|
|  Get related patents on CD |
| United States Patent | 5922591 |
| Link to this page | http://www.wikipatents.com/5922591.html |
| Inventor(s) | Anderson; Rolfe C. (Mountain View, CA);
Lipshutz; Robert J. (Palo Alto, CA);
Rava; Richard P. (San Jose, CA);
Fodor; Stephen P. A. (Palo Alto, CA) |
| Abstract | The present invention provides a miniaturized integrated nucleic acid
diagnostic device and system. The device of the invention is generally
capable of performing one or more sample acquisition and preparation
operations, in combination with one or more sample analysis operations.
For example, the device can integrate several or all of the operations
involved in sample acquisition and storage, sample preparation and sample
analysis, within a single integrated unit. The device is useful in a
variety of applications, and most notably, nucleic acid based diagnostic
applications and de novo sequencing applications. |
| |
|
Title Information  |
|
|
|
|
|
Drawing from US Patent 5922591 |
|
|
Integrated nucleic acid diagnostic device |
|
|
|
|
|
| Publication Date |
July 13, 1999 |
|
|
|
|
|
| Filing Date |
June 27, 1996 |
|
|
|
|
|
|
|
|
|
|
|
| Parent Case |
CROSS REFERENCE TO RELATED APPLICATIONS
The present application is a regular application claiming priority from
Provisional U.S. patent application Ser. No. 60/000,703, filed Jun. 29,
1995, and Provisional U.S. patent application Ser. No. 60/000859, filed
Jul. 3, 1995. This application is also a continuation-in-part of U.S.
patent application Ser. No. 08/589,027, filed Jan. 19, 1996, now U.S. Pat.
No. 5,856,174. Each of these applications is incorporated herein by
reference in its entirety for all purposes. |
|
|
|
|
|
|
|
|
|
|
|
|
|
Title Information  |
|
|
References  |
|
|
| *references marked with an asterisk below are user-added references |
|
U.S. References |
|
|
| Add a new US reference: |
| | Reference | Relevancy | Comments | Reference | Relevancy | Comments | 5700637 Southern 435/6 Dec,1997 |      Your vote accepted [0 after 0 votes] | | 5660993 Cathey 435/7.9 Aug,1997 |      Your vote accepted [0 after 0 votes] | | 5653939 Hollis 422/50 Aug,1997 |      Your vote accepted [0 after 0 votes] | | 5593130 Hansson 251/61.1 Jan,1997 |      Your vote accepted [0 after 0 votes] | | 5589350 Bochner 435/29 Dec,1996 |      Your vote accepted [0 after 0 votes] | | 5587128 Wilding 422/50 Dec,1996 |      Your vote accepted [0 after 0 votes] | | 5498392 Wilding 422/68.1 Mar,1996 |      Your vote accepted [0 after 0 votes] | | 5486335 Wilding 422/55 Jan,1996 |      Your vote accepted [0 after 0 votes] | | 5436129 Stapleton 435/6 Jul,1995 |      Your vote accepted [0 after 0 votes] | | 5424186 Fodor 435/6 Jun,1995 |      Your vote accepted [0 after 0 votes] | | 5384261 Winkler 436/518 Jan,1995 |      Your vote accepted [0 after 0 votes] | | 5382511 Stapleton 435/6 Jan,1995 |      Your vote accepted [0 after 0 votes] | | 5375979 Trah 417/52 Dec,1994 |      Your vote accepted [0 after 0 votes] | | 5346672 Stapleton 422/102 Sep,1994 |      Your vote accepted [0 after 0 votes] | | 5313264 Ivarsson 356/73 May,1994 |      Your vote accepted [0 after 0 votes] | | 5304487 Wilding 435/29 Apr,1994 |      Your vote accepted [0 after 0 votes] | | 5296375 Kricka
Mar,1994 |      Your vote accepted [0 after 0 votes] | | 5281516 Stapleton 435/3 Jan,1994 |      Your vote accepted [0 after 0 votes] | | 5277556 van Lintel 417/413.2 Jan,1994 |      Your vote accepted [0 after 0 votes] | | 5271724 van Lintel 417/413.2 Dec,1993 |      Your vote accepted [0 after 0 votes] | | 5252294 Kroy 422/102 Oct,1993 |      Your vote accepted [0 after 0 votes] | | 5230866 Shartle 422/103 Jul,1993 |      Your vote accepted [0 after 0 votes] | | 5188963 Stapleton 435/288.3 Feb,1993 |      Your vote accepted [0 after 0 votes] | | 5171132 Miyazaki 417/413.1 Dec,1992 |      Your vote accepted [0 after 0 votes] | | 5143854 Pirrung 436/518 Sep,1992 |      Your vote accepted [0 after 0 votes] | | 5126022 Soane 204/458 Jun,1992 |      Your vote accepted [0 after 0 votes] | | 4426451 Columbus 436/518 Dec,1969 |      Your vote accepted [0 after 0 votes] | | 5451500 Stapleton 435/6 Dec,1969 |      Your vote accepted [0 after 0 votes] | | |
|
|
|
|
U.S. References |
|
|
Foreign References |
|
|
|
|
|
|
Foreign References |
|
|
Other References |
|
|
|
|
|
|
Other References |
|
|
|
|
|
References  |
|
|
Claims  |
|
|
What is claimed is:
1. A miniature fluidic system, comprising:
a body having at least two discrete reaction chambers, each of said
reaction chambers comprising at least one vent port, and wherein each of
said reaction chambers is fluidly connected to a common chamber or channel
by a fluidic inlet having a controllable diaphragm valve disposed
thereacross; and
a pneumatic system for selectively applying a pressure differential between
said common channel or chamber and at least a selected one of said at
least two discrete chambers, whereby said pressure differential directs a
fluid sample in said body between said common channel or chamber and said
at least one selected chamber.
