IP Library Granted Patent US 9,539,202
Granted Patent B2
US 9,539,202 · App. 11/796,747 · Granted Jan 10, 2017

Formulation of liposomal vesicles in aqueous solutions with lachrymal film characteristics

Inventors: Rocio Herrero Vanrell (Madrid, ES); Jose Benitez Del Castillo (Madrid, ES); Eva Vico Ruiz (Madrid, ES); Marta Vicario De La Torre (Madrid, ES); Irene Teresa Molina Martinez (Madrid, ES)
Assignee: UNIVERSIDAD COMPLUTENSE DE MADRID
A61K9/0048A61K9/127A61K31/07A61K31/20A61K31/375A61K31/56A61K33/00A61K38/1709A61K38/1808A61K38/1825A61K38/1841A61K38/30A61K38/38A61K38/40A61K38/47A61K38/57
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Quick Facts
Patent No.
US 9,539,202
App. No.
11/796,747
Granted
Jan 10, 2017
Kind
B2
Abstract

The present invention involves the preparation of a pharmaceutical liposomal system in an aqueous solution which contains a substance or polymer with mucomimetic and/or mucoadhesive properties. Due to the components and characteristics of the formulation described in this present patent it can be used as a precorneal tear film substitute. This invention is included in the pharmacy and medicine areas.

Claims (19)

1. An ophthalmic composition for use as a precorneal film substitute, comprising phosphatidylcholine liposomal vesicles obtained from soy lecithin containing α-tocopherol and cholesterol, wherein the liposomal vesicles, once formed, are dispersed in aqueous solution with trehalose and hyaluronic acid, and wherein the trehalose is present in the composition in an amount effective to render the ophthalmic composition isotonic or hypotonic in clinical use in a human eye.

2. The composition of claim 1 , comprising neutral lipids, low polarity lipids as wax, cholesterol esters, triglycerides, free fatty acids and hydrocarbons.

3. The composition of claim 1 , comprising lipocalins.

4. The composition of claim 1 , comprising vitamin A.

5. The composition of claim 1 , comprising the following ions: Sodium, Potassium, Calcium, Chloride and Bicarbonate.

6. The composition of claim 1 , comprising vitamin C.

7. The composition of claim 1 , comprising lactoferrine.

8. The composition of claim 1 , comprising albumin or prealbumin.

9. The composition of claim 1 , comprising immunoglobulin A (IgA).

10. The composition of claim 1 , comprising an antibacterial agent selected from the group consisting of Immunoglobulin G (IgG), lysozyme and a complement thereof.

11. The composition of claim 1 , comprising a long chain fatty acid selected from the group consisting of gadoleic, palmitic, palmitoleic, estearic, oleic, linoleic, araquidic, linolenic, eicosenic, lignoceric, lactic and miristic.

12. The composition of claim 1 , comprising a hydrophilic lipid selected from the group consisting of phospholipids, sphingomyelin, ceramides and cerebrosides.

13. The composition of claim 1 , comprising a growth factor.

14. The composition of claim 13 , wherein the growth factor comprises epithelial growth factor: EGF.

15. The composition of claim 13 , wherein the growth factor comprises beta transforming growth factor (TGF-β), acidic fibroblast growth factor (aFGF), basic fibroblast growth factor (bFGF), or Substance P insulin-like growth factor.

16. The composition of claim 13 , which comprises an antiprotease.

17. The ophthalmic composition according to claim 1 , wherein the trehalose is present in the composition in an amount effective to render the ophthalmic composition isotonic in clinical use in a human eye.

18. The ophthalmic composition according to claim 1 , wherein the trehalose is present in the composition in an amount effective to render the ophthalmic composition hypotonic in clinical use in a human eye.

19. A method for treating dry eye syndrome in a patient in need of such treatment comprising providing the composition of claim 1 , and applying the composition to an eye of the patient.

Continuity (2)
Provisional Application 60796118 · Apr 28, 2006
Related Publication 20070292496A1 · Dec 20, 2007