A dentrifice composition containing a water-dispersible, membrane-forming material which, when applied to tooth surfaces in an oral environment, attaches thereto and forms a substantially continuous, hydrophobic barrier thereon which substantially reduces elution of a previously applied therapeutic agent.
|
1. A dentifrice composition for substantially effectively coating previously fluoride-treated teeth and thereby reducing elution of said fluoride from said teeth, said composition comprising
a fluoride-containing caries prophylactic agent provided that said agent is substantially free from polyvalent metal atoms; and at least about 0.05% by weight of an anionic water-dispersible membrane-forming material which, when applied to the surface of said previously fluoride-treated teeth in an oral environment, complexes with the calcium of said teeth and forms a substantially continuous hydrophobic barrier thereon which substantially reduces the elution of said previously applied fluoride from said teeth and which, when at equilibrium with the complex, has a formation constant in the range of about 0.5 to 8, said anionic membrane-forming material being a non-polymeric fluorinated material selected from the group
(Rf SO2 N(R2)R3 O)m PX(XB)3-m (Cg F2g+1 CH2 O)k PO(OM)q Rf COOM Rf R3 COOM Rf SO2 OM Rf SO2 OY wherein Rf is a monovalent, stable, inert, fluorinated, saturated aliphatic non-polar radical containing from about 4 to 16 carbon atoms; R2 is selected from hydrogen and alkyl groups containing from about 2 to 3 carbon atoms; R3 is selected from alkylene, chloro- substituted alkylene and alkarylene groups that contain from about 1 to 10 carbon atoms; X is selected from oxygen and sulfur; B is selected from hydrogen, alkali metal, ammonium and amine groups, and alkyl, aryl, cycloalkyl, alkaryl, and aralkyl groups each containing up to 20 carbon atoms; M is selected from hydrogen, alkali metal, ammonium and amine groups; Y is an aryl group; m is 1 or 2; g is an integer of from 1 to 10; k is 1 or 2; and q is 3-k. 2. A dentifrice composition according to
3. A dentifrice composition according to
4. A dentifrice composition according to
(C8 F17 SO2 N(C2 H5)C2 H4 O)2 PSSH (C8 F17 SO2 N(C2 H5)C2 H4 O)2 POOH C8 F17 SO2 N(C2 H5)C2 H4 OPO(OH2) C8 F17 SO2 N(C2 H5)C2 H4 OPO(OH)2 C8 F17 SO2 N(C2 H5)C10 H20 OPO(OH)2 C8 F17 SO2 N(C2 H5)C2 H4 OP(OH)(O)OC18 H37 C8 F17 SO2 N(C4 H9)C2 H4 OPO(OH)2. 5. A dentifrice composition according to
C8 F17 SO2 N(C2 H5)C2 H4 OPO(OH)2. 6. A dentifrice composition according to
Rf COOM. 7. A dentifrice composition according to
C8 F17 COOH C11 F23 COOH. 8. A dentifrice composition according to
Rf R3 COOM. 9. A dentifrice composition according to
C8 F17 CH2 CHCl8 H16 COOH C8 F17 C10 H20 COOH. 10. A dentifrice composition according to
C8 F17 C10 H20 COOH. 11. A dentifrice composition according to
12. A dentifrice composition to
|
This is This is a reissue of application Ser. No. 176,680 filed Aug. 11, 1980, now U.S. Pat. No. 4,304,766, which was a division of application Ser. No. 26,402 filed Apr. 2, 1979, now U.S. Pat. No. 4,243,658, which was a continuation-in-part of Ser. No. 865,681 filed Dec. 29, 1977, now abandoned.
This invention relates to compositions for topical application to teeth. More particularly it relates to compositions and methods which substantially reduce the elution of a previously applied therapeutic agent from teeth. The compositions and methods of the invention are especially useful in inhibiting the growth of cariogenic bacteria and preventing the formation of plaque on teeth in an oral environment.
Dental plaque results when cariogenic bacteria (e.g., Streptococcus mutans) collect in colonies and form deposits on tooth surfaces. The presence of the bacteria and deposits is extremely detrimental to the health of the tooth for, if left unchecked, they may result in infected gingival tissue, the formation of dental caries and possibly periodontal disease. In extreme cases their presence may even result in the loss of teeth. Many attempts have been made to control or prevent both the occurrence of dental caries and the formation of dental plaque. For example, fluoride solutions or gels have been used. Treatment with these materials is typically performed in a dental office at periodic, but not frequent, intervals. Such treatments are primarily intended to render tooth enamel more resistant to the acid action caused by plaque. They do not, however, result in plaque control for an extended period since plaque reestablishes itself on the teeth shortly after ingestion of food.
Even when the frequency of application of such solutions and gels is increased only partial control has been shown. For example, studies wherein a fluoride-containing solution (1% fluoride concentration) was applied four to five times in the course of a year have demonstrated that this technique had only limited success due to the rapid reestablishment of plaque in the oral cavity. Moreover, the daily application of a fluoride gel by means of a custom-fitted polyvinyl mouthpiece for a period of twenty-one months also showed no substantial change in plaque formation among treated and untreated patients. See "Clinical Anticaries Effect of A Repeated Sodium Fluoride Application by Mouthpiece," Journal of the American Dental Association, V. 75, No. 3, September, 1967, pages 638-644.
As a result, there has been no truly effective prophylactic treatment for teeth made available. However, the present invention provides such a treatment.
