WO2006100073A1 - Dentifrice compositions comprising as a soluble calcium sequestring agent a derivative comprising a phosphonate group - Google Patents

Dentifrice compositions comprising as a soluble calcium sequestring agent a derivative comprising a phosphonate group Download PDF

Info

Publication number
WO2006100073A1
WO2006100073A1 PCT/EP2006/002667 EP2006002667W WO2006100073A1 WO 2006100073 A1 WO2006100073 A1 WO 2006100073A1 EP 2006002667 W EP2006002667 W EP 2006002667W WO 2006100073 A1 WO2006100073 A1 WO 2006100073A1
Authority
WO
WIPO (PCT)
Prior art keywords
composition
abrasive
dentifrice
agent
composition according
Prior art date
Application number
PCT/EP2006/002667
Other languages
French (fr)
Inventor
Jonathan Edward Creeth
Original Assignee
Glaxo Group Limited
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Glaxo Group Limited filed Critical Glaxo Group Limited
Priority to BRPI0609712-0A priority Critical patent/BRPI0609712A2/en
Priority to US11/909,207 priority patent/US20080175799A1/en
Priority to CA002602401A priority patent/CA2602401A1/en
Priority to EP06723658A priority patent/EP1863575A1/en
Priority to AU2006226507A priority patent/AU2006226507A1/en
Priority to JP2008502327A priority patent/JP2008533184A/en
Priority to MX2007011686A priority patent/MX2007011686A/en
Publication of WO2006100073A1 publication Critical patent/WO2006100073A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/19Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/24Phosphorous; Compounds thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/55Phosphorus compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q11/00Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses

