JPH0477415A - Dental calcus preventing composition - Google Patents

Dental calcus preventing composition

Info

Publication number
JPH0477415A
JPH0477415A JP2187944A JP18794490A JPH0477415A JP H0477415 A JPH0477415 A JP H0477415A JP 2187944 A JP2187944 A JP 2187944A JP 18794490 A JP18794490 A JP 18794490A JP H0477415 A JPH0477415 A JP H0477415A
Authority
JP
Japan
Prior art keywords
composition
casein phosphopeptide
calcus
dental
formation
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
JP2187944A
Other languages
Japanese (ja)
Other versions
JPH0699294B2 (en
Inventor
Seiji Fukuda
福田 清司
Yasuo Tanaka
康雄 田中
Hideaki Miyawaki
宮脇 英昭
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.)
TAIYO KORYO KK
Original Assignee
TAIYO KORYO 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 TAIYO KORYO KK filed Critical TAIYO KORYO KK
Priority to JP2187944A priority Critical patent/JPH0699294B2/en
Publication of JPH0477415A publication Critical patent/JPH0477415A/en
Publication of JPH0699294B2 publication Critical patent/JPH0699294B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Cosmetics (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Confectionery (AREA)

Abstract

PURPOSE:To obtain dental calcus-preventing composition having excellent dental calcus formation-preventing action and high safety even in continuous use for a long time containing casein phosphopeptide as an active ingredient. CONSTITUTION:Casein phosphopeptide used in an amount of >=0.01wt.%, preferably 0.1-5wt.% to total of the composition and other well-known excipient, auxiliary, flavor, antibacterial agent or antiseptic agent, etc., are suitably mixed, then prepared to afford the objective composition. Said composition can be used in adding to dentifrice, mouth wash, a troche, a gargle, an ointment or chewing gum, etc. Casein phosphopeptide suppresses precipitation of calcium phosphate regarded as a cause of dental calcus formation, suppresses the transformation from amorphous calcium phosphate to hydroxyapatite and further effectively suppresses the crystal growth of hydroxyapatite.

Description

【発明の詳細な説明】 〈産業上の利用分野〉 本発明は、歯石防止組成物に関し、更に詳細には練り歯
みがき、マウスウォッシュ、トローチなどの口腔用組成
物等に添加して歯石形成を抑制する歯石防止組成物に関
する。
DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to an anti-tartar composition, and more particularly, to an anti-tartar composition that can be added to oral compositions such as toothpaste, mouthwash, troches, etc. to suppress the formation of tartar. The present invention relates to an anti-tartar composition.

〈従来の技術〉 歯石はその表面の粗造さのため、歯肉に対して、機械的
な刺激因子となるとともに、歯肉炎、歯周炎の病因とな
ることが知られている。歯石形成の詳細については必ず
しも明らかにされているわけではないが、プラークを構
成する細菌や唾液糖タンパク等の有機基質に唾液や、浸
出液から供給されるカルシウムやリンが沈着し、これが
結晶化するプラークの石灰化現象としてとらえることが
できる。一方、唾液や血清中に存在するカルシウムやリ
ンの濃度が歯や骨の主成分であるリン酸カルシウムに対
して過飽和であり、歯や前厄外の組織が石灰化しないの
は体液中にピロリン酸塩が存在するからだと考えられて
いる。このことから、歯石形成を抑制するために、ピロ
リン酸ナトリウム(pp)やトリポリリン酸ナトリウム
(TPP)などについて、例えばran Vitroお
よび動物実験によるポリリン酸ナトリウムの歯石形成抑
制効果にかんする研究」 (三宅幹雄、大里文夫、臼歯
周誌第30巻3号p、860〜867)等が提案されて
いる。
<Prior Art> Due to its rough surface, dental calculus is known to be a mechanical irritating factor for the gums and to be a cause of gingivitis and periodontitis. Although the details of tartar formation are not necessarily clear, calcium and phosphorus supplied from saliva and exudate are deposited on organic substrates such as bacteria and salivary glycoproteins that make up plaque, and this crystallizes. It can be understood as a calcification phenomenon of plaque. On the other hand, the concentration of calcium and phosphorus present in saliva and serum is supersaturated with respect to calcium phosphate, which is the main component of teeth and bones. It is thought that this is because it exists. Therefore, in order to suppress tartar formation, we conducted research on the inhibitory effects of sodium polyphosphate on tartar formation using sodium pyrophosphate (PP) and sodium tripolyphosphate (TPP), for example, in ran vitro and animal experiments.'' (Mikio Miyake) , Fumio Osato, Journal of Periodontology Vol. 30, No. 3, p. 860-867), etc. have been proposed.

