Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F265/00—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00
  • C08F265/04—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00 on to polymers of esters
  • C08F265/06—Polymerisation of acrylate or methacrylate esters on to polymers thereof
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K6/00—Preparations for dentistry
  • A61K6/80—Preparations for artificial teeth, for filling teeth or for capping teeth
  • A61K6/884—Preparations for artificial teeth, for filling teeth or for capping teeth comprising natural or synthetic resins
  • A61K6/887—Compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S528/00—Synthetic resins or natural rubbers -- part of the class 520 series
  • Y10S528/92—Polymers useful for replacing hard animal tissues, e.g. dentures, bones

Definitions

• This invention relates to a provisional crown-and- bridge resin comprising a powder-liquid restorative system.
• Provisional crown-and-bridge resins are used in the mouth after a dentist has prepared the tooth, as a short- term filling-like structure for the patient to use during the time the laboratory is manufacturing the permanent crown or other prosthesis. Typically these resins are supposed to remain in place for several weeks, but may, in some cases, remain for as long as two years or more.
• the present invention provides a provisional or temporary crown-and-bridge resin based, in most instances, upon an ethyl methacrylate resin and a poly (ethyl methacrylate) powder.
• the material has been made radio- paque by adding barium glass to the poly (ethyl methacrylate) powder.
• the resin usually based on ethyl methacrylate monomer, has a high percentage of tetrahydrofurfuryl methacrylate.
• the tetrahydrofurfuryl methacrylate is the sole resin component, except for some minor ingredients, such as anti-oxident, accelerator, etc.
• the resin also may contain ethoxylated bisphenol A dimethacrylate as a major component.
• the material is easy to handle. It sets into a putty or rubbery stage about 60 seconds to 2 1/2 minutes after activation and sets hard in about 3 1/2 to 6 minutes.
• the invention comprises a liquid or resin and a powder which are mixed in proper proportions, typically in a ratio of about two parts of liquid to seven parts of powder, but this ratio may vary from about two to five parts of powder per part of liquid.
• composition of the liquid resin lies within the following ranges: LIQUID RESIN
• the powder is mixed with the liquid to achieve a thick but still favorable consistency, in an amount by weight of two to five parts of powder per part of liquid, typically in the ratio of seven parts of powder to two parts of liquid.
• the powder may be varied by adding suitable color materials, suitable dyes or pigments so as to match the color of the teeth, especially when used for a portion of a tooth that is to be at the front of the mouth and exposed to viewers. Suitable materials include brown and yellow. dyes, titanium dioxide, cadmium sulfide, and black iron oxide, all used in small amounts.
• Tetrahydrofurfuryl methacrylate 40 Ethyl methacrylate 60 2-hydroxy ⁇ thyl-p-toluidine 0. .5 Powder:
• Powder Same as Example 13. Powder-to-R.esin ratio 3.5:1.0 Liquid Resin Cure Characteristics Example Ratio of A:B Stringy Rubbery Hard 15 1/9 200 sec 220 sec 16 2/8 200 230 17 3/7 170 185 18 4/6 80 180 210 19 5/5 80 175 255 20 6/4 80 135 265 21 7/3 55 100 273 22 8/2 70 100 280 23 9/1 60 135 345 EXAMPLE 24
• the benzoyl peroxide can be used at quantities from about 0.1% to about 5%. As the tertiary amine content decreases, the peroxide should increase.
• the butylated hydroxytoluene can be used in amounts from about 0.01 to about 1.0%.
• Other usable antioxidents include:
• Methyl ether of hydroquinone at about 0.1 to about 5%.
• N,N-dimethyl-p-toluidine at about 1/4-1/2 concentration of 2-HEPT.
• the material has been found to be non-irritative to the gingival tissue, which is very important, and it has excellent stability with virtually no shrinkage on curing, as will be shown below. This enables it to remain in place for periods of even longer duration than are ordinarily expected for the laboratory to make the prosthesis. Its hardness is quite satisfactory. Its toughness enables it to be used for its purpose with very satisfactory results, although it can easily be removed in the same manner as other previously used materials. The fact that it is X-ray. opaque means that it not only can be detected by X-ray but also that it will look normal in the mouth when its appearance must be relied upon. Cure Shrinkage
• a quick and reproduceable measurement of cure- shrinkage of polymeric dental restorative materials may be made with the aid of a quartz-tube dilatometer, such as that manufactured by Tinius-Olsen of Willow Grave, Pa.
• the device comprises a quartz tube into which a quartz rod is fitted.
• a fixture attached to the quartz tube enables positioning and locking of a dial indicator gage.
• a sample is placed into the bottom of the quartz tube, the quartz rod is placed atop the sample, and the dial gage is positioned to a mid-scale reading and locked. Any changes in sample length are recorded with an accuracy of 0.001 mm.
• 3-ml. glass syringes manufactured by MPL Corporation, Chicago IL. These syringes have a silicone-coated glass barrel, two end fixtures of polyethylene, and a silicone rubber plunger. The syringes were modified by removing the plunger and twisting off the rear polyethylene closure.
• Enough material was mixed to fill a syringe to a depth of approximately 10 mm. In practice, some trial and error may be required to determine the correct amount.

Landscapes

• Health & Medical Sciences (AREA)
• Oral & Maxillofacial Surgery (AREA)
• Chemical & Material Sciences (AREA)
• Animal Behavior & Ethology (AREA)
• Public Health (AREA)
• Organic Chemistry (AREA)
• Medicinal Chemistry (AREA)
• Plastic & Reconstructive Surgery (AREA)
• Epidemiology (AREA)
• Life Sciences & Earth Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Health & Medical Sciences (AREA)
• Polymers & Plastics (AREA)
• Veterinary Medicine (AREA)
• Dental Preparations (AREA)
• Stringed Musical Instruments (AREA)
• Polymerisation Methods In General (AREA)
• Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
• Golf Clubs (AREA)
• Developing Agents For Electrophotography (AREA)
• Materials For Medical Uses (AREA)
• Multicomponent Fibers (AREA)
• Investigating Or Analyzing Materials By The Use Of Ultrasonic Waves (AREA)

Priority Applications (2)

Applications Claiming Priority (2)

Publications (1)

Family

ID=22339858

Family Applications (1)

Country Status (8)

Cited By (4)

Families Citing this family (20)

Citations (3)

Family Cites Families (5)

• 1980
  • 1980-01-14 US US06/111,677 patent/US4264489A/en not_active Expired - Lifetime
  • 1980-12-30 EP EP80108252A patent/EP0032249B2/en not_active Expired
  • 1980-12-30 AT AT80108252T patent/ATE6735T1/de not_active IP Right Cessation
  • 1980-12-30 DE DE8080108252T patent/DE3067228D1/de not_active Expired
• 1981
  • 1981-01-02 BR BR8105861A patent/BR8105861A/pt unknown
  • 1981-01-02 JP JP56500699A patent/JPH0261492B2/ja not_active Expired - Lifetime
  • 1981-01-02 WO PCT/US1981/000030 patent/WO1981002022A1/en not_active Ceased
  • 1981-01-13 CA CA000368370A patent/CA1134532A/en not_active Expired

Patent Citations (3)

Non-Patent Citations (1)

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