In accordance with the present invention there is provided a dentrifice composition for substantially reducing elution of a previously applied therapeutic agent from teeth, said composition comprising:
at least one ingredient selected from the group consisting of therapeutic agents, polishing agents, surfactants, flavoring agents, sweetening agents, thickening agents and humectants, and at least about 0.05% by weight, and preferably from about 0.1 to 5% by weight, of a water-dispersible, membrane-forming material which, when applied to the surface of teeth in an oral environment, forms a substantially continuous hydrophobic barrier thereon which substantially reduces the elution of said previously applied therapeutic agent from said tooth.
In another embodiment of the present invention there is provided a method for inhibiting plaque formation on teeth which comprises contacting the teeth with an effective amount of the above-described composition.
As they are used herein, the following terms have the following meanings:
Compositions for topical application to the teeth such as mouthwashes or rinses, toothpastes, gels, etc.
Materials which may be either dispersed or dissolved in aqueous media at a level at least about 10 parts of such material per one million parts of media (i.e., 0.001%), and preferably at a level of at least about 100 parts of such material per one million parts of media (i.e., 0.01%).
A layer which does not adsorb or absorb water.
The present invention provides a simple and effective composition and process by which cariogenic bacteria and plaque formation may be controlled. The barrier formed by compositions of the invention substantially reduces the elution of a previously applied therapeutic agent (i.e., dental fluoride treatments), thereby prolonging the effectiveness of such agents. Moreover, compositions of the invention need be applied only periodically (e.g., once daily) in order to achieve the desired reduction in elution and resultant control of caries and plaque.
A variety of membrane-forming materials are useful in the present invention. They include polymeric and nonpolymeric, ionic and nonionic materials. Ionic materials are those which when provided in aqueous solution, are attracted to either the positive or negative electrode during electrolysis. Thus, anionic materials are attracted to the positive electrode and cationic materials are attracted to the negative electrode. Nonionic materials are those materials which, when provided in aqueous solution, are not normally attracted to either the positive or negative electrode during electrolysis.
Anionic membrane-forming materials useful in the present invention are believed to attach to tooth surfaces and form a substantially continuous barrier thereon by complexing with calcium present in the teeth. The strength of the complex structure formed may be represented by the formation constant of the complexing agent. This constant is expressed in terms of log10 K and is based upon the complex formed between the membrane-forming material and a ligand on the tooth surface. The formation constant is measured at about 25°C and an ionic strength approaching 0 from the following equation: ##EQU1## In these formulae W represents the membrane-forming material, L represents the ligand which complexes with W and WL represents the complex formed between W and L. The bracketed symbols indicate the concentration of the indicated material at equilibrium.
The formation constant of useful anionic membrane-forming materials is in the range of about 0.5 to 8. Preferably, it is in the range of about 0.6 to 6. A formation constant greater than 8 indicates a very strong calcium complexor. Such complexors tend to decalcify the tooth (i.e., withdraw the calcium from the tooth), thereby weakening its resistance to disease and wear.
The polymeric anionic membrane-forming materials useful in the present invention comprise a class of polymers having a polyolefinic main chain with acidic functionalities pendant therefrom. Typical of the materials which can comprise the polyolefinic main chain are polymers of ethylene, propylene, styrene, unsaturated carboxylic acids, (especially those containing up to about 5 carbon atoms) and copolymers of two or more of these materials.
The acid functionalities pendant from the polyolefinic main chain are selected from
--COOM,
--PO(OM)2
--OPO(OM)2
--SO3 M
--OSO3 M
wherein M is selected from hydrogen, alkali metal (e.g., sodium, potassium, lithium, etc.), ammonium and amine groups.
Representative polymeric anionic membrane-forming materials useful in the present invention are:
(a) Polyacrylic acid, having the repeating unit ##STR1## a molecular weight in the range of 2,000 to 4,000,000, available from the Aldrich Chemical Company;
(b) "Separan AP 30," having the repeating unit ##STR2## and a molecular weight of about 2,000,000, available from the Dow Chemical Company;
(c) Sodium polystyrenesulfonate, having the repeating unit ##STR3## and a molecular weight in the range of about 5,000 to 6,000,000, available from the Dow Chemical Company;
(d) "Gantrez AN", having the repeating unit ##STR4## available from GAF Corporation;
(e) "EMA" polymers, having the repeating unit ##STR5## available from the Monsanto Chemical Company;
(f) Polyvinyl phosphate, having the repeating unit ##STR6## commercially available from Polysciences, Incorporated; and
(g) Copolymers of acrylates which contain pendant carboxyl groups, such as the "Carboset" resins available from the B. F. Goodrich Chemical Company.
The nonpolymeric anionic membrane-forming materials useful in the present invention comprise a class of materials having a nonionic aliphatic portion and an anionic terminal group. They may be generally represented by the formula R1 Z wherein R1 is the aliphatic portion of the compound and Z is the anionic terminal group.
The aliphatic portion may be saturated or unsaturated and it may be straight or branched chain. Additionally, it may be a hydrocarbon or fluorocarbon radical. Moreover, the aliphatic portion may contain hetero atoms selected from oxygen, nitrogen and sulfur.
Z may be joined directly to R' or, alternatively, there may be a divalent linking group Q which joins R' and Z. Q must not interfere with the formation of the complex structure between the anionic material and the tooth surface.
The Z groups useful in the nonpolymeric membrane-forming materials are selected from
--COOM
--PO(OM)2
═POOM
--OPO(OM)2
--SO2 OM
--OSO2 OM
--PS(SM)2
═PSSM
wherein M is as defined previously.
Representative of useful Q groups are hydrocarbon groups containing from 1 to about 30 carbon atoms, oxygen, sulfur and --SO2 O--. The hydrocarbon groups may be straight chain or branched chain and may include unsaturation and aromatic (e.g., cyclic) groups. Moreover, the hydrocarbon groups may contain heteroatoms in the skeletal chain. Typically the hetero atoms are selected from the group consisting of oxygen, nitrogen and sulfur.
