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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
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The present invention provides a microchip with channels for biological analysis. The main channel is the separation channel, while the detecting channel has a conductive element for electrochemical detection. Additional channels and reservoirs are provided for injecting sample and buffer during analysis procedures. The method for forming the microchip involves forming the main channel, detecting channel, and reservoirs, placing conductive elements in the detecting channel and reservoir, and attaching the microchip to a biological microfluid. The invention allows for efficient and accurate analysis of biological samples.

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

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Examples

Experimental program
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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...

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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

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Application Information

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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
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