USRE35413E - Electrospray ion source with reduced neutral noise and method - Google Patents

Electrospray ion source with reduced neutral noise and method Download PDF

Info

Publication number
USRE35413E
USRE35413E US08/220,963 US22096394A USRE35413E US RE35413 E USRE35413 E US RE35413E US 22096394 A US22096394 A US 22096394A US RE35413 E USRE35413 E US RE35413E
Authority
US
United States
Prior art keywords
skimmer
ions
ion source
droplets
low pressure
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US08/220,963
Inventor
Iain C. Mylchreest
Mark E. Hail
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Thermo Finnigan LLC
Original Assignee
Finnigan Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Finnigan Corp filed Critical Finnigan Corp
Priority to US08/220,963 priority Critical patent/USRE35413E/en
Application granted granted Critical
Publication of USRE35413E publication Critical patent/USRE35413E/en
Assigned to THERMO FINNIGAN LLC reassignment THERMO FINNIGAN LLC CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: FINNIGAN CORPORATION
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/62Detectors specially adapted therefor
    • G01N30/72Mass spectrometers
    • G01N30/7293Velocity or momentum separators
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/62Detectors specially adapted therefor
    • G01N2030/621Detectors specially adapted therefor signal-to-noise ratio
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/62Detectors specially adapted therefor
    • G01N30/72Mass spectrometers
    • G01N30/7233Mass spectrometers interfaced to liquid or supercritical fluid chromatograph
    • G01N30/724Nebulising, aerosol formation or ionisation
    • G01N30/7246Nebulising, aerosol formation or ionisation by pneumatic means
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/62Detectors specially adapted therefor
    • G01N30/72Mass spectrometers
    • G01N30/7233Mass spectrometers interfaced to liquid or supercritical fluid chromatograph
    • G01N30/724Nebulising, aerosol formation or ionisation
    • G01N30/7266Nebulising, aerosol formation or ionisation by electric field, e.g. electrospray
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/62Detectors specially adapted therefor
    • G01N30/72Mass spectrometers
    • G01N30/7233Mass spectrometers interfaced to liquid or supercritical fluid chromatograph
    • G01N30/7273Desolvation chambers

Definitions

  • This invention relates generally to electrospray ion sources and more particularly to sources having reduced neutral noise.
  • the electrospray process consists of flowing sample liquid through a small tube or capillary which is maintained at a high voltage with respect to a nearby surface.
  • the liquid is dispersed into fine electrically charged droplets or by the voltage gradient of the tip of the capillary.
  • the ionization mechanism involves the desorption at atmospheric pressure of ions from the fine electrically charged particles.
  • a heated gas is flowed in counter-current to the electrospray to enhance dissolution of the electrospray droplets.
  • the ions created by the electrospray are then mass analyzed in a mass analyzer such as a mass spectrometer.
  • FIG. 4 is an enlarged view of the region 4--4 of FIG. 1.
  • an electrospray ion source 11 is schematically shown as associated with an analyzer chamber 12.
  • the source includes an input needle 13 into which a liquid sample 14 is introduced.
  • the needle includes an inner tube 16 in which the liquid sample is introduced. Surrounding the tube is a second tube 17 which defines with the first tube an annular region through which a liquid is introduced for mixing with the sample liquid to reduce the surface tension and form droplets.
  • An outer tube 18 forms a second annulus through which a focusing gas is introduced to focus the droplets as they exit the needle towards a capillary tube 19.
  • the needle, or capillary is maintained at a high voltage with respect to the nearby surfaces forming the ionization chamber 21 and as the liquid is dispersed, the droplets or particles are charged by the voltage gradient at the tip of the capillary.
  • the ionization mechanism involves the desorption at atmospheric pressure of ions from the fine electrically charged particles.
  • a counter-flow of gas indicated by the arrow 22 enhances the desorption process.
  • the gas flows through a chamber 23 past the end of the capillary 19 and exits the ionization chamber 21 as indicated schematically at 24.
  • the end of the tube 19 is supported by, for example, three supports 29 disposed at 120° with respect to one another.
  • the end of the capillary is opposite a skimmer 31 which separates the low pressure region 26 from a lower pressure region in the analyzer 12.
  • the skimmer includes a central orifice or aperture 32 which normally is aligned with the axis of the bore of the capillary.
  • the skimmer is followed by ion optics which may comprise a second skimmer 33 and lenses 34, which direct ions into the analyzing chamber and into a suitable analyzer.
  • the solvated droplets or particles flow into the capillary and acquire kinetic energy which allows them to pass through the skimmer aperture 32 into the lens region including skimmer 33 and lenses 34. These droplets or particles impact on the surfaces of the skimmer 33 or the lenses 34 and create secondary ions. These ions are random and find their way into the detector and cause noise to be observed at the detector, thereby decreasing the signal-to-noise level and producing electronic spikes in the mass spectrum.
  • the axis of the capillary is altered or directed as shown in FIG. 4 by adjusting the supports 29 so that the axis is offset from the skimmer orifice or aperture. In this way, there is no alignment between the bore of the capillary and the orifice of the skimmer.
  • the tendency is for the large droplets or particles to move to the center of the flow in the capillary and travel in a straight line. These droplets or particles traveling in a straight line strike the skimmer. This is illustrated in FIG. 4, which shows that large particles 36 travel a straight line and impinge upon the skimmer 31.
  • the droplets or particles are thereafter pumped away by the vacuum pump associated with the chamber 26 as illustrated by the arrow 37.
  • the realignment of the axis of the capillary tube does not cause any significant loss in the observed signal intensity of the ions being analyzed. This is due to the fact that the analyzed ions and gases undergo a free jet expansion and are deviated from the axis to travel through the orifice or aperture 32.

