EP1663054A4 - TREATMENT, COMPOSITIONS AND DEVICES WITH A SOLID STAINLESS AND TREATMENT GEL - Google Patents

TREATMENT, COMPOSITIONS AND DEVICES WITH A SOLID STAINLESS AND TREATMENT GEL

Info

Publication number
EP1663054A4
EP1663054A4 EP04752965A EP04752965A EP1663054A4 EP 1663054 A4 EP1663054 A4 EP 1663054A4 EP 04752965 A EP04752965 A EP 04752965A EP 04752965 A EP04752965 A EP 04752965A EP 1663054 A4 EP1663054 A4 EP 1663054A4
Authority
EP
European Patent Office
Prior art keywords
treatment
teeth
adhesive
composition
person
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP04752965A
Other languages
German (de)
English (en)
French (fr)
Other versions
EP1663054A1 (en
Inventor
Peter M Allred
Neil T Jessop
Dan E Fischer
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ultradent Products Inc
Original Assignee
Ultradent Products Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US10/646,443 external-priority patent/US7052275B2/en
Priority claimed from US10/692,117 external-priority patent/US7011523B2/en
Priority claimed from US10/728,525 external-priority patent/US6997708B2/en
Priority claimed from US10/784,063 external-priority patent/US6981874B2/en
Application filed by Ultradent Products Inc filed Critical Ultradent Products Inc
Publication of EP1663054A1 publication Critical patent/EP1663054A1/en
Publication of EP1663054A4 publication Critical patent/EP1663054A4/en
Withdrawn legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04—Dispersions; Emulsions
    • A61K8/042—Gels
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61C—DENTISTRY; APPARATUS OR METHODS FOR ORAL OR DENTAL HYGIENE
    • A61C19/00—Dental auxiliary appliances
    • A61C19/06—Implements for therapeutic treatment
    • A61C19/063—Medicament applicators for teeth or gums, e.g. treatment with fluorides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61C—DENTISTRY; APPARATUS OR METHODS FOR ORAL OR DENTAL HYGIENE
    • A61C19/00—Dental auxiliary appliances
    • A61C19/06—Implements for therapeutic treatment
    • A61C19/063—Medicament applicators for teeth or gums, e.g. treatment with fluorides
    • A61C19/066—Bleaching devices; Whitening agent applicators for teeth, e.g. trays or strips
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/42—Amides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8147—Homopolymers or copolymers of acids; Metal or ammonium salts thereof, e.g. crotonic acid, (meth)acrylic acid; Compositions of derivatives of such polymers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/817—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
    • A61K8/8176—Homopolymers of N-vinyl-pyrrolidones. Compositions of derivatives of such polymers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/86—Polyethers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q11/00—Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses

Definitions

  • the Field of the Invention is in the field of treatment compositions and devices used to _ treat a person's teeth and/or gums. More particularly, the invention relates to treatment compositions and devices that include a substantially solid adhesive composition, a treatment gel, and optionally a moisture-resistant barrier layer.
  • non- customized dental trays can be used without the need for a professional customization procedure by a dentist, such trays tend to be more bulky and less comfortable than custom-fitted trays.
  • Dental trays that can be self-customized e.g., so-called "boil- and-bite" trays
  • Another alternative tooth bleaching method involves painting a bleaching composition directly onto the surfaces of a person's teeth to be bleached. An advantage of this procedure is that it eliminates the need to obtain a customized tray, or even a non-custom fray.
  • the main disadvantage is that the bleaching composition remains directly exposed to the person's saliva and disruptive forces and movements normally found within a person's mouth. The result is that a significant portion of the bleaching composition does not remain on the tooth where bleaching is desired. Instead, some or all of the composition can dissolve away into the person's saliva' and/or be transferred to adjacent oral tissues. Because paint-on dental bleaching compositions, like all dental bleaching compositions, contain peroxide- based bleaching agents, irritation to soft oral tissues within the user's mouth and throat is a potential problem when using such compositions. Yet another alternative tooth bleaching method involves placing a flexible bleaching strip over a user's tooth surfaces.
  • Bleaching strips typically comprise a flexible plastic strip coated with a moist dental bleaching gel of moderate viscosity and relatively low stickiness on the side of the strip facing the user's teeth.
  • a portion of the bleaching strip is first placed over the front surfaces of the user's teeth, followed by folding the remainder of the strip around the occlusal edges of the teeth and back against a portion of the lingual surfaces.
  • this procedure does not require the user to obtain a customized tray, or even a non-custom tray, into which a bleaching composition must be placed by the user prior to use.
  • bleaching strips include a barrier that, at least in theory, protects the dental bleaching gel from diffusing into the user's mouth.
  • a barrier that, at least in theory, protects the dental bleaching gel from diffusing into the user's mouth.
  • Conventional bleaching strips are prone to slip off the teeth as a result of even minimal movement of the user's mouth, jaw or tongue. Indeed, it is recommended that the user not eat, drink, smoke or sleep while wearing the bleaching strip. In practice, it is difficult to talk and maintain the bleaching strips properly oriented over the teeth to be bleached.
  • the bleaching Even if a user successfully maintains a conventional bleaching strip in its proper position during the recommended bleaching period, the bleaching often diffuses into the person's saliva, potentially causing a poor taste in the user's mouth and possibly discomfort to soft oral and throat tissues.
  • the tendency of the bleaching gel to diffuse into the user's mouth can be accelerated through even minimal shifts of the bleaching strip over the user's teeth, with each shift potentially causing bleaching gel that remains adhered to the user's teeth, but not covered by the plastic strip, to be exposed to saliva in the user's mouth.
  • the bleaching strip can become so dislodged or mangled that it must be removed by the user and replaced with a fresh bleaching strip to complete the recommended bleaching time.
  • the main impediment to successful bleaching or other oral treatments is the failure of users to complete the prescribed treatment regimen. If the treatment apparatus is difficult to use, requires numerous repetitions to achieve observable results, or is simply uncomfortable or a hassle to wear, the user may simply give up and abort the treatment process altogether. Thus, even if significant dental bleaching or other treatment is possible using a particular treatment product, it is less likely to occur where the inadequacies of the treatment apparatus or method causes a user to become discouraged before desired results are attained. In view of the foregoing, there is an ongoing need for improved treatment compositions and apparatus that are simple and easy to use, that reliably remain in position over the user's teeth so as to reduce diffusion of bleaching composition into a user's oral cavity.
  • Treatment compositions according to the invention include an adhesive layer comprising a substantially solid adhesive composition in the form of a dental tray, strip, patch or other desired shape that becomes more adhesive to teeth when moistened (e.g., by saliva or water), and a treatment gel adjacent to the adhesive composition layer.
  • the treatment gel includes an active agent for treating teeth and/or gums and may comprise a bead, a continuous layer, or a plurality of discontinuous regions or islands.
  • Treatment devices include a moisture-resistant barrier layer, such as a dental tray, strip, patch, or a thin membrane having no predefined shape, an adhesive composition comprising a substantially solid adhesive composition that becomes more adhesive to teeth when moistened (e.g., by saliva or water) adjacent to the barrier layer, and a treatment gel adjacent to at least one of the adhesive layer or barrier layer.
  • the treatment gel may comprise a bead, a continuous layer, or a plurality of discontinuous regions or islands.
  • the adhesive layer may be a continuous layer or a plurality of discontinuous regions.
  • the adhesive layer is advantageously shaped like a dental fray, strip or patch to give the treatment device form.
  • the bleaching composition may be considered to be an intermediate to the finished treatment device comprising the treatment composition and the barrier layer.
  • the optional barrier layer advantageously comprises a thin, flexible membrane formed from a moisture-resistant polymer material. Nevertheless, it is within the scope of the invention to provide barrier layers having any desired thickness or rigidity.
  • the barrier layer comprises a thin layer of a polyolefin, polyester, EVA, polyurethane, or similar moisture-resistant material.
  • the barrier layer may comprise a conventional dental tray, examples of which include both customized and non-custom dental trays, or it may comprise a substantially flat strip or patch.
  • the barrier layer may be as simple as a layer of a moisture resistant barrier-forming material that is sprayed or painted on, applied by dipping, or otherwise applied to an existing adhesive layer comprising a substantially solid adhesive composition (e.g. , one that is in the form of a dental tray, strip or patch).
  • the substantially solid adhesive composition comprises at least one tooth adhesion agent that contributes or provides increased adhesiveness to teeth when moistened by saliva or water and optionally at least one active agent.
  • the moistened adhesive composition or layer may optionally be formulated to release a bleaching agent activator that reacts with and destabilizes a bleaching agent within a bleaching gel, in the case where the active agent is a dental bleaching agent.
  • a barrier layer is advantageously provided to protect the adhesive composition and treatment gel from diffusing away from the person's teeth into the oral cavity as a result of ambient saliva or moisture found within the person's mouth.
  • the adhesive composition advantageously comprises one or more coherent regions or masses that do not readily run or flow, as opposed to a liquid, gel, or dry particulate or powdery composition.
  • a substantially solid and coherent adhesive composition in combination with a treatment gel better adheres to a person's teeth and does not readily diffuse into the surrounding oral cavity on its own, absent becoming diluted by saliva or moisture in a person's mouth, compared to a gel used by itself. This helps maintain the adhesive composition and treatment gel between the barrier layer and a person's teeth and/or gums being treated and helps prevent diffusion of the active agent into the surrounding oral cavity. This, in turn, promotes more effective treatment and better patient compliance, and it reduces the tendency of the user to taste the treatment composition when in use.
  • the tooth adhesion agent within the adhesive composition contributes or provides increased adhesiveness to teeth when moistened with saliva or water.
  • the tooth adhesion agent advantageously remains substantially non- adhesive when the adhesive composition is in a dry or substantially solid condition but becomes more adhesive to teeth when the adhesive composition is moistened with, e.g., water or saliva.
  • a non-limiting example of a suitable tooth adhesion agent is polyvinyl pyrrolidone (PVP), although it is within the scope of the invention to use other tooth adhesion agents known in the art.
  • PVP polyvinyl pyrrolidone
  • the adhesive composition, as well as intermediate compositions used to make the substantially solid adhesive composition may include other components as desired to yield a final composition having desired properties. These include both inert components and active agents.
  • inert components include, but are not limited to, plasticizers and humectants (e.g., glycerin, sorbitol, and polyethylene glycol), volatile solvents (e.g., water and alcohols), neutralizing agents, thickening agents (e.g., fumed silica), flavorants, sweeteners, and the like.
  • plasticizers and humectants e.g., glycerin, sorbitol, and polyethylene glycol
  • volatile solvents e.g., water and alcohols
  • neutralizing agents e.g., water and alcohols
  • thickening agents e.g., fumed silica
  • active agents examples include desensitizing agents (e.g., potassium nitrate), remineralizing agents (e.g., sodium fluoride or other fluoride salts), dental bleaching agents (e.g., aqueous hydrogen peroxide, carbamide peroxide, sodium perborate, and sodium percarbonate), bleaching agent stabilizers (e.g., EDTA, citric acid, or alkyl sulfates), bleaching agent activators, antimicrobial agents (e.g., chlorhexidine), antiplaque agents, anti-tartar agents, or other medicaments.
  • desensitizing agents e.g., potassium nitrate
  • remineralizing agents e.g., sodium fluoride or other fluoride salts
  • dental bleaching agents e.g., aqueous hydrogen peroxide, carbamide peroxide, sodium perborate, and sodium percarbonate
  • bleaching agent stabilizers e.g., EDTA, citric acid, or al
  • the treatment gel comprises an active agent and a tackifying agent, typically dispersed within a liquid carrier or vehicle.
  • active agents include one or more of a desensitizing agent, remineralizing agent, dental bleaching agent, antimicrobial agent, anti-plaque agent, anti-tartar agent, or other medicament (e.g., the active agents that may optionally be included within the adhesive composition or layer).
  • Exemplary tackifying agents include PVP, carboxypolymethylene (e.g., CARBOPOL, sold by Novean, Inc.), polyethylene oxide (e.g., POLYOX, made by Union Carbide), polyacrylic acid polymers or copolymers (e.g., PEMULEN, sold by Novean, Inc.), polyacrylates, polyacrylamides, copolymers of polyacrylic acid and polyacrylamide, PVP-vinyl acetate copolymers, carboxymethylcellulose, carboxypropylcellulose, polysaccharide gums, proteins, and the like. It is, of course, within the scope of the invention to use any tackifying agent known in the art.
  • Exemplary liquid carriers or vehicles include water, alcohols, polyols (e.g., glycerin, sorbitol, polyethylene glycol, propylene glycol, and polypropylene glycol), and the like.
  • the substantially solid adhesive composition is made by first forming a flowable liquid or gel composition intermediate that is subsequently dried to form a substantially solid adhesive composition. This may be performed by heating or otherwise causing one or more volatile solvents to be driven off by evaporation, thus leaving behind the substantially solid composition or layer. The drying process may be performed before or after the adhesive composition intermediate is placed into contact with a barrier layer.
  • the intermediate composition is cast onto a forming surface, dried and removed to yield a substantially solid sheet that is cut, stamped or otherwise formed into a desired shape (e.g., tray, strip or patch).
  • a treatment gel is attached or applied to an inner surface of the adhesive composition, and a barrier layer is optionally applied or attached to an outer surface of the adhesive composition.
  • the treatment gel can be applied to the adhesive composition before or after the barrier layer, or in the absence of a barrier layer. At least a portion of the treatment gel can be applied directly adjacent to the barrier layer.
  • An advantage of providing a treatment gel that is separate from the adhesive composition, rather than an active agent that is contained within the adhesive composition, is that it provides a treatment composition or device that is more stable or consistent relative to the amount of active agent, particularly where the active agent is sensitive to heat. Heating the adhesive composition intermediate to drive off the water so as to yield a substantially solid adhesive composition can destabilize a bleaching agent or other heat-sensitive active agent contained therein and cause it to become less potent. Because the treatment gel is generally not heated during manufacture of treatment composition and devices according to the invention, greater stability and potency of a heat-sensitive active agent can be maintained.
  • the adhesive composition may optionally contain a bleaching agent activator that diffuses or leaches out of the adhesive composition and activates the bleaching gel upon moistening at least one of the bleaching gel or adhesive layer with saliva or water.
