BIOACTIVE GLASS COMPOSITIONS AND DENTIN HYPERSENSITIVITY REMEDIATION
A dental formulation including: a bioactive glass composition as defined herein, in an effective amount; and a suitable carrier as defined herein, in an effective amount. Also disclosed is a method of making and using the dental formulation to treat, for example, dentin sensitivities.
This application is a Continuation of U.S. application Ser. No. 16/203,002, filed on Nov. 28, 2018, which claims the benefit of priority under 35 U.S.C. § 119 of U.S. Provisional Patent Application No. 62/591,423 filed Nov. 28, 2017, the content of which is incorporated herein by reference in its entirety.
CROSS-REFERENCE TO RELATED APPLICATIONSThe present application is related commonly owned and assigned USSN Provisional application Nos., filed May 25, 2016:
62/342,384, entitled “BIOACTIVE ALUMINOBORATE GLASSES”;
62/342,377, entitled “MAGNETIZABLE GLASS CERAMIC COMPOSITION AND METHODS THEREOF”;
62/342,381, entitled “LITHIUM DISILICATE GLASS-CERAMIC COMPOSITIONS AND METHODS THEREOF”;
62/342,391, entitled “BIODEGRADABLE MICROBEADS”; and
62/342,411, entitled “BIOACTIVE GLASS MICROSPHERES”; but does not claim priority thereto.
The present application is also related to commonly owned and assigned USSN Application No. 62/189,880, filed Jul. 7, 2015, entitled “ANTIMICROBIAL PHASE-SEPARATING GLASS AND GLASS CERAMIC ARTICLES AND LAMINATES,” which mentions a copper containing laminate having a degradable phase, which phase liberates cooper ion, and a non-degradable phase, but does not claim priority thereto.
The present application is also related commonly owned and assigned USSN application Nos.:
62/591,446, filed Nov. 28, 2017, entitled “HIGH LIQUIDUS VISCOSITY BIOACTIVE GLASS”; and
62/591,438, filed Nov. 28, 2017, entitled “CHEMICALLY STRENGTHENED BIOACTIVE GLASS-CERAMICS”;
62/591,429, filed Nov. 28, 2017, entitled “BIOACTIVE BORATE GLASS AND METHODS THEREOF”, filed concurrently herewith, but does not claim priority thereto.
The entire disclosure of each publication or patent document mentioned herein is incorporated by reference.
BACKGROUNDThe disclosure relates to a glass composition, a bioactive glass composition, and to methods of making and using the compositions.
SUMMARYIn embodiments, the disclosure provides a glass composition, a bioactive glass composition, a bioactive dental formulation (e.g., toothpaste), and to methods of making and using the compositions.
In embodiments, the disclosure provides a composition and method for treating dentin hypersensitivity.
In embodiments, the disclosure provides a group of borate and borosilicate bioactive glasses, an oral care product, for example, a toothpaste, a mouthwash, and like formulations, for the treatment of dentin hypersensitivity.
In embodiments, the disclosure provides a glass composition that has a significantly higher rate of occluding of exposed dentin tubules than a 45S5-containing toothpaste, demonstrating excellent properties for treating dentin hypersensitivity.
In embodiments, the present disclosure provides: a bioactive glass composition as defined herein, including or excluding selected source additives.
In embodiments of the disclosure:
Various embodiments of the disclosure will be described in detail with reference to drawings, if any. Reference to various embodiments does not limit the scope of the invention, which is limited only by the scope of the claims attached hereto. Additionally, any examples set forth in this specification are not limiting and merely set forth some of the many possible embodiments of the claimed invention.
In embodiments, the disclosed compositions, articles, and methods of making and using provide one or more advantageous features or aspects, including for example as discussed below. Features or aspects recited in any of the claims are generally applicable to all facets of the invention. Any recited single or multiple feature or aspect in any one claim can be combined or permuted with any other recited feature or aspect in any other claim or claims.
Definitions“Dentin hypersensitivity,” (DH) “dentin sensitivity,” (DS) or like terms refer to a short, sharp pain caused by cold and heat, air, touch, or chemical or osmotic stimuli, e.g., sweets.
