EP0764014A1 - Mundspülung zusammensetzungen - Google Patents

Mundspülung zusammensetzungen

Info

Publication number
EP0764014A1
EP0764014A1 EP95922943A EP95922943A EP0764014A1 EP 0764014 A1 EP0764014 A1 EP 0764014A1 EP 95922943 A EP95922943 A EP 95922943A EP 95922943 A EP95922943 A EP 95922943A EP 0764014 A1 EP0764014 A1 EP 0764014A1
Authority
EP
European Patent Office
Prior art keywords
mixtures
group
composition according
mouthrinse
preferably selected
Prior art date
Legal status (The legal status 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 status listed.)
Withdrawn
Application number
EP95922943A
Other languages
English (en)
French (fr)
Inventor
Kevin Thomas Mclaughlin
Stephen Joseph Hunter-Rinderle
William Gerald Hall
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Procter and Gamble Co
Original Assignee
Procter and Gamble Co
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 Procter and Gamble Co filed Critical Procter and Gamble Co
Publication of EP0764014A1 publication Critical patent/EP0764014A1/de
Withdrawn legal-status Critical Current

Links

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
    • A61K8/34Alcohols
    • A61K8/345Alcohols containing more than one hydroxy group
    • 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
    • A61K8/34Alcohols
    • A61K8/347Phenols

