Methods and compositions for thiol-acrylate based matertals for 3D cell culturing in a microfluidic device

Patent metadata

Field	Value
Publication number	US-11767516-B2
Application number	US-202017116289-A
Country	US
Kind code	B2
Filing date	Dec 9, 2020
Priority date	Dec 11, 2019
Publication date	Sep 26, 2023
Grant date	Sep 26, 2023

Abstract

Provided are thiol-acrylate hydrogels and tunable cell culture materials including thiol-acrylate hydrogels, and methods of making thereof. Also provided are systems for forming three-dimensional cell culture scaffolds including the materials, and methods of culturing cells, including cancer cells, using thiol-acrylate hydrogels and tunable cell culture materials. The materials herein can be used in microfluidic droplet-generating devices.

First claim

What is claimed is:

1. A tunable cell culture material comprising a hydrogel,
wherein the hydrogel is a product of a reaction between a thiol and an acrylate;
wherein the thiol comprises ethoxylated trimethylolpropane tri (3-mercapto-propionate) (ETTMP), and the acrylate comprises poly(ethylene glycol) diacrylate (PEGDA); and
when the hydrogel weight percent is about 8.5 and the molar ratio is about 1.0, the gelation time is about 150 minutes;
when the hydrogel weight percent is about 8.5 and the molar ratio is about 1.05, the gelation time is about 40 minutes;
when the hydrogel weight percent is about 9 and the molar ratio is about 1.0, the gelation time is about 80 minutes;
when the hydrogel weight percent is about 9 and the molar ratio is about 1.05, the gelation time is about 30 minutes;
when the hydrogel weight percent is about 9.5 and the molar ratio is about 1.0, the gelation time is about 30 minutes; and
when the hydrogel weight percent is about 9.5 and the molar ratio is about 1.05, the gelation time is about 25 minutes.

2. A tunable cell culture material of claim 1 , wherein the reaction is a base-catalyzed Michael addition occurring at a pH of about 7.6 to 8.2.

3. The tunable cell culture material of claim 1 , further comprising a liquid medium;
wherein the liquid medium comprises an extracellular buffer (ECB) comprising the following components: HEPES, NaCl, KCl, MgCl 2 ·6H 2 O, CaCl 2 ·2H 2 O, and glucose.

4. The tunable cell culture material of claim 3 , wherein the hydrogel comprises from about 8.5 to about 10.5 wt % of the material.

5. The tunable cell culture material of claim 4 , wherein the thiol and acrylate are present in a molar ratio of about 1 to about 1.05 thiol groups per acrylate group.

6. The tunable cell culture material of claim 5 , wherein:
when the molar ratio is about 1.0, the material has a swelling ratio of about 2.5 to about 4.0 after 4 hours; and
when the molar ratio is about 1.05, the material has a swelling ratio of about 4 to about 7 after 24 hours.

7. The tunable cell culture material of claim 3 , wherein:
a relative weight of the material decreases to no greater than one millionth of an original weight of the material in pH 8.05 DMEM in about 60 to about 200 hours; and
a relative weight of the material decreases no greater than one millionth of an original weight of the material in pH 7.9 phosphate buffered saline in about 100 to about 425 hours.

8. A method for culturing cells, the method comprising:
a. providing a tunable cell culture material comprising a hydrogel according to claim 1 ;
b. seeding the cells in the hydrogel to form a seeded hydrogel;
c. contacting the hydrogel with a culture medium; and
d. allowing the cells to grow for a period of from about 4 days to about 17 days.

9. The method of claim 8 , wherein about 95 to about 97% of cells seeded in the hydrogel are viable after 17 days.

10. The method of claim 8 , wherein the culture medium comprises HEPES, NaCl, KCl, MgCl 2 ·6H 2 O, CaCl 2 ·2H 2 O, and glucose.

11. The method of claim 8 , wherein the seeded hydrogel is provided to a microfluidic droplet-generating device in an aqueous phase and the seeded hydrogel gelates inside the microfluidic droplet-generating device.

12. The method of claim 8 , wherein the cells form spheroids having a diameter of about 100 μm to about 300 μm.

13. The method of claim 8 , further comprising introducing the seeded hydrogel to a microfluidic device after step b, such that the contacting with the culture medium occurs inside the microfluidic device.

14. A tunable cell culture material comprising:
a hydrogel and a liquid medium;
wherein the hydrogel is a product of a reaction between a thiol and an acrylate;
wherein the thiol comprises ethoxylated trimethylolpropane tri (3-mercapto-propionate) (ETTMP), and the acrylate comprises poly(ethylene glycol) diacrylate (PEGDA); and
wherein the liquid medium comprises an extracellular buffer (ECB) comprising the following components: HEPES, NaCl, KCl, MgCl 2 ·6H 2 O, CaCl 2 ·2H 2 O, and glucose.

15. The tunable cell culture material of claim 14 , wherein:
a relative weight of the material decreases to no greater than one millionth of an original weight of the material in pH 8.05 DMEM in about 60 to about 200 hours; and
a relative weight of the material decreases no greater than one millionth of an original weight of the material in pH 7.9 phosphate buffered saline in about 100 to about 425 hours.

16. The tunable cell culture material of claim 14 , wherein the hydrogel comprises from about 8.5 to about 10.5 wt % of the material.

17. The tunable cell culture material of claim 16 , wherein the thiol and acrylate are present in a molar ratio of about 1 to about 1.05 thiol groups per acrylate group.

18. The tunable cell culture material of claim 17 , wherein:
when the molar ratio is about 1.0, the material has a swelling ratio of about 2.5 to about 4.0 after 4 hours; and
when the molar ratio is about 1.05, the material has a swelling ratio of about 4 to about 7 after 24 hours.

Assignees

• Univ Louisiana State
• Board Of Supervisors Of Louisiana State Univ

Inventors

• Melvin Adam
• Pojman John
• Khan Anowar

Classifications

• C12N5/0693 Primary

  Tumour cells; Cancer cells · CPC title

• C08G75/04

  from mercapto compounds or metallic derivatives thereof (C08G75/0204 takes precedence) · CPC title

• C12M23/16

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

• C12N5/0062

  General methods for three-dimensional culture · CPC title

• C12N2500/05

  Inorganic components · CPC title