Definitions

  • the present invention relates to dentifrice compositions, in particular compositions comprising a fluoride source and a soluble calcium sequestering agent that is not an 5 oxidising agent, for cleaning natural teeth and dentures.
  • dentifrice compositions in particular compositions comprising a fluoride source and a soluble calcium sequestering agent that is not an 5 oxidising agent, for cleaning natural teeth and dentures.
  • Such compositions show excellent cleaning properties whilst at the same time low abrasion characteristics.
  • the compositions are also useful for combating the problems associated with acid erosion and/or tooth wear
  • Dentifrices have been used for more than 2000 years and the principal purpose of a dentifrice has always been the removal of surface deposits from the teeth. It is known that removal of surface deposits from the teeth can be achieved through the use of either a chemical or mechanical cleaning agent. An example of a chemical cleaning
  • agent is a calcium-sequestering agent, for example a polyphosphate salt, such as tripolyphosphate, and the mechanical agents are the abrasive materials, e.g. precipitated silica or calcium carbonate.
  • abrasive cleaning agent is amorphous hydrated silica . Bleaching agents are sometimes included in dentifrice compositions to decolourise tooth stains. This will not however remove the stain
  • Hydrogen peroxide is a well-known bleaching agent but with peroxide-containing dentifrices the lifetime of peroxide in the oral cavity is very short.
  • Human plaque contains a significant level of the peroxide-degrading enzyme catalase, which means that it is very difficult to maintain
  • abrasive agents for 30 example abrasive agents, humectants, fluoride sources, binders, anti plaque agents, dyes, flavours, preservatives, water and other optional ingredients.
  • Fluoride is an important aid to oral health, particularly for the health of the tooth's enamel.
  • the effective removal of surface deposited stains from the teeth or a dental prosthesis is always associated with substantially abrasive formulations. It is however recognised 35 that dentifrice compositions containing abrasive materials can damage the tooth surface as well as the surface of dental prosthetics so it is very important that a dentifrice formulation should provide effective cleaning without subjecting the tooth or prosthetic to excessive abrasion.
  • WO-A-95/17158 describes and claims a composition for reducing or removing surface deposited stains from natural teeth or dental prostheses comprising a dentally acceptable preparation comprising 5 to 15% by weight of a water soluble alkali metal tripolyphosphate.
  • All dentifrice formulation examples shown in WO-A-95/17158 include conventional dental abrasives, for example abrasive silica, is disclosed in the range 5-80 wt.%.
  • the established method for determining the abrasivity of a dentifrice formulation is by measuring the Relative Dentine Abrasivity (RDA) (Hefferen, JJ. A laboratory method for measuring dentifrice abrasivity. J. Dent. Res. 55 563-573, 1976.).
  • RDA Relative Dentine Abrasivity
  • This assay measures loss of dentine due to extended brushing with a 25:40 w/w slurry of test toothpaste from prepared samples of human dentine.
  • the dentine samples are irradiated to generate 32 P in the mineral.
  • the assay measures radioactivity in the supernatant after brushing, relative to radioactivity liberated by brushing with a standard slurry of calcium pyrophosphate.
  • IVSR in- vitro stain removal
  • This assay aims to maximise the relevance of the assay to the in vivo situation by using untreated naturally stained bovine teeth as substrate. The teeth are brushed for an extended period with a 1 :3 slurry of test toothpaste in water. Stain removal is quantified using a chromameter.
  • Performance may be measured relative to a Control dentifrice formulation containing 14% Zeodent 113TM abrasive silica (available from J.M. Huber Corporation) in a conventional base containing water, sorbitol, glycerin, PEG, flavour, SLS, sodium saccharin, Xanthum gum and sodium fluoride.
  • IVSR is also known as the natural extrinsic stain removal assay or NESR and is referred to as such in some publications.
  • Cleaning efficiency may therefore be described as the ratio of the FVSR to the RDA.
  • IVSR values that are quoted herewith are relative to a control formulation that has been assigned an arbitrary value of 100.
  • the efficacy of dentifrices of the present invention in combating dental erosion can be assessed by measuring their ability to reduce the solubility of enamel when treated with lactic acid using a standard FDA method 33 for sodium fluoride silica dentifrices. This is know as the Enamel Solubility Reduction Assay.
  • EP 0 835 223B discloses an amorphous silica that has a low abrasivity value which, when incorporated into a dentifrice composition, maintains good cleaning characteristics. This publication however considers the abrasive silica as the only cleaning material of the composition and describes the amorphous silica in terms of its physical properties. Accordingly EP 0 835 223B claims an amorphous silica characterized by: an RDA value of between 30 and 70, an oil absorption capacity of between 100 and 155cm 3 /100g, and a BET surface area of up to 200m 2 /g.
  • EP-A-O 396 460 describes in Example 1 an amorphous silica in terms of BET surface area, oil uptake, pore volume, pH, refractive index and translucence.
  • EP-A-O 002 184 discloses the use of a sodium polyphosphate in fine granulate form for tooth cleaning, either by itself or in combination with a commercial toothpaste formulation, referring to the abrasive effect of the sodium polyphosphate and intensification of tooth cleaning by this material without damaging the substance of the teeth.
  • the present invention concerns the use of other calcium sequestering agents, such as polymeric materials that comprise a phosphonate group.
  • It is an object of the present invention to provide a dentifrice composition comprising as a soluble calcium sequestering agent that is not an oxidising agent, a polymeric material comprising a phosphonate group wherein the composition has an RDA value of below 30 and an IVSR value greater than 50 (when compared to a Control) and an orally acceptable vehicle, wherein the calcium sequestering agent is present in a proportion of 1-20 wt % and an abrasive is present in a proportion of 0-5 wt % of the composition.
  • the composition is a toothpaste being a viscous extrudable fluid which can be provided in a collapsible container e.g. a tube or a pump and extruded therefrom onto a toothbrush for use.
  • a collapsible container e.g. a tube or a pump and extruded therefrom onto a toothbrush for use.
  • the RDA value is below 25, preferably below 20, and most preferably as low as possible, e.g. so that the composition is substantially non-abrasive.
  • the IVSR value is up to 250, preferably 200 and more preferably greater than 100, for example being in the range 75-150, e.g. 75-120.
