Acoustic separation for bioprocessing

Patent metadata

Field	Value
Publication number	US-11291756-B2
Application number	US-201916452191-A
Country	US
Kind code	B2
Filing date	Jun 25, 2019
Priority date	Jul 28, 2016
Publication date	Apr 5, 2022
Grant date	Apr 5, 2022

Abstract

A method for separating cells in a biofluid includes pretreating the biofluid by introducing an additive comprising a cell activator, flowing the pretreated biofluid through a microfluidic separation channel, and applying acoustic energy to the microfluidic separation channel to accumulate target cells in a primary stream and non-target cells in a secondary stream. A system for microfluidic cell separation capable of separating target cells from non-target cells in a biofluid includes at least one microfluidic separation channel, a source of biofluid, a source of additive comprising a cell activator, and at least one acoustic transducer coupled to the microfluidic separation channel.

First claim

What is claimed is:

1. A method of separating target cells from non-target cells in a biofluid, comprising:
selecting the target cells to be a desired cell type;
pretreating the biofluid comprising mixed cells by introducing an additive to alter at least one of size of the target cells, size of the non-target cells, compressibility of the biofluid, compressibility of the target cells, compressibility of the non-target cells, aggregation potential of the target cells, and aggregation potential of the non-target cells, the additive comprising a cell activator;
flowing the pretreated biofluid into an inlet of a microfluidic separation channel; and
applying acoustic energy to the pretreated biofluid within the microfluidic separation channel, such that the target cells accumulate within at least one primary stream along the separation channel and the non-target cells accumulate within at least one secondary stream along the separation channel.

2. The method of claim 1 , comprising selecting the cell activator to comprise a B cell activator.

3. The method of claim 2 , wherein the B cell activator comprises CpG oligodeoxynucleotides.

4. The method of claim 1 , comprising selecting the cell activator to comprise a T cell activator.

5. The method of claim 4 , wherein the T cell activator comprises at least one of a soluble CD3 antibody, a bead coated with humanized CD3 and CD28 agonist antibodies, and Interleukin 2.

6. The method of claim 1 , wherein the additive comprises at least one of a cell aggregator, deionized water, a detergent, a surfactant, a solution to regulate salinity of the biofluid, a solution to regulate tonicity of the biofluid, a solution to regulate viscosity of the biofluid, a solution to regulate osmolarity of the biofluid, a solution to regulate ion concentration of the biofluid, and combinations thereof.

7. The method of claim 6 , further comprising selecting the additive to be a platelet activator or a cell adhesion molecule.

8. The method of claim 7 , further comprising selecting the additive to be adenosine diphosphate.

9. A system for microfluidic cell separation configured to separate target cells from non-target cells in a biofluid, comprising:
at least one microfluidic separation channel comprising an inlet, a first outlet, and a second outlet;
a source of the biofluid comprising the target cells and the non-target cells in fluid communication with the inlet of the at least one microfluidic separation channel;
a source of a predetermined volume of an additive comprising a cell activator in fluid communication with the source of the biofluid, the additive being effective to alter at least one of size of the target cells, size of the non-target cells, compressibility of the biofluid, compressibility of the target cells, compressibility of the non-target cells, aggregation potential of the target cells, and aggregation potential of the non-target cells; and
at least one acoustic transducer coupled to a wall of the at least one microfluidic separation channel positioned and configured to apply a standing acoustic wave transverse to the microfluidic separation channel at selected parameters including wavelength, frequency, amplitude, and power level effective to accumulate the target cells within at least one primary stream along the microfluidic separation channel directed to the first outlet and accumulate the non-target cells within at least one secondary stream along the microfluidic separation channel directed to the second outlet.

10. The system of claim 9 , wherein the cell activator comprises a B cell activator.

11. The system of claim 10 , wherein the B cell activator comprises CpG oligodeoxynucleotides.

12. The system of claim 9 , wherein the cell activator comprises a T cell activator.

13. The system of claim 12 , wherein the T cell activator comprises at least one of a soluble CD3 antibody, a bead coated with humanized CD3 and CD28 agonist antibodies, and Interleukin 2.

14. The system of claim 9 , wherein the additive comprises at least one of a cell aggregator, deionized water, a detergent, a surfactant, a solution to regulate salinity of the biofluid, a solution to regulate tonicity of the biofluid, a solution to regulate viscosity of the biofluid, a solution to regulate osmolarity of the biofluid, a solution to regulate ion concentration of the biofluid, and combinations thereof.

15. The system of claim 14 , wherein the additive comprises a platelet activator or a cell adhesion molecule.

16. The system of claim 15 , wherein the additive comprises adenosine diphosphate.

17. The system of claim 9 , further comprising at least one input sensor configured to measure a concentration of target cells or non-target cells in the biofluid.

18. The system of claim 17 , further comprising at least one output sensor configured to measure at least one parameter of an output suspension, the at least one parameter comprising at least one of hematocrit (HCT %) of the output suspension, concentration of target cells in the output suspension, and concentration of non-target cells in the output suspension.

19. The system of claim 18 , further comprising a control module in electrical communication with the at least one input sensor, the at least one output sensor, and the source of the additive, configured to introduce the predetermined volume of the additive into the biofluid in response to a measurement of at least one of the concentration of the target cells or the non-target cells in the biofluid and the parameter of the output suspension being outside tolerance of a target value.

20. A method of separating target cells from non-target cells in a biofluid, comprising:
selecting the target cells to be leukocytes selected from the group consisting of mononuclear cells, lymphocytes, monocytes, granulocytes, agranulocytes, macrophages, T cells, B cells, NK cells, subclasses thereof, and combinations thereof;
pretreating the biofluid comprising mixed cells by introducing a predetermined volume of an additive effective to alter at least one of size of the target cells, size of the non-target cells, compressibility of the biofluid, compressibility of the target cells, compressibility of the non-target cells, aggregation potential of the target cells, and aggregation potential of the non-target cells, the additive comprising a cell activator;
flowing the pretreated biofluid into an inlet of a microfluidic separation channel; and
applying acoustic energy to the pretreated biofluid comprising the mixed cells within the microfluidic separation channel, such that the target cells accumulate within at least one primary stream along the separation channel and the non-target cells accumulate within at least one secondary stream along the separation channel.

21. The method of claim 20 , further comprising selecting the target cells to be a class of lymphocytes.

Assignees

• Charles Stark Draper Laboratory Inc

Inventors

• Fiering Jason O
• Kotz Kenneth T
• Moore Nathan Francis

Classifications

• B01L2200/0652

  Sorting or classification of particles or molecules · CPC title

• B01L2300/0864

  comprising only one inlet and multiple receiving wells, e.g. for separation, splitting · CPC title

• B01L3/502753

  characterised by bulk separation arrangements on lab-on-a-chip devices, e.g. for filtration or centrifugation · CPC title

• A61M1/362

  changing physical properties of target cells by binding them to added particles to facilitate their subsequent separation from other cells, e.g. immunoaffinity · CPC title

• B01L3/502761

  specially adapted for handling suspended solids or molecules independently from the bulk fluid flow, e.g. for trapping or sorting beads or physically stretching molecules · CPC title