KR100246832B1 - Oral compositions - Google Patents

Abstract

Cream toothpaste, powder toothpaste, liquid toothpaste, dental toothpaste, denture cleaner comprising a lipophilic compound selected from flavors, physiological coolants and antimicrobial compounds and aminoalkyl silicones having an aminoalkylsiloxane content of about 0.1% -2% based on repeat units Oral composition in the form of chewing gum or candy. The composition provides improved antiplaque and antimicrobial activity with improved realism, effects and / or potency of lipophilic ingredients on the tooth or carcass.

Description

[Name of invention]

Household composition

[Technical Field]

The present invention relates to oral compositions such as cream toothpaste, powder toothpaste, liquid toothpaste, gargle, denture cleaner, chewing gum, candy and the like. In particular, the present invention relates to compositions for oral cavity with improved anti-plaque activity in addition to good cleaning performance, physical properties and in-use performance properties.

[Background]

Plaques are initiated when bacteria engrossing the thin film form a proteinaceous film on the tooth surface. Transgenic bacteria metabolize, multiply, and aggregate dietary constructs to form adherent waste known as plaques. Plaques generally consist of bacteria, bacterial end products such as polysaccharides, inorganic salts and saliva proteins. Plaque bacteria ferment dietary carbohydrates with organic acids that demineralize enamel, causing teeth to rot.

Stones are essentially plaque mineralized with calcium phosphate salts. As the stones mature and harden, they are visibly colored due to the adsorption of dietary chromagen. Along with its unpleasant appearance, stone waste in the gum line is a major cause of gingivitis and periodontal disease. In addition to the above-mentioned hypocrisy and health problems due to plaque, investigations have shown that the primary cause of bad breath is degradation following retention of dead cell material that continues to escape from normal, healthy mouths.

Modern dental hygiene and denture preparations typically include antiplaque and / or antitartar preparations in addition to antibacterial and flavoring agents. Antimicrobial action can affect plaque formation by reducing the number of bacteria in the mouth / dentures or killing bacteria trapped in the membrane to prevent further growth and metabolism.

Flavors can alleviate the problem of bad breath through deodorizing action. Some antimicrobials, such as menthol, also act as bad breath deodorants. However, the efficacy of the antimicrobial agent depends largely on the retention of the antimicrobial agent in the oral cavity / denture, in particular on the surface of the tooth or denture where plaque is formed.

A typical disadvantage of known dentifrices is that only relatively short periods of time during brushing or rinsing teeth in formulations that have an effect are useful as antimicrobials. The problem is caused by the fact that toothpaste is rarely used: mostly once or perhaps twice a day. As a result, for most people the long time between brushing provides optimal plaque formation conditions.

Therefore there has been a need to develop oral formulations with prolonged, residual antimicrobial and / or strong flavor effects.

In order to coat so-called teeth and to prevent tooth decay and pigmentation, it is known to include silicone in the toothpaste composition. In one example, GB-A-689,679 discloses gargles containing organic polysiloxanes for removing or preventing tar, coloring, tartar and food debris from teeth. This gargling medicine may include antiseptic compounds such as thymol, flavoring agents and flavoring agents.

US-A-2.806.814 discloses dentifrices comprising a combination of a higher aliphatic acyl amide of an amino carboxylic acid and a silicone compound as an active agent. The patent teaches that silicone compounds have been proposed to facilitate the prevention or removal of tars, colorings, tar tars, and the like from teeth. Silicone compounds are said to act as synergists in enhancing the antimicrobial and acid inhibitory activity of the active ingredient. Dimethylpolysiloxanes are said to be particularly effective. Flavor oils and / or menthol may be included.

US-A-3624120 discloses quaternary ammonium salts of cyclic siloxane polymers for use as cationic surfactants, fungicides and anti-carticides.

Accordingly, the present invention provides an oral composition having improved efficacy on plaque, mucus and bacterial waste while at the same time having good cleaning performance, physical properties and performance characteristics in use.

The present invention also provides compositions for oral cavity containing lipophilic compounds such as flavoring agents, physiological coolants or antibacterial agents and having improved substantivity, strong effect and / or efficacy on teeth and dentures.

