Patent Application
20230099063
The present invention relates to self-healing shells comprising amphiphilic molecules having metal-coordinating group or groups reversibly cross-linked with suitable metal cations, their uses and processes to produce them.
Surfactants (or surface active agents) are amphiphilic molecules comprising both a hydrophobic and a hydrophilic group. The surfactant therefore contains both a water soluble portion and a water insoluble (oil soluble) portion so that a surfactant will self-assemble at a water or gas and oil interface, with the hydrophilic group extending into the water phase and the hydrophobic group extending into the oil or gas phase.
Surfactants have many uses, including as detergents, wetting agents, emulsifiers, foaming agents, and dispersants.
However, there remains a need to develop surfactant systems containing enhanced properties.
In a first aspect of the present invention there is provided a self-healing shell at an interface between a first fluid phase and a second fluid phase; wherein the first fluid phase is a liquid phase or a gas phase and the second fluid phase is a liquid phase; said shell comprising amphiphilic molecules and metal cations; wherein the amphiphilic molecules comprise one or more hydrophilic group(s) and one or more hydrophobic group(s), and wherein the amphiphilic molecules comprise one or more metal-coordinating group(s); wherein the metal cations comprise metal ions, metal oxides, metal hydroxides, metal carbides, metal nitrides, and/or metal nanoparticles; and wherein amphiphilic molecules in the shell are reversibly cross-linked via the one or more metal-coordinating group(s) and metal cations.
It has surprisingly been discovered that by using amphiphilic molecules with a metal coordinating group, it is possible to combine the interfacial activity of surfactants with the reversible gelling and/or self-healing properties of the meal coordinating groups.
This allows the surfactants to reversibly cross-link (self-heal) only at interfaces, thereby forming shells that display self-healing properties.
In a yet further aspect of the present invention, there is provided a method of manufacturing self-healing shells as defined herein; the method comprising forming a system comprising: an interface between a first fluid phase and a second fluid phase, amphiphilic molecules and metal cations; wherein the first fluid phase is a liquid phase or a gas phase and the second fluid phase is a liquid phase; such that the metal-coordinating group(s) and metal cation(s) reversibly cross-link at the interface to form a self-healing shell.
In a yet further aspect of the present invention, there is provided a method of transporting material from a first closed system to a second closed system within a surrounding solvent using self-healing shells described herein; comprising forming a first self-healing capsule comprising a shell to encapsulate a first fluid and form a first closed system; forming a second self-healing capsule comprising shell to encapsulate a second fluid and form a second closed system; bringing the first and second self-healing capsules into contact such that the first and second fluids fuse bringing the first and second closed systems into contact with each other while still being protected from the surrounding solvent by the self-healing shell.
In a yet further embodiment of the present invention, there is provided the use of a self-healing shell as described herein in a screening assay. Screening assays which use self-healing shells according to the present invention may to reduce cross-talk between droplets caused by material leakage. The present invention can be used to stabilise emulsion drops used in screening assays.
In a yet further embodiment of the present invention, there is provided the use of self-healing shell as described herein as a vehicle for drug delivery and/or for encapsulation of drugs, food ingredients, nutraceuticals, cosmetics, pesticides, nutrients, fragrances, catalysts, agrichemicals, biological material such as cells, DNA, RNA, proteins, enzymes, antibodies, reagents to form proteins, coatings, paints, or waste products.
In a yet further embodiment of the present invention, there is provided three-dimensional hydrogel material comprising self-healing shells as described herein.
In a yet further embodiment of the present invention, there is provided an amphiphilic molecule as described herein, comprising one or more hydrophilic group(s) and one or more hydrophobic group(s); and wherein the amphiphilic molecule comprises one or more metal-coordinating group(s) as claimed in; wherein the amphiphilic molecule is a block copolymer; and wherein the metal-coordinating group is a metal-coordinating group selected from the group consisting of: benzenediol or derivatives thereof, preferably catechol or derivatives thereof; and benzenetriol or derivatives thereof, preferably gallol or derivatives thereof; histidines and derivatives thereof; ethylenediaminetetraacetic acid and derivatives thereof and wherein the metal-coordinating group may optionally be further substituted.
In a yet further aspect of the present invention there is provided a shell at an interface between a first fluid phase and a second fluid phase; wherein the first fluid phase is a liquid phase or a gas phase and the second fluid phase is a liquid phase; said shell comprising amphiphilic molecules and metal cations; wherein the amphiphilic molecules comprise one or more hydrophilic group(s) and one or more hydrophobic group(s), and wherein the amphiphilic molecules comprise one or more metal-coordinating group(s); wherein the metal cations comprise metal ions, metal oxides, metal hydroxides, metal carbides, metal nitrides, and/or metal nanoparticles; and wherein amphiphilic molecules in the shell are cross-linked via the one or more metal-coordinating group(s) and metal cations.
In a yet further aspect of the present invention, the reaction conditions may be modified to enable covalent cross-linking between amphiphilic molecules, including by adjusting the pH and/or by the presence of a catalysts including ions that serve as a catalyst or another oxidising agent.
In a yet further aspect of the present invention, there is provided the use of shells and/or amphiphilic molecules of the present invention or precursor materials thereof, in stabilizing emulsion drops, particularly for screening assays or high throughput screening applications. Such applications include drug discovery, antibody screening, protein screening, biotechnology, biology and chemistry. In a yet further aspect of the present invention, there is provided screening assays or high throughput screening devices incorporating shells and/or amphiphilic molecules of the present invention or precursor materials thereof.
The shells themselves can be used to measure properties of solutions. For example, shells according to the present invention may be formed and their buckling measured to determine the concentration of ions in a solution. Such an approach can be used to detect and/or quantify the presence of ions in a solution. As such, in a yet further aspect of the present invention, there is provided a method of detecting the presence and/or concentration of ion or ions, said method comprising measuring properties of a shell made according to the present invention which vary according to ion concentration, and using said property to determine the presence and/or concentration of ion or ions.
In a yet further aspect of the present invention, a second or further amphiphilic molecules according to the present invention can be used in the shells and methods of the present invention. Such an approach can further tune the properties of the shell, for example to make a stronger shell. In an embodiment, one amphiphilic molecule may be soluble in an aqueous phase and a second amphiphilic molecule may be soluble in a non-aqueous phase. Such an approach enables linking, via metal-coordinating groups, of amphiphilic molecules from both phases and can form strong shells.
In a yet further aspect of the present invention, there is provided a shell at an interface between a first fluid phase and a second fluid phase; wherein the first fluid phase is a liquid phase or a gas phase and the second fluid phase is a liquid phase; said shell comprising amphiphilic molecules; wherein the amphiphilic molecules comprise one or more hydrophilic group(s) and one or more hydrophobic group(s), and wherein the amphiphilic molecules comprise one or more coordinating group(s); and wherein amphiphilic molecules in the shell are covalently cross-linked by suitable conditions including suitable pH conditions and/or through the use of suitable catalysts including suitable oxidising agents. The coordinating group(s) may be the same as the metal coordinating group(s) as described herein. As such, the amphiphilic molecules in this aspect may be the same as the amphiphilic molecules described in relation to reversible binding.
In a yet further aspect of the present invention there is provided a shell at an interface between a first fluid phase and a second fluid phase; wherein the first fluid phase is a liquid phase or a gas phase and the second fluid phase is a liquid phase; said shell comprising amphiphilic molecules and metal cations; wherein the amphiphilic molecules comprise one or more fluorophilic group(s) and one or more hydrophobic group(s), and wherein the amphiphilic molecules comprise one or more metal-coordinating group(s); wherein the metal cations comprise metal ions, metal oxides, metal hydroxides, metal carbides, metal nitrides, and/or metal nanoparticles; and wherein amphiphilic molecules in the shell are cross-linked via the one or more metal-coordinating group(s) and metal cations.
The following embodiments apply to all aspects of the present invention.
In the present application, a number of general terms and phrases are used, which should be interpreted as follows.
“Self-healing” means the shell is able to spontaneously repair if it is breached. The shell is able to reform cross-links either with the shell and/or via further surfactant molecules and cations within the liquid(s) to reform an intact shell. The repair may reform the shell to its original structure or it may reform the shell in a slightly different structure that nevertheless repairs the breach. The property of self-healing can make the shell “sticky”.
