Oral mucosal carriers and protectants

Abstract

Oral mucosal carriers and protectants. [Solution] An oral mucosal carrier comprising a combination of dimethicone components of two different viscosities, the difference between the two different viscosities being about 2 million cP or more, and at least one active agent.

Description

[Technical field]

[0001] CROSS-REFERENCE TO RELATED APPLICATIONS This application claims the benefit of U.S. Provisional Application No. 62 / 755,722, filed November 5, 2018, and U.S. Provisional Application No. 62 / 846,763, filed May 13, 2019, the entire contents of each of which are incorporated herein by reference.

[0002] The present invention relates generally to oral mucosal carriers and protectants that are suitable for oral use, particularly for providing an additive or therapeutic agent to the oral mucosa, comprising at least two dimethicone components of different viscosities and at least one excipient for application to the oral mucosa. [Background technology]

[0003] Oral-based care products, including mouthwashes, prophylactic pastes, gels, toothpastes, lozenges, etc., are marketed to meet the diverse needs of patients. Toothpaste is one of the most common oral care products, specifically utilized to reduce and prevent caries by brushing with a gel or paste that contains fluoride and other ingredients. These products are often sold in over-the-counter strengths and are used worldwide for their protective and restorative properties.

[0004] While toothpaste is ubiquitous, other oral care products are necessary to meet the needs of patients, including those for orthodontic bracket treatment, dry mouth, halitosis treatment, ulcerative stomatitis, tooth sensitivity, dry socket treatment, whitening, and those for caring for the oral mucosa against fissures, bleeding, cuts, sores, fungal, viral, and bacterial infections, sun damage, skin damage, and cancerous growths. These products come in many different forms, such as sprays that contain the active ingredient, while other products include lozenges, foams, gels, pastes, or other materials for oral application. Unfortunately, many of these products are drugs that temporarily address or mask the problem without actually treating the cause of the illness or problem the patient is facing.

[0005] The treatment of the oral mucosa can affect a wide range of problems and new products are needed that provide a carrier with sufficient properties for use in treating these afflictions of the oral mucosa. Thus, new products are needed to create safe, reliable and highly effective products for oral mucosa treatment and oral application. Summary of the Invention

[0006] In a preferred embodiment, the oral mucosal carrier comprises a first and a second dimethicone, the first dimethicone having a viscosity of 1,000 to 25,000 cP and the second dimethicone having a viscosity of 2 million cP to 3 million cP, and an active agent suitable for oral application, in a preferred embodiment, the active agent is selected from the group consisting of fluoride donors, calcium donors, phosphate donors, antimicrobial agents, and combinations thereof.

[0007] The oral mucosal carrier comprises 25-99% 12,500 cP dimethicone and 1%-50% 2.5 million cP dimethicone, 0.1%-1.5% fluoride donor, antimicrobial agent, or a combination thereof.

[0008] The oral mucosal carrier comprises 25-99% 1,000 cP dimethicone and 1%-75% 2.5 million cP dimethicone, 0.1%-1.5% sodium fluoride, benzalkonium chloride, or a combination thereof.

[0009] In certain embodiments, the concentration of the fluoride donor is 800-1500 ppm, as permitted under FDA regulations for commercial applications. In preferred embodiments, the concentration of the fluoride agent is about 1000 ppm fluoride or about 1100 ppm fluoride. In certain embodiments, 1000 ppm fluoride is obtained by incorporating a concentration of about 0.4% stannous fluoride, about 0.22% sodium fluoride, and about 0.76% sodium monofluorophosphate. In certain embodiments, 1100 ppm fluoride is obtained by incorporating a concentration of about 0.454% stannous fluoride, about 0.243% sodium fluoride, or about 0.836% sodium monofluorophosphate. In certain applications, prescription strength materials may be provided at concentrations of 5000 ppm or less. In certain embodiments, the fluoride donor is selected from the group consisting of sodium fluoride, stannous fluoride, sodium monofluorophosphate, ACPF (amorphous calcium phosphate fluoride), amine 297 fluoride, and combinations thereof.

[0010] The oral mucosal carrier comprises two dimethicone polymers and a fluoride, a first dimethicone polymer having the formula Me3-O-[SiMe2]n-Me3, where "n" is the number of repeating units, and having a viscosity of about 1,000 to 25,000 cP, and a second dimethicone polymer having a formula where n is greater than the first dimethicone polymer and having a higher viscosity of about 2 million cP to 3 million cP, the first dimethicone polymer comprising 10 to 99 percent of the total weight of the formulation, and the second dimethicone polymer comprising 1 to 90 percent of the total weight of the formulation.

[0011] The oral mucosal carrier comprises two dimethicone polymers and a fluoride, the first dimethicone polymer having the formula Me3-O-[SiMe2]n-Me3 with "n" repeat units, the second dimethicone polymer having a higher viscosity and more "n" repeat units than the first dimethicone polymer, and the ratio of the first dimethicone polymer to the second dimethicone polymer is 100:1 to 1:8. Preferably, the ratio is about 50:1 to about 1:2, or about 40:1 to about 1:1.

[0012] The method of compounding the oral mucosa carrier comprising first and second dimethicones includes: adding an amount of first dimethicone into a centrifugal mixer, the first dimethicone having a lower viscosity than the second dimethicone; adding an amount of at least one excipient to the first dimethicone, mixing the first dimethicone with the at least one excipient in the centrifugal mixer; adding an amount of the second dimethicone to the mixed first dimethicone and the at least one excipient, and mixing the resulting material in the centrifugal mixer.In a particular embodiment, the second dimethicone is mixed into the first dimethicone in at least two portions, the first portion and the second portion.The first and second portions may be equal or unequal amounts. In certain embodiments, the second dimethicone is mixed in 2, 3, 4, 5, 6, 7, 8, 9, 10, or more portions, with the mixture being mixed in the centrifugal mixer between each additional amount of the second dimethicone.

[0013] In certain embodiments, the active ingredient is an antibiotic, a sulfur compound, a skin healing compound, a bone growth promoting compound, an antimicrobial agent, a local anesthetic, an antifungal agent, CoQ 10, vitamin D, chlorhexidine, FDA monograph compounds recognized at the web address https: / / www.fda.gov / downloads / AboutFDA / CentersOffices / CDER / UCM135688.pdf, chitosan, hemostatic materials, anti-inflammatory, topical steroids, anti-inflammatory compounds, hemp-based extracts including cannabinoids and terpenes including, but not limited to, THC and CBD, silver nitrate, essential oils, skin protectants, pain relievers or blockers, zinc oxide, small molecules, nitroglycerin, nicotine, hormones, or combinations thereof.

[0014] In one embodiment, the oral mucosal carrier further comprises a phosphate donor, wherein the phosphate donor is selected from the group consisting of potassium dihydrogen phosphate, dipotassium hydrogen phosphate, dicalcium phosphate, tricalcium phosphate, sodium dihydrogen phosphate, disodium hydrogen phosphate, monomagnesium phosphate, dimagnesium phosphate, and combinations thereof.

[0015] In one embodiment, the oral mucosal carrier further comprises a calcium donor selected from the group consisting of calcium nitrate, calcium chloride, calcium citrate, calcium sulfate, calcium oxalate, calcium fluoride, dicalcium phosphate, tricalcium phosphate, calcium gluconate, and combinations thereof. In a further embodiment, the calcium donor can further comprise at least one amino acid. In a further embodiment, the amino acid is lysine.

[0016] In one embodiment, the oral mucosal carrier further comprises a potassium donor selected from the group consisting of potassium nitrate, potassium chloride, potassium dihydrogen phosphate, dipotassium hydrogen phosphate, and combinations thereof.

[0017] In one embodiment, the oral mucosal carrier further comprises a flavoring or sweetener selected from the group consisting of spearmint oil, oil of wintergreen, peppermint oil, bubble gum, cherry, vanilla, chlorophyll, acesulfame K, sucralose, xylitol, saccharin, sodium cyclamate, and combinations thereof.

[0018] In one embodiment, the oral mucosal carrier further comprises an antimicrobial agent selected from the group consisting of benzalkonium chloride, cetylpyridinium chloride, trans-farnesol, chitosan, chlorhexidine, quaternary ammonium compounds, phenols, bisguanides, and combinations thereof.

[0019] In one embodiment, the oral mucosal carrier further comprises one or more of a bulking agent, a flow agent, a preservative, or a combination thereof. As with the case of including flavoring, it may be preferable to provide a small amount of a bulking agent or texturizing agent to the product to give the material a texture or improve its consistency for application to the surface of the teeth. For example, the patient may prefer the material to have a slight texture so that the patient can "feel" that the material is remaining on the surface of the oral mucosa. The bulking agent may be necessary simply to provide the product with a good consistency and overall feel. Similarly, flow agents or glidants may be added to the compositions herein to give and modify the physical properties of the material. For example, magnesium stearate, stearic acid, silicon dioxide, glycerin, palmitate, and others known to those skilled in the art.

[0020] In one embodiment, the oral mucosal carrier further comprises one or more whitening agents selected from the group consisting of urea peroxide, calcium peroxide alone or in combination with an amino acid, such as L-lysine, titanium dioxide, hydrogen peroxide, and a complex of polyvinylpyridine (PVP), hydrogen peroxide, and combinations thereof.

[0021] In a preferred embodiment, the dimethicone-based oral mucosal carrier comprises a first dimethicone material having a viscosity of about 1,000 cP to 25,000 cP and a second dimethicone material having a viscosity of about 2 million to 3 million cP, and at least one active agent. In a preferred embodiment, the at least one active agent is selected from the group consisting of a fluoride donor, cetylpyridinium chloride, benzalkonium chloride, and combinations thereof. In a preferred embodiment, the fluoride donor is selected from the group consisting of sodium fluoride, stannous fluoride, ACPF, and combinations thereof. In a preferred embodiment, the carrier has a ratio of the first dimethicone to the second dimethicone of 100:1 to 1:10, 50:1 to 1:2, or 40:1 to 1:1. In a preferred embodiment, the oral mucosal carrier has a fluoride donor concentration of 0.1-1.5%, or a fluoride donor concentration of 1-1500 ppm, more specifically 800 ppm-1500 ppm. In a preferred embodiment, the oral mucosal carrier further comprises a calcium donor. In a further preferred embodiment, the oral mucosal carrier further comprises a potassium donor. In a further preferred embodiment, the oral mucosal carrier further comprises a flavoring or sweetening agent. In a further preferred embodiment, the oral mucosal carrier further comprises cetylpyridinium chloride. In a further preferred embodiment, the oral mucosal carrier further comprises a bulking agent, a flow agent, a preservative, or a combination thereof. In a further preferred embodiment, the oral mucosal carrier further comprises a phosphate donor.

