US4443497A
Expired / Lapsed
US
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Method of preparing microcapsules
Assignee: Tanabe Pharma Corp
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Filing: 1981-12-21
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Granted: 1984-04-17
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Expires: 2001-12-21
Abstract
Abstract Microcapsules are prepared by conducting the phase-separation of a coating polymer material in the presence of ethylcellulose. Ethylcellulose present in the phase separation system minimizes the coagulation of the coating polymer material.
Inventors
- 👤 Masayoshi Samejima
- 👤 Goichi Hirata
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-26 13:56
CPC Classifications
A; A61; A61K; A61K9/00; A61K9/14; A61K9/16; A61K9/1682; A61K9/1694; A61K9/1605; A61K9/1629; A61K9/1635; A61K9/1652; B; B01; B01J; B01J13/00; B01J13/02; B01J13/06; B01J13/08
Claims Analysis
Total Claims: 11
Claim 1
Independent Claim
215 words
A method of preparing microcapsules which comprises: (i) dissolving a coating polymer material which is selected from the group consisting of (a) water-insoluble, acid-soluble coating polymer material, (b) enteric coating polymer material and (c) amphoteric coating polymer material; and 0.05 to 5 grams of ethylcellulose having an ethoxy content of 44-55 w/w % per gram of said coating polymer material; in a solvent selected from the class consisting of a chlorinated hydrocarbon having one to three carbon atoms, an alkanol having one to four carbon atoms, an alkanone having three to five carbon atoms, a mixture of said alkanol and said alkanone, 2-methoxyethanol, 2-ethoxyethanol, 2-butoxyethanol, dioxane, epihalohydrin, trimethyl phosphate, triethyl phosphate, tetrahydrofuran and diacetone alcohol to form a solution; (ii) dispersing particles of a pharmaceutically active compound as a core material in said solution to form a dispersion; (iii) adding an organic liquid which is miscible with said solvent and which is a nonsolvent for said coating polymer material and the pharmaceutically active compound to said dispersion thereby forming coating walls of said coating polymer material on and around said particles of said core material, whereby the ethyl cellulose present minimizes the coagulation of the coating polymer material and/or the adhesion or agglomeration of the thus-formed microcapsules, and then (iv) recovering the thus-formed microcapsules therefrom.
Claim 2
Independent Claim
215 words
A method of preparing microcapsules which comprises: (i) dissolving a coating polymer material which is selected from the group consisting of (a) water-insoluble, acid-soluble coating polymer material, (b) enteric coating polymer material and (c) amphoteric coating polymer material; and 0.05 to 5 grams of ethylcellulose having an ethoxy content of 44-55 w/w % per gram of said coating polymer material; in a solvent selected from the class consisting of a chlorinated hydrocarbon having one to three carbon atoms, an alkanol having one to four carbon atoms, an alkanone having three to five carbon atoms, a mixture of said alkanol and said alkanone, 2-methoxyethanol, 2-ethoxyethanol, 2-butoxyethanol, dioxane, epihalohydrin, trimethyl phosphate, triethyl phosphate, tetrahydrofuran and diacetone alcohol to form a solution; (ii) dispersing particles of a pharmaceutically active compound as a core material in said solution to form a dispersion; (iii) adding an organic liquid which is miscible with said solvent and which is a nonsolvent for said coating polymer material and the pharmaceutically active compound to said dispersion thereby forming coating walls of said coating polymer material on and around said particles of said core material, whereby the ethyl cellulose present minimizes the coagulation of the coating polymer material and/or the adhesion or agglomeration of the thus-formed microcapsules, and then (iv) recovering the thus-formed microcapsules therefrom.
