Systems and methods for generation of emulsions with suitable clarity with applications of use
The inventions cover systems and methods for generation of emulsions having suitable clarity without requiring refractive index matching between emulsion components. Systems can include: a substrate including a set of openings; a reservoir facing the substrate at a first side and containing a sample fluid configured for droplet formation upon interacting with the set of openings of the substrate; and a collecting container facing the substrate at a second side and containing a set of fluid layers configured with a density gradient and suitable immiscibility characteristics. One or more components of the system(s) can support methods for emulsion generation, in relation to enabling interactions between multiple continuous phases and a dispersed droplet phase to generate clear emulsions. Applications of the inventions(s) can include performance of droplet-based digital PCR in an improved manner (e.g., without requiring implementation of correction factors based upon Poisson statistics).
1. A method for generation of an emulsion having clarity above a threshold level of clarity, the method comprising:
generating a set of droplets from a sample fluid; and
generating an emulsion upon processing the set of droplets with a set of fluid layers configured with a density gradient across the set of fluid layers, wherein each fluid layer of the set of fluid layers is immiscible with adjacent fluid layers of the set of fluid layers, and
wherein upon measuring clarity of the emulsion with a transmission detector, the emulsion is characterized with clarity above the threshold level of clarity along an axis in which measurement of clarity is performed, wherein the threshold level is 70% optical transmittance of light, and wherein clarity of the emulsion is produced without refractive index matching of the set of fluid layers and the sample fluid.
2. The method of claim 1 , wherein generating the set of droplets comprises:
retaining the sample fluid within a reservoir aligned with a substrate comprising a set of openings and a collecting container downstream of the substrate; and
applying a force to the sample fluid, thereby driving the sample fluid through the set of openings and into the set of fluid layers.
3. The method of claim 2 , wherein applying the force comprises at least one of: a) centrifuging an assembly comprising the reservoir, the substrate, and the collecting container; and b) pressurizing the sample fluid through the set of openings and into the collecting container.
4. The method of claim 3 , wherein the sample fluid is composed of an aqueous solution, and wherein the set of fluid layers comprises a first non-aqueous liquid having a first density and a first aqueous liquid having a second density greater than the first density, and wherein the sample fluid includes a density medium and has a third density greater than the first density and the second density.
5. The method of claim 4 , wherein the sample comprises an aqueous biological solution, and wherein the first non-aqueous liquid comprises an oil with a surfactant, and wherein the first aqueous liquid comprises water with at least one of a solute and a surfactant.
6. The method of claim 1 , wherein generating the set of droplets comprises generating an early stage emulsion comprising the sample fluid as a dispersed phase within a first continuous phase, the early stage emulsion having clarity below the threshold level of clarity, and
wherein generating the emulsion having clarity above the threshold level of clarity comprises processing the early stage emulsion with a second continuous phase that is immiscible with and denser than the first continuous phase.
7. The method of claim 6 , wherein processing the early stage emulsion with the second continuous phase comprises centrifuging the early stage emulsion with the second continuous phase, thereby displacing an excess volume of the first continuous phase away from the dispersed phase and producing the emulsion having clarity above the threshold level of clarity.
8. The method of claim 6 , wherein second continuous phase is denser than the first continuous phase and less dense than the dispersed phase.
9. The method of claim 1 , wherein at least one of the set of fluid layers is configured to form a film about individual droplets formed from the sample fluid, the film having a thickness less than a wavelength of light used to observe the emulsion.
10. The method of claim 1 , wherein the sample fluid comprises a solution comprising components for polymerase chain reaction (PCR), the method further comprising performing droplet digital PCR with the emulsion within the collecting container.
11. The method of claim 1 , wherein the sample fluid comprises a fluorescent compound reactive with target material of the sample fluid, the method further comprising performing fluorescent imaging of the emulsion generated from the sample fluid, within the collecting container, and processing readout signals from individual droplets of the emulsion within the collecting container.
12. The method of claim 1 , wherein generating the emulsion comprises generating at least one of a synthetic biological component and a set of microparticles with shells from the sample fluid and the set of fluid layers.
13. The method of claim 1 , wherein each of the set of droplets has a characteristic diameter from 10 microns to 100 microns, and wherein clarity of the emulsion is produced without refractive index matching of the set of fluid layers and the sample fluid.