US3203097A - Germicidal dental pad - Google Patents
Germicidal dental pad Download PDFInfo
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- US3203097A US3203097A US275511A US27551163A US3203097A US 3203097 A US3203097 A US 3203097A US 275511 A US275511 A US 275511A US 27551163 A US27551163 A US 27551163A US 3203097 A US3203097 A US 3203097A
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- United States
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- germicidal
- wax
- oil
- plasticizer
- gms
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- Expired - Lifetime
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- 230000002070 germicidal effect Effects 0.000 title claims description 30
- 239000000203 mixture Substances 0.000 claims description 37
- 239000004014 plasticizer Substances 0.000 claims description 21
- 239000000463 material Substances 0.000 claims description 19
- 230000036760 body temperature Effects 0.000 claims description 5
- 239000012188 paraffin wax Substances 0.000 claims description 4
- 238000012360 testing method Methods 0.000 description 21
- 239000001993 wax Substances 0.000 description 19
- 239000003921 oil Substances 0.000 description 16
- 235000019198 oils Nutrition 0.000 description 15
- 239000003925 fat Substances 0.000 description 13
- 235000019197 fats Nutrition 0.000 description 13
- 239000002285 corn oil Substances 0.000 description 12
- 235000005687 corn oil Nutrition 0.000 description 12
- 239000004744 fabric Substances 0.000 description 12
- 239000007787 solid Substances 0.000 description 10
- ACGUYXCXAPNIKK-UHFFFAOYSA-N hexachlorophene Chemical compound OC1=C(Cl)C=C(Cl)C(Cl)=C1CC1=C(O)C(Cl)=CC(Cl)=C1Cl ACGUYXCXAPNIKK-UHFFFAOYSA-N 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 241000894006 Bacteria Species 0.000 description 5
- 229960004068 hexachlorophene Drugs 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000011369 resultant mixture Substances 0.000 description 4
- 229920006395 saturated elastomer Polymers 0.000 description 4
- IGQQQAUZPNTQFP-UHFFFAOYSA-N 1-chloro-1-phenylpropan-1-ol Chemical compound CCC(O)(Cl)C1=CC=CC=C1 IGQQQAUZPNTQFP-UHFFFAOYSA-N 0.000 description 3
- 241001465754 Metazoa Species 0.000 description 3
- 235000019483 Peanut oil Nutrition 0.000 description 3
- 229930182555 Penicillin Natural products 0.000 description 3
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 241000191967 Staphylococcus aureus Species 0.000 description 3
- 230000002421 anti-septic effect Effects 0.000 description 3
- CYDMQBQPVICBEU-UHFFFAOYSA-N chlorotetracycline Natural products C1=CC(Cl)=C2C(O)(C)C3CC4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O CYDMQBQPVICBEU-UHFFFAOYSA-N 0.000 description 3
- 229960004475 chlortetracycline Drugs 0.000 description 3
- CYDMQBQPVICBEU-XRNKAMNCSA-N chlortetracycline Chemical compound C1=CC(Cl)=C2[C@](O)(C)[C@H]3C[C@H]4[C@H](N(C)C)C(O)=C(C(N)=O)C(=O)[C@@]4(O)C(O)=C3C(=O)C2=C1O CYDMQBQPVICBEU-XRNKAMNCSA-N 0.000 description 3
- 235000019365 chlortetracycline Nutrition 0.000 description 3
- 235000012343 cottonseed oil Nutrition 0.000 description 3
- 239000002385 cottonseed oil Substances 0.000 description 3
- 239000012467 final product Substances 0.000 description 3
- 239000004006 olive oil Substances 0.000 description 3
- 235000008390 olive oil Nutrition 0.000 description 3
- 239000000312 peanut oil Substances 0.000 description 3
- 229940049954 penicillin Drugs 0.000 description 3
- 230000002062 proliferating effect Effects 0.000 description 3
- 235000015112 vegetable and seed oil Nutrition 0.000 description 3
- 238000009631 Broth culture Methods 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- DCXXMTOCNZCJGO-UHFFFAOYSA-N tristearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 2
- 239000008158 vegetable oil Substances 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
- LHJGJYXLEPZJPM-UHFFFAOYSA-N 2,4,5-trichlorophenol Chemical compound OC1=CC(Cl)=C(Cl)C=C1Cl LHJGJYXLEPZJPM-UHFFFAOYSA-N 0.000 description 1
- GOJCZVPJCKEBQV-UHFFFAOYSA-N Butyl phthalyl butylglycolate Chemical compound CCCCOC(=O)COC(=O)C1=CC=CC=C1C(=O)OCCCC GOJCZVPJCKEBQV-UHFFFAOYSA-N 0.000 description 1
- 241000287828 Gallus gallus Species 0.000 description 1
- PVNIQBQSYATKKL-UHFFFAOYSA-N Glycerol trihexadecanoate Natural products CCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCC PVNIQBQSYATKKL-UHFFFAOYSA-N 0.000 description 1
- 241000699696 Meriones Species 0.000 description 1
- 229930193140 Neomycin Natural products 0.000 description 1
- 235000004347 Perilla Nutrition 0.000 description 1
