WO2001037797A1 - Toothpaste - Google Patents

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Publication number
WO2001037797A1
WO2001037797A1 PCT/GB2000/004488 GB0004488W WO0137797A1 WO 2001037797 A1 WO2001037797 A1 WO 2001037797A1 GB 0004488 W GB0004488 W GB 0004488W WO 0137797 A1 WO0137797 A1 WO 0137797A1
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WO
WIPO (PCT)
Prior art keywords
alumina
toothpaste
abrasive
abrasivity
surface area
Prior art date
Application number
PCT/GB2000/004488
Other languages
French (fr)
Inventor
Kevin John Wills
Iain Stewart Duncan
Original Assignee
Alcan International 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 Alcan International Limited filed Critical Alcan International Limited
Priority to AU15365/01A priority Critical patent/AU1536501A/en
Priority to KR1020027006701A priority patent/KR20020069192A/en
Priority to EP00977730A priority patent/EP1231891B1/en
Priority to DE60013887T priority patent/DE60013887T2/en
Priority to DE1231891T priority patent/DE1231891T1/en
Priority to US10/111,179 priority patent/US6682717B1/en
Priority to AT00977730T priority patent/ATE275928T1/en
Priority to CA002387315A priority patent/CA2387315A1/en
Priority to JP2001539413A priority patent/JP2003514838A/en
Priority to DK00977730T priority patent/DK1231891T3/en
Publication of WO2001037797A1 publication Critical patent/WO2001037797A1/en

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Classifications

    • 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
    • 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
    • A61K8/26Aluminium; Compounds thereof