“Occlude,” “occluding,” “occlusion,” or like terms refer, for example, to close up or block off, to obstruct.
“Glass,” “glasses,” or like terms can refer to a glass or a glass-ceramic.
“Glass article,” or like terms can refer to any object made wholly or partly of glass or a glass-ceramic.
“Flavorant,” “flavor” or like terms can refer to any natural or synthetic substance that provides organoleptic properties to the disclosed composition when a user has contact with the composition. The flavorant can be, for example, a single compound or a mixture of compounds. The flavorant can be selected to give the composition or product a unique flavor or to maintain flavor consistency between different product batches or after recipe changes. The flavorant can be any known or discovered compound, for example, diacetyl, acetylpropionyl, acetoin, isoamyl acetate, benzaldehyde, cinnamaldehyde, ethyl propionate, methyl anthranilate, limonene, ethyl decadienoate, allyl hexanoate, ethyl maltol, ethyl vanillin, methyl salicylate, and like compounds, or mixtures thereof.
Other typical composition components or formulation ingredients are known to one of skill in the art such as an abrasive, a humectant, a colorant, an antibacterial agent, a surfactant, a whitening agent, a binder, and like components or ingredients, see for example, en.wikipedia.org/wiki/Toothpaste.
“Angiogenesis ability,” “angiogenic,” “angiogenesis,” or like terms, refer to the physiological process by which new blood vessels form from pre-existing vessels.
“Include,” “includes,” or like terms means encompassing but not limited to, that is, inclusive and not exclusive.
“About” modifying, for example, the quantity of an ingredient in a composition, concentrations, volumes, process temperature, process time, yields, flow rates, pressures, viscosities, and like values, and ranges thereof, or a dimension of a component, and like values, and ranges thereof, employed in describing the embodiments of the disclosure, refers to variation in the numerical quantity that can occur, for example: through typical measuring and handling procedures used for preparing materials, compositions, composites, concentrates, component parts, articles of manufacture, or use formulations; through inadvertent error in these procedures; through differences in the manufacture, source, or purity of starting materials or ingredients used to carry out the methods; and like considerations. The term “about” also encompasses amounts that differ due to aging of a composition or formulation with a particular initial concentration or mixture, and amounts that differ due to mixing or processing a composition or formulation with a particular initial concentration or mixture.
“Optional” or “optionally” means that the subsequently described event or circumstance can or cannot occur, and that the description includes instances where the event or circumstance occurs and instances where it does not.
The indefinite article “a” or “an” and its corresponding definite article “the” as used herein means at least one, or one or more, unless specified otherwise.
Abbreviations, which are well known to one of ordinary skill in the art, may be used (e.g., “h” or “hrs” for hour or hours, “g” or “gm” for gram(s), “mL” for milliliters, and “rt” for room temperature, “nm” for nanometers, and like abbreviations).
Specific and preferred values disclosed for components, ingredients, additives, dimensions, conditions, times, and like aspects, and ranges thereof, are for illustration only; they do not exclude other defined values or other values within defined ranges. The composition and methods of the disclosure can include any value or any combination of the values, specific values, more specific values, and preferred values described herein, including explicit or implicit intermediate values and ranges.