また、従来よりカゼインホスホペプチドは、カルシウム
吸収促進因子として知られており、例えばβ−カゼイン
由来のペプチドやα−カゼイン由来のペプチドが知られ
ている。しかしながら該カゼインホスホペプチドが、歯
石形成防止作用を有することについては知られていない
のが現状である。
Furthermore, casein phosphopeptides have been conventionally known as calcium absorption promoting factors, and for example, peptides derived from β-casein and peptides derived from α-casein are known. However, at present, it is not known that the casein phosphopeptide has an effect of preventing dental calculus formation.

〈発明が解決しようとする課題〉 従って、本発明の目的は、歯石形成防止作用に優れ、且
つ長時間にわたる連続使用においても安全性の高い歯石
防止組成物を提供することにある。
<Problems to be Solved by the Invention> Therefore, an object of the present invention is to provide an anti-tartar composition that has an excellent effect of preventing tartar formation and is highly safe even during continuous use over a long period of time.

〈課題を解決するための手段〉 本発明によれば、カゼインホスホペプチドを有効成分と
することを特徴とする歯石防止組成物が提供される。
<Means for Solving the Problems> According to the present invention, there is provided an anti-tartar composition characterized by containing casein phosphopeptide as an active ingredient.

以下本発明を更に詳細に説明する。The present invention will be explained in more detail below.

本発明において、有効成分として用いるカゼインホスホ
ペプチド(Casein Phosphopeptid
e)は、歯石形成の初期に生ずるリン酸カルシウムの沈
殿を抑制し1次に生ずる非晶質リン酸カルシウムからハ
イドロキシアパタイトの転移を抑制し、更にハイドロキ
シアパタイトの結晶成長も効果的に抑制する成分であっ
て、該リン酸カルシウム沈殿抑制については、カゼイン
ホスホペプチドがCa”イオンとキレート結合し、リン
酸カルシウムの形成を抑制するからだと考えられる。こ
のメカニズムは、キレート作用により、Ca”+イオン
が減少し、リン酸カルシウムの表面に吸着して結晶成長
点をブロックして結晶成長を押さえるがらである。
In the present invention, casein phosphopeptide is used as an active ingredient.
e) is a component that suppresses the precipitation of calcium phosphate that occurs at the initial stage of tartar formation, suppresses the transition of hydroxyapatite from the primary amorphous calcium phosphate, and further effectively suppresses the crystal growth of hydroxyapatite, This inhibition of calcium phosphate precipitation is thought to be due to casein phosphopeptide chelating with Ca'' ions and suppressing the formation of calcium phosphate. It adsorbs and blocks crystal growth points, suppressing crystal growth.

さらにカゼインホスホペプチドはカゼインを原料とした
ペプチドであり極めて安全性の高い物質であって、口腔
に何ら刺激を与えず、トリポリリン酸、ピロリン酸のよ
うな骨の脱灰を刺激することがない物質である。
Furthermore, casein phosphopeptide is a peptide made from casein and is an extremely safe substance that does not cause any irritation to the oral cavity and does not stimulate bone demineralization like tripolyphosphate and pyrophosphate. It is.

本発明に用いる該カゼインホスホペプチドは、公知の方
法、例えば結晶トリプシンでβ−カゼインを加水分解し
、精製する方法[R,F、Peterson。
The casein phosphopeptide used in the present invention can be obtained by a known method, for example, by hydrolyzing β-casein with crystalline trypsin and purifying it [R, F, Peterson.

