Drug delivery devices and methods
View Patent ↗This disclosure relates generally to methods and devices for use in treating eye conditions with implantable drug delivery devices. One method includes introducing an implant into the suprachoroidal space, wherein the interior volume of the implant is plugged with a drug-release material comprising at least one active agent that elutes through at least one opening in the implant, wherein the drug-release material degrades from the interior volume of the implant over a period time.
1. A method of implanting an ocular implant for treating an ocular disorder of an eye, comprising:
forming a self-sealing incision in the cornea of the eye into the anterior chamber of the eye;
introducing an implant through the incision into the anterior chamber, the implant comprising:
a proximal end with at least one inflow port;
a distal end with at least one outflow port; and
an internal lumen extending through the implant between the at least one inflow port and at least one outflow port,
wherein the implant is mounted on an implantation instrument having a delivery wire extending through the internal lumen of the implant;
positioning the implant in the eye using the implantation instrument and the delivery wire on which the implant is mounted, wherein the implant is positioned between a first and second tissue layer and into fluid communication with the suprachoroidal space using the delivery wire on which the implant is mounted;
withdrawing the delivery wire from the internal lumen of the implant;
injecting drug-release material through the delivery wire as the delivery wire is being withdrawn from the internal lumen of the implant filling the internal lumen of the implant with the drug-release material, wherein injecting drug-release material includes creating a lake of the drug-release material near the distal end of the implant;
eluting the at least one active agent from the drug-release material to treat the eye as the drug-release material degrades, wherein the space is maintained after the lake of drug-release material degrades.
2. The method of claim 1 , further comprising preventing fluid flow through the internal lumen of the implant with the drug-release material.
3. The method of claim 2 , wherein the drug-release material is configured to degrade over a period of time from the internal lumen of the implant.
4. The method of claim 3 , wherein the period of time is selected from the group consisting of at least 12 hours, at least 24 hours, at least 3 days, at least 14 days, at least 30 days, at least 120 days, and at least one year.
5. The method of claim 3 , further comprising creating a flow pathway through the internal lumen of the implant between the at least one inflow port and the at least one outflow port upon degradation of the drug-release material over the period of time.
6. The method of claim 3 , wherein the drug-release material is impregnated with at least one therapeutic agent.
7. The method of claim 6 , wherein the at least one therapeutic agent is released over the period of time.
8. The method of claim 6 , wherein the drug-release material comprises nanostructures facilitating zero order kinetic release of the at least one therapeutic agent.
9. The method of claim 1 , further comprising releasing the implant from the delivery wire.
10. The method of claim 9 , further comprising conducting fluid through the flow pathway from the anterior chamber into the suprachoroidal space.
11. The method of claim 1 , wherein the drug-release material is a biodegradable polymer, including a poly(lactic-co-glycolic acid).
12. The method of claim 1 , wherein injecting drug-release material through the delivery wire comprises injecting drug-release material through a bore in the delivery wire.