WO2006136196A1 - Gellan seamless breakable capsule and process for manufacturing thereof - Google Patents

Gellan seamless breakable capsule and process for manufacturing thereof Download PDF

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Publication number
WO2006136196A1
WO2006136196A1 PCT/EP2005/008502 EP2005008502W WO2006136196A1 WO 2006136196 A1 WO2006136196 A1 WO 2006136196A1 EP 2005008502 W EP2005008502 W EP 2005008502W WO 2006136196 A1 WO2006136196 A1 WO 2006136196A1
Authority
WO
WIPO (PCT)
Prior art keywords
anyone
breakable capsule
shell
agent
capsule according
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.)
Ceased
Application number
PCT/EP2005/008502
Other languages
French (fr)
Inventor
Jean-Michel Hannetel
Didier Hartmann
Jean Mane
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.)
V Mane Fils SAS
Original Assignee
V Mane Fils SAS
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 V Mane Fils SAS filed Critical V Mane Fils SAS
Priority to PCT/EP2005/008502 priority Critical patent/WO2006136196A1/en
Priority to PCT/EP2005/009226 priority patent/WO2006136198A1/en
Priority to US11/922,574 priority patent/US20090208568A1/en
Priority to AP2007004284A priority patent/AP2876A/en
Priority to NZ564191A priority patent/NZ564191A/en
Priority to CA2612615A priority patent/CA2612615C/en
Priority to AT06809049T priority patent/ATE444740T1/en
Priority to KR1020077030403A priority patent/KR101430018B1/en
Priority to PL06809049T priority patent/PL1898889T3/en
Priority to UAA200800631A priority patent/UA89543C2/en
Priority to DE602006009655T priority patent/DE602006009655D1/en
Priority to PCT/IB2006/002905 priority patent/WO2007012981A2/en
Priority to MX2007016511A priority patent/MX2007016511A/en
Priority to BRPI0611742A priority patent/BRPI0611742B8/en
Priority to DK06809049.7T priority patent/DK1898889T3/en
Priority to ZA200711060A priority patent/ZA200711060B/en
Priority to RU2008102115/15A priority patent/RU2428971C2/en
Priority to PT06809049T priority patent/PT1898889E/en
Priority to ES06809049T priority patent/ES2333822T3/en
Priority to EP06809049A priority patent/EP1898889B1/en
Priority to JP2008517632A priority patent/JP5529415B2/en
Priority to AU2006273701A priority patent/AU2006273701B2/en
Priority to CN2006800224576A priority patent/CN101203213B/en
Priority to SI200630508T priority patent/SI1898889T1/en
Publication of WO2006136196A1 publication Critical patent/WO2006136196A1/en
Anticipated expiration legal-status Critical
Priority to CY20091101337T priority patent/CY1109690T1/en
Priority to US16/575,865 priority patent/US20200078274A1/en
Ceased legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/11—Encapsulated compositions
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
    • A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
    • A23L27/70—Fixation, conservation, or encapsulation of flavouring agents
    • A23L27/72—Encapsulation
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
    • A23L29/00—Foods or foodstuffs containing additives; Preparation or treatment thereof
    • A23L29/20—Foods or foodstuffs containing additives; Preparation or treatment thereof containing gelling or thickening agents
    • A23L29/269—Foods or foodstuffs containing additives; Preparation or treatment thereof containing gelling or thickening agents of microbial origin, e.g. xanthan or dextran
    • A23L29/272—Gellan
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23P—SHAPING OR WORKING OF FOODSTUFFS, NOT FULLY COVERED BY A SINGLE OTHER SUBCLASS
    • A23P10/00—Shaping or working of foodstuffs characterised by the products
    • A23P10/30—Encapsulation of particles, e.g. foodstuff additives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/4816—Wall or shell material
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/4833—Encapsulating processes; Filling of capsules
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q11/00—Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00—Preparations for care of the skin
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J13/00—Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
    • B01J13/02—Making microcapsules or microballoons
    • B01J13/04—Making microcapsules or microballoons by physical processes, e.g. drying, spraying
    • B01J13/046—Making microcapsules or microballoons by physical processes, e.g. drying, spraying combined with gelification or coagulation
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/4841—Filling excipients; Inactive ingredients
    • A61K9/4858—Organic compounds
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
    • Y10T428/2991—Coated

Definitions

  • the present invention relates to a breakable capsule for release of its content upon crushing.
  • Such capsules are useful for numerous applications, such as in oral care application (toothpaste, mouthwash, gums...) , in food applications such as confectionary, dairy, bakery, savoury, or in personal care products such as cosmetic products and the like.
  • capsule will be used to designate any size of capsules, from 0.5 up to 8 mm, including macrocapsules and microcapsules . It is of particular interest to obtain seamless capsules, as the breakability of a welded capsule may be influenced by the easy rupture of the weld.
  • Fuji patent application JP10291928 describes a capsule obtained through a co-extrusion process, wherein the external liquid phase comprises gellan and calcium salts .
  • Gellan gum first discovered in 1978, is produced by the microorganism Sphingomonas elodea.
  • the Applicant has found that the production of gellan capsule through the Fuji process was not satisfactory and resulted in poor quality capsules and in processing difficulties, because the gellan was actually gelling during the co-extrusion, and it was not possible to obtain spherical and homogeneous breakable capsules. For this reason, the Applicant tried to improve the Fuji process and found that the drawbacks of the prior art process may be due to the presence of calcium salts, and more generally to divalent metal salts in gellan during the co-extrusion step.
