|
|
|
| United States Patent | 5965410 |
| Link to this page | http://www.wikipatents.com/5965410.html |
| Inventor(s) | Chow; Calvin Y. H. (Portola Valley, CA), Kopf-Sill; Anne R. (Portola Valley, CA), Parce; J. Wallace (Palo Alto, CA) |
| Abstract | A novel method and device for transporting and/or monitoring a fluid in a
multi-port device 400, 800, 1000 used in a microfluidic system is
provided. The multi-port device includes a substrate having a novel
channel configuration. A first channel region 413 having a first port and
a second port for transporting fluid therebetween is defined in the
substrate. A second channel region 421 having a first port and a second
port for applying electric current for heating fluid or for monitoring a
fluid parameter therebetween is also defined in the substrate. In some
embodiments, the first channel intersects 407 with the second channel. The
heating or monitoring aspect of the invention can be used with a variety
of biological reactions such as PCR, LCR, and others. |
|
|
|
Title Information  |
|
|
|
|
|
Drawing from US Patent 5965410 |
|
|
Electrical current for controlling fluid parameters in microchannels |
|
|
|
|
|
| Publication Date |
October 12, 1999 |
|
|
|
|
|
| Filing Date |
November 25, 1997 |
|
|
|
|
|
|
|
|
|
|
|
| Parent Case |
This application claims the benefit of U.S. Provisional Application No.
60/056,058, filed Sep. 2, 1997, which 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 | 5810985 Bao et al.
Sep,1998 |      Your vote accepted [0 after 0 votes] | | 5800690 Chow et al.
Sep,1998 |      Your vote accepted [0 after 0 votes] | | 5779868 Parce et al.
Jul,1998 |      Your vote accepted [0 after 0 votes] | | 5699157 Parce
Dec,1997 |      Your vote accepted [0 after 0 votes] | | 5674742 Northrup et al.
Oct,1997 |      Your vote accepted [0 after 0 votes] | | 5646039 Northrup et al.
Jul,1997 |      Your vote accepted [0 after 0 votes] | | 5639423 Northrup et al.
Jun,1997 |      Your vote accepted [0 after 0 votes] | | 5641400 Kaltenbach et al.
Jun,1997 |      Your vote accepted [0 after 0 votes] | | 5637469 Wilding et al.
Jun,1997 |      Your vote accepted [0 after 0 votes] | | 5607832 Stanley et al.
Mar,1997 |      Your vote accepted [0 after 0 votes] | | 5603351 Cherukuri et al.
Feb,1997 |      Your vote accepted [0 after 0 votes] | | 5585069 Zanzucchi et al.
Dec,1996 |      Your vote accepted [0 after 0 votes] | | 5589136 Northrup et al.
Dec,1996 |      Your vote accepted [0 after 0 votes] | | 5587128 Wilding et al.
Dec,1996 |      Your vote accepted [0 after 0 votes] | | 5571410 Swedberg et al.
Nov,1996 |      Your vote accepted [0 after 0 votes] | | 5527670 Stanley
Jun,1996 |      Your vote accepted [0 after 0 votes] | | 5529752 Pontis et al.
Jun,1996 |      Your vote accepted [0 after 0 votes] | | 5498392 Wilding et al.
Mar,1996 |      Your vote accepted [0 after 0 votes] | | 5346672 Stapleton et al.
Sep,1994 |      Your vote accepted [0 after 0 votes] | | 5333675 Mullis et al.
Aug,1994 |      Your vote accepted [0 after 0 votes] | | 5281516 Stapleton et al.
Jan,1994 |      Your vote accepted [0 after 0 votes] | | 5270183 Corbett et al.
Dec,1993 |      Your vote accepted [0 after 0 votes] | | 5207886 Lauer et al.
May,1993 |      Your vote accepted [0 after 0 votes] | | 5194133 Clark et al.
Mar,1993 |      Your vote accepted [0 after 0 votes] | | 5176203 Larzul
Jan,1993 |      Your vote accepted [0 after 0 votes] | | 5126022 Soane et al.
Jun,1992 |      Your vote accepted [0 after 0 votes] | | 4965188 Mullis et al.
Oct,1990 |      Your vote accepted [0 after 0 votes] | | 4963498 Hillman et al.
Oct,1990 |      Your vote accepted [0 after 0 votes] | | 4908112 Pace
Mar,1990 |      Your vote accepted [0 after 0 votes] | | 4800159 Mullis et al.
Jan,1989 |      Your vote accepted [0 after 0 votes] | | 4683195 Mullis et al.
Jul,1987 |      Your vote accepted [0 after 0 votes] | | 4683202 Mullis et al.
Jul,1987 |      Your vote accepted [0 after 0 votes] | | 4675300 Zare et al.
Jun,1987 |      Your vote accepted [0 after 0 votes] | | 3987362 McCann et al.
