Alloplastic injectable dermal filler and methods of use thereof
A composition comprising an alloplastic injectable suspension for use as a dermal filler comprising a biocompatible and pliable material and a physiologically acceptable suspending agent is provided. A method of making a composition comprising an alloplastic injectable suspension for use as a dermal filler comprising a biocompatible and pliable material and a physiologically acceptable suspending agent, said method comprising admixing a biocompatible and pliable material with a physiologically acceptable suspending agent, is also provided. A method of augmenting soft tissue to provide long-term reduction of a skin defect, said method comprising stimulating collagen beneath the skin defect is further provided. In an embodiment of the method of augmenting soft tissue, the stimulation of collagen production is effected by injecting into the deep reticular dermis an a dermal filler, said dermal filler being an alloplastic injectable suspension and comprising a biocompatible and pliable material and a physiologically acceptable suspending agent.
1. A composition comprising: an alloplastic injectable suspension for use as a dermal filler comprising a biocompatible and pliable material and a physiologically acceptable suspending agent; wherein the biocompatible and pliable material is a copolymer of phenylethyl acrylate and phenylethyl methacrylate.
2. The composition of claim 1 , wherein the copolymer is a powder, a non-porous microbead, or a microsphere.
3. The composition of claim 1 , wherein the copolymer is in the form of particles each having a diameter of about 10μ to about 100μ; about 0.01μ to about 10μ, or about 0.01μ to about 5μ.
4. The composition of claim 1 , wherein the physiologically acceptable suspending agent is resorbable.
5. The composition of claim 4 , wherein the physiologically acceptable suspending agent is a buffered physiological solution, cross-linked sodium hyaluronate, a non cross-linked sodium hyaluronate, isolated collagen, collagen isolated from an animal, collagen isolated from a bird, or genetically engineered collagen.
6. The composition of claim 1 , wherein said composition further comprises a local anesthetic.
7. The composition of claim 1 , wherein the phenylethyl acrylate and the phenylethyl methacrylate are present in the copolymer at a molar ratio of about 1:1000; about 1:100; about 1:10; about 1:9; about 1:8; about 1:7; about 1:6; about 1:5; about 1:4; about 1:3; about 1:2; or about 1:1.
8. The composition of claim 1 , wherein said copolymer is cross-linked.
9. A method of making the composition of claim 1 comprising an alloplastic injectable suspension for use as a dermal filler comprising a biocompatible and pliable material and a physiologically acceptable suspending agent, comprising admixing a biocompatible and pliable material with a physiologically acceptable suspending agent; wherein the biocompatible and pliable material is a copolymer of phenyl ethyl acrylate and phenylethyl methacrylate.
10. The method of claim 9 , wherein the copolymer is a powder, a non-porous microbead, or a microsphere.
11. The method of claim 10 , wherein the copolymer is in the form of particles each having a diameter of about 10μ to about 100μ; about 0.01μ to about 10μ, or about 0.01μ to about 5μ.
12. The method of claim 9 , wherein the phenylethyl acrylate and the phenylethyl methacrylate are present in the copolymer at a molar ratio of about 1:1000; about 1:100; about 1:10; about 1:9; about 1:8; about 1:7; about 1:6; about 1:5; about 1:4; about 1:3; about 1:2; or about 1:1.
13. The method of claim 9 , wherein said copolymer is cross-linked.
14. A method of augmenting soft tissue to provide long-term reduction of a skin defect, said method comprising injecting into the deep reticular dermis the composition of claim 1 .
15. The method of claim 14 , wherein the injected dermal filler produces little immunologic response in the host tissue or no immunologic response in the host tissue.
16. The method of claim 14 , wherein comprising injecting the dermal filler below the skin defect at a junction of the dermis and subcutaneous fat.
17. The method of claim 14 , wherein the skin defect is a result of loss of collagen and hyaluronic acid in the skin during the aging process.
18. The method of claim 14 , wherein the skin defect is a result of premature aging, said premature aging caused by overexposure to sunlight, overexposure to environmental pollutants, smoking tobacco products, exposure to cigarette smoke, poor nutrition and skin disorders.
19. The method of claim 14 , wherein the skin defect is a dynamic wrinkle, a fine wrinkles or a static wrinkle.
20. The method of claim 14 , wherein the skin defect is an acne scar, a surgical scar, a large pore, or a soft tissue contour defect.
21. The method of claim 14 , wherein the long-term reduction of the skin defect is of a duration of at least one year.