Tooth whitening product

Information

  • Patent Grant
  • 10493016
  • Patent Number
    10,493,016
  • Date Filed
    Tuesday, December 13, 2016
    8 years ago
  • Date Issued
    Tuesday, December 3, 2019
    5 years ago
Abstract
A tooth whitening product is provided. The tooth whitening product has a backing layer and a tooth whitening composition. The tooth whitening composition includes first and second water soluble polymers, water, and a tooth whitening agent, wherein the first water soluble polymer is polyethelene oxide and the second water soluble polymer is polyvinyl alcohol.
Description
FIELD OF THE INVENTION

The present invention relates to products for whitening teeth, and, more particularly, to products for whitening teeth that have a whitening agent incorporated therein.


BACKGROUND OF THE INVENTION

Tooth whitening has become very popular over the past few years. More and more consumers are choosing to whiten their teeth. Options for tooth whitening include toothpastes, mouthrinses, chewing gums, in-office bleaching, and most commonly tooth whitening solutions used with a tray obtained either over-the-counter or from a dentist. Tooth whitening products using a strip of material in combination with a chemical whitening active are known in the art. For example, U.S. Pat. No. 6,419,906, the substance of which is incorporated herein by reference, describes a tooth whitening product comprising a strip of material formed from a water hydratable polymer and a tooth whitening agent. While these whitening products may function for their intended purpose, there is continuing desire to improve the handling and aesthetics of these tooth whitening products.


SUMMARY OF THE INVENTION

A tooth whitening product is provided. The tooth whitening product has a backing layer and a tooth whitening composition. The tooth whitening composition includes first and second water soluble polymers, water, and a tooth whitening agent, wherein the first water soluble polymer is polyethelene oxide and the second water soluble polymer is polyvinyl alcohol.





BRIEF DESCRIPTION OF THE DRAWINGS

While the specification concludes with claims particularly pointing out and distinctly claiming the invention, it is believed that the present invention will be better understood from the following description taken in conjunction with the accompanying drawings in which:



FIG. 1 is a cross-sectional side view of tooth whitening product made in accordance with the present invention, wherein a coating of a tooth whitening agent has been applied to a film;



FIG. 2 is a perspective view of another embodiment of a tooth whitening product of the present invention, wherein the tooth whitening product comprises a web and a coating that completely bridges the void spaces of the web and wherein a portion of the coating has been removed to reveal features there below;



FIG. 3 is a cross-sectional side view of the tooth whitening product of FIG. 2, wherein the void spaces are shown as partially filled;



FIG. 4 is a cross-sectional side view of the tooth whitening product of FIG. 2, wherein the void spaces are shown as completely filled;



FIG. 5 is a perspective view of another embodiment of a tooth whitening product of the present invention, wherein the tooth whitening product comprises a web and a coating that partially bridges the void spaces of the web;



FIG. 6 is a perspective view of another embodiment of a tooth whitening product of the present invention, wherein the tooth whitening product comprises a web and a coating that does not bridge the void spaces of the web;



FIG. 7 is a cross-sectional side view of another embodiment of a tooth whitening product of the present invention that comprises a perforated film; and



FIG. 8 is a perspective view of another embodiment of a tooth whitening product of the present invention that comprises a first layer and a second layer.





DETAILED DESCRIPTION OF THE INVENTION

All weight percentages herein refer to the tooth whitening composition after processing (e.g., after drying, cooling, curing, extrusion, or casting). Reference will now be made in detail to embodiments of the invention, examples of which are illustrated in the accompanying drawings wherein like numerals indicate the same elements throughout the views and wherein elements having the same two last digits (e.g., 20 and 120) connote similar elements. The present invention is directed to tooth whitening products comprising a tooth whitening composition including a tooth whitening or bleaching agent and one or more water soluble polymers and, optionally, water, and a plasticizer. In another embodiment, the invention is directed to a tooth bleaching composition comprising a tooth whitening agent and a polyethylene oxide polymer and a polyvinyl alcohol polymer. As used herein, the phrase “water soluble” preferably means a compound or composition whose solubility in water is greater than 5 wt %, preferably greater than 10 wt %, or more preferably greater than 15 wt % when measured in water at 20 C without the aid of pH adjusting agents, including solutes which are require temperatures greater than 20 C to solubilize in water but which still have the above-stated weight percentages when the solution is cooled to 20 C. Solubility is determined by More preferably, “water soluble” means a compound or composition whose solubility in water is greater than 5 wt %, preferably greater than 10 wt %, or more preferably greater than 15 wt % when first mixed in water at 20 C without the aid of pH adjusting agents. The water soluble polymers are also preferably water hydratable. As used herein, the phrase “water hydratable” is intended to refer to a compound or composition that absorbs water. While the present invention will be described herein with respect to these films or strips, it is contemplated that the present invention can be used with other tooth whitening products, such as dental trays. Water soluble polymers, which are also water hydratable, suitable for use with the present invention include ethylene oxide polymers, homopolymers or mixtures of ethylene oxide polymers of varying molecular weight ranging from about 10,000 Daltons and up to about 10,000,000 Daltons and preferably in the range of about 100,000 to about 1,500,000 Daltons. Such ethylene oxide polymers are commercially available from various sources. Polyethylene oxide in the molecular weight range of 10,000 to 1,000,000 Daltons is available from the Union Carbide Company under the tradename “Polyox”. Other suitable polymers include polypropylene oxide, cross-linked polyacrylic acid, e.g., Carbopol, linear polyacrylic acid, polyvinyl alcohol, sodium alginate, methyl methacrylate, xanthan gum, pectin, pullulan, guar gum, agar, polyvinyl pyrolidone (PVP), carrageanan, celluloses (e.g., hydroxypropylcellulose, hydroxyethyl cellulose, hydroxypropylmethyl cellulose and hydroxymethyl cellulose), polyethylene oxide polypropylene oxide copolymers (e.g., poloxamer), microcrystalline cellulose, polyvinyl pyrolidone polyvinyl acetate copolymers, poly vinyl ester-methyl_copolymers, polyoxyethelene-polyoxypropylene block copolymer, and mixtures thereof. While the thickness of the film may vary, as described more fully hereafter, the film may have a thickness between about 0.1 micrometer and about 1500 micrometer (μm). The tooth whitening composition may be provided as a standalone film or may be applied to, coated on, or otherwise provided with a backing layer or strip of material. The backing layer can be provided as a single layer or as a laminate formed from a plurality of layers, such as any combination of a foam, mesh, or a strip of material. The backing layer can be water permeable, water impermeable, or partially water permeable. The backing layer can be continuous or discontinuous (i.e., formed from a plurality of discrete segments). Examples of some suitable backing layers are described in U.S. Pat. Nos. 5,891,453; 5,989,569; and 2004/0005277.


Hydration of the water soluble polymer by saliva in the oral cavity allows release (e.g., solubilizes, diffuses, or mobilizes) of the whitening agent incorporated in the polymer matrix. The whitening agent releases from the tooth whitening product to the tooth surfaces to which the tooth whitening composition is applied. Whitening or bleaching agents suitable for the practice of the present invention include peroxides, metal chlorites, perborates, percarbonates, peroxyacids, persulfates, and combinations thereof. Suitable peroxide compounds include hydrogen peroxide, urea peroxide, calcium peroxide, and mixtures thereof. Suitable metal chlorites include calcium chlorite, barium chlorite, magnesium chlorite, lithium chlorite, sodium chlorite, and potassium chlorite. The preferred chlorite is sodium chlorite. A preferred percarbonate is sodium percarbonate. Preferred persulfates are oxones.


Optionally, the water soluble polymer may be mixed with a plasticizer. Suitable plasticizers include glycols such as propylene glycol, polyethylene glycol, methoxypolyethylene glycol, polyhydric alcohols such as glycerin sorbitol, and xylitol, and glycerol esters such as glycerol triacetate. Glycerin can be used as well as propylene glycol or polyethylene glycol such as is available from Union Carbide Corporation as their series of Carbowaxes that range in molecular weight from 200 to 600 Daltons. Other plasticizers include cellulose esters, sebacate esters, castor oil, tricresyl phosphate, phthalate, adipate, ethyl citrate, ethanolamine, and oligosaccharides.


Optionally, any of the tooth whitening compositions described herein may further include an amount of water. The amount of water that is present may be varied by the amount of drying or curing that occurs. The embodiments of the present may include greater than about 2%, or about 4%, or about 6% or about 10% and/or less than about 90%, or about 40%, or about 30% of water by weight percent of the tooth whitening composition after drying.


In one embodiment of the present invention, a tooth whitening product 20 comprises a water soluble polymeric film 22 and a solid whitening agent that has been applied as a coating 24 to one side of the water soluble polymeric film 22, as shown in FIG. 1. The solid tooth whitening agent can be applied while the film is still tacky or after the film has dried, cured, or cooled. Application of the tooth whitening agent in this manner reduces exposure of the tooth whitening agent to any water that may have been used as a solvent in forming the film and also reduces the amount of contact between the water soluble polymer and the tooth whitening agent in comparison to a water hydratable film having a tooth whitening agent dispersed there throughout. In addition, this embodiment has an increased concentration of the tooth whitening agent at the surface that is applied to the teeth. Such a coating can also assist in the diffusion of the tooth whitening agent toward the tooth surface since the coating is directly adjacent and/or in contact with the tooth surface during use. Suitable solid tooth whitening agents that can be applied to one side of a water soluble polymeric film include carbimide peroxide, calcium peroxide, percarbonate, sodium percarbonate, perborates, persulfates, and mixtures thereof. These tooth whitening agents can be sprayed, applied by gravure printing, mist grinding, drop powdering, and other processes known in the art.