  • the bleaching gel is initially substantially anhydrous and/or does not initially contact the adhesive composition in order to minimize diffusion or leaching of the bleaching agent activator out of the adhesive activation layer and into the bleaching gel prior to use.
  • a dental tray or barrier strip can be coated with a flowable adhesive composition intermediate, such as by painting or spreading, which is then heated or allowed to dry at room temperature to form the substantially solid adhesive composition.
  • the treatment gel may then be applied to the inside surface of the dried adhesive composition.
  • the size and shape of treatment compositions and devices according to the invention can be tailored to more readily fit a person's upper or lower dental arch. They may also be tailored to fit persons having differently-sized or shaped dental arches.
  • the treatment compositions and devices are advantageously designed so as to substantially cover the front and lingual surfaces of the teeth and/or gums to be treated. Treating both the front and lingual surfaces helps in treating the interproximal spaces between adjacent teeth.
  • treatment compositions and devices are advantageously flexible and adhesive so as to readily conform to a wide variety of differently-sized teeth and dental arches.
  • Treatment compositions and devices according to one embodiment are in the shape of a dental tray having a front side wall, a rear side wall, and a trough between the front and rear side walls. Having the shape of a dental tray facilitates placement of the treatment composition or device over a person's teeth by minimizing the amount of manipulation that is necessary to obtain a good fit between the composition or device and the person's teeth.
  • the treatment compositions and devices are in the shape of substantially flat strips or patches prior to use.
  • the inventive treatment compositions and devices are designed to more reliably remain in place over the person's teeth and/or gums compared to conventional bleaching strips. The result is more effective treatment and better patient compliance.
  • the treatment composition or device has a horseshoe shape and a U-shaped trough like a conventional dental tray.
  • the treatment composition or device has an L-shaped profile or "trough". It will be appreciated, however, that treatment compositions and devices according to the invention can have any longitudinal profile or shape (e.g., they can be straight or have any desired degree of longitudinal curvature from one end of the composition or device to the other).
  • the trough may have any desired cross-sectional shape (e.g., the trough can be V-shaped, trapezoidal, rectangular, or other geometric shape).
  • the treatment composition or device may include mechanical features such as a notch within the front side wall, preferably within an edge near the center of the front side wall, and/or a notch within the rear side wall, preferably within an edge near the center of the rear side wall. Notches allow a tray-like treatment composition or device to more easily conform to differently-sized dental arches.
  • the treatment composition or device can be designed so as to be "one-size fits all.”
  • the treatment compositions and devices according to the invention can be designed to be worn for any desired time period. Increasing the concentration of active agent within the treatment gel generally reduces the required treatment time. Nevertheless, due to the extremely comfortable fit and reliable adhesion between the inventive treatment compositions and devices and the person's teeth, it is possible to wear such compositions and devices for extended periods of time in order to ensure even and thorough treatment.
  • Treatment compositions and devices according to the invention can be designed to be worn while, e.g., talking, sleeping, eating, drinking, smiling, frowning, grimacing, yawning, coughing, smoking, or making virtually any facial expression or mouth contortion.
  • the treatment compositions or devices can be designed to be worn for as little as a few minutes or as long as several hours.
  • a typical treatment session of fast duration may last from about 10 to about 30 minutes.
  • a treatment session of intermediate duration may last from about 30 minutes to about 2 hours.
  • a treatment session of long duration including professional treatment or overnight treatment while a person is sleeping, may last from about 2 hours to about 12 hours.
  • Treatment sessions may be repeated as many times as are needed to obtain a desired degree of treatment. In the case of tooth bleaching, a clinical whitening effect has been observed after only 1-3 whitening sessions.
  • a typical treatment regimen will preferably include 1-20 treatment sessions, more preferably 2-15 treatment sessions, and most preferably 3-10 treatment sessions.
  • multiple treatment compositions and/or devices may be packaged together and sold as a kit.
  • the number of treatment compositions and/or devices provided with each kit can equal the number of sessions that represent a prescribed treatment regimen.
  • multiple treatment compositions and/or devices can be stacked, internested, or laid together within a package.
  • the treatment compositions and/or devices can be sealed collectively or individually as desired. They may contain a removable protective layer on their interior surfaces to protect the adhesive composition and the treatment gel from contamination or moisture, both of which can possibly cause premature decomposition or degradation of the active agent.
  • the adhesive composition may be a dry or substantially solid insert or it may be a liquid or gel that is applied to a barrier layer and allowed to dry prior to placement of the treatment gel adjacent to the adhesive layer and placement of the finished treatment device over the person's teeth and/or gums.
  • Figure 1 is a perspective view of an exemplary treatment device according to the invention in the shape of a dental tray comprising a barrier layer, an adhesive layer, and a treatment gel
  • Figure 2A is a cross-sectional view of the treatment device depicted in Figure i
  • Figure 2B is a cross-sectional view of en exemplary treatment composition according to the invention in the shape of a dental tray, but without a barrier layer
  • Figure 2C is a cross-sectional view of an exemplary treatment device according to the invention that includes a barrier layer and multiple spots or regions of adhesive composition interspersed with multiple spots or regions of a treatment gel
  • Figure 3 illustrates a fray-like treatment composition or device according to the invention contained within a sealed protective package having a peelable cover
  • Figure 4 is a perspective view of an exemplary treatment composition or device that is similar to the treatment device depicted in Figure 1, or the freatment composition of Figure 2B, but that further includes a terminal side
  • inventive treatment compositions include an adhesive composition that becomes more adhesive to teeth when moistened with water or saliva and a treatment gel adjacent to the adhesive composition.
  • inventive treatment devices include a moisture- resistant barrier layer, an adhesive composition that becomes more adhesive to teeth when moistened with water or saliva, and a freatment gel adjacent to at least one of adhesive composition or barrier layer.
  • the optional barrier layer protects the adhesive layer and treatment gel from diffusing away from the person's teeth as a result of ambient saliva or moisture found within the person's mouth.
  • the inventive treatment compositions and devices are more adhesive to teeth than conventional dental bleaching strips. Such compositions and devices are also less intrusive than bulky, over-the-counter, non-custom or boil-and-bite dental trays. In some ways they are as reliable as, or even more reliable than, custom-fitted dental trays in maintaining a treatment gel against a person's teeth. In some cases, they are also as comfortable as, or even more comfortable than, custom-fitted trays.
  • barrier layer refers to one or more layers of a moisture-resistant material that protects the adhesive layer and treatment gel from ambient moisture and saliva found within a person's mouth when the treatment device is placed over the person's teeth and/or gums.
  • the barrier layer may also serve to protect the adhesive layer and treatment gel from moisture or other contaminants during storage and prior to use.
  • the barrier layer may be in any desired form including, but not limited to, a sheet laminated to a surface of the adhesive layer, a coating applied to a pre-formed adhesive layer or treatment composition, a dental treatment tray, or a strip or patch.
  • strip and "patch” are essentially synonymous.
  • adheresive layer and “adhesive composition”, as used herein, refer to one or more regions of a composition that has been formulated or processed so as to be substantially solid, coherent, and non-flowable.
  • the adhesive composition or layer may comprise a single continuous region or layer adjacent to the treatment gel and, optionally, a barrier layer, or it may comprise a plurality of discontinuous regions or layers adjacent to a barrier layer and spaced-apart by random or predetermined intervals.
  • substantially solid refers to an adhesive composition or layer that is in a solid or semi-solid condition.
  • a "substantially solid" adhesive composition or layer can be characterized as a cohesive mass that does not readily flow or separate when subjected to gravitational forces and which cannot be readily expressed through a syringe outlet or other similarly-sized opening or orifice.
  • the term “substantially solid” excludes runny adhesive liquids, viscous adhesive liquids, and even thick adhesive gels that are able to flow when subjected to gravity and/or which can be readily expressed through a syringe outlet or other similarly-sized opening or orifice.
  • substantially solid when used in the context of an adhesive composition or layer, also excludes dry particulate adhesive compositions or powders because dry particulates and powders readily flow when subjected to gravity and/or are readily separated (i.e., the particles as a whole have little or no internal cohesion). Moreover, powders or particulates, when viewed as a whole, are not coherent or solid.
  • One characteristic of the "substantially solid” adhesive compositions or layers is that they become more adhesive when an exposed surface thereof is moistened with, e.g., saliva or water. When moistened, the surface of the adhesive composition or layer turns into a sticky material that is able to more strongly adhere to teeth compared to a substantially solid adhesive composition or layer that has not been moistened.
  • the adhesive composition at the surface may become a viscous liquid, paste or gel, at least temporarily, depending on the amount of moisture that is applied to the surface of the "substantially solid” adhesive composition or layer. Nevertheless, the consistency of the moistened surface can remain “substantially solid” depending on the degree of initial moistening, or it can stiffen and even revert back to being “substantially solid” as the initial quantity of surface moisture diffuses into a remaining portion of the "substantially solid” adhesive composition or layer over time (e.g., during a bleaching procedure in which the adhesive layer or composition is protected from saliva and ambient moisture in a person's mouth by a moisture-resistant barrier layer).
  • a bleaching agent activator may be initially locked or retained within a solid matrix of the adhesive composition or layer prior to moistening with saliva but which leaches, diffuses, or is otherwise made available for contacting, mixing or reacting with a bleaching gel when moistened with saliva or water in order to activate the bleaching agent and accelerate bleaching.
  • treatment gel refers to a treatment composition that has been formulated or processed so as to be flowable (e.g., it can be expressed out of a syringe orifice or other dispensing means known in the art).
  • the treatment gels according to the invention are, however, preferably sufficiently thick or viscous that they will not run off an an adhesive layer onto which the treatment gel is placed.
  • the treatment gel is rubbery or highly viscous.
  • the two dissimilar compositions may tend to reach an equilibrium wherein some of the liquid carrier of the treatment gel diffuses into the adhesive layer, thus further increasing the viscosity and stiffness of the treatment gel.
  • the treatment gel may comprise a single continuous bead or layer adjacent to the adhesive composition or layer, or it may comprise a plurality of discontinuous regions or layers spaced-apart by random or predetermined intervals. In some cases, at least a portion of the treatment gel may directly contact the barrier layer (e.g., through one or more discontinuities in the adhesive activation composition or layer).
  • a “dental tray” or “tray-like” composition or device includes a front side wall configured to engage front surfaces of a person's teeth when in use, a rear side wall extending laterally from the front side wall, either abruptly by one or more distinct angles or non-abruptly by a curved transition portion, configured to engage lingual surfaces of the person's teeth, and a trough between said front and rear side walls.
  • a “dental tray” may be configured so that a portion of the front side wall, rear side wall, or a transition portion thereof (e.g., a bottom wall), engages the incisal or occlusal edges of the person's teeth when in use.
  • the dental tray may be curved or straight in a longitudinal dimension.
  • the term "trough”, as used herein, refers to the region that is at least partially bounded by the front side wall, the rear side wall, and a plane or imaginary curved dome extending from an upper edge of the front side wall and an upper edge of the rear side wall.
  • a "trough" can theoretically exist whenever the front and rear side walls have a space therebetween and are laterally offset by an angle of less than 180°.
  • the front and rear side walls will be offset by an angle that is preferably less than about 150°, more preferably less than about 120°, and most preferably less than about 90°.
  • a transition portion e.g., a trough having a U-shaped or rectangular cross section
  • at least a portion of the front and rear side walls may be substantially parallel (i.e., be offset by an angle of approximately 0°) or offset by a very small angle.
  • at least a portion of the front and rear side walls may be offset by an acute angle (i.e., by an angle between 0-90°).
  • a trough having an L-shaped cross section at least a portion of the front and rear side walls may be offset by an angle centered around approximately 90° (e.g., by an angle in a range of about 70° to about 110°).
  • a trough having an L-shaped cross section can be a subset or slight variation of a trough having a V-shaped cross section.
  • the tray or device may be straight in the "longitudinal dimension” or it may be horseshoe-shaped or otherwise “longitudinally curved” in the longitudinal dimension so as to approximate the curvature of a person's dental arch, or at least facilitate placement of the tray or device over the dental arch.
  • shaped adhesive composition refers to a composition that has been formulated or processed so that at least a portion of the composition is substantially solid, coherent, and non-flowable.
  • the "shape" of the adhesive layer, treatment composition, or treatment device is primarily determined by the shape and relative rigidity of the barrier layer and/or adhesive layer.
  • the treatment gel typically does not determine or contribute to the "shape” of the treatment compositions and devices but conforms to the shape of the adhesive layer and/or barrier layer.
  • strip or “patch” are used interchangeably and shall refer to any treatment composition or device that is substantially flat, or that has a slight curvature or bend but that does not constitute a "dental tray", as that term is understood in the art.
  • a “strip” or “patch”, with or without a barrier layer, includes an inner surface or region configured to engage the front and/or rear surfaces of a person's teeth and/or gums when in use and an outer surface that is generally oriented away from the person's teeth and/or gums.
  • a “strip” or “patch” may be configured so that a portion of the inner surface engages the incisal or occlusal edges of the person's teeth when in use.
  • the strip or patch may be curved or straight in one or both of the lengthwise and widthwise directions in order to fit over a user's teeth and/or gums in a desired manner.
  • the term "molecular weight”, as used herein, shall refer to number average molecular weight expressed in Daltons, unless otherwise specified.
  • Treatment compositions according to the invention can exist alone or in combination with a barrier layer as part of a treatment device.
  • Treatment compositions according to the invention include an adhesive layer that becomes more adhesive to teeth when moistened by, e.g., saliva or water, and a freatment gel adjacent to an inner surface of the adhesive layer.
  • a moisture-resistant barrier layer adjacent to an outer surface of the adhesive layer protects the adhesive layer and treatment gel from ambient moisture within a person's mouth during use.
  • the barrier layer comprises a thin, flexible membrane formed from a moisture-resistant polymer material.
  • the barrier layer comprises a thin, flexible layer of a polyolefin or similarly moisture-resistant material, such as wax, metal foil, paraffin, ethylene-vinyl acetate copolymer (EVA), ethylene-vinyl alcohol copolymer (EVAL), polycaprolactone (PCL), polyvinyl chloride (PVC), polyesters, polycarbonates, polyamides, polyurethanes, or polyesteramides.