A number of nonpolymeric anionic materials are useful as the membrane-forming material. One group of such materials contains substantial quantities of fluorine in the main chain. Thus, for example, the perfluoroalkanesulfonamidoalkyl esters of phosphorous acids have been found useful. These compounds have the formula
[Rf SO2 N(R2)R3 0]m PX(XB)3-m
wherein Rf is a monovalent, stable, inert, fluorinated, saturated aliphatic nonpolar radical; R2 is hydrogen, alkyl of from 1 to 6 carbon atoms, aryl, cycloalkyl, aralkyl or alkaryl; R3 is an alkylene, arylene, alkarylene or aralkylene bridging group containing from 1 to 12 carbon atoms, m is 1 or 2; X is oxygen or sulfur; and B is hydrogen, alkyl, aryl, cycloalkyl, alkaryl, or aralkyl (each of up to 20 carbon atoms) alkali metals (e.g., sodium, potassium, lithium, etc.), ammonium, or amine groups.
The Rf radical can be straight chain, branched chain or, if sufficiently large, cyclic. Additionally, it can be a combination of cyclic, branched and straight chain, (e.g., alkylcycloaliphatic). The skeletal chain of the Rf radical can include catenary oxygen and/or trivalent nitrogen hetero atoms bonded only to carbon atoms. Such hetero atoms provide stable linkages between fluorocarbon groups and do not interfere with the inert character of the radical.
The Rf radical has from about 4 to 16 carbon atoms; preferably from about 6 to 12 carbon atoms; and most preferably 8 carbon atoms. Moreover, Rf generally contains from about 40 to 80 weight percent, and preferably from about 50 to 80 weight percent, fluorine. Correspondingly the fluorochemical material of formula I will contain from about 4 to 70 weight percent fluorine.
The most preferred Rf radicals are fully or substantially fully fluorinated. Thus they are perfluoroalkyl groups (e.g., Cn F2n+1 --). Additionally the terminal portion of the Rf group preferably contains a --CF3 group, and most preferably the terminal portion also has at least three fully fluorinated carbon atoms, (e.g., CF3 CF2 CF2 --).
R2 may be hydrogen or a straight or branched chain alkyl, aryl, cycloalkyl, alkaryl or aralkyl group. Preferably it is a straight chain alkyl group containing 2-3 carbon atoms.
R3 is a divalent bridging group. It may be straight chain or branched chain and preferably is an alkylene group that contains from 2 to 8 carbon atoms.
Representative examples of useful perfluoroalkanesulfonamidoalkyl esters of phosphorous acids useful in the present invention include
[C8 F17 SO2 N(C2 H5)C2 H4 0]2 PSSH
[C8 F17 SO2 N(C2 H5)C2 H4 0]2 POOH
C8 F17 SO2 N(C2 H5)C2 H4 OPO(OH)2
C8 F17 SO2 N(C2 H5)C10 H20 OPO(OH)2
C8 F17 SO2 N(C2 H5)C2 H4 OP(OH)(O)OC18 H37
C8 F17 SO2 N(C4 H9)C2 H4 OPO(OH)2
The preparation of these compounds is described in U.S. Pat. No. 3,094,547 (for those wherein X is oxygen). Thus the appropriate perfluoroalkyl alcohol may be reacted with phosphorous oxytrichloride above 50°C to produce the corresponding dichloride. The dichloride may, in turn, be hydrolyzed to produce the phosphate.
The preparation of these compounds when X is sulfur is also known and may be carried out by reacting the appropriate perfluoroalkyl alcohol with phosphorous pentasulfide followed by refluxing in a non-reactive solvent such as benzene or isopropyl ether. Additional details on the preparation of dithiophosphate esters may be found in Inorganic Synthesis, Vol. 6, p. 142 (McGraw-Hill, 1960).
Yet other nonpolymeric anionic fluorochemicals useful as the membrane-forming material are the fluoroalkanephosphates which may be represented by the formula
[C8 F2g+1 CH2 O]k PO(OM)q (II)
wherein M is selected from hydrogen, alkali metal (e.g., sodium, potassium, lithium), ammonium and amine groups, and g is an integer of from 1 to 10, k is 1 or 2 and q is 3-k. These materials are commercially available from E. I. Du Pont de Nemours as "Zonyl FSP."
Another class of nonpolymeric anionic materials useful in the present invention is the perfluoroalkanesulfonamidoalkyl carboxylic acids of the formula
Rf SO2 N(R2)R3 COOM (III)
wherein Rf, R2 and R3 are as defined in formula I and M is as defined in formula II. The preparation of these compounds is described in U.S. Pat. No. 2,809,990. Thus the appropriate perfluoroalkanesulfonamide may be converted to a sulfonamide salt which may then be converted to an ester of the desired acid which may in turn be hydrolyzed to the acid or the salt.
Representative examples of perfluoroalkanesulfonamidoalkyl carboxylic acids useful in the present invention include
C8 F17 SO2 N(CH3)(CH2)10 COOH
C8 F17 SO2 N(C2 H5)CH2 COOH ##STR7##
Yet another class of the nonpolymeric anionic fluorochemicals useful as the membrane-forming material are the fluorocarbon monocarboxylic acids of the formula
Rf COOM (IV)
wherein Rf is as defined in formula I and M is as defined in formula II. The preparation of these compounds is described in U.S. Pat. No. 2,567,011.