  • the Applicant experimented a process wherein the co-extrusion liquid phase containing gellan was performed in absence of calcium salts, and observed that, surprisingly, the resulting capsules had the required spherical shape and homogeneous size.
  • the obtained capsules cannot be used as such, because the shell is too soft and the resulting capsules are not breakable capsules; the Applicant found a solution to this subsequent technical problem by contacting the capsules with divalent metal ions, preferably calcium or magnesium ions, once the co-extrusion process is finished, and this finally lead to satisfactory breakable capsules.
  • this invention relates to a process for manufacturing seamless breakable capsules and to new breakable capsules.
  • the process of the invention comprises a step (A) of co-extrusion of an external and hydrophilic liquid phase and an internal and lipophilic liquid phase, in order to form a capsule having a core comprising the internal and lipophilic phase and a shell comprising the external and hydrophilic phase; and a step (B) of washing and immersing the capsules into an aqueous solution containing a curing agent, suitable for making the shell breakable as required for the intended use; optionally a step (C) of drying the obtained capsules in a dry air or optionally a step (D) of suspending the capsules into an aqueous medium to obtain a slurry form.
  • the co-extrusion process consists of three main stages: compound drop formation, shell solidification and capsule collection.
  • the compound drop is a sphere of the liquid fill phase inside the shell phase.
  • the liquid fill phase is hereinafter referred to as "the core”.
  • the shell phase is hereinafter referred to as "the shell”.
  • the external liquid phase includes a gelling agent comprising gellan gum alone or in combination with another gelling agent, a filler, and a metal sequestering agent, the liquid being water, preferably desionized or osmozed water.
  • gelling agent in the meaning of this invention, it is referred to an agent able to convert an aqueous phase from a flowable liquid to a solid or a gel.
  • sequestering agent in the meaning of this invention it is referred to any agent complexing, chelating or sequestering bivalent ions such as calcium or magnesium.
  • breakable in the meaning of this invention, it is referred to a capsule which crush strength is comprised between 0.01 and 5 kp.
  • the crush strength of the capsule is measured by continuously applying a load vertically onto one particle until rupture.
  • the crush strength of the capsules in the present invention is measured by using a texturometer TA.XT plus from Micro Stable System in compression mode or a LLOYD - CHATILLON Digital Force Gauge, Model DFIS 50, having a capacity of 25Kg, a resolution of 0.02 Kg, and an accuracy of +/- 0,15 %.
  • the force gauge is attached to a stand; the capsule is positioned in the middle of a plate that is moved up with a manual thread screw device. Pressure is then applied manually and the gauge records the maximum force applied at the very moment of the rupture of the capsule, (measured in Kg or in Lb) . Rupture of the capsule results in the release of the core.
  • Gellan gum is a hydrocolloid which, according to the invention, can be used as the sole gelling agent of the external liquid phase, or in combination with other gelling agents.
  • Other suitable gelling agents may be alginates, agar, carragheenan, xanthan gum, dextran, curdlan, welan gum, rhamsan gum or modified starches.
  • Suitable gellan gums are for example, but not limited to deacylated gellan gum.
  • Kelcogel® can be mentioned as a suitable gellan gum.
  • the filler is any suitable material that can increase the percentage of dry material in the external liquid phase and thus after co-extrusion in the obtained shell. Increasing the dry material amount in a shell results in solidifying the shell, and in making it physically more resistant.
  • the filler is selected from the group comprising starch derivatives such as dextrin, maltodextrin, cyclodextrin (alpha, beta or gamma) , or cellulose derivatives such as hydroxypropylmethylcellulose (HPMC) , hydroxypropylcellulose
  • HPC methylcellulose
  • CMC carboxymethylcellulose
  • polyvinyl alcohol polyols or mixture thereof.
  • a divalent metal sequestering or complexing agent allows to trap the divalent metal ions which are possibly present in the components of the liquid phase including water and which have a gelling effect on gellan.
  • a divalent metal sequestering agent preferably of a calcium ion sequestering agent, allows the gellan to be co-extruded without undesirable or uncontrolable gelling during the coextrusion.
  • the water used for the external phase is deionized water or osmozed water; using processing water remains possible but needs adjusting the amount of divalent metal sequestering agent.
  • the sequestering agent is a metal salt, preferably selected from the group comprising trisodium citrate, trisodium phosphate, tetrasodium pyrophosphate, sodium hexametaphosphate and mixtures thereof.
  • the hydrophilic external liquid phase may further comprise at least one plasticizer, which may be glycerol, sorbitol, maltitol, triacetine or polyethylene glycol type, or another polyalcohol with plasticizing or humectant properties, and advantageously a coloring agent or pigment in a form of powder or suspension stable in aqueous medium.
  • plasticizer which may be glycerol, sorbitol, maltitol, triacetine or polyethylene glycol type, or another polyalcohol with plasticizing or humectant properties, and advantageously a coloring agent or pigment in a form of powder or suspension stable in aqueous medium.
  • the co-extrusion step (A) of the process can be performed at a temperature being from room temperature to 100 0 C.
  • room temperature which means between 18 and 30 0 C, preferably 20-25 0 C under atmospheric pressure.