Oct,1976 |      Your vote accepted [0 after 0 votes] | | |
|
|
|
|
U.S. References |
|
|
Foreign References |
|
|
|
|
|
|
Foreign References |
|
|
Other References |
|
|
| Add a new Other reference: |
| Post related web sites and other references in this section |
| | Reference | Relevancy | Comments | Moeller et al Chemistry with Inorganic Qualitative Analysis p. 565, 1980.
. Feb,2007 |      Your vote accepted [0 after 0 votes] | | Dasgupta, P.K. et al., "Electroosmosis: A Reliable Fluid Propulsion System for Flow Injection Analysis," Anal. Chem. 66:1792-1798 (1994).
. Feb,2007 |      Your vote accepted [0 after 0 votes] | | Manz, A. et al., "Electroosmotic pumping and electrophoretic separations for miniaturized chemical analysis systems," J. Micromech. Microeng. 4:257-265 (1994).
. Feb,2007 |      Your vote accepted [0 after 0 votes] | | Ramsey, J.M. et al., "Microfabricated chemical measurement systems," Nature Medicine 1 (10):1093-1096 (1995).
. Feb,2007 |      Your vote accepted [0 after 0 votes] | | Seiler, K. et al., "Electroosomotic Pumping and Valveless Control of Fluid Flow within a Manifold of Capillaries on a Glass Chip," Anal. Chem. 66 (20):3485-3491 (1994).. Feb,2007 |      Your vote accepted [0 after 0 votes] | | |
|
|
|
|
Other References |
|
|
|
|
|
References  |
|
|
|
|
|
| Market Size |
|
Estimate the gross annual revenues of the relevant market
sector:
|
| | |
| |
|
|
| Market Share |
|
Estimate the percentage of the relevant market sector this invention will capture:
|
| | |
| |
|
|
| Reasonable Royalty |
|
What percentage of gross sales should the inventor or assignee be paid?
|
| | |
| |
|
|
|
Public's "Guesstimation" of Royalty Value
|
| Market Size | N/A | [No votes] | | x | Market Share | N/A | [No votes] | | x | Reasonable Royalty | N/A | [No votes] |
| | N/A | |
| |
|
|
|
|
|
|
|
|
|
|
|
|
Market Review  |
|
|
Technical Review  |
|
|
Claims  |
|
|
What is claimed is:
1. A method of elevating temperature in at least a portion of a fluid-filled channel disposed in a substrate, to a selected elevated temperature, comprising:
applying a selectable current through a fluid in the at least a portion of the fluid-filled channel, the portion of the fluid-filled channel having a electrical resistance;
controlling at least one of the selectable current or the electrical resistance to elevate the temperature in the portion of the channel to the selected elevated temperature.
2. The method of claim 1, further comprising transporting a material through at least the portion of the channel to elevate the temperature of the material to the selected elevated temperature.
3. The method of claim 1, wherein the portion of the channel is at least a first portion and the selected elevated temperature is a first selected elevated temperature, and further comprising maintaining at least a second portion of the channel
at a second temperature lower than the first selected elevated temperature.
4. The method of claim 3, further comprising providing the first portion of the channel with a narrowed cross-sectional area relative to the second portion of the channel; and
wherein the controlling step comprises applying a constant current through a fluid in the first and second portions of the channel.
5. The method of claim 3, comprising repeatedly transporting a material between the at least first portion of the channel and the at least second portion of the channel to cycle a temperature of the material between the first selected elevated
temperature and the second temperature.
6. The method of claim 5, wherein the material comprises reagents for performing a nucleic acid amplification reaction.
7. The method of claim 6, wherein the nucleic acid amplification reaction is selected from the group consisting of a polymerase chain reaction and a ligase chain reaction.
8. The method of claim 2, wherein the transporting of the material comprises electrokinetically transporting the material through the at least first portion.
9. The method of claim 8, wherein the selectable current is a first selectable current, and wherein the step of electrokinetically transporting the material comprises applying a second selectable current through the channel to electrokinetically
transport a material along the first channel.
10. The method of claim 9, wherein the first selectable current comprises an alternating current and the second selectable current comprises a direct current.
11. The method of claim 8, wherein electrokinetically transporting the material through the channel comprises electroosmotically transporting the material through the channel.
12. The method of claim 8, wherein electrokinetically transporting the material through the channel comprises electrophoretically transporting the material through the channel.
13. The method of claim 1, wherein the fluid-filled channel is disposed in a substrate, and further comprising the step of maintaining a global temperature of the substrate at a selected level above or below ambient temperature.
14. The method of claim 1, wherein the channel is a first channel, and the applying step comprises:
providing at least a second channel intersecting the first channel at the portion of the first channel; and
applying the first selectable current through the second channel and the portion of the first channel.
15. The method of claim 1, wherein the controlling step further comprises sensing a temperature in the portion of the channel, and increasing or decreasing the selectable current based upon the temperature sensed.