  • a polyolefin or similarly moisture-resistant material such as wax, metal foil, paraffin, ethylene-vinyl acetate copolymer (EVA), ethylene-vinyl alcohol copolymer (EVAL), polycaprolactone (PCL), polyvinyl chloride (PVC), polyesters, polycarbonates, polyamides, polyurethanes, or polyesteramides.
  • EVA ethylene-vinyl acetate copolymer
  • EVAL ethylene-vin
  • such sheets may be applied or attached to an existing adhesive composition or a treatment composition comprising a substantially solid adhesive layer and a treatment gel.
  • a treatment composition comprising a substantially solid adhesive layer and a treatment gel.
  • barrier layers having any desired material, thickness or rigidity so long as the barrier layer provides at least some moisture protection relative to the adhesive composition or layer and treatment gel.
  • the barrier layer may comprise a conventional dental tray, examples of which include both customized and non-custom dental trays, or it may initially be a strip or patch, or have some other configuration.
  • the barrier layer may be as simple as a layer of a moisture resistant material that is sprayed or painted on, applied by dipping, or otherwise applied to an existing shaped adhesive or treatment composition (e.g., one that is in the form of a dental tray or that otherwise has a desired shape).
  • suitable polyolefins for use in making the barrier layer include, but are not limited to, polyethylene (PE), high density polyethylene (HDPE), low density polyethylene (LDPE), ultra low density polyethylene (ULDPE), polypropylene (PP), and polytetrafluoroethylene (PTFE) (e.g., TEFLON).
  • a suitable polyester for use in making the barrier layer includes, but is not limited to, polyethylene terephthalate (PET), an example of which is MYLAR, sold by DuPont.
  • PET polyethylene terephthalate
  • MYLAR MYLAR
  • An example of a suitable polyurethane barrier material is a polyurethane film manufactured by ArgoTech, which is located in Greenfield, Massachusetts. Plasticizers, flow additives, and fillers known in the art can be used as desired to modify the properties of any of the foregoing polymers used to form the barrier layer.
  • the barrier layer is formed of a mixture of ethylene-vinyl acetate copolymer (EVA) and polypropylene (PP), preferably comprising about 5% to about 35% PP, more preferably about 10% to about 30% PP, more especially preferably about 15% to about 25% PP, and most preferably about 20% PP, with the balance comprising ethylene-vinyl acetate (EVA), and optionally other polymers and/or small quantities of additives such as plasticizers.
  • EVA ethylene-vinyl acetate copolymer
  • PP polypropylene
  • barrier layers that are formed onto a surface of a previously formed adhesive layer or treatment composition, such as by adhering a sheet or fray-like barrier layer to the adhesive layer or freatment composition.
  • the barrier layer may itself be initially flowable and later hardened, such as a lacquer that contains a barrier material (e.g., a cellulosic ether, cellulose acetate, wax, plastic, polyvinyl acetate, polyvinyl alcohol, or shellac) dissolved in one or more solvents that are later removed; a chemical or light-cure material (e.g., a methacrylate or acrylate resin); or a thermoplastic melt (e.g., any thermoplastic resin).
  • a barrier material e.g., a cellulosic ether, cellulose acetate, wax, plastic, polyvinyl acetate, polyvinyl alcohol, or shellac
  • a chemical or light-cure material e.g., a methacrylate or acrylate resin
  • a thermoplastic melt e.g., any thermoplastic resin
  • adhesive compositions and layers within treatment compositions and devices according to the invention preferably comprise a substantially solid and coherent adhesive composition, as opposed to a liquid, a flowable gel, or a dry powder or particulate.
  • the adhesive composition or layer may comprise a single coherent mass or region, or it may comprise a plurality of coherent masses or regions.
  • substantially solid and coherent adhesive composition or layer better maintains the treatment gel against the teeth and/or gums being treated instead of diffusing into the surrounding oral cavity, as compared to treatment gels that are loaded without an adhesive layer into customized or non-customized dental trays or that are applied using a flexible strip of plastic without an adhesive layer. This, in turn, promotes better treatment of the teeth and/or gums and patient compliance by, e.g., reducing irritation to surrounding oral tissues and/or at least some of the bad taste normally associated with freattnent compositions.
  • Substantially solid adhesive compositions include at least one tooth adhesion agent and, optionally, one or more inert component or active agents.
  • the adhesive composition may also include a bleaching agent activator.
  • the bleaching agent activator and any optional active agents may be dispersed within a substantially solid matrix comprising the tooth adhesion agent.
  • an active agent in the form of a liquid or solution can be spread, sprayed, or otherwise applied to an exposed surface of the adhesive composition prior to or after applying the treatment gel thereto.
  • the adhesive composition may include multiple layers or regions, with one layer or region comprising a bleaching agent activator and another layer or region omitting the bleaching agent activator so as to shield a bleaching gel in contact with the adhesive composition from the bleaching agent activator.
  • the adhesive composition may include a water soluble surface coating (e.g., a candy shell) that is non-adhesive or less adhesive that prevents interaction between the bleaching agent activator and bleaching gel prior to moistening the adhesive composition and/or bleaching gel with water or saliva prior to or during use.
  • the adhesive composition includes both a bleaching agent activator and a bleaching agent stabilizer and is formulated so that the effects of the bleaching agent stabilizer predominate prior to moistening the adhesive composition and/or bleaching gel with water or saliva. Thereafter, moistening the adhesive composition and/or bleaching gel with water or saliva causes the effects of the bleaching agent activator to predominate.
  • the bleaching agent stabilizer can act to raise the activation energy requirement just enough to prevent or inhibit activation of the bleaching agent prior to moistening the adhesive composition and/or bleaching gel with water or saliva but not so much as to prevent or inhibit activation after moistening occurs. This careful balance can be determined and optimized by testing adhesive compositions having varying concentrations of bleaching agent activator and bleaching agent stabilizer.
  • the bleaching agent activator can be concentrated within the interior (e.g., inner adhesive layer) of the adhesive composition and/or the bleaching agent stabilizer can be concentrated at the surface of the protective adhesive composition (e.g. as a coating by itself or within an outer adhesive layer).
  • the tooth adhesion agent may comprise any known tackifying agent that is substantially non-adhesive, or less adhesive, when the adhesive composition or layer is substantially solid but which becomes more adhesive to teeth when the adhesive composition or layer is moistened with, e.g., water or saliva.
  • a presently preferred tooth adhesion agent is polyvinyl pyrrolidone (PVP).
  • PVP polymers have been found to provide excellent adhesion to polymer barrier layers made from PE, PET, polyurethane, and paraffin, to be substantially non-adhesive when the adhesive composition is dry to the touch, and to have superior adhesion to teeth when a surface of a substantially solid adhesive composition is moistened with saliva or water.
  • Non-limiting examples of polyvinyl pyrrolidone polymers that have been used in formulating adhesive compositions and layers according to the invention include Kollidon 30, a polyvinyl pyrrolidone polymer sold by BASF having a molecular weight of 50,000, Kollidon VA 60, a polyvinyl pyrrolidone polymer having a molecular weight of 60,000, and Kollidon 90 F, a polyvinyl pyrrolidone polymer having a molecular weight of 1.3 million.
  • PVP polymers having widely varying molecular weights have been found to provide similar adhesion and wetting properties, it is believed that PVP polymers of any molecular weight, at least those having a molecular weight between 50,000 and 1.3 million, will be useful in formulating substantially solid adhesive compositions or layers according to the invention.
  • tooth adhesion agents that may be used in addition to, or instead of, PVP within the scope of the invention include, but are not limited to, carboxypolymethylene (e.g., CARBOPOL, sold by Novean, Inc.), polyethylene oxide (e.g., POLYOX, made by Union Carbide), polyacrylic acid polymers or copolymers (e.g., PEMULEN, sold by Novean, Inc.), polyacrylates, polyacrylamides, copolymers of polyacrylic acid and polyacrylamide, PVP-vinyl acetate copolymers, carboxymethylcellulose, carboxypropylcellulose, polysaccharide gums, proteins, and the like.
  • carboxypolymethylene e.g., CARBOPOL, sold by Novean, Inc.
  • polyethylene oxide e.g., POLYOX, made by Union Carbide
  • polyacrylic acid polymers or copolymers e.g., PEMULEN, sold by Novean, Inc
  • polyethylene oxide polymers comprises a less preferred tooth adhesion agent
  • a polyethylene oxide polymer having a molecular weight of 1 million provides better adhesion to barrier layers such as MYLAR than a polyethylene oxide polymer having a molecular weight of 100,000.
  • the one or more tooth adhesion agents are preferably included in an amount in a range of about 10% to about 90% by weight of the substantially solid adhesive composition (exclusive of any bound water or other solvent), more preferably in a range of about 20% to about 80% by weight of the substantially solid adhesive composition, and most preferably in a range of about 40% to about 75% by weight of the substantially solid adhesive composition. 2.
  • the adhesive compositions and layers may include inert components in addition to the tooth adhesion agent, as desired, to yield a final composition or layer having desired properties.
  • inert components include, but are not limited to, plasticizers and humectants (e.g., glycerin, sorbitol, polyethylene glycol, propylene glycol, and polypropylene glycol), volatile solvents (e.g., water and alcohols, such as ethanol), stabilizing agents (e.g., EDTA, salts of EDTA, citric acid and its salts, phosphoric acid and its salts, phenolphosphonic acid and its salts, gluconic acid and its salts, alkali metal pyrophosphates, alkali metal pyrophosphates, alkyl sulfates, such as sodium lauryl sulfate, tin salts, such as sodium stannate, and tartrates), neutralizing agents (e.g., sodium hydrox
  • water When water is used as a solvent when manufacturing adhesive compositions or layers according to the invention and then driven off by evaporation to yield a substantially solid adhesive composition, it is postulated that a significant amount of water remains bound or associated with the hydrophilic components within the adhesive composition, including the tooth adhesion agent, any inert components (e.g., polyols added as humectants, stabilizing agents, neutralizing agents, and/or thickening agents), and any hydrophilic active agents (e.g., bleaching agent, desensitizing agents or other active agents).
  • any inert components e.g., polyols added as humectants, stabilizing agents, neutralizing agents, and/or thickening agents
  • any hydrophilic active agents e.g., bleaching agent, desensitizing agents or other active agents.
  • Active Agents A wide variety of active agents known in the dental and oral arts can be included within the adhesive composition or layer. Examples of include bleaching agents (e.g., hydrogen peroxide or solid complexes or analogues of hydrogen peroxide, such as carbamide peroxide or sodium perborate), desensitizing agents (e.g., potassium nitrate), remineralizing agents (e.g., sodium fluoride or other fluoride salts), antimicrobial agents (e.g., chlorhexidine, froclosan, and tefracycline), antiplaque agents, anti-tartar agents, other medicaments, and bleaching agent activators (e.g., metals, metal salts, and bases).
  • bleaching agents e.g., hydrogen peroxide or solid complexes or analogues of hydrogen peroxide, such as carbamide peroxide or sodium perborate
  • desensitizing agents e.g., potassium nitrate
  • remineralizing agents e.g
  • substantially solid adhesive compositions and layers that include one or more active agents are disclosed in U.S. application Serial No. 10/446,235, filed May 27, 2003; U.S. application Serial No. 10/446,471, filed May 27, 2003; U.S. application Serial No. 10/637,237, filed August 8, 2003; U.S. application Serial No. 10/646,484, filed August 22, 2003; and U.S. application Serial No. 10/646,443, filed Augusts 22, 2003.
  • one or more bleaching agents are included within the substantially solid adhesive composition, they are preferably included in an amount in a range of about 5% to about 80% by weight of the substantially solid adhesive composition, more preferably in a range of about 10% to about 60% by weight of the substantially solid adhesive composition, and most preferably in a range of about 20% to about 50% by weight of the substantially solid adhesive composition.
  • potassium nitrate is included within the substantially solid adhesive composition as a desensitizing agent, it is preferably included in an amount in a range of about 0.01% to about 50% by weight of the substantially solid adhesive composition, more preferably in a range of about 0.1% to about 25% by weight of the substantially solid adhesive composition, and most preferably in a range of about 0.5% to about 10% by weight of the substantially solid adhesive composition.
  • potassium nitrate When included in combination with a dental bleaching agent, potassium nitrate is preferably included in an amount in a range of about 0.01% to about 2% by weight of the substantially solid adhesive composition, more preferably in a range of about 0.05% to about 1% by weight of the substantially solid adhesive composition, and most preferably in an amount of about 0.5% by weight of the substantially solid adhesive composition. It has been found that including potassium nitrate in these amounts creates a synergistic effect with the dental bleaching agent that appears to enhance tooth whitening. It also provides the highest level of tooth desensitization when used with a bleaching agent.
  • chlorhexidine gluconate is a preferred medicament and is preferably included in an amount in a range of about 0.01 to about 50% by weight of the substantially solid adhesive composition, more preferably in a range of about 0.05% to about 25% by weight of the substantially solid adhesive composition, and most preferably in a range of about 0.1% to about 10% by weight of the substantially solid adhesive composition.
  • Other anti-bacterial agents or medicaments may be included in the same concentration ranges.
  • Adhesive compositions and layers may comprise a bleaching agent activator capable of destabilizing a dental bleaching agent in order to accelerate bleaching in the case where the freatment gel includes a dental bleaching agent. When peroxides are destabilized they more rapidly release oxygen radicals, which cause tooth bleaching.
  • the bleaching agent activator may be retained within the substantially solid adhesive composition prior to use (e.g., locked within a substantially solid matrix), but then diffuse, leach, or otherwise contact, mix or react with the bleaching gel upon moistening the dental bleaching gel and/or adhesive composition with saliva or water.
  • the bleaching gel is initially substantially anhydrous and/or does not initially touch the adhesive composition in order to prevent diffusion or leaching of the bleaching agent activator into the bleaching gel prior to use.
  • One class of bleaching agent activators includes bases (i.e., substances that raise the pH in aqueous systems).
  • Examples of useful bases that can destabilize bleaching agents and thereby accelerate bleaching include oxides, hydroxides, carbonates, and bicarbonates of alkali metals and alkaline earth metals, and amines.
  • Non-limiting examples include sodium oxide, sodium hydroxide, potassium oxide, potassium hydroxide, sodium carbonate, sodium bicarbonate, ammonium hydroxide, magnesium hydroxide, sodium phosphate tribasic, and ethanolamine.
  • Bases, when used as bleaching agent activators are preferably included in an amount in a range of about 0.1% to about 20% by weight of the adhesive composition, more preferably in a range of about 1 % to about 10% by weight, and most preferably about 7% by weight.