2. The system of claim 1, wherein said vent port comprises a gas permeable
fluid barrier disposed across said vent port.
3. The system of claim 2, wherein said gas permeable fluid barrier is a
hydrophobic membrane.
4. The system of claim 1, wherein at least one of said at least two
chambers is a debubbling chamber, said debubbling chamber comprising at
least two vent ports, one of said at least two vent ports being disposed
at an intermediate position in said chamber, whereby a bubble separating
at least two discrete fluid plugs in said chamber may exit said chamber
allowing said at least two discrete fluid plugs to connect.
5. The system of claim 1, wherein said pneumatic system is further capable
of applying a pressure differential to said diaphragm valve to deflect
said diaphragm valve.
6. The system of claim 5, wherein deflection of said diaphragm valve opens
said fluid connection.
7. The system of claim 1, wherein each of said chambers has a cross
sectional dimension of from about 0.05 to about 20 mm, and a depth
dimension of from about 0.05 to about 5 mm.
8. The system of claim 1, wherein said at least two chambers are fluidly
connected via a fluid passage, said fluid passage having a cross-sectional
dimension of from about 10 .mu.m to about 1000 .mu.m, and a depth
dimension of from about 1 to 500 .mu.m.
9. The system of claim 1, wherein said pneumatic system comprises a
pneumatic manifold for applying a differential pressure between said at
least first chamber and said at least second chamber, to move said fluid
sample from said at least first chamber to said at least second chamber.
10. The system of claim 1, wherein said pneumatic system comprises a
differential pressure delivery system for maintaining said at least first
chamber at a first pressure and said second chamber at a second pressure,
said first pressure being greater than ambient pressure and said second
pressure being greater than said first pressure, whereby when said second
chamber is brought to ambient pressure, said first pressure forces a
liquid sample in said first chamber into said second chamber.
11. The system of claim 10 wherein said differential pressure delivery
system comprises:
a pressure source;
at least first and second passages fluidly connecting said pressure source
to said at least first and second chambers, respectively;
a first fluidic resistance disposed in said first passage between said
pressure source and said first chamber, said first fluidic resistance
transforming a pressure from said pressure source to said first pressure;
a second fluidic resistance disposed in said second passage between said
pressure source and said second chamber, said second fluidic resistance
transforming said pressure from said pressure source to said second
pressure; and
first and second openable closures in said first and second chambers,
respectively, whereby opening of said first or second closures allows said
first or second chambers to achieve ambient pressure.
12. The miniature system of claim 11, wherein said first and second fluidic
resistances independently comprise one or more fluid passages connecting
said first and second passages to said first and second chambers, said
first fludic reistance having a smaller cross-sectional area than said
second fluidic resistance.
13. The system of claim 1, wherein said pneumatic system comprises a
differential pressure delivery system for maintaining said first chamber
at a first pressure and said second chamber at a second pressure, said
second pressure being less than ambient pressure and said first pressure
being less than said second pressure, whereby when said first chamber is
brought to ambient pressure, said second pressure draws a liquid sample in
said first chamber into said second chamber.
14. The system of claim 13, wherein said differential pressure delivery
system comprises:
a pressure source;
at least first and second passages fluidly connecting said pressure source
to said at least first and second chambers, respectively;
a first fluidic resistance disposed in said first passage between said
pressure source and said first chamber, said first fluidic resistance
transforming a pressure from said pressure source to said first pressure;
a second fluidic resistance disposed in said second passage between said
pressure source and said second chamber, said second fluidic resistance
transforming said pressure from said pressure source to said second
pressure; and
first and second openable closures in said first and second chambers,
respectively, whereby opening of said first or second closures allows said
first or second chambers to achieve ambient pressure.
