EP2654664A2 - Wässriges mundpflegeprodukt - Google Patents

Wässriges mundpflegeprodukt

Info

Publication number
EP2654664A2
EP2654664A2 EP11793808.4A EP11793808A EP2654664A2 EP 2654664 A2 EP2654664 A2 EP 2654664A2 EP 11793808 A EP11793808 A EP 11793808A EP 2654664 A2 EP2654664 A2 EP 2654664A2
Authority
EP
European Patent Office
Prior art keywords
care product
oral care
group
particles
agents
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Withdrawn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
EP11793808.4A
Other languages
English (en)
French (fr)
Inventor
Peter STEINRÜCKE
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.)
Bio-Gate AG
Original Assignee
Bio-Gate AG
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 Bio-Gate AG filed Critical Bio-Gate AG
Priority to EP11793808.4A priority Critical patent/EP2654664A2/de
Publication of EP2654664A2 publication Critical patent/EP2654664A2/de
Withdrawn legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8147—Homopolymers or copolymers of acids; Metal or ammonium salts thereof, e.g. crotonic acid, (meth)acrylic acid; Compositions of derivatives of such polymers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/0241—Containing particulates characterized by their shape and/or structure
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8129—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical; Compositions of hydrolysed polymers or esters of unsaturated alcohols with saturated carboxylic acids; Compositions of derivatives of such polymers, e.g. polyvinylmethylether
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/817—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
    • A61K8/8182—Copolymers of vinyl-pyrrolidones. Compositions of derivatives of such polymers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q11/00—Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/41—Particular ingredients further characterized by their size
    • A61K2800/412—Microsized, i.e. having sizes between 0.1 and 100 microns

