This invention relates to a dentifrice and more particularly to a dentifrice containing rapidly water hydratable film flakes suspended in the dentifrice composition which impart to the dentifrice decorative, cosmetic and therapeutic benefits.
Aesthetic effects have been acknowledged to play an important role in consumer acceptance of many products. In many cases ornamental effects have been used to distinguish particular products in the marketplace and identify products having particular distinct properties. In the dentifrice field, substantially clear dentifrice products such as toothpastes and gels which have incorporated therein contrasting colored flakes are known. Such flakes provide an aesthetic effect which the consumer finds pleasing and promotes the use of the dentifrice, particularly by children. Although such products have met with consumer approval, the art seeks to further improve the aesthetic effects as well as the cosmetic and therapeutic benefits of these products so as to encourage the use of dentifrices in practicing oral hygiene.
In accordance with the present invention there is provided a dentifrice having suspended therein flakes of a water hydratable film (hereinafter film flakes) comprised of a homogeneous mixture of a water soluble hydroxyalkyl cellulose polymer and starch, the film matrix having entrained therein an agent selected from therapeutic, cosmetic and decorative agents.
In one embodiment of the invention there is provided an aesthetically decorative dentifrice having distributed throughout film flakes in which a decorative colorant is entrained in the film matrix, the dentifrice vehicle being substantially clear so that the aesthetically decorative effect can be viewed by the user.
In a second embodiment, therapeutic agents such as antibacterial agents and fluoride anticaries salts, are entrained in the film flake matrix.
In a third embodiment cosmetic agents such as sweetening agents, breath freshening agents, are entrained in the film flake matrix which flavorants are rapidly released as the flakes disintegrate during toothbrushing, delivering a pleasing burst of sweetness or breath freshening flavor into the oral cavity.
The entrainment of the therapeutic and cosmetic agents in the film flake matrix suspended in the dentifrice isolates these agents from interaction with reactive ingredients present in the dentifrice so that the agents are maintained substantially separate from the reactive dentifrice ingredients daring manufacture and storage while subsequently being released from the film matrix when the dentifrice containing the film flakes is topically applied to the tooth surface as by tooth brushing.
The term “substantially clear” when used in to describe the present invention shall mean translucent or transparent. The term “dentifrice” shall include toothpastes and gels.
The film flakes of the present invention are formed from a matrix comprised of hydroxyalkyl methylcellulose starch and starch film forming agents in which is entrained a colorant such a dye or pigment, a flavorant, sweetener and/or a therapeutic agent such as an antibacterial agent or a breath freshening agent. The film matrix can further comprise water, additional film forming agents, plasticizing agents, surfactants and emulsifying agents.
In preparing the film matrix according to the present invention the hydroxyalkylmethyl cellulose, a starch ingredient, a colorant, flavor, sweetener and/or therapeutic agents and other film forming ingredients are dissolved in a compatible solvent to form a film forming composition. The film forming composition is cast on a releasable carrier and dried to form a sheet of film matrix material. The carrier material must have a surface tension which allows the film solution to spread evenly across the intended carrier width without soaking to form a destructive bond between the film carrier substrates. Examples of suitable carrier materials include glass, stainless steel, Teflon and polyethylene-impregnated paper. Drying of the film may be carried out at high temperature using a drying oven, drying terminal, vacuum drier, or any other suitable drying equipment which does not adversely effect the ingredients of which the film is composed.
The film thickness ranges in size front 0.5 to 10 microns and preferably 2 to 3 microns. The dried film of the present invention is then cut or punched into shaped flakes having a particle size of 0.01 to 0.50 inches preferably 0.08 to 0.25 inches.
Additional stability can be provided to the shapes formed from the dried film, by applying to the film, before shaping into flakes, a protective barrier overcoat such as a food grade shellac or ethyl cellulose.
When the film is to be used for decorative effect, the film once formed is punched into various attractive shaped flakes such as hearts, stars, diamonds and circles. The film flakes are incorporated in the base dentifrice of the present invention at a concentration of about 0.05 to 1.0% by weight and preferably 0.1 to about 0.5% by weight.
The major film forming agent used to prepare the film matrix of the present invention is an hydroxylkyl cellulose such as hydroxypropyl methyl cellulose, hydroxyethylpropyl cellulose, hydroxybutyl methyl cellulose, hydroxy propyl methyl cellulose and carboxymethyl cellulose. Preferably the cellulose polymer is a low viscosity hydropropylmethyl cellulose polymer (HPMC). When HPMC is used as the film forming agent, it is preferred that the HPMC have a viscosity in the range of about 1 to about 40 millipascal seconds (mPa□s) as determined as a 2% by weight aqueous solution of the HPMC at 20° C. using a Ubbelohde tube viscometer. Preferably the HPMC has a viscosity of about 3 to about 20 mPa□s at 20° C.
HPMC is available commercially from the Dow Chemical Company under the trade designation Methocel E5 LV. Methocel E5 LV is a USP grade, low viscosity HPMC having 29.1% methoxyl groups and 9% hydroxyproxyl group substitution. It is a white or off-white free-flowing dry powder. As a 2 wt % solution in water as measured with a Ubbelohde tube viscometer it has a viscosity of 5.1 mPa□s at 20° C.