Definitions

  • Dentifrice any substance or combination of substances specially prepared for the public for cleaning the accessible surfaces of teeth.
  • Toothpaste any semi-solid dentifrice preparation presented in the form of a paste, cream or gel.
  • Toothpaste invariably contains an abrasive powder for cleaning purposes.
  • the cleaning and abrasive properties of the toothpaste depend on the concentration of the powder, on the Moh's hardness of the abrasive, and on the shape and particle size and size distribution of the powder.
  • the cleaning effect of toothpaste concerns its effectiveness in removing adventitious stains and other deposits from the surface of teeth and other parts of oral cavity.
  • the abrasive effect or abrasivity concerns undesired removal of surface components of teeth including enamel and dentine, and undesired damage in the oral cavity.
  • a toothpaste having a high cleaning effect generally has a rather high abrasivity, and vice versa.
  • ISO1 1609 provides methods for testing abrasivity and sets limits on dentifrices marketed in Europe.
  • An earlier British standard BS5136 of 1981 also sets limits on abrasivity by comparison with a standard reference toothpaste, which is also used as a reference in ISO1 1609, and which has the formulation:-
  • Abrasive powders used or contemplated for use in toothpaste formulations include silicas, including gels and precipitates, sodium bicarbonate, calcium and magnesium carbonates, calcium phosphates, alumina and hydrates thereof, alummosilicates, aluminium and magnesium silicates, and thermosetting urea-formaldehyde and other plastics materials.
  • silicas including gels and precipitates, sodium bicarbonate, calcium and magnesium carbonates, calcium phosphates, alumina and hydrates thereof, alummosilicates, aluminium and magnesium silicates, and thermosetting urea-formaldehyde and other plastics materials.
  • GB-A-2155333 teaches the use of calcium hydrogenphosphate anhydride and an aluminium oxide having an average particle size of 0.5 ⁇ m to 10 ⁇ m.
  • the alumina has a high ⁇ -content, as measured by X-ray diffraction.
  • WO-A-95/33441 teaches the use of cationically charged colloids of a metal compound.
  • the colloid has a particle size of 0.001 ⁇ m to 0.2 ⁇ m.
  • GB-A-2037162 and GB-A-2009596 disclose the use of hydrated aluminas in dentifrice products.
  • alumina is sometimes loosely used to cover a number of aluminium oxide, oxide hydroxide and trihydroxide compounds.
  • the correct designations and some crystalline phases are shown below:
  • This invention is concerned with alumina that is essentially Corundum.
  • Corundum is produced by calcination of aluminium trihydroxides and oxide hydroxides.
  • a number of forms of alumina (often described as activated aluminas) are produced before corundum is formed.
  • Another form of alumina chemical is aluminium hydroxide gel, which is often formed by the neutralisation of an aluminium salt solution.
  • the invention provides a toothpaste comprising as an abrasive an alumina in the form of particles having dio below 3.5 ⁇ m, d 50 below 1.0 ⁇ m, and specific surface area below 6m 2 /g.
  • alumina as an abrasive in toothpaste, wherein the alumina is in the form of particles having d 10 below 3.5 ⁇ m, d 50 below 1.0 ⁇ m, and a specific surface area below 6m 2 /g.
  • alumina as a whitening agent in toothpaste, wherein the alumina is in the form of particles having dio below 3.5 ⁇ m, d 50 below 1.O ⁇ m, and a specific surface area below 6m 2 /g.
  • the alumina may serve the purpose of replacing titania or the like in conventional products, thus resulting in a cost saving.
  • the surface area is measured by the following method.
  • a sample of alumina of sufficient weight to give an estimated surface area of about 0.5 to 25m 2 is degassed in a Micrometrics Desorb 2300B at about 150°C until a stable reading is obtained.
  • the sample is then transferred to a Micrometrics Flowsorb II 2300, cooled and immersed in a mixture of 30% N and 70% He gas.
  • the total amount of N absorbed is measured from the change in thermal conductivity of the gas mixture preferably during de- sorption as the temperature is raised again to room temperature. Surface area per gram is then calculated from the total gas absorbed and the weight of the sample.
  • the particle size is measured as follows. Particle size distribution of a sample of alumina is measured in a Sedigraph 5100 instrument supplied by Micrometrics Products.
  • the abrasive is preferably an anhydrous alumina, generally a calcined alumina or alternatively a tabular or fused alumina. Calcination is effected at a temperature of at least 900°C. Higher calcination temperatures result in harder products.
  • the alumina used in this invention is preferably fairly hard, such as may be obtained by calcination at above 1000°C.
  • the alumina in this invention is an ⁇ - alumina.
  • the ⁇ content is greater than 90%, preferably greater than 93%, even more preferably greater than 95% as measured by X-ray diffraction. In a preferred embodiment, the ⁇ -content is less than 1 %.
