WO2016070016A1 - Compositions and methods for forming emulsions - Google Patents
Compositions and methods for forming emulsions Download PDFInfo
- Publication number
- WO2016070016A1 WO2016070016A1 PCT/US2015/058268 US2015058268W WO2016070016A1 WO 2016070016 A1 WO2016070016 A1 WO 2016070016A1 US 2015058268 W US2015058268 W US 2015058268W WO 2016070016 A1 WO2016070016 A1 WO 2016070016A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- temperature
- components
- emulsion
- phase
- amphiphilic compound
- 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
Links
Classifications
-
- 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
- A61K9/10—Dispersions; Emulsions
- A61K9/107—Emulsions ; Emulsion preconcentrates; Micelles
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L35/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical, and containing at least one other carboxyl radical in the molecule, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L35/02—Homopolymers or copolymers of esters
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/003—Organic compounds containing only carbon and hydrogen
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/007—Organic compounds containing halogen
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/54—Silicon compounds
-
- 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
Definitions
- the present invention generally relates to emulsions and methods for forming emulsions.
- Emulsification is a powerful age-old technique for mixing and dispersing immiscible components within a continuous liquid phase. Consequently, emulsions are central components of medicine, food, and performance materials. Complex emulsions, including multiple emulsions and Janus droplets, are of increasing importance in pharmaceuticals and medical diagnostics, in the fabrication of microdroplets and capsules for food, in chemical separations, for cosmetics, and for dynamic optics. As complex emulsion properties and functions are related to the droplet geometry and composition, the development of rapid and facile fabrication approaches allowing precise control over the droplets' physical and chemical characteristics is critical.
- the present invention provides emulsions and methods for forming emulsions.
- emulsions are provided.
- the emulsion comprises an outer phase, a plurality of droplets dispersed within the outer phase, wherein the plurality of droplets comprise two or more components, wherein the two or more components are substantially miscible at a first temperature, and wherein the two or more components are substantially immiscible at a second temperature.
- the method comprises adjusting the temperature of a fluid to a first temperature, wherein the fluid comprises a first phase and a second phase substantially immiscible in the first phase, wherein the second phase comprises two or more components that are substantially miscible with each other, emulsifying the fluid, and adjusting the temperature of the fluid to a second temperature, such that the two or more components become substantially immiscible.
- FIGs. 1A-1B illustrate the formation of complex emulsions, according to one set of embodiments.
- FIG. 2 shows photographs of the formation of complex emulsions comprising hexane and perfluorohexane, according to certain embodiments.
- FIG. 3A shows photographs of a complex emulsion comprising hexane and perfluorohexane, formed according to one set of embodiments.
- FIG. 3B shows a photograph of a complex emulsion comprising hexane and perfluorohexane, formed according to one set of embodiments.
- FIG. 4A shows a photograph of Janus droplets, formed according to one set of embodiments.
- FIG. 4B shows a scanning electron micrograph of particles formed from polymerized Janus droplets, formed according to one set of embodiments.
- FIG. 4C shows a scanning electron micrograph (top) and an energy dispersive x- ray map highlighting fluorine (bottom) of a Janus particle, formed according to one set of embodiments.
- FIG. 5 shows a four-phase emulsion, formed according to one set of
- Embodiments described herein may be useful in the formation of emulsions (e.g., complex emulsions).
- the methods may allow for one- step fabrication of multi-phase (e.g., three-phase, four-phase) emulsions (e.g., complex emulsions), and may be useful in numerous applications including food manufacturing, drug delivery, medical diagnostics, performance materials, cosmetics, MRI and ultrasound contrast agents, artificial blood, among other applications.
- methods and emulsions described herein may allow for forming emulsions with controlled and reconfigurable morphologies.
- Emulsions and methods described herein are the ability to readily incorporate additional components (e.g., magnetic nanoparticles, biological materials, polymers, metals, etc.) into various applications.
- Emulsions e.g., complex emulsions are also provided.
- the methods and emulsions comprise an outer phase and a plurality of droplets dispersed within the outer phase.
- the plurality of droplets comprise two or more components.
- the two or more components may be substantially miscible over a range of temperatures (e.g., below a critical temperature, above a critical temperature).
- the two or more components may also be substantially immiscible over a different range of temperatures (e.g., above the critical temperature, below the critical temperature) than the range of temperatures over which they are miscible.
- emulsions e.g., complex emulsions
- unconstrained by the limits of previous methods e.g., low yield of microfluidic devices, multi-step processes, the need for solvent addition and/or extraction, etc.
- the plurality of droplets comprise two or more
- the critical temperature is an upper consolute temperature of the two or more components. That is to say, in some such embodiments, the two components are substantially miscible above the upper consolute temperature of the two or more components and substantially immiscible below the upper consolute temperature of the two or more components.
- the critical temperature is a lower consolute temperature of the two or more components. That is to say, in some such embodiments, the two components are substantially miscible below the lower consolute temperature of the two or more components and substantially immiscible above the lower consolute temperature of the two or more components.
- the miscibility of the two or more components is reversible. That is to say, the miscibility of the two or more components can be changed, in some embodiments, by increasing or decreasing the temperature to a temperature greater than, or less than, the critical temperature.
- two or more components may have an upper consolute temperature greater than or equal to about 0 °C, greater than or equal to about 5 °C, greater than or equal to about 8 °C, greater than or equal to about 10 °C, greater than or equal to about 15 °C, greater than or equal to about 18 °C, greater than or equal to about 20 °C, greater than or equal to about 22 °C, greater than or equal to about 25 °C, greater than or equal to about 27 °C, greater than or equal to about 30 °C, greater than or equal to about 35 °C, greater than or equal to about 40 °C, greater than or equal to about 50 °C, greater than or equal to about 55 °C, or greater than or equal to about 60 °C.