The hydroxyalkyl methyl cellulose is incorporated in the film matrix in amounts ranging from about 10 to about 60% by weight and preferably about 15 to about 40% by weight.
Cold water swellable, physically modified and pregelatenized starches are particularly useful as texture modifier to increase the stiffness of the hydroxyalkyl methyl cellulose film matrix of the present invention. In the preparation of such starch products, the granular starch is cooked in the presence of water and possibly an organic solvent at a temperature not higher than 10° C. higher than the gelatinization temperature. The obtained starch is then dried.
Pregelatinized corn starch is available commercially. A preferred starch is available under the trade designation Cerestar Polar Tex-instant 12640 from the Cerestar Company. This Cerestar starch is a pregelaterized, stabilized and crosslinked waxy maize starch. It is readily dispersible and swellable in cold water. In its dry form, it is a white free flowing powder with an average flake size no greater than 180 micrometers and 85% of the flakes are smaller than 75 micrometers. It has a bulk density of 44 lbs/ft3.
The Cerestar starch has excellent cold storage and freeze-thaw stability. It has a rapid hydration rate and can reach extremely high viscosity without cooking. It has a smooth and creamy texture similar to cook-up starches. It also has excellent paste clarity and a bland flavor.
The pregelatinized starch is present in the film matrix of the present invention in an amount ranging from about 5 to about 50% by weight and preferably about 10 to about 35% by weight.
The hydroxyalkyl cellulose to starch ratio (by weight) may vary from about 1:3 to about 4:1 and preferably about 1:1.5 to about 2.5:1.
Colorants used to prepare the film flakes as well as the dentifrice into which the film flakes may be suspended, are pharmacologically and physiologically non-toxic when used in the suggested amounts. The colorants include both pigments and dyes. Pigments useful in the practice of the present invention include non-toxic, water insoluble inorganic pigments such as titanium dioxide, titanium dioxide coated mica (Timiron), chromium oxide greens, ultramarine blues and pinks and ferric oxides as well as water insoluble dye lakes prepared by extending calcium or aluminum salts of FD&C, dyes on alumina such as FD&C Green #1 lake, FD&C Blue #2 lake, FD&C R&D #30 lake and FD&C # Yellow 15 lake. The pigments have a flake size in the range of 5 to 1000 microns, preferably 250 to 500 microns. Pigments are incorporated in the decorative film matrix of the present invention in an amount ranging from about 1 to about 10% by weight and preferably about 2 to about 5% by weight.
A particularly preferred class of dyes are those available from Micropowders, Inc. under the trade designation Spectra bead which are high molecular weight polyethylene powders permanently colored with dyes such as FD&C Blue #1 aluminum lake.
Dyes used in the practice of the present invention are distributed uniformly throughout the film flake matrix or the dentifrice and are desirably food color additives presently certified under the Food Drug & Cosmetic Act for use in food and ingested drugs, including dyes such as FD&C Red No. 3 (sodium salt of tetraiodofluorescein), Food Red 17, disodium salt of 6-hydroxy-5-{(2-methoxy-5-methyl-4-sulphophenyl)azo}-2-naphthalenesulfonic acid, Food Yellow 13, sodium salt of a mixture of the mono and disulphonic acids of quinophtalone or 2-(2-quinolyl) indanedione, FD&C Yellow No. 5 (sodium salt of 4-p-sulfophenylazo-1-p-sulfophenyl-5-hydroxypyrazole-3 carboxylic acid), FD&C Yellow No. 6 (sodium salt of p-sulfophenylazo-B-naphtol-6-monosulfonate), FD&C Green No. 3 (disodium salt of 4-{[4-(N-ethyl-p-sulfobenzylamino)-phenyl]-(4-hydroxy-2-sulfoniumphenyl)-methylene}-[1N-ethyl-N-p-sulfobenzyl)-Δ-3,5-cyclohexadienimine], FD&C Blue No. 1 (disodium salt of dibenzyldiethyl-diaminotriphenylcarbinol trisulfonic acid anhydrite), FD&C Blue No. 2 (sodium salt of disulfonic add of indigotin) and mixtures thereof in various proportions.
The concentration of the dye is present in the Min matrix in an amount ranging from about 0.5 to about 5 and preferably about 1 to about 4% by weight.
The dentifrice base in which the film flakes are suspended is preferably substantially clear and contains a dye or pigment contrasting to that incorporated in the film flakes. Concentration of a contrasting dye or pigment in the dentifrice can range in an amount from about 0.05 percent to about 10 percent by weight with respect to the weight of the base dentifrice and preferably present from about 0.1 percent to about 5 percent by weight of the weight of the dentifrice base.
The film matrix of the present invention is rupturable during tooth brushing so that flavors, sweeteners as well as therapeutic agents may be maintained substantially separate from the dentifrice ingredients during manufacture and storage, while subsequently being released when the dentifrice is applied topically to tooth surfaces, the mechanical agitation created during tooth brushing effecting rupture of the film matrix whereby the entrained ingredient is released to the tooth surface.
