Method and system for alleviating joint pain
AssigneeEmboMedics, Inc.
InventorsJafar Golzarian, Lihui Weng, Omid Souresrafil
Life of this patent
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Abstract
A system for providing a drug-eluting resorbable hydrogel for treating chronic pain, the system including carboxymethyl chitosan and oxidized carboxymethyl cellulose solutions, which together with one or more bioactive agents, can be mixed and delivered at the time of use in order to gel in situ within a joint space. Once delivered, the hydrogel can provide bioactive agents such as NSAIDs directly to the areas commonly associated with chronic pain, including to the spine, knee, shoulder, and elbow. The hydrogel is substantially non-inflammatory, and substantially biodegradable over time, to provide prolonged drug release.
Claims10
A system for intraarticular drug delivery, comprising:
- a) a deliverable composition comprising a plurality of parts adapted to be mixed at the time of use in order to be delivered to an intraarticular space under conditions suitable to form a hydrogel in situ, b) one or more active agents included within the deliverable composition, and c) a device for mixing the composition parts, including active agent(s), in order to deliver the mixed composition to the intraarticular space. A system according to claim 1, wherein the plurality of parts comprises a first solution comprising between about 0.5% and about 3% weight per volume (w/v) carboxymethyl chitosan (CCN) in a first solvent, and a second solution comprising between about 0.5% and about 3% w/v oxidized carboxymethyl cellulose (OCMC) in a second solvent, and the first and second parts are mixed to form a single liquid phase that can be delivered to the joint space in order to form a hydrogel at the targeted joint site.
A system according to claim 2, wherein the bioactive agent comprises One or more NSAIDS.
A method of intraarticular drug delivery, comprising:
- a) providing a deliverable composition comprising a plurality of parts adapted to be mixed at the time of use in order to be delivered to an intraarticular space under conditions suitable to form a hydrogel in situ, b) providing one or more active agents adapted to be included within the deliverable composition, and c) providing a device adapted to mix the composition parts, including active agent(s), d) mixing the plurality of parts to form a deliverable composition, and e) delivering the composition to the intraarticular space in a manner sufficient to form a hydrogel in situ.
Dependencies are inferred from the claim text.