Representative examples of fluorocarbon monocarboxylic acids useful in the present invention include
C8 F17 COOH
C11 F23 COOH
Still another class of nonpolymeric anionic fluorochemicals useful as the membrane-forming material are represented by the formula
Rf R3 COOM (V)
wherein Rf and R3 are as defined in formula I and M is as defined in formula II. These compounds are described in U.S. Pat. No. 2,951,051.
Representative examples of compounds of formula V include
C8 F17 CH2 CHClC8 H16 COOH
C8 F17 C10 H20 COOH
Yet another class of nonpolymeric anionic fluorochemicals useful in the present invention are the perfluoroalkanesulfonate esters of the formula
Rf SO2 OY (VI)
wherein Rf is as defined in formula I and Y is an aryl group. The preparation of these compounds is described in U.S. Pat. No. 3,346,612. Thus, these compounds may be prepared by reacting an appropriate phenolic compound with an appropriate perfluoroalkanesulfonyl fluoride.
Representative of useful perfluoroalkanesulfonate esters are ##STR8##
Still another class of nonpolymeric anionic fluorochemicals useful in the present invention are the fluorocarbon sulfonic acids and their derivatives. These compounds have the formula
Rf SO2 OM (VII)
wherein Rf is as defined in formula I and M is as defined in formula II. The preparation of these compounds is described in U.S. Pat. No. 2,732,398. A particularly useful compound of this type is C8 F17 SO2 OK.
Nonfluorinated materials are also useful as nonpolymeric anionic materials in the present invention. One class of such materials is the carboxylic acids of the formula
R5 COOM (VIII)
wherein R5 is a hydrocarbon group, preferably alkyl, containing from 6 to 24 carbon atoms and M is as defined in formula II. The R5 group may be straight or branched chain and may contain unsaturation. Preferably, however, the carboxylic acids are saturated. When the compositions employing materials of formula VIII as the membrane-forming material are formulated in water, the acid should be provided in its water-soluble salt form.
Representative examples of useful carboxylic acids of formula VIII include lauric, myristic, palmitic, stearic and oleic acids.
Another class of nonfluorinated material useful as the membrane-forming material comprises the organic phosphates, of the formula
[R6 O]m PO(OM)3-m (IX)
wherein R6 is a hydrocarbon group containing from about 10 to 20 carbon atoms, M is as defined in formula II and m is 1 or 2. Representative examples of useful organic phosphates of formula IX include (C16 H33 O)2 POOH and (C18 H37 O)2 POOH.
Still other anionic non-polymeric materials may be used as the membrane-forming material. Thus, aliphatic sulfonates of the formula
R6 SO2 OM (X)
wherein R6 is as defined in formula IX and M is as defined in formula II are also useful. Representative examples of useful aliphatic sulfonates include C12 H25 SO2 ONa and sodium dioctyl sulfosuccinate, i.e., ##STR9## Sodium dioctyl sulfosuccinate is commercially available as "Aerosol OT" from American Cyanamide Company.
Another useful class of nonpolymeric, anionic, membrane-forming materials is the N-acyl alkylaminoalkanoic acids of the formula
R6 CON(R2)R3 COOM (XI)
wherein R6 is as defined in formula IX, R2 and R3 are as defined in formula I and M is as defined in formula II. A particularly useful alkylaminoalkanoic acid is C11 H23 CON(CH3)CH2 COONa.
Yet another useful class of nonpolymeric, anionic, membrane-forming materials is the hydroxamic acids of the formula
R6 CONHOH (XII)
wherein R6 is as defined in formula IX. Particularly useful hydroxamic acids are the fatty acid hydroxamic acids.
Amine salts of fatty acids have also been found useful as the membrane-forming material. These compounds are known and may be prepared by reacting an amine (e.g., triethanol amine) with a fatty acid (e.g., stearic acid). One particularly useful compound of this type is the triethanol amine salt of stearic acid.
Cationic membrane-forming materials useful in the present invention are believed to attach to tooth surfaces via a complexing interaction between the cationic portion of the material and the proteinaceous portion of the tooth. A variety of cationic materials may be used as the membrane-forming material. They include polymeric and nonpolymeric materials.
The polymeric cationic membrane-forming materials useful in the invention comprise a class of polymers containing nitrogen in their backbone. They may have molecular weights as low as about 100 or higher than about 100,000.
Representative polymeric cationic membrane-forming materials are:
(a) Polydimeryl polyamine, a polydimeryl polyamide which has a molecular weight of about 8000, and an amine number of about 120 and is commercially available from General Mills Chemical Co;
(b) Polyethylene imine which has the repeating unit --CH2 -CH2 NH--n, and a molecular weight of about 100,000 and is commercially available from Dow Chemical Co.;
(c) 1,5-dimethyl diazaundecamethylene polymethobromine hexadimethrine bromide, a quaternary composition which has the repeating unit ##STR10## and is commercially available from Aldrich Chemical Company as Polybrene;
(d) Poly(N,N-dimethyl-3,5-dimethylenepiperidinium chloride) which has the repeating unit ##STR11## and is commercially available from Aldrich Chemical Company; and
(e) "Protamine" a grouping of simple proteins which yield only amino acids, especially diamino acids, upon cleavage by enzymes or acids and is commercially available from Pflatz and Bauer, Inc.
The nonpolymeric cationic membrane-forming materials useful in the present invention comprise a class of materials having a non-ionic aliphatic portion and a cationic terminal group. They may be generally represented by the formula R1 D wherein R1 is the aliphatic portion of the compound and is as defined previously and D is the cationic terminal group.
D may be joined directly to R1 or, alternatively, there may be a divalent linking group Q which joins R1 and D. Q must not interfere with the formation of the complex structure between the cationic material and the two surfaces and is as defined previously herein.