The coating of the solid tooth whitening agent can cover all or a portion of the water soluble polymeric film. The thickness of the coating can be greater than about 0.001 microns, or greater than about 0.005 microns, or greater than about 0.01 microns or greater than about 0.05 microns, or greater than about 0.1 microns, or greater than about 1 micron, or greater than 5 microns and/or less than about 100 microns, or less than about 50 microns, or less than about 10 microns, or less than about 1 micron. The dose per unit area of the tooth whitening agent is at least about 0.001 mg/cm2, or at least about 0.005 mg/cm2, or at least about 0.01 mg/cm2, or at least about 0.05 mg/cm2, or at least about 0.1 mg/cm2, or at least about 1 mg/cm2, or at least about 10 mg/cm2, or at least about 100 mg/cm2 and/or less than about 500 mg/cm2, or less than about 250 mg/cm2, or less than about 100 mg/cm2, or less than about 10 mg/cm2. Other materials can be mixed with the solid tooth whitening agent or applied sequentially before or after application of the solid tooth whitening agent. For example, binders, adherents, starches, sweeteners and flavorants, colorants (e.g., to aid in distinguishing the active side of the strip from the non-active side), release agents (e.g., talc powder, manitol powder, lecithin, corn oil, bees wax, silica, calcium monostearate, glycerol monostearate, alkali salts of long chain fatty acids) which facilitate release of the tooth whitening composition from a surface such as a casting plate, pH adjusting agents, including alkalizing agents or acidifying agents, surfactants (e.g., polysorbate 80 and glyceryl oleate), and other oral care actives can be applied as part of the application step. While the solid tooth whitening agent can be applied in a dry form, it is contemplated that a solvent could be used with the tooth whitening agent during application. In one embodiment, a solvent that solubilizes both the water soluble polymer and the tooth whitening agent can be employed when applying the tooth whitening agent to the surface of the water soluble film. In this process, the tooth whitening is solubilized in the solvent and then applied to the surface of the water soluble film so that the tooth whitening agent is dispersed at least partly within the film as the solvent can solubilize a portion of the film. Alternatively, the solvent may only solublize the tooth whitening agent, in which case a discrete coating would be formed on one side of the film after solvent evaporation or removal. Suitable solvents could include solvents that can solubilize the tooth whitening agent at a given temperature but which do not solubilize the water soluble polymer at that temperature. Some examples include Cellosolve acetate, anisole, 1,4 dioxane, ethyl acetate, ethylenediamine, dimethyl Cellosolve, Cellosolve solvent, alcohols such as ethanol, methanol, or iso-propanol, Carbitol solvent, n-butanol, cuyl Cellosolve, n-butyl acetate, 2-propanol, and methyl Cellosolve, and mixtures thereof.


The water soluble polymeric film 22 can be prepared using a conventional extrusion, calendaring, pressing or solvent casting processes. For example, to prepare a film by solvent casting polyethylene oxide, the ethylene oxide polymer or mixture of polymers is dissolved in a sufficient amount of a solvent which is compatible with the polymer. Examples of suitable solvents include water, alcohols, acetone, ethyl acetate or mixtures thereof. After a solution has been formed, a plasticizer is added with stirring, and heat is applied if necessary to aid dissolution, until a clear and homogeneous solution has been formed, followed by the addition of the whitening agent and any other ingredients such as flavors. The solution is coated onto a suitable carrier material and dried to form a film. The carrier material must have a surface properties that allow the polymer solution to spread evenly across the intended carrier width without soaking in to form a destructive bond between the two substrates. Examples of suitable carrier materials include glass, stainless steel, teflon, polyethylene-impregnated kraft paper. The solution can also be cast onto the previously described backing layers, a pouch or a portion of a package for the tooth whitening composition. Drying of the film may be carried out in a high-temperature air-bath using a drying oven, drying tunnel, vacuum drier, or any other suitable drying equipment, after which the tooth whitening agent can be sprayed onto the film.


In another embodiment of the present invention, the efficacy and/or stability of the tooth whitening agent can be increased by forming the water soluble film with a solvent other than water so that the tooth whitening agent does not come into contact with water during the formation process and there is no residual water left in the film post manufacture. As used herein, the term “stability” is intended to refer to the propensity of a material to maintain its original concentration or structure over a fixed period of time. As used herein, the term “efficacy” is intended to refer to the amount of tooth whitening per unit time. In one process, the water soluble polymer and the tooth whitening agent are mixed and then fed to an extruder whose screw, through mechanical action, melts the water-hydatratable polymer. The melted polymer is then extruded into a film to be formed into the tooth whitening product.


The efficacy of the tooth whitening agent can also be increased by reducing the amount of water soluble polymer that forms the film. In one embodiment, the water soluble polymer film further comprises water insoluble organic and/or inorganic additives to reduce the amount of the water soluble polymer so that solubilization of the tooth whitening agent is maximized during use. Suitable water insoluble organic materials include polyolefins (e.g., polyethylene, polypropylene, polybutenes, polyisoprenes, and copolymers thereof) and polyester. Suitable water insoluble inorganic materials include calcium phosphate, calcium pyrophosphate, and titanium dioxide, and silica. The water insoluble additives can comprise at least about 10%, or at least about 20%, or at least about 30% and/or less than about 90%, or less than about 80%, or less than about 70%, or less than about 50% or less than about 40%, or less than about 30% by weight of the film. In these embodiments, the amount of the water soluble polymer is at least about 5%, or at least about 10%, or at least about 20%, or at least about 30% and/or less than about 90%, or less than about 80%, or less than about 70% by weight of the film. The water insoluble additives can be ground prior to incorporation into the film. In one embodiment, the average particle size of the water insoluble additives is at least about 1 micron, or at least about 20 microns, or at least about 25 microns and/or less than about 100 microns, or less than about 50 microns, or less than about 25 microns, or less than about 10 microns. In addition to decreasing the amount of water soluble polymer that is available to react with the tooth whitening agent, the concentration of tooth whitening agent available at the surface of the tooth can be increased during hydration, because more water is available to solubilize the tooth whitening agent rather than hydrating or otherwise solubilizing the water soluble polymer. The tooth whitening agent can be admixed with the water soluble polymer as described in U.S. Pat. No. 6,419,906 or coated onto the film as previously described.


In yet another embodiment of the present invention, a web, scrim, or mesh is incorporated in the tooth whitening product to improve the hydration of the film. The web, scrim, or mesh can be formed from fibers that are aligned in random or repeating geometric patterns. Referring to FIG. 2, a tooth whitening product 120 comprising a web 32 is illustrated. The web 32 is formed from fibers 34 that are arranged in a repeating geometric pattern. The fibers can be formed from one or more water insoluble, water soluble, or water hydratable polymers and may have a tooth whitening agent incorporated therein. If the fibers are formed from water insoluble materials, the web may function in a manner similar to the previously described films that incorporate water insoluble materials. The fibers are arranged in a manner to provide void spaces 36 between the fibers. The void spaces can facilitate hydration of the web 32 and therefore solubilization of the tooth whitening agent. The void spaces can vary in size or have a substantially constant size over the web. For example, the void spaces might be smaller in one region and larger in another region depending upon the desired rate of hydration. The fibers 34 can have a diameter of at least about 1 micron, or at least about 5 microns, or at least about 10 microns, or at least about 20 microns, or at least about 50 microns and/or less than about 200 microns, or less than about 100 microns, or less than about 50 microns, or less than about 20 microns. The spacing 38 between fibers is at least about 1 micron, or at least about 5 microns, or at least about 10 microns, or at least about 20 microns, or at least about 50 microns, or at least about 1 mm, or at least about 1.5 mm and/or less than about 5 mm, or less than about 2.5 mm, or less than about 1.5 mm, or less than about 50 microns.


In an alternate embodiment, a tooth whitening product 220, shown in FIG. 3, comprises a web 32 having a coating or layer 44 applied thereto. The web 32 can be formed a water soluble, water insoluble, or water hydratable polymer or other material, such as other polymers (e.g., polypropylene, polyethylene, etc.) and cellulose. The fibers 34 of the web 32 can be arranged in a random or repeating pattern. The coating 44 comprises a water soluble polymer and a tooth whitening agent. Other materials can be included in the coating, such as a plasticizer, water, water insoluble additives, etc. The coating can bridge the void spaces 36 such that a substantially solid layer is formed on web 32. The coating might completely fill the void spaces as shown in FIG. 3 or partially fill the void spaces as shown in FIG. 4 with respect to tooth whitening product 320. When the void spaces are partially filled, the pocket 50 that is formed can facilitate hydration of the web and therefore solubilization and release of the tooth whitening agent. Alternatively, the coating 44 can only partially bridge the void spaces, as shown in FIG. 5 for the tooth whitening product 420. In yet another embodiment, a coating 44 does not bridge the void spaces 36 of web 32 but merely coats the fibers 34, either wholly or partially, as shown by way of example in FIG. 6 for the tooth whitening product 520.


The concentration of the tooth whitening agent within the coating and/or the fibers and the amount of water soluble polymer can be varied within these web embodiments depending upon the extent to which the coating bridges the void spaces and/or coats the fibers and based upon the desired rate of solibilization of the tooth whitening agent. As will be appreciated, any combination of completely filling the voids, partially filling the voids, partially bridging the voids, and coating the fibers can be provided in one embodiment.


In a related embodiment, a perforated film without a distinct web or scrim might be provided, as shown in FIG. 7. In the tooth whitening product 620, a single or multilayer film might be provided comprising a water soluble polymer, a tooth whitening agent, a plasticizer, and optionally water. The film can be perforated after it has dried or cured. The void spaces, holes, or apertures 630 that are formed during the perforation process can pass completely through the thickness of the film or might only partially penetrate the film thickness. The void spaces 636 can have the same dimensions as previously described with respect the void spaces of the web. The void spaces 636 can be provided in a random or repeating pattern and vary in size and shape as previously described. Further, this embodiment can include a coating of a tooth whitening agent as previously described or other features of the embodiments discussed above.


