WO2000030591A1 - Self etching adhesive primer composition and polymerizable surfactants - Google Patents
Self etching adhesive primer composition and polymerizable surfactants Download PDFInfo
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- WO2000030591A1 WO2000030591A1 PCT/US1999/020945 US9920945W WO0030591A1 WO 2000030591 A1 WO2000030591 A1 WO 2000030591A1 US 9920945 W US9920945 W US 9920945W WO 0030591 A1 WO0030591 A1 WO 0030591A1
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/67—Unsaturated compounds having active hydrogen
- C08G18/671—Unsaturated compounds having only one group containing active hydrogen
- C08G18/672—Esters of acrylic or alkyl acrylic acid having only one group containing active hydrogen
- C08G18/673—Esters of acrylic or alkyl acrylic acid having only one group containing active hydrogen containing two or more acrylate or alkylacrylate ester groups
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/40—Primers
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/331—Polymers modified by chemical after-treatment with organic compounds containing oxygen
- C08G65/332—Polymers modified by chemical after-treatment with organic compounds containing oxygen containing carboxyl groups, or halides, or esters thereof
Definitions
- the invention relates to dental adhesive primers.
- the invention provides a self-etching dental adhesive primer composition and polymerizable surfactants.
- the primer composition is used in a method of coating a water insoluble polymerizable monomer mixture on a tooth or bone substance.
- the primer composition is useful as an adhesive or adhesion promoter to affix dental f ⁇ iling materials or bone cements to tooth material.
- Other uses include forming a protective film on the tooth or bone, or for fixing bone cements in position.
- the composition essentially comprises an emulsion of water immisible polymerizable monomers, oligomers and adhesion promoters in water.
- an emulsion of the polymerizable substances in water the need for volatile organic solvents is avoided and biocompatability is enhanced.
- a further advantage is that independent of the resin phase, the pH of the aqueous phase can be adjusted to provide a self-etching action on the tooth and bone substance, thus enhancing adhesion of the layer to the tooth or bone without requiring a separate etching step.
- the composition preferably further comprises initiators, accelerators, and inhibitors as often used in unsaturated polymerizable mixtures. Further, the composition preferably comprises surfactants and colloidal silica particles to aid in the formulation of an emulsion and to help keep this stable.
- fluoride releasing agents, bactericidal substances or medicinally beneficial materials may also be included in either aqueous or the resin phase of the
- the emulsion will typically contain droplets with diameters of less than 30 microns of the polymerizable monomers, oligomers and adhesion promoters. More preferably most of the droplets have a diameter less than 10 microns. Preferably a portion of the droplets will have a diameter less than 1 micron.
- the film On applying the composition to the tooth or bone substance the film may first be left for a few seconds to allow an etching action to occur. The water may then be gently blown away, whereby the droplets of polymerizable monomers, oligomers and adhesion promoters coalesce to form a continuous film. No washing of the treated surface is required.
- the present invention provides surfactants containing polymerizable monomers for use in compositions.
- the surfactants are able to polymerize into the matrix to become part of the polymer, and are thereby immobilised.
- Applications for surfactants containing polymerizable monomers are wide and varied, and include for instance paints and coatings, inks, and glues, particularly those where the coating, ink, or glue is cured by exposure to light.
- the surfactants of the present invention are useful in dental restorative materials.
- Prior art water-soluble hydrophilic materials form very weak spongy polymers, and have undesirable physical characteristics in the cured film layer.
- the polymerizable resin mixtures and composites used for the repair and replacement of tooth substance, or for the fixation of prosthesis into bone do not adhere of themselves to the tooth or bone substance, and some means is needed to keep them in place. This has long been a problem, and various methods have been developed to overcome it. Initially the attachment method was purely mechanical, and in dental practice large volumes of tooth had to be drilled away to provide sufficient anchorage to keep the filling material in place.
- US Patent 4,514,342 discloses adhesion promoters such as PENTA.
- US Patent 5,645,429 discloses primer and adhesive combined into one formulation.
- a common example is washing-up liquid, which enables water to spread out on a greasy surface, and also helps to keep the loosened globules of fat suspended in the water.
- surfactant There are many types of surfactant, but all consist basically of a hydrophobic part and a hydrophilic part. Both the hydrophobic and hydrophilic parts can comprise either a long chain, or a compact "head". In addition, the hydrophilic part can be either ionic or non- ionic. There are many possible ways of combining these different hydrophobic and hydrophilic parts, leading to a wide range of possible surfactants.