Flavor agents incorporated in the film matrix of the present invention are known to the prior art, such as natural and artificial flavors. These flavorings may be chosen from synthetic flavor oils and flavoring aromatics, and/or oils, oleo resins and extracts derived mint plants, leaves, flowers, fruits and so forth, and combinations thereof. Representative flavor oils include: spearmint oil, cinnamon oil, peppermint oil, clove oil, bay oil, thyme oil, cedar leaf oil, oil of nutmeg, oil of sage, and oil of bitter almonds. These flavor agents can be used individually or in admixture. Commonly used flavors include mints such as peppermint, artificial vanilla, cinnamon derivatives, and various fruit flavors, whether employed individually or in admixture. Generally, any flavoring or food additive, such as those described in Chemicals Used in Food Processing, publication 1274 by the National Academy of Sciences, pages 63-258, may be used. Generally the flavoring agent is incorporated in the film of the present invention in an amount ranging from about 1 to about 30% by weight and preferably about 15 to about 25% by weight.
Sweeteners may also be incorporated in the film matrices of the present invention include both natural and artificial sweeteners. Suitable sweetener include water soluble sweetening agents such as monosaccharides disaccharides and plysaccharides such as xylose, ribose, glucose (dextrose), mannose, glatose, fructose (levulose), sucrose (sugar), maltose, water soluble artificial sweeteners such as the soluble saccharin salts, i.e., sodium or calcium saccharin salts, cyclamate salts dipeptide based sweeteners, such a L-aspartic acid derived sweeteners, such as L-aspartyl-L-phenylalaine methyl ester (aspartame).
In general, the effective amount of sweetener is utilized to provide the level of sweetness desired for a particular film matrix composition, will vary with the sweetener selected. This amount will normally be about 0.01% to about 2% by weight of the composition.
Therapeutic agents incorporated in the film flake matrix of the present invention are compounds that are reactive with dentifrice ingredients and must therefore be isolated from the dentifrice ingredients during manufacture and storage.
The therapeutic agents entrained in the film matrix maintained substantially separate from the ingredients of the base dentifrice during manufacture and storage are subsequently released into the dentifrice during tooth brushing. Entrainment of the therapeutic agent in the film matrix prevents premature leakage into the dentifrice so that in the case of therapeutic agents which are reactive ingredients, interaction with dentifrice ingredients is avoided.
For example, reaction of a cationic therapeutic agent such as cetyl pyridinium chloride or chlorhexidene with an anionic surfactant such as sodium lauryl sulfate, which surfactant is conventionally included in dentifrice compositions, inactivates the therapeutic agent thereby reducing the antibacterial efficacy of the dentifrice composition.
In the use of fluoride salts as anticavities agents, one of the methods used to achieve enhanced fluoridation known to the art (U.S. Pat. No. 5,045,305 and U.S. Pat. No. 5,145,668), is to mix, immediately before use, separate solutions containing fluoride and calcium salts. Such a procedure is a time consuming daily chore which discourages its use. Combining the calcium and fluoride salts into a single dentifrice composition will not provide an effective means for fluoridation as the presence of the calcium salt reacts with and removes bioactive soluble ionic fluoride from the dentifrice by forming insoluble and inactive calcium fluoride thereby reducing the antiocariogenic effectiveness of the fluoride dentifrice. Incorporating the calcium salt in the flakes formed from the film matrix of the present invention isolates the fluoride ion in the dentifrice from interaction with the calcium salt until the film matrix disintegrates during tooth brushing.
Typically, in the case of calcium salts, these salts are present in the film flake matrix in an amount up to about 30% by weight, based on the weight of the film matrix, and preferably in the amount of about 18% to 22%.
In addition to fluoride or calcium salts, there may also be included in the film flake matrix anticalculus agents such as pyrophosphate salts including dialkali or tetraalkali metal pyrophosphate salts such as Na4P207, K4P207, Na2K2P207, Na2H2P207 and K2H2P207, long chain polyphosphates such as sodium hexametaphosphate and cyclic phosphates such as sodium trimetaphosphate which are included in the film matrix at a concentration of about 15 to 20% by weight.
Other active agents which may be incorporated, it he film matrix of this invention include antibacterial agents such as Triclosan, breath freshening agents such as zinc gluconate, zinc citrate and/or alpha ionone, desensitizers such as potassium nitrate, vitamins such as pantheon, retinyl palmitate, tocopherol acetate, herbs such as chamomilla recutita, mentha piperita, salvia officinalis, commiphora myrrha, whitening agents such as hydrogen peroxide and urea peroxide, high cleaning silica, preservatives, silicones, chlorophyll compounds.
The active agents are incorporated in the film matrix of the present invention at a concentration of about 0.1 to about 2.0% by weight and preferably about 0.15 to about 5% by weight.
The present invention is illustrated by the following examples.
In the preparation of the base dentifrice in accordance with the present invention there is utilized an orally acceptable vehicle, including a water-phase with humectant which is preferably glycerine or sorbitol or an alkylene glycol such as polyethylene glycol or propylene glycol, wherein the water is present typically in amount of about 5 to about 10% by weight and the glycerine, sorbitol and/or the alkylene glycol ingredients typically total about 30 to about 80% by weight of the dentifrice, more typically about 50 to about 70% by weight.