- the upper consolute temperature of the two or more components is less than about 70 °C, less than about 60 °C, less than about 55 °C, less than about 50 °C, less than about 40 °C, less than about 35 °C, less than about 30 °C, less than about 27 °C, less than about 25 °C, less than about 22 °C, less than about 20 °C, less than about 18 °C, less than about 15 °C, less than about 10 °C, less than about 8 °C, or less than about 5 °C.
- two or more components may have a lower consolute temperature greater than or equal to about 0 °C, greater than or equal to about 5 °C, greater than or equal to about 8 °C, greater than or equal to about 10 °C, greater than or equal to about 15 °C, greater than or equal to about 18 °C, greater than or equal to about 20 °C, greater than or equal to about 22 °C, greater than or equal to about 25 °C, greater than or equal to about 27 °C, greater than or equal to about 30 °C, greater than or equal to about 35 °C, greater than or equal to about 40 °C, greater than or equal to about 50 °C, greater than or equal to about 55 °C, or greater than or equal to about 60 °C.
- the lower consolute temperature of two components is less than about 70 °C, less than about 60 °C, less than about 55 °C, less than about 50 °C, less than about 40 °C, less than about 35 °C, less than about 30 °C, less than about 27 °C, less than about 25 °C, less than about 22 °C, less than about 20 °C, less than about 18 °C, less than about 15 °C, less than about 10 °C, less than about 8 °C, or less than about 5 °C. Combinations of the above-referenced ranges are also possible (e.g., a lower consolute temperature of greater than or equal to about 0 °C and less than about 70 °C). Other ranges are also possible. Those skilled in the art would be capable of selecting suitable methods for determining the lower consolute temperature of two or more components.
- the two or more components have a greater miscibility at a first temperature as compared to a second temperature. That is to say, at the first temperature, the two or more components may be miscible to some extent, and miscible to some lesser extent (e.g., immiscible to some extent) at the second temperature.
- the two or more components may be substantially miscible over a range of pressures (e.g., below a critical pressure, above a critical pressure).
- the two or more components may also be substantially immiscible over a different range of pressure (e.g., above the critical pressure, below the critical pressure) than the range of pressures over which they are miscible.
- the use of two or more components with differing miscibility at different pressures may allow for the one-step formation (e.g., bulk) of emulsions (e.g., complex emulsions), unconstrained by the limits of previous methods (e.g., low yield of microfluidic devices, multi-step processes, the need for solvent addition and/or extraction, etc.)
- a suitable temperature and/or suitable pressure range for forming the emulsions described herein based upon the teachings of the specification and the examples below, and would generally understand these temperature ranges and/or pressure ranges to include ranges in which the two or more components remain substantially fluid (e.g., below the boiling point of the two or more components, above the freezing point of the two or more components.) In some embodiments, the two or more components are immiscible with the outer phase over the suitable temperature range and/or pressure range.
- Immiscible refers to two components (or a phase and a component) having an interfacial tension of greater than or equal to 0.01 mN/m as determined by an inverted pendant drop goniometer.
- miscible refers to two components (or a phase and a component) having an interfacial tension of less than 0.01 mN/m as determined by an inverted pendant drop goniometer.
- the two or more components comprise a first component and a second component at least partially encapsulated within the first component.
- the two or more components do not encapsulate each other but interface with the outer phase (or an additional component at least partiallyencapsulating the two or more components) to form Janus droplets.
- Janus droplets are generally droplets where the droplet is divided into two or more distinct parts comprising two or more different components that do not encapsulate each other.
- the emulsion comprises an aqueous phase and a plurality of droplets comprising a hydrocarbon and a fluorocarbon, wherein the plurality of droplets are Janus droplets.
- component generally refers to a portion of a droplet comprising a group of substantially similar molecules, a group of substantially similar compounds, and/or a phase (e.g., a non-aqueous phase, an aqueous phase).
- a phase e.g., a non-aqueous phase, an aqueous phase.
- the component is a liquid phase (e.g., a gas phase, an aqueous phase, a non-aqueous phase) comprising a group of substantially similar compounds and/or molecules.
- each component may occupy at least about 1 vol , at least about 2 vol , at least about 5 vol , at least about 10 vol , at least about 20 vol , at least about 50 vol , at least about 70 vol , at least about 90 vol , at least about 95 vol , or at least about 99 vol of the total volume of the two or more components.
- At least one of the two or more components comprises a hydrocarbon.
- suitable hydrocarbons include alkanes (e.g., hexane, heptane, decane, dodecane, hexadecane), alkenes, alkynes, aromatics (e.g., benzene, toluene, xylene, benzyl benzoate, diethyl phalate), oils (e.g., natural oils and oil mixtures including vegetable oil, mineral oil, and olive oil), liquid monomers and/or polymers (e.g., hexanediol diacrylate, butanediol diacrylate, polyethylene glycols, trimethylolpropane ethoxylate triacrylate), alcohols (e.g., butanol, octanol, pentanol, ethanol, isopropanol), ethers (e.g., diethyl ether,
- At least one of the two or more components comprises a fluorocarbon.
- suitable fluorocarbons include fluorinated compounds such as perfluoroalkanes (e.g., perfluorohexanes, perfluorooctane, perfluorodecalin, perfluoromethylcyclohexane), perfluoroalkenes (e.g.,
- perfluorobenzene perfluoroalkynes
- branched fluorocarbons e.g.,
- fluorocarbons include partially fluorinated compounds such as methoxyperfluorobutane, ethyl nonafluorobutyl ether, 2H,3H-perfluoropentane, trifluorotoluene, perfluoroidodide, fluorinated or partially fluorinated oligomers, 2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9- hexadecafluorodecane-l,10-diyl bis(2-methylacrylate), perfluoroiodide, and 2-
- At least one of the two or more components comprises a silicone such as silicone oil.
