Microfluidic device and method for transporting electrically charged substances through a microchannel of a microfluidic device

• US 20050161327A1
• Filed: 12/20/2004
• Published: 07/28/2005
• Est. Priority Date: 12/23/2003
• Status: Abandoned Application

• Current Assignee: STMicroelectronics SRL (STMicroelectronics NV)
• Original Assignee: STMicroelectronics SRL (STMicroelectronics NV)
• Inventors: Palmieri, Michele
• Application Number:
  US11/017,272
• Publication Number:
  US 20050161327A1
• Time in Patent Office: Days
• US Class Current: 204/450
• CPC Class Codes: B01L 2300/087 Multiple sequential chambers
• CPC Class Codes: B01L 2400/0424 Dielectrophoretic forces
• CPC Class Codes: B01L 2400/0496 Travelling waves, e.g. in combination with electrical or acoustic forces
• CPC Class Codes: B01L 3/50273 characterised by the means or forces applied to move the fluids micropumps F04B19/006, of the membrane type F04B43/043
• CPC Class Codes: B01L 7/52 with provision for submitting samples to a predetermined sequence of different temperatures, e.g. for treating nucleic acid samples amplification or hybridisation processes per se C12Q1/68; controlling sequential reactions for synthesis B01J19/0046
• CPC Class Codes: B03C 5/022 Non-uniform field separators
• CPC Class Codes: F04B 19/006 Micropumps F04B43/043 and F04B43/095 take precedence

Abstract

A microfluidic device includes an inlet reservoir, for receiving electrically charged substances dispersed in a fluid medium, a microfluidic circuit in fluidic connection with the inlet reservoir, and an electric transport device for moving the electrically charged substances along the microfluidic circuit. The electric transport device comprises a number of conductive regions arranged along the microfluidic circuit and separated by regions of opposite type, said regions of conductivity electrically connected to a voltage source for providing pulsed voltage that carries charged substances along the microfluidic circuit.

Claims

1. ) A microfluidic device, comprising an inlet reservoir, for receiving electrically charged substances dispersed in a fluid medium, and a microfluidic circuit fluidly coupled to said inlet reservoir, characterized in that it comprises an electric transport device, arranged along said microfluidic circuit for moving said electrically charged substances along said microfluidic circuit away from said inlet reservoir.

2. ) The microfluidic device of claim 1, wherein said electric transport device comprises at least three conductive regions, arranged adjacent along said microfluidic circuit, and periodic biasing means for periodically biasing said conductive regions according to a predetermined sequence.

3. ) The microfluidic device of claim 2, wherein said periodic biasing means comprises a voltage source, having a number N of outputs and periodically supplying N voltage pulses having different amplitudes on said outputs, such that voltage levels on said outputs are phase-shifted with respect to each other.

4. ) The microfluidic device of claim 3, wherein each of said outputs is connected to one conductive region every N and immediately adjacent conductive regions are connected to different outputs.

5. ) The microfluidic device of claim 4, wherein immediately adjacent conductive regions are connected to outputs providing voltage pulses which are phase-shifted 360°

/N.

6. ) The microfluidic device of claim 5, wherein the voltage levels on said outputs are uniformly phase-shifted.

7. ) The microfluidic device of claim 6, wherein said microfluidic circuit is housed in a semiconductor chip and is upwardly delimited by an epitaxial layer having a first type of conductivity, and wherein said conductive regions extend through said epitaxial layer and have a second type of conductivity, opposite to said first type of conductivity.

13. ) A method of performing a biological test, wherein a biological fluid is applied to the integrated microreactor of claim 7 and a biological test is performed.

14. ) A method of claim 13, wherein the biological test is amplification.

15. ) A method of claim 14, wherein the amplification is DNA amplification.

8. ) A method for moving electrically charged substances dispersed in a fluid medium through a microfluidic circuit of a microfluidic device, comprising the step of providing an electric field within said microfluidic circuit, a component of said electric field being directed substantially parallel to an axis of said microfluidic circuit and having uniform orientation at least in a region of said a microfluidic circuit.

9. ) A method of claim 8, further comprising the step of shifting said electric field along said microfluidic circuit.

10. ) A method of claim 9, wherein said step of providing an electric field comprises establishing a non-uniform voltage distribution within said microfluidic circuit, said non-uniform voltage distribution being periodic in time and in space, along said microfluidic circuit.

11. ) A method of claim 10, wherein said step of establishing a non-uniform voltage distribution comprises periodically providing a number N of voltage pulses at space intervals along said microfluidic circuit, according to a predetermined sequence.

12. ) A method of claim 11, wherein said step of periodically providing a number N of voltage pulses comprises periodically providing said voltage pulses to at least three conductive regions arranged adjacent along said microfluidic circuit and spaced apart by said space intervals, such that immediately adjacent conductive regions receive said voltage pulses with a phase-shift of 360°

/N.

16. ) A microfluidic device, comprising:

a) a semiconductor body;

b) an inlet reservoir in said semiconductor body, for receiving a biological sample including an electrically charged molecule;

c) a detection chamber in said semiconductor body;

d) a microfluidic circuit fluidly coupled to said inlet reservoir and to said detection chamber and including one or more processing chambers;

e) an electric transport device comprising a plurality of conductive regions arranged sequentially and adjacent said microfluidic circuit;

f) a voltage source electrically connected to said conductive regions for providing a pulsed voltage to move said electrically charged molecule along said microfluidic circuit.

17. ) The microfluidic device of claim 16, wherein said processing chambers include an amplification chamber for nucleic acid amplification.

18. ) The microfluidic device of claim 17, comprising heating elements and a temperature sensor associated with said amplification chamber, wherein said heating elements are connected to an external power source heating said biological sample in said amplification chamber.

19. ) The microfluidic device according to claim 18, wherein said detection chamber includes an array of probes for nucleic acid detection.

20. ) The microfluidic device according to claim 19, wherein said microfluidic circuit includes a microchannel buried in said semiconductor body.

21. ) The microfluidic device according to claim 16, wherein said conductive regions are spaced apart from each other by a distance which is approximately equal to a depth of said microfluidic circuit.

22. ) The microfluidic device according to claim 16, wherein said conductive regions are spaced apart from each other by at least 2 μ

m.

23. ) The microfluidic device according to claim 22, wherein said distance is at least 10 μ

m.