  • polymeric material comprising aphosphonate group examples include those described and referred to in published patent application WO 2004/054529 (The Procter + Gamble Company).
  • the polymeric material may also be mixed with other calcium sequestering agents such as polyphosphates as described and referred to in PCT/EP2004/010629.
  • Preferred polymeric materials comprising a phosphonate group are azacycloheptane diphosphonate and ethanehydroxy bisphosphonate.
  • the soluble calcium-sequestering agent may be present in a proportion 1-20 wt %, preferably 2-15 wt%, more preferably 5-15 wt% of the dentifrice composition.
  • a proportion of the calcium-sequestering agent in the composition below the solubility limit thereof a gel or liquid compositions may be provided in which the calcium sequestering agent is in solution, so that the gel or liquid may include no undissolved solid particles, and may be a clear gel or liquid.
  • the composition may include a fluoride ion source.
  • Fluoride ion may stabilise polyphosphates in the mouth.
  • a fluoride ion source may be provided by an alkali metal fluoride, preferably sodium fluoride, an alkali metal monofluorophosphate, stannous fluoride and the like.
  • the fluoride ion source is an alkali metal fluoride, most preferably sodium fluoride.
  • the fluoride ion source serves in a known manner for caries protection.
  • the fluoride ion source will be used in an amount to provide an anti-caries effective amount and a phosphatase enzyme inhibiting amount, such as an amount sufficient to provide from about 25 ppm to about 3500 ppm, preferably about 1100 ppm, as fluoride ion.
  • a phosphatase enzyme inhibiting amount such as an amount sufficient to provide from about 25 ppm to about 3500 ppm, preferably about 1100 ppm, as fluoride ion.
  • the formulation may contain 0.1 - 0.5 wt % of an alkali metal fluoride such as sodium fluoride.
  • the pH of the composition is from 6 to 10.5, more preferably from 7 to 9.5.
  • the composition may contain up to 0.5 wt.% of sodium hydroxide to provide a suitable pH.
  • the orally acceptable vehicle may be of a generally conventional composition e.g. comprising a thickening agent, a binding agent and a humectant.
  • Preferred binding agents include for example natural and synthetic gums such as xanthan gums, carageenans, alginates, cellulose ethers and esters.
  • Preferred humectants include glycerin, sorbitol, propylene glycol and polyethylene glycol.
  • a preferred humectant system consists of glycerin, sorbitol and polyethylene glycol.
  • the orally acceptable vehicle may optionally comprise one or more surfactant, sweetening agent, flavouring agent, anticaries agent (in addition to the fluoride ion source), anti-plaque agent, anti-bacterial agent such as triclosan or cetyl pyridinium chloride, tooth desensitizing agent, colouring agents and pigment.
  • useful surfactants include the water-soluble salts of alkyl sulphates having from 10 to 18 carbon atoms in the alkyl moiety, such as sodium lauryl sulphate, but other anionic surfactants as well as non-ionic, zwitterionic, cationic and amphoteric surfactants may also be used.
  • a toothpaste composition of the present invention suitably contains from about 10 to about 80 wt % humectant such as sorbitol, glycerin, polyethylene glycol or xylitol; from about 0.25 to about 5 wt % detergent; from 0 to about 2 wt % sweetener and flavouring agents; together with water and an effective amount of binding and thickening agents, such as from about 0.1 to about 15 wt %, to provide the toothpaste of the invention with the desired stability and flow characteristics. It is preferred to use a thickening silica as the thickening agent.
  • thickening silicas are known silicas which have relatively little abrasive effect compared with known abrasive silicas such as Zeodent 113TM, but provide a thickening effect on the composition.
  • Suitable thickening silicas are known and include those marketed by Huber under the tradename Zeodent, e.g. Zeodent 167, by Degussa AG under the trade name SDDENT®, e.g. SE)ENT 22S®, and by Grace-Davison Chemical Division under the trade name SYLOBLANC®, e.g. SYLOBLANC 15®, respectively.
  • the composition may contain up to ca. 20wt % of a thickening silica, typically 5-15 wt %.
  • the composition of the invention may contain an abrasive material, for example known types of "abrasive silica” commonly used in toothpaste compositions e.g. Zeodent 113TM as mentioned above.
  • an abrasive material for example known types of "abrasive silica” commonly used in toothpaste compositions e.g. Zeodent 113TM as mentioned above.
  • an abrasive material may be defined as a material having an RDA of 30 or above. Larger amounts of silica may be incorporated, more typical of abrasive silica incorporation levels in toothpastes (up to e.g. 25%), if that silica has an RDA below 30.
  • the slurry conditions used to determine the RDA of an abrasive raw material differ from those used to determine the RDA of a formulated toothpaste.
  • the slurry conditions for a raw material are 1Og abrasive plus 50ml of a 0.5% carboxymethyl cellulose slurry in 10% glycerin, whereas the slurry conditions for a formulated toothpaste are 25g toothpaste plus 40ml water. Care should therefore be taken when comparing RDA figures for abrasives as raw materials with RDA figures for fully formulated toothpastes.
  • a preferred dentifrice composition of this invention comprises as a soluble calcium sequestering agent that is not an oxidising agent, a polymeric material comprising a phosphonate group wherein the composition has an RDA value of below 30 and an IVSR value greater than 50 (when compared to a Control) and an orally acceptable vehicle, wherein the calcium sequestering agent is present in a proportion 1-20 wt %, preferably 5-10 wt % of the composition, with 0 - 5 wt %, preferably 0 wt % of an abrasive, typically an abrasive silica.
  • the dentifrice composition may be presented as either a single or dual phase composition.
  • the composition is in the form of a conventional toothpaste-type composition that can be squeezed from a collapsible tube. It is also suitable for dispensing from a pressurised aerosol container.
  • Toothpaste-type compositions according to the present invention may be prepared by admixing according to conventional practice the calcium sequestering agent, and the fluoride ion source if present, with the orally acceptable dental vehicle, which may be anhydrous but is preferably an aqueous orally acceptable dental vehicle, to form a storage-stable semi-solid extrudable material useful as a dentifrice.
  • the orally acceptable dental vehicle which may be anhydrous but is preferably an aqueous orally acceptable dental vehicle, to form a storage-stable semi-solid extrudable material useful as a dentifrice.
  • Example 1 is a formulation in which the calcium-sequestering chemical cleaning system is azacycloheptane diphosphonate. Thickening silica is increased to account for the lower level of solids in the formulation. Other calcium sequestering agents may be used as chemical cleaning agent and/or anticaries agent.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Oral & Maxillofacial Surgery (AREA)
  • Cosmetics (AREA)