  • Another class of bleaching agent activators includes metals and metal compounds. Examples of metals and metal compounds include transition metals
  • Another class of bleaching agent activator includes enzymes, particularly organo-metallic enzymes containing transition metals, such as iron.
  • Catalase which is described more particularly in U.S. Patent No. 6,485,709 to Banerjee et al.
  • Metals, metal compounds, and organo-metallic enzymes when used as a bleaching agent activator, are preferably included in an amount in a range of about 0.01% to about 20% by weight of the adhesive composition, more preferably in a range of about 0.05% to about 10% by weight, and most preferably in a range of about 0.1 % to about 5% by weight.
  • the treatment compositions and devices according to the invention may include any treatment gel known in the art.
  • the treatment gel may comprise a continuous layer or bead positioned so as to cover a person's front tooth surfaces, rear tooth surfaces, or both, or it may comprise separate beads, layers or islands of gel separated by a space.
  • Preferred treatment gels are those that are substantially viscous and tacky in order to assist the adhesive layer in retaining the treatment composition or device against a person's teeth during use.
  • the treatment gels according to the invention may comprise at least one active agent and any of the adhesive composition intermediates used to manufacture the substantially solid adhesive compositions or layers described herein.
  • Exemplary dental treatment gels, and methods for making such gels, which may be used to manufacture treatment compositions and devices according to the invention are disclosed in U.S. Patent No. 5,376,006; U.S. Patent No. 5,785,527; U.S. Patent No. 5,851,512; U.S. Patent No. 5,858,332; U.S. Patent No. 5,985,249; U.S. Patent No.
  • the treatment gels will include at least one active agent, at least one tackifying agent, and a liquid or gel carrier or vehicle into which the active agent and tackifying agent are dispersed.
  • An advantage of providing a treatment gel separate from the adhesive layer is that it provides a treatment composition or device that is more stable or consistent relative to the amount of active agent, at least in the case where the active agent is sensitive to heat. Heating an adhesive composition intermediate to drive off the water so as to yield a substantially solid adhesive composition can destabilize or decompose an active agent that is sensitive to heat and render it less potent. Because the treatment gel is generally not heated during manufacture of treatment compositions and devices according to the invention, greater stability and potency of the active agent may be achieved.
  • a bleaching gel is initially substantially anhydrous in order to prevent, inhibit or minimize diffusion or leaching of a bleaching agent activator from the adhesive composition or layer into the bleaching gel.
  • the bleaching device is manufactured in a manner so that the bleaching gel directly contacts the barrier layer but not the adhesive composition, thereby preventing or inhibiting premature activation of the bleaching gel.
  • active agents tackifying agents, and carriers or vehicles.
  • the active agent comprises at least one dental bleaching agent.
  • a common dental bleaching agent that is known to bleach teeth and that has been found to be safe for oral use is hydrogen peroxide. However, hydrogen peroxide does not itself exist free in nature, but only as an aqueous solution or as a complex. Aqueous hydrogen peroxide is an acceptable dental bleaching agent to the extent that an anhydrous bleaching gel is not desired.
  • Non-limiting examples of complexed hydrogen peroxide include carbamide peroxide and metal perborates.
  • Other bleaching agents that can be used to bleach teeth include, but are not limited to, metal percarbonates, peroxides, chlorites, and hypochlorites, peroxy acids, and peroxy acid salts.
  • Bleaching agents within the dental bleaching gels according to the invention can have any desired concentration, e.g., between 1-90% by weight of the dental bleaching gel. The concentration of the dental bleaching agent can be adjusted depending on the intended treatment time for each bleaching session. In general, the shorter the treatment time, the more bleaching agent will be added to accelerate dental bleaching so as to effect bleaching in a shorter time period.
  • the one or more bleaching agents are preferably included in an amount in a range of about 1% to about 60% by weight of the treatment gel, more preferably in a range of about 3% to about 40% by weight of the treatment gel, and most preferably in a range of about 5% to about 30% by weight of the treatment gel.
  • the freatment gels according to the invention may include one or more other active agent as desired to yield a treatment gel having desired properties.
  • Examples of other active agents include desensitizing agents (e.g., potassium nitrate, other potassium salts, citric acid, citrates, and sodium fluoride), antimicrobial agents, remineralizing agents, antiplaque agents, anti-tartar agents, and other medicaments known in the art.
  • desensitizing agents e.g., potassium nitrate, other potassium salts, citric acid, citrates, and sodium fluoride
  • antimicrobial agents e.g., potassium nitrate, other potassium salts, citric acid, citrates, and sodium fluoride
  • antimicrobial agents e.g., potassium nitrate, other potassium salts, citric acid, citrates, and sodium fluoride
  • antimicrobial agents e.g., remineralizing agents, antiplaque agents, anti-tartar agents, and other medicaments known in the art.
  • Exemplary remineralizing agents capable of preventing caries include, but are not limited to, sodium fluoride, sodium monofluorophosphate, stannous fluoride, other fluoride salts, and calcium phosphate.
  • Exemplary anti-tartar agents include, but are not limited to, pyrophosphates, polypyrophosphates, polyvinyl methyl ether malic acid, sodium hexametal phosphate, alkali metal phosphates, calcium lactate, and friclosan.
  • Exemplary anticalculus or antiplaque agents include, but are not limited to, 8-hydroxyquinoline sulfate, dicitrate cyclic ester, and zinc citrate.
  • potassium nifrate When potassium nifrate is included within the freatment gel as a desensitizing agent, it is preferably included in an amount in a range of about 0.01% to about 50% by weight of the treatment gel, more preferably in a range of about 0.1 % to about 25% by weight of the treatment gel, and most preferably in a range of about 0.5% to about 10% by weight of the treatment gel.
  • potassium nitrate When potassium nitrate is included in combination with a dental bleaching agent, the potassium nitrate is preferably included in an amount in a range of about 0.01% to about 2% by weight of the treatment gel, more preferably in a range of about 0.05%) to about 1% by weight of the treatment gel, and most preferably in an amount of about 0.5%) by weight of the treatment gel.
  • chlorhexidine gluconate is a preferred medicament and is preferably included in an amount in a range of about 0.01 to about
  • Tackifying Agents Useful tackifying agents that may be used in the freatment gel include any of the tooth adhesion agents disclosed herein for use in manufacturing the substantially adhesive compositions or layers according to the invention. The main difference between a "tackifying agent" within a "freatment gel", and a “tooth adhesion agent” within an "adhesive composition” or “adhesive layer”, is the physical state.
  • a tackifying agent within a treatment gel is already mixed with a liquid or gel carrier or vehicle such that the resulting treatment gel is immediately sticky and tacky to the touch as a result of the tackifying agent.
  • an adhesive composition or layer typically becomes much more adhesive to teeth when the adhesive composition or layer is moistened by saliva or water as a result of the tooth adhesion agent.
  • the adhesive composition or layer may initially be non-adhesive and dry to the touch prior to moistening with saliva or water.
  • One useful tackifying agent is polyvinyl pyrrolidone (PVP).
  • Non-limiting examples of polyvinyl pyrrolidone polymers that have been used in formulating dental bleaching gels according to the invention include Kollidon 30, a polyvinyl pyrrolidone polymer sold by BASF having a molecular weight of 50,000, Kollidon VA 60, a polyvinyl pyrrolidone polymer having a molecular weight of 60,000, and Kollidon 90 F, a polyvmyl pyrrolidone polymer having a molecular weight of 1.3 million.
  • carboxypolymethylene e.g., CARBOPOL, sold by Novean, Inc.
  • polyethylene oxide e.g., POLYOX, made by Union Carbide
  • polyacrylic acid polymers or copolymers e.g., PEMULEN, sold by Novean,
  • the one or more tackifying agents are preferably included in an amount in a range of about 1% to about 50% by weight of the treatment gel, more preferably in a range of about 3% to about 30% by weight of the treatment gel, and most preferably in a range of about 5% to about 20% by weight of the treatment gel.
  • Carriers and Vehicles The dental bleaching gel will typically include one or more liquid or gel carriers or vehicles into which the active agent, tackifying agent, and other components are dispersed.
  • liquid or gel carriers or vehicles include, but are not limited to, water, alcohols (e.g., ethyl alcohol), and polyols (e.g., glycerin, sorbitol, polyethylene glycol, polyethylene oxide, propylene glycol, and polypropylene glycol).
  • the carrier or vehicle will typically comprise the balance of components in the treatment gel in addition to the active agent, tackifying agent, and any other components. 4.
  • the treatment gels according to the invention may optionally include other components as desired to yield a treatment, gel having desired properties.
  • stabilizing agents e.g., EDTA, salts of EDTA, citric acid and its salts, phosphoric acid and its salts, phenolphosphonic acid and its salts, gluconic acid and its salts, alkali metal pyrophosphates, alkali metal pyrophosphates, alkyl sulfates, such as sodium lauryl sulfate, tin salts, such as sodium stannate, and tartrates), neutralizing agents (e.g., sodium hydroxide and triethanolamine), thickening agents (e.g., fumed silica), desensitizing agents (e.g., potassium nitrate, other potassium salts, citric acid, citrates, and sodium fluoride), remineralizing agents (e.g., sodium fluoride, stannous fluoride, sodium monofluorophosphate, and other fluoride salts), antimicrobial agents (e.g., chlorhexidine, froclosan, and phosphat
  • the treatment compositions and devices according to the invention are preferably in the shape of a dental fray having a front side wall, a rear side wall, and a frough between the front and rear side walls. Having the shape of a dental tray facilitates placement of the treatment composition or device over a person's teeth by reducing the amount of manipulation that is necessary to obtain a good fit between the composition or device and the person's teeth.
  • the freatment compositions and devices are in the shape of a patch or strip. It is within the scope of the invention for the treatment compositions and devices to have any desired shape or configuration.
  • Treatment compositions and devices that have a substantially solid adhesive layer that becomes more adhesive when moistened with water or saliva are easier to install over a person's teeth compared to conventional bleaching strips or patches, which do not reliably adhere to a user's teeth. That is because the inventive treatment compositions and devices are designed to more reliably adhere and remain in place over the person's teeth compared to conventional bleaching strips, which employ a dental bleaching gel immediately adjacent to a plastic sheet. The result is more effective freatment and better patient compliance.
  • freatment compositions and devices according to the invention can be designed so as to be worn while talking, sleeping, eating, drinking, smiling, frowning, grimacing, yawning, coughing, smoking, or making virtually any facial expression or mouth contortion.
  • the treatment compositions and devices have a horseshoe shaped longitudinal profile and a trough with a U-shaped cross section, much like a conventional dental tray.
  • An exemplary freatment device in the form of a dental tray is depicted in Figures 1 and 2A.
  • Figure 1 is a perspective view of a freatment device 10 having a front side wall 12 and a rear side wall 14 that together have a generally horseshoe shape in a longitudinal dimension and that define a trough 16 having a generally U-shaped cross section.
  • the U-shaped cross section of the trough is seen more clearly in Figure 2A.
  • the treatment device 10 further includes a barrier layer 18, preferably comprising a moisture-resistant material, an adhesive composition or layer 20, preferably comprising a substantially solid adhesive composition, and a treatment gel 28.
  • the adhesive layer 20 includes an outer surface 22, which is adjacent to an interior surface 24 of the barrier layer 18, and an inner surface 26, which is adjacent to the treatment gel 28.
  • both the treatment gel 28 and a portion of the inner surface 26 of the adhesive layer 20 are designed to directly contact a person's teeth when the treatment device 10 is in use.
  • An upper edge of the front side wall 12 can be designed so as to terminate at or shy of the gingival margin of a person's dental arch when the freatment device 10 is in use. Alternatively, it may extend beyond the gingival margin and extend at least partially over a person's gums.
  • FIG 2B alternatively depicts a treatment composition 19 comprising an adhesive composition or layer 20' in the shape of a dental tray, so as to have a front side wall 12' and a rear side wall 14', and a treatment gel 28 adjacent to an inner surface 26' of the adhesive layer 20'.
  • the treatment composition 19 differs from the treatment device 20 of Figures 1 and 2A in that it includes no barrier layer.
  • the adhesive layer 20' also includes an exterior surface 22' that may optionally be coated with a water-resistant barrier layer or material if desired (see Figure 2A) to protect the treatment composition (more particularly the adhesive layer 20' and treatment gel 28) from saliva or ambient moisture (see Figure 2A).
  • the treatment composition 19 may be sold alone or together with a moisture-resistant barrier layer, or a material used to make a barrier, that can be placed adjacent to the exterior surface 22' of the adhesive layer 20' prior to or during use.
  • Figure 2C alternatively depicts a freatment device 10' that includes a barrier layer 18, regions or spots of an adhesive composition 20' interspersed with regions or spots of a treatment gel 28'. Both the adhesive composition 20' and treatment gel 28' are located adjacent to the barrier layer. In this way, the adhesive composition 20' and treatment gel 28' do not initially touch prior to use. According to one embodiment, this helps prevent or inhibit contact between a bleaching agent activator within the adhesive composition 20' and a bleaching agent within the treatment gel 28' prior to use.
  • the freatment compositions or devices can be packaged within a sealed container or package.
  • a treatment device or freatment composition according to the invention can be sealed within a protective package 30 that includes a rigid support layer 32 and a peelable cover 34.
  • the peelable cover 34 is removed and the freatment device or composition is removed or separated from the support layer 32.
  • the treatment device or composition may alternatively include a removable protective layer (not shown) that is temporarily placed within the frough adjacent to the freatment gel.
  • FIG 4 illustrates a treatment composition or device 40 that is a variation of the U-shaped freatment device 10 of Figures 1 and 2A or the treatment composition 19 of Figure 2B. The main difference is that each longitudinal end 42 of the treatment composition or device 40 is raised so as to at least partially enclose the last tooth on each side of a person's dental arch when the treatment composition or device 40 is in use.
  • Figure 5 illustrates an alternative embodiment of a freatment composition or device 50 according to the invention that has an L-shaped cross section.
  • the treatment composition or device 50 includes a front side wall 52 and a rear side wall 54 extending laterally from the front side wall 52 so as to form a frough 56 having an approximate L-shaped cross section.