  • the abrasive is used in the form of particles having dio below
  • the alumina abrasive is a sub-micron product, having d 50 of 0.1-1.0 ⁇ m.
  • the alumina abrasive has a relatively narrow particle size distribution, e.g. with dio being no greater than four times d 50 .
  • the alumina abrasive has a specific surface area below 6m 2 /g, preferably in the range of 4.5-5.0 m 2 /g.
  • the specific surface area is related to the aforesaid parameters of hardness (harder products have lower specific surface areas) and particle size (more finely divided products have larger specific surface areas).
  • Alumina products of the kind described are readily available commercially, for they are produced in substantial quantities mainly for use in refractories and ceramics. Grinding may conveniently be effected by fluid energy or vibratory milling (micronising) or preferably by ball milling.
  • an abrasive powder has excellent stain removal properties in one toothpaste, it is generally the case that it will be found to have excellent stain removal properties in others.
  • the abrasivity of a toothpaste does depend to a significant extent on the whole formulation, and not merely on the nature and concentration of the abrasive present in it, nevertheless an abrasive which shows high or low abrasivity in one toothpaste formulation may generally be expected to show correspondingly high or low abrasivity in others.
  • the alumina abrasive is preferably present in the toothpaste at a concentration of 1-15% w/w, preferably higher than 2%, even more preferably higher than 3%, e.g. 3-12% w/w. Toothpastes include a wide variety of components in a wide variety of concentrations. The alumina should be compatible with other ingredients. The following list is intended to be exemplary rather than definitive or restrictive.
  • Toothpastes are generally water-based.
  • a binder or thickener is generally present.
  • suitable materials are carboxyvinyl polymers, carrageenan, hydroxyethyl cellulose and water soluble salts of cellulose ethers such as sodium carboxymethylcellulose and sodium carboxymethyl hydroxyethyl cellulose.
  • Natural gums and colloidal silica or silicate materials can also be used.
  • Binders or thickeners are generally present in an amount from about 0.15 to about 5.0% w/w of the total composition.
  • a humectant is also generally used to keep the formulation from hardening on exposure to air.
  • suitable humectants are glycerine, sorbitol, xylitol, polyethylene glycols and propylene glycol.
  • Humectants are generally present in an amount from about 10% to about 70% w/w of the weight of the composition.
  • One or more particulate materials regarded as abrasives or abrasive polishers or fillers, are also present.
  • the alumina abrasive described above is one such, but others may also be present as noted above. Examples are:
  • Silicas including gels and precipitates, sodium bicarbonate, calcium and magnesium carbonates, dicalcium phosphate dihydrate, alumina and hydrates thereof, aluminosilicates, aluminium and magnesium silicates, and thermosetting urea-formaldehyde and other plastics materials. It is preferred that the alumina is not present in combination with calcium hydrogenphosphate anhydride.
  • Abrasives are generally present at a level of about 10% to about 70%, preferably from about 15% to about 25%, w/w of the formulation.
  • a source of fluoride ion is preferably provided. Regulatory authorities in various countries may stipulate a maximum and/or a minimum total fluoride ion concentration.
  • compositions include sweeteners, flavours, colours, peroxides or other bleaching agents, anti-calculus agents, anti-plaque agents, anti-bacterial agents, preservatives and effervescence generators.
  • Toothpaste may be manufactured by conventional techniques.
  • the alumina abrasives with which this invention is concerned are rather easy to incorporate for, unlike some other abrasive powders, they are generally not prone to lumping.
  • the alumina abrasives used in the experimental section below are either commercial products or development products (designated BAX) available from Alcan Chemicals Limited, and are here identified by means of their trade names. This invention is based on the discovery that the development product BAX842 has unexpectedly and outstandingly good properties.
  • silica-based toothpaste was used.
  • the formulation was as shown in Table 1.
  • samples were subjected to an in-vitro test developed and performed by the Health Science Research Centre at Indiana University - Purdue University. This test involves staining teeth using a broth containing instant coffee, instant tea, gastric mucin3 and a micrococcus leteus culture. The colour of the stained teeth is measured using a Minolta colourmeter. The teeth are then brushed with the toothpaste and the colour measured. A measurement of stain removal is then calculated.
  • the enamel abrasivity (Designated REA) was measured by Missouri Analytical Laboratories, using a method described by R J Grabenstetter et al. (J D Res. Vol. 37, Nov-Dec 1958, No. 6, pages 1060- 8).