Without wishing to be bound by theory, the self-healing properties are believed to be due to the ionic nature of the bonds formed. However, in some embodiments, the self-healing nature of the shells due to ionic interactions, although present, are not a critical characteristic of the shell. Thus, in embodiments of the invention, reference to “self-healing shells” may be considered a reference to a “shell”. As an example, the present invention encompasses a shell at an interface between a first fluid phase and a second fluid phase; wherein the first fluid phase is a liquid phase or a gas phase and the second fluid phase is a liquid phase; said shell comprising amphiphilic molecules and metal cations; wherein the amphiphilic molecules comprise one or more hydrophilic group(s) and one or more hydrophobic group(s), and wherein the amphiphilic molecules comprise one or more metal-coordinating group(s); wherein the metal cations comprise metal ions, metal oxides, metal hydroxides, metal carbides, metal nitrides, and/or metal nanoparticles; and wherein amphiphilic molecules in the shell are cross-linked via the one or more metal-coordinating group(s) and metal cations.
Furthermore, in embodiments, the conditions may be present or adjusted such that covalent bonds form between amphiphilic molecules. In these situations, the shell will no longer be considered self-healing.
“Shell” means the amphiphilic molecules at the interface are ionically cross-linked via the metal coordinating group and the metal cation to form a responsive shell which separates the first phase and the second phase. The shell may encapsulate the first phase from the second phase. The shell may form a capsule. The shell may form a membrane between the first phase and second phase. The membrane may be planar or another shape. There may be multiple phases beyond the first and second phase.
The shell protects the inner phase from the outer phase (and vice versa) and provides a resilient but flexible shell. The shell is stable and strong enough to be moved within a system and will self-heal if it is breached by the reformation of further ionic coordination bonds.
“Capsule” according to the present invention means an inner phase encapsulated by a shell that is formed at the interface between the first phase and the second phase. For example, in an oil-in-water emulsion, drops of oil may be encapsulated by a shell according to the present invention thereby protecting the inner oil from the outer water phase. Equally, in a water-in-oil emulsion, drops of water may be encapsulated by a capsule according to the present invention to protect the inner water phase from an outer oil phase. Water-in-oil-in-water and oil-in-water-in-oil emulsions or emulsion drops encompassing more than one smaller drop are also possible. Further, it is possible to form capsules according to the present invention when the first and second phases have some solubility in each other, provided the interfacial tension is sufficiently high for drops to form. If mechanical agitation is used to form drops, the interfacial tension between two liquids can be quite small.
Once capsules have been formed, they can be transferred (or the medium surrounding them can be replaced). This could include removing them from the system into air or moving them into any suitable medium. It is therefore possible in embodiments to remove formed capsules and move them into a different system, or to form capsules and then change the system in which they are placed. The shell of the present invention protects the encapsulated contents from the medium and vice versa. As an example, formed capsules encapsulating a liquid could be introduced into the same liquid contained in the core of the capsule, but the inner liquid is still separated since it is encapsulated by the shell.
“Membrane” according to the present invention means that the shell forms at the interfacial boundary. This may be planar or conform to a different shape. An example of a membrane is where a first phase is introduced into a second phase via, for example, a needle. A shell will form at the interfacial boundary but will not fully encapsulate the inner material since it is still attached to the needle. In this example, ultimately, if the drop releases from the needle the shell may fully encapsulate the inner material forming a capsule.
“Amphiphilic molecule”: the shell according to the present invention is formed from amphiphilic molecules coordinated via metal cations which undergo molecular self-assembly at interfaces to form self-healing shells. By molecular self-assembly it is intended to mean that the amphiphilic molecules form a suitable structure to enable a shell to form. Examples of suitable structures include monolayers, bilayers or aggregates. Examples of further suitable structures include multilayers.
The amphiphilic molecules according to the present invention may be considered surfactants. As such, reference in the present application to amphiphilic molecule may be substituted with surfactant. An example is an amphiphilic compound that contains hydrophobic and hydrophilic groups, reduce the interfacial tension between two liquids and the surface tension between a liquid and a gas. A further example of a surfactant is an amphiphilic compound that contains a hydrophobic group and a flourophilic group which adsorbs at the interfacial tension between a fluorinated solvent and a non-aqueous solvent. The molecules of the present invention assemble at the interfacial tension between two liquids or surface tension between a liquid and a gas.
Amphiphilic molecules comprise: a hydrophilic group and a hydrophobic group. The group may be a group, tail or block. Thus, any suitable amphiphilic molecules are encompassed by the present invention. The amphiphilic molecule may comprise a hydrophilic head, a hydrophilic tail or include a hydrophilic block polymer. The amphiphilic molecule may comprise a hydrophobic head, a hydrophobic tail or include a hydrophobic block polymer.
Amphiphilic molecules may also comprise: a flourophilic group and a hydrophobic group. The present invention therefore also encompasses amphiphilic molecules comprising one or more flourophilic group(s) and one or more hydrophobic group(s), and wherein the amphiphilic molecules comprise one or more metal-coordinating group(s). As such, reference to hydrophilic group in the present invention may be replaced with flourophilic group where appropriate.
In a preferred embodiment, the amphiphilic molecule may be a block copolymer incorporating at least one hydrophobic and hydrophilic block. The amphiphilic molecule may be a block copolymer. The amphiphilic molecule may be a diblock copolymer. The amphiphilic molecule may be a triblock copolymer.
The amphiphilic molecules also comprise one or more metal coordinating group(s). Incorporating metal coordinating group or groups into the amphiphilic molecules enables the combination of interfacial activity of surfactants with the reversible gelling and self-healing properties of the metal coordinating groups. These groups allow the surfactants to reversibly cross-link (self-heal) at interfaces, thereby converting the surfactants into shells that display self-healing properties. It is at the interface that the surfactants will self-assemble and begin to cross-link which is where the shell will begin to form. The shell may then grow through the attachment of additional surfactants at or near the interface.
Under suitable conditions, the amphiphilic molecules according to the present invention self-assemble and reversibly cross-link with suitable metal cations into shells. This may be pH dependent, and the present invention therefore provides for the formation of materials which are pH responsive. The properties of the shells may also be tunable depending on the cation introduced into the system.
The pH dependent nature of the molecules means that it is possible to include the reagents into a system and, upon shifting the pH to a suitable value (for example a suitable basic pH), the molecules will cross-link to form the shell.
“Hydrophilic group” means a polar component which is soluble in water or other polar solvents. Suitable hydrophilic groups include hydrophilic polymers, or hydrophilic block polymers. Suitable hydrophilic groups include polyethyleneglycol (PEG) polyacrylicacid (PAA), polyethyleneimine (PEI), polyvinylalcohol (PVA), Poly(N-isopropylacrylamide) (PNIPAM), poly(2-methyl-2-oxazoline) (PMOXA), polyglycols, natural hydrophilic polysaccharides including dextran, alginate, and peptides.
The amphiphilic molecule may include two or more hydrophilic groups. The metal coordinating group may itself constitute the or a hydrophilic group. As an example, the amphiphilic molecule may comprise a hydrophilic block polymer and a hydrophilic metal coordinating group (e.g catechol or derivatives thereof).
“Hydrophobic group” means a non-polar group which is a water-insoluble (or oil soluble) component. Suitable hydrophobic groups include substituted or unsubstituted lipophilic hydrocarbon chains, fluorinated chains, hydrophobic polymer(s), liquid crystals and the like.
Lipophilic hydrocarbon chains are preferably branched or unbranched having from 6 to 18 carbon atoms. The carbon chain may be saturated or unsaturated. The carbon chains may optionally be substituted with one or more functional groups and may contain one or more heteroatoms. Suitable lipophilic hydrocarbon chains include short saturated or unsaturated aliphatic chains (for example the hydrophobic part of lipids).
Hydrophobic polymers include: aliphatic chains (saturated and unsaturated), acrylics, amides and imides, carbonates, dienes, esters, ethers, fluorocarbons, perfluorinated polyethers, olefins, styrenes, vinyl acetals, vinyl and vinylidene chlorides, vinyl esters, vinyl ethers and ketones, vinylpyridine and vinypyrrolidone polymers. Hydrophobic polymers may preferably be selected from polypropyleneglycol (PPG), polystyrene, (PS), polylacticacid (PLA), fluorocarbons, methacrylates, polyethylene, polydimethylsiloxane (PDMS), chitosan and cellulose.
