Claims for Patent: 6,036,976

Summary for Patent: 6,036,976

Title:	Sustained release microspheres and preparation thereof
Abstract:	Disclosed is a method of producing microspheres which comprises subjecting a w/o/w emulsion or o/w emulsion to an in-water drying method under the following conditions: 1) the amount of microspheres per m.sup.3 of an external aqueous phase is about 0.1 to about 500 kg, 2) the square root of the area (unit: m.sup.2) of the liquid surface in contact with the gas phase is about 0.2 to about 4.5 per the cube root of the volume (unit: m.sup.3) of an external aqueous phase, 3) the w/o/w emulsion or o/w emulsion is replaced at the replacement frequency of about 0.01 to about 10 times/minutes, 4) a gas is blown to the w/o/w emulsion or o/w emulsion at the gas transfer rate near the liquid surface of about 0.1 to about 300 m/second, and 5) the gas is replaced at the replacement frequency of not less than about 0.5 times/minutes; and the method of the present invention increases the rate of solvent removal from microspheres in in-water drying, reduces the amount of solvent in microspheres in a short time.
Inventor(s):	Takechi; Nobuyuki (Osaka, JP), Ohtani; Seiji (Osaka, JP), Nagai; Akihiro (Osaka, JP)
Assignee:	Takeda Chemical Industries, Ltd. (Osaka, JP)
Application Number:	09/154,164
Patent Claims:	1. A sustained-release microsphere comprising a physiologically active substance and a biodegradable polymer, which is produced by a process which comprises: subjecting a w/o/w emulsion or o/w emulsion wherein said physiologically active substance is in an inner aqueous phase and said biodegradable polymer is in an external oil phase to an in-water drying method under the following conditions: 1) the amount of microspheres per m.sup.3 in an external aqueous phase is about 0.1 to about 500 kg, 2) the square root of the area (unit: m.sup.2) of the liquid surface in contact with the gas phase is about 0.2 to about 4.5 per the cube root of the volume (unit: m.sup.3) of the external aqueous phase, 3) the w/o/w emulsion or o/w emulsion is replaced at a replacement frequency of about 0.01 to about 10 times/minute, 4) a gas is blown toward the w/o/w emulsion or o/w emulsion so that the gas transfer rate near the liquid surface is about 10 to 300 m/second, and 5) the gas is replaced at a replacement frequency of not less than about 0.5 times/minute. 2. The microsphere according to claim 1, wherein the amount of microspheres per m.sup.3 in the external aqueous phase is about 0.5 to about 100 kg. 3. The microsphere accordingly to claim 1, wherein the square root of the area (unit: m.sup.2) of the liquid surface in contact with the gas phase is about 0.5 to about 3.0 per the cube root of the volume (unit: m.sup.3) of the external aqueous phase. 4. The microsphere according to claim 1, wherein the physiologically active substance is a physiologically active peptide. 5. The microsphere according to claim 1, wherein the physiologically active substance is an LH-RH agonist or an LH-RH antagonist. 6. The microsphere according to claim 1, wherein the biodegradable polymer is a biodegradable polymer having a free terminal carboxyl group. 7. The microsphere according to claim 1, wherein the biodegradable polymer is a lactic acid/glycolic acid polymer. 8. The microsphere according to claim 1, wherein the gas transfer rate near the liquid surface is about 10 to about 200 m/second. 9. The microsphere according to claim 1, wherein the gas transfer rate near the liquid surface is about 50 to about 150 m/second. 10. The microsphere according to claim 7, wherein the composition ratio of a lactic acid/glycolic acid is from about 90/10 to about 50/50. 11. The microsphere according to claim 1, wherein the physiologically active substance is a substance selected from the group consisting of LH-RH agonist, LH-RH antagonist, antitumor agent, antibiotic, antipyretic agent, analgesic, anti-inflammatory agent, antitussive expectorant, sedative, muscle relaxant, antiepileptic, antiulcer agent, antidepressant, anti-allergic agent, cardiotonic, antiarrhythmic agent, vasodilator, hypotensive diuretic, antidiabetic, antihyperlipidemic agent, anticoagulant, hemolytic, antituberculosis agent, hormone, narcotic antagonist, bone resorption suppressor, osteogenesis promoter and angiogenesis inhibitor. 12. The microsphere according to claim 1, wherein the physiologically active substance is: (1) a peptide represented by the formula: wherein R.sub.1 represents His, Tyr, Trp or p-NH.sub.2 -Phe; R.sub.2 represents Tyr or Phe; R.sub.3 represents Gly or a D- amino acid residue; R.sub.4 represents Leu, Ile or Nle; R.sub.5 represents (a) Gly-NH--R.sub.6 wherein R.sub.6 is H or an alkyl group with or without a hydroxyl group or (b) NH--R.sub.7 wherein R.sub.7 is H, an alkyl group with or without an amino or a hydroxyl group, or (c) ureido (--NH--CO--NH.sub.2); or (2) a peptide represented by the formula: ##STR13## wherein X represents hydrogen atom or tetrahydrofuryl-carboxamide; Q represents hydrogen atom or methyl; A represents nicotinoyl or N,N'-diethylamidino; B represents isopropyl or N,N'-diethylamidino; or a salt thereof. 13. The microsphere according to claim 1, wherein the physiologically active substance is leuprorelin or leuprorelin acetate. 14. A sustained-release microsphere comprising a physiologically active substance and a biodegradable polymer, which is produced by a process which comprises: subjecting a w/o/w emulsion or o/w emulsion wherein said physiologically active substance is in an inner aqueous phase and said biodegradable polymer in an external oil phase to an in-water-drying method under the following conditions: 1) the amount of microspheres per m.sup.3 in an external aqueous phase is about 0.1 to about 500 kg, 2) the square root of the area (unit: m.sup.2) of the liquid surface in contact with the gas phase is about 0.2 to about 4.5 per the cube root of the volume (unit: m.sup.3) of the external aqueous phase, 3) the w/o/w emulsion or o/w emulsion is replaced at a replacement frequency of about 0.01 to about 10 times/minute, 4) a gas is blown toward the w/o/w emulsion or o/w emulsion so that the gas transfer rate near the liquid surface is about 10 to about 200 m/second, and 5) the gas is replaced at a replacement frequency of not less than about 0.5 times/minute, wherein the physiologically active substance is leuprorelin or leuprorelin acetate, and the biodegradable polymer is a lactic acid/glycolic acid polymer having a composition ratio of about 90/10 to 50/50. 15. A sustained-release preparation, comprising the microsphere according to any one of claims 1 to 14 together with a pharmaceutically acceptable dispersant, excipient, disintegrating agent, binder, lubricant, thickening agent or base.