Summary of the Invention

According to a first aspect of the invention, at least one family composition composition component selected from abrasives, binders, wetting agents, surfactants, fluoride ion sources, anti-calculators and sweeteners, and additionally alkyl- and alkoxy- of formula (I) There is provided a spherical composition in the form of a cream toothpaste, powder toothpaste, liquid toothpaste, gargle, denture cleaner, chewing gum or candy, consisting of a dimethicone copolyol selected from dimethicone copolyols:

[Wherein X is selected from hydrogen and alkyl, alkoxy and acyl groups having from about 1 to about 16 carbon atoms, Y is selected from alkyl and alkoxy groups having from about 8 to about 22 carbon atoms, and n is about 0 To about 200, m is about 1 to about 40, q is about 1 to about 100, and the molecular weight of residue (C ₂ H ₄ O-) _x (C ₃ H ₆ O-) _y X is about 50 to about 2000, preferably about 250 to about 1000, and x and y are values such that the weight ratio of oxyethylene: oxypropylene is from about 100: 0 to about 0: 100, preferably from about 100: 0 to about 20:80 to be].

According to another aspect of the invention, a cream toothpaste comprising a lipophilic compound selected from flavors, physiological coolants and antibacterial compounds, and a dimethicone copolyol selected from alkyl- and alkoxy-dimethicone copolyols of the formula (I) Oral compositions are provided in the form of powder, toothpaste, liquid toothpaste, gargle, denture cleaner, chewing gum or candy.

All percentages and ratios herein are values over the weight of the total composition unless otherwise indicated.

The oral compositions of the present invention thus comprise dimethicone copolyol antiplaque formulations, and preferred compositions are additionally lipophilic compounds and / or abrasives, binders, wetting agents, surfactants, fluoride ion sources, anti-calcite agents and It further comprises at least one composition composition for oral cavity selected from sweetening agents. Each of these will be discussed in turn.

In general terms, dimethicone copolyols are selected from alkyl- and alkoxy-dimethicone copolyols of Formula (I):

[Formula I]

[Wherein X is selected from hydrogen and alkyl, alkoxy and acyl groups having from about 1 to about 16 carbon atoms, Y is selected from alkyl and alkoxy groups having from about 8 to about 22 carbon atoms, and n is about 0 To about 200, m is about 1 to about 40, q is about 1 to about 100, and the molecular weight of residue (C ₂ H ₄ O-) _x (C ₃ H ₆ O-) _y X is about 50 to about 2000, preferably about 250 to about 1000, and x and y are values such that the weight ratio of oxyethylene: oxypropylene is from about 100: 0 to about 0: 100, preferably from about 100: 0 to about 20:80 to be].

In a preferred embodiment, the dimethicone copolyol is selected from C ₁₂ to C ₂₀ alkyl dimethicone copolyols and mixtures thereof. Very preferred are cetyl dimethicone copolyols available under the trade name of Abil EM90. Generally, the dimethicone copolyol is present at a concentration of about 0.01% to about 25% by weight, preferably about 0.1% to about 5% by weight, more preferably about 0.5% to about 1.5% by weight.

In addition, the composition for oral cavity of the present invention includes a lipophilic compound. In general terms, lipophilic compounds suitable for use herein are oily forms that can be dissolved or dissolved in dimethicone copolyol at a concentration of preferably at least about 1% by weight, more preferably at least about 5% by weight at 25 ° C. It is a substance. Preferred lipophilic compounds are selected from flavoring agents, physiological coolants and antibacterial compounds. Dimethicone copolyols act to enhance the reality of lipophilic compounds to teeth and / or dentures, thereby providing long lasting and improved flavor effects and efficacy.

The lipophilic flavoring agents suitable for use herein are wintergreen oils, oregano oils, laurel leaf oils, peppermint oils, spearmint oils, cloves oils, sage oils, sasafrase oils, lemon oils, orange oils, anise oils, benzaldehydes, high amygdala. Bitter almond oil, camphor, cedar leaf oil, marjoram oil, citronella oil, lavender oil, mustard oil, pine oil, pine needle oil, rosemary oil, thyme oil, broiler At least one flavor component selected from leaf oil, and mixtures thereof.

Suitable lipophilic antimicrobial compounds for use herein are thymol, menthol, triclosan, 4-hexylesorcinol, phenol, eucalyptol, benzoic acid, benzoyl peroxide, butyl paraben, methyl paraben, propyl paraben, salicyamide and these It contains a mixture of.

Suitable physiological coolants for use herein include carboxamides, mentan esters and mentan ethers, and mixtures thereof.

Suitable mentan ethers for use herein are selected from those having the formula:

[Wherein R ₅ is an aliphatic radical containing up to 25 carbon atoms, preferably up to 5 carbon atoms and may be substituted by hydroxy and X is hydrogen or hydroxy (e.g., Takasago International Corp. Sold under the trade name "Takasago").

Particularly preferred coolants for use in the compositions of the present invention are 10 [3-1-mentoxy propane-1,2-diol (MPD)]. MPD is a monoglycerine derivative of 1-menthol and has excellent cooling activity.