Representative examples of cationic terminal groups (D) useful in the present invention include
--NHC2 H4 NHC2 H4 NH2
--NH2
--NHC2 H4 NH2 ##STR12##
N(CH3)2 C2 H4 OH.H2 PO4.crclbar.
--N(CH3)3.Cl.crclbar.
A number of nonpolymeric cationic materials are useful as the membrane-forming material. One group of useful materials contains substantial quantities of fluorine in the main chain. Thus, for example, the distally perfluoroalkanesulfonamido amines described in U.S. Pat. No. 3,458,571 have been found useful. These compounds have the formula
Rf SO2 N(R2)R3 NHA (XIII)
wherein Rf, R2 and R3 are as described in formula I and A is a proton (e.g., hydrogen) or a poly(alkylamino) group.
Representative examples of compounds according to formula XIII include
C8 F17 SO2 N(C2 H5)C2 H4 NHC2 H4 NH2
C8 F17 SO2 NHC2 H4 NH2 ##STR13##
C8 F17 SO2 N(C2 H5)C2 H4 NHC2 H4 NH2
Another class of nonpolymeric cationic fluorinated materials useful in the present invention are the quaternary derivatives of the perfluoroalkanesulfonamidopolymethylenedialkylamine compounds. These derivatives are described in U.S. Pat. No. 2,759,019. They may be represented by the formula
Rf SO2 N(R2)R3 N+ R37 E-(XIV)
wherein Rf, R2, and R3 are as described in formula I, R7 is an alkyl group containing from 1 to 6 carbon atoms and E is an anion. Typical anions include H2 PO4.crclbar., NO3.crclbar. and halogens such as iodide, bromide, and chloride.
Representative examples of perfluoroalkanesulfonamidopolymethylenedialkylamine quaternary derivates include
C8 F17 SO2 N(CH3)C2 H4 N30 (CH3)3.Cl-
C8 F17 SO2 NHC3 H6 N+ (CH3)3.Cl-
C8 F17 SO2 NHC3 H6 N+ (CH3)2 C2 H4 OH.H2 PO4-
Nonfluorinated materials are also useful as nonpolymeric cationic membrane-forming materials in the present invention. Thus, for example, alkyl amines of the formula Cn H2n+1 NH2, wherein n is from 4 to 20, have been found useful.
Alkyl guanidines have also been found useful as membrane-forming materials of the present invention. For example, C16 H33 NHC(NH)NH2.HCl has been found useful as a membrane-forming material.
Useful nonionic membrane-forming materials are believed to attach to tooth surfaces by interacting with either or both of (i) the hydroxyl groups of the hydroxyapetite (i.e., C10 (PO4)6 (OH)2) or (ii) the hydroxyl groups present on the tooth surfaces from water or saliva in the mouth. In any event, useful nonionic membrane-forming materials may be represented by the formulae
[R8 ]b -Si-[R9 ]4-b (XV)
[R10 ]x -Ti-[OR11 ]4-x (XVI)
[R12 ]x Ti[R11 ]4-x (XVII)
In these formulae R8 is selected from hydrocarbon and fluorocarbon groups or combinations of hydrocarbon and fluorocarbon groups which may contain up to 25 carbon atoms. When R8 contains fluorocarbon terminal groups it is preferred that they be separated from the Si atom by an alkylene group. R8 may be aliphatic, aromatic or a combination of aliphatic and aromatic groups which may contain heteroatoms selected from nitrogen, sulfur, oxygen and silicone. Preferably no two of said hetero atoms are adjacent, and the oxygen atoms present are in the form of ether linkages. R9 is an alkoxy group containing from 1 to 6, and preferably from 1 to 3, carbon atoms. R10 is selected from hydrocarbon groups, preferably alkoxy groups, containing from 1 to 20 carbon atoms and preferably from 1 to 10 carbon atoms. R11 is selected from hydrocarbon groups of 1 to 20 carbon atoms which may be aliphatic, aromatic or aliphatic and aromatic and which may contain nitrogen, phosphorous, oxygen and sulfur substitution. R12 is a heterocyclic group containing carbon oxygen and hydrogen. The value of b and x is 0, 1, 2 or 3.
One class of materials according to formulae XV and XVI useful in the present invention include fluorocarbon siloxanes of the type described in U.S. Pat. No. 3,442,664 and having the formula
Rf R13 Si(OR14)3 (XVIII)
wherein Rf is as defined in formula I, R13 is an alkylene group of from 2 to 4 carbon atoms and R14 is an alkyl group of from 1 to 4 carbon atoms.
Representative examples of useful fluorocarbon siloxanes according to formula XVIII include
C8 F17 CH2 CHClSi(OCH3)3
C8 F17 CH2 CHClSi(OC2 H5)3
Other fluorocarbon siloxanes useful as the membrane-forming material in the present invention include: ##STR14##
C7 F15 CONHC3 H6 Si(OC2 H5)3
(H5 C2 O)3 SiC3 H6 NHCO(CF2 O)x (CF2 CF2 O)y CFCONHC3 H6 Si(OC2 H5)3
C18 H37 N(CH3)2 C3 H6 Si (OCH3)3 Cl-
This last compound is commercially available from Dow Corning Corporation as Q9-5700.
Compounds according to formulae XVI and XVII useful in the invention include the organotitanates. Examples of these compounds include ##STR15## The foregoing titanium compounds are available from Kenrich Petro-chemicals as the Ken-react titanates.