  • the co-extrusion step is a synchronous extrusion of two liquids: the external and hydrophilic liquid phase, and the internal and lipophilic liquid phase which can be performed using an apparatus and a process as described in EP 513603, the disclosure of which is herein incorporated by reference.
  • the solidification step is performed by keeping cold the capsules in order to ensure correct gelling of the shell, for example by contacting them with a cold bath.
  • the cold bath may preferably be cold oil or cold emulsion.
  • the capsules may then be centrifuged in order to remove the surplus oil, and/or dried and washed with organic solvent (such as acetone, ethyl acetate, ethanol, petroleum ether, etc.) also to remove the surplus oil, and optionally dried in a current or air at controlled temperature and humidity .
  • organic solvent such as acetone, ethyl acetate, ethanol, petroleum ether, etc.
  • the relative humidity of the drying air is 20% to 60%, preferably 30 to 50%; the temperature of the drying air is of 15 to 60 0 C, preferably 35 to 45 °C.
  • capsules are then immersed into an aqueous solution or an emulsion containing a curing agent which comprises a divalent salt and optionally an acid.
  • a curing agent which comprises a divalent salt and optionally an acid.
  • the capsules are dried in the same conditions as mentioned above.
  • the curing agent preferably comprises divalent metal ions, or a mixture of divalent metal ions, such as calcium ions or magnesium ions.
  • the aqueous solution containing the curing agent is preferably a divalent metal salt solution, preferably containing calcium or magnesium salts, more preferably, calcium dichloride, calcium carbonate, calcium sulfate or dicalcium phosphate.
  • This solution may be the aqueous phase of an oil-in-water emulsion.
  • This solution can be at a temperature comprised between 2 0 C and room temperature.
  • the aqueous solution containing the curing agent is maintained under acid conditions of pH, and preferably at a pH less than 5, more preferably from 3 to 4.
  • the aqueous solution containing a curing agent is a calcium chloride solution having a pH of 3 to 4.
  • the aqueous solution containing the curing agent can also contain preservatives or bactericides such as benzoate, parabens, diols, cetylpyridinium chloride, diazolidinyl urea or any preservatives used for food, pharmaceutical or cosmetic products.
  • preservatives or bactericides such as benzoate, parabens, diols, cetylpyridinium chloride, diazolidinyl urea or any preservatives used for food, pharmaceutical or cosmetic products.
  • the process comprises the steps of co-extruding the above mentioned external and internal liquid phases, optionally solidifying and/or gelling the surface of the shell by keeping the capsule under cold conditions, optionally centrifugating, optionally washing the so-obtained capsules with an organic solvent, immersing the resulting capsules into an aqueous solution containing a curing agent, and drying the capsules.
  • the solidifying/gelling/curing steps can be gathered into a single step, for example by dipping the capsules into a bath, under cold conditions, containing the divalent metal salts, preferably calcium or magnesium salts, more preferably, calcium dichloride, calcium sulfate or dicalcium phosphate.
  • This bath may be an oil-in-water emulsion.
  • the capsules manufactured through the process according to the invention are essentially or perfectly spherical and very homogeneous in size.
  • This invention also relates to breakable capsules which are preferably seamless capsules susceptible to be obtained through the process according to the invention.
  • the capsule of the invention comprises a core and a shell, and said shell includes a gelling agent comprising gellan gum alone or in combination with another gelling agent, a filler, and a divalent metal sequestering agent.
  • the gelling agent of the shell is a combination of gellan and of at least one other gelling agent selected from the group consisting of gelatin and hydrocolloids such as agar, carragheenan, xanthan gum, alginate, dextran, curdlan, welan gum, rhamsan gum or modified starches.
  • gelatin and hydrocolloids such as agar, carragheenan, xanthan gum, alginate, dextran, curdlan, welan gum, rhamsan gum or modified starches.
  • the filler and the sequestering agent are as described hereinabove.
  • the shell further comprises a plasticizer as described hereinabove and advantageously a coloring agent.
  • the shell may contain other additives such as perfumes, aromas, etc.
  • the breakable capsule according to the invention has a crush strength from 0.01 to 5, preferably from 0.01 to 2.5 kp.
  • the shell thickness of the capsule is 10-500 microns, preferably 30-150 microns, more preferably 50-60 microns.
  • the ratio diameter of the capsule / thickness of the shell is in the range of 10 to 100, preferably 50 to 70.
  • the core of the capsule is preferentially composed of a mixture of materials or products which are lipophilic or partially soluble in ethanol, or of molecules formulated as oil/water/oil emulsions.
  • the core of a breakable capsule according to the invention represents by weight 50 to 92% of said capsule, preferably 60 to 90%, more preferably 70 to 80%.
  • the core of the capsule may be composed of one or more lipophilic solvents conventionally used in the food, pharmaceutical or cosmetic industries.
  • these lipophilic solvents may be triglycerides, especially medium chain triglycerides, and in particular triglycerides of caprylic and capric acid, or mixtures of triglycerides such as vegetable oil, olive oil, sunflower oil, corn oil, groundnut oil, grape seed oil, wheat germ oil, mineral oils and silicone oils.
  • the amount of lipophilic solvent in the core of a capsule according to the invention is of the order of 0.01 to 90%, preferentially 25 to 75%, of the total weight of the capsule.