- 244000124853 Perilla frutescens Species 0.000 description 1
- KIPLYOUQVMMOHB-MXWBXKMOSA-L [Ca++].CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C([O-])[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c1c(O)cccc1[C@@]3(C)O.CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C([O-])[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c1c(O)cccc1[C@@]3(C)O Chemical compound [Ca++].CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C([O-])[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c1c(O)cccc1[C@@]3(C)O.CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C([O-])[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c1c(O)cccc1[C@@]3(C)O KIPLYOUQVMMOHB-MXWBXKMOSA-L 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- VFGRALUHHHDIQI-UHFFFAOYSA-N butyl 2-hydroxyacetate Chemical compound CCCCOC(=O)CO VFGRALUHHHDIQI-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- -1 fatty acid esters Chemical class 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 201000005562 gingival recession Diseases 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229960004927 neomycin Drugs 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 125000001557 phthalyl group Chemical group C(=O)(O)C1=C(C(=O)*)C=CC=C1 0.000 description 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 229940063650 terramycin Drugs 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
- 239000005418 vegetable material Substances 0.000 description 1
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/60—Preparations for dentistry comprising organic or organo-metallic additives
- A61K6/69—Medicaments
-
- 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
- A61K8/0208—Tissues; Wipes; Patches
Definitions
- This invention relates to dental cushions for use with artificial dentures in order to compensate for looseness of fit of the denture, due in the main to gum recession.
- the primary object of the present invention is to provide a dental cushion such as that described in our prior Patents No. 2,664,631, No. 2,897,592, and No. 2,897,593 in which the fabric is impregnated with a wax-plasticizergermicide composition which renders the cushion softer and more pliable and hence more adaptable or conformable to the denture.
- the cushions of our previous patents have proved to be highly successful and are presently in wide use.
- the cushions are not only soft and pliable but are also adaptable and conformable to the denture.
- the cushion of the present invention likewise possesses these properties.
- a satisfactory cushion should possess a requisite tackiness and should be resistant to fraying, crystallization and flasking at body temperautre. In addition it should possess a satisfactory taste, color and appearance.
- Still another object of the present invention is to provide a dental cushion in which the fabric is impregnated with a wax-plasticizer-germicide composition which renders the cushion softer and more pliable and hence more adaptable or conformable to the denture.
- Another object of the invention is to provide a dental cushion of the character described which is more adherent Yet, it is not so
- a further object of the invention is to provide a dental cushion of the character described which is not only pliable but which is also unusually resistant to fraying and to crystallization or flaking.
- a further object of the invention is to provide a novel wax-plasticizer-germicide composition per se which is flake-resistant and pliable at body temperatures and unusually durable, and hence can be applied to fabrics or other fibrous materials for use other than as dental cushions.
- the present invention is applicable todental cushions of varying shapes and especially to the shape and con- 3,203,097 Patented Aug. 31, 1965 ice struction as set forth in Patent No. 2,664,631. Hence special drawings are not deemed necessary for inclusion herein.
- compositions comprising a water-insoluble wax which is combined with a minor amount of a fat or oil plasticizer comprising saturated, unsaturated and partly saturated animal, vegetable and synthetic fats and oils, and an associated germicidal material.
- the germicidal material is present in a quantity such that the final composition exhibits the necessary germicidal characteristics.
- the germicidal material is added to a sufiicient quantity of the fat or oil plasticizer, and the resulting mixture is then incorporated into the Wax which has been previously liquefied under conditions of heat. In this manner, a composition is prepared which yields a satisfactory product upon solidification at room temperature.