Abstract

An electrospray ion source having a capillary tube for directing ions from an ionizing region to an analyzing region including a skimmer in which the capillary tube is oriented to cause undesolvated droplets to strike the skimmer.

Description

BRIEF DESCRIPTION OF THE INVENTION
This invention relates generally to electrospray ion sources and more particularly to sources having reduced neutral noise.
BACKGROUND OF THE INVENTION
The electrospray process consists of flowing sample liquid through a small tube or capillary which is maintained at a high voltage with respect to a nearby surface. The liquid is dispersed into fine electrically charged droplets or by the voltage gradient of the tip of the capillary. The ionization mechanism involves the desorption at atmospheric pressure of ions from the fine electrically charged particles. In many cases, a heated gas is flowed in counter-current to the electrospray to enhance dissolution of the electrospray droplets. The ions created by the electrospray are then mass analyzed in a mass analyzer such as a mass spectrometer.
Under the appropriate conditions, the electrospray resembles a symmetrical cone consisting of a very fine mist (or fog) of droplets (ca. 1 μm diameter). Excellent sensitivity and ion current stability can be obtained if the fine mist is produced. Unfortunately, the electrospray "quality" is highly dependent on the bulk properties of the solution being analyzed. The most important of which are surface tension and conductivity. A poor quality electrospray may contain larger droplets (>10 μm diameter) or a non-dispersed droplet stream.
The use of sheath liquid and a focusing gas are often used to insure stable sprays when electrospraying high aqueous content sample solutions. One type of electrospray interface apparatus includes an inner needle for transferring a liquid sample to an ionizing region at one end of the needle, a first outer tube surrounding and spaced from said needle for flowing a liquid past the tip of said needle, and a second outer tube surrounding the first tube to define a second cylindrical space for flowing a gas past the end of said first tube and needle to focus the electrospray.
In U.S. Pat. No. 4,542,293 there is described the use of a tube made of an electrical insulator for conducting ions in the ionizing electrospray region at atmospheric pressure and a low pressure region. A glass or quartz capillary is suitable. Ions and gas are caused to flow from the ionization region through the tube into the low pressure region where free jet expansion occurs. A conductive coating is formed on the ends of the insulating tube and a voltage is applied thereacross to accelerate ions which flow through the tube. A conducting skimmer is disposed adjacent the end of the tube and is maintained at a voltage which causes further acceleration of the ions through and into a lower pressure region including focusing lenses and analyzing apparatus.
The electrospray process employing a sheath liquid and focusing gas provides small droplets or particle which are desolvated by the addition of a counter current drying gas. Occasionally, larger undesolvated droplets or particles will traverse into the capillary and will acquire substantial kinetic energy which will allow it to pass through the skimmer and into the lens region. The droplets or particles impinge upon surfaces and forms secondary ions. These ions are random and cause noise to be observed at the analyzer detector, thereby decreasing the signal to noise levels and producing noise spikes in the ion chromatogram.
OBJECTS AND SUMMARY OF THE INVENTION
It is a general object of this invention to provide an ion source and method in which high velocity droplets or particles are prevented from flowing into the lens region of an associated analyzer.
It is another object of the invention to provide an ion source which includes a skimmer and means for directing high velocity droplets or particles away from the skimmer aperture.
The foregoing and other objects of this invention are achieved in an electrospray ion source of the type which includes a tube communicating between the ionizing region and a low pressure region with a skimmer having an aperture through which ions pass, the skimmer separating the low pressure region from a lower pressure region which includes lenses and an analyzer, where analysis is carried out. The capillary is oriented so that undesolvated droplets or particles travelling through the capillary are prevented from passing through the skimmer aperture into the analysis region.
