CA1198680A - Anticalculus oral composition - Google Patents

Abstract

ANTICALCULUS ORAL COMPOSITION
ABSTRACT OF THE DISCLOSURE

A substantially anhydrous oral composition is disclosed which is substantially devoid of normally staining antibacterial antiplaque agents and which contains an effective anticalculus amount of a bis(o-carboxyphenyl) ester of a C2-8 aliphatic dicarboxylic acid such as bis(o-carboxyphenyl) succinate.

Description

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This application is rela~ed to United States Patent 4,080,441.
This invention relates to oral compositions containing an anticalculus agent.
Calculus is a hard, mineralized formation which forms on the teeth. Regular brushing prevents a rapid build-up of these deposits, but even regular brushing is not sufficient to remove all of the calculus deposits which adhere to the teeth.
Calculus is formed on the teeth when crystals of calcium phos-phates begin to be deposited in the pellicle and extracellularmatrix of the dental pla~ue and become sufficiently closely packed together for the aggregates to become resistant to defor-mation. I'here is no complete agreement on the route by which calcium and orthophosphate ultimately become the crystalline material called hydroxyapatite (HAP). It is generally agreed, however, that at higher saturations, that is, above the critical saturation limit, the precursor to crystalline hydroxyapatite is an amorphous or microcrystalline calcium phosphate. "Amor-phous calcium phosphate" although related to hydroxyapatite differs Erom it in atomic structure, particle morphology, and stoichiometry. The X-ray diffraction pattern of amorphous cal-cium phosphate shows broad peaks typical of amorphous materials, which lack the long-range atomic order characteristic of all crystalline materials, including hydroxyapatite. A suggested mechanism by which the nontoxic anticalculus agents of this in-vention inhibit calculus formation probably involves such agents functioning to bind the amino groups in the matrix system in the oral cavity at physiological pH and temperatures and also cross-links the protein.

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A suk;stantial number of different types of compounds and compositions have been developed for use as antibacterial, and antiplaque and anticalculus agents in oral compositions, in-cluding for example such cationic materials as the bis-biguanide compounds and quaternary ammonium compounds, e.g. ben~ethonium chloride and cetyl pyridinium chloride, disclosed in United States 4,080,4~1. These cationic materials however tend to stain the teeth with continued use.
It is an object of this invention to provide an improved anticalculus oral composition which will have relatively little or no tendency to stain the teeth.
A further object of the invention is to provide an oral composition which inhibits the transformation of amorphous cal-cium phosphate to hydroxyapatite crystal structure normally associated with calculus.
Another object o~ this invention is the provision of an improved method for inhibiting the formation of calculus.
Other objects and advantages will appear as the descrip-tion proceeds.
The invention provides a substantially anhydrous oral composition devoid of stain-inducing antibacterial antiplaque agents and comprising an orally acceptable vehicle and in an effective amount as an anticalculus agent at least one bis(o-carbox~ phenyl) ester of a C2 8 aliphatic dicarboxylic acid.
The antlcalculus agents of this invention may be represented, in their free acid form, by the formula:

OOC ~C~3n C~O
COOH HOOC

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wherein preferably the R's are independently H or Cl 4 alkyl, pre~erably H, and n is an integer of O to 6, pre~erably 2, the preferred anticalculus agent accordingly being bis(o-carboxyphenyl) succinate (BOCS). The -~CRR~-ngroup may however be a single bond when n is O as in the bisesters o~ oxalic acid, or may be any Cl_6 alkylene or alkenylene group, i.e. straight or branched saturated or unsaturated, O or S chain interrupted, Cl 4 alkoxy substituted, or the like. When -the ~ CRR group is part of an ethylenic group, one or both R's may be ~ero, i.e. replaced by a valence bond. The bis(o-carboxyphenyl) esters of the following aliphatic dicarboxylic acids are only illus-trati~e of the anticaiculus agents of this inrention:
oxalic (ethanedioic) malonic (propanedioic) succinic ~butanedioic) glutaric (pentanedioic) adipic (hexanedioic) pimelic (heptanedioic) suberic (octanedioic) maleic (1,2-ethylenedicarboxylic HOOCCH:CH-COOH) itaconic (methylenesuccinic HOOCC(:CH2)CH2-COOH) isosuccinic (2-methylpropanedioic) muconic (2,1l-hexadienedioic HOOCCH: CHCH: CH-COOH ) dihydromuconic (HooccH2cH2cx:cHcooH) dihydroitaconic (methylsuccinic) 3-ethylhexanedioic ~urther, one or both phenyl moieties in this agent may be nuclearly substituted with one or more Cl_~ alkyl or alkoxy groups such as methyl or isobutoxy, or halo such as chloro, bromo, iodo or fluoro.
Suitable methods for preparing these anticalculus agents are disclosed in the a~orementioned U.S. 4,080,441. Another improved method for such preparation is described in Example A below.
It will be understood that the ~ree acid form of these anticalculus agente may be converted to and employed in their equivalent salt form by treatment with any base containing an orally acceptable cation such as alkali metal (e.g. sodium~
potassium), alkaline earth metal (e.g. calcium, magnesium), me'al, ammonium, mono-di-or tri- Cl_lg alkyl or alkanol- aubstituted ammonium or organic amine (e.g. methyl, ethyl, hydroxyethyl substituents).
The anticalculus agents of this invention are anti-nucleating agents, oral compositions of this invention containingthem are effective in reducing formation of dental calculus without unduly decalcifying the dental enamel, and in contrast to the above-mentioned cationic an~tibacterial, antiplaque and anticalculus agents, such agents and compositions have little or no tendency to stain the teeth, and can further be found to e~fectively reduce or inhibit gingivitis.
The concentration of these an-ticalculus agentsin oral compositions can range widely, typically upward from about 0.01%
by weight, with no upper limit on the amount -that can be utilized except as dictated by cos-t or incompatibility with the vehicle.
Generally, concentrations from about 0.01% to about 10%, preferably about 0.05% to about 8.o%~ and more prefera~ly about 0.1% to about 4% by weight are utilized. Oral compositions which in the ordinary course of usage could be accidentally ingested preferably contain concentra-tions in the lower portions of the foregoing ranges.
Although these anticalculus agents vary in water solubility depend-ing upon their molecular weight, identity and proportions of salt-forming cations, etc, they are sufficiently soluble in aqueous media, e.g. in the oral cavity, in the low concentrations employed herein to be termed water soluble to that extent. It has however been unexpectedly found that oral compositions containing such agents in an aqueous medium undergo significant hydrolysis or other deterioration in storage. In accordance with a further aspect of this invention, it is preferred to provide oral compositions which are substantially anhydrous, e.g. containing 0 to less than about 0.2 moles of water per mole of the anticalculus agent.
When the oral compositions of this invention are in liquid, paste or cream form, as in mouthwashes and rinses, toothpastes and dental creams, a water-miscible (preferably water soluble) organic normally liquid orally acceptable vehicle is preferably employed. Typically, such vehicles include water soluble C2 ~ monohydric and polyhydric alkanes and Cl 4 alkyl ethers thereof such as ethanol, ethyiene glycol, methyl, ethyl and butyl ethers thereof (methyl, ethyl and butyl Cellusolve*), propylene glycol, tetra-methylene glycol, and glycerin, and water soluble poly (ethylene glycols)such as diethylene glycol, methyl, ethyl, diethyl and butyl ethers thereof (methyl, ethyl, diethyl and butyl Carbitol*), triethylene glycol, low mole-cular weight polyethylene glycols, e.g. 400, 600, and mixtures thereof etc.

