Non-Fluidic Microdetection Device and Uses Thereof

a non-fluidic microdetection and detection device technology, applied in the field of microchips, can solve problems such as optical instrumentation cos

Inactive Publication Date: 2008-06-12
COLORADO STATE UNIVERSITY
View PDF0 Cites 37 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0009]According to a third broad aspect of the invention, there is provided a method for performing electrophoresis. Electrophoresis is performed by attaching at least first conductive element and a second conducive element to a microchip having a biologic microfluid thereon, wherein the microchip comprises at least one main channel formed in a channel forming medium, the main channel containing at least one biologic microfluid; at least one detecting channel containing the first conductive element for performing electrochemical detecting, the detecting channel being formed in the channel forming medium and adjoining the main channel; and at least one reservoir containing the second conductive element for serving as a reference to the first conductive element, the reservoir being formed in the channel forming medium and containing biologic waste; and applying either continuous or pulsed amperometric detection to the microchip using the conductive elements to thereby cause biologic specimens within the biologic microfluid to migrate toward the first conductive element and, when in electrical contact with the first conductive element, to generate a measurable signal.

Problems solved by technology

However, the cost of optical instrumentation, the need for analyte derivatization, and the limited portability of LIF has led to the investigation of electrochemical detection (ECD), an attractive alternative for microchip devices, see Verpoorte, E., Electrophoresis 2002, 23, 677-712; Wang, J., Talanta 2002, 56, 223-231; Rossier, J., Reymond, F., Michel, P. E., Electrophesis 2002, 23, 858-867; Lacher, N. A., Garrison, K. E., Martin, R. S., Lunte, S. M., Electrophoresis 2001, 22, 2526-2536; Vandaveer, W. R. I. V., Pasas, S. A., Martin, R. S., Lunte, S. M., Electrophoresis 2002, 23, 3667-3677; and Wang, J., Trends in Anal. Chem. 2002, 21, 226-232, the entire contents and disclosures of which are hereby incorporated by reference.
However, when a constant potential is applied, the electrode may be fouled by the accumulation of adsorbed carbonaceous material, resulting in an unstable signal, see Fanguy, J. C., Henry, C. S., Analyst 2002, 127, 1021-1023; Garcia, G., Garcia, C. D., Ortiz, P. I., De Pauli, C. P., J. Electroanal. Chem. 2002, 519, 53-59, the entire contents and disclosures of which are hereby incorporated by reference.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Non-Fluidic Microdetection Device and Uses Thereof
  • Non-Fluidic Microdetection Device and Uses Thereof
  • Non-Fluidic Microdetection Device and Uses Thereof

Examples

Experimental program
Comparison scheme
Effect test

example i

Injection Procedure

[0063]A solution of 1 .μM fluorescein, prepared in the running electrolyte, was used to follow the injection. For the present experiments, injection times of 10 seconds were used to ensure plug homogeneity because at the slowest electroosmotic flow (EOF) conditions, the double-T was filled in 7 seconds. Injection times are dependent on the sample and the chip and may vary from about 1 second to about 1 minute.

example ii

Analysis of Carbohydrates

[0064]It is well known that activation barriers for oxidation of some compounds may be decreased at a clean Au electrode, see LaCourse, W. R., Pulsed Electrochemical Detection in High-Performance Liquid Chromatography, Wiley J. & Sons: New York, 1997, the entire contents and disclosure of which is hereby incorporated by reference. These surfaces stabilize free-radical oxidation products by adsorption and, thereby, may promote faradaic reactions. Once a clean surface is obtained, a potential should be chosen in order to maximize the electrode response. The effect of the detection potential on the signal was analyzed between −0.3 to +1.1V for glucose (GLU), lactose (LAC) and sucrose (SUC) as shown in FIG. 5. As may be seen, the peak current increases as the potential increases until a maximum in the signal is obtained. The following current decrease observed at higher potentials may be explained as the result of the formation of oxide on the working electrode ...

example iii

Analysis of Amino Acids

[0070]The direct detection of unlabeled amino acids has the potential to simplify quantification of these important analytes. The effect of the potential applied to the working electrode was analyzed between −0.3 and +1.1 V for the three amino acids. As was observed for carbohydrates, the peak current increased as the potential increased until a maximum in the signal was obtained at around 0.7 V. Since similar profiles were found between the selected amino acids, 0.7 V was chosen as a suitable detection potential. As part of the detection potential determination, a higher cleaning potential was selected when sulfur-containing compounds were injected in order to decrease the peak tailing produced by the high interaction between the sulfur group and the Au.

[0071]The electrolyte conditions may not only affect the separation process but also the detection step. It was previously reported that the adsorption of the amines through the free pair of electrons may be r...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
angleaaaaaaaaaa
90° angleaaaaaaaaaa
electrical potentialaaaaaaaaaa
Login to view more

Abstract

The present invention provides a microchip for performing electrophoresis with electrochemical means, such as by pulsed amperometric detection (PAD), for the separation and detection of underivatized carbohydrates, amino acids, sulfur-containing antibiotics, etc. The present methods permit the direct detection of amines, thiols, alcohols and carbohydrates and therefore is a useful technique for the development of electrochemical detection for microchip electrophoresis.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]This application claims priority to U.S. Provisional Patent Application No. 60 / 496,673, entitled “Direct Determination of Carbohydrates, Amino Acids and Antibiotics by Microchip Electrophoresis with Pulsed Amperometric Detection,” filed Aug. 21, 2003, and to PCT / US2004 / 021740, filed Jul. 8, 2004, and to U.S. Utility patent application Ser. No. 10 / 568,975, filed Sep. 12, 2006, the entire contents and disclosure of all of which is hereby incorporated by reference.BACKGROUND[0002]1. Field of Invention[0003]The present invention relates generally to electrophoresis, and more particularly to a microchip that performs electrophoresis, a method to produce a microchip with integrated electrodes, and a method for performing electrophoresis using a microchip with integrated electrodes.[0004]2. Related Art[0005]Microanalytical devices open up new possibilities for the miniaturization of conventional chemical and biochemical analysis systems. Since t...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(United States)
IPC IPC(8): B01D57/02G01N27/447
CPCG01N27/4473Y10T29/49155Y10T29/49117
Inventor HENRY, CHARLES S.GARCIA, CARLOS D.
Owner COLORADO STATE UNIVERSITY
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products