  • the L-shaped treatment composition or device 50 of Figure 5 is somewhat easier to initially place over a person's dental arch compared to the U-shaped treatment composition or devices of Figures 1-4. This is due to the approximately planar orientation of the rear side wall 54 relative to the occlusal or incisal edges of a person's teeth when the front side wall 52 of the treatment composition or device 50 is initially placed and adhered against the front surfaces of a person's teeth.
  • the L- shaped freatment composition or device 50 is generally required to form and adhere the rear side wall 54 against the lingual surfaces of the person's teeth as a result of the greater initial offset angle between the front side wall 52 and rear side wall 54.
  • the ability of treatment compositions or devices according to the invention to adhere to tooth surfaces immediately after placement over a person's teeth, and even more so after initial wetting of the adhesive layer facilitates the process of conforming the front side wall 52 and rear side wall 54 to the person's tooth surfaces.
  • the freatment composition or device 50 having an L-shaped cross section it may be more correct to say that the rear side wall 54 extending laterally from the front side wall 52 is really a bottom wall rather than a rear side wall.
  • the side wall 54 shall constitute, and fall within the definition of, a "rear side wall".
  • the treatment composition or device may include mechanical features such as one or more notches within the front or rear side walls.
  • the treatment composition or device 50 includes a notch 58 in an outer edge near the center of the front side wall 52 and a notch 59 in an outer edge near the center of the rear side wall 54. Notches 58 and 59 allow the tray- like treatment composition or device to more easily spread open or compress when being conformed to differently-sized dental arches. In this way, the treatment composition or device 50 can more easily be a "one-size fits all" composition or device.
  • Figure 6 depicts an alternative embodiment of a treatment composition or device 60 according to the invention, which includes a front side wall 62 and a rear side wall 64 that define a U-shaped trough 66 into which a bead of treatment gel 28 is placed.
  • the treatment composition or device 60 of Figure 6 has a substantially straight or linear longitudinal profile.
  • Figure 7 depicts yet another alternative embodiment of a treatment composition or device 70 according to the invention.
  • the treatment composition or device 70 includes a front side wall 72 and a rear side wall 74 that define a V-shaped frough 76 and a curved longitudinal profile.
  • the main difference between the V- shaped treatment composition or device 70 of Figure 7 and the L-shaped freatment composition or device 50 of Figure 5 is the angle at which the front and rear side walls are laterally offset from each other.
  • FIG 8 is a perspective view of a treatment strip or patch 110 comprising a barrier layer 112, which preferably comprises a moisture-resistant material, an adhesive layer 114, which preferably comprises a substantially solid adhesive composition, and a treatment gel 116.
  • the adhesive layer 114 includes an outer surface 120, which is adjacent to an inner surface 122 of the barrier layer 112, and an inner surface 124, which is adjacent to the treatment gel 116. It is within the scope of the invention for the treatment gel 116 to directly contact the adhesive layer 114, the barrier layer 112, or both depending on where the treatment gel 116 is located relative to the adhesive layer 114.
  • both the treatment gel 116 and at least a portion of the inner surface 124 of the adhesive layer 114 are designed to directly contact a person's teeth when the treatment strip 110 is in use.
  • An upper edge 126 of the freatment strip 110 can be designed so as to terminate at or shy of the gingival margin of a person's dental arch when in use.
  • Figure 9B alternatively depicts a treatment composition 111 comprising an adhesive layer 114' in the shape of a strip or patch, so as to have an outer surface 120' and an inner surface 124', and a treatment gel 116' adjacent to the inner surface 124' of the adhesive layer 114'.
  • the treatment composition 111 differs from the freatment strip 110 of Figures 8 and 9 A in that it includes no barrier layer.
  • the outer surface 120' of the adhesive layer 114' may optionally be coated with a water-resistant barrier layer or material if desired (see Figure 9A) to protect the freatment composition 111 (more particularly the adhesive layer 114' and freatment gel 116') from saliva or ambient moisture.
  • the freatment composition 111 may be sold alone or together with a moisture-resistant barrier layer, or a material used to make a barrier layer, that can be placed adjacent to the outer surface 120' of the adhesive layer 114' prior to or during use.
  • Figure 9C alternatively depicts a treatment device 110' that includes a barrier layer 112, regions or spots of an adhesive composition 114' interspersed with regions or spots of a treatment gel 116'.
  • Both the adhesive composition 114' and treatment gel 116' are located adjacent to the barrier layer. In this way, the adhesive composition 114' and treatment gel 116' do not initially touch prior to use. In the case where the freatment gel 116' includes a dental bleaching agent, this helps prevent or inhibit contact between a bleaching agent activator within the adhesive composition 114' and the bleaching agent within the treatment gel 116' prior to use.
  • the freatment gel 116' includes a dental bleaching agent
  • this helps prevent or inhibit contact between a bleaching agent activator within the adhesive composition 114' and the bleaching agent within the treatment gel 116' prior to use.
  • they can be packaged within a sealed container or package. As illustrated in Figure 10, one or more treatment strips 110 (or treatment compositions) can be sealed within a protective package 130 that includes a rigid support layer 132 and peelable cover 134.
  • the peelable cover 134 is removed and the freatment strip 110 or composition is removed or separated from the support layer 132.
  • the treatment strip 110 or composition may alternatively include a removable protective layer (not shown) that is temporarily placed adjacent to the treatment gel.
  • the removable protective layer is removed so as to expose the treatment gel.
  • Figure 11 shows a treatment strip 142 being optionally manipulated (such as by bending, curving or folding) so as to have an approximate V-shaped cross section in order to facilitate placement of the treatment strip 142 over a person's teeth and/or gums.
  • treatment compositions and devices according to the invention can have any profile and longitudinal shape (e.g., they can be flat or have a 3-dimensional shape; they can have a straight or curved longitudinal profile from one end to the other).
  • the front and rear side walls of a fray may define a trough of any desired cross-sectional shape (e.g., the frough can be trapezoidal, rectangular, or any other desired geometric shape).
  • the size and shape of treatment compositions and devices according to the invention can be tailored to more readily fit either a person's upper dental arch or lower dental arch. They can be sized so as to treat all or merely a subset of a person's teeth and/or gums.
  • the freatment compositions and devices may be sufficiently adhesive and flexible so as to readily conform to a wide variety of differently-sized teeth and dental arches.
  • the treatment compositions and devices are advantageously designed so as to substantially cover the front and lingual surfaces of the teeth and/or gums to be treated. Treating both the front and lingual surfaces helps in treating (e.g. , bleaching) the interproximal spaces between adjacent teeth. If left unbleached, stained inte ⁇ roximal spaces can form a dark ring or silhouette around each tooth.
  • the thickness of the barrier layer and/or the adhesive layer can be selected to yield a treatment device having a desired strength and flexibility.
  • the barrier layer In order for the barrier layer to remain flexible so as to conform to a person's teeth, the barrier layer will generally have a thickness ranging from about 0.025 mm to about 1.5 mm, preferably in a range of about 0.05 to about 1 mm.
  • the adhesive layer will generally have a thickness ranging from about 0.1 mm to about 3 mm.
  • the thickness of the adhesive layer can also be selected depending on the intended duration of each treatment session. In generally, increasing the thickness of the adhesive layer will provide a longer adhesion of the freatment device or composition to a person's teeth. By way of example, for short wear times, the adhesive layer will preferably have a thickness ranging from about 0.1 mm to about 0.5 mm.
  • the adhesive layer will preferably have a thickness ranging from about 0.5 mm to about 2 mm.
  • the adhesive layer will preferably have a thickness ranging from about 2 mm to about 3 mm.
  • the amount of treatment gel can be selected to yield a treatment composition or device having a desired tackiness and/or potency.
  • the treatment gel will be required to provide the sum total of the active treatment. In such cases, the thickness of the freatment gel may be increased, all things being equal.
  • the adhesive layer also includes an active agent, the treatment gel will not be required to provide the entirety of the active agent. In such cases, the thickness of the treatment gel may be decreased, all things being equal.
  • the more viscous and tacky the treatment gel the less deleterious will be the freatment gel on the overall ability of the freatment composition or device to adhere to a person's teeth.
  • the cross-sectional thickness of the freatment gel may be increased, all things being equal.
  • the less viscous and tacky the treatment gel the less the freatment gel will tend to adhere to a person's teeth.
  • the cross-sectional thickness of the treatment gel may be advantageously decreased, all things being equal.
  • a shaped adhesive composition or layer is first made by forming a flowable adhesive composition intermediate that is then shaped and dried to form a substantially solid adhesive composition or layer in the form of a dental tray, fray-like device, strip, patch or other desired shape. This may be performed by heating or otherwise causing one or more volatile solvents to be driven off by evaporation, thus leaving behind the substantially solid adhesive layer. Thereafter, a freatment gel is placed against an inner surface of the adhesive layer and/or the barrier layer.
  • the treatment gel may directly contact the barrier layer to the extent that the adhesive layer has one or more discontinuities or otherwise does not cover the entire barrier layer.
  • An optional barrier layer may also be placed against an outer surface of the adhesive layer in order to protect the adhesive layer and freatment gel from ambient moisture within a person's mouth.
  • the barrier layer may be placed against the adhesive layer either before or after the adhesive composition is dried so as to become substantially solidified.
  • the barrier layer may comprise a preformed dental fray. In another, it may comprise a thin, flexible sheet, strip or patch.
  • the barrier layer may initially comprise a flowable barrier material or precursor that is later cured or hardened, such as by removing a solvent by evaporation, by chemical or light curing, or by cooling a thermoplastic melt.
  • the adhesive intermediate composition can be cast onto a forming surface and dried to form a substantially solid sheet, which is subsequently molded, stamped, cut or otherwise formed into a desired shape. Thereafter, a treatment gel is attached or applied to an inner surface of the adhesive layer, and a barrier layer is optionally applied or attached to an outer surface of the adhesive layer. The treatment gel can be applied to the adhesive layer before or after the barrier layer, or in the absence of a barrier layer.
  • the adhesive layer can be made by spreading a flowable adhesive composition intermediate onto the surface of a large or continuous polymeric sheet (e.g., using a screeding device).
  • the polymeric sheet and adhesive composition intermediate are then placed into a forced air oven or other appropriate desiccation device in order to heat and drive off a substantial portion of the water or other solvent used to form the flowable adhesive composition intermediate. Removal of the volatile solvent yields an adhesive layer comprising a substantially solid adhesive composition.
  • individual intermediate tray-like devices, patches or strips can be molded, stamped or cut from the large or continuous polymeric sheet coated with the substantially solid adhesive composition or layer and then separated as individual devices.
  • a solid sheet comprising the adhesive composition or layer can be separated from the polymer sheet and molded, stamped, cut or otherwise formed into a desired shape.
  • the treatment gel may be applied or placed adjacent to an inner surface of the adhesive layer.
  • a barrier layer in the form of a dental tray, tray-like device e.g., a customized or non-custom fray
  • strip, patch or other desired shape can be coated with a flowable adhesive composition intermediate. The adhesive composition intermediate is then heated together with the barrier layer or otherwise allowed to dry in order to form an adhesive layer comprising a substantially solid adhesive composition.
  • a treatment gel is applied to an inner surface of the adhesive layer and/or the barrier layer in order to yield a finished freatment device according to the invention.
  • Any or all of these assembly processes can be performed during commercial manufacture of the treatment device, or by an end user as part of using a bleaching kit.
  • IV. METHODS OF USING TREATMENT COMPOSITIONS AND DEVICES INCORPORATING SUCH COMPOSITIONS
  • the treatment compositions and devices according to the invention can be designed to be worn for any desired time period. Increasing the concentration of the one or more active agents generally reduces the time required to effect bleaching.
  • inventive freatment compositions or devices due to the extremely comfortable fit and reliable adhesion between the inventive freatment compositions or devices and the person's teeth, it is possible to wear such compositions or devices for extended periods of time in order to ensure more uniform freatment.
  • They may be designed to be worn while performing normal daily activities, such as talking, eating, drinking, smoking, coughing, smiling, frowning, grimacing, or while sleeping. This greatly decreases their intrusiveness into everyday activities compared to conventional bleaching strips, which do not reliably adhere to teeth, or intrusive treatment devices such as large, bulky dental treatment appliances.
  • the dental treatment compositions or devices according to the invention may be worn over a person's upper dental arch, lower dental arch, or both simultaneously.
  • FIG 12 illustrates a person 80 placing a treatment composition or device 82 over the person's upper dental arch.
  • the treatment composition or device 82 can be in the form of a dental tray, strip, patch or other desired shape.
  • Figure 13 illustrates the person 80 placing a treatment composition or device 92 over the person's lower dental arch after having placed the freatment composition or device 82 over the upper dental arch. It will be appreciated, however, that the treatment compositions or devices can be placed over a person's upper and lower dental arches in any desired order.
  • the adhesive composition or layer of a bleaching composition or device contains a bleaching agent activator
  • contacting the bleaching composition or device with saliva or water causes the bleaching agent activator to leach or diffuse out of the adhesive composition, or otherwise become available, so as to react with or otherwise destabilize the bleaching agent within the dental bleaching gel in order to accelerate bleaching.
  • the bleaching may advantageously be initially substantially anhydrous in order to prevent or inhibit diffusion or leaching of the bleaching agent activator from the adhesive composition into the bleaching gel.
  • the bleaching gel may include a stabilizing agent, such as EDTA, in a sufficient quantity to prevent premature activation of the bleaching agent prior to use but not so much as to entire prevent activation during use.
  • the bleaching agent can occupy discontinuities within the adhesive layer so as to directly contact the barrier layer rather than the adhesive layer, thereby preventing or inhibiting contact between the bleaching gel and adhesive layer prior to use.
  • a user can pry open a corner of the barrier layer and/or adhesive layer using a fingernail or rigid tool and then pull the remainder off. Any residual adhesive composition and/or treatment gel that remains adhered to the person's teeth can be removed by washing or flushing water over the person's teeth, and/or by brushing.
  • inventive treatment compositions are very adhesive to teeth when protected from excessive moisture, they can be formulated to quickly break down and dissolve when flushed with excess water and/or by gentle mechanical action (e.g., brushing).
  • the treatment compositions or devices can be worn for as little as a few minutes or as long as several hours.
  • a typical freatment session of fast duration may last from about 10 to about 30 minutes.
  • a treatment session of intermediate duration may last from about 30 minutes to about 2 hours.
