Polyvinylsiloxane based curable dental retraction composition

Patent metadata

Field	Value
Publication number	US-9044288-B2
Application number	US-201314133703-A
Country	US
Kind code	B2
Filing date	Dec 19, 2013
Priority date	Dec 19, 2012
Publication date	Jun 2, 2015
Grant date	Jun 2, 2015

Abstract

Disclosed herein is a two part retraction system that can be inserted into the sulcus to form a semi-rigid porous elastomer releasing a hemostatic agent suitable for sulcus retraction such that a dental impression may be completed by a dental practitioner.

First claim

I claim:

1. A two part retraction system comprising:
a base paste and a catalyst paste, wherein
the base paste comprises (1) a crosslinker capable of releasing hydrogen gas upon combination with the catalyst paste having a hydrosilation catalyst at room temperature, (2) a vinyl fluid, (3) a non-reinforcing filler, (4) a reinforcing filler, (5) optionally a hydroxy terminated polydimethylsiloxane, and (6) optionally a hydrophilic additive, and
the catalyst paste comprises (1) a vinyl fluid, (2) a hemostatic agent, (3) a non-reinforcing filler, (4) a reinforcing filler, (5) a platinum complex hydrosilation catalyst, and (6) a retarder,
wherein the hemostatic agents is ferric sulfate, ferric chloride, a mixture of ferric sulfate and ferric chloride, permanganates, zinc chloride or a water soluble astringent aluminum salt.

2. The two part retraction system of claim 1 , wherein the crosslinker has a hydrogen content of at least 7 mmol/g.

3. The two part retraction system of claim 1 , wherein the crosslinker is polymethylhydrosiloxane.

4. The two part retraction system of claim 1 , wherein the water soluble astringent aluminum salt is potassium aluminum sulfate (AlKSO4), aluminum ammonium sulfate, aluminum sulfate, aluminum chlorohydrate, aluminum acetate, or a mixture thereof.

5. The two part retraction system of claim 1 , wherein the hydrophilic additive is potassium polyacrylate, sodium polyacrylate, or siloxylated polyethers.

6. A method of retracting a sulcus of a patient, the method comprising applying a two-part retraction system that expands upon curing using a dispensing device having about a 1 mm outside diameter that can be inserted into the sulcus to form a semi-rigid foam cord, and slowly withdrawing the dispensing device while emptying the two part retraction composition,
the two-part retraction composition comprising a base paste and a catalyst paste, wherein
the base paste comprises (1) a crosslinker capable of releasing hydrogen gas upon combination with the catalyst paste having a hydrosilation catalyst at room temperature, (2) a vinyl fluid, (3) a non-reinforcing filler, (4) a reinforcing filler, (5) optionally a hydroxy terminated polydimethylsiloxane, and (6) optionally a hydrophilic additive, and
the catalyst paste comprises (1) a vinyl fluid, (2) a hemostatic agent, (3) a non-reinforcing filler, (4) a reinforcing filler, (5) a platinum complex hydrosilation catalyst, and (6) a retarder;
the dispensing device comprising first and a second longitudinally juxtaposed barrels; each said barrel having a first and a second end; each said first and second barrels having a quantity of at least one of the materials initially contained therein; each said barrel having an open end and a dispensing end; a sealing plunger disposed in each said barrel such that the material in each said barrel is initially positioned between said dispensing end of said barrels and the respective ones of said sealing plungers; a snap cap contiguously formed to initially close each of said dispensing ends of said barrels; such that said snap cap may be broken from said barrels to form a secondary open end at said dispensing end of said barrels, thereby facilitating the material contained in each said barrel to flow through and be dispensed; wherein the dispensing ends and the snap cap form a neck area as a section of reduced thickness which is defined by a V-groove that runs around the perimeter of the neck area in a figure 8 shape, whereby the V-groove acts to concentrate the stress across the neck in such a way that said snap cap may be broken from said barrels along a breaking plane; wherein said snap cap includes a tab portion opposite the neck area, the tab portion being of a sufficient size to allow a user to apply enough leverage to the tab portion to break said snap cap at the section of reduced thickness.

7. A two part retraction system comprising:
a base paste and a catalyst paste, wherein
the base paste comprises (1) a crosslinker capable of releasing hydrogen gas upon combination with the catalyst paste having a hydrosilation catalyst at room temperature, (2) a vinyl fluid, (3) a non-reinforcing filler, (4) a reinforcing filler, (5) optionally a hydroxy terminated polydimethylsiloxane, and (6) optionally a hydrophilic additive, and the catalyst paste comprises (1) a vinyl fluid, (2) a non-reinforcing filler, (3) a reinforcing filler, (4) a platinum complex hydrosilation catalyst, and (5) a retarder, and
wherein at least one of the base paste or the catalyst paste further includes an encapsulated hemostatic agent.

8. The two part retraction system of claim 7 , wherein the crosslinker has a hydrogen content of at least 7 mmol/g.

9. The two part retraction system of claim 7 , wherein the crosslinker is polymethylhydrosiloxane.

10. The two part retraction system of claim 7 , wherein the hemostatic agent is a water soluble astringent aluminum salt.

11. The two part retraction system of claim 10 , wherein the water soluble astringent aluminum salt is potassium aluminum sulfate (AlKSO4), aluminum ammonium sulfate, aluminum sulfate, aluminum chlorohydrate, aluminum acetate, or a mixture thereof.

12. The two part retraction system of claim 7 , wherein the hemostatic agent is ferric sulfate, ferric chloride, a mixture of ferric sulfate and ferric chloride, permanganates or zinc chloride.

13. The two part retraction system of claim 7 , wherein the hemostatic agent is a mixture of tannins, adrenaline or 8-hydroxyquinoline derivatives.

14. The two part retraction system of claim 7 , wherein the hydrophilic additive is potassium polyacrylate, sodium polyacrylate, or siloxylated polyethers.

Assignees

• Dentsply Int Inc

Inventors

• Angeletakis Christos

Classifications

• A61K6/71

  Fillers · CPC title

• A61K6/69

  Medicaments · CPC title

• A61K6/18

  causing dental retraction, e.g. compositions for widening the sulcus for making dental impressions or removing teeth · CPC title

• A61C9/0033 Primary

  Gingival retraction appliances · CPC title

• A61K6/19 Primary

  Self-expanding, e.g. for filling teeth · CPC title