- This sequence of preparation is usually preferable as the germicidal material is generally soluble in the plasticizer, and the resultant mixture soluble in the wax.
- the germicidal material is preferably one which is soluble to the extent necessary in the plasticizer employed and whereby the resultant mixture will be compatible with the wax so that the resultant product exhibits the desired properties including the requisite germicidal activity.
- the germicidal compound or composition may be diaphene (ASC4 Brand manufactured by the Stecker Company, Inc., of Ridgewood, New Jersey), acrifiavin, chlorophenyl propanol (Millmaster), penicillin, Aureomycin, streptomycin, Terramycin and neomycin, etc.
- hexachlorophene a compound sold under the trademark G-l 1. It is known chemically as 2,2 methylenebis 3,4,6 trichlorophenol; bis(3,5,6-trichloro-2-hydroxyphenyl)methane; or 2,2-dihydroxy-3,6,3',5, -hexachlorodiphenylmethane.
- the germicidal compound or composition should be present in such a proportion that the resultant mixture or solution exhibits germicidal properties.
- the lower limit of the germicidal material is about 0.01% by weight of total solids although somewhat lower amounts may be employed depending upon the germicidal activity desired in the final product.
- the upper limit of the germicidal material is also dependent upon the desired germicidal properties of the finished product.
- An upper limit of .02% by weight of total solids has proved to be satisfactory under severe test conditions although still greater amounts may be employed and is limited only by considerations of compatibility with the other components.
- the germicidal material is preferably placed in solution in the plasticizer and the resulting mixture placed in solution with the wax. Heat or solvents may be employed where necessary. In this manner the germicidal material is uniformly and thoroughly distributed throughout the Wax.
- the germicidal material may be incorporated in the wax and the plasticizer then added to the resultant mixture. With this sequence of preparation, the final product may be a dispersion. Such a product is still satisfactory so long as the desired germicidal properties are exhibited.
- the fat or oil plasticizer is present in such proportion as to give the requisite softness, pliability and tackiness and is preferably present in a proportion of about 2% by weight of total solids. In the preferred embodiments, this amount of plasticizer is sufiicient to dissolve the germicidal material.
- the fat or oil plasticizer is a saturated, unsaturated or partly saturated animal, vegetable or similar synthetic fat or oil basically comprising a mixture of fatty acids and fatty acid esters (usually triglycerides). These fats and oils are usually subdivided into three groups: solid (mainly stearin), semi-solid (mainly palmitin) and liquid (mainly olein). Animal fats and oils which may be used are beef, chicken and mutton fats and lard.
- Vegetable fats and oils are generally preferred because Examples of satisfactory vegetable materials are corn oil, cottonseed oil, peanut oil, olive oil, flaxseed oil, perilla, oiticica and mixtures thereof. In addition certain hydrogenated materials known as Crisco and Spry have proved to be satisfactory.
- wax-plasticizer-germicide composition Any wax having the desired minimum melting point may be employed in the wax-plasticizer-germicide composition but we have found that the best wax is a 50-50 mixture of Atlantic Refining Company 131 wax and Cities Service Pacemaker D-30.
- Atlantic 131 wax is a low melting, fully refined paraffin wax having the following physical properties:
- the fat or oil plasticizer is'preferably present in a proportion of 2% by weight of total solids, the percentage may vary depending upon the degree of softness and pliability desired in the finished product. In employing the plasticizer in proportion less than 2%, it i preferable that enough plasticizer still be employed so as to completely dissolve the germicidal material. If this is not done, it will be necessary to disperse the germicidal material in the Wax. In this connection a 50-50 mixture of Atlantic 131 wax and Cities Service D-30 as well as other varied blends may be employed.
- the plasticizer and the germicidal material are preferably initially combined and the resulting mixture added to the melted wax with constant agitation and heat Where necessary until thorough dispersion or solution is obtained.
- a relatively thin piece of cloth, such as flannel is dipped in the composition while the latter is still hot and under continuous agitation.
- the coated cloth while hot is conveyed between plates which remove the ex-
- the coated cloth is then air cooled until the composition hardens.
- the excess composition may be manually removed by rolling the cloth while it is impregnated with the hot composition.
- the cloth is then stamped, cut or otherwise formed into U-shaped upper and lower denture cushions as illustrated in Patent No. 2,664,631. The cushions are then nested and packaged for storage and shipment.