  • a treatment session of long duration, including professional treatment or overnight treatment while a person is sleeping may last from about 2 hours to about 12 hours.
  • Treatment sessions according to the invention may be repeated as many times as needed to obtain a desired degree of treatment.
  • a clinical whitening effect has been observed after only 1-3 whitening sessions.
  • a typical treatment regimen will preferably include 1-20 treatment sessions, more preferably 2-15 treatment sessions, and most preferably 3-10 freatment sessions.
  • V. DENTAL TREATMENT KITS For convenience of use, multiple freatment compositions or devices may be packaged together and sold as a kit. In the case of treatment compositions that do not initially include a barrier layer, a separate barrier layer, or material used to form a barrier layer, may be optionally included within the kit. In one embodiment, the number of treatment compositions or devices provided with each kit may equal the number of sessions that represent a prescribed freatment regimen. Because of the ease of placing the inventive treatment compositions or devices over a person's teeth, coupled with the reliability with which they adhere to teeth, the likelihood that a particular treatment composition or device will fail, or otherwise not work as intended, is greatly diminished compared to conventional bleaching strips.
  • freatment compositions or devices can be stacked or interested together.
  • the treatment compositions or devices can be sealed collectively or individually as desired.
  • a protective package 30 is depicted in Figure 3, and a protective package 130 is depicted in Figure 10.
  • the treatment compositions or devices may optionally contain a removable protective layer on an interior surface to protect the freatment gel from contamination or moisture. It is within the scope of the invention to provide barrier layers and treatment composition that are initially separate and that are brought together by the end user.
  • the freatment composition may comprise a pre-shaped insert in the shape of a horse-shoe that is placed into a trough of a tray-like barrier layer, with or without actually adhering the adhesive layer to the barrier layer.
  • a flowable adhesive composition intermediate can be placed within the trough of a dental tray or tray-like barrier layer and allowed to dry prior to placement of the treatment gel against an inner surface of the substantially solid adhesive layer. Thereafter, a treatment gel is placed adjacent to an inner surface of the substantially solid adhesive layer.
  • a treatment gel may also be placed by a user adjacent to an inner surface of a shaped adhesive layer or composition in the absence of a barrier layer, or prior to placing a barrier layer adjacent to an outer surface of the adhesive layer.
  • Examples 1-21 are directed to the manufacture of adhesive dental bleaching layers that become more adhesive when moistened by saliva or water.
  • Examples 22- 26 are directed to the manufacture of adhesive dental desensitizing layers that become more adhesive when moistened by saliva or water.
  • Examples 27-29 are directed to the manufacture of adhesive antimicrobial layers that become more adhesive when moistened by saliva or water.
  • the adhesive bleaching, desensitizing and antimicrobial layers of Examples 1-29 therefore comprise exemplary adhesive compositions or layers according to the invention.
  • exemplary treatment compositions or devices according to the invention can be manufactured by placing any treatment gel disclosed herein, or known in the art, adjacent to an inner surface of the bleaching, desensitizing, or antimicrobial layers of Examples 1-29.
  • Examples 30-37 are directed to the manufacture of adhesive compositions or layers that do not include any active agent.
  • Exemplary treatment compositions or devices according to the invention can be manufactured by placing any treatment gel disclosed herein, or known in the art, adjacent to an inner surface of the adhesive layers of Examples 30-37.
  • Examples 38-43 are directed to exemplary treatment gels that are suitable for use in manufacturing treatment compositions or devices according to the invention.
  • treatment compositions or devices according to the invention can be manufactured by placing the treatment gels of Examples 38-43 adjacent to any of the adhesive layers described herein, including those formed according to Examples 1-37.
  • Examples 44-50 describe further variations of exemplary treatment compositions according to the invention.
  • EXAMPLE 1 An initially flowable intermediate composition suitable for use in manufacturing a substantially solid, cohesive, and non-flowable adhesive bleaching layer was formed by mixing together the following components: Carbamide Peroxide 16% Polyvinyl pyrrolidone (M.W.
  • the resulting intermediate composition was spread over the surfaces of three types of flexible polymer sheets: polyethylene sheets having a thickness of approximately 0.15 to 0.18 mm; sheets made of paraffin having a thickness of approximately 0.05 to 0.08 mm; and MYLAR sheets having a thickness of approximately 0.38 mm.
  • the composition was spread using a spatula.
  • the coated sheets were heated in a forced air oven heated to a temperature of 50-70° C. for approximately 1 hour.
  • the coated sheets were removed from the oven and inspected.
  • the intermediate composition had dried sufficiently so as to form a solid, coherent bleaching layer on the surface of the polymer sheets.
  • the dried bleaching layer adhered well to each of the polymer sheets.
  • the coated sheets were placed back into the oven overnight to remove additional water.
  • the coated sheets were removed from the oven a second time, cut apart into smaller-sized pieces, and either used as strips or shaped into tray-like devices suitable for placement over a person's teeth.
  • the tray-like devices included front and rear side walls that defined a trough having an approximate U- or V-shaped cross section and were curved in the longitudinal dimension to roughly approximate the curvature of a dental arch.
  • the strips and tray-like devices were tested by placing them over a person's teeth.
  • the residual saliva present on the tooth surfaces moistened the exposed surface of the bleaching layer and caused it to become sticky and very adhesive to teeth almost immediately.
  • the bleaching devices were pressed against the teeth, which caused them to conform to the natural irregularities of the dental arch and adhere firmly against the teeth.
  • the bleaching layer formed in this example comprises an excellent adhesive layer.
  • a treatment gel is placed within the trough of a tray-like device of this example, adjacent to an inner surface of the adhesive bleaching layer, to yield a traylike treatment device according to the invention.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • the freatment gel is not heated prior to placing the treatment device over a person's teeth and/or gums, which helps preserves the potency and concentration of the active agent within the treatment gel.
  • Treatment devices are worn for varying time periods ranging from several minutes to several hours without becoming dislodged. In some cases a noticeable treatment effect is detected after just one treatment session (e.g., a 2-hour bleaching session).
  • the bleaching layer of Example 2 did not adhere strongly to the polymer sheets but was easily separated therefrom.
  • the coated sheets were placed back into the oven overnight.
  • the coated sheets were removed from the oven a second time, cut apart into smaller-sized pieces, and used as strips or shaped into tray-like devices suitable for placement over a person's teeth.
  • the tray-like devices included front and rear side walls that defined a frough having an approximate U- or V-shaped cross section and were curved in the longitudinal dimension to roughly approximate the curvature of a dental arch.
  • the bleaching devices were tested by placing them over a person's teeth.
  • the residual saliva present on the tooth surfaces moistened the exposed surface of the bleaching layer and caused it to become sticky and adhesive to teeth within a few seconds.
  • Example 2 The results of Example 2 indicate that, while polyethylene oxide was a satisfactory teeth adhesion agent, it was less satisfactory in promoting adhesion between a bleaching layer and a polymer sheet.
  • a treatment gel is placed within the frough of a tray-like device of this example, adjacent to an inner surface of the adhesive bleaching layer, to yield a traylike freatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • EXAMPLE 3 An initially flowable intermediate composition suitable for use in manufacturing a substantially solid, cohesive, and non-flowable adhesive bleaching layer was formed by mixing together the following components: Carbamide Peroxide 16% Carbopol 974P 5% Aqueous NaOH (50%) 6% Water 73% The resulting intermediate composition was spread over the surface of MYLAR sheets using a spatula. The coated sheets were heated in a forced air oven heated to a temperature of 50-70° C. for approximately 1 hour. The coated sheets were removed from the oven and inspected. Although the intermediate composition dried sufficiently to form a solid, it shrunk considerably, probably because of the large amount of water that was needed to cause Carbopol to form a gel.
  • Shrinkage of the intermediate composition caused the polymer sheet to become partially shriveled up.
  • using carboxypolymethylene as a tooth adhesion agent resulted in a dried bleaching composition that adhered to a polymer sheet.
  • the coated sheets were removed from the oven after heating overnight, cut apart into smaller-sized pieces, and used as strips or shaped into tray- like devices suitable for placement over a person's teeth.
  • the bleaching layer When placed over a person's teeth it took about 5 seconds for the bleaching layer to become moistened enough to start becoming sticky and adhesive to teeth.
  • the strips and fray-like devices were able to conform to the person's teeth and remain in place after being pressed against the teeth for about 30-60 seconds.
  • Example 3 The results of Example 3 indicate that, while Carbopol 974 P is able to adhere to a MYLAR sheet and appears to be a satisfactory tooth adhesion agent once the adhesive bleaching layer is sufficiently moistened, it presents a shrinkage problem that can cause undesirable deformation of thin, flexible polymer sheets. One would expect Carbopol 974 P to work better when used with less flexible sheets and/or preformed dental trays of sufficient rigidity to avoid shriveling or unwanted deformation.
  • a freatment gel is placed within the trough of a tray-like device of this example, adjacent to an inner surface of the adhesive bleaching layer, to yield a traylike treatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • the bleaching layer of Example 4 did not adhere at all to the MYLAR sheets. This indicates that the lower molecular weight polyethylene oxide of Example 4 was even less adhesive to MYLAR sheets than the higher molecular weight polyethylene oxide of Example 2. Sheets comprising an adhesive bleaching layer could also be formed by spreading the intermediate composition on a solid surface such as glass, drying the composition, and then peeling off the dried adhesive layer. By comparison, when the intermediate composition of Example 1 was applied to a glass surface and then dried, it adhered so strongly that it could not readily be peeled off the glass surface. Instead, it had to be forcefully chipped or pried off using a razor blade.
  • the dried bleaching layer of Example 4 did, however, adhere to a person's teeth when moistened, although not as well as the bleaching layers of Examples 1-3. This indicates that the bleaching layer of Example 4 might have commercial application as an adhesive layer in a tray-like dental bleaching device to the extent that problems adhering to the barrier layer are overcome or are not an issue.
  • a treatment gel is placed within the frough of a fray-like device of this example, adjacent to an inner surface of the adhesive bleaching layer, to yield a fraylike treatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • the intermediate composition was dry in less than time than the intermediate compositions of Examples 1-4.
  • the inclusion of glycerin helped the bleaching layer remain more flexible and less brittle after drying.
  • the bleaching layer adhered well to each of the polymer sheets.
  • the coated sheets were placed back into the oven overnight.
  • the coated sheets were removed from the oven a second time, cut apart into smaller-sized pieces, and used as strips or shaped into tray-like devices suitable for placement over a person's teeth.
  • the tray-like devices included front and rear side walls that defined a trough having an approximate U- or V-shaped cross section and were curved in the longitudinal dimension to roughly approximate the curvature of a dental arch.
  • a treatment gel is placed within the trough of a fray-like device of this example, adjacent to an inner surface of the adhesive bleaching layer, to yield a tray- like treatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • An initially flowable intermediate composition suitable for use in manufacturing a substantially solid, cohesive, and non-flowable adhesive bleaching layer was formed by mixing together the following components: Carbamide Peroxide 10% Water 21% Ethanol 21% Kollidon VA 64 (M.W.
  • Kollidon VA 64 is a polyvinyl pyrrolidone polymer sold by BASF.
  • the resulting intermediate composition was spread over the surfaces of polyethylene, paraffin, and MYLAR sheets as described in Example 1.
  • the coated sheets were heated in a forced air oven heated to a temperature of 50-70° C. for approximately 45 minutes.
  • the coated sheets were removed from the oven and inspected.
  • the intermediate composition had dried sufficiently so as to form a solid, coherent bleaching layer on the surface of the polymer sheets.
  • the inclusion of polyethylene glycol helped the bleaching layer remain more flexible and less brittle after drying.
  • the bleaching layer adhered well to each of the polymer sheets.
  • the coated sheets were cut apart into smaller-sized pieces and used as strips or shaped into fray-like devices suitable for placement over a person's teeth.
  • the traylike devices included front and rear side walls that defined a trough having an approximate U- or V-shaped cross section and were curved in the longitudinal dimension to roughly approximate the curvature of a dental arch.
  • the fray-like devices and strips adhered almost immediately when placed over a person's teeth.
  • a treatment gel is placed within the frough of a fray-like device of this example, adjacent to an inner surface of the adhesive bleaching layer, to yield a fray- like freatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • the bleaching layer adhered well to each of the polymer sheets.
  • the coated sheets were cut apart into smaller-sized pieces and used as strips or shaped into tray-like devices suitable for placement over a person's teeth.
  • the traylike devices included front and rear side walls that defined a frough having an approximate U- or V-shaped cross section and were curved in the longitudinal dimension to roughly approximate the curvature of a dental arch.
  • the fray-like devices and strips adhered almost immediately when placed over a person's teeth.
  • a freatment gel is placed within the frough of a tray-like device of this example, adjacent to an inner surface of the adhesive bleaching layer, to yield a fraylike treatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • the coated sheets were heated in a forced air oven heated to a temperature of 50-70° C. for approximately 30 minutes.
  • the coated sheets were removed from the oven and inspected.
  • the intermediate composition had dried sufficiently so as to form a solid, coherent bleaching layer on the surface of the polymer sheets.
  • the bleaching layer adhered well to each of the polymer sheets.
  • the coated sheets were cut apart into smaller-sized pieces and used as strips or shaped into fray-like devices suitable for placement over a person's teeth.
  • the traylike devices included front and rear side walls that defined a trough having an approximate U- or V-shaped cross section and were curved in the longitudinal dimension to roughly approximate the curvature of a dental arch.
  • the fray-like devices and strips adhered almost immediately when placed over a person's teeth.
  • a freatment gel is placed within the trough of a fray-like device of this example, adjacent to an inner surface of the adhesive bleaching layer, to yield a traylike treatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • the coated sheets were heated in a forced air oven heated to a temperature of 50-70° C. for approximately 30 minutes.
  • the coated sheets were removed from the oven and inspected.
  • the intermediate composition had dried sufficiently so as to form a solid, coherent bleaching layer on the surface of the polymer sheets.
  • the bleaching layer adhered well to each of the polymer sheets.
  • the coated sheets were cut apart into smaller-sized pieces and used as strips or shaped into fray-like devices suitable for placement over a person's teeth.
  • the traylike devices included front and rear side walls that defined a trough having an approximate U- or V-shaped cross section and were curved in the longitudinal dimension to roughly approximate the curvature of a dental arch. The tray-like devices and strips adhered almost immediately when placed over a person's teeth.
