Substrates for isolating, reacting and microscopically analyzing materials

• US 7,297,497 B2
• Filed: 05/08/2006
• Issued: 11/20/2007
• Est. Priority Date: 08/16/2002
• Status: Active Grant

• Current Assignee: Medicinal Genomics Corporation (Courtagen Life Sciences, Inc.)
• Original Assignee: Decision Biomarkers Incorporated (Courtagen Life Sciences, Inc.)
• Inventors: Montagu, Jean I., Dowd, Roger, Root, David
• Primary Examiner(s): Lam; Ann Y.
• Application Number:
  US11/431,997
• Publication Number:
  US 20060286550A1
• Time in Patent Office: 561 Days
• Field of Search: 435/6, 435/4, 435/7.1, 435/7.92, 4352871-2873, 435/287.7, 436/518, 386/244, 386/248, 422/50, 422/55
• US Class Current: 435/6.19
• CPC Class Codes: G01N 33/54366 Apparatus specially adapted for solid-phase testing
• CPC Class Codes: G01N 33/544 the carrier being organic

Abstract

An immobilizing device for biological material comprises a rigid support (12) carrying a substrate layer (20, 20′) of polymer having biological immobilizing properties, e.g. for amino and nucleic acids. Substantially solid ultra-thin substrate layers (20′) having a thickness less than about 5 micron, preferably between about 0.1 and 0.5 micron, and micro-porous, ultra-thin substrate layers (20′) having a thickness less than about 5 micron, preferably less than 3 micron, 2 or 1 micron are shown, which may be segmented by isolating moats M. The substrate layer is on a microscope slide (302), round disc (122), bio-cassette, at the bottom of a well of a multiwell plate, and as a coating inside a tube. Fluorescence or luminescence intensity and geometric calibration spots (420) are shown. Reading is enhanced by the intensity calibration spots. (420) to enable normalization of readings under uneven illumination conditions, as when reading by dark field, side illumination mode. The reference spots are shown being printed simultaneously with printing an array of biological spots or with the same equipment. Methods of forming layers of the device include controlled drawing from a bath of coating composition and drying, and spinning of C-D shaped substrates. Post-forming treatment is shown by corona treatment and radiation. Adherent metal oxides (14), silica-based materials and other materials are used to unite layers of the composite. In multi-well plates the oxide promotes joining of a bottom plate (95, 95′) and upper, well-defining structure (94) of dissimilar material. The oxides (14) also provide beneficial opacity to prevent light entering the glass support, for applying potential to the substrate, etc.

Claims

1. A device constructed for immobilizing material for exposure to liquid during an assay, the device comprising a polymer layer on a rigid support, the layer having an outer deposit-receiving region that has binding properties for a bio-material, wherein the layer comprises nitrocellulose in the form of a coating of substantially solid film of thickness less than about 1 micron and a deposit of the biomaterial is immobilized on the deposit-receiving region.

2. The device of claim 1 in which the substantially solid film is less than about 0.5 micron in thickness.

3. The device of claim 1 in which the substantially solid film is between about 0.1 and 0.5 micron in thickness.

4. The device of claims 1, 2 or 3 in which the substantially solid film is a dried residue of a coating solution of nitrocellulose and volatile solvent, the dried residue of the coating solution adhered throughout a continuous extent to a continuous surface on the rigid support.

5. The device of claim 1 having, as the deposit of bio-material, an array of individual deposits of material.

6. The device of claim 5 in which the bio-material comprises protein, peptides, antibodies, viruses, or nucleic acid or other genetic material, receptors, cDNA clones, DNA probes, oligonucleotides including synthetic oligonuceleotides, or polymerase chain reaction (PCR) products, or plant, animal, human, fungal or bacterial cells, or malignant cells or cells from biopsy tissue.

7. This device of claim 5 in which the individual deposits comprise spots of biomaterial between about 100 and 400 micron in diameter.

8. The device of claim 1 in which the substantially solid film transmits light without substantial scatter.

9. The device of claim 5 in which the rigid support is glass.

10. The device of claim 5 in which the rigid support is plastic.

11. The device of claim 1 constructed to expose the deposit of the bio-material on the substantially solid film for direct illumination or optical inspection from the exterior.

12. The device of claim 11 in which a portion of the device below the substantially solid film is substantially opaque to light from the solid film.

13. The device of claim 12 in which the rigid support is substantially transparent and an adherent intervening layer between the solid film and the rigid support is substantially opaque.

14. The device of claim 1 in which the deposit of bio-material on the substantially solid film is subject to illumination or inspection via the rigid support, the device being functionally transparent so that light can pass through the rigid support and the substantially solid film to the deposit.

15. The device of claim 14 in which there is at least one substantially transparent intervening adherent layer between the substantially solid film and the rigid support.

16. The device of claim 1 in which the substantially solid film of nitrocellulose is adhered to a substantially continuous surface on the rigid support via one or more adherent intervening layers.