- Another common use of surfactants is in cosmetic creams and medicaments, where they are used to keep for instance paraffin oil or other water insoluble materials suspended in an aqueous base.
- This type of formulation is also known as an oil in water emulsion.
- surfactant By suitable choice of surfactant it is also possible to keep droplets of water suspended and stable in a non water miscible oil, and this is known as a water in oil emulsion.
- surfactants are also often used in paints, glues, and other surface coatings, and sometimes two or more surfactants are used together to provide optimum surface wetting properties as well as optimum emulsion stability. With a paint, or other coating that is intended to dry, it is usually desirable that when the coating is dry, the surfactant is de-activated or immobilised in some way.
- a surfactant is a material which contains both a non polar hydrophobic end and a polar hydrophilic end, and which is able to form an interface between two surfaces of differing polarity.
- surfaces is used broadly when applied to surfactants, and can mean either two solid surfaces, two liquid surfaces, or one solid and one liquid surface. However, not all materials which have both polar and non-polar ends are effective surfactants.
- the non polar end for instance has to be large enough to keep it firmly attached to a non polar solid surface, or to keep it directed towards or within the surface of a non polar liquid surface. Likewise, the polar end has to be large enough to keep it within the polar environment.
- the ratio of the polarity of the hydrophilic end to the non polarity of the hydrophobic end also has to be correct and ideally should be optimised for each application. Because it is often hard to find one single surfactant with the ideal properties, mixtures of two or more surfactants are often used in practical formulations.
- the polar - nonpolar properties of the surfactants are approximately additive, and by choice of a suitable ratio of suitable surfactants a wide range of applications can be covered.
- surfactants are known, for instance those known as the Spans, which consist of esters of long chain fatty acids with sorbitan. By changing the length of the fatty acid and the number attached to the sorbitan group, a range of surfactants with varying properties is obtained.
- Another group of commonly used surfactants are those known as the Tweens. These also consist of esters of fatty acids with sorbitan, but with the addition of a polyethylenoxide chain attached to the sorbitan. By changing the length and number of the fatty acids and also the length of the polyethylenoxide chain, a further range of surfactants is produced.
- surfactants comprises esters of fatty acids directly with polyethylenoxide.
- the surfactants described above all come within the general group known as non - ionic surfactants.
- surfactants may also be produced by combining non-polar groups with polar ionic groups such as phosphates, sulfates, quaternary amines, and carboxylic groups.
- a well known example of this class is sodium lauryl sulphate.
- none of the above surfactants contains an easily polymerisable group which would enable it to be incorporated permanently into the matrix of which it is part.
- Water dispersible polyurethanes containing polyalkylene oxide polyether chains and sulfonate groups are already know, as illustrated in USP 4190566, USP 4303774, and USP 5624758. However these materials do not contain unsaturated polymerizable groups, and are not polymerizable.
- It is an object of the invention to provide a method for coating a tooth comprising forming an emulsion of droplets of water immiscible monomers in water by high shear mixing for at least 5 minutes, applying the emulsion to a surface of a tooth in a patient's mouth and evaporating the water.
- the primer is applied to unetched enamel of a dental tooth and polymerizing the polymerizable material to form a dental product having adhesion to the enamel of more than 13 MPa.
- R represents a polymerizable moiety
- R] is a hydrophobic hydrocarbon moiety
- X is an ether group
- a and b each independently is an integer from 1 to 50
- L' is a linking group capable of linking R to Rj
- L" is a linking group capable of linking Ri to X
- neither L' nor L" is a carbon to carbon bond or an ether group.
- High shear mixing typically uses a mixing blade rotated adjacent to a stationary plate with small holes therethrough.
- the rotating blade of the high shear mixer is rotated at about 22,000 revolutions per minute in a container having a volume of about 500 ml.
- High shear mixing to form compositions in accordance with the invention is preferably for at least 1 minute, more preferably for at least 3 minutes and most preferably for about 5 minutes.
- PENTA dipentaerythritolpentacrylate phosphoric acid ester, prepared according to Example 2 of US Patent 4,816,495.
- G750 For convenience and easy reference herein, the various surfactants have been given a code such as G750, whereby G stands for glycerol dimethacrylate, and 750 is the mean molecular weight of the polyethyleneglycol chain moiety used.
- BHT refers to 2,6-di-tert-butyl-4-methyl phenol.