L、V、Nouman and T、L、McMeek
in、Journal of theA+++eric
an  Che+*1cal  5ociety  8
0 9595−99(195又はR,Na1to an
d H,5uzuki、AgriculturalBi
ological  Chemistry  38 1
543−1545(1974)]、 各種酸カゼイン、
カゼインナトリウム、カゼインカルシウム等を原料とし
、トリプシン又はトリプシンを含む酵素剤を作用させた
後、分画操作して得る方法(特開昭59−159792
号公報、特開昭59−159793号公報)等により調
製することができる他、例えば商品名「明治CPP−I
J(CPP含有量12重量%以上)、[明治cpp−2
J  (CPP含有量12重量%以上)、r明治CPP
−31(CPP含有量85重量%以上)(以上明治製菓
株式会社製)等の市販品をそのまま用いることもできる
L, V, Nouman and T, L, McMeek
in, Journal of theA+++eric
an Che+*1cal 5ociety 8
0 9595-99 (195 or R, Na1to an
d H, 5uzuki, Agricultural Bi
Logical Chemistry 38 1
543-1545 (1974)], various acid caseins,
A method in which sodium caseinate, calcium caseinate, etc. are used as raw materials, treated with trypsin or an enzyme containing trypsin, and then fractionated (Japanese Patent Laid-Open No. 159792
In addition, for example, the product name "Meiji CPP-I" can be prepared according to
J (CPP content 12% by weight or more), [Meiji cpp-2
J (CPP content 12% by weight or more), r Meiji CPP
Commercially available products such as -31 (CPP content: 85% by weight or more) (manufactured by Meiji Seika Co., Ltd.) can also be used as they are.

本発明の歯石防止組成物において、有効成分として用い
るカゼインホスホペプチドの含有割合は、歯石形成を防
止できる量以上であれば特に限定されるものではなく1
組成物全体に対して0.01重量%以上、好ましくは0
.1〜5重量%であれば良い6本発明においてカゼイン
ホスホペプチド以外に含有させることができる成分とし
ては、例えば公知の賦形剤、補助剤、香料、抗菌剤、防
腐剤等を添加することもできる。
In the tartar prevention composition of the present invention, the content of casein phosphopeptide used as an active ingredient is not particularly limited as long as it is at least an amount that can prevent tartar formation.
0.01% by weight or more based on the entire composition, preferably 0
.. 1 to 5% by weight is sufficient6 In the present invention, components that can be included other than casein phosphopeptide include, for example, known excipients, adjuvants, fragrances, antibacterial agents, preservatives, etc. can.

本発明の歯石防止組成物の作用形態は、例えば公知の口
腔用製剤、具体的には歯みがき剤、マウスウォッシュ、
トローチ剤、うがい薬塗布液剤、チューインガム等とし
て使用することができる。
The mode of action of the anti-tartar composition of the present invention is, for example, known oral preparations, specifically dentifrices, mouthwashes,
It can be used as a lozenge, gargle solution, chewing gum, etc.

〈発明の効果〉 本発明の歯石防止組成物は、カゼインホスホペプチドを
有効成分として含有するので、歯肉炎の病因として知ら
れる歯石形成を有効に防止することができ、しかもカゼ
インホスホペプチドが天然物であり、極めて安全性に優
れているので、口腔用衛生品、食品添加剤として極めて
有用である。
<Effects of the Invention> Since the tartar prevention composition of the present invention contains casein phosphopeptide as an active ingredient, it can effectively prevent tartar formation, which is known as the cause of gingivitis.Moreover, casein phosphopeptide is a natural product. Since it is extremely safe, it is extremely useful as oral hygiene products and food additives.

〈実施例〉 以下本発明を試験例及び実施例により更に詳細に説明す
るが、本発明はこれらに限定されるものではない。
<Examples> The present invention will be explained in more detail below using test examples and examples, but the present invention is not limited thereto.

ヌ」1匠 歯石形成の原因と考えられるリン酸カルシウムの沈殿形
成と非晶質リン酸−カルシウムからハイドロキシアパタ
イトへの転移、更にハイドロキシアパタイトの結晶成長
、夫々についてその抑制効果を調べるために、カゼイン
ホスホペプチドとして、市販の商品名「明治CPP−I
J 、r明治cpp−2」、「明治CPP−34’ (
以上明治製菓株式会社製)を用いて以下のとおり行った
In order to investigate the inhibitory effects of calcium phosphate precipitate formation, the transition from amorphous calcium phosphate to hydroxyapatite, and the crystal growth of hydroxyapatite, which are considered to be the causes of dental calculus formation, casein phosphopeptide was used. Commercially available product name “Meiji CPP-I”
J, rMeiji CPP-2", "Meiji CPP-34' (
The above was carried out as follows using Meiji Seika Co., Ltd.).

