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US3965033A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for the production of oil-containing microcapsules

Assignee: Fujifilm Holdings Corp
•
Filing: 1974-01-31
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Granted: 1976-06-22
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Expires: 1994-01-31
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Abstract

Abstract In a process for producing oil-containing microcapsules by coacervation comprising A. INTRODUCING A FINE POWDER OR HYDROPHOBIC LIQUID INTO A HIGH MOLECULAR WEIGHT ELECTROLYTIC WALL-FORMING COLLOID; B. COACERVATING THE RESULTING DISPERSION OR EMULSION; C. COOLING THE RESULTING COACERVATE TO GEL IT AND FORM THE WALL OF SAID MICROCAPSULES; AND D. HARDENING SAID WALL OF SAID MICROCAPSULES; THE IMPROVEMENT WHICH COMPRISES ADDING A PHENOLIC COMPOUND TO THE SYSTEM.

Inventors

  • 👤 Hiroharu Matsukawa
  • 👤 Keiso Saeki

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-26 15:41
CPC Classifications
A; A61; A61K; A61K8/00; A61K8/02; A61K8/11; A61K9/00; A61K9/48; A61K9/50; A61Q; A61Q13/00; B; B01; B01J; B01J13/00; B01J13/02; B01J13/06; B01J13/08; A61K2800/00; A61K2800/40; A61K2800/41; A61K2800/412; Y; Y10; Y10T; Y10T428/00; Y10T428/29; Y10T428/2982; Y10T428/2984; Y10T428/2985; Y10T428/2987