- suitable silicone oils include polydimethylsiloxane and cyclosiloxane fluids.
- At least one of the two or more components comprises water.
- At least one of the two or more components comprises an ionic liquid (e.g., an electrolyte, a liquid salt).
- at least one of the two or more inner phases comprises an ionic liquid (e.g., an electrolyte, a liquid salt, 1- allyl-3-methylimidazolium bromide, l-allyl-3-methylimidazolium chloride,
- the outer phase comprises water.
- at least one of the two or more components comprises a deuterated compound (e.g., a deuterated hydrocarbon).
- At least one of the two or more components comprises a chlorinated solvent (e.g. chloroform, carbon tetrachloride).
- a chlorinated solvent e.g. chloroform, carbon tetrachloride
- At least one of the two or more components comprises a polymer (e.g., polyethylene glycol).
- the polymer is a block copolymer.
- the polymer is a liquid crystal polymer (e.g., a thermo tropic liquid crystal polymer).
- the polymer is a biopolymer (e.g. gelatin, alginate)
- Non-limiting examples of combinations of components present in the emulsion described herein include hexane and perfluorohexane, carbon tetrachloride and perfluorohexane, chloroform and perfluorohexane, hexane and perfluorodecalin, hexane and perfluoromethylcyclohexane, hexane and perfluorotributylamine, isopropanol and hexadecane, ethyl lactate and heptane, acetic acid and decane, and triethylamine and water. Other combinations and materials are also possible.
- At least one of the two or more components comprises a gas (e.g., a perfluoropentane gas).
- a gas e.g., a perfluoropentane gas
- At least one of the two or more components comprises a combination of the materials described above (e.g., comprising a hydrocarbon, a fluorocarbon, a silicone, or combinations thereof).
- a combination of the materials described above e.g., comprising a hydrocarbon, a fluorocarbon, a silicone, or combinations thereof.
- Non-limiting examples of combinations of components present in the emulsion described herein include hexane and perfluorohexane, carbon tetrachloride and perfluorohexane, chloroform and perfluorohexane, hexane and perfluorodecalin, hexane and
- perfluoromethylcyclohexane hexane and perfluorotributylamine
- isopropanol and hexadecane ethyl lactate and heptane
- acetic acid and decane acetic acid and decane
- triethylamine and water Other combinations and materials are also possible.
- At least one of the two or more components comprises a combination of the materials described above (e.g., comprising a hydrocarbon, a fluorocarbon, a silicone, or combinations thereof).
- the outer phase may comprise any suitable material.
- the two or more components comprising the plurality of droplets may be substantially immiscible with the outer phase.
- the outer phase is an aqueous phase (e.g., comprising water).
- the outer phase is a non-aqueous phase.
- the non-aqueous phase comprises a hydrocarbon, a fluorocarbon, a silicone, or the like, as described above in the context of the two or more components, substantially immiscible with the two or more components.
- an outer phase based upon the miscibility of those materials (e.g., such that the two or more components are substantially immiscible with the outer phase).
- the use of an non-aqueous outer phase may be advantageous in certain applications where the emulsion is used in low humidity environments.
- a plurality of droplets comprising fluorocarbon/hydrocarbon phases can be created in a liquid silicone matrix.
- the silicone can be crosslinked of polymerized to change its mechanical properties.
- at least a portion of the droplets may be deformed and/or aligned by mechanically deforming (e.g., applying a mechanical force to) the outer phase.
- the emulsion comprises an amphiphilic compound.
- the amphiphilic compound is miscible in the outer phase.
- the amphiphilic compound is miscible in at least one of the two or more components.
- the amphiphilic compound has a greater miscibility in at least one of the two or more components than a miscibility in the outer phase.
- the amphiphilic compound is disposed at the interface between the outer phase and the plurality of droplets.
- the amphiphilic compound is disposed at the interface between at least two of the two or more components. The amphiphilic compound may preferentially interact with one or more components or the outer phase. Those skilled in the art would be capable of selecting a suitable amphiphilic compound based upon the teachings of the specification and examples below.
- the amphiphilic compound is a surfactant.
- suitable surfactants include ionic surfactants, non-ionic surfactants, and zwitterionic surfactants.
- the surfactant is a fluoro surfactants (e.g., commercially available fluorosurfactants such as Zonyl® or Capstone®), .
- the surfactant is anionic surfactants (e.g., sodium dodecyl sulfate (SDS))., cationic surfactants (e.g., alkyltrimethyl ammonium chloride, alkylmethyl ammonium bromide), non-ionic surfactants (e.g., alkyl poly(ethylene oxide)), zwitterionic surfactants (e.g., alkyl betain, C8-lecitin), polymeric surfactants, gemini surfactants, particulate surfactants (e.g., graphene oxide, silica particles), and combinations thereof. Other surfactants are also possible.
- anionic surfactants e.g., sodium dodecyl sulfate (SDS)
- cationic surfactants e.g., alkyltrimethyl ammonium chloride, alkylmethyl ammonium bromide
- non-ionic surfactants e.g., alkyl poly(ethylene oxide)
- the amphiphilic compound is a nucleic acid (e.g., DNA, RNA). In certain embodiments the amphiphilic compound comprises an amino acid (e.g., a peptide, a protein). In some embodiments, the amphiphilic compound comprises a biomaterial.
