Self-contained microfluidic biochip and apparatus

a microfluidic biochip and microfluidic technology, applied in biochemistry apparatus and processes, fluid controllers, laboratory glassware, etc., can solve the problems of multiple reagent delivery, poor sensitivity and reliability of all commercially available point of care testing analyzers, and problems in closed confinement. achieve the effect of convenient implementation

Inactive Publication Date: 2005-09-08
HO WINSTON Z +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Benefits of technology

[0016] In accordance with preferred embodiments of the present invention, a self-contained microfluidic disposable biochip is provided for performing a variety of chemical and biolo...

Problems solved by technology

All the commercially available point of care testing (POCT) analyzers have poor sensitivity and reliability in comparison with the large laboratory systems.
The key p...

Method used

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  • Self-contained microfluidic biochip and apparatus
  • Self-contained microfluidic biochip and apparatus
  • Self-contained microfluidic biochip and apparatus

Examples

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example no.1

EXAMPLE NO. 1

[0071] The system as shown in FIG. 7 is designed and configured to simultaneously synthesize and label probes from two samples and hybridize the two probes to an integrated array of 400 spotted DNA elements. These elements would represent 400 well characterized unique genes and are selected so that according to preliminary data (FIG. 10), ⅔ of the genes are known to be highly expressed between normal human kidney (Asterand, Detroit, Mich.) and the Universal Human Reference RNA™ (Stratagene, La Jolla, Calif.). While ⅓ are known to show a low to no differential expression (between 0.5- and 1.5-fold) between the two specimens. The expression profiles have been generated using the Agilent Human 1A Oligo Microarray™ (22K array) and the Agilent platform for probe synthesis, hybridization and scanning. The slight bias of the data points towards the Reference RNA is caused by the fact that the Universal RNA is a pool of total RNAs of 10 different human tissues. Thus for the maj...

example no.2

EXAMPLE NO. 2

[0073] cDNA Synthesis & Amplification: cDNA synthesis includes three different reaction steps: (A) a reverse transcription (RT) step; (B) the formation of double-stranded cDNA step; and (C) the isothermal amplification (IA) step. In the RT, the mRNA (poly A+) portion within the total RNA is transcribed into single-stranded cDNA using a chimeric RNA-DNA primer. The primer binds with its DNA part to the poly(A) tail of the mRNA but the RNA part stays single-stranded. In this way the resulting RNA-cDNA complex has a unique RNA target sequence at the 5′ end of the cDNA. After fragmentation of the RNA in the RNA-cDNA complex, DNA polymerase is used to synthesize a second strand including DNA complementary to the unique 5′ RNA sequence of the first strand. The result is a double-stranded cDNA with a unique RNA / DNA heteroduplex at the 5′ end. In the IA part of the unique 5′ RNA sequence is removed by added RNase H. The exposed cDNA sequence is then available for binding a seco...

example no.3

EXAMPLE NO. 3

[0074] Fluorescent Dye Coupling: The fluorescence labeling of the cDNA is achieved in a simple chemical by coupling of NHS-ester cyanine 3 (Cy3) or cyanine 5 (Cy5) to aminoallyl groups of the cDNA. The uncoupled dye is removed by purification with magnetic beads process (Dynal).

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Abstract

A biochip and apparatus is disclosed for performing biological assays in a self-contained microfluidic platform. The disposable biochip for multi-step reactions comprises a body structure with a plurality of reagent cavities and reaction wells connected via microfluidic channels; the reagent cavities with reagent sealing means for storing a plurality of reagents; the reagent sealing means being breakable and allowing a sequence of reagents to be released into microfluidic channel and reaction well; and the reaction well allowing multi-step reactions to occur by sequentially removing away the residual reagents. The analysis apparatus can rapidly, automatically, sensitively, and simultaneously detect and identify multiple analytes or multiple samples in a very small quantity.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS [0001] This application is a continuation-in-part application of U.S. patent application Ser. No. 10 / 338,451, filed Jan. 8, 2003, entire contents of which are incorporated herein by reference.FIELD OF THE INVENTION [0002] The invention is related to a method using a self-contained biochip that is preloaded with necessary reagents, and utilizes microfluidic and micro-pressure actuator mechanisms to perform biological reactions and assays, particularly for gene expression profiling or screening of candidate genes for a genetic study. The biochip analysis apparatus is configured rapidly and automatically measuring the quantities of chemical and biological species in a sample. BACKGROUND OF THE INVENTION [0003] Current hospital and clinical laboratories are facilitated with highly sophisticate and automated systems with the capability to run up to several thousand samples per day. These high throughput systems have automatic robotic arms, pumps, t...

Claims

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Application Information

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IPC IPC(8): B01L3/00
CPCB01L3/5025B01L3/502738B01L2200/16B01L2300/0672B01L2400/0683B01L2300/0864B01L2300/0867B01L2400/049B01L2300/0803
Inventor HO, WINSTON Z.TAJBAKHSH, JIAN
Owner HO WINSTON Z
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