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Oral & Maxillofacial Surgery (AREA)
  • Cosmetics (AREA)
  • Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)

Abstract

There is disclosed a toothpaste comprising as an abrasive an alumina in the form of particles having d10 below 3.5νm, d50 below 1.0νm and a specific surface area below 6m2/g.

Description

TOOTHPASTE
International standard ISO11609 of 1995 contains the following definitions:-
Dentifrice: any substance or combination of substances specially prepared for the public for cleaning the accessible surfaces of teeth.
Toothpaste: any semi-solid dentifrice preparation presented in the form of a paste, cream or gel.
This invention is concerned with toothpaste. Toothpaste invariably contains an abrasive powder for cleaning purposes. The cleaning and abrasive properties of the toothpaste depend on the concentration of the powder, on the Moh's hardness of the abrasive, and on the shape and particle size and size distribution of the powder. The cleaning effect of toothpaste concerns its effectiveness in removing adventitious stains and other deposits from the surface of teeth and other parts of oral cavity. The abrasive effect or abrasivity concerns undesired removal of surface components of teeth including enamel and dentine, and undesired damage in the oral cavity. A toothpaste having a high cleaning effect generally has a rather high abrasivity, and vice versa. ISO1 1609 provides methods for testing abrasivity and sets limits on dentifrices marketed in Europe. An earlier British standard BS5136 of 1981 also sets limits on abrasivity by comparison with a standard reference toothpaste, which is also used as a reference in ISO1 1609, and which has the formulation:-
Precipitated calcium carbonate 40%w/w. Glycol 25% w/w
Sodium carboxymethylcellulose 1.40% w/w Dodecyl sodium sulphate 1.00% w/w
Sodium silicate (80° TW of approximately pH 7) 0.05% w/w
Saccharin sodium 0.15% w/w
Formalin (40% (m/m) formaldehyde) 0.10 w/w Peppermint flavouring 0.80% w/w
Water 33.05% w/w
Abrasive powders used or contemplated for use in toothpaste formulations include silicas, including gels and precipitates, sodium bicarbonate, calcium and magnesium carbonates, calcium phosphates, alumina and hydrates thereof, alummosilicates, aluminium and magnesium silicates, and thermosetting urea-formaldehyde and other plastics materials. There is a need in the industry for an abrasive for inclusion in toothpaste formulations, which provides good cleaning properties, in particular stain removal, while showing relatively low abrasivity. In particular, there is a need for an abrasive which can be incorporated in a concentration large enough to provide an excellent cleaning effect in a toothpaste with low abrasivity which nevertheless complies with the abrasivity requirements of the above-stated standard specifications. This invention addresses that need. US 3957968 teaches the use of flat flakes of α-aluminium oxide in toothpaste. The flakes have a median particle size of 2 to 7 μm. US 4060599 discloses the use of a finer aluminium oxide (median 1 to 2μm) and specifically uses Reynolds RC152DBM which has a median size of around 1.7μm. US 4632826 teaches the use of a weakly calcined alumina polishing agent. This polishing agent consists of 10% to 50% by weight γ aluminium oxide and 50% to 90% by weight α aluminium oxide.
GB-A-2155333 teaches the use of calcium hydrogenphosphate anhydride and an aluminium oxide having an average particle size of 0.5μm to 10μm. The alumina has a high α-content, as measured by X-ray diffraction. WO-A-95/33441 teaches the use of cationically charged colloids of a metal compound. The colloid has a particle size of 0.001 μm to 0.2μm.
GB-A-2037162 and GB-A-2009596 disclose the use of hydrated aluminas in dentifrice products.
The phrase "alumina" is sometimes loosely used to cover a number of aluminium oxide, oxide hydroxide and trihydroxide compounds. The correct designations and some crystalline phases are shown below:
Mineral Name Chemical Composition Accepted
Crvstalloqraphic and Chemical Designation
Gibbsite Aluminium trihydroxide γ - AI(OH)3
Bayerite Aluminium trihydroxide α - AI(OH)3
Nordstrandite Aluminium trihydroxide AI(OH)3
Boehmite Aluminium oxide hydroxide γ - AIOOH
Diaspore Aluminium oxide hydroxide α - AIOOH
Corundum Aluminium oxide α - AI2O3
This invention is concerned with alumina that is essentially Corundum. Corundum is produced by calcination of aluminium trihydroxides and oxide hydroxides. Depending on the form of aluminium trihydroxide and oxide hydroxide starting material, a number of forms of alumina (often described as activated aluminas) are produced before corundum is formed. Another form of alumina chemical is aluminium hydroxide gel, which is often formed by the neutralisation of an aluminium salt solution. The invention provides a toothpaste comprising as an abrasive an alumina in the form of particles having dio below 3.5μm, d50 below 1.0μm, and specific surface area below 6m2/g.