BRIEF DESCRIPTION OF THE DRAWINGS
The foregoing and other objects of the invention will be more clearly understood from the description to follow when read in conjunction with the accompanying drawings of which:
FIG. 1 shows an electrospray ion source coupled to an analyzing region via a capillary tube;
FIG. 2 is an enlarged view of the region 2--2 of FIG. 1;
FIG. 3 is a sectional view taken along the line 3--3 of FIG. 1 showing the tube support; and
FIG. 4 is an enlarged view of the region 4--4 of FIG. 1.
DETAILED DESCRIPTION OF THE INVENTION
Referring to FIG. 1, an electrospray ion source 11 is schematically shown as associated with an analyzer chamber 12. The source includes an input needle 13 into which a liquid sample 14 is introduced.
Referring particularly to FIG. 2, the needle includes an inner tube 16 in which the liquid sample is introduced. Surrounding the tube is a second tube 17 which defines with the first tube an annular region through which a liquid is introduced for mixing with the sample liquid to reduce the surface tension and form droplets. An outer tube 18 forms a second annulus through which a focusing gas is introduced to focus the droplets as they exit the needle towards a capillary tube 19. As previously explained, the needle, or capillary, is maintained at a high voltage with respect to the nearby surfaces forming the ionization chamber 21 and as the liquid is dispersed, the droplets or particles are charged by the voltage gradient at the tip of the capillary. The ionization mechanism involves the desorption at atmospheric pressure of ions from the fine electrically charged particles. A counter-flow of gas indicated by the arrow 22 enhances the desorption process. The gas flows through a chamber 23 past the end of the capillary 19 and exits the ionization chamber 21 as indicated schematically at 24.
A chamber 26 maintained at a lower pressure than the atmosphere pressure of the chamber 21 communicates with the ionization chamber via the capillary tube 19. Due to the differences in pressure, ions and gas are caused to flow through the capillary 19 into the chamber 26. A voltage is applied between conductive sleeves 27 and 28 to provide a voltage gradient. The end of the tube 19 is supported by, for example, three supports 29 disposed at 120° with respect to one another.
The end of the capillary is opposite a skimmer 31 which separates the low pressure region 26 from a lower pressure region in the analyzer 12. The skimmer includes a central orifice or aperture 32 which normally is aligned with the axis of the bore of the capillary. The skimmer is followed by ion optics which may comprise a second skimmer 33 and lenses 34, which direct ions into the analyzing chamber and into a suitable analyzer.
As described above, the solvated droplets or particles flow into the capillary and acquire kinetic energy which allows them to pass through the skimmer aperture 32 into the lens region including skimmer 33 and lenses 34. These droplets or particles impact on the surfaces of the skimmer 33 or the lenses 34 and create secondary ions. These ions are random and find their way into the detector and cause noise to be observed at the detector, thereby decreasing the signal-to-noise level and producing electronic spikes in the mass spectrum.
In accordance with this invention, the axis of the capillary is altered or directed as shown in FIG. 4 by adjusting the supports 29 so that the axis is offset from the skimmer orifice or aperture. In this way, there is no alignment between the bore of the capillary and the orifice of the skimmer. The tendency is for the large droplets or particles to move to the center of the flow in the capillary and travel in a straight line. These droplets or particles traveling in a straight line strike the skimmer. This is illustrated in FIG. 4, which shows that large particles 36 travel a straight line and impinge upon the skimmer 31. The droplets or particles are thereafter pumped away by the vacuum pump associated with the chamber 26 as illustrated by the arrow 37. The realignment of the axis of the capillary tube does not cause any significant loss in the observed signal intensity of the ions being analyzed. This is due to the fact that the analyzed ions and gases undergo a free jet expansion and are deviated from the axis to travel through the orifice or aperture 32.
Thus, there has been provided a method and apparatus for reducing neutral noise in an electrospray.