15. The system of claim 14, wherein said first and second fluidic
resistances independently comprise one or more fluid passages connecting
said first and second passages to said first and second chambers, said
first fludic reistance having a larger cross-sectional area than said
second fluidic resistance.
16. The system of claim 1, wherein said system further includes a
temperature controller disposed adjacent at least one of said at least two
chambers, for controlling a temperature within said at least one chamber.
17. The system of claim 16, wherein said temperature controller comprises a
thermoelectric temperature controller.
18. The system of claim 16, wherein said temperature controller comprises a
resistive heater.
19. The system of claim 18, wherein said resistive heating element is a
NiCr/polyimide/copper laminate heating element.
20. The system of claim 16, further comprising a temperature sensor
disposed within said temperature controlled chamber.
21. The system of claim 20, wherein said temperature sensor is a
thermocouple.
22. The system of claim 20, wherein said temperature sensor is a resistance
thermometer.
23. The system of claim 1, wherein at least one of said at least two
chambers is a cell lysis chamber and comprises a cell lysis system
disposed therein, for lysing cells in a fluid sample.
24. The system of claim 23, wherein said cell lysis system comprises an
acoustic energy source disposed adjacent said cell lysis chamber.
25. The system of claim 23, wherein said cell lysis chamber includes
microstructures fabricated on an internal surface of said cell lysis
chamber for enhancing cell lysis.
26. The system of claim 23, wherein said cell lysis chamber includes an
electrolytic pH control system for altering a pH of said cell lysis
chamber.
27. The system of claim 1, wherein at least one of said at least two
chambers is a hybridization chamber for analyzing a component of a fluid
sample, said hybridization chamber including a polymer array, said polymer
array including a plurality of different polymer sequences coupled to a
surface of a single substrate, each of said plurality of different polymer
sequences being coupled to said surface in a different, known location.
28. The system of claim 27, wherein said polymer array comprises at least
100 different polymer sequences coupled to said surface of said single
substrate, each of said plurality of different polymer sequences being
coupled to said surface in a different, known location.
29. The system of claim 27, wherein said polymer array comprises at least
1000 different polymer sequences coupled to said surface of said single
substrate, each of said plurality of different polymer sequences being
coupled to said surface in a different, known location.
30. The system of claim 27, wherein said polymer array comprises at least
10,000 different polymer sequences coupled to said surface of said single
substrate, each of said plurality of different polymer sequences being
coupled to said surface in a different, known location.
31. The system of claim 1, wherein at least one of said at least two
chambers comprises a nucleic acid amplification system.
32. The system of claim 31, wherein said nucleic acid amplification
includes a system for cycling a fluid sample in said at least one chamber
between at least two different temperatures.
33. The system of claim 32, wherein said system for cycling comprises at
least two separate temperature controlled chambers, said at least two
chambers being maintained at at least two different temperatures, whereby
said sample is cycled between said at least two temperatures by moving
said fluid sample back and forth between said at least two temperature
controlled chambers.
34. The system of claim 1, wherein at least one of said at least two
chambers comprises a nucleic acid purification system for separating
nucleic acids in said sample from other contaminants in said sample.
35. The system of claim 34, wherein said nucleic acid purification system
comprises a separation matrix for separating said nucleic acids from said
contaminants.
36. The system of claim 35, wherein said separation matrix comprises
functional groups for preferentially binding said nucleic acids in said
sample.
37. The system of claim 36, wherein said functional groups comprise poly-T
oligonucleotides.
38. The system of claim 35, wherein said nucleic acid purification system
further comprises an electrophoretic system for applying an electric field
to said fluid sample to separate said nucleic acids from said
contaminants.
39. The system of claim 35, wherein said separation matrix comprises a gel
matrix.
40. The system of claim 35, wherein said separation matrix comprises a
membrane disposed between said sample and an anode of said electrophoretic
system.
41. The system of claim 1, wherein at least one of said at least two
chambers is a reverse transcription chamber, said reverse transcription
chamber having disposed therein an effective amount of a reverse
transcriptase enzyme and the at least four deoxynucleoside triphosphates.
42. The system of claim 1, wherein at least one of said at least two
chambers is an in vitro transcription chamber, said in vitro transcription
chamber having an effective amount of an RNA polymerase and at least four
different nucleoside triphosphates, disposed therein.
43. The system of claim 1, wherein at least one of said at least two
chambers comprises a nucleic acid fragmentation system, for fragmenting a
nucleic acid in a fluid sample.
44. The system of claim 43, wherein said fragmentation system comprises a
focused piezoelectric element disposed adjacent said fragmentation
chamber.
45. The system of claim 44, wherein said fragmentation system further
comprises a series of microstructures fabricated on a first surface of
said chamber.
46. The system of claim 43, wherein said fragmentation system comprises at
least one channel through which said fluid sample is pumped, said channel
having a submicron cross-sectional dimension for generating a high-shear
rate.
