BRPI1003240B1 - Compositions for treatment of dental sensitivity and non-therapeutic method for treatment of sensitive teeth - Google Patents

Description

Report of the Invention Patent for "COMPOSITIONS FOR TREATMENT OF DENTAL SENSITIVITY AND NON-THERAPEUTIC METHOD FOR TREATMENT OF SENSITIVE TEETH".

FIELD OF THE INVENTION The present invention relates to compositions for treating dental sensitivity, which have a dentin affinity and cause effective occlusion of open dentinal tubules.

BACKGROUND OF THE INVENTION

Many people suffer from tooth sensitivity, and this condition is often called dentinal hypersensitivity, which is a common problem in the adult population. This is defined as a temporary pain from exposed dentin, typically in response to chemical, thermal, tactile or osmotic stimuli, and which cannot be explained by any other dental defect or pathology. Erosion of the external surface (enamel) of the teeth and / or gingival retraction often results in exposure of dentinal tubules, resulting in routes between the oral cavity and the nerve fibers present in the pulp. It has been shown in vivo that there is a pressure gradient across dentin, which causes outward fluid flow. This fluid flow is disturbed or increased in response to tactile, thermal (heat or cold) and osmotic (high sugar, etc.) stimuli believed to result in a response of the mechanoreceptors in the pulp nerve fibers, which may lead to the development of the fluid. is detected as pain. Nerve-wheezing and dental tubule occlusion agents have been used to treat dental sensitivity. Special toothpastes, which contain potassium and / or bivard nitrate, amorphous calcium phosphate etc., are regularly used by consumers suffering from dentinal sensitivity. Another occlusive agent that is also used to treat dental sensitivity is potassium oxalate. None of these occlusive agents, however, is completely effective in mitigating dentinal sensitivity, since effective occlusion of dentinal tubules depends on different variables. There is therefore a continuing need for dental sensitivity treatment compositions which have a dentin optimized affinity and which effectively occlude the dentinal tubules.

SUMMARY OF THE INVENTION

It has been found that the above objective can be achieved by selecting specific compounds that provide a protective barrier to the teeth and / or effectively occlude the exposed inner tubules, thereby decreasing tooth sensitivity. In certain embodiments, the present invention provides an buccal composition comprising: a) at least one compound of formula I wherein: M1 and M3 are independently a monovalent or divalent metal, M2 is a polyvalent metal or metal oxide, and A and B are independently selected from the group consisting of C2 -C6 diacids, triacids and tetra acids, b) optionally a taste, c) optionally a sweetener, d) optionally a pH buffer, ee) at least one orally acceptable solvent, wherein the buccal composition has a pH greater than (or at least) 2.0 (or about 2).

In other embodiments, the compositions of the present invention relate to an buccal composition, comprising: a) at least one compound of formula I wherein: M1 and M3 are independently a monovalent or divalent metal, M2 is a polyvalent metal or metal oxide, and A and B are independently selected from the group consisting of C 2 -C 6 diacids, triacids and tetra acids, and b) at least one orally acceptable solvent, wherein the The composition is substantially free of water.

In still other embodiments, the compositions of the present invention pertain to buccal compositions comprising: a) at least one compound of formula I wherein: M1 and M3 are independently a monovalent or divalent metal, M2 is a polyvalent metal or metal oxide, and A and B are independently selected from the group consisting of C 2 -C 6 diacids, triacids and tetra acids, b) at least one additional desensitizing agent, and c) at least an orally acceptable solvent.

In another embodiment, the compositions of the present invention relate to a method for treating sensitive teeth, comprising the steps of applying to them for at least two consecutive applications a composition comprising: a) at least one compound of formula I M1 -A-M2-B-M3 (I) wherein: M1 and M3 are independently a monovalent or divalent metal, a monovalent or divalent metal, M2 is a polyvalent metal or metal oxide, and A and B are independently selected from the group. consisting of C 2 -C 6 diacids, triacids and tetraacids, and b) at least one orally acceptable solvent, wherein the applications are spaced no more than (or less than) 12 (or about 12) hours apart.

In yet another embodiment, the compositions of the present invention are directed to a method for occluding dentinal tubules of the teeth, comprising the steps of applying to the teeth for at least two consecutive applications a composition comprising: a) at least one compound of wherein: M1 and M3 are independently a monovalent or divalent metal or a monovalent or divalent metal, M2 is a polyvalent metal or metal oxide, and A and B are independently selected from the group consisting of C 2 -C 6 diacids, triacids and tetraacids, and b) contact the teeth with the composition for at least (or more than) 10 (or about 10) seconds in which the tubules are at least ( or more than) about 5% occluded.

In yet another embodiment, the compositions of the present invention are directed to a method for occluding dentinal tubules of the teeth, comprising the steps of applying to the teeth for at least two consecutive applications a composition comprising: a) at least one compound of wherein: M1 and M3 are independently a monovalent or divalent metal, M2 is a polyvalent metal or a metal oxide, and A and B are independently selected from the group consisting of: in C2 - C6 diacids, triacids and tetra acids, and (b) contact the teeth with the composition in the presence of calcium for at least 20 seconds when the compound forms a calcium precipitate on or near the teeth. , so that at least (or more than) 30% (or about 30%) of the precipitate formed remains in the teeth after sonication for 2 (or about 2) minutes.