- suitable biomaterials include carbohydrates or derivatives thereof, saccharides or derivatives thereof (e.g., sialic acid), lipids or derivatives thereof, enzymes, chromophores or the like. Those skilled in the art would be capable of selecting suitable biomaterials based upon the teachings of the specification and the examples below.
- the amphiphilic compound comprises a perfluorinated segment. In some embodiments, the amphiphilic compound comprises ethylene glycol.
- the amphiphilic compound is capable of forming metal complexes.
- the amphiphilic compound is graphene oxide.
- the amphiphilic compound may be a particle (e.g., a silica particle, a polymer particle, a Janus particle, a nanoparticle, a gel particle).
- a particle e.g., a silica particle, a polymer particle, a Janus particle, a nanoparticle, a gel particle.
- the one or more components and/or the outer phase comprises an additional compound dispersed in the one or more components and/or the outer phase.
- the additional compound is miscible dispersible in the a first component and immiscible not dispersible in the a second component.
- at least a portion of the additional compound is dispersible in the first component and not dispersible in the second component (e.g., a surfactant).
- the additional compound may be dispersible or not dispersible in the outer phase.
- Non-limiting examples of suitable additional compounds include particles (e.g., magnetic particles/nanoparticles, silica particles), biological molecules (e.g., insulin), pharmaceutical compounds, polymers, surfactants, cells, bacteria, viruses, active pharmaceutical ingredients, and metals or metal particles.
- particles e.g., magnetic particles/nanoparticles, silica particles
- biological molecules e.g., insulin
- pharmaceutical compounds e.g., polymers, surfactants, cells, bacteria, viruses, active pharmaceutical ingredients, and metals or metal particles.
- Other additional compounds are also possible and those skilled in the art would be capable of selecting such compounds based upon the teachings of this specification.
- the emulsion can be formed by adjusting the temperature of a fluid comprising the outer phase and the two or more immiscible components such that the two or more components become substantially miscible with each other, and emulsifying the fluid (e.g., thus forming the plurality of droplets).
- the method comprises adjusting the temperature of the fluid comprising the plurality of droplets such that the two or more components become substantially immiscible.
- a fluid 100A comprises first component 110 (e.g., a hydrocarbon) and second component 120 (e.g., a fluorocarbon) which are immiscible at a first temperature T 0 .
- T 0 is adjusted to a second temperature T ⁇ (e.g., where T ⁇ is greater than T 0 , or where T ⁇ is less than T 0 ) such that the first component and second component form a miscible mixture 130 in fluid 100B.
- the first component and the second component which are initially substantially immiscible, may be heated such that they are miscible.
- the first component and the second component which are initially substantially immiscible, may be cooled such that they are miscible.
- Miscible mixture 130 can, in certain embodiments, be emulsified to form emulsion lOOC comprising plurality of droplets 132.
- Plurality of droplets 132 may comprise miscible mixture 130 and be present in an outer phase 140.
- outer phase 140 may be added prior to changing the temperature from To to TV In certain embodiments, outer phase 140 may be added after changing the temperature but prior to emulsification.
- T ⁇ is adjusted to a temperature T 2 (e.g., where T 2 is greater than T ⁇ or where T 2 is less than T such that droplet 132 comprises first component 110, and second component 120 substantially immiscible with first component 110, contained within the droplet.
- first component 110 may be at least partially encapsulated by second component 120.
- first component 110 and second component 120 are not
- FIG. IB a Janus particle
- ⁇ is greater than a critical temperature of the two or more components (e.g., an upper consolute temperature of the two or more components). In certain embodiments, T ⁇ is less than a critical temperature of the two or more
- components e.g., a lower consolute temperature.
- Those skilled in the art will be capable of selecting suitable methods for determining the critical temperature (e.g., the upper consolute temperature, the lower consolute temperature) of two or more components.
- Suitable methods for emulsifying the fluid are known in the art and may comprise sonication, high shear mixing, shaking, passing the fluid through a membrane, or injecting the two or more components into the outer phase through a small diameter channel.
- a portion of the plurality of droplets can be solidified (e.g., polymerized) such that a first configuration, a second configuration different than the first configuration, and/or a Janus droplet configuration solid droplets can be fabricated.
- a crosslinker e.g., a fluorinated acrylate
- solidifying droplets comprises adding a gelling agent (e.g., calcium-crosslinked alginate, gelatin, agar, or the like).
- solidifying droplets comprises drying the droplets.
- solidifying droplets comprises changing the temperature such that one or more components solidify (e.g., a component comprising a liquid crystal or liquid crystal polymer that solidifies below the new temperature, a component comprising a liquid with a relatively high freezing point such that changing the temperature solidifies the liquid).
- components solidify e.g., a component comprising a liquid crystal or liquid crystal polymer that solidifies below the new temperature, a component comprising a liquid with a relatively high freezing point such that changing the temperature solidifies the liquid.
- Other methods of solidifying droplets are also possible and are known in the art.
- the following example describes the general formation of an emulsion.
- hydrocarbon and fluorocarbon liquids were heated until miscible and emulsified. The temperature required varied depending on the solutions. Solutions were emulsified either in bulk by shaking or by coaxial glass capillary microfluidics and cooled to induce phase separation.
- hexane-perfluorohexane emulsions the emulsions were chilled on ice prior to imaging and often imaged while immersed in a cool water bath to maintain a temperature below 20°C.
- syringe pumps were used to inject the outer phase and inner phase using a glass capillary microfluidic device made from an outer square capillary and inner cylindrical capillary pulled to a 30 ⁇ tip using a Micropipette Puller (Sutter Instrument Company).
- the microfluidic setup was heated above the T c of the inner phase solution using a heat lamp.
