WO2007132258A1 - Applications of encapsulated oil emulsions and method of prepation therefor - Google Patents

Applications of encapsulated oil emulsions and method of prepation therefor Download PDF

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Publication number
WO2007132258A1
WO2007132258A1 PCT/GB2007/001854 GB2007001854W WO2007132258A1 WO 2007132258 A1 WO2007132258 A1 WO 2007132258A1 GB 2007001854 W GB2007001854 W GB 2007001854W WO 2007132258 A1 WO2007132258 A1 WO 2007132258A1
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Prior art keywords
product
oils
oil
active ingredient
mixture
Prior art date
Application number
PCT/GB2007/001854
Other languages
French (fr)
Inventor
Kenneth Albert Banks
Stephen Terrence Moore
Original Assignee
Zone Innovation Limited
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 Zone Innovation Limited filed Critical Zone Innovation Limited
Publication of WO2007132258A1 publication Critical patent/WO2007132258A1/en

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Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/26Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests in coated particulate form
    • A01N25/28Microcapsules or nanocapsules

Definitions

  • This invention relates to encapsulated oil emulsions and methods of preparation of said encapsulated oil emulsions and applications therefor, and in particular encapsulated oil emulsion systems for encapsulating an active ingredient.
  • the present invention is suited for encapsulation of active ingredients, such as biocidally active products that are directed towards infection/bacterial control, and the use of such products in relation to user products supplied for use in particular environments where such control of infection/bacterial contamination is important, for example, in the Healthcare Industry.
  • active ingredients such as biocidally active products that are directed towards infection/bacterial control
  • Encapsulated materials have been used for several years in various applications, and consequently, the methodology in creating such encapsulated materials is already in the public domain.
  • the present invention utilises already known encapsulation techniques in creating new and inventive encapsulated products and applications therefor.
  • tissue that include within their infrastructure aloe vera oil extract to act as a softener/lubricator of peoples skin. This application would reduce the effect of wear damage to the skin caused by rubbing of the skin with the bare tissue material.
  • the aloe vera oil extract is directly located in the infrastructure of the tissue and is not deployed as an encapsulated material. Consequently, these tissues have a shelf life and degrade after a short time.
  • the present invention is concerned with providing an encapsulation system and technique that can readily be used producing products for use in particular applications. Further said products would have an extended shelf life for the active material and which become activated at the point of use either on dispersal or after a period of time.
  • a product including a particulate material, which particulate material comprises a microencapsulated active ingredient and the encapsulating material forms a shell to seal the active ingredient from the surrounding atmosphere and the active ingredient is released when the encapsulating shell is ruptured or broken and wherein the encapsulated active material is carried in one or more oils selected from aromatic oils, aliphatic oils, paraff ⁇ nic oils or napthenic oils.
  • the particulate materials are manufactured and suited for dispersal into a particular environment. That environment could require for the most effective operation of the material that the particulate material is capable of being retained in situ for a long period of time. Consequently the properties of the encapsulating material would need to meet certain external factors as well as sealing the active material against premature release and/or loss of efficacy.
  • it may be important to secure the particulate material in place and to enhance this the adherence of the encapsulate material may be further enhanced by the addition of an additional resin, polymeric material or natural adhesive to the encapsulate material. This may be applied at a secondary stage in the manufacture.
  • the active ingredient may be selected from the following groups of materials
  • Lubricant additives such as polyiosbutaliene, or polytetrafluoroethylene (PTFE) or graphite and molybdenum disulphide dispersions; Tracers, for example UV fluorescent tracers; silicone oils: or natural waxes.
  • PTFE polytetrafluoroethylene
  • Tracers for example UV fluorescent tracers
  • silicone oils or natural waxes.
  • the active ingredient may include a mixture of active ingredients including one or more of the above examples.
  • a product made in accordance with the present invention may comprise a mixture of particulate materials, at least one of which is made in accordance with the present invention.
  • the particulate material of the present invention may have a particle size in the range of 5 to 30 microns, and more preferably in the range of 10 to 20 microns, and most preferable in the range of 10 to 15 microns.
  • the active ingredient includes biocidic material and the active biocide is selected from the group of triclosan (2,4,4'-trichloro-2'- hydroxydiphenyl ether); trichlorocarban (l-(3',4'-dichlorophenyl)-3-(4'- chlorophenyl)urea); PCMX (p-Chloro-m-xylenol); Hexahydro- 1 ,3 ,5,-Tris(2- Hydroxyethyl)-S-Triazine, and DCMX (2,4-Dichloro-3,5-xylenol).
  • triclosan 2,4,4'-trichloro-2'- hydroxydiphenyl ether
  • trichlorocarban l-(3',4'-dichlorophenyl)-3-(4'- chlorophenyl)urea
  • PCMX p-Chloro-m-xylenol
  • the oil used to carry the encapsulated active material is preferably selected from the group of materials comprising essential oils; naturally derived oils; or petroleum oils.