  • the core may also comprise one or more aromatic or fragrance molecules as conventionally used in the formulation of flavoring or fragrance compositions. Mention will in particular be made of aromatic, terpenic and/or sesquiterpenic hydrocarbons, and more particularly essential oils, alcohols, aldehydes, phenols, carboxylic acids in their various forms, aromatic acetals and ethers, nitrogenous heterocycles, ketones, sulfides, disulfides and mercaptans which may be aromatic or non aromatic. It may also comprise one or more molecules or extracts for cosmetic use.
  • the core may also comprise one or more fillers as used in aromatic emulsions. Mention will be made of dammar gum, wood resins of the ester gum type, sucrose acetate isobutyrate (SAIB) or brominated vegetable oils. The function of these weighting agents is to adjust the density of the liquid core.
  • the core may also comprise one or more sweeteners, which may be provided in the form of a solution or suspension in ethanol.
  • suitable sweeteners may be, but is not limited to, aspartame, saccharine, NHDC, sucralose, acesulfame, neotame, etc.
  • the core may also comprise one or more "sensate" aromatic agents, which provide either a freshening effect or a hot effect in the mouth.
  • Suitable freshening agents may be, but are not limited to, menthyl succinate and derivatives thereof, in particular Physcool® marketed by the Applicant.
  • a suitable hot effect agent may be, but is not limited to, vanillyl ethyl ether.
  • the flavoring agents that can be solubilized in the solvent of the core of the capsule include, but are not limited to, natural or synthetic aromas and/or fragrances -
  • suitable fragrances are fruity, confectionery, floral, sweet, woody fragrances.
  • suitable aromas are vanilla, coffee, chocolate, cinnamon, mint.
  • the capsules according to the invention can be used in many applications such as food, pharmaceutical, cleaning and cosmetic products.
  • Menthol Capsules (referred as 3039/A1) are prepared by co- extruding an outer liquid phase and an internal liquid phase presenting the following compositions:
  • the obtained capsules are separated into two batches referred as Ala and Alb.
  • crush strength of the capsules' is measured using a texturometer in compression mode.
  • the obtained capsules present the following physical characteristics : diameter : 2mm, thickness of the shell : 0.096mm, total weight : 4mg, weight of the core: 2.8mg (70%), weight of the shell : 1.2mg (30%).
  • Example 2
  • Cinnamon Capsules (referenced as 4053/F1) are prepared by co-extruding an outer liquid phase and an internal liquid phase presenting the following compositions:
  • the obtained capsules present the following physical characteristics : diameter : 1.2mm, thickness of the shell : 0.053mm, total weight : 0.87mg, weight of the core: 0.62mg (71.98%), weight of the shell : 0.24mg (28.02%),
  • Capsules are then incorporated into a toothpaste base containing mint flavour and cinnamon capsules 4053/F1 at a
  • cinnamon flavour is clearly identified showing good breakability of the capsules.

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Abstract

The invention relates to a process for manufacturing a seamless breakable capsule, comprising co-extruding an external and hydrophilic liquid phase, and an internal and lipophilic liquid phase, in order to form a capsule constituted of a core comprising the internal and lipophilic phase, and a shell comprising the external and hydrophilic phase, wherein the external liquid phase includes a gelling agent comprising gellan gum alone or in combination with another gelling agent, a filler, and a divalent metal sequestering agent, and to breakable capsules comprising a core and a shell, wherein the shell includes a gelling agent comprising gellan gum alone or in combination with another gelling agent, a filler, and a divalent metal sequestering agent.

Description

GELIAN SEAMLESS BREAKABLE CAPSULE AlStD PROCESS FOR MANUFACTURING THEREOF.
The present invention relates to a breakable capsule for release of its content upon crushing. Such capsules are useful for numerous applications, such as in oral care application (toothpaste, mouthwash, gums...) , in food applications such as confectionary, dairy, bakery, savoury, or in personal care products such as cosmetic products and the like.
In the present patent application, the term "capsule" will be used to designate any size of capsules, from 0.5 up to 8 mm, including macrocapsules and microcapsules . It is of particular interest to obtain seamless capsules, as the breakability of a welded capsule may be influenced by the easy rupture of the weld.
Fuji patent application JP10291928 describes a capsule obtained through a co-extrusion process, wherein the external liquid phase comprises gellan and calcium salts .
Gellan gum, first discovered in 1978, is produced by the microorganism Sphingomonas elodea.
The Applicant has found that the production of gellan capsule through the Fuji process was not satisfactory and resulted in poor quality capsules and in processing difficulties, because the gellan was actually gelling during the co-extrusion, and it was not possible to obtain spherical and homogeneous breakable capsules. For this reason, the Applicant tried to improve the Fuji process and found that the drawbacks of the prior art process may be due to the presence of calcium salts, and more generally to divalent metal salts in gellan during the co-extrusion step. Thus, the Applicant experimented a process wherein the co-extrusion liquid phase containing gellan was performed in absence of calcium salts, and observed that, surprisingly, the resulting capsules had the required spherical shape and homogeneous size. However, the obtained capsules cannot be used as such, because the shell is too soft and the resulting capsules are not breakable capsules; the Applicant found a solution to this subsequent technical problem by contacting the capsules with divalent metal ions, preferably calcium or magnesium ions, once the co-extrusion process is finished, and this finally lead to satisfactory breakable capsules.
Thus, this invention relates to a process for manufacturing seamless breakable capsules and to new breakable capsules.