Hydrophobic polymer(s) are particularly preferably fluorinated. Preferred fluorinated polymers include perfluoropolyether groups. Particular polymers include perfluorinated polyethers with carboxylic acid-, methyl ester-, methylene alcohol- or allyl ether end groups. Further particular polymers include different poly(perfluoroalkyl-methacrylates). Examples of suitable perfluoropolyether fuorinated polymers include Krytox FSH 157, Krytox FSM 157, Krytox FSL 157, FC40. Preferred fluorinated polymers include perflourinated oligomer or polymer, such as poly(perfluoro propyleneoxide), e.g. KRYTOX® by Chemours. “Flourophilic group” means a component which is soluble in a fluorinated solvent. Examples of fluorophilic groups include the fluorinated polymers described herein.
Fluorinated polymers may comprise any fluorinated compound such as a linear, branched, cyclic, saturated, or unsaturated fluorinated hydrocarbon. The fluorinated molecule can optionally include at least one heteroatom. In some cases, the fluorophilic compound may be highly fluorinated, for example at least 30%, at least 50%, at least 70%, or at least 90% of the hydrogen atoms are replaced by fluorine atoms. In a further embodiment, all of the hydrogen atoms on the fluorinated part of the molecule are replaced by fluorine atoms.
Fluorinated polymers may include one or more fluorinated compounds selected from: perfluorodecalin, perfluoromethyldecalin, perfluoroindane, perfluorotrimethyl bicyclo[3.3.1]nonane, perfluoromethyl adamantine, perfluoro-2,2,4,4-tetra-methylpentane; 9-12C perfluoro amines, e.g., perfluorotripropyl amine, perfluorotributyl amine, perfluoro-1-azatricyclic amines; bromofluorocarbon compounds, e.g., perfluorooctyl bromide and perfluorooctyl dibromide; F-4-methyl octahydroquinolidizine and perfluoro ethers, including chlorinated polyfluorocyclic ethers, perfluoro-4-methylmorpholine, perfluorotriethylamine, perfluoro-2-ethyltetrahydrofuran, perfluoro-2-butyltetrahydrofuran, perfluoropentane, perfluoro(2-methylpentane), perfluorohexane, perfluoro-4-isopropylmorpholine, perfluorodibutyl ether, perfluoroheptane, perfluorooctane, perfluorotripropylamine, perfluorononane, perfluorotributylamine, perfluorodihexyl ether, perfluoro[2-(diethylamino)ethyl-2-(N-morpholino)ethyl]ether, n-perfluorotetradecahydrophenanthrene, and mixtures thereof. In some instances, the fluorophilic component can be straight-chained, branched, cyclic, etc., and/or have a combination of such structures.
The amphiphilic molecule may be a block copolymer. Suitable block copolymers include: diblock copolymers, triblock copolymers, and/or random block copolymers. Suitable diblock copolymers include: AB diblock copolymers, PEG diblock copolymers, polystyrene diblock copolymers. Examples of suitable diblock polymers include such as PEG-poly(propylene glycol), PNIPAM-poly(propylene glycol), PMOXA-poly(propylene glycol), PEG-poly(lactic acid), PEG-poly(lactic-co-glycolic acid) or any combination of said blocks. Suitable triblock copolymers include: ABA triblock copolymers, ABC triblock copolymers, biodegradable triblock copolymers, PEG/PPG triblock copolymers, polystyrene triblock copolymers, multi-arm PEG block copolymers, dendrimer-based block-copolymers; PNIPAM-based block copoylmers, PIMOXA based block-copolymers, light responsive block copolymers, temperature responsive block copolymers, PPG, perfluorinated polyether, perfluorinated polyether-PEG. Suitable random block copolymers include any combination of the blocks outlined above, provided at least one block is hydrophobic and at least one block is hydrophilic. Particular random block polymers include perfluorinatedpolyether and polypropyleneglycol.
The amphiphilic molecule may be a bipolar amphiphilic molecule.
The respective properties of the hydrophobic and hydrophilic groups may be adjusted depending on the requirements of the system. For example, the amphiphilic molecule may be designed such that it is soluble in the aqueous phase. Alternatively, the amphiphilic molecule may be designed such that it is soluble in the non-aqueous phase. Such modifications enable tuning of the properties of the amphiphilic molecules and the shells they subsequently form. As disclosed herein, it is possible to combine more than one amphiphilic molecule type in a system to further tune shell properties. It is also possible more generally to vary the surfactant properties to achieve different mechanical properties as desired.
“Metal coordinating group” means a group which is able to coordinate with a metal cation by forming a reversible ionic bond between the coordinating group and the cation. In aspects of the present invention, “Metal coordinating group(s)” may be “coordinating group(s)”.
The metal coordinating group may be connected to the amphiphilic molecule, either directly or via a spacer. The metal coordinating group may itself form the (or a) hydrophilic group. A metal coordinating group may be located at or near the hydrophilic region(s) of the amphiphilic molecule. A metal coordinating group may be located at or near the hydrophobic region(s) of the amphiphilic molecule. Metal coordinating groups may be located at or near both the hydrophilic and hydrophobic region(s) of the amphiphilic molecule.
The spacer or linking group, if used, may be a small molecule chosen to link the groups together. Suitable linkers include, for example, PEG, aliphatic chains, short hydrocarbon-based chains, morpholino groups and/or a phosphate groups. The linker may be selected to assist with self-assembly and/or coordination.
The number of metal coordinating groups present on the amphiphilic molecule will vary in number and location depending on the desired properties. There could be one, two, three or more metal coordinating groups. If the molecule includes repeating units, the metal coordinating group could be present in the repeating portion thereby leading to a number of groups per molecule. In an embodiment, there is one metal coordinating group per amphiphilic molecule. In a further embodiment, there are two metal coordinating groups per amphiphilic molecule. In a yet further embodiment, there are three or more metal coordinating groups per amphiphilic molecule. In a further embodiment, the metal coordinating group is incorporated into the repeating unit of a polymer.
The ratio of metal coordinating group(s) to metal ions can be tuned. There may be one, two or three coordinating groups per metal ion. Preferred metal coordinating groups are benzenediol or derivatives thereof. Further preferred metal coordinating groups are benzenetriol or derivatives thereof. Further metal coordinating groups might be histidines or derivatives thereof, groups comprising a carboxyl group; and ethylenediaminetetraacetic acid and derivatives thereof. Preferred metal coordinating groups are benzenediol or benzenetriol. Particularly preferred metal coordinating groups are benzenediol or derivatives thereof.
“Benzenediol” means a benzene ring substituted with two hydroxyl groups and “Benzenetriol” means a benzene ring substituted with three hydroxyl groups. The benzene ring may optionally be further substituted. To provide sufficient complexation, the hydroxyl groups are adjacent to each other, e.g. in a benzenediol the ortho (catechol) isomer. Thus, in a preferred embodiment, the metal coordinating group is catechol (also known as 1,2-benzenediol) or a derivate thereof. For a benzenetriol, a preferred molecule is gallol.
In a preferred embodiment, two hydroxyl groups are in the ortho-meta positions vs the hydrophobic chain. In an alternative embodiment, two catechol hydroxyl groups are in the meta-para positions vs the hydrophobic chain. The meta-para position is especially preferred.
By using a benzenediol or benzenetriol as metal coordinating group it is not necessary to have a separate hydrophilic group. That is, the metal coordinating group functions as the hydrophilic group in the amphiphilic molecule. However, it may be desirable to nevertheless still have separate hydrophilic group or groups, for example a hydrophilic block polymer.
Further metal coordinating groups include specific catechols (such as dopamine, hydrocaffeic acid, and tiron (disodium 4,5-dihydroxy-1,3-benzenedisulfonate).
Yet further metal coordinating groups include amino acids. Suitable amino acids include, but are not limited to, histidine, serine, threonine, asparagine, glutamine, lysine, or cysteine.
“Metal cation” can be any metal cation suitable to coordinate with a metal coordinating group. The metal cation forms reversible ionic bonds with metal coordinating group(s). Suitable metal cations include metal ions, metal oxides, metal hydroxides, metal carbides, metal nitrides and/or metal nanoparticles.
Particular metal ions include beryllium, magnesium, calcium, strontium, barium, chromium, manganese, iron, cobalt, nickel, copper, silver, gold, zinc, cadmium, mercury, aluminium, gallium, indium, tin, lead, bismuth and lithium. Particularly preferred metal cations include iron, aluminium or titanium, with iron especially preferred.
