阅读说明：本技术 口腔护理组合物和用于提高其稳定性的方法 (Oral care compositions and methods for improving the stability thereof ) 是由 费林 普拉卡萨劳·曼达迪 苏曼·乔普拉 于 2017-12-13 设计创作，主要内容包括：公开了无水口腔护理组合物和防止无水口腔护理组合物中的相分离的方法。口腔护理组合物可包含口腔可接受的媒介物、增稠体系和增白剂。口腔可接受的媒介物可包含丙二醇,增稠体系可包含聚合物增稠剂。聚合物增稠剂可以是或可包括2-丙烯酰胺基甲基丙磺酸或其盐的共聚物。(Disclosed are anhydrous oral care compositions and methods of preventing phase separation in anhydrous oral care compositions. The oral care composition may comprise an orally acceptable vehicle, a thickening system, and a whitening agent. The orally acceptable vehicle can comprise propylene glycol and the thickening system can comprise a polymeric thickener. The polymeric thickener may be or may include a copolymer of 2-acrylamidomethylpropanesulfonic acid or a salt thereof.)

1. An anhydrous oral care composition comprising:

an orally acceptable vehicle comprising propylene glycol;

a thickening system comprising a polymeric thickener, wherein the polymeric thickener is a copolymer of 2-acrylamidomethylpropanesulfonic acid or a salt thereof; and

a whitening agent.

2. The anhydrous oral care composition of claim 1, wherein the polymeric thickener is a block copolymer.

3. The anhydrous oral care composition of claim 1 or 2, wherein the polymeric thickener comprises a block copolymer of a first monomer and a second monomer,

wherein the first monomer comprises the 2-acrylamidomethylpropanesulfonic acid or a salt thereof, and

wherein the second monomer comprises a vinyl monomer having a nitrogen-containing side chain.

4. The anhydrous oral care composition of claim 3, wherein the vinyl monomer is at least one of methacrylic acid, a methacrylate ester, a methacrylamide, a methacrylate salt and a vinyl pyrrolidone.

5. The anhydrous oral care composition of claim 4, wherein the first monomer is an ammonium salt of 2-acrylamidomethylpropanesulfonic acid.

6. The anhydrous oral care composition of any one of claims 3 to 5, wherein the second monomer comprises a vinyl monomer having an amide functional group.

7. The anhydrous oral care composition of claim 6, wherein the second monomer is N-vinyl pyrrolidone.

8. The anhydrous oral care composition of any one of claims 1 to 7, wherein the polymeric thickener comprises a copolymer of an ammonium salt of 2-acrylamido methylpropane sulfonic acid and N-vinyl pyrrolidone.

9. The anhydrous oral care composition according to any one of claims 1 to 8, wherein the thickening system consists of a copolymer of an ammonium salt of 2-acrylamidomethylpropanesulfonic acid and N-vinylpyrrolidone.

10. The anhydrous oral care composition according to any one of claims 1 to 9, wherein the polymeric thickener is present in an amount of from about 0.1% to about 1% by weight of the anhydrous oral care composition.

11. The anhydrous oral care composition according to any one of claims 1 to 10, wherein the polymeric thickener is present in an amount of from about 0.25% to about 0.75%, optionally 0.4% or 0.55%, by weight of the anhydrous oral care composition.

12. The anhydrous oral care composition according to any one of claims 1 to 11, wherein the anhydrous oral care composition is substantially free of fluoride, and optionally free of fluoride.

13. The anhydrous oral care composition of any one of claims 1 to 12, wherein the anhydrous oral care composition does not comprise fumed silica and/or crosslinked polyvinylpyrrolidone.

14. The anhydrous oral care composition according to any one of claims 1 to 13, wherein the oral care composition comprises less than 5.0% by weight water, preferably less than 1.0% by weight water, more optionally less than 0.1% by weight water.

15. The anhydrous oral care composition of any one of claims 1 to 14, wherein the whitening agent comprises a crosslinked polyvinylpyrrolidone (PVP) hydrogen peroxide complex.

16. A method of preventing phase separation in an anhydrous oral care composition, the method comprising:

contacting an orally acceptable vehicle comprising propylene glycol and a whitening agent with one another to form the oral care composition; and

contacting the anhydrous oral care composition with a polymeric thickener.

17. A method for whitening teeth of a subject in need of whitening teeth, the method comprising: contacting an oral surface of the subject with the anhydrous oral care composition of any one of claims 1 to 15.