The process of the invention comprises a step (A) of co-extrusion of an external and hydrophilic liquid phase and an internal and lipophilic liquid phase, in order to form a capsule having a core comprising the internal and lipophilic phase and a shell comprising the external and hydrophilic phase; and a step (B) of washing and immersing the capsules into an aqueous solution containing a curing agent, suitable for making the shell breakable as required for the intended use; optionally a step (C) of drying the obtained capsules in a dry air or optionally a step (D) of suspending the capsules into an aqueous medium to obtain a slurry form.
The co-extrusion process consists of three main stages: compound drop formation, shell solidification and capsule collection. The compound drop is a sphere of the liquid fill phase inside the shell phase. The liquid fill phase is hereinafter referred to as "the core". The shell phase is hereinafter referred to as "the shell". According to the invention, the external liquid phase includes a gelling agent comprising gellan gum alone or in combination with another gelling agent, a filler, and a metal sequestering agent, the liquid being water, preferably desionized or osmozed water.
By "gelling agent" in the meaning of this invention, it is referred to an agent able to convert an aqueous phase from a flowable liquid to a solid or a gel.
By "sequestering agent" in the meaning of this invention it is referred to any agent complexing, chelating or sequestering bivalent ions such as calcium or magnesium.
By "breakable" in the meaning of this invention, it is referred to a capsule which crush strength is comprised between 0.01 and 5 kp. The crush strength of the capsule is measured by continuously applying a load vertically onto one particle until rupture. The crush strength of the capsules in the present invention is measured by using a texturometer TA.XT plus from Micro Stable System in compression mode or a LLOYD - CHATILLON Digital Force Gauge, Model DFIS 50, having a capacity of 25Kg, a resolution of 0.02 Kg, and an accuracy of +/- 0,15 %. The force gauge is attached to a stand; the capsule is positioned in the middle of a plate that is moved up with a manual thread screw device. Pressure is then applied manually and the gauge records the maximum force applied at the very moment of the rupture of the capsule, (measured in Kg or in Lb) . Rupture of the capsule results in the release of the core.
Gellan gum is a hydrocolloid which, according to the invention, can be used as the sole gelling agent of the external liquid phase, or in combination with other gelling agents. Other suitable gelling agents may be alginates, agar, carragheenan, xanthan gum, dextran, curdlan, welan gum, rhamsan gum or modified starches. Suitable gellan gums are for example, but not limited to deacylated gellan gum. Kelcogel® can be mentioned as a suitable gellan gum.
The filler is any suitable material that can increase the percentage of dry material in the external liquid phase and thus after co-extrusion in the obtained shell. Increasing the dry material amount in a shell results in solidifying the shell, and in making it physically more resistant. Preferably, the filler is selected from the group comprising starch derivatives such as dextrin, maltodextrin, cyclodextrin (alpha, beta or gamma) , or cellulose derivatives such as hydroxypropylmethylcellulose (HPMC) , hydroxypropylcellulose
(HPC) , methylcellulose (MC) , carboxymethylcellulose (CMC) , polyvinyl alcohol, polyols or mixture thereof. Using a divalent metal sequestering or complexing agent allows to trap the divalent metal ions which are possibly present in the components of the liquid phase including water and which have a gelling effect on gellan. Thus, the use of a divalent metal sequestering agent, preferably of a calcium ion sequestering agent, allows the gellan to be co-extruded without undesirable or uncontrolable gelling during the coextrusion.
Preferably, the water used for the external phase is deionized water or osmozed water; using processing water remains possible but needs adjusting the amount of divalent metal sequestering agent.
The sequestering agent is a metal salt, preferably selected from the group comprising trisodium citrate, trisodium phosphate, tetrasodium pyrophosphate, sodium hexametaphosphate and mixtures thereof.
The hydrophilic external liquid phase may further comprise at least one plasticizer, which may be glycerol, sorbitol, maltitol, triacetine or polyethylene glycol type, or another polyalcohol with plasticizing or humectant properties, and advantageously a coloring agent or pigment in a form of powder or suspension stable in aqueous medium.
According to one embodiment of the invention, the co-extrusion step (A) of the process can be performed at a temperature being from room temperature to 1000C. Advantageously, it is performed at room temperature, which means between 18 and 300C, preferably 20-25 0C under atmospheric pressure.
The co-extrusion step is a synchronous extrusion of two liquids: the external and hydrophilic liquid phase, and the internal and lipophilic liquid phase which can be performed using an apparatus and a process as described in EP 513603, the disclosure of which is herein incorporated by reference. According to an embodiment of the invention, after the co-extrusion step (A) , the solidification step is performed by keeping cold the capsules in order to ensure correct gelling of the shell, for example by contacting them with a cold bath. The cold bath may preferably be cold oil or cold emulsion. The capsules may then be centrifuged in order to remove the surplus oil, and/or dried and washed with organic solvent (such as acetone, ethyl acetate, ethanol, petroleum ether, etc.) also to remove the surplus oil, and optionally dried in a current or air at controlled temperature and humidity . The relative humidity of the drying air is 20% to 60%, preferably 30 to 50%; the temperature of the drying air is of 15 to 60 0C, preferably 35 to 45 °C.
The thus obtained capsules are then immersed into an aqueous solution or an emulsion containing a curing agent which comprises a divalent salt and optionally an acid. The effect of the immersion step is to wash out the oil remaining at the periphery of the capsule, and to gradually strengthen the shell, notably through dehydration and osmotic equilibrium.