Abstract

A dentifrice composition is disclosed comprising a soluble calcium sequestering agent that is not an oxidising agent, wherein the soluble calcium sequestering agent is a polymeric material comprising a phosphonate group. The composition has an RDA value of below 30 and an IVSR value greater than 50 (when compared to a Control) and an orally acceptable vehicle, wherein the calcium sequestering agent is present in a proportion of 1-20 wt % and an abrasive is present in a proportion of 0-5 wt % of the composition. The composition is highly effective in removing stains from natural teeth and prosthetics and will not damage the tooth or prosthetic due to excessive abrasion. The compositions are also useful for combating the problems associated with acid erosion and/or tooth wear.

Description

DENTIFRICE COMPOSITIONS COMPRISING AS A SOLUBLE CALCIUM SEQUESTRING AGENT A DERIVATIVE COMPRISING A PHOSPHONATE GROUP
The present invention relates to dentifrice compositions, in particular compositions comprising a fluoride source and a soluble calcium sequestering agent that is not an 5 oxidising agent, for cleaning natural teeth and dentures. Such compositions show excellent cleaning properties whilst at the same time low abrasion characteristics. The compositions are also useful for combating the problems associated with acid erosion and/or tooth wear
10
Dentifrices have been used for more than 2000 years and the principal purpose of a dentifrice has always been the removal of surface deposits from the teeth. It is known that removal of surface deposits from the teeth can be achieved through the use of either a chemical or mechanical cleaning agent. An example of a chemical cleaning
15 agent is a calcium-sequestering agent, for example a polyphosphate salt, such as tripolyphosphate, and the mechanical agents are the abrasive materials, e.g. precipitated silica or calcium carbonate. An example of an abrasive cleaning agent is amorphous hydrated silica . Bleaching agents are sometimes included in dentifrice compositions to decolourise tooth stains. This will not however remove the stain
20 effectively and, furthermore, effective bleaching agents can damage the oral tissues and are difficult to formulate successfully. Hydrogen peroxide is a well-known bleaching agent but with peroxide-containing dentifrices the lifetime of peroxide in the oral cavity is very short. Human plaque contains a significant level of the peroxide-degrading enzyme catalase, which means that it is very difficult to maintain
25 an effective level of peroxide on the tooth surface for sufficient time for stain to be bleached. Use of more aggressive bleaching agents than peroxides however bring concerns over tissue damage.
Traditional dentifrice formulations contain a number of specific components for 30 example abrasive agents, humectants, fluoride sources, binders, anti plaque agents, dyes, flavours, preservatives, water and other optional ingredients. Fluoride is an important aid to oral health, particularly for the health of the tooth's enamel. The effective removal of surface deposited stains from the teeth or a dental prosthesis is always associated with substantially abrasive formulations. It is however recognised 35 that dentifrice compositions containing abrasive materials can damage the tooth surface as well as the surface of dental prosthetics so it is very important that a dentifrice formulation should provide effective cleaning without subjecting the tooth or prosthetic to excessive abrasion. WO-A-95/17158 describes and claims a composition for reducing or removing surface deposited stains from natural teeth or dental prostheses comprising a dentally acceptable preparation comprising 5 to 15% by weight of a water soluble alkali metal tripolyphosphate. All dentifrice formulation examples shown in WO-A-95/17158 include conventional dental abrasives, for example abrasive silica, is disclosed in the range 5-80 wt.%.
The established method for determining the abrasivity of a dentifrice formulation is by measuring the Relative Dentine Abrasivity (RDA) (Hefferen, JJ. A laboratory method for measuring dentifrice abrasivity. J. Dent. Res. 55 563-573, 1976.). This assay measures loss of dentine due to extended brushing with a 25:40 w/w slurry of test toothpaste from prepared samples of human dentine. The dentine samples are irradiated to generate 32P in the mineral. The assay measures radioactivity in the supernatant after brushing, relative to radioactivity liberated by brushing with a standard slurry of calcium pyrophosphate.
Cleaning performance is closely linked to stain removal and can be measured in various ways. There is a very useful published in- vitro stain removal (IVSR) assay (Layer TM, McConville PS and Wicks MA. Stain removal efficacy of whitening toothpastes - in vitro studies. J. Dent. Res. 79: 216 abstract 581, 2000) that is used in the present invention. This assay aims to maximise the relevance of the assay to the in vivo situation by using untreated naturally stained bovine teeth as substrate. The teeth are brushed for an extended period with a 1 :3 slurry of test toothpaste in water. Stain removal is quantified using a chromameter. Performance may be measured relative to a Control dentifrice formulation containing 14% Zeodent 113™ abrasive silica (available from J.M. Huber Corporation) in a conventional base containing water, sorbitol, glycerin, PEG, flavour, SLS, sodium saccharin, Xanthum gum and sodium fluoride. IVSR is also known as the natural extrinsic stain removal assay or NESR and is referred to as such in some publications.
Cleaning efficiency may therefore be described as the ratio of the FVSR to the RDA.