In another embodiment of the present invention, a tooth whitening product 720 is provided in the form of a laminated film as shown in FIG. 8. The laminated film comprises two or more layers comprising water hydratable polymers. A first layer 64, which is to be applied to the teeth, further comprises a tooth whitening agent. The water hydratable polymer comprises at least about 1%, or at least about 10%, or at least about 20% and/or less than about 90%, or less than about 70%, or less than about 50% by weight of the first layer. The tooth whitening agent comprises at least about 1%, or at least about 10%, or at least about 15% and/or less than about 70%, or less than about 60%, or less than about 50% by weight of the first layer. The balance of the first layer can comprise water or other materials, such as the previously described water insoluble additives or a plasticizer. The second layer 66, which is positioned adjacent the lips and/or cheeks during use, preferably does not comprise a tooth whitening agent. The water hydratable polymer of the second layer 66 comprises at least about 20%, or at least about 30%, or at least about 40% and/or less than about 100%, or less than about 90%, or less than about 80% by weight of the second layer. A plasticizer comprises at least about 0.1%, or at least about 1%, or at least about 2% and/or less than about 40%, or less than about 30%, or less than about 20% by weight of the second layer. The balance of the second layer 66 can comprise other materials, such as water, water insoluble additives, or oral care actives other than a tooth whitening agent. Examples of other oral care actives suitable for use with the present invention include phosphates (e.g., pyrophosphates, polyphosphate, polyphosphonates, and mixtures thereof), fluoride ion sources, antimicrobial agent, anti-imflamatory agents, nutrients, and enzymes. These oral care actives are further described in U.S. Pat. No. 6,096,328 (and the patents cited therein), the substances of which are incorporated herein by reference. These other oral care actives could also be incorporated into a film comprising only a single layer and formed from a water-hydratable polymer (e.g., polyethyylene oxide) and a plasticizer, the basic formation of which is described in U.S. Pat. No. 6,419,906.


The composition of the first layer 64 and the second layer 66 of the tooth whitening product 720 can be adapted to provide different functionalities. For example, the first layer 64 might comprise less of the water hydratable polymer than the second layer 66 so that the first layer 64 hydrates more quickly thereby solubilizing the tooth whitening agent more quickly and more effectively (i.e., providing a greater concentration more quickly). The second layer can contain relatively more of the water hydratable polymer so that it functions as a barrier layer preventing diffusion of the solubilized tooth whitening agent away from a tooth while still permitting some hydration from the back side of the tooth whitening product. Also, since the second outer layer comprises more of the water soluble polymer, it will remain in a film-like state longer than the first layer 64 so that the tooth whitening agent will have a longer period of time in which to act upon the teeth. The absence of the tooth whitening agent from the second layer could also improve tissue tolerablity as a peroxide source would not be directly adjacent the soft tissue of the lips and cheeks. The tooth whitening product 720 can be formed by casting the first layer first followed by the second layer being cast on top of the first layer either before or after the first layer has dried or cured. The layers can be pressed together by rollers aligned so that there is nip of gap there between through which the first and second layers pass. The first and second layers can comprise the same water soluble polymer or distinct water soluble polymers.


In another aspect of the present invention, a film comprising a water soluble polymer and a tooth whitening agent is provided in a thin form and with an increased concentration of the tooth whitening agent. The thickness of the film is at least about 1 μm, or at least about 5 μm, or at least about 10 μm, or least about 15 μm and/or less than about 2 mm, or less than about 1 mm, or less than about 0.5 mm, or less than about 0.25 mm, or less than about 0.1 mm, or less than about 20 μm, or less than about 15 μm. The concentration of the tooth whitening agent is at least about 1%, or at least about 10% or at least about 15%, or at least about 20%, or least about 25% and/or less than about 70%, or less than about 60%, or less than about 50%, or less than about 40%, or less than about 30%. Surprisingly, these increased concentration levels of the tooth whitening agent can be utilized while still maintaining acceptable soft tissue tolerability without the need for cumbersome rubber dams or other artificial soft tissue barriers. As used herein, the phrase “artificial barrier” is intended to refer to any physical means that prevents or is intended to prevent a tooth whitening agent from migrating onto the soft tissue adjacent the teeth during a bleaching operation. Other artificial barriers can include light cured resins. As used herein, the phrase “soft tissue tolerability” is intended to refer to the degree to which a user experiences a sensation often described as burning or stinging or experiences irritation of the gingival tissues. This sensation can range from minor to severe. In addition, one or more layers, preferably without a tooth whitening agent, can be provided adjacent the previously described layer containing the tooth whitening agent.


In another embodiment, the tooth whitening composition comprises two or more water soluble polymers, a tooth whitening agent, and optionally a plasticizer, and/or water. The tooth whitening composition may be provided as a layer on a backing layer, as as a stand-alone film, or in other forms. In a preferred embodiment, the first water soluble polymer is a polyethylene oxide polymer and the second water soluble polymer is polyvinyl alcohol. The polyethylene oxide may have an average molecular weight greater than about 100,000, or about 200,000, or about 300,000, or about 600,000 and or less than about 10,000,000, or about 4,000,000, or about 1,500,000, or about 900,000. The tooth whitening composition may comprise greater than about 10%, or about 20%, or about 30% or about 40% and/or less than about 90%, or about 60%, or about 50% by weight of polyethylene oxide. The tooth whitening composition may comprise mixtures of polyethylene oxides have different average molecular weights. The tooth whitening composition may comprise greater than about 0.5%, or about 2%, or about 5% and/or less than about less than about 90% or about 50%, or about 20%, or about 15% or about 10% by weight of polyvinyl alcohol. The ratio of the first water soluble polymer to the second water soluble polymer is between about 10:90 and about 90:0.5 or between about 50:2 and about 30:20. The polyvinyl alcohol may have varying degrees of hydrolysis. The degree of hydrolysis signifies the extent of conversion of polyvinyl acetate to polyvinyl alcohol. A mixture of polyethylene oxide and polyvinyl alcohol will be more adhesive and less cohesive as the degree of hydrolysis of the polyvinyl alcohol increases. Thus, for the same amount of polyethylene oxide, less polyvinyl alcohol is required as the degree of hydrolysis of the polyvinyl alcohol increases in order to provide the same level of adhesiveness. The polyvinyl alcohol may be super hydrolyzed, fully hydrolyzed, intermediately hydrolyzed, or partially hydrolyzed. Typically, the range of hydrolysis, from partially hydrolyzed to super hydrolyzed, is between about 70% (partially hydrolyzed) and about 99.5% (super hydrolyzed). In one embodiment, the range of hydrolysis is greater than about 70%, or about 80%, or about 87% and/or less than about 99%, or about 95%, or about 91%. As used herein, the phrase “hydrolysis” is intended to refer to the level of hydrolysis of the raw material before manufacture of the tooth whitening composition. In another embodiment, the range of hydrolysis is between about 87% and about 91% and the amount of polyvinyl alcohol between about _5_% and about _50_% by weight of the tooth whitening composition. The tooth whitening composition may also optionally include a plasticizer. In one embodiment, the tooth whitening composition may comprise greater than about 1%, or about 10%, or about 20% and/or less than about 80%, or about 60%, or about 80% by weight of a plasticizer. A preferred plasticizer is polyethylene glycol. A more preferred plasticizer is a polyethylene glycol having a molecular weight between about 200 and about 9,000. The tooth whitening composition may also optionally include water at the same levels as previously discussed herein. The tooth whitening composition. The tooth whitening composition may include hydrogen peroxide greater than about 0.5%, or about 3%, or about 6% and/or less than about 40%, or about 20%, or about 10% by weight of the tooth whitening composition. The foregoing embodiments of a tooth whitening composition comprising two water soluble polymers may also incorporate aspects of any of the other embodiments described herein, such as a mesh or scrim, water insoluble organic or inorganic additives, perforations, etc.


Non-limiting examples of the foregoing embodiments incorporating a mixture of polyethylene oxide and polyvinyl alcohol are set forth below. It will be appreciated that these compositions may include additional ingredients or other ingredients may be substituted for those listed. Each example sets forth the tooth whitening composition formulation before drying and after drying.


EXAMPLE 1

















Polyethylene
Polyvinyl






oxide
alcohol






WSR-1105
Gohsenol






(MW
GL-05S


Hydrogen



900,000)
(86.5%-89%)
PEG 600
Water
peroxide




















% wt before
6
2
6.5
82.5
3


drying







% wt after
30
10
35
10
15


drying









EXAMPLE 2

















Polyethylene
Polyvinyl






oxide
alcohol






WSR-205
Gohsenol






(MW
NH-26


Hydrogen



600,000)
(99.4%)
PEG 600
Water
peroxide




















% wt before
7.5
0.5
5
85
2


drying







% wt after
40
2.5
25
22.5
10


drying









EXAMPLE 3

















Polyethylene
Polyvinyl






oxide
alcohol






WRS-1105
Gohsenol






(MW
KH-17


Hydrogen



900,000)
(78.5-81.5%)
PEG 600
Water
peroxide




















% wt before
4
5
6
84
1


drying







% wt after
20
25
30
19
6


drying









EXAMPLE 4

















Polyethylene
Polyvinyl






oxide
alcohol






WSR-N750
Gohsenol






(MW
GL-05S


Hydrogen



300,000)
(86.5-89%)
PEG 600
Water
peroxide




















% wt before
6.5
3
6
81.5
3


drying







% wt after
34
15
30
6
15


drying









Embodiments of the polyethylene oxide/polyvinyl alcohol mixtures of the present invention, including examples 1 to 4, can be made by preparing a first mixture comprising polyethylene oxide and a solvent, such as water, and a second mixture comprising polyvinyl alcohol and a solvent, such as water. It will be appreciated that a mixture of solvents might also be used herein. Both mixtures are separately stirred until both the polyethylene oxide and the polyvinyl alcohol are fully hydrated. The first and second mixtures are combined and a tooth whitening agent (e.g., hydrogen peroxide) and optionally a plasticizer (e.g., PEG 600) are added. This tooth whitening composition may be cast on a backing layer or a suitable drying surface. The tooth whitening composition is then dried until a desired amount of the solvent has been removed. The tooth whitening composition can be freeze dried or a drying tunnel incorporating radiant or convective heating can be used. In one embodiment, the tooth whitening composition can be dried in drying box using a nitrogen air mixture at room temperature at a flow rate between about 0.085 m3/min and about 0.3 m3/min. The drying time may be between about 15 minutes and about 2 hours or between about 20 minutes and about 60 minutes.