According to one embodiment of the invention, after immersion, the capsules are dried in the same conditions as mentioned above.
The curing agent preferably comprises divalent metal ions, or a mixture of divalent metal ions, such as calcium ions or magnesium ions.
The aqueous solution containing the curing agent is preferably a divalent metal salt solution, preferably containing calcium or magnesium salts, more preferably, calcium dichloride, calcium carbonate, calcium sulfate or dicalcium phosphate. This solution may be the aqueous phase of an oil-in-water emulsion. This solution can be at a temperature comprised between 20C and room temperature. Advantageously, the aqueous solution containing the curing agent is maintained under acid conditions of pH, and preferably at a pH less than 5, more preferably from 3 to 4. According to a preferred embodiment of the invention, the aqueous solution containing a curing agent is a calcium chloride solution having a pH of 3 to 4.
The aqueous solution containing the curing agent can also contain preservatives or bactericides such as benzoate, parabens, diols, cetylpyridinium chloride, diazolidinyl urea or any preservatives used for food, pharmaceutical or cosmetic products.
According to one embodiment of the invention, the process comprises the steps of co-extruding the above mentioned external and internal liquid phases, optionally solidifying and/or gelling the surface of the shell by keeping the capsule under cold conditions, optionally centrifugating, optionally washing the so-obtained capsules with an organic solvent, immersing the resulting capsules into an aqueous solution containing a curing agent, and drying the capsules.
According to one embodiment of the invention, the solidifying/gelling/curing steps can be gathered into a single step, for example by dipping the capsules into a bath, under cold conditions, containing the divalent metal salts, preferably calcium or magnesium salts, more preferably, calcium dichloride, calcium sulfate or dicalcium phosphate. This bath may be an oil-in-water emulsion.
The capsules manufactured through the process according to the invention are essentially or perfectly spherical and very homogeneous in size.
This invention also relates to breakable capsules which are preferably seamless capsules susceptible to be obtained through the process according to the invention.
The capsule of the invention comprises a core and a shell, and said shell includes a gelling agent comprising gellan gum alone or in combination with another gelling agent, a filler, and a divalent metal sequestering agent.
Preferably the gelling agent of the shell is a combination of gellan and of at least one other gelling agent selected from the group consisting of gelatin and hydrocolloids such as agar, carragheenan, xanthan gum, alginate, dextran, curdlan, welan gum, rhamsan gum or modified starches.
According to a preferred embodiment of the invention the filler and the sequestering agent, are as described hereinabove. According to another embodiment, the shell further comprises a plasticizer as described hereinabove and advantageously a coloring agent. According to the intended use of said capsules, the shell may contain other additives such as perfumes, aromas, etc.
According to a preferred embodiment, the breakable capsule according to the invention has a crush strength from 0.01 to 5, preferably from 0.01 to 2.5 kp.
Advantageously, the shell thickness of the capsule is 10-500 microns, preferably 30-150 microns, more preferably 50-60 microns. The ratio diameter of the capsule / thickness of the shell is in the range of 10 to 100, preferably 50 to 70.
The core of the capsule is preferentially composed of a mixture of materials or products which are lipophilic or partially soluble in ethanol, or of molecules formulated as oil/water/oil emulsions.
The core of a breakable capsule according to the invention represents by weight 50 to 92% of said capsule, preferably 60 to 90%, more preferably 70 to 80%.
The core of the capsule may be composed of one or more lipophilic solvents conventionally used in the food, pharmaceutical or cosmetic industries. In a preferred embodiment, these lipophilic solvents may be triglycerides, especially medium chain triglycerides, and in particular triglycerides of caprylic and capric acid, or mixtures of triglycerides such as vegetable oil, olive oil, sunflower oil, corn oil, groundnut oil, grape seed oil, wheat germ oil, mineral oils and silicone oils. The amount of lipophilic solvent in the core of a capsule according to the invention is of the order of 0.01 to 90%, preferentially 25 to 75%, of the total weight of the capsule.
The core may also comprise one or more aromatic or fragrance molecules as conventionally used in the formulation of flavoring or fragrance compositions. Mention will in particular be made of aromatic, terpenic and/or sesquiterpenic hydrocarbons, and more particularly essential oils, alcohols, aldehydes, phenols, carboxylic acids in their various forms, aromatic acetals and ethers, nitrogenous heterocycles, ketones, sulfides, disulfides and mercaptans which may be aromatic or non aromatic. It may also comprise one or more molecules or extracts for cosmetic use. The core may also comprise one or more fillers as used in aromatic emulsions. Mention will be made of dammar gum, wood resins of the ester gum type, sucrose acetate isobutyrate (SAIB) or brominated vegetable oils. The function of these weighting agents is to adjust the density of the liquid core.
The core may also comprise one or more sweeteners, which may be provided in the form of a solution or suspension in ethanol. Examples of suitable sweeteners may be, but is not limited to, aspartame, saccharine, NHDC, sucralose, acesulfame, neotame, etc.
The core may also comprise one or more "sensate" aromatic agents, which provide either a freshening effect or a hot effect in the mouth. Suitable freshening agents may be, but are not limited to, menthyl succinate and derivatives thereof, in particular Physcool® marketed by the Applicant. A suitable hot effect agent may be, but is not limited to, vanillyl ethyl ether.
