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Publication numberUS2700636 A
Publication typeGrant
Publication dateJan 25, 1955
Filing dateJan 13, 1953
Priority dateMay 14, 1949
Publication numberUS 2700636 A, US 2700636A, US-A-2700636, US2700636 A, US2700636A
InventorsAshton William Howard
Original AssigneeJohnson & Johnson
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Gum-impregnated dental floss
US 2700636 A
Abstract  available in
Previous page
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Claims  available in
Description  (OCR text may contain errors)

United States Patent 2,700,636 GUM-IMPREGNATED DENTAL FLOSS William Howard Ashton, Philadelphia, Pa., assignor to Johnson & Johnson, a corporation of New Jersey No Drawing. Original application May 14, 1949, Serial No. 93,413, now Patent No. 2,667,443, dated January 26, 1954. Divided and this application January 13, 1953, Serial No. 331,111

7 Claims. 01. 167-93) The present invention relates to dental floss and dental tape impregnated with chemicals for the purpose of increasing the resistance of teeth to deteriorating influences.

The interproximal regions are of particular concern to the dental profession where continual prophylaxis should be maintained to insure greatest resistance to deteriorating conditions. Particles of food (carbohydrates, meat fibers, etc.) are trapped in these regions and often become incapable of removal by natural reflexes. Dental floss or dental tape is used to remove these trapped bodies from these regions where other means such as brushing cannot penetrate. Subsequent disintegration of these food particles, if not removed, provide a media for the growth of detrimental microorganisms which give ofi acids, or enzymes which cause acids, and therefore account for deteriorating conditions in these interproximal regions.

It is, therefore, an object of the invention to incorporate chemical agents in dental floss designed to assist in maintaining conditions which are beneficial to the teeth. More specifically, the invention involves the incorporation or impregnation of dental floss or dental tape, or any similar suitable yarn or tape, with chemicals which will act as medicaments to:

1. Assist in enamel growth and thereby increase resistance to detrimental conditions;

2. Protect enamel or dentine by the preferential coating of insoluble precipitates;

3. React with, neutralize, sequester, buffer, or counteract acids which are present in the saliva or those which are produced therein by bacteria or subsequent enzymatic disintegration of foreign particles lodged in the interproximal regions of the teeth.

Sodium biphosphate up to 20% by weight can be incorporated into yarns to assist in the topical application of this salt to the teeth or their interproximal regions. When a yarn has a coating or a binder such as beeswax, a petroleum wax, a resin, resinous wax-like material or a water soluble wax-like material (e. g., solid ethylene glycol polymer or derivative) this salt may be incorporated in the binder. Water soluble cellulose derivatives such as methyl cellulose or sodium carboxymethyl cellulose are also efiicient binders for yarns impregnated with this salt.

Such salts or mixtures may be incorporated or impregnated in the yarn by dry mechanical impregnation of the powdered salt or mixture; solution in water of the salt and water soluble binder in which the yarn is soaked; mixture of the salt in a molten bath of the binder through which the yarn is drawn and subsequently allowed to cool to permit solidification of the binder and salt mixture.

There has been developed a method of coating the teeth which is felt to produce an impenetrable film over the enamel and thus make it more resistant to attack. This method consists in coating the treated teeth with zinc chloride and subsequently with potassium ferrocyanide which presumably forms an insoluble precipitate of zinc ferrocyanide as a protective coating. The use of zinc chloride has also been investigated. Zinc chloride appears to have an alfinity for the proteolytic components of the teeth.

Zinc chloride or potassium ferrocyanide may be incorporated or impregnated in dental floss or dental tape by the methods described in the above section as well as with any of the binders mentioned.

Chemicals may be incorporated or impregnated in dental floss or dental tape which when forced into the mterproximal regions of the teeth will neutralize, sequester, bufler, or counteract any acids occluded therein.