[0022] In a further preferred embodiment, the method includes placing the entire first dimethicone component in a mixing vessel and adding thereto an amount of an active ingredient; mixing the two components in a centrifugal mixer at 3,000 RPM for about 10 minutes; after mixing for 10 minutes, adding a portion of the second dimethicone to the now mixed material, adding one-fifth of the total concentration of the second dimethicone in discrete increments; and mixing the resulting material at 3,000 RPM in 5 minute increments until all of the second dimethicone has been added and mixed into the oral mucosal carrier, followed by adding another incremental portion of the second dimethicone.

[0023] In a preferred embodiment, the method includes adding a calcium donor with the first dimethicone and the active agent before mixing the ingredients.In a preferred embodiment, the method includes adding a fluoride, calcium, potassium donor, cetylpyridinium, chloride, or a combination thereof with the first dimethicone and the fluoride before mixing the ingredients.In a further preferred embodiment, the method includes adding benzalkonium chloride or cetylpyridinium chloride with the first dimethicone before mixing the ingredients.

[0024] In a further preferred embodiment, the oral mucosal carrier composition consists essentially of a dimethicone-based oral mucosal carrier comprising a first dimethicone material having a viscosity of about 1,000 cP to 25,000 cP and a second dimethicone material having a viscosity of about 2 million to 3 million cP, and at least one active agent. In a further embodiment, the composition combines the first dimethicone and the second dimethicone in a ratio of 100:1 to 1:10. In a further embodiment, the composition consists essentially of at least one active agent.

[0025] In a further preferred embodiment, the oral mucosal carrier is a therapeutic agent selected from the group consisting of sodium fluoride, difluorosilane, stannous fluoride, APF (acid fluoride phosphate), ACPF (amorphous calcium fluoride phosphate), ACP (amorphous calcium phosphate), sodium monofluorophosphate, benzalkonium chloride, dipotassium hydrogen phosphate, calcium nitrate, cetylpyridinium chloride, phosphate donors, potassium donors, and antibacterial, antifungal, antiviral, small molecule, antiemetic, biological, self-replicating peptide, cannabinoid, terpene, and combinations thereof. In a further embodiment, the active agent is hemp extract.

[0026] In further embodiments, the therapeutic agent may be selected from agents that treat dry mouth selected from the group consisting of pilocarpine, acetylcholine, electrolytes such as sodium, potassium, calcium, magnesium, chloride, phosphate, and carbonate. In further embodiments, the therapeutic agent may be a saliva enhancer selected from the group consisting of essential oil extracts, scutellaria baicalensis, xylitol, carboxymethylcellulose, and variations thereof for improving saliva flow. In further embodiments, the therapeutic agent is a halitosis treatment selected from the group consisting of antibacterial compounds, natural or synthetic oils, odor destroyers, or odor masking agents.

[0027] In a further embodiment, the composition for treating ulcerative stomatitis is characterized in that the therapeutic agent is aluminum powder (potassium aluminum sulfate), baking soda, probiotics, honey, coconut oil or other natural oils with antimicrobial properties, magnesium hydroxide, chamomile, echinacea, sage, deglycyrrhizinized licorice (DGL), zinc, vitamin B 12 The agent for treating oral ulcers is selected from the group consisting of antimicrobial compounds, antifungal agents, and combinations thereof.

[0028] In a further embodiment, the composition is a dry socket treatment and the therapeutic agent is a dry socket treatment agent selected from the group consisting of an analgesic, an antibacterial agent, a tissue growth agent, In a further embodiment, the therapeutic agent is selected from the group consisting of an NSAID, an opioid, acetaminophen, chlorhexidine, metronidazole, guaiacol, eugenol, balsam of peru, chlorobutanol, iodoform, butamben, polymyxin B sulfate, tyrothricin, neomycin sulfate, tetracaine hydrochloride, and combinations thereof.

[0029] In a further embodiment, the composition has a whitening agent, specifically, the therapeutic agent is a peroxide.

[0030] Use of the oral mucosal carrier of any embodiment herein for treating oral fungal, bacterial, or viral infections. [Brief description of the drawings]

[0031] [Figure 1] 1 shows a diagram of the formula for PDMS (dimethicone) having n repeating siloxane units. [Diagram 2] 1 shows the release profiles of several different blends of the present disclosure for release of a therapeutic agent such as cetylpyridinium chloride over a 24 hour period. [Diagram 3] 1 shows the release profiles of several different blends of the present disclosure in terms of CBD release over a 24 hour period. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0032] Oral mucosa is constantly bombarded by sugar, alcohol, low and high pH foods and beverages, and substances that stain or damage the teeth, enamel, and gums of individuals. Fortunately, as described herein, oral mucosa carrier products create useful materials for several ailments of the oral mucosa. Some ailments include, for example, the treatment of the tooth surface to prevent caries and reduce tooth sensitivity. However, oral mucosa is more than just teeth and gums, and many individuals face painful, uncomfortable, or embarrassing afflictions that require treatment with certain active or inactive ingredients.

[0033] For example, orthodontic tooth surface treatment is often required before applying cement to the tooth, and the tooth is etched to allow for better and more secure attachment of the bracket. Etching simply removes a layer of dentin or enamel from the tooth surface, which may otherwise create sensitivity or access to the tooth. Thus, after the tooth has been orthodontally treated, a material that can be applied around the bracket, to the tooth surface, and to the oral mucosa can help remineralize the tooth surface to repair any damage that may have been accidentally caused.

[0034] Many individuals also suffer from dry mouth. Dry mouth may occur in individuals who suffer from allergies, may occur simply with age, may occur due to occupational activities, ambient relative humidity, the presence of pollutants in the air, medication, or other social endeavors.For example, people who use certain cannabinoid products often complain of the side effect of dry mouth, despite the relief provided by the drug.As described herein, oral mucosa carriers provide a barrier while providing a lubricating feel and delivery of excipients or other therapeutic agents, reducing the need for multiple oral care.

[0035] A large portion of the population also suffers from bad breath. Sufferers are not only those who may have secondary medical concerns, including concerns caused by sleep apnea or snoring, but also those who have problems breathing through the nose, or simply from the buildup of bacteria in the oral mucosa that leads to bad breath. Treatment is often by better care habits, including brushing and flossing, but also by the use of certain oral mouthwashes, which too often simply mask the problem for a short period of time.

[0036] Many individuals also face the burden of canker sores forming, or other mouth sores that form from abuse, misuse, or the progression of viral or bacterial diseases. Canker sores are particularly frustrating because they form out of nowhere and cause open wounds that are painful for days. Existing techniques typically coat the open wounds, often with materials such as cyanoacrylate, to promote healing. However, the formulations of the present embodiments can further treat aphthous ulcers, as well as other mouth sores, including sores from lichen planus, canker sores, and herpes. New formulations with protective properties are welcomed in the field to better treat canker sores and other mouth and oral sores.

[0037] Tooth sensitivity is a significant problem for people who have suffered from dentin removal or gum recession, exposing the tubules on the tooth surface that connect to the nerve endings in the mouth. Such sensitivity makes eating and drinking painful, as many materials cause discomfort to the individual. Materials that treat both the underlying problem, typically from periodontal disease or damage to the tooth surface, as well as the protective barrier, could dramatically change treatment options for patients suffering from sensitivity.

[0038] Dry sockets (alveolar osteitis) occur fairly frequently after tooth extraction procedures. Although modern dental practice aims to prevent tooth extraction, sometimes tooth extraction is necessary to prevent further pain, discomfort, or to relieve damaged or diseased tissue. A dry socket occurs when the blood clot that formed after tooth extraction is released, exposing the bone in the socket. Treatment is often provided by rinsing with saltwater and packing the wound with gauze, gelatin, or another sealant. Clove oil or other antiseptics are frequently added to prevent bacterial infection and to soothe the open wound. Once the pain subsides, the wound will heal naturally. However, such problems are better treated with oral carriers that are mucoadhesive and can form a better barrier and provide relief to the specific site of injury.

[0039] Canker sores or oral thrush is caused by the fungus Candida albicans, which builds up on the lining of the mouth. It is a normal organism in the mouth, but sometimes the oral mucosa develops an overgrowth, typically causing discomfort to infants and young children. Therapeutic treatment with an oral carrier and an antifungal agent provides a fast and efficient way to control this discomfort and eliminate the fungal infection.

[0040] Tooth surface whitening is often provided by peroxides, which effectively bleach the tooth surface and remove stains. The present embodiments provide an improved mucoadhesive material that will increase retention time and contact with the tooth surface, increasing the efficiency of the peroxide and whitening agent.

[0041] In reality, each of these issues alone is a significant problem faced by both the individual and the dental professional who treats them. The ability to reduce caries, reduce dentin hypersensitivity, treat dry mouth, bad breath, canker sores, fungal, viral, or bacterial sores, as well as reduce dry socket concerns, is invaluable. In reality, these afflictions are faced by a wide range of patients, including children with immature teeth, and children and adults with mature teeth.

[0042] A common theme in many oral mucosal concerns is to provide two features, one is a protectant to protect the area of ​​interest from discomfort from hot or cold foods, sugar, salt, ingested substances from the mouth itself, from the tongue touching the surfaces in the mouth, or simply from pain, and a material that provides coating and barrier protection to the oral mucosa would provide immediate and sustained relief for many pains. At the same time, one that simply provides protection or a coating would prevent the ingress of other products into the oral mucosa that may reduce the body's ability to heal or provide therapeutic relief to the individual. Here, embodiments are directed to oral mucosal carrier and protectant products that provide carriers and reservoirs for excipients or therapeutics for pain treatment, as well as barrier materials to provide skin protection within the oral mucosa.