(a)リン酸カルシウム沈殿の抑制試験まず16本の1
0−試験管に、各々のカゼインホスホペプチドと、比較
試験として、従来歯石形成を防止する有効成分として知
られるトリポリリン酸とが夫々試験溶液全体に対して0
.05wt%、O,1wt%、0.25wt%、0 、
5 w t%となるように、リン酸カルシウム溶液(p
H7,4)と共に入れ、ミキサーで混合した後、塩化カ
ルシウム溶液0.25−を夫々添加混合して、試験溶液
全体を5mQとした。得られた各溶液を商品名「日立U
−1100J(日立製作所株式会社)を用いて550n
mにおける吸光度を測定した。
(a) Calcium phosphate precipitation inhibition test First, 1 of 16
0 - In a test tube, each casein phosphopeptide and, as a comparative test, tripolyphosphoric acid, which is conventionally known as an active ingredient for preventing tartar formation, were added to the entire test solution.
.. 05wt%, O, 1wt%, 0.25wt%, 0,
Calcium phosphate solution (p
After mixing with a mixer, 0.25 ml of calcium chloride solution was added and mixed to make the entire test solution 5 mQ. Each of the obtained solutions was
-550n using 1100J (Hitachi, Ltd.)
The absorbance at m was measured.

この測定時においても各溶液をミキサーで撹拌し、生成
する沈殿が均一に分散した状態で測定を行った。得られ
た吸光度と、各有効成分との関係を第1図に示す、第1
図において、吸光度が高いほどリン酸カルシウムの沈殿
抑制効果が高いことを示す。従って第1図の結果より、
カゼインホスホペプチドは、従来のトリポリリン酸より
、微量でリン酸カルシウムの沈殿の抑制効果を示すこと
が判った。
Also during this measurement, each solution was stirred with a mixer, and the measurement was carried out in a state in which the generated precipitate was uniformly dispersed. The relationship between the obtained absorbance and each active ingredient is shown in Figure 1.
In the figure, the higher the absorbance, the higher the effect of suppressing precipitation of calcium phosphate. Therefore, from the results in Figure 1,
Casein phosphopeptide was found to be more effective in inhibiting calcium phosphate precipitation than conventional tripolyphosphate at a trace amount.

(b)ハイドロキシアパタイト形成の抑制試験2mQの
O,1Mリン酸カリウム水溶液と、表1に示す商品名「
明治CPP−IJ  (カゼインホスホペプチド含有量
12重量%)、「明治CPP−2J(カゼインホスホペ
プチド含有量12重量%)。
(b) Hydroxyapatite formation inhibition test 2 mQ of O, 1M potassium phosphate aqueous solution and the product name "
Meiji CPP-IJ (casein phosphopeptide content: 12% by weight), “Meiji CPP-2J (casein phosphopeptide content: 12% by weight).

「明治CPP−34(カゼインホスホペプチド含有量8
5重量%)及び比較としてトリポリリン酸(TPP)が
サンプル液全体(22mQ)に対して夫々0.02.0
.04.0.08重量%となるように混和した後、2m
Qの0.1M塩化カルシウム水溶液を添加した。反応は
、商品名rHM−7E  PHツメ−−」 (東亜電波
株式会社製)を用いて、前記塩化カルシウムを加えた時
点からpHを測定し、ハイドロキシアパタイト形成の時
間を測定した。その結果を表1に示す。尚カゼインホス
ホペプチド又はトリポリリン酸を添加しない場合には1
6分でハイドロキシアパタイトが形成された。
"Meiji CPP-34 (casein phosphopeptide content 8
5% by weight) and for comparison, tripolyphosphoric acid (TPP) was 0.02.0% relative to the entire sample solution (22mQ).
.. 04. After mixing to 0.08% by weight, 2m
Q 0.1M aqueous calcium chloride solution was added. For the reaction, the pH was measured from the time the calcium chloride was added using a product named "rHM-7E PH Tsume" (manufactured by Toa Denpa Co., Ltd.), and the time for hydroxyapatite formation was measured. The results are shown in Table 1. In addition, if casein phosphopeptide or tripolyphosphate is not added, 1
Hydroxyapatite was formed in 6 minutes.

表1の結果より、カゼインホスホペプチドは、トリポリ
リン酸と同等若しくはそれ以上のハイドロキシアパタイ
トの形成を抑制する効果が得られると推定できる。尚商
品名「明治CPP−IJ及び「明治CPP−24では、
ハイドロキシアパタイトの形成時間がトリポリリン酸よ
りかなり速いが、これは、有効成分であるカゼインホス
ホペプチドの濃度が12重量%とトリポリリン酸濃度の
約1/8の濃度であるからであり、同程度の濃度、即ち
「明治CPP−3Jを用いた場合にはそれ以上の効果が
得られることがわかる。
From the results in Table 1, it can be estimated that casein phosphopeptide has the same or greater effect of suppressing hydroxyapatite formation than tripolyphosphate. In addition, the product name "Meiji CPP-IJ" and "Meiji CPP-24"
The formation time of hydroxyapatite is considerably faster than that of tripolyphosphate, but this is because the concentration of the active ingredient, casein phosphopeptide, is 12% by weight, which is approximately 1/8 of the concentration of tripolyphosphate; That is, it can be seen that even greater effects can be obtained when Meiji CPP-3J is used.