Claims Analysis

Total Claims: 21
Claim 1
Independent Claim 595 words
A process for producing oil-containing microcapsules by coacervation, which comprises: 1. dispersing a hydrophobic fine powder or emulsifying a hydrophobic liquid into an aqueous solution of at least one type of high molecular weight electrolytic colloid for use in forming the capsule wall; 2. subjecting dispersion or emulsion obtained in Step (1) to water dilution, and/or pH adjustment to achieve coacervation and optionally, adding an aqueous solution of a high molecular weight colloid, if desired; 3. cooling the formed coacervate to gel the same; 4. adding a phenolic compound thereto at a temperature above 5°C., during Steps (2) and (3); 5. adding a hardening agent to the system; 6. adding a shock-preventing agent to the system at a temperature lower than the gelling point of gelatin, said shock-preventing agent being capable of preventing a rapid increase in the viscosity of the system during pre-hardening of the coacervate when the pH of the system approaches a value of no less than about 6; 7. adjusting the pH of the system to the alkali side, said Steps (5) through (7) constituting the pre-hardening treatment; and 8. optionally elevating the temperature of the system to more effectively harden the coacervate, the order of Steps (5) through (7) being capable of being freely modified with respect to each other, and Step (5) further being capable of being conducted prior to Step (4), said shock-preventing agent being present in an amount sufficient to prevent a rapid increase in viscosity during pre-hardening, when the pH of the system approaches a value of no less than about 6 and being a member selected from the group consisting of a modified cellulose comprising polysaccharides having β-1,4-glucoside bonds of glucoses and having anionic functional groups, an anionic starch derivative composed of a linear polysaccharide amylose formed by only α-1,4-bonds of D-glucose, and a branched polysaccharide amylopectin formed by mainly α-1,4 bonds of D-glucose and a partially side chain branched by α-1,6 bonds, an anionic acid polysaccharide, obtained by polycondensing linearly D-galacturonic acid between the α-1,4 bonds thereof, said acid polysaccharide containing pectin, pectic acid, and pectinic acid, a condensate of naphthalene sulfonic acid and Formalin, which condensate is represented by the formula: ##SPC3## wherein X is a hydrogen atom, an alkali metal, or an ammonium group, and n is a positive integer, a hydroxyethyl cellulose derivative selected from the group consisting of the carboxymethyl ether of hydroxyethyl cellulose, hydroxyethyl cellulose sulfate, and hydroxyethyl cellulose phosphate, a vinylbenzene sulfonate copolymer selected from the group consisting of a vinylbenzene sulfonate-acryloylmorpholine copolymer, a vinylbenzene sulfonate-morpholinoethylacrylamide copolymer, a vinylbenzene sulfonate acrylamide copolymer, a vinylbenzene sulfonate-vinylpyrrolidone copolymer, and a vinylbenzene sulfonatemethyloxy-methylacrylamide, said copolymer having the following group within its molecular structure: ##SPC4## wherein M is an alkali metal and n is a positive integer and, an acrylic acid copolymer selected from the group consisting of an acrylic acid-acryloylmorpholine copolymer, an acrylic acid-morpholinomethylacrylamide copolymer, an acrylic acid-acrylamide copolymer, an acrylic acid-vinylpyrrolidone copolymer, an acrylic acid-methoxymethylacrylamide copolymer, said copolymer having the following group within its molecular structure: ##EQU2## wherein X is a hydrogen atom or an alkali metal, and n is a positive integer, a maleic acid copolymer of maleic acid anhydride and at least one monomer having at least one unsaturated bond which is subjected to addition polymerization with said anhydride or a salt thereof, and a nucleic acid compound, said phenolic compound being present in an amount ranging from 1/500 to 3/4 part by weight based on one part by weight of gelatin used to form the capsule wall, at least one of the hydrophilic colloids employed being gelatin.
Claim 2
Dependent Claim 595 words