[0043] The oral mucosal carrier and protectant includes a first dimethicone product having a first viscosity. FIG. 1 details the general formula of dimethicone with "n" repeat units. The higher the number of repeat units "n", the higher the viscosity of the material. The oral mucosal carrier and protectant further includes a second dimethicone product having a second viscosity, the viscosity of the second dimethicone product being at least 2 million cP higher than the viscosity of the first dimethicone product, preferably at least 2.1 million, 2.2 million, 2.3 million, 2.4 million, or 2.5 million cP higher than the first dimethicone product. In certain embodiments, the difference is 2.5 million to 3 million cP. The cP unit (centipoise) is a unit of dynamic viscosity. The combination of the two viscosities provides a material that provides a physical barrier by forming a layer that mucoadheres to the tooth surface or oral mucosa, and when coated on the tooth surface or mucosal surface, the material has resistance to being removed due to strong adhesion. Thus, the material forms a barrier of this coating on the tooth surface and oral mucosa, but it also functions as a vehicle or reservoir for therapeutic agents for the treatment of one or many of the ailments described herein.

[0044] For example, the oral mucosal carrier and protectant may be in the form of a paste, gel, foam, aerosol, liquid, or may be provided as a food material such as a lozenge or gummies. Each of these forms allows for application to the mouth, where the oral mucosal carrier coats the surface of the oral mucosa. The material mixed into the dimethicone can then be released onto the oral mucosa or teeth surface, allowing the effectiveness of such a product to treat the oral mucosa.

[0045] The embodiments of the present disclosure detail a carrier material that is rosin-free, does not require the use of alcohol as a solvent, and is aqueous-free. In fact, the ability to remove rosin and solvent provides a new product for those who are allergic to rosin or sensitive to alcohol residues from existing products. The embodiments herein allow for the formation of a carrier that is highly adhesive to teeth and oral mucosal surfaces, allowing for the delivery of active agents that precipitate on the tooth surface.

[0046] As used herein, the terms active agent, additive, and excipient are used interchangeably to mean any material added to the carrier product of the present embodiment other than the dimethicone component. This term includes additional excipients and therapeutic agents, including, but not limited to, flavors, colorants, binders, bulking agents, preservatives, alcohol, titanium dioxide, sweeteners, dimethacrylates, waxes, fats, oils, Gantrez® (a synthetic alternating copolymer of methyl vinyl ether [MVE] and maleic anhydride), flow agents, stabilizers, saliva promoters, and the like.

[0047] As used herein, the term therapeutic agent or compound refers to a material that provides a medicinal, healing, or therapeutic effect to at least one cell of the oral mucosa, as understood by those skilled in the art.Non-limiting examples include certain fluoride or calcium donors, sodium fluoride, difluorosilane, stannous fluoride, APF (acid fluoride phosphate), ACPF (amorphous calcium phosphate fluoride), ACP (amorphous calcium phosphate), sodium monofluorophosphate, benzalkonium chloride, dipotassium hydrogen phosphate, calcium compounds, calcium nitrate, cetylpyridinium chloride, phosphate donors, potassium donors, as well as antibacterial agents, antifungal agents, antiviral agents, antibiotics, small molecules, antiemetic agents, biological materials, self-replicating peptides, cannabinoids, terpenes, and combinations thereof.

[0048] Components of the Oral Mucosal Carrier of the Present Disclosure Dimethicone, also known as polydimethylsiloxane or PDMS, is a silicone-based polymer of various sizes based on the number of repeating units of the polymer. Dimethicone has a wide range of applications, for example, in antiperspirants, skin creams, skin lotions, sunscreen lotions, bath oils, hair care products, and coatings for oral products. Skin care products have a wide range of applications, and dimethicone is trusted for its properties as the base of a wide range of cosmetic formulations, its hydrophobicity, range of viscosities, lubricating properties, low surface tension, transparent, tasteless, odorless, inert, and because it is miscible with a wide range of other materials.

[0049] In fact, dimethicone of various viscosities is trusted in many cosmetic formulations, used to fill in uneven texture and fine lines, such as in primers, foundations, or lotions. Additionally, as a silicone oil, it provides a protective cover on the skin, such as in sunscreen lotions or other skin lotions.

[0050] Dimethicone is also used in hair care products to provide smoothness, especially in conditioner or detangling products.In fact, the incorporation of dimethicone into the product makes hair smooth and reduces or makes it easier to remove tangles.In addition, many hair care products use dimethicone to leave hair shiny or glossy.This is because the product coats hair and leaves a small layer of material on the hair itself.

[0051] PDMS has a typical formula, [ka] The number of "n" repeat units affects the viscosity of the material. Dimethicone products are often sold in various formulations depending on their viscosity. Here, we combine dimethicones of at least two different viscosities, one preferably having a viscosity of about 1,000 cP to 25,000 cP, and the other preferably having a viscosity of about 2 million cP to 3 million cP, most preferably about 2.1 million to 2.9 million, or 2.2 million to 2.8 million, or 2.3 million to 2.7 million, or 2.4 million to 2.6 million, or most preferably about 2.5 million cP. When purchasing these materials, a typical Certificate of Analysis will provide the viscosity determined by rotational testing, and each Certificate of Analysis will typically provide the specification limits for the material within about 10%, or about 5%, or about 1% of the stated specification. For example, for a described material having a viscosity of 2.5 million cP, materials used in embodiments herein included a specification range of 2,312,500 to 2,687,500 cP.

[0052] The FDA has approved dimethicone for personal care products, and the material is generally considered safe for use. In fact, the FDA lists at least 16 entries for topical, transdermal, and oral applications of dimethicone. Of these, four are specifically listed for oral applications, namely Dimethicone 100, 350, 350, and 1000, with the overlapping 350 entry being one for capsules and one for "prolonged action capsules." Thus, dimethicone has a known expected safety profile with the FDA.

[0053] The difference in viscosity of dimethicones is simply in the number of repeating polymer units in the molecule. For example, polymers with a higher number of repeating units tend to restrict the movement of the polymer and therefore will be more viscous than polymers with a lower number of repeating units. However, when purchasing these dimethicone products commercially, in almost every instance, the materials are sold by their viscosity, with a range or variation of about 1-10% of the stated viscosity.

[0054] In creating a formulation for the present oral mucosal carrier product, all of the above considerations must be considered, i.e., rate or release of active ingredient, adhesion, as well as the aesthetic and tactile response of the materials to produce a superior product. As detailed in Formulations 1-9 and Table 3 below, we tested several different base formulations, the first using 1,000 cP ingredients with 2.5 million cP dimethicone, and the second substituting 1,000 cP dimethicone with 12,500 dimethicone. We also tested variants using 25,000, 50,000 cP, and 100,000 cP mixed with 2.5 million dimethicone. Finally, 1,000 and 12,500 dimethicone were tested with the lower 1.5 million cP dimethicone to evaluate the materials with various base materials at different concentrations.

[0055] In summary, compositions containing a first dimethicone with a viscosity of less than 50,000 cP were more effective than compositions with a viscosity of 50,000 cP or more, regardless of whether a second dimethicone with a viscosity of 1.5 million, 2 million, 2.5 million, or 3 million cP was used. Furthermore, the difference in viscosity also seemed to be important to some extent, that is, the one using the 2.5 million cP dimethicone performed better than the one mixed with the 1.5 million cP product. However, this does not mean that the 50,000 cP material, as a low viscosity dimethicone, was not significantly better than the currently available material. Thus, in the broadest sense, the combination of two dimethicone materials with different viscosities provides important advantages.

[0056] In a preferred embodiment, a first dimethicone of 1,000 cP to 50,000 cP, optimally 1,000 cP to 25,000 cP, was mixed with a second dimethicone of 2.5 million cP to provide optimal retention and adhesion to the oral mucosa while allowing for the appropriate feel, physical properties, and release profile.

[0057] In a preferred embodiment, the oral mucosal carrier composition comprises a dimethicone-based oral mucosal carrier comprising a first dimethicone material having a viscosity of about 1,000 cP to 25,000 cP and a second dimethicone material having a viscosity of about 2 million to about 3 million, and at least one active agent.

[0058] In a further preferred embodiment, the composition is a combination of the first dimethicone and the second dimethicone in a ratio of 100:1 to 1:10. In a further preferred embodiment, the composition comprises two or more active agents. In a further preferred embodiment, the composition comprises at least one therapeutic agent.

[0059] In a further preferred embodiment, the composition is such that the active agent is a bulking agent. In a further preferred embodiment, the bulking agent is an edible wax. In a further preferred embodiment, the bulking agent comprises 0.01 to 15% of the total weight of the composition.

[0060] In a further preferred embodiment, the composition is a therapeutic agent selected from the group consisting of sodium fluoride, difluorosilane, stannous fluoride, APF (acid fluoride phosphate), ACPF (amorphous calcium fluoride phosphate), ACP (amorphous calcium phosphate), sodium monofluorophosphate, benzalkonium chloride, dipotassium hydrogen phosphate, calcium nitrate, cetylpyridinium chloride, phosphate donor, potassium donor, antibacterial agent, antifungal agent, antiviral agent, antibiotic, small molecule, antiemetic agent, biological material, self-replicating peptide, cannabinoid, terpene, and combinations thereof.In a further preferred embodiment, the composition is a therapeutic agent selected from the group consisting of sodium fluoride, difluorosilane, stannous fluoride, APF (acid fluoride phosphate), ACPF (amorphous calcium fluoride phosphate), ACP (amorphous calcium phosphate), sodium monofluorophosphate, benzalkonium chloride, dipotassium hydrogen phosphate, calcium nitrate, cetylpyridinium chloride, phosphate donor, potassium donor, antibacterial agent, antifungal agent, antiviral agent, antibiotic, small molecule, antiemetic agent, biological material, self-replicating peptide, cannabinoid, terpene, and combinations thereof.

[0061] Product Formulation for Oral Mucosal Carrier Use When preparing oral formulations, typically the formulation includes not only the carrier but also the active ingredient specifically.In further embodiments, the carrier and the active ingredient are further combined with one or more excipients, which are typically added to produce a specific formulation, or to improve the formulation, its consistency, viscosity, texture, taste, feel, or to incorporate the inclusion of other active ingredients for oral treatment.

[0062] The primary application of these oral mucosal carriers and protective materials is tooth remineralization. For example, as previously mentioned, orthodontic bracket treatment may require some etching or damage to the tooth enamel surface. Thus, treatment of the tooth surface after the brackets are attached would be advantageous to aid in remineralization and prevent sensitivity or caries due to weakening or removal of the enamel surface for orthodontic application of the brackets. Commercial strengths, i.e., less than 1,500 ppm, may be suitable for long-term use, but concentrations of 5,000 ppm may also be suitable for application under prescription in a dental office, where higher ppm concentrations can be ordered by prescription. Application of such materials is typically via liquid, paste, foam, or gel-like application to the tooth surface or adjacent to the brackets placed on the tooth surface. Studies have confirmed that high concentrations of fluoride have been shown to dramatically prevent the development of caries on both immature and mature tooth surfaces when fluoride is applied in a dental office.