Definitions

  • the present invention relates to a mouthrinse and methods of use providing improved activity and thereby reducing oral bacteria, mouth malodor and further promoting oral health.
  • Dental plaque is a mixed matrix of bacteria, epithelial cells, leukocytes, macro- phages and other oral exudate. Bacteria comprise approximately three-quarters of the plaque matrix. Any given sample of dental plaque could contain as many as 400 different varieties of microorganisms. This mix includes both aerobic and anaerobic bacteria, fungi and protozoa. Viruses have also been found in samples of dental plaque.
  • This matrix of organisms and oral exudate continues expanding and coalesces with other plaque growths situated nearby.
  • the bacteria synthesize levans and glucans from sucrose found in the oral cavity providing energy for the microorgan- isms.
  • These glucans, levans and microorganisms form an adhesive skeleton for the continued proliferation of plaque.
  • the present invention relates to improved mouthrinse compositions com ⁇ bining thymol and a polyhydric alcohol.
  • Talwar et al. discloses compositions comprising thymol together with an anethole and sugar alcohol combination to mask thymol's bitter taste.
  • the oral composition is a toothpaste, dental cream or gel
  • the disclosure also suggests the use of a suitable humectant (e.g. propylene glycol).
  • Dills et al. discloses compositions comprising a combination of thymol with hexetidine together with a suitable humectant (e.g. propylene glycol).
  • the present invention is directed at a good tasting mouthrinse composition providing improved activity using thymol without the need for additional antimicrobials and/or taste masking agents such as anethole.
  • a still further object of the present invention is to provide an effective method of treating or preventing plaque and related periodontal diseases such as gingivitis.
  • the present invention relates to a clear mouthrinse composition
  • a clear mouthrinse composition comprising: a.) from about 0.01% to about 0.4% of thymol; b.) from about 5% to about 30% of a polyhydric alcohol selected from among the group consisting of propylene glycol, butylene glycol, hexylene glycol and mixtures thereof; and c.) an orally acceptable carrier wherein the viscosity of said composition is below about 5 centipoise and further wherein the levels of hexetidine and anethole in said composition are less than about 0.01%.
  • mouthrinse compositions of the present invention are preferably clear.
  • “clear” as used herein does not mean colorless, but means substantially lacking the presence of particles of sufficient size to scatter visible light as detected visually.
  • orally acceptable carrier means a suitable vehicle which can be used to apply the present compositions to the oral cavity in a safe and effective manner.
  • the pH of those compositions herein described range from about 4.0 to about 9.5, with the preferred pH being from about 4.0 to about 9.0 and the most preferred pH being 4.5 to about 8.5.
  • Thymol also known as 5-methyl-2-(l-methylethyl)-phenol, is obtained from the essential oil of Thym s vulgari Linne 1 and Monarch punctata Linne 1 , Labiataer or from other botanical sources by fractional distillation. Alternatively, thymol may be synthesized from ?-cymene, and by interaction of w-cresol and isopropyl chloride. Essential oils are generally plant derived volatile oils and usually carry the odor or flavor of the plant. Thymol is a white crystalline powder with an aromatic odor and taste and is soluble in organic solvents and only slightly soluble in water. Thymol is incorporated in the present invention at levels of about 0.01% to about 0.4%, prefer ⁇ ably from about 0.05% to below about 0.1%, more preferably from about 0.06% to about 0.08%.
  • Another essential ingredient of the present invention is the polyhydric alcohol.
  • Polyhydric alcohols are best known for their solvent and humectant properties.
  • the polyhydric alcohols useful in the present invention include those selected from among the group consisting of propylene glycol, butylene glycol, hexylene glycol and rriixtures thereof.
  • the polyhydric alcohols comprise from about 5% to about 30% of the inven ⁇ tive compositions, preferably from about 10% to about 20%.
  • Water is also present in the mouthrinse compositions of the present invention.
  • Water comprises from about 50% to about 90%, preferably from about 70% to about 85% of the mouthrinse compositions described herein. These amounts of water include the free water which is added, plus that amount which is introduced with other materials such as with sorbitol.
  • the water, used in the present invention should preferably be deionized, distilled, free of organic impurities and bacteria and substan ⁇ tially free of metal ions.
  • the present invention may optionally include antitartar (anticalculus or chelat- ing) agents.
  • Antitartar agents are able to complex calcium found in the mixed matrix layers of plaque. This facilitates the loosening of plaque.
  • Suitable antitartar agents include: di- and/or tri- carboxylic acids such as tartaric acid, citric acid, pharmaceuti ⁇ cally acceptable salts thereof and mixtures thereof; polymeric polycarboxylates such as methyl vinyl ether; and the various soluble pyrophosphate salts, including tetra- alkali metal pyrophosphate, di-alkali metal diacid pyrophosphate, tri-alkali metal monoacid pyrophosphate and mixtures thereof.
  • the present invention may optionally include a water-soluble fluoride compound present in the composition in an amount sufficient to give a fluoride ion concentration in the composition at 25°C of from about 0.0025% to about 5.0% by weight, preferably from about 0.005% to about 2.0% by weight when it is used to provide additional anticaries effectiveness.
  • a fluoride ion-yielding material can be employed as sources of soluble fluoride in the present compositions. Examples of suitable fluoride ion-yielding materials are found in U.S. Patent No. 3.535.421. October 20, 1970 to Briner et al. and U.S. Patent No. 3.678.154.
  • Representative fluoride ion sources include: stannous fluoride, sodium fluo- ride, potassium fluoride, sodium monofluorophosphate and many others. Stannous fluoride and sodium fluoride are particularly preferred, as well as mixtures thereof.
  • Abrasives useful in abrading grinding and polishing teeth may also be option ⁇ ally incorporated into compositions of the present invention.
  • Typical dentally ac- ceptable abrasives include insoluble calcium salts, alumina, silica, synthetic resins and mixtures thereof. Suitable silica abrasives are described in U.S. Patent 5.176.900. herein incorporated by reference.