IVSR values that are quoted herewith are relative to a control formulation that has been assigned an arbitrary value of 100.
The efficacy of dentifrices of the present invention in combating dental erosion can be assessed by measuring their ability to reduce the solubility of enamel when treated with lactic acid using a standard FDA method 33 for sodium fluoride silica dentifrices. This is know as the Enamel Solubility Reduction Assay.
EP 0 835 223B discloses an amorphous silica that has a low abrasivity value which, when incorporated into a dentifrice composition, maintains good cleaning characteristics. This publication however considers the abrasive silica as the only cleaning material of the composition and describes the amorphous silica in terms of its physical properties. Accordingly EP 0 835 223B claims an amorphous silica characterized by: an RDA value of between 30 and 70, an oil absorption capacity of between 100 and 155cm3/100g, and a BET surface area of up to 200m2/g.
From the literature it appears that many formulations that are dependent for their cleaning properties upon their abrasive content are described and claimed in terms of the physical properties of the abrasive material. For example EP-A-O 396 460 describes in Example 1 an amorphous silica in terms of BET surface area, oil uptake, pore volume, pH, refractive index and translucence.
EP-A-O 002 184 discloses the use of a sodium polyphosphate in fine granulate form for tooth cleaning, either by itself or in combination with a commercial toothpaste formulation, referring to the abrasive effect of the sodium polyphosphate and intensification of tooth cleaning by this material without damaging the substance of the teeth.
A highly effective dentifrice formulation without the traditional amounts of abrasive material has been described in PCT/EP2004/010629. In this application calcium sequestering agents, such as sodium tripolyphosphate are described in formulations that have no or very low levels of abrasive material. Such compositions have good cleaning characteristics with an abrasivity (measured as RDA) of below 30.
The present invention concerns the use of other calcium sequestering agents, such as polymeric materials that comprise a phosphonate group.
It is an object of the present invention to provide a dentifrice composition comprising as a soluble calcium sequestering agent that is not an oxidising agent, a polymeric material comprising a phosphonate group wherein the composition has an RDA value of below 30 and an IVSR value greater than 50 (when compared to a Control) and an orally acceptable vehicle, wherein the calcium sequestering agent is present in a proportion of 1-20 wt % and an abrasive is present in a proportion of 0-5 wt % of the composition.
Preferably the composition is a toothpaste being a viscous extrudable fluid which can be provided in a collapsible container e.g. a tube or a pump and extruded therefrom onto a toothbrush for use.
Preferably the RDA value is below 25, preferably below 20, and most preferably as low as possible, e.g. so that the composition is substantially non-abrasive. Preferably the IVSR value is up to 250, preferably 200 and more preferably greater than 100, for example being in the range 75-150, e.g. 75-120.
Examples of the polymeric material comprising aphosphonate group include those described and referred to in published patent application WO 2004/054529 (The Procter + Gamble Company). The polymeric material may also be mixed with other calcium sequestering agents such as polyphosphates as described and referred to in PCT/EP2004/010629.
Preferred polymeric materials comprising a phosphonate group are azacycloheptane diphosphonate and ethanehydroxy bisphosphonate.
When high levels of soluble calcium-sequestering agents are used in a formulation, there is often a certain amount of undissolved solids in the formulation. Any undissolved calcium-sequestering agent in compositions of the present invention will thus during use dissolve rapidly and provide a cleaning effect in its dissolved state.
The soluble calcium-sequestering agent may be present in a proportion 1-20 wt %, preferably 2-15 wt%, more preferably 5-15 wt% of the dentifrice composition. By using a proportion of the calcium-sequestering agent in the composition below the solubility limit thereof a gel or liquid compositions may be provided in which the calcium sequestering agent is in solution, so that the gel or liquid may include no undissolved solid particles, and may be a clear gel or liquid.
The composition may include a fluoride ion source. Fluoride ion may stabilise polyphosphates in the mouth. For a composition for use in cleaning natural teeth the inclusion of a fluoride ion source is also desirable because of its caries protection activity, but for a composition for use in cleaning artificial dentures such activity is not necessary. The fluoride ion source may be provided by an alkali metal fluoride, preferably sodium fluoride, an alkali metal monofluorophosphate, stannous fluoride and the like. Preferably, however, the fluoride ion source is an alkali metal fluoride, most preferably sodium fluoride. The fluoride ion source serves in a known manner for caries protection. Preferably, the fluoride ion source will be used in an amount to provide an anti-caries effective amount and a phosphatase enzyme inhibiting amount, such as an amount sufficient to provide from about 25 ppm to about 3500 ppm, preferably about 1100 ppm, as fluoride ion. For example the formulation may contain 0.1 - 0.5 wt % of an alkali metal fluoride such as sodium fluoride.