More particularly, suitable cations include Be2+ beryllium ion, Mg2+ magnesium ion, Ca2+ calcium ion, Sr2+ strontium ion, Ba2+ barium ion, Ti2+ titanium (II), Ti4+ titanium (IV), Cr2+ chromium (II), Cr3+ chromium (III), Cr6+ chromium (VI), Mn2+ manganese (II), Mn3+ manganese (III), Mn4+ manganese (IV), Fe2+ iron (II), Fe3+ iron (III), Co2+ cobalt (II), Co3+ cobalt (III), Ni2+ nickel (II), Ni3+ nickel (III), Cu+ copper (I), Cu2+ copper (II), Ag+ silver ion, Au+ gold (I), Au+3 gold (III), Zn2+ zinc ion, Cd2+ cadmium ion, Hg22+ mercury (I), Hg2+ mercury (II), Al3+ aluminium ion, Ga3+ gallium ion, In+ indium (I), ln3+ indium (III), Sn2+ tin (II), Sn4+ tin (IV), Pb2+ lead (II), Pb4+ lead (IV), Bi3+ bismuth (III), Bi5+ bismuth (V) and Li+ lithium ion. Particularly preferred metal cations include Fe3+ iron (III).
The metal may be added in the form of a metal salt. Suitable metal salts include but are not limited to halides, nitriles, hydroxides and the like.
The metal cation may be in the form of an oxide or nanoparticle. For example, iron oxide nanoparticles may be used. Other suitable oxides or nanoparticles include iron oxides, iron nitrides, iron carbides, nickel oxides, nickel carbides, titanium oxides, titanium metal particles, titanium nitrides, titanium carbides.
Using nanoparticles allows for larger numbers of metal coordinating groups to ionically bond with a single nanoparticle. This impacts the properties of the shell, namely increasing the relaxation time, and may increase the stability of the shell.
“Metal complexed” or “metal coordinated” means amphiphilic molecules coordinate via their metal coordinating groups and metal cations through ionic bonds. Through this coordination, the amphiphilic molecule form self-assembling, reversibly cross-linked shells that can self-heal via further reversible cross-linking.
“Viscoelastic” means the property of a substance of exhibiting both elastic and viscous behaviour, the application of stress causing temporary deformation if the stress is quickly removed but permanent deformation if it is maintained. The shells of the present invention may be viscoelastic.
The present invention provides for the first time a self-healing shell at an interface between a first fluid phase and a second fluid phase; wherein the first fluid phase is a liquid phase or a gas phase and the second fluid phase is a liquid phase; said shell comprising amphiphilic molecules and metal cations; wherein the amphiphilic molecules comprise one or more hydrophilic group(s) and one or more hydrophobic group(s), and wherein the amphiphilic molecules comprise one or more metal-coordinating group(s); wherein the metal cations comprise metal ions, metal oxides, metal hydroxides, metal carbides, metal nitrides and/or metal nanoparticles; and wherein amphiphilic molecules in the shell are reversibly cross-linked via the one or more metal-coordinating group(s) and metal cations.
It has surprisingly been discovered that by having metal-coordinating groups on amphiphilic molecules, these molecules can ionically cross-link at the interface with metal cations to form self-healing shells. These shells have a number of advantageous properties. The shells are self-healing meaning that in the event of rupture; new coordinations will occur reforming the intact shell. The shells are robust and will self-heal in the event of a rupture. In addition, the self-healing properties mean that a shell (for example in the form of a capsule) can be brought into contact with an adjacent shell (for example an adjacent capsule) and the shells can be fused. In the case of capsules, this enables the capsules to merge.
Furthermore, the mechanical properties of the shell can be adjusted depending on the choice of: metal-coordinating group; metal cation; the ratio of metal cation to metal coordinating group; and/or by varying other conditions like pH and temperature. The mechanical properties can also be modified by the number of metal coordinating groups attached to the amphiphilic molecule together with the location of their placement on the molecule. Properties can also be adjusted by the length and flexibility of spacers connecting metal coordinating groups to the surfactants. Properties can also be adjusted by the selection of hydrophobic and hydrophilic groups.
The robust self-healing nature of the shells together with their tuneable mechanical properties make the present invention useful in a variety of areas including transportation, storage or movement of target materials, for example drugs, foodstuffs, agrochemicals, cosmetics, biological matter and the like.
Any suitable metal-coordinating group can be chosen. The metal-coordinating group may be the hydrophilic group on the amphiphilic molecule or may be otherwise attached to the amphiphilic molecule. The amphiphilic molecule may comprise one, two, three or more metal-coordinating groups. The groups may be at the end or ends of the molecule or may be in a repeating unit of a polymer. The amphiphilic molecule may be a bipolar amphiphilic molecule. Such molecules may assemble into a U shape at an interface, impacting their packing density at the interface.
One preferred metal-coordinating group is benzenediol or derivative thereof. The dual hydroxy groups on the molecule enable coordination with metal ions. In a preferred embodiment, it has been found that preferably catechol or derivatives thereof are particularly useful. Catechols having the two hydroxyl groups in the ortho and para positions relative to the hydrophobic chain are especially preferred. The benzenediol may be gallol having three adjacent hydroxy groups.
Catechols form reversible ionic bonds with metal cations. An example is shown in
Alternatively, if the metal ion is, for example, a nanoparticle like iron oxide nanoparticles, then many more catechols can bind to a single nanoparticle. Such an approach may improve the stability of the shell, and may do so by shifting the relaxation time of the resultant structure.
Any suitable hydrophobic chain may be selected and the properties of the chain can be tuned to suit the needs of the self-healing shell.
In a particular embodiment, amphiphilic molecules include the following compounds of Formula I (a-f):
Formula I (a), FSHDopa, was synthesized by linking Dopamine to Krytox 157 FSH a perfluorinated polyether with a carboxylic acid end group. This synthesis is a two step synthesis. Formula I (b), FSHPEGHA, a PEG-spacer was added that separates the fluorinated block from the catechol. Formula I (c) stearic acid-dopa. Formula I (d), Oleic acid-dopa, the unsaturated bond in the hydrobarbon chain changes the stiffness of the molecule and therefore its packing density and propensity to form aggregates. Formula I (e), DiDopa-PPG, this surfactant contains two catechols that are separated by polypropylene glycol. Formula I (f), FSHPEG900HA, to increase the size of the hydrophilic part, a PEG-spacer was added that separates the fluorinated block from the catechol.
Generally the FSH is the name of the commercial product Krytox FSH 157 from Chemours which is the fluorinated green part of the surfactant. Dopa stands for dopamine which represents the blue catechol group, PEG for polyethyleneglycol, SA for stearic acid (just instead of the acid we added the dopa, OA oleic acid, PPG Polypropyleneglycol.
As discussed above, the mechanical properties of the shell can be modified by adjusting the properties of the amphiphilic molecules, the metal cation, and the solvent conditions like pH, temperature or ionic strength. Adjustment of these conditions impacts the degree to which the amphiphilic molecules cross link in the shell and this degree of cross-linking impacts the mechanical properties.
By increasing the degree of cross-linking, it is estimated that the mesh size of the cross-linked molecules decreases which can increase the stability of the shell and/or decrease its permeability.
Increasing the number of metal coordinating groups on the amphiphilic molecules can increase the degree of cross-linking, associated with a corresponding increase in the number of available ions. Furthermore, selection of particular metal coordinating groups will also increase the degree and strength of cross-linking.
Modifying the metal cation will also impact the cross-linking and the mechanical properties of the shell by affecting the dissipation times of the complex-ion pair. A preferred metal cation is Fe3+ iron (III) but any suitable cation can be used.
Modifying the hydrophobic group(s) and/or hydrophilic group(s) can enable tuning of the shell's properties. For example, modification can influence the shell thickness, the mechanical stability (rigidity) and/or permeability.
Varying the ratio of metal-coordinating group to cation will impact the cross-linking and therefore the mechanical properties and permeability of the shell. This ratio can be impacted by the stoichiometric ratio of metal-coordinating group and cation present in the system. The ratio is also affected by pH. For example, for an amphiphilic molecule with catechol as metal-coordinating group and iron (III) as metal cation, at lower pH the molecules form a 1:1 mono structure as shown in
As previously discussed, by modifying the pH of the system it is possible to affect cross-linking and to change the degree of cross-linking. As such, it is possible to tune the properties of the shell by modifying the pH. It also makes shells according to the present invention sensitive to pH. Such shells find use as, for example, drug delivery vehicles which are sensitive to pH changes enabling precise drug delivery depending on conditions. Preferred pH ranges include 1-14, 5-14, 9-14, 10-14, 9-12, 10-12, around 9, around 12, 12-14.