Carboxamides that have been found to be the most useful are those described in US Pat. No. 4,136,163 to Wasson et al., January 23, 1979, and US Pat. No. 4,230,688 to Oct. 28, 1980, Rawsell et al.

The concentration of the lipophilic compound in the composition of the present invention is generally from about 0.01% to about 10% by weight, preferably from about 0.05% to about 5% by weight, more preferably from about 0.1% to about 3% by weight. to be.

Compositions in the form of creamy toothpastes, denture cleaners, creams and the like generally comprise a binder and a thickener. Suitable binders for use herein include carboxyvinyl polymers, carrageenan, hydroxyethyl cellulose and water-soluble salts of cellulose ethers such as sodium carboxymethyl cellulose and sodium carboxymethyl hydroxyethyl cellulose. Natural gums such as karaya gum, xanthan gum, arabian gum and tragacanth gum can also be used. To further enhance the texture, colloidal magnesium aluminum silicate or finely divided silica can be used as part of the thickener. The binder / thickener may be used in an amount of about 0.1% to about 5.0%, preferably about 0.1 to about 1% by weight of the total composition.

It is also desirable to include certain wetting substances in cream dentifrices to prevent the composition from curing upon exposure to air. Certain humectants may also impart desirable sweetness to cream dentifrice compositions. Liquid toothpastes and mouthwashes may also include large amounts of humectants. Suitable humectants include glycerin, sorbitol, xylitol, polyethylene glycol, propylene glycol, other edible polyalcohols, and mixtures thereof. When wetting agents are present, they generally represent about 10% to about 70% by weight of the composition of the present invention.

Cream toothpastes, liquid toothpastes and denture cleaners in liquid or cream form generally include an abrasive polish material. An abrasive polish material contemplated for use herein may be any material that does not excessively polish dental or denture acrylics. These include, for example, calcium ortho, fatigue such as silica, calcium and magnesium carbonates, dicalcium orthophosphate dihydrate, calcium pyrophosphate, tricalcium phosphate and calcium polymethaphosphate, including xerogels, hydrogels, aerogels and precipitates. -Hydrates such as meta- and polyphosphates, insoluble sodium polymethaphosphate, alumina and alpha alumina trihydrate, aluminosilicates such as calcined aluminum silicate and aluminum silicate, magnesium and zirconium silicates such as magnesium trisilicate, urea And particulate condensation products of formaldehyde, polymethylmethacrylate, powdered polyethylene and thermosetting polymeric resins such as those disclosed on December 25, 1962, US-A-3,070,510. In addition, mixtures of abrasives may be used. The abrasive polish materials generally have an average particle size of about 0.1 to about 30 microns, preferably about 5 to 15 microns.

Various types of silica tooth abrasives provide excellent tooth cleaning and gloss performance without excessive removal of tooth enamel or tooth quality. Silica abrasives include the silica xerogels described in US Pat. No. 2, 1970, US-A-3,538.230, Digiulio, US Pat. No. 21,1975, US Pat. Silica gel such as silica xerogel sold under the trade name " Syloid " by Grace & Company, Division Chemical Division. Suitable precipitated silica materials are described in J.M. Including those marketed as "Zeodent" by Huber Corporation, in particular the silica including the name "Zeodent 119:". Such silica abrasives are disclosed in US-A-4,340,583, July 29, 1982.

In view of providing good cleaning performance with good compatibility with anti-plaque formulations, calcium carbonate abrasives are highly preferred here.

The abrasive is generally present in the toothpaste formulations of the present invention at a concentration of about 10% to about 70% by weight, preferably about 15% to about 25% by weight.

The composition of the present invention may also contain a surfactant. Suitable surfactants include non-soap anionic, nonionic, cationic, zwitterionic and zwitterionic organic synthetic detergents and are those that are moderately stable and foam over a wide range of pH ranges. Many of these suitable detergents are disclosed in US Pat. No. 4,051,234, September 27, 1977 to Gieske et al.

Examples of suitable surfactants include alkyl sulfates; Ethylene oxide and fatty acids, fatty alcohols, fatty amides, polyhydric alcohols (e.g. sorbitan monostearate, sorbitan oleate), alkyl phenols (e.g. Tergitol) and polypropylene oxide or polyoxybutylene (e.g. Pluronics) Condensation products of; Amine oxides such as dimethyl cocamine oxide, dimethyl lauryl amine oxide and cocoalkyldimethyl amine oxide (Aromox); Polysorbates such as Tween 40 and Tween 80 (Hercules); Sorbitan stearate, sorbitan monooleate and the like; Sarcosinates such as sodium cocoyl sarcosinate and sodium lauroyl sarcosinate (Hamposyl-95 ex W.R. Grace); Cationic surfactants such as cetyl pyridinium chloride, cetyl trimethyl ammonium bromide, di-isobutyl phenoxyethoxy ethyl-dimethyl benzyl ammonium chloride and coconut alkyl trimethyl ammonium nitrate.