Preferably the pH of the composition is from 6 to 10.5, more preferably from 7 to 9.5. Typically the composition may contain up to 0.5 wt.% of sodium hydroxide to provide a suitable pH.
In compositions of the present invention i.e. those which can be extruded onto a toothbrush, the orally acceptable vehicle may be of a generally conventional composition e.g. comprising a thickening agent, a binding agent and a humectant. Preferred binding agents include for example natural and synthetic gums such as xanthan gums, carageenans, alginates, cellulose ethers and esters. Preferred humectants include glycerin, sorbitol, propylene glycol and polyethylene glycol. A preferred humectant system consists of glycerin, sorbitol and polyethylene glycol.
In addition, the orally acceptable vehicle may optionally comprise one or more surfactant, sweetening agent, flavouring agent, anticaries agent (in addition to the fluoride ion source), anti-plaque agent, anti-bacterial agent such as triclosan or cetyl pyridinium chloride, tooth desensitizing agent, colouring agents and pigment. Useful surfactants include the water-soluble salts of alkyl sulphates having from 10 to 18 carbon atoms in the alkyl moiety, such as sodium lauryl sulphate, but other anionic surfactants as well as non-ionic, zwitterionic, cationic and amphoteric surfactants may also be used.
If an aqueous orally acceptable vehicle is employed, a toothpaste composition of the present invention suitably contains from about 10 to about 80 wt % humectant such as sorbitol, glycerin, polyethylene glycol or xylitol; from about 0.25 to about 5 wt % detergent; from 0 to about 2 wt % sweetener and flavouring agents; together with water and an effective amount of binding and thickening agents, such as from about 0.1 to about 15 wt %, to provide the toothpaste of the invention with the desired stability and flow characteristics. It is preferred to use a thickening silica as the thickening agent. So called "thickening silicas" are known silicas which have relatively little abrasive effect compared with known abrasive silicas such as Zeodent 113™, but provide a thickening effect on the composition. Suitable thickening silicas are known and include those marketed by Huber under the tradename Zeodent, e.g. Zeodent 167, by Degussa AG under the trade name SDDENT®, e.g. SE)ENT 22S®, and by Grace-Davison Chemical Division under the trade name SYLOBLANC®, e.g. SYLOBLANC 15®, respectively. For example the composition may contain up to ca. 20wt % of a thickening silica, typically 5-15 wt %.
The composition of the invention may contain an abrasive material, for example known types of "abrasive silica" commonly used in toothpaste compositions e.g. Zeodent 113™ as mentioned above. However to achieve the RDA below 30 it is preferred to include as little of this type of abrasive material as possible, preferably less than 5 wt.%, more preferably less than 2 wt.% abrasive, most preferably 0 wt.% abrasive material, in addition to any mild abrasive effect produced by other solid particles in the composition, e.g. undissolved calcium sequestering agent and e.g. any thickening silica present. For the purposes of this invention an abrasive material may be defined as a material having an RDA of 30 or above. Larger amounts of silica may be incorporated, more typical of abrasive silica incorporation levels in toothpastes (up to e.g. 25%), if that silica has an RDA below 30.
Regarding the RDA values given in the preceding paragraph, it should be noted that the slurry conditions used to determine the RDA of an abrasive raw material differ from those used to determine the RDA of a formulated toothpaste. The slurry conditions for a raw material are 1Og abrasive plus 50ml of a 0.5% carboxymethyl cellulose slurry in 10% glycerin, whereas the slurry conditions for a formulated toothpaste are 25g toothpaste plus 40ml water. Care should therefore be taken when comparing RDA figures for abrasives as raw materials with RDA figures for fully formulated toothpastes.
Therefore a preferred dentifrice composition of this invention comprises as a soluble calcium sequestering agent that is not an oxidising agent, a polymeric material comprising a phosphonate group wherein the composition has an RDA value of below 30 and an IVSR value greater than 50 (when compared to a Control) and an orally acceptable vehicle, wherein the calcium sequestering agent is present in a proportion 1-20 wt %, preferably 5-10 wt % of the composition, with 0 - 5 wt %, preferably 0 wt % of an abrasive, typically an abrasive silica. The dentifrice composition may be presented as either a single or dual phase composition.
Suitably the composition is in the form of a conventional toothpaste-type composition that can be squeezed from a collapsible tube. It is also suitable for dispensing from a pressurised aerosol container.
Toothpaste-type compositions according to the present invention may be prepared by admixing according to conventional practice the calcium sequestering agent, and the fluoride ion source if present, with the orally acceptable dental vehicle, which may be anhydrous but is preferably an aqueous orally acceptable dental vehicle, to form a storage-stable semi-solid extrudable material useful as a dentifrice. The composition of the invention will now be described by way of non-limiting examples only.
Table 1. Examples of the present invention
Figure imgf000008_0001
Example 1 is a formulation in which the calcium-sequestering chemical cleaning system is azacycloheptane diphosphonate. Thickening silica is increased to account for the lower level of solids in the formulation. Other calcium sequestering agents may be used as chemical cleaning agent and/or anticaries agent.