Compounds which may be used and applied in or onto the yarn or fabric by the above described methods, with olr gvithout any of the binders or mixtures thereof, inc u e:

1. Aliphatic amines, e. g., tricetyl amine; 2. Cyclic amines, e. g., hexamethylene tetramine; 3. Fatty acid amides containing less than 25 carbon atoms, e. g., stearamide; 4. Basic amino acids, e. g., lysine; 5. Polypeptides, e. g., glycylglycine; 6. Inorganic basic salts such as (NH4)2CO3, Na2HPO4,

(NH4)2HPO4, CHsCOONa, KzHPOi, etc.; t 7. Compounds which will give rise to basic products as a result of reaction or disintegration in the interproximal regions, e. g., urea or biuret; 8. Mixtures of any of the above to total 20% of the yarn; 9. The specific combination of urea dibasic ammonium phosphate as disclosed by Kesel; 10. Coating with cellulosic ether amides to act as neutralizing agents.

by weight the manner in which it may be carried into practice,

several specific examples will now be described in detail. It should be clearly understood, however, that these examples are included solely for purposes of illustration and not with the object of delineating the breadth of the mvention or limiting the scope of the appended claims.

Example I.Dry impregnation A. Urea or dibasic ammonium phosphate or any mixtures thereof in the dry state and finely divided condition is impregnated in silk or nylon of 300 to 2500 totaldenier by being mechanically forced into the yarn.

This impregnation is accomplished best by the use of wooden wringer rolls, preferably end grain maple, onto which, or prior to which, the urea dibasic ammonium phosphate is dusted, on the yarn or rollers, or picked up thereby. The vertical pressure of the rollers is adjusted to force the dry urea dibasic ammonium phosphate into the interstices of the yarn depending on the yarn or the torque of the wringer rolls. The impregnation proceeds satisfactorily up to 20% by weight urea dibasic ammonium phosphate based on the weight of the yarn. A desirable degree of impregnation is 3 to 7% on a dry weight basis. Specific mixtures of 5 parts urea to 3 parts dibasic ammonium phosphate are dusted onto the moving wringer rolls, through which a Welded yarn, e. g., Nymo, is drawn.

B. Zinc chloride, potassium ferrocyanide, or any mixtures thereof are impregnated as above described, into dry silk or a welded nylon monocord such as that sold by Belding Heminway Corticelli, under the trade-mark Other fibers are also satisfactory as previously Nymoj: described.

Example lI.-Water solution impregnation mentioned"Ny mo 1s mixture .conslsting of:

20 parts (NHs)2HPO4 20 parts (NHzhCO l -part sodium carboxymethyl cellulose 0.1 part C4H9CH(C2H5).CH2SO4N3 (Te'rgitol O8) 200 parts water .0. The above formulation is used except that in place of sodium carboxymethyl cellulose, one of the following or related binders or mixtures thereof is employed:

(1) Glue (4) Tragacanth (2) Gelatin (5) Gum arabic (3) Methyl cellulose (6) Algin Example Ill-Jmpregnation with waxes A. Medicaments are mixed with molten wax through which theyarnis drawn and the waxcoating containing the salts allowed to set, resulting in a yarn bound with wax containing the medicaments in solid suspension, solid solution, or partial solution. For example, dry crystalline urea, dibasic ammonium phosphate or other solid compounds mentioned previously of 100 mesh or finer is. added to molten beeswax maintained at 10 F. to 50 F. above the setting point. 35-filament end 70 denier or total 1050 denier nylon yarn is drawn through the .wax medicament mixture containing byweight of medicament. A waxed medicament coated yarn results yielding up to 60% coating per weight of untreated yarn.

B. Medicaments are sifted or dusted onto the waxed yarn while wax is still semi-solid or tacky enough to provide adequate adhesion.

A mixture of 5 'parts urea to 3 parts dibasic ammonium phosphate is sifted onto 1050 total denier wax coated nylon yarn at a high enough temperature to maintain the wax soft. Dusting is controlled to give-a salt content of 6% of the total weight of treated yarn. Cooling below its setting temperature sets the-wax on the yarn and the medicaments are distributed thereon.