Background

Conventional oral care products or compositions thereof (e.g., toothpastes, gels, etc.) containing whitening agents are typically employed to whiten teeth. For example, conventional toothpastes containing peroxide (e.g., hydrogen peroxide) are typically employed to oxidize tooth surface bound chromophores, thereby whitening the teeth. However, peroxides are often unstable and susceptible to degradation. Thus, peroxides are often incorporated into non-aqueous oral care products and/or compositions to help stabilize the peroxide. Although non-aqueous oral care compositions such as non-aqueous toothpastes have proven effective for stabilizing peroxides, there are limitations to gelling agents and/or thickening agents that are compatible with propylene glycol.

In view of the foregoing, non-aqueous oral care compositions incorporating hydrogen peroxide often utilize limited conventional thickener options to promote thickening and/or gelling of the oral care composition. For example, non-aqueous oral care compositions often incorporate fumed silica and/or a cross-linked polymer (e.g., cross-linked PVP) to thicken and/or gel the oral care composition. However, conventional thickeners are not capable of forming a network with each other. As a result, solids contained in oral care compositions can often settle, resulting in phase separation within the oral care composition.

Thus, there is a need for improved non-aqueous oral care compositions incorporating whitening agents and methods of preventing phase separation therein.

Disclosure of Invention

This summary is intended only to introduce a simplified summary of some aspects of one or more embodiments of the disclosure. Further areas of applicability of the present disclosure will become apparent from the detailed description provided hereinafter. This summary is not an extensive overview, is not intended to identify key or critical elements of the teachings or to delineate the scope of the disclosure. Rather, its sole purpose is to present one or more concepts in a simplified form as a prelude to the more detailed description that is presented later.

The foregoing and/or other aspects and utilities embodied in the present disclosure may be achieved by providing an anhydrous oral care composition comprising an orally acceptable vehicle, a thickening system, and a whitening agent. The orally acceptable vehicle can comprise propylene glycol, and the thickening system can comprise a polymeric thickener, which can be a copolymer of 2-acrylamidomethylpropanesulfonic acid or a salt thereof.

In at least one embodiment, the polymeric thickener may be a block copolymer.

In another embodiment, the polymeric thickener may comprise a block copolymer of a first monomer and a second monomer. The first monomer may include 2-acrylamidomethylpropanesulfonic acid or a salt thereof, and the second monomer may include a vinyl monomer having a nitrogen-containing side chain.

In another embodiment, the vinyl monomer may be or include at least one of methacrylic acid, methacrylate esters, methacrylamide, methacrylate salts, vinyl pyrrolidone, and combinations thereof.

In another embodiment, the first monomer can be an ammonium salt of 2-acrylamidomethylpropanesulfonic acid.

In another embodiment, the second monomer may include a vinyl monomer having an amide functional group.

In another embodiment, the second monomer may be N-vinyl pyrrolidone.

In another embodiment, the polymeric thickener can be a copolymer of an ammonium salt of 2-acrylamidomethylpropanesulfonic acid and N-vinylpyrrolidone.

In another embodiment, the thickening system may comprise or consist of a copolymer of an ammonium salt of 2-acrylamidomethylpropanesulfonic acid and N-vinylpyrrolidone.

In another embodiment, the anhydrous oral care composition can be substantially free of fluoride.

In another embodiment, the anhydrous oral care composition may be free or non-pyrogenic silica and crosslinked polyvinylpyrrolidone.

In another embodiment, the oral care composition may comprise less than 5.0% water by weight, preferably less than 1.0% water by weight, more preferably less than 0.1% water by weight.

In another embodiment, the whitening agent may comprise a crosslinked polyvinylpyrrolidone (PVP) hydrogen peroxide complex.

The foregoing and/or other aspects and utilities embodied in the present disclosure may be achieved by providing a method for preventing phase separation in an anhydrous oral care composition. The method can include contacting an orally acceptable vehicle comprising propylene glycol and a whitening agent with one another to form an oral care composition, and contacting the anhydrous oral care composition with a polymeric thickening agent.

In at least one embodiment, the polymeric thickener may comprise a block copolymer of a first monomer and a second monomer, wherein the first monomer may comprise acrylamide having a sulfo group, and wherein the second monomer may comprise a vinyl monomer having a nitrogen-containing side chain, preferably the polymeric thickener is a copolymer of an ammonium salt of 2-acrylamidomethylpropanesulfonic acid and N-vinylpyrrolidone.

Further areas of applicability of the present disclosure will become apparent from the detailed description provided hereinafter. It should be understood that the detailed description and specific examples, while indicating some exemplary aspects of the disclosure, are intended for purposes of illustration only and are not intended to limit the scope of the disclosure.

Detailed Description

The following description of the various aspects is merely exemplary in nature and is in no way intended to limit the disclosure, its application, or uses.

Ranges are used throughout as a shorthand way of describing each and every value that is within the range. Any value within the range can be selected as the terminus of the range. In addition, all references cited herein are hereby incorporated by reference in their entirety. In the event that a definition in this disclosure conflicts with a definition in a cited reference, the present disclosure controls.

