Method for indicating shelf-life after mixing pre-dosed, pre-packaged two-part dental compositions

• US 7,569,185 B2
• Filed: 10/02/2006
• Issued: 08/04/2009
• Est. Priority Date: 10/25/2005
• Status: Expired due to Fees

• Current Assignee: Ultradent Products Incorporated
• Original Assignee: Ultradent Products Incorporated
• Inventors: Fischer, Dan E.
• Primary Examiner(s): ALEXANDER, LYLE
• Application Number:
  US11/537,807
• Publication Number:
  US 20070106210A1
• Time in Patent Office: 1,037 Days
• Field of Search: 422/55, 422/58, 422/61, 436 1- 2, 436164-165, 604/82, 424/10.1, 433/80, 433/226
• US Class Current: 422/430
• CPC Class Codes: A61C 5/62 Applicators, e.g. syringes or guns
• CPC Class Codes: A61M 2005/3125 specific display means, e.g. to indicate dose setting
• CPC Class Codes: A61M 2205/50 with microprocessors or computers
• CPC Class Codes: A61M 2205/583 by visual feedback
• CPC Class Codes: A61M 5/284 comprising means for injection of two or more media, e.g. by mixing
• CPC Class Codes: A61M 5/3129 Syringe barrels A61M5/3205 and A61M5/50 take precedence
• CPC Class Codes: A61M 5/31511 Piston or piston-rod constructions, e.g. connection of piston with piston-rod A61M5/5066 takes precedence
• CPC Class Codes: B05C 17/0052 Accessories therefor
• CPC Class Codes: B05C 17/00593 Hand tools of the syringe type
• CPC Class Codes: B65D 2203/12 Audible, olfactory or visual signalling means B65D51/248, B65D55/028, B65D79/02 and B65D81/24 take precedence
• CPC Class Codes: G09F 2003/0273 Labels for bottles, flasks
• CPC Class Codes: G09F 2003/028 Labels containing microcapsules, e.g. ink microcapsules for indicia transfer
• CPC Class Codes: G09F 3/0291 Labels or tickets undergoing a change under particular conditions, e.g. heat, radiation, passage of time
• CPC Class Codes: G09F 3/0297 including a machine-readable marking, e.g. a bar code digitally marked record carriers in general G06K19/00

Abstract

A pre-dosed, pre-packaged mixing system and associated method for mixing, storing, and dispensing a two-part dental composition that becomes less stable upon mixing. The mixing system includes a pre-dosed, pre-packaged quantity of a first component contained within a first chamber, and a pre-dosed, pre-packaged quantity of a second component contained within a second chamber. The chambers are separated by separation means so as to separate the two-components prior to mixing. Once mixed, the practitioner is able to record a mixing and/or expiration date on at least a portion of the mixing system so as to indicate a shelf-life of the less stable mixed dental composition.

Claims

1. A syringe system for mixing and for recording the mixing date to permit monitoring of the shelf life of a mixed two-part dental composition, the syringe system comprising:

a first pre-dosed composition pre-packaged so as to be contained in a first syringe having a barrel with a first plunger slidable within the first barrel;

a second pre-dosed composition pre-packaged so as to be contained in a second syringe having a barrel, with a second plunger slidable within the second barrel, and the separate compositions each having a shelf life significantly greater than the shelf life of the two compositions after they are mixed;

the first and second plungers being operable so that by first sliding the first plunger into the first syringe barrel the first pre-dosed composition is introduced into the second syringe barrel so that it contacts the second pre-dosed composition, the two compositions thereafter being either further mixed using one or both syringe barrels, or else applied in a dental procedure by expressing the mixed contents from the second syringe barrel; and

time and temperature sensitive marking means, disposed on one of the first or second syringes, which, when activated upon mixing the two compositions, thereafter provides a visual indication which automatically changes over time so as to indicate the lapsed time and temperature conditions from when the two compositions were mixed, and which also changes as a function of temperature, so that the shelf life of the mixed compositions is easily ascertainable from the visual indication.

