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Publication numberUS2425118 A
Publication typeGrant
Publication dateAug 5, 1947
Filing dateApr 30, 1945
Priority dateApr 30, 1945
Publication numberUS 2425118 A, US 2425118A, US-A-2425118, US2425118 A, US2425118A
InventorsNoyes Stanley E
Original AssigneeNoyes Stanley E
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Dental impression composition
US 2425118 A
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Description  (OCR text may contain errors)

Patented Aug. 5, 1947 DENTAL IMPRESSION COMPOSITION Stanley E. Noyes, Los Angeles, Calif.

No Drawing. Application April 30, 1945, Serial No. 591,221

7 Claims. (01. 18-47) This invention relates to a new dental impression compound and the method of producing the same.

For many dental purposes such as making of full dentures, partial dentures, bridges, etc., it is necessary for the dentist to be able to accurately reproduce portions of the mouth of the subject. Such reproductions often involve the duplication of undercuts of more or less severity, as for instance in the case where a tooth or teeth have been extracted and the adjacent teeth have crowded together.

For many years dental impressions have been taken with materials such as plaster of Paris, or various shellac or wax compositions. These materials have little or no elasticity and. while it is not difficult to take some impressions with them, such as for most full dentures, it is not possible to reproduce accurately undercuts without either breaking the impression and i e-assembling it as is done with plaster, or taking the impression in sections as is the practice in the use ofshellac and Wax compounds. The foregoing methods obviously involve time and there is the danger of inaccuracy, as well as discomfort to the patient.

By the use of an impression material which may be introduced in the mouth in a fluid or plastic condition and cooled to an elastic state, it is possible to take an impression which will accurately reproduce all details of the portion of the mouth under examination, and which due to its elasticity, can be removed from any undercuts present without losing the accuracy of the impression.

Due to the narrow range of temperature which the human mouth can stand, rather strict limitations are placed on the types of elastic materials which can be used. These materials must obviously be either fluid or plastic when they are seated to place in the mouth and must change by cooling to an elastic gel which will permit removal from the undercuts without permanent distortion. They must also either harden to a solid or be a sufficiently tough and rigid gel so that they may be used as molds for models of plaster or other compounds to be poured into them.

My dental impression material is composed of a suitable gel forming agent which may be obtained, for example, from the various marine algae in-'- cluding gigartina, chondrus, bladder wrack, kelp, gracilaria, or agar-agar. If the gel forming agent is alginic acid it may be converted into the form 'of a salt, as for example, sodium alginate, potassium alginate, ammonium alginate or mixtures thereof. The salts of alginic acid are used in the impression material to render the product elastic.

To the gel forming agent then is added a heavy metal silicate such as for example lead silicate or zinc silicate. The exact chemical reaction which takes place on the addition of the lead or zinc silicate to the dental composition is not fully understood but it is definitely known to affect the conversion of the gel forming agent from the soluble to the insoluble form. For example water soluble alkali metal salts of alginic acid are converted over to the insoluble form.

To the foregoing composition then is also added a water soluble phosphate such as sodium, potassium or lithium phosphate sodium hexametaphosphate may also be employed. Sodium tetrapyrophosphate has also been found to be especially satisfactory by reason of its limited solubility in Water.

To the foregoing composition then is also added sodium fiuosilicate, however other silico fluorides may be used as for example zinc, manganese, or calcium.

Zinc nitrate is also added to my composition to produce an insoluble compound with the gel forming constituents such as the alginates. The ordinary commercia] U. S. P. zinc nitrate may be used but in order to control the action of the zinc nitrate it has been found advantageous to pretreat the zinc nitrate in the following manner. The zinc nitrate is first dissolved in a low boiling aliphatic alcohol such as ethyl or methyl alcohol and this solution is evaporated at a temperature of about 200 F. until all of the alcohol present has been vaporized. The resulting residue is then Water Washed, dried and ground. Again it is not understood exactly why the zinc nitrate pretreated in the above manner is aliected. It is definitely known, however, that the Zinc nitrate pretreated with alcohol, as described above is less water soluble and reacts more slowly with the gel forming agent (for example sodium or potassium alginate).

To the above composition there is finally added a filler such as diatomaceous earth, manganese carbonate, or talc which is insoluble in water and which is easily Wetted.