Unless otherwise indicated, all percentages and amounts expressed herein and elsewhere in this specification are to be understood as referring to weight percentages. The amounts given are based on the effective weight of the material.

In addition, all numerical values are "about" or "approximately" the stated value, and experimental error and variation as contemplated by one of ordinary skill in the art are contemplated. It is to be understood that all values and ranges disclosed herein are approximate values and ranges, regardless of whether "about" is used in connection therewith.

Composition comprising a metal oxide and a metal oxide

The present inventors have surprisingly and unexpectedly found that polymers or polymeric thickeners will effectively prevent phase separation in oral care compositions incorporating whitening agents (e.g., peroxides). The polymeric thickener may be or include a copolymer of a first monomer, such as 2-acrylamidomethylpropanesulfonic acid or a salt thereof, and a second monomer, such as methacrylic acid, methacrylate esters, methacrylamide, methacrylate salts and vinylpyrrolidone, which will effectively prevent phase separation in an oral care composition incorporating a whitening agent (e.g., peroxide). In particular, the present inventors have surprisingly and unexpectedly found that block copolymers of 2-acrylamidomethylpropanesulfonate and N-vinylpyrrolidone are effective in preventing phase separation in non-aqueous oral care compositions incorporating a whitening agent (e.g., peroxide). The present inventors have also surprisingly and unexpectedly found that block copolymers of 2-acrylamidomethylpropanesulfonate and N-vinylpyrrolidone are effective thickeners for non-aqueous oral care compositions. The present inventors have also surprisingly and unexpectedly found that block copolymers of 2-acrylamidomethylpropanesulfonate and N-vinylpyrrolidone are compatible with and/or maintain the stability of a whitening agent of an oral care composition. It has also been surprisingly and unexpectedly found that oral care compositions exhibit stability (e.g., no phase separation) for at least two months when exposed to accelerated aging conditions.

The compositions disclosed herein may be or may include an oral care product and/or an oral care composition thereof. The oral care composition may be a non-aqueous oral care composition, such as a non-aqueous dentifrice or toothpaste. The oral care composition may comprise an orally acceptable vehicle such as propylene glycol, one or more whitening agents, and a thickening agent. In at least one embodiment, the thickening agent of the oral care composition does not include fumed silica and/or a cross-linked polymer such as cross-linked polyvinylpyrrolidone.

The oral care composition may be anhydrous prior to use. For example, the oral care composition may be free or substantially free of water. As used herein, "free" or "substantially free" may refer to a composition containing less than 5.0 wt.%, less than 3.0 wt.%, less than 1.0 wt.%, less than 0.1 wt.%, less than 0.05 wt.%, less than 0.01 wt.%, less than 0.005 wt.%, or less than 0.0001 wt.%, based on the total weight of the oral care composition. The oral care composition prior to use may have a "low water content". As used herein, "low water content" may refer to compositions containing greater than about 5 wt% and less than about 7 wt% or less than about 10 wt% water.

Orally acceptable vehicle

The oral care composition may form at least a part of or be used in one or more oral care products. Illustrative oral care products can include, but are not limited to, toothpaste (dentifrice), prophylaxis paste, tooth powder, tooth polish, tooth gel (e.g., whitening gel), chewing gum, lozenge, mouthwash, whitening strip, paint-on gel, varnish, veneer and tube, syringe or tray containing gel or paste, or gel or paste coated on an application support such as a dental floss or toothbrush (e.g., manual, electric, sonic, combinations thereof, or ultrasonic toothbrush). In a typical embodiment, the oral care composition may form at least a portion of or be used with a toothpaste. For example, the oral care composition may generally be a gel of a toothpaste, or a whitening gel to be combined with a toothpaste. The oral care composition may comprise or be combined with an orally acceptable vehicle to form an oral care product (e.g., toothpaste). In an exemplary embodiment, the orally acceptable vehicle can be or include propylene glycol.

In at least one embodiment, the orally acceptable vehicle can include one or more humectants. Illustrative humectants can be or include, but are not limited to, glycerin, propylene glycol, and combinations thereof. In a preferred embodiment, the orally acceptable vehicle can be or include, but is not limited to, propylene glycol. The propylene glycol may be present in an amount of 20 wt% to about 75 wt%, based on the total weight of the oral care composition. For example, the propylene glycol may be present in an amount of about 20 wt.%, about 25 wt.%, about 30 wt.%, about 35 wt.%, about 40 wt.%, or about 45 wt.% to about 50 wt.%, about 55 wt.%, about 60 wt.%, about 65 wt.%, about 70 wt.%, or about 75 wt.%. In another example, the propylene glycol may be present in an amount of about 20 wt.% to about 75 wt.%, about 25 wt.% to about 70 wt.%, about 30 wt.% to about 65 wt.%, about 35 wt.% to about 60 wt.%, about 40 wt.% to about 55 wt.%, or about 45 wt.% to about 50 wt.%. In a preferred embodiment, the propylene glycol may be present in an amount of about 45% to about 50% by weight or in an amount of about 60% to about 70% by weight.

