Systems and methods for encapsulation and multi-step processing of biological samples

Patent metadata

Field	Value
Publication number	US-11860076-B2
Application number	US-202016934045-A
Country	US
Kind code	B2
Filing date	Jul 21, 2020
Priority date	Jun 20, 2019
Publication date	Jan 2, 2024
Grant date	Jan 2, 2024

Abstract

The present invention relates to methods and systems for isolation of species in semi-permeable capsules and processing of encapsulated species through series of steps and/or reactions. To produce capsules, first aqueous two-phase system (ATPS) droplets are generated using microfluidics system and then the hydrogel shell layer is hardened by inducing polymerization. As exemplified in this invention to achieve concentric ATPS droplet formation density-matched PEGDA and Dextran polymer solutions can be used. Once a capsule is formed, its composition can be changed by adding new reagents or replacing out old ones (e.g. by resuspending capsules in desired aqueous solution). The hydrogel shell of semi-permeable capsules can be dissolved at selected step during multi-step procedures in order to release the encapsulated species. The present invention exemplifies the isolation of individual cells within capsules and using the encapsulated cells for genotypic and phenotypic analysis. Finally, the present invention also exemplifies the use of capsules in multi-step procedures to perform complex biological reactions.

First claim

The invention claimed is:

1. A method for isolating species in microscopic compartments comprising a semi-permeable shell and an aqueous inner phase, and processing encapsulated species in a series of reactions/procedures, wherein the method comprises:
forming a liquid droplet on a microfluidic chip, wherein a first aqueous phase, a second aqueous phase, and a carrier oil are injected into the chip to form the liquid droplet, and wherein the species is in the first or second aqueous phase;
forming an aqueous two-phase system passively, wherein the first and second aqueous phases are miscible and form an inner phase and an outer phase, respectively;
hardening the outer phase using physical or chemical stimulus, thereby creating a hardened shell encapsulating the species in the aqueous inner phase; and
performing one or more biological or biochemical reactions on the encapsulated species in microscopic compartments, wherein performing the one or more biological or biochemical reactions on the encapsulated species in the microscopic compartments comprises resuspending the microscopic compartments in assay reagents, and wherein the hardened shell provides a semi-permeable shell allowing for exchange of compounds having molecular weights of less than 200,000 MW through the shell and retention of compounds having molecular weight greater than 300,000 MW.

2. The method according to claim 1 , wherein the physical or chemical stimulus is light or a chemical compound.

3. The method according to claim 1 , wherein the liquid droplets are contained within a carrier oil.

4. The method according to claim 1 , wherein the liquid droplets contain an inner aqueous phase enriched in dextran polymer and an outer aqueous phase enriched in modified polyethylene glycol polymer.

5. The method according to claim 4 , wherein the modified polyethylene glycol polymer is cross-linked.

6. The method according to claim 4 , wherein the first and second aqueous phases are chosen to have similar densities and to achieve high concentricity of the aqueous two-phase system.

7. The method according to claim 1 , wherein the microscopic compartments are liquid droplets, aqueous two-phase system droplets or capsules and have diameter in the range from 1 μm to 100 μm size, preferably in the range 10-60 μm and more preferably in the range of 20-40 μm.

8. The method according to claim 1 , wherein processing one or more biological or biochemical reactions comprises treating the encapsulated species enzymatically.

9. The method according to claim 1 , wherein processing one or more biological or biochemical reactions comprises processing the capsules carrying encapsulated species through multi-step reactions and/or operations off-chip.

10. The method according to claim 1 , wherein processing one or more biological or biochemical reactions comprises releasing the encapsulated species from the microscopic compartments into surrounding fluid.

11. The method of claim 1 , wherein processing one or more biological or biochemical reactions comprises performing phenotypic and/or genotypic analysis on encapsulated species.

12. The method of claim 1 , wherein the species are one or more of selected from the list consisting of cells, bacteria, viruses, DNA, RNA, proteins, biological material, or biochemical compounds.

13. The method of claim 1 , wherein a reaction of the one or more biological or biochemical reactions comprises reverse transcription.

14. The method of claim 1 , wherein a reaction of the one or more biological or biochemical reactions comprises nucleic acid amplification.

15. The method of claim 1 , wherein a reaction of the one or more biological or biochemical reactions comprises a cell lysis.

Assignees

• Univ Vilnius
• Droplet Genomics

Inventors

• Mazutis Linas
• Stonyte Greta
• Leonavicius Karolis
• Zelvyte Ausra

Classifications

• G01N1/4077 Primary

  by other techniques involving separation of suspended solids · CPC title

• B01J13/046 Primary

  combined with gelification or coagulation · CPC title

• B01J13/206

  Hardening; drying · CPC title

• C12Q1/6806

  Preparing nucleic acids for analysis, e.g. for polymerase chain reaction [PCR] assay (C12Q1/6804 takes precedence) · CPC title