[0063] For example, prescription strength fluoride oral mucosal carrier and protectant products are applied or spread through a number of different applications to smear or coat each tooth surface and usually remain in place for about 1-8 hours, whereas a typical treatment would have the product on the tooth surface for 4-6 hours. Eating and drinking a limited meal is permitted immediately after application, but brushing the tooth surfaces, or other food or drink materials that rub against the tooth surfaces, will remove some of the product from the tooth surfaces more quickly than normal.

[0064] This product is different from existing fluoride products that often use natural resins that dry to a color such as yellow or brown that is problematic for most users due to appearance, and it also eliminates or reduces the unpleasant taste and texture due to resin-based fluoride products. In fact, the oral mucosal carrier and protectant described herein leaves a smooth coating on the tooth surface and can be flavored with a number of flavorings. Specifically, this product excludes rosin and therefore also eliminates the alcohol solvent required for rosin-based products.

[0065] The oral mucosal carrier of this embodiment is developed to adhere to oral mucosal surfaces, with the material itself acting as a reservoir for therapeutic agents such as cetylpyridinium chloride to allow for the desired antimicrobial activity in the oral environment. In fact, as shown in Figure 2, a graph provides values ​​for chloride release from cetylpyridinium chloride material based on three different formulations, the first having a 1:1 ratio of 2.5 million cP to 1,000 cP dimethicone, the second having a 1:4 ratio of 2.5 million to 1,000 cP dimethicone, and the third being 100% 1,000 cP dimethicone. Both the time and release profiles serve to allow chloride to leave the carrier and release of the therapeutic agent to the mucosal surface.

[0066] Table 3 below details several different formulations of the present disclosure, each with a different amount of force (peak adhesion) and (total adhesion) that provides each material's value for its adhesion.Those with greater adhesion typically remain on mucosal surfaces for a longer period of time than those with lower peak adhesion.Thus, formulations that use a higher proportion of higher viscosity dimethicone have greater adhesion properties compared to those that use a lower proportion of higher viscosity dimethicone.

[0067] At the same time, there must be a balance between peak adhesion and the dissolution rate of the drug, which in FIG. 2 is the chloride. FIG. 2 shows that the higher amount of 2.5 million cP dimethicone results in a slower dissolution rate of chloride from the carrier. At a 1:1 ratio of the two dimethicone materials, the chloride release rate is nearly half the rate with the other two tested release profiles of this disclosure. Thus, the product containing only 1,000 cP dimethicone had the fastest release profile from 0-5 hours, but at 24 hours, its total release was nearly identical to the product with a 4:1 (low viscosity:high viscosity dimethicone) ratio. Also, the 4:1 ratio product had a dramatic and significant improvement in adhesion over the 1,000 cP material. Thus, the effective release to the oral mucosa is much higher with the material with 2.5 million cP dimethicone, which is retained on the oral mucosa for a longer period of time than the material without the high viscosity dimethicone.

[0068] At 24 hours, the release profile for the 1:1 ratio product reached over 40 ppm chloride per gram of carrier. The importance of these release profiles is to evaluate the two-fold concern of release rate that allows for uptake of released chloride while balancing the need for adhesion to maintain the material on the oral mucosal surface. For example, if only a 1,000 cP material washes off the oral mucosal surface in 30 minutes, then that fast release rate will be insufficient as there will not be enough time to allow release of the therapeutic agent. Similarly, too fast a release may simply release material into the saliva, preventing sufficient uptake of the therapeutic agent into the oral mucosal tissue. Thus, a slightly slower release may be beneficial and ultimately outweigh a faster release when considering the oral mucosal surface.

[0069] To confirm the release profile, a second active agent was tested to determine the release profile, i.e., the release of CBD from the material, as shown in Figure 3. Figure 3 details a very similar set of study results compared to those in Figure 2, i.e., the lowest viscosity material has a faster release profile, but the total release profile is nearly the same as that of the product using a 4:1 ratio of low and high viscosity dimethicone. In fact, although not shown in the figure, the release of fluoride was also tested in a similar study, and the same general principles were confirmed regarding release. Thus, several different materials all show similar, consistent release profiles from the material.

[0070] For application to the tooth surface, for paste, gel, foam, liquid, aerosol, or food material purposes, the oral mucosal carrier of the present disclosure must also have a profile that allows application of the material at room temperature. In fact, ease of application is necessary not only to ensure that the material is applied correctly, but also to aid in its ultimate use. Materials that require heating or cooling, or application with specialized applicators, are likely to face the burden of professionals applying these materials, so the benefit of the product will remain unused in a drawer, not on the tooth surface. Thus, if the material is in the form of a paste, gel, or foam, it is preferably of a gel or paste-like consistency that can be brushed or applied to the tooth surface. If it is a liquid, it must be able to be swished in the mouth and coated, or if it is an aerosol, it must be easily sprayed into the mouth for coating purposes. For food materials, one that can maintain its shape or coat the material would be advantageous. Finally, materials in contact with the oral mucosa must adhere to the teeth and oral tissues and then tolerate the properties of saliva and oral mucosa to allow release of excipients and therapeutic agents from the carrier.

[0071] The dimethicone carrier product of the present embodiment reduces many of the undesirable side effects of existing resin-based oral materials. Moreover, these natural resins require alcohol or other solvents for application, and then leave a yellow or brown film on the tooth surface. This is a real aesthetic problem, but children, adolescents, and adults who use such products often have a reluctance to keep the product on the tooth surface for the period of time required to allow fluoride to migrate to the tooth surface. Thus, the material is scraped off by washing, brushing, flossing, or simply tongue movements. In practice, existing resin-based oral products often suffer from a staining or dirty feel on the tooth surface, and therefore subject the tooth surface to tongue movements, which ultimately removes a higher percentage of the oral mucosa carrier. The present embodiment includes an oral mucosa carrier and protectant that has a transparent color after application to the tooth surface, thus eliminating the brown or yellow coloring present in many resin-based materials.

[0072] Furthermore, the use of dimethicone material provides a smooth and clean-feeling coating on tooth surface and oral mucosa surface.In fact, dimethicone products are frequently used for their ability to act as lubricants or smooth texture.Therefore, by creating a smooth surface on tooth and oral mucosa surface, tongue action is reduced, and therefore removal of the dimethicone-based formulation of the present disclosure is reduced, compared to those that rely on natural resins as carriers.Reducing removal of formulation naturally increases the time that material is on tooth or oral mucosa surface, and therefore improves the release of material to tooth surface and oral mucosa.

[0073] The main therapeutic component of the oral mucosa carrier may include fluoride. Fluoride, which is available in several different forms, is provided in a dimethicone carrier that is placed in close proximity to the tooth surface, and will provide remineralization properties when the oral mucosa carrier is applied and adheres (or is adjacent) to the tooth surface. For example, sodium fluoride is a common fluoride additive. Other fluorides known to those skilled in the art may also be utilized, such as stannous fluoride, ACPF, etc., which are known and used in other oral care products. Each of these may be suitably added as a fluoride donor for remineralization purposes.

[0074] In certain embodiments, flavoring or sweetening agents are often used to provide a pleasant taste when applying the material.In some of the above embodiments, the dental varnish composition of the present invention can further include one or more sweeteners, flavoring agents, and coloring agents.Any suitable flavoring or sweetening agent material can be used.Examples of suitable flavoring components include natural or artificial flavors, such as natural flavors, spearmint, peppermint, wintergreen, clove, sage, eucalyptus, marjoram, cinnamon, citrus, vegetable, nut, fruit, and bramble oils, but are not limited to these. Other flavorings may include oleoresins, essences or extracts containing flavor constituents derived from spices, fruits or fruit juices, vegetables or vegetable juices, edible yeasts, herbs, bark, buds, roots, leaves, or similar plant materials, meat, seafood, poultry, eggs, dairy products, or fermentation products thereof, protein hydrolysates, distillates, or any product of roasting, cooking, or enzymatic degradation, as well as other natural and synthetic flavorings known to those skilled in the art.

[0075] Suitable sweeteners include nutritive and non-nutritive sweeteners such as sucrose, fructose, dextrose, high fructose corn syrup, sugar alcohols such as xylitol, maltitol, sorbitol, mannitol, erythritol, sucralose, aspartame, acesulfame potassium, saccharin, sedum saccharin, and synthetics such as neotame, others include, but are not limited to, lactose, maltose, sodium cyclamate, perillartine, AMP (aspartic acid phenylalanine methyl ester), and other natural and synthetic sweeteners known to those skilled in the art.

[0076] Suitably, the flavor and / or sweetener, each or together, may comprise up to 10% by weight of the composition, or up to 5%, or up to 4%, or up to 3%, or up to 2%, or up to 1%, or 0.5% to 1% by weight. In certain embodiments, it may be preferable to provide the material without flavor or sweetener, in which case the material has little or no flavor, which may cause the patient to worry that the material is not on the tooth surface. Thus, a small amount of either sweetener or flavor may help the patient understand that the material is present.

[0077] A potential problem with the addition of flavorings is that they can increase the rate at which the material is washed off the oral mucosal surface, thus reducing the time that the active ingredient or material is present on the teeth or oral mucosal surface, including, but not limited to, the patient's gums, tongue, cheeks, upper and lower parts of the mouth, and throat area. Often, saliva flow is necessary to ensure application of the material to all oral surfaces, but washing the material off quickly reduces the effectiveness of the product. Therefore, the mucoadhesive properties of the dimethicone carrier are important to ensure that the material remains adjacent to the oral mucosal or dental surface for a sufficient period of time to allow release of the excipient or therapeutic agent.

[0078] Addition of bulking agents or textures. As with the inclusion of flavorings, it may be suitable to provide a small amount of bulking agents or texturizing agents to the product to give it mass and substance, to give the material texture, or to improve its consistency for application to the dental surface. For example, the addition of beeswax, other natural waxes, fats, oils, Gantrez® (a synthetic alternating copolymer of methyl vinyl ether [MVE] and maleic anhydride), and other agents that can modify the flow, texture, and viscosity of the final product. Other bulking agents may include mannitol, dicalcium phosphate, calcium sulfate, dry starch, cellulose, kaolin, sodium chloride, anhydrous lactose, sorbitol, sucrose, and the like. Those skilled in the art recognize that bulking agents are frequently used in the formulation of pharmaceutical and oral products, and therefore understand the meaning of the term as used herein.