Whitening agent

The oral care composition may comprise one or more whitening agents. The whitening agent may be or include, but is not limited to, hydrogen peroxide or one or more sources of hydrogen peroxide. For example, the whitening agent may be hydrogen peroxide and/or a hydrogen peroxide releasing substance. The one or more sources of hydrogen peroxide may be or include any compound or material configured to release hydrogen peroxide. Preferably, the whitening agent includes, but is not limited to, solid whitening agents and combined whitening agents, which are substantially anhydrous oxygen generating compounds. Solid whitening agents useful herein include peroxides, persulfates. Exemplary peroxide phases include hydroperoxides, hydrogen peroxide, peroxides of alkali and alkaline earth metals, organic peroxy compounds, peroxy acids, pharmaceutically-acceptable salts thereof, and mixtures thereof. Peroxides of alkali and alkaline earth metals include, but are not limited to, lithium peroxide, potassium peroxide, sodium peroxide, magnesium peroxide, calcium peroxide, barium peroxide, and mixtures thereof. Organic peroxy compounds include, but are not limited to, urea peroxide, glyceryl hydroperoxide, alkyl hydroperoxides, dialkyl peroxides, alkyl peroxy acids, peroxy esters, diacyl peroxides, benzoyl peroxide, and monoperoxyphthalate, and mixtures thereof. Peroxy acids and salts thereof include, but are not limited to, organic peroxy acids such as alkyl peroxy acids, monoperoxyphthalic acidSalts and mixtures thereof, and inorganic peroxy acid salts such as perborate salts of alkali and alkaline earth metals such as lithium, potassium, sodium, magnesium, calcium and barium, and mixtures thereof. Preferred solid peroxides are sodium perborate, urea peroxide and mixtures thereof. The whitening agent may preferably be conjugated. For example, peroxides can bind to polymers such as PVP (poly (N-vinylpyrrolidone)). Suitable PVP complexes are disclosed, for example, in U.S. patent No. 5,122,370, the contents of which are incorporated herein by reference. In some embodiments, it may be desirable to use any known whitening agent other than sodium percarbonate and/or any percarbonate. The hydrogen peroxide source or brightener may also be or include, but is not limited to, peroxolone^TMX L10 complex orX L10F, commercially available from Ashland Inc.

The amount or concentration of the hydrogen peroxide source can vary widely. In at least one example, the hydrogen peroxide source can be present in an amount to provide a hydrogen peroxide concentration of less than or equal to 4 weight%, less than or equal to 3.5 weight%, less than or equal to 3 weight%, less than or equal to 2.5 weight%, less than or equal to 2 weight%, less than or equal to 1.5 weight%, based on the total weight of the oral care composition. In at least one embodiment, the source of hydrogen peroxide can be present in an amount greater than or equal to 1 weight percent and less than or equal to 30 weight percent based on the total weight of the oral care composition. For example, the hydrogen peroxide source may be present in an amount of about 1 wt.%, about 3 wt.%, about 5 wt.%, about 7 wt.%, about 9 wt.%, about 11 wt.%, about 13 wt.%, or about 15 wt.% to about 17 wt.%, about 19 wt.%, about 21 wt.%, about 22 wt.%, about 23 wt.%, about 25 wt.%, about 27 wt.%, about 29 wt.%, or about 30 wt.%. In another example, the hydrogen peroxide source may be present in an amount of about 1 wt% to about 30 wt%, about 3 wt% to about 29 wt%, about 5 wt% to about 27 wt%, about 7 wt% to about 25 wt%, about 9 wt% to about 23 wt%, about 11 wt% to about 21 wt%, about 13 wt% to about 19 wt%, or about 15 wt% to about 17 wt%. In other embodiments, the source of hydrogen peroxide is crosslinked PVP complexed with hydrogen peroxide and is present in an amount of from about 15 wt.% to about 17 wt.%, preferably from about 16 wt.% to about 17 wt.%, more preferably about 16.5 wt.%. In a further embodiment, the hydrogen peroxide source is crosslinked PVP complexed with hydrogen peroxide and is present in an amount of from about 20 wt.% to about 30 wt.%, preferably from about 21 wt.% to about 25 wt.%, more preferably about 22 wt.%.

