Method of soft tissue augmentation
Particles made of a viscoelastic medium, are injectable gel particles, and have a size, when subjected to a physiological salt solution, in the range of from 1 to 5 mm. The particles are useful in a soft tissue augmentation implant. The implant includes particles of a viscoelastic medium, wherein a major volume of the particles are injectable gel particles The implant is useful in a method of soft tissue augmentation in a mammal, including man, comprising subepidermal administration at a site in said mammal where soft tissue augmentation is desirable, of an implant.
1. A method of tissue augmentation, comprising administering subepidermally by injection 1 to 10 ml of a viscoelastic medium through a 10-20 gauge needle at a site of a human subject,
wherein the viscoelastic medium comprises gel particles comprising cross-linked hyaluronic acid and derivatives thereof,
wherein the concentration of the cross-linked hyaluronic acid and derivatives thereof in the gel particles, when subjected to a physiological salt solution, is in the range of 15 to 40 mg/ml, and
wherein at least 50% (v/v) of the gel particles has a size range, when subjected to a physiological salt solution, in the range of 1.5 to 5 mm,
whereby migration of the gel particles from the administration site is prevented or decreased, relative to migration of smaller gel particles.
2. The method according to claim 1 , wherein the administration is subcutaneous administration.
3. The method according to claim 1 , wherein the size range is 1.5 to 2.5 mm.
4. The method according to claim 1 , wherein the tissue augmented is tissue that connects, supports or surrounds an organ of the body.
5. The method according to claim 1 , wherein the injection is through a 16-20 gauge needle.
6. The method according to claim 1 , wherein the concentration of the cross-linked hyaluronic acid and derivatives thereof in the gel particles, when subjected to a physiological salt solution, is in the range of 20 to 25 mg/ml.
7. The method according to claim 1 , wherein the concentration of the cross-linked hyaluronic acid and derivatives thereof in the gel particles, when subjected to a physiological salt solution, is approximately 20 mg/ml.
8. The method according to claim 1 , wherein the injection is through a 20 gauge needle.
9. The method according to claim 1 , wherein the concentration of the cross-linked hyaluronic acid and derivatives thereof in the gel particles, when subjected to a physiological salt solution, is approximately 15 to 22 mg/ml.
10. The method according to claim 1 , wherein the concentration of the cross-linked hyaluronic acid and derivatives thereof in the gel particles, when subjected to a physiological salt solution, is approximately 22 to 30 mg/ml.
11. The method according to claim 1 , wherein at least 50% (v/v) of the gel particles has a size range of 2.5 to 5 mm.
12. The method according to claim 1 , wherein at least 50% (v/v) of the gel particles has a size range of 1.5 to 4 mm.
13. The method according to claim 1 , wherein the administration is a single injection.
14. The method according to claim 1 , wherein the administration comprises multiple injections.
15. The method according to claim 1 , wherein the administration comprises one or more injections into one or more subepidermal layers.
16. The method according to claim 1 , wherein the viscoelastic medium comprises one or more drugs.
17. The method according to claim 16 , wherein the one or more drugs are selected from the group consisting of a local anesthetic, an anti-inflammatory, an antibiotic, and a growth factor.
18. The method according to claim 1 , wherein the viscoelastic medium further comprises cells.
19. A method of tissue augmentation, comprising administering submuscularly by injection 1 to 10 ml of a viscoelastic medium through a 10-20 gauge needle at a site of a human subject,
wherein the viscoelastic medium comprises gel particles comprising cross-linked hyaluronic acid and derivatives thereof,
wherein the concentration of the cross-linked hyaluronic acid and derivatives thereof in the gel particles, when subjected to a physiological salt solution, is in the range of 15 to 40 mg/ml, and
wherein at least 50% (v/v) of the gel particles has a size range, when subjected to a physiological salt solution, in the range of 1.5 to 5 mm,
whereby migration of the gel particles from the administration site is prevented or decreased, relative to migration of smaller gel particles.
20. A method of tissue augmentation, comprising administering supraperiosteally by injection 1 to 10 ml of a viscoelastic medium through a 10-20 gauge needle at a site of a human subject,
wherein the viscoelastic medium comprises gel particles comprising cross-linked hyaluronic acid and derivatives thereof,
wherein the concentration of the cross-linked hyaluronic acid and derivatives thereof in the gel particles, when subjected to a physiological salt solution, is in the range of 15 to 40 mg/ml, and
wherein at least 50% (v/v) of the gel particles has a size range, when subjected to a physiological salt solution, in the range of 1.5 to 5 mm,
whereby migration of the gel particles from the administration site is prevented or decreased, relative to migration of smaller gel particles.