  • U.S. Patent 4.623.536 discloses sodium bicarbonate, baking soda, as a mild abrasive and is herein incorporated by reference.
  • Other compounds useful as abrasives are described in U.S. Patent 5.176.901 which is also herein incorporated by reference. Mixtures of the above described abrasives may also be used.
  • compositions of the present invention are other stannous salts such as stannous pyrophosphate and stannous gluconate and other antimicrobials such as bis-biquanide salts, copper bisglycinate and nonionic antimicrobial salts.
  • enzymes including endoglycosidase, papain, dextranase, mutanase and mixtures thereof. Such agents are disclosed in U.S. Patent No. 2.946.725. July 26, 1960, to Norris et al. and U.S. Patent No. 4.051.234. Sep ⁇ tember 27, 1977 to Gieske et al., both of which are herein incorporated by reference.
  • Surfactants useful as optional components of the present invention include nonionic surfactants, betaines, zwitterionic surfactants or mixtures thereof. Suitable nonionic surfactants are described in U.S. Patent 4.992.276. February 12, 1991, Dills et al., incorporated herein by reference. Most preferred from among the nonionic surfactants are the poloxamer surfactants. A particularly preferred poloxamer is Poloxamer 407, which is sold under the tradename Pluronic F-127 by BASF-Wyan- dotte, Parsippany, N.J.
  • Betaine surfactants are also useful in the compositions of the present invention.
  • Preferred betaine surfactants are disclosed in U.S. Patent 5.180.577. January 19, 1993, to Polefka et al., incorporated herein by reference.
  • Typical alkyl dimethyl betaines include decyl betaine or 2-(N-decyl-N,N-dimethylammonio) acetate, coco betaine or 2-(N-coc-N, N-dimethyl ammonio) acetate, myristyl betaine, palmityl betaine, lauryl betaine, cetyl betaine, cetyl betaine, stearyl betaine, etc.
  • amido- betaines are exemplified by cocoamidoethyl betaine, cocoamidopropyl betaine, lauramidopropyl betaine and the like.
  • the betaines of choice are preferably the cocoamidopropyl betaine and, more preferably, the lauramido propyl betaine.
  • Zwitterionic surfactants, like betaines, carry both a charged acidic and a charged basic moiety on the same molecule.
  • Preferred zwitterionic synthetic surfac ⁇ tants can be broadly described as derivatives of aliphatic quaternary ammonium, phosphonium, and sulfonium compounds, in which the aliphatic radicals can be straight chain or branched, and wherein one of the aliphatic substituents contains from about 8 to 18 carbon atoms and one contains an anionic water-solubilizing group, e.g., carboxy, sulfonate, sulfate, phosphate or phosphonate.
  • Zwitterionic surfactants suitable for use in the present invention are further described in U.S. Patent 4.198.392. April 15, 1980, to Juneja, incorporated herein by reference.
  • humectants are well known in the art.
  • the humectant may be a single agent or a mixture of compatible humectants
  • suitable humectants include xylitol, glycerin and sorbitol as well as other polyhydroxy alcohols other than the required alcohols of the present in ⁇ vention. While it is feasible to use a combination of humectants, the preferred embodiment incorporates the use of a single humectant.
  • Humectants provide from about 0% to about 55%, and most preferably from about 5% to about 20% of the herein described invention.
  • the preferred humectants include glycerin and/or sorbi- tol.
  • compositions of the present invention can also incorporate a flavoring agent or a mixture of compatible flavoring agents other than thymol.
  • flavoring agents are well known in the art.
  • Preferable flavoring agents are selected from among the group of essential aromatic flavor oils consisting of eucalyptol, methyl salicylate, menthol and mixtures thereof. These essential aromatic flavoring agents are included at levels of from about 0.01 to about 0.5%, preferably from about 0.04% to about 0.3%.
  • flavoring agents also suitable for use in the present invention include: anise, cassia, clove, dihydroanethole, es- tragole, peppermint, oxanone, phenyl ethyl alcohol, sweet birch, eugenol, spearmint, cinnamic aldehyde, menthone, alpha-ionone, ethyl vanillin, limonene, isoamylacetate, benzaldehyde, ethylbutyrate and many others.
  • flavoring agents comprise from about 0.01% to about 5.0%, preferably from about 0.05% to about 2.0% and most preferably from about 0.1% to about 1.0% of the herein described composition.
  • Another preferred nonessential component of the present invention is a cool ⁇ ing agent or a combination of cooling agents. Suitable cooling agents are those des ⁇ cribed in U.S. Patent 4.136.163. January 23, 1979, to Watson et al., U.S. Patent 4.230.688. October 28, 1980, to Rowsell et al. and U.S. Patent 4.032.661. to Rowsell et al., all of which are herein incorporated by reference.
  • Particularly pre- ferred cooling agents are N-ethyl-p-menthane-3-carboxamide (WS-3 supplied by Sterling Organics), taught by the above incorporated U.S. Patent 4.136.163 and N,2,3-trimethyl-2-isopropylbutanamide which is commercially available as WS-23 from Wilkinson Sword Limited and taught by the above incorporated U.S. Patent 4.230.688.
  • Another particularly preferred cooling agent is 3-1-menthoxypropane 1,2-diol (TK-10 supplied by Takasago Perfumery Co., Ltd., Tokyo, Japan). This material is described in detail in U.S. Patent 4.459.425. July 10, 1984 to Amano et al. and incorporated herein by reference.
  • optional components include, but are not limited to: coloring agents; sweeteners, including saccharin, dextrose, levulose, cyclamate and aspartate, along with many others; buffering systems such as benzoic acid and sodium benzoate, citric acid and sodium citrate, bicarbonates, peroxides, nitrate salts such as sodium and potassium nitrate and any other buffering system compatible with the invention's herein described essential components. These agents, if present, are included at levels of from about 0.01% to about 30%.
  • Another optional component of the present invention is ethyl alcohol. Ethyl alcohol provides several functions when combined in the compositions of the present invention. Its inclusion can be, but is not limited to use as an additional antibacterial or as an astringent. Ethyl alcohol can be incorporated in the present invention at a level of less than about 40%, preferably less than about 10% and most preferably in concentrations of less than about 2%.
  • a mouthrinse of the present invention is prepared by sequentially dissolving each of the following ingredients with agitation in a stainless steel or glass mixing tank containing the butylene glycol:
  • Poloxamer-407 0.5000 Eucalyptol 0.0900
  • Examples II -VI are combinations made by incorporating the components using conventional mixing technology similar to that described in Example I.