2. The system of claim 1 wherein the time sensitive means comprises an activatable label having a length of microporous material and a tinted liquid contained within a sealed blister, such that when the blister is activated to release the liquid, it will migrate along the length of the microporous material as a function of time that shows how much time has lapsed since the two compositions were mixed, and thus how much shelf life remains for the mixed compositions.

3. The system of claim 1 wherein the time sensitive means comprises first and second compositions contained in first and second sealed blisters, respectively, that are separated by a membrane which, when broken, activates mixing of the first and second compositions in the two blisters by mixing them, so that thereafter the mixed compositions create a first color that progressively changes to a second color over time, the second color indicating elapsed time and thus the end of the shelf life of the mixed dental compositions.

4. The system of claim 3, wherein the rate at which the mixed compositions change color from the first to the second color will be delayed when the mixed dental compositions are refrigerated to extend the shelf life of the mixed dental compositions.

5. The system of claim 1 wherein the time sensitive means comprises an activatable label having a material which, when exposed by pealing back a cover, begins to change from a first to a second color as a function of time, the second color indicating elapsed time and thus the end of the shelf life of the mixed dental compositions.

6. The system of claim 5, wherein the rate at which the material of the label changes color from the first to the second color will be delayed when the mixed dental compositions are refrigerated to extend the shelf life of the mixed dental compositions.

7. The system of claim 1 wherein the time sensitive means comprises an activatable label having a microchip readable by an associated microchip reader which indicates to a user the time lapsed since mixing the two dental compositions.

8. The system of claim 7 wherein the microchip is configured to account for differences in temperature so that the lapsed time recorded by the microchip will be delayed when the mixed dental compositions are refrigerated to extend the shelf life of the mixed dental compositions.

9. The system of claim 1 wherein the first syringe barrel is connected end-to-end with the second syringe barrel so as to form a syringe-to-syringe mixing system.

10. The system of claim 1 wherein the first syringe barrel fits within the second syringe barrel so that the first syringe barrel also functions as the plunger for the second syringe barrel, thus forming a syringe-in-syringe mixing system.

11. The system of claim 10 wherein an outlet end of the first syringe barrel comprises a rupturable membrane so that when the plunger is pushed into the first syringe barrel, the pre-dosed dental composition packaged within the first syringe barrel will be expelled under pressure sufficient to create turbulence, into the second syringe barrel, thus mixing the two dental compositions in the second syringe barrel.

12. The system of claim 10 wherein the plunger of the first syringe barrel comprises a locking structure so that when the plunger is pushed into the first syringe barrel a sufficient distance, the syringe plunger inhibits the plunger from thereafter being withdrawn from the first syringe barrel.

13. The system of claim 12 wherein the locking structure comprises an annular ring formed on a circumference of the plunger of the first syringe barrel which cooperates with a corresponding groove formed inside the first syringe barrel for receiving the annular ring when the plunger is pushed far enough into the first syringe barrel.

18. The method of claim 1 wherein the time sensitive means comprises an activatable label having a color-changing material, and wherein the step for activating the label comprises pealing back a cover to expose the color-changing material to that it begins to change from a first to a second color as a function of time, the second color indicating elapsed time and thus the end of the shelf life of the mixed dental compositions.

19. The method of claim 18, wherein the rate at which the material of the label changes color from the first to the second color will be delayed when the mixed dental compositions are refrigerated to extend the shelf life of the mixed dental compositions.

14. In a syringe system for mixing for recording the mixing date to permit monitoring of the shelf life of a mixed two-part dental composition, a method comprising steps for:

providing a first pre-dosed composition pre-packaged so as to be contained in a first syringe having a barrel with a first plunger slidable within the first barrel;

providing a second pre-dosed composition pre-packaged so as to be contained in a second syringe having a barrel, with a second plunger slidable within the second barrel, and the separate compositions each having a shelf life significantly greater than the shelf life of the two compositions after they are mixed;

providing a time sensitive and temperature-dependent marking means, disposed on one of the first or second syringes;

operating the first and second plungers so that by first sliding the first plunger into the first syringe barrel the first pre-dosed composition is introduced into the second syringe barrel so that it contacts the second pre-dosed composition, the two compositions thereafter being either further mixed using one or both syringe barrels, or else applied in a dental procedure by expressing the mixed contents from the second syringe barrel;

upon mixing the two dental composition, activating the time and temperature sensitive markings, means in order to provide a visual indication which automatically changes over time so as to indicate the lapsed time and temperature conditions from when the two compositions were mixed, so that the shelf life of the mixed compositions is easily ascertainable from the visual indication.