Thickening system

The oral care composition may comprise a thickening system having one or more thickening agents. The one or more thickening agents may be any orally acceptable thickening or thickening agent configured to at least partially form a network and thereby prevent phase separation in the oral care composition. An exemplary thickener may be or may include a polymeric thickener such as a copolymer of at least two monomers, where the first monomer may be an acrylamide having a sulfonic acid group and the second monomer may be a vinyl monomer having a nitrogen-containing side chain. Illustrative vinyl monomers can be or include, but are not limited to, methacrylic acid, methacrylates, methacrylamides, methacrylates, vinyl pyrrolidone, and the like, and combinations thereof. For example, the thickener may be or include a copolymer of 2-acrylamidomethylpropanesulfonic acid or a salt thereof such as an ammonium or sodium salt and a vinyl monomer having a nitrogen-containing cyclic side chain or a vinyl monomer having an amide functional group such as N-vinylpyrrolidone. In a preferred embodiment, the thickener may be a copolymer of an ammonium salt of 2-acrylamidomethylpropanesulfonic acid and N-vinylpyrrolidone, which may beAVC is commercially available from Clariant International L td. (Charlotte, N.C.. Block copolymer thickener may have the INCI designation Acrylyldimethyltaura/VP copolymer or correspond to CAS reference number 335383-60-3. Another preferred thickenerCan be a block copolymer of the sodium salt of 2-acrylamidomethylpropanesulfonic acid with N-vinylpyrrolidone, which can beAVS is commercially available from Clariant International L td (Charlotte, N.C.) and has the INCI designation sodium acryloyl dimethyl taurate/VP crosslinked polymer in yet another preferred embodiment, the polymeric thickener can beHMB、B L V and/orIn yet another preferred embodiment, the polymeric thickener may be or include polyacrylate crosspolymer-6, which may be SEPIMAX^TMZEN is commercially available from SEPPIC s.a. a subsidiary of Air L iquide group (puteaux, france).

In at least one embodiment, the oral care composition can be free or substantially free of fumed silica. In another embodiment, the oral care composition may be free or substantially free of crosslinked PVP prior to use. It is to be understood that in at least one embodiment, the oral care composition may comprise crosslinked PVP complexed with hydrogen peroxide as a source of hydrogen peroxide prior to use, but may also be free or substantially free of crosslinked PVP. In yet another embodiment, the oral care composition may be free or substantially free of both fumed silica and crosslinked PVP prior to use. In yet another embodiment, the oral care composition may comprise fumed silica and crosslinked PVP.

The amount or concentration of the thickening system or thickening agent thereof in the oral care composition can vary widely. In at least one embodiment, the thickening agent can be present in the oral care composition in an amount greater than or equal to 0.1 weight% and less than or equal to 1.0 weight%, based on the total weight of the oral care composition. For example, the thickening agent may be present in the oral care composition in an amount of about 0.1 weight%, about 0.2 weight%, about 0.3 weight%, about 0.4 weight%, or about 0.5 weight% to about 0.6 weight%, about 0.7 weight%, about 0.8 weight%, about 0.9 weight%, or about 1.0 weight%. In another example, the thickening agent may be present in the oral care composition in an amount of from about 0.1% to about 1.0%, from about 0.2% to about 0.9%, from about 0.3% to about 0.8%, from about 0.4% to about 0.7%, or from about 0.5% to about 0.6% by weight. In some embodiments, the thickening agent may be present in the oral care composition in an amount of about 0.4 wt% to about 0.6 wt%, optionally about 0.4 wt% or about 0.55 wt%.

In another embodiment, the thickening agent can be present in the oral care composition in an amount greater than 0% and less than or equal to 20% by weight, based on the total weight of the oral care composition. For example, the thickening agent can be present in the oral care composition in an amount greater than 0% and less than or equal to 20%, less than or equal to 18%, less than or equal to 16%, less than or equal to 14%, less than or equal to 12%, less than or equal to 10%, less than or equal to 8%, less than or equal to 6%, less than or equal to 5%, less than or equal to 4%, less than or equal to 3%, less than or equal to 2%, less than or equal to 1.8%, less than or equal to 1.6%, less than or equal to 1.4%, less than or equal to 1.2%, less than or equal to 1.0%, less than or equal to 0.8%, less than or equal to 0.6%, or less than or equal to 0.4% by weight.

In at least one embodiment, the oral care composition can comprise an additional and/or optional thickening agent. Illustrative additional or optional thickeners may also be or include, but are not limited to, carbomers (e.g., carboxyvinyl polymers), carrageenans (e.g., irish moss, carrageenan, iota carrageenan, etc.), high molecular weight polyethylene glycols (e.g.,commercially available from Dow Chemical Company (midland, michigan), cellulosic polymers, hydroxyethylcellulose, carboxymethylcellulose and salts thereof (e.g., CMC sodium), natural gums (e.g., karaya, xanthan, gum arabic, and gum tragacanth), colloidal magnesium aluminum silicate, and the like, as well as mixtures or combinations thereof.