17. The device of claim 16 in which an intervening layer is comprised of an adherent metal oxide.

18. The device of claim 16 in which an intervening layer is comprised of tantalum oxide.

19. The device of claim 16 in which the rigid support is of glass and an adherent intervening layer is an adhesion-promoting layer comprised of silane, epoxy silane, polylisine, PEI, GAP, an adherent metal oxide, colloidal silica or a soluble silicate.

20. The device of claim 1 in which the substantially solid film has, as its outer deposit-receiving region, an outer surface in treated state for enhanced immobilization of the material.

21. The device of claim 20 in which the treated state is the result of exposure of the surface to an energetic surface-altering condition.

22. The device of claim 21 in which the treated state is the result of exposure of the surface to corona treatment.

23. The device of claim 21 in which the treated stated is the result of exposure of the surface to charged particles.

24. The device of claim 21 in which the treated state is the result of exposure of the surface to gamma radiation.

25. The device of claim 21 in which the treated state is the result of exposure of the outer surface to at least one of corona treatment, flame treatment, bombardment by charged particles comprising electrons, ions or sub-atomic particles, or electromagnetic radiation of ultraviolet, gamma or X-ray wavelength.

26. The device of claim 1 in which the immobilized bio-material is capable of being associated with a fluorophore tag for optically-stimulated fluorescent emission analysis.

27. The device of claim 26 in combination with a reader for fluorescence from fluorescent labels associated with at least some of the individual deposits.

28. The combination of claim 27 in which the reader comprises a CCD sensor.

29. The device of claim 1 in which the nitrocellulose film is a drawn coating.

30. The device of claim 1 in which the outer surface of the nitrocellulose film is generally flat, the deposit comprising a spotted two-dimensional array of bio-material.

31. The device of claim 1 constructed for analysis based on optically-stimulated light emission from a fluorescent tag that is or becomes associated with the bio-material deposit, wherein, in the deposit-receiving region of the substantially solid nitrocellulose film,the film is adhered continuously to a continuous surface of the rigid support and is substantially transparent.

32. The device of claim 31 wherein said deposit-receiving region of said substantially solid film has binding properties for protein, and the deposit comprises protein, peptides, antibodies or viruses.

33. The device of claim 31 wherein the device is constructed to enable effective light to pass in at least one direction between the deposit on said substrate layer and though said rigid support.

34. The device of claim 31 in which the substantially solid film is less than about 0.5 micron in thickness.

35. The device of claim 31, wherein the substantially solid film is generally flat, the deposit comprising a spotted two-dimensional array of bio-material.

36. The device of claim 31, wherein the deposit-receiving region of said substantially solid film is a deposit-receiving surface of the film in a treated state as the result of exposure of the surface to an energetic surface altering treatment.

37. The device of claim 31, wherein said rigid support is selected from the group consisting of glass, fused quartz, silicon, plastic, PMMA, polystyrene, ceramic or a solid metal.

44. The device of claim 33 constructed and arranged to enable illumination of a deposit of biological material on said substrate layer via said rigid support.

45. The device of claim 33 constructed and arranged to enable microscopic inspection of a deposit of biological material on said substrate layer via said rigid support.

46. The device of claim 5 in which the individual deposits are in unreacted state.

47. The device of claim 5 in which the individual deposits are in a reacted state as a result of performance of an assay, at least some of the said deposits being associated with fluorescent or luminescent label.

48. The device claim 31 wherein the deposit receiving surface of the substantially solid nitrocellulose film is in a treated state as the result of exposure to corona treatment.

49. The device of claim 31 wherein the deposit-receiving surface of the substantially solid nitrocellulose film is in a treated state as the result of exposure to charged ions.

50. The device of claim 31 wherein the deposit-receiving surface of the substantially soild nitrocellulose film is in a treated state as the result of exposure to gamma radiation.

51. The device of claim 13 in which the intervening layer is a substantially opaquc layer of tantalum oxide.

52. The device of claim 15 in which the intervening layer is a substantially transparent layer of tantalum oxide.

53. The device of claim 16 in which an intervening layer is comprised of a silicon-based material.

54. The device of claim 16 in which an intervening layer is comprised of silane.

55. The device of claim 28 constructed for direct optical inspection by the CCD sensor from the exterior, and a portion of the device below the substantially solid film is substantially opaque.

56. The device of claim 55 in which the rigid support is substantially transparent and an adherent intervening layer between the solid film and the rigid support is substantially opaque.

57. The device of claim 56 in which the intervening layer is a substantially opaque layer of tantalum oxide.

58. The device of claim 31 wherein said deposit-receiving region of said substantially solid film has binding properties for nucleic acid and the deposit comprises nucleic acid or other genetic material, receptors, cDNA clones, DNA probes, oligonucleotides including synthetic oligonucleotides, or polymerase chain reaction (PCR) products.

