US2019021958A1PendingUtilityA1
Method for creating a mineral trioxide aggregate material with improved biological effects
Est. expiryApr 29, 2035(~8.8 yrs left)· nominal 20-yr term from priority
A61L 27/165A61K 6/76A61K 6/887A61K 6/851A61K 6/17A61L 27/32A61L 2420/02C04B 2103/0067A61L 27/306C23C 14/22C04B 28/04A61L 2430/12A61L 2420/08B28B 1/14C04B 2111/00836B28B 11/24A61K 6/0606A61K 6/083A61K 6/0088A61K 6/0008C23C 14/082C23C 14/34C23C 14/24A61L 27/30A61C 13/0835A61C 13/0006A61C 8/0013A61C 5/50
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Claims
Abstract
A dental device is improved in its ability to produce hydroxyl apatite by having a layer of mineral trioxide aggregate (MTA) deposited thereon. A tile of MTA is prepared, heat treated and sintered to produce a micronized tile of MTA that can then be deposited by physical vapor depositions, hot isostatic pressing, molding or other conventional technique.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . An implantable dental device comprising a layer of mineral trioxide aggregate that produces hydroxyl apatite in the presence of phosphate buffered saline.
2 . An implantable dental device as in claim 1 wherein said device is an obturation point.
3 . An implantable device as in claim 1 wherein said obturation point comprises gutta-percha.
4 . A method for producing hydroxyl apatite on a dental device comprising the step of preparing a tile of mineral trioxide aggregate.
5 . A method as in claim 4 further comprising forming a mixture by mixing Portland cement and deionized water in an amount of from about 10:1 to about 1:10.
6 . A method as in claim 5 wherein said mixture is placed into a mold and cured in a humidity chamber.
7 . A method as in claim 6 wherein said humidity chamber is set at 36 degrees Celsius with about a 90 percent relative humidity for from about 5 hours to about 10 days.
8 . A method as in claim 7 wherein said cured mixture is subjected to a second heating by heating to from about 50 to about 500 degrees Celsius for from about 15 minutes to about 2 days.
9 . A method as in claim 8 wherein said method includes micronizing said cured tile.
10 . A method as in claim 9 wherein said micronizing includes ball-mill grinding said tile to a particle size of from about 1 to about 200 microns.
11 . A method as in claim 10 wherein said micronizing includes ball-mill grinding said tile to a particle size of from about 10 to about 100 microns.
12 . A method as in claim 11 wherein said micronizing includes ball-mill grinding said tile to a particle size of about 53 microns.
13 . A method as in claim 9 wherein said micronized tile is sintered at a temperature of from about 25 to about 400 degrees Celsius for a period of from about 5 minutes to about 5 hours.
14 . A method as in claim 13 wherein said sintered, micronized tile is subjected to a second sintering temperature of from about 275 to about 650 degrees Celsius for from about 5 minutes to about 12 hours.
15 . A method as in claim 14 wherein said second sintering step is conducted at a pressure of from about 5000 psi to about 50,000 psi.
16 . A method as in claim 14 wherein said sintered, micronized tile is subjected to a third sintering temperature of from about 550 to about 1100 degrees Celsius for from about 30 minutes to about 2 days.
17 . A method as in claim 16 wherein said third sintering step is conducted at a pressure of from about 1000 psi to about 50,000 psi.
18 . A method as in claim 9 wherein said step of depositing includes physical vapor deposition of said micronized tile.
19 . A method as in claim 9 wherein said step of depositing includes hot isostatic pressing of said micronized tile.
20 . A method as in claim 9 wherein said step of depositing includes hot isostatic pressing of said micronized tile.
21 . A method as in claim 9 wherein said step of depositing includes molding of said micronized tile.Join the waitlist — get patent alerts
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