Spinal disc implants with reservoirs for delivery of therapeutic agents
Nucleus pulposus implants that contain reservoirs for receiving, holding, and releasing therapeutic agents are provided. In one form of the invention, a spinal implant is provided with reservoirs positioned at least partially beneath the external surface of the implant. The reservoirs are provided to receive, hold, and release therapeutic and/or pharmaceutical agents into the surrounding tissues.
1 . A spinal implant, comprising:
a load bearing body, having an outer surface, sized for placement at least partially into an intervertebral disc space; and
at least one reservoir positioned at least partially within the body for holding and releasing therapeutic agents;
whereby the at least one reservoir is in fluid communication with at least a portion of the outer surface of the body, thereby providing for in vivo release of the therapeutic agents.
2 . The implant of claim 1 , wherein the body has one or more predetermined injection sites for depositing the therapeutic agents.
3 . The implant of claim 2 , wherein the one or more predetermined injection sites include a sealing mechanism to prevent release of the therapeutic agents into the surrounding tissues.
4 . The implant of claim 2 , wherein the one or more predetermined injection sites are marked with at least one x-ray marker.
5 . The implant of claim 1 , the implant further comprising one or more channels between the at least one reservoir and the outer surface of the body to permit fluid communication therebetween.
6 . The implant of claim 1 , wherein the at least one reservoir comprises more than one reservoir.
7 . The implant of claim 6 , wherein the more than one reservoir are not in fluid communication with each other.
8 . The implant of claim 1 , wherein the body is comprised of one or more materials providing load bearing properties and release of therapeutic agents.
9 . The implant of claim 1 , wherein the therapeutic agent is selected from the group consisting of therapeutic agents, pharmaceutical agents, biological agents, growth factors, and combinations thereof.
10 . The implant of claim 9 , wherein the therapeutic agent is selected from the group consisting of antibiotics, analgesics, anesthetics, anti-inflammatory drugs, steroids, anti-viral and anti-retroviral compounds, therapeutic proteins or peptides, therapeutic nucleic acids, and combinations thereof.
11 . A spinal implant, comprising:
a load bearing body, having an outer surface, sized for placement at least partially into an intervertebral disc space;
a plurality of sets of reservoirs positioned at least partially within the body;
wherein each set of reservoirs comprises at least one reservoir for holding and releasing therapeutic agents;
and wherein plurality of reservoirs are in fluid communication with at least a portion of the outer surface of the body the body, thereby providing for in vivo release of the therapeutic agents.
12 . The implant of claim 11 , wherein the body has one or more injection sites for depositing the therapeutic agents.
13 . The implant of claim 12 , wherein the one or more injection sites include a sealing mechanism to prevent release of the therapeutic agents into the surrounding tissues.
14 . The implant of claim 12 , wherein the one or more injection sites are marked with at least one x-ray marker.
15 . The implant of claim 11 , the implant further comprising one or more channels between the at least one reservoir and the outer surface of the body to permit fluid communication therebetween.
16 . The implant of claim 15 , wherein each set of reservoirs has its own unique set of channels that permit fluid communication between the set of reservoirs and the outer surface.
17 . The implant of claim 11 , wherein the degree of fluid communication between the reservoirs and the outer surface is different for each set of reservoirs.
18 . The implant of claim 11 , wherein at least one set of reservoirs is not in fluid communication with any other set of reservoirs.
19 . The implant of claim 11 , wherein at least one set of reservoirs is in fluid communication with at least one other set of reservoirs.
20 . The implant of claim 11 , wherein at least one set of reservoirs comprises a plurality of reservoirs, wherein the plurality of reservoirs within that set of reservoirs are in fluid communication with each other.
21 . The implant of claim 11 , wherein at least one set of reservoirs comprises a plurality of reservoirs, wherein the plurality of reservoirs within that set of reservoirs are not in fluid communication with each other.
22 . The implant of claim 11 , wherein the body is comprised of one or more materials providing load bearing properties and release of therapeutic agents.
23 . The implant of claim 11 , wherein the therapeutic agent is selected from the group consisting of therapeutic agents, pharmaceutical agents, biological agents, growth factors, and combinations thereof.
24 . The implant of claim 23 , wherein the therapeutic agent is selected from the group consisting of antibiotics, analgesics, anesthetics, anti-inflammatory drugs, steroids, anti-viral and anti-retroviral compounds, therapeutic proteins or peptides, therapeutic nucleic acids, and combinations thereof.
25 . A method for inserting therapeutic agents into a spinal implant, comprising:
inserting a hypodermic needle into-a spinal implant that includes at least one reservoir positioned at least partially within the spinal implant;
providing an agent through the needle and into the at least one reservoir, the agent being in the form of a liquid solution or suspension;
filling the reservoir at least partially with the agent; and
removing the needle.
26 . The method of claim 25 , wherein the hypodermic needle is inserted through a predetermined injection site.
27 . The method of claim 26 , wherein the predetermined injection site includes at least one x-ray marker, and the hypodermic needle is inserted under fluoroscopic guidance.
28 . A method for inserting therapeutic agents into a spinal implant, comprising:
creating a pellet containing at least one therapeutic agent in substantially solid; and
fabricating the spinal implant around the pellet so as to embed the pellet at least partially within the spinal implant.
29 . The method of claim 28 , wherein the pellet is water soluble.
30 . A spinal implant prepared by the method of claim 28 , wherein the spinal implant has an outer surface and the pellet is in fluid communication with the outer surface of the implant.
31 . The method of claim 28 , wherein creating the pellet comprises mixing the at least one therapeutic agent with a binder.