Claims

1. A dentifrice composition comprising as a soluble calcium sequestering agent that is not an oxidising agent, a polymeric material comprising a phosphonate group wherein the composition has an RDA value of below 30 and an IVSR value greater than 50 (when compared to a Control), and an orally acceptable vehicle, wherein the calcium sequestering agent is present in a proportion of 1- 20 wt % and an abrasive is present in a proportion of 0-5 wt % of the composition.
2. A dentifrice composition according to claim 1, further comprising an abrasive silica that has an RDA below 30.
3. A dentifrice composition according to claim 2, wherein the RDA value is below 20 and the IVSR value is up to 250.
4. A dentifrice composition according to claim 3, wherein the calcium sequestering agent is present in an amount of from 2-15 wt % of the composition.
5. A dentifrice composition according to claim 4, wherein 0 wt% of the abrasive is present in the composition.
6. .A dentifrice composition according to claim 5, wherein the IVSR value is measured relative to a Control dentifrice containing 14% Zeodent 113 abrasive silica in a conventional base containing water, sorbitol, glycerin, PEG, flavour, SLS, sodium saccharin, Xanthum gum and sodium fluoride.
7. A dentifrice composition according to any one of the above claims for use in treating natural teeth or a dental prosthetic.
8. A dentifrice composition according to any one of the above claims in the form of a viscous extrudable fluid which can be provided in a collapsible container.
PCT/EP2006/002667 2005-03-21 2006-03-17 Dentifrice compositions comprising as a soluble calcium sequestring agent a derivative comprising a phosphonate group WO2006100073A1 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
BRPI0609712-0A BRPI0609712A2 (en) 2005-03-21 2006-03-17 toothpaste composition
US11/909,207 US20080175799A1 (en) 2005-03-21 2006-03-17 Dentifrice Compositions Comprising as a Soluble Calcium Sequestering Agent a Derivative Comprising a Phosphonate Group
CA002602401A CA2602401A1 (en) 2005-03-21 2006-03-17 Dentifrice compositions comprising as a soluble calcium sequestring agent a derivative comprising a phosphonate group
EP06723658A EP1863575A1 (en) 2005-03-21 2006-03-17 Dentifrice compositions comprising as a soluble calcium sequestring agent a derivative comprising a phosphonate group
AU2006226507A AU2006226507A1 (en) 2005-03-21 2006-03-17 Dentifrice compositions comprising as a soluble calcium sequestring agent a derivative comprising a phosphonate group
JP2008502327A JP2008533184A (en) 2005-03-21 2006-03-17 Dentifrice composition comprising a derivative having a phosphonic acid group as a soluble calcium scavenger
MX2007011686A MX2007011686A (en) 2005-03-21 2006-03-17 Dentifrice compositions comprising as a soluble calcium sequestring agent a derivative comprising a phosphonate group.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB0505758.3 2005-03-21
GBGB0505758.3A GB0505758D0 (en) 2005-03-21 2005-03-21 Novel compositions

Publications (1)

Publication Number Publication Date
WO2006100073A1 true WO2006100073A1 (en) 2006-09-28

Family

ID=34531589

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2006/002667 WO2006100073A1 (en) 2005-03-21 2006-03-17 Dentifrice compositions comprising as a soluble calcium sequestring agent a derivative comprising a phosphonate group

Country Status (11)

Country Link
US (1) US20080175799A1 (en)
EP (1) EP1863575A1 (en)
JP (1) JP2008533184A (en)
AU (1) AU2006226507A1 (en)
BR (1) BRPI0609712A2 (en)
CA (1) CA2602401A1 (en)
GB (1) GB0505758D0 (en)
MX (1) MX2007011686A (en)
RU (1) RU2007135124A (en)
WO (1) WO2006100073A1 (en)
ZA (1) ZA200708052B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070122357A1 (en) * 2005-11-29 2007-05-31 The Procter & Gamble Company Dentifrice composition

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1421064A (en) * 1973-03-09 1976-01-14 Procter & Gamble Oral compositions for calculus retardation
US4575456A (en) * 1984-11-30 1986-03-11 Colgate-Palmolive Company Gel dentifrice of desirable consistency
EP0236827A2 (en) * 1986-03-07 1987-09-16 Blendax GmbH Toothpaste
EP0341662A2 (en) * 1988-05-09 1989-11-15 The B.F. Goodrich Company Tartar inhibiting oral compositions and method
US4996042A (en) * 1987-05-04 1991-02-26 Blendax Gmbh Toothpaste
US5849267A (en) * 1997-05-20 1998-12-15 Colgate-Palmolive Company Stable desensitizing antitartar dentifrice
WO2004054529A1 (en) * 2002-12-13 2004-07-01 The Procter & Gamble Company Method of protecting teeth against erosion