- Emulsions were then cooled below T c to induce phase separation.
- Emulsions were observed to be stable during the time periods used (e.g., on the order days).
- Example 1 The following example describes the formation of an emulsion. According to the methods described in Example 1.
- Fluorocarbons are generally lipophobic as well as hydrophobic and many fluorocarbon and hydrocarbon liquids are immiscible at room temperature but have a low upper consolute temperature (T c ) and mix with gentle heating.
- T c upper consolute temperature
- perfluorohexane for example, have a T c of 22.65°C.
- a 1: 1 volume ratio of hexane and perfluorohexane was mixed and emulsified above T c in an aqueous solution of Zonyl FS- 300 fluorosurfactant (FIG. 2, top left). Cooling below T c induced phase separation and yielded structured complex droplets (FIGs. 2. Bottom right). Above T c , hexane and perfluorohexane are miscible and emulsified in 0.1% Zonyl (FIG. 2, top left).
- hexane and perfluorohexane phase separate to create a hexane-in-perfluorohexane-in- water (H/F/W) double emulsion (FIG. 2, bottom right).
- H/F/W hexane-in-perfluorohexane-in- water
- Fig. 3A surfactant solution
- Liquid droplets and solid droplets with asymmetric properties were created by affecting different chemistries in the separate compartments of a fluorous-hydrocarbon Janus droplet.
- magnetic Fe 3 C"4 nanoparticles stabilized with oleic acid were synthesized for preferential partitioning into the hydrocarbon phase.
- Magnetite nanoparticles were made as follows: 25 mL of concentrated NH30H was added to an acidified solution of 1.6 g of FeCl 3 and 1 g of FeCl 2 *4H 2 0 in 50 mL of water at 80°C. The magnetite nanoparticle precipitate was collected with a magnet, washed with water, and redispersed.
- the nanoparticle/dichlorobenzene hemispheres are rapidly oriented and move in the direction of a magnet (Fig. 4A).
- an emulsion consisting of a liquid polymer precursor, 1,6-hexanediol diacrylate, as the hydrocarbon phase and
- methoxyperfluorobutane as the fluorous phase, was polymerized (Fig. 4B).
- 1- 6,hexanediol diacrylate with 4% Darocur 1173 photoinitiator was heated with equal volume methoxyperfluorobutane above the Tc and emulsified.
- 1% SDS and 1% Zonyl in a 3:2 ratio yielded Janus droplets which were then polymerized under a UV lamp while kept cold on ice.
- methoxyperfluorobutane with a fluorinated acrylate oligomer and crosslinker, spherical solid Janus droplets with fluorinated and non- fluorinated sides were created (Fig. 4C).
- silicone oil Si
- hydrocarbon oil H, mineral oil and octadecane
- fluorinated oil F, ethyl nonafluorobutyl ether
- a reference to "A and/or B,” when used in conjunction with open-ended language such as “comprising” can refer, in one embodiment, to A without B (optionally including elements other than B); in another embodiment, to B without A (optionally including elements other than A); in yet another embodiment, to both A and B (optionally including other elements); etc.
- the phrase "at least one,” in reference to a list of one or more elements, should be understood to mean at least one element selected from any one or more of the elements in the list of elements, but not necessarily including at least one of each and every element specifically listed within the list of elements and not excluding any combinations of elements in the list of elements.
- This definition also allows that elements may optionally be present other than the elements specifically identified within the list of elements to which the phrase "at least one" refers, whether related or unrelated to those elements specifically identified.
- At least one of A and B can refer, in one embodiment, to at least one, optionally including more than one, A, with no B present (and optionally including elements other than B); in another embodiment, to at least one, optionally including more than one, B, with no A present (and optionally including elements other than A); in yet another embodiment, to at least one, optionally including more than one, A, and at least one, optionally including more than one, B (and optionally including other elements); etc.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Dispersion Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Polymers & Plastics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Preparation (AREA)
- Colloid Chemistry (AREA)
- Cosmetics (AREA)
- Manufacturing Of Micro-Capsules (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2017522834A JP6914192B2 (ja) | 2014-10-31 | 2015-10-30 | 乳剤形成のための組成および方法 |
| EP15855674.6A EP3212315A4 (en) | 2014-10-31 | 2015-10-30 | Compositions and methods for forming emulsions |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462073896P | 2014-10-31 | 2014-10-31 | |
| US62/073,896 | 2014-10-31 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2016070016A1 true WO2016070016A1 (en) | 2016-05-06 |
Family
ID=55858388
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2015/058268 Ceased WO2016070016A1 (en) | 2014-10-31 | 2015-10-30 | Compositions and methods for forming emulsions |
