WO2003009824A1 - Oral composition comprising peroxyamidophthalamide derivatives - Google Patents

Oral composition comprising peroxyamidophthalamide derivatives Download PDF

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Publication number
WO2003009824A1
WO2003009824A1 PCT/EP2002/006980 EP0206980W WO03009824A1 WO 2003009824 A1 WO2003009824 A1 WO 2003009824A1 EP 0206980 W EP0206980 W EP 0206980W WO 03009824 A1 WO03009824 A1 WO 03009824A1
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WO
WIPO (PCT)
Prior art keywords
formulation
peroxy
oral composition
agents
phthalamide
Prior art date
Application number
PCT/EP2002/006980
Other languages
French (fr)
Inventor
Andrew Joiner
David William Thornthwaite
Philip Christopher Waterfield
Original Assignee
Unilever N.V.
Unilever Plc
Hindustan Lever Ltd
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 Unilever N.V., Unilever Plc, Hindustan Lever Ltd filed Critical Unilever N.V.
Priority to EP02738175A priority Critical patent/EP1408920A1/en
Priority to BR0211663-4A priority patent/BR0211663A/en
Publication of WO2003009824A1 publication Critical patent/WO2003009824A1/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
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/38Percompounds, e.g. peracids

Definitions

  • the invention provides an oral composition with an improved teeth whitening effect, comprising a first formulation comprising an effective amount of a peroxy amido phthalamide having the structural formula: N-(CHR) n -C0 3 H Formula 1
  • This formulation has a pH of 4. pH-adjusting formulation

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

Abstract

An oral composition with an improved teeth whitening effect, comprising a first formulation comprising an effective amount of a peroxy amido phthalamide having the structural formula: in which R is hydrogen or C1-C4 alkyl; n is 1 to 5; and X is C=O or SO2,wherein said first formulation has a pH of from 2 to 6and a second formulation formulated such that when said second formulation is mixed with the first formulation the pH of the mixture is from 6.5 to 8.5.

