Biochip and fabrication thereof

• US 20130315782A1
• Filed: 11/08/2012
• Published: 11/28/2013
• Est. Priority Date: 11/08/2011
• Status: Abandoned Application

• Current Assignee: Jung-Tang Huang
• Original Assignee: Jung-Tang Huang
• Inventors: HUANG, JUNG-TANG
• Application Number:
  US13/671,644
• Publication Number:
  US 20130315782A1
• Time in Patent Office: Days
• US Class Current: 422/69
• CPC Class Codes: B01L 2300/0645 Electrodes
• CPC Class Codes: B01L 2300/0816 Cards, e.g. flat sample carriers usually with flow in two horizontal directions
• CPC Class Codes: B01L 2400/0406 capillary forces
• CPC Class Codes: B01L 3/502715 characterised by interfacing components, e.g. fluidic, electrical, optical or mechanical interfaces
• CPC Class Codes: B81C 1/00015 for manufacturing microsystems
• CPC Class Codes: G01N 27/00 Investigating or analysing materials by the use of electric, electrochemical, or magnetic means G01N3/00 – G01N25/00 take precedence; measurement or testing of electric or magnetic variables or of electric or magnetic properties of materials G01R
• CPC Class Codes: G01N 27/128 Microapparatus
• CPC Class Codes: G01N 33/487 of liquid biological material
• CPC Class Codes: H01L 23/31 characterised by the arrangement or shape
• CPC Class Codes: H01L 2924/00 Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
• CPC Class Codes: H01L 2924/0002 Not covered by any one of groups H01L24/00, H01L24/00 and H01L2224/00

Abstract

A biochip comprising a plastic substrate, an IC chip, and a sealing cover is disclosed in this invention. The plastic substrate combines the function of sample inlet area, separating structure, micro-fluidic channel, flow resistor, detection area, and capillary pump or suction area. Sealing the plastic substrate with porous cover could make the structure of micro-fluidic to form the capillary effect or degas-driven effect, and drive the sample naturally without extra pump. The detection area is constituted by the IC chip which is embedded into the plastic substrate, and the IC chip includes the amplifier circuit and detection structure. In the detection area, there uses the biological specific conjugates to catch the bio-particles, nano-particles, or macromolecule sensitively. And finally, transfer the detected electric signal to a mobile communication device.

Claims

1. A biochip, comprising:

a plastic substrate, having a variety of microfluidic structures, including at least a inlet region of the fluid sample, a separation structure, a mixer structure, a detection zone groove, a capillary pump or suction area, outlet, therebetween are connected by microfluidic channels;

further at the edge of the plastic substrate golden fingers are set and extended with convergent spacing to the edge of the detection zone groove;

at least one integrated circuit (IC) chip is embedded in the detection zone groove of the plastic substrate, the IC chip has at least one detection structure, which is modified by using biological conjugates;

each detection structure measures nanoscale particles or biopolymers in the fluid sample with high specificity and sensitivity;

the I/O pads of the IC chip are wire bonded to the corresponding golden fingers on the edge of the plastic substrate detection zone groove to obtain the external power source and output a detection signal to the outside;

a sealing cover made of Polydimethyisiloxane (PDMS) or porous polymer is used to seal the plastic substrate embedded with the IC chip into the biochip, the bottom side of the sealing cover thereof corresponding to the test structure of the IC chip has a microfluidic channel, which is leakage-free connected to input/output port of the microfluidic channel on the plastic substrate;

the fluid sample in the tubular microfluidic channel of the biochip moves by degas-driven flow or capillary flow through test structures at the IC chip without leakage.

2. The biochip according claim 1 wherein the nano sensing material is selected from the group consists of carbon nanotubes, silicon nanowire, InP nanowire, GaN nanowire or semiconductor nanowire, graphene or nanometer semiconductor film.

3. The biochip according claim 1 wherein the defection structure is based on electrical sensing mechanism selected from the group consists of resistor-type, capacitor-type, or transistor-type.

4. The biochip according claim 1 wherein the biological conjugates are selected from the group consists of antibodies, aptamers, carbohydrates, and their combinations,

5. The biochip according claim 1 wherein the fluid sample is body fluid, selected from the group consist of blood, cerebrospinal fluid, gastric juice, a variety of digestive juices, semen, saliva, tears, sweat, urine, vaginal fluids, or a solution containing the specimen.

6. The biochip according claim 1 wherein the top sides of the sealing cover is further deposited with a layer of airtight polymer or material, which enhances the reliability of the degas-driven flow.

7. The biochip according claim 1 wherein, a reader is further added for catching the detected signal from the biochip, the reader is separated into two part:

one is a mobile communication device;

the other is a signal processing device connected to the golden fingers on the edges of the plastic substrate of the biochip;

the signal processing device comprising a microcontroller (μ

C), analog-to-digital converter (ADC);

through a USB interface the mobile communication device provides power to the signal processing device and the IC chip and read the detection signal;

after analog to digital conversion, the digitized signal is displayed as the detected concentration in the mobile communication device, and achieve the point-of-care diagnosis.

8. The biochip according claim 1 wherein a reader is further added for catching the detected signal from the biochip;

the reader is separated into two parts;

one is a mobile communication device;

the other is a signal processing device connected to the golden fingers on the edges of the plastic substrate of the biochip;

the signal processing device includes a multiplexer, a current amplifier, a microcontroller (μ

C), power supply (battery), further adding a wireless communication module;

the signals of sensing elements on the biochip are scanned and amplified, and transmitted through the wireless communication module to the mobile communications device.

9. A method for fabricating a biochip consisting of a plastic substrate, an IC chip, and a sealing cover, comprising;

step 1, the IC chip is directly embedded into the plastic substrate with the insert mold injection method by letting the detection area of embedded IC chip be faced downward;

the plastic substrate containing a variety of microfluidic structures;

the IC chip before inserting has already contained nano-sensing materials deposited on its detection structures;

step 2, clean the injection-molded microfluidic channel on the plastic substrate and modify the surface of the overall plastic substrate into hydrophilic condition;

step 3, following embedded IC chip in step 2 a precision dispenser dispatches and immobilizes biological conjugates onto nano-sensing materials;

step 4, cover and bond the sealing cover with the plastic substrate by the aid of alignment holes on the sealing cover and the alignment pins on the plastic substrate;

step 5, the IC chip is wire bonded, to the plastic substrate and then dispensed with glue to protect the bonding wires, which completes fabrication of the biochip;

step 6, the fabricated biochip is loaded into a vacuum bag for further vacuum packaging.

10. The method according claim 9 wherein the nano-sensing material is selected from the group consists of carbon nanotubes, silicon nanowire, InP nanowire, GaN nanowire or semiconductor nanowire, graphene or nanometer semiconductor film.

11. The fabrication method according claim 9 wherein the detection structure is based on electrical sensing mechanism selected from the group consists of resistor-type. capacitor-type, or transistor-type.

12. The method according claim 9 wherein the biological conjugates are selected from the group consists of antibodies, aptamers, carbohydrates, and their combinations.

13. The method according claim 9 wherein the sealing cover is made of Polydimethylsiloxane (PDMS) or porous polymer.