Country Status (4)
| Country | Link |
|---|---|
| US (2) | US10252231B2 (enExample) |
| EP (1) | EP3212315A4 (enExample) |
| JP (2) | JP6914192B2 (enExample) |
| WO (1) | WO2016070016A1 (enExample) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105997572A (zh) * | 2016-05-19 | 2016-10-12 | 曾新民 | 一种含纳米石墨烯洗面奶及其制备方法 |
| CN106512875A (zh) * | 2016-11-17 | 2017-03-22 | 陕西师范大学 | Janus型多级孔SiO2微球及其制备方法和应用 |
| CN106880502A (zh) * | 2017-03-20 | 2017-06-23 | 北京大学口腔医学院 | 一种Janus纳米颗粒作为粘接剂用于牙科修复填充材料的应用 |
| WO2018222138A1 (en) * | 2017-05-30 | 2018-12-06 | Orica International Pte Ltd | Explosives composition |
| WO2022121042A1 (zh) * | 2020-12-10 | 2022-06-16 | 广东省科学院化工研究所 | 一种复合型乳液及其制备方法与应用 |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11119098B2 (en) | 2014-10-31 | 2021-09-14 | Massachusetts Institute Of Technology | Systems including Janus droplets |
| US10060913B2 (en) | 2016-09-19 | 2018-08-28 | Massachusetts Institute Of Technology | Systems including janus droplets capable of binding an analyte and changing orientation to provide a detectable change |
| US20210041425A1 (en) * | 2014-10-31 | 2021-02-11 | Massachusetts Institute Of Technology | Complex liquid crystal droplets |
| EP3212315A4 (en) | 2014-10-31 | 2018-07-11 | Massachusetts Institute of Technology | Compositions and methods for forming emulsions |
| WO2016070027A1 (en) | 2014-10-31 | 2016-05-06 | Massachusetts Institute Of Technology | Compositions and methods for arranging colloid phases |
| US20190170737A1 (en) | 2016-09-19 | 2019-06-06 | Massachusetts Institute Of Technology | Systems including janus droplets |
| US20180246314A1 (en) | 2017-02-03 | 2018-08-30 | Massachusetts Institute Of Technology | Tunable microlenses and related methods |
| US11434381B2 (en) | 2017-03-06 | 2022-09-06 | Bic-Violex Sa | Coating |
| CN108079896A (zh) * | 2018-02-07 | 2018-05-29 | 广州中健健康科技有限公司 | 一种利用生物基离子液体将水油体电聚合的方法 |
| US11654404B2 (en) | 2018-05-18 | 2023-05-23 | Massachusetts Institute Of Technology | Light emitting droplets and related methods |
| US12274993B2 (en) | 2019-09-18 | 2025-04-15 | Massachusetts Institute Of Technology | Systems and methods for affecting interactions of electromagnetic radiation with janus droplets for sensitive detection of species |
| EP4037816A4 (en) * | 2019-10-04 | 2023-10-18 | The Regents Of The University Of Colorado, A Body Corporate | Micron sized droplets with solid endoskeleton or exoskeleton which tunes the thermal stability of the liquid droplets |
| CN116410614B (zh) * | 2023-03-27 | 2025-03-18 | 华中科技大学 | 一种具有温度响应性的全内反射结构色液滴及其制备与应用 |
Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1992017179A1 (en) * | 1991-03-28 | 1992-10-15 | Micro Vesicular Systems, Inc. | Lipid vesicle containing water-in-oil emulsions |
| US5217648A (en) | 1988-08-19 | 1993-06-08 | Illinois Institute Of Technology | Process for preparation of hemoglobin multiple emulsions |
| US5980936A (en) | 1997-08-07 | 1999-11-09 | Alliance Pharmaceutical Corp. | Multiple emulsions comprising a hydrophobic continuous phase |
| WO2009061372A1 (en) * | 2007-11-02 | 2009-05-14 | President And Fellows Of Harvard College | Systems and methods for creating multi-phase entities, including particles and/or fluids |
| WO2009101113A2 (en) * | 2008-02-12 | 2009-08-20 | L'oreal | Oil-in-water emulsion comprising an amphiphilic polymer |
| US20090232856A1 (en) | 2008-03-11 | 2009-09-17 | Mary Kay Inc. | Stable three-phased emulsions |
| US20120248020A1 (en) | 2007-12-06 | 2012-10-04 | The Board Of Trustees Of The University Of Illinois | Chromatography devices and methods |
| US20120319043A1 (en) * | 2010-01-29 | 2012-12-20 | Braster Sa | Liquid-crystal emulsion oil in water type and a preparation method of the liquid-crystal emulsion |
| US20120328654A1 (en) * | 2009-09-02 | 2012-12-27 | National Health Research Institutes | Multi-phase emulsions based on amphiphilic block copolymers |
Family Cites Families (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4870026A (en) | 1982-09-16 | 1989-09-26 | The General Hospital Corporation | Non-A, non-B. hepatitis, virus, methods of identification purification, characterization, diagnosis and immunization |
| US4912034A (en) | 1987-09-21 | 1990-03-27 | Biogenex Laboratories | Immunoassay test device and method |
| US5066465A (en) | 1989-12-27 | 1991-11-19 | Olympus Optical Co., Ltd. | Reaction apparatus |
| US5332661A (en) | 1991-07-31 | 1994-07-26 | Abbott Laboratories | Reagents and methods for the quantification of total doxepins in biological fluids |
| JP3097866B2 (ja) | 1991-10-15 | 2000-10-10 | マルティライト リミティド | 標識試薬を使用した結合検定法 |
| US5387676A (en) | 1992-03-11 | 1995-02-07 | Ciba Corning Diagnostics Corp. | MN gene and protein |
| US5573994A (en) | 1994-05-13 | 1996-11-12 | University Of Cincinnati | Superabsorbent foams, and method for producing the same |
| US6271202B1 (en) | 1996-04-19 | 2001-08-07 | University Of Tennessee Research Corporation | Reduction of impairment of respiratory tract mucosal immunity |