[0079] Furthermore, flow agent can be added to modify the final physical properties of material, giving it higher or lower viscosity, or the ability of product to flow or remain at its target position when contacted with aqueous saliva in mouth.For example, magnesium stearate, stearic acid, silicon dioxide, glycerin, palmitate, and others known to those skilled in the art.Those skilled in the art recognize that flow agent is frequently used in the formulation of pharmaceutical products, and therefore understand the meaning of the term used herein.

[0080] Additional therapeutic materials may be suitably incorporated into the oral formulations of the present invention, such as whitening agents, urea peroxide, potassium peroxide, titanium dioxide, hydrogen peroxide, polyvinylpyridine (PVP) and hydrogen peroxide complexes, preservatives, vitamins, e.g., vitamin B6, B 12Examples of suitable additives include, but are not limited to, EDTA, E, and K, silicones, chlorophyll compounds, potassium salts for the treatment of dentin hypersensitivity, e.g., potassium nitrate, and anti-tartrate agents, e.g., sodium tripolyphosphate, and di- and tetra-alkali metal pyrophosphates, e.g., disodium and tetrasodium pyrophosphate, and calcium-based salts, e.g., dicalcium phosphate, tricalcium phosphate, precipitated calcium carbonate, either alone or in combination with amino acids such as L-arginine and L-lysine. These agents, when present, are incorporated into the compositions of the present invention in amounts that do not substantially adversely affect the desired properties and characteristics, and thus are typically added at 0.1 to 10 weight percent of the total composition.

[0081] Benzalkonium chloride may also be added as a therapeutic material for its use as an antiseptic and disinfectant, and for its preservative properties. However, when used in sufficient concentrations, it can be used as an oral mucosal disinfectant to reduce the number of bacteria that can damage the oral mucosa. Other antibacterial agents may include, but are not limited to, cetylpyridinium chloride, transfarnesol, chitosan, chlorhexidine, quaternary ammonium compounds, phenols, bisguanides, and combinations thereof.

[0082] Calcium nitrate and other calcium donor materials can be used in conjunction with fluoride ion donor.The purpose of providing both fluoride and calcium donors is to allow more remineralization to the tooth surface.The carrier described herein does not include aqueous.Therefore, unless a specific additive does not include water, the entire composition does not include water.

[0083] In certain embodiments, it may be suitable to add potassium donors such as dipotassium hydrogen phosphate or other potassium salts for tooth sensitivity treatment.Additional potassium donors such as potassium nitrate, potassium chloride, and potassium dihydrogen phosphate are effective and commonly used to reduce tooth sensitivity.In addition, arginine and lysine, as well as fluoride, oxalates such as potassium oxalate, bioglass, ACP, or casein-phosphopeptide-ACP, and other known materials can be used to treat tooth sensitivity.

[0084] In certain embodiments, it may be suitable to add a phosphate donor, including, for example, ACP, casein-phosphopeptide-ACP, potassium dihydrogen phosphate, dipotassium hydrogen phosphate, dicalcium phosphate, tricalcium phosphate, sodium dihydrogen phosphate, sodium dihydrogen phosphate, disodium hydrogen phosphate, monomagnesium phosphate, dimagnesium phosphate, and other donors, salts thereof, and combinations thereof known to those of skill in the art.

[0085] Oral mucosa carrier and protective material can be formulated under conditions that will prevent bacterial growth or prevent spoilage.Indeed, the inclusion of certain antibacterial agents may provide improved safety and improved shelf life.The material can be formulated under normal procedures known to those skilled in the art of oral care products, and then sterilized.Alternatively, no sterilization process is required.

[0086] Dry mouth or thirst treatments may include pilocarpine, acetylcholine, electrolytes such as sodium, potassium, calcium, magnesium, chloride, phosphate, and carbonate. Saliva enhancers may be advantageously included in the mucosal carrier formulations of the present disclosure, including, for example, essential oil extracts, acanthus persica, xylitol, carboxymethylcellulose, and variations thereof to enhance saliva flow.

[0087] Halitosis treatments may include any number of antimicrobial compounds described herein, and / or natural or synthetic oils or odor destroyers or odor masking agents.

[0088] The canker sore treatment is provided without any additional compounds, as the carrier itself will protect and cover the canker sore, but may also contain additional excipients or therapeutic compounds. Aluminum powder (potassium aluminum sulfate), baking soda, probiotics, honey, coconut oil or other natural oils with antimicrobial properties, magnesium hydroxide, chamomile, echinacea, sage, deglycyrrhizinized licorice (DGL), zinc, vitamin B 12 and other antimicrobial materials as described herein.

[0089] Dry socket treatment often includes analgesics as a first line of defense. For example, common NSAIDs or other analgesics, and other analgesic materials including acetaminophen, or opioid-based materials. Additionally, antibacterial or antimicrobial agents may be suitable. Additionally, agents for tissue growth and healing may be suitable. For example, the following compounds are a non-limiting list of possible additives: NSAIDs, opioids, acetaminophen, chlorhexidine, metronidazole, guaiacol, eugenol, balsam of peru, chlorobutanol, iodoform, butamben, polymyxin B sulfate, tyrothricin, neomycin sulfate, tetracaine hydrochloride, and combinations thereof.

[0090] As known to those skilled in the art, peroxides (whitening) may suitably be added. In some cases, peroxides may also be used for their antibacterial and antimicrobial properties.

[0091] Certain embodiments herein include a portion of a hemp extract. By hemp extract is meant a material that includes a portion of a material extracted from a hemp plant that contains at least one or more of certain cannabinoid or terpene molecules. Specifically, hemp extracts are believed to contain either cannabidiol (CBD) or delta-9-tetrahydrocannabinol (THC). In certain embodiments, low-THC hemp extracts mean those that have less than 0.30% THC. High-THC hemp extracts mean those that contain more than 0.30% THC. Typically, hemp extracts are ethanol or CO2 extracted from cannabis plants and contain multiple cannabinoid and terpene molecules. These can be diluted with another carrier oil or solvent, if necessary.

[0092] Cannabinoids, including CBD and THC infused topicals, only penetrate the skin layer easily, whereas the oral mucosa offers the opportunity to rapidly take up the material, thus providing an opportunity to enhance bioavailability via oral administration, but avoiding first-pass metabolism. Thus, the carrier materials defined herein are effective in delivering cannabinoid compounds and other compounds to the body.

[0093] Oral absorption of THC is slow, with peak concentrations occurring 1-5 hours after administration. Bioavailability of THC was 6% when administered orally, compared with a maximum of 27% when inhaled. Maximum plasma THC concentrations ranged from 4.4 to 11.0 μg / L after a 20 mg dose of oral THC. Once absorbed, THC is oxidized by the cytochrome P450 hepatic mixed function oxidase system to equipotent 11-hydroxy-THC (11-OH-THC), which is further metabolized to the inactive 11-nor-9-carboxy-THC (THCCOOH).

[0094] CBD has oral absorption and bioavailability similar to THC. After administration of 10 mg CBD + 10 mg THC in an oral capsule, the mean (SD) peak plasma concentrations were 2.5 (2.2) μg / L CBD and 6.4 (3.1) μg / L THC, and after buccal Sativex (10 mg THC + 10 mg CBD), they were 3.0 (3.1) μg / L CBD and 6.1 (5.4) μg / L THC. Time to maximum concentration (T max ) were 1.3 (0.8) hours for CBD and 1.0 (0.6) hours for THC after oral administration, and 2.8 (1.3) hours for CBD and 2.4 (1.1) hours for THC after buccal administration.

[0095] Therefore, a new strategy is needed to deliver cannabinoids orally, by adsorption through the oral mucosa. In the mouth, there are three areas of absorption: the mucosa inside the entire mouth, the area under the tongue (sublingual), and the tongue itself. Cannabis products placed under the tongue (sublingually) will take effect sooner than products absorbed through the general mucosal tissue lining the mouth or placed on the tongue itself. With this method of intake, the effects of cannabis should be felt in 15 to 60 minutes. Replacing oral forms of administration (by digestion) with forms for delivery to the oral mucosa would therefore be highly advantageous.

[0096] The main use of these oral mucosa carriers and protective materials is the delivery of cannabinoid compounds, with the supplemental effect of any additional oral effects. These may include remineralization to prevent or reduce caries, or as mentioned above, orthodontic bracket treatment may require etching or damage to the enamel surface of the tooth. Therefore, after the bracket is attached, treatment of the tooth surface will be advantageous to help remineralization and prevent sensitivity or caries due to weakening or removal of the enamel surface for orthodontic application of the bracket.

[0097] Method for manufacturing dimethicone oral mucosal carrier products A mixture of two different viscosity dimethicone products, especially products with such a dramatic viscosity difference, presents significant obstacles in the manufacture and mixing of ingredients. In reality, one cannot simply add all ingredients to a mixing bowl, mix / stir the ingredients, and create an instant formulation. Several different protocols were tested to allow the ingredients to be thoroughly mixed until a suitable process was produced.

[0098] As an example, the ingredients of Example 1 below were tested in several different mixing applications. Initially, all ingredients were placed together in a single mixing vessel and mixed with a magnetic mixing bar. Due to the viscosity of the materials, mixing was not possible. Further testing attempted to use a spinning / rotating mixing blade. However, except for the smallest amount of 2.5 million cP material, the viscosity of the materials made this difficult and the blade introduced a large amount of air into the product, making it unsuitable for use. After trial and error, a bladeless mixing system that utilizes centrifugal force to assist mixing was found to be effective in mixing two different viscosities of silicone material with additional excipients in the following examples. EXAMPLES

[0099] Example 1 The following compounds were mixed using a Flacktek centrifugal mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Sodium Fluoride. First, 17.6 grams of the 1,000 cP Dimethicone were added to the mixing cup. Next, 0.02 grams of Sodium Fluoride were added to the mixing cup. The two compounds were mixed at 3,000 RPM for 10 minutes. Next, 2.4 grams of the 2.5 million cP Dimethicone were added in five increments of 0.48 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0100] Subsequent formulation examples were prepared following the same procedure as Example 1. The following table lists the proportions of ingredients used in specific formulation examples.

