Mucoadhesive nanoparticle composition comprising immunosuppresant and methods of use thereof
Disclosed is a mucoadhesive nanoparticle delivery system for delivering an immunosuppressant, such as cyclosporine A, to a mucosal site for treatment of a disease or condition involving inflammation or excess immune activity. The system comprises nanoparticles formed from a plurality of linear amphiphilic block copolymers, each having a hydrophobic block comprising polylactide (PLA) and a hydrophilic block comprising dextran. The nanoparticles are surface-functionalized with a mucosal targeting moiety, such as a phenylboronic acid derivative, for targeted delivery and enhanced retention at the mucosal site. Pharmaceutical compositions, methods, and uses thereof comprising the mucoadhesive nanoparticle delivery system are disclosed. The compositions can be administered in an effective amount for treating the disease or condition while substantially preserving or restoring the function and/or integrity of the mucosal lining. The composition may be formulated as an aqueous suspension for administration to an anterior surface of the eye in the treatment of dry eye syndrome.
1. A method for treating a disease or condition involving inflammation, comprising topically administering to the anterior surface of an eye of a subject a composition comprising nanoparticles capable of releasing cyclosporine A, the nanoparticles comprising a plurality of linear amphiphilic PLA-b-Dex diblock copolymers and being functionalized with phenylboronic acid (PBA), wherein the concentration of cyclosporine A in the composition is about 0.001% to about 0.1% wt/vol.
2. The method of claim 1 , wherein the copolymers comprise PLA-b-Dex-g-PBA.
3. The method of claim 1 , wherein the nanoparticles have an average particle size of less than about 1000 nm, less than about 100 nm, less than about 50 nm, or less than about 30 nm.
4. The method of claim 1 , wherein the disease or condition is dry eye syndrome.
5. The method of claim 1 , wherein the composition is administered at a dose and/or administration frequency that provides a therapeutic effect while substantially preserving the function and integrity of the mucosal lining.
6. The method of claim 1 , wherein the composition is administered at a dose and/or administration frequency that improves hydration of the mucosal lining.
7. The method of claim 1 , wherein the composition is formulated as an aqueous suspension.
8. The method of claim 1 , wherein the concentration of cyclosporine A in the composition is about 0.01 to about 0.1% wt/vol or about 0.01% to about 0.05% wt/vol.
9. The method of claim 1 , wherein the cyclosporine A is administered at a dose of about 0.1 μg to about 125.0 μg per week, about 0.1 μg to about 100.0 μg per week, about 0.1 μg to about 75.0 μg per week, about 0.1 μg to about 50.0 μg per week, about 0.1 to about 20.0 μg per week, about 0.1 to about 10.0 μg/week, about 0.1 to about 5.0 μg/week.
10. The method of claim 1 , wherein the composition is administered once every 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19 or 20 days.
11. The method of claim 1 , wherein the composition is administered once per week.
12. The method of claim 1 , wherein the composition is administered at an overall dose of less than about 150.0 μg per week at an administration frequency of less than 10 times per week.
13. The method of claim 1 , wherein the composition is administered less than 5 times per week.
14. The method of claim 1 , wherein the composition is administered less than 2 times per week.
15. The method of claim 1 , wherein the composition is administered at an overall dose of about 0.1 μg to about 75.0 μg cyclosporine A per week.
16. The method of claim 1 , wherein the composition is administered at an overall dose of about 0.1 μg to about 20.0 μg cyclosporine A per week.
17. The method of claim 1 , wherein the composition is administered once every 1, 3, 7 or 14 days.
18. The method of claim 1 , wherein the surface density of PBA is about 1 per nm 2 to 15 per nm 2 .
19. The method of claim 1 , wherein the nanoparticles have an average particle size of less than about 100 nm.
20. A method for treating a disease or condition involving inflammation, comprising topically administering to the anterior surface of an eye of a subject a composition comprising nanoparticles capable of releasing cyclosporine A, the nanoparticles comprising copolymers consisting essentially of linear amphiphilic PLA-b-Dex diblock copolymers and being surface-functionalized with phenylboronic acid (PBA), wherein the concentration of cyclosporine A in the composition is about 0.001% to about 0.1% wt/vol, and wherein the composition is administered at an overall dose of about 0.1 μg to about 20.0 μg cyclosporine A per week at an administration frequency of less than 10 times per week.