According to a further aspect of the present invention, there is provided the use of alumina as an abrasive in toothpaste, wherein the alumina is in the form of particles having d10 below 3.5μm, d50 below 1.0μm, and a specific surface area below 6m2/g.
According to a further aspect of the present invention, there is provided the use of alumina as a whitening agent in toothpaste, wherein the alumina is in the form of particles having dio below 3.5μm, d50 below 1.Oμm, and a specific surface area below 6m2/g. In this way the alumina may serve the purpose of replacing titania or the like in conventional products, thus resulting in a cost saving.
The surface area is measured by the following method. A sample of alumina of sufficient weight to give an estimated surface area of about 0.5 to 25m2 is degassed in a Micrometrics Desorb 2300B at about 150°C until a stable reading is obtained. The sample is then transferred to a Micrometrics Flowsorb II 2300, cooled and immersed in a mixture of 30% N and 70% He gas. The total amount of N absorbed is measured from the change in thermal conductivity of the gas mixture preferably during de- sorption as the temperature is raised again to room temperature. Surface area per gram is then calculated from the total gas absorbed and the weight of the sample.
The particle size is measured as follows. Particle size distribution of a sample of alumina is measured in a Sedigraph 5100 instrument supplied by Micrometrics Products.
The abrasive is preferably an anhydrous alumina, generally a calcined alumina or alternatively a tabular or fused alumina. Calcination is effected at a temperature of at least 900°C. Higher calcination temperatures result in harder products. The alumina used in this invention is preferably fairly hard, such as may be obtained by calcination at above 1000°C. The alumina in this invention is an α - alumina. Preferably, the α content is greater than 90%, preferably greater than 93%, even more preferably greater than 95% as measured by X-ray diffraction. In a preferred embodiment, the γ-content is less than 1 %. The abrasive is used in the form of particles having dio below
3.5μm, preferably below 2.5 μm. (dio, d5o and d90 are used in conventional manner to indicate that 10, 50 or 90 wt % of the product has a particle size above the stated value). Preferably, the alumina abrasive is a sub-micron product, having d50 of 0.1-1.0 μm. Preferably the alumina abrasive has a relatively narrow particle size distribution, e.g. with dio being no greater than four times d50.
The alumina abrasive has a specific surface area below 6m2/g, preferably in the range of 4.5-5.0 m2/g. The specific surface area is related to the aforesaid parameters of hardness (harder products have lower specific surface areas) and particle size (more finely divided products have larger specific surface areas).
Alumina products of the kind described are readily available commercially, for they are produced in substantial quantities mainly for use in refractories and ceramics. Grinding may conveniently be effected by fluid energy or vibratory milling (micronising) or preferably by ball milling. When an abrasive powder has excellent stain removal properties in one toothpaste, it is generally the case that it will be found to have excellent stain removal properties in others. Although the abrasivity of a toothpaste does depend to a significant extent on the whole formulation, and not merely on the nature and concentration of the abrasive present in it, nevertheless an abrasive which shows high or low abrasivity in one toothpaste formulation may generally be expected to show correspondingly high or low abrasivity in others.
The alumina abrasive is preferably present in the toothpaste at a concentration of 1-15% w/w, preferably higher than 2%, even more preferably higher than 3%, e.g. 3-12% w/w. Toothpastes include a wide variety of components in a wide variety of concentrations. The alumina should be compatible with other ingredients. The following list is intended to be exemplary rather than definitive or restrictive.
Toothpastes are generally water-based. A binder or thickener is generally present. Examples of suitable materials are carboxyvinyl polymers, carrageenan, hydroxyethyl cellulose and water soluble salts of cellulose ethers such as sodium carboxymethylcellulose and sodium carboxymethyl hydroxyethyl cellulose. Natural gums and colloidal silica or silicate materials can also be used. Binders or thickeners are generally present in an amount from about 0.15 to about 5.0% w/w of the total composition.
A humectant is also generally used to keep the formulation from hardening on exposure to air. Examples of suitable humectants are glycerine, sorbitol, xylitol, polyethylene glycols and propylene glycol. Humectants are generally present in an amount from about 10% to about 70% w/w of the weight of the composition.