[0101] [Table 1]

[0102] Example 6 The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (12,500 cP), Sodium Fluoride. First, 17.6 grams of the 12,500 cP Dimethicone were added to the mixing cup. Next, 0.02 grams of Sodium Fluoride were added to the mixing cup. The two compounds were mixed at 3,000 RPM for 10 minutes. Next, 2.4 grams of the 2.5 million cP Dimethicone were added in five increments of 0.48 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0103] [Table 2]

[0104] The mucoadhesion of the nine dimethicone oral mucosal formulations was measured using a tensile test method described in the literature. A Brookfield CT3 Texture Analyzer instrument was used at room temperature (23±1° C.). 20 grams of sample was used in the container and measurements were taken within 2 minutes of filling the container. Peak adhesion was measured (n=6) for each formulation. These values ​​are reported in Table 3 below. Total adhesion was measured (n=6) for each oral mucosal formulation. These values ​​are reported in Table 3 below. More negative numbers represent greater adhesion and greater total adhesion.

[0105] [Table 3]

[0106] Example 10 Example of dimethicone for orthodontic bracket treatment The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Sodium Fluoride. First, 15 grams of the 1,000 cP dimethicone were added to the mixing cup. Next, 20 milligrams of sodium fluoride were added to the mixing cup. The two compounds were mixed at 3,000 RPM for 10 minutes. Next, 5 grams of the 2.5 million cP dimethicone were added in five 1.0 gram increments. After each increment was added, the formulation was mixed for 5 minute increments.

[0107] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Sodium Fluoride, Calcium Nitrate. First, 10 grams of 1,000 cP Dimethicone were added to the mixing cup. Next, 20 milligrams of Sodium Fluoride were added to the mixing cup. Next, 20 milligrams of Calcium Nitrate were added to the mixing cup. The three compounds were mixed at 3,000 RPM for 10 minutes. Next, 10 grams of 2.0 gram Dimethicone was added in five increments. After each increment was added, the formulation was mixed for 5 minutes.

[0108] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Sodium Fluoride, Calcium Nitrate, and Dipotassium Hydrogen Phosphate. First, 10 grams of 1,000 cP Dimethicone were added to the mixing cup. Next, 20 milligrams of Sodium Fluoride were added to the mixing cup. Next, 20 milligrams of Calcium Nitrate were added to the mixing cup. Next, 10 milligrams of Dipotassium Hydrogen Phosphate were added to the mixing cup. The four compounds were mixed at 3,000 RPM for 10 minutes. Next, 10 grams of 2.0 gram Dimethicone were added in five increments. After each increment was added, the formulation was mixed for 5 minute increments.

[0109] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Sodium Fluoride, Calcium Nitrate, Dipotassium Hydrogen Phosphate, and Spearmint Oil. First, 18 grams of 1,000 cP Dimethicone were added to the mixing cup. Next, 20 milligrams of Sodium Fluoride were added to the mixing cup. Next, 20 milligrams of Calcium Nitrate were added to the mixing cup. Next, 10 milligrams of Dipotassium Hydrogen Phosphate were added to the mixing cup. Next, 80 milligrams of Spearmint Oil were added to the mixing cup. The five compounds were mixed at 3,000 RPM for 10 minutes. Next, 2 grams of 2.5 million cP Dimethicone were added in five increments of 0.4 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0110] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Sodium Fluoride, Calcium Nitrate, Dipotassium Hydrogen Phosphate, Spearmint Oil, and Cetylpyridinium Chloride. First, 19 grams of 1,000 cP dimethicone were added to the mixing cup. Next, 20 milligrams of sodium fluoride were added to the mixing cup. Next, 20 milligrams of calcium nitrate were added to the mixing cup. Next, 10 milligrams of dipotassium hydrogen phosphate were added to the mixing cup. Next, 80 milligrams of spearmint oil were added to the mixing cup. Next, 100 milligrams of cetylpyridinium chloride were added to the mixing cup. The six compounds were mixed at 3,000 RPM for 10 minutes. Next, 1 gram of 2.5 million cP dimethicone was added in five separate additions of 0.2 grams each. After each increment was added, the formulation was mixed for 5 minutes.

[0111] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), and Stannous Fluoride. First, 10 grams of the 1,000 cP dimethicone were added to the mixing cup. Next, 20 milligrams of stannous fluoride were added to the mixing cup. The two compounds were mixed at 3,000 RPM for 10 minutes. Next, 10 grams of the 2.5 million cP dimethicone were added in five 2.0 gram increments. After each increment was added, the formulation was mixed for 5 minute increments.

[0112] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Stannous Fluoride, Calcium Nitrate, Dipotassium Hydrogen Phosphate, Spearmint Oil, and Cetylpyridinium Chloride. First, 19.5 grams of 1,000 cP dimethicone were added to the mixing cup. Next, 20 milligrams of stannous fluoride were added to the mixing cup. Next, 20 milligrams of calcium nitrate were added to the mixing cup. Next, 10 milligrams of dipotassium hydrogen phosphate were added to the mixing cup. Next, 80 milligrams of spearmint oil were added to the mixing cup. Next, 100 milligrams of cetylpyridinium chloride were added to the mixing cup. The six compounds were mixed at 3,000 RPM for 10 minutes. Next, 0.5 grams of 2.5 million cP dimethicone were added in two separate additions of 0.25 grams each. After each increment was added, the formulation was mixed for 5 minutes.

[0113] Dimethicone Dry Mouth Treatment The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Citric Acid, Sodium Citrate, Tartaric Acid, and Baking Soda. First, 9.5 grams of 1,000 cP Dimethicone were added to the mixing cup. Next, 0.5 grams of baking soda were added to the mixing cup. Next, 0.5 grams of tartaric acid were added to the mixing cup. Next, 0.5 grams of citric acid were added to the mixing cup. Next, 0.5 grams of sodium citrate were added to the mixing cup. These five compounds were mixed at 3,000 RPM for 10 minutes. Next, 9.5 grams of 2.5 million cP Dimethicone were added in five increments of 1.9 grams each. After each increment was added, the formulation was mixed for 5 minutes.

[0114] Using a Flacktek mixer, the following compounds were mixed: Dimethicone (2.5 million cP), Dimethicone (12,500 cP). First, 9.5 grams of the 12,500 cP dimethicone were added to the mixing cup. Next, 9.5 grams of the 2.5 million cP dimethicone were added in five increments of 1.9 grams each. After each increment was added, the blend was mixed for 5 minutes. The mixture of the two dimethicones together is the lubricating blend.

[0115] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Gentian, Capsicum, and Statherin. First, 18.5 grams of the 1,000 cP Dimethicone were added to the mixing cup. Next, 0.2 grams of Gentian were added to the mixing cup. Next, 0.1 grams of Capsicum were added to the mixing cup. Next, 0.01 grams of Statherin were added to the mixing cup. These four compounds were mixed at 3,000 RPM for 10 minutes. Next, 0.5 grams of the 2.5 million cP Dimethicone were added in five increments of 0.1 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0116] Example of dimethicone for preventing bad breath The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), and Peppermint Oil. First, 10.1 grams of the 1,000 cP Dimethicone were added to the mixing cup. Next, 0.04 grams of Peppermint Oil were added to the mixing cup. The two compounds were mixed at 3,000 RPM for 10 minutes. Next, 9.5 grams of the 2.5 million cP Dimethicone were added in five increments of 1.9 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0117] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), and Cinnamon Oil. First, 10.1 grams of 1,000 cP Dimethicone were added to the mixing cup. Next, 0.04 grams of Cinnamon Oil were added to the mixing cup. The two compounds were mixed at 3,000 RPM for 10 minutes. Next, 9.5 grams of 2.5 million cP Dimethicone were added in five increments of 1.9 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0118] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), and Wintergreen Oil. First, 10.1 grams of 1,000 cP Dimethicone were added to the mixing cup. Next, 0.04 grams of Wintergreen Oil were added to the mixing cup. The two compounds were mixed at 3,000 RPM for 10 minutes. Next, 9.5 grams of 2.5 million cP Dimethicone were added in five increments of 1.9 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0119] Examples of Dimethicone Use in Canker Sores and Mouth Sores (Aphthous Ulcers, Herpes, Canker Sores, Lichen Planus) The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), and Fluocinonide. First, 10.1 grams of 1,000 cP Dimethicone were added to the mixing cup. Next, 50 milligrams of Fluocinonide were added to the mixing cup. The two compounds were mixed at 3,000 RPM for 10 minutes. Next, 9.5 grams of 2.5 million cP Dimethicone were added in five 1.9 gram increments. After each increment was added, the formulation was mixed for 5 minute increments.

[0120] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Benzocaine. First, 16.1 grams of the 1,000 cP dimethicone were added to the mixing cup. Next, 2 grams of benzocaine were added to the mixing cup. The two compounds were mixed at 3,000 RPM for 10 minutes. Next, 3.5 grams of the 2.5 million cP dimethicone were added in three increments of 1.67 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0121] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (12,500 cP), Silver Nitrate. First, 15.1 grams of the 12,500 cP Dimethicone were added to the mixing cup. Next, 0.4 grams of Silver Nitrate were added to the mixing cup. The two compounds were mixed at 3,000 RPM for 10 minutes. Next, 4.5 grams of the 2.5 million cP Dimethicone were added in five increments of 0.9 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0122] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Triamcinolone, Chlorhexidine, and Lidocaine. First, 18.1 grams of 1,000 cP Dimethicone were added to the mixing cup. Next, 0.1 grams of Triamcinolone were added to the mixing cup. Next, 0.1 grams of Chlorhexidine were added to the mixing cup. Next, 1 gram of Lidocaine was added to the mixing cup. The four compounds were mixed at 3,000 RPM for 10 minutes. Next, 1.5 grams of 2.5 million cP Dimethicone were added in three increments of 0.5 grams. After each increment was added, the formulation was mixed for 5 minute increments.