Soluble fluoride ion sources may also be incorporated into the present compositions. The soluble fluoride ion source is used in an amount sufficient to provide about 50 to about 3500 ppm of fluoride ions. Preferred fluorides are sodium fluoride, fluoride of the second tin, indium fluoride, zinc ammonium fluoride, tin ammonium fluoride, calcium fluoride and sodium monofluoro phosphate. US-A-2,946,735 to Norris et al., Issued July 26, 1960, and US-A-3,678,154 to Widder et al., Issued July 18, 1972, disclose such salts along with others. .

The composition may also include an anti-stone agent. Suitable anti-calcite agents include di- and tetra-alkali metal pyrophosphates as set forth in EP-A-97476. Specific salts include tetraalkali metal pyrophosphate, dialkali metal diacid pyrophosphate, trialkali metal monoacid pyrophosphate and mixtures thereof, wherein the alkali metal is sodium or potassium. The salts are useful in both hydrated and non-hydrated forms. The amount of pyrophosphate salts useful in these compositions is any effective amount and is generally at least about 1.0 wt%, preferably from about 1.5 wt% to about 10 wt%, more preferably from about wt% to about 6 wt%, based on the composition. It is sufficient to provide% P ₂ O ₇ ^-4 in the preparation. Pyrophosphate salts are described in more detail in "Kirk & Othmer, Encyclopedia of Chemical Technology, 2nd Edition, Vol. 15, Interscience Publishers (1968)".

Other anti-stone stones suitable here are zinc salts. Salt salts are disclosed in US-A-4,100,269, US-A-4,416,867, US-A-4,425,325 and US-A-4,339,432. Among the various zinc materials, the preferred formulation is zinc citrate. The zinc compound may be present in an amount sufficient to provide about 0.01 wt% to about 4 wt%, preferably 0.05 wt% to about 1 wt% zinc ions.

Other suitable anti-calcite agents are copolymers of polyacrylates and maleic acid or their anhydrides and methyl vinyl ethers such as Gantrez, polyamino propane sulfonic acids, polyphosphates such as tripolyphosphate, as described in US-A-4,627,977. Synthetic anionic polymers, including hexametaphosphate), diphosphonates (eg EHDP, AHP), polypeptides (eg polyaspartic acid and polyglutamic acid), and mixtures thereof.

Sweeteners that may be used include aspartame, acesulfame, saccharin, dextrose, levose and sodium cyclamate. Generally, sweeteners are used at concentrations from about 0.005% to about 2% by weight of the composition.

Any other optional component suitable for use herein is a water soluble source of chlorhexidine digluconate, quaternary ammonium bacterial compounds and some metal ions such as zinc, copper, silver and second tin (e.g. zinc, copper And second water soluble antibacterial agents such as tin chloride, and silver nitrate); Pigments such as titanium dioxide; Orally acceptable dyes / colorants such as FD & C Blue # 1, FD & C Yellow # 10, FE & C Red # 40; Antioxidants, vitamins such as vitamins C and E, other antiflag preparations such as secondary tin salts, copper salts, strontium salts and magnesium salts; pH modifiers, urea, calcium glycerophosphate, sodium trimethaphosphate, anti-caring agents such as plant extracts, sensitive dental desensitizers such as potassium nitrate and potassium citrate, and mixtures thereof.

Typically, gargles include water / alcohol solutions, fragrances, wetting agents, sweeteners, foaming agents, and colorants, as described above. The gargling medicine may comprise ethanol at a concentration of 0 to 60% by weight, preferably 5 to 30% by weight.

The denture cleaning composition of the present invention may additionally include one or more bleaches, organic peroxy acid precursors, boiling agents, chelating agents and the like.

Bleaches take the form of inorganic oversalts and can be selected from any of the known bleaches known for use in denture cleaners such as alkali metal and ammonium persulfates, perborates, percarbonates and perphosphates and alkali metal alkaline earth metal peroxides. have. Examples of suitable bleaches include carium, ammonium, sodium and lithium persulfate and perborate mono- and tetrahydrates, sodium pyrophosphate peroxyhydrate and magnesium, calcium, strontium and zinc peroxide. Of these, however, alkali metal persulfates, perborates and mixtures thereof are preferred for excitation and use, more preferably alkali metal perborates. Indeed, it is a feature of the present invention that the tablet composition provides excellent antimicrobial activity even in the absence of alkali metal persulfate.