Claim 3
Dependent Claim
113 words
The method according to claim 1, wherein said coating polymer material is selected from the class consisting of carboxyalkyl alkylcellulose; phthalic or succinic acid ester of alkyl cellulose, hydroxyalkyl alkylcellulose, cellulose acetate; copolymers of acrylic or methacrylic acid and alkyl esters of acrylic or methacrylic acid; copolymers of acrylic or methacrylic acid, alkyl acrylate and alkyl methacrylate; copolymers of (A) dialkylaminoalkyl methacrylate and (B) an alkyl methacrylate; copolymers of (A) dialkylaminoalkyl methacrylate, (B) a first alkyl methacrylate, and (C) a second alkyl methacrylate; polyvinylacetal dialkylaminoacetate; and copolymers of (A) vinylpyridine or alkylvinylpyridine, (B) acrylic or methacrylic acid, and (C) a monomer selected from acrylonitrile, styrene and alkyl ester of acrylic or methacrylic acid.
Claim 4
Dependent Claim
73 words
The method according to claim 1, wherein said coating polymer material is selected from carboxyalkyl alkylcellulose; phthalic acid ester of hydroxyalkyl alkylcellulose or cellulose acetate; copolymers of methacrylic acid and alkyl acrylate; copolymers of methacrylic acid and alkyl methacrylate; copolymers of methacrylic acid, alkyl acrylate and alkyl methacrylate; copolymers of dialkylaminoethyl methacrylate, butyl methacrylate and methyl methacrylate; polyvinylacetal dialkylaminoacetate; and copolymers of (A) vinylpyridine or alkylvinylpyridine, (B) methacrylic acid and (C) alkyl acrylate.
Claim 5
Dependent Claim
24 words
The method according to claim 2 or 3, where the alkyl group contained in the coating polymer material has 1 to 4 carbon atoms.
Claim 6
Dependent Claim
73 words
The method according to claim 1, wherein said coating polymer material is selected from carboxymethyl ethylcellulose, cellulose acetate phthalate, hydroxypropyl methylcellulose phthalate, polyvinylacetal diethylaminoacetate, copolymers of dimethylaminoethyl methacrylate, methyl methacrylate and butyl methacrylate; copolymers of methacrylic acid, methyl acrylate and methyl methacrylate; copolymers of methacrylic acid and methyl methacrylate; copolymers of methacrylic acid and ethyl acrylate; copolymers of 2-vinylpyridine, methacrylic acid and methyl acrylate; and copolymers of 2-methyl-5-vinylpyridine, methyl acrylate and methacrylic acid.
Claim 7
Dependent Claim
30 words
The method according to claim 1, wherein said coating polymer material is present in an amount of about 0.02 to about 10 grams per gram of the pharmaceutically active compound.
Claim 8
Dependent Claim
55 words
The method according to claim 1, 2 or 3, wherein said pharmaceutically active compound has a particle size of about 5 to about 100μ, and said ethylcellulose has a viscosity of about 3 to about 500 cP when measured at 25° C. with respect to a 5 w/w % solution of said ethylcellulose in toluene-ethanol.
Claim 9
Dependent Claim
40 words
The method according to claim 1, 2 or 3, wherein said solvent is an alkanol having 1 to 4 carbon atoms, an alkanone having 3 to 5 carbon atoms, a mixture of said alkanol and said alkanone, or ethyl acetate.
Claim 10
Dependent Claim
17 words
The method according to claim 1, 2, or 3 further comprising adding a plasticizer to said solution.
Claim 11
Dependent Claim
63 words
The method according to claim 9, wherein said plasticizer is selected from the class consisting of glycerin monoacetate, glycerin diacetate, glycerin triacetate, propyleneglycol, polyvinylacetate, an ester of glycerin or acetylglycerin with an alkanoic acid having 10 to 18 carbon atoms; polyethyleneglycol, dialkylpolysiloxane, and polylactic acid, and is added in an amount of 0.01 to 1.0 gram per gram of said coating polymer material.
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USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1987-04-17 | 1987-10-17 | 1988-04-17 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1991-04-17 | 1991-10-17 | 1992-04-17 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1995-04-17 | 1995-10-17 | 1996-04-17 | $7700.00 | Window Closed / Lapsed |