In another embodiment, the compositions of the present invention relate to a method of depositing a precipitate on the teeth and / or dentinal tubules of the teeth, comprising the steps of applying to the teeth for at least two consecutive applications a composition comprising (a) at least one compound of formula I M1-A-M2-B-M3 (I) wherein: M1 and M3 are independently a monovalent or divalent metal, M2 is a polyvalent metal or metal oxide, and A and B are independently selected from the group consisting of C 2 -C 6 diacids, triacids and tetra acids, and b) contact the teeth with the composition in the presence of calcium for at least (or more than) 20 (or about 20) seconds. wherein M2 is present in the precipitate at a concentration of at least (or more than) 5% (or about 5%) of the deposited precipitate. BRIEF DESCRIPTION OF THE DRAWINGS Figure 1 is a scanning electron microscope image of a corroded dentin chip taken after 7 treatments with 0.5% potassium oxalate formulation and showing minimal surface oxalate precipitation dentin splinter and / or occlusion of the dentinal tubule after treatment. Figure 2 is a scanning electron microscope image of a corroded dentin chip taken after 14 treatments with 0.5% potassium oxalate formulation and showing a minimum precipitation of oxalate over the dentin chip surface. and / or occlusion of the dentinal tubule after treatment. Figure 3 is a scanning electron microscope image of a corroded dentin chip taken after 21 treatments with 0.5% potassium oxalate formulation and showing a minimum precipitation of oxalate over the dentin chip surface. and / or occlusion of the dentinal tubule after treatment. Figure 4 is a scanning electron microscope image of a corroded dentin chip taken after 28 treatments with 0.5% potassium oxalate formulation and showing a minimum precipitation of oxalate over the dentin chip surface. and / or occlusion of the dentinal tubule after treatment. Figure 5 is a scanning electron microscope image of a corroded dentin chip taken after 7 treatments with 0.5% potassium oxide and titanium oxalate formulation showing substantial precipitation of titanium oxide oxalate over the surface of the dentin flake and / or a virtually complete occlusion of the dentinal tubules after treatment. Figure 6 is a scanning electron microscope image of a corroded dentin chip taken after 14 treatments with 0.5% potassium oxide titanium formulation, showing substantial precipitation of titanium oxide oxalate over the surface of the dentin flake and / or a virtually complete occlusion of the dentinal tubules after treatment. Figure 7 is a scanning electron microscope image of a corroded dentin chip taken after 21 treatments with 0.5% potassium oxide and titanium oxalate formulation showing substantial precipitation of titanium oxide oxalate over the surface of the dentin flake and / or a virtually complete occlusion of the dentinal tubules after treatment. Figure 8 is a scanning electron microscope image of a corroded dentin chip taken after 28 treatments with 0.5% potassium oxide and titanium oxalate formulation showing substantial precipitation of titanium oxide oxalate over the surface of the dentin flake and / or a virtually complete occlusion of the dentinal tubules after treatment. Figure 9 is a scanning electron microscope image of a corroded dentin chip taken prior to treatment with a formulation having the same ingredients as those used to treat the dentin chips of Figures 1 to 8 but free of oxalate. potassium or titanium oxide oxalate and not showing any change in precipitation on the surface of the dentin flake and / or occlusion of the dentinal tubule before treatment and after treatment. Figure 10 is a scanning electron microscope image of a corroded dentin chip taken after 28 treatments with a formulation that has the same ingredients as those used to treat the dentin chips of Figures 1 to 8, but free of oxalate. potassium or titanium oxide oxalate and not showing any change in precipitation on the surface of the dentin flake and / or occlusion of the dentinal tubule before treatment and after treatment. Figure 11 is a scanning electron microscope image of a corroded dentin chip that has undergone 28 treatments with a formulation containing 0.5% potassium oxalate (formulation B) and then sonicated for 2 minutes with the use of a normal pulse sounder. Figure 12 is a scanning electron microscope image of a corroded dentin chip that has undergone 28 treatments with a formulation containing 0.5% titanium oxide (formulation D) and then sonicated for 2 minutes with the use of a normal pulse sounder. Comparison between these dentin flake images in Figures 11 and 12 and their respective images after 28 days of treatment, as shown in Figures 4 and 8, illustrates the increased stability of the precipitates generated by the potassium oxide versus titanium formulation versus the formulation of potassium oxalate.

DETAILED DESCRIPTION OF THE INVENTION

The compositions of the present invention may comprise, consist of, or consist essentially of, essential elements and limitations of the invention described herein, as well as any of the additional or optional ingredients, components or limitations described herein.

All documents incorporated herein by reference in their entirety are incorporated herein only to the extent that they are not inconsistent with this descriptive report.

All percentages, parts and ratios are based on the total weight of the composition of the present invention, unless otherwise specified. All of these weights, for the mentioned ingredients, are based on the active content and therefore do not include vehicles or by-products that may be included in commercially available materials, unless otherwise specified. The term "safe and effective amounts" for use in the present invention means an amount of a compound or composition, such as a topical or systemic active, that is sufficient to significantly induce a positive benefit, for example tooth desensitization, but lowers sufficient to avoid serious side effects, that is, to provide a reasonable benefit / risk ratio within the scope of sound judgment in the art. The term "occluded" or "occlusion" for use in the present invention means that the exposed openings in or out of the inner tubules are partially, substantially or completely obstructed.

The compositions of the present invention comprise at least one compound of formula I wherein M1 and M3 are independently a monovalent or divalent metal, M2 is a polyvalent metal or metal oxides of the invention. same; and A and B are independently selected from the group consisting of C 2 -C 6 diacids, triacids and tetraacids, optionally C 2 -C 4 diacids or triacids, optionally C 2 -C 3 diacids or triacids or optionally C 2 diacids.

