Cross-linking composition delivered by iontophoresis, useful for the treatment of keratoconus
An improved formulation of an ophthalmic composition contains riboflavin, as cross-linking agent of corneal collagen, administered by corneal iontophoresis, able to guarantee an increased capacity of permeation of riboflavin of the corneal stroma and therefore greater therapeutic efficacy in the treatment of keratoconus.
1. An ophthalmic composition useful for the treatment of keratoconus to be administered by corneal iontophoresis, wherein the cross-linking agent is riboflavin, the pH is between 6.9 and 7.2, and the value of osmolarity is between 90 and 100 mOsm/l, and the following formulation:
Riboflavin sodium phosphate
0.147
g
Sodium-EDTA
0.1
g
Tris-(hydroxymethyl)aminomethane
0.05
g
NaH 2 PO 4 •2H 2 O
0.385
g
Na 2 HPO 4 •2H 2 O
0.217
g
Distilled water
up to 100
g.
2. The ophthalmic composition according to claim 1 , wherein the pH is 7.0, and the osmolarity is 96 mOsm/l.
3. The ophthalmic composition according to claim 2 , wherein the pH value equal to 7.0 is obtained through a buffering system comprising sodium phosphate monobasic dihydrate and/or sodium phosphate dibasic dihydrate, in appropriate amounts.
4. The ophthalmic composition according to claim 1 , wherein the composition is prepared in a technical form of collirium, eye drops, gels, and in all pharmaceutical forms that enable a corneal application followed by corneal iontophoresis.
5. The ophthalmic composition according to claim 1 , wherein the ophthalmic composition is dextran free.
6. The ophthalmic composition according to claim 1 , wherein the ophthalmic composition is NaCl free.
7. An ophthalmic composition useful for the treatment of keratoconus to be administered by corneal iontophoresis, wherein the cross-linking agent is riboflavin, the pH is between 6.9 and 7.2, the value of osmolarity is between 90 and 100 mOsm/l, and the composition is NaCl free and the following formulation:
Riboflavin sodium phosphate 0.147 g
Sodium-EDTA 0.1 g
Tris-(hydroxymethyl)aminomethane 0.05 g
NaH PO 4 .2H 2 O 0.385 g
Na HPO 4 .2H 2 O 0.217 g
Distilled water up to 100 g.
8. The ophthalmic composition according to claim 7 , wherein the ophthalmic composition is dextran free.
9. The ophthalmic composition according to claim 7 , wherein the pH is 7.0, and the osmolarity is 96 mOsm/l.
10. The ophthalmic composition according to claim 7 , wherein the pH value equal to 7.0 is obtained through a buffering system comprising sodium phosphate monobasic dihydrate and/or sodium phosphate dibasic dihydrate, in appropriate amounts.
11. The ophthalmic composition according to claim 7 , wherein the composition is prepared in a technical form of collirium, eye drops, gels, and in all pharmaceutical forms that enable a corneal application followed by corneal iontophoresis.