Description

ORAL COMPOSITION COMPRISING PEROXYAMIDOPHTHALAMIDE DERIVATIVES
The present invention relates to an oral composition comprising a peroxy compound in a multi-component format.
The use of peroxy compounds in oral care compositions has already been proposed in the prior art. Many peroxy compounds have been suggested for whitening/bleaching human teeth, and representative examples of such peroxy compounds are hydrogen peroxide, urea peroxide, organic peracids such as perphthalic acid, diperoxycarboxylic acids, 1,12- dodecanedioic peroxy acid, peroxy acetic acid and systems comprising a peroxy compound and a peroxy acid precursor which generate peroxy acetic acid in situ, such as sodium perborate and tetraacetylethylene diamine (TAED) . The use of peroxy acetic acid is suggested in particular in e.g. EP-A-0545, 594 (Colgate), which also sets out the various prior proposals, made in the art for several peroxy compounds as bleaching/whitening agent for human teeth.
Peroxy amido phthalamides have the structural formula:
N-(CHR)n-C03H Formula 1
Figure imgf000002_0001
0
in which R is hydrogen or C1-C4 alkyl; n is 1 to 5/ and X is C=0 or SO2, are known per se and have been described in EP-A-325,288 and EP-A-325, 289. A preferred compound of this formula is N-phthalimido hexanoic peroxy acid ("PAP") of Formula 1, in which R is H, n is 5 and X is C=0. An alternative example of a compound according to Formula 1 wherein x is SO2 is saccharin-perhexanoic acid ("saccharin PAP"), as described in EP-A-485, 927.
For the sake of clarity, the term Λperoxy amido phthalamides' hereinafter means those peroxy amido phthalamides according to Formula 1.
WO 00/16737 (McLaughlin) discloses the use of potassium based inorganic persalts and peroxide bleaching agents in a two component system. This system effects the whitening of teeth, but does not damage the surrounding tissue.
US 6165448 A, (Chesebrough-Ponds) discloses a tooth whitening method using an organic peroxy compound in combination with an imine quaternary salt acting as a catalyst.
We have now found that the provision of peroxy amido phthalamides as oral care actives can be improved when formulated in a multi-component product in which the component comprising the peroxy amido phthalamide has a pH ranging from 2 to 6 and is mixed with another formulation just prior to use such that the mixture of the two formulations has a pH ranging from 6.5 to 8.5.
Without wishing to be bound by theory we believe that peroxy amido phthalamide bleaching agents, notably PAP, have special characteristics that make them particularly suitable for use in this system. Having mixed the components so that they are within the pH range from 6.5 to 8.5, the peroxy amido phthalamide is only sparingly soluble. This property of peroxy amido phthalamide means at any one time there is only a small amount of bleaching agent in solution and thus available to bleach the substrate. Once this activated bleach has reacted it is then replaced by some more of the insoluble material. This keeps the solution concentration of the peroxy amido phthalamide at its saturation level.
The slow dissolution of the peroxy amido phthalamide in this manner extends the time period over which the peroxy amido phthalamide will be effective at bleaching.
This property of the peroxy amido phthalamide also remedies the problem of the bleaching agent not being stable within the pH range specified for the mixture, namely pH from 6.5 to 8.5. Therefore the pH of the solution can be instantaneously increased to from pH 6.5 to 8.5, (which is the optimum conditions for the bleaching agent active to work) , without compromising the stability of the peroxy amido phthalamide, i.e. the stability of the peroxy amido phthalamide in a system whose pH changes is not dependent on the new pH.
Accordingly, the invention provides an oral composition with an improved teeth whitening effect, comprising a first formulation comprising an effective amount of a peroxy amido phthalamide having the structural formula: N-(CHR)n-C03H Formula 1
Figure imgf000005_0001
in which R is hydrogen or C1-C4 alkyl; n is 1 to 5; and X is C=0 or SO2,
wherein said first formulation has a pH of from 2 to 6
and a second formulation formulated such that when said second formulation is mixed with the first formulation the pH of the mixture is from 6.5 to 8.5.
Preferably, the peroxy amido phthalamide is PAP.
Preferably the second formulation has a pH ranging from 9 to 12.
More preferably, the pH of the mixture of the first formulation and the second formulation ranges from 7 to 8.
Most preferably, there is only one second formulation.
The amount of peroxy amido phthalamide, used in the present invention, may vary from 0.0001 to 99 % by weight of the total oral composition, preferably from 0.001 to 30 % by weight, particularly preferably from 0.01-10 % by weight and especially preferably from 0.1 to 5% by weight of the total oral composition.
Further the first and second formulations of the oral care composition according to the invention are packaged independently from one another, i.e. they are stored separately and mixed only immediately prior to use. The separate packagings may be part of a greater packaging presentation which allows for two formulations to be dispensed simultaneously and mixed for the first time on the brush such as that used by Mentadent® in their so called double pump mechanisms. The packages may also be completely independent from one another and be part of a whitening kit which contains a container of bleaching active and a container of buffering agent from which the contents can be independently dispensed and mixed before use.
The composition according to the invention is meant to be used in the oral cavity and as such will comprise an oral care benefit agent selected from the group consisting of anti-caries agent, anti-tartar agent, gum-health agent, antimicrobial agent and anti-oral malodour agent. The oral care benefit agent may be in either of the formulations according to the invention, though preferably the pH adjusting formulation, i.e. the formulation not comprising the bleaching agent. Preferably the oral composition will comprise a fluoride source as anti-caries agent.
The oral composition can be formulated in any suitable application form, such as gels, mouthwashes and toothpastes. The composition may also be a so called leave-on product whereby it is dispensed into a gum shield and then applied directly to the teeth and left for several minutes before being removed.
The oral care compositions of the present invention may furthermore comprise optional, conventional ingredients such as pharmaceutically acceptable carriers like starch, sucrose, water or water/alcohol systems etc. Small amounts of surfactants may also be included, such as anionic, non- ionic and amphoteric surfactants. When formulated into a dentifrice, such formulation may contain all the usual dentifrice ingredients.
Thus, they may comprise particulate abrasive materials such as silicas, aluminas, calcium carbonates,' dicalciumphosphates, calcium pyrophosphates hydroxyapatites, trimetaphosphates, insoluble hexametaphosphates and so on, usually in amounts between 5 and 60 % by weight of the total oral composition.
Furthermore, the oral care composition formulations may comprise humectants such as glycerol, sorbitol, propyleneglycol, xylitol, lactitol and so on.
Binders and thickeners such as sodium carboxymethyl- cellulose, xanthan gum, gum arabic, etc. may also be included, as well as synthetic polymers such as polyvinyl pyrrolidone, Gantrez®, polyacrylates and carboxyvinyl polymers such as Carbopol®. Flavours such as peppermint and spearmint oils may also be included, as well as preservatives, opacifying agents, colouring agents, pH-adjusting agents, sweetening agents and so on. Stabilising agents for the organic peroxy acids such as dipicolinic acid or sodium stannate may also be usefully included.
Anti-bacterial agents may also be included such as Triclosan, chlorhexidine, copper-, zinc- and stannous salts such as zinc citrate, sodium zinc citrate and stannous pyrophosphate, sanguinarine extract, metronidazole. Further examples of anti-bacterial agents are quaternary ammonium compounds such as cetylpyridinium chloride; bis-guanides such as chlorhexidine digluconate, hexetidine, octenidine, alexidine; halogenated bisphenolic compounds such as 2,2' methylenebis- (4-chloro-6-bromophenol) .
Polymeric compounds which can enhance the delivery of active ingredients such as anti-bacterial agents can also be included. Examples of such polymers are copolymers of polyvinylmethylether with maleic anhydride and other similar delivery enhancing polymers, e.g. those described in DE-A-3,942,643 (Colgate).
Furthermore anti-inflammatory agents such as ibuprofen, flurbiprofen, aspirin, indomethacin etc. may also be included.
Anti-caries agents such as sodium- and stannous fluoride, aminefluorides, monosodiumfluorophosphate, casein, plaque buffers such as urea, calcium lactate, calcium glycerophosphate, strontium polyacrylates may also be included. Other optional ingredients include vitamins such as Vitamin C, and plant extracts. Desensitising agents such as potassium citrate, potassium chloride, potassium tartrate, potassium bicarbonate, potassium oxalate, potassium nitrate as well as strontium salts may also be included.
Buffers and salts to buffer the pH and ionic strength of the compositions may also be included. Liposomes and other encapsulates may also be used to improve delivery or stability of active ingredients.
Furthermore, the oral compositions may comprise anti- calculus agents such as alkalimetal pyrophosphates, hypophosphite-containing polymers, organic phosphonates, phosphocitrates etc.
In addition, the compositions may comprise functional biomolecules such as bacteriocins, antibodies, enzymes and so on.
Other optional ingredients that may be included are e.g. bleaching agents, e.g. those described in EP-A-0 545,594, effervescing systems such as sodium bicarbonate/citric acid systems, colour change systems, and so on.
When formulated as a mouthwash, the oral care composition usually comprises a water/alcohol solution, flavour, humectant, sweetener and colorant. Since the peroxyacids of the invention also have an antimicrobial property, the composition of the invention are also effective to combat plaque and caries.
Particular embodiments according to the present invention will further be illustrated by way of Example.
EXAMPLE 1
The following oral composition comprises two formulations: a PAP-gel formulation and a pH-adjusting formulation.
PAP-gel formulation
Figure imgf000010_0001
PAP is commercially available as Eureco HC-17 (ex. Ausimont) .
This formulation has a pH of 4. pH-adjusting formulation
Figure imgf000011_0001
When both the PAP-formulation and the pH-adjusting formulation are mixed together the pH of the resulting composition is between about 6.5 and 8.5.