* Trade Mark Polyhydric compounds in the aforementioned group, especially propylene glycol, glycerin, and the low molecular weight poly-ethylene glycols, generally function also as humectants which are desirable components of the oral compositions of this invention.
Other types of such water miscible liquid vehicles which may be employed are the polar aprotic solvents such as dimethyl ~ormamide and sulfoxide, N-methyl pyrrolidone, sulfolane, tetramethyl sulfone, acetorlitrile, and preferably et~ylene and propylene carbonate.
Essentially water-immiscible organic liquid vehicles may also be employed representative of which are hydrocarbon, fatty acid and fatty acid ester oils such as mineral oil, tetradecane, pentane, caproic, acid~ oe~anthylic acid 7 methyl caproate and laurate, ethylene glycol dicaprylate and the like.
Mixtures of the same types and/or of different types of liquid vehicles as described above may of course be employed.
The proportion of the aforementioned liquid vehicle employed in these oral compositions will obviously depend for the mos-t part upon the desired degree of fluidity or viscosity and will be readily determinable in routine manner in any particular instance.
Typically, liquid compositions such as mouthwashes and rinses contain about 70% to about 99.9%, and toothpastes and dental creams contain about 10% to about 80%, by weight of such liquid vehicle, about 10%
to about l00% of which may be a humectant. ~ormally solid humectants such as sorbitol may also be included.
The oral compositions o~ this invention typically have, in aqueous medium, e.g. in the oral cavity or in the form o~ a 20%
aqueous slurry or solution, a pH oI' about 3.5 to about 8, pre~erably about 4 to about 7, more pre-ferably about 4 to 6. Such pH can be controlled by inclusion of the re~uired amounts of acidic substances such as citric or benzoic acid, basic substances such as sodium hydroxide, and/or buffering agents such as sodium citrate, benzoate, bicarbonate or carbonate, disodium hydrogen phosphate, sodium dihydrogen phosphate, or mixtures thereof.
The vehicle i.n solid or pasty compositions such as toothpowders, tablets, toothpastes and dental creams generally contains polishing material.
Examples of polishing materials are water-insoluble sodium metaphosphate (IMP), potassium metaphosphate, tricalcium phosphate, anhydrous, mono-hydrated and dihydrated calcium and dicalcium phosphate, calcium pyrophos-phate, magnesium orthophosphate, trimagnesium phosphate, magnesium and cal-cium carbonate and sulfate, alumina, hydrated alumina, aluminum silicate, alkali metal and alkaline earth metal aluminosilicates, zirconium silicate, silica, bentonite, and mixtures thereof. Preferred polishing materials in-clude crystalline and colloidal silica, silica gel, complex amorphous alkali metal aluminosilicate, hydrated alumina and IMP.
Alumina, particularly the hydrated alumina sold by Alcoa* as C333, which has an alumina content of 64.9% by weight, a silica content of 0.008%, a ferric oxide content of 0.003%; and a moi.sture content of 0.37%, at ll0 C., and which has a specific gravity of 2.42 and a particle size such that 100%
of the particles are less than 50 microns and 84% of the particles are less than 20 microns, is very ef:Eective.
When visually clear gels are employed, a polishing agent of col-loidal silica, such as those sold under the trademark SYLOID as Syloid 72, 74 or 244 or under the trademark SANTOCEL as Santocel l00 * Trade Mark and alkali metal aluminosilicate complexes are par-ticularly use~ul, since they have re~ract:ive indices close to the refractive indices of gelling agent-liquid systems commonly used in dentifrices.
Many of the so-called "water-insoluble" polishing material are anionic in character and also include small amounts of soluble material. Thus, insoluble sodium metaphospha-te may be formed in any suitable manner, as illustrated by Thorpe's Dictionary of Applied Chemistry, ~lolume ~ 9 4th Edition, pp. 510-511. The forms of insoluble sodium me-taphosphate known as Madrell's salt and Kurrol's salt are further examples o~ suitable materials. These metaphosphate salts exhibit a minute so~ubility in water, and there~ore are commonly referred to as insoluble metaphosphates. There is present therein a minor amount of soluble phosphate rnaterial as impurities~
usually a few percent such as up to 4% by weight. The amount of soluble phosphate material, which is believed to include a soluble sodium trimetaphosphate in the case o~ insoluble metaphosphate, may be reduced by washing with water if desired. The insoluble alkali metal metaphosphate is typically employed in powder form o~ a particle size such that no more than abou-t 1% of the material is larger than about 37 microns.
The polishing material is generally present in amounts ranging from about 20% to about ~% by weight of the oral prepar~tion.
Preferably, it is present in amoun-ts ranging from 20% to about 75%
in toothpaste, and from about 70% to about ~% in toothpowder.
In the preparation of toothpowders, it is usually sufficient to admix mechanically, e.g., by milling, the various solld ingredients in appropriate quantities and par-ticle sizes.
In a too-thpaste, cream or gel, the liquids and solids typically are suitably proportioned to form a creamy or gelled mass which is extrudable from a pressurized container or from a collapsible tube. Thickening -to the proper desired viscosity or ~lowability is typically facilitated or achieved by lnclusion of a binding, t~ic~ening or gelling agent such as natural or synthetic gums or gum-like materials, typically Irish moss, Pluronics , sodium carbox~methylcellulose and carboxyethylcellu-lose, methylcellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, hydroxypropyl methylcellulose, hydroxybu~yl methyl-*