  • the essential oils include peppermint oil; eucalyptus oils; jojoba oils; and sweet almond oil or a mixture thereof.
  • the naturally derived oils may be selected from coconut oil; corn oil; and olive oil or a mixture thereof.
  • the oil used with the present invention may include a mixture of one or more essential oils and one or more naturally derived oils.
  • the petroleum oils may be selected from paraffin waxes or polyolefin based oils.
  • the product made in accordance with the present invention may be a coating material or dispersion such as an aqueous suspension.
  • oils include glycerides, turpenes, esters and/or hetero-cyclic materials, and the most suitable types of oils selected from each of the groupings will be a liquid material at or below 7O 0 C, and also as the preferred method for encapsulating the material comprises and aqueous based dispersion/suspension, the material is preferable not soluble in water and not miscible with water.
  • micro-encapsulation is melamine/formaldehyde encapsulation.
  • standard quality melamine and 37% formaldehyde were used as microencapsulate raw materials with suitable surfactant materials and stabilisers, as well as PH controllers. More detail concerning the exact method and materials used to provide example materials of the present invention is provided below.
  • Suitable final use products for the product of the present invention include paper towels having a coating including the product of the present invention, as well as other fibrous materials (natural or synthetic), to which the product of the present invention can be adhered; temporary lacquers and coatings; and air fresheners.
  • the particulate material is broken, so releasing the active materials. This is particularly suited for applications where infection/bacterial control is the primary feature to be considered.
  • the invention is directed to use of biocides, which are released over a period of time, so preventing micro-organisms from developing on the treated surface.
  • the encapsulated material is expelled in the aerosol with the particles towards the periphery of the spray being ruptured/broken on ejection, and the particles in the central area of the spray being allowed to fall and rest on surrounding surfaces.
  • the particles allowed to fall and rest will be ruptured/broken subsequently by, for example, people walking in he room and crushing the settled particles.
  • One particular example of the invention envisaged would be as a means to supply treatment agents or paliative materials for the control of asthma where the aerosol is sprayed over the patients pillow and the particular material is ruptured through the night by the movement of the patient.
  • the method used to encapsulate the active materials is as follows.
  • Standard quality melamine, 37% formaldehyde were used as the micro-encapsulate wall material; sodium lauryl sulphate (SLS) and Tween 20 were used as surfactants; and poly vinyl alcohol (PVA) as a stabiliser. Further, sodium hydroxide and citric acid were used as pH controllers.
  • micro-capsules In order to prepare the micro-capsules for encapsulation, two sets of equipment were required to produce the micro-encapsulates.
  • the specification for the apparatus comprised an overhead stirrer, capable of stirring a maximum of 15 litres at 2000 rpm; a hot plate with a temperature range of 20 to 200 0 C and a balance capable of weighing a minimum of 200 grams with an accuracy of at least 0.01 grams were provided.
  • Other equipment included one litre beakers, 0 to HO 0 C thermometers, stirring rods, paddle heads and a PH probe.
  • a solution of melamine, formaldehyde and water was prepared and heated to approximately 85 0 C, whilst continuously stirring at 200 rpm. Once a clear liquid had formed, the PH was adjusted to be between 8.7 and 8.9.
  • An oil in water emulsion was prepared using the selected oil.
  • a solution of SLS dissolved in water was prepared.
  • a solution of Tween 20 in the selected oil was also prepared. The SLS solution and the Tween 20 solution were steadily added to one another, with continuous stirring at 200 rpm.
  • a small quantity of PVA emulsion was added after approximately ten minutes stirring to assist the emulsion stability.
  • the PH of the resultant emulsion was adjusted to approximately 7.5 and the solution heated to a temperature of approximately 5O 0 C.
  • the melamine/forrnaldehyde solution was slowly added to the emulsion mentioned above, and the PH adjusted to approximately 5.5 to 6. Throughout this process, a steady temperature of 50 0 C was maintained and the reaction allowed to progress for a period of two to four hours whilst maintaining this steady temperature. A few drops of isopropyl alcohol were added to the resultant solution to terminate the reaction.
  • the emulsion described in example 3 was prepared in a formulation of 20.33%, with isopropyl alcohol 36.88% and water 42.79%.
  • the formulation When the formulation is dispensed from the aerosol, the product is dispersed to form a fine mist of micro-capsules which settle on the sprayed surface to produce a fine film, and the capsules are bound to the surface on drying by the included PVA resin.
  • the micro-capsules towards the periphery of the spray plume are ruptured/broken, providing immediate activation of the active material contained within the formulation.
  • Paper Towel In this particular derived product, the material details in example 1 above were used to produce a coating on commercially available paper towels.
  • the particulate matter of the present invention is disbursed into the interstices of the fibres make up of the towel, so that when the towel is used for cleaning hand, the micro-capsulate particulate is broken, so that the towels sanitise the skins surface.
  • the present invention can be provided for supply as a hard surface coating for coating of, for example, concrete surface.
  • a biocidal particulate material and examples of formula used in these flooring surfaces are as follows.

