# US 6,120,787 A · Sustained release particles > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 6,120,787 A - Document ID: US6120787A - Status: Granted - Kind: A - Application number: 09/051,709 - Filed: 1998-04-17 - Granted: 2000-09-19 - Earliest claimed: 1995-10-19 - Assignees: Biogram AB - Inventors: Nils-Ove Gustafsson; Timo Laakso; Peter Fyhr; Monica Jonsson - Web page: https://patentgrep.com/patent/US6120787A ## CPC - A61K 9/5031: {obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, poly(lactide-co-glycolide)} - A61K 9/1647: {Polyesters, e.g. poly(lactide-co-glycolide)} - A61K 9/1652: {Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin (homeopathic globules A61K9/1623)} - A61K: PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES (devices or methods specially adapted for bringing pharmaceutical products into particular physical or administering forms A61J3/00; chemical aspects of, or use of materials for deodorisation of air, for disinfection or sterilisation, or for bandages, dressings, absorbent pads or surgical articles A61L; soap compositions C11D) ## Abstract A method of preparing parenterally administrable sustained release microparticles, which comprises preparing core particles in an aqueous medium that is essentially free from organic solvent, a biologically active substance being entrapped therein during or after said preparation, drying the core particles and coating the same with a release-controlling polymer by air suspension technique so as to create a shell on the core particles without any detrimental exposure of the active substance to organic solvent. Microparticles obtainable by such a method also are provided. ## Claims ### Claim 1 A method for preparing parenterally administerable, sustained release microparticles containing a biologically active substance, which method comprises (i) preparing core particles from a biodegradable material in an aqueous medium which substantially lacks any organic solvents which are detrimental to the activity of said active substance; such that said biologically active substance becomes entrapped in said particles during or after said preparation; (ii) drying said core particles containing said active substance; and (iii) coating said core particles with a film-forming, biodegradable, release-controlling polymer by an air suspension technique which results in the creation of a shell comprised of said polymer containing said core particles under condition that avoid exposure of the active substance to any detrimental organic solvent potentially detrimental to the activity of said active substance. ### Claim 2 (depends on 1) The method of claim 1, which includes a washing step intervening steps (i) and (ii). ### Claim 3 (depends on 1) The method of claim 1, wherein said parenterally administrable microparticles are administrable via injection. ### Claim 4 (depends on 1) The method of claim 1, wherein said microparticles have a mean diameter ranging from 10 to 100 .mu.m. ### Claim 5 (depends on 4) The method of claim 4, wherein said particles have a mean diameter ranging from 20 to 100 .mu.m. ### Claim 6 (depends on 1) The method of claim 1, wherein said core particle material is selected from the group consisting of starches, and modified forms thereof. ### Claim 7 (depends on 1) The method of claim 1, wherein said polymer is selected from the group consisting of homo- or copolymers prepared from (.alpha.-hydroxy acids and/or cyclic dimers of .alpha.-hydroxy acids. ### Claim 8 (depends on 7) The method of claim 7, wherein said .alpha.-hydroxy acid is selected from the group consisting of lactic acid and glycolic acid. ### Claim 9 (depends on 7) The method according to claim 7, wherein said cyclic dimers are selected from the group consisting of glycolides and lactides. ### Claim 10 (depends on 1) The method of claim 1, wherein said core particles are prepared by a method comprising an aqueous two-phase system. ### Claim 11 (depends on 1) The method of claim 1, wherein said polymer is applied to the core particles in the form of a solution, a pseudolatex, or an emulsion. ### Claim 12 (depends on 11) The method according to claim 11, wherein said coating solution is an aqueous solution. ### Claim 13 (depends on 11) The method of claim 11, wherein said pseudolatex comprises an aqueous polymer composition. ### Claim 14 (depends on 11) The method of claim 11, wherein said emulsion is an aqueous emulsion. ### Claim 15 (depends on 14) The method of claim 14, wherein said emulsion comprises an aqueous emulsion wherein one of the phases comprises a polymer dissolved in a solvent. ### Claim 16 (depends on 1) The method according to claim 1, wherein said air suspension technique is selected from the group consisting of fluidized bed techniques, spouted bed techniques, and Wurster process techniques. ### Claim 17 (depends on 16) The method of claim 16, wherein said fluidized bed technique comprises a vacuum fluidized bed technique. ### Claim 18 (depends on 1) The method of claim 1, wherein said cores particles further comprise agents which stabilize the active substance contained therein. ### Claim 19 (depends on 1) The method according to claim 1, wherein at least one additional additive is incorporated into the release-controlling polymer shell during application thereof, and wherein said at least one additive is selected from the group consisting of film property modifying agents and release-controlling agents. ### Claim 20 (depends on 19) The method of claim 19, wherein said film property modifying agent is a plasticizer or surfactant. ### Claim 21 (depends on 1) The method according to claim 1, wherein the amount of said polymer shell material ranges from 1 to 200 percent by weight relative to the core weight. ### Claim 22 (depends on 21) The method according to claim 21, wherein the amount of the polymer shell material ranges from 5 to 100 percent by weight relative to the core weight. ### Claim 23 (depends on 1) A method according to claim 1, wherein said biologically active substance is a substance which is sensitive to exposure to organic solvents. ### Claim 24 (depends on 1) A method according to claim 1, wherein said active substance is selected from the group consisting of peptides, polypeptides, and proteins. ### Claim 25 A method of coating small particles comprising applying to said small particles by an air suspension technique an emulsion comprising a polymeric coating material wherein one of the phases of said emulsion is a liquid of said polymeric coating material comprised in a solvent and the other phase is water. ### Claim 26 (depends on 25) The method of claim 25, wherein said small particles are microparticles. ### Claim 27 Parenterally administrable sustained release microparticles, which comprise: (a) core particles of a biodegradable material and entrapped therein a biologically active substance which is sensitive to exposure to organic solvents, said core particles having been prepared in an aqueous medium essentially free from organic solvent to which said biologically active substance is sensitive; and (b) a shell, on said core particles, from a film-forming, biodegradable, release-controlling polymer; said shell having been applied on the core particles by means of air-suspension technique. ### Claim 28 (depends on 27) Microparticles of claim 27, wherein said biologically active substance is selected from the group consisting of peptides, polypeptides and proteins. ### Claim 29 (depends on 27) Microparticles of claim 27, which have a mean diameter ranging from 10 to 100 .mu.m. ### Claim 30 (depends on 27) Microparticles of claim 27, wherein said core particle material is selected from the group consisting of starches and modified forms thereof. ### Claim 31 (depends on 27) Microparticles of claim 27, wherein said shell-forming polymer is selected from the group consisting of homo- or copolymers prepared from .alpha.-hydroxy acids and/or cyclic dimers or .alpha.-hydroxy acids. ### Claim 32 (depends on 27) Microparticles of claim 27, wherein said shell-forming polymer has been applied to the core particles in the form of an aqueous emulsion thereof.