Examples of suitable monovalent metals include, but are not limited to Na, K and Li, optionally Na or K or optionally K.

Examples of suitable divalent metals include, but are not limited to, Mg, Ca, Sr, Ba and Zn, optionally Mg, Ba and Zn or optionally Mg.

Examples of suitable polyvalent metals include, but are not limited to Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Tc, Re, Os, Ir, Hg, Ce, Sn, Eu, Yb, Pa and U, optionally Ti, Sn, Mn and Fe or optionally Ti.

Examples of suitable metal oxides include, but are not limited to, the corresponding oxides of Ba, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Tc, Re, Os, Ir, Hg, Ce, Sm, Eu. Yb, Pa and U, optionally the corresponding oxides of Ba, Ti, Sr, Sn, Zr, Mn and Fe, optionally the corresponding oxides of Ba, Ti, Sr, Sn, Zr or optionally the corresponding oxides of Ti.

In certain embodiments, M1 and / or M3 are independently selected from the group consisting of Na, K and Li. Optionally, both M1 and M3 are K.

In certain embodiments, M2 is selected from the group consisting of Ti, Sr, Sn, Mg, Ca, Mn and Zr. Optionally, M2 is selected from the group consisting of Ti, Sr, Sn, Mg, Ca, Mn and Zr oxides. In other embodiments, M2 is selected from the group consisting of Ti or Ti oxide.

Examples of suitable diacids include, but are not limited to, oxalic acid, succinic acid, methyl succinic acid, diglycolic acid, glutaric (i.e. pentanedioic) acid, 3,5,5-trimethyl pentanedioic acid, hexanedioic acid, 3, 5,5-trimethylhexanedioic acid, 2,4,4-trimethylhexanedioic acid, decanedioic acid, undecanedioic acid, dodecanedioic acid, 1,4-cyclohexane dicarboxylic acid, cyclohexane-1,4-diacetic acid, maleic acid, citric acid, itaconic acid, fumaric acid, oxalic acid, terephthalic acid, phthalic acid and isophthalic acid, hydroxy succinic acid, malonic acid, adipic acid, sebacic acid and tartaric acid, optionally oxalic acid, succinic acid or optionally acid oxalic.

Examples of suitable triacids include, but are not limited to, citric acid.

Examples of suitable tetra acids include, but are not limited to, 1,1,2,2-ethane tetracarboxylic acid, 1,1,2,3-propane tetracarboxylic acid, 1,1,4,4-butane acid tetracarboxylic acid, 1,2,4,5-benzene tricarboxylic acid and ethylenediamine tetraacetic acid or optionally 1,1,2,2-ethane tetracarboxylic acid.

In certain embodiments, the compound of formula I is selected from the group consisting of potassium titanium oxide oxalate ("KTO") (also called potassium titanium oxalate), potassium titanium oxide citrate, calcium oxalate and titanium, and calcium and titanium potassium oxalate, optionally potassium titanium oxide oxalate ("KTO"), titanium potassium oxide citrate or, optionally, potassium oxide and titanium oxalate ("KTO").

The compositions of the present invention include, based on the total weight of the composition, from 0.01% (or about 0.01%) to 10.0% (or about 10.0%), optionally 0.1%. (or about 0.1%) to 7.0% (or about 7.0%) or optionally from 1% (or about 1%) to 5.0% (or about 5.0% ) of at least one compound of formula I.

In certain embodiments, the compositions of the invention include an orally acceptable solvent. Orally acceptable solvents include, but are not limited to, water, ethanol, n-propanol or polyhydric alcohols such as glycerine, sorbitol and polyethylene glycol, and any mixtures thereof, and may be present in concentrations of about 0.1 % to about 99.9%, optionally from about 1% to about 90% or optionally from about 10% to about 75% of the orally acceptable solvent.

In certain other embodiments, the compositions of the present invention are substantially free of water. The term "substantially free" for use in the present invention means less than 5% (or about 5%), optionally less than 3% (or about 3%), optionally less than 1% (or about 1%). ), optionally less than 0.5% (or about 0.5%) and optionally zero (or anhydrous).

In certain embodiments, the compositions of the present invention have a pH of at least 2 (or about 2), optionally from 2.5 (or about 2.5) to 7.0 (or about 7.0), optionally from 3.5 (or about 3.5) to 6.0 (or about 6.0) or optionally from 3.2 (or about 3.2) to 4.5 (or about 4, 5).

In certain embodiments, the pH of the composition of the present invention may be buffered using conventional acid / salt systems. Conventional buffer systems include phosphoric acid and sodium phosphate salts, or citric acid and sodium citrate. Suitable acid / salt salt buffer combinations suitable for use in the present invention include citric acid sodium citrate, sodium phosphoric acid phosphate, monobasic sodium phosphate, dibasic sodium phosphate, acetic acid sodium acetate, succinic acid-sodium succinate, sodium aconitic acid-sodium aconitate and sodium benzoic acid benzoate, in amounts of up to about 1 wt%, optionally from about 0.05 wt% to about 0 75 wt% of the composition and / or optionally from about 0.1 wt% to about 0.5 wt% of the composition.