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  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Toxicology (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Agronomy & Crop Science (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

A product suitable for use in certain products such as coated or impregnated paper towels; coating or impregnated fibrous materials (natural or synthetic); lacquers and coatings; or air fresheners and which includes a particulate material. The particulate material comprising a micro-encapsulated active ingredient with the encapsulating material which is carried in one or more oils selected from aromatic oils, aliphatic oils, paraffinic oils or napthenic oils, forming a shell to seal the active ingredient from the surrounding atmosphere. In use the active ingredient is released when the encapsulating shell of the particular material is ruptured or broken.

Description

Applications of Encapsulated Oil Emulsions and Method of Preparation Therefor
This invention relates to encapsulated oil emulsions and methods of preparation of said encapsulated oil emulsions and applications therefor, and in particular encapsulated oil emulsion systems for encapsulating an active ingredient.
The present invention is suited for encapsulation of active ingredients, such as biocidally active products that are directed towards infection/bacterial control, and the use of such products in relation to user products supplied for use in particular environments where such control of infection/bacterial contamination is important, for example, in the Healthcare Industry.
Encapsulated materials have been used for several years in various applications, and consequently, the methodology in creating such encapsulated materials is already in the public domain. The present invention utilises already known encapsulation techniques in creating new and inventive encapsulated products and applications therefor.
For a number of years some user products have included additional materials that provide the user product with an enhanced or beneficial property in order to make the user product more suitable for its particular application. One typical example of this type of enhanced user product would be tissues that include within their infrastructure aloe vera oil extract to act as a softener/lubricator of peoples skin. This application would reduce the effect of wear damage to the skin caused by rubbing of the skin with the bare tissue material. In this application, the aloe vera oil extract is directly located in the infrastructure of the tissue and is not deployed as an encapsulated material. Consequently, these tissues have a shelf life and degrade after a short time.
The present invention is concerned with providing an encapsulation system and technique that can readily be used producing products for use in particular applications. Further said products would have an extended shelf life for the active material and which become activated at the point of use either on dispersal or after a period of time. In accordance with a first aspect of the present invention, there is provided a product including a particulate material, which particulate material comprises a microencapsulated active ingredient and the encapsulating material forms a shell to seal the active ingredient from the surrounding atmosphere and the active ingredient is released when the encapsulating shell is ruptured or broken and wherein the encapsulated active material is carried in one or more oils selected from aromatic oils, aliphatic oils, paraffϊnic oils or napthenic oils.
The particulate materials are manufactured and suited for dispersal into a particular environment. That environment could require for the most effective operation of the material that the particulate material is capable of being retained in situ for a long period of time. Consequently the properties of the encapsulating material would need to meet certain external factors as well as sealing the active material against premature release and/or loss of efficacy. In one potential usage of the particulate material it may be important to secure the particulate material in place and to enhance this the adherence of the encapsulate material may be further enhanced by the addition of an additional resin, polymeric material or natural adhesive to the encapsulate material. This may be applied at a secondary stage in the manufacture.
The active ingredient may be selected from the following groups of materials
Biocides;
Lubricant additives, such as polyiosbutaliene, or polytetrafluoroethylene (PTFE) or graphite and molybdenum disulphide dispersions; Tracers, for example UV fluorescent tracers; silicone oils: or natural waxes.