Dentin hypersensitivity is a global oral health issue and its treatment remains a significant challenge for most dental professionals. Dentin hypersensitivity is caused by the absence of the smear layer of dentin tubules, which exposes dentinal tubules to thermal, chemical, mechanical, or osmotic stimuli. The movement of the fluid within the tubules stimulates mechanical receptors that are sensitive to fluid pressure, resulting in the transmission of the stimuli to the pulpal nerves and ultimately the pain response. Dentin hypersensitivity can generally be treated, for example, by chemical desensitization of the tooth nerve endings, tubule occluding agents or barriers to reduce dentin permeability, or both (see S. B. Low, “Reduction in dental hypersensitivity with nano-hydroxyapatite, potassium nitrate, sodium monoflurophosphate and antioxidants,” Open Dent J, 2015; (9): 92-97; S. Miglani, “Dentin hypersensitivity: Recent trends in management,” J Consery Dent. 2010, 13(4): 218-224; A. R. Davari, “Dentin hypersensitivity: Etiology, diagnosis and treatment; a literature review,” J Dent (Shiraz), 2013, 14(3): 136-145). The use of potassium nitrate (KNO3) as a chemical desensitization agent can eliminate the potassium ion concentration gradient across the nerve cell membrane. Therefore, the nerve cells will not depolarize and will not respond to stimuli (see S. B. Low, supra.). Current tubule occluding agents include fluorides (i.e., formation of calcium fluoride crystals), oxalates (i.e., formation of calcium oxalate), and strontium chloride (i.e., has affinity for dentine due to the high permeability and possibility for absorption into or onto the organic connective tissues and the odontoblast processes) (see S. Miglani, supra.). Additionally, Pro-Argin-based toothpastes can form a dentin-like mineral deposition layer due to the binding of arginine and calcium carbonate to the negatively charged dentine surface (see R Kulal, “An in-vitro comparison of nano hydroxyapatite, Novamin and Proargin desensitizing toothpastes—a SEM study” J Clin Diagn Res, 2016, 10(10): ZC51-ZC54). Recently, silicate glass based toothpastes such as Novamin® and BioMin® (having for example less than 40% mol SiO2, greater than 8% mol P2O5), were found to react with saliva and release calcium, phosphate, or in the presence of fluoride ions to form hydroxycarbonated apatite or fluorapatite, respectively, over the exposed dentin and within dentin tubules (see S. Miglani, supra.; L. J. Litkowski, “Compositions containing bioactive glass and their use in treating tooth hypersensitivity,” U.S. Pat. No. 6,338,751; and R. Hill, “Bioactive glass composition,” U.S. Pat. No. 9,168,272)(see also H. E. Strassler, et al., “Dentinal Hypersensitivity: Etiology, Diagnosis and Management” Contin. Ed. Pub.; and M. Han, et al., “In vivo remineralization of dentin using an agarose hydrogel biomimetic mineralization system,” 7 Feb. 2017, in nature.com/srep/).
Dentin treatment using bioactive glass-containing toothpastes is believed to be the only treatment method that can provide long period protection. Unlike other occluding reagents of dentin tubules, a bioactive glass can reliably relieve the pain of dental hypersensitivity for extended periods permanently. Recently developed aluminoborate glasses have been demonstrated to have excellent biocompatability, enhanced angiogenesis, and can promote wound healing, see for example, the abovementioned commonly owned and assigned copending patent applications: 62/342,411 and 62/342,384.
In embodiments, the present disclosure provides an array of borate and borosilicate glass compositions that have superior properties and a capacity to treat dentin hypersensitivity compared to known bioactive glasses.
In embodiments, the present disclosure provides a dental formulation, for example, for oral topical applications, comprising:
a bioactive glass composition in an effective amount, e.g., from 0.1 to 10 wt %, comprising a source of:
2 to 70% B2O3,
1 to 60% SiO2,
2 to 16% Al2O3,
5 to 30% CaO,
1 to 6% P2O5,
1 to 20% Na2O,
1 to 20% K2O, and
1 to 20% MgO, based on a 100 mol % total of the composition; and
a suitable carrier, in an effective amount of from 99.9 to 90 wt % based on a 100 wt % total of the composition. The mol % of the source has the equivalent weight percentages of 1 to 60% B2O3, 1 to 60% SiO2, 2 to 20% Al2O3, 5 to 25% CaO, 1 to 10% P2O5, 1 to 20% Na2O, 1 to 25% K2O, and 1 to 15% MgO, based on a 100 wt % total of the composition.
In embodiments, the disclosure provides a bioactive glass comprising a source of from 5 to 50 mol % SiO2 (4 to 40 wt %), and the suitable carrier comprises a source of from 5 to 25 mol % SiO2 (4 to 20 wt %) (e.g., as an abrasive), based on a 100 mol % (100 wt %) total of the composition.