- the final product is a cushion which readily conforms to the denture with good adherence thereto while possessing, at the same time, unusual resistance to flaking, fraying and disintegration in the mouth. Attention is called to the fact that while the cushions are sufficiently tacky to adhere to the dentures, they are not so tacky as to adhere one to another during nesting.
- Example I The following tests were run using corn oil as an exemplary fat or oil plasticizer:
- the Alantic and Cities Service waxes used herein are as previously indicated.
- the diaphene employed is Stecker Company ASC4.
- the B-16 employed is Santicizer B-16 disclosed in Patent No. 2,897,593 for use as a plasticizer for wax.
- B-16 is the trade designation of butyl phthalyl butyl glycollate.
- test culture is embodied in a test broth prepared in accordance with the standard F.D.A. procedure.
- the test culture has a 24 hour broth culture, sub-cultured at least six times prior to the test.
- the inoculated loop employed is a 4 mm. ID. loop of platinum wire US. No. 23 B. & S. guage.
- test culture prior to use, must be tested for resistance to phenol and must resist 1-80 phenol for 5 minutes exposure and 1-90 phenol for 15 minutes exposure.
- Cloth such as flannel as previously described of a substantially U-shape was dipped in all of the foregoing mixes including the control to form pads and antiseptic test repeated. Substantially the same results were obtained. Where no corn oil was employed (Mixes 3, 3A, and 6), the diaphene was first incorporated in the wax and the 13-16 added thereafter. 25
- Example II The tests of Example I were run using cotton seed oil, peanut oil and olive oil, and satisfactory results similar to those of Example I were obtained. These pads were checked after several weeks of actual use in the mouth and the test pads were found to possess the essential properties of a newly prepared pad.
- Example 111 Example IV Example I was repeated using .01 and .02% by weight acrifiavin, 25 ppm. Aureomycin, .01 and .02% by weight penicillin and chlorophenyl propanol. Antiseptic tests on these compositions were also quite satisfac- I is further to be noted that a control was run in conjunction with tests of Examples 11, III and IV. The
- Example V Example TV was repeated using .01, .02, .05% by weight hexachlorophene. Antiseptic tests on this formulation yielded excellent results. A control was run in conjunction with the tests of this example, and indicated that the normal growth of bacteria under test conditions is prolific for the control. However, the formulations containing the hexachlorophene exhibited essentially an absence of bacteria growth.
- a cushion for an artificial denture comprising a relatively thin layer of cloth of a substantially U-shape, and impregnated with a composition including a waterinsoluble parafiin wax which does not melt at body temperature a fat or oil plasticizer and an effective amount of a germicidal material compatible with said wax and said plasticizer.
- said fat or oil plasticizer is a vegetable oil.
- said vegetable oil is selected from the group consisting of corn oil, cotton seed oil, olive oil and peanut oil.
- germicidal material is selected from the group consisting of hexachlorophene, diaphene, acrifiavin, chlorophenyl propanol, penicillin and Aureomycin.
- a cushion for an artificial denture comprising a relatively thin layer of cloth of a substantially U-shape and impregnated with a composition including a major portion of water-insoluble paraffin wax which does not melt at body temperature, two per cent by weight of total solids of corn oil and 0.02 percent by weight of total solids of diaphene.
- a cushion for an artificial denture comprising a relatively thin layer of cloth of a substantially U-shape, and impregnated with a composition including a major portion of water-insoluble paraffin wax which does not melt at body temperature, two percent by weight of total solids of corn oil and 0.02 percent by weight of total solids of hexachlorophene.
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Birds (AREA)
- Dental Preparations (AREA)
Description
to the denture because it is tackier. tacky as to prevent separation of the cushions one from another when they are nested in packaged form.
United States Patent 3,203,097 GERMICIDAL DENTAL PAD Julius Hollander, Merion Station, and Bernard S. Sabreen,
Philadelphia, Pa., assignors, by direct and mesne assignments, to The Denver Chemical Manufacturing Company, Stamford, Conn., a corporation of Colorado No Drawing. Filed Apr. 25, 1963, Ser.'No. 275,511 6 Claims. (Cl. 32--2) This application is a continuation-in-part based on ap plication Serial No. 125,391, filed July 20, 1961, now abandoned.
This invention relates to dental cushions for use with artificial dentures in order to compensate for looseness of fit of the denture, due in the main to gum recession.