| US6180418B1 (en) | 1998-01-20 | 2001-01-30 | The United States Of America As Represented By The Secretary Of The Navy | Force discrimination assay |
| AU2001257001A1 (en) | 2000-04-10 | 2001-10-23 | Mount Sinai School Of Medicine Of New York University | Screening methods for identifying viral proteins with interferon antagonizing functions and potential antiviral agents |
| ES2251487T3 (es) | 2000-06-05 | 2006-05-01 | Syngenta Limited | Nuevas emulsiones. |
| US7625951B2 (en) | 2000-07-13 | 2009-12-01 | University Of Kentucky Research Foundation | Stimuli-responsive hydrogel microdomes integrated with genetically engineered proteins for high-throughput screening of pharmaceuticals |
| CN1231758C (zh) | 2000-10-19 | 2005-12-14 | 泰博特克公司 | 操作用于识别目的的微载体的方法 |
| JP3595805B2 (ja) | 2001-08-07 | 2004-12-02 | キヤノン株式会社 | 刺激応答性組成物、並びに該組成物を用いた画像形成方法および装置 |
| GB0315991D0 (en) | 2003-07-08 | 2003-08-13 | Dakocytomation Denmark As | Standard |
| US8241651B2 (en) | 2004-11-10 | 2012-08-14 | The Regents Of The University Of Michigan | Multiphasic biofunctional nano-components and methods for use thereof |
| US7947772B2 (en) | 2004-11-10 | 2011-05-24 | The Regents Of The University Of Michigan | Multiphasic nano-components comprising colorants |
| JP4690418B2 (ja) | 2004-11-10 | 2011-06-01 | ザ リージェンツ オブ ザ ユニバーシティ オブ ミシガン | 多相ナノ粒子 |
| KR20160129919A (ko) | 2008-06-05 | 2016-11-09 | 더 어드미니스트레이터즈 오브 더 튜래인 어듀케이셔널 훤드 | 중합체 기능성 진화를 합성 동안 모니터하기 위한 방법 및 장치 |
| US8278040B2 (en) | 2008-07-30 | 2012-10-02 | Wisconsin Alumni Research Foundation | Optically responsive and mechanically tunable colloid-in-liquid crystal gels |
| KR101796906B1 (ko) | 2009-03-24 | 2017-11-10 | 유니버시티 오브 시카고 | 반응을 수행하기 위한 방법 |
| US20110104777A1 (en) | 2009-11-03 | 2011-05-05 | Manuel Marquez | Method of making an artificial micro-gland that is anisotropic |
| WO2011087916A2 (en) | 2010-01-15 | 2011-07-21 | Willson Richard C | Force mediated assays |
| US8318105B2 (en) | 2010-02-10 | 2012-11-27 | Selinfreund Richard H | Systems and methods for biomarker analysis |
| WO2012075033A2 (en) | 2010-11-29 | 2012-06-07 | President And Fellows Of Harvard College | Environmentally responsive optical microstructured hybrid actuator assemblies and applications thereof |
| US9387446B2 (en) | 2011-09-22 | 2016-07-12 | Ariel-University Research And Development Company Ltd. | Emulsions and methods of making emulsions |
| WO2013059294A1 (en) | 2011-10-17 | 2013-04-25 | The Regents Of The University Of Michigan | Methods and devices for detecting and separating target analyte species using anisotropic micro-particles |
| KR20230003659A (ko) | 2013-02-08 | 2023-01-06 | 10엑스 제노믹스, 인크. | 폴리뉴클레오티드 바코드 생성 |
| US10285940B2 (en) | 2013-10-02 | 2019-05-14 | The Regents Of The University Of California | Multicomponent, internally structured nanoemulsions and methods of production |
| US9642923B2 (en) | 2014-02-24 | 2017-05-09 | Verily Life Sciences Llc | Engineered particles with polarization contrast and alignment control for enhanced imaging |
| CN104023407B (zh) | 2014-05-23 | 2017-09-29 | 大唐移动通信设备有限公司 | 上行频选调度方法和装置 |
| US10060913B2 (en) | 2016-09-19 | 2018-08-28 | Massachusetts Institute Of Technology | Systems including janus droplets capable of binding an analyte and changing orientation to provide a detectable change |
| US11119098B2 (en) | 2014-10-31 | 2021-09-14 | Massachusetts Institute Of Technology | Systems including Janus droplets |
| WO2016070027A1 (en) | 2014-10-31 | 2016-05-06 | Massachusetts Institute Of Technology | Compositions and methods for arranging colloid phases |
| EP3212315A4 (en) | 2014-10-31 | 2018-07-11 | Massachusetts Institute of Technology | Compositions and methods for forming emulsions |
| US20190170737A1 (en) | 2016-09-19 | 2019-06-06 | Massachusetts Institute Of Technology | Systems including janus droplets |
| US20200166503A1 (en) | 2018-11-27 | 2020-05-28 | Massachusetts Institute Of Technology | Selective reflection of light from colloidal droplets and particles for biological and chemical detection |
-
2015
- 2015-10-30 EP EP15855674.6A patent/EP3212315A4/en not_active Withdrawn
- 2015-10-30 WO PCT/US2015/058268 patent/WO2016070016A1/en not_active Ceased
- 2015-10-30 US US14/929,117 patent/US10252231B2/en active Active
- 2015-10-30 JP JP2017522834A patent/JP6914192B2/ja not_active Expired - Fee Related
-
2019
- 2019-02-25 US US16/284,722 patent/US11229892B2/en active Active
-
2020
- 2020-09-07 JP JP2020149719A patent/JP2020199503A/ja active Pending
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5217648A (en) | 1988-08-19 | 1993-06-08 | Illinois Institute Of Technology | Process for preparation of hemoglobin multiple emulsions |
| WO1992017179A1 (en) * | 1991-03-28 | 1992-10-15 | Micro Vesicular Systems, Inc. | Lipid vesicle containing water-in-oil emulsions |
| US5980936A (en) | 1997-08-07 | 1999-11-09 | Alliance Pharmaceutical Corp. | Multiple emulsions comprising a hydrophobic continuous phase |