Other ingredients may be added to the compositions of the present invention. For example, therapeutic agents, such as caries prophylactic agents, polishing agents, surfactants, flavoring and sweetening agents, thickening agents and humectants may be included using techniques which are known to the art.
When such other ingredients are employed with (i) the anionic membrane-forming materials or (ii) the cationic membrane-forming materials which have a calcium complexing moiety D, the other ingredients must be substantially free of polyvalent metal atoms, (e.g., calcium, magnesium, etc.). These atoms interact with these particular types of membrane-forming materials and prevent them from forming the barrier. Thus while a minor amount of such atoms may be present, the total amount present must not prevent the membrane-forming material from interacting with the teeth. Preferably these compositions are free of polyvalent metal atoms.
With these factors in mind, then, suitable therapeutic agents, such as caries prophylactic agents, include sodium fluoride, stannous fluoride, potassium fluoride, hexylamine, hydrofluoride, myristylamine hydrofluoride, betaine fluoride, glycine potassium fluoride, etc. A particularly preferred fluoride is sodium fluoride.
When such other ingredients are employed with (i) the nonionic membrane-forming materials or (ii) the cationic membrane-forming materials which are free from calcium complexing moieties, such ingredients need not be substantially free from polyvalent metal atoms.
The therapeutic agents, when employed, are typically present in sufficient concentration so as to provide an available fluoride ion concentration of up to about 2% by weight, and preferably in the range of about 0.5-2% by weight, of the dentifrice composition. Additionally, it is preferred that the weight ratio of therapeutic ingredient to membrane-forming material be in the range of about 1:0.5 to 1:5 and most preferably in the range of about 1:0.5 to 1:1.
Suitable polishing agents include abrasive materials such as nonionic polymers. Representative of such materials are water-impervious crosslinked thermosetting resins (e.g., the condensation product of melamine and urea with formaldehyde), powdered polymethylmethacrylate and powdered polyethylene. Preferably the polishing agent is not so abrasive so as to scratch or unduly abrade the tooth surface or the dentin. Rather it only cleans the tooth surface. The polishing agents may comprise up to 95% by weight of the dentifrice composition.
Surfactants useful in the present invention include, for example, nonionic surfactants which are known to the art. These materials typically comprise up to about 5% by weight of the dentifrice composition.
Flavoring and sweetening agents useful in the invention include, for example, the oils of wintergreen, peppermint, spearmint, sassafras and anise. Additionally small amounts of sweetening agents such as saccharin, dextrose, levulose, etc., may also be added to the compositions. The flavoring and sweetening agents may comprise up to about 5% by weight of the dentifrice composition.
Gelling or thickening agents useful in the invention include, for example, water-soluble salts of cellulose ethers such as sodium carboxy methyl cellulose and sodium carboxy methyl hydroxy ethyl cellulose, natural gums such as gum karaya, gum arabic, and gum tragacanth; and colloidal magnesium-aluminum silicate or finely divided silica. Such thickening agents may comprise up to about 5% by weight of the dentifrice composition.
When provided in solution, dentifrices of the present invention typically comprise a solution of the membrane-forming material in water or a mixture of water and an alcohol. Typically the alcohol is a lower alkanol (e.g., ethanol, propanol, etc.). These compositions are particularly useful as mouthwashes or rinses.
The present invention is further illustrated in the following examples.
This example demonstrates that compositions of the invention form substantially continuous barriers that reduce the elution of a previously applied fluoride treatment from the teeth.
Separate bovine central incisors were used in the tests. A flat surface was provided on each tooth by first polishing each with 240 grit silicon carbide abrasive paper; and then with 400 grit silicon carbide abrasive paper. The teeth were then given a 5 minute soak with a 2% by weight solution of sodium fluoride (NaF) in deionized water. One-half of the number of the teeth were then given a 5 minute soak with a 1% by weight solution of membrane-forming material (C16 H33 O)2 -POOH, in deionized water. The remaining teeth were given no treatment with the membrane-forming composition. All of the teeth were then tested for initial water contact angle, initial fluoride level, water contact angle after a 26 hour water soak and fluoride content after a 26 hour water soak.
The water contact angle was measured by placing a drop of water on the flat polished surface of the tooth using a Model 710 "Hamilton" microliter syringe. The drop was then photographed using a PolaroidR camera which had a telescopic lens. The maximum perpendicular height (h) of the drop from the surface of the tooth to the top of the drop and the maximum length (l) of the drop in contact with the surface of the tooth were measured. These values were used to calculate the contact angle--by inserting them in the formula
(tan θ/2)=2h/l.
As the water contact angle increases the water repellancy of the surfaces increases. High water contact angles (e.g., at least about 70°) are characteristic of the anionic membrane-forming materials.
The fluoride content was measured with an electron microprobe Model 400 available from Materials Analysis Co. This was a destructive test so that duplicate sets of teeth were tested in order to determine the initial fluoride content and the fluoride content after water soak. The results obtained are given in Table V.
TABLE V |
__________________________________________________________________________ |
INITIAL 26 HOUR WATER SOAK |
CONTACT |
FLUORIDE CONTACT |
FLUORIDE |
ANGLE ON TOOTH ANGLE ON TOOTH |
TOOTH TREATMENT |
(°) |
(COUNTS/SEC) |
(°) |
(COUNTS/SEC) |
__________________________________________________________________________ |
A. |
NaF 21 1.7 -- -- |
B. |
NaF + (C16 H33 O)2 POOH |
100.4 1.2 -- -- |
Composition |
C. |
NaF 34 -- 35.4 0.5 |
D. |
NaF + (C16 H33 O)2 POOH |
89 -- 66.2 0.9 |
Composition |
__________________________________________________________________________ |
Comparison of treatments A and B shows the dramatic increase in water contact angle caused by the addition of the membrane-forming material (C16 H33 O)2 -POOH. Comparison of treatments C and D shows that, even after soaking the teeth for 26 hours in water, the membrane remains on the surface and that it substantially reduces elution of the initial fluoride treatment.