The primary object of the present invention is to provide a dental cushion such as that described in our prior Patents No. 2,664,631, No. 2,897,592, and No. 2,897,593 in which the fabric is impregnated with a wax-plasticizergermicide composition which renders the cushion softer and more pliable and hence more adaptable or conformable to the denture.
The cushions of our previous patents have proved to be highly successful and are presently in wide use. The cushions are not only soft and pliable but are also adaptable and conformable to the denture. The cushion of the present invention likewise possesses these properties.
Moreover, a satisfactory cushion should possess a requisite tackiness and should be resistant to fraying, crystallization and flasking at body temperautre. In addition it should possess a satisfactory taste, color and appearance.
It has been noted, however, that the prior cushions sometimes exhibited an unpleasant odor upon prolonged or repeated contact and use in the mouth of the wearer. This odor is due to the ordinary bacteria which is usually to be found in the mouth.
It is accordingly an object of the present invention to provide a dental cushion which possesses the desirable properties of previous dental cushions and which in addition will resist the effect of mouth bacteria and retain a pleasant taste and odor in spite of of repeated and protracted use and contact in the users mouth.
Still another object of the present invention is to provide a dental cushion in which the fabric is impregnated with a wax-plasticizer-germicide composition which renders the cushion softer and more pliable and hence more adaptable or conformable to the denture.
Another object of the invention is to provide a dental cushion of the character described which is more adherent Yet, it is not so A further object of the invention is to provide a dental cushion of the character described which is not only pliable but which is also unusually resistant to fraying and to crystallization or flaking.
And yet a further object of the invention is to provide a novel wax-plasticizer-germicide composition per se which is flake-resistant and pliable at body temperatures and unusually durable, and hence can be applied to fabrics or other fibrous materials for use other than as dental cushions.
The present invention is applicable todental cushions of varying shapes and especially to the shape and con- 3,203,097 Patented Aug. 31, 1965 ice struction as set forth in Patent No. 2,664,631. Hence special drawings are not deemed necessary for inclusion herein.
The aforementioned objects and other objects of the invention are obtained by providing a composition comprising a water-insoluble wax which is combined with a minor amount of a fat or oil plasticizer comprising saturated, unsaturated and partly saturated animal, vegetable and synthetic fats and oils, and an associated germicidal material.
The germicidal material is present in a quantity such that the final composition exhibits the necessary germicidal characteristics. The germicidal material is added to a sufiicient quantity of the fat or oil plasticizer, and the resulting mixture is then incorporated into the Wax which has been previously liquefied under conditions of heat. In this manner, a composition is prepared which yields a satisfactory product upon solidification at room temperature. This sequence of preparation is usually preferable as the germicidal material is generally soluble in the plasticizer, and the resultant mixture soluble in the wax.
The germicidal material is preferably one which is soluble to the extent necessary in the plasticizer employed and whereby the resultant mixture will be compatible with the wax so that the resultant product exhibits the desired properties including the requisite germicidal activity.
The germicidal compound or composition may be diaphene (ASC4 Brand manufactured by the Stecker Company, Inc., of Ridgewood, New Jersey), acrifiavin, chlorophenyl propanol (Millmaster), penicillin, Aureomycin, streptomycin, Terramycin and neomycin, etc.
Another germicidal compound which is used in connection with the present invention is hexachlorophene, a compound sold under the trademark G-l 1. It is known chemically as 2,2 methylenebis 3,4,6 trichlorophenol; bis(3,5,6-trichloro-2-hydroxyphenyl)methane; or 2,2-dihydroxy-3,6,3',5, -hexachlorodiphenylmethane.
The germicidal compound or composition should be present in such a proportion that the resultant mixture or solution exhibits germicidal properties. The lower limit of the germicidal material is about 0.01% by weight of total solids although somewhat lower amounts may be employed depending upon the germicidal activity desired in the final product.
The upper limit of the germicidal material is also dependent upon the desired germicidal properties of the finished product. An upper limit of .02% by weight of total solids has proved to be satisfactory under severe test conditions although still greater amounts may be employed and is limited only by considerations of compatibility with the other components.
The germicidal material is preferably placed in solution in the plasticizer and the resulting mixture placed in solution with the wax. Heat or solvents may be employed where necessary. In this manner the germicidal material is uniformly and thoroughly distributed throughout the Wax.