In an embodiment, the pH of the system is at or is adjusted to a pH range within about 6 to about 12. Within this range, the amphiphilic molecules will reversibly cross-link. It is possible to hold the system at a pH below this level to prevent reversible cross-linking. Such an approach may be desirable to control when cross-linking occurs or to reverse cross-linking. It is also possible to increase the pH to above about 12 as discussed further below which will lead to the formation of covalent bonds between molecules.
It is possible to make the shell dissociate by varying parameters like pH or temperature. The addition of chelates such as but not limited to EDTA, EDDA, DTPA, HEDTA may also cause dissociation of the shell as the chelate traps the metal ion thereby affecting shell cross-linking.
It is also possible to cause the shell to irreversibly bind. This can be achieved by, for example, raising pH to a high pH which causes irreversible bonds to form. Such an approach may have advantages where it is no longer desired to have a self-healing reversible shell. This can also be achieved at lower pH values through the use of an appropriate oxidising agent.
Where irreversible cross-linking is required, the shell may initially be formed using reversible binding and steps taken to then form irreversible bonds. Alternatively, the amphiphilic molecules according to the present invention may be used directly in irreversible binding without the need for a metal ion to be present. Such irreversible binding can be achieved by the use of suitable pH conditions and/or through the use of suitable catalysts including suitable oxidising agents.
The self-healing shell of the present invention may be present in a system comprising the first fluid phase, the second fluid phase (and any further phases) and a self-healing shell at the interface between the phases.
The first fluid phase may be a liquid phase. This provides for a liquid/liquid phase system. The system may be an emulsion. In this embodiment, the first liquid phase may be an aqueous phase and the second liquid phase may be a non-aqueous phase. In a further embodiment, the first liquid phase may be a non-aqueous phase and the second liquid phase may be an aqueous phase. In a yet further embodiment, the first liquid phase and the second liquid phase may both be aqueous phases. In a yet further embodiment, the first liquid phase and the second liquid phase may both be non-aqueous phases. For example, in in a fluorinated/non fluorinated organic solvent. In such an embodiment, the amphiphilic molecule would be hydrophobic and fluorophilic.
It is possible to produce water-in-oil emulsions and oil-in-water emulsions according to the present invention. As such, it is possible to encapsulate an oil phase from an aqueous solvent or to encapsulate a water phase from an oil solvent. Also encompassed within the present invention are water-in-oil-in-water systems and oil-in-water-in-oil systems. Further emulsions are also possible including triple emulsions, multiple emulsions, double emulsions with multiple cores and the like.
In an alternate embodiment, the first fluid phase may be a gas phase. This provides for a liquid/gas phase system. The system may be a foam.
Suitable aqueous solvents include water. Further suitable aqueous solvents include low molecular weight poly(ethylene glycol) which is liquid under atmospheric conditions at suitable temperatures.
Suitable non-aqueous solvents may include but are not limited to aliphatic solvents such as hexane, decane, dodecane, hexadecane, alcohols, such as ethanol, methanol, hexanol, decanol, dodecanol, hexadecanol, alkenes, toluene, perfluorinated oils, fluorinated oils, perfluorocarbons, perfluoropolyethers, chloroform, ethers, dimethylformaide, dimethylsulfoxide, dichlormethane, pentane, cyclopentane, acetonitrile, isopropanol, methoxy-nonafluorobutaneethyl acetate, mineral oil, silicon-based oils, food grade oils including fish oil, sunflower oil, olive oil. Particular fluorinated products include 3M Fluorinert such as FC-40, 3M Novec engineering fluid such as Novec 7500 or Novec 7100. Fluorinert FC-40 is a clear colourless, thermally stable fully flourinated liquid with an average molecular weight of 650 and a liquid density of 1855 kg/m3. Novec 7500 has a molecular weight of 414 and a liquid density of 1614 kg/m3.
Further fluorinated solvents include the Fluorinet electronic liquids and Novec engineering fluids. Examples are included in the tables below:
3M™ Fluorinert™ Electronic Liquids (All values determined at 25° C. unless otherwise specified)
3M™ Novec™ Engineered Fluids (All values determined at 25° C. unless otherwise specified)
The self-healing shells as described herein can be made by forming a system comprising an interface between a first fluid phase and a second fluid phase, amphiphilic molecules as defined herein, and metal cations as defined herein; wherein the first fluid phase is a liquid phase or a gas phase and the second fluid phase is a liquid phase; such that the metal-coordinating group(s) and metal cation(s) reversibly cross-link at the interface to form a self-healing shell.
The system may contain a third phase or further phases.
The first fluid phase may be a liquid. The first fluid phase may be an aqueous phase and the second fluid phase may be a non-aqueous phase. The first fluid phase may be a non-aqueous phase and the second fluid phase may be an aqueous phase. The first liquid phase and the second liquid phase may both be aqueous phases. The first liquid phase and the second liquid phase may both be non-aqueous phases. The first fluid phase may be a gas. The first fluid phase may be a gas and the second fluid phase may be an aqueous phase. The first fluid phase may be a gas and the second fluid phase may be a non-aqueous phase.
The interface may be formed by any suitable means. The interface will from when two phases are brought into contact with sufficient interfacial tension. Suitable means include adding one phase into the other phase, including dropwise addition; emulsifying the first phase and the second phase, including high pressure emulsification; microfluidics; shaking; stirring; or the use of a membrane.
For example, the first phase may be added dropwise into the second phase. By introducing a drop into the second phase, an interface is created between the two phases. At this interface, the amphiphilic molecules will adsorb, lowering the interfacial tension. At an appropriate pH, the metal-coordinating groups will reversibly cross-link with the metal cation and form a shell around the drop containing the first phase and shielding it from the second phase. The shell is self-healing because, in the event of shell rupture, the broken ionic bonds can reform and/or further amphiphilic molecules and cations present in the phases can coordinate to reform an intact shell.
The metal cations and amphiphilic molecules may be in the same phase or a different phase. Preferably, the metal cations and amphiphilic molecules are in a different phase. This helps to ensure that they only react at the interface.
In an embodiment, the metal cations may be in an aqueous phase and the amphiphilic molecules may be in a non-aqueous phase. In an embodiment, the metal cations may be in an aqueous phase and the amphiphilic molecules are in an aqueous phase. In an embodiment, the metal cations may be metal oxide or nanoparticles and may be in a non-aqueous phase and the amphiphilic molecules may be in an aqueous phase. In an embodiment, the metal cations may be metal oxide or nanoparticles and may be in an aqueous phase and the amphiphilic molecules may be in a non-aqueous phase. In a further embodiment, the metal cations may be metal oxide or nanoparticles and may be in a non-aqueous phase and the amphiphilic molecules may be in a second non-aqueous phase that is immiscible in the first non-aqueous phase.
For example, the amphiphilic molecules and metal cation may be contained in the first phase. Upon addition of the first phase into the second phase, an interface is created which causes the amphiphilic molecules to self-assemble at the interface. The presence of the metal cations enables reversible cross-linking of the amphiphilic molecules. Thus, by addition of the first phase into the second phase, the first phase contains the components necessary to form the shell.
Alternatively, amphiphilic molecules and metal cation may be contained in the second phase, into which the first phase is added. In the same way as previously, an interface is created which causes self-assembly of the amphiphilic molecules and cross-linking but in this embodiment, the components necessary to form the shell are contained in the phase into which the first phase is added.
As a further preferred embodiment, the amphiphilic molecules may be contained in one phase and the metal cations contained in another phase. This way, the components do not interact until the phases are brought together and thereafter the components will react at the interface. In the same way as previously, an interface is created which causes self-assembly of the amphiphilic molecules and cross-linking but in this embodiment, the components necessary to form the shell come into contact at the interface.
As discussed, the ability to cross-link to form a shell is impacted by pH. An system can be prepared at one pH and the pH be subsequently adjusted to effect cross linking.
Once the shell has been formed, it is possible to remove fluid within the system to retain the intact shell. If the shell is encapsulating an inner liquid then this will retain intact thereby allowing the shell to be removed from the system.
It is also possible after formation to increase the pH such that irreversible bonds form within the shell thereby producing a covalently cross-linked shell. Such an approach does not require the presence of metal cations. Thus, the present invention encompasses both a process which initially forms reversible cross-linked shells which are subsequently covalently cross-linked or produces covalently cross-linked shells from the outset.
The shells of the present invention can be used to encapsulate a material and thereby to form a capsule.
In an embodiment, after formation of the self-healing shells of the present invention, for example capsules, the external phase can be removed or replaced leaving intact capsules containing the inner phase.