The base dentifrice also contains an inorganic or a natural or synthetic thickener or gelling agent in proportions of about 0.10 to about 5% by weight, preferably about 0.2 to about 1% by weight. These proportions of thickeners in the dentifrice compositions of the present invention in which the film flakes of the present invention are suspended are sufficient to form an extrudable, shape-retaining product which can be squeezed from a tube onto a toothbrush and will not fall between the bristles of the brush but rather, will substantially maintain its shape thereon. Suitable thickeners or gelling agents useful in the practice of the present invention include inorganic thickening silicas such as amorphous silicas available from Huber Corporation under the trade designation Zeodent 165, Irish moss, iota-carrageenan, gum tragacamb, and polyvinylpyrrolidone.
Polishing agents such as silica, calcined alumina, sodium bicarbonate, calcium carbonate, dicalcium phosphate and calcium pyrophosphate may be included in the base dentifrice compositions used in the practice of the present invention. Visually clear dentifrice compositions are obtained by using polishing agents such as collodial silica, such as those sold under the trade designation Zeodent 115 available from the Huber Corporation or alkali metal aluminosilicate complexes (that is, silica containing alumina combined in its matrix) which have refractive indices close to the refractive indices of gelling agent-liquid (including water and/or humectant) systems used in dentifrice compositions.
The polishing agent is generally present in the base dentifrice composition in weight concentrations of about 3% to about 50% by weight.
Surfactants are used in the base dentifrice compositions of the present invention to achieve increased prophylactic action and render the instant compositions more cosmetically acceptable. Suitable examples of surfactants include water-soluble salts of higher fatty acid monoglyceride monosulfates, such as the sodium salt of the monsulfated monoglyceride of hydrogenated coconut oil fatty acids, cocamidopropyl betaine, higher alkyl sulfates such as sodium lauryl sulfate, alkyl aryl sulfonates such as sodium dodecyl benzene sulfonate, higher alkyl sulfoacetates, sodium lauryl sulfoacetate, higher fatty acid esters of 1,2-dihydroxy propane sulfonate, and the substantially saturated higher aliphatic acyl amides of lower aliphatic amino carboxylic acid compounds, such as those having 12 to 16 carbons in the fatty acid, alkyl or acyl radicals, and the like. Examples of the last mentioned amides are N-lauroyl sarcosine, and the sodium, potassium, and ethanolamine salts of N-lauroyl, N-myristoyl, or N-palmitoyl sarcosine.
The anionic surfactants are typically present in the dentifrice compositions of the present invention in an amount of about 0.3 to about 5% by weight, preferably about 0.5 to about 2.0% by weight.
To prepare the dentifrice base of the present invention, water, humectants, e.g. glycerin, sorbitol polyethylene glycol are dispersed in as conventional mixer until the mixture becomes a homogeneous gel phase. Into the gel phase are added the polishing agent. These ingredients are mixed until a homogeneous phase is obtained. Thereafter the thickener, any flavor and surfactant ingredients are added and the ingredients mixed at high speed until vacuum of about 20 to 100 mmHg. The shaped film flakes are added to the dentifrice constituents as a last step, so as to minimize the shear to which the dentifrice ingredients are subjected to during the prior mixing steps.
Silver colored film flakes were prepared by using the ingredients listed in Table 1 below. In preparing the film, the HMPC polymer Methocel E5LV having a viscosity of 5.1 mPa□s (2% aqueous solution) was added to deionized water at 23° C., and the solution stirred for 5 minutes. To this solution was added the pregelatized starch Cerestar Polar Tex Instant 12640 and stirred vigorously for about one hour until the starch was completely dispersed and a homogeneous mixture was formed. To this mixture was added the titanium coated mica and mixed for 10 minutes after which the sodium lauryl sulfate surfactant was added and mixed for an additional 15 minutes. Thereafter spearmint flavor was thoroughly mixed for an additional 40 minutes to form a slurry emulsion. The weight ratio of HPMC to Starch was 2:1. The emulsion was then cast on a polyethylene coated paper at 25° C. and dried at 110° C. to form a solid thin film having a thickness of 2.5 microns. Star shaped flakes punched from the dried film had a particle size of 0.25 inches.
A transparent green colored base dentifrice composition having the ingredients listed in Table II was prepared, wherein a vehicle solution of the sorbitol and water was made and subjected to 28-30 lbs. applied vacuum and a mixture of saccharin sodium fluoride and was added thereto. Subsequently, a green dye was Wended with the vehicle. The mixture was degassed at 28-30 lbs. applied vacuum over a 5 minute period. Then Zeodent 115 silica abrasive and Zeodent 165, an amorphous silica thickening agent and sodium lauryl sulfate (SLS) were added after preliminary degassing. The ingredients were mixed. After about 5 minutes mixing, with application of vacuum, the dentifrice preparation was considered to be complete and thereafter 0.3% by weight of the star shaped film flakes were suspended in the dentifrice.