Polymer and method of making same

In at least one embodiment, the oral care composition can comprise one or more polymers or polymeric additives. For example, the oral care composition can comprise one or more block copolymers of polyethylene glycol and polyethylene glycol (e.g., of molecular weight at least 5000Da), polypropylene glycol and polyethylene glycol, and the like, and combinations thereof. In at least one embodiment, the oral care composition comprises a block copolymer of ethylene oxide and propylene oxide represented by formula (1),

(ethylene oxide)_x- (propylene oxide)_y(1)

Where x is an integer from about 80 to about 150 (e.g., x is 100-130, or about 118) and y is an integer from about 30 to about 80 (e.g., y is 60-70, or about 66). The block copolymer of ethylene oxide and propylene oxide may have an average molecular weight greater than or equal to about 5,000Da and less than or equal to about 20,000 Da. For example, the block copolymer of ethylene oxide and propylene oxide may have a molecular weight of about 8,000Da to about 13,000 Da. In another example, the molecular weight of the block copolymer of ethylene oxide and propylene oxide may be about 9,800Da or about 10,000 Da. In yet another example, the block copolymer of ethylene oxide and propylene oxide may have a molecular weight of about 8,000Da to about 10,000 Da. In at least one embodiment, the oral care composition does not comprise a block copolymer of ethylene oxide and propylene oxide having a molecular weight of less than 5,000 Da. For example, at least 99.5%, at least 99.0%, or at least 99.9% of the block copolymers of ethylene oxide and propylene oxide present in the oral care composition have a molecular weight greater than or equal to 5,000 Da. In at least one embodiment, the polymer or polymer additive (if included in the composition) may be or may includeL4370 andl1220, both of which are commercially available from BASF (Wooden, Mich.).

The amount or concentration of polymer or polymer additive (e.g., block copolymer) present in the oral care composition can vary widely. In at least one embodiment, the polymer or polymer additive (e.g., block copolymer) can be present in the oral care composition in an amount from about 5% to about 10% by weight. For example, the amount of polymer or polymer additive (e.g., block copolymer) present in the oral care composition can be about 5.0 wt.%, about 5.5 wt.%, about 6.0 wt.%, about 6.5 wt.%, about 7.0 wt.%, or about 7.5 wt.% to about 8.0 wt.%, about 8.5 wt.%, about 9.0 wt.%, about 9.5 wt.%, or about 10.0 wt.%. In another example, the polymer or polymer additive may be present in the oral care composition in an amount from about 5.0 wt% to about 10.0 wt%, from about 5.5 wt% to about 9.5 wt%, from about 6.0 wt% to about 9.0 wt%, from about 6.5 wt% to about 8.5 wt%, or from about 7.0 wt% to about 8.0 wt%. In another embodiment, the polymer or polymer additive may be present in the oral care composition in an amount of from about 5 weight% to about 15 weight%, based on the total weight of the oral care composition. For example, the amount of polymer or polymer additive (e.g., block copolymer) present in the oral care composition can be about 5.0, about 5.5, about 6.0, about 6.5, about 7.0, about 7.5, about 8.0, about 8.5, about 9.0, about 9.5, or about 10.0 to about 10.5, about 11.0, about 11.5, about 12.0, about 12.5, about 13.0, about 13.5, about 14.0, about 14.5, or about 15.0 weight percent.

In at least one embodiment, the polymer or polymer additive may be or may compriseComprisesL1220, which is commercially available from BASF (Wynoddt, Mich.) in another embodiment, the polymer or polymer additive may be or include polyethylene glycol (e.g., about 400Da or about 600 Da.) in yet another embodiment, the polymer or polymer additive may be or include a low or medium molecular weight polyethylene glycol having a molecular weight greater than or equal to about 400Da and less than or equal to about 1000 Da. for example, the polymer or polymer additive may be or include PEG 400, PEG600, PEG 800, PEG 100, and the like, as well as mixtures or combinations thereof.

Surfactants or surface-active agents

The oral care composition may comprise a surfactant or a surfactant system comprising one or more surfactants. The surfactant may be configured to at least partially aid or facilitate mixing or contact between one or more components of the oral care composition. For example, the surfactant may aid in or facilitate contact between the hydrophobic and hydrophilic components/phases of the oral care composition. The surfactant may be or may include an anionic, nonionic, cationic, amphoteric surfactant, or a combination thereof.