cellulose t Laponite CP or SP (synthetic hectorite clay of Laporte Industries Ltd.), viscarin, gelatin, glucose, sucrose,Carbopols (e.g. 934,940,941), gum karaya, gum arabic, gum tragacanth, polyvinylpyrrolidone, polyvinyl alcohol and starch.
They are usually present, singly or plurally, in an amount up to about 10~ by weight, preferably in the range of from about 0.5 to about 5%. The preferred gelling agents are Pluronics and hydroxypropyl cellulose. Pluronics such as F108 and F127 are polyoxypropylene polyoxyethylene block polymers which simul-taneously function as nonionic surfactants.

The oral compositions of this invention may contain a non-soap synthetic sufficiently water soluble organic anionic or nonionic surfactant in concentrations generally ranging ~rom about 0.05 ~ about 10, preferably about 0.5 to about 5, weight percent, to promote wetting, detersive and foaming properties.
United States Patent No. 4,041,149 discloses such suitable anio-nic surfactants in col. 4, lines 31-38 and such suitable non-ionic surfactants in col. 8, lines 30-68 and col. 9, lines 1-12 n In certain forms of this invention a fluorine-providing compound is present in the oral prepara-tion. These compounds may be slightly soluble in water or may be fully water-soluble. They * Trade Marks f/~r,ne C:~"~al~J In~
are characterized by their abili-ty to release fluoridc ions in water and by substantial freedom ~rom reaction with other compounds of the oral preparation. Among these materials are inorganic fluoride salts,, such as soluble alkali me-tal, alkaline earth metal and heavy metal sal-ts, for example, sodium fluoride, potassium fluoride, ammonium fluoride, calcium fluoride, a copper ~luoride such as cuprous fluoride, zinc fluoride, a tin fluoride such as stannic fluoride or stannous chlorofluoride, barium rluoride 9 sodium ~luorsilicate, ammonium fluorosilicate, sodium fluorozirconate, sodium monofluorophosphate, aluminum mono-,and di-fluorophosphate, and fluorinated sodium calcium pyrophospha-te. Alkali metal and tin fluorides, such as sodium and stannous fluorides, sodium monofluorophosphate and mixtures thereof, are preferred.
The amount of' the fluorine-providing compound is dependent to some extent upon the type of compound, its solubility, and the type of oral preparation, but it must be nontoxic amount.
In a thickened or solid oral preparation, such as toothpaste or toothpowder, an amount of such compound, which releases a maximum of about 1% by weight o~ the preparation is considered satisfactory.
Any suitable minimum amount of such compound may be used,but it is preferable to employ sufficient compound to release about 0.005%
to 1%, and pre~erably abou-t 0.1% of fluoride ion. Typically, in the cases of alkali metal fluorides and stannous fluoride, this component is present in an amount up to about 2% by weight, based on -the weight of the preparation, and preferably in the range of about 0.05% to 1%. In the case of sodium monofluorophosphate, the compound may be present in an amount up to 7.6% by weight, more typically about 0.5 to about 1% by weight.