- FTIR refers to Fourier - Transform Infra red Spectroscopy.
- the invention provides a self etching adhesive dental primer composition, a method of use of the primer composition and a product formed from the primer.
- the dental product is formed from the primer composition which includes water, surfactant and polymerizable material in suspension in the water.
- the polymerizable material includes monomers which are water immiscible. Preferably at least a portion of the monomers have a moiety selected from the group consisting of phosphoryl and a salt of phosphoryl.
- the monomers have an average molecular weight less than 1000.
- the primer is used by applying to unetched dental tooth enamel and the polymerizable material is polymerized to form a dental product having adhesion to the enamel of more than 13 MPa.
- the invention provides polymerizable surfactant compounds within the scope of general formula:
- R represents a polymerizable moiety
- Ri is a hydrophobic hydrocarbon moiety
- X is an ether group
- a and b each independently is an integer of 1, or more and L' is a linking group capable of linking, R to Ri
- L" is a linking group capable of linking Ri to X and neither L' nor L" is a carbon to carbon bond.
- the size of the largest dimension of each droplet of resin in the suspension is preferably less than 30 microns and more preferably less than about 10 microns.
- Such a suspension of a water immisible component in water is generally referred to as an oil-in-water emulsion.
- one or more surfactants or other surface active agents are added either singly or in combination to help keep the suspension stable.
- the restriction of water solubility of the resin is removed, the wide range of monomers commonly used in dentistry can be employed in the present invention, and the physical characteristics of the cured resin layer can adjusted or optimized without restriction.
- the pH of the aqueous phase can be adjusted independently of the resin phase as required.
- a wide range of ethenically unsaturated monomers, polymerization initiators, and surfactants are useful in compositions in accordance with the invention.
- Bond strength to tooth dentin and enamel is measured herein including the Examples as follows:
- Human extracted teeth without significant anatomical alterations, defects or restorations were cleaned and disinfected by soaking in 1% sodium hypochlorite solution for 18 to 24 hours, rinsed, and then stored at from 1 to 8°C in 1% sodium chloride I water (saline solution) until used within six months.
- Teeth were prepared for adhesion to dentin by hand sanding them using wet 300 grit silicon carbide paper, to expose an area of dentin at a plane just below the original interface between the enamel and the dentin. This area was then polished by hand sanding with wet 600 grit silicon carbide paper. The teeth were kept in water until used within 1 to 12 hours. When adhesion to enamel was to be tested, the teeth were chosen so that an approximately flat area of enamel about 5 mm in diameter was present. This area was washed and cleaned using wet 1200 grit silicon carbide powder and a bristle brush rotating in a dental handpiece. The teeth were then used within 6 hours as below.
- the surface to be adhered to was dried lightly with a paper tissue, and the treatment solution or emulsion applied using a felt applicator as supplied by DENTSPLY for 10 to 30 seconds and then the remaining solvent or water was evaporated by gently blowing with a stream of dry oil free air.
- the layer of remaining resin was light cured by irradiating it for ten seconds with light from a dental light curing unit having a minimum output of 350 milliwatt/square centimetre in the 500 to 500 nm wavelength range (for instance a Spectrum curing unit sold by DENTSPLY International Inc. ).
- a portion of plastic straw of 5 mm internal diameter and about 4 mm long was placed end on the prepared surface
- the filling material was cured by irradiating for forty seconds from the exposed end with the dental light.
- the prepared samples were stored for 24 hours in water at 37°C before being thermocycled 500 times between water baths held at 5°C and 55°C with a dwell time in each bath of 20 seconds.
- the thermocycled samples were then left in water at 37°C overnight before being tested in shear using a Zwick universal testing machine model Z010 with a cell having a maximum load of 500 Newtons, a crosshead speed of 1 mm per minute and a 2 mm diameter chisel.
- the chisel has a tip point formed at the lower end by grinding and positioning a planar surface across the end of the cylinder at a 45 degree angle to the central axis of the cylinder. In test position, the tip point of the chisel was applied against the composite. Each tooth was mounted vertically in plaster for the test. A minimum of six samples were prepared for each test, and the mean adhesion was calculated.
- sorbitan monooleate commercially available from many sources including Adrich
- Tween 80 manufactured by Atlas Powder Company
- polyoxyethlene(20)-sorbitan monooleate also available commercially from many sources, including Aldrich.