After packaging, the dentifrice product was squeezed from a tube and was extruded as a distinctive green, aesthetically pleasing ribbon product having suspended therein clearly visible star shaped silver colored flakes extending throughout the extruded product.
A second film flake wed prepared following the procedure of Example 1. The ingredients of the film matrix are listed in Table III below.
The thickness of the film was 3.0 microns. Thereafter 0.2% by weight of heart shaped flakes having a particle size of 0.125 inches were die cut from the film. Shellac (100% non-bleached) was applied to the film before the heart shapes were die cut from the matrix. The heart shaped flakes were then incorporated into the dentifrice base of Table II as the last step, so as to minimize the shear to which they are subjected to during mixing.
After packaging, the dentifrice product was squeezed from a tube and was extruded as a distinctive blue, aesthetically pleasing product having suspended therein clearly visible heart shaped red colored flakes extending randomly throughout the extruded product.
Film flakes suitable for the delivery of a flavor burst having a high flavor concentration (23.75 wt %) was prepared following the procedure of Example 1, the ingredients of which are listed in Table IV. Flakes in the shape of circles formed from the film were suspended in a base dentifrice of type disclosed in Table II. When brushed on teeth the dentifrice emitted a burst of flavor as the brushing caused the mechanical rupture of the film with the immediate release of its flavor constituent.
A film of 2.5 microns thickness containing a high concentration of calcium acetate (21.4% by weight) was papered following the procedure of Example 1 having the ingredient's listed in Table V below:
0.3% by weight film flakes of 0.25 inch particle size of Table V were suspended in a commercial fluoride toothpaste containing 1100 parts per million (ppm) fluoride ion. The toothpaste containing the film flakes designated “Paste A”, was then aged at 120° F. for 2 to 8 weeks and analyzed for fluoride content at weekly intervals. For purposes of comparison, the same toothpaste to which the film flakes had not been incorporated designated “Paste B”, was also analyzed for fluoride levels during the same two week interval.
The presence of fluoride ion in the dentifrice at each week interval was determined by separating the base from the flakes first then analyzing the base for the presence of fluoride using F− ion selective electrodes. The results of these assays are recorded in Table VI below.
The fluoride assays of the two toothpastes are recorded in Table VI below.
The results recorded in Table VI show a minimal loss of fluoride ion over the 8 week assay period in Paste A containing film entrained calcium acetate as compared to Paste B which did not contain any calcium salt. When brushed on teeth of the film suspended in the dentifrice will rapidly disintegrate whereby calcium ion will be released to interact with the fluoride ion to enhance the anticaries efficacy of the fluoride ion on the teeth being brushed.
Cetyl pyridinium chloride (CPC) is incompatible with sodium lauryl sulfate (SLS) a surfactant widely used in dentifrice compositions. Because of this incompatibility CPC has not found application in most dentifrice formulations. In Table VII below there is listed the ingredients of a film matrix in which CPC is entrained. The film when suspended in a SLS containing dentifrice will not react with the SLS present in the dentifrice. The CPC will be released during tooth brushing without being inactivated by the presence of SLS in the toothpaste base.
This application is a continuation of U.S. Ser. No. 11/967,878 filed Dec. 31, 2007, now U.S. Pat. No. 8,475,771, which is a divisional application of U.S. Ser. No. 10/720,462 filed Nov. 24, 2003, now U.S. Pat. No. 7,763,235, which is a continuation of U.S. Ser. No. 10/331,312 filed Dec. 30, 2002, now U.S. Pat. No. 6,669,929 B1. The disclosures of the above applications are incorporated herein by reference.