In an embodiment, it is possible to form layers of self-healing capsules followed by removal of the external phase to produce a hydrogel with unique biomechanical properties. By ionically linking adjacent capsules, thereby producing larger materials with well-defined compositions and locally varying compositions, advantageous materials can be prepared that mimic natural materials. The mechanical properties of the hydrogel can be tuned depending on the selection of materials used to make the shell, as well as the configuration of capsules both in terms of the orientation of the capsules in a layer, and the ability to stack layers on top of each other to form hydrogels with unique properties.
There are multiple uses for the self-healing shells according to the present invention. The shells can encapsulate material with a robust and self-healing shell. This allows materials to be protected. It also allows materials to be stored and/or selectively transported/moved. For example, it is desirable in many applications to be able to encapsulate a material into a first closed system and then manipulate the closed system to selectively allow the material to come into contact with a second closed system. This could be used, for example, to selectively allow a shell containing a fluid (liquid or gas) and defining a first closed system to come into contact with a second shell containing a second fluid and defining a second closed system. The self-healing nature of the shell enables the two shells to fuse and bring the first and second fluids into contact with each other forming a new shell that surrounds the newly formed mixed fluid. Such manipulations can be used for research on investigatory purposes.
As such, in an embodiment, there is provided a method of transporting material from a first closed system to a second closed system within a surrounding system using self-healing capsules described herein; comprising forming a first self-healing capsule comprising a shell to encapsulate a first fluid and form a first closed system; forming a second self-healing capsule comprising shell to encapsulate a second fluid and form a second closed system; bringing the first and second self-healing capsules into contact such that the first and second shells fuse bringing the first and second closed systems into contact with each other while still being protected from the surrounding system by the self-healing shell.
Such a system allows for the controlled transportation of material. This material could be drugs, food ingredients, nutraceuticals, cosmetics, pesticides, nutrients, fragrances, catalysts, agrichemicals, reagents to form proteins, biological material such as DNA, RNA, proteins, antibodies, coatings, paints, waste products and the like. While the material within each closed system can be mixed and fused, it does not come into contact with the surrounding system since it is always encapsulated by the shell.
A specific embodiment is the use of self-healing shell as described herein in droplet based screening assays. By forming self-healing shells around target material, cross-talk between droplets caused by material leakage is reduced, improving the accuracy of the assay. This allows for more sensitive measurements since the target analyte and any reagents can be contained within the shell and will not leak into the surrounding solvent or another drop. Particular screening uses include high-throughput screening, high throughput drug screening, high throughput antibody screening, DNA sequencing or single cell sequencing. As discussed herein, in an embodiment, the shells need not be self-healing.
Droplet based screening assays rely on each water in oil or water in oil in water drop to be a closed container to conduct a biological or chemical reaction. Common used surfactants which stabilize the emulsion drops can also facilitate the transport of material in form of aggregates or tiny emulsion drops through the oil phase possible from one drop to another which results in less accurate assays. This transport of material through the liquid/liquid interface can be reduced by cross-linking the interface as described herein.
An example of a screening assay is biology screening which currently uses individual well plates to separate target analytes. By using a droplet based screening assay, throughput can be dramatically increased and the present invention retains droplet stability and integrity over a sufficient timescale to enable experiments to be undertaken with sufficient confidence that cross-contamination is minimised. High throughput screening assays can use individual drops as containers for biological or chemical experiments in analogy to well plates but on a much smaller scale, enabling lower costs due to less reagents and a higher throughput.
The self-healing shells according to the present invention may be used as a vehicle for drug delivery or for the encapsulation of drugs, biomaterial such as cells, DNA, RNA, proteins, enzymes, antibodies, food ingredients, nutraceuticals, cosmetics, pesticides, nutrients, fragrances, catalysts, agrichemicals, reagents to form proteins, coatings, paints, waste products and the like. Due to their pH sensitive nature, the shells according to the present invention are particularly suited to situations where pH controlled release is desired. The shell can also show temperature sensitivity enabling temperature controlled release.
The shells of the present invention may be used to produce high stability emulsions or foams. An advantage of these emulsions or foams is their ability to withstand changes to osmotic pressure or other mechanical forces.
In a yet further embodiment, there is provided an amphiphilic molecule as defined herein comprising one or more hydrophilic group(s) and one or more hydrophobic group(s); and wherein the amphiphilic molecule comprises one or more metal-coordinating group(s); wherein the amphiphilic molecule is a block copolymer; and wherein the metal-coordinating group is a metal-coordinating group selected from the group consisting of: benzenediol or derivatives thereof, preferably catechol or derivatives thereof; and benzenetriol or derivatives thereof, preferably gallol or derivatives thereof; and wherein the metal-coordinating group may optionally be further substituted.
Such amphiphilic molecule have not previously been identified and allow for the formation of self-healing shells as described herein when coordinated with a metal cation.
The hydrophilic group(s), hydrophobic group(s), and metal-coordinating group(s) may be as defined herein.
The invention will now be described by way of the following non-limiting examples.
All chemicals, namely fluorinated oils HFE-7100 and HFE-7500 (3M, USA), the fluorinated block of the surfactant FSH (Krytox 157 FSH, Chemours, USA), polypropylene glycol (PPG 2000 g/mol, Acros Organics), thionyl chloride and chloroform (Merck, Germany), dichloromethane (DCM), anhydrous Ethyl acetate (EtAc), methanol (MeOH), triethylamine, dopamine hydrochloride (Dopa), N,N-dicyclohexylcarbodiimid (DCC) (Sigma-Aldrich), anhydrous N,N-Dimethylformamide (DMF) and 3-(3,4,-Dihydroxyphenyl)propionic acid (hydrocaffeic acid, HA) (Abcr, Germany), and N-Hydroxysuccinimide (NHS) and stearoyl Chloride (TCI, Japan) were used as received.
All the reactions were performed under argon atmosphere using dry glassware.
The fluorinated surfactant (FSHDopa) was synthesized following previously published work: Holtze, C. et al. Biocompatible surfactants for water-in-fluorocarbon emulsions. Lab Chip 8, 1632-1639 (2008). One equivalent of the perfluorinated polyether Krytox FSH 157 (6500 g/mol, Chemours, USA) was dissolved in Novec HFE-7100 (3M, USA) under Argon. 10 mol equivalent of thionylchloride (Sigma-Aldrich, USA) was added to the clear solution and refluxed at 65° C. for 2 hours to activate carboxylic acid end group of the Krytox by transforming it into an acid chloride. The excess solvent and excess thionylchloride is subsequently removed by keeping the solution at 90° C. and a reduced pressure for 1 h. After the activated Krytox has cooled to room temperature it was redispersed in HFE-7100 at 0.1 g/ml. To this solution of anhydrous dimethyl formamide (abcr, Germany) containing 4 mol equivalent (0.05 g/ml) of Dopamine HCl (Sigma-Aldrich, USA) was cooled to 0° C. before 6 mol equivalent of trimethylamine (Sigma-Aldrich, USA) was added. This solution was stirred at room temperature for 30 min before it was added to the activated Krytox under inert atmosphere. The reaction was stirred at 65° C. overnight. The product was filtered through a filter paper, put in a separating funnel and washed three times with water and HFE-7100.
An alternative synthesis for FSHDopa is: 1 mol equivalent of FSH was dissolved at 0.2 gmL−1 in HFE-7100, dried with molecular sieves, and the solution degassed with argon. 10 mol equivalents of thionyl chloride was added to the solution under argon atmosphere to activate the carboxylic end group of the FSH. This reaction was refluxed at 65° C. for 2 hours. Under reduced pressure and at 90° C. the excess thionyl chloride was removed, resulting in the pure activated FSH. The FSH was subsequently re-dissolved in HFE-7100. 2.5 mol equivalents of dopamine was dissolved in DMF and the solution degassed with argon before it was mixed with activated FSH. 2.5 mol equivalents of triethylamine was added to the reaction to drive the reaction to completion. The reaction was refluxed overnight at 65° C. The solution was filtered through a filter paper, and all the solvents removed under reduced pressure. The product was purified using a mixture of water and HFE-7100 and subsequently washed using a mixture of HFE-7100 and methanol. The precipitates were removed through centrifugation at 3000 g for 15 min (Mega Star, 1.6R, VWR). This washing step was repeated three times before the product was dried using a rotary evaporator (Hei-VAP, Heidolph, Germany) and freeze dryer (FreeZone 2.5, Labconco, USA).