Claims (1)

What is claimed is: .[.
1. An ion source of the type which includes an ionization chamber and an adjacent low pressure region including a skimmer having an orifice, a capillary tube having an axial bore communicating between the ionization chamber and the low pressure region whereby ions and gases in said ionization chamber flows through said bore into said low pressure region, directing the axis of the capillary tube away from the skimmer orifice whereby droplets and/or particles flowing through the bore are not allowed to pass through the skimmer, while ions are transmitted into the low pressure chamber..]..[.2. An electrospray ion source as in claim 1 in which said ionization chamber includes means for electrospraying a sample to be analyzed..]..Iadd.3. A method of operating an ion source, said ion source including a low pressure chamber having a skimmer with an orifice and a capillary tube having a bore with an axis, said method comprising the steps of:
desolvating charged droplets in said ion source to produce a flow of ions and undesolvated droplets;
causing said flow of ions and undesolvated droplets to flow from said bore along said axis of said bore into said low pressure chamber; and
offsetting said axis of said bore from said orifice of said skimmer so that said ions flow through said orifice while said undesolvated droplets impinge upon said skimmer. .Iaddend..Iadd.4. A method of operating an ion source, said ion source including a low pressure chamber having a skimmer with an orifice, and means to communicate with the low pressure chamber, said method comprising the steps of:
desolvating charged droplets in said ion source to produce a flow of ions and undesolvated droplets;
causing said flow of ions and undesolvated droplets to flow from said communicating means along an axis of said communicating means into said low pressure chamber; and
offsetting said axis of said communicating means from said orifice of said skimmer so that said ions flow through said orifice while said undesolvated droplets impinge upon said skimmer. .Iaddend.
US08/220,963 1991-05-17 1994-03-30 Electrospray ion source with reduced neutral noise and method Expired - Lifetime USRE35413E (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US08/220,963 USRE35413E (en) 1991-05-17 1994-03-30 Electrospray ion source with reduced neutral noise and method

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US07/703,471 US5171990A (en) 1991-05-17 1991-05-17 Electrospray ion source with reduced neutral noise and method
US08/220,963 USRE35413E (en) 1991-05-17 1994-03-30 Electrospray ion source with reduced neutral noise and method

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US07/703,471 Reissue US5171990A (en) 1991-05-17 1991-05-17 Electrospray ion source with reduced neutral noise and method

Publications (1)

Publication Number Publication Date
USRE35413E true USRE35413E (en) 1996-12-31

Family

ID=24825524

Family Applications (2)