The amount of bleach in the total composition is generally about 5% to about 70%, preferably about 10% to about 50%. In compositions consisting of a mixture of alkali metal persulfates and perborates, the total persulfate: perborate ratio is suitably about 5: 1 to about 1: 5, more specifically about 2: 1 to about 1: 2.

In addition, the denture cleaning composition may incorporate a release of carbon dioxide or oxygen with boiling in the presence of a boiling generator, ie water. Boiling generators may be selected from effective launching agents under acidic, neutral or alkaline pH conditions, but preferably this is a combination of effective or most effective generators under acidic or neutral pH conditions and effective or most effective generators under alkaline pH conditions. Made of water. Boiling agents effective under acidic or neutral pH conditions include tartaric acid, fumaric acid, citric acid, malic acid, maleic acid, gluconic acid, succinic acid, salicylic acid, adipic acid or sulfamic acid, sodium fumarate, sodium or potassium acid phosphate, betaine hydro One or more non-toxic, physiologically acceptable organic acids, such as chlorides or mixtures thereof, and one or more alkali metal carbonates, such as sodium bicarbonate, sodium carbonate, sodium sesquicarbonate, potassium carbonate, carium bicarbonate, or mixtures thereof Or combinations mixed with bicarbonates. Of these, malic acid is preferred. Boiling generators that are effective under alkaline pH conditions include, as described above, perchlorates such as alkali and alkaline earth metal peroxoborate, perborate, persulfate, percarbonate, perphosphonate and mixtures thereof, for example monopersulfate, II du Plint de Nemours Co., which is a 2: 1: 1 mixture of carium sulphate and carium bisulfate, having an active coral content of about 4.5%. Mixtures of alkali metal perborate (anhydrous, mono- or tetrahydrate) with monopersulfate, such as Caroat ^R sold by the company.

In preferred denture cleaning compositions in tablet form, the boiling generator has the form of a solid base material which releases carbon dioxide or coral with boiling in the presence of water. Suitably the solid base material incorporates (non) carbonate / acid boiling couples, optionally mixed with perborate / persulfate coral boiling generators. Mixing of the generator is useful to achieve optimal dissolution properties, and pH conditions are useful to achieve optimal cleaning and antimicrobial activity. The (non) carbonate component generally comprises from 5% to about 65%, preferably from about 25% to 55%, of the total composition; The acid component generally comprises about 5% to about 50%, preferably about 10% to about 30% of the total composition.

The denture cleaning composition of the present invention may be supplemented with other known ingredients of such formulations. A particularly preferred additional component is the organic peroxy acid precursor, which term can generally be defined as a compound in which the appropriate amount of 0.1 N sodium thiosulfate is at least 1.5 ml in the following peracid preparation test.

Test solutions are prepared by dissolving the following materials in 1000 ml distilled water:

Sodium pyrophosphate (Na ₄ P ₂ O ₇ .10H ₂ O) 2.5 g

0.615 g sodium perborate with 10.4% free oxygen

(NaBO ₂ H ₂ O ₂ 3 H ₂ O)

0.5 g sodium dodecylbenzenesulfonate

An amount of activator is added to this solution at 60 ° C. so that one level of activator is introduced for each atom of available oxygen present.

The mixture obtained by the addition of the active agent is stirred vigorously and maintained at 60 ° C. Five minutes after the addition, 100 ml fractions of the total solution are recovered and immediately titrated onto a mixture of 250 g of crushed ice and 15 ml of glacial acetic acid. Potassium iodide (0.4 g) is then added and the free iodine is titrated immediately, using 0.1 N sodium thiosulfate with starch as indicator until the blue color first disappears. The amount of sodium thiosulfate solution used in ml is the appropriate amount of the bleach activator.

Organic peracid precursors are typically compounds comprising one or more acyl groups that can be perhydrolyzed. Preferred active agents are those of the N-acyl or O-acyl compound type comprising acyl radicals R-CO, wherein R is a hydrocarbon or substituted hydrocarbon group, said hydrocarbon group preferably having from about 1 to about 20 carbon atoms. to be. Examples of suitable peracid precursors include:

1) Acyl organamides of the formula RCONR ₁ R ₂ as disclosed in US-A-3,117,148, wherein RCO is a carboxyl acyl radical, R ₁ is an acyl radical, and R ₂ is an organic radical. Examples of compounds included in the group include the following:

a) N, N-diacetylaniline and N-acetylphthalimide;

b) N-acylhydantoin, such as N, N'-diacetyl-5,5-dimethylhydantoin;

c) polyacylated alkylene diamines as disclosed in GB-A-907,356, GB-A-907,357 and GB-A-907,358, such as N, N, N ', N'-tetraacetylethylenediamine (TAED) and the corresponding Hexamethylenediamine (TAHD) derivatives.

d) Acylated glycuril as described in GB-A-4,246,338, GB-A-1,246,339 and GB-A-1,247,429, such as tetraacetylglycoluril.