The active ingredient may include a mixture of active ingredients including one or more of the above examples.
A product made in accordance with the present invention may comprise a mixture of particulate materials, at least one of which is made in accordance with the present invention.
The particulate material of the present invention may have a particle size in the range of 5 to 30 microns, and more preferably in the range of 10 to 20 microns, and most preferable in the range of 10 to 15 microns.
In one embodiment of the present invention, the active ingredient includes biocidic material and the active biocide is selected from the group of triclosan (2,4,4'-trichloro-2'- hydroxydiphenyl ether); trichlorocarban (l-(3',4'-dichlorophenyl)-3-(4'- chlorophenyl)urea); PCMX (p-Chloro-m-xylenol); Hexahydro- 1 ,3 ,5,-Tris(2- Hydroxyethyl)-S-Triazine, and DCMX (2,4-Dichloro-3,5-xylenol).
The oil used to carry the encapsulated active material is preferably selected from the group of materials comprising essential oils; naturally derived oils; or petroleum oils.
In accordance with one embodiment of the present invention, the essential oils include peppermint oil; eucalyptus oils; jojoba oils; and sweet almond oil or a mixture thereof.
In accordance with one embodiment of the present invention, the naturally derived oils may be selected from coconut oil; corn oil; and olive oil or a mixture thereof.
The oil used with the present invention may include a mixture of one or more essential oils and one or more naturally derived oils.
In accordance with another embodiment of the present invention, the petroleum oils may be selected from paraffin waxes or polyolefin based oils.
The product made in accordance with the present invention may be a coating material or dispersion such as an aqueous suspension.
It will be noted that all of the above mentioned oils include glycerides, turpenes, esters and/or hetero-cyclic materials, and the most suitable types of oils selected from each of the groupings will be a liquid material at or below 7O0C, and also as the preferred method for encapsulating the material comprises and aqueous based dispersion/suspension, the material is preferable not soluble in water and not miscible with water.
The preferred method for micro-encapsulation is melamine/formaldehyde encapsulation. In this system, standard quality melamine and 37% formaldehyde were used as microencapsulate raw materials with suitable surfactant materials and stabilisers, as well as PH controllers. More detail concerning the exact method and materials used to provide example materials of the present invention is provided below.
Suitable final use products for the product of the present invention, include paper towels having a coating including the product of the present invention, as well as other fibrous materials (natural or synthetic), to which the product of the present invention can be adhered; temporary lacquers and coatings; and air fresheners.
With the use of the invention as a coating for paper towels, as the towel is used the particulate material is broken, so releasing the active materials. This is particularly suited for applications where infection/bacterial control is the primary feature to be considered.
With regard to the use of the invention in temporary lacquers and coatings, the invention is directed to use of biocides, which are released over a period of time, so preventing micro-organisms from developing on the treated surface.
In similar regard to the use of the invention, directed towards biocides whose actions might be activated by the passing contact of the surface by persons, animals or objects thereby destroying any micro-organisms.
With regards to use in an air freshener, the encapsulated material is expelled in the aerosol with the particles towards the periphery of the spray being ruptured/broken on ejection, and the particles in the central area of the spray being allowed to fall and rest on surrounding surfaces. The particles allowed to fall and rest will be ruptured/broken subsequently by, for example, people walking in he room and crushing the settled particles. One particular example of the invention envisaged would be as a means to supply treatment agents or paliative materials for the control of asthma where the aerosol is sprayed over the patients pillow and the particular material is ruptured through the night by the movement of the patient.
The invention will now be described by way of example.
The method used to encapsulate the active materials is as follows.