Optional Components In certain embodiments, the compositions of the present invention further include other dental desensitizing agents. Examples of additional dental desensitizing agents include, but are not limited to, potassium citrate, potassium chloride, potassium nitrate, citric acid, citric acid salts, strontium chloride and mixtures thereof. Also useful in the present invention are bioactive glass materials as described in US Patent Nos. 5735942, 5891233, 6086374, 6244871, 6338751 and 6365132, each of which is hereby incorporated by reference in its entirety and phosphopeptides as described in U.S. Patent Nos. 5,015,628, 5981475, 6448374 and 6780844, each of which is incorporated herein by reference in its entirety.

In certain embodiments, the additional dental desensitizing agent is potassium nitrate. In certain embodiments, the concentration of the additional dental desensitizing agent is from 0.1% (or about 0.01%) to 10% (or about 10%), optionally 0.1% (or about 0.1%). %) to 8% (or about 8%) or optionally from 1% (or about 1%) to 7% (or about 7%) by weight of the composition.

Fluoride ion sources are well known for use in oral care compositions as anti-caries actives and may also be incorporated into the compositions of the present invention. Fluoride ions are contained in numerous oral care compositions for this purpose, particularly toothpastes. Patents describing toothpastes include US Patent Nos. 3538230, 3689637, 3711604, 3911104, 3935306 and 4040858, each of which is incorporated herein by reference in its entirety. Applying fluoride ions to tooth enamel protects teeth against tooth decay. A wide variety of materials which provide fluoride ions may be employed as a source of fluorides in the compositions of the present invention. Examples of suitable materials which provide fluoride ions are found in US Patent No. 3,535,421 issued to Briner et al. on October 20, 1970 and US Patent No. 3,678,154 issued to Widder et al. on July 28, 1972, both patents incorporated herein by reference in their entirety. In certain embodiments, fluoride ion sources for use in the present invention include stannous fluoride, monofluorophosphate, sodium fluoride, potassium fluoride and ammonium fluoride. In other embodiments, sodium fluoride is incorporated. In certain embodiments, the compositions of the present invention provide from about 50 ppm to 10,000 ppm, optionally from about 100 to 3,000 ppm, of fluoride ions in aqueous solutions that come in contact with dental surfaces.

Also useful in the compositions of the present invention are phosphates. Phosphates include pyrophosphates, polyphosphates, polyphosphonates and mixtures thereof. Pyrophosphates are among the best known for use in dental care products. Pyrophosphate ions applied to teeth are derived from pyrophosphate salts. Pyrophosphate salts useful in the compositions of the present invention include dialcaline metal pyrophosphate salts, tetraalkaline metal pyrophosphate salts and mixtures thereof. Preferred species are disodium dihydrogen pyrophosphate (Na2H2P207), tetrasodium pyrophosphate (Na4P207) and tetrapotassium pyrophosphate (IQP4), in their unhydrated and hydrated forms. In certain embodiments, the tetrasodium pyrophosphate salt is pyrophosphate.

Pyrophosphate salts are described in more detail in Kirk & Othmer, "Encyclopedia of Clinical Technology", third edition, volume 17, Wiley-Interscience Publishers (1982), incorporated herein by reference in its entirety, including all incorporated references. Additional anti-calculating agents induce pyrophosphates or polyphosphates disclosed in US Patent No. 4590066, polyacrylates and other polycarboxylates such as those disclosed in US Patent Nos. 3429963,4304766 and 4661341, polyeoxy succinates such as those disclosed in US Pat. 4846650, ethylenediamine tetraacetic acid as disclosed in British Patent No. 490,384 dated February 15, 1937, nitri-lotriacetic acid and related compounds as disclosed in US Patent No. 3678154, and polyphosphonates as set forth in US Patent Nos. 3737533, 3,988,443 and 4,877,603, all patents cited herein being incorporated by reference in their In certain embodiments, phosphates include potassium and sodium pyrophosphates; sodium tripolyphosphate; diphosphonates, such as ethane-1-hydroxy-1,1-diphosphonate, 1-azacycloheptane-1,1-diphosphonate, and linear alkyl diphosphonates; tricalcium phosphates, linear carboxylic acids; sodium zinc citrate and mixtures of any of the above phosphates. In certain embodiments, the phosphate is tricalcium phosphate plus sodium lauryl sulfate as described in US 20080187500 A1, published August 7, 2008 by Karlinsey, Robert L, and whose publication is incorporated herein by reference in its entirety.

When incorporated into the compositions of the present invention, phosphates may be present at concentrations of from about 0.01% to about 10%, optionally from about 0.1% to about 7%, and optionally from about 0%. 5% to about 5%.

In certain embodiments, the compositions of the present invention also include essential oils. Essential oils are volatile aromatic oils that are synthetic or derived from plants by distillation, expression or extraction. Essential oils usually have the odor or taste of the plant from which they were obtained. If used in the dentifrice compositions of the present invention, the essential oils offer anti-gingivitis activity. Some of these essential oils also act as flavoring agents. The essential oils of the present invention include, but are not limited to, thymol, menthol, methyl salicylate (wintergreen oil) and eucalyptol. Thymol, also known by the chemical formula 5-methyl 2- (1-methylethyl) phenol, is obtained from the essential oils of Thymus vulgaris Labiatae and Monarda punctata Labiatae. Thymol is a crystalline white powder with aromatic odor and taste. Thymol is soluble in organic solvents, but only slightly soluble in deionized water. Menthol is mainly isolated from Mentha arvensis oil. In its commercial form, menthol is available as L-menthol crystals, obtained from a process involving the cooling of the oil. Fractional distillation of peppermint oil, which usually contains from about 40% to about 65% menthol, represents another important source of menthol. Synthetic sources of L-menthol are also available. Eucalyptol is derived from the eucalyptus tree. Endowed with a camphoric odor and a refreshing taste, this essential oil is often combined with other essential oils such as menthol in confectionery formulations to give a medicinal effect. The combinations of menthol and eucalyptol are widely used. Particularly preferred uses of the menthol-eucalyptus combination! include, according to the present invention, dentifrices such as toothpastes or dental gels. Methyl salicylate is the main ingredient in many essential oils, comprising about 99% of wintergreen (Gaultheria procumbens) and sweet birch (Slow birch) oil. Methyl salicylate, which has a distinctive refreshing aroma, is widely used in mouthwashes, chewing gums and other oral and pharmaceutical preparations.