59. The device of claim 31 wherein said deposit-receiving region of said substantially solid film has binding properties for cells and the deposit comprises plant, animal, human, fungal or bacterial cells or malignant cells or cells from biopsy tissue.

60. The device of claim 31 wherein the solid nitrocellulose film is adhered to said rigid support via an adherent intervening layer that is substantially opaque.

61. The device of claim 60 in which the intervening layer comprises a substantially opaque layer of tantalum oxide.

62. The device of claim 31 in which the substantially solid film is between about 0.1 and 0.5 micron in thickness.

63. The device of claim 1, 2, or 3 in which the rigid support is constructed and arranged to comprise a microscope slide for optical analysis.

64. The device of claim 1, 2, or 3 comprising an optically readable component of a bio-cassette, the component combined with other components to define the bio-cassette.

65. The device of claim 1, 2, or 3 defining an optically readable bottom portion of a multi well plate.

66. The device of claim 1, 2, or 3 in which the substantially solid nitrocellulose film is adhered to a substantially continuous surface of a rigid support via at least one adherent intervening layer, the outer deposit-receining region of the substantially solid film being in treated state for enhanced immobilization of the bio-material as the result of exposure of the outer surface to an energetic surface-altering condition.

67. The device of claim 66 constructed to expose the deposit of the material for direct illumination or optical inspection from the exterior, a portion of the device below the coating being substantially opaque to light.

68. The device of claim 67 in which the adherent intermediate layer is substantially opaque.

69. The device of claim 68 in which the substantially opaque intermediate layer is comprised of tantalum oxide.

70. The device of claim 66 in which at least one adherent intervening layer comprises tantalum oxide,

and the outer deposir-receining surface of the substantially solid nitrocellulose film is in treated state for enhanced immobilization of the material as the result of exposure of the surface to an energetic surface-altering condition comprising corona treatment.

71. The device of claim 70 constructed to expose deposits of the material for direct illumination or optical inspection from the exterior, the intervening adherent tantalum oxide layer being substantially opaque to light.

38. A method of forming a device constructed for immobilizing material for exposure to liquid during an assay, the device comprising a polymer layer on a rigid support, the layer having an outer deposit-receiving region that has binding properties for a bio-material, wherein the layer comprises nitrocellulose in the form of a coating of substantially solid film of thickness less than about 1 micron and a deposit of the biomaterial is immobilized on the deposit-receiving region, the method including applying directly or indirectly to said rigid support a coating composition comprising nitrocellulose and at least one solvent while maintaining forming conditions to produce a substantially solid film coating of nitrocellulose of thickness less than about 1 micron.

39. The method of claim 38 including forming the substantially solid film coating of nitrocellulose with thickness between about 0.5 micron.

40. The method of claim 38 including forming the substantially solid film coating of nitrocellulose with thickness between about 0.1 and 0.5 micron.

41. The method of claim 38, 39 or 40 comprising:

(a) at least partially immersing a rigid member that bears a straight support surface in a vat containing a coating solution comprising a biologically compatible organic film-forming composition of nitrocellulose winch includes at least one volatile solvent,

(b) progressively drawing the member from the solution along a fixed path into a still environment,

(c) the fixed path being generally parallel to said straight support surface, the method

(d) including maintaining conditions to enable said solvent to evaporate to leave a drawn substantially solid film of nitrocellulose adhered to said support surface.

74. The method of claim 41 in which, the following forming the solid film of nitrocellulose, exposing its exposed surface to an energetic surface-altering condition.

42. A method of conducting an assay including providing a device constructed for immobilizing material for exposure to liquid during an assay, the device comprising a polymer layer on a rigid support, the layer having an outer deposit-receiving region that has binding properties for a bio-material, wherein the layer comprises nitrocellulose in the form of a coating of substantially solid film of thickness less than about 1 micron and a deposit of the bio-material is immobilized on the deposit-receining region, the deposit comprising an array of spots of biomaterial, conducting an assay which tags at least some of the spots with a fluorescent label, and, after washing the array, reading the array by optically stimulating emission from the fluorescent labels and fluorescent detection of the stimulated emission.

43. The method of claim 42 conducted with the device wherein the substantially solid nitrocellulose film is adhered to said rigid support via an adherent intervening layer that is substantially opaque and wherein the reading is accomplished directly from the exterior with a CCD sensor.

75. The method of claim 42 in which the assay is based on protein-protein interaction.

76. The method of claim 42 in which the assay is based on interaction of nucleic acid or other genetic material.

77. The method of claim 42 in which the assay is based on cells from a living organism.

78. The method of claim 42 in which the assay is based on a virus.

72. The method of claom 41 in which the rigid support comprises a glass body bearing a layer of adhesion promoting substance that defines the support surface.

73. The method of claim 72 in which the layer of adhesion promoting substance is tantalum oxide.