 3.7) as acidic drinking water. The demineralization inhibition rate was 35%.

(比較例3:PMD無添加例)
PMDの代わりに砂糖を0.1g溶解した以外は実施例4と同様の操作を行った。脱灰抑制率は0%であった。
実施例1〜5、比較例1〜3の結果を表4にまとめた。
(Comparative example 3: PMD additive-free example)
The same operation as in Example 4 was performed except that 0.1 g of sugar was dissolved instead of PMD. The demineralization inhibition rate was 0%.
The results of Examples 1 to 5 and Comparative Examples 1 to 3 are summarized in Table 4.

Figure 2005330270
Figure 2005330270

(実施例6)
本実施例は歯のモデルをヒドロキシアパタイト(SIGMA社)から、より歯に近い構造物であるヒドロキシアパタイト成型品(ペンタックス社製CELLYARD HA scaffold)に代えて脱灰抑制試験を行った例である。
飲食物(酸性飲料水:スポーツドリンク)
酸性飲料水であるスポーツドリンク(pH3.5)10mlにPMDを0.01g溶解したものを試験液、何も添加していないものを対照液とし両液にヒドロキシアパタイト成型品を一錠添加、攪拌した後、36℃で2時間脱灰反応させた。反応終了後、その上澄み液の可溶性カルシウム濃度を測定した。前述の脱灰抑制試験の計算式より脱灰抑制率を求めた。脱灰抑制率は47%であった。
(Example 6)
In this example, a decalcification suppression test was performed by replacing the hydroxyapatite (SIGMA) with a hydroxyapatite molded product (CELLYARD HA scaffold manufactured by PENTAX), which is a structure closer to a tooth.
Food and drink (acidic water: sports drink)
A test drink is prepared by dissolving 0.01 g of PMD in 10 ml of sports drink (pH 3.5), which is an acidic drinking water, and one tablet of hydroxyapatite molded product is added to both solutions, with nothing added as a control solution, and stirred. After that, decalcification was performed at 36 ° C. for 2 hours. After completion of the reaction, the soluble calcium concentration of the supernatant was measured. The demineralization inhibition rate was calculated from the formula for the demineralization inhibition test described above. The decalcification inhibition rate was 47%.

(実施例7)
酸性飲料水であるスポーツドリンク(pH3.5)10mlにPMD0.05g溶解した以外は実施例6と同様の操作を行った。脱灰抑制率は65%であった。
(Example 7)
The same operation as in Example 6 was performed except that 0.05 g of PMD was dissolved in 10 ml of sports drink (pH 3.5) which is acidic drinking water. The decalcification inhibition rate was 65%.

(実施例8)
酸性飲料水であるスポーツドリンク(pH3.5)10mlにPMD0.03gとともに塩化カルシウムを0.01g溶解したものを試験液とした以外は実施例6と同様の操作を行った。脱灰抑制率は65%であった。
(Example 8)
The same operation as in Example 6 was performed, except that 0.01 g of calcium chloride was dissolved together with 0.03 g of PMD in 10 ml of sports drink (pH 3.5) which is an acidic drinking water. The decalcification inhibition rate was 65%.

(比較例4:PMD無添加例)
PMDの代わりにキシリトールを0.1g溶解した以外は実施例6と同様の操作を行った。脱灰抑制率は0%であった。
(Comparative example 4: PMD additive-free example)
The same operation as in Example 6 was performed except that 0.1 g of xylitol was dissolved instead of PMD. The demineralization inhibition rate was 0%.

(実施例9)
飲食物(酸性飲料水:ピーチジュース)
酸性飲料水であるピーチジュース(pH3.6)10mlに還元PMDを0.05g溶解したものを試験液、何も添加していないものを対照液とし両液にヒドロキシアパタイト成型品を一錠添加、攪拌した後、36℃で2時間脱灰反応させた。反応終了後、その上澄み液の可溶性カルシウム濃度を測定した。前述の脱灰抑制試験の計算式より脱灰抑制率を求めた。脱灰抑制率は37%であった。
Example 9
Food and drink (acidic drinking water: peach juice)
A solution of 0.05 g of reduced PMD dissolved in 10 ml of peach juice (pH 3.6), which is acidic drinking water, was added to the test solution, and one tablet of hydroxyapatite molded product was added to both solutions. After stirring, the reaction was decalcified at 36 ° C. for 2 hours. After completion of the reaction, the soluble calcium concentration of the supernatant was measured. The demineralization inhibition rate was calculated from the formula for the demineralization inhibition test described above. The decalcification inhibition rate was 37%.

(比較例5:PMD無添加例)
還元PMDの代わりにパラチニットを0.1g溶解した以外は実施例8と同様の操作を行った。脱灰抑制率は0%であった。
実施例6〜9、比較例4、5の結果を表5にまとめた。
(Comparative Example 5: PMD-free example)
The same operation as in Example 8 was performed except that 0.1 g of paratinite was dissolved instead of reduced PMD. The demineralization inhibition rate was 0%.
The results of Examples 6 to 9 and Comparative Examples 4 and 5 are summarized in Table 5.

Figure 2005330270
Figure 2005330270

Claims (5)

リン酸マルトデキストリン、還元リン酸マルトデキストリン、リン酸オリゴ糖、還元リン酸オリゴ糖、リン酸澱粉及びそれらの塩から選ばれる少なくとも1種を含有する脱灰抑制用組成物。   A composition for suppressing demineralization, comprising at least one selected from maltodextrin phosphate, reduced maltodextrin phosphate, oligosaccharide phosphate, reduced phosphate oligosaccharide, phosphate starch and salts thereof. 更に、少なくとも1種の水溶性カルシウム塩を含有する請求項1記載の脱灰抑制用組成物。   Furthermore, the composition for demineralization suppression of Claim 1 containing at least 1 sort (s) of water-soluble calcium salt. 脱灰抑制用組成物がpH4以下において脱灰抑制作用を有する請求項1又は請求項2記載の脱灰抑制用組成物。   The demineralization-suppressing composition according to claim 1 or 2, wherein the demineralization-suppressing composition has a decalcification-suppressing action at a pH of 4 or less. 食品、飲料、調味料、口腔剤、医薬品、化粧品、飼料又は肥料に添加するための請求項1〜3のいずれか1項に記載の脱灰抑制用組成物。   The composition for demineralization suppression according to any one of claims 1 to 3, which is added to foods, beverages, seasonings, oral preparations, pharmaceuticals, cosmetics, feed or fertilizers. 請求項1〜3のいずれか1項に記載の脱灰抑制用組成物を含有する食品、飲料、調味料、口腔剤、医薬品、化粧品、飼料又は肥料。   A food, beverage, seasoning, oral preparation, pharmaceutical, cosmetic, feed or fertilizer containing the composition for suppressing demineralization according to any one of claims 1 to 3.
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JP2007020567A (en) * 2005-06-16 2007-02-01 Oji Paper Co Ltd Phosphorylated saccharide composition and method for producing the same
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