Drug delivery methods, structures, and compositions for nasolacrimal system
A drug insert is configured for use with an implant. The implant is configured for insertion into a lacrimal canaliculus. The drug insert includes a drug core comprising a therapeutic agent and a polymer; and a sheath body comprising material substantially impermeable to the therapeutic agent, wherein the drug core is positioned within the sheath body. The sheath body is configured to provide an exposed end of the drug core that releases therapeutic agent to an eye when the drug insert is disposed within the implant and the implant is positioned in the lacrimal canaliculus. A distal end of the drug core is sealed with a medical-grade adhesive.
1. A punctal plug configured for insertion into a lacrimal canaliculus of a patient, the punctal plug comprising:
a silicone plug body comprising a drug insert;
the drug insert comprising:
a drug core comprising a therapeutic agent contained in a matrix, and
an impermeable sheath body partially covering the drug core,
wherein when the punctal plug is inserted into the lacrimal canaliculus of the patient an exposed surface of the drug core is in direct contact with tear fluid to permit diffusion of the therapeutic agent into the tear fluid of the eye.
2. The implant of claim 1 , wherein the sheath body is comprised of at least one of polyimide or polyethylene terephthalate.
3. The implant of claim 1 , wherein the sheath body includes a distinguishing color that shows placement of one or more of the implant in the lacrimal canaliculus or the insert in the implant.
4. The implant of claim 1 , wherein the therapeutic agent comprises one or more of an anti-glaucoma medication, a prostaglandin, a non-steroidal anti-inflammatory drug (NSAID), a lubricant, a surfactant, an inhibitor of angiogenesis, peptides, proteins, or enzymes.
5. The implant of claim 1 , wherein the therapeutic agent is selected from the group consisting of latanoprost, bimatoprost, timolol maleate, NSAID, travoprost, and cyclosporin.
6. The implant of claim 5 , wherein about 3 micrograms to about 135 micrograms of latanoprost is present in the drug core.
7. The implant of claim 5 , wherein about 50 micrograms to about 100 micrograms of latanoprost is present in the drug core.
8. The implant of claim 1 , wherein the drug core comprises inclusions of the therapeutic agent in a polymer.
9. The implant of claim 8 , wherein the inclusions comprise droplets and the therapeutic agent is latanoprost.
10. The implant of claim 1 , wherein the drug insert is further configured to release the therapeutic agent for at least 21 days.
11. The implant of claim 1 , wherein the sheath body comprises a polyimide sheath body, and wherein the drug core comprises: silicone and latanoprost.
12. The implant of claim 1 , wherein the matrix comprises a non-biodegradable polymer.
13. The implant of claim 12 , wherein the non-biodegradable polymer is selected from the group consisting of silicone, an acrylate, a polyethylene, polyurethane, and polyester.
14. The implant of claim 1 , wherein the concentration of therapeutic agent in the drug core is at least 20% by weight of the drug core.
15. The implant of claim 1 , wherein the drug core comprises a non-homogenous mixture of silicone and the therapeutic agent.
16. The implant of claim 1 , wherein the drug insert has a diameter of about 0.006 inches to about 0.025 inches.
17. A method for the treatment of glaucoma in an eye, the method comprising: placing a punctal plug in a lacrimal canaliculus of the eye, wherein the punctal plug comprises;
a silicone plug body comprising a drug insert;
the drug insert comprising:
a drug core comprising a therapeutic agent contained in a matrix; and
an impermeable sheath body, wherein the drug core is positioned within the sheath body, wherein the sheath body is configured to provide aproximal exposed proximal end of the drug insert in direct contact with tear fluid that releases therapeutic agent to the eye when the drug insert is disposed within the punctal plug and the punctal plug is inserted into the lacrimal canaliculus of a patient.