Reversible, on-demand generation of aqueous two-phase microdroplets
The present invention provides methods of on-demand, reversible generation of aqueous two-phase microdroplets core-shell microbeads, microparticle preparations comprising the core-shell microbeads, and drug delivery formulation comprising the microparticle preparations. Because these aqueous microdroplets have volumes comparable to those of cells, they provide an approach to mimicking the dynamic microcompartmentation of biomaterial that naturally occurs within the cytoplasm of cells. Hence, the present methods generate femtoliter aqueous two-phase droplets within a microfluidic oil channel using gated pressure pulses to generate individual, stationary two-phase microdroplets with a well-defined time zero for carrying out controlled and sequential phase transformations over time. Reversible phase transitions between single-phase, two-phase, and core-shell microbead states are obtained via evaporation-induced dehydration and water rehydration.
1. A method for forming an aqueous two-phase microdroplet, the method comprising:
providing a microfluidic device comprising a central microchannel having a communication junction with a first side microchannel, wherein said first side microchannel contains an aqueous solution comprising a single-phase mixture of first and second solutes capable of phase separation with each other but present at concentrations sufficiently below the binodal curve of the single-phase mixture in order for the first and second solutes to remain in a single phase in said aqueous solution at the time of microdroplet formation, and said central microchannel contains an aqueous-immiscible phase, and wherein the height and width of said first side microchannel at said communication junction are sufficiently smaller than the height and width of said central microchannel;
generating a single-phase aqueous microdroplet, composed of said aqueous solution, into said central microchannel by applying a pressure pulse through said first side microchannel of the microfluidic device, wherein the pressure pulse creates an interfacial tension induced force sufficient for said first aqueous microdroplet to have a diameter of from about 0.2 μm to about 100 μm, and
allowing passive water evaporation from said single-phase aqueous microdroplet to occur until a two-phase aqueous microdroplet containing first and second aqueous phases is formed in said central microchannel.
2. The method of claim 1 , comprising:
providing a microfluidic device comprising a central microchannel having a communication junction with a first side microchannel and, approximately opposing said first side microchannel, having a communication junction with a second side microchannel, said central microchannel containing an aqueous-immiscible phase, said first side microchannel containing a first aqueous solution and said second side microchannel containing a second aqueous solution, wherein said first and second aqueous phases solutions contain first and second solutes, respectively, capable of phase separation with each other but present in said first and second aqueous solutions at concentrations sufficiently below the binodal curve of a mixture of said first and second aqueous solutions in order for the two solutes to be in a single phase when combined into a microdroplet, and wherein the height and width of said first and second side microchannels at said communication junctions are sufficiently smaller than the height and width of said central microchannel;
generating a first aqueous microdroplet composed of the first aqueous solution, into said central microchannel by applying a pressure pulse through said first side microchannel of the microfluidic device, wherein the pressure pulse creates an interfacial tension induced force sufficient for said first aqueous microdroplet to have a diameter of from about 0.2 μm to about 100 μm;
generating a second aqueous microdroplet composed of the second aqueous solution, into said central microchannel by applying a pressure pulse through said second side microchannel in said microfluidic device, wherein the pressure pulse creates an interfacial tension induced force sufficient for said first aqueous microdroplet to have a diameter of from about 0.2 μm to about 100 μm;
allowing said first and second aqueous microdroplets to coalesce in said central microchannel to form a single-phase aqueous microdroplet that contains a mixture of said first and second solutes in a single phase; and
allowing passive water evaporation from said single-phase aqueous microdroplet to occur until a two-phase microdroplet containing first and second aqueous phases is formed in said central microchannel.
3. The method of claim 1 , wherein said aqueous-immiscible phase is an oil or mixture of oils.
4. The method of claim 3 , wherein said oil is soybean oil.
5. The method of claim 1 , wherein said pressure pulse creates an interfacial tension induced force sufficient to form a microdroplet having a diameter of from about 1 μm to about 20 μm.
6. The method of claim 5 , wherein said pressure pulse creates an interfacial tension induced force sufficient to form a microdroplet having a diameter of from about 5 μm to about 15 μm.
7. The method of claim 1 , wherein the height and width of the first side microchannel independently ranges from about 0.2 μm to about 3 μm, and the height and width of the central microchannel independently ranges from about 10 μm to about 40 μm.
8. The method of claim 1 , wherein the height and width of said first side microchannel independently ranges from approximately 0.1 μm to about 5 μm.
9. The method of claim 1 , wherein the height and width of said central microchannel independently ranges from about 1 μm to about to about 300 μm.
10. The method of claim 1 , wherein one or both of said first or second aqueous phases comprise one or more biomolecules capable of partitioning between said first and second aqueous phases.
11. The method of claim 1 , further comprising one or more biomolecules that do not partition between said first and second aqueous phases, and one or more biomolecules that partition between said first and second aqueous phases.
12. The method of claim 1 , further comprising one or more biomolecules that do not partition between said first and second aqueous phases.
13. A method of making a microparticle preparation, the method comprising:
(a) applying multiple pressure pulses to generate aqueous two-phase microdroplets according to the method of claim 1 ;
(b) applying a backing pressure to the central microchannel to move the aqueous two-phase microdroplets into a collection reservoir while allowing passive water evaporation to occur until each aqueous two-phase microdroplet remains at a constant size to form core-shell microbeads,
(c) recovering said core-shell microbeads from said collection reservoir to thereby produce a microparticle preparation.
14. The method of claim 13 wherein one or more of said aqueous solutions used in forming said aqueous two-phase microdroplets comprise a drug.
15. A drug delivery formulation which comprises a microparticle preparation prepared by the method of claim 13 and a pharmaceutically-acceptable carrier.
16. The method of claim 1 , further comprising reversible conversion of said two-phase aqueous microdroplet into a single-phase aqueous microdroplet by fusing said two-phase aqueous microdroplet with a microdroplet of water.
17. The method of claim 1 , wherein said first and second solutes are first and second polymers, respectively.
18. The method of claim 17 , wherein said first polymer is PEG and said second polymer is dextran.