One or more particulate materials, regarded as abrasives or abrasive polishers or fillers, are also present. The alumina abrasive described above is one such, but others may also be present as noted above. Examples are:
Silicas, including gels and precipitates, sodium bicarbonate, calcium and magnesium carbonates, dicalcium phosphate dihydrate, alumina and hydrates thereof, aluminosilicates, aluminium and magnesium silicates, and thermosetting urea-formaldehyde and other plastics materials. It is preferred that the alumina is not present in combination with calcium hydrogenphosphate anhydride.
Abrasives are generally present at a level of about 10% to about 70%, preferably from about 15% to about 25%, w/w of the formulation. A source of fluoride ion is preferably provided. Regulatory authorities in various countries may stipulate a maximum and/or a minimum total fluoride ion concentration.
Other components which may also be included in toothpaste formulations in accordance with conventional practice, include sweeteners, flavours, colours, peroxides or other bleaching agents, anti-calculus agents, anti-plaque agents, anti-bacterial agents, preservatives and effervescence generators.
Toothpaste may be manufactured by conventional techniques. The alumina abrasives with which this invention is concerned are rather easy to incorporate for, unlike some other abrasive powders, they are generally not prone to lumping.
Here is an example of a toothpaste formulation:-
Dicalcium phosphate 40% w/w Alumina 10%
Sorbitol 25%
Polyethylene glycol 2%
Carboxymethylcellulose 1.1%
Sodium Saccharin 0.2% Sodium Lauryl Sulphate 1.5%
Benzoic Acid 0.15%
Sodium Benzoate 0.2%
Water 19.5%
This formulation based on dicalcium phosphate polishing agent/filler, has been used to test the properties of various alumina abrasives. In the experimental section below, a different formulation based on a silica polishing agent/filler was used. Although the results obtained with the two formulations were different in absolute terms, they were generally the same in relative terms, i.e. any particular alumina abrasive generally had the same or a similar effect on the properties of both formulations. This justifies the assertion that an abrasive showing valuable properties in one toothpaste may reasonably be expected to show corresponding valuable properties in others.
The alumina abrasives used in the experimental section below are either commercial products or development products (designated BAX) available from Alcan Chemicals Limited, and are here identified by means of their trade names. This invention is based on the discovery that the development product BAX842 has unexpectedly and outstandingly good properties.
EXAMPLE 1
In this example, a silica-based toothpaste was used. The formulation was as shown in Table 1.
Table 1 Silica-based toothpaste formulation
Figure imgf000009_0001
The alumina products used in this example are given in Table 2. Table 2
Figure imgf000010_0001
For stain removal, samples were subjected to an in-vitro test developed and performed by the Health Science Research Centre at Indiana University - Purdue University. This test involves staining teeth using a broth containing instant coffee, instant tea, gastric mucin3 and a micrococcus leteus culture. The colour of the stained teeth is measured using a Minolta colourmeter. The teeth are then brushed with the toothpaste and the colour measured. A measurement of stain removal is then calculated.
The enamel abrasivity (Designated REA) was measured by Missouri Analytical Laboratories, using a method described by R J Grabenstetter et al. (J D Res. Vol. 37, Nov-Dec 1958, No. 6, pages 1060- 8).
The abrasivity and stain removal results are shown in Table 3. Table 3 Abrasivity and stain removal results
Figure imgf000011_0001
Discussion The comparative performance of the aluminas in terms of abrasivity (REA value) and stain removal is shown in Figure 1. BAX 842 is outstanding.
The relationship between particle size dio and enamel abrasivity is shown in Figure 2. For the ball milled products, it can be seen in Figure 2 that there is a linear relationship (R2 = 0.96, equation y =
18.985x + 25.109) between REA value and d10 with REA falling as the dio decreases. BAX842 does not fit this linear relationship as the abrasivity is much less than would be expected for its dio, i.e. for a d10 value of 2.35μm, the linear regression equation calculates an enamel abrasivity of 69 versus 46 obtained with BAX842. There is no relationship between enamel abrasivity and dio for the micronised aluminas. The relationship between stain removal and dι0 for the ball milled and micronised aluminas shows significant scatter in performance with no linear relationship.