In embodiments, the disclosure provides a dental formulation composition further comprising a source of fluoride ion in an amount of from 1 to 25 mol % (1 to 30 wt %) (see, e.g., U.S. Pat. No. 9,168,272).
In embodiments, the disclosure provides a dental formulation composition wherein the source of fluoride ion is selected, for example, from NaF, SnF2, CaF2, and like sources, or a mixture of selected sources.
In embodiments, the disclosed bioactive glass composition and dental formulation composition containing the disclosed bioactive glass composition can be substantially free-of or entirely free-of a source of fluoride ion.
In embodiments, the disclosed bioactive composition and dental formulation composition containing the disclosed bioactive glass composition can be substantially free-of or entirely free-of a source of titanium oxide.
In embodiments, the disclosure provides a dental formulation composition wherein the bioactive glass composition in an effective amount is from 1 to 20 wt % (e.g., from 1 to 10 wt %) and the suitable carrier in an effective amount is from 80 to 99 wt % (e.g., from 90 to 99 wt %).
In embodiments, the disclosure provides a preferred dental formulation composition wherein the bioactive glass composition comprises:
40 to 60% B2O3,
0.1 to 5% SiO2,
6 to 10% Al2O3,
15 to 25% CaO,
1.5 to 2.0% P2O5,
4 to 8% Na2O,
6 to 10% K2O, and
6 to 10% MgO, based on a 100 mol % total of the composition. The mol % of the source has the equivalent weight percentages of 30 to 50% B2O3, 0.1 to 5% SiO2, 8 to 15% Al2O3, 15 to 25% CaO, 1.5 to 5% P2O5, 4 to 8% Na2O, 6 to 15% K2O, and 3 to 8% MgO, based on a 100 wt % total of the composition.
In embodiments, the disclosure provides a dental formulation composition wherein the suitable carrier comprises one or more ingredients selected from: an abrasive, a humectant, i.e., an anti-drying agent such as glycerol, sorbitol, xylitol, 1,2-propylene glycol, polyethyleneglycol, and like compounds, a flavorant, a colorant, an antibacterial agent, a surfactant, a whitening agent, and other like suitable ingredients known in the art, or a mixture thereof.
In embodiments, the disclosure provides a dental formulation composition wherein the suitable carrier comprises one or more forms selected from: a gum, a paste, a powder, a toothpaste, a mouthwash, a poultice, a tea, a sucker, a spray, and like forms, or a mixture thereof.
In embodiments, the disclosure provides a remineralizing composition comprising: any one of the abovementioned bioactive glass compositions or combinations thereof, and optionally a suitable carrier such as non-aqueous carrier for the remineralizing composition.
In embodiments, the disclosure provides a remineralizing composition comprising: the abovementioned bioactive glass composition and an optional suitable carrier.
In embodiments, the disclosure provides a method of treating dentin hypersensitivity or sensitivity comprising:
contacting a dental surface and any of the abovementioned dental formulations comprising the remineralizing composition.
In embodiments, the contacting the dental formulation has a higher relative rate of from 50 to 95% of occluding exposed dentin tubules compared to a dental formulation base formula that is free-of the bioactive glass, i.e., without the bioactive glass present.
In embodiments, contacting the dental formulation can be selected from at least one of: polishing with a paste formula, rinsing with a liquid formula, injecting with a liquid formula, filling a tooth with a composite, e.g., typically made of powdered bioactive glass and acrylic resin, or a combination thereof.
In embodiments, the dental surface can have at least one of, for example: a dentin surface, a dentin tubule, or a combination thereof.
In embodiments, the disclosure provides a dental formulation comprising:
a bioactive glass composition in an effective amount comprising a source of:
2 to 70% B2O3,
2 to 16% Al2O3,
5 to 30% CaO,
1 to 6% P2O5,
1 to 20% Na2O, and
1 to 20% MgO, based on a 100 mol % total of the composition; and a suitable carrier, in an effective amount based on the combined 100 weight % of the bioactive glass and the carrier. The mol % of the source has the equivalent weight percentages of 1 to 60% B2O3, 1 to 60% SiO2, 2 to 20% Al2O3, 5 to 25% CaO, 1 to 10% P2O5, 1 to 20% Na2O, 1 to 25% K2O, and 1 to 15% MgO, based on a 100 wt % total of the composition.