- Surfactants of the present invention have polymerizable groups such as hydroxyethyl methacrylate, hydroxypropyl methacrylate, glycerol dimethacrylate, pentaerythritol triacrylate and the like which have been attached via urethane linkages and a hexyl, cyclohexyl, pentyl, octyl or other hydrocarbon group moiety to polyethylenegycol chains of varying length and numbers.
- the methacrylate or acrylate moiety (hereafter written as (meth)acrylate) together with the hydrocarbon group moiety form a non polar hydrophobic end, while the polyethyleneglycol chain forms a polar hydrophilic end.
- surfactants with a wide variety of properties may be produced.
- other non polar groups such as fatty acids may also be incorporated to provide an even more hydrophobic end when this is required.
- the polyethyleneglycol chain may further be broken in several short chains if desired.
- a common method of determining the suitability of a surfactant for a particular use is to measure or calculate its HLB value. There are several methods to estimate the HLB value of materials, but for surfactants containing polythylenglycol chains, the HLB value is approximately given by the relationship:
- HLB is equal to the mole percent of hydrophilic group divided by five.
- the HLB value of a material may be approximately calculated by adding together the so called "group number" of the individual chemical groups contained in the compound.
- group number the HLB value is approximately given by the relationship:
- HLB is equal to seven added to the sum of the hydrophilic groups numbers and the sum of the lipophilic group numbers
- the invention provides polymerizable surfactant compounds within the scope of general formula:
- Ri is a hydrophobic hydrocarbon moiety
- X is a ether group, a and b each independently is an integer of 1 , or more and
- L' is a linking group capable of linking, R to Ri
- L" is a linking group capable of linking Ri to X and neither L' nor L" is a carbon to carbon bond.
- the polymerizable surfactants have a multitude of possible uses, they are preferably used as stabilisers for emulsions of water immiscible monomers in water, and also to aid in the spreading out of such monomers onto a hydrophilic surface.
- the emulsions are preferably adhesives and coatings.
- surfactants such as the Tweens and Spans are already available and are capable of providing stable emulsions and aiding in the spreading of monomers on a hydrophilic surface, they are not ideal. As described earlier, these surfactants are not polymerizable and are able to leach out of the cured formulation.
- Isophoronediisocyanate was stirred with 50 grams polyethylene glycol monomethylether 2000 (mean molecular weight 2000) and warmed to about 60°C until the PEGME melted. 0.25 grams Dibutyl tin dilaurate was added and the mixture stirred further. A clear liquid was formed which solidified on cooling. This was warmed again to 65°C, 0.05 grams of BHT was added, followed by adding 5.7 grams of glycerine dimethacrylate. The mixture was heated to 90°C and stirred for about 2 hours, after which an FTIR showed that all the isocyanate had been consumed. The product was a white hard waxy solid, partially soluble in water to give a light foam on shaking. The material had a melting range of about 49 - 51°C. The HLB value is calculated to be approximately 16.
- Example 2 The method of Example 2 was repeated except for the amount of each component, 75 grams polyethylene glycol monomethyl ether with a mean molecular weight of about 5000 was used, together with 3.33 grams of isophorone diisocyanate, 0.1 gram of dibutyl tin dilaurate. After completion of this first reaction, 3.5 grams glycerol dimethacrylate and 0.05 grams BHT were added. As in example 2, the mixture was stirred at 90°C for about 2 hours after which the reaction was complete.
- the polymerizable surfactant (G5000) product was a hard waxy solid, partially soluble in water to give a light foam on shaking. The material had a melting range of about 58 - 60°C. The HLB value was calculated to be approximately 18. Preparation of surfactant HP2000
- Example 4 The reaction of Example 4 was repeated except for using an equimolar amount of monomethyl ether 750 in place of the monomethyl ether 2000 and, due to the lower melting point of the monomethyl ether 750, the mixture was stirred at 50°C instead of 65°C.
- the polymerizable surfactant (HP750) product material formed had a melting range of about 31.4°C - 33.1°C.
- the HLB value was calculated to be approximately 13.
- Example 4 The reaction of Example 4 was repeated except for using an equimolar amount of hydroxyethyl methacrylate in place of the hydroxypropylmethacrylate to form a polymerizable surfactant (HE2000) product.
- the HLB value was calculated to be approximately 17.
- the mixture was stirred and held at 45°C for 2 hours, after which time an FTIR spectrum showed that all of the isocyanate had been consumed. Because the pentaerythritol ethoxylate contains four -OH groups, these still showed strongly in the FTIR spectrum.
