JPH0477415A - Dental calcus preventing composition - Google Patents
Dental calcus preventing compositionInfo
- 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
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 16
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 claims abstract description 29
- 235000021240 caseins Nutrition 0.000 claims abstract description 29
- 239000005018 casein Substances 0.000 claims abstract description 28
- 108010001441 Phosphopeptides Proteins 0.000 claims abstract description 27
- 239000004480 active ingredient Substances 0.000 claims abstract description 9
- 208000006558 Dental Calculus Diseases 0.000 claims description 21
- 230000015572 biosynthetic process Effects 0.000 abstract description 18
- 239000001506 calcium phosphate Substances 0.000 abstract description 14
- 229910000389 calcium phosphate Inorganic materials 0.000 abstract description 14
- 235000011010 calcium phosphates Nutrition 0.000 abstract description 14
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 abstract description 14
- 229910052588 hydroxylapatite Inorganic materials 0.000 abstract description 13
- XYJRXVWERLGGKC-UHFFFAOYSA-D pentacalcium;hydroxide;triphosphate Chemical compound [OH-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O XYJRXVWERLGGKC-UHFFFAOYSA-D 0.000 abstract description 13
- 239000013078 crystal Substances 0.000 abstract description 8
- 238000001556 precipitation Methods 0.000 abstract description 6
- 239000002324 mouth wash Substances 0.000 abstract description 4
- 229940051866 mouthwash Drugs 0.000 abstract description 3
- 239000003242 anti bacterial agent Substances 0.000 abstract description 2
- 229940112822 chewing gum Drugs 0.000 abstract description 2
- 235000015218 chewing gum Nutrition 0.000 abstract description 2
- 239000000551 dentifrice Substances 0.000 abstract description 2
- 239000000546 pharmaceutical excipient Substances 0.000 abstract description 2
- 239000004599 antimicrobial Substances 0.000 abstract 1
- -1 auxiliary Substances 0.000 abstract 1
- 239000000796 flavoring agent Substances 0.000 abstract 1
- 235000019634 flavors Nutrition 0.000 abstract 1
- 239000002674 ointment Substances 0.000 abstract 1
- 230000009466 transformation Effects 0.000 abstract 1
- 108010076119 Caseins Proteins 0.000 description 29
- 102000011632 Caseins Human genes 0.000 description 29
- 235000019832 sodium triphosphate Nutrition 0.000 description 11
- 239000000047 product Substances 0.000 description 10
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 10
- 238000012360 testing method Methods 0.000 description 9
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 239000011574 phosphorus Substances 0.000 description 7
- 229910052698 phosphorus Inorganic materials 0.000 description 7
- 230000002401 inhibitory effect Effects 0.000 description 5
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 4
- 239000011575 calcium Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 3
- 206010044029 Tooth deposit Diseases 0.000 description 3
- 102000004142 Trypsin Human genes 0.000 description 3
- 108090000631 Trypsin Proteins 0.000 description 3
- 238000002835 absorbance Methods 0.000 description 3
- 229910052791 calcium Inorganic materials 0.000 description 3
- 230000005764 inhibitory process Effects 0.000 description 3
- 108090000765 processed proteins & peptides Proteins 0.000 description 3
- 239000012588 trypsin Substances 0.000 description 3
- 108090000672 Annexin A5 Proteins 0.000 description 2
- 210000000988 bone and bone Anatomy 0.000 description 2
- 239000001110 calcium chloride Substances 0.000 description 2
- 229910001628 calcium chloride Inorganic materials 0.000 description 2
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 2
- 235000011180 diphosphates Nutrition 0.000 description 2
- 208000007565 gingivitis Diseases 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 102000004196 processed proteins & peptides Human genes 0.000 description 2
- 210000003296 saliva Anatomy 0.000 description 2
- 239000012085 test solution Substances 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 2
- 235000021247 β-casein Nutrition 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 102000003886 Glycoproteins Human genes 0.000 description 1
- 108090000288 Glycoproteins Proteins 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000002308 calcification Effects 0.000 description 1
- 108010033929 calcium caseinate Proteins 0.000 description 1
- 229940021722 caseins Drugs 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004737 colorimetric analysis Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000005115 demineralization Methods 0.000 description 1
- 230000002328 demineralizing effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 210000000416 exudates and transudate Anatomy 0.000 description 1
- 235000013373 food additive Nutrition 0.000 description 1
- 239000002778 food additive Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 230000009036 growth inhibition Effects 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 239000007937 lozenge Substances 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 210000000214 mouth Anatomy 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 201000001245 periodontitis Diseases 0.000 description 1
- 229910000160 potassium phosphate Inorganic materials 0.000 description 1
- 239000008057 potassium phosphate buffer Substances 0.000 description 1
- 235000011009 potassium phosphates Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 229940048084 pyrophosphate Drugs 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 229940080237 sodium caseinate Drugs 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- 235000019830 sodium polyphosphate Nutrition 0.000 description 1
- 229940048086 sodium pyrophosphate Drugs 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- 239000000606 toothpaste Substances 0.000 description 1
- 229940034610 toothpaste Drugs 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 235000021249 α-casein Nutrition 0.000 description 1
Landscapes
- Cosmetics (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Confectionery (AREA)
Abstract
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
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)
する歯石防止組成物。An anti-tartar composition characterized by containing casein phosphopeptide as an active ingredient.
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)
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)
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 |
-
1990
- 1990-07-18 JP JP2187944A patent/JPH0699294B2/en not_active Expired - Lifetime
Patent Citations (1)
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)
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 |
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