The following is a specific example of my new dental composition: 10 grams of diatomaceous earth, 1.75 grams of sodium fluosilicate, 4.0 grams of sodium or potassium alginate, 6.75 grams of lead silicate, 0.5 gram of sodium tetrapyrophosphate and 0.5 gram of zinc nitrate (either as purchased in the U. S. P. form or pretreated with alcohol as described above) are placed in a finely divided and dry form in a tumbling keg or mixer and mixed until a uniform blend is obtained. This mixing should be so conducted that the temperature in the tumbler or mixing device does not exceed 100 to 110 F., otherwise the final composition may be damaged. The blended material is then withdrawn from the tumbling or mixing device and thoroughly mixed with 50 cubic centimeters of water with a spatula until, a smooth creamy mixture is obtained which sets in a short time to an elastic gel. In practice this creamy mixture is placed in a dental tray which is placed in the mouth of the patient where it sets up in the form of the elastic gel in from three to six minutes. The setting time can be varied by varying the temperature of the Water used. Cold water will retard the set and warm water will hasten it. This control can also be maintained by varying the amount of the powdered composition used in combination with water. The greater amount of powder used in relationshi to the water the more time will be required to obtain the proper set.

An impression containing the above composition can be removed from the mouth after setting without breaking, tearing or distorting and will allow dental stone or plaster of Paris to set hard against its surface with extreme accuracy. This impression material also possesses the quality of not requiring a separating medium or fixing bath before pouring dental stone or plaster of Paris into the impression. Furthermore, it can be stored over a long period without deteriorating.

The specific mixture of ingredients set forth above in the example can be modified without departing from the spirit of the invention.

I claim:

1. A composition of matter comprising an alkali metal alginate, lead silicate and zinc nitrate, which has been dissolved in a lower aliphatic alcohol and recovered therefrom by evaporation of the alcohol.

2. A composition of matter comprising an alkali metal alginate, lead silicate, sodium fiuosilicate and zinc nitrate which has been rendered substantitally insoluble in water by treatment with a lower aliphatic alcohol.

3. A composition of matter comprising an alkali metal alginate, lead silicate, sodium fluosilicate, an inorganic phosphate salt, and zinc nitrate which has been dissolved in ethyl alcohol and recovered therefrom by evaporation of the alcohol.

4. A composition of matter comprising an alkali metal alginate, lead silicate and zinc nitrate which is substantially insoluble in water.

5. A composition of matter comprising a gel forming material selected from the class consistingof alginates and agar-agar, lead silicate and zinc nitrate which has been dissolved in ethyl alcohol and recovered therefrom by evaporation of the alcohol.

6. A composition of matter comprising an alkali metal alginate, a heavy metal silicate, and zinc nitrate which has been dissolved in ethyl alcohol and recovered therefrom by evaporation of the alcohol.

7. A composition of matter comprising an alkali metal alginate, a heavy metal silicate, sodium fiuosilicate, sodium tetra pyrophosphate a filler and zinc nitrate which has been dissolved in ethyl alcohol and recovered therefrom by evaporation of the alcohol at a temperature not substantially in excess of 200 F.


REFERENCES CITED The following references are of record in the file of this patent:

UNITED STATES PATENTS Number Name Date 2,249,694 Wilding July 15, 1941 2,298,835 Noyes Oct. 13, 1942 2,325,051 Gross July 2'7, 1943

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US2249694 *Sep 18, 1939Jul 15, 1941Amalgamated Dental CoMaterial for taking impressions for dental or other purposes
US2298835 *Nov 7, 1941Oct 13, 1942Noyes Stanley EDental impression composition
US2325051 *May 31, 1940Jul 27, 1943White S Dental Mfg CoDental impression compound
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US2568752 *Jul 28, 1947Sep 25, 1951Dental Perfection CompanyDental impression composition
US2678280 *Mar 21, 1952May 11, 1954Dental Perfection CompanyGel point indicating impression materials
US2681860 *Jan 8, 1952Jun 22, 1954Int Nickel CoMold and mold composition
US4608088 *Mar 22, 1984Aug 26, 1986Dento-Med Industries IncorporatedDenture adherent powder
U.S. Classification106/38.51, 106/217.9, 106/205.2, 106/38.35
International ClassificationA61K6/10
Cooperative ClassificationA61K6/10
European ClassificationA61K6/10