Application Number Title Priority Date Filing Date
US07/703,471 Ceased US5171990A (en) 1991-05-17 1991-05-17 Electrospray ion source with reduced neutral noise and method
US08/220,963 Expired - Lifetime USRE35413E (en) 1991-05-17 1994-03-30 Electrospray ion source with reduced neutral noise and method

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US07/703,471 Ceased US5171990A (en) 1991-05-17 1991-05-17 Electrospray ion source with reduced neutral noise and method

Country Status (4)

Country Link
US (2) US5171990A (en)
JP (1) JP2604087B2 (en)
CA (1) CA2068849C (en)
GB (1) GB2256523B (en)

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5736740A (en) * 1995-04-25 1998-04-07 Bruker-Franzen Analytik Gmbh Method and device for transport of ions in gas through a capillary
US20040217280A1 (en) * 2003-02-14 2004-11-04 Mds Sciex Atmospheric pressure charged particle discriminator for mass spectrometry
US20050258358A1 (en) * 2004-05-21 2005-11-24 Thakur Rohan A Electrospray ion source apparatus
US20060255264A1 (en) * 2005-05-16 2006-11-16 Belford Michael W Enhanced ion desolvation for an ion mobility spectrometry device
US20080001082A1 (en) * 2006-06-08 2008-01-03 Richard Syms Microengineered vacuum interface for an ionization system
US20080104064A1 (en) * 2006-10-10 2008-05-01 Gangqiang Li Electrospray Ionization Mass Spectrometer Interface
WO2009149182A1 (en) 2008-06-04 2009-12-10 The Board Of Regents Of The University Of Texas System Modulation of gene expression through endogenous small rna targeting of gene promoters
WO2010124231A2 (en) 2009-04-24 2010-10-28 The Board Of Regents Of The University Of Texas System Modulation of gene expression using oligomers that target gene regions downstream of 3' untranslated regions
WO2011053994A1 (en) 2009-11-02 2011-05-05 Alnylam Pharmaceuticals, Inc. Modulation of ldl receptor gene expression with double-stranded rnas targeting the ldl receptor gene promoter
US8642946B2 (en) 2006-11-17 2014-02-04 Thermo Finnigan Llc Apparatus and method for a multi-stage ion transfer tube assembly for use with mass spectrometry
WO2022091025A1 (en) 2020-10-30 2022-05-05 Pfizer Inc. Methods for measuring dystrophin in tissue samples
WO2022130172A1 (en) 2020-12-15 2022-06-23 Pfizer Inc. Hilic uplc-ms method for separating and analyzing intact adeno-associated virus capsid proteins