The above described embodiments of the present invention can be further combined with other layers such as a thin protective coating layer, e.g., of 10 nanometers (nm) to 500 microns (um) thickness or a backing layer formed from a strip of material. The coating material is applied in a sufficiently thin layer so as not to interfere with the flexibility of the film and to allow the whitening strip to conform to an arrangement of a row of teeth. The coating materials can be one or a combination of high molecular weight (that is, molecular weights greater than 1,000,000 Dalton) and include, ethyl cellulose, propyl cellulose, isopropyl cellulose, butyl cellulose, t-butyl cellulose, cellulose acetate, and derivatives of polyvinyl alcohol such as polyvinyl acetate and shellac.


The tooth whitening products of the present invention can be packaged in pouches as individual strips or a roll of film can be provided in a tape-like dispenser, wherein individuals strips can be cut from the roll for use in the oral cavity or the film can be provided with perforations or other frangible features to permit separation of predetermined length strips from the roll of film. Optionally, the tooth whitening products of the present invention can further include a release liner. The release liner can be formed from any material that exhibits less affinity for the film and/or web than the film or web exhibits for itself. The release liner can be formed from polymer films, paper, foils, woven, non-wovens, and other suitable materials known in the art. Optionally, the release liner can include a coating such as wax, silicone, Teflon®, fluoropolymers, etc. The films of the present invention can be formed directly on the release liner. The release liner can be cut to the desired size either before or after formation of the film thereupon. The tooth whitening products of the present invention can also be provided as liner for dental trays, such as those described in U.S. Pat. No. 5,098,303, wherein the strips are incorporated into the trough of the dental tray.


To use the tooth whitening products of the present invention, the film when applied to the teeth surface when hydrated by saliva in the oral cavity or prewetted by dipping the strip in water will adhere to the teeth in an appropriate manner. In this regard, the tooth whitening product is formed to have a width dimension suitable to cover a row of teeth (upper or lower). Therefore, the tooth whitening product may be applied to the upper set of teeth, or to the lower set of teeth either separately or simultaneously. The length dimension of the tooth whitening product is determined by the amount of coverage desired. In this regard, the number of teeth which it is desired to whiten will determine the dimensions of the product. For instance, it may be desired to only whiten the front teeth, which are most easily seen by others. Accordingly, the length of tooth whitening product can be reduced in this case, as compared to the case where it is desired to whiten all of the teeth. The duration of application of product to the teeth will depend upon the type and concentration of the tooth whitening agent, as well as the type and intensity of extrinsic or intrinsic stain.


The embodiments described herein were chosen and described to provide the best illustration of the principles of the invention and its practical application to thereby enable one of ordinary skill in the art to utilize the invention in various embodiments and with various modifications as are suited to the particular use contemplated. All such modifications and variations are within the scope of the invention as determined by the appended claims when interpreted in accordance with the breadth to which they are fairly, legally and equitably entitled.


The dimensions and values disclosed herein are not to be understood as being strictly limited to the exact numerical values recited. Instead, unless otherwise specified, each such dimension is intended to mean both the recited value and a functionally equivalent range surrounding that value. For example, a dimension disclosed as “40 mm” is intended to mean “about 40 mm.”


Every document cited herein, including any cross referenced or related patent or application and any patent application or patent to which this application claims priority or benefit thereof, is hereby incorporated herein by reference in its entirety unless expressly excluded or otherwise limited. The citation of any document is not an admission that it is prior art with respect to any invention disclosed or claimed herein or that it alone, or in any combination with any other reference or references, teaches, suggests or discloses any such invention. Further, to the extent that any meaning or definition of a term in this document conflicts with any meaning or definition of the same term in a document incorporated by reference, the meaning or definition assigned to that term in this document shall govern.


While particular embodiments of the present invention have been illustrated and described, it would be obvious to those skilled in the art that various other changes and modifications can be made without departing from the spirit and scope of the invention. It is therefore intended to cover in the appended claims all such changes and modifications that are within the scope of this invention.