The flavoring agents that can be solubilized in the solvent of the core of the capsule include, but are not limited to, natural or synthetic aromas and/or fragrances - Examples of suitable fragrances are fruity, confectionery, floral, sweet, woody fragrances. Examples of suitable aromas are vanilla, coffee, chocolate, cinnamon, mint. The capsules according to the invention can be used in many applications such as food, pharmaceutical, cleaning and cosmetic products.
They can be presented and sold in a slurry containing them, in suspension in a gel formed with a gel forming agent such as CMC or Carbopol, and optionally comprising preservatives and stabilizers.
The invention is hereunder illustrated by the following examples, which should not be considered as limiting the scope of the invention.
EXAMPLES
Example 1
Menthol Capsules (referred as 3039/A1) are prepared by co- extruding an outer liquid phase and an internal liquid phase presenting the following compositions:
Figure imgf000011_0001
Figure imgf000012_0001
The obtained capsules are separated into two batches referred as Ala and Alb. Capsules from each batch are cooled at 40C for Ih, washed with desionised water and then immersed in a bath containing an aqueous solution of calcium chloride (0.1% for Ala and 1% for Alb) at pH=3.5 at T=20°C during 15 minutes.
Wet capsule crush strength (gel strength) is then measured for both capsules Ala and Alb using a texturometer TA.XT plus from Micro Stable System to compare influence of concentration of calcium (the results are presented on Figure 1) .
Wet capsule strength is higher using 1% CaC12 solution than using 0.1% CaC12 solution.
After drying, crush strength of the capsules' is measured using a texturometer in compression mode.
Figure imgf000012_0002
The obtained capsules present the following physical characteristics : diameter : 2mm, thickness of the shell : 0.096mm, total weight : 4mg, weight of the core: 2.8mg (70%), weight of the shell : 1.2mg (30%). Example 2
Cinnamon Capsules (referenced as 4053/F1) are prepared by co-extruding an outer liquid phase and an internal liquid phase presenting the following compositions:
Figure imgf000013_0001
The obtained capsules are cooled at 40C for Ih, washed with desionised water and then immersed in a bath containing an aqueous solution containing 1.25% of calcium chloride at pH=3 at T=20°C during 30 minutes.
The obtained capsules present the following physical characteristics : diameter : 1.2mm, thickness of the shell : 0.053mm, total weight : 0.87mg, weight of the core: 0.62mg (71.98%), weight of the shell : 0.24mg (28.02%),
Capsules are then incorporated into a toothpaste base containing mint flavour and cinnamon capsules 4053/F1 at a
0.2% use level. During brushing, cinnamon flavour is clearly identified showing good breakability of the capsules.

Claims

1. A breakable capsule comprising a core and a shell, wherein the shell includes a gelling agent comprising gellan gum alone or in combination with another gelling agent, a filler, and a divalent metal sequestering agent .
2. The breakable capsule according to claim 1, wherein the gelling agent is a combination of gellan and one gelling agent selected from the group consisting of gelatin and hydrocolloids such as agar, carrageenan, xanthan gum, alginate, dextran, curdlan, welan gum, rhamsan gum or modified starches .
3. The breakable capsule according to anyone of claims 1 or 2, wherein the filler is a starch derivative such as dextrin, maltodextrin, cyclodextrin and/or a cellulose derivative such as hydroxypropylmethylcellulose (HPMC) , hydroxypropylcellulose (HPC) , methylcellulose (MC) , polyvinyl alcohols, polyols or mixtures thereof.
4. The breakable capsule according to anyone of claims 1 to 3, wherein the sequestering agent is a metal salt, preferably selected from the group comprising trisodium citrate, trisodium phosphate, tetrasodium pyrophosphate, sodium hexametaphosphate and mixtures thereof.
5. The breakable capsule according to anyone of claims 1 to 4, wherein the shell further comprises an acid salt selected from the group comprising such as citrate, glucuronate, adipate, fumarate, gluconate and salt of glucono-delta-lactone, and mixtures thereof.
6. The breakable capsule according to anyone of claim 1 to 5, wherein the shell further comprises a plasticizer, preferably selected from the group consisting of glycerol, sorbitol, maltitol, triacetine or PEG type, or another polyol with plasticizing properties, and mixtures thereof.
7. The breakable capsule according to anyone of claim 1 to 6, having an crush strength from 0.01 to 5 kp.
8. A process for manufacturing a seamless breakable capsule, comprising
- co-extruding an external and hydrophilic liguid phase, and an internal and lipophilic liquid phase, in order to form a capsule constituted of a core comprising the internal and lipophilic phase, and a shell comprising the external and hydrophilic phase,
- immersing into an aqueous solution containing a curing agent, wherein the external liquid phase includes a gelling agent comprising gellan gum alone or in combination with another gelling agent, a filler, and a divalent metal sequestering agent.
9. The process for manufacturing a seamless breakable capsule according to claim 8, comprising:
- co-extruding an external and hydrophilic liquid phase, and an internal and lipophilic liquid phase, in order to form a capsule constituted of a core comprising the internal and lipophilic phase and a shell comprising the external and hydrophilic phase, optionally solidifying and/or gelling the surface of the shell by keeping the capsule under cold conditions, - optionally washing the so-obtained capsule with an organic solvent,
- immersing into an aqueous solution containing a curing agent.
- optionally drying the capsule.