Families Citing this family (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5306910A (en) * 1992-04-10 1994-04-26 Millipore Corporation Time modulated electrified spray apparatus and process
US20060277017A1 (en) * 1993-11-04 2006-12-07 Sproch Norman K Method for the characterization of the three-dimensional structure of proteins employing mass spectrometric analysis and computational feedback modeling
US5504327A (en) * 1993-11-04 1996-04-02 Hv Ops, Inc. (H-Nu) Electrospray ionization source and method for mass spectrometric analysis
US7047171B1 (en) 1995-12-08 2006-05-16 Sproch Norman K Method for the characterization of the three-dimensional structure of proteins employing mass spectrometric analysis and computational feedback modeling
US5750988A (en) * 1994-07-11 1998-05-12 Hewlett-Packard Company Orthogonal ion sampling for APCI mass spectrometry
US5495108A (en) * 1994-07-11 1996-02-27 Hewlett-Packard Company Orthogonal ion sampling for electrospray LC/MS
GB9525507D0 (en) * 1995-12-14 1996-02-14 Fisons Plc Electrospray and atmospheric pressure chemical ionization mass spectrometer and ion source
DE19655304B8 (en) * 1995-12-14 2007-05-31 Micromass Uk Ltd. Mass spectrometers and methods for mass spectrometry
US5917184A (en) * 1996-02-08 1999-06-29 Perseptive Biosystems Interface between liquid flow and mass spectrometer
US5672868A (en) * 1996-02-16 1997-09-30 Varian Associates, Inc. Mass spectrometer system and method for transporting and analyzing ions
US5986259A (en) * 1996-04-23 1999-11-16 Hitachi, Ltd. Mass spectrometer
US5750993A (en) * 1996-05-09 1998-05-12 Finnigan Corporation Method of reducing noise in an ion trap mass spectrometer coupled to an atmospheric pressure ionization source
EP0925601B1 (en) * 1996-09-10 2010-11-10 PerkinElmer Health Sciences, Inc. Improvements to atmospheric pressure ion sources
GB2324906B (en) * 1997-04-29 2002-01-09 Masslab Ltd Ion source for a mass analyser and method of providing a source of ions for analysis
GB2328074B (en) * 1997-08-06 2001-11-07 Masslab Ltd Ion source for a mass analyser and method of cleaning an ion source
US6392225B1 (en) 1998-09-24 2002-05-21 Thermo Finnigan Llc Method and apparatus for transferring ions from an atmospheric pressure ion source into an ion trap mass spectrometer
JP3578041B2 (en) * 2000-03-23 2004-10-20 株式会社島津製作所 Liquid chromatograph mass spectrometer
US6465776B1 (en) 2000-06-02 2002-10-15 Board Of Regents, The University Of Texas System Mass spectrometer apparatus for analyzing multiple fluid samples concurrently
US6872940B1 (en) 2002-05-31 2005-03-29 Thermo Finnigan Llc Focusing ions using gas dynamics
JP5073168B2 (en) * 2002-05-31 2012-11-14 ウオーターズ・テクノロジーズ・コーポレイシヨン A fast combined multimode ion source for mass spectrometers.
CA2470452C (en) 2003-06-09 2017-10-03 Ionics Mass Spectrometry Group, Inc. Mass spectrometer interface
US7015466B2 (en) 2003-07-24 2006-03-21 Purdue Research Foundation Electrosonic spray ionization method and device for the atmospheric ionization of molecules
US7009176B2 (en) * 2004-03-08 2006-03-07 Thermo Finnigan Llc Titanium ion transfer components for use in mass spectrometry
US7424980B2 (en) * 2004-04-08 2008-09-16 Bristol-Myers Squibb Company Nano-electrospray nebulizer
US7547878B2 (en) * 2006-06-29 2009-06-16 Ionwerks, Inc. Neutral/Ion reactor in adiabatic supersonic gas flow for ion mobility time-of-flight mass spectrometry
US7391019B2 (en) * 2006-07-21 2008-06-24 Thermo Finnigan Llc Electrospray ion source
US7868289B2 (en) * 2007-04-30 2011-01-11 Ionics Mass Spectrometry Group Inc. Mass spectrometer ion guide providing axial field, and method
US8507850B2 (en) 2007-05-31 2013-08-13 Perkinelmer Health Sciences, Inc. Multipole ion guide interface for reduced background noise in mass spectrometry
US20100154568A1 (en) * 2008-11-19 2010-06-24 Roth Michael J Analytical Instruments, Assemblies, and Methods
CN103858201A (en) 2011-03-04 2014-06-11 珀金埃尔默健康科学股份有限公司 Electrostatic lenses and systems including the same
US9851333B2 (en) 2013-05-29 2017-12-26 Dionex Corporation Nebulizer for charged aerosol detection (CAD) system
US9230786B1 (en) 2014-06-11 2016-01-05 Bruker Daltonics, Inc. Off-axis channel in electrospray ionization for removal of particulate matter
US9768006B2 (en) 2016-01-20 2017-09-19 Thermo Finnigan Llc Ion transfer tube flow and pumping system load
CN110289202B (en) * 2019-04-08 2024-04-09 天津大学 Ion guiding device