Number | Name | Date | Kind |
---|---|---|---|
124902 | Lounsbery | Mar 1872 | A |
309209 | Driscoll | Dec 1884 | A |
446491 | Weston | Feb 1891 | A |
449457 | Yeo | Mar 1891 | A |
502144 | Scoular | Jul 1893 | A |
919736 | Loesch | Apr 1909 | A |
982946 | Gardner | Jan 1911 | A |
1059162 | Janik | Apr 1913 | A |
1321514 | Erickson | Nov 1919 | A |
1429405 | Carter et al. | Sep 1922 | A |
1605903 | Schuler | Nov 1926 | A |
1785078 | Gibson | Dec 1930 | A |
1947124 | Clauss | Feb 1934 | A |
2062867 | Cosier | Dec 1936 | A |
2137170 | Levey | Nov 1938 | A |
2353594 | Seagren | Jul 1944 | A |
2394322 | McKee | Feb 1946 | A |
2503280 | Lockwood | Apr 1950 | A |
2507088 | Bradley | May 1950 | A |
2526811 | Dawson | Oct 1950 | A |
2610588 | Seagren et al. | Sep 1952 | A |
2624277 | Sunkoz | Jan 1953 | A |
2645049 | Brown | Jul 1953 | A |
2791960 | Pietropinto | May 1957 | A |
2846314 | Aichele et al. | Aug 1958 | A |
2895832 | Bersey | Jul 1959 | A |
3009812 | Ganz | Nov 1961 | A |
3260744 | Ito et al. | Jul 1966 | A |
3320174 | Rubinfeld | May 1967 | A |
3372188 | Alston et al. | Mar 1968 | A |
3711604 | Cologney et al. | Jan 1973 | A |
3741911 | Shane | Jun 1973 | A |
3852494 | Williamson | Dec 1974 | A |
3928261 | Ashidaga et al. | Dec 1975 | A |
3929988 | Barth | Dec 1975 | A |
3934000 | Barth | Jan 1976 | A |
3944661 | Colodney et al. | Mar 1976 | A |
3951821 | Davidson | Apr 1976 | A |
3954961 | Cologney et al. | May 1976 | A |
3957964 | Grimm, III | May 1976 | A |
3957968 | Cordon | May 1976 | A |
4003971 | Mannara | Jan 1977 | A |
4048299 | Litchfield et al. | Sep 1977 | A |
4075316 | Cordon | Feb 1978 | A |
4089943 | Roberts et al. | May 1978 | A |
4129520 | Peterson | Dec 1978 | A |
4136162 | Fuchs et al. | Jan 1979 | A |
4185106 | Dittmar et al. | Jan 1980 | A |
4209417 | Whyte | Jun 1980 | A |
4285978 | Quinlivan | Aug 1981 | A |
4376762 | Hauschild et al. | Mar 1983 | A |
4440877 | Hauschild et al. | Apr 1984 | A |
4470982 | Winkler | Sep 1984 | A |
4597959 | Barr | Jul 1986 | A |
4642197 | Kruse et al. | Feb 1987 | A |
4650685 | Persson et al. | Mar 1987 | A |
4820506 | Kleinberg et al. | Apr 1989 | A |
4837008 | Rudy et al. | Jun 1989 | A |
4839157 | Mei-King Ng et al. | Jun 1989 | A |
4849212 | Glandorf et al. | Jul 1989 | A |
RE33093 | Schiraldi et al. | Oct 1989 | E |
4876092 | Mizobuchi et al. | Oct 1989 | A |
4897258 | Rudy et al. | Jan 1990 | A |
4950479 | Hill et al. | Aug 1990 | A |
4956404 | Pelzig | Sep 1990 | A |
4971782 | Rudy et al. | Nov 1990 | A |
5017394 | MacPherson et al. | May 1991 | A |
5035906 | Persson et al. | Jul 1991 | A |
5045305 | Clarkson et al. | Sep 1991 | A |
5047244 | Sanvordeker et al. | Sep 1991 | A |
5062986 | Fujita et al. | Nov 1991 | A |
5071704 | Fischel-Ghodsian | Dec 1991 | A |
5089269 | Noda et al. | Feb 1992 | A |
5145668 | Chow et al. | Sep 1992 | A |
5185106 | Chen et al. | Feb 1993 | A |
5242615 | Urfer et al. | Sep 1993 | A |
5266306 | Ohtsuki et al. | Nov 1993 | A |
5354551 | Schmidt | Oct 1994 | A |
5425953 | Sintov et al. | Jun 1995 | A |
5447584 | Shakespeare et al. | Sep 1995 | A |
5455043 | Fischel-Ghodsian | Oct 1995 | A |
5538663 | Kihara et al. | Jul 1996 | A |
5616315 | Masterman et al. | Apr 1997 | A |
5643603 | Bottenberg et al. | Jul 1997 | A |
5695746 | Garlick, Jr. | Dec 1997 | A |
5700449 | Katayama et al. | Dec 1997 | A |
5700478 | Biegajski et al. | Dec 1997 | A |
5711943 | Grossman | Jan 1998 | A |
5792446 | Ashley | Aug 1998 | A |
5843415 | Klar | Dec 1998 | A |
5866531 | Assmann et al. | Feb 1999 | A |
5869029 | Graff-Andersen et al. | Feb 1999 | A |
5869437 | Wolfersberger | Feb 1999 | A |
5900399 | Seiter et al. | May 1999 | A |
5910472 | Elliott et al. | Jun 1999 | A |
5931999 | Aisner | Aug 1999 | A |
5939093 | Park et al. | Aug 1999 | A |
5948430 | Zerbe et al. | Sep 1999 | A |