In embodiments, the dental formulation is free of silica such as a source of SiO2, and free of inorganic potassium salts such as a source of K2O.
In embodiments, the present disclosure is advantaged in several aspects, including for example: the disclosed borate and borosilicate glass compositions can have a significantly higher rate of occluding of the exposed dentin tubules compared to a 45S5-containing toothpaste, which result(s) demonstrate excellent potential of the disclosed bioactive glass for treating dentin hypersensitivity or dentin sensitivity; the disclosed bioactive glass compositions can be free-of inorganic potassium salts, and the disclosed bioactive glass compositions, and dentin treatment formulations, can be silicate free. Novamin® and Biomin® are silicate-containing bioactive glasses.
In embodiments, the disclosure provides borate and borosilicate bioactive glass compositions, for example, as listed in Table 1, that can react with mammalian saliva and can release calcium and phosphate to form hydroxycarbonated apatite, or if fluoride ions are present to form fluorapatite (see
Fluoride can be incorporated into the glass compositions in a precursor form of, for example, sodium fluoride (NaF), stannous fluoride (SnF2), calcium fluoride (CaF2), and like fluorides or mixtures thereof. The fluoride incorporated glasses can release fluoride and form fluorapatite in an oral fluid. Fluorapatite is more resistant to acid dissolution than hydroxycarbonated apatite.
The fluoride incorporated glasses can also be added into non-aqueous dentifrice matrix, for example, in combination with another bioactive glass. Fluoride ions are known to aid apatite formation and can stimulate osteoblast division.
In addition to their re-mineralizing toothpaste effect, the disclosed glass compositions and formulations can also be antimicrobial, which property permits, for example, prevention of dental caries, reduce plaque formation, control gingivitis, suppress breath malodor, and like beneficial effects. The disclosed glass compositions and formulations can also be incorporated in other professionally applied dental products, such as cleaning and polishing pastes, varnishes, re-mineralizing filling materials, and like formulations.
In embodiments, the disclosure provides a remineralizing composition comprising, for example:
a bioactive glass composition in an effective amount, e.g., from 0.1 to 10 wt %, comprising a source of:
2 to 70% B2O3,
1 to 60% SiO2,
2 to 16% Al2O3,
5 to 30% CaO,
1 to 6% P2O5,
1 to 20% Na2O,
1 to 20% K2O, and
1 to 20% MgO, based on a 100 mol % total of the composition, and optionally further comprising a suitable carrier in from 80 to 99.9 wt % to the bioactive glass in from 0.1 to 20 wt % based on the total weight of the composition and carrier. The mol % of the source has the equivalent weight percentages of 1 to 60% B2O3, 1 to 60% SiO2, 2 to 20% Al2O3, 5 to 25% CaO, 1 to 10% P2O5, 1 to 20% Na2O, 1 to 25% K2O, and 1 to 15% MgO, based on a 100 wt % total of the composition.
Referring to the Figures,
Each glass composition of Table 1 was separately melted and ground to 1 to 10 microns using, for example, an air jet mill.
Each ground glass composition of Table 1 was separately formulated into a dental formulation such as listed in Table 2.
Each dental formulation was evaluated for the ability to occlude dentine discs made of human molars as detailed in Example 9, i.e., the discs having dentin tubules were exposed to the dental formulation and compared to a dental formulation base (control) that was free-of the disclosed bioactive glass.
Raw materials, equipment, or both, used to produce the compositions of the present disclosure, can introduce certain impurities or components that are not intentionally added, and can be present in the final glass composition. Such materials can be present in the disclosed compositions in minor amounts and are referred to as “tramp materials.”
Disclosed compositions can comprise the tramp materials, typically in trace amounts. Similarly, “iron-free,” “sodium-free,” “lithium-free,” “zirconium-free,” “alkali earth metal-free,” “heavy metal-free,” or like descriptions, mean that the tramp material was not purposefully added to the composition, but the composition may still comprise iron, sodium, lithium, zirconium, alkali earth metals, or heavy metals, etc., but in approximately tramp or trace amounts.