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4300044A (en) * 1980-05-07 1981-11-10 Iribarne Julio V Method and apparatus for the analysis of chemical compounds in aqueous solution by mass spectroscopy of evaporating ions
US4542293A (en) * 1983-04-20 1985-09-17 Yale University Process and apparatus for changing the energy of charged particles contained in a gaseous medium
US4861988A (en) * 1987-09-30 1989-08-29 Cornell Research Foundation, Inc. Ion spray apparatus and method
US4885076A (en) * 1987-04-06 1989-12-05 Battelle Memorial Institute Combined electrophoresis-electrospray interface and method
US4963735A (en) * 1988-11-11 1990-10-16 Hitachi, Ltd. Plasma source mass spectrometer
US4994165A (en) * 1989-02-16 1991-02-19 Cornell Research Foundation, Inc. Liquid junction coupling for capillary zone electrophoresis/ion spray spectrometry
US5349186A (en) * 1993-06-25 1994-09-20 The Governors Of The University Of Alberta Electrospray interface for mass spectrometer and method of supplying analyte to a mass spectrometer

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8404683D0 (en) * 1984-02-22 1984-03-28 Vg Instr Group Mass spectrometers
US4999493A (en) * 1990-04-24 1991-03-12 Vestec Corporation Electrospray ionization interface and method for mass spectrometry

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4300044A (en) * 1980-05-07 1981-11-10 Iribarne Julio V Method and apparatus for the analysis of chemical compounds in aqueous solution by mass spectroscopy of evaporating ions
US4542293A (en) * 1983-04-20 1985-09-17 Yale University Process and apparatus for changing the energy of charged particles contained in a gaseous medium
US4885076A (en) * 1987-04-06 1989-12-05 Battelle Memorial Institute Combined electrophoresis-electrospray interface and method
US4861988A (en) * 1987-09-30 1989-08-29 Cornell Research Foundation, Inc. Ion spray apparatus and method
US4963735A (en) * 1988-11-11 1990-10-16 Hitachi, Ltd. Plasma source mass spectrometer
US4994165A (en) * 1989-02-16 1991-02-19 Cornell Research Foundation, Inc. Liquid junction coupling for capillary zone electrophoresis/ion spray spectrometry
US5349186A (en) * 1993-06-25 1994-09-20 The Governors Of The University Of Alberta Electrospray interface for mass spectrometer and method of supplying analyte to a mass spectrometer

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
Bruins, A. P., et al., "Ion Spray Interface for Combined Liquid Chromatography/Atmospheric Pressure Ionization Mass Spectrometry", Analytical Chemistry, 59(22):2642-2646 (1987). No Month.
Bruins, A. P., et al., Ion Spray Interface for Combined Liquid Chromatography/Atmospheric Pressure Ionization Mass Spectrometry , Analytical Chemistry , 59(22):2642 2646 (1987). No Month. *