表   1 (c)ハイドロキシアパタイト結晶成長の抑制試験 食塩0.05M、塩化カルシウム1.06mMを含む0
.63mMリン酸カリウム緩衝液(pH7,4)20−
に、商品名「明治CPP−IJ、「明治CPP−2J 
 r明治CPP−3J又はTPPを0.5〜5PPMの
濃度になるように添加し、更に種結晶として商品名rN
oH−0252゜TypelJ  (シグマ株式会社製
)のハイドロキシアパタイト251Kgを撹拌下加えた
。リン濃度の測定は、1時間毎に各上澄液を採取し、モ
リブデンブルー比色定量法により定量した。その結果を
夫々第2a”−d図に示す。
Table 1 (c) Hydroxyapatite crystal growth inhibition test containing 0.05M common salt and 1.06mM calcium chloride.
.. 63mM potassium phosphate buffer (pH 7,4) 20-
The product name "Meiji CPP-IJ", "Meiji CPP-2J"
Add rMeiji CPP-3J or TPP to a concentration of 0.5 to 5 PPM, and further use the product name rN as a seed crystal.
251 kg of hydroxyapatite oH-0252°Type J (manufactured by Sigma Corporation) was added under stirring. The phosphorus concentration was measured by collecting each supernatant every hour and quantifying it by molybdenum blue colorimetric method. The results are shown in Figures 2a''-d, respectively.

第2 a −d図の結果より、カゼインホスホペプチド
は、トリポリリン酸と同様なハイドロアパタイトの結晶
成長を抑制する効果が得られることが判った。
From the results shown in Figures 2a to 2d, it was found that casein phosphopeptide has the same effect of inhibiting hydroapatite crystal growth as tripolyphosphate.

ヌ】11L二」− 試験例において、リン酸カルシウム阻害活性を示した各
々のカゼインホスホペプチドを配合した実施例を以下に
示す。
[11L2] - Examples in which each of the casein phosphopeptides that showed calcium phosphate inhibitory activity in the test examples were blended are shown below.

(以下余白) (実施例1) ムj4酌り形 (実施例4) チ」二二乙企ゴ偉k (実施例2) マウスウオ・シュ (実施例5) 鼓 (実施例3) 上o −f赳(Margin below) (Example 1) Muj4 cupcake (Example 4) Chi' 22 (Example 2) Mouthwash (Example 5) drum (Example 3) 上 o -f 赳

【図面の簡単な説明】[Brief explanation of drawings]

第1図は、試験例で行ったカゼインホスホペプチド及び
トリポリリン酸の濃度と透過率とを示すグラフ、第2a
図は、試験例で行った商品名「明治CPP−1」を用い
た各濃度における時間とリン濃度とを示すグラフ、第2
b図は、同じく商品名「明治CPP−2Jを用いた各濃
度における時間とリン濃度とを示すグラフ、第2C図は
、同じく商品名[明治CPP−3Jを用いた各濃度にお
ける時間とリン濃度とを示すグラフ、第2d図は同じく
トリポリリン酸を用いた各濃度における時間とリン濃度
とを示すグラフである。 特許呂願人
FIG. 1 is a graph showing the concentration and transmittance of casein phosphopeptide and tripolyphosphoric acid conducted in test examples;
The figure is a graph showing the time and phosphorus concentration at each concentration using the product name "Meiji CPP-1" in the test example,
Figure b is a graph showing time and phosphorus concentration at each concentration using Meiji CPP-2J, also under the trade name, and Figure 2C is a graph showing time and phosphorus concentration at each concentration using Meiji CPP-3J, also under the trade name. Figure 2d is a graph showing the time and phosphorus concentration at each concentration using tripolyphosphoric acid.