This synthesis was performed in 3 steps. The Krytox FSH was activated using thionylchloride as explained above following protocols that have previously been published in Etienne, G., Kessler, M. & Amstad, E. Influence of Fluorinated Surfactant Composition on the Stability of Emulsion Drops. Macromol. Chem. Phys. 218, 1-10 (2017). The Jeffamine diamine (hydrophilic group) was coupled to the Krytox and purified as described. Subsequently, 1 mol equivalent Hydrocaffeic acid (abcr, Germany) was dissolved in DMF at 0.005 g/ml and cooled to 0° C. before 1.1 mol equivalent of N-Hydroxysuccinimide (NHS, TCI, Japan) and 1.1 mol equivalent of N,N-Dicyclohexylcarbodiimid (Sigma-Aldrich, USA) were added. This solution was stirred for 2 h at 0° C. before it was heated to room temperature and stirred at this temperature for 1 h. The FSHPEG900-amine was added to this solution at 0.5 mol equivalent (0.04 g/ml) and the mixture was stirred overnight before the solution is filtered and the solvents are removed in the rotary evaporator. We purified the product with a 10:1 methanol:HFE7100 mixture before the product is dried in vacuum. Additionally the reaction can also be done by first linking the hydrocaffeic acid to the PEG by DCC/NHS coupling and then linking it to the fluorinated Krytox FSH 157.
To increase the size of the hydrophilic part, a PEG-spacer was added that separates the fluorinated block from the catechol.
An alternative synthesis for FSHPEG900HA is: 1 mol equivalent of hydrocaffeic acid was dissolved in dry ethyl acetate at 0.04 gmL-1, and 1 mol equivalent NHS was added to the reaction. 1 mol equivalent of DCC was dissolved in ethyl acetate and added to the NHS HA mixture that was stirred overnight under inert atmosphere. The product HA-NHS was filtered through a filter paper and dried under reduced pressure. 1 mol equivalent of HA-NHS was dissolved at 0.11 gmL-1 in dry ethyl acetate and bubbled with argon. 0.95 mol equivalent of the Jeffamine ED-900 (Huntsman, USA) was dissolved in dry ethyl acetate and added to the HA-NHS solution and stirred overnight. Jeffamine ED900, a poly(propylene oxide)-poly(ethylene oxide)-poly(propylene) (PPO-PEO-PPO) triblock copolymer was used as a hydrophilic block. The solvent was removed using a rotary evaporator, resulting in the intermediate product H2N-PEG-HA.
FSH was activated as described for the alternative synthesis of FSHDopa. 1.5 mol equivalent of H2N-PEG-HA was dissolved in DCM and added to the activated FSH. 1 mol equivalent of triethylamine was added to drive the reaction to completion, and everything was refluxed overnight at 65° C. The solvent was removed, and the product was washed using a mixture of HFE-7100 and methanol, and they were centrifuged at 3000 g. This washing step was repeated three times. The final product was dried using a rotary evaporator and a freeze dryer.
FSHPEGHA was synthesis following the alternative synthetic route for FSHPEG900HA but the Jeffamine ED-900 (Huntsman, USA) was replaced with Amine-PEG-Amine Mw 600 (CreativePEG works, USA), which was used as the hydrophilic block.
1 mol equivalent of stearoyl chloride (TCI, Japan) was dissolved in anhydrous dimethyl formamide (abcr, Germany) at 0.05 g/ml under dry conditions. 1.5 mol equivalent of Dopamine HCl (Sigma-Aldrich, USA) was dissolved in anhydrous DMF at 0.2 g/ml under argon. While cooling the solution to 0° C. 3 mol equivalent of trimethylamine (Sigma-Aldrich, USA) was added to the DMF-based solution containing dopamine. This solution was subsequently added to the solution containing stearoyl chloride and stirred overnight at 65° C. under inert atmosphere. The solution was filtered while it was before the DMF was removed using a Rotary evaporator. The product was purified using water and ethyl acetate (Sigma-Aldrich, USA). The washing was repeated 3 times and before the product was washed once with 1M HCl to remove the excess trimethylamine.
An alternative synthesis for SA-Dopa is: 1 mol equivalent of stearyl chloride was dissolved in anhydrous DMF under argon at 0.2 gmL−1. 1.5 mol equivalents of dopamine was dissolved at 0.06 gmL−1 in DMF and cooled to 0° C. 3 mol equivalents of triethylamine was added to the dopamine and mixed with stearyl chloride. The mixture was heated to 65° C. and stirred overnight under argon atmosphere. The reaction product was extracted with water and ethyl acetate. This cleaning step was repeated three times before everything was dried in a rotary evaporator and a freeze dryer
1 mol equivalent of oleic acid (Sigma-Aldrich, USA) was dissolved in anhydrous chloroform (Sigma-Aldrich, USA) at 0.1 g/ml under dry conditions. 10 mol equivalent of thionylchloride (Sigma-Aldrich, USA) was added and stirred for 2 h at 60° C. 3 mol equivalent of Dopamine HCl (Sigma-Aldrich, USA) was dissolved in anhydrous DMF at 0.2 g/ml under argon. This solution was subsequently added to the solution containing stearoyl chloride and stirred overnight at 65° C. under inert atmosphere. When mixed together 3 mol equivalent of trimethylamine (Sigma-Aldrich, USA) was added to the mixture. The solution was filtered while it was before the DMF was removed using a Rotary evaporator. The product was purified using water and chloroform (Sigma-Aldrich, USA).
The unsaturated bond in the hydrobarbon chain changes the stiffness of the molecule and therefore its packing density and propensity to form aggregates
This synthesis of DiDopa-PPG was performed using protocols established for the synthesis of FSHDopa. Instead of using a fluorinated solvent (HFE-7100) we employed chloroform (for the activation) and dimethyl formamide (for the coupling reaction). The extraction was done with diethyl ether and water.
An alternatie synthesis for DiDopa-PPG is: 1 mol equivalent of propyleneglycol was dissolved in chloroform, and 10 mol equivalent of thionyl chloride added. The solution was refluxed at 65° C. for 2 hours. The excess thionyl chloride was removed under reduced pressure at 90° C. 4 mol equivalents of dopamine was dissolved in DMF, 1.5 mol equivalents of triethylamine was added, and the mixture was stirred overnight. The product was extracted with diethylether and water. Extraction was repeated three times before the solvents were removed using a rotary evaporator and freeze dryer.
To observe the behaviour of the surfactants at the water-oil interface, oil containing the surfactants was injected into a water bath, as shown in
When the surfactant is not crosslinked because the outer solution is at a low pH and the liquid is retracted, the drop shrinks as seen in
An oil phase (HFE 7100) containing 1 wt. % FSHDopa and 1:2 catechol:Fe by adding 1M FeCl3 in EtOH to the surfactant solution is prepared. The outer water phase was at pH=7.7. First a drop of oil solution is deposited on the bottom of the cuvette. Next, a second drop is formed at the needle by injecting oil phase and retracting it.
When two oil drops comprising the shells made from the ionically crosslinked surfactants of the present invention are brought in contact, the drops fuse and allow exchange of liquids contained in them, as exemplified in
Upon contact of the two interfaces (
Example 2 demonstrates the use of the shells of the present invention in the controlled transportation of reagents, nutrients, and waste products between different drops.
An oil phase (HFE 7100) containing 1 wt. % FSHDopa and 1:2 catechol:Fe by adding 1M FeCl3 in EtOH to the surfactant solution was prepared. The outer water phase was at pH=7.7. First a drop of oil solution is deposited on the bottom of the cuvette, the drop contains an air bubble as a model system to transport. Next, a second drop is formed at the needle by injecting oil phase and retracting it.
Viscoelastic capsules of high stability and with self-healing properties were fabricated and allow for transportation of material from one closed container to another as shown in
An air bubble (used as a model) is trapped in an oil drop on the surface of a glass vial. The air bubble can be seen in the drop on the surface of the glass cuvette in
Double emulsions are formed using a microfluidic device. To form these double emulsions, an aqueous phase containing 10 wt. % PVA (for responsive test at pH=8.5) was used as an outer phase and a perfluorinated oil (HFE7100) containing 1 mM FSHPEG900HA (responsive) or 1 mM DiFSHPEG900 (non responsive surfactant) was employed as a middle phase and an aqueous phase containing 20 wt. PEG+0.1 wt % Fluorescein was employed as an inner phase. After producing the double emulsions they are washed with a water and sucrose solution at equal osmotic pressure as the inner phase and for the responsive surfactant adapted to pH=8.5. The leakage of the dye over times is observed with the responsive compared to the non-responsive surfactant.