Claims

An oral composition with an improved teeth whitening effect, comprising a first formulation comprising an effective amount of a peroxy amido phthalamide having the structural formula:
N-(CHR)n-C03H Formula 1
Figure imgf000012_0001
0
in which R is hydrogen or C1-C alkyl; n is 1 to 5; and X is C=0 or SO2,
wherein said first formulation has a pH of from 2 to 6
and a second formulation formulated such that when said second formulation is mixed with the first formulation the pH of the mixture is from 6.5 to 8.5.
2. Oral composition according to claim 1, wherein the second formulation has a pH ranging from 9 and 12.
3. Oral composition according to any preceding claim, wherein the pH of the mixture is from 7 to 8.
4. Oral composition according to any preceding claim, wherein the peroxy amido phthalamide is PAP.
PCT/EP2002/006980 2001-07-26 2002-06-25 Oral composition comprising peroxyamidophthalamide derivatives WO2003009824A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
EP02738175A EP1408920A1 (en) 2001-07-26 2002-06-25 Oral composition comprising peroxyamidophthalamide derivatives
BR0211663-4A BR0211663A (en) 2001-07-26 2002-06-25 Oral composition

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP01306397 2001-07-26
EP01306397.9 2001-07-26

Publications (1)

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WO2003009824A1 true WO2003009824A1 (en) 2003-02-06

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EP (1) EP1408920A1 (en)
CN (1) CN1533266A (en)
BR (1) BR0211663A (en)
WO (1) WO2003009824A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020217054A1 (en) * 2019-04-21 2020-10-29 Biofilm Limited Tooth whitening film, process of manufacture thereof and a method of using such a film