2) Acylated sulfonamides as disclosed in GB-A-3,183,266, such as N-methyl-N-benzoyl-mentane sulfonamide and N-phenyl-N-acetyl mentane sulfonamide.

3) Carboxylic esters as disclosed in GB-A-836,988, GB-A-963,135 and GB-A-1,147,871. Examples of compounds of this type include phenyl acetate, sodium acetoxy benzene sulfonate, trichloroethyl acetate, sorbitol hexaacetate, fructose pentaacetate, p-nitrobenzaldehyde diacetate, isopropaneyl acetate, acetyl aceto hydroxamic acid , And acetyl salicylic acid. Others include esters of phenols or substituted phenols with alpha-chlorinated lower aliphatic carboxylic acids, such as chloroacetylphenol and chloroacetylsalicylic acid, as disclosed in US Pat. No. 3,130,165.

Carboxylic esters having the formula Ac L, wherein Ac is an acyl of an organic carboxylic acid containing a straight or branched C ₆ -C ₂₀ alkyl or alkenyl moiety or a C ₆ -C ₂₀ alkyl-substituted aryl moiety And L is a leaving group, the conjugate acid of which has a pKa in the range of 4 to 13, for example oxybenzenesulfonate or oxybenzoate). Preferred compounds of this type are as follows;

a) Ac is R ₃ -CO, R ₃ is a straight or branched chain alkyl group having 6 to 20, preferably 6 to 12, more preferably 7 to 9 carbon atoms, wherein the longest comprising carbonyl carbon Straight chain alkyl chains contain 5 to 18, preferably 5 to 10, carbon atoms and R ₃ is optionally substituted by Cl, Br, OCH ₃ or OC ₂ H ₅ (preferably alpha in the carbonyl moiety) Substituted). Examples of substances in this class include sodium 3,5,5-trimethylhexanoyloxybenzene sulfonate, sodium 3,5,5-trimethylhexanoyloxybenzoate, sodium 2-ethylhexanoyl oxybenzenesulfonate, sodium furnace It is preferable that nanoyl oxybenzene sulfonate and sodium octanoyl oxybenzenesulfonate are included, and in each example, an acyloxy group is p-substituted.

b) Ac is a formula R ₃ (AO) mXA wherein R ₃ is a straight or branched chain alkyl or alkylaryl group having 6 to 20, preferably 6 to 15 carbon atoms in the alkyl moiety, R ₅ is Cl, _May be substituted by Br, OCH ₃ or OC ₂ H ₅ , AO is oxyethylene or oxypropylene, m is 0 to 10, X is O, NR ₄ or CO-NR ₄ , and A is CO, CO -CO, R ₆ -CO, CO-R ₆ -CO or CO-NR ₄ -R ₆ -CO, wherein R ₄ is C _1-4 alkyl, R ₆ is from 1 to 8 alkylene or alkenyl moieties Alkylene, alkenylene, arylene or alkylene having a carbon atom) Bleach activator compounds of this type are carboxylic acid derivatives of formula R ₃ (AO) _m OCOL, formula R ₃ OCO (CH ₂ ) of ₂ COL acid derivatives, of formula R ₃ OCH ₂ COL-hydroxy acid derivatives, R a ₃ OCOCOL oxalic acid derivative of formula R ₃ OCOCH = CHCOL maleic acid and fumaric acid derivatives of the formula _{R 3 CONR 1 (CH 3)} 6 COL of Acyl Aminocaproic acid derivatives, acyl glycine derivatives of formula R ₃ CONR ₁ CH ₂ COL, and amino-6-oxocapronic acid derivatives of formula R ₃ N (R ₁ ) CO (CH ₂ ) ₄ COL. m is preferably 0 to 10, R ₃ is preferably C _6-12 , more preferably, m is preferably 0 to 10, R ₃ is preferably C _6-12 , more preferably, C _6-10 alkyl when m is 0 and C _9-15 alkyl when m is not 0. The leaving group L is as defined above.

5) Acyl-cyanurates, such as triacetyl- or tribenzoylcyanurate, as disclosed in US Pat. No. 3,332,882.