[0123] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Fluocinonide, Spearmint Oil, and Chitosan. First, 10.1 grams of 1,000 cP Dimethicone were added to the mixing cup. Next, 50 milligrams of Fluocinonide were added to the mixing cup. Next, 40 milligrams of Spearmint Oil were added to the mixing cup. Next, 0.1 grams of Chitosan were added to the mixing cup. The four compounds were mixed at 3,000 RPM for 10 minutes. Next, 9.5 grams of 2.5 million cP Dimethicone were added in five increments of 1.9 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0124] Examples of Dimethicone Dry Socket Treatment The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Acetaminophen, Chlorhexidine, and Metronidazole. First, 19.1 grams of 1,000 cP Dimethicone were added to the mixing cup. Next, 0.5 grams of Ibuprofen were added to the mixing cup. Next, 0.1 grams of Chlorhexidine were added to the mixing cup. Next, 0.5 grams of Metronidazole were added to the mixing cup. The four compounds were mixed at 3,000 RPM for 10 minutes. Next, 0.5 grams of 2.5 million cP Dimethicone were added in two increments of 0.25 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0125] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Guaiacol, Eugenol, Balsam of Peru, and Chlorobutanol. First, 10.1 grams of 1,000 cP Dimethicone were added to the mixing cup. Next, 0.5 grams of Ibuprofen were added to the mixing cup. Next, 1 gram of Guaiacol was added to the mixing cup. Next, 0.4 grams of Eugenol were added to the mixing cup. Next, 0.4 grams of Chlorobutanol were added to the mixing cup. The five compounds were mixed at 3,000 RPM for 10 minutes. Next, 9.5 grams of 2.5 million cP Dimethicone were added in five increments of 1.9 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0126] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Iodoform, Eugenol, and Butamben. First, 10.1 grams of 1,000 cP Dimethicone were added to the mixing cup. Next, 0.4 grams of Iodoform were added to the mixing cup. Next, 0.4 grams of Eugenol were added to the mixing cup. Next, 0.8 grams of Butamben were added to the mixing cup. The four compounds were mixed at 3,000 RPM for 10 minutes. Next, 9.5 grams of 2.5 million cP Dimethicone were added in five increments of 1.9 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0127] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Polymyxin B Sulfate, Tyrothricin, Neomycin Sulfate, and Tetracaine Hydrochloride. First, 10.1 grams of 1,000 cP Dimethicone were added to the mixing cup. Next, 0.5 grams of Polymyxin B were added to the mixing cup. Next, 0.5 grams of Tyrothricin were added to the mixing cup. Next, 0.5 grams of Neomycin Sulfate were added to the mixing cup. Next, 0.4 grams of Tetracaine Hydrochloride were added to the mixing cup. The five compounds were mixed at 3,000 RPM for 10 minutes. Next, 9.5 grams of 2.5 million cP Dimethicone were added in five increments of 1.9 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0128] Examples of dimethicone used to treat mucositis The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Chlorhexidine Gluconate, and Lidocaine. First, 18.5 grams of the 1,000 cP Dimethicone were added to the mixing cup. Next, 0.3 grams of Chlorhexidine Gluconate were added to the mixing cup. Next, 1.5 grams of Lidocaine were added to the mixing cup. The three compounds were mixed at 3,000 RPM for 10 minutes. Next, 0.5 grams of the 2.5 million cP Dimethicone were added in one portion and the formulation was mixed for 5 minutes.

[0129] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Chlorhexidine Gluconate, Lidocaine, and Palifermin. First, 9.5 grams of 1,000 cP Dimethicone were added to the mixing cup. Next, 0.3 grams of Chlorhexidine Gluconate were added to the mixing cup. Next, 1.5 grams of Lidocaine were added to the mixing cup. Next, 5 milligrams of Palifermin were added to the mixing cup. The four compounds were mixed at 3,000 RPM for 10 minutes. Next, 9.5 grams of 2.5 million cP Dimethicone were added in five increments of 1.9 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0130] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Chlorhexidine Gluconate, Lidocaine, Palifermin, Dipotassium Hydrogen Phosphate, and Calcium Chloride. First, 9.5 grams of 1,000 cP Dimethicone were added to the mixing cup. Next, 0.3 grams of Chlorhexidine Gluconate were added to the mixing cup. Next, 1.5 grams of Lidocaine were added to the mixing cup. Next, 5 milligrams of Palifermin were added to the mixing cup. Next, 0.5 grams of Dipotassium Hydrogen Phosphate were added to the mixing cup. Next, 0.5 grams of Calcium Chloride were added to the mixing cup. The six compounds were mixed at 3,000 RPM for 10 minutes. Next, 9.5 grams of 2.5 million cP Dimethicone were added in five separate additions of 1.9 grams each. After each increment was added, the formulation was mixed for 5 minutes.

[0131] Examples of Dimethicone Providing Whitening Treatments The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), and Carbamide Peroxide. First, 9.5 grams of the 1,000 cP dimethicone were added to the mixing cup. Next, 1 gram of the carbamide peroxide was added to the mixing cup. The two compounds were mixed at 3,000 RPM for 10 minutes. Next, 9.5 grams of the 2.5 million cP dimethicone were added in five increments of 1.9 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0132] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Carbamide Peroxide, and Spearmint Oil. First, 18.5 grams of 1,000 cP Dimethicone were added to the mixing cup. Next, 1 gram of Carbamide Peroxide was added to the mixing cup. Next, 40 milligrams of Spearmint Oil were added to the mixing cup. The three compounds were mixed at 3,000 RPM for 10 minutes. Next, 0.5 grams of 2.5 million cP Dimethicone were added in five 0.1 gram increments. After each increment was added, the formulation was mixed in increments of 5 minutes.

[0133] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (12,500 cP), Carbamide Peroxide, Spearmint Oil, and Potassium Nitrate. First, 9.5 grams of 12,500 cP Dimethicone were added to the mixing cup. Next, 1 gram of Carbamide Peroxide was added to the mixing cup. Next, 40 milligrams of Spearmint Oil were added to the mixing cup. Next, 0.75 grams of Potassium Nitrate was added to the mixing cup. The four compounds were mixed at 3,000 RPM for 10 minutes. Next, 9.5 grams of 2.5 million cP Dimethicone were added in five increments of 1.9 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0134] Examples of how dimethicone provides treatment for tooth sensitivity The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Potassium Nitrate. First, 9.5 grams of the 1,000 cP Dimethicone were added to the mixing cup. Next, 1 gram of Potassium Nitrate was added to the mixing cup. The two compounds were mixed at 3,000 RPM for 10 minutes. Next, 9.5 grams of the 2.5 million cP Dimethicone were added in five increments of 1.9 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0135] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Potassium Nitrate, and Spearmint Oil. First, 14.5 grams of 1,000 cP Dimethicone were added to the mixing cup. Next, 1 gram of Potassium Nitrate was added to the mixing cup. Next, 40 milligrams of Spearmint Oil were added to the mixing cup. The three compounds were mixed at 3,000 RPM for 10 minutes. Next, 4.5 grams of 2.5 million cP Dimethicone were added in three 1.5 gram increments. After each increment was added, the formulation was mixed for 5 minute increments.

[0136] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Potassium Nitrate, Spearmint Oil, and Zinc Chloride. First, 18.5 grams of 1,000 cP Dimethicone were added to the mixing cup. Next, 1 gram of Potassium Nitrate was added to the mixing cup. Next, 40 milligrams of Spearmint Oil were added to the mixing cup. Next, 0.5 grams of Zinc Chloride was added to the mixing cup. The four compounds were mixed at 3,000 RPM for 10 minutes. Next, 0.5 grams of 2.5 million cP Dimethicone were added in five increments of 0.1 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0137] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (12,500 cP), Potassium Nitrate, Spearmint Oil, Zinc Chloride, and Calcium Phosphate. First, 14.5 grams of 12,500 cP Dimethicone were added to the mixing cup. Next, 1 gram of Potassium Nitrate was added to the mixing cup. Next, 40 milligrams of Spearmint Oil were added to the mixing cup. Next, 0.5 grams of Zinc Chloride was added to the mixing cup. Next, 0.4 grams of Calcium Phosphate was added to the mixing cup. The five compounds were mixed at 3,000 RPM for 10 minutes. Next, 4.5 grams of 2.5 million cP Dimethicone were added in five increments of 0.9 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0138] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (25,000 cP), Potassium Nitrate, Spearmint Oil, Zinc Chloride, Calcium Phosphate, Sodium Fluoride. First, 9.5 grams of 25,000 cP Dimethicone were added to the mixing cup. Next, 1 gram of Potassium Nitrate was added to the mixing cup. Next, 40 milligrams of Spearmint Oil were added to the mixing cup. Next, 0.5 grams of Zinc Chloride were added to the mixing cup. Next, 0.4 grams of Calcium Phosphate were added to the mixing cup. Next, 20 milligrams of Sodium Fluoride were added to the mixing cup. The six compounds were mixed at 3,000 RPM for 10 minutes. Next, 9.5 grams of 2.5 million cP Dimethicone were added in five increments of 1.9 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0139] Adding CBD Example 11: The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (12,500 cP), Hemp Extract. First, 17.1 grams of 12,500 cP Dimethicone were added to the mixing cup. Next, 25 mg of CBD extract was added to the mixing cup via 1 mL of non-aqueous hemp extract oil. The two ingredients were mixed at 3,000 RPM for 10 minutes. Next, 1.9 grams of 2.5 million cP Dimethicone were added in five increments of 0.38 grams each. After each increment was added, the formulation was mixed for 5 minutes.

[0140] Subsequent formulations were prepared following the same procedure as Example 11. The following table lists the proportions of ingredients used in specific formulations.

[0141] [Table 4]

[0142] Example 16 The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (12,500 cP), CBD. First, 17.1 grams of 12,500 cP Dimethicone were added to the mixing cup. Next, 12.5 mg of Benzalkonium Chloride were added to the mixing cup. The two compounds were mixed at 3,000 RPM for 10 minutes. Next, 1.9 grams of 2.5 million cP Dimethicone were added in five increments of 0.38 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0143] [Table 5]

[0144] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), 12.5 mg CBD, and Nystatin. First, 10.1 grams of 1,000 cP Dimethicone were added to the mixing cup. Next, 0.5 mL (12.5 mg CBD) and 0.4 grams of Nystatin were added to the mixing cup. The two compounds were mixed at 3,000 RPM for 10 minutes. Next, 9.5 grams of 2.5 million cP Dimethicone were added in five increments of 1.9 grams each. After each increment was added, the formulation was mixed for 5 minutes.