Claims
  • 1. A tooth whitening product, comprising: a first layer comprising a tooth whitening composition comprising first and second polymers, water, and a tooth whitening agent, wherein said first polymer is polyethylene oxide with an average molecular weight of from about 300,000 to about 900,000 and said second polymer is polyvinyl alcohol, wherein the first layer contacts at least one tooth;a second layer that does not comprise a tooth whitening agent.
  • 2. The tooth whitening product of claim 1, wherein the concentration of said first polymer is between about 10% and about 90% by weight of said tooth whitening composition.
  • 3. The tooth whitening product of claim 1, wherein the concentration of said second polymer is between about 0.5% and about 50% by weight of said tooth whitening composition.
  • 4. The tooth whitening product of claim 1, wherein the concentration of said water is between about 2% and about 90% by weight of said tooth whitening composition.
  • 5. The tooth whitening product of claim 1, wherein said tooth whitening composition further comprises a plasticizer having a concentration between about 1% and about 80% by weight of said tooth whitening composition.
  • 6. The tooth whitening product of claim 5, wherein said plasticizer is polyethylene glycol.
  • 7. The tooth whitening product of claim 1, wherein said polyvinyl alcohol has a hydrolysis between about 70% and about 91%.
  • 8. The tooth whitening product of claim 1, wherein the second layer is a laminate.
  • 9. The tooth whitening product of claim 1, wherein said tooth whitening composition comprises a mixture of two or more polyethylene oxides and wherein said polyethylene oxides have different average molecular weights.
  • 10. The tooth whitening product of claim 1, wherein said tooth whitening agent of the first layer is hydrogen peroxide.
  • 11. The tooth whitening product of claim 1, wherein said first and second polymers are water soluble.
  • 12. The tooth whitening product of claim 1, wherein the second layer comprises at least about 20%, by weight of the second layer, of a water hydratable polymer.
  • 13. The tooth whitening product of claim 12, wherein the water hydratable polymer is polyethylene oxide with an average molecular weight of from about 300,000 to about 900,000.
  • 14. The tooth whitening product of claim 13, wherein there is more polyethylene oxide in the second layer than in the first layer, by total weight of the tooth whitening product.
  • 15. The tooth whitening product of claim 1, wherein the second layer comprises an oral care active other than the tooth whitening agent.
US Referenced Citations (520)
Number Name Date Kind
1979119 Radzinsky Oct 1934 A
2560724 Harrison Jul 1951 A
2835628 Saffir May 1958 A
2994362 Hall Aug 1961 A
3047966 Greenspan Aug 1962 A
3070102 MacDonald Dec 1962 A
3096202 De Groot Von Arx Jul 1963 A
3256014 Kelsey Jun 1966 A
3444858 Russell May 1969 A
3598123 Zaffaroni Aug 1971 A
3625215 Quisling Dec 1971 A
3640741 Etes Feb 1972 A
3657413 Rosenthal et al. Apr 1972 A
3659928 MacFarlane May 1972 A
3688406 Porter et al. Sep 1972 A
3711182 Jasgur Jan 1973 A
3729839 Bourdier May 1973 A
3754332 Warren Aug 1973 A
3784390 Hijiya Jan 1974 A
3844286 Cowen Oct 1974 A
3859987 Holstad Jan 1975 A
3902509 Tundermann et al. Sep 1975 A
3955281 Weitzman May 1976 A
3964164 Hesselgren Jun 1976 A
3972995 Tsuk Aug 1976 A
3998215 Anderson Dec 1976 A
4029757 Miodozeniec Jun 1977 A
4029758 Miodozeniec Jun 1977 A
4031200 Reif Jun 1977 A
4032627 Suchan Jun 1977 A
4072551 Dabal Feb 1978 A
4084700 Dunchock Apr 1978 A
4136145 Fuchs Jan 1979 A
4136162 Fuchs et al. Jan 1979 A
4138314 Patil et al. Feb 1979 A
4138814 Weitzman Feb 1979 A
4139627 Lane Feb 1979 A
4182222 Stahl Jan 1980 A
4211330 Strock Jul 1980 A
4232334 Dyson Nov 1980 A
4251400 Columbus Feb 1981 A
4273418 Gillespie et al. Jun 1981 A
4292299 Suzuki Sep 1981 A
4294820 Keith Oct 1981 A
4307075 Martin Dec 1981 A
4308250 Griffin Dec 1981 A
4324547 Arcan et al. Apr 1982 A
4325855 Dickmann Apr 1982 A
4331576 Colon May 1982 A
4335731 Bora Jun 1982 A
4363843 Crofts Dec 1982 A
4373036 Chang Feb 1983 A
4376628 Aardse Mar 1983 A
4428373 Seid Jan 1984 A
4431631 Clipper Feb 1984 A
4438258 Graham Mar 1984 A
4442258 Sunakawa Apr 1984 A
4460562 Keith Jul 1984 A
4503070 Eby, III Mar 1985 A
4513243 Novak Apr 1985 A
4515162 Yamamoto May 1985 A
4517173 Kizawa May 1985 A
4518721 Dhabhar May 1985 A
4522593 Fischer Jun 1985 A
4522805 Gordon Jun 1985 A
4522806 Muhlemann Jun 1985 A
4528180 Schaeffer Jul 1985 A
4529748 Wienecke Jul 1985 A
4532063 Gueldenzopf Jul 1985 A
4537778 Clipper Aug 1985 A
4544354 Gores Oct 1985 A
4554154 White Nov 1985 A
4557692 Chorbajian Dec 1985 A
4560351 Osborne Dec 1985 A
4568536 Kronenthal Feb 1986 A
4592487 Simon Jun 1986 A
4592488 Simon Jun 1986 A
4592726 Brilliant Jun 1986 A
4593053 Jevne Jun 1986 A
4623394 Nakamura Nov 1986 A
4640685 Croll Feb 1987 A
4650665 Kronenthal Mar 1987 A
4661070 Friedman Apr 1987 A
4687663 Schaeffer Aug 1987 A
4690996 Shih Sep 1987 A
4695465 Kazuo Sep 1987 A
4696757 Blank Sep 1987 A
4712460 Allen Dec 1987 A
4713239 Babaian Dec 1987 A
4713243 Schiraldi Dec 1987 A
4722761 Cartmell Feb 1988 A
4728291 Golub Mar 1988 A
4741700 Barabe May 1988 A
4741941 Englebert et al. May 1988 A
4755385 Etienne Jul 1988 A
4755386 Hsiao Jul 1988 A
4765983 Takayanagi Aug 1988 A
4770634 Pellico Sep 1988 A
4772470 Inoue Sep 1988 A
4777046 Iwakura Oct 1988 A
4786253 Morals Nov 1988 A
4788052 Ng Nov 1988 A
4797283 Allen Jan 1989 A
4799888 Golub Jan 1989 A
4812308 Winston Mar 1989 A
4828113 Friedland et al. May 1989 A
4837008 Rudy Jun 1989 A
4839156 Ng Jun 1989 A
4839157 Mei-King Ng Jun 1989 A
4849213 Schaeffer Jul 1989 A
4849246 Schmidt Jul 1989 A
4860754 Sharik Aug 1989 A
RE33093 Schiraldi et al. Oct 1989 E
4876092 Mizobuchi Oct 1989 A
4891400 Schwabe Jan 1990 A
4895517 Fischer Jan 1990 A
4895721 Drucker Jan 1990 A
4900253 Landis Jan 1990 A
4900552 Sanvordeker Feb 1990 A
4900554 Yanagibashi Feb 1990 A
4902227 Smith Feb 1990 A
4910247 Haldar Mar 1990 A
4915950 Miranda Apr 1990 A
4919615 Croll Apr 1990 A
4925670 Schmidt May 1990 A
4927634 Sorrentino May 1990 A
4927636 Hijiya May 1990 A
4931282 Asmus Jun 1990 A
4949580 Browing Aug 1990 A
4950479 Hill Aug 1990 A
4968251 Darnell Nov 1990 A
4971782 Rudy Nov 1990 A
4972946 Whittaker Nov 1990 A
4980152 Frazier Dec 1990 A
4983379 Schaeffer Jan 1991 A
4983381 Zaragoza Jan 1991 A
4988500 Hunter Jan 1991 A
4990089 Munro Feb 1991 A
5001170 Keegan Mar 1991 A
5008106 Merianos Apr 1991 A
5009881 Hill Apr 1991 A
5015180 Randklev May 1991 A
5024701 Desmarais Jun 1991 A
5032387 Hill Jul 1991 A
5047244 Sanvordeker Sep 1991 A
5059120 Lee Oct 1991 A
5059417 Williams Oct 1991 A
5064717 Suzuki Nov 1991 A
5076791 Madray, Jr. Dec 1991 A
5084268 Thaler Jan 1992 A
5098303 Fischer Mar 1992 A
5122365 Murayama Jun 1992 A
5158825 Altwirth Oct 1992 A
5160737 Friedman Nov 1992 A
5165424 Silverman Nov 1992 A
5166233 Kuroya et al. Nov 1992 A
5171564 Nathoo Dec 1992 A
5186938 Sablotsky Feb 1993 A
RE34196 Munroe Mar 1993 E
5192802 Rencher Mar 1993 A
5211559 Hart et al. May 1993 A
5229164 Pins Jul 1993 A
5234342 Fischer Aug 1993 A
5240415 Haynie Aug 1993 A
5246371 Fischer Sep 1993 A
5252334 Chiang Oct 1993 A
5256402 Prencipe Oct 1993 A
5271940 Cleary Dec 1993 A
5288231 Kuehn et al. Feb 1994 A
5288498 Stanley Feb 1994 A
5290566 Schow Mar 1994 A
5310563 Curtis et al. May 1994 A
5314915 Rencher May 1994 A
5320831 Majeti et al. Jun 1994 A
5326685 Gaglio et al. Jul 1994 A
5330746 Friedman Jul 1994 A
5332576 Mantelle Jul 1994 A
5340314 Tarvis Aug 1994 A
5340581 Tseng et al. Aug 1994 A
5344702 Haubs Sep 1994 A
5354551 Schmidt Oct 1994 A
5356291 Darnell Oct 1994 A
5364267 Fischer Nov 1994 A
5376006 Fischer Dec 1994 A
5380198 Suhonen Jan 1995 A
5387103 Fischer Feb 1995 A
5393528 Staab Feb 1995 A
5401495 Murayama Mar 1995 A
5401528 Schmidt Mar 1995 A
5409631 Fischer Apr 1995 A
5409703 McAnalley Apr 1995 A
5420197 Lorenz May 1995 A
5425641 Fischer Jun 1995 A
5425953 Sintov Jun 1995 A
5427770 Viccaro Jun 1995 A
5438076 Friedman et al. Aug 1995 A
5455043 Fischel-Ghodsian Oct 1995 A
5456745 Roreger Oct 1995 A
5462749 Rencher Oct 1995 A
5464348 Fischer Nov 1995 A
5472704 Santus Dec 1995 A
5474780 Chang Dec 1995 A
5505933 Norfleet Apr 1996 A
5509800 Cunningham Apr 1996 A