Where the germicidal material is not soluble in the plasticizer, the germicidal material may be incorporated in the wax and the plasticizer then added to the resultant mixture. With this sequence of preparation, the final product may be a dispersion. Such a product is still satisfactory so long as the desired germicidal properties are exhibited.
of superior taste and odor characteristics.
cess to the desired coating thickness.
The fat or oil plasticizer is present in such proportion as to give the requisite softness, pliability and tackiness and is preferably present in a proportion of about 2% by weight of total solids. In the preferred embodiments, this amount of plasticizer is sufiicient to dissolve the germicidal material.
The fat or oil plasticizer is a saturated, unsaturated or partly saturated animal, vegetable or similar synthetic fat or oil basically comprising a mixture of fatty acids and fatty acid esters (usually triglycerides). These fats and oils are usually subdivided into three groups: solid (mainly stearin), semi-solid (mainly palmitin) and liquid (mainly olein). Animal fats and oils which may be used are beef, chicken and mutton fats and lard.
Vegetable fats and oils are generally preferred because Examples of satisfactory vegetable materials are corn oil, cottonseed oil, peanut oil, olive oil, flaxseed oil, perilla, oiticica and mixtures thereof. In addition certain hydrogenated materials known as Crisco and Spry have proved to be satisfactory.
Any wax having the desired minimum melting point may be employed in the wax-plasticizer-germicide composition but we have found that the best wax is a 50-50 mixture of Atlantic Refining Company 131 wax and Cities Service Pacemaker D-30.
Atlantic 131 wax is a low melting, fully refined paraffin wax having the following physical properties:
Melting point, F. (AMP) 127 Saybolt color (ASTM D-l56) +30 Durometer hardness 95 F. Oil percent (ASTM D-72l) 0.6 Penetration 100 F. (suggested TAPPI Semi- Muro Method) 140 Taste and odor a- None Cities Service Pacemaker D-30 is a low melting refined microcrystalline wax having the following physical properties:
Melting point, F. (AMP) 128-130 Saybolt color, min. 28 Tensile, min. 73 F p.s.i. 300 Heat stability min. 180 F. days Oil content, max. percent 0.25 Carbonizable substance Pass Taste and odor Nil Although the fat or oil plasticizer is'preferably present in a proportion of 2% by weight of total solids, the percentage may vary depending upon the degree of softness and pliability desired in the finished product. In employing the plasticizer in proportion less than 2%, it i preferable that enough plasticizer still be employed so as to completely dissolve the germicidal material. If this is not done, it will be necessary to disperse the germicidal material in the Wax. In this connection a 50-50 mixture of Atlantic 131 wax and Cities Service D-30 as well as other varied blends may be employed.
In use, the plasticizer and the germicidal material are preferably initially combined and the resulting mixture added to the melted wax with constant agitation and heat Where necessary until thorough dispersion or solution is obtained. A relatively thin piece of cloth, such as flannel, is dipped in the composition while the latter is still hot and under continuous agitation. The coated cloth while hot is conveyed between plates which remove the ex- The coated cloth is then air cooled until the composition hardens. The excess composition may be manually removed by rolling the cloth while it is impregnated with the hot composition. The cloth is then stamped, cut or otherwise formed into U-shaped upper and lower denture cushions as illustrated in Patent No. 2,664,631. The cushions are then nested and packaged for storage and shipment.
The final product is a cushion which readily conforms to the denture with good adherence thereto while possessing, at the same time, unusual resistance to flaking, fraying and disintegration in the mouth. Attention is called to the fact that while the cushions are sufficiently tacky to adhere to the dentures, they are not so tacky as to adhere one to another during nesting.
The following examples relating to the preparation and testing of various compositions and pads within the scope of the present invention is merely exemplary thereof and is not to be construed in a limiting manner.
Example I The following tests were run using corn oil as an exemplary fat or oil plasticizer:
The Alantic and Cities Service waxes used herein are as previously indicated. The diaphene employed is Stecker Company ASC4. The B-16 employed is Santicizer B-16 disclosed in Patent No. 2,897,593 for use as a plasticizer for wax. B-16 is the trade designation of butyl phthalyl butyl glycollate.
The following were employed.