Unless otherwise specified, the concentrations of all constituents recited herein are expressed in terms of weight percent (wt %).
EXAMPLESThe following Examples demonstrate making, use, and analysis of the disclosed compositions, formulations, and methods in accordance with the above general procedures.
Example 1Glass 1
The composition of Example 1 in Table 1 was prepared as follows: The source batch materials in the indicated amounts, including silicon dioxide, boric acid, alumina, sodium oxide, potassium oxide, limestone, magnesium oxide, and calcium phosphate, were individually combined. The batch source materials were vigorously mixed in a plastic jar using a Turbular mixer. Then they were transferred to a platinum crucible with an internal volume of approximately 650 cc. The crucible was then loaded into an annealing furnace to calcine the batch at 250° C. for 24 hr. The calcined batches were then melted at 1100 to 1300° C. for 6 hr and then the glass melt was poured on a steel plate, and annealed at 400 to 500° C.
Examples 2 to 6Glasses 2 through 6 were likewise prepared as in Example 1 with the exception that the composition or amount used in the batch was different and as listed in Table 1.
Comparative Example 7Comparative Glass 7
The composition of Comparative Example 7 in Table 1 was prepared as in Example 1 with the exception that: there is no boric acid or alumina batched in the comparative glass, see for example US 20140186274, which mentions a non-aqueous base composition in combination with a bioactive glass.
Example 8Dental Formulation
The dental formulations of Table 2 were prepared as follows: Glycerol and PEG 400 were added to the glass composition first, then the remaining ingredients of the formulation were separately added and thoroughly mixed with a spatula.
Example 9Evaluation of Dental Formulation
The dental formulations of Table 2 were evaluated as follows: Human molars were lawfully obtained from bforbones (bforbones.com). Dentine discs having a thickness of 1 mm were cut perpendicularly to the long axis of the tooth above the cemento-enamel junction using a Buehler low-speed water cooled diamond saw. A smear layer was created on both sides of the dentine discs by sanding 30 seconds using 500-grit sanding paper. The smear was subsequently removed by treating with 6% citric acid for 3 mins, then rinsed with water, and dried at 37° C. The dentine discs were randomly divided into control or experiment groups, each containing at least 3 specimens, which received either a non-aqueous toothpaste base formulation or a toothpaste containing 5% of 45S5; and the toothpaste containing a disclosed glass composition, as listed in Tables 1 and 2. The toothpaste and a powered tooth brush were used to brush against both sides of the dentin discs for 1 min per side. The specimens were then rinsed with distilled water to remove visible traces of toothpaste, and then stored in artificial saliva (1.5 mM CaCl2), 0.9 mM KH2PO4, 130 mM KCl, and 20 mM HEPES with pH 7.4). The procedure of brushing, rinsing, and storing each specimen in artificial saliva was repeated twice a day for 7 days, then the specimens were dried at 37° C. for 16 hrs and stored at RT before SEM.
The disclosure has been described with reference to various specific embodiments and techniques. However, many variations and modifications are possible while remaining within the scope of the disclosure.
Claims
1. A dental formulation comprising:
- a bioactive glass composition in an effective amount comprising a source of: 2 to 70% B2O3, 2 to 16% Al2O3, 5 to 30% CaO, 1 to 6% P2O5, 1 to 20% Na2O, and 1 to 20% MgO, based on a 100 mol % total of the composition; and
- a carrier, in an effective amount based on the combined weight of the bioactive glass and the carrier.
2. The dental formulation of claim 1, wherein:
- the bioactive glass further comprises a source of from 5 to 50% SiO2, based on a 100 mol % total of the composition, and
- the carrier comprises a source of silica of from 1 to 25 wt % SiO2 by super addition to the bioactive glass.
