Method of Bonding Orthodontic Brackets

FIG. 1 is a top plan view of a conventional small base orthodontic bracket of the type which may be used with the method of the present invention.

FIG. 2 is a right side view of the bracket of FIG. 1.

FIG. 3 is a bottom plan view of the orthodontic bracket of FIG. 1.

FIG. 4 is an illustration showing the placement of the light source adjacent the bracket and the tooth during polymerization.

FIG. 5 is an illustration showing the placement of a bracket in cross section using a reinforced bonding technique in accordance with the present invention.

FIG. 6 is a top plan view showing a wide base bracket of the prior art.

FIG. 7 is a top plan view showing another prior art wide base bracket.

As previously discussed, it is the purpose of the present invention to disclose a method for attaching orthodontic brackets to teeth in a manner which permits conventional small based brackets including those of the mesh, dimpled or dovetail type to be used with a photopolymerizable bonding agents in a technique where bonding of the brackets may be accomplished within ten to twenty seconds or less by use of a primarily visible blue light source. Additionally, ceramic, plastic and the newer reduced base metal brackets may also be bonded to teeth using the same photopolymerizable bonding agents and curing techniques. In an effort to give background into the difference between the types of orthodontic brackets which have been developed for use with various bonding agents, reference is made to FIGS. 1-3, 6 and 7 of the drawings.

With specific reference to FIGS. 1-3, a conventional bracket 10 is disclosed having an imperforate base portion 11 and a pair of upstanding wire engaging anchors 13 and 14. The type of orthodontic bracket disclosed in FIGS. 1-3 is similar to one manufactured by Ormco and includes a dimpled or meshed pad 15 which is braised to the base, as shown in FIG. 2, so as to form a generally concave undersurface 16. As noted from the top plan view of FIG. 1, the base portion with the underlying wire mesh braised thereto does not extend significantly beyond the wire anchors or wings 13 and 14. In this regard, the mounting portion of the bracket covers a minimal amount of tooth surface area as compared with the prior art orthodontic brackets shown in FIGS. 6 and 7.

In an effort to obtain quicker bonding time and stronger bonds between dental mounting brackets and teeth, photopolymerized bonding agents have been developed which are cured by the application of light or other radiation within a given wavelength. A problem encountered with such bonding agents is that the agent must be exposed to the light or radiation in order to be cured. In order to make it possible to use the stronger and more quickly cured photopolymers in fixing dental brackets to teeth, prior dental brackets were redesigned to include enlarged base or mounting portions. The enlarged base portions also had openings therethrough to permit light or other radiation to pass therethrough in order to cure a polymeric compound which was applied to the underside of the base and acted as the bonding agent for the bracket.

In FIG. 6, a first type of enlarged base orthodontic bracket 17 is disclosed having a base portion 17 and a pair of upwardly extending wire engaging portions 19 and 20. Although the wire engaging portions 19 and 20 of this bracket are substantially the same dimension as those of the bracket shown in FIGS. 1-3, the base portion 17 extends well beyond the perimeter defined by the upstanding brackets 19 and 20. The outwardly extending base portion permits a plurality of openings 21 to be made around the periphery of the base. The openings permit a polymeric material to pass therethrough as the bracket is pushed against a tooth so that such polymeric material can be directly exposed to light waves or radiation being used to polymerize the polymeric bonding agent.

In FIG. 7, another variation of an enlarged base dental bracket is identified as number 25. This dental bracket includes a base portion 26 which is defined by a wire mesh or screen which is shown as being generally rectangular in configuration (although other configurations including circular may be used) and having a plurality of openings 27 therein. A pair of upstanding wire engaging members 28 and 29 extend upwardly from the base and are of substantially the same size as the upstanding wire engaging flanges discussed with respect to the other dental brackets above. In this embodiment, it is noted that the wire mesh extends well beyond the area defined by the wire engaging portions of the bracket and thus covers a substantially greater area of tooth surface when applied for use. The wire mesh has the same function as the openings discussed with respect to the prior art structure shown in FIG. 6 and permits a polymeric material to be directly exposed therethrough to radiation or light being used to polymerize the same.

The use of photopolymerized or light activated bonding agents is generally preferred in that it permits a thicker composite bonding agent to be used than with conventional bonding techniques. The thicker composite permits the orthodontic bracket to be positioned more accurately and retained in position until curing can be accomplished. The problem still exists, however, with prior art direct and indirect bonding techniques, that such bonding was not or could not be accomplished without increasing the width of the base of the brackets being used. The increase in bracket size has the disadvantages of covering a greater portion of the surface area of the tooth thereby being less desirable in appearance; requiring that more of the tooth area be cleaned after removal of the bracket; and further providing a larger perimeter area in which to trap food and other particles which may lead to surface damage of the tooth.

It has been found, however, that one type of photopolymerizable material offers significant advantages for attaching orthodontic brackets to teeth. This bonding agent includes a resin blend of Bis-GMA reacted with an aliphatic diisocyanate as the primary polymerizing agent. Bis-GMA being the common term for 2,2-bis [4-(2-hydroxy-3-methacryloxypropoxy) phenyl] propane.