5958525 | Green et al. | Sep 1999 | A |
5990058 | Bac et al. | Nov 1999 | A |
5990205 | Cordova | Nov 1999 | A |
6007795 | Masterman et al. | Dec 1999 | A |
6051059 | Aisner | Apr 2000 | A |
6117419 | Vernice | Sep 2000 | A |
6138315 | Schmitt et al. | Oct 2000 | A |
6210699 | Acharya et al. | Apr 2001 | B1 |
6221832 | Casteel et al. | Apr 2001 | B1 |
6232285 | Casteel et al. | May 2001 | B1 |
6241974 | White, Jr. et al. | Jun 2001 | B1 |
6251452 | Weinstein et al. | Jun 2001 | B1 |
6258342 | Harcum et al. | Jul 2001 | B1 |
6258343 | Hiczek, Sr. et al. | Jul 2001 | B1 |
6294509 | Meiwa et al. | Sep 2001 | B1 |
6315986 | Wong et al. | Nov 2001 | B1 |
6352701 | Scholz et al. | Mar 2002 | B1 |
6365209 | Cherukuri | Apr 2002 | B2 |
6379654 | Gebreselassie et al. | Apr 2002 | B1 |
6403543 | George | Jun 2002 | B1 |
6419903 | Xu et al. | Jul 2002 | B1 |
6447761 | Ramin | Sep 2002 | B1 |
6451754 | Rowland et al. | Sep 2002 | B1 |
6492320 | Guo et al. | Dec 2002 | B2 |
6497899 | Thombre et al. | Dec 2002 | B2 |
6503495 | Alwattari et al. | Jan 2003 | B1 |
6506720 | Blasey et al. | Jan 2003 | B1 |
6509007 | Rajaiah et al. | Jan 2003 | B2 |
6524562 | Guskey | Feb 2003 | B2 |
6531119 | Hall-Puzzio et al. | Mar 2003 | B1 |
6541441 | Mumoli | Apr 2003 | B2 |
6544943 | Ricci et al. | Apr 2003 | B1 |
6548473 | Thoen et al. | Apr 2003 | B1 |
6569261 | Aubay et al. | May 2003 | B1 |
6576225 | Kilcher | Jun 2003 | B1 |
6585997 | Moro et al. | Jul 2003 | B2 |
6586013 | Victor | Jul 2003 | B2 |
6589924 | Schmidt et al. | Jul 2003 | B2 |
6596298 | Leung et al. | Jul 2003 | B2 |
6620777 | Heibel et al. | Sep 2003 | B2 |
6635702 | Schmucker-Casatner | Oct 2003 | B1 |
6638521 | Dobrozsi | Oct 2003 | B2 |
6664217 | Puvvada et al. | Dec 2003 | B1 |
6664225 | Mumoli | Dec 2003 | B2 |
6669929 | Boyd et al. | Dec 2003 | B1 |
6682756 | Horstmann et al. | Jan 2004 | B1 |
6706675 | Demson et al. | Mar 2004 | B1 |
6797683 | Shana'a et al. | Sep 2004 | B2 |
6957964 | Chiang | Oct 2005 | B2 |
7025983 | Leung et al. | Apr 2006 | B2 |
7049274 | Ranade et al. | May 2006 | B2 |
7132113 | Zerbe et al. | Nov 2006 | B2 |
7181588 | Johnson | Feb 2007 | B2 |
7323162 | Martin et al. | Jan 2008 | B2 |
7410649 | Yoshimi et al. | Aug 2008 | B2 |
20010022964 | Leung et al. | Sep 2001 | A1 |
20010048965 | Cherukuri | Dec 2001 | A1 |
20020001569 | Dromard et al. | Jan 2002 | A1 |
20020034542 | Thombre | Mar 2002 | A1 |
20020048553 | Baumgartner | Apr 2002 | A1 |
20020051797 | Jezior | May 2002 | A1 |
20020064541 | Noa et al. | May 2002 | A1 |
20020110536 | Osumi | Aug 2002 | A1 |
20020169270 | Amberg Schwab | Nov 2002 | A1 |
20020187108 | Rajaiah et al. | Dec 2002 | A1 |
20030008144 | Whitney et al. | Jan 2003 | A1 |
20030053962 | Zerbe et al. | Mar 2003 | A1 |
20030171232 | Freeman et al. | Sep 2003 | A1 |
20040086468 | Prosise | May 2004 | A1 |
20040126332 | Boyd et al. | Jul 2004 | A1 |
20040136924 | Boyd et al. | Jul 2004 | A1 |
20040139624 | Chickering et al. | Jul 2004 | A1 |
20040219119 | Wei | Nov 2004 | A1 |
20040236924 | Johnson et al. | Nov 2004 | A1 |
20050019273 | Boyd et al. | Jan 2005 | A1 |
20050043209 | Schmiedel et al. | Feb 2005 | A1 |
20050106112 | Boyd et al. | May 2005 | A1 |
20050281757 | Ibrahim et al. | Dec 2005 | A1 |
20060018845 | Edelstein | Jan 2006 | A1 |
20060189503 | Gambogi et al. | Aug 2006 | A1 |
20060292088 | Maitra-Prithwiraj | Dec 2006 | A1 |
20070010415 | Kinscherf et al. | Jan 2007 | A1 |
20070066507 | Fleckenstein et al. | Mar 2007 | A1 |
20070148213 | Ibrahim et al. | Jun 2007 | A1 |
20070196313 | Scala et al. | Aug 2007 | A1 |
20080014393 | Denome et al. | Jan 2008 | A1 |
20080024281 | Shimura | Jan 2008 | A1 |
20080138369 | Boyd et al. | Jun 2008 | A1 |
20080160056 | Boyd | Jul 2008 | A1 |
Number | Date | Country |
---|---|---|
982943 | Feb 1976 | CA |
982946 | Feb 1976 | CA |
2512159 | Jul 2004 | CA |
2548386 | Jun 2005 | CA |
1303259 | Jul 2001 | CN |
1422147 | Jun 2003 | CN |
735096 | May 1943 | DE |
103 52 845 | Jun 2005 | DE |
