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Patent 2236199 Summary

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(12) Patent: (11) CA 2236199
(54) English Title: HIGH PRESSURE MS/MS SYSTEM
(54) French Title: SYSTEME SM/SM HAUTE PRESSION
Status: Deemed expired
Bibliographic Data
(51) International Patent Classification (IPC):
  • H01J 49/26 (2006.01)
  • H01J 49/42 (2006.01)
(72) Inventors :
  • JAVAHERY, GHOLAMREZA (Canada)
  • JOLLIFFE, CHARLES (Canada)
  • THOMSON, BRUCE (Canada)
(73) Owners :
  • DH TECHNOLOGIES DEVELOPMENT PTE. LTD. (Singapore)
(71) Applicants :
  • MDS INC. (Canada)
(74) Agent: BERESKIN & PARR LLP/S.E.N.C.R.L.,S.R.L.
(74) Associate agent:
(45) Issued: 2006-10-03
(22) Filed Date: 1998-04-28
(41) Open to Public Inspection: 1999-10-28
Examination requested: 2003-01-31
Availability of licence: N/A
(25) Language of filing: English

Patent Cooperation Treaty (PCT): No

(30) Application Priority Data: None

Abstracts

English Abstract

A mass spectrometer system in which ions are mass selected in an RF-only quadrupole at relatively high pressure (1 to 7 torr) using FNF or SWIFT, and are then fragmented in a following collision cell which is in the same vacuum chamber, thus reducing pumping needs. The fragments can be mass analyzed in any desired way, including by another RF-only quadrupole in the same vacuum chamber and also using FNF or SWIFT. Triple MS can be performed in the same way.


French Abstract

Un système de spectromètre de masse dans lequel les ions sont sélectionnés en masse dans un quadripôle RF uniquement à une pression relativement élevée (1 à 7 torrs) à l'aide de FNF SWIFT, et sont ensuite fragmentés dans une cellule de collision suivante qui est dans la même chambre à vide, réduisant ainsi les besoins de pompage. Les fragments peuvent être analysés en masse de manière voulue quelconque, y compris par un autre quadripôle RF uniquement dans la même chambre à vide et aussi en utilisant FNF ou SWIFT. MS triple peut être réalisé de la même manière.

Claims

Note: Claims are shown in the official language in which they were