US2011238016A1PendingUtilityA1
Drug delivery to a joint
Assignee: HOSPITAL FOR SPECIAL SURGERYPriority: Jan 13, 2004Filed: Jun 8, 2011Published: Sep 29, 2011
Est. expiryJan 13, 2024(expired)· nominal 20-yr term from priority
A61K 9/0024A61L 2300/41A61L 31/16A61M 37/0069A61P 29/00A61L 2300/402A61L 2300/222A61P 31/04
55
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Claims
Abstract
A drug delivery device may include a base to be percutaneously affixable in an attachment zone of a synovial joint and a sustained-release drug carrier coupled to the base. The drug delivery device may also include an access device to provide access to the attachment zone. The attachment zone may comprise a non-articulating portion of a bone and/or cartilage with the synovial joint and the drug carrier may elute the drug into the synovial fluid sufficient to sustain a therapeutically effective concentration of the drug in the synovial fluid for at least 8 hours.
Claims
exact text as granted — not AI-modified1 . A sustained-release intra-articular drug delivery device, comprising:
a base, so sized and shaped as to be percutaneously affixable in an attachment zone of a synovial joint, the attachment zone comprising a non-articulating portion of bone and/or cartilage with the synovial joint; and a sustained-release drug carrier coupled to the base, the carrier including a drug, the carrier so formed as to elute the drug into synovial fluid, upon implantation of the device in a joint, sufficient to sustain a therapeutically effective concentration of the drug in the synovial fluid for at least 8 hours.
2 . The drug delivery device of claim 1 , wherein the base comprises at least one barb.
3 . The drug delivery device of claim 2 , wherein the at least one barb is retractable.
4 . The drug delivery device of claim 2 , wherein the at least one barb is expandable.
5 . The drug delivery device of claim 1 , wherein the base has a variable diameter.
6 . The drug delivery device of claim 5 , wherein a first diameter is selected to facilitate insertion and a second diameter is selected to facilitate affixation.
7 . The drug delivery device of claim 1 , wherein the base is configured to be substantially flush with the bone surface after affixation.
8 . The drug delivery device of claim 1 , wherein the drug carrier is replaceable.
9 . The drug delivery device of claim 1 , wherein the attachment zone comprises a band of bone and/or cartilage adjacent to an articulating surface within the synovial joint.
10 . The drug delivery device of claim 9 , wherein the band extends from about 0.5 millimeters to about 1 centimeter away from the articulating surface.
11 . The drug delivery device of claim 1 , wherein the synovial joint is a hip joint, and the attachment zone comprises a non-articulating portion of bone and/or cartilage within the hip.
12 . The drug delivery device of claim 11 , wherein the attachment zone comprises a band of bone and/or cartilage adjacent to at least one of a femoral head, and an acetabulum.
13 . The drug delivery device of claim 1 , wherein the synovial joint is a knee joint, and the attachment zone comprises a non-articulating portion of bone and/or cartilage within the knee.
14 . The drug delivery device of claim 13 , wherein the attachment zone comprises a band of bone and/or cartilage adjacent to at least one of a tibial plateau, a femoral condyle, a patellofemoral area, the medial rim of a femoral trochlea, the lateral rim of a femoral trochlea, and the periphery of an intercondylar notch.
15 . The drug delivery device of claim 1 , wherein the synovial joint is a shoulder joint, and the attachment zone comprises a non-articulating portion of bone and/or cartilage within the shoulder.
16 . The drug delivery device of claim 15 , wherein the attachment zone comprises a band of bone and/or cartilage adjacent to at least one of the anatomical neck of a humerus, a glenoid cavity, and a glenoid neck.
17 . The drug delivery device of claim 1 , wherein the synovial joint is an arthroplastic joint comprising at least one prosthesis, and the attachment zone comprises a non-articulating portion of bone and/or cartilage within the joint.
18 . The drug delivery device of claim 17 , wherein the attachment zone comprises a band of bone and/or cartilage adjacent to the at least one prosthesis.
19 . A sustained-release intra-articular drug delivery device, comprising:
a base, so sized and shaped as to be percutaneously affixable in an attachment zone of a synovial joint, the attachment zone comprising a non-articulating portion of bone and/or cartilage with the synovial joint; a sustained-release drug carrier coupled to the base, the carrier including a drug, the carrier so formed as to elute the drug into synovial fluid, upon implantation of the device in a joint, sufficient to sustain a therapeutically effective concentration of the drug in the synovial fluid for at least 8 hours; and an access device, so sized and shaped as to provide access to the attachment zone.
20 . The drug delivery device of claim 19 , wherein the base comprises at least one barb.
21 . The drug delivery device of claim 20 , wherein the at least one barb is retractable.
22 . The drug delivery device of claim 20 , wherein the at least one barb is expandable.
23 . The drug delivery device of claim 19 , wherein the base has a variable diameter.
24 . The drug delivery device of claim 23 , wherein a first diameter is selected to facilitate insertion and a second diameter is selected to facilitate affixation.
25 . The drug delivery device of claim 19 , wherein the base is configured to be substantially flush with the bone surface after affixation.
26 . The drug delivery device of claim 19 , wherein the drug carrier is replaceable.
27 . The drug delivery device of claim 19 , wherein the attachment zone comprises a band of bone and/or cartilage adjacent to an articulating surface within the synovial joint.
28 . The drug delivery device of claim 27 , wherein the band extends from about 0.5 millimeters to about 1 centimeter away from the articulating surface.
29 . The drug delivery device of claim 19 , wherein the synovial joint is a hip joint, and the attachment zone comprises a non-articulating portion of bone and/or cartilage within the hip.
30 . The drug delivery device of claim 29 , wherein the attachment zone comprises a band of bone and/or cartilage adjacent to at least one of a femoral head, and an acetabulum.
31 . The drug delivery device of claim 19 , wherein the synovial joint is a knee joint, and the attachment zone comprises a non-articulating portion of bone and/or cartilage within the knee.
32 . The drug delivery device of claim 31 , wherein the attachment zone comprises a band of bone and/or cartilage adjacent to at least one of a tibial plateau, a femoral condyle, a patellofemoral area, the medial rim of a femoral trochlea, the lateral rim of a femoral trochlea, and the periphery of an intercondylar notch.
33 . The drug delivery device of claim 19 , wherein the synovial joint is a shoulder joint, and the attachment zone comprises a non-articulating portion of bone and/or cartilage within the shoulder.
34 . The drug delivery device of claim 33 , wherein the attachment zone comprises a band of bone and/or cartilage adjacent to at least one of the anatomical neck of a humerus, a glenoid cavity, and a glenoid neck.
35 . The drug delivery device of claim 19 , wherein the synovial joint is an arthroplastic joint comprising at least one prosthesis, and the attachment zone comprises a non-articulating portion of bone and/or cartilage within the joint.
36 . The drug delivery device of claim 35 , wherein the attachment zone comprises a band of bone and/or cartilage adjacent to the at least one prosthesis.Cited by (0)
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