The aliphatic diisocyanate is preferably a hexamethylene diisocyanate although other diiocyanates may be used such as other aliphatic and aromatic diisocyanates.

The resin binder compound is blended with a diluent monomer in order to achieve a viscosity of approximately 40,000 to 60,000 centipoise. The diluent monomers are chosen from photopolymerizable monomers including di and tri acrylates such as diethylene, triethylene, or ethylene glycol dimethacrylates and the like. Generally, the ratio of diluent monomer to resin being 1:6 to 1:1.

The binder resin compound and diluent monomer are then blended with a photosensitizing agent which consists of an alpha diketone photosensitizer, an amine reducing agent and an ultraviolet photosensitizer. The alpha diketone should be capable of initiating photopolymerization of the binder resin compound and may preferably be camphoroquinone which is present in an amount of between generally 0.10% to 0.25% by weight with the resin compound, monomer and photosensitizing agent. Benzil and other quinones including naphthoquinone may also be used.

The amine reducing agent need only be present in amounts by weight of 0.30% to 0.60% of the total resin binder, monomer and photosensitizing agent. Various trialkanolamines, and alkyldialkanolamines may be selected although the preferred are N-methyldiethanolamines.

The ultraviolet photosensitizers are present in an amount of between 0.20% to 0.60% by weight of the resin compound, diluent monomer and photosensitizing agent. The ultraviolet sensitizers are selected from benzoin alkyl ethers and especially benzoin methyl, ethyl, isopropyl, and isobutyl ethers.

The above formulation which is a combination of the resin binder compound, diluent monomer and photosensitizing agent will hereinafter be referred to as a liquid bonding mixture. One commercially available liquid bonding agent having the foregoing composition is marketed under the name Prisma-Bond, a product of L. D. Caulk Company.

The liquid bonding mixture is subsequently blended with a filler material of glass particles having sizes of less than 50 microns and preferably less than approximately 10-15 microns with the average being approximately 4-5 microns in order to form a bonding agent compound. The filler is selected from various silicates including barium silicate, and barium aluminum silicate. Quartz and the like may also be used. The filler material should preferably be silanated.

The appropriate pigment to match the color of the teeth being treated may be added to the bonding agent compound. Such pigments may be selected from a number of iron oxide or other acceptable dental pigments. The amount of the filler material may vary with the greater percentage of filler material added to strengthen the overall bonding agent. However, the increased amount of filler material also makes it more difficult to place the composite into the bracket mesh or base and manipulate the bracket prior to curing of the compound. Generally, the filler material should be present in the mixture from between 70%-85% by weight and preferably approximately 76% by weight of the total liquid bonding mixture and filler material.

When selecting the pigment, it should be noted that the lighter the pigment, the faster the curing or polymerization time that will be possible using the method of the invention.

A commercially available photopolymerizable bonding agent compound having the foregoing composition is distributed under the name of Prisma-Fil. Prisma-Fil is a known bonding agent distributed by the L. D. Caulk Company which is polymerized using a visible blue light having primary light emissions waves in approximately 360-500 nanometer range. One type of instrument which is available to optically transmit such blue light in the desired range is marketed under the name of Prisma-Lite also distributed by L. D. Caulk Company. Application of the Prisma-Lite to the preferred bonding compound such as Prisma-Fil will permit the Prisma-Fil to be polymerized within a matter of seconds.

In preparing the teeth for application of a small imperforate base bracket using the photopolymerizable bonding agent compound and method of the present invention, it is first necessary that the surface of the teeth be cleaned such as using a prophy brush with a flour pumice and water solution and then thoroughly rinsed and dried with compressed air. The surface to which the bracket is to be attached is then etched with a conventionally available etching solution and preferably with an etching solution of 50% phosphoric acid neutralized with 7% zinc oxide with applications being made for approximately sixty seconds after which the etching solution is rinsed thoroughly with water and the surface is dried. It should be noted that conventional etching solutions have strength equating to approximately 35%-37% phosphoric acid. Thereafter, the surface of the tooth is treated with the liquid bonding mixture (i.e., Prisma-Bond) discussed above which includes the resin bonding agent, diluent monomers and photosensitizing agent. Any excess liquid is then dried using compressed air. The bonding agent compount (i.e. Prisma-Fil) is then pressed into the base portion of the bracket in a manner to carefully insure that all voids are filled. An additional measure of compound or composite is then added to the previously placed thin layer of composite on the mesh base. Care should be taken when preparing the bracket to avoid, as much as possible, exposure of the bonding agent compound to the surrounding light.

The bracket with the bonding agent composite applied thereto is then placed on the prepared tooth surface and pressure is applied to expel the excess bonding agent compound or composite. The excess bonding agent compound is removed with a tool such as an explorer and the bracket positioned in the appropriate location. Additional pressure is subsequently applied to the bracket, after it is properly positioned, to insure intimate contact between the bracket base and the tooth surface and to expel any possible air or excess composite which may have been trapped therebetween.

