Injectable flowable composition comprising buprenorphine
View Patent ↗The present invention is directed to a buprenorphine sustained release delivery system capable of delivering buprenorphine, a metabolite, or a prodrug thereof for a duration of about 14 days to about 3 months. The buprenorphine sustained release delivery system includes a flowable composition and a solid implant for the sustained release of buprenorphine, a metabolite, or a prodrug thereof. The implant is produced from the flowable composition. The buprenorphine sustained release delivery system provides in situ 1-month and 3-month release profiles characterized by an exceptionally high bioavailability and minimal risk of permanent tissue damage and typically no risk of muscle necrosis.
1. An injectable flowable composition comprising:
(i) 8 wt % to about 22 wt % of buprenorphine free base;
(ii) about 25 wt % to about 50 wt % of a poly(DL-lactide-co-glycolide) biodegradable thermoplastic polymer; wherein the polymer has an average molecular weight of about 5,000 Daltons to about 40,000 Daltons; and
(iii) about 30 wt % to about 70 wt % of N-methyl-2-pyrrolidone.
2. The composition of claim 1 , wherein the composition is transformed in situ into a solid implant by contact with water or a bodily fluid.
3. The composition of claim 1 , wherein the polymer is a 50/50 poly(DL-lactide-co-glycolide) biodegradable thermoplastic polymer.
4. The composition of claim 1 , wherein the polymer has an average molecular weight of about 9,000 Daltons to about 20,000 Daltons.
5. The composition of claim 1 , wherein the polymer has a carboxy terminal group.
6. The composition of claim 1 , wherein the weight ratio of buprenorphine to polymer is between 0.01:1 and 2:1.
7. A method for treating a patient having an opioid dependency comprising parenterally administering to the patient a therapeutically effective amount of the composition of claim 1 once per month to treat the opioid dependency.