In a li~uid oral preparation such as a mouthwash~ the ~luorine-providlng compound is typical~y present in an amount su~ficien-t to release up to about 0.()005 to about 0.2%, pre~erably about 0.001 -to about 0.1~ and more pre~erably about 0.0013% by weight of f`luoride ion.
Various other materials may be incorporated in the oral preparations of this invention such as whitening agents~ pre~erYatives silicones, chlorophyll compounds, o-ther anticalculus agents~ an-ti-bacterial antiplaque agents, and/or ammoniated material such as urea, diammonium phosphate, and mixtures thereof. These adjuv~nts 7 where present, are incorpora-ted in the preparations in amounts which do not substantially adversely a~fect the properties and characteristics desired.
Any suitable ~lavoring or sweetening material may also be employed.
Examples o~ suitable ~la~oring constituents are flavoring oils, e.g., oils of spearmint, peppermint~ wintergreen~
sassa~ras, clove, sage~ eucalyptus, mar~oram, cinnamon, lemon? and orange3menthol, eugenol, cineol, and methyl salicylate. Suitable sweetening agents include sucrose, fructose, lactose, maltose~
sorbitol, xylitol, sodium cyclamate, perillartine, APM (aspartyl phenyl alanine, methyl ester) and saccharine. Suitably 7 ~lavor and sweetening agents may together comprise ~rom about 0.01% to 5%
or more o~ the preparation.
In preparing the oral compositions o~ this invention, it is preferred but not essential to add the anticalculus agent ' a~ter the other ingredients ~except perhaps so~e o~ the water~ are mixed or contacted with each other to avoid a tendency ~or such agent to be precipitated.

It will be understood that 7 as is conventional, the oral preparations are to be sold or otherwise distributed in suitable labelled packages. Thus a ~ar of mouthrinse will have a label describing itg in substance, as a mouthrinse or mouthwash and having directions Por its use; and a toothpaste will usually be in a collapsible tube, typically aluminum, lined lead or plastic, or other squeeze dispenser ~or metering out the contents, having a label describing it, in substance, as a toothpaste or dental cream.
In the practice of this invention an oral composition according to this invention such as a mouthwash or toothpaste containing the de~cribed anticalculus agent in an amount effective to inhibit calculus on den-tal surPaces is applied regularly to the oral cavity, especially dental enamel, preferably from about 1 to 3 times daily.
Example A
Preparation of Bis(o-carboxyphenyl)succinate 0.4 moles salicylic acid (55.2 grams) 0.4 moles pyridine (31.2 ml~) n . 2 moles succinyl chloride (31.0 grams) The salicylic acid and pyridine are dissolved in 90 ml.
of acetone. To the resulting clear solution, the succinyl chloride in 90 ml. of acetone is added, with stirring, at a rate to keep acetone refluxing for half an hour. During this addition, the desired BOCS product begins to separate and the mixture turns dark -purple. ~he reaction slurry is stirred for half an hour after all -the succinyl chloride has been added. Then 200 ml. of water are added, the acetone evaporated from the slurry in a rotary evaporator at 35C. and the desired BOCS product collected on a suction Pilter, washed with water and dried in vacuum at 60C.

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Yield - 66.5 grams ~93%) M.P. 177 -177.5C.
Neutral Equivalent 179.9*
Saponification Eq. 186.8*
*calculated for C18H14 8 The following examples are further illustrative of the nature of the present invention, but it is understood that the invention is not limited thereto. All amounts and proportions referred to heTein and in the appended claims are by weight, and temperatures are in C., unless otherwise indicated.
Example 1 The following formulation is illustrative of a toothpaste in accord-ance with this invention effective for inhibiting calculus.
Parts by Weight Propylene glycol 42.0 Hydroxypropyl cellulose 1.0 Polyethylene glycol 60010.0 Sodium saccharin 0.2

2 0.
IMP 28.0 Syloid 244 12.0 Sodium lauryl sulfate Flavor 1.0 BOCS 3.0 The following formulations, given in parts by weight, are illustra-tive of mouthwashes in accordance with this invention effective for inhibit-ing calculus.