- the material was warmed briefly to 60°C to reduce the viscosity and poured out into a bottle.
- the product was a colourless highly viscous honey-like material, which was insoluble in water, but soluble in a range of methacrylate resins.
- the HLB value was calculated to be approximately 7.
- Example 7 The procedure of Example 7 was followed, except that pentaerythritol triallyl ether (3.85 gram) was used in place of the pentaerythritol diacrylate stearate.
- the product was a soft wax like substance.
- the HLB value is calulated to be about 17.
- a mixture of monomers was made up for use as a dental adhesive. This was stirred until it was homogenous.
- Example 13 The method of Example 13 was repeated except that 1 gram (rather than 0.5 gram) of the polymerizable surfactant product formed by following the proecedure of Example 1 was used. An emulsion was easily formed by stirring, but it did not have long term stability.
- Example 13 The method of Example 13 was repeated except that 1 gram of the polymerizable surfactant from Example 2 was used. An emulsion was easily formed which was more stable than that in Example 13, but long term stability over a period of several weeks was still not obtained. A light foam formed on the surface of the emulsion.
- Example 13 The method of Example 13 was repeated except that 1.5 grams (rather than 0.5 grams of the product formed in Example 1) of the polymerizable surfactant formed by following the proecedure of Example 2 was used. An emulsion was easily formed, and stability was better than with Example 15. A light foam formed on the surface of the emulsion.
- Example 13 The method of Example 13 was repeated except that 2 grams of the polymerizable surfactant from Example 2 was used in place of the polymerizable surfactants formed by following the procedures of Example 1. An emulsion was easily formed. A light foam formed on the surface of the emulsion. The emulsion was stable for extended periods of more than 1 month.
- Example 10 10 grams of the resin from Example 10 and 40 grams of the water added. The mixture was shaken briefly, after which a white emulsion was obtained. This was treated for 5 minutes with ultrasound, and then for 5 minutes with a Ultra Torrax high speed mixer. No foaming was observed, but a creamy layer formed on the surface of the emulsion.
- Example 20 The procedure of Example 20 was followed except that the enamel was treated with 36% phosphoric acid solution for 30 seconds, washed, and then dried before the procedure of Example 20 was carried out on the enamel. Results are given in Table 1.
- compositions of Examples 11 and 12 provide adhesion to unetched enamel of 13.9 MPa and 14.5 MPa (maximum value 23.2 MPa), almost twice as high as the 7.9 MPa of the composition of Example 20 (maximum value 11.6 MPa). This approaches the value of 19.35 MPa obtained in Example 21 when the enamel was separately etched, and demonstrates a self-etching action on enamel taking place in the procedures of Examples 11 and 12.
- Example 22 4 grams of the material prepared by following the procedure of Example 22 and 19 grams of the mixture prepared by following the procedure of Example 10 were warmed and mixed together to give a homogenous liquid. 18 grams of water was added and the mixture shaken to give a white emulsion. This was treated with ultrasound for five minutes, then reshaken. The emulsion was then further treated for five minutes with a high shear mixer. The resulting emulsion, containing about 43% resin part, was stable and showed no signs of separation. The droplet size was measured and found to have a mean size of 1.5 microns with 90% of the droplets below 2.9 microns.
- Example 7 The material formed by following the procedure of Example 7 (the adduct between polyethyleneglycol 2000 monomethyl ether, isophorone diisocyante, and pentaerythritol diacrylate stearate)(lgram), and 10 grams of the mixture formed by following the procedure of Example 10 were warmed and mixed together until homogenous. [2-(methacryloyloxy)ethyl]trimethylammonium chloride (75% aqueous solution, available from Aldrich) (1.33 grams) and 18 grams of water were added and the mixture shaken vigorously. After treatment with ultrasound the mixture was then treated with a high shear mixer for 5 minutes. The resin part quickly separated out when stirring ceased and a stable emulsion could not be achieved. Since a stable emulsion was previously easily prepared using the material from Example 7, this illustrates the strong destabilizing effect of quaternary amines in this composition.
- Example 17 The method of Example 17 was repeated except that 0.1 grams of cetylamine hydrofluoride was dissolved in the resin mixture before addition of the water. In this case the resin part quickly separated out and, unlike Example 17, a stable formulation was not achieved. This again illustrates the strong destabilizing effect of quaterniary amines.