The amounts of essential oils that may be used in the compositions of the present invention are from 0.001 (or about 0.001) to 1% (or about 1%) thymol, 0.001 (or about 0.001) to 1% (or about 0.001). Methyl salicylate, 0.001 (or about 0.001) to 15% (or about 15%) menthol and 0.001 (or about 0.001) to 1% (or about 1%) eucalyptol, where Such amounts are clinically effective for inhibiting gingivitis. Optionally, a composition according to the present invention contains about 0.064% thymol, about 0.060% methyl salicylate, about 0.042% menthol and about 0.092% eucalyptol, wherein said amounts are clinically effective for the inhibition of gingivitis.

Alternatively or in addition to essential oils, the compositions of the present invention may also include a microbicidal effective amount of a microbicidal agent selected from the group consisting of polyphenols (e.g. triclosan), zinc salts, stannous fluoride, chlorhexidine, hexetidine, sanguinarine , benzalkonium chloride, salicylanilide, domiphene bromide, cetylpyridinium chloride, tetradecylpyridinium chloride (CTP), N-tetradecyl-4-ethylpyridinium chloride (CTDEP), octe-nidine, delmopinol, octapinol and other piperidine preparations, niacin, zinc / tin ion agents, antibiotics such as augmentin, amoxicillin, tetracycline, doxycycline, minocycline and metronidazole, and analogs and salts of the aforesaid, essential oils including eugenol, geraniol, charcoal, citral, hyquinchiol, catechol, peroxide hydrogen, metal salts of chlorite, or any combinations of all of the above.

Mixtures of any of the above mentioned agents may also be used.

The compositions of the invention may also contain a surfactant selected from anionic, nonionic, amphoteric, betaine, cationic and mixtures thereof. Suitable anionic surfactants include alkyl sulfates, alkyl ether sulfates, sulfosuccinates, isethionates, acyl amides, alkyl ether carboxylates and alkyl phosphates, wherein the alkyl group has from about 6 carbon atoms to about 30 carbon atoms. . Suitable cationic surfactants include cetyl pyridinium chloride. The total amount of surfactants suitable for use in the composition of the present invention may be in the range, based on the total weight of the total composition, from about 1% to about 50%, optionally from about 5% to about 40%. or optionally from about 8% to about 25%.

Types of nonionic surfactants that are suitable for use in the present invention include fatty alcohol acid or amide ethoxylates, monoglyceride ethoxylates, sorbitan ester ethoxylates and alkyl polyglycosides. Such nonionic surfactants may be used in the composition of the present invention in an amount based on the total weight of the composition from about 0.0% to about 30%, for example from about 0.1% to about 30%. 20% and from about 0.1% to about 15%.

The classes of amphoteric surfactants that are suitable for use in the present invention include alkylimino diproprionates, alkyl amphoglycinates (mono- or di-), alkyl amphoproprionates (mono- or di-), alkyl amphacetates (mono- or di-), N acids alkyl b-aminopropriionics, alkyl polyamino carboxylates, and phosphorylated imidazolines. Such amphoteric surfactants may be used in the composition of the present invention in an amount based on the total weight of the composition from about 0.1% to about 20%, for example from about 0.1% to about 15%. , and from about 0.1% to about 10%.

Types of betaines which are suitable for use in the present invention include alkyl betaines, alkylamido betaines, alkyl sultaines and alkylamido sultaines, wherein the alkyl group has from about 6 carbon atom to about 30 carbon atom, with about preferably from 10 to about 14 carbon atoms. Such betaine surfactants may be used in the composition of the present invention in an amount based on the total weight of the cleaning composition from about 0.1% to about 15%, for example about 0.1%. about 10% and from about 0.1% to about 8%.

Cationic surfactant classes which are suitable for use in the present invention include alkyl (mono-, di- or tri-) quaternaries, benzyl quaternaries (e.g. cetyl pyridinium chloride), ester quaternaries, ethoxylated quaternaries, alkylamines and mixtures. thereof, wherein the alkyl group has from about 6 carbon atoms to about 30 carbon atoms, with from 8 to about 22 carbon atoms being preferred. Such cationic surfactants may be used in the composition of the present invention in an amount, based on the total weight of the composition, from about 0.01% to about 20%, optionally from about 0.05% to about 15%. / or optionally from about 0.1% to about 10%.

The compositions of the present invention may also non-exclusively include one or more optional ingredients, including a thickening agent, wetting agents, chelating agents and additives such as flavorings, preservatives and the like.

Commercially available thickening agents, which are capable of imparting the proper viscosity to the compositions, are suitable for use in the present invention. Examples of suitable thickening agents include, but are not limited to: 1) polyethylene glycol mono- or diesters of the formula: wherein Z is an integer from about 3 to about 200; and 2) fatty acids containing from about 16 to about 22 carbon atoms; fatty acid esters of ethoxylated polyols; ethoxylated derivatives of glycerine mono- and diesters of fatty acids; hydroxy alkyl celluloses; alkyl celluloses; hydroxyalkyl alkyl cellulose; and mixtures thereof. Preferred thickeners include polyethylene glycol esters and, more preferably PEG-150 diestaerate which is available from Stepan Company of Northfield, Illinois, (USA), or from Comiel, SpA of Bologna, Italy under the trade name of "PEG 6000 DS".

In certain embodiments, thickening agents may be included in the compositions of the present invention at concentrations of from about 0.01% to about 10%, optionally from about 0.1 to about 5% or optionally from about 0%. , 2% to about 2.0%.

Commercially available humectants are suitable for use in the present invention for their humectant properties, in addition to their use as potential solvents as detailed above. The humectant may be present in an amount from about 0% to about 10%, preferably from about 0.5% to about 5%, and more preferably from about 0.5% to about 3%. %, based on the weight of the composition as a whole. Examples of suitable humectants include, but are not limited to: 1) water-soluble liquid polyols selected from the group consisting of: glycerine, propylene glycol, hexylene glycol, butylene glycols, dipropylene glycol, and mixtures thereof; 2) polyalkylene glycol of the formula: wherein R 'is an alkylene group having from about 2 to about 3 carbon atoms and b is an integer from about 2 to about 10; 3) polyethylene glycol methyl glucose ether of formula CH 3 -C 6 H 10 O 5 - (OCH 2 CH 2) c-OH, wherein c is an integer from about 5 to about 25; 4) urea; and 5) mixtures thereof, with glycerin being the preferred humectant.

In certain embodiments, humectants may be incorporated into the compositions of the present invention at concentrations of from about 0.1% to about 40%, optionally from about 1.0% to about 30%, or optionally from about 5%. % to about 25%.

In certain embodiments, chelating agents may be incorporated into the compositions of the present invention. Examples of suitable chelating agents include those capable of protecting and preserving the compositions of this invention. Optionally, in addition to its possible use as a tetra acid in the compounds of formula I, ethylene diamine tetraacetic acid ("EDTA") may be used as a chelating agent. In certain embodiments, the chelating agent is tetrasodium EDTA, commercially available from the Dow Chemical Company of Midland, Michigan, USA under the trade name "Versene 100XL", and may be present in an amount based on the total weight of the composition, from about 0 to about 0.5% and optionally from about 0.05% to about 0.25%.

Suitable preservatives include sodium benzoate and polysorbate, and are present in the composition in an amount based on the total weight of the composition from about 0 to about 0.2% and preferably about 0.05%. at about 0.10%.

The compositions of the present invention may be in the form of mouthwashes, mouthwash, toothpastes, pastes such as toothpastes, powders such as dental powders, gels, tablets, lozenges, microcapsules, sprays, varnishes or strips (such as remineralization strips as shown in US Patent Publication No. 20070128130, Kropt et al., issued June 7, 2007, incorporated herein by reference in its entirety, or with or without teeth whitening strips as disclosed in US Patent Publication No. 20080003248, of Georgiades et al., issued January 3, 2008, and US Patent No. 6949240, to Sagel et al., issued September 27, 2005, both patent documents being incorporated herein by reference. reference coatings in their entirety), coatings for these strips and the like. As mentioned above, the compositions of the present invention may also be applied by conventional oral care devices including toothbrushes, toothpicks, floss, dental sprinklers or nebulizers and dental pens as described in US Patent Publication No. No. 20080044363, by Montgomery, published February 21, 2008, incorporated herein by reference in its entirety.

The compositions of the present invention may also be useful as a coating for or as an impregnant for impregnation in dental devices selected from the group consisting of toothbrushes (manual or mechanical), toothbrush bristles, dental floss, toothpicks and similar. The compositions of the present invention may also be useful as coatings or impregnants for dental composite materials, dental fillings and the like. Method for Use of the Compositions of the Present Invention The invention illustrated herein may be practiced in the absence of any component, ingredient or step that is not specifically disclosed herein.

In certain embodiments, the compositions of the present invention are applied to sensitive teeth for at least two consecutive applications, optionally at least (or more than) 7 (or about 7) consecutive applications or optionally 14 (or about 14). consecutive applications or optionally 21 (or about 21) consecutive applications or optionally 28 (or about 28) consecutive applications.

When applied to a sensitive tooth (or teeth), in certain embodiments, the composition is allowed to remain in contact with the sensitive teeth for at least (or more) 10 (or about 10) seconds, optionally 20 (or about 20). ) seconds, optionally 30 (or about 30) seconds, optionally 50 (or about 50) seconds or optionally 60 (or about 60) seconds.

In certain embodiments, the time between consecutive applications must be no more than (or less) than 12 (or about 12) hours, optionally 8 (or about 8) hours, optionally 4 (or about 4) hours, optionally 2 (or about 2) hours or, optionally, one (or about one) hour.

In certain embodiments, the compositions of the present invention are applied to sensitive teeth such that the compounds of formula I form precipitated deposits with available calcium in the teeth so that at least (or more than) 5% occlusion occurs. (or about 5%), optionally 25% (or about 25%), optionally 40% (or about 40%), optionally 60% (or about 60%), optionally 75% (or about 75%) ), optionally 85% (or about 85%) or optionally 95% (or about 95%) of the dentinal tubules of the teeth.

In certain embodiments, the M2 of formula I is present in the precipitate deposit formed by the compounds of formula I and calcium at a concentration of at least (or above) 5% (or about 5%), optionally 10% (or about 10%), optionally 20% (or about 20%) or optionally 35% (or about 35%).

Once formed on the teeth, the stability exhibited by the precipitate deposit (s) comprising the compounds of formula I and calcium is such that at least (or more than) 5% (or about 5%), optionally 30%. % (or about 30%), optionally 35% (or about 35%), optionally 50% (or about 50%), optionally 75% (or about 75%) or optionally 90% (or about 90%) remain on the teeth after sonication for 2 (or about 2) minutes using a CD-4800 (Digital Professional Ultrasonic Cleaner [CD-4800]) produced by Best And More Electronics [Shenzhen] Co ., Ltd., China), with a normal pulse of about 42 KHz. In this pulse, the sonicator usually provides greater force than typically used for sonic or manual tooth brushing. The phrase "precipitate deposits" for use in the present invention means the deposit formed on the teeth and / or occluding the teeth tubules by precipitating the compounds of formula I with calcium present in the oral cavity fluids after application. of compositions comprising the compounds of formula I as presented in the present application. The formation of precipitate deposits with the compounds of formula I may also be generated or facilitated by the separate addition of calcium to the oral cavity as water-soluble calcium salts before or after the addition of the compositions of the present invention. The invention comprising the compounds of formula I. Examples of suitable water soluble calcium salts include, but are not limited to calcium chloride, calcium nitrate, calcium bromide and calcium dihydrogen phosphate, as well as mixtures thereof. The amount of the water-soluble calcium salt must exceed, on a molar basis, the amount of the compounds of formula I provided by the compositions of the present invention. Several examples are shown below to further illustrate the nature of the invention and the embodiment thereof.

Examples The compositions of the present invention as described in the following examples illustrate specific embodiments of compositions of the present invention, but are not intended to be a limitation thereto. Other modifications may be made by one skilled in the art without departing from the character and scope of the present invention.

Preparation of Mouth Rinse Formulations Liquid mouth rinse formulations were prepared, and the efficacy for dentinal occlusion of potassium oxide titanium (KTO) formulations was evaluated. The method of preparation is described as follows: In a formulation tank, water, KTO, benzoic acid and poloxamer were added and mixed until dissolved. Once the poloxamer was dissolved, alcohol, n-propanol, sorbitol and water were added, followed by sodium benzoate and then mixed until dissolved. The pH was verified and determined to be about 4.2. To the above formulation mixture was added menthol, thymol, eucalyptol and methyl salicylate and mixed until homogeneous. Once a homogeneous solution was formed, sodium saccharin and Green FDC No. 3 (1% solution adjusted for purity) were added. The formulation was mixed until homogeneous. The final pH of the formulation was 4.2. The composition of the liquid mouthwash formulations are described in table 1.

Table 1 Preparation of Dentin and Artificial Saliva Samples The dentin occlusion efficacy of the KTO compounds and formulations of the present invention has been demonstrated as follows: dentin chips (polished and non-corroded) were obtained from Dental Product Testing, a division of Thermametric Technologies Inc. of Indianapolis, Indiana, USA. Dentin chips have been corroded to completely remove the dirt layer (or debris layer caused by cutting dentin or enamel) by dipping the dentin chips in 6% citric acid for up to 2 minutes, followed by rinsing and sonication. in deionized water. Potassium oxalate (KO) was obtained from Fluka, St. Louis, MO, USA (lot 430462/1). Potassium titanium oxide oxalate (KTO) dihydrate was obtained from Sigma, St. Louis MO, USA (lot 51740). Artificial saliva was prepared using conventional equipment and protocols routinely used in laboratory protocols, and having the composition as shown in Table 2: Table 2 pH = 7.0 Comparison and analysis test All corroded dentin flake samples (10 in total) were randomized and divided into five treatment groups. Scanning electron microscopy (SEM) and surface chemical analysis were used using electron dispersion spectroscopy (EDS) to monitor tubule occlusion and surface deposition generated by KTO formulations. The five treatment groups were as follows: Group 1: treated with formulation A Group 2: treated with formulation B Group 3: treated with formulation C Group 4: treated with formulation D Group 5: treated with formulation E (ie without KTO or KO) The treatment regimen for groups 1 to 5 consisted of the following: 1. treat the chip samples in each group with 20 ml of the respective treatment formulation under agitation for 30 seconds. . 2. Rinse the chip samples in each group with deionized H2O for 1 minute. 3. Dip the chip samples into the artificial saliva composition between treatments, and no more than two treatments were performed per day. 4. Repeat steps 1 through 3 for a total of 28 treatments. 5. Dentin samples were analyzed by SEM and / or EDS after 7, 14, 21 and 28 treatments. Prior to analysis, the chips were rinsed in deionized H2 O for 3 minutes, and air dried during SEM analysis.

The data obtained from the EDS analysis of 2 chip samples per group (chip 1 and chip 2) are summarized in tables 3 and 4 below. After 7 treatments, samples treated with 0.5% KTO (formulation D) show the highest affinity for eroded dentin surfaces, as evidenced by the reduction in the sulfur percentage detected in the EDS reading (the spectrum). EDS of the corroded dentin surface typically has about 45 to 50% sulfur). The percentage of sulfur detected is reduced as sulfur present on the surface of the dentin flake is covered or masked by surface deposition generated by KTO formulation treatments. Although not completely absent, the percentage of sulfur detected is dramatically reduced in the 0.1% KTO treated sample (Formulation C). After 14 treatments, the percentage of sulfur detected remained low in the 0.5% KTO-treated sample (formulation D), and most significantly reduced in the 0.1% KTO-treated sample (formulation C). Scanning electron microscopy performed on these samples suggests the initiation or formation of surface precipitation on the dentin surface for formulation D samples, and the degree of tubule occlusion increases with the number of treatments. SEM analysis, image classification and calculation of tubule occlusion percentage were performed to obtain a semi-quantitative comparison of occlusion efficacy of dentinal tubules of different formulations. Methods and calculations for analyzing SEM data, classifying images, and obtaining tubule occlusion percentage were performed according to the methods described in West NX, Addy, M, Hughes, J. (1998) J. Oral Rehabil, 25 , 885, and confirmed by the methods described in Lee SY, Kwon HK, Kim BI (2008) J. Oral Rehabil, 35, 847. Based on the above described analyzes of SEM data, the percentage of tubule occlusion was determined for the formulations A to E in treatments 7,14,21 and 28, being summarized in table 5.

Table 5 Percentage of tubule occlusion A comparison analyzing data for pre- and post-treatment scanning electron micrographs at different times of the treatment cycle and at different KTO concentrations (as shown in table 5 and the figures). from 1 to 4 (KO treatment), from 5 to 8 (KTO treatment) and 9 and 10 (oxalate free treatment) clearly demonstrated an increase in surface precipitation leading to an optimized and effective increase in tubule occlusion.

Determination of Adherence to Formed Precipitate Deposits The following procedures were performed to determine the adhesion (or ability of the precipitate to remain on the dental surface) of the KTO precipitate deposited on the dentin flake samples during the treatment cycle. Dentin chips treated with formulation B (0.5% KO) and formulation D (0.5% KTO) for 28 treatments were sonicated for 2 minutes (about 2 minutes can also be used) with of a normal pulse CD-4800 ultrasound (about 42 KHz). Comparison between the sonicated chip images (Figures 11 and 12) and their respective images on day 28 of the treatment, as shown in Figures 4 and 8, demonstrate that KTO generated precipitate deposits were more resistant to sonication (about 92% KTO-generated precipitate remained on the flake sample) whereas KO-generated precipitates (about 38% of the KO-generated precipitate remained on the flake sample), indicating that KTO-generated precipitate deposits offer increased stability, on the other. compared to KO generated precipitate deposits. Without sticking to the theory, it is believed that this optimized stability of precipitate deposits generated by the compounds of formula I not only offer a higher degree of dental desensitization, but also a longer lasting dental desensitization.

Tables 6 and 7 show the examples from F to O, illustrating additional examples of mouthwashes of the compositions of the present invention. Examples F to O can be prepared as described for examples A to E above. Table 8 presents the examples from P to S illustrating the dentifrice examples of the compositions of the present invention. Examples of P to S may be prepared using conventional toothpaste mixing technologies. Example S illustrates an anhydrous dentifrice embodiment of the present invention.

Table 8 CLAIMS

Claims (11)

Composition for the treatment of dental sensitivity, characterized in that it comprises: (a) at least one compound of formula I wherein M1 and M3 are independently a monovalent metal or divalent, M2 is selected from the group consisting of titanium (Ti) and titanium oxide (Ti); and A and B are independently selected from the group consisting of C2 - ββ diacids, triacids and tetra acids, and b) at least one orally acceptable solvent, wherein the composition for treating dental sensitivity contains less than 3% of Water. Composition according to Claim 1, characterized in that M2 is titanium (Ti). Composition according to Claim 1, characterized in that M2 is titanium oxide (Ti). Composition according to Claim 1, characterized in that the compound of formula I is selected from the group consisting of titanium potassium oxide oxalate, titanium calcium oxalate, titanium potassium oxide citrate, oxalate. potassium, calcium and titanium and mixtures thereof. Composition according to Claim 4, characterized in that the compound of formula I is potassium oxide and titanium oxalate. Composition according to Claim 4, characterized in that the compound of formula I is titanium potassium oxide citrate. Composition according to Claim 1, characterized in that it is in the form of a mouthwash, a mouthwash, a dentifrice, a paste, a powder, a gel, a tablet, a tablet, a microcapsule, a strip or strip coating. Composition according to Claim 1, characterized in that the composition is a coating or impregnation for dental devices selected from the group consisting of toothbrushes, toothbrush bristles, dental floss and toothpicks. A non-therapeutic method for treating sensitive teeth, characterized in that it comprises the step of bringing sensitive teeth into contact with a composition as defined in claim 1 for at least about 10 seconds. A composition for the treatment of dental sensitivity, characterized in that it comprises: (a) at least one desensitizing agent of formula I wherein: M1 and M3 are independently a metal monovalent or divalent, M2 is selected from the group consisting of titanium (Ti) and titanium oxide (Ti); and A and B are independently selected from the group consisting of C 2 -C 6 diacids, triacids and tetra acids, and b) at least one additional desensitizing agent, and c) at least one orally acceptable solvent, wherein the composition for treatment Dental sensitivity contains less than 3% water. Composition according to Claim 10, characterized in that the additional desensitizing agent is selected from the group consisting of potassium citrate, potassium chloride, potassium nitrate, citric acid, citric acid salts, strontium chloride, bioactive glass materials, phosphopeptides and mixtures thereof.