Syringe for extrusion of wetted, particulate material

• US 4,645,488 A
• Filed: 11/30/1983
• Issued: 02/24/1987
• Est. Priority Date: 08/12/1982
• Status: Expired due to Fees

• Current Assignee: UAB Research Foundation The Non-Profit Corporation
• Original Assignee: Board of Trustees of The University of Alabama (University of Alabama System)
• Inventors: Matukas, Victor J.
• Primary Examiner(s): YASKO JR, JOHN D
• Application Number:
  US06/556,725
• Time in Patent Office: 1,182 Days
• Field of Search: 604/59, 604/55, 604/60, 604/48, 604/904, 604/57, 604/49, 604/54, 604/287, 604/11-18, 604/230, 604/218, 604/222
• US Class Current: 604/59
• CPC Class Codes: A61M 31/00 Devices for introducing or retaining media, e.g. remedies, in cavities of the body A61M25/00 takes precedence ; introducing or retaining ophthalmic products into the ocular cavities A61F9/0008

Abstract

The invention relates to a syringe for extrusion of a semi-plastic, particulate mass comprising a barrel of flexible material having one or more longitudinal slits therein and provided at its upper end with a piston with means for making positive engagement with a plunger rod, the barrel being optionally fitted with a closure plug.

Claims

1. A dental restorative dispensing syringe for extruding a wetted particulate mass therefrom which comprises:

(A) a barrel of flexible plastic material having at least one longitudinal slit therein at its open end in combination with (B) a piston slidable within the bore of said barrel providing a seal between said piston and the inside wall of the barrel along its entire length and having means for making positive engagement with (C) a plunger rod, the length of said slit being approximately equal to the length of the wetted particulate mass to be extruded therefrom and being operative to allow said barrel to expand under the influence of said wetted particulate mass when said piston is extruding said mass, thereby reducing barrel resistance.

2. A dispensing syringe according to claim 1 wherein said barrel has one longitudinal slit therein.

3. A dispensing syringe according to claim 1 which is fitted with a closure plug at its lower end.

4. A dispensing syringe according to claim 1 which is pre-loaded with a particulate material.

5. A dispensing syringe according to claim 1 wherein said particulate material is hydroxylapatite.

6. A dispensing syringe according to claim 2 wherein said particulate material is hydroxylapatite.

7. A dispensing syringe according to claim 3 wherein said particulate material is hydroxylapatite.

8. A dispensing syringe according to claim 4 wherein said particulate material is hydroxylapatite.

9. An alveolar ridge augmentation device comprising:

(a) a barrel member of flexible material defining a bore, said barrel member having an open end;

(b) a wetted mass of particulate ridge augmentation material within said bore;

(c) means operatively coupled with said barrel member for expressing said wetted mass from said bore through said open end;

(d) said barrel member having at least one expansion slit extending longitudinally from said open end, the length of said slit being approximately equal to the length of the wetted particulate mass to be expressed therefrom and being operative to allow said barrel member to expand under the influence of said wetted mass when said means is expressing said wetted mass, thereby reducing barrel resistance to said wetted mass.

10. The device according to claim 9 wherein said barrel member is flexible plastic material.

11. The device according to claim 9 wherein said barrel member is circular in cross-section.

12. The device according to claim 9 wherein said barrel member has one slit therein.

13. The device according to claim 10 wherein said barrel member has one slit therein.

14. The device according to claims 11 wherein said barrel member has one slit therein.

15. The device according to claim 9 wherein said particulate mass is ceramic hydroxylapatite.

16. The device according to claim 10 wherein said particulate mass is ceramic hydroxylapatite.

17. The device according to claim 11 wherein said particulate mass is ceramic hydroxylapatite.

18. A method of delivering a wetted mass of particulate dental restorative material with a dispensing syringe in alveolar ridge augmentation procedures in a patient requiring such treatment, said dispensing syringe comprising:

(A) a barrel for containing said material, said barrel being of flexible material fitted with a closure plug at its lower end and having at least one longitudinal slit therein extending from its lower end towards its upper end in combination with (B) a piston having means for making positive engagement with (C) a plunger rod, the length of said slit being approximately equal to the length of the wetted particulate mass to be delivered therefrom and being operative to allow said barrel to expand under the influence of said wetted mass when said piston is extruding said mass thereby reducing barrel resistance, which method comprises;

(1) producing a wetted mass of the particulate material by addition of delivery fluid to said particulate material, (2) inserting the syringe barrel into a mucoperiosteal tunnel on the lateral aspect of the patient'"'"'s jaw after removal of said closure plug and (3) extruding said wetted, particulate material into said mucoperiosteal tunnel while withdrawing said syringe barrel from said tunnel.

19. A method according to claim 18 wherein said delivery fluid is saline.

20. A method according to claim 18 wherein said delivery fluid is distilled water.

21. A method according to claim 18 wherein said delivery fluid is blood.

22. A method according to claim 18 wherein said barrel is flexible plastic material.

23. A method according to claim 18 wherein said particulate material is hydroxylapatite.

24. A method according to claim 19 wherein said particulate material is hydroxylapatite.

25. A method according to claim 20 wherein said particulate material is hydroxylapatite.

26. A method according to claim 21 wherein said particulate material is hydroxylapatite.

27. A method according to claim 22 wherein said particulate material is hydroxylapatite.

32. A method according to claim 26 wherein the particulate material is wetted with saline.

33. A method according to claim 26 wherein the particulate material is wetted with the patient'"'"'s blood.

28. A method for augmenting the alveolar ridge in an edentulous patient comprising the steps of:

(1) providing a charge of particulate dental restorative material;

(2) providing a delivery fluid;

(3) mixing said delivery fluid with said charge to form a wetted extrudable mass;

(4) forming a mucoperiosteal tunnel on the lateral aspect of the patient'"'"'s jaw;

(5) depositing said wetted mass in said tunnel by extruding it from a barrel having at least one expansion slit extending longitudinally from its open end, the length of said slit being approximately equal to the length of the wetted mass to be extruded therefrom and being operative to allow said barrel member to expand under the influence of said wetted mass as it is extruded, thereby reducing barrel resistance to said wetted mass.

29. A method according to claim 28 further comprising the step of withdrawing the barrel from said tunnel while extruding said mass.

30. A method according to claim 28 wherein said particulate material is hydroxylapatite, whitlockite or mixtures thereof.

31. A method according to claim 29 wherein said particulate material is hydroxylapatite, whitlockite or mixtures thereof.

34. A method of alveolar ridge augmentation in a patient requiring such treatment by use of a dispensing syringe for dispensing a wetted particulate material, said syringe comprising (a) a barrel of flexible material defining a bore, said barrel member having an open end;

(b) a mass of particulate ridge augmentation material within said bore;

(c) means operatively coupled with said barrel member for expressing said particulate material from said bore through said open end;

(d) said barrel member having at least one expansion slit extending longitudinally from said open end, the length of said slit being approximately equal to the length of the wetted particulate material to be expressed therefrom and being operative to allow said barrel member to expand under the influence of said wetted material when said means is expressing said wetted material, thereby reducing barrel resistance to said wetted material, which method comprises (1) drawing saline or distilled water into the syringe by withdrawal of said plunger rod while immersing the tip of the same in either saline or distilled water or by addition of the patient'"'"'s blood to the syringe to thereby produce a wetted mass of the particulate material, (2) inserting the syringe barrel into a mucoperiosteal tunnel on the lateral aspect of the patient'"'"'s jaw and (3) extruding said wetted, particulate material into said mucoperiosteal tunnel while withdrawing said syringe from said tunnel.