Exploiting oxygen inhibited photopolymerization within emulsion droplets for the fabrication of microparticles with customizable properties
Described are methods and devices for the generation of hydrogel particles with micrometer and submicrometer dimensions using oxygen-inhibited partial polymerization, and the particles generated therefrom. The described methods generate particles with dimensions independent of the starting polymerizable solution dimension, for example, a microdroplet. Further, microfluidic flow parameters (e.g. viscosity, flow rate) and photopolymerization process parameters (e.g. optical exposure intensity and duration) are controlled to generate particles with tunable crosslinking density-determined properties including elasticity, diffusivity, and biomolecular display for diverse applications such as drug delivery, tissue engineering cell scaffolds, and single- and multiple- cell therapeutics. Similarly, gradients of crosslinking density-determined properties can be created within single particles through the selection of optical exposure intensity and duration. In addition to conventional spherical shapes, a suite of non-spherical shapes may be generated by manipulating the dimensions of the microfluidic channels and other related physical and process parameters.
1. A method of generating a plurality of microparticles comprising:
providing a continuous phase comprising a non-aqueous liquid and a dispersed phase comprising an aqueous solution including a functionalized monomer or a macromer and a photoinitiator;
forming a composition comprising microdroplets of said aqueous solution dispersed in said non-aqueous liquid via a surfactant;
diffusing oxygen through said non-aqueous liquid into said microdroplets;
partially polymerizing a first microdroplet, thereby generating a first microparticle covered in an unpolymerized layer of aqueous solution, the first microparticle being smaller than the first microdroplet; and
removing the unpolymerized layer of aqueous solution to expose a surfactant-free functionalized surface;
wherein the functionalized monomer or macromer and the functionalized surface comprise functional groups configured for selective molecular binding.
2. The method of claim 1 , wherein the step of diffusing oxygen into said microdroplets generates an oxygen concentration gradient in the first microdroplet.
3. The method of claim 2 , wherein said oxygen concentration gradient results in a crosslinking gradient in the first microparticle.
4. The method of claim 3 , comprising controlling the crosslinking gradient via oxygen concentration during the partially polymerizing step such that molecules larger than a predetermined size are prevented from diffusing into the microparticle.
5. The method of claim 1 , wherein said step of partially polymerizing the first microdroplet comprises inhibiting polymerization via oxygen.
6. The method of claim 1 , wherein said step of partially polymerizing the first microdroplet comprises exposing the first microdroplet to UV light.
7. The method of claim 1 , wherein the composition is formed in a microfluidic device, the method comprising flowing the microdroplets through one or more channels of the microfluidic device.
8. The method of claim 1 , wherein said microdroplets have an average primary cross-sectional dimension of less than or equal to 100 μm and wherein the microparticle has a primary cross-sectional dimension of less than or equal to 20 μm.
9. The method of claim 1 comprising treating the functionalized surface of said microparticle with a biological material.
10. The method of claim 1 , wherein said aqueous phase further comprises a biological material.
11. A microparticle generated using the method of claim 1 .
12. The method of claim 1 , wherein the aqueous solution includes the functionalized monomer or a macromer and a crosslinking hydrogel backbone monomer or macromer.
13. The method of claim 12 , wherein the partially polymerizing step comprises forming a crosslinked copolymer with functional groups of the crosslinked copolymer exposed to an exterior of the microparticle.
14. The method of claim 1 , wherein the functionalized surface of the microparticle is configured to exhibit at least one of: selective binding of particular species, biological functions, pharmacological functions and combinations thereof.
15. The method of claim 1 , wherein the partially polymerizing step comprises controlling the extent of conversion to below a threshold value in order to allow a target molecule to diffuse into a core of the microparticle.
16. The method of claim 15 , wherein the threshold value is selected based on a size of the target molecule.
17. The method of claim 16 wherein the threshold value is less than 50%.
18. The method of claim 16 wherein the threshold value is 38%.
19. The method of claim 1 , wherein the functional groups are configured for the detection of bioactive macromolecules.
20. The method of claim 1 , wherein the functional groups are configured for molecular recognition.
21. The method of claim 20 , wherein the molecular recognition comprises ligand-protein binding.
22. The method of claim 1 , wherein the functional groups comprise ligands.