5522726 Hodosh Jun 1996 A
5529782 Staab Jun 1996 A
5534562 Fischer Jul 1996 A
5560379 Pieczenik Oct 1996 A
5565190 Santalucia Oct 1996 A
5575654 Pontenot Nov 1996 A
5575655 Darnell Nov 1996 A
5579523 Tanaka Nov 1996 A
5593684 Baker Jan 1997 A
5599553 Chung Feb 1997 A
5603701 Fischer Feb 1997 A
5611687 Wagner Mar 1997 A
5613942 Lucast Mar 1997 A
5616027 Jacobs et al. Apr 1997 A
5618273 Fischer Apr 1997 A
5620322 Lococo Apr 1997 A
5626866 Ebert et al. May 1997 A
5629003 Horstmann May 1997 A
5631000 Pellico May 1997 A
5631055 Vines et al. May 1997 A
5635162 Fischer Jun 1997 A
5639445 Curtis et al. Jun 1997 A
5648064 Gaffar et al. Jul 1997 A
5660178 Kantner Aug 1997 A
5662758 Hamilton Sep 1997 A
5678273 Porcelli Oct 1997 A
5685712 Fischer Nov 1997 A
5686094 Acharya Nov 1997 A
5692900 Fischer Dec 1997 A
5700148 Fischer Dec 1997 A
5700478 Biegajski Dec 1997 A
5707235 Knutson Jan 1998 A
5707736 Levy et al. Jan 1998 A
5708052 Fischer Jan 1998 A
5713738 Yarborough Feb 1998 A
5722833 Fischer Mar 1998 A
5723132 Tseng et al. Mar 1998 A
5725843 Fischer Mar 1998 A
5746598 Fischer May 1998 A
5759037 Fischer Jun 1998 A
5759038 Fischer Jun 1998 A
5766011 Sibner Jun 1998 A
5770105 Fischer Jun 1998 A
5770182 Fischer Jun 1998 A
5770219 Chiang Jun 1998 A
5780045 McQuinn Jul 1998 A
5785955 Fischer Jul 1998 A
5788579 Cherry et al. Aug 1998 A
5800832 Tapolsky Sep 1998 A
5816804 Fischer Oct 1998 A
5819765 Mittiga Oct 1998 A
5827525 Liao et al. Oct 1998 A
5827591 Blok Oct 1998 A
5846058 Fischer Dec 1998 A
5851512 Fischer Dec 1998 A
5851551 Tseng Dec 1998 A
5855870 Fischer Jan 1999 A
5856282 Hughes Jan 1999 A
5858332 Jensen Jan 1999 A
5860809 Meehan Jan 1999 A
5863202 Fontenot Jan 1999 A
5879591 Nagoh et al. Mar 1999 A
5879691 Sagel et al. Mar 1999 A
5888480 Homola et al. Mar 1999 A
5891453 Sagel Apr 1999 A
5894017 Sagel Apr 1999 A
5902568 Ryles May 1999 A
5922307 Montgomery Jul 1999 A
5948430 Zerbe Sep 1999 A
5950830 Trigger Sep 1999 A
5953885 Berman Sep 1999 A
5968500 Robinson Oct 1999 A
5968633 Hamilton Oct 1999 A
5908868 Homola et al. Nov 1999 A
5980249 Fontenot Nov 1999 A
5980932 Chiang Nov 1999 A
5981499 Hau Nov 1999 A
5985249 Fischer Nov 1999 A
5989526 Dorrit Nov 1999 A
5989569 Dirksing Nov 1999 A
6008171 Hughes Dec 1999 A
6019962 Rabe Feb 2000 A
6024891 Hughes Feb 2000 A
6030222 Tarver Feb 2000 A
6036943 Fischer Mar 2000 A
6045811 Dirksing et al. Apr 2000 A
6071503 Drechsler Jun 2000 A
6072100 Mooney Jun 2000 A
6074654 Drechsler Jun 2000 A
6077502 Witt Jun 2000 A
6083421 Huang Jul 2000 A
6086855 Fischer Jul 2000 A
6090401 Gowan, Jr. Jul 2000 A
6094889 VanLoon Aug 2000 A
6096328 Sagel et al. Aug 2000 A
6106293 Wiesel Aug 2000 A
6123950 Hughes Sep 2000 A
6126443 Burgio Oct 2000 A
6129929 Wick Oct 2000 A
6132702 Witt Oct 2000 A
6136297 Sagel et al. Oct 2000 A
6139820 Fischer Oct 2000 A
6139823 Drechsler Oct 2000 A
6142780 Burgio Nov 2000 A
6146655 Ruben Nov 2000 A
6149895 Kutsch Nov 2000 A
6155825 Fischer Dec 2000 A
6155832 Wiesel Dec 2000 A
6159498 Tapolsky Dec 2000 A
6177096 Zerbe Jan 2001 B1
6182420 Berman Feb 2001 B1
6183251 Fischer Feb 2001 B1
6197331 Lerner Mar 2001 B1
6210699 Acharya Apr 2001 B1
6211296 Frate Apr 2001 B1
6217335 Rittan Apr 2001 B1
6231957 Zerbe May 2001 B1
6234793 Fischer May 2001 B1
6248363 Patel Jun 2001 B1
6261679 Chen et al. Jul 2001 B1
6274122 McLaughlin Aug 2001 B1
6277458 Dirksing Aug 2001 B1
6284264 Zerbe Sep 2001 B1
6287120 Wiesel Sep 2001 B1
6306206 Fischer Oct 2001 B1
6306370 Jensen Oct 2001 B1
6309625 Jensen Oct 2001 B1
6312671 Jensen Nov 2001 B1
6322360 Burgio Nov 2001 B1
6331292 Montgomery Dec 2001 B1
6337086 Kanios Jan 2002 B1
6340466 Drechsler Jan 2002 B1
6343932 Wiesel Feb 2002 B1
6368576 Jensen Apr 2002 B1
6375963 Repka Apr 2002 B1
6379155 Rittano Apr 2002 B1
6379654 Gebreselassie Apr 2002 B1
6391283 Jensen May 2002 B1
6402514 Fischer May 2002 B1
6400801 Fischer Jun 2002 B1
6406683 Drechsler Jun 2002 B1
6419903 Xu Jul 2002 B1
6419906 Xu et al. Jul 2002 B1
6461158 Sagel Oct 2002 B1
6468079 Fischer Oct 2002 B1
6488914 Montgomery Dec 2002 B2
6500004 Jensen Dec 2002 B2
6500408 Chen Dec 2002 B2
6503486 Xu Jan 2003 B2
6514483 Xu Feb 2003 B2
6517350 Diasti Feb 2003 B2
6537565 Swanbom Mar 2003 B2
6585997 Moro Mar 2003 B2
6551579 Sagel Apr 2003 B2
6552024 Chen Apr 2003 B1
6576712 Feldstein Jun 2003 B2
6582708 Sagel Jun 2003 B1
6589512 Yue Jul 2003 B1
6592887 Zerbe Jul 2003 B2
6596298 Leung Jul 2003 B2
6625839 Fischer Sep 2003 B2
6635272 Leaderman Oct 2003 B2
6649147 Ye et al. Nov 2003 B1
6652282 Jensen Nov 2003 B2
6669930 Hoic Dec 2003 B1
6682721 Kim et al. Jan 2004 B2
6682756 Horstmann Jan 2004 B1
6685921 Lawlor Feb 2004 B2
6689344 Chang Feb 2004 B2
6692727 Yue et al. Feb 2004 B1
6703040 Katsarava Mar 2004 B2
6709671 Zerbe Mar 2004 B2
6719995 Rajaiah Apr 2004 B2
6729879 Allred May 2004 B2
6730316 Chen May 2004 B2
6737080 Schumann May 2004 B1
6756417 Allred Jun 2004 B2
6814794 Allred Nov 2004 B2
6860736 Allred Mar 2005 B2
6884426 Sagel Apr 2005 B2
6916463 Lee et al. Jul 2005 B2
6946142 Chang Sep 2005 B2
6949240 Sagel et al. Sep 2005 B2
6981874 Allred Jan 2006 B2
6994546 Fischer Feb 2006 B2
6997706 Jessop Feb 2006 B2
6997708 Allred Feb 2006 B2
7011523 Allred Mar 2006 B2
7018622 Goodhart et al. Mar 2006 B2
7025983 Leung Apr 2006 B2
7040893 Fischer May 2006 B2
7040897 Fischer May 2006 B2
7048543 Allred May 2006 B2
7052275 Allred May 2006 B2
7056118 Allred Jun 2006 B2
7059857 Allred Jun 2006 B2
7059858 McLean Jun 2006 B2
7074042 Allred Jul 2006 B2
7094393 Montgomery Aug 2006 B2
7097449 Jessop Aug 2006 B2
7121828 Fischer Oct 2006 B2
7122199 Sagel Oct 2006 B2
7128899 Chen Oct 2006 B2
7144250 Fischer Dec 2006 B2
7168951 Fischer Jan 2007 B2
7172423 Allred Feb 2007 B2
7192276 Fischer Mar 2007 B2
7192280 Allred Mar 2007 B2
7198623 Fischer Apr 2007 B2
20010009755 Fischer Jul 2001 A1
20010021828 Fischer Sep 2001 A1
20010024657 Lerner Sep 2001 A1
20020006387 Sagel et al. Jan 2002 A1
20020126785 Sagel et al. Jan 2002 A1
20020018754 Sagel Feb 2002 A1
20020081556 Tseng Jun 2002 A1
20020127190 Zerbe Sep 2002 A1
20020127254 Fotinos Sep 2002 A1
20020131990 Barkalow Sep 2002 A1
20020141950 Chen Oct 2002 A1
20020146666 Sagel et al. Oct 2002 A1
20020187111 Xu et al. Dec 2002 A1
20020187181 Godbey Dec 2002 A1
20030035841 Dzija Feb 2003 A1
20030049209 Tseng Mar 2003 A1
20030054039 Zyck Mar 2003 A1
20030082115 Allred May 2003 A1
20030099690 Awamura May 2003 A1
20030145863 Allred Aug 2003 A1
20030147258 Fischer Aug 2003 A1
20030148242 Fischer Aug 2003 A1
20030152528 Singh Aug 2003 A1
20030156980 Fischer Aug 2003 A1
20030170308 Cleary Sep 2003 A1
20030194382 Chang Oct 2003 A1
20030199605 Fischer Oct 2003 A1
20030211056 Sagel Nov 2003 A1
20030212372 Fischer Nov 2003 A1
20030215766 Fischer Nov 2003 A1
20030219389 Sagel Nov 2003 A1
20030219390 Santarpia Nov 2003 A1
20030228264 Perna Dec 2003 A1
20040005277 Willison Jan 2004 A1
20040022755 Kamar Feb 2004 A1
20040043134 Corriveau Mar 2004 A1
20040062724 Moro Apr 2004 A1
20040086468 Prosise May 2004 A1
20040091432 Dulin May 2004 A1
20040096569 Barkalow May 2004 A1
20040101496 Chen May 2004 A1
20040105834 Singh Jun 2004 A1
20040120903 Sagel Jun 2004 A1
20040122377 Fischer Jun 2004 A1
20040136927 Kim Jul 2004 A1
20040209229 Jensen Oct 2004 A1
20040214130 Fischer Oct 2004 A1
20040214131 Fischer Oct 2004 A1
20040214140 Fischer Oct 2004 A1
20040219190 Kosti Nov 2004 A1
20040223933 Chen Nov 2004 A1
20040249016 Allread Dec 2004 A1
20040258723 Singh Dec 2004 A1
20050016884 Stout Jan 2005 A1
20050019275 Sagel Jan 2005 A1
20050019277 Sagel et al. Jan 2005 A1
20050031554 Kim Feb 2005 A1
20050031675 Spence Leung Feb 2005 A1
20050048102 Tapolsky Mar 2005 A1
20050064371 Soukos Mar 2005 A1
20050069837 Lewis Mar 2005 A1
20050100515 Sagel May 2005 A1
20050130096 Stout Jun 2005 A1
20050136373 Fischer Jun 2005 A1
20050137109 Quan Jun 2005 A1
20050137110 Scott Jun 2005 A1
20050147658 Tapolsky Jul 2005 A1
20050163820 Fischer Jul 2005 A1
20050186150 Allred Aug 2005 A1
20050196726 Fischer Aug 2005 A1
20050208110 Singh Sep 2005 A1
20050215727 Feldstein Sep 2005 A1
20050238591 Sagel Oct 2005 A1
20050249677 Malcmacher Nov 2005 A1
20050249680 Goodhart Nov 2005 A1
20050249780 Goodhart Nov 2005 A1
20050260544 Jones et al. Nov 2005 A1
20050287086 Sagel Dec 2005 A1
20060263307 Robillard Nov 2006 A1
20070003495 Sagel Jan 2007 A1
20070086891 Sagel Apr 2007 A1
