GB929408A - Encapsulated emulsions and processes for their preparation - Google Patents

Encapsulated emulsions and processes for their preparation

Info

Publication number
GB929408A
GB929408A GB4022459A GB4022459A GB929408A GB 929408 A GB929408 A GB 929408A GB 4022459 A GB4022459 A GB 4022459A GB 4022459 A GB4022459 A GB 4022459A GB 929408 A GB929408 A GB 929408A
Authority
GB
United Kingdom
Prior art keywords
hydrophilic
styrene
oil
emulsion
units
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
GB4022459A
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 GB929408A publication Critical patent/GB929408A/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
    • B01J13/08Simple coacervation, i.e. addition of highly hydrophilic material
    • 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

Abstract

Particles of a (primary) hydrophilic liquid-in-oil emulsion containing an anti-inversion agent in the oil phase are encapsulated by dispersing the said primary emulsion to form a secondary emulsion in an aqueous dispersion of at least two coacervating colloids at least one of which is a hydrophilic colloid and at least one of which is a linear macromolecular synthetic polymer and causing a coacervate of the polymers to deposit about the particles of the primary emulsion and, if desired, subsequently drying and/or hardening the capsules. The primary emulsion may contain conventional emulsifying agents e.g. esters of polyhydric alcohols, sorbitan derivatives, and sorbitan polyoxyethylene derivatives and advantageously contains a thickening agent, e.g. acacia, methyl cellulose, magnesium aluminium silicate, glycium and syrups in the hydrophilic liquid phase. As anti-inversion agents there are mentioned surface-active agents (preferably non-ionic), and conventional oil-gelling and oil-thickening agents, e.g. waxes, solid fats and sterols. Suitable hydrophilic colloids are naturally occurring gelable and nongelable hydrophilic colloids and derivatives thereof, e.g. gelatine, agar, albumen, deacetylated chitins, pectins, acacia, starch and fibrinogen. Suitable linear macromolecular synthetic polymers are those whose structure comprises both lipophilic units and hydrophilic units, e.g. styrene-maleic amide copolymers, sulphonated polystyrenes, carbohydrate acetate phthalates and (preferably) hydrolysed styrenemaleic anhydride copolymers of general formula [-R-R1-]n, wherein R represents lipophilic units of which more than 70% are styrene residues and R1 represents hydrophilic units of which more than 50% are maleic acid residues. Coacervation may be induced by alteration of the pH of the polymer dispersion or by dilution thereof with water. Either or both phases of the primary emulsion may contain dissolved or suspended "active" ingredients which render the encapsulated products useful, e.g. as sustained release fertilizers, plant growth regulants, pesticides, bactericides, food additives, cosmetic ingredients, vitamin preparations and pharmaceutical materials. Specific examples include: (a) aqueous chloral hydrate-in-mineral oil emulsion in gelatine and styrene-maleic acid copolymer; (b) glycerine suspension of rotenone in mineral oil in serum albumin and styrene-maleic amide copolymer and (c) aqueous urea solution-in-peanut oil in gelatine and styrene-maleic acid copolymer. Specification 751,600 is referred to.
GB4022459A 1958-12-22 1959-11-26 Encapsulated emulsions and processes for their preparation Expired GB929408A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US78192258A 1958-12-22 1958-12-22

Publications (1)

Publication Number Publication Date
GB929408A true GB929408A (en) 1963-06-19

Family

ID=25124384

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4022459A Expired GB929408A (en) 1958-12-22 1959-11-26 Encapsulated emulsions and processes for their preparation

Country Status (3)

Country Link
CH (1) CH396841A (en)
DE (1) DE1185154B (en)
GB (1) GB929408A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1989000812A1 (en) * 1987-07-28 1989-02-09 Micro-Pak, Inc. Method of manufacturing unilamellar lipid vesicles
US5019392A (en) * 1988-03-03 1991-05-28 Micro-Pak, Inc. Encapsulation of parasiticides
US5023086A (en) * 1987-03-13 1991-06-11 Micro-Pak, Inc. Encapsulated ionophore growth factors
US5234767A (en) * 1987-03-13 1993-08-10 Micro-Pak, Inc. Hybrid paucilamellar lipid vesicles
US5628936A (en) * 1987-03-13 1997-05-13 Micro-Pak, Inc. Hybrid paucilamellar lipid vesicles
US20170065497A1 (en) * 2014-03-31 2017-03-09 Givaudan Sa Organic compounds
WO2017059508A1 (en) * 2015-10-07 2017-04-13 Oxiteno S.A. Indústria E Comércio Emulsifying powder

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE530009A (en) * 1953-06-30

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5023086A (en) * 1987-03-13 1991-06-11 Micro-Pak, Inc. Encapsulated ionophore growth factors
US5234767A (en) * 1987-03-13 1993-08-10 Micro-Pak, Inc. Hybrid paucilamellar lipid vesicles
US5628936A (en) * 1987-03-13 1997-05-13 Micro-Pak, Inc. Hybrid paucilamellar lipid vesicles
WO1989000812A1 (en) * 1987-07-28 1989-02-09 Micro-Pak, Inc. Method of manufacturing unilamellar lipid vesicles
US4853228A (en) * 1987-07-28 1989-08-01 Micro-Pak, Inc. Method of manufacturing unilamellar lipid vesicles
US5019392A (en) * 1988-03-03 1991-05-28 Micro-Pak, Inc. Encapsulation of parasiticides
US20170065497A1 (en) * 2014-03-31 2017-03-09 Givaudan Sa Organic compounds
WO2017059508A1 (en) * 2015-10-07 2017-04-13 Oxiteno S.A. Indústria E Comércio Emulsifying powder

Also Published As

Publication number Publication date
DE1185154B (en) 1965-01-14
CH396841A (en) 1965-08-15

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