Oil gelling agent and cosmetic
US-2024252417-A1 · Aug 1, 2024 · US
US2016331669A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016331669-A1 |
| Application number | US-201315106507-A |
| Country | US |
| Kind code | A1 |
| Filing date | Dec 20, 2013 |
| Priority date | Dec 20, 2013 |
| Publication date | Nov 17, 2016 |
| Grant date | — |
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Provided is an oral care composition comprising a phosphate/acrylate co-polymer, a tin salt, and an orally acceptable carrier, and methods of using the same.
Opening claim text (preview).
1 . An oral care composition comprising a phosphate/acrylate co-polymer, a tin salt, and an orally acceptable carrier. 2 . The composition of claim 1 wherein the wherein the phosphate/acrylate co-polymer is a co-polymerized product of a mixture of acrylic acid, methacrylic acid, and 2-hydroxyethyl methacrylate phosphates of Formula 1: wherein n is 0, 1 or 2. 3 . The composition of claim 2 , wherein the phosphate/acrylate co-polymer is a co-polymerized product of a mixture of acrylic acid, methacrylic acid, and 2-hydroxyethyl methacrylate phosphates of Formula 1 comprising acrylic acid in a molar percentage of 70-90%; methacrylic acid in a molar percentage of 5-20%, and hydroxyethyl methacrylate phosphates of Formula 1 in a molar percentage of 1-10%, 4 . The composition of claim 2 , wherein the phosphate/acrylate co-polymer is a co-polymerized product of a mixture of acrylic acid, methacrylic acid, and 2-hydroxyethyl methacrylate phosphates of Formula 1 comprising acrylic acid in a molar percentage of 80-90% or 85%; methacrylic acid in a molar percentage of 5-15% or 11%, and hydroxyethyl methacrylate phosphates of Formula 1 in a molar percentage of 2-6% or 4%. 5 . The composition of claim 1 , wherein the phosphate/acrylate copolymer is a random copolymer having a weight average molecular weight of 10,000 to 500,000, and the phosphate/acrylate copolymer is below it glass transition temperature. 6 . The composition of claim 5 , wherein the weight average molecular weight is 10,000 to 200,000 grams per mole, optionally, 10,000 to 40,000, 15,000 to 25,000, or 17,000 to 23,000 grams per mole. 7 . The composition of claim 1 wherein the tin salt is selected from stannous chloride, stannous fluoride and mixtures thereof. 8 . The composition of claim 1 , wherein the tin salt comprises SnCl 2 . 9 . The composition of claim 1 , wherein the composition comprises 0.1 to 10 weight % SnCl 2 , optionally 0.1 to 5 weight %, 0.1 to 3 weight %, 0.1 to 1.5 weight %, or 0.5 to 1.2 weight % SnCl 2 . 10 . The composition of claim 1 , wherein the composition comprises one or more of water, a thickener, a buffer, a humectant, a surfactant, an abrasive, a sweetener, a flavorant, a pigment, a dye, an anti-caries agent, an anti-bacterial, a whitening agent, a desensitizing agent, a vitamin, a preservative, an enzyme, or a mixture thereof. 11 . The composition of claim 10 , wherein the anti-bacterial agent is selected from the group consisting of triclosan, cetylpyridinium chloride (CPC), chlorhexidine (CHX), water soluble zinc salts, water insoluble zinc salts, zinc oxide, zinc citrate, or a mixture thereof. 12 . The composition of claim 1 , wherein the composition is a mouthwash, toothpaste, tooth gel, tooth powder, non-abrasive gel, mousse, foam, mouth spray, lozenge, oral tablet, dental implement, or pet care product. 13 . A method for the treatment and/or inhibition of a chemical stain, plaque, acid erosion, and/or tartar on a dental surface, comprising contacting the dental surface with a composition of claim 1 . 14 . A use of any of the compositions of claim 1 for the treatment and/or inhibition of a chemical stain, plaque, acid erosion, and/or tartar on a dental surface comprising contacting the dental surface with the composition. 15 . A method for the treatment and/or inhibition of gum disease comprising contacting the oral cavity with a composition of claim 1 . 16 . A use of any of the compositions of claim 1 for the treatment and/or inhibition of gum disease in an oral cavity comprising contacting the oral cavity with the composition. 17 . A method for the treatment and/or inhibition of halitosis comprising contacting the oral cavity with a composition of claim 1 . 18 . A use of any of the compositions according to claim 1 for the treatment and/or inhibition of halitosis in an oral cavity comprising contacting the oral cavity with the composition. 19 . A method for the inhibition of biofilm formation on a dental surface comprising contacting the oral cavity with a composition of claim 1 . 20 . A use of any of the compositions according to claim 1 for the inhibition of biofilm formation on a dental surface comprising contacting the dental surface with the composition. 21 . A method for treating and/or inhibiting bacteria from sticking together and growing into bigger colonies in an oral cavity comprising contacting the oral cavity with a composition of claim 1 . 22 . A use of any of the compositions according to claim 1 for treating and/or inhibiting bacteria from sticking together and growing into bigger colonies in an oral cavity.
Antibacterial agents · CPC title
Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis · CPC title
At least two compounds being classified in the same subclass of A61K8/18 · CPC title
having six membered rings · CPC title
containing atoms other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur or phosphorus · CPC title
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