Standard quality melamine, 37% formaldehyde were used as the micro-encapsulate wall material; sodium lauryl sulphate (SLS) and Tween 20 were used as surfactants; and poly vinyl alcohol (PVA) as a stabiliser. Further, sodium hydroxide and citric acid were used as pH controllers.
In order to prepare the micro-capsules for encapsulation, two sets of equipment were required to produce the micro-encapsulates. The specification for the apparatus comprised an overhead stirrer, capable of stirring a maximum of 15 litres at 2000 rpm; a hot plate with a temperature range of 20 to 2000C and a balance capable of weighing a minimum of 200 grams with an accuracy of at least 0.01 grams were provided. Other equipment included one litre beakers, 0 to HO0C thermometers, stirring rods, paddle heads and a PH probe.
A solution of melamine, formaldehyde and water was prepared and heated to approximately 850C, whilst continuously stirring at 200 rpm. Once a clear liquid had formed, the PH was adjusted to be between 8.7 and 8.9.
An oil in water emulsion was prepared using the selected oil. A solution of SLS dissolved in water was prepared. A solution of Tween 20 in the selected oil was also prepared. The SLS solution and the Tween 20 solution were steadily added to one another, with continuous stirring at 200 rpm.
A small quantity of PVA emulsion was added after approximately ten minutes stirring to assist the emulsion stability. The PH of the resultant emulsion was adjusted to approximately 7.5 and the solution heated to a temperature of approximately 5O0C.
The melamine/forrnaldehyde solution was slowly added to the emulsion mentioned above, and the PH adjusted to approximately 5.5 to 6. Throughout this process, a steady temperature of 500C was maintained and the reaction allowed to progress for a period of two to four hours whilst maintaining this steady temperature. A few drops of isopropyl alcohol were added to the resultant solution to terminate the reaction.
Using the above-mentioned methodology, the following examples of emulsion materials were prepared. All the composition detail provided below is provided as W/W%.
The following examples were prepared by the methodology above where the selected biocide was incorporated to fall within the range 0.25% - 2.00% expressed on the weight of the incorporated oil.
Example 1
Figure imgf000007_0001
Figure imgf000008_0001
Example 2
Figure imgf000008_0002
Example 3
Figure imgf000009_0001
Example 4
Figure imgf000009_0002
Figure imgf000010_0001
Example 5
Figure imgf000010_0002
The above-mentioned sample materials were then used to produce certain derived products examples of which are given below. It should be noted that any of the examples above can be substituted in the product examples. The actual choice will depend on the particular application or use that is being considered and a particular system can be applied to particular circumstances.
Aerosol Coating
Samples of the above mentioned bases were diluted with water and an alcohol solvent to form a base material for packing into aerosol sprays. The propellant material used was that typically used with current aerosols, namely (1,1 Dichloro-1-Fluoroethane, 1,1,1,2 Tetrafluoroethane , or Butane/Propane mixtures).
The emulsion described in example 3, was prepared in a formulation of 20.33%, with isopropyl alcohol 36.88% and water 42.79%.
When the formulation is dispensed from the aerosol, the product is dispersed to form a fine mist of micro-capsules which settle on the sprayed surface to produce a fine film, and the capsules are bound to the surface on drying by the included PVA resin. On disbursal from the aerosol, the micro-capsules towards the periphery of the spray plume are ruptured/broken, providing immediate activation of the active material contained within the formulation.
Paper Towel In this particular derived product, the material details in example 1 above were used to produce a coating on commercially available paper towels. The particulate matter of the present invention is disbursed into the interstices of the fibres make up of the towel, so that when the towel is used for cleaning hand, the micro-capsulate particulate is broken, so that the towels sanitise the skins surface.
Hard Surface Coating
The present invention can be provided for supply as a hard surface coating for coating of, for example, concrete surface. In this particular example, a biocidal particulate material and examples of formula used in these flooring surfaces are as follows. Example A
Jojoba oil / PCMX base 20.5; Acrylic resin solution 8.8; and Water 71.7
Example B
Peppermint oil / triclosan base 19.5; Acrylic resin emulsion 10; and Water 70.5