Bovine teeth were prepared and treated with NaF as described in Example 1. Certain of the teeth were then soaked for 5 minutes with compositions containing various membrane-forming materials. Each of the teeth were then soaked in separate 100 ml deionized water baths for 24 hours. The teeth were removed from the baths and each bath was then analyzed for fluoride ion content using a fluoride ion electrode. The results of these tests are set forth in Table VI.
TABLE VI |
______________________________________ |
FLUORIDE |
CONTENT |
IN WATER |
TOOTH TREATMENT (μg/ml) |
______________________________________ |
A 2% NaF 1.04 |
B 2% NaF + 0.55 |
0.5% C8 F17 SO2 N(C2 H5)C2 H4 |
OPO(OH)2 + |
97.5% deionized water |
C 2% NaF 0.72 |
D 2% NaF + 1% Polyacrylic Acid (CH2 CH) + |
0.21 |
97% deionized water COOH |
E NaF + 0.43 |
1% [C18 H37+N(CH3)2 C3 H6 Si(OCH.su |
b.3)3 ]Cl- + |
97% deionized water |
______________________________________ |
Comparison of treatments A and B (run simultaneously) graphically illustrates the decrease in elution of the NaF as a result of the presence of the membrane-forming material. Comparison of treatments D and E with treatment C (run simultaneously but at a different time than tests A and B) further graphically illustrate the decrease in elution of the NaF as a result of the presence of the membrane-forming material.
This example demonstrates the durability of the membrane. Bovine central incisors were prepared and the initial water contact angle measured as described in Example 1. The teeth were then soaked for 5 minutes with 0.1% by weight solutions of various membrane-forming materials in deionized water. The water contact angle was then measured after the teeth had been soaked in deionized water for 10 and 60 minutes and 24 hours. The results are given in Table VII.
TABLE VII |
______________________________________ |
Water Contact Angle (°) |
10 60 24 |
Membrane-forming ini- min min hour |
Material tial soak soak soak |
______________________________________ |
##STR16## 33.4 90 91 92.8 |
C8 F17 C10 H20 COOH |
38.5 114 102 110.4 |
C8 F17 SO2 N(C2 H5)C2 H4 OPO(OH)2 |
34.2 101.5 93 50 |
______________________________________ |
The high water contact angles, even after 24 hours of water soaking, demonstrate that the membranes retain their integrity for extended periods of time.
The procedures of Example 3 were repeated except that the teeth were given a fluoride treatment before being soaked for 5 minutes with a 0.1% by weight solution of membrane-forming material in deionized water. The fluoride treatment consisted of a 5 minute soak with an acidulated phosphate fluoride which comprised 40 grams (g) of NaF, 11.8 ml of HF, 126 ml of H3 PO4 and 1400 ml of deionized water. The results of the water contact angle measurements are given in Table VIII.
TABLE VIII |
__________________________________________________________________________ |
MEMBRANE-FORMING WATER CONTACT ANGLE (°) |
MATERIAL Initial* |
4 Min |
5 Hrs |
24 Hrs |
5 days |
__________________________________________________________________________ |
C8 F17 SO2 H(C2 H5)C2 H4 OPO(OH)2 |
43.6 |
101.4 |
94 104 87.6 |
Triethanolamine salt of |
38 102 78.4 |
80 -- stearic acid |
__________________________________________________________________________ |
This data demonstrates the durability of membranes formed form membrane-forming materials according to the invention.
Bovine central incisors were sequentially polished with 120 grit, 400 grit and 600 grit SiC abrasive papers so as to obtain a smooth, flat, uniform surface. The polished teeth were exposed to fluoride solution. One half of the number of the teeth were then used as controls while the remaining teeth were coated with various membrane-forming materials by dipping the teeth in an aqueous solution (0.5% by weight) for 5 minutes and then air-drying the treated teeth. All of the teeth were then exposed to water by soaking them in two separate 5 microliter portions of water for 15 minutes each. The fluoride remaining on the teeth after soaking was recovered by etching the teeth with a 5 microliter portion of 0.5 M perchloric acid which had been further diluted to 100 microliters by volume. The amount of fluoride recovered was determined by the hanging-drop fluoride electrode technique (P. Venkateswarlu, Analytical Chemistry: 46 878, 1974).
The amount of fluoride retained on the coated teeth and the control teeth was then compared by dividing the amount retained on the coated teeth by the amount retained on the control teeth.
The fluoride treatments, membrane-forming materials and results of the hanging drop test are set forth in Table IX.
TABLE IX |
______________________________________ |
FLUO- |
RIDE RE- |
TENTION |
(Ratio |
FLUORIDE MEMBRANE-FORMING Coated: |
TREATMENT MATERIAL Control) |
______________________________________ |
4% NaF, 5 min. |
C8 F17 (CH2)10 COOH |
2.3 |
4% NaF, 5 min. |
Protamine Sulfate 18 |
4% NaF, 5 min. |
(C16 H33 O)2 POOH |
1.7 |
1.4 |
4% NaF, 5 min. |
(CH3)2 CHOTi[OCOC16 H32 CH3 ]3 |
1.8 |
5% SnF2, 5 min. |
(CH3)2 CHOTi[OCOC16 H32 CH3 ]3 |
1.2 |
2.6 |
2.3 |
2.8 |
3.0 |
______________________________________ |
As can be seen from the data, the compositions of the invention substantially reduce the elution of a previously applied fluoride.