1 502 144 | Feb 1978 | EP |
0449457 | Oct 1991 | EP |
0711544 | May 1996 | EP |
1051962 | Nov 2000 | EP |
1059162 | Dec 2000 | EP |
1 153 594 | Nov 2001 | EP |
1319706 | Jun 2003 | EP |
1321514 | Jun 2003 | EP |
446491 | Dec 1912 | FR |
446491 | Apr 1936 | GB |
1309209 | Mar 1973 | GB |
1465190 | Feb 1977 | GB |
1502144 | Feb 1978 | GB |
2124902 | Feb 1984 | GB |
58-216109 | Dec 1983 | JP |
2000116843 | Oct 2002 | RU |
WO 9820862 | May 1998 | WO |
9922710 | May 1999 | WO |
WO 9936478 | Jul 1999 | WO |
WO 0006089 | Feb 2000 | WO |
WO 0018365 | Apr 2000 | WO |
WO 0042992 | Jul 2000 | WO |
0117488 | Mar 2001 | WO |
WO 0117488 | Mar 2001 | WO |
WO 0180821 | Nov 2001 | WO |
WO 0180823 | Nov 2001 | WO |
WO 0180832 | Nov 2001 | WO |
0202128 | Jan 2002 | WO |
WO 0202128 | Jan 2002 | WO |
WO 02041765 | Sep 2002 | WO |
WO 02092028 | Nov 2002 | WO |
WO 03030881 | Apr 2003 | WO |
WO 03034979 | May 2003 | WO |
WO 2004006967 | Jan 2004 | WO |
WO 2004020566 | Mar 2004 | WO |
2004060335 | Jul 2004 | WO |
WO 2004060290 | Jul 2004 | WO |
2005110344 | Nov 2005 | WO |
2006013081 | Feb 2006 | WO |
WO 2006089057 | Aug 2006 | WO |
WO 2007022229 | Feb 2007 | WO |
WO 2007130684 | Nov 2007 | WO |
Entry |
---|
European Search Report for Application No. EP091158190 dated Sep. 1, 2009. |
American Dental Association (http://www.ada.org/public/topics/bad—breath.asp)pp. 1-2 Dec. 2003. |
American Academy of Periodontology http://www.perio.org/consumer/faq—general.htm, pp. 1-4 Oct. 2004. |
Your dictionary.com http://www.yourdictionary.com/ahd/d/d0136300.html, (2007) p. 1. |
U.S. Appl. No. 11/963,292, filed Dec. 21, 2007. |
BASF The Chemical Company, 2009, Kollicoat® SR 30 D Poly (Vinyl Acetate) Dispersion 30 Per Cent Ph. Eur. Technical Information. |
DOW, 1999, “A Formulator's Guide to Methocel Cellulose Ethers in Personal Care Products”. |
DOW, 2010, METHOCEL™ Products, Dow Excipients http://www.dow.com/dowexcipients/products/methocel.htm, accessed Apr. 8, 2010. |
Grain Processing Corp's “Instant Pure-Cote® B793 Modified Starch,” Product Bulletin, undated. |
International Search Report and Written Opinion in International Application No. PCT/US03/040562, dated Sep. 30, 2004. |
International Search Report and Written Opinion in International Application No. PCT/US04/042442, dated Mar. 29, 2005. |
International Search Report and Written Opinion in International Application No. PCT/US06/031922, dated Dec. 6, 2006. |
International Search Report and Written Opinion in International Application No. PCT/US06/062539, dated Jun. 20, 2007. |
International Search Report and Written Opinion in International Application No. PCT/US10/031717, dated Aug. 18, 2010. |
International Search Report and Written Opinion in International Application No. PCT/US10/032189, dated Aug. 17, 2010. |
McClelland, 1997, “Defining Colors,” MacWorld Photoshop 4 Bible, Chapter 5, pp. 157-184. |
National Adademy of Sciences, 1965, “Group 11: Flavoring Agents, Sub-Group A: Synthetic Flavors,” Chemicals Used in Food Processing, Publication 1274, pp. 63-258. |
Salsa et al., 1997, “Oral Controlled-Release Dosage Forms. I. Cellulose Ether Polymers in Hydrophilic Matrices,” Drug Development and Industrial Pharmacy 23(9):929-938. |
The Herbarie, 2012, http://theherbarie.com/Hydroxypropyl-Methycellulose-HPMC-pr-230.html, retrieved Feb. 24, 2012, pp. 1-2. |
U.S. Appl. No. 10/720,462 File History to Jun. 3, 2013. |
U.S. Appl. No. 11/014,571 File History to Jun. 3, 2013. |
U.S. Appl. No. 11/316,626 File History to Jun. 3, 2013. |
U.S. Appl. No. 11/465,525 File History to Jun. 3, 2013. |
U.S. Appl. No. 11/967,878 File History to Jun. 3, 2013. |
Number | Date | Country | |
---|---|---|---|
20130272973 A1 | Oct 2013 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 10720462 | Nov 2003 | US |
Child | 11967878 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 11967878 | Dec 2007 | US |
Child | 13910060 | US | |
Parent | 10331312 | Dec 2002 | US |
Child | 10720462 | US |