Claims

1 A product including a particulate material, which particulate material comprises a micro-encapsulated active ingredient and the encapsulating material forms a shell to seal the active ingredient from the surrounding atmosphere, and, the active ingredient is released when the encapsulating shell is ruptured or broken wherein the encapsulated active material is carried in one or more oils selected from aromatic oils, aliphatic oils, paraffinic oils or napthenic oils.
2 A product as claimed in claim 1 wherein the properties of the encapsulating material can be modified.
3 A product as claimed in claim 2 wherein the properties of the encapsulating material are enhanced by modifying the adhesive/adherence of said material.
4 A product as claimed in claim 3 wherein the encapsulating material is modified by addition of an additional resin, polymeric material or natural adhesive to the encapsulate material.
5 A product as claimed in any of claim 2 to 5, wherein the modification of the encapsulating material is carried out at a secondary stage in the manufacture to the forming of the encapsulate shell.
6 A product as claimed in any of the preceding claims wherein the active ingredient is selected from the following groups of materials: Biocides;
Lubricant additives; Tracers
7 A product as claimed in claim 6 wherein the active ingredient is a Lubricant additives selected from polyiosbutaliene, polytetrafluoroethylene (PTFE), graphite or molybdenum disulphide dispersions.
8 A product as claimed in claim 6 wherein the active ingredient is a tracer and is selected from UV fluorescent tracers, silicone oils, or natural waxes.
9 A product as claimed in any preceding claim, wherein the active ingredient encapsulated in the particulate material comprises a mixture of active ingredients,
10 A product wherein the dispersed material may comprise a mixture of particulate materials each having different active material and at least one of which is made in accordance with any of the preceding claims.
11 A product as claimed in any preceding claim wherein the particulate material has a particle size in the range of 5 to 30 microns.
12 A product as claimed in any preceding claim wherein the particulate material has a particle size in the range of 10 to 20 microns.
13 A product as claimed in any preceding claim wherein the particulate material has a particle size in the range of 10 to 15 microns.
14 A product as claimed in claim in any preceding claim in which the active ingredient includes a biocide material and the active biocide is selected from the group of triclosan (2,4,4'-trichloro-2'-hydroxydiphenyl ether); trichlorocarban (l-(3',4'- dichlorophenyl)-3-(4'-chlorophenyl) urea); PCMX (p-Chloro-m-xylenol); Hexahydro- 1,3,5,-Tris(2-Hydroxyethyl)-S-Triazine, or DCMX (2,4-Dichloro-3,5-xylenol) or a mixture thereof.
15 A product as claimed in any preceding claim in which the oil used to carry the encapsulated active material is preferably selected from the group of materials comprising essential oils; naturally derived oils; or petroleum oils. 16 A product as claimed in claim 15 wherein the oil is an essential oil selected from peppermint oil; eucalyptus oils; jojoba oils; and sweet almond oil or a mixture thereof.
17 A product as claimed in claim 15 wherein the oil is a naturally derived oils selected from coconut oil; corn oil; and olive oil or a mixture thereof.
18 A product as claimed in claim 15 wherein the oil comprises a mixture of one or more essential oils and/or one or more naturally derived oils.
19 A product as claimed in claim 15 wherein the oil is a petroleum oil selected from paraffin waxes or polyolefin based oils or a mixture thereof.
20 A product as claimed in any preceding claim wherein the oil comprises glycerides, turpenes, esters or hetero-cyclic materials or a mixture thereof which oil or mixture is liquid at or below 7O0C.
21 A product as claimed in any preceding claim in which the encapsulation method comprises an aqueous based dispersion/suspension, with the active ingredient not being soluble in water and not miscible with water.
22 A product as claimed in claim 21 in which the method for micro-encapsulation is melamine/formaldehyde encapsulation.
23 A product as claimed in any preceding claim wherein the finished product is a coating material or dispersion such as an aqueous suspension.
24 The use of a product formed in accordance with any of the preceding claims which use comprises one of the following: coating or impregnated paper towels; coating or impregnated fibrous materials (natural or synthetic); lacquers and coatings; or air fresheners.
PCT/GB2007/001854 2006-05-17 2007-05-17 Applications of encapsulated oil emulsions and method of prepation therefor WO2007132258A1 (en)

