GB911483A - Encapsulated emulsions and processes for their preparation - Google Patents

Encapsulated emulsions and processes for their preparation

Info

Publication number
GB911483A
GB911483A GB3793959A GB3793959A GB911483A GB 911483 A GB911483 A GB 911483A GB 3793959 A GB3793959 A GB 3793959A GB 3793959 A GB3793959 A GB 3793959A GB 911483 A GB911483 A GB 911483A
Authority
GB
United Kingdom
Prior art keywords
oil
emulsion
coacervating
colloid
agent
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB3793959A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pharmacia and Upjohn Co
Original Assignee
Upjohn Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Upjohn Co filed Critical Upjohn Co
Publication of GB911483A publication Critical patent/GB911483A/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J13/00Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
    • B01J13/02Making microcapsules or microballoons
    • B01J13/06Making microcapsules or microballoons by phase separation
    • B01J13/10Complex coacervation, i.e. interaction of oppositely charged particles
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J13/00Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
    • B01J13/02Making microcapsules or microballoons
    • B01J13/06Making microcapsules or microballoons by phase separation
    • B01J13/08Simple coacervation, i.e. addition of highly hydrophilic material

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Dispersion Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Manufacturing Of Micro-Capsules (AREA)
  • Colloid Chemistry (AREA)

Abstract

Microcapsules composed of a gellable hydrophilic colloid enclosing a water-in-oil emulsion containing an "anti-inversion agent" in the oil phase and prepared by a coacervation process (see Group VI) comprise the dye D and C Green No. 5 dissolved in the aqueous phase of the emulsion. Suitable colloids are gelatin, agar, casein, albumin, pectins, starch and fibrinogen and the anti-inversion agent may be non-ionic surfactant, hydrogenated castor oil, a solid fat, a sterol or a natural or synthetic wax. Specification 751,600 is referred to.ALSO:Microcapsules for use in fertilizers as a source of nitrogen consist of an aqueous urea-in-oil emulsion contained within a mantle of a gellable hydrophilic colloid, e.g. gelatin, agar, albumen, casein, pectins, starch or fibrinogen, the oil phase of the emulsion (e.g. corn oil) containing an "anti-inversion agent", e.g. hydrogenated castor oil or a solid fat, sterol or natural or synthetic wax or a non-ionic surfactant. They are produced by a concervation process whereby the colloid is caused to deposit from an aqueous roll thereof on to emulsion particles suspended therein the capsule walls subsequently being gelled and hardened (see Group VI). Specification 751,600 is referred to.ALSO:Particles of a hydrophilic liquid-in-oil emulsion are encapsulated by a process wherein the said emulsion containing an anti-inversion agent in the oil phase is dispersed in a coacervating solution comprising a coacervating agent and an aqueous sol of a coacervating colloid at a temperature above the gel point of the said colloid to form a secondary emulsion upon which the coacervate is deposited and which may subsequently be gelled and hardened by cooling and treatment with a hardener or plasticizer e.g. aqueous formaldehyde. A conventional thickening agent e.g. acacia, tragacanth, methyl- or carboxymethyl-cellulose, magnesium aluminium silicate, polyglycols, glycerin or syrups may be added to both the internal hydrophilic liquid phase and to the coacervating solution, and conventional emulsifying agents may be used in the preparation of the primary emulsion. The anti-inversion agent may be any which is capable of preventing the inversion of the primary emulsion on its dispersion in the coacervating solution e.g. surface active agents (preferably non-ionic) e.g. sorbitan fatty acid esters, polyoxyethylene sorbitan fatty acid esters and oil thickening agents e.g. natural and synthetic waxes, solid fats, sterols and ethyl cellulose. Suitable coacervating colloids are gelable hydrophilic colloids e.g. gelatin (preferred), agar-agar, alginates, casein, pectins, starch and fibrinogen. The coacervating agent may be an electrolyte e.g. a salt having an alkali or alkali metal cation and an organic or inorganic anion or a water soluble solvent in which the coacervating colloid is less soluble than it is in water. The primary emulsion particles may contain additional materials dissolved or suspended in either or both phases, e.g. pharmaceuticals, vitamins, cosmetic ingredients, fertilizers, plant growth hormones, fungicides, bactericides, viricides and pesticides. Specific examples relate inter alia to encapsulated emulsions comprising: (a) urea in an internal aqueous phase (fertilizer preparation); (b) cod liver oil (oil phase) and ascorbic acid (aqueous phase) for incorporation into dry cereals; (c) neomycin (aqueous phase) for incorporation into ointments; (d) an ethanolic solution of ethylene dibromide in peanut oil (nematocidal preparation). Reference is also made to orally and parenterally administrable pharmaceutical forms which may have sustained release characteristics. Detailed examples of the preparation of the capsules are given. Specification 751,600 is referred to.
GB3793959A 1958-12-22 1959-11-09 Encapsulated emulsions and processes for their preparation Expired GB911483A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US78191958A 1958-12-22 1958-12-22

Publications (1)

Publication Number Publication Date
GB911483A true GB911483A (en) 1962-11-28

Family

ID=25124371

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3793959A Expired GB911483A (en) 1958-12-22 1959-11-09 Encapsulated emulsions and processes for their preparation

Country Status (4)

Country Link
BR (1) BR5915720D0 (en)
CH (1) CH395938A (en)
DE (1) DE1185153B (en)
GB (1) GB911483A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003032749A1 (en) * 2001-10-18 2003-04-24 Firmenich Sa Spray-dried compositions and method for their preparation
US7994110B2 (en) 2005-05-03 2011-08-09 Evonik Degussa Gmbh Solid redispersible emulsion

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3959464A (en) * 1971-06-03 1976-05-25 Pennwalt Corporation Microencapsulated methyl and ethyl parathion insecticide in aqueous carrier
US4908233A (en) * 1985-05-08 1990-03-13 Lion Corporation Production of microcapsules by simple coacervation
US4777089A (en) * 1985-05-08 1988-10-11 Lion Corporation Microcapsule containing hydrous composition

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE530010A (en) * 1953-06-30
US2800457A (en) * 1953-06-30 1957-07-23 Ncr Co Oil-containing microscopic capsules and method of making them

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003032749A1 (en) * 2001-10-18 2003-04-24 Firmenich Sa Spray-dried compositions and method for their preparation
US6723359B2 (en) 2001-10-18 2004-04-20 Firmenich Sa Spray-dried compositions and method for their preparation
US7994110B2 (en) 2005-05-03 2011-08-09 Evonik Degussa Gmbh Solid redispersible emulsion

Also Published As

Publication number Publication date
DE1185153B (en) 1965-01-14
CH395938A (en) 1965-07-31
BR5915720D0 (en) 1973-05-24

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