U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Sheathless interface for capillary electrophoresis/electrospray ionization-mass spectrometry using an in-capillary electrode

Patent 6863790 Issued on March 8, 2005. Estimated Expiration Date: Icon_subject August 5, 2019. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

Method for the electrochemical analysis of electrolytic components in a sample liquid
Patent #: 4838999
Issued on: 06/13/1989
Inventor: Haar ,   et al.

Capillary electrophoresis flow control system
Patent #: 5482608
Issued on: 01/09/1996
Inventor: Keely, et al.

Electrochemical detector cell, method and pyrolysis furnace
Patent #: 5525197
Issued on: 06/11/1996
Inventor: Coulson

Device for separating polynucleotides having a plurality of electrode-containing cells and movable collecting capillary
Patent #: 5607646
Issued on: 03/04/1997
Inventor: Okano, et al.

Electrolytic cell and capillary gap electrode for gas-developing or gas-consuming electrolytic reactions and electrolysis process therefor
Patent #: 5650058
Issued on: 07/22/1997
Inventor: Wenske, et al.

Capillary electrophoresis electrospray ionization mass spectrometry interface Patent #: 5993633
Issued on: 11/30/1999
Inventor: Smith, et al.

Inventors

Assignee

Application

No. 09370781 filed on 08/05/1999

US Classes:

204/452, With detailed detection204/454, With adjustment or alteration of electro-osmotic bulk flow204/603, With detailed detection system (e.g., including a light source and a camera, etc.)250/288With sample supply means

Examiners

Primary: Warden, Robert J.
Assistant: Olsen, Kaj K.

Attorney, Agent or Firm

International Classes

G01N027/447
G01N030/72

Abstract

A simple and rugged sheathless interface for capillary electrophoresis/electrospray ionization-mass spectrometry (CE/ESI-MS) was designed using common laboratory tools and chemicals. The interface uses a small platinum (Pt) wire which is inserted into the CE capillary through a small hole near the terminus. The position of the wire inside the CE capillary and within the buffer solution is analogous to standard CE separation operations where the terminus of the CE capillary is placed inside a buffer reservoir along with a grounded platinum electrode. By combining the use of the in-capillary electrode interface with sharpening of the fused silica tip of the CE capillary outlet, a stable electrospray current was maintained for an extended period of time. The design was successfully applied to CE/ESI-MS separations and analysis of mixtures of peptides and proteins. A detection limit of approximately 4 femtomole (S/N=3) was achieved for detection of myoglobin utilizing a 75 μm-i.d. aminopropylsilane treated CE column and using a wide scan range of 550-1350 Da. The advantages of this new design include: (1) a stable CE and ESI current, (2) durability, (3) a reduced risk of sparking between the capillary tip and the inlet of the mass spectrometer, (4) lack of any dead volume, and (5) facile fabrication with common tools and chemicals.

Other References

  • P.W. Atkins, “Physical Chemistry”, 4th Edition, 1990, pp. 147-151.
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