20070086961 Sagel Apr 2007 A1
20070218015 Hardy Sep 2007 A1
20070253990 Sagel Nov 2007 A1
20070259011 Sagel Nov 2007 A1
20070269388 Sagel Nov 2007 A1
20070269471 Sagel Nov 2007 A1
20070269491 Sagel Nov 2007 A1
20070269520 Sagel Nov 2007 A1
20070269521 Sagel Nov 2007 A1
20070275023 Sagel Nov 2007 A1
20070275041 Sagel Nov 2007 A1
20070297994 Sagel Dec 2007 A1
20070298088 Sagel Dec 2007 A1
20080011636 St. John Jan 2008 A1
20080025923 Sagel Jan 2008 A1
20080025924 Sagel Jan 2008 A1
20080025927 Sagel Jan 2008 A1
20080025928 Sagel Jan 2008 A1
20080026021 Sagel Jan 2008 A1
20080031910 Sagel Feb 2008 A1
20080038211 Sagel Feb 2008 A1
20080226567 Sagel Sep 2008 A1
20090181071 St. John Jan 2009 A1
20090092564 Sagel et al. Apr 2009 A1
20110014252 Sagel et al. Jan 2011 A1
20120189680 Sagel et al. Jul 2012 A1
Foreign Referenced Citations (134)
Number Date Country
601478 Sep 1990 AU
681997 Mar 1964 CA
1209761 Aug 1986 CA
2078960 Oct 1993 CA
2095445 Jul 1995 CA
2000040 Oct 1995 CA
2162536 May 1996 CA
2162812 May 1996 CA
2162885 May 1996 CA
871818 Mar 1953 DE
1104116 Apr 1961 DE
2330869 Jan 1975 DE
29701552 May 1997 DE
00636604 Nov 1982 EP
0 063 604 Mar 1984 EP
0 109 269 May 1984 EP
0 109 269 Jul 1986 EP
0 200 508 Dec 1986 EP
0 219 762 Apr 1987 EP
0 232 006 Aug 1987 EP
0 252 459 Jan 1988 EP
0 273 069 Jul 1988 EP
0 288 420 Oct 1988 EP
0 328 317 Aug 1989 EP
0 381 194 Aug 1990 EP
0 273 069 Oct 1992 EP
0 511 782 Nov 1992 EP
0 539 751 May 1993 EP
0 569 797 Nov 1993 EP
0 599 435 Jun 1994 EP
0 636 378 Feb 1995 EP
0 637 446 Feb 1995 EP
0 743 059 Nov 1996 EP
0 763 358 Mar 1997 EP
0 854 112 Jul 1998 EP
0 864 315 Sep 1998 EP
0 899 208 Mar 1999 EP
1 153 594 Nov 2001 EP
0250187 Sep 2003 EP
2637 175 Apr 1990 FR
2701397 Feb 1998 FR
1142325 Feb 1969 GB
1240411 Jul 1971 GB
2108841 May 1983 GB
2 115 431 Sep 1983 GB
2 159 052 Nov 1985 GB
42604 Sep 1980 IE
57-028102 Feb 1982 JP
58-213709 Dec 1983 JP
60005159 Jan 1985 JP
60005160 Jan 1985 JP
61280423 Dec 1986 JP
62-142113 Jun 1987 JP
62-225417 Nov 1987 JP
630005756 Jan 1988 JP
63-054318 Mar 1988 JP
64-040423 Feb 1989 JP
1-279838 Nov 1989 JP
1279838 Nov 1989 JP
03-264522 Mar 1990 JP
02-202814 Aug 1990 JP
2250826 Oct 1990 JP
3198754 Aug 1991 JP
3-264522 Nov 1991 JP
3-264523 Nov 1991 JP
5-124954 May 1993 JP
06-321774 May 1993 JP
5220203 Aug 1993 JP
5-236885 Sep 1993 JP
7-100186 Apr 1995 JP
7126133 May 1995 JP
8183732 Jul 1996 JP
08325128 Dec 1996 JP
10-017448 Jan 1998 JP
10226639 Aug 1998 JP
1222420 Aug 1999 JP
2003137756 May 2003 JP
20030059552 Jul 2009 KR
2075965 Sep 1994 RU
WO 8806879 Sep 1988 WO
WO 8910740 Nov 1989 WO
WO 9015592 Dec 1990 WO
WO 9103236 Mar 1991 WO
WO 9106270 May 1991 WO
WO 9106289 May 1991 WO
WO 9116041 Oct 1991 WO
WO 9210161 Jun 1992 WO
WO 9301790 Feb 1993 WO
WO 9505416 Feb 1995 WO
WO 9509603 Apr 1995 WO
WO 9515158 Jun 1995 WO
WO 9517158 Jun 1995 WO
WO 9524872 Sep 1995 WO
WO 9625910 Aug 1996 WO
WO 9717059 May 1997 WO
WO 9725968 Jul 1997 WO
WO 9817263 Apr 1998 WO
WO 9855044 Dec 1998 WO
WO 9855079 Dec 1998 WO
WO 9920237 Apr 1999 WO
WO 9927895 Jun 1999 WO
WO 9962472 Dec 1999 WO
WO 9966870 Dec 1999 WO
WO 0042992 Jul 2000 WO
WO 00044845 Aug 2000 WO
WO 0054699 Sep 2000 WO
WO 0101942 Jan 2001 WO
WO 01001958 Jan 2001 WO
WO 0101958 Jan 2001 WO
WO 01030263 May 2001 WO
WO 01134107 May 2001 WO
WO 0168045 Sep 2001 WO
WO 0168045 Sep 2001 WO
WO 0200182 Jan 2002 WO
WO 0202085 Jan 2002 WO
WO 0204570 Jan 2002 WO
WO 0207636 Jan 2002 WO
WO 0226196 Apr 2002 WO
WO 0240068 May 2002 WO
WO 0202085 Jun 2002 WO
WO 0243657 Jun 2002 WO
WO 02060779 Aug 2002 WO
WO 02087645 Nov 2002 WO
WO 02092049 Nov 2002 WO
WO 03011259 Feb 2003 WO
WO 03043659 May 2003 WO
WO 03072075 Sep 2003 WO
WO 03086337 Oct 2003 WO
WO 03101360 Dec 2003 WO
WO 2004071323 Aug 2004 WO
WO 2004103201 Dec 2004 WO
WO 2005027768 Mar 2005 WO
WO 2005074894 Aug 2005 WO
WO 06124983 Nov 2006 WO
Non-Patent Literature Citations (90)
Entry
J.H. Briston, “Plastic Films”, 1974, pp. 96-97.
G. McLaughlin, et al., “Materials” and “Clinical Techniques”, Color Atlas of Tooth Whitening, 1991, pp. 35-38 & 45-50, Ishiyaku EuroAmerica, Inc.
S.M. Newman, et al., “Tray-Forming Technique for Dentist-Supervised Home Bleaching”, Quintessence International, 1995, pp. 447-453, vol. 26, No. 7.
3M Dental Products 2000 Product Catalog, 32 pages.
Besner, E., et al., Practical Endodontics, 1994, pp. 7-15, 178-180; Mosby-Year Book, Inc.
Howard Frysh, BDS, DDS., “Chemistry of Bleaching”, Complete Dental Bleaching, 1995, pp. 25-32 & 90-97, Quintessence Publishing Co, Inc.
V.B. Haywood, et al., “Nightguard Vital Bleaching”, Quintessence International, 1989, vol. 20, No. 3, pp. 173-176, 19th International Meeting on Dental Implants and Transplants, Bologna, Italy.
V.B. Haywood, “History, Safety, and Effectiveness of Current Bleaching Techniques and Applications of the Nightguard Vital Bleaching Technique”, Quintessence International, 1992, vol. 23, No. 7, pp. 471-488.
V.B. Haywood, “Nightguard Vital Bleaching”, Dentistry Today, 1997, pp. 88-91.
“Tooth Bleaching, Home-Use Products”, Clinical Research Associates Newsletter, 1989, vol. 3, Issue 12.
Ralph H. Leonard Jr., et al, “Risk factors for developing tooth sensitivity and gingival irritation associated with nightguard vital bleaching”, Esthetic Dentistry, 1997, vol. 28,No. 8, pp. 527-534.
Van B. Haywood, et al, “Nightguard vital bleaching: how safe is it?”, Esthetic Dentistry, 1991, vol. 22, No. 7, pp. 515-523.
Van B. Haywood, “Bleaching of vital and not vital teeth”, Periodontology and Restorative Dentistry, 1992, pp. 142-149.
Van B. Haywood, “Nightquard vital bleaching, a history and products update: Part 1”, Esthestic Dentistry Update, 1991, vol. 2, No. 4, pp. 63-66.
Van B. Haywood, “Nightguard vital bleaching, a history and products update: Part 2”, Esthestic Dentistry Update, 1991, vol. 2, No. 5, pp. 82-85.
Claudia Paula Drew, “Teeth Bleaching . . . a Vital technique for you to know”, 1988, Sep./Oct., pp. 23-25.
Van Benjamin Haywood, “Overview and Status of Mouthguard Bleaching” Journal of Esthetic Dentistry, 1991, vol. 3, No. 5, pp. 157-161.
Van B. Haywood, “Nightguard vital bleaching: current information and research”, Esthetic Dentistry Update, 1990, vol. 1, No. 2, pp. 20-25.
Carolyn F. G. Wilson, et al, “Color change following vital bleaching of tetracycline-stained teeth” Pediatric Dentistry, 1985, vol. 7, No. 3, pp. 205-208.
“Tooth Bleaching, Home-Use Products”, Clinical Research Associates Newsletter, Jul. 1989, pp. 1-4.
Sue Ellen Richardson, “Home bleaching: effectiveness, history, technique, bleaches, cost and safety” The Journal of the Greater Houston Dental Society, 1989, pp. 22-26.
Van B. Haywood, “The food and drug administration and its influence on home bleaching”, ADA, 1993, pp. 12-18.
Van B. Haywood, “Efficacy of foam liner in 10% carbamide peroxide bleaching technique”, Esthetic Dentistry, 1993, vol. 24, No. 9, pp. 663-666.
Christopher J. Woolverton, “Toxicity of two carbamide peroxide products used in nightguard vital bleaching”, American Journal of Dentistry, 1993, vol. 6, No. 6, pp. 310-314.
Van B. Haywood, “Response of normal and tetracycline-stained teeth with pulp-size variation to nightguard vital bleaching”, Journal of Esthetic Dentistry, 1994, vol. 6, No. 3, pp. 109-114.
Ralph H. Leonard, et al, “Salivary pH changes during 10% carbamide peroxide bleaching” Dental Research, 1994, vol. 25, No. 8, pp. 547-550.
Ralph H. Leonard, et al, “Change in pH of plaque and 10% carbamide peroxide solution during nightguard vial bleaching treatment” Esthetic Dentistry, 1994, vol. 25, No. 12, pp. 819-823.
Van B. Haywood, “Historical development of whiteners: clinical safety and efficacy”, Aesthetics, 1997, pp. 98-104.
Van B. Haywood, “Effectiveness, side effects and long-term status of nightguard vital bleaching”, JADA, 1994, vol. 125, pp. 1219-1226.
James W. Curtis, et al, “Assessing the effects of 10 percent carbamide peroxide on oral soft tissues”, JADA, 1996, vol. 127, pp. 1218-1223.
Fonda G. Robinson, et al, “Effect of 10 percent carbamide peroxide on color of provisional restoration materials”, JADA, 1997, vol. 128, pp. 727-731.
Van B. Haywood, “Commonly asked questions about nightguard vital bleaching”, IDA Journal, 1993, pp. 28-33.
Van B. Haywood, “Nightguard vital bleaching: current concepts and research”, JADA, 1997, vol. 128, pp. 19s-25s.