It is extremely important that the second application of pressure be applied to force the bracket against the tooth after initial placement. The application of pressure may cause the resin mixture or bonding agent to lower the viscosity of the mixture thereby making the mixture flow better. The result of the second application of pressure will be: First, that a greater degree of agent bonding penetration is achieved with respect to the etched enamel surface of the tooth and the base of the bracket; and second, that a thinner layer of composite will be created between the bracket and tooth. Due to the viscosity of the bonding agent compound or composite, the bracket will not easily shift once it has been applied to the surface of the tooth thereby insuring that the bracket will not drift prior to curing of the bonding compound.

Once the bracket has been applied to the tooth as discussed above, a source of visible light S having principle wave light emissions L in approximately the 360-500 nonometer range is brought in close proximity to the bracket and to the tooth surface face as shown in FIG. 4. Although the process preferably uses a light source in the visible range, a source having visible and/or ultraviolet radiation may be used in some instances. The light source is directed at two angles or placements between the base of the bracket and the surface of the tooth T. It has been found more preferable to direct the light source first along the occlusal aspect of the tooth bracket interface and thereafter directed at a second ang1e along the gingival aspect of the tooth bracket interface. However, the light could be directed from the mesial and distal aspects of the tooth bracket interface as well. It has been found during testing that the light should be directed from two spaced angles for a period of approximately ten seconds. Thereafter the bracket will be bonded to the tooth with such bonding being complete throughout the width of the base even though the upper surface of the base is solid metal or opaque as shown in FIG. 1.

With particular reference to FIG. 5, the method of attaching orthodontic brackets in accordance with the present invention is also adaptable to permit plastic and ceramic brackets to be securely bonded to the surface of a tooth. In FIG. 5, the plastic or ceramic bracket 30 is shown as having a base portion 31 which is secured by a thin layer of bonding agent compound 32 to the surface of the tooth T. As the bond between the base 31 and the surface of the tooth is not as great when using plastic or ceramic materials, the bonding agent compound is applied in excess so as to form a continuous bead 33 which extends over the edge and to the upper surface 34 of the base member of the bracket. After the bead the bonding agent is properly shaped, a light source S is directed in the area between the brackets and tooth interface, to thereby polymerize the bonding agent composite or compound.

In preparing a plastic or ceramic bracket for mounting to the surface of a tooth, the same steps as discussed with respect to the preferred embodiment are followed with the exception that the excess bonding agent compound need not be removed, but is formed into a retaining bead or lock which surrounds the side and upper edge portions of the base of the bracket.

In an effort to make the brackets more appealing, manufacturers are currently marketing metal brackets having even smaller bases than those disclosed in FIGS. 1 through 3. Where it is necessary to increase the bond strength between the bracket and tooth interface because of the relatively small area of contact therebetween, the same bead forming technique discussed above may be used to obtain additional bonding strength and improve the esthetic appearances as well. It should be noted, however, that due to the increased bond strength obtainable using the liquid bonding mixture and bonding agent compound and techniques discussed above, it is possible to secure small base brackets, such as those marketed under the name of Attract, to teeth and obtain strong and lasting bonds.

Prior to the concept of the method of the present invention, it was not believed possible to polymerize a bonding agent mixture or compound such as Prisma-Bond, and Prisma-Fil where such bonding agents were covered by a reflective metal or opaque imperforate surface. It has been found, however, through testing, that not only do these photopolymerizable compounds cure when exposed to the proper light which is directed or aimed between the base of the bracket and the tooth but that the bonds created exceed the bonding strength normally achievable using other photopolymerizable or self-curing compounds and orthodontic bracket applying techniques.

In addition to the benefits obtained using the bonding agent mixture and compound and technique of the present invention, it has also been found that when a mesh based bracket, such as shown in FIG. 3, is removed from the tooth surface that the bonding agent has a tendency to be retained by the mesh material leaving little or no trace deposits of the compounds on the tooth. This makes it possible for the cleanup of the tooth surface to be more easily accomplished as very little composite or compound must be removed from the tooth.

From the foregoing, it can be seen that the method of applying orthodontic brackets in accordance with the teaching of the present invention permits the preferred small base brackets to be used thereby adding significantly to the enhanced appearance of the dental applicance and also reduces the affective area of the tooth which must be covered by the base of the brackets. In addition to the net affects achieved relative to the tooth surface, the present method permits an initial placement of the bracket on a tooth which placement will be insured by the viscosity of the uncured polymerizable compound. Polymerization and bonding of the bracket is thereafter quickly achieved in a period of approximately twenty seconds or less by directing an ultraviolet and/or visible light source from two aspects or sides of the tooth bracket interface thereby curing the bonding agent compound and bonding the bracket securely to the tooth that light sources such as Prisma-Lite, having emissions principally in the 360-500 nanometer range, do not or are not known to cause irritation to the surrounding area of a patient's mouth, gum, eyes or skin, and are not harmful to the pulp of living human teeth.