CPC A61K 9/0024 (2013.01) [A61K 9/0019 (2013.01); A61K 9/0029 (2013.01); A61K 9/204 (2013.01); A61K 9/2031 (2013.01); A61K 31/167 (2013.01); A61K 31/445 (2013.01); A61K 31/519 (2013.01); A61K 31/5415 (2013.01); A61K 31/7048 (2013.01); A61K 38/12 (2013.01); A61K 47/34 (2013.01); C08G 63/664 (2013.01)] | 31 Claims |
1. An injectable biodegradable drug delivery composition comprising:
(i) a mixture of at least three different block copolymers, wherein each block copolymer is:
(a) a biodegradable triblock copolymer having the formula:
Av-Bw-Ax
wherein A is a polyester and B is polyethylene glycol and v and x are the number of repeat units ranging from 1 to 3,000 and w is the number of repeat units ranging from 3 to 300 and v=x or v≠x; or
(b) a biodegradable diblock copolymer having the formula:
Cy-Az
wherein A is a polyester and C is an end-capped polyethylene glycol and y and z are the number of repeat units with y ranging from 2 to 250 and z ranging from 1 to 3,000; and
wherein the mixture comprises at least one (a) and at least one (b); and the weight ratio of the sum of the biodegradable triblock copolymers of (a) and the sum of the biodegradable diblock copolymers of (b) is 1:19 to 5:1; and wherein for at least one of the copolymers according to (a) or (b) A is poly(lactic-co-glycolic acid) (PLGA); and
(ii) at least one pharmaceutically active ingredient; wherein the release kinetics of said at least one active ingredient from said biodegradable drug delivery composition can be modulated without adversely affecting injectability and/or viscosity before injection of the injectable biodegradable drug delivery composition and/or depot robustness after injection of the biodegradable drug delivery composition, compared to a composition having a single biodegradable triblock of the copolymer of (a) and a single biodegradable diblock of the copolymer of (b).
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