3. The dental formulation of claim 1, wherein the bioactive glass further comprises a source of from 1 to 20% K2O.
4. The dental formulation of claim 1, wherein the bioactive glass is essentially free of silica as a source of SiO2, and free of inorganic potassium salts as a source of K2O.
5. The dental formulation of claim 1, further comprising a source of fluoride ion in an amount of from 1 to 25 mol % by super addition to the composition.
6. The dental formulation of claim 5, wherein the source of fluoride ion is selected from NaF, SnF2, CaF2, or a combination thereof.
7. The dental formulation of claim 1, wherein the bioactive glass is essentially free of a source of fluoride ion.
8. The dental formulation of claim 1, wherein the bioactive glass composition in an effective amount is from 0.1 to 10 wt %, and the suitable carrier in an effective amount is from 90 to 99.9 wt %.
9. The dental formulation of claim 1, wherein the carrier comprises at least one of an abrasive, a humectant, a flavorant, a colorant, an antibacterial agent, a surfactant, a whitening agent, a binder, or a mixture thereof.
10. The dental formulation of claim 1, wherein the suitable carrier comprises one or more forms selected from: a gum, a paste, a powder, a toothpaste, a mouthwash, a poultice, a tea, a sucker, a spray, or a mixture thereof.
11. The dental formulation of claim 1, wherein the bioactive glass composition in an effective amount comprising a source of:
- 6 to 10% Al2O3,
- 15 to 25% CaO,
- 1.5 to 2% P2O5,
- 4 to 8% Na2O,
- 6 to 10% K2O, and
- 6 to 10% MgO, based on a 100 mol % total of the composition.
12. The dental formulation of claim 1, wherein the bioactive glass composition comprises:
- 40 to 60% B2O3, and
- 0 to 10% SiO2, based on a 100 mol % total of the composition.
13. The dental formulation of claim 1, wherein the bioactive glass composition comprises:
- 20 to 40% B2O3, and
- 10 to 30% SiO2, based on a 100 mol % total of the composition.
14. The dental formulation of claim 1, wherein the bioactive glass composition comprises:
- 5 to 20% B2O3, and
- 30 to 50% SiO2, based on a 100 mol % total of the composition.
15. A method of treating dental hypersensitivity, comprising:
- reacting a borate or borosilicate glass composition with mammalian saliva to form hydroxycarbonated apatite or fluorapatite on a dentin surface, a dentin tubule, or combination thereof.
16. The method of claim 15, wherein the borate or borosilicate glass composition comprises:
- 2 to 70% B2O3,
- 2 to 16% Al2O3,
- 5 to 30% CaO,
- 1 to 6% P2O5,
- 1 to 20% Na2O, and
- 1 to 20% MgO, based on a 100 mol % total of the composition.
17. The method of claim 16, wherein the borate or borosilicate glass composition in an effective amount comprising a source of:
- 6 to 10% Al2O3,
- 15 to 25% CaO,
- 1.5 to 2% P2O5,
- 4 to 8% Na2O,
- 6 to 10% K2O, and
- 6 to 10% MgO, based on a 100 mol % total of the composition.
18. The method of claim 16, wherein the borate or borosilicate glass composition comprises:
- 40 to 60% B2O3, and
- 0 to 10% SiO2, based on a 100 mol % total of the composition.
19. The method of claim 16, wherein the borate or borosilicate glass composition comprises:
- 20 to 40% B2O3, and
- 10 to 30% SiO2, based on a 100 mol % total of the composition.
20. The method of claim 16, wherein the borate or borosilicate glass composition comprises:
- 5 to 20% B2O3, and
- 30 to 50% SiO2, based on a 100 mol % total of the composition.
21. The method of claim 16, wherein the borate or borosilicate glass composition comprises:
- a source of fluoride ion in an amount of from 1 to 25 mol % by super addition to the composition.
Type: Application
Filed: Nov 6, 2020
Publication Date: May 6, 2021
Inventors: Huayun Deng (Painted Post, NY), Ye Fang (Painted Post, NY), Qiang Fu (Painted Post, NY), John Christopher Mauro (Boalsburg, PA), Michael S Pambianchi (Corning, NY)
Application Number: 17/091,573