A water in oil in water double emulsions containing fluorescein as a dye in the inner phase was produced. The leakage of fluorescein dye from double emulsions stabilized with a non-functionalized fluorinated surfactant (DiFSHPEG9000) was analysed by observing them under fluorescent microscope over time. It was observed that after 2 hours most of the dye had leaked out of the double emulsion as seen in
In contrast, when the same experiment was performed using capsules of the present invention using surfactant (FSHPEG900HA) cross-linked with iron, leakage was drastically reduced as shown in
The experiment was repeated over a longer timeframe of 14 days in
By preparing capsules of the present invention, cross-talk between drops was reduced thereby improving the accuracy of screening assays.
To verify that catechols are coupled to the perfluorinated block-copolymers, the block-copolymer is dissolved in a fluorinated solvent (HFE7100). FeCl3 is dissolved in ethanol and added to the surfactant containing solution. Because the catechol is bound to the perfluorinated block-copolymers, it is soluble in the fluorinated solvent such that it forms complexes with the Fe3+ ions and the solution becomes green, as shown on the left side of
To test the influence of the pH on the interfacial tension between a fluorinated solvent, HFE7500 containing 1 wt % FSHDopa and water, we perform pendant drop measurements. If the pH is low such that most of the catechols are protonated, the interfacial tension is high, approximately 35 mN/m. By contrast if we increase the pH above the pKa values of DOPA, the interfacial tension strongly decreases, as shown in
To test if the shells composed of FSHDOPA/Fe3+ complexes display a self-healing behaviour, we form a drop composed of HFE7100 that contains 1wt %. FSHDopa. The drop is immersed in an aqueous solution containing Fe3+. We observe the formation of a thin shell at the liquid-liquid interface, as shown in
To test the influence of the hydrophobic chain of catechol-functionalized surfactants on their ability to form self-healing shells, we synthesized a surfactant composed of stearic acid that is linked to a catechol. This surfactant was dissolved in ethyl acetate containing Fe3+ ions and the solution was used to form a drop that is surrounded by an aqueous phase (pH=7.7). Also in this case, we observe that a shell that buckles forms at the liquid-liquid interface, as indicated by the time lapse micrographs in
Similarly, we observed the formation of a shell if a surfactant composed of two catechols that are interspaced by poly(propylene glycol) (diDOPA-PPG) is dispersed in toluene containing Fe3+ and this phase is used to form a drop in an aqueous phase as shown in the time lapse micrographs in
To test the influence of the surfactant on the permeability of water-oil-water double emulsions, we formed double emulsions composed of an aqueous core, a perfluorinated shell, and a surrounding aqueous phase. The diameter of the double emulsion was approximately 90 μm, the shell thickness was approximately 10 μm. To quantify the permeability, we loaded fluorescein into the core of the double emulsions.
We observed that double emulsions stabilized with non-functionalized surfactants, such as DiFSHPEG900 were highly permeable and the majority of fluorescein was released within 100 min. By contrast, if double emulsions were stabilized with the catechol-modified surfactant, FSHPEG900HA and Fe3+ ions were added to link these surfactants, thereby forming a shell, only a very small fraction of fluorescein was released within 100 min. Indeed, these double emulsions retained the vast majority of the encapsulants for more than 1500 min, as shown in
Further capsules made according to the present invention are shown in Example 10 with perfluorinated drops using a pendant drop set-up. Fluorinated drops encompassing 2 mM of the catechol-functionalized surfactant FSHPEG900HA were formed in an aqueous solution containing 1 mM FeCl3. Catechol-Fe3+ complexes form when the pH was increased to basic values using NaOH where catechols are deprotonated. Under basic conditions, the formation of thin solid shells at the drop surface were formed within 30 s. The shell start to buckle if liquid is retracted, as shown in the time-lapse micrographs in
To confirm the generality of the approach, a non-fluorinated hydrocarbon-based surfactant was synthesized composed of polypropylene glycol whose two ends are functionalized with catechols (DiDopaPPG), as shown in
These results confirm that the formation of viscoelastic shells is not limited to fluorinated surfactants but also occurs if hydrocarbon-based catechol-functionalized surfactants are employed. Note that if the amount of added base is increased, thin, rather fragile shells become apparent, even for drops that do not encompass any surfactant or those that contain catechol-free surfactants. This shell formation most likely is caused by Fe3+ ions that aggregate. The resulting particles accumulate at the surface, thereby forming Pickering emulsions.
To test if catechol-functionalized surfactants are indeed ionically crosslinked, UV-VIS spectroscopy was performed on SADopa that was dissolved in ethanol at 4 mM. In the absence of any Fe3+ ions, an absorption peak at 280 nm, typical for catechols, is observed. Upon addition of Fe3+ the absorption peak shifts to 246 nm, as shown in
Aqueous drops (pH 8) were dispersed in HFE-7100 containing 2 mM of the catechol-functionalized FSHPEG900HA surfactant and 0.6 mM Fe3+. To closely control the size of the drops, they are formed in polydimethylsiloxane (PDMS)-based microfluidic flow focusing devices. These monodisperse drops with a diameter of 114 μm are deposited onto a layer of an aqueous solution (pH=8) where they self-assemble into a densely packed monolayer, as shown in the optical micrograph in
The stability of the capsules was assessed under mechanical compression by centrifuge them at 13500 g. No significant rupture or merging was observed indicating mechanical stability.
The stability was also tested against rupture if dried. 114 μm diameter water drops were produced that encompass fluorescein. Drops were deposited onto an aqueous solution containing 0.6 mM Fe3+ that is buffered to pH=8.5 using BICINE. Drops stabilized with the catechol-functionalized FSHPEG900HA surfactant self-assemble into a hexagonal close-packed monolayer. Even though they are in direct contact with their neighbours, these aqueous drops retain their integrity even if the surrounding oil is evaporated, as shown in
Water-oil-water double emulsions, containing fluorescein in their cores were produced and assessed in ionically crosslinked FSHPEG900HA against a non-ionically crosslinked equivalents.
By contrast, fluorescein is very rapidly released if double emulsions are stabilized with catecholfunctionalized surfactants, FSHPEG900HA, that are not ionically crosslinked, as shown by the upward pointing triangles in
By way of further comparison, the plots shown in
To test the potential for the shells of the present invention at higher concentrations to be useful as inks that can be 3D printed, an experiment was conducted to confirm that capsules can be processed into macroscopic materials using 3D printing. Aqueous drops that are dispersed in HFE-7100 containing 2 mM of the catechol-functionalized FSHPEG900HA surfactant and 0.6 mM Fe3+ were assembled. The drops were up-concentrated and ejected through a pipette tip at a controlled flow rate to form a 3D hydrogel, as shown in the time-lapse photographs in
The stability of capsules according to the present invention was further increased by created emulsion drops containing two different catechol functionalized surfactants: one in the aqueous phase and one in the fluorinated oil phase. An example of a capsule that has been mechanically stressed with a razor blade is shown in
By replacing FSHPEG900HA with a FSHDopa, stable capsules were created that attain non-spherical shapes. These results demonstrates that capsules made from two different types of catechol-functionalized surfactants are mechanically more stable than those made of only one type of surfactant, as shown in
In conclusion, self-healing shells according to the present have been identified which offer new opportunities. The presence of metal coordinating groups and metal ions allows for the formation of self-healing shells which have tunable mechanical properties and can advantageously be used in a number of applications including as encapsulants, novel materials, and in the pharmaceutical, screening, agrichemical, fragrance, coatings, food and other sectors.
The invention will now be described in the following clauses:
The present invention produces novel viscoelastic, sticky capsules that are deformable and mechanically sufficiently robust to be additive manufactured into macroscopic granular materials. Capsules possess ionically crosslinked shells which in some embodiments are composed of catechol-functionalized block copolymer based surfactants. These mechanically stable shells are for practical purposes impermeable even towards low molecular weight encapsulants, thereby enabling the use of these capsules as truly closed yet dynamic containers that do not suffer from cross-contaminations and enable triggered release of reagents. Importantly, the mechanical stability, flexibility, and viscoelastic behaviour of these capsules open up a new field of their use in additive manufacturing: they can be 3D printed into proto-tissue-like cm-sized granular materials. This feature offers new possibilities for additive manufacturing of functional granular soft materials possessing locally varying compositions and structures that are well-defined over many length scales.
| Number | Date | Country | Kind |
|---|---|---|---|
| 18170186.3 | Apr 2018 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2019/061130 | 4/30/2019 | WO |
