Methods for local drug delivery by microinjection
This invention provide novel compositions, methods and devices for sustained drug delivery. The microencapsulated sustained drug delivery compositions are deposited using oscillating needle apparatus oscillating at 10-12000 minutes per minutes. The injected compositions may undergo variety of physical chemical changes upon deposition. The physical and chemical changes enables improved drug encapsulation and sustained drug release. Also described are new methods to form polymer microparticles or polymer films/implants in situ inside the tissue. The invention also describes colored biodegradable microparticle based compositions wherein the compositions comprise drug encapsulated microparticles and coloring agent encapsulated microparticles mixed in any proportion. Medical applications of the compositions and methods described in this invention are also described.
1. A method for delivering an injectable composition at a local site in a tissue, the method comprising:
providing an injectable composition having a bioactive agent; and
injecting the injectable composition in the tissue at an amount of 1.0E-03 ml to 1.0E-16 ml per injection,
wherein the bioactive agent is encapsulated in a plurality of biodegradable microparticles, the microparticles being dispersed in a fluid carrier.
2. The method according to claim 1 , wherein the microparticles in the injectable composition have an average particle size in the range of 500 nm to 300 microns.
3. The method according to claim 2 , wherein the microparticles in the injectable composition are of substantially spherical, semispherical, elliptical, circular disk, or irregular shape.
4. The method according to claim 1 , wherein the fluid carrier of the injectable composition is an aqueous based medium.
5. The method according to claim 1 , wherein the injected microparticles are deposited in a pre-determined two or three-dimensional pattern in the tissue.
6. The method according to claim 1 , wherein the microparticles have a visualization agent.
7. The method according to claim 6 , wherein the visualization agent is a coloring composition, a fluorescent composition or a radio opaque contrast agent or an NMR contrast agent.
8. The method according to claim 1 , wherein the biodegradable microparticles are prepared from a biodegradable polymer selected from a group comprising of polymers, dendramers, copolymers or oligomers of glycolide, dl-lactide, d-lactide, l-lactide, caprolactone, dioxanone and trimethylene carbonate; degradable polyurethanes; polyamides; polyesters; polypeptides; polyhydroxyacids; polyorthocarbonates, polylactic acid; polyglycolic acid; polyanhydrides; and polylactones.
9. The method of claim 1 , wherein the injectable composition is injected in the tissue at a depth of 10 microns to 5 mm.