A process for producing oil-containing microcapsules by coacervation, which comprises: 1. dispersing a hydrophobic fine powder or emulsifying a hydrophobic liquid into an aqueous solution of at least one type of high molecular weight electrolytic colloid for use in forming the capsule wall; 2. subjecting dispersion or emulsion obtained in Step (1) to water dilution, and/or pH adjustment to achieve coacervation and optionally, adding an aqueous solution of a high molecular weight colloid, if desired; 3. cooling the formed coacervate to gel the same; 4. adding a phenolic compound thereto at a temperature above 5°C., during Steps (2) and (3); 5. adding a hardening agent to the system; 6. adding a shock-preventing agent to the system at a temperature lower than the gelling point of gelatin, said shock-preventing agent being capable of preventing a rapid increase in the viscosity of the system during pre-hardening of the coacervate when the pH of the system approaches a value of no less than about 6; 7. adjusting the pH of the system to the alkali side, said Steps (5) through (7) constituting the pre-hardening treatment; and 8. optionally elevating the temperature of the system to more effectively harden the coacervate, the order of Steps (5) through (7) being capable of being freely modified with respect to each other, and Step (5) further being capable of being conducted prior to Step (4), said shock-preventing agent being present in an amount sufficient to prevent a rapid increase in viscosity during pre-hardening, when the pH of the system approaches a value of no less than about 6 and being a member selected from the group consisting of a modified cellulose comprising polysaccharides having β-1,4-glucoside bonds of glucoses and having anionic functional groups, an anionic starch derivative composed of a linear polysaccharide amylose formed by only α-1,4-bonds of D-glucose, and a branched polysaccharide amylopectin formed by mainly α-1,4 bonds of D-glucose and a partially side chain branched by α-1,6 bonds, an anionic acid polysaccharide, obtained by polycondensing linearly D-galacturonic acid between the α-1,4 bonds thereof, said acid polysaccharide containing pectin, pectic acid, and pectinic acid, a condensate of naphthalene sulfonic acid and Formalin, which condensate is represented by the formula: ##SPC3## wherein X is a hydrogen atom, an alkali metal, or an ammonium group, and n is a positive integer, a hydroxyethyl cellulose derivative selected from the group consisting of the carboxymethyl ether of hydroxyethyl cellulose, hydroxyethyl cellulose sulfate, and hydroxyethyl cellulose phosphate, a vinylbenzene sulfonate copolymer selected from the group consisting of a vinylbenzene sulfonate-acryloylmorpholine copolymer, a vinylbenzene sulfonate-morpholinoethylacrylamide copolymer, a vinylbenzene sulfonate acrylamide copolymer, a vinylbenzene sulfonate-vinylpyrrolidone copolymer, and a vinylbenzene sulfonatemethyloxy-methylacrylamide, said copolymer having the following group within its molecular structure: ##SPC4## wherein M is an alkali metal and n is a positive integer and, an acrylic acid copolymer selected from the group consisting of an acrylic acid-acryloylmorpholine copolymer, an acrylic acid-morpholinomethylacrylamide copolymer, an acrylic acid-acrylamide copolymer, an acrylic acid-vinylpyrrolidone copolymer, an acrylic acid-methoxymethylacrylamide copolymer, said copolymer having the following group within its molecular structure: ##EQU2## wherein X is a hydrogen atom or an alkali metal, and n is a positive integer, a maleic acid copolymer of maleic acid anhydride and at least one monomer having at least one unsaturated bond which is subjected to addition polymerization with said anhydride or a salt thereof, and a nucleic acid compound, said phenolic compound being present in an amount ranging from 1/500 to 3/4 part by weight based on one part by weight of gelatin used to form the capsule wall, at least one of the hydrophilic colloids employed being gelatin.
Claim 3
Dependent Claim 15 words
The process of claim 1 where the coacervate is hardened between steps (7) and (8).
Claim 4
Dependent Claim 25 words
The process of claim 1, wherein said phenolic compound is a member selected from the group consisting of a phenol monomer and a phenol resin.
Claim 5
Dependent Claim 30 words
The process of claim 3, wherein said phenol monomer is an aromatic compound in which the hydrogen atom attached to the ring is substituted with at least one hydroxyl group.
Claim 6
Dependent Claim 25 words
The process of claim 4, wherein said phenolic monomer is a member selected from the group consisting of polyhydric phenols, phenolcarboxylic acids, nitrophenols and biphenols.
Claim 7
Dependent Claim 62 words
The process of claim 4, wherein said phenol monomer is a phenol compound having as a substituent a member selected from the group consisting of an alkyl group, an allyl group, a halogen atom, a halogen-substituted alkyl group, a cycloalkyl group, a phenyl group, a halogen-substituted phenyl group, an alkyl-substituted phenyl group, a biphenyl group, a benzyl group and a alpha-alkylbenzyl group.
Claim 8
Dependent Claim 47 words