6) Anhydrides of benzoic acid or phthalic acid, which may be substituted, such as benzoic anhydride, m-chlorobenzoic anhydride and phthalic anhydride.

Of all the above, organic peracid precursors of type 1 (c) and 4 (a) are preferred.

If a peroxy bleaching precursor is present, the concentration of the peroxy bleaching precursor relative to the total composition is preferably from about 0.1% to about 10% by weight, more preferably from about 0.5% to about 5% by weight, in general As a bleach precursor aggregate.

Preferred bleaching precursor aggregates for use herein generally comprise a binder or flocculant at a concentration of about 5% to about 40%, preferably about 10% to about 30%, as their weight percent. Suitable flocculants include polyvinylpyrrolidone, poly (oxyethylene) having a molecular weight of 20,000 to 500,000, polyethylene glycols having a molecular weight of about 1,000 to about 50,000, carbowax having a molecular weight of 4,000 to 20,000, nonionic surfactants, fatty acids, sodium Carboxymethyl cellulose, gelatin, fatty alcohols, phosphates and polyphosphates, clays, aluminosilicates and polymeric polycarboxylates. Among them, polyethylene glycol is very preferred, and particularly preferably a molecular weight of about 1,000 to about 30,000, preferably 2,000 to about 10,000.

In terms of optimal dissolution and pH properties, from about 10% to about 75%, preferably from about 20% to about 60%, by weight of peroxy acid bleaching precursor, from about 5% to about 60%, preferably from about 5 % To about 50%, more preferably about 10% to about 40% (non) carbonate / acid boiling couple, about 0% to about 20% peroxoboroate, and about 5% to about 40%, preferably Is a bleaching precursor aggregate comprising from about 10% to about 30% flocculant.

The final bleaching precursor granules preferably have an average particle size of about 500 to about 1500, preferably about 500 to 1,000 μm, which is valuable in terms of optimum dissolution performance and aesthetics. Furthermore, the concentration of aggregates of bleach precursors is preferably about 1% to about 20% by weight, more preferably about 5% to about 15% by weight relative to the composition.

Denture cleaning compositions of the present invention may be in the form of creams, tablets, granules or powders, although tablet-like compositions are highly preferred. Tablet compositions may be monolayer or multilayer tablets.

Denture cleaning compositions of the invention may be supplemented with other conventional ingredients of the formulations, in particular surfactants, chelating agents, enzymes, flavors, physiological coolants, antimicrobial compounds, pigments, sweeteners, tablet binders and fillers, dimethylpolysiloxanes Foaming sedatives such as, foaming stabilizers such as fatty acid sugar esters, preservatives, lubricants such as talc, magnesium stearate, finely divided amorphous pyrogenic silica and the like. The free moisture content of the final composition is preferably about 1% or less, in particular about 0.5% or less.

Tablet binders and fillers suitable for use herein include polyvinylpyrrolidone, poly (oxyethylene) having a molecular weight of 20,000 to 500,000, polyethylene glycols having a molecular weight of about 1,000 to about 50,000, carbowax of a molecular weight of 4,000 to 20,000, nonionic surfactants, Fatty acids, sodium carboxymethyl cellulose, gelatin, fatty alcohols, clays, polymerizable polycarboxylates, sodium carbonate, calcium carbonate, calcium hydroxide, magnesium oxide, magnesium hydroxide carbonate, sodium sulfate, proteins, cellulose ethers, cellulose esters, Polyvinyl alcohol, alginic acid esters, and similar colloidal vegetable fatty substances. Of these, polyethylene glycol is very preferred, and particularly preferably has a molecular weight of about 1,000 to about 30,000, preferably about 12,000 to about 30,000.

The surfactant used in the denture cleaning composition of the present invention may be selected from many solubles that are miscible with other components of the denture cleaner, both in dry condition and in solution. The material helps to improve the effectiveness of other components of the composition by helping to penetrate the inner surface of the denture. Dry powders or granular anionic surfactants such as sodium lauryl sulfate, sodium N-lauroyl sarcosinate, sodium lauryl sulfoacetate or dioctyl sodium sulfosuccinate or ricinole sodium sodium sulfosuccinate For example, 0.1% to 5% by weight of the dry composition can be included in the composition, preferably the surfactant comprises 0.5 to 4% by weight of the composition.