Mix #1:
124 gms. Atlantic 123 gms. Cities Service 6 gms. corn oil, 0.05 gm. diaphene (0.02%) No B-16 Mix #2:
124 gms. Atlantic 123 gms. Cities Service 6 gms. corn oil, 0.05 gms. diaphene (0.02%) 3 gms. B-16 Mix #3:
124 gms. Atlantic 123 gms. Cities Service 0.05 gm. diaphene (0.02%) added to paraflin 3 gms. B16 No corn oil Mix #3A:
247 gms. Atlantic parafi'in only 0.05 gm. diaphene (0.02%) added to paraflin 3 gms. B-16 No corn oil Mix #4:
124 gms. Atlantic 123 gms. Cities Service 3 gms. corn oil, 0.0 25 gm. diaphene (0.01%) No B-l6 Mix #5:
124 gms. Atlantic 123 gms. Cities Service 3 gms. oil, 0.025 gm. Diaphene (0.01%) 3 gms. B-16 Mix #6:
124 gms. Atlantic 123 gms. Cities Service 0.025 gm. diaphene added to parafiin (0.01%) 3 gms. B16 No corn oil The foregoing mixtures including a control preparation were placed in tubes which were in turn placed in an autoclave, heated to 250 F. for 15 minutes, cooled to 98 F. and then inoculated with one loop each of a 24 hour broth culture Staphylococcus aureus.
Other well known test cultures are:
(a) M. pyogenes a ureus (b) M. pyogenes aurgus (c) M. p yogenes varians a'ureus (F.D.A. Strain No. 209) The test culture is embodied in a test broth prepared in accordance with the standard F.D.A. procedure. The test culture has a 24 hour broth culture, sub-cultured at least six times prior to the test. The inoculated loop employed is a 4 mm. ID. loop of platinum wire US. No. 23 B. & S. guage.
The test culture, prior to use, must be tested for resistance to phenol and must resist 1-80 phenol for 5 minutes exposure and 1-90 phenol for 15 minutes exposure.
The results of the tests are as follows:
- No growth visible. Fair growth. Moderate growth.
+++ Prolific growth.
Cloth such as flannel as previously described of a substantially U-shape was dipped in all of the foregoing mixes including the control to form pads and antiseptic test repeated. Substantially the same results were obtained. Where no corn oil was employed (Mixes 3, 3A, and 6), the diaphene was first incorporated in the wax and the 13-16 added thereafter. 25
The foregoing tests establish that a product of satisfactory color, taste, softness, pliability and tackiness can be prepared which will also exhibit satisfactory germicidal activity.
These pads were checked several weeks of actual use in the mouth and the test pads were found to possess the essential properties of a newly prepared pad.
Example II The tests of Example I were run using cotton seed oil, peanut oil and olive oil, and satisfactory results similar to those of Example I were obtained. These pads were checked after several weeks of actual use in the mouth and the test pads were found to possess the essential properties of a newly prepared pad.
Example 111 Example IV Example I was repeated using .01 and .02% by weight acrifiavin, 25 ppm. Aureomycin, .01 and .02% by weight penicillin and chlorophenyl propanol. Antiseptic tests on these compositions were also quite satisfac- I is further to be noted that a control was run in conjunction with tests of Examples 11, III and IV. The
control indicated that the normal growth of bacteria under test conditions is prolific.
Example V Example TV was repeated using .01, .02, .05% by weight hexachlorophene. Antiseptic tests on this formulation yielded excellent results. A control was run in conjunction with the tests of this example, and indicated that the normal growth of bacteria under test conditions is prolific for the control. However, the formulations containing the hexachlorophene exhibited essentially an absence of bacteria growth.
Obviously many modifications and variations of the present invention are possible in the light of the above teachings. It is, therefore, to be understood that within the scope of the appended claims, the invention may be practiced otherwise than as specifically described.
What is claimed as the invention is:
1. A cushion for an artificial denture comprising a relatively thin layer of cloth of a substantially U-shape, and impregnated with a composition including a waterinsoluble parafiin wax which does not melt at body temperature a fat or oil plasticizer and an effective amount of a germicidal material compatible with said wax and said plasticizer.
2. The invention of claim 1 wherein said fat or oil plasticizer is a vegetable oil.
3. The invention of claim 2 wherein said vegetable oil is selected from the group consisting of corn oil, cotton seed oil, olive oil and peanut oil.
4. The invention of claim 2 wherein said germicidal material is selected from the group consisting of hexachlorophene, diaphene, acrifiavin, chlorophenyl propanol, penicillin and Aureomycin.
5. A cushion for an artificial denture comprising a relatively thin layer of cloth of a substantially U-shape and impregnated with a composition including a major portion of water-insoluble paraffin wax which does not melt at body temperature, two per cent by weight of total solids of corn oil and 0.02 percent by weight of total solids of diaphene.
