Methods and apparatuses for purification of gel droplets supporting biological tissue

Patent metadata

Field	Value
Publication number	US-11628382-B2
Application number	US-202117233950-A
Country	US
Kind code	B2
Filing date	Apr 19, 2021
Priority date	Aug 26, 2020
Publication date	Apr 18, 2023
Grant date	Apr 18, 2023

Abstract

Method and apparatuses for forming gel droplets including biological tissue (e.g., cells), and in particular, methods and apparatuses for removing oil from the gel droplets comprising dissociated cells (including micro-organospheres) are described herein. Although it is beneficial to use oil in the formation of these gel droplets, and particularly micro-organospheres, oil may inhibit growth and survival of the cells within the gel droplets. The methods and apparatuses described herein may permit the removal of oil and may enhance survival and quality of the resulting gel droplets.

First claim

What is claimed is:

1. A method of processing gel droplets containing cells, the method comprising:
forming a plurality of gel droplets in an oil, wherein the gel droplets comprise cells from a dissociated tissue sample distributed within a polymerized sphere of matrix material, the gel droplets having the cells distributed therein; and
contacting the gel droplets against a hydrophobic membrane so that the oil is removed from the gel droplets through or into the hydrophobic membrane.

2. The method of claim 1 , wherein the gel droplets comprise micro-organospheres having a diameter of between 50-500 μm.

3. The method of claim 1 , wherein contacting the gel droplets against a hydrophobic membrane comprises removing at least 99% of the oil from the gel droplets.

4. The method of claim 1 , wherein contacting the gel droplets against a hydrophobic membrane comprises passing the gel droplets through a chamber at least partially formed by the hydrophobic membrane.

5. The method of claim 4 , wherein the chamber comprises a tunnel or tube formed by the hydrophobic membrane.

6. The method of claim 1 , wherein contacting the gel droplets against a hydrophobic membrane comprises eluting the gel droplets into a funnel formed by the hydrophobic membrane.

7. The method of claim 1 , wherein contacting the gel droplets against a hydrophobic membrane comprises filtering the gel droplets against the hydrophobic membrane.

8. The method of claim 1 , wherein contacting the gel droplets against a hydrophobic membrane comprises passing a solution including the gel droplets over the hydrophobic membrane.

9. The method of claim 1 , wherein the hydrophobic membrane has a pore size that is between 0.1 and 5 μm.

10. The method of claim 1 , wherein contacting the gel droplets against a hydrophobic membrane comprises retaining the gel droplets in an aqueous medium.

11. The method of claim 1 , wherein the gel droplets each comprises between 1 and 200 of the cells distributed therein.

12. The method of claim 1 , further comprising washing the gel droplets on the hydrophobic membrane with an aqueous medium.

13. The method of claim 1 , further comprising culturing the gel droplets in a culture medium.

14. A method of processing gel droplets, the method comprising:
forming a plurality of gel droplets in an oil, wherein the gel droplets comprise cells from a dissociated tissue sample distributed within a sphere of matrix material, the gel droplets having a diameter of between 50 and 500 μm with between 1 and 200 of the cells distributed therein; and
contacting the gel droplets against a hydrophobic membrane so that at least 98% of the oil is removed from the gel droplets on or into the hydrophobic membrane;
washing the gel droplets on the hydrophobic membrane with an aqueous medium; and
culturing the gel droplets in a culture medium.

15. The method of claim 14 , wherein the gel droplets comprise micro-organospheres having a diameter of between 50-500 μm.

16. The method of claim 14 , wherein contacting the gel droplets against a hydrophobic membrane comprises removing at least 99% of the oil from the gel droplets.

17. The method of claim 14 , wherein contacting the gel droplets against a hydrophobic membrane comprises passing the gel droplets through a chamber at least partially formed by the hydrophobic membrane.

18. The method of claim 17 , wherein the chamber comprises a tunnel or tube formed by the hydrophobic membrane.

19. The method of claim 14 , wherein contacting the gel droplets against a hydrophobic membrane comprises eluting the gel droplets into a funnel formed by the hydrophobic membrane.

20. The method of claim 14 , wherein contacting the gel droplets against a hydrophobic membrane comprises filtering the gel droplets against the hydrophobic membrane.

21. The method of claim 14 , wherein contacting the gel droplets against a hydrophobic membrane comprises passing a solution including the gel droplets over the hydrophobic membrane.

22. The method of claim 14 , wherein the hydrophobic membrane has a pore size that is between 0.1 and 5 μm.

23. The method of claim 14 , wherein contacting the gel droplets against a hydrophobic membrane comprises retaining the gel droplets in an aqueous medium.

24. The method of claim 14 , further comprising washing the gel droplets on the hydrophobic membrane with an aqueous medium.

Assignees

• Univ Duke

Inventors

• Wang Zhaohui
• Shen Xiling

Classifications

• B01D2325/02834

  more than 0.1 and up to 1 µm · CPC title

• C12M29/04

  Filters; Permeable or porous membranes or plates, e.g. dialysis · CPC title

• C12M25/01 Primary

  Drops · CPC title

• C12M23/16

  Microfluidic devices; Capillary tubes (integrated microfluidic structures B01L3/5027; microreactors B01J19/0093) · CPC title

• B01D69/02

  characterised by their properties · CPC title