[0145] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (12,500 cP), CBD, Bacitracin, Omycin, Polymyxin B. First, 18.5 grams of 12,500 cP Dimethicone were added to the mixing cup. Next, 12.5 mg of CBD and 1.45 grams of Bacitracin were added to the mixing cup. Next, 70 mg of Neomycin were added to the mixing cup. Next, 14 mg of Polymyxin B was added to the mixing cup. The four compounds were mixed at 3,000 RPM for 10 minutes. Next, 0.5 grams of 2.5 million cP Dimethicone were added in five increments of 0.1 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0146] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), CBD, Tranexamic Acid. First, 9.5 grams of 1,000 cP Dimethicone were added to the mixing cup. Next, 12.5 mg of CBD and 1 gram of Tranexamic Acid were added to the mixing cup. The two compounds were mixed at 3,000 RPM for 10 minutes. Next, 9.5 grams of 2.5 million cP Dimethicone were added in five increments of 1.9 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0147] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (25,000 cP), CBD. First, 9.5 grams of 25,000 cP Dimethicone were added to the mixing cup. Next, 25 mg of CBD were added to the mixing cup. The two compounds were mixed at 3,000 RPM for 10 minutes. Next, 9.5 grams of 2.5 million cP Dimethicone were added in five increments of 1.9 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0148] THC-providing formulation The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (12,500 cP), 25% THC. First, 9.5 grams of 1,000 cP dimethicone were added to the mixing cup. Then, 25 mg of THC was added to the mixing cup via 1 mL of oil carrier containing THC. The two compounds were mixed at 3,000 RPM for 10 minutes. Next, 9.5 grams of 2.5 million cP dimethicone were added in five increments of 1.9 grams each. After each increment was added, the formulation was mixed for 5 minutes. In a preferred embodiment, the oil carrier is hemp oil, coconut oil, or grain oil.

[0149] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Spearmint Oil, and Hemp Extract. First, 9.5 grams of 1,000 cP Dimethicone were added to the mixing cup. Next, 40 milligrams of Spearmint Oil were added to the mixing cup. Next, 25 milligrams of CBD were added to the mixing cup. The compounds were mixed at 3,000 RPM for 10 minutes. Next, 9.5 grams of 2.5 million cP Dimethicone were added in five increments of 1.9 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0150] In one particular embodiment, 5-25 mg of THC via hemp extract was added to the combination and mixed therein.

[0151] In certain embodiments, different flavor oils can be mixed for flavor.

[0152] The following compounds were mixed using a Flacktek mixer: Dimethicone (2.5 million cP), Dimethicone (1,000 cP), Spearmint Oil, Hemp Extract, and Wax. First, 9.5 grams of 1,000 cP Dimethicone were added to the mixing cup. 5 mg of wax and 40 milligrams of Spearmint Oil were added to the mixing cup. Next, 25 milligrams of CBD were added to the mixing cup. The compounds were mixed at 3,000 RPM for 10 minutes. Next, 9.5 grams of 2.5 million cP Dimethicone were added in five increments of 1.9 grams each. After each increment was added, the formulation was mixed for 5 minute increments.

[0153] In a further embodiment, the wax is a plant-based wax. In a further embodiment, the wax is beeswax in concentrations of 10 mg, 15, 20, and 25 mg, and was added to the mixture. In one particular embodiment, THC was further included in a concentration of 5-25 mg.

[0154] Discussion When each formulation was evaluated, a pattern emerged in which the more dimethicone with high viscosity 2.5 million cP was mixed into the formulation, the less ability it had to work with the material in terms of spreading the material, in terms of formulating liquid, gel, paste, and foam materials.However, as the viscosity increased with increasing amounts of dimethicone with 2.5 million cP, the more food formulations could be incorporated, for example, materials incorporating gelatin for formulating materials such as gummies, or for forming solid or nearly solid materials for oral treatment as lozenges.For fluid materials, mixtures of 100:1, 50:1, 40:1, 20:1, 10:1, 5:1, 1:1, 1:2, 1:5, and 1:8 were evaluated for their effectiveness (1,000:2.5 million cP).Additional mixtures were also evaluated in various other examples.

[0155] However, in the 1:1 ratio sample of 1,000 cP and 2.5 million cP dimethicone, the consistency and ease of use of the material was significantly reduced in applications such as liquids, gels, pastes, or foams. At the 1:1 ratio, the material could still be applied to the tooth surface, but was not as practical as the lower ratio materials for application in liquid form. However, the inclusion of other excipients and even larger amounts of 2.5 million cP dimethicone produced a new material that was intended as a food material (lollipops, lozenges, gummies, etc.) and could be placed on the oral mucosa. The accumulation of saliva on the oral mucosa releases the ingredients from within the carrier material. Thus, the food material allows for the coating and subsequent release of the material in the same manner as a liquid, gel, or other application form.

[0156] Thus, the amount of each of the first and second dimethicone products varied depending on the final formulation, whether it was a liquid, gel, paste, foam, or gummy or solid consistency. In certain preferred embodiments, the material may also be formulated into an aerosol and sprayed into the mouth for application. The aerosolized particles allow for rapid and broad application to oral mucosal surfaces.

[0157] In certain preferred embodiments, the oral mucosal carrier composition consists essentially of a dimethicone-based oral mucosal carrier comprising a first dimethicone material having a viscosity of about 1,000 cP to 25,000 cP and a second dimethicone material having a viscosity of about 2 million to about 3 million, and at least one active agent. In preferred embodiments, the first dimethicone and the second dimethicone are combined in a ratio of 100:1 to 1:10, preferably 50:1 to 1:1. In preferred embodiments, the composition consists essentially of at least one excipient.

[0158] In certain preferred embodiments, the oral mucosal carrier composition comprises a dimethicone-based oral mucosal carrier comprising a first dimethicone material having a viscosity of about 1,000 cP to 25,000 cP and a second dimethicone material having a viscosity of about 2 million to about 3 million, and at least one active agent. In preferred embodiments, the first dimethicone and the second dimethicone are combined in a ratio of 100:1 to 1:10. In preferred embodiments, the composition comprises two or more active agents. In preferred embodiments, the composition comprises at least one excipient.

Claims

1. 1. A dimethicone-based oral mucosal carrier comprising a first dimethicone material having a viscosity of 1,000 cP to 25,000 cP and a second dimethicone material having a viscosity of 2 to 3 million cP, and at least one active agent, wherein the ratio of the first dimethicone material to the second dimethicone material is 100:1 to 1:

10.

2. 10. The oral mucosal carrier of claim 1, wherein the at least one active agent is selected from the group consisting of fluoride donors, cetylpyridinium chloride, benzalkonium chloride, and combinations thereof.

3. 3. The oral mucosal carrier of claim 2, wherein the fluoride donor is selected from the group consisting of sodium fluoride, stannous fluoride, ACPF (amorphous calcium phosphate fluoride), and combinations thereof.

4. The oral mucosal carrier according to any one of claims 1 to 3, wherein the ratio of the first dimethicone material to the second dimethicone material is from 50:1 to 1:

2.

5. The oral mucosal carrier according to claim 2 or 3, wherein the concentration of the fluoride donor is 0.1 to 1.5%.

6. The oral mucosal carrier according to claim 2 or 3, wherein the concentration of the fluoride donor is 1 to 1500 ppm.

7. The oral mucosal carrier according to claim 2 or 3, wherein the concentration of the fluoride donor is 800 ppm to 1500 ppm.

8. The oral mucosal carrier according to any one of claims 1 to 7, further comprising a calcium donor, a potassium donor, or a phosphate donor.

9. The oral mucosal carrier according to any one of claims 1 to 8, further comprising a flavouring or sweetening agent.

10. The oral mucosal carrier according to any one of claims 1 to 9, further comprising cetylpyridinium chloride.

11. The oral mucosal carrier of any one of claims 1 to 10, further comprising a bulking agent, a flow agent, a preservative, or a combination thereof.

12. 12. A method of formulating an oral mucosal carrier according to any one of claims 1 to 11, comprising: placing the entirety of the first dimethicone material in a mixing vessel and adding thereto an amount of an active ingredient; mixing the two ingredients in a centrifugal mixer at 3,000 RPM for 10 minutes; adding a portion of the second dimethicone material to the now mixed material after the 10 minutes of mixing, the portion of the second dimethicone material being added in discrete increments of one-fifth of the total concentration of the second dimethicone material; and mixing the resulting material at 3,000 RPM in 5 minute increments until all of the second dimethicone material has been added and mixed into the oral mucosal carrier, followed by adding another incremental portion of the second dimethicone material.

13. The oral mucosal carrier of any one of claims 1 to 11, wherein the oral mucosal carrier comprises two or more active agents.

14. The oral mucosal carrier according to any one of claims 1 to 11 and 13, comprising a bulking agent, said bulking agent being an edible wax.

15. 15. The oral mucosal carrier of any one of claims 1 to 11, 13 and 14, wherein the active agent is a therapeutic agent selected from the group consisting of sodium fluoride, difluorosilane, stannous fluoride, APF (acid phosphate fluoride), ACPF (amorphous calcium phosphate fluoride), ACP (amorphous calcium phosphate), sodium monofluorophosphate, benzalkonium chloride, dipotassium hydrogen phosphate, calcium nitrate, cetylpyridinium chloride, phosphate donors, potassium donors, and antibacterial, antifungal, antiviral, antiemetic, self-replicating peptides, cannabinoids, terpenes, and combinations thereof.

16. The oral mucosal carrier according to any one of claims 1 to 11 and 13 to 15, wherein the active agent is a hemp extract.

17. The activator is (1) a drug for treating dry mouth selected from the group consisting of pilocarpine, acetylcholine, sodium, potassium, calcium, magnesium, chloride, phosphate, and carbonate electrolytes; and / or (2) a saliva enhancer selected from the group consisting of essential oil extracts, spirantes, xylitol, carboxymethylcellulose, and modifications thereof to enhance saliva flow; and / or (3) an agent for treating halitosis selected from the group consisting of antibacterial compounds, natural or synthetic oils, odor destroyers, or odor masking agents; and / or (4) Aluminum powder (potassium aluminum sulfate), baking soda, probiotics, honey, coconut oil, antimicrobial oil, magnesium hydroxide, chamomile, echinacea, sage, deglycyrrhizinized licorice (DGL), zinc, vitamin B 12 and / or an agent for treating oral ulcers selected from the group consisting of: (5) a drug for treating dry socket selected from the group consisting of analgesics, antibacterial agents, and tissue growth agents; and / or (6) NSAIDs, opioids, acetaminophen, chlorhexidine, metronidazole, guaiacol, eugenol, balsam of peru, chlorobutanol, iodoform, butamben, polymyxin B sulfate, tyrothricin, neomycin sulfate, tetracaine hydrochloride, and combinations thereof; and / or (7) The oral mucosal carrier according to any one of claims 1 to 11 and 13 to 16, which is a peroxide.

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