Compositions and methods of using lamellar bodies for modifying linear biological macromolecules
Compositions comprising therapeutically effective amounts of lamellar bodies to restore lubricity and non-stick properties to mucous surfaces for conditions characterized by dry adherent surfaces, particularly those surfaces close to the body openings and conditions of the eye.
1. A method of treating areas affected by mucositis to restore lubricity and non-stick properties to dry adherent surfaces or to decrease the viscosity of pathological exudates which can cause crusting and synechiae wherein the method comprises applying a composition including lamellar bodies in suspension to the mucous surfaces in a subject in need thereof wherein the lamellar bodies comprise about 44-70% phosphatidylcholine about 15-23% sphingomyelin about 6-10% phosphatidyl ethanolamine about 2-6% phosphatidyl serine about 2-4% phosphatidyl inositol and about 4-12% cholesterol by weight.
2. The method of claim 1 wherein the mucositis is characterised by dryness of mucous surfaces.
3. The method of claim 2 wherein the dryness of mucous surfaces is of the buccal cavity, oropharynx or larynx.
4. The method of claim 1 wherein the lamellar bodies are provided in a form selected from the group consisting of an aerosol spray, a suspension, and a gel.
5. The method of the claim 1 wherein the mucositis is caused by radiation, chemotherapeutic agents, drugs, auto-immunity, allergies and infections.
6. The method of claim 1 wherein the characteristic feature of the mucositis is dryness of the surfaces which become covered with sticky exudates consisting of viscous mucus, viscous DNA and actin from dead cells and bacteria.
7. The method of claim 1 wherein the mucositis is caused by one of Stevens-Johnson syndrome, Pemphigus, Behcet's disease, systemic lupus erythematosis.
8. The method of claim 1 wherein the area affected is the external surfaces of the eye.
9. The method of claim 1 wherein the area affected is the mucous membrane of the eyelids and the conjunctive.
10. The method of claim 8 wherein the external surface of the eye is dry and/or covered by thickened viscous secretion or exudates.
11. The method of claim 10 wherein the exudates form crusts whose abrasive effect further excoriates and traumatises the surface.
12. The method of claim 8 wherein the dryness of the eye is keratoconjunctivitis sicca.
13. The method of claim 8 wherein the dryness of the eye is blepharitis and conjunctivitis.
14. The method of claim 8 wherein the dryness of the eye is caused by an autoimmune disorder selected from the group consisting of rheumatoid disease and Sjogren's syndrome.
15. The method of claim 8 wherein the lamellar bodies are applied in the form of gel, matrices or slow release devices or excipients.
16. The method of claim 1 wherein said composition further comprises about 0-3% by weight of lysophosphatidyl choline.
17. The method of claim 1 wherein said lamellar bodies comprise about 54% phosphatidylcholine, about 19% sphingomyelin about 8% phosphatidyl ethanolamine about 4% phosphatidyl serine about 3% phosphatidyl inositol and about 10% cholesterol by weight.
18. The method of claim 1 wherein said composition further comprises about 2% by weight lysophosphatidyl choline.