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5736740A (en) * 1995-04-25 1998-04-07 Bruker-Franzen Analytik Gmbh Method and device for transport of ions in gas through a capillary
US7462826B2 (en) 2003-02-14 2008-12-09 Mds Sciex Atmospheric pressure charged particle discriminator for mass spectrometry
US20040217280A1 (en) * 2003-02-14 2004-11-04 Mds Sciex Atmospheric pressure charged particle discriminator for mass spectrometry
US20060118715A1 (en) * 2003-02-14 2006-06-08 Mds Sciex Atmospheric pressure charged particle discriminator for mass spectrometry
US7098452B2 (en) 2003-02-14 2006-08-29 Mds Sciex Atmospheric pressure charged particle discriminator for mass spectrometry
US20060226354A1 (en) * 2003-02-14 2006-10-12 Mds Sciex Atmospheric pressure charged particle discriminator for mass spectrometry
US20050258358A1 (en) * 2004-05-21 2005-11-24 Thakur Rohan A Electrospray ion source apparatus
US7199364B2 (en) 2004-05-21 2007-04-03 Thermo Finnigan Llc Electrospray ion source apparatus
US20060255264A1 (en) * 2005-05-16 2006-11-16 Belford Michael W Enhanced ion desolvation for an ion mobility spectrometry device
US7351960B2 (en) 2005-05-16 2008-04-01 Thermo Finnigan Llc Enhanced ion desolvation for an ion mobility spectrometry device
US20080001082A1 (en) * 2006-06-08 2008-01-03 Richard Syms Microengineered vacuum interface for an ionization system
US7786434B2 (en) 2006-06-08 2010-08-31 Microsaic Systems Limited Microengineered vacuum interface for an ionization system
US20080104064A1 (en) * 2006-10-10 2008-05-01 Gangqiang Li Electrospray Ionization Mass Spectrometer Interface
US8642946B2 (en) 2006-11-17 2014-02-04 Thermo Finnigan Llc Apparatus and method for a multi-stage ion transfer tube assembly for use with mass spectrometry
WO2009149182A1 (en) 2008-06-04 2009-12-10 The Board Of Regents Of The University Of Texas System Modulation of gene expression through endogenous small rna targeting of gene promoters
WO2010124231A2 (en) 2009-04-24 2010-10-28 The Board Of Regents Of The University Of Texas System Modulation of gene expression using oligomers that target gene regions downstream of 3' untranslated regions
WO2011053994A1 (en) 2009-11-02 2011-05-05 Alnylam Pharmaceuticals, Inc. Modulation of ldl receptor gene expression with double-stranded rnas targeting the ldl receptor gene promoter
WO2022091025A1 (en) 2020-10-30 2022-05-05 Pfizer Inc. Methods for measuring dystrophin in tissue samples
WO2022130172A1 (en) 2020-12-15 2022-06-23 Pfizer Inc. Hilic uplc-ms method for separating and analyzing intact adeno-associated virus capsid proteins

Also Published As

Publication number Publication date
GB9210609D0 (en) 1992-07-01
GB2256523B (en) 1995-04-19
JP2604087B2 (en) 1997-04-23
JPH06215727A (en) 1994-08-05
US5171990A (en) 1992-12-15
GB2256523A (en) 1992-12-09
GB2256523A8 (en) 2000-03-17
CA2068849A1 (en) 1992-11-18
CA2068849C (en) 1999-02-02

Similar Documents

Publication Publication Date Title
USRE35413E (en) Electrospray ion source with reduced neutral noise and method
US5122670A (en) Multilayer flow electrospray ion source using improved sheath liquid
US5157260A (en) Method and apparatus for focusing ions in viscous flow jet expansion region of an electrospray apparatus
US6812459B2 (en) Ion sampling for APPI mass spectrometry
CA1340133C (en) Combined electrophoresis-electrospray interface and method
USRE36892E (en) Orthogonal ion sampling for electrospray .[.LC/MS.]. mass spectrometry
USRE34757E (en) Combined electrophoresis-electrospray interface and method
US4842701A (en) Combined electrophoretic-separation and electrospray method and system
US4861988A (en) Ion spray apparatus and method
US6770875B1 (en) Apparatus and method for desolvating and focussing ions for introduction into a mass spectrometer
CA1218472A (en) Method and apparatus for the mass spectrometric analysis of solutions
JP5073168B2 (en) A fast combined multimode ion source for mass spectrometers.
JP4657451B2 (en) Vortex gas flow interface for electrospray mass spectrometry
US5447553A (en) Method for interfacing liquid chromatography-mass spectrometry systems
US20050056781A1 (en) Ion source and mass spectrometric apparatus
US7391019B2 (en) Electrospray ion source
US5975426A (en) Use of porous beads as a tip for nano-electrospray
JPH06331616A (en) Housing for converting electric spray to ion current
JPH07306193A (en) Ion source and mass spectrograph

Legal Events

Date Code Title Description
FPAY Fee payment

Year of fee payment: 8

AS Assignment

Owner name: THERMO FINNIGAN LLC, CALIFORNIA

Free format text: CHANGE OF NAME;ASSIGNOR:FINNIGAN CORPORATION;REEL/FRAME:011898/0886

Effective date: 20001025

FPAY Fee payment

Year of fee payment: 12