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Example Flavor 0.22 0.22 0.22 Ethanol 15.0 15.0 15.0 Pluronic F108 3.0 3.0 3.0 Glycerine 10.0 10.0 10.0 Sodium saccharin 0.03 0.03 0.03 BOCS 0.05 0.50 1.0 The mouthwash formulations of Examples 2-4 above may be applied to the oral cavity as is or after dilution with about 2 to 4 times their volumes of water, i.e. volume ratios of formulation: water of about 1:2 to about 1:4.
Substitution of equivalent amounts of the following bis ester-containing compounds for the BOCS employed in the formulations of Examples 2-5 yield formulations also effective for inhibiting dental calculus.
Example Bis Ester-Containing Compound bis(2-carboxy-4-butoxyphenyl)oxalate 6 bis(2-carboxy-4-propyl-6-chlorophenyl)glutarate 7 bis(2-carboxy-4-methyl-6-bromophenyl)adipate 8 bis(2-carboxy-4-iodo-6-ethoxyphenyl)suberate 9 bis(2-carboxyphenyl)pimelate bis(2-carboxy-5-methoxyphenyl)malonate 11 bis(2-carboxy-6-butylphenyl)maleate 12 bis(2-carboxyphenyl)itaconate 13 bis(2-carboxy-4-fluorophenyl)muconate Example 14 In this study on 24 rats, a placebo of water and an 0.1% solution of BOCS in dimethyl sulfoxide, pH 7.10, as the test anticalculus mouthrinse are evaluated for effectiveness against formation of calculus for a 30 day period. Litter matured Osborne-Mendel rats are used. On days 21 and 22 they t6~q~

are inoculated intraorally with Strep-mutans and Actinomyces viscous and feces from caries-active Osborne-Mendel rats, placed on calculogenic diet 580F supplemented with 0.2% P as Na2pO4~ and the placebo and the test mouth-rinse each applied to molars of a group of 12 such rats twice daily on Monday to Friday and once daily on Saturday and Sunday for a period oE 30 days. The animals are weighed at the beginning and at the end of the study to assure that the rats remain in otherwise normal condition. At the end of the period, calculus formation is assessed according to routine procedures and the following results are found:

Mean No. Mean Terminal Calculus Animals Weight Gain Units*Significance Placebo (Water) 12 128 grams 17.9 Mouthrinse 12 135 grams 14.8 ~<0.01 (0.1% BOCS) *20 units at risk The above results establish that BOCS at 0.1% level when applied topically is significantly eEfective (at tha +99% level) in reducing calculus formation.
This invention has been described with respect to preferred embodi-ments and it will be understood that modifications and variations thereof obvious to those skilled in the art are to be included wi~hin the spirit and purview of this application and the scope of the appended claims.

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Claims (6)

THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:

1. A substantially anhydrous oral composition devoid of stain inducing antibacterial antiplaque agents and comprising an orally acceptable vehicle and in an effective amount as an anticalculus agent at least one bis(o-carboxyphenyl)ester of a C2-8 aliphatic dicarboxylic acid.

2. The oral composition of claim 1 wherein said anti-calculus agent is bis(o-carboxyphenyl) succinate.

3. The oral composition of claim 1 or 2 containing;
approximately by weight, 0.01% to 10% of said anticalculus agent.

4. The oral composition of claim 1 or 2 containing, approximately by weight, 0.05% to 5% of said anticalculus agent.

5. The oral composition of claim 1 or 2 which is a mouth-wash containing a liquid vehicle and having, in aqueous medium, a pH of about 3.5 to about 8.

6. The oral composition of claim 1 or 2 which is a tooth-paste containing a liquid vehicle, a gelling agent and a dentally acceptable polishing agent and having, in aqueous medium, a pH
of about 3.5 to about 8.