Claims (1)

【特許請求の範囲】[Claims] カゼインホスホペプチドを有効成分とすることを特徴と
する歯石防止組成物。
An anti-tartar composition characterized by containing casein phosphopeptide as an active ingredient.
JP2187944A 1990-07-18 1990-07-18 Tartar prevention composition Expired - Lifetime JPH0699294B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2187944A JPH0699294B2 (en) 1990-07-18 1990-07-18 Tartar prevention composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2187944A JPH0699294B2 (en) 1990-07-18 1990-07-18 Tartar prevention composition

Publications (2)

Publication Number Publication Date
JPH0477415A true JPH0477415A (en) 1992-03-11
JPH0699294B2 JPH0699294B2 (en) 1994-12-07

Family

ID=16214907

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2187944A Expired - Lifetime JPH0699294B2 (en) 1990-07-18 1990-07-18 Tartar prevention composition

Country Status (1)

Country Link
JP (1) JPH0699294B2 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU721548B3 (en) * 1999-01-13 2000-07-06 Pacific Biolink Pty Limited Protective peptide formulation
WO2000057842A3 (en) * 1999-03-25 2001-11-29 Warner Lambert Co Oral care chewing gums and confections
JP2002521415A (en) * 1998-07-29 2002-07-16 パシフィック バイオリンク ピーティーワイ.リミテッド Casein compositions for delivery of bioactive ingredients
US6733818B2 (en) * 1999-03-25 2004-05-11 Cadbury Adams Usa Llc Oral care confections and method of using
US6863882B2 (en) 2002-01-03 2005-03-08 The Procter & Gamble Company Stable oral compositions comprising casein phosphopeptide complexes and fluoride

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60156620A (en) * 1983-12-22 1985-08-16 ザ ユニヴアーシテイ オブ メルボルン Dental caries controller

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60156620A (en) * 1983-12-22 1985-08-16 ザ ユニヴアーシテイ オブ メルボルン Dental caries controller

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002521415A (en) * 1998-07-29 2002-07-16 パシフィック バイオリンク ピーティーワイ.リミテッド Casein compositions for delivery of bioactive ingredients
AU721548B3 (en) * 1999-01-13 2000-07-06 Pacific Biolink Pty Limited Protective peptide formulation
WO2000057842A3 (en) * 1999-03-25 2001-11-29 Warner Lambert Co Oral care chewing gums and confections
US6733818B2 (en) * 1999-03-25 2004-05-11 Cadbury Adams Usa Llc Oral care confections and method of using
US6846500B1 (en) 1999-03-25 2005-01-25 Cadbury Adams Usa Llc Oral care chewing gums and method of use
US6863882B2 (en) 2002-01-03 2005-03-08 The Procter & Gamble Company Stable oral compositions comprising casein phosphopeptide complexes and fluoride

Also Published As

Publication number Publication date
JPH0699294B2 (en) 1994-12-07

Similar Documents

Publication Publication Date Title
KR100225820B1 (en) Phosphopeptides for the treatment of dental calculus
US3004897A (en) Dental preparation
CA2116225C (en) Anticalculus dentifrices
KR100238551B1 (en) Treatment for sensitive teeth
WO1993007852A1 (en) Methods of reducing plaque and gingivitis with reduced staining
WO1993007850A1 (en) Methods of reducing plaque and gingivitis with reduced staining
EP0471396A1 (en) Dental compositions containing stabilized copper
CZ156795A3 (en) Mouth preparation containing agents against formation of microbial plaque, tartar, gingivitis and foetor ex ore
US20080152598A1 (en) Oral composition for stabilization, (re)calcification and (re)mineralization of tooth enamel and dentine
EP0089136A2 (en) Oral hygiene products
JPS6136211A (en) Composition for oral cavity application
JP2007527867A (en) Prevention of crystal formation in toothpaste
JPH01207227A (en) Tartar preventing composition
JPH10182389A (en) Dentifrice composition
JPH0477415A (en) Dental calcus preventing composition
EP0265186A2 (en) Anticalculus compositions
US5032389A (en) Zinc tripolyphosphate compounds as anticalculus and antiplaque agents
JP2887636B2 (en) Oral preparation
US4175120A (en) Dentifrice
WO2018206211A1 (en) Oral care compositions
GB2412586A (en) Polyaspartate to treat dental tartar
JPH02311413A (en) Composition for tooth paste
JP2960176B2 (en) Oral composition
GB1522158A (en) Process for the stabilisation of calcium hydrogenphosphate-dihydrate against hydrolysis
JPH0710726A (en) Composition for oral cavity