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2343196C3 (en) * 1973-08-27 1980-01-10 Henkel Kgaa, 4000 Duesseldorf Aiacycloalkan-2 ^ -diphosphonic acids or their water-soluble salts
US5302375A (en) * 1992-11-19 1994-04-12 Colgate-Palmolive Company Oral composition having improved tooth whitening effect
MY136424A (en) * 2002-07-23 2008-09-30 Glaxo Group Ltd Aerosol dentifrice formulation
DE10311171A1 (en) * 2003-03-12 2004-09-23 Henkel Kgaa Oral and dental care composition with antitartar, antiplaque and anti-discoloration action, containing cationic antibacterial agent, aza-cycloalkane-diphosphonic acid and xanthan gum or carboxymethyl cellulose

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1421064A (en) * 1973-03-09 1976-01-14 Procter & Gamble Oral compositions for calculus retardation
US4575456A (en) * 1984-11-30 1986-03-11 Colgate-Palmolive Company Gel dentifrice of desirable consistency
EP0236827A2 (en) * 1986-03-07 1987-09-16 Blendax GmbH Toothpaste
US4996042A (en) * 1987-05-04 1991-02-26 Blendax Gmbh Toothpaste
EP0341662A2 (en) * 1988-05-09 1989-11-15 The B.F. Goodrich Company Tartar inhibiting oral compositions and method
US5849267A (en) * 1997-05-20 1998-12-15 Colgate-Palmolive Company Stable desensitizing antitartar dentifrice
WO2004054529A1 (en) * 2002-12-13 2004-07-01 The Procter & Gamble Company Method of protecting teeth against erosion

Also Published As

Publication number Publication date
CA2602401A1 (en) 2006-09-28
AU2006226507A1 (en) 2006-09-28
JP2008533184A (en) 2008-08-21
MX2007011686A (en) 2007-11-15
US20080175799A1 (en) 2008-07-24
BRPI0609712A2 (en) 2011-10-18
EP1863575A1 (en) 2007-12-12
RU2007135124A (en) 2009-04-27
GB0505758D0 (en) 2005-04-27
ZA200708052B (en) 2008-11-26

Similar Documents

Publication Publication Date Title
EP2753292B1 (en) Tooth remineralizing dentifrice
JPH09503506A (en) Oral composition
JPH0784374B2 (en) Anti-tartar toothpaste
US10285921B2 (en) Dentrifrice compositions having dental plaque mitigation or improved fluoride uptake
MX2010012386A (en) Oral compositions and uses thereof.
CA2946054C (en) Dentifrice compositions having dental plaque mitigation or improved fluoride uptake
WO2012047781A1 (en) Multi-purposed dentifrice
ZA200602359B (en) A dentifrice composition comprising a soluble calcium sequestering agent
JP2007527867A (en) Prevention of crystal formation in toothpaste
WO2002002060A2 (en) Oral compositions
US20080175799A1 (en) Dentifrice Compositions Comprising as a Soluble Calcium Sequestering Agent a Derivative Comprising a Phosphonate Group
CN113038992A (en) Oral care compositions comprising charcoal
CA2334623C (en) Clear dentrifrice gels
KR20000007808A (en) Whitening toothpaste composition
WO2024104743A1 (en) Oral care composition
WO2022184874A1 (en) Oral care composition
GB2413493A (en) Oral hygiene composition
MXPA06004261A (en) Prevention of crystal formation in toothpaste

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 561698

Country of ref document: NZ

Ref document number: 2006226507

Country of ref document: AU

Ref document number: 2008502327

Country of ref document: JP

WWE Wipo information: entry into national phase

Ref document number: 2602401

Country of ref document: CA

Ref document number: 11909207

Country of ref document: US

WWE Wipo information: entry into national phase

Ref document number: MX/a/2007/011686

Country of ref document: MX

NENP Non-entry into the national phase

Ref country code: DE

WWE Wipo information: entry into national phase

Ref document number: 07104796

Country of ref document: CO

WWE Wipo information: entry into national phase

Ref document number: 2006723658

Country of ref document: EP

ENP Entry into the national phase

Ref document number: 2006226507

Country of ref document: AU

Date of ref document: 20060317

Kind code of ref document: A

WWP Wipo information: published in national office

Ref document number: 2006226507

Country of ref document: AU

WWE Wipo information: entry into national phase

Ref document number: 2007135124

Country of ref document: RU

WWP Wipo information: published in national office

Ref document number: 2006723658

Country of ref document: EP

ENP Entry into the national phase

Ref document number: PI0609712

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20070920