Illustrative surfactants can be or include, but are not limited to, C_8-20Water-soluble salts of alkyl sulfates, C_8-20Sulfonated monoglycerides of fatty acids, sarcosinates, taurates, sodium lauryl sulfate, sodium cocoyl monoglyceride sulfonates, sodium lauryl sarcosinate, sodium lauryl isethionate, sodium laureth carboxylate and sodium dodecylbenzenesulfonate, and cocamidopropyl betaine. Illustrative surfactants or surface active agents may also be or include, but are not limited toL35、L43、L64、L10、L44、L62、10R5、17R4、L25R4、P84、P65、P104、P105, and the like, and combinations thereof, which are commercially available from BASF (ontolifu, new jersey). In a typical embodiment, the surfactant is or comprises poly (ethylene glycol) -block-poly (propylene glycol) -block-poly (ethylene glycol) or PEG-PPG-PEG(s) ((s))L-35)。

The amount of surfactant present in the oral care composition can vary widely. In at least one embodiment, the one or more surfactants can be present in the oral care composition in an amount greater than or equal to 0.0 weight% and less than or equal to 10.0 weight%, based on the total weight of the oral care composition. For example, the amount of surfactant present in the oral care composition can be from about 0.0 weight%, about 1 weight%, about 2 weight%, about 3 weight%, about 4 weight%, or about 4.5 weight% to about 5.5 weight%, about 6 weight%, about 7 weight%, about 8 weight%, about 9 weight%, or about 10 weight%, based on the total weight of the oral care composition. In another example, the surfactant can be present in the oral care composition in an amount of from about 0.0 wt% to about 10 wt%, from about 1 wt% to about 9 wt%, from about 2 wt% to about 8 wt%, from about 3 wt% to about 7 wt%, from about 4 wt% to about 6 wt%, or from about 4.5 wt% to about 5.5 wt%, based on the total weight of the oral care composition. In a preferred embodiment, the surfactant may be present in the oral care composition in an amount of from about 4 wt% to about 6 wt%, more preferably from about 4.5 wt% to about 5.5 wt%, more preferably about 5.0 wt%, based on the total weight of the oral care composition.

Abrasive material

In at least one embodiment, the oral care composition can comprise one or more abrasives or dental abrasives. As used herein, the term "abrasive" may also refer to materials commonly referred to as "polishing agents".

Any suitable orally acceptable abrasive can be used, but preferably the type, fineness (particle size), and amount of abrasive should be selected so that tooth enamel is not excessively abraded in normal use of the oral care composition.

Suitable abrasives include, but are not limited to, silica (e.g., in the form of silica gel, hydrated silica, or precipitated silica), alumina, insoluble phosphates, calcium carbonate, resinous abrasives such as urea-formaldehyde condensation products, and the like. Among the insoluble phosphates that may be used as abrasives are orthophosphates, polymetaphosphates and pyrophosphates. Illustrative examples are dicalcium orthophosphate dihydrate, calcium pyrophosphate, (3-calcium pyrophosphate, tricalcium phosphate, calcium polymetaphosphate, and insoluble sodium polymetaphosphate. if present, the abrasive typically has an average particle size of from about 0.1 to about 30 μm, for example from about 1 to about 20 μm or from about 5 to about 15 μm.

In at least one embodiment, the amount or concentration of abrasive can be from about 5 weight% to about 40 weight%, based on the total weight of the oral care composition. For example, the abrasive can be present in the oral care composition in an amount of about 5.0 wt%, about 5.5 wt%, about 6.0 wt%, about 6.5 wt%, about 7.0 wt%, about 7.5 wt%, about 8.0 wt%, about 8.5 wt%, about 9.0 wt%, about 9.5 wt%, about 10.0 wt%, about 10.5 wt%, about 11.0 wt%, about 11.5 wt%, or about 12.0 wt% to about 12.5 wt%, about 13.0 wt%, about 13.5 wt%, about 14.0 wt%, about 14.5 wt%, about 15.0 wt%, about 15.5 wt%, about 16.0 wt%, about 16.5 wt%, about 17.0 wt%, about 17.5 wt%, about 18.0 wt%, about 18.5 wt%, about 19.0 wt%, about 19.5 wt%, or about 20.0 wt%. In another example, the abrasive can be present in the oral care composition in an amount of about 5 weight%, about 10 weight%, about 15 weight%, or about 20 weight% to about 25 weight%, about 30 weight%, about 35 weight%, or about 40 weight%.

