SELF-CONTAINED BIOLOGICAL ASSAY APPARATUS, METHODS, AND APPLICATIONS
First Claim
1. A self-contained, biological assay apparatus, comprising:
- a housing;
a dispensing platform including a controllably-movable reagent dispensing system, disposed in the housing;
a reagent supply component disposed in the housing;
a pneumatic manifold removably disposed in the housing in a space shared by the dispensing platform, removably coupled to a fluidic transport layer and a plurality of reservoirs,wherein the fluidic transport layer, the reservoirs, and a test sample to be introduced therein are disposed in the housing in the space separate from the dispensing platform;
a pneumatic supply system removably coupled to the pneumatic manifold in the housing in a space separate from the dispensing platform; and
a control system coupled to at least one of the dispensing platform and the pneumatic supply system, disposed in the housing,wherein the apparatus is characterized as a self-contained, fully automated biological assay-performing apparatus.
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Accused Products
Abstract
A self-contained, fully automated, biological assay-performing apparatus includes a housing; a dispensing platform including a controllably-movable reagent dispensing system, disposed in the housing; a reagent supply component disposed in the housing; a pneumatic manifold removably disposed in the housing in a space shared by the dispensing platform, removably coupled to a fluidic transport layer and a plurality of reservoirs, wherein the fluidic transport layer, the reservoirs, and a test sample to be introduced therein are disposed in the housing in the space separate from the dispensing platform; a pneumatic supply system removably coupled to the pneumatic manifold in the housing in a space separate from the dispensing platform; and a control system coupled to at least one of the dispensing platform and the pneumatic supply system, disposed in the housing.
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Citations
39 Claims
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1. A self-contained, biological assay apparatus, comprising:
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a housing; a dispensing platform including a controllably-movable reagent dispensing system, disposed in the housing; a reagent supply component disposed in the housing; a pneumatic manifold removably disposed in the housing in a space shared by the dispensing platform, removably coupled to a fluidic transport layer and a plurality of reservoirs, wherein the fluidic transport layer, the reservoirs, and a test sample to be introduced therein are disposed in the housing in the space separate from the dispensing platform; a pneumatic supply system removably coupled to the pneumatic manifold in the housing in a space separate from the dispensing platform; and a control system coupled to at least one of the dispensing platform and the pneumatic supply system, disposed in the housing, wherein the apparatus is characterized as a self-contained, fully automated biological assay-performing apparatus. - View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25)
wherein the reagent dispensing system includes a reagent dispenser component having a distal dispensing end; and a camera connected to the reagent dispensing system having a field of view that includes at least a selected region of interest of the reservoirs.
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3. The apparatus of claim 2, wherein the reagent dispenser component is an elongate needle structure having a length, L, and a selected bore size.
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4. The apparatus of claim 3, wherein the reagent dispensing system further includes a reagent storage structure fluidly connected to the reagent dispenser component, wherein the reagent storage structure has a selected dimension that operatively coincides with the selected bore size.
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5. The apparatus of claim 4, wherein the reagent storage structure is a length of tubing.
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6. The apparatus of claim 2, wherein the reagent dispenser component is a plurality of elongate needle structures of length, L, having different respective, selected bore sizes.
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7. The apparatus of claim 6, wherein the reagent dispensing system further includes a plurality of reagent storage structures that are respectively fluidly connected to the plurality of reagent dispenser components, wherein each reagent storage structure has a selected dimension that operatively coincides with the respective selected bore size.
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8. The apparatus of claim 7, wherein each of the reagent storage structures is a length of tubing.
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9. The apparatus of claim 7, having only two reagent storage structures that are respectively fluidly connected to two reagent dispenser components, wherein one of the reagent dispenser components has a bore diameter b1, 0.003≦
- b1≦
0.018 inches and the other reagent dispenser component has a bore diameter b2, 0.015≦
b2≦
0.030 inches.
- b1≦
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10. The apparatus of claim 1, wherein the pneumatic manifold is interfaced with a microfluidic system having at least one assay capacity.
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11. The apparatus of claim 10, wherein the microfluidic system further comprises a multi-layer, monolithic, polymeric, non-elastomeric microfluidic component having a given configuration of microfeatures including a plurality of pneumatically-activated diaphragms.
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12. The apparatus of claim 11, wherein the pneumatic manifold has a plurality of pneumatic only ports on an underside thereof, and a plurality of pneumatic only channels disposed therein in fluid connection with a plurality of valves in the fluidic transport layer and the plurality of pneumatic only ports, wherein said plurality of pneumatic ports have a fixed configuration, and said plurality of pneumatic only channels have a given configuration specifically corresponding to a given configuration of the plurality of pneumatically-activated diaphragms in the fluidic transport layer.