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Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3778383A (en) * 1970-05-26 1973-12-11 Ciba Geigy Ag Process for the encapsulation of substances which are finely distributed in a liquid and capsule compositions produced thereby
WO2000048465A1 (en) * 1999-02-19 2000-08-24 Thies Technology Pest controlling
WO2001005926A1 (en) * 1999-07-20 2001-01-25 The Procter & Gamble Company Improved encapsulated oil particles
WO2002051536A1 (en) * 2000-12-27 2002-07-04 Cognis Deutschland Gmbh & Co. Kg Encapsulation of emulsions
WO2004009054A2 (en) * 2002-07-24 2004-01-29 General Mills, Inc. Encapsulation of sensitive components using pre-emulsification
WO2004081222A2 (en) * 2003-03-14 2004-09-23 Sol-Gel Technologies Ltd. Agent-encapsulating micro- and nanoparticles, methods for preparation of same and products containing same
US20050065238A1 (en) * 2003-09-23 2005-03-24 Lark John C. Encapsulated nanoparticles, products containing the same, and methods for using the same

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3778383A (en) * 1970-05-26 1973-12-11 Ciba Geigy Ag Process for the encapsulation of substances which are finely distributed in a liquid and capsule compositions produced thereby
WO2000048465A1 (en) * 1999-02-19 2000-08-24 Thies Technology Pest controlling
WO2001005926A1 (en) * 1999-07-20 2001-01-25 The Procter & Gamble Company Improved encapsulated oil particles
WO2002051536A1 (en) * 2000-12-27 2002-07-04 Cognis Deutschland Gmbh & Co. Kg Encapsulation of emulsions
WO2004009054A2 (en) * 2002-07-24 2004-01-29 General Mills, Inc. Encapsulation of sensitive components using pre-emulsification
WO2004081222A2 (en) * 2003-03-14 2004-09-23 Sol-Gel Technologies Ltd. Agent-encapsulating micro- and nanoparticles, methods for preparation of same and products containing same
US20050065238A1 (en) * 2003-09-23 2005-03-24 Lark John C. Encapsulated nanoparticles, products containing the same, and methods for using the same

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