15. The method of claim 14 wherein the time sensitive means comprises an activatable label having a length of microporous material and a tinted liquid contained within a sealed blister, and wherein the step for activating the label comprises bursting the sealed blister to release the liquid, so that the liquid will then migrate along the length of the microporous material as a function of time that shows how much time has lapsed since the two compositions were mixed, and thus how much shelf life remains for the mixed compositions.

16. The method of claim 14 wherein the time sensitive means comprises first and second compositions contained in first and second sealed blisters, respectively, that are separated by a membrane, and wherein the step for activating the label comprises bursting at least one of the blisters to cause mixing of the first and second compositions in the two blisters, so that thereafter the mixed compositions create a first color that progressively changes to a second color over time, the second color indicating elapsed time and thus the end of the shelf life of the mixed dental compositions.

17. The method of claim 16, wherein the rate at which the mixed compositions change color from the first to the second color will be delayed when the mixed dental compositions are refrigerated to extend the shelf life of the mixed dental compositions.

20. The method of claim 14 wherein the time sensitive means comprises an activatable label having a microchip readable by an associated microchip reader, and wherein the step for activating the label comprises initiating the microchip so that it indicates to a user the time lapsed since mixing the two dental compositions.

21. The method of claim 20 wherein the microchip is configured to account for differences in temperature so that the lapsed time recorded by the microchip will be delayed when the mixed dental compositions are refrigerated to extend the shelf life of the mixed dental compositions.

22. The method of claim 14 wherein the first syringe barrel is connected end-to-end with the second syringe barrel so as to form a syringe-to-syringe mixing system, and wherein the step for operating the first and second plungers comprises sliding the first plunger into the first syringe barrel at one end of the syringe barrels that are connected end-to-end, and then sliding the second plunger at the opposite end of the connected syringe barrels into the second syringe barrel so that the two dental compositions are mixed as they move back and forth from one syringe barrel into the other.

23. The method of claim 14 wherein the first syringe barrel fits within the second syringe barrel so that the first syringe barrel also functions as the plunger for the second syringe barrel, thus forming a syringe-in-syringe mixing system, and wherein the step for operating the first and second plungers comprises sliding the first plunger into the first syringe barrel and then using the first syringe barrel as a plunger for the second syringe barrel, sliding the first syringe barrel into the second syringe barrel to either further mix or else expel the mixed contents, as desired.

24. The method of claim 23 wherein an outlet end of the first syringe barrel comprises a rupturable membrane so that when the plunger is pushed into the first syringe barrel, the pre-dosed dental composition packaged within the first syringe barrel will be expelled under pressure sufficient to create turbulence, into the second syringe barrel, thus mixing the two dental compositions in the second syringe barrel.

25. The method of claim 23 wherein the plunger of the first syringe barrel comprises a locking structure so that when the plunger is pushed into the first syringe barrel a sufficient distance, the syringe plunger inhibits the plunger from thereafter being withdrawn from the first syringe barrel, and wherein the method further comprises locking the plunger of the first syringe barrel into the first syringe barrel.

26. The method of claim 25 wherein the locking structure comprises an annular ring formed on a circumference of the plunger of the first syringe barrel which cooperates with a corresponding groove formed inside the first syringe barrel for receiving the annular ring when the plunger is pushed far enough into the first syringe barrel, and wherein locking the plunger of the first syringe barrel into the first syringe barrel comprises pushing the plunger far enough into the first syringe barrel so that the annular ring mates with the annular groove.