MICROFLUIDIC DEVICE HAVING ONBOARD TISSUE OR CELL SAMPLE HANDLING CAPABILITY

• US 20110003324A1
• Filed: 07/06/2010
• Published: 01/06/2011
• Est. Priority Date: 07/06/2009
• Status: Abandoned Application

• Current Assignee: Sony Corporation (Sony Group Corp.), Sony Corporation Of America (Sony Group Corp.)
• Original Assignee: Sony Corporation (Sony Group Corp.), Sony Corporation Of America (Sony Group Corp.)
• Inventors: Durack, Gary P.
• Application Number:
  US12/830,887
• Publication Number:
  US 20110003324A1
• Time in Patent Office: Days
• US Class Current: 435/29
• CPC Class Codes: B01L 2200/0647 Handling flowable solids, e.g. microscopic beads, cells, particles
• CPC Class Codes: B01L 2300/0816 Cards, e.g. flat sample carriers usually with flow in two horizontal directions
• CPC Class Codes: B01L 2300/0864 comprising only one inlet and multiple receiving wells, e.g. for separation, splitting
• CPC Class Codes: B01L 2400/0439 ultrasonic vibrations, vibrating piezo elements
• CPC Class Codes: B01L 3/5027 by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip B01L3/5023 takes precedence; micromixers B01F33/30; microreactors for synthesis B01J19/0093; microcapillary devices in general B81B1/00
• CPC Class Codes: G01N 15/1484 microstructural devices
• CPC Class Codes: G01N 15/149 specially adapted for sorting particles, e.g. by their size or optical properties
• CPC Class Codes: G01N 2015/1006 for cytology
• CPC Class Codes: G01N 2015/149 Sorting the particles

Abstract

The present disclosure is generally directed to systems for the storage and preservation of an original tissue or cell sample onboard a microfluidic device, such as a cytometry chip. In some embodiments, the sample may be disassociated while onboard the microfluidic device.

Claims

1. A microfluidic device, comprising:

a substrate;

a microfluidic flow channel formed in said substrate, wherein said flow channel extends through a portion of said substrate adapted to facilitate cytometry analysis of cells flowing in said flow channel; and

a sample repository onboard said substrate and containing material operative to preserve cells in a tissue sample placed within said sample repository.

2. The microfluidic device of claim 1, wherein a location of said sample repository is selected from the group consisting of:

on said substrate and in said substrate.

3. The microfluidic device of claim 1, wherein said material is selected from the group consisting of:

chemicals and reagents.

4. The microfluidic device of claim 1, wherein said sample repository comprises a well formed in said substrate.

5. The microfluidic device of claim 4, further comprising:

a cover affixed to said substrate and substantially sealing said well.

6. A method for analyzing cells, comprising the steps of:

a) providing a tissue sample;

b) disassociating cells from said tissue sample;

c) analyzing said disassociated cells by cytometry while said cells are onboard a microfluidic device having a substrate; and

d) placing a non-disassociated portion of said tissue sample in a sample repository onboard said microfluidic device.

7. The method of claim 6, wherein a location of said sample repository is selected from the group consisting of:

on said substrate and in said substrate.

8. The method of claim 6, further comprising the step of:

e) placing material in said sample repository, said material operative to preserve cells in said tissue sample placed within said sample repository.

9. The method of claim 8, wherein said material is selected from the group consisting of:

chemicals and reagents.

10. The method of claim 8, wherein step (e) is performed prior to step (d).

11. The method of claim 6, further comprising the step of:

e) placing a cover over said sample repository.

12. The method of claim 6, further comprising the step of:

e) after step (c), conducting a morphological review of said non-disassociated portion of said tissue sample in said sample repository.

13. The method of claim 6, further comprising the step of:

e) disassociating cells from said non-disassociated portion of said tissue sample in said sample repository; and

f) testing said cells disassociated at step (e).

14. The method of claim 13, wherein step (f) further comprises conducting a cytometry analysis on said cells disassociated at step (e).

15. A microfluidic device, comprising:

a substrate;

a sample well onboard said substrate for holding a tissue sample;

means for disassociating cells from said tissue sample while said tissue sample is in said sample well; and

a microfluidic flow channel formed in said substrate and operatively coupled to said sample well for receiving said disassociated cells, wherein said flow channel extends through a portion of said substrate adapted to facilitate cytometry analysis of said cells flowing in said flow channel.

16. The microfluidic device of claim 15, wherein a location of said sample well is selected from the group consisting of:

on said substrate and in said substrate.

17. The microfluidic device of claim 15, wherein said means for disassociating cells comprises:

an input port operatively coupled to said substrate and operatively coupled to said sample well for transfer of fluid thereto;

a supply of chemicals coupled to said input port;

wherein said chemicals are operative to disassociate cells from said tissue sample while said tissue sample is in said sample well.

18. The microfluidic device of claim 15, wherein said means for disassociating cells comprises:

a source of vibratory energy operative to apply at least a portion of said vibratory energy to said tissue sample in said sample well;

wherein said vibratory energy is operative to disassociate cells from said tissue sample while said tissue sample is in said sample well.

19. The microfluidic device of claim 18, wherein said source of vibratory energy produces ultrasonic energy.

20. A method for analyzing cells, comprising the steps of:

a) placing a tissue sample in a sample well onboard a microfluidic device;

b) disassociating cells from said tissue sample within said sample well; and

c) analyzing said disassociated cells by cytometry while said cells are onboard said microfluidic device.

21. The method of claim 20, wherein a location of said sample repository is selected from the group consisting of:

on said substrate and in said substrate.

22. The method of claim 20, wherein step (b) comprises applying a chemical to said sample well to disassociate said cells from said tissue sample.

23. The method of claim 20, wherein step (b) comprises applying vibratory energy to said sample well to disassociate said cells from said tissue sample.

24. The method of claim 20, wherein step (b) comprises applying a chemical and vibratory energy to said sample well to disassociate said cells from said tissue sample.

25. A microfluidic device, comprising:

a substrate;

an input port operatively coupled to said substrate for accepting a quantity of cells;

a microfluidic flow channel formed in said substrate, wherein said flow channel extends through a portion of said substrate adapted to facilitate cytometry analysis of said cells flowing in said flow channel; and

a sample repository onboard said substrate and in fluid communication with said microfluidic flow channel;

wherein a portion of said cells may be routed to said sample repository through said flow channel without undergoing cytometry analysis.

26. The microfluidic device of claim 25, wherein a location of said sample repository is selected from the group consisting of:

on said substrate and in said substrate.

27. A method for analyzing cells, comprising the steps of:

a) providing a quantity of cells into a microfluidic flow channel formed in a substrate of a microfluidic device;

b) depositing a first portion of said cells in a sample well onboard said substrate and in fluid communication with said microfluidic flow channel; and

c) analyzing a second portion of said cells by cytometry while said cells are onboard a microfluidic device.

28. The method of claim 27, wherein a location of said sample repository is selected from the group consisting of:

on said substrate and in said substrate.