APPARATUS AND METHOD FOR SEPARATING A BIOLOGICAL ENTITY FROM A SAMPLE VOLUME

• US 20150118728A1
• Filed: 04/19/2013
• Published: 04/30/2015
• Est. Priority Date: 04/20/2012
• Status: Abandoned Application

• Current Assignee: Agency For Science Technology and Research
• Original Assignee: Agency For Science Technology and Research
• Inventors: Rahman, Abdur Rub Abdur, Jegatha, Chandran, Wong, Chee Chung, Shankar, Lakshmi
• Application Number:
  US14/395,602
• Publication Number:
  US 20150118728A1
• Time in Patent Office: Days
• US Class Current: 435/173.9
• CPC Class Codes: B01L 2200/06 Fluid handling related problems
• CPC Class Codes: B01L 2300/0681 Filter
• CPC Class Codes: B01L 3/502753 characterised by bulk separation arrangements on lab-on-a-chip devices, e.g. for filtration or centrifugation separation in general B01D; microapparatus for analysis using electrophoresis G01N27/44791; sample preparation G01N1/28
• CPC Class Codes: B03C 1/30 Combinations with other devices, not otherwise provided for
• CPC Class Codes: B03C 2201/22 characterised by the magnetical field, special shape or generation
• CPC Class Codes: C12N 13/00 Treatment of microorganisms or enzymes with electrical or wave energy, e.g. magnetism, sonic waves
• CPC Class Codes: G01N 33/54333 Modification of conditions of immunological binding reaction, e.g. use of more than one type of particle, use of chemical agents to improve binding, choice of incubation time or application of magnetic field during binding reaction
• CPC Class Codes: G01N 33/54386 Analytical elements
• CPC Class Codes: G01N 33/56966 Animal cells
• CPC Class Codes: G01N 35/0098 involving analyte bound to insoluble magnetic carrier, e.g. using magnetic separation magnetic particles used in immunoassays G01N33/54326; magnetic separation in general B03C

Abstract

According to embodiments of the present invention, an apparatus for separating a biological entity from a sample volume is provided. The apparatus includes an input chamber including an inlet configured to receive the volume sample, and an outlet, at least one magnetic element adjacent a portion of the input chamber, the magnetic element configured to provide a magnetic field in a vicinity of the portion of the input chamber to trap at least some leukocytes from the sample volume, and a filter in fluid communication with the outlet, the filter configured to separate the biological entity. According to further embodiments of the present invention, a method for separating a biological entity from a sample volume is also provided.

Claims

1. An apparatus for separating a biological entity from a sample volume, the apparatus comprising:

an input chamber comprising;

an inlet configured to receive the sample volume; and

an outlet;

at least one magnetic element adjacent a portion of the input chamber, the magnetic element configured to provide a magnetic field in a vicinity of the portion of the input chamber to trap at least some leukocytes from the sample volume; and

a filter in fluid communication with the outlet, the filter configured to separate the biological entity.

2. The apparatus according to claim 1, wherein the input chamber further comprises a layer comprising leukocyte specific biomarkers coated on at least a section of an inner wall of the input chamber, the leukocyte specific biomarkers configured to couple to leukocytes from the sample volume.

3. The apparatus according to claim 2, wherein the layer further comprises an azide.

5. The apparatus according to claim 1, wherein the magnetic element is arranged to at least substantially surround the portion of the input chamber.

6. The apparatus according to claim 1, further comprising a plurality of magnetic elements arranged along a length of the input chamber.

7. The apparatus according to claim 1, wherein the input chamber and the filter form a closed pathway for the sample volume.

8. The apparatus according to claim 1, wherein the filter is comprised in a microfluidic device.

9. The apparatus according to claim 8, wherein the outlet of the input chamber is coupled to the filter via at least one microchannel.

10. The apparatus according to claim 9, further comprising at least one further magnetic element adjacent a portion of the microchannel, the magnetic element configured to provide a magnetic field in a vicinity of the portion of the microchannel.

12. The apparatus according to claim 8, wherein the microfluidic device comprises a piezoelectric substrate.

13. The apparatus according to claim 1, wherein the input chamber further comprises a plurality of magnetic beads couplable to leukocyte specific biomarkers configured to couple to the leukocytes from the sample volume.

16. The apparatus according to claim 1, wherein the filter comprises a single porous layer comprising a plurality of pores, each of the plurality of pores having a dimension between about 0.5 μ

m and about 30 μ

m.

17. The apparatus according to claim 1, wherein the filter comprises:

a first porous layer and a second porous layer arranged one over the other,

wherein the first porous layer comprises a plurality of first pores defined through the first porous layer,

wherein the second porous layer comprises a plurality of second pores defined through the second porous layer,

wherein one or more respective second pores are arranged to at least substantially overlap with each respective first pore such that a respective opening defined between a perimeter of the each respective first pore and a perimeter of each of the one or more respective second pores is smaller than a diameter of each first pore.

18. The apparatus according to claim 17, wherein each second pore has a diameter that is smaller than the diameter of each first pore.

19. The apparatus according to claim 18, wherein the one or more respective second pores are arranged to be within the perimeter of each respective first pore.

20. The apparatus according to claim 1, wherein the filter comprises:

a plurality of first channels arranged in a first row; and

a plurality of second channels arranged in a second row adjacent to the first row,

wherein one or more respective second channels are arranged to at least substantially overlap with each respective first channel such that a respective opening defined between an edge of the each respective first channel and an edge of each of the one or more respective second channels is smaller than a width of each first channel.

21. The apparatus according to claim 20, wherein the filter further comprises:

a plurality of third channels arranged in a third row,

wherein the second row is arranged between the first row and the third row, and

wherein one or more respective third channels are arranged to at least substantially overlap with each respective second channel such that a respective opening defined between an edge of the each respective second channel and an edge of each of the one or more respective third channels is smaller than a width of each second channel.

24. The apparatus according to claim 1, wherein the input chamber is a syringe or a vacutainer.

4. (canceled)

11. (canceled)

14. (canceled)

15. (canceled)

22. (canceled)

23. (canceled)

25-28. -28. (canceled)

29. A method for separating a biological entity from a sample volume, the method comprising:

supplying the sample volume to an input chamber;

supplying a plurality of magnetic beads to the input chamber, the plurality of magnetic beads couplable to leukocyte specific biomarkers;

trapping leukocytes from the sample volume that are coupled to the plurality of magnetic beads at a portion of the input chamber via at least one magnetic element; and

filtering the sample volume by means of a filter for separating the biological entity.

30-32. -32. (canceled)

33. A method for separating a biological entity from a sample volume, the method comprising:

supplying the sample volume to an input chamber;

filtering the sample volume by means of a filter for trapping the biological entity and at least some of leukocytes, fetal cells or stem cells on the filter;

supplying a plurality of magnetic beads couplable to leukocyte specific biomarkers to the filter;

flowing the trapped contents of the filter into the input chamber;

trapping the leukocytes from the sample volume that are coupled to the plurality of magnetic beads at a portion of the input chamber via at least one magnetic element; and

filtering the sample volume by means of the filter for separating the biological entity.

34. (canceled)