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)
  • Emergency Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Oral & Maxillofacial Surgery (AREA)
  • Cosmetics (AREA)
EP95922943A 1994-06-10 1995-06-02 Mundspülung zusammensetzungen Withdrawn EP0764014A1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US25792694A 1994-06-10 1994-06-10
US257926 1994-06-10
PCT/US1995/007007 WO1995034276A1 (en) 1994-06-10 1995-06-02 Mouthrinse compositions

Publications (1)

Publication Number Publication Date
EP0764014A1 true EP0764014A1 (de) 1997-03-26

Family

ID=22978377

Family Applications (1)

Application Number Title Priority Date Filing Date
EP95922943A Withdrawn EP0764014A1 (de) 1994-06-10 1995-06-02 Mundspülung zusammensetzungen

Country Status (4)

Country Link
EP (1) EP0764014A1 (de)
JP (1) JPH10501265A (de)
CA (1) CA2191573A1 (de)
WO (1) WO1995034276A1 (de)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX9706958A (es) * 1995-03-16 1997-11-29 Procter & Gamble Composiciones refrigerantes.
EE9800110A (et) * 1995-10-11 1998-10-15 Warner-Lambert Company Vähendatud etanoolisisaldusega ja etanoolivaba antimikroobne kompositsioon
US6103683A (en) * 1996-01-12 2000-08-15 The Procter & Gamble Co. Disinfecting compositions and processes for disinfecting surfaces
US6348187B1 (en) * 1996-01-24 2002-02-19 Warner-Lambert Company Peroxide/essential oils containing mouthwash compositions and two-part mouthwash systems
EP0791362A3 (de) * 1996-02-23 1998-03-04 The Procter & Gamble Company Desinfizierende Zusammensetzungen und Verfahren zum Entkeimen von Oberflächen
AU5355296A (en) * 1996-02-23 1997-09-10 Warner-Lambert Company Reduced alcohol mouthwash
AUPN862596A0 (en) * 1996-03-12 1996-04-04 F.H. Faulding & Co. Limited Pharmaceutical compositions
US5891422A (en) * 1996-10-10 1999-04-06 Warner-Lambert Company Antimicrobial composition containing a C3 -C6 alcohol
US6261540B1 (en) * 1997-10-22 2001-07-17 Warner-Lambert Company Cyclodextrins and hydrogen peroxide in dental products
US20070140992A1 (en) * 2005-12-21 2007-06-21 Lynn Schick Taste masking of essential oils using a hydrocolloid
US7596836B2 (en) * 2007-05-02 2009-10-06 Schwartz Steve W Nose and throat anti-influenza solution and method of use
US9974722B2 (en) * 2016-10-20 2018-05-22 Johnson & Johnson Consumer Inc. Reduced-ethanol mouth rinse formulations

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5356615A (en) * 1991-01-30 1994-10-18 Colgate Palmolive Company Antiplaque oral compositions
ZA937353B (en) * 1992-10-07 1994-04-29 Warner Lambert Co Taste masking of thymol
WO1994016674A1 (en) * 1993-01-27 1994-08-04 Warner-Lambert Company Reduced alcohol mouthwash antiseptic and antiseptic preparations
ZA94438B (en) * 1993-02-19 1994-08-29 Warner Lambert Co Pre-brushing rinse composition
CN1137750A (zh) * 1993-12-22 1996-12-11 普罗克特和甘保尔公司 用于高效释放抗菌剂的浓缩漱口液
EP0737059A1 (de) * 1993-12-29 1996-10-16 The Procter & Gamble Company Zahnreinigungsmittel enthaltend thymol zur verhinderung von zahnstein
US5407662A (en) * 1994-01-03 1995-04-18 Mackles; Leonard Aqueous monophasic compositions containing aromatic lipophiles

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9534276A1 *

Also Published As

Publication number Publication date
CA2191573A1 (en) 1995-12-21
WO1995034276A1 (en) 1995-12-21
JPH10501265A (ja) 1998-02-03

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