  • a freatment gel is placed within the frough of a fray-like device of this example, adjacent to an inner surface of the adhesive bleaching layer, to yield a fraylike treatment device according to the invention that is very adhesive to a person's teeth and or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • An initially flowable intermediate composition suitable for use in manufacturing a substantially solid, cohesive, and non-flowable adhesive bleaching layer was formed by mixing together the following components: Carbamide Peroxide 10% Ethanol 64% Kollidon VA 90 F (M.W.
  • Aerosil 200 was added as a tackifying agent to promote adhesion of the intermediate composition to the polymer sheets.
  • the coated sheets were heated in a forced air oven heated to a temperature of 50-70° C. for approximately 30 minutes. The coated sheets were removed from the oven and inspected.
  • the intermediate composition had dried sufficiently so as to form a solid, coherent bleaching layer on the surface of the polymer sheets. The bleaching layer adhered well to each of the polymer sheets.
  • the coated sheets were cut apart into smaller-sized pieces and used as strips or shaped into tray-like devices suitable for placement over a person's teeth.
  • the traylike devices included front and rear side walls that defined a trough having an approximate U- or V-shaped cross section and were curved in the longitudinal dimension to roughly approximate the curvature of a dental arch.
  • the tray-like devices and strips adhered almost immediately when placed over a person's teeth.
  • a treatment gel is placed within the frough of a tray-like device of this example, adjacent to an inner surface of the adhesive bleaching layer, to yield a traylike freatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • the bleaching layer adhered well to each of the polymer sheets.
  • the coated sheets were cut apart into smaller-sized pieces and used as strips or shaped into tray-like devices suitable for placement over a person's teeth.
  • the traylike devices included front and rear side walls that defined a trough having an approximate U- or V-shaped cross section and were curved in the longitudinal dimension to roughly approximate the curvature of a dental arch.
  • the fray-like devices and strips adhered almost immediately when placed over a person's teeth.
  • a freatment gel is placed within the trough of a tray-like device of this example, adjacent to an inner surface of the adhesive bleaching layer, to yield a traylike treatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • Example 12 MYLAR sheets as in Example 2.
  • the coated sheets were heated in a forced air oven heated to a temperature of 50-70° C. for approximately 1 hour.
  • the coated sheets were removed from the oven and inspected.
  • the intermediate composition had dried sufficiently so as to form a solid, coherent bleaching layer on the surface of the polymer sheets.
  • the bleaching layer of Example 12 did not adhere well to the MYLAR sheets. It also shrunk somewhat after extended drying.
  • the bleaching layer of Example 12 was able to adhere to a person's teeth when moistened.
  • a freatment gel is placed within the trough of a tray-like device of this example, adjacent to an inner surface of the adhesive bleaching layer, to yield a fray- like treatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • the resulting intermediate composition was spread over the surfaces of polyethylene, paraffin, and MYLAR sheets as described in Example 1.
  • the coated sheets were heated in a forced air oven heated to a temperature of 50-70° C. for approximately 1 hour.
  • the coated sheets were removed from the oven and inspected.
  • the intermediate composition had dried sufficiently so as to form a solid, coherent of bleaching layer on the surface of the polymer sheets.
  • the bleaching layer adhered well to each of the polymer sheets.
  • the coated sheets were cut apart into smaller-sized pieces and used as strips or shaped into fray-like devices suitable for placement over a person's teeth.
  • the traylike devices included front and rear side walls that defined a trough having an approximate U- or V-shaped cross section and were curved in the longitudinal dimension to roughly approximate the curvature of a dental arch.
  • the tray-like devices and strips adhered almost immediately when placed over a person's teeth.
  • a freatment gel is placed within the frough of a tray-like device of this example, adjacent to an inner surface of the adhesive bleaching layer, to yield a fraylike treatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • the coated sheets were cut apart into smaller-sized pieces and used as strips or shaped into tray-like devices suitable for placement over a person's teeth.
  • the traylike devices included front and rear side walls that defined a trough having an approximate U- or V-shaped cross section and were curved in the longitudinal dimension to roughly approximate the curvature of a dental arch.
  • the tray-like devices and strips adhered almost immediately when placed over a person's teeth.
  • a treatment gel is placed within the frough of a tray-like device of this example, adjacent to an inner surface of the adhesive bleaching layer, to yield a tray- like treatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • the coated sheets were cut apart into smaller-sized pieces and used as strips or shaped into tray-like devices suitable for placement over a person's teeth.
  • the traylike devices included front and rear side walls that defined a trough having an approximate U- or V-shaped cross section and were curved in the longitudinal dimension to roughly approximate the curvature of a dental arch.
  • the fray-like devices and strips adhered almost immediately when placed over a person's teeth.
  • a treatment gel is placed within the trough of a fray-like device of this example, adjacent to an inner surface of the adhesive bleaching layer, to yield a traylike treatment- device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • the intermediate composition had dried sufficiently so as to form a solid, coherent bleaching layer on the surface of the polymer sheets.
  • the bleaching layer adhered well to each of the polymer sheets.
  • the coated sheets were cut apart into smaller-sized pieces and used as strips or shaped into tray-like devices suitable for placement over a person's teeth.
  • the traylike devices included front and rear side walls that defined a trough having an approximate U- or V-shaped cross section and were curved in the longitudinal dimension to roughly approximate the curvature of a dental arch. The tray-like devices and strips adhered almost immediately when placed over a person's teeth.
  • a treatment gel is placed within the frough of a tray-like device of this example, adjacent to an inner surface of the adhesive bleaching layer, to yield a fraylike freatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • An initially flowable intermediate composition suitable for use in manufacturing a substantially solid, cohesive, and non-flowable adhesive bleaching layer was formed by mixing together the following components: Carbamide Peroxide 15% Polyvinyl pyrrolidone (M.W.
  • the resulting intermediate composition was spread over the surfaces of polyethylene, paraffin, and MYLAR sheets as described in Example 1.
  • the coated sheets were heated in a forced air oven heated to a temperature of 50-70° C. for approximately 1 hour.
  • the coated sheets were removed from the oven and inspected.
  • the intermediate composition had dried sufficiently so as to form a solid, coherent bleaching layer on the surface of the polymer sheets.
  • the bleaching layer adhered well to each of the polymer sheets.
  • the coated sheets were cut apart into smaller-sized pieces and used as strips or shaped into tray-like devices suitable for placement over a person's teeth.
  • the traylike devices included front and rear side walls that defined a trough having an approximate U- or V-shaped cross section and were curved in the longitudinal dimension to roughly approximate the curvature of a dental arch.
  • the tray-like devices and strips adhered almost immediately when placed over a person's teeth.
  • a freatment gel is placed within the frough of a tray-like device of this example, adjacent to an inner surface of the adhesive bleaching layer, to yield a fraylike treatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a freatment gel is placed adjacent to the adhesive layer of a strip.
  • Carbamide Peroxide 15% Polyvinyl pyrrolidone (M.W. 1.3 million) 32% Water 13.8% Ethanol 20% Glycerin 12% Aerosil 200 5% Calcium EDTA 0.2% Silwet L-7001 2%
  • the resulting intermediate composition was spread over the surfaces of polyethylene, paraffin,
  • the intermediate composition had dried sufficiently so as to form a solid, coherent bleaching layer on the surface of the polymer sheets.
  • the bleaching layer adhered well to each of the polymer sheets.
  • the coated sheets were cut apart into smaller-sized pieces and used as strips or shaped into tray-like devices suitable for placement over a person's teeth.
  • the traylike devices included front and rear side walls that defined a trough having an approximate U- or V-shaped cross section and were curved in the longitudinal dimension to roughly approximate the curvature of a dental arch.
  • the tray-like devices and sfrips adhered almost immediately when placed over a person's teeth.
  • a treatment gel is placed within the trough of a tray-like device of this example, adjacent to an inner surface of the adhesive bleaching layer, to yield a traylike freatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • An initially flowable intermediate composition suitable for use in manufacturing a substantially solid, cohesive, and non-flowable adhesive bleaching layer was formed by mixing together the following components: Calcium Peroxide 20% Carbamide Peroxide 4% Polyvmyl pyrrolidone (M.W.
  • the resulting intermediate composition was spread over the surfaces of polyethylene, paraffin, and MYLAR sheets as described in Example 1.
  • the coated sheets were heated in a forced air oven heated to a temperature of 50-70° C. for approximately 1 hour.
  • the coated sheets were removed from the oven and inspected.
  • the intermediate composition had dried sufficiently so as to form a solid, coherent bleaching layer on the surface of the polymer sheets.
  • the bleaching layer adhered well to each of the polymer sheets.
  • the coated sheets were cut apart into smaller-sized pieces and used as strips or shaped into tray-like devices suitable for placement over a person's teeth.
  • the traylike devices included front and rear side walls that defined a trough having an approximate U- or V-shaped cross section and were curved in the longitudinal dimension to roughly approximate the curvature of a dental arch.
  • the tray-like devices and strips adhered almost immediately when placed over a person's teeth.
  • a treatment gel is placed within the trough of a tray-like device of this example, adjacent to an inner surface of the adhesive bleaching layer, to yield a traylike treatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a freatment gel is placed adjacent to the adhesive layer of a strip.
  • the bleaching layer adhered well to each of the polymer sheets.
  • the coated sheets were cut apart into smaller-sized pieces and used as strips or shaped into tray-like devices suitable for placement over a person's teeth.
  • the traylike devices included front and rear side walls that defined a frough having an approximate U- or V-shaped cross section and were curved in the longitudinal dimension to roughly approximate the curvature of a dental arch.
  • the tray-like devices and strips adhered almost immediately when placed over a person's teeth.
  • a freatment gel is placed within the trough of a tray-like device of this example, adjacent to an inner surface of the adhesive bleaching layer, to yield a traylike freatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • the intermediate composition had dried sufficiently so as to form a solid, coherent bleaching layer on the surface of the polymer sheets.
  • the bleaching layer adhered well to each of the polymer sheets.
  • the coated sheets were cut apart into smaller-sized pieces and used as strips or shaped into tray-like devices suitable for placement over a person's teeth.
  • the tray- like devices included front and rear side walls that defined a frough having an approximate U- or V-shaped cross section and were curved in the longitudinal dimension to roughly approximate the curvature of a dental arch.
  • the tray-like devices and strips adhered almost immediately when placed over a person's teeth.
  • a treatment gel is placed within the frough of a tray-like device of this example, adjacent to an inner surface of the adhesive bleaching layer, to yield a traylike treatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • An initially flowable intermediate composition suitable for use in manufacturing a substantially solid, cohesive, and non-flowable adhesive desensitizing layer was formed by mixing together the following components: Sodium Fluoride 0.25% Polyvinyl pyrrolidone (M.W.
  • the resulting intermediate composition was spread over the surfaces of three types of flexible polymer sheets: polyethylene sheets having a thickness of approximately 0.15 to 0.18 mm; sheets made of paraffin having a thickness of approximately 0.05 to 0.08 mm; and MYLAR sheets having a thickness of approximately 0.38 mm.
  • the intermediate composition was spread using a screeding device.
  • the coated sheets were heated in a forced air oven heated to a temperature of 50-70° C. for approximately 1 hour.
  • the coated sheets were removed from the oven and inspected.
  • the intermediate composition had dried sufficiently so as to form a solid, coherent desensitizing layer on the surface of the polymer sheets.
  • the dried desensitizing composition adhered well to each of the polymer sheets.
  • the coated sheets were cut apart into smaller-sized pieces and used as strips or shaped into tray-like devices suitable for placement over a person's teeth.
  • the tray- like devices included front and rear side walls that defined a frough having an approximate U- or V-shaped cross section and were curved in the longitudinal dimension to roughly approximate the curvature of a dental arch.
  • the tray-like devices and strips were tested by placing them over a person's teeth.
  • the residual saliva present on the tooth surfaces moistened the exposed surface of the desensitizing layer and caused it to become sticky and very adhesive to teeth almost immediately.
  • the tray-like devices and strips were pressed against the teeth, which caused them to conform to the natural irregularities of the dental arch and adhere firmly against the teeth.
  • the desensitizing layer formed in this example comprises an excellent adhesive layer.
  • a freatment gel is placed within the frough of a tray-like device of this example, adjacent to an inner surface of the adhesive desensitizing layer, to yield a fray-like freatment device according to the invention.
  • a freatment gel is placed adjacent to the adhesive layer of a strip.
  • the treatment gel is not heated prior to placing the treatment device over a person's teeth and/or gums, which helps preserves the potency and concentration of the active agent within the treatment gel.
  • the tray-like treatment device (or strip) is worn for varying time periods ranging from several minutes to several hours without becoming dislodged.
  • the desensitizing layer adhered well to the barrier layers comprising polymer sheets.
  • the tray-like devices and strips were tested by placing them over a person's teeth.
  • the residual saliva present on the tooth surfaces moistened the exposed surface of the desensitizing layer and caused it to become sticky and very adhesive to teeth almost immediately.
  • the tray-like devices and strips were pressed against the teeth, which caused them to conform to the natural irregularities of the dental arch and adhere firmly against the teeth.
  • a treatment gel is placed within the trough of a tray-like device of this example, adjacent to an inner surface of the adhesive desensitizing layer, to yield a tray-like treatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a freatment gel is placed within the trough of a tray-like device of this example, adjacent to an inner surface of the adhesive desensitizing layer, to yield a tray-like treatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • a treatment gel is placed within the trough of a tray-like device of this example, adjacent to an inner surface of the adhesive desensitizing layer, to yield a tray-like treatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • a treatment gel is placed within the frough of a tray-like device of this example, adjacent to an inner surface of the adhesive desensitizing layer, to yield a tray-like treatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • a freatment gel is placed within the frough of a tray-like device of this example, adjacent to an inner surface of the adhesive antimicrobial layer, to yield a tray-like freatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • a treatment gel is placed within the frough of a tray-like device of this example, adjacent to an inner surface of the adhesive antimicrobial layer, to yield a tray-like treatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • An initially flowable intermediate antimicrobial composition suitable for use in manufacturing a substantially solid, cohesive, and non-flowable adhesive antimicrobial layer was formed by mixing together the following components: Phenol 3% Polyvmyl pyrrolidone (M.W.
  • the resulting intermediate antimicrobial composition was manufactured into tray-like devices and strips according to the method described in Examples 1 or 22.