Definitions

  • the invention concerns an aqueous oral care product comprising a copolymer.
  • an oral composition containing a substantially water insoluble noncationic antibacterial antiplaque agent and a synthetic cross-linked polymer such as cross-linked poly (methylvinyl ether/maleic acid or anhydride) as antibacterial-enhancing agent to enhance delivery of said antibacterial agent to, and the
  • noncationic antibacterial antiplaque agent an agent comprising a halogenated diphenyl ether, in particular triclosan.
  • triclosan is known to be able to enrich in fat tissue of the human body and the use of triclosan is not undisputed among toxicologists.
  • Polymers as those disclosed in this patent application are distributed under the name "Gantrez” by International Specialty Products (ISP, Wayne, New Jersey, USA) . All of these polymers are negatively charged at pH 7. They are used as adhesive resins for toothpaste. The negative charge supports an adhesion to the surface of teeth. If a cationic antibacterial agent or antibacterial agent comprising a cationic group would be used together with these polymers this agent could weaken the adhesion to the teeth.
  • oligomer composition comprising a first oligomer and a second oligomer
  • the first oligomer comprises a plurality of polymerized monomer units having pendent, free-radically polymerizable functional groups, and a plurality of polymerized monomer units having pendent, hydrophilic poly (alkylene oxide) groups.
  • the second oligomer comprises a plurality of polymerized monomer units having pendent photoinitiator groups.
  • the first oligomer and second oligomer can be photochemically crosslinked by forming covalent bonds between said pendent, free-radically polymerizable functional groups of said first oligomer and said photoinitiator groups of said second oligomer.
  • the oligomer composition may be used for wound dressings or as material for dental moldings or impressions. When the composition is used to prepare hydrophilic gel materials for medical
  • the gel can include one or more active agents such as antibacterial agents like antibiotics, iodine, silver, silver chloride and chlorhexidine .
  • active agents such as antibiotics, iodine, silver, silver chloride and chlorhexidine .
  • Other additives that can be incorporated into the gel material are viscosity modifiers such as polymeric thickeners, e.g. Gantrez resin. After crosslinking of the oligomer composition the Gantrez resin is fixed within the
  • the body care product may be a toothpaste.
  • the effect of the silver in such a toothpaste is restricted to the time of use of the toothpaste and a short time thereafter.
  • the object of the present invention is to provide an oral care product having a long lasting antibacterial effect such as the oral composition known from US 5,334,375 but without the disadvantages of the halogenated diphenyl ether such as triclosan.
  • Embodiments of the invention are characterized by the features of claims 2 to 12.
  • an aqueous oral care product comprising particles which consist of metal and which contain metallic silver, and a completely polymerized copolymer is provided.
  • “Completely polymerized” means that polymerization has been completed and no further chain elongation takes place.
  • the copolymer is a copolymer of maleic acid or derivative thereof and alkyl vinyl ether or alkyl alcohol vinyl ether or N-vinylpyrrolidone or acrylic acid or acrylic acid ester comprising the repeating structural unit
  • Ri represents a Ci - C alkyl group or Ci - C alkyl alcohol group
  • R 2 and R3 represent independently from each other a COOR 5 - or a S0 2 0R6-group
  • R5 and R6 represent independently from each other hydrogen, a Ci - C alkyl group or Ci - C alkyl alcohol group or another Ci - C4 aliphatic hydrocarbon
  • R4 represents hydrogen or a Ci - C4 alkyl group or Ci - C4 alkyl alcohol group or another Ci - C4 aliphatic hydrocarbon
  • n is an integer greater than 1 representing the number of repeat occurrences of this structural unit in a molecule of this copolymer and wherein the molecular weight of the copolymer is 80.000 to 2.000.000, wherein at least R 2 and/or R 3 are negatively charged at pH 7.
  • R 2 or R 3 can be present as free acid that is dissociated at pH 7 or as an ester.
  • aqueous means that the oral care product is contained in a composition comprising water in an amount exceeding trace amounts.
  • the copolymer provides a film. Supported by the negative charge of R 2 and/or R 3 the film is secured against the dental surface.
  • the aqueous oral care product according to the invention does not have the disadvantages of an oral care product containing triclosan. Instead of bringing an
  • the particles are continuously producing silver ions, which are
  • antimicrobially active and can also behave anti- inflammatorily . This makes it possible to create a depot using metallic silver, without the need to maintain a high local silver ion concentration that could impair the beneficial effect of the negatively charged copolymer.
  • the silver ions are cations that should bind to the negatively charged groups of the copolymer and thereby weaken adherence of the copolymer to the teeth inventors surprisingly found that the metallic particles are very effectively retained by the copolymer on the teeth and can provide an antimicrobial and anti ⁇ inflammatory effect.
  • the reason for that may be that the tendency of the silver ions to bind to the negatively charged groups of the copolymer is much lower than the high tendency to react with sulfhydryl groups of proteins in tissue, bacteria and saliva.
  • the oral care product according to the invention may provide, with respect to the concentration required to achieve an antimicrobial effect, a relatively high local concentration of silver ions on the teeth and gingiva accompanied by a high antimicrobial and anti-inflammatory effect in this area.
  • this triclosan can penetrate skin and mucosa and enter into blood. It might therefore more severely affect the oral germ flora than silver ions.
  • triclosan is able to enriche in fat tissue and may be degraded in the organism into toxic products.
  • antibacterial agent should be noncationic according to US 5,334,375 inventors found that an
  • antibacterial substance producing cations can be used to provide an antibacterial effect without preventing an effective adhesion to teeth.
  • Inventors found that locally produced ions prefer reacting with protein structures instead of binding to the copolymer.
  • the copolymer comprising silver ions releasing particles is more effective in providing a long lasting antimicrobial effect to teeth than the same copolymer comprising only silver ions that neutralize the negative charge and thereby weaken binding of the copolymer to teeth.
  • Ri is a methyl group.
  • R. 2 may be a carboxy group and/or R 3 may be a carboxy group, a COOC 2 H 5 group or a COOC 4 H 9 group.
  • the mean outer diameter of the single particles is 10 nm to 100 ⁇ , in particular 1 to 50 ⁇ , in particular 10 to 40 ⁇ .
  • the particles may have a mean internal porosity of at least 65%, in particular between 65 and 95%, in particular between 65 and 90%, in particular between 70 and 85%, in particular between 75 and 85%, or between 85 and 95%, in particular between 90 and 95%.
  • Internal porosity is understood as meaning the percentage of the volume of the particle which is not filled with metal.
  • the mean internal porosity of the particles can be determined using the following method:
  • step 4 can be effected by means of a computer-assisted image analysis of the TEM photographs.
  • the beat density of a powder of the particles is first of all determined.
  • the beat density is the mass of a unit volume of a powder which is layered as densely as possible by means of beating.
  • the beat density can be determined in accordance with DIN ISO 3953.
  • the value which is determined in this connection is calculated as a percentage of the density of the metal forming the particles and subtracted from 100%. The value which is calculated in this way constitutes the total porosity of the particles.
  • the choice of the porosity can be used to specify the quantity of silver ions which are released by a particle in a particular unit of time. If a high porosity is chosen, this thereby releases many silver ions which means that, overall, the antimicrobial and
  • the particles may consist of metallic silver to an extent of at least 99% (w/w) , in particular of at least 99.9% (w/w) .
  • the oral care product according to the invention may further comprise at least one additive selected from the group consisting of sodium carboxymethylcellulose, waxes, oils, preservatives, flavoring agents, viscosity
  • sweeteners modifiers, sweeteners, colorants, polyphosporic acids, quaternary ammonium compounds, biguanides, surfactants, whitening agents, anticaries agents, tartar control agents, antiplaque agents, periodontal actives,
  • abrasives abrasives, breath freshening agents, malodor control agents, tooth desensitizers, salivary stimulants orally acceptable carriers, and mixtures thereof.
  • the oral care product according to the invention may be formulated as a paste, gel, or liquid.
  • the oral care product may be a mouthrinse or a dentifrice, in
  • the invention further relates to the oral care product according to the invention for use as a medicament.
  • the oral care product according to the invention may be for the treatment of ailment caused by germs in the oral cavity.
  • the ailment may be
  • Periodontosis gingivitis, dental plaque, stomatitis, or halitosis.
  • An aqueous oral care product according to the invention has been mixed from the following components in the following proportions: Abrasive silica 12% (w/w) ,
  • porous silver particles (average diameter about 10 ⁇ ) 0.05% (w/w) and
  • a further aqueous oral care product according to the invention has been mixed from the following components in the following proportions:
  • porous silver particles (average diameter about 10 ⁇ ) 0.05% (w/w) and
  • Gantrez S is the commercial name of a copolymer of maleic acid and methyl vinyl ether distributed by
  • the porous silver particles are distributed by Bio- Gate AG, Neumeyerstr . 28 - 34, 90411 Nuremberg, Germany under the commercial name "MicroSilver BG" .
  • the oral care product according to example 2 has been used in a clinical study with two groups of test persons.
  • Group 1 used the oral care product according to example 2 for oral care.
  • Group 2 used the same composition but without Gantrez S.
  • Two and 14 hours after the application of the oral care product samples of the dental plaque were taken from the test persons.
  • ICP-MS inductively coupled plasma mass spectrometry
  • the samples were examined for their content of silver to evaluate which percentage of the silver contained in the sample of dental plaque taken after two hours is still present in the sample of the dental plaque taken after 14 hours of the same test person.
  • Fig. 1 shows the result of this study.
  • the right column of Fig. 1 represents the average percentage of silver in the samples of dental plaque taken from test persons of group 2 and the left column the average percentage of silver in the samples of dental plaque taken from test persons of group 1.
  • Gantrez S increased the percentage of silver retained on the teeth.