Van B. Haywood, “Commonly asked questions about nightguard vital bleaching”, The Dental Assistant, Mar./Apr. 1996, pp. 6-12.
M.S. McCracken, “Demineralization effects of 10 percent carbamide peroxide”, Journal of Dentistry, 1996, vol. 24, No. 6, pp. 395-398.
Van B. Haywood, “Achieving, maintaining and recovering successful tooth bleaching”, Journal of Esthetic Dentistry, 1996, vol. 8, No. 1, pp. 31-38.
Van B. Haywood, “Considerations and variations of dentist-prescribed, home-applied tooth-bleaching techniques”, Compound Educ Dent., 1994, Suppl. No. 17, pp. s616-s621.
Van B. Haywood, “Efficacy of six months of nightguard vital bleaching of tetracycline-stained teeth”, Journal of Esthetic Dentistry, 1997, vol. 9, No. 1, pp. 13-19.
Carl M. Russell, et al, “Dentist-supervised home bleaching with ten percent carbamide peroxide gel: a six month study”, Journal of Esthetic Dentistry, 1996, vol. 8, No. 4, pp. 177-182.
R.E. Goldstein, et al., “Chemistry of Bleaching”, Complete Dental Bleaching, 1995, pp. 25-32 & 90-97, Quintessence Publishing Co., Inc.
Paul A. Sagel, et al., Vital Tooth Whitening With a Novel Hydrogen Peroxide Strip System: Design, Kinetics, and Clinical Response, Compendium, Supplement No. 29, vol. 21, 2000.
Office Action from the United States Patent & Trademark Office, dated Jun. 18, 2002, issued on U.S. Appl. No. 09/864,640, filed May 24, 2001, assignee—The Procter & Gamble Company, now abandoned.
Office Action from the United States Patent & Trademark Office, dated Sep. 5, 2002, issued on U.S. Appl. No. 09/864,686, filed May 24, 2001, assignee—The Procter & Gamble Company, now abandoned.
Office Action from the United States Patent & Trademark Office, dated May 28, 2003, issued on U.S. Appl. No. 09/864,686, filed May 24, 2001, assignee—The Procter & Gamble Company, now abandoned.
International Search Report, dated Sep. 24, 1998, issued on International Application No. PCT/US 98/11113.
International Search Report, dated Jan. 13, 1999, issued on International Application No. PCT/US 98/10967.
International Search Report, dated Apr. 14, 1999, issued on International Application No. PCT/US 98/17774.
International Search Report, dated Jul. 17, 2000, issued on International Application No. PCT/US 00/06604.
International Search Report, Jul. 26, 2000, issued on International Application No. PCT/US 00/06605.
International Search Report, dated Oct. 13, 2000, issued on International Application No. PCT/US 00/15891.
International Search Report, dated Oct. 13, 2000, issued on International Application No. PCT/US 00/18189.
International Search Report, dated Oct. 17, 2000, issued on International Application No. PCT/US 00/18187.
PCT Written Opinion, dated May 3, 2001, issue on International Application No. PCT/US00/18188.
International Preliminary Examination Report, dated Jul. 30, 2001, issued on International Application No. PCT/US00/18188.
International Search Report, dated Aug. 6, 2001, issued on International Application No. PCT/US 00/29384.
International Search Report, dated Apr. 5, 2002, issued on International Application No. PCT/US 01/19060.
International Search Report, dated Sep. 19, 2002, issued on International Application No. PCT/US 02/10630.
International Search Report, dated Oct. 9, 2002, issued on International Application No. PCT/US 01/24558.
Office Action from the United States Patent & Trademark Office, dated May 11, 2006, issued on U.S. Appl. No. 10/927,655, filed Aug. 26, 2004, assignee—The Procter & Gamble Company.
Office Action from the United States Patent & Trademark Office dated Nov. 30, 2006, issued on U.S. Appl. No. 10/927,655, filed Aug. 26, 2004, assignee—The Procter & Gamble Company.
Office Action from the United States Patent & Trademark Office dated Aug. 3, 2007, issued on U.S. Appl. No. 10/927,655, filed Aug. 26, 2004, assignee—The Procter & Gamble Company.
Office Action from the United States Patent & Trademark Office dated Apr. 17, 2008, issued on U.S. Appl. No. 10/927,655, filed Aug. 26, 2004, assignee—The Procter & Gamble Company.
Office Action from the United States Patent & Trademark Office dated Feb. 21, 2008, issued on U.S. Appl. No. 11/888,176, filed Jul. 31, 2007, assignee—The Procter & Gamble Company.
International Search Report, PCT/US 03/28612.
International Search Report, dated Sep. 25, 2003, issued on International Application No. PCT/US 03/16372.
International Search Report, dated Nov. 7, 2003, issued on International Application No. PCT/US 03/25354.
International Search Report, dated Jan. 7, 2004, issued on International Application No. PCT/US 03/26269.
International Search Report, dated Mar. 15, 2004, issued on International PCT/US2004/036322.
PCT Written Opinion, dated Mar. 21, 2005, issued on International Application No. PCT/ US2004/036322.
International Search Report, dated Oct. 31, 2006, issued on International Application No. PCT/US 06/019057.
Written Opinion of International Searching Authority dated Oct. 31, 2006, issued on International Application No. PCT/US2006/019057.
Declaration of Non-Establishment of International Search Report, dated Dec. 28, 2006, issued on International Application No. PCT/IB2006/05217.
Written Opinion of International Searching Authority dated Dec. 28, 2006, issued International Application No. PCT/IB2006/05217.
International Search Report, dated Feb. 18, 2008, issued on International Application No. PCT/IB2007/052834.
Written Opinion of International Searching Authority dated Feb. 18, 2008, issued on International Application No. PCT/IB2007/052834.
Newman, S.M. et al., “Tray—forming technique for Dentist—supervised home bleaching”, Quintessence International, vol. 26, No. 7, pp. 447-453 (1995).
Messing, J.J., et al., Color Atlas of Endodontics, 1988, pp. 106-107, 135-140, 173-175, 257-259, The C.V. Mosby Company, Ltd.
Office Action from the United States Patent & Trademark Office dated Aug. 3, 2007, issued on U.S. Appl. No. 09/268,185, filed Mar. 15, 1999, assignee—The Procter & Gamble Company.
Office Action from the United States Patent & Trademark Office dated Sep. 24, 2002, issued on U.S. Appl. No. 09/268,185, filed Mar. 15, 1999, assignee—The Procter & Gamble Company.
Office Action from the United States Patent & Trademark Office dated Oct. 4, 2001, issued on U.S. Appl. No. 09/268,185, filed Mar. 15, 1999, assignee—The Procter & Gamble Company.
Office Action from the United States Patent & Trademark Office dated Oct. 20, 2001, issued on U.S. Appl. No. 09/864,640, filed May 24, 2001, 1999, assignee—The Procter & Gamble Company.
Office Action from the United States Patent & Trademark Office dated Jun. 18, 2002, issued on U.S. Appl. No. 09/864,640, filed May 24, 2001, 1999, assignee—The Procter & Gamble Company.
Office Action from the United States Patent & Trademark Office dated Jul. 1, 2004, issued on U.S. Appl. No. 10/321,252, filed Dec. 17, 2002, assignee—The Procter & Gamble Company.
Office Action from the United States Patent & Trademark Office dated Nov. 21, 2005, issued on U.S. Appl. No. 11/099,738, filed Apr. 6, 2005, assignee—The Procter & Gamble Company.
Office Action from the United States Patent & Trademark Office dated Jun. 29, 2006, issued on U.S. Appl. No. 11/157,769, filed Jun. 21, 2005, assignee—The Procter & Gamble Company.
Office Action from the United States Patent & Trademark Office dated Mar. 8, 2007, issued on U.S. Appl. No. 11/157,769, filed Jun. 21, 2005, assignee—The Procter & Gamble Company.
Office Action from the United States Patent & Trademark Office dated Sep. 25, 2007, issued on U.S. Appl. No. 11/157,769, filed Jun. 21, 2005, assignee—The Procter & Gamble Company.
Office Action from the United States Patent & Trademark Office dated Oct. 2, 2008, issued on U.S. Appl. No. 11/157,769, filed Jun. 21, 2005, assignee—The Procter & Gamble Company.
DC Chemical Co., Ltd., http://www.oci.co.kr/english/product/p_petr/p_petr8.htm pp. 1-10.
Dow Chemicals, http://www.dow.com/polyox/intro.htm pp. 1-2, Aug. 2002.
Related Publications (1)
Number Date Country
20170087079 A1 Mar 2017 US
Provisional Applications (1)
Number Date Country
60409862 Sep 2002 US
Continuations (2)
Number Date Country
Parent 13953879 Jul 2013 US
Child 15377577 US
Parent 10820590 Apr 2004 US
Child 13953879 US
Continuation in Parts (1)
Number Date Country
Parent 10659100 Sep 2003 US
Child 10820590 US