16. The method of claim 15, wherein the sensing step comprises determining a relative electrical resistance through the fluid in the portion of the channel, the relative electrical resistance being indicative of the temperature of the fluid in
at least the portion of the channel.
17. A method of heating fluid in a microfluidic system, said method comprising steps of;
providing a channel having a first end, a second end, and a region defined therebetween, said channel being disposed in a substrate;
providing fluid in said region of said channel;
applying an electric current through said fluid to heat said fluid at said region;
wherein said electric current selectively heats said fluid in said region of said channel while preventing substantial heating of said fluid outside said region.
18. The method of claim 17, wherein said channel is an annular region.
19. The method of claim 17, wherein said current is applied using a voltage bias applied directly to said fluid.
20. The method of claim 19, wherein said voltage bias is applied directly to said fluid using a pair of electrodes.
21. The method of claim 17, wherein said region has a smaller cross-section relative to a cross-section of said channel at said first end.
22. The method of claim 17, wherein said region has a smaller cross-section relative to a cross-section of said channel at said second end.
23. The method of claim 17, wherein said current is DC, AC, or arbitrary.
24. The method of claim 17, wherein said fluid contains materials selected from the group consisting of samples, analytes, buffers and reagents.
25. The method of claim 17, wherein said channel comprises a cross-section ranging from about 0.1 .mu.m to about 500 .mu.m.
26. The method of claim 17, wherein said region is disposed in said substrate adjacent to a second fluid-filled channel disposed in said substrate, but wherein said region is not in direct fluid communication with said second channel.
27. The method of claim 17, further comprising a step of moving said fluid in said channel, said step of moving comprising the steps of applying a voltage bias to said fluid to move said fluid between said first end and said second end.
28. The method of claim 17, wherein said voltage bias is provided by DC.
29. The method of claim 17, wherein said applying step occurs successively to heat and cool said fluid in said region; wherein said applying step selectively heats and cools said fluid in said region of said channel while preventing substantial
heating of said fluid outside said region.
30. The method of claim 29, wherein said fluid comprises a nucleic acid material.
31. The method of claim 29, wherein said steps occur in a nucleic acid amplification process.
32. The method of claim 31, wherein the nucleic acid amplification process is selected from the group consisting of PCR and LCR.
33. A method of controlling temperature of fluid in a channel defined in a substrate of a microfluidic system, said method comprising steps of:
applying an electrical energy source to begin heating said fluid in said channel; and
adjusting a first parameter applied from said electrical energy source to said fluid to provide a relatively constant second parameter in said fluid, wherein said first parameter is current, voltage, power or a combination thereof, and the second
parameter is resistance and conductivity; and
wherein said fluid is heated without substantially increasing a temperature of said substrate.
34. The method of claim 33, wherein said first parameter is voltage.
35. The method of claim 33, wherein said first parameter is electric current.
36. The method of claim 33, wherein said second parameter is conductivity.
37. The method of claim 33, wherein said applying step occurs successively to heat and cool said fluid in said channel.
38. The method of claim 33, wherein said fluid is heated in a portion of said channel. |
|
|
|
|
Claims  |
|
|
Description  |
|
|
BACKGROUND OF THE INVENTION
The present invention generally relates to microfluidic systems. More particularly, the present invention provides a technique, including methods and devices, for providing and controlling heat to fluid in a channel of a microfluidic system in
an efficient manner. Merely by way of example, the invention is applied to a polymerase chain reaction process, commonly termed PCR, but it will be recognized that the invention has a much wider range of applicability. The invention also provides
techniques for monitoring and controlling a variety of process parameters using resistivity and/or conductivity measurements.
There has been a growing interest in the manufacture and use of microfluidic systems for the acquisition of chemical and biochemical information. Techniques commonly associated with the semiconductor electronics industry, such as
photolithography, wet chemical etching, etc., are being used in the fabrication of these microfluidic systems. The term, "microfluidic", refers to a system or device or "chip" having channels and chambers which are generally fabricated at the micron or
submicron scale, e.g., having at least one cross-sectional dimension in the range of from about 0.1 .mu.m to about 500 .mu.m. Early discussions of the use of planar chip technology for the fabrication of microfluidic systems are provided in Manz et al.,
Trends in Anal. Chem. (1990) 10(5):144-149 and Manz et al., Adv. in Chromatog. (1993) 33:1-66, which describe the fabrication of such fluidic devices and particularly microcapillary devices, in silicon and glass substrates.
Applications of microfluidic systems are myriad. For example, International Patent Appln. WO 96/04547, published Feb. 15, 1996, describes the use of microfluidic systems for capillary electrophoresis, liquid chromatography, flow injection
analysis, and chemical reaction and synthesis. U.S. Appln. No. 08/671,987, entitled "HIGH THROUGHPUT SCREENING ASSAY SYSTEMS IN MICROSCALE FLUIDIC DEVICES", filed o | | |