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)
EP11793808.4A 2010-12-23 2011-12-12 Wässriges mundpflegeprodukt Withdrawn EP2654664A2 (de)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP11793808.4A EP2654664A2 (de) 2010-12-23 2011-12-12 Wässriges mundpflegeprodukt

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
EP10196729 2010-12-23
EP11151697 2011-01-21
EP11164961 2011-05-05
EP11178523A EP2468236A3 (de) 2010-12-23 2011-08-23 Wässriges Mundpflegeprodukt
PCT/EP2011/072409 WO2012084563A2 (en) 2010-12-23 2011-12-12 Aqueous oral care product
EP11793808.4A EP2654664A2 (de) 2010-12-23 2011-12-12 Wässriges mundpflegeprodukt

Publications (1)

Publication Number Publication Date
EP2654664A2 true EP2654664A2 (de) 2013-10-30

Family

ID=45023534

Family Applications (2)

Application Number Title Priority Date Filing Date
EP11178523A Withdrawn EP2468236A3 (de) 2010-12-23 2011-08-23 Wässriges Mundpflegeprodukt
EP11793808.4A Withdrawn EP2654664A2 (de) 2010-12-23 2011-12-12 Wässriges mundpflegeprodukt

Family Applications Before (1)

Application Number Title Priority Date Filing Date
EP11178523A Withdrawn EP2468236A3 (de) 2010-12-23 2011-08-23 Wässriges Mundpflegeprodukt

Country Status (2)

Country Link
EP (2) EP2468236A3 (de)
WO (1) WO2012084563A2 (de)

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5334375A (en) 1988-12-29 1994-08-02 Colgate Palmolive Company Antibacterial antiplaque oral composition
DE10340277B4 (de) * 2003-08-29 2006-11-23 Bio-Gate Bioinnovative Materials Gmbh Körperpflegemittel mit Silber-Agglomeraten
US20050070688A1 (en) 2003-09-26 2005-03-31 3M Innovative Properties Company Reactive hydrophilic oligomers

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2012084563A2 *

Also Published As

Publication number Publication date
WO2012084563A2 (en) 2012-06-28
EP2468236A2 (de) 2012-06-27
WO2012084563A3 (en) 2012-10-26
EP2468236A3 (de) 2012-10-17

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