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7601002B2 (en) 2004-03-29 2009-10-13 Colgate-Palmolive Co Dental whitening method
US7270805B1 (en) * 2006-03-30 2007-09-18 Conopco, Inc. Skin lightening agents, compositions and methods
BE1020399A5 (en) * 2012-07-04 2013-09-03 Sylphar Nv NEW COMPOSITION FOR MAKING WHITE TEETH.
CN106726702A (en) * 2017-03-13 2017-05-31 广州欧诺洁个人护理用品有限公司 A kind of tooth whitening products without hydrogen peroxide
CN113476333A (en) * 2020-08-19 2021-10-08 唯艺科学研究(深圳)有限公司 PAP-containing gel

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EP0325289A1 (en) * 1988-01-20 1989-07-26 AUSIMONT S.p.A. Bleaching agents comprising imido-aromatic percarboxylic acids
US4990329A (en) * 1985-05-24 1991-02-05 The Procter & Gamble Company Composition for treating oral diseases
EP0485927A1 (en) * 1990-11-16 1992-05-20 Hoechst Aktiengesellschaft Sulfimidoperoxycarboxylic acids
WO1996005802A2 (en) * 1994-08-22 1996-02-29 Unilever N.V. Teeth whitening composition containing organic peroxyacids
EP0895777A2 (en) * 1997-08-05 1999-02-10 Ausimont S.p.A. Compositions based on peroxyacids
WO2000016737A1 (en) * 1998-09-18 2000-03-30 Mclaughlin Gerald G Composition and method for whitening teeth without damaging soft tissue
WO2000018366A1 (en) * 1998-09-23 2000-04-06 Unilever N.V. Oral composition with an improved teeth whitening effect
EP1050294A1 (en) * 1999-03-12 2000-11-08 Farmaceutici Dott. Ciccarelli S.p.A. Tooth pastes
US6165448A (en) * 1998-09-25 2000-12-26 Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. Oral composition with an improved teeth whitening effect

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JP3783364B2 (en) * 1996-11-20 2006-06-07 株式会社デンソー Starter
US5928628A (en) * 1997-10-23 1999-07-27 Pellico; Michael A. Two-component dental bleaching system and method

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US4990329A (en) * 1985-05-24 1991-02-05 The Procter & Gamble Company Composition for treating oral diseases
EP0325289A1 (en) * 1988-01-20 1989-07-26 AUSIMONT S.p.A. Bleaching agents comprising imido-aromatic percarboxylic acids
EP0485927A1 (en) * 1990-11-16 1992-05-20 Hoechst Aktiengesellschaft Sulfimidoperoxycarboxylic acids
WO1996005802A2 (en) * 1994-08-22 1996-02-29 Unilever N.V. Teeth whitening composition containing organic peroxyacids
EP0895777A2 (en) * 1997-08-05 1999-02-10 Ausimont S.p.A. Compositions based on peroxyacids
WO2000016737A1 (en) * 1998-09-18 2000-03-30 Mclaughlin Gerald G Composition and method for whitening teeth without damaging soft tissue
WO2000018366A1 (en) * 1998-09-23 2000-04-06 Unilever N.V. Oral composition with an improved teeth whitening effect
US6165448A (en) * 1998-09-25 2000-12-26 Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. Oral composition with an improved teeth whitening effect
EP1050294A1 (en) * 1999-03-12 2000-11-08 Farmaceutici Dott. Ciccarelli S.p.A. Tooth pastes

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020217054A1 (en) * 2019-04-21 2020-10-29 Biofilm Limited Tooth whitening film, process of manufacture thereof and a method of using such a film
CN114126567A (en) * 2019-04-21 2022-03-01 必修复有限公司 Tooth whitening film, process for preparing the same and method of using the same
JP2022530375A (en) * 2019-04-21 2022-06-29 ビーソルブ リミテッド Tooth whitening film, its manufacturing process and how to use such film
CN114126567B (en) * 2019-04-21 2024-01-30 必修复有限公司 Tooth whitening film, preparation process thereof and method for using tooth whitening film
JP7474423B2 (en) 2019-04-21 2024-04-25 ビーソルブ リミテッド Teeth whitening film, process for making same and method for using such film

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US20030215403A1 (en) 2003-11-20
EP1408920A1 (en) 2004-04-21
CN1533266A (en) 2004-09-29
BR0211663A (en) 2004-07-13

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