10. The process for manufacturing a seamless breakable capsule according to claim 8 or 9, wherein the curing agent comprises divalent ions, preferably calcium ions.
11. The process for manufacturing a seamless breakable capsule according to anyone of claims 8 to 10, wherein the aqueous solution containing a curing agent is a calcium chloride solution, which pH is preferably of 3 to 4.
12. The process for manufacturing a seamless breakable capsule according to anyone of claims 8 to 11, wherein the gelling agent is a combination of gellan and at least one other gelling agent selected from the group consisting of gelatin and hydrocolloids such as agar, carragheenan, xanthan gum, alginate, dextran, curdlan, welan gum, rhamsan gum or modified starches, and mixtures thereof .
13. The process for manufacturing a seamless breakable capsule according to anyone of claims 8 to 12, wherein the filler is a starch derivative such as dextrin, maltodextrin, cyclodextrin, a cellulose derivative such as HPMC, HPC, MC and mixtures thereof.
14. The process for manufacturing a seamless breakable capsule according to anyone of claims 8 to 13, wherein the sequestering agent is a metal salt, preferably selected from the group comprising sodium carbonate, trisodium citrate, trisodium phosphate, tetrasodium pyrophosphate, sodium hexametaphosphate and mixtures thereof.
15. The process for manufacturing a seamless breakable capsule according to anyone of claims 8 to 14, wherein the external hydrophilic liquid phase further comprises a plasticizer, preferably selected from the group consisting of glycerol, sorbitol, maltitol, triacetine or PEG type, or another polyol with plasticizing properties, and mixtures thereof.
16. Slurry containing breakable capsules according to anyone of claims 1 to 7, in suspension in a gel formed with a gel forming agent such CMC or Carbopol, and optionally comprising preservatives and stabilizers.
PCT/EP2005/008502 2005-06-21 2005-06-21 Gellan seamless breakable capsule and process for manufacturing thereof Ceased WO2006136196A1 (en)

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PCT/EP2005/008502 WO2006136196A1 (en) 2005-06-21 2005-06-21 Gellan seamless breakable capsule and process for manufacturing thereof
PCT/EP2005/009226 WO2006136198A1 (en) 2005-06-21 2005-08-05 Gellan seamless breakable capsule and process for manufacturing thereof
BRPI0611742A BRPI0611742B8 (en) 2005-06-21 2006-06-21 one-piece gellan breakable capsule and process for making it
ZA200711060A ZA200711060B (en) 2005-06-21 2006-06-21 Gellan seamless breakable capsule and process for manufacturing thereof
NZ564191A NZ564191A (en) 2005-06-21 2006-06-21 Gellan seamless breakable capsule and process for manufacturing thereof
CA2612615A CA2612615C (en) 2005-06-21 2006-06-21 Gellan seamless breakable capsule and process for manufacturing thereof
AT06809049T ATE444740T1 (en) 2005-06-21 2006-06-21 SEAMLESS RUSSIBLE GELLAN CAPSULE AND PRODUCTION METHOD THEREOF
KR1020077030403A KR101430018B1 (en) 2005-06-21 2006-06-21 Gellan seamless breakable capsule and process for manufacturing thereof
PL06809049T PL1898889T3 (en) 2005-06-21 2006-06-21 Gellan seamless breakable capsule and process for manufacturing thereof
UAA200800631A UA89543C2 (en) 2005-06-21 2006-06-21 Gellan seamless breakable capsule and process for manufacturing thereof
DE602006009655T DE602006009655D1 (en) 2005-06-21 2006-06-21 SEAMLESS BREAKABLE YELLOW CAPSULE AND MANUFACTURING METHOD THEREFOR
PCT/IB2006/002905 WO2007012981A2 (en) 2005-06-21 2006-06-21 Gellan seamless breakable capsule and process for manufacturing thereof
MX2007016511A MX2007016511A (en) 2005-06-21 2006-06-21 Gellan seamless breakable capsule and process for manufacturing thereof.
US11/922,574 US20090208568A1 (en) 2005-06-21 2006-06-21 Gellan Seamless Breakable Capsule and Process for Manufacturing Thereof
DK06809049.7T DK1898889T3 (en) 2005-06-21 2006-06-21 Fragile, jointless gelatin capsule and a process for making them
AP2007004284A AP2876A (en) 2005-06-21 2006-06-21 Gellan seamless breakable capsule and process for manufacturing thereof
RU2008102115/15A RU2428971C2 (en) 2005-06-21 2006-06-21 Gellan seamless, able for mechanical destruction capsule and method of obtaining it
PT06809049T PT1898889E (en) 2005-06-21 2006-06-21 Gellan seamless breakable capsule and process for manufacturing thereof
ES06809049T ES2333822T3 (en) 2005-06-21 2006-06-21 FRANGIBLE CAPSULA OF GELANO WITHOUT SEWING AND MANUFACTURING PROCEDURE OF THE SAME.
EP06809049A EP1898889B1 (en) 2005-06-21 2006-06-21 Gellan seamless breakable capsule and process for manufacturing thereof
JP2008517632A JP5529415B2 (en) 2005-06-21 2006-06-21 Gellan seamless collapsible capsule and method for producing the same
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CY20091101337T CY1109690T1 (en) 2005-06-21 2009-12-22 COLLABORATIVE CAPE GELANN WITHOUT WELDING AND PROCEDURE FOR ITS CONSTRUCTION
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