47. The system of claim 1, further comprising a fluid mixing system for
mixing said fluid sample within at least one of said at least two
chambers.
48. The system of claim 47, wherein said fluid mixing system comprises a
piezoelectric element disposed adjacent at least one of said at least two
chambers.
49. The system of claim 47, wherein said fluid mixing system comprises a
separate chamber adjacent to and fluidly connected to said at least one of
said at least two chambers, whereby said fluid sample is flowed between
said at least one chamber and said separate chamber to mix said fluid
sample.
50. The system of claim 47, wherein said mixing system comprises:
a plurality of metallic particles disposed within said at least one
chamber;
an electromagnetic field generator adjacent said at least one chamber,
whereby when said electromagnetic field generator is activated, said
metallic particles are vibrated within said at least one chamber mixing
contents of said chamber.
51. The system of claim 47, wherein said mixing system mixes a fluid sample
contained in a hybridization chamber.
52. A miniature fluidic system, comprising:
a body having at least first and second chambers disposed therein, at least
one of said first and second chambers having a vent port with a gas/liquid
separator disposed thereacross, each of said at least first and second
chambers having a fluid inlet with a controllable diaphragm valve disposed
thereacross, said at least first and second chambers being in fluid
connection, and at least one of said at least first and second chamber
being a hybridization chamber for analyzing a component of a fluid sample,
said hybridization chamber including a polymer array, said polymer array
including a plurality of different polymer sequences coupled to a surface
of a single substrate, each of said plurality of different polymer
sequences being coupled to said surface in a different, known location;
a sample inlet, fluidly connected to at least one of said first and second
chambers, for introducing a fluid sample into said system;
a fluid transport system for moving a fluid sample from said at least first
chamber to said at least second chamber.
53. The system of claim 52, wherein said polymer array comprises at least
100 different polymer sequences coupled to said surface of said single
substrate, each of said plurality of different polymer sequences being
coupled to said surface in a different, known location.
54. The system of claim 52, wherein said polymer array comprises at least
1000 different polymer sequences coupled to said surface of said single
substrate, each of said plurality of different polymer sequences being
coupled to said surface in a different, known location.
55. The system of claim 52, wherein said polymer array comprises at least
10,000 different polymer sequences coupled to said surface of said single
substrate, each of said plurality of different polymer sequences being
coupled to said surface in a different, known location.
56. The system of claim 52, wherein said body further comprises a
transparent region disposed over said hybridization chamber for detecting
hybridization of a component of said fluid sample to said polymer array.
57. The system of claim 52, wherein said fluid transport system comprises a
micropump disposed in said body and fluidly connected to at least one of
said plurality of chambers.
58. The system of claim 57, wherein said micropump comprises an
electrophoretic pump. |
|
|
|
|
Claims  |
|
|
Description  |
|
|
BACKGROUND OF THE INVENTION
The relationship between structure and function of macromolecules is of
fundamental importance in the understanding of biological systems. These
relationships are important to understanding, for example, the functions
of enzymes, structure of signalling proteins, ways in which cells
communicate with each other, as well as mechanisms of cellular control and
metabolic feedback.
Genetic information is critical in continuation of life processes. Life is
substantially informationally based and its genetic content controls the
growth and reproduction of the organism. The amino acid sequences of
polypeptides, which are critical features of all living systems, are
encoded by the genetic material of the cell. Further, the properties of
these polypeptides, e.g., as enzymes, functional proteins, and structural
proteins, are determined by the sequence of amino acids which make them
up. As structure and function are integrally related, many biological
functions may be explained by elucidating the underlying structural
features which provide those functions, and these structures are
determined by the underlying genetic information in the form of
polynucleotide sequences. In addition to encoding polypeptides,
polynucleotide sequences can also be specifically involved in, for
example, the control and regulation of gene expression.
The study of this genetic information has proved to be of great value in
providing a better understanding of life processes, as well as diagnosing
and treating a large number of disorders. In particular, disorders which
are caused by mutations, deletions or repeats in specific portions of the
genome, may be readily diagnosed and/or treated using genetic techniques.
Similarly, disorders caused by external agents may be diagnosed by
detecting the presence of genetic material which is unique to the external
agent, e.g., bacterial or viral DNA.
While current genetic methods are generally capable of identifying these
genetic sequences, such methods generally rely on a multiplicity of
distinct processes to elucidate the nucleic acid sequences, with each
process introducing a potential for error into the overall process. These
processes also draw from a large number of distinct disciplines, including
chemistry, molecular biology, medicine and others. It would therefore be
desirable to integrate the various process used in genetic diagnosis, in a
single process, at a minimum cost, and with a maximum ease of operation.
Interest has been growing in the fabrication of microfluidic devices.
Typi | | |