- Example 13 The method of Example 13 was repeated except that 2 gram of polyethylenglycol monomethyl ether 2000 was used in place of the polymerizable surfactant. However the resin phase separated from the water as soon as mechanical agitation ceased, and it was not possible to obtain an emulsion. This demonstrates that the polyethylenglycol monomethyl ether 2000 itself is not a suitable emulsifier in this application.
- a self etching adhesive dental primer composition comprising water, surfactant and polymerizable material in suspension in the water.
- the polymerizable material comprises monomers.
- the monomers are water immiscible. At least a portion of the monomers have a moiety selected from the group consisting of phosphoryl and a salt of phosphoryl.
- the monomers have an average molecular weight less than 1000.
- the composition includes polymerization initiators, such as camphorquinone.
- the composition includes polymerization accelerators, such as tertiary amine compounds.
- the size of the individual droplets of polymerizable monomer suspended in the water is less than thirty microns.
- the polymerization initiator and accelerator are contained within separate suspended droplets of the water immiscible polymerizable monomer or mixture of monomers.
- the monomers are dispersed within droplets having a largest droplet dimension less than 30 microns. More preferably, the monomers are dispersed within droplets having a largest droplet dimension less than 10 microns.
- a method for coating a tooth comprising forming an emulsion of droplets of water immiscible monomers in water by high shear mixing for at least 5 minutes, applying the emulsion to a surface of a tooth in a patient's mouth and evaporating the water.
- the emulsion of water immiscible monomer in water comprises a self etching adhesive primer dental composition for coating tooth substance or bone comprising water, surfactant and a suspension in the water of a water immiscible polymerizable monomers at least a portion of the monomers having an average molecular weight less than 1000.
- the emulsion of water immiscible monomers comprise PENTA.
- a self-etching adhesive dental primer formed by high shear mixing for at least 5 minutes.
- the primer is a self etching adhesive primer dental composition for coating tooth substance or bone comprising water, surfactant and a suspension in the water of a water immiscible polymerizable monomers having at least a portion of the monomers having an average molecular weight less than 1000.
- a dental product formed by providing a self etching adhesive dental primer composition, comprising water, surfactant and polymerizable material in suspension in said water, the polymerizable material comprising monomers which are water immiscible, at least a portion of the monomers having an average molecular weight less than 1000, applying the primer to unetched enamel of a dental tooth and polymerizing the polymerizable material to form a dental product having adhesion to the enamel of more than 13 MPa.
- polymerizable dental restorative material is applied to the dental product.
- a self etching adhesive dental primer product made by the process comprising high shear mixing a composition, comprising water, surfactant and polymerizable material in suspension in the water.
- the polymerizable material comprises monomers.
- the monomers are water immiscible.
- Preferably at least a portion of the monomers have a moiety selected from the group consisting of phosphoryl and a salt of phosphoryl.
- the monomers have an average molecular weight less than 1000 to form a self-etching adhesive dental primer product consisting essentially of a suspension of droplets of polymerizable material in water.
- the droplets have a largest dimension less than 50 microns.
- the suspension is stable for at least one month at 23°C.
- a preferred embodiment of the invention provides a method of simultaneously etching and priming previously unetched tooth enamel which consists essentially of providing a self etching adhesive dental primer composition, comprising water, surfactant and polymerizable material in suspension in the water.
- the polymerizable material comprises monomers.
- the monomers are water immiscible.
- Preferably at least a portion of the monomers have a moiety selected from the group consisting of phosphoryl and a salt of phosphoryl.
- the monomers have an average molecular weight less than 1000.
- the self-etching primer is applied to unetched tooth enamel.
- the polymerizable material is polymerized to form a dental product having adhesion to the enamel of more than 13 MPa.
- the tooth to which the primer is applied is in a patient's mouth.
- R is a polymerizable group or groups such as acrylate, methacrylate, vinyl, or vinyl ether
- Ri is a non polar hydrocarbon moiety such as cyclohexane, isophorone, hexane, trimethylhexane, octane,
- L' and L" are linking groups, such as ester, urethane, amide, or ether, and may be the same or different
- X is a hydrophylic group such as polyethylene oxide, polythethyleneglycol, pentaerythritol, pentaerythritol ethoxylate and derivatives of the forgoing.
- the number of polymerizable groups (a) must be at least 1, and preferably 2 or more.