Example 5 was repeated except a different water washing technique was employed. In this example the water washing comprised drip washing the teeth with water for a period of time and followed by etching the teeth to recover the retained fluoride. Two etchings with the perchloric acid were performed. The first gave a measure of the fluoride retained by the coated teeth while the second gate a measure of the depth of fluoride treatment.
The fluoride treatments, membrane-forming materials and results of the hanging drop test are set forth in Table X.
TABLE X |
__________________________________________________________________________ |
FLUORIDE MEMBRANE-FORMING |
WASHING |
TREATMENT MATERIAL TIME(HRS) |
L1 |
L2 |
__________________________________________________________________________ |
4% NaF, 5 min. |
C8 F17 (CH2)10 COOH |
36 2.2 |
1.7 |
9.7 |
1.3 |
4% NaF, 5 min. |
(C16 H33 O)2 POOH |
36 2.5 |
1.6 |
1.2 |
1.3 |
4% NaF, 5 min. |
(C3 H)2 CHOTi[OCOC16 H32 CH3 ]3 |
36 7.5 |
1.5 |
1.9 |
1.4 |
4% NaF, 5 min. |
C8 F17 SO2 N(C2 H5)CH2 COOK |
36 1.4 |
1.0 |
Na2 PO3 F (0.1% F) |
C8 F17 SO2 N(C2 H5)CH2 COOK |
44 1.7 |
1.0 |
2.3 |
1.3 |
1.7 |
1.7 |
SnF2 (0.1% F) |
C8 F17 SO2 N(C2 H5)CH2 COOK |
60 1.8 |
1.4 |
3 min. 1.4 |
1.3 |
__________________________________________________________________________ |
L1 = first etching |
L2 = second etching |
As can be seen from the data, treated teeth are resistant to elution of a previously applied fluoride treatment.
Patent | Priority | Assignee | Title |
4792211, | Sep 18 1985 | SEIKO INSTRUMENTS & ELECTRONICS LTD , 31-1, KAMEIDO 6-CHOME, KOTO-KU, TOKYO, JAPAN | Ferroelectric liquid crystal electro-optical device having high water repellent alignment layer |
4960586, | Nov 15 1989 | Gillette Canada Company | Aqueous stannous fluoride non-abrasive home treatment gel compositions |
4961924, | Nov 15 1989 | Gillette Canada Company | Stabilized stannous fluoride toothpaste |
4970065, | Nov 15 1989 | Gillette Canada Company | Stabilized aqueous stannous fluoride mouthwash |
5009883, | Nov 15 1989 | Gillette Canada Company | Aqueous stannous fluoride non-abrasive home treatment gel compositions |
5009884, | Nov 15 1989 | Gillette Canada Company | Stabilized aqueous stannous fluoride mouthwash |
5017363, | Nov 15 1989 | Gillette Canada Company | Stabilized stannous fluoride toothpaste |
5211559, | Jul 18 1991 | Gillette Canada Company | Dental treatment tray for holding medicament gel |
5283924, | Sep 21 1990 | Gillette Canada Company | Interdental foam brush and treatment gel combination therewith |
5662887, | Dec 01 1994 | Minnesota Mining and Manufacturing Company | Fluorocarbon containing coatings, compositions and methods of use |
5665333, | Jan 17 1995 | ProVSeal LLC | Methods, compositions, and dental delivery systems for the protection of the surfaces of teeth |
5888480, | Jan 17 1995 | ProVSeal LLC | Methods, compositions, and dental delivery systems for the protection of the surfaces of teeth |
5961958, | Jul 16 1996 | ProVSeal LLC | Methods, compositions, and dental delivery systems for the protection of the surfaces of teeth |
5980868, | Jan 17 1995 | ProVSeal LLC | Methods, compositions, and dental delivery systems for the protection of the surfaces of teeth |
Patent | Priority | Assignee | Title |
2580473, | |||
2829086, | |||
2955985, | |||
3120469, | |||
3429963, | |||
3431208, | |||
3507955, | |||
3624120, | |||
3751568, | |||
3956480, | Jul 01 1974 | Colgate-Palmolive Company | Treatment of teeth |
3969499, | May 24 1971 | Lee Pharmaceuticals | Dental adhesive materials containing fluoride compounds |
4036950, | Jan 15 1975 | Colgate-Palmolive Company | Oral preparations |
4170636, | Dec 29 1977 | Minnesota Mining and Manufacturing Company | Composition and method for inhibiting plaque formation |
DE2164383, |
Executed on | Assignor | Assignee | Conveyance | Frame | Reel | Doc |
May 07 1982 | Minnesota Mining and Manufacturing Company | (assignment on the face of the patent) | / |
Date | Maintenance Fee Events |
Date | Maintenance Schedule |
Jan 01 1988 | 4 years fee payment window open |
Jul 01 1988 | 6 months grace period start (w surcharge) |
Jan 01 1989 | patent expiry (for year 4) |
Jan 01 1991 | 2 years to revive unintentionally abandoned end. (for year 4) |
Jan 01 1992 | 8 years fee payment window open |
Jul 01 1992 | 6 months grace period start (w surcharge) |
Jan 01 1993 | patent expiry (for year 8) |
Jan 01 1995 | 2 years to revive unintentionally abandoned end. (for year 8) |
Jan 01 1996 | 12 years fee payment window open |
Jul 01 1996 | 6 months grace period start (w surcharge) |
Jan 01 1997 | patent expiry (for year 12) |
Jan 01 1999 | 2 years to revive unintentionally abandoned end. (for year 12) |