MULTIPLEX ANALYSIS OF CELLS, PARTICLES, AND OTHER ANALYTES

• US 20120244529A1
• Filed: 04/21/2010
• Published: 09/27/2012
• Est. Priority Date: 04/21/2009
• Status: Abandoned Application

• Current Assignee: Advanex Incorporated
• Original Assignee: Advanex Incorporated
• Inventors: Fuchs, Martin, Stender, Henrik, Meltzer, Michelle, Janeen, Shepard, Huang, Richard
• Application Number:
  US13/265,176
• Publication Number:
  US 20120244529A1
• Time in Patent Office: Days
• US Class Current: 435/6.11
• CPC Class Codes: B01L 2200/04 Exchange or ejection of cartridges, containers or reservoirs
• CPC Class Codes: B01L 2200/0668 Trapping microscopic beads
• CPC Class Codes: B01L 2200/10 Integrating sample preparation and analysis in single entity, e.g. lab-on-a-chip concept
• CPC Class Codes: B01L 2300/0627 Sensor or part of a sensor is integrated
• CPC Class Codes: B01L 2300/0681 Filter
• 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 2300/0887 Laminated structure
• CPC Class Codes: B01L 2400/0487 fluid pressure, pneumatics
• CPC Class Codes: B01L 2400/0677 phase change valves; Meltable, freezing, dissolvable plugs; Destructible barriers
• CPC Class Codes: B01L 2400/0683 mechanically breaking a wall or membrane within a channel or chamber
• CPC Class Codes: B01L 2400/084 Passive control of flow resistance
• 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: B01L 3/502746 characterised by the means for controlling flow resistance, e.g. flow controllers, baffles B01L3/502738 takes precedence

Abstract

In general, the invention features multiplexed devices, systems, methods, and kits for analysis of cells, particles, and other analytes on a porous membrane. Preferred devices detect, identify and quantify low levels of microorganisms in complex biological samples, such as blood. An exemplary device includes a housing having a fluid inlet that is in fluid communication with a plurality of channels, e.g., having substantially the same fluidic resistance. Each of the plurality of channels is in fluid communication with a reservoir containing reagents for analyzing cells, particles, or other analytes bound to particles, one or more substantially planar, porous membranes through which the cells or particles do not pass, and one or more outlets, wherein liquid flowing away from the inlet is divided between the plurality of channels and flows through the one or more membranes towards the outlet, and wherein the reservoir is disposed upstream of the one or more membranes.

Claims

1. A device comprising a housing having a fluid inlet that is in fluid communication with a plurality of channels, wherein each of said plurality of channels is in fluid communication with a reservoir containing reagents for analyzing cells, particles, or analytes bound to said particles, one or more substantially planar, porous membranes through which said cells or particles do not pass, and one or more outlets, wherein liquid flowing away from said inlet is divided between said plurality of channels and flows through said one or more membranes towards said outlet, and wherein said reservoir is disposed upstream of said one or more membranes.

2. The device of claim 1, wherein said reagents for analyzing bind to a target analyte bound to said particles.

3. The device of claim 1, further comprising at least one reservoir for said particles, wherein said reservoir is disposed between said inlet and one of said one or more membranes, and wherein said reservoir for said particles is in fluid communication with at least one of said plurality of channels.

4. The device of claim 1, wherein said housing comprises a portion through which optical analysis of said cells or particles on one of said one or more membranes may occur.

5. The device of claim 1, further comprising electrodes disposed adjacent to or on one of said one or more membranes for electrical analysis of said cells or particles.

6. The device of claim 1, further comprising a magnetic resonance detector adjacent to one of said one or more membranes for magnetic relaxation analysis of said cells or particles.

7. The device of claim 1, further comprising a reservoir for waste disposed between one of said one or more membranes and said outlet.

8. The device of claim 1, further comprising a reservoir containing liquid reagents disposed between said inlet and one of said one or more membranes and separated from said plurality of channels by a valve.

9. The device of claim 1, further comprising a reservoir for containing a sample disposed between said inlet and one of said one or more membranes and in fluid communication with said plurality of channels.

10. The device of claim 9, further comprising a reservoir containing liquid reagents separated from said sample reservoir by a valve.

11. The device of claim 1, further comprising a temperature sensor and/or a heating or cooling element.

12. The device of claim 1, further comprising a passive mixer or an active mixer element disposed between said inlet and one of said one or more membranes.

13. The device of claim 1, wherein each of said plurality of channels has substantially the same fluidic resistance.

14. The device of claim 1, wherein, for at least one of said plurality of channels, said reservoir is disposed within said channel.

15. The device of claim 1, further comprising a plurality of reservoirs of reagents for analyzing, wherein each reservoir is in fluid communication with at least one of said plurality of channels.

16. The device of claim 15, wherein each of said plurality of reservoirs is in fluid communication with one, and only one, of said plurality of channels.

17. The device of claim 16, wherein each of said reservoirs is disposed within said channel.

18. The device of claim 1, wherein, for at least one of said plurality of channels, said reservoir is separated from said channel by a valve.

19. The device of claim 1, wherein said reservoir of reagents for analyzing is in fluid communication with each of said plurality of channels, so that flow of said reagents for analyzing away from said inlet is divided between said plurality of channels.