  • the antimicrobial layer adhered well to the barrier layers comprising polymer sheets.
  • the tray-like devices and strips were tested by placing them over a person's teeth.
  • the residual saliva present on the tooth surfaces moistened the exposed surface of the antimicrobial layer and caused it to become sticky and very adhesive to teeth almost immediately.
  • the tray-like devices and strips were pressed against the teeth, which caused them to conform to the natural i ⁇ egularities of the dental arch and adhere firmly against the teeth.
  • a freatment gel is placed within the trough of a tray-like device of this example, adjacent to an inner surface of the adhesive antimicrobial layer, to yield a tray-like freatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • a treatment gel is placed within the trough of a tray-like device of this example, adjacent to an inner surface of the adhesive layer, to yield a tray-like treatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • An initially flowable adhesive composition intermediate suitable for use in manufacturing a substantially solid adhesive layer was formed by mixing together the following components: Water 20% Ethanol 30% Glycerin 15% Polyvinyl py ⁇ olidone (M.W.
  • the resulting adhesive composition intermediate was manufactured into tray- like compositions, strips or intermediate devices according to the methods described in Examples 1 or 22.
  • the adhesive layer adhered well to the ba ⁇ ier layers comprising polymer sheets.
  • a freatment gel is placed within the trough of a tray-like device of this example, adjacent to an inner surface of the adhesive layer, to yield a tray-like treatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • a freatment gel is placed within the trough of a tray-like device of this example, adjacent to an inner surface of the adhesive layer, to yield a tray-like treatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • a treatment gel is placed within the trough of a tray-like device of this example, adjacent to an inner surface of the adhesive layer, to yield a tray-like treatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • An initially flowable adhesive composition intermediate suitable for use in manufacturing a substantially solid adhesive layer was formed by mixing together the following components: Ethanol 63.6% Glycerin 9.1% Polyvinyl pyrrolidone (M.W.
  • the resulting adhesive composition intermediate was manufactured into fray- like compositions, strips or intermediate devices according to the methods described in Examples 1 or 22.
  • the adhesive layer adhered well to the ba ⁇ ier layers comprising polymer sheets.
  • a treatment gel is placed within the trough of a tray-like device of this example, adjacent to an inner surface of the adhesive layer, to yield a tray-like treatment device according to the invention that is very adhesive to a person's teeth and or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • An initially flowable adhesive composition intermediate suitable for use in manufacturing a substantially solid adhesive layer was formed by mixing together the following components: Ethanol 44% Polyvinyl py ⁇ olidone (M.W.
  • EXAMPLE 37 An initially flowable adhesive composition intermediate suitable for use in manufacturing a substantially solid adhesive layer was formed by mixing together the following components: Ethanol 31.95% Water 10% Polyvinyl py ⁇ olidone (M.W. > 1 million) 27% Polyvinyl pyrrolidone (M.W. « 60,000) 10% Sodium Lauryl Sulfate 0.5% Glycerin 15% Sucralose (25% solution) 0.5% Peach Flavor 4% Potassium Nifrate 0.8% Sodium Fluoride 0.25% The resulting adhesive composition intermediate was manufactured into tray- like compositions, strips or intermediate devices according to the methods described in Examples 1 or 22. The adhesive layer adhered well to the barrier layers comprising polymer sheets.
  • a treatment gel is placed within the trough of a tray-like device of this example, adjacent to an inner surface of the adhesive layer, to yield a tray-like treatment device according to the invention that is very adhesive to a person's teeth and/or gums.
  • a treatment gel is placed adjacent to the adhesive layer of a strip.
  • the treatment gel was sticky and viscous it was able to adhere and retain the flexible, thin-walled dental tray reasonably well against the person's teeth for a desired period of time (e.g., 1 hour or more).
  • a desired period of time e.g. 1 hour or more.
  • the dental tray of this example was easily dislodged from the person's mouth.
  • the treatment gel was easily expressed out of the dental tray and into the person's oral cavity by normal mouth movements, such as talking, yawning or clenching of teeth.
  • the treatment gel was used to form treatment compositions or devices according to the invention by being placed adjacent to one or more adhesive layers of Examples 30-37. A treatment device was tested by placing it over a person's teeth.
  • the freatment device adhered very strongly to the person's teeth such that it could only be dislodged by intentionally pealing it off the person's teeth.
  • the treatment gel was firmly held between the barrier layer and the person's teeth such that it did not readily spill out of the treatment device and into the person's oral cavity.
  • One reason for this was the much stronger seal between the adhesive layer and the person's teeth than is possible when using the treatment gel and the dental tray only.
  • Another reason was that the strong adhesion between the adhesive layer and the person's teeth greatly diminished the freedom of movement of the treatment device relative to the person's teeth.
  • EXAMPLE 39 A treatment gel suitable for use in manufacturing treatment compositions and devices according to the invention was formed by mixing together the following components: Water 19.2% Edetate Disodium 0.1 % Carbamide Peroxide 18.5% Xylitol C 7% Glycerin 25.4% CARBOPOL 974 5.3% NaOH (50% in water) 4.5% Carboxy Methyl Cellulose 4% Kollidon 90F 10% Peach Flavor 3% Sucralose (25% in water) 3% The resulting treatment gel was extremely thick. The treatment gel was used to form treatment devices according to the invention by being placed adjacent to one or more adhesive layers of Examples 30-37. A treatment device was tested by placing it over a person's teeth.
  • the treatment device adhered very strongly to the person's teeth such that it could only be dislodged by intentionally pealing it off the person's teeth.
  • the freatment gel was firmly held between the barrier layer and the person's teeth such that it did not readily spill out of the freatment device and into the person's oral cavity.
  • EXAMPLE 40 A treatment gel suitable for use in manufacturing freatment compositions and devices according to the invention was formed by mixing together the following components: Water 18% Edetate Disodium 0.1% Carbamide Peroxide 18.5% Sucralose (25% in water) 3% Glycerin 41.6% CARBOPOL 974 5.3% NaOH (50% in water) 4.5% Kollidon 90F 2% Carboxy Methyl Cellulose 4% Peach Flavor 3% The resulting treatment gel had a very good consistency and was able to be easily loaded into a dental fray and then hold the dental tray against a person's teeth. The freatment gel was used to form freatment devices according to the invention by being placed adjacent to one or more adhesive layers of Examples 30-37.
  • a treatment device was tested by placing it over a person's teeth.
  • the treatment device adhered very strongly to the person's teeth such that it could only be dislodged by intentionally pealing it off the person's teeth.
  • the treatment gel was firmly held between the ba ⁇ ier layer and the person's teeth such that it did not readily spill out of the treatment device and into the person's oral cavity.
  • a treatment gel suitable for use in manufacturing treatment compositions and devices according to the invention was formed by mixing together the following components: Water 18% EDTA 0.1% Carbamide Peroxide 22% Sucralose (25% in water) 2% Glycerin 37.1% CARBOPOL 974 5.3% NaOH (50% in water) 4.5% Kollidon 90F 2% Carboxy Methyl Cellulose 5% Peach Flavor 4%
  • the resulting treatment gel had a very good consistency and was able to be easily loaded into a dental tray and then hold the dental tray against a person's teeth.
  • the treatment gel was used to form treatment devices according to the invention by being placed adjacent to one or more adhesive layers of Examples 30-37. A treatment device was tested by placing it over a person's teeth.
  • the treatment device adhered very strongly to the person's teeth such that it could only be dislodged by intentionally pealing it off the person's teeth.
  • the treatment gel was firmly held between the ba ⁇ ier layer and the person's teeth such that it did not readily spill out of the treatment device and into the person's oral cavity.
  • EXAMPLE 42 A treatment gel suitable for use in manufacturing treatment compositions and devices according to the invention was formed by mixing together the following components: Water 18% EDTA 0.1% Carbamide Peroxide 22% Sucralose (25% in water) 2% Glycerin 40.1% CARBOPOL 974 5.3% NaOH (50% in water) 4.5% Kollidon 90F 2% Carboxy Methyl Cellulose 5% Peppermint Oil 1% The resulting treatment gel had a very good consistency and was able to be easily loaded into a dental tray and then hold the dental tray against a person's teeth.
  • the freatment gel was used to form treatment devices according to the invention by being placed adjacent to one or more adhesive layers of Examples 30-37.
  • a treatment device was tested by placing it over a person's teeth.
  • the freatment device adhered very strongly to the person's teeth such that it could only be dislodged by intentionally pealing it off the person's teeth.
  • the treatment gel was firmly held between the barrier layer and the person's teeth such that it did not readily spill out of the treatment device and into the person's oral cavity.
  • EXAMPLE 43 A treatment gel suitable for use in manufacturing treatment compositions and devices according to the invention was formed by mixing together the following components: Water • 22.5% EDTA 0.1% Carbamide Peroxide 18.5% Sucralose (25% in water) 0.75% Glycerin 41.6% CARBOPOL 974 5.3% NaOH (50% in water) 2.25% Polyvinyl Py ⁇ olidone (M.W. > 1 million) 2% Carboxy Methyl Cellulose 4% Flavor (peach, watermelon or peppermint) 3% The resulting treatment gel had a very good consistency and was able to be easily loaded into a dental tray and then hold the dental tray against a person's teeth.
  • the treatment gel was used to form freatment devices according to the invention by being placed adjacent to one or more adhesive layers of Examples 30-37.
  • a freatment device was tested by placing it over a person's teeth. The treatment device adhered very strongly to the person's teeth such that it could only be dislodged by intentionally pealing it off the person's teeth. The freatment gel was firmly held between the ba ⁇ ier layer and the person's teeth such that it did not readily spill out of the treatment device and into the person's oral cavity.
  • EXAMPLE 44 Any of the treatment gels of Examples 38-43 is placed adjacent to an inner surface of any of the adhesive layers of Examples 1-29 in order to form freatment compositions and devices according to the invention.
  • EXAMPLE 45 Any of the treatment gels of Examples 38-43 are modified by adding one or more of a desensitizing agent, remineralizing agent, antimicrobial agent, antiplaque agent, anti-tartar gent, or other medicament in addition to, or instead of at least a portion of, the bleaching agent to yield a freatment gel having desired properties.
  • EXAMPLE 46 Any of the foregoing compositions or devices are modified by including, adjacent to the adhesive layers, one or more dental bleaching or treatment gels disclosed in one or more of the following U.S. patents: U.S. Patent No. 5,376,006: U.S. Patent No. 5,770,182; U.S. Patent No. 5,785,527; U.S. Patent No.
  • EXAMPLE 47 Dental treatment devices are manufactured by placing any of the adhesive compositions or layers according to Examples 1-37 adjacent to a fray, strip or patch comprising a mixture of ethyl vinyl acetate (80%) and polypropylene (20%) and placing a treatment gel according to any of Examples 38-43 and 45-46 adjacent to a surface of the adhesive composition or layer opposite the tray, strip or patch.
  • EXAMPLE 48 Any of the adhesive compositions or layers according to Examples 1-37 is modified by adding an effective amount of one or more bleaching agent activators as discussed elsewhere in the disclosure (e.g., 5% of a an alkali metal or alkaline earth metal base and/or 1% of a metal, metal compound or organo-metallic enzyme) to yield an adhesive activation composition or layer.
  • Adhesive compositions in the examples above that originally included a bleaching agent are modified by omitting the bleaching agent.
  • a treatment composition comprising a bleaching gel if placed adjacent to the adhesive composition of this example, is substantially anhydrous and/or contains a stabilizing agent for the bleaching agent.
  • the combination of the adhesive activation composition or layer and bleaching gel comprises a dental bleaching composition according to the invention.
  • EXAMPLE 49 A bleaching device is manufactured so as to include the dental bleaching composition of Example 48 and a barrier layer adjacent to the adhesive composition or layer.
  • EXAMPLE 50 A bleaching device is manufactured so as to include regions or spots of an adhesive activation composition as set forth in Example 48 interspersed with a treatment gel comprising a bleaching agent according to any of Examples 38-43 and 45-46.
  • the present invention may be embodied in other specific forms without departing from its spirit or essential characteristics.
  • the described embodiments are to be considered in all respects only as illustrative and not restrictive.
  • the scope of the invention is, therefore, indicated by the appended claims rather than by the foregoing description. All changes which come within the meaning and range of equivalency of the claims are to be embraced within their scope. What is claimed is:

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EP04752965A 2003-08-22 2004-05-07 TREATMENT, COMPOSITIONS AND DEVICES WITH A SOLID STAINLESS AND TREATMENT GEL Withdrawn EP1663054A4 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US10/646,443 US7052275B2 (en) 2003-05-27 2003-08-22 Kits and methods for bleaching and desensitizing teeth
US10/692,117 US7011523B2 (en) 2003-10-22 2003-10-22 Bleaching compositions and devices having a solid adhesive layer and bleaching gel adjacent thereto
US10/728,525 US6997708B2 (en) 2003-10-22 2003-12-05 Treatment compositions and strips having a solid adhesive layer and treatment gel adjacent thereto
US10/784,063 US6981874B2 (en) 2003-10-22 2004-02-19 Dental bleaching compositions and devices having a solid activation adhesive layer or region and bleaching gel layer or region
PCT/US2004/016065 WO2005023142A1 (en) 2003-08-22 2004-05-07 Treatment compositions and devices having a solid adhesive layer and a treatment gel

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EP1663054A4 true EP1663054A4 (en) 2009-03-04

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AU (1) AU2004270099A1 (pt)
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KR101248282B1 (ko) 2012-11-06 2013-03-27 한국엔지니어링플라스틱 주식회사 치과용품
WO2014097046A1 (en) * 2012-12-18 2014-06-26 Koninklijke Philips N.V. Seal for teeth whitening trays
EP2964142B1 (en) 2013-03-08 2021-12-22 Ultradent Products, Inc. Dental articles containing wax-thermoplastic elastomer compositions and methods of manufacture and use
US10913853B2 (en) * 2013-10-11 2021-02-09 Ultradent Products, Inc. Wax-based compositions, articles made therefrom, and methods of manufacture and use

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EP1663054A1 (en) 2006-06-07
WO2005023142A1 (en) 2005-03-17
BRPI0413753A (pt) 2006-10-31
JP2007503251A (ja) 2007-02-22
AU2004270099A1 (en) 2005-03-17

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