The process of claim 4, wherein said phenol monomer is selected from the group consisting of o-cresol, m-cresol, p-cresol, o-ethylphenol, p-t-butylphenol, p-nonylphenol, p-dodecylphenol, p-octylphenol, p-fluoro-phenol, p-chlorophenol, p-bromophenol, m-chlorophenol, p-cyclohexylphenol, o-phenylphenol, p-phenylphenol, o-(o-chlorophenyl)-phenol, p-(p-bromophenyl)-phenol, o-(2-biphenylyl)-phenol, alpha-phenyl-o-cresol, 2,4-xylenol, 3,4-xylenol, 2-allyl-p-cresol, 2,4-dichlorophenol, 2,5-dichlorophenol, 4-chloro-m-cresol, 2-chloro-4-phenylphenol, 2,3,5-trimethylphenol, 2,3,5,6-tetramethylphenol, alpha-naphthol and beta-naphthol.
Claim 9
Dependent Claim 39 words
The process of 5, wherein said polyhyric phenol is a member selected from the group consisting of resorcinol, catechol, hydroquinone, pyrogallol, fluoroglucinol, 1,2-dihydroxy-4-methylbenzene, 1,3-dihydroxy-5-methylbenzene, 3,4-dihydroxy-1-methylbenzene, 3,5-dihydroxy-1-methylbenzene, 2,4-dihydroxyethyl-benzene, t-butylhydroxyquinone, 1,3-naphthalenediol, 1,4-naphthalenediol, 1,5-naphthalenediol, 1,6-naphthalenediol, 1,7-naphthalenediol, 4-phenylpyrocatechol, 4-chloroesorcinol, phenyl-hydroquinone, 4,6-dichloroesorcinol and tetrachorohydroquinone.
Claim 10
Dependent Claim 39 words
The process of 5, wherein said polyhyric phenol is a member selected from the group consisting of resorcinol, catechol, hydroquinone, pyrogallol, fluoroglucinol, 1,2-dihydroxy-4-methylbenzene, 1,3-dihydroxy-5-methylbenzene, 3,4-dihydroxy-1-methylbenzene, 3,5-dihydroxy-1-methylbenzene, 2,4-dihydroxyethyl-benzene, t-butylhydroxyquinone, 1,3-naphthalenediol, 1,4-naphthalenediol, 1,5-naphthalenediol, 1,6-naphthalenediol, 1,7-naphthalenediol, 4-phenylpyrocatechol, 4-chloroesorcinol, phenyl-hydroquinone, 4,6-dichloroesorcinol and tetrachorohydroquinone.
Claim 11
Dependent Claim 38 words
The process of claim 5, wherein said phenol carboxylic acid is a member selected from the group consisting of m-oxybenzoic acid, p-oxybenzoic acid, protocatechuic acid, alpha-resorcylic acid, beta-resorcylic acid, orsellinic acid, caffeic acid, umbellic acid and gallic acid.
Claim 12
Dependent Claim 21 words
The process of claim 5, wherein said nitrophenol is a member selected from the group consisting of p-nitrophenol, m-nitrophenol and o-nitrophenol.
Claim 13
Dependent Claim 32 words
The process of claim 5 wherein said biphenol is a member selected from the group consisting of biphenol, bicresol, dibenzylbiphenol, diethylbiphenol, dipropylbiphenol, diallylbiphenol, dihalobiphenol, diphenyltetrol, methylenediphenol, methylenebis (alkylphenol), methylenebis(benzylphenol), methylenebis(phenylphenol) and methylenebis(halophenol).
Claim 14
Dependent Claim 38 words
The process of claim 5 wherein said biphenol is a member selected from the group consisting of o-o'-biphenol, m-m'-biphenol, p-p'-biphenol, 4,4'-bi-o-cresol, 4,4'-bi-m-cresol, 6,6'-o-cresol, 2,2'-diethyl-p-p'-biphenol, 2,2'-diallyl-p-p'-biphenol, 3,3'5,5'-biphenyltetrol, 4,4'-methylenediphenol, 2,4'-methylenediphenol, 2,2'-methylenediphenol, 4,4'-isopropylidenediphenol, 4,4'-cyclopentylidenephenol, 4,4'-cyclohexylidenediphenol, methylenediresorcinol, 4,4'-methylene-di-o-cresol, 4,4'-methylenebis(2-chlorophenol), 4,4'-methylenebis(2,5-dichlorophenol), and 4,4'-thiodiphenol.
Claim 15
Dependent Claim 13 words
The process of claim 3, wherein said phenol resin is a phenol-aldehyde resin.
Claim 16
Dependent Claim 11 words
The process of claim 13, wherein said phenol-aldehyde resin is water-soluble.
Claim 17
Dependent Claim 28 words
The process of claim 13, wherein said phenol of said phenolaldehyde resin is a member selected from the group consisting of phenol, cresol, xylenol, an alkylphenol and resorcinol.
Claim 18
Dependent Claim 14 words
The process of claim 13, wherein said aldehyde of said phenol-aldehyde resin is formaldehyde.
Claim 19
Dependent Claim 36 words
The process of claim 1, wherein said phenol compound is present in an amount ranging from 1/100 to 1/2 parts by weight based on one part by weight of colloid used to form the capsule wall.
Claim 20
Dependent Claim 37 words
The process of claim 1, wherein said colloid is a member selected from the group consisting of gelatin, casein, alginate, gum arabic, carrageenan, a maleic acid-styrene copolymer, a maleic acid-methylvinyl ether copolymer, and a maleic acid-ethylene copolymer.
Claim 21
Dependent Claim 16 words
The process of claim 1, wherein said phenolic compound is a resol-type or novolak-type phenolic resin.

References Cited (Backward Citations)

US2800457A Cited
US2969331A Cited
US2886445A Cited
US3069370A Cited
GB929405A Cited
US3803045A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1979-06-22 1979-12-22 1980-06-22 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1983-06-22 1983-12-22 1984-06-22 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1987-06-22 1987-12-22 1988-06-22 $7700.00 Window Closed / Lapsed

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