20. The device of claim 1, wherein one of said one or more membranes is substantially nonfluorescent.

21. The device of claim 1, wherein one of said one or more membranes is resistant to degradation by alcohol, acid, or base.

22. he device of claim 1, further comprising a plurality of reservoirs of reagents for analyzing, wherein each of said plurality of channels is separated from one of said reservoirs of reagents by a reservoir valve, and further comprising a plurality of channel valves that when closed prevent flow between said channel and said inlet.

23. The device of claim 22, further comprising a sample chamber and a liquid reagent chamber, wherein said sample chamber and said liquid reagent chamber are separated by a valve and are disposed between said inlet and said plurality of channels.

24. The device of claim 1, wherein said reservoir is a mechanically deformable chamber, and compression of said chamber expels its contents.

25. The device of claim 1, wherein said outlet allows the passage of gas but not liquid.

26. A system having a receptacle for mating to a device of any of the preceding claims and comprising (i) actuators for pumping fluids from said inlet of said device towards said outlet of said device;

(ii) a temperature controller configured to interface with said device to control the temperature in at least a portion of said device; and

(iii) a detector configured to interface with said device for analysis of cells, particles, or analytes bound to said particles on said membrane.

27. The system of claim 26, further comprising an active mixer element configured to interface with said device to mix two fluids between said inlet and said membrane.

28. The system of claim 26, wherein said detector is an optical detector, electrical detector, or a magnetic relaxation or magnetic resonance detector.

29. The system of claim 26, further comprising a reservoir for fluids and a pump to deliver fluids from said reservoir to said inlet of said device.

48. A kit comprising a device of claim 1 and a diluent, lysis buffer, hybridization buffer, or control particles.

30. A method of analyzing a sample, said method comprising the steps of:

(i) introducing said sample into a device comprising a housing having a fluid inlet that is in fluid communication with a plurality of channels, wherein each of said plurality of channels is in fluid communication with a reservoir containing reagents for analyzing cells, particles, or analytes bound to said particles, one or more substantially planar, porous membranes through which said cells or particles do not pass, and one or more outlets, wherein liquid flowing away from said inlet is divided between said plurality of channels and flows through said one or more membranes towards said outlet, and wherein said reservoir is disposed upstream of said one or more membranes,

wherein said sample comprises said cells, particles or analytes that bind to said particles;

(ii) allowing said reagents for analyzing to contact said cells, particles, or analytes;

(iii) capturing said cells or particles on said membrane; and

(iv) analyzing said cells or particles on said membrane.

31. The method of claim 30, wherein said reagents for analyzing comprise probes for nucleic acids or antibodies.

32. The method of claim 31, wherein said probes comprise PNA, DNA, or LNA.

33. The method of claim 32, wherein said cells, particles, or analytes bound to said particles are further contacted with reagents that bind to said probes or antibodies, resulting in signal amplification.

34. The method of claim 30, wherein said reagents for analyzing are labeled for optical, electrical, or magnetic detection.

35. The method of claim 30, wherein said reagents for analyzing comprise a plurality of reagents that are optically distinguishable and that bind to different cells, particles, or analytes bound to said particles.

36. The method of claim 30, further comprising, after step (i) and prior to step (iv), treating said sample with a liquid reagent.

37. The method of claim 36, wherein said device further comprises a passive mixer disposed so that said liquid reagent and said sample mix while flowing through said device and before contacting said membrane.

38. The method of claim 36, wherein said treating step further comprises actively mixing said sample with said liquid reagent.

39. The method of claim 38, wherein said device further comprises a sample reservoir and a liquid reagent reservoir separated by a valve from said sample reservoir, wherein said sample is introduced into said sample reservoir in step (i), said liquid reagent is stored in said liquid reagent reservoir, and said active mixing comprises actuating said valve and transferring said liquid reagent to said sample reservoir or said sample to said liquid reagent reservoir.

40. The method of claim 36, wherein said liquid reagent comprises a diluent, lysis buffer, or said particles comprising binding moieties to said analytes.

41. The method of claim 40, wherein said sample is contacted with said particles comprising binding moieties under conditions in which said analytes of said sample bind to said particles, which are captured by said membrane in step (iii).

42. The method of claim 30, wherein said sample is contacted with control particles that are subsequently divided between said plurality of channels proportionally with said sample, wherein said control particles are captured by said membrane in step (iii).

43. The method of claim 30, wherein said device further comprises a plurality of reservoirs containing reagents for analyzing, wherein one of said plurality of reservoirs is disposed within each of said plurality of channels, and said reagents for analyzing are released from said reservoir by flow of adjacent liquid in step (ii).

44. The method of claim 30, wherein said device further comprises a plurality of reservoirs containing reagents for analyzing, wherein one of said plurality of reservoirs is separated by a valve from each of said plurality of channels, and step (ii) comprises actuating said valve.

45. The method of claim 30, wherein said cells are microorganisms and are analyzed.

46. The method of claim 30, wherein said cells are analyzed and are produced by a subject as a result of disease.

47. The method of claim 30, wherein said sample comprises a culture, an environmental sample, or a biological sample.

49. A device that can detect, identify, and quantify a low-level of microorganisms in complex biological samples.