| WO2009061372A1 (en) * | 2007-11-02 | 2009-05-14 | President And Fellows Of Harvard College | Systems and methods for creating multi-phase entities, including particles and/or fluids |
| US20120248020A1 (en) | 2007-12-06 | 2012-10-04 | The Board Of Trustees Of The University Of Illinois | Chromatography devices and methods |
| WO2009101113A2 (en) * | 2008-02-12 | 2009-08-20 | L'oreal | Oil-in-water emulsion comprising an amphiphilic polymer |
| US20090232856A1 (en) | 2008-03-11 | 2009-09-17 | Mary Kay Inc. | Stable three-phased emulsions |
| US20120328654A1 (en) * | 2009-09-02 | 2012-12-27 | National Health Research Institutes | Multi-phase emulsions based on amphiphilic block copolymers |
| US20120319043A1 (en) * | 2010-01-29 | 2012-12-20 | Braster Sa | Liquid-crystal emulsion oil in water type and a preparation method of the liquid-crystal emulsion |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105997572A (zh) * | 2016-05-19 | 2016-10-12 | 曾新民 | 一种含纳米石墨烯洗面奶及其制备方法 |
| CN105997572B (zh) * | 2016-05-19 | 2021-02-02 | 广州靓美莲美容科技有限公司 | 一种含纳米石墨烯洗面奶及其制备方法 |
| CN106512875A (zh) * | 2016-11-17 | 2017-03-22 | 陕西师范大学 | Janus型多级孔SiO2微球及其制备方法和应用 |
| CN106880502A (zh) * | 2017-03-20 | 2017-06-23 | 北京大学口腔医学院 | 一种Janus纳米颗粒作为粘接剂用于牙科修复填充材料的应用 |
| CN106880502B (zh) * | 2017-03-20 | 2019-10-08 | 北京大学口腔医学院 | 一种Janus纳米颗粒作为粘接剂用于牙科修复填充材料的应用 |
| WO2018222138A1 (en) * | 2017-05-30 | 2018-12-06 | Orica International Pte Ltd | Explosives composition |
| AU2018276886B2 (en) * | 2017-05-30 | 2022-05-19 | Orica International Pte Ltd | Explosives composition |
| WO2022121042A1 (zh) * | 2020-12-10 | 2022-06-16 | 广东省科学院化工研究所 | 一种复合型乳液及其制备方法与应用 |
Also Published As
| Publication number | Publication date |
|---|---|
| US11229892B2 (en) | 2022-01-25 |
| JP6914192B2 (ja) | 2021-08-04 |
| EP3212315A1 (en) | 2017-09-06 |
| US20160151753A1 (en) | 2016-06-02 |
| JP2018501944A (ja) | 2018-01-25 |
| US20190184356A1 (en) | 2019-06-20 |
| EP3212315A4 (en) | 2018-07-11 |
| US10252231B2 (en) | 2019-04-09 |
| JP2020199503A (ja) | 2020-12-17 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US11229892B2 (en) | Compositions and methods for forming emulsions | |
| Sheth et al. | Multiple nanoemulsions | |
| Eastoe et al. | Surfactants and nanoscience | |
| Golemanov et al. | Selection of surfactants for stable paraffin-in-water dispersions, undergoing solid− liquid transition of the dispersed particles | |
| Gupta et al. | A general route for nanoemulsion synthesis using low-energy methods at constant temperature | |
| Hunter et al. | Pickering emulsifiers based on block copolymer nanoparticles prepared by polymerization-induced self-assembly | |
| Tcholakova et al. | Efficient self-emulsification via cooling-heating cycles | |
| US10005058B2 (en) | Compositions and methods for arranging colloid phases | |
| Ku et al. | Dynamically reconfigurable, multifunctional emulsions with controllable structure and movement | |
| WO2009037482A2 (en) | Microcapsules and methods | |
| Cholakova et al. | Multilayer formation in self-shaping emulsion droplets | |
| Cholakova et al. | “Self-shaping” of multicomponent drops | |
| Wu et al. | Modeling the interfacial energy of surfactant-free amphiphilic Janus nanoparticles from phase inversion in Pickering emulsions | |
| Valkova et al. | Mechanisms and control of self-emulsification upon freezing and melting of dispersed alkane drops | |
| Cheon et al. | Particle stabilization of oil–fluorocarbon interfaces and effects on multiphase oil-in-water complex emulsion morphology and reconfigurability | |
| Mulligan et al. | Deformation and breakup of micro-and nanoparticle stabilized droplets in microfluidic extensional flows | |
| Song et al. | Controlled formation of all-aqueous Janus droplets by liquid–liquid phase separation of an aqueous three-phase system | |
| Nonomura et al. | Multiple pickering emulsions stabilized by microbowls | |
| Xu et al. | Microfluidic preparation and structure evolution of double emulsions with two-phase cores | |
| Zhang et al. | Large-scale single-cell encapsulation in microgels through metastable droplet-templating combined with microfluidic-integration | |
| Birrer et al. | Ionic liquid-in-water emulsions stabilized by molecular and polymeric surfactants | |
| Zhang et al. | Inhibiting Ostwald ripening by scaffolding droplets | |
| Raju et al. | Pickering Janus emulsions stabilized with gold nanoparticles | |
| Sakamoto et al. | Surface freezing of cetyltrimethylammonium chloride–hexadecanol mixed adsorbed film at dodecane–water interface | |
| EP4037816A1 (en) | Micron sized droplets with solid endoskeleton or exoskeleton which tunes the thermal stability of the liquid droplets |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 15855674 Country of ref document: EP Kind code of ref document: A1 |
|
| ENP | Entry into the national phase |
Ref document number: 2017522834 Country of ref document: JP Kind code of ref document: A |
|
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| REEP | Request for entry into the european phase |
Ref document number: 2015855674 Country of ref document: EP |