Therapeutic microparticles
Biodegradable, compression resistant microparticles adapted for injection through a catheter system, such as is useful for selective embolization procedures. The microparticles can optimally be neutrally buoyant relative to a target bodily fluid. Various active agents may be included in the microparticles, such an anesthetic which can reduce pain during an embolization procedure. The invention further comprises methods and equipment for testing and delivering compression resistant microparticles.
1 . A microparticle comprising:
a homopolymer of at least a poly(a-hydroxy ester) or a copolymer of at least a poly(a-hydroxy ester) having a trimethylene carbonate moiety; the microparticle adapted for catheter delivery.
2 . A microparticle according to claim 1 , wherein said microparticle is an embolic agent.
3 . A microparticle according to claim 1 , wherein said microparticle is substantially neutrally buoyant relative to a target bodily fluid for a time necessary to deliver a bolus of particles.
4 . A microparticle according to claim 1 , having at least one bioactive agent.
5 . A microparticle according to claim 1 , having at least one additive.
6 . A microparticle according to claim 1 , further comprising at least one coating.
7 . A microparticle according to claim 1 , having a number of distributed voids.
8 . A microparticle according to claim 1 , having a convoluted surface.
9 . A catheter deliverable microparticle comprising: at least one bioresorbable base polymer and a void volume, wherein the microparticle is compression resistant.
10 . A microparticle according to claim 9 , wherein said microparticle is an embolic agent.
11 . A microparticle according to claim 9 , wherein said microparticle is substantially neutrally buoyant relative to a target bodily fluid for a time necessary to deliver a bolus of particles.
12 . A microparticle according to claim 9 , having at least one bioactive agent.
13 . A microparticle according to claim 9 , having at least one additive.
14 . A microparticle according to claim 9 , further comprising at least one coating.
15 . A microparticle according to claim 9 , having a number of distributed voids.
16 . A microparticle according to claim 9 , having a convoluted surface.
17 . A bolus of embolic microparticles, comprising: a plurality of catheter deliverable microparticles, said catheter deliverable microparticles being compression resistant and having at least one bioresorbable base polymer and having a void volume.
18 . A bolus of embolic microparticles according to claim 17 , wherein a number of said catheter deliverable microparticles have a density which is between 0.9 g/cc and 1.4 g/cc.
19 . A bolus of embolic microparticles according to claim 17 , wherein a number of said catheter deliverable microparticles have a specific gravity of 0.6 to 1.4 relative to a target bodily fluid.
20 . A bolus of embolic microparticles according to claim 17 , wherein a therapeutically effective number of said catheter deliverable microparticles are neutrally buoyant relative to a target bodily fluid.
21 . A bolus of embolic microparticles according to claim 17 , wherein a number of said catheter deliverable microparticles have at least one bioactive agent.
22 . A bolus of embolic microparticles according to claim 17 , wherein a number of said catheter deliverable microparticles have an external diameter and are resistant to a deformation of said external diameter of greater than 10%.
23 . A catheter deliverable microparticle comprising:
at least one bioresorbable base polymer,
a second material which is different from said at least one bioresorbable base polymer,
a void volume in which said second material is present, and
wherein said microparticle is compression resistant.
24 . A method of making microparticles comprising
providing an organic solvent;
mixing the organic solvent and a solvated polymer in an aqueous solution;
maintaining the organic solvent in the aqueous solution in a quantity and under conditions that maintain the organic solvent below an organic solvent saturation point of the aqueous solution; and
creating microparticles in the aqueous solution while maintaining the solution below the saturation point.
25 . The method of claim 24 that further comprises providing as the organic solvent ethyl acetate.
26 . The method of claim 24 that further comprises providing as the organic solvent methylene chloride.
27 . A method of testing a microparticle for compression resistance comprising
providing a sample of microparticles suspended in a solution, the microparticles having a given nominal cross-sectional dimension of x;
providing a test apparatus that includes at least one constriction with an effective opening size with a dimension less than x;
passing the sample of microparticles and solution through the at least one constriction in the test apparatus under pressure;
sampling the solution downstream of the at least one constriction to determine if the microparticles passed through the constriction without permanent damage to the microparticles;
wherein particles of dimension x that do not pass through the constriction are deemed compression-resistant.