6. A cushion for an artificial denture comprising a relatively thin layer of cloth of a substantially U-shape, and impregnated with a composition including a major portion of water-insoluble paraffin wax which does not melt at body temperature, two percent by weight of total solids of corn oil and 0.02 percent by weight of total solids of hexachlorophene.
References Cited by the Examiner UNITED STATES PATENTS 1,050,561 1/13 Moore 32-2 2,159,218 5/39 MacLaren 106-245 2,392,513 1/46 Town 32-2 2,664,631 1/54 Hollander et a1. 32-2 3,029,188 4/62 Cyr et al 167-60 RICHARD A. GAUDET, Primary Examiner.
ROBERT E. MORGAN, Examiner.
Claims (1)
1. A CUSHION FOR AN ARTIFICIAL DENTURE COMPRISING A RELATIVELY THIN LAYER OF CLOTH OF A SUBSTANTIALLY U-SHAPE, AND IMPREGNATED WITH A COMPOSITION INCLUDING A WATERINSOLUBLE PARAFFIN WAX WHICH DOES NOT MELT AT BODY TEMPERATURE A FAT OR OIL PLASTICIZER AND AN EFFECTIE AMOUNT OF A GERMICIDAL MATERIAL COMPATIBLE WITH SAID WAX AND SAID PLASTICIZER.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US275511A US3203097A (en) | 1963-04-25 | 1963-04-25 | Germicidal dental pad |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US275511A US3203097A (en) | 1963-04-25 | 1963-04-25 | Germicidal dental pad |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3203097A true US3203097A (en) | 1965-08-31 |
Family
ID=23052627
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US275511A Expired - Lifetime US3203097A (en) | 1963-04-25 | 1963-04-25 | Germicidal dental pad |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3203097A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4808410A (en) * | 1987-12-16 | 1989-02-28 | Richardson-Vicks Inc. | Pharmaceutical compositions containing dyclonine HC1 and phenol |
| WO1990006745A1 (en) * | 1988-12-16 | 1990-06-28 | James Copelan | Disposable personal dental hygiene assembly |
| US5133971A (en) * | 1988-12-14 | 1992-07-28 | Phoebe Copelan | Personal dental hygiene assembly |
| WO1998023205A1 (en) | 1996-11-25 | 1998-06-04 | Mdi Instruments, Inc. | Inner ear diagnostic apparatus and method |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1050561A (en) * | 1908-06-16 | 1913-01-14 | John Moore | Pad for artificial teeth. |
| US2159218A (en) * | 1937-09-25 | 1939-05-23 | Standard Oil Co | Wax |
| US2392513A (en) * | 1942-04-08 | 1946-01-08 | Edward W Town | Cushion for artificial dentures |
| US2664631A (en) * | 1946-11-02 | 1954-01-05 | Hollander Julius | Cushion for artificial dentures |
| US3029188A (en) * | 1958-02-20 | 1962-04-10 | Olin Mathieson | Gelatin adhesive pharmaceutical preparations |
-
1963
- 1963-04-25 US US275511A patent/US3203097A/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1050561A (en) * | 1908-06-16 | 1913-01-14 | John Moore | Pad for artificial teeth. |
| US2159218A (en) * | 1937-09-25 | 1939-05-23 | Standard Oil Co | Wax |
| US2392513A (en) * | 1942-04-08 | 1946-01-08 | Edward W Town | Cushion for artificial dentures |
| US2664631A (en) * | 1946-11-02 | 1954-01-05 | Hollander Julius | Cushion for artificial dentures |
| US3029188A (en) * | 1958-02-20 | 1962-04-10 | Olin Mathieson | Gelatin adhesive pharmaceutical preparations |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4808410A (en) * | 1987-12-16 | 1989-02-28 | Richardson-Vicks Inc. | Pharmaceutical compositions containing dyclonine HC1 and phenol |
| US5133971A (en) * | 1988-12-14 | 1992-07-28 | Phoebe Copelan | Personal dental hygiene assembly |
| WO1990006745A1 (en) * | 1988-12-16 | 1990-06-28 | James Copelan | Disposable personal dental hygiene assembly |
| WO1998023205A1 (en) | 1996-11-25 | 1998-06-04 | Mdi Instruments, Inc. | Inner ear diagnostic apparatus and method |
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