- the multiplier (b) should be such that the total of the X groups have a polarity and water solubilising ability at least equivalent to about four -[CH2-CH2-O]- groups.
- (b) is more preferably at least 10.
- the hydrophobic group X can comprise either a single chain as for example in polyethylenglycol, or multiple chains attached to one central atom as in pentaerythritol ethoxylate.
- the groups R, R ls and X can be joined together by methods to join the groups, for example ester, urethane, ethers, or amides linkages can be used within the scope of the present invention.
- R is glycerol dimethacrylate where (a) is 2, L' and L" are urethane links, R ⁇ is isophorone, and X is -[CH2-CH2-O]- with (b) approximately 17.
- One of the possible isomers is shown in general structure II below, where n is approximately 17 and R IV is methyl . When n is approximately 45, the structure shows one possible isomer of the invention of Example 2, while with n approximately equal to 113 a possible isomer of the invention of Example 3 is illustrated. It is understood by those skilled in the art that in reactions such as these, a mixture of products is formed which also contains a mixture of isomers. The reaction conditions can be adjusted for production of the desired compound and isomer, but totally pure compounds with precisely defined structures are usually not obtained.
- the structures below serve to illustrate compounds within the scope of general structure II.
- Example 4 HP2000, R is hydroxypropylmethacrylate where L' and L" are urethane links, Ri is isophorone, X is -[CH2-CH2-O]- and a is 1, and b approximately 45. Possible isomers of this structure are within the scope of the following general formula III:
- Example 5 The product of Example 5 is within the scope of the structure within the scope of formula III wherein one of R', R" or R'" is methyl, and the others are H, R IV is methyl and n is approximately 17.
- group P can comprise multiply unsaturated moieties such as pentaerythritol triacrylate, pentaerythritol diacrylate stearate, pentaerythritol triallyl ether.
- Preferred compounds within the scope of the general Formula I are compounds within the scope of general formula IV:
- R is H or a carbohydryl group having from 1 to 6 carbon atoms and n is an integer from to 10 to 50.
- R is vinyl ether.
- X comprises -(CH -CH -O) m - groups wherein m is an integer from 10 to 50.
- L' and L" are urethane linkages.
- P is methacrylate or acrylate
- X comprises -
- compounds within the scope of the general formula V is produced by reaction between a hydroxyl (meth)acrylate, a diisocyanate, and a hydroxyl terminated compound selected from the group consisting of polyethyleneoxide and polyethyleneglycol.
- hydroxyl acrylate comprises hydroxy propyl methacrylate.
- the diisocyanate comprises isophorone diisocyanate.
- the hydroxyl acrylate is hyroxyl methacrylate.
- the hydroxyl terminated compound comprises polyethyleneglycol monomethyl ether.
Abstract
Description
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Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2000583476A JP2002530308A (en) | 1998-11-23 | 1999-09-13 | Self-etching adhesive primer composition and polymerizable surfactant |
AU62468/99A AU767362B2 (en) | 1998-11-23 | 1999-09-13 | Self etching adhesive primer composition and polymerizable surfactants |
EP99949633A EP1133272A1 (en) | 1998-11-23 | 1999-09-13 | Self etching adhesive primer composition and polymerizable surfactants |
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US09/198,315 US6387982B1 (en) | 1998-11-23 | 1998-11-23 | Self etching adhesive primer composition and polymerizable surfactants |
US09/198,315 | 1998-11-23 |
Publications (1)
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WO2000030591A1 true WO2000030591A1 (en) | 2000-06-02 |
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Family Applications (1)
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PCT/US1999/020945 WO2000030591A1 (en) | 1998-11-23 | 1999-09-13 | Self etching adhesive primer composition and polymerizable surfactants |
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US (1) | US6387982B1 (en) |
EP (1) | EP1133272A1 (en) |
JP (1) | JP2002530308A (en) |
AU (1) | AU767362B2 (en) |
WO (1) | WO2000030591A1 (en) |
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US7666593B2 (en) | 2005-08-26 | 2010-02-23 | Helicos Biosciences Corporation | Single molecule sequencing of captured nucleic acids |
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Also Published As
Publication number | Publication date |
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JP2002530308A (en) | 2002-09-17 |
AU767362B2 (en) | 2003-11-06 |
US6387982B1 (en) | 2002-05-14 |
EP1133272A1 (en) | 2001-09-19 |
AU6246899A (en) | 2000-06-13 |
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