Claims

1. A toothpaste comprising as an abrasive an alumina in the form of particles having d-io below 3.5 μm, d5o below 1.0μm, and a specific surface area below 6 m2/g.
2. The toothpaste of claim 1 wherein dio is below 2.5 μm.
3. The toothpaste of claim 1 or claim 2 wherein the specific surface area is 4.5-5.0 m2/g.
4. The toothpaste of any one of claims 1 to 3, wherein the particles have d5o of 0.1 -1.0 μm.
5. The toothpaste of claim 4, wherein the ratio of d10 to d50 is not more than 4.0.
6. The toothpaste of any one of claims 1 to 5, wherein the abrasive is present in a proportion of 1-15% w/w.
7. The toothpaste of any one of claims 1 to 6, wherein the alumina is anhydrous.
8. The toothpaste of any one of claims 1 to 7, wherein the alumina is ball-milled.
9. The toothpaste of any one of claims 1 to 8, wherein the alumina is a calcined alumina.
10. The toothpaste of claim 9, wherein the alumina has been calcined at a temperature of at least 900°C.
11. The toothpaste of any one of claims 1 to 10, wherein the alumina has an α content of greater than 90%.
12. The toothpaste of claim 11 , wherein the alumina has an α content of greater than 93%.
13. The use of alumina as an abrasive in toothpaste, wherein the alumina is in the form of particles having dio below 3.5μm, d50 below 1.0μm, and a specific surface area below 6m2/g.
14. The use of alumina as a whitening agent in toothpaste, wherein the alumina is in the form of particles having d10 below 3.5μm, d5o below 1.0μm, and a specific sur ace area below 6m2/g.
PCT/GB2000/004488 1999-11-26 2000-11-27 Toothpaste WO2001037797A1 (en)

Priority Applications (10)

Application Number Priority Date Filing Date Title
AU15365/01A AU1536501A (en) 1999-11-26 2000-11-27 Toothpaste
KR1020027006701A KR20020069192A (en) 1999-11-26 2000-11-27 Toothpaste
EP00977730A EP1231891B1 (en) 1999-11-26 2000-11-27 Toothpaste
DE60013887T DE60013887T2 (en) 1999-11-26 2000-11-27 TOOTHPASTE
DE1231891T DE1231891T1 (en) 1999-11-26 2000-11-27 TOOTHPASTE
US10/111,179 US6682717B1 (en) 1999-11-26 2000-11-27 Toothpaste of selected calcined alumina particles
AT00977730T ATE275928T1 (en) 1999-11-26 2000-11-27 TOOTHPASTE
CA002387315A CA2387315A1 (en) 1999-11-26 2000-11-27 Toothpaste
JP2001539413A JP2003514838A (en) 1999-11-26 2000-11-27 Toothpaste
DK00977730T DK1231891T3 (en) 1999-11-26 2000-11-27 Toothpaste

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GBGB9928057.0A GB9928057D0 (en) 1999-11-26 1999-11-26 Toothpaste
GB9928057.0 1999-11-26

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JP (1) JP2003514838A (en)
KR (1) KR20020069192A (en)
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AU (1) AU1536501A (en)
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BRPI0707046A2 (en) * 2006-03-02 2011-04-12 Unilever Nv toothpaste composition
US9005585B2 (en) 2006-09-29 2015-04-14 The Procter & Gamble Company Oral compositions containing gel networks
US8518381B2 (en) * 2008-03-28 2013-08-27 The Procter & Gamble Company Processes of making oral compositions containing gel networks
GB201005508D0 (en) * 2010-03-31 2010-05-19 Glaxo Group Ltd Novel composition
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AU1536501A (en) 2001-06-04
DE60013887T2 (en) 2005-08-18
GB9928057D0 (en) 2000-01-26
EP1231891A1 (en) 2002-08-21
ES2180465T3 (en) 2005-04-01
JP2003514838A (en) 2003-04-22
DE1231891T1 (en) 2003-03-20
ATE275928T1 (en) 2004-10-15
DE60013887D1 (en) 2004-10-21
ES2180465T1 (en) 2003-02-16
KR20020069192A (en) 2002-08-29
EP1231891B1 (en) 2004-09-15
DK1231891T3 (en) 2004-12-06
US6682717B1 (en) 2004-01-27
CA2387315A1 (en) 2001-05-31

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