Fluoride ion source

In at least one embodiment, the oral care product and/or oral care composition thereof can be free or substantially free of fluoride (e.g., soluble fluoride salts). In another embodiment, the oral care product and/or oral care composition thereof may further comprise fluoride, such as one or more fluoride ion sources (e.g., soluble fluoride salts). A variety of fluoride ion-generating materials may be employed as the soluble fluoride source. Examples of suitable fluoride ion-generating materials can be found in U.S. Pat. No. 3,535,421 to Briner et al, U.S. Pat. No. 4,885,155 to Parran, Jr et al, and U.S. Pat. No. 3,678,154 to Widder et al, the disclosures of which are incorporated herein by reference. Illustrative fluoride ion sources include, but are not limited to, fluoride, stannous fluoride, sodium fluoride, potassium fluoride, sodium monofluorophosphate, fluorosilicates such as sodium and ammonium fluorosilicate, amine fluoride, ammonium fluoride, and combinations thereof. In one exemplary embodiment, the fluoride ion source comprises sodium fluoride. The amount of fluoride ion source in the oral care composition can be less than 0.08 wt.%, less than 0.07 wt.%, less than 0.06 wt.%, less than 0.05 wt.%, or less than 0.04 wt.%. For example, the amount of fluoride ion source may be about 0.05 wt%. In another embodiment, the fluoride ion source is present in an amount to provide a total of about 100 to about 20,000ppm, about 200 to about 5,000ppm, or about 500 to about 2,500ppm fluoride ion.

Additional ingredients

It will be appreciated by those of ordinary skill in the art that the oral care product and/or oral care composition thereof may comprise other additional ingredients/components. For example, the oral care product and/or oral care composition thereof can comprise anticaries agents, desensitizing agents, viscosity modifiers, diluents, pH modifying agents, humectants, mouth feel agents, sweeteners, flavors, colors, preservatives, and the like, as well as combinations and mixtures thereof. In some embodiments, the compositions described herein are substantially free of volatile flavoring agents. In other embodiments, the compositions described herein are completely free of volatile flavoring agents. It will also be appreciated by those of ordinary skill in the art that while the general attributes of each of the above categories of materials may differ, there may be some common attributes and any given material may serve multiple purposes within two or more of these categories of materials.

In at least one embodiment, the additional ingredients/components can include one or more active materials configured to prevent and/or treat one or more diseases and/or conditions of the oral cavity. For example, the one or more active materials can be configured to prevent and/or treat one or more diseases and/or conditions of the hard and/or soft tissues of the oral cavity. The active material can also be configured to prevent and/or treat one or more physiological conditions and/or diseases, and/or provide aesthetic benefits to the oral cavity.

In at least one embodiment, the oral care product and/or oral care composition thereof can comprise an anticalculus agent. Typically, the anticalculus agent may be incompatible with some oral care compositions, however, embodiments of the present disclosure may incorporate the anticalculus agent with an oral care composition in a single phase oral care product. Illustrative anticalculus agents may include, but are not limited to, phosphates and polyphosphates (e.g., pyrophosphate), polyaminopropanesulfonic Acid (AMPS), hexametaphosphate, zinc citrate trihydrate, polypeptides, polyolefin sulfonates, polyolefin phosphates, bisphosphonates. In a typical embodiment, the anticalculus agent comprises tetrasodium pyrophosphate (TSPP), Sodium Tripolyphosphate (STPP), or a combination thereof.

The oral care product or oral care composition thereof may comprise an antioxidant. Any orally acceptable antioxidant may be used, including but not limited to: butylated Hydroxyanisole (BHA), Butylated Hydroxytoluene (BHT), vitamin a, carotenoids, vitamin E, flavonoids, polyphenols, ascorbic acid, herbal antioxidants, chlorophyll, melatonin, and the like, and combinations and mixtures thereof.

It is understood that all ingredients used in the compositions described herein are orally acceptable. As used herein, the expression "orally acceptable" can define ingredients that are present in the compositions as described in amounts and forms that do not render the use of the compositions in the oral cavity unsafe.

Method of producing a composite material

The present disclosure can provide methods for preventing phase separation in oral care products or oral care compositions thereof incorporating whitening agents (e.g., peroxides). The method can include contacting the oral care composition with a polymeric thickener having a first monomer such as 2-acrylamidomethylpropanesulfonic acid or a salt thereof and a second monomer such as methacrylic acid, a methacrylate, methacrylamide, a methacrylate and vinylpyrrolidone. The oral care composition may be a non-aqueous or propylene glycol-based oral care composition. The method may include the absence of the incorporation of at least one other thickening agent, such as fumed silica and crosslinked polyvinylpyrrolidone. The method may further include forming an intermolecular bonding network between the plurality of polymers of the polymeric thickener to prevent phase separation. The method can include preventing separation under accelerated aging conditions, for example at a temperature of about 40 ℃ to about 50 ℃. The method may include preventing separation under accelerated aging conditions for at least two months. The method may further comprise maintaining viability, stability and/or compatibility with the whitening agent under accelerated aging conditions. For example, the method may comprise maintaining viability, stability, and/or compatibility with the whitening agent for at least three months.