Another method of treating the above consists in drawingthe'waxed yarn at ahigh enough temperature to maintain the wax soft through a pile of the sifted medicaments.

. Waxes giving suitable adhesion are:

Beeswax- Microcrystalline waxes Synthetic waxes Water-soluble waxes Solid .polyethyleneglycols (Carbowax,) are suitable vehicles and watensolublebinders for impregnated yarns.

Impregnation is efiectedusing a mixture consisting of:

40 parts Carbowax 4000 10 parts =Carbowax 1540 5 "parts (NH2)2CO: (NI-I4) zHPO': :5:3

treated by drawing it through a 4' Example IV.-Resin binders and impregnation Yarns to be impregnated with medicaments using a resinous binder are drawn through a suitable solution of the resin, the solvent serving as a vehicle as well as being volatile. After the resin coating is applied the solvent is evaporated and temperature regulated and velocity of yarn controlled to apply the dry medicaments at a point where the resin is just under cured or still tacky enough to retain the medicaments on the surface of the yarn. Subsequent cooling or baking converts the resin to stable form.

Nylon yarn is drawn through a solution containing 64% water, 31% resorcinol-formaldehyde, 5% formaldehyde at 70 F. The coated yarn is heated at 180 F. for two minutes or until curing has just occurred. Finely divided medicament is then dusted onto the coated yarn or forced therein by rollers resulting in a resin bound and coated yarn treated with medicament. Other resins may be substitutedfor resorcinol-formaldehyde.

It will be apparent to those skilledzin the art that many variations may be made in the procedures .andcompositions described in the foregoing examples,.without departing from the spiritor scope of the inventive concept. I, therefore, intend to be limited only insofar. as required bythe prior art and the appended patent claims.

This is a divisionalapplication of my copending application Serial Number 93,413, filed May 14, 1949, now Patent No. 2,667,443.

The claims are:

1. Dental floss comprising a single strand of material impregnatedwith amedicament mixture of urea and dibasieammonium phosphate in a water-soluble solid gum.

2. Dental floss comprising a single strand of material impregnated with from 0.1% .to 20% by weight of a medicament mixture of urea and dibasic ammonium phosphate inmethyl cellulose.

3. Dental floss .comprisinga single strand of material impregnated with from 0.1%. to 20% by weight of a medicament mixture of urea. and dibasic ammonium phosphate in sodium ,carboxymethyl cellulose.

4. Dental. floss comprising a single strand of material impregnated with a dental medicament ina water-soluble solid gum.

5. Dental floss comprising .a single strand of material impregnated with adental medicament in a water-soluble solid vegetable gum.

6. Dental floss comprising a single strand of material impregnated with adental medicament in a water-soluble solid cellulosic gum.

7. Dental floss comprisinga single strand of material impregnated with a dental medicament in methyl cellulose.

References Cited inthefile of this patent UNITED STATES'PATENTS 185,666 Brown Dec. 26, 1876 1,069,874 Hanscomb Aug. 12, 1913 1,285,988 Gudebrod Nov. 26, 1918 1,839,486 Lawton Jan. 5, 1932 1,989,895 Gilder. Feb. 5, 1935 2,224,489 Rosenbroek Dec. 10, 1940 2,464,755 Taub Mar. 15, 1949 OTHER REFERENCES Seydel, Cotton, vol. (1946), No. 8, pp. 63-66, 69; 13109. 9, pp. 65-69,; No. 11.. Pp. 59-63; No. 12,, PP 82-4,

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Referenced by
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US2772205 *Sep 7, 1954Nov 27, 1956Colgate Palmolive CoDental floss containing higher aliphatic acyl amide of an aminocarboxylic acid compound
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U.S. Classification424/443, 424/54, 424/57
International ClassificationA61K8/02, A61K6/02, A61Q11/00, A61C15/04
Cooperative ClassificationA61Q11/00, A61K6/02, A61C15/041, A61K8/02
European ClassificationA61C15/04B, A61Q11/00, A61K8/02, A61K6/02