IP Library Granted Patent US 11,471,397
Granted Patent B2
US 11,471,397 · App. 16/319,876 · Granted Oct 18, 2022

Process for the preparation of microcapsules

Inventors: Florence Vigouroux Elie (Geneva, CH); Sonia Godefroy (Geneva, CH); Murray Osborne (Geneva, CH)
Assignee: Firmenich SA
A61K8/87A01N25/28A23L27/72A61K8/11A61K8/64A61K8/645A61K8/65A61K8/731A61K8/732A61K8/84A61K9/5031A61K9/5089A61Q13/00A61Q19/10C11D3/3703C11D3/3726C11D3/505C11D17/0039A61K2800/412A61K2800/594A61K2800/805B01J13/16B01J13/206
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Quick Facts
Patent No.
US 11,471,397
App. No.
16/319,876
Granted
Oct 18, 2022
Kind
B2
Abstract

The present invention relates to a new process for the preparation of microcapsules. Microcapsules obtainable by said process are also an object of the invention. Perfuming compositions and consumer products comprising said capsules, in particular perfumed consumer products in the form of home care or personal care products, are also part of the invention.

Claims (33)

1. A process for the preparation of a polyurea-based core-shell microcapsule slurry comprising the steps of:

1) admixing a hydrophobic active ingredient with at least one polyisocyanate having at least three isocyanate functional groups to form an oil phase, provided that the oil phase is essentially free from diisocyanate;

2) dissolving an ionic or non-ionic emulsifier in water to form a water phase, wherein the ionic emulsifier is chosen in the group consisting of gum Arabic, carboxymethyl cellulose, soy protein, sodium caseinate, gelatin, bovine serum albumin, sugar beet pectin, hydrolyzed soy protein, hydrolyzed sericin, Pseudo collagen, Biopolymer SA-N, Pentacare-NA PF, and mixtures thereof and wherein the non-ionic emulsifier is chosen in the group consisting of polyvinyl alcohol, modified polyvinyl alcohol, modified starch, modified cellulose, polysaccharides and mixtures thereof;

3) adding the oil phase to the water phase to form an oil-in-water dispersion; and

4) applying conditions sufficient to induce interfacial polymerisation and form microcapsules in form of a slurry;

wherein

the at least one polyisocyanate having at least three isocyanate functional groups is present in an amount comprised between 1 and 15 wt % of the oil phase,

no substantial amount of amine or polyamine is added at any stage of the process,

the process does not comprise a further step of adding a cationic polymer to form an outer coating to the microcapsule, and

no substantial amount of water-soluble reactant is added at any stage of the process, wherein the water-soluble reactant is selected from the group consisting of polyols, thiols, ureas, urethanes and mixtures thereof.

2. The process according to claim 1 , further comprising the step of drying the microcapsule slurry to obtain dried microcapsules.

3. The process according to claim 1 , wherein the at least one polyisocyanate having at least three isocyanate functional groups is present in an amount comprised between 2 and 8 wt % of the oil phase.

4. The process according to claim 1 , wherein the at least one polyisocyanate having at least three isocyanate functional groups is present in an amount comprised between 2 and 6 wt % of the oil phase.

5. The process according to claim 1 , wherein the at least one polyisocyanate having at least three isocyanate functional groups is a mixture of at least one aliphatic polyisocyanate and at least one aromatic polyisocyanate, the aliphatic polyisocyanate and the aromatic polyisocyanate being in a respective molar ratio ranging from 80:20 to 10:90.

6. The process according to claim 1 , wherein the at least one polyisocyanate having at least three isocyanate functional groups is an aromatic polyisocyanate.

7. The process according to claim 1 , wherein the oil phase consists essentially of the hydrophobic active ingredient with the at least one polyisocyanate having at least three isocyanate functional groups.

8. The process according to claim 1 , wherein the hydrophobic active ingredient is selected from the group consisting of a perfume, flavor, nutraceuticals, cosmetics, insect control agents, biocide actives and mixtures thereof.

9. A polyurea-based microcapsule slurry obtainable by a process as defined in claim 1 .

10. A polyurea-based microcapsule powder obtained by drying the microcapsule slurry as defined in claim 9 .

11. The microcapsule slurry according to claim 1 comprising microcapsules having a core-shell morphology and comprising:

an oil-based core comprising a hydrophobic active ingredient wherein the hydrophobic active ingredient is selected from the group consisting of a perfume or flavour oil;

a shell consisting essentially of polymerised polyisocyanate formed from at least one polyisocyanate comprising at least three isocyanate functional groups in the absence of a polyamine or an amine, and an emulsifier as defined in claim 1 and wherein the microcapsules do not comprise a cationic coating.

12. A perfuming composition comprising

(i) a microcapsule slurry as defined in claim 1 , wherein the oil comprises a perfume;

(ii) at least one ingredient selected from the group consisting of a perfumery carrier and a perfumery co-ingredient; and

(iii) optionally at least one perfumery adjuvant.

13. A liquid perfumed consumer product, selected from the group consisting of: a laundry care product, a home care product, a body care product, a skin care product, an air care product, and a hygiene product, the consumer product comprising:

a) from 2 to 65% by weight, relative to the total weight of the consumer product, of at least one surfactant;

b) water or a water-miscible hydrophilic organic solvent; and

c) a microcapsule slurry as defined in claim 9 .

14. A powder perfumed consumer product, selected from the group consisting of: a laundry care product, a home care product, a body care product, a skin care product, an air care product, and a hygiene product, said consumer product comprising:

a) from 2 to 65% by weight, relative to the total weight of the consumer product, of at least one surfactant; and

b) a microcapsule powder as defined in claim 10 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 4, 2022
From: VIGOUROUX ELIE, FLORENCE; GODEFROY, SONIA; OSBORNE, MURRAY
To: FIRMENICH SA
Reel/Frame 061306/0967 →
Priority Claims (1)
EP 16181447 · Jul 27, 2016 · regional
Continuity (1)
Related Publication 20190269603A1 · Sep 5, 2019