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13. The apparatus of claim 12, wherein the pneumatic supply system further comprises
a plurality of aperture tubes that provide a passage of the pneumatic signal there through, in fluid connection with said plurality of pneumatic only ports, wherein said plurality of aperture tubes have a fixed configuration specifically corresponding to the fixed configuration of the plurality of pneumatic only ports of the pneumatic manifold, removably connected to the pneumatic manifold. -
14. The apparatus of claim 11, wherein each multi-layer, monolithic microfluidic component further comprises:
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a polymeric, non-elastomeric substrate having a plurality of fluid channels disposed therein, each of the fluid channels having an inlet end and an outlet end; at least one reagent reservoir of a type capable of holding a reagent material; at least one bi-directional diaphragm pump comprising at least three non-elastomeric membrane-based diaphragm valve structures; and a valve disposed in fluid coupling with the at least one reagent reservoir and at least one of the inlet ends, wherein the valve is adapted to controllably direct a flow of the material from the at least one reagent reservoir to a plurality of reservoirs via at least one of the channels coupled to the valve, further wherein each multi-layer, monolithic microfluidic component consists of a non-elastomeric, polymeric material.
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15. The apparatus of claim 14, wherein each substrate further comprises a plurality of analysis reservoirs, each analysis reservoir including an analysis system disposed therein.
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16. The apparatus of claim 14, wherein the analysis system is one of colorimetric, fluorescent colorimetric, chemiluminescent, electrochemical, electrophoretic, lateral flow, protein microarray, nucleic acid microarray, fluorescent.
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17. The apparatus of claim 14, further comprising a securing-ring structure having a plurality of perimeter indentations, wherein the analysis membrane is operatively engaged with the securing-ring structure.
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18. The apparatus of claim 17, wherein the reservoir has at least a partial inner perimetal shelf upon which the analysis membrane is disposed.
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19. The apparatus of claim 17, wherein the securing-ring structure comprises two opposing ring structures each having a plurality of perimeter indentations, further wherein the analysis membrane is disposed intermediate the two opposing ring structures.
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20. The apparatus of claim 15, further comprising a heater.
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21. The apparatus of claim 20, wherein the heater is disposed in heating proximity to a heatable, magnetically engageable reservoir.
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22. The apparatus of claim 14, further comprising:
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a lumen mounting layer attached to a bottom surface of the substrate including a plurality of lumens each having a proximal end that is fluidly connected to a respective fluidic channel and a distal end projecting downwardly perpendicularly from the substrate; and a respective plurality of amplification/reaction chambers attached at a top region thereof to the tube mounting layer such that the distal end of each tube is disposed substantially near a bottom region thereof.
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23. The apparatus of claim 22, further comprising a heater for elevating a temperature in each of the amplification/reaction chambers.
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24. The apparatus of claim 11, further comprising a magnetic assembly operably disposed under a reservoir or channel, wherein the magnetic assembly further comprises a magnet, a magnet holder, a piston rod, and a pneumatic piston assembly (alternatively the piston assembly may be motor or electromagnetically activated).
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25. The apparatus of claim 24, further comprising a heater assembly operably connected to the magnetic assembly.
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26. An automated process for isolating, amplifying, and analyzing a target nucleic acid sequence that may be present in a fluid test sample, comprising:
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providing a pneumatic manifold that operates a microfluidic system having a fluidic transport layer and a fluidic channel disposed therein, and reservoirs attached thereto; introducing the fluid test sample into the fluidic channel; providing at least one reagent to the channel from at least one respective reservoir that is in fluid connection with the fluidic transport layer; combining the fluid test sample and the at least one reagent in a region of the fluidic transport layer, reservoir or amplification reactor; transporting the fluid test sample to a temperature-controlled amplification/reaction reactor that is in operative communication with the fluidic transport layer; incubating the fluid test sample in the amplification/reaction reactor under conditions sufficient to permit the target nucleic acid sequence to be amplified; transporting the fluid test sample to an analysis reservoir; and analyzing the amplified target nucleic acid sequence from the test sample, wherein the test sample is transported from a starting location in the fluidic transport layer to the analysis reservoir separately from any other samples and separately from the pneumatic manifold and the dispensing system. - View Dependent Claims (27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39)
sensitivity to a drug, pharmaceutical composition, chemical or compound of interest.
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Specification