Suitable cationic, nonionic and zwitterionic surfactants include quaternary ammonium compounds such as cetyltrimethylammonium bromide, alkylene oxides such as ethylene or propylene oxide and fatty alcohols, phenols, fatty amines or fatty acid alkanolamides; Condensates of fatty acids, fatty acid alkanolamides themselves, esters of long-chain (C _8-22 ) fatty acids with polyalcohols or sugars, for example glyceryl monostearate or saccharose monolaurate or sorbitol polyoxyethylene mono- or di-stea Late, betaine, sulfobetaine or long chain alkylaminocarboxylic acid.

Chelating agents advantageously aid in cleaning and bleaching stability by retaining metal ions such as calcium, magnesium and heavy metal cations in solution. Examples of suitable chelating agents are: aminopolycarboxylates such as sodium tripolyphosphate, sodium acid pyrophosphate, tetrasodium pyrophosphate, nitrilotriacetic acid and ethylenediaminetetraacetic acid and salts thereof, and hydroxyethanediphosphonic acid, ethylenediamine Polyphosphonates and aminopolyphosphonates such as tetramethylenephosphonic acid, diethylenetriaminepentamethylenephosphonic acid and salts thereof. The chelating agent chosen is not critical except that it must be compatible with other components of the denture cleaner when in the dry and aqueous state. Advantageously, the chelating agent accounts for 0.1 to 60% by weight, preferably 0.5 to 30% by weight of the composition. However, the phosphonic acid chelating agent preferably comprises from about 0.1% to about 1%, preferably from about 0.1% to about 0.5% by weight of the composition.

Enzymes suitable for use herein are exemplified by proteases, alkylases, amylases, lipases, dextranases, mutanases, glucanases and the like.

EXAMPLE

The following examples further describe and describe preferred embodiments within the scope of the present invention.

[Examples I to V]

The following are representative denture cleansing tablets according to the present invention. Percent is the weight relative to the total tablets. Tablets are made through compression of the granulation component mixture in a punch and colored tablet press at a pressure of about 10 ⁵ kPa.

1.Ethylenediaminetetramethylenephosphonic acid

2. Tetraacetylethylene Diamine

3. Sodium 3,5,5-trimethylhexanoyloxybenzene sulfonate

4. Cetyl Dimethicone Copolyol

5. Peppermint-Based Incense

In Examples I to V above, the total tablet weight is 3 g and the diameter is 25 mm.

The denture cleansing tablets in Examples I to V exhibit improved antiplaque, cleansing and antibacterial activity with good cohesion, other physical properties and performance characteristics in use.

[Examples VI to VIII]

The following is a representative cream toothpaste / denture cleansing cream according to the present invention. Percent is the weight relative to the total composition.

The cream toothpaste / denture cleansing creams of Examples VI-X show improved antiplaque, strong flavor effect, and antimicrobial activity with good cleaning properties.

Claims (11)

A composition containing at least one family composition composition component selected from abrasives, binders, wetting agents, surfactants, fluoride ion sources, anti-calcite agents and sweeteners, wherein the composition is selected from alkyl- and alkoxy-dimethicone copolyols of Formula (I) An oral composition further comprising dimethicone copolyol: [Formula I]

[Wherein X is selected from hydrogen and alkyl, alkoxy and acyl groups having 1 to 16 carbon atoms, Y is selected from alkyl and alkoxy groups having 8 to 22 carbon atoms, n is 0 to 200, m Is 1 to 40, q is 1 to 100, the molecular weight of residue (C ₂ H ₄ O-) _x (C ₃ H ₆ O-) _y X is 50 to 2000, and x and y are oxyethylene: oxypropylene Is a value such that the weight ratio is from 100: 0 to 0: 100. The composition of claim 1 wherein the dimethicone copolyol is selected from C ₁₂ to C ₂₀ alkyl dimethicone copolyols and mixtures thereof. The composition according to claim 1 or 2, wherein the dimethicone copolyol is cetyl dimethicone copolyol. 3. The composition of claim 1, wherein the composition comprises 0.01% to 25% by weight of dimethicone copolyol. 10 wt% according to claim 4 selected from silica, alumina, aluminosilicates, magnesium and zirconium silicates, calcium ortho-, pyro-, meta- and polyphosphates, calcium and magnesium carbonates, insoluble metaphosphates and thermosetting polymeric resins. To 70% by weight of the composition comprising a dental abrasive. The composition of claim 5 comprising from 0.1 wt% to 1 wt% of the binder. The composition of claim 4 comprising 0.1% to 5% by weight of dimethicone copolyol. The oral composition according to claim 1, which is in the form of a cream toothpaste, a powder toothpaste, a liquid toothpaste, or a gargle. The oral composition of claim 1 in the form of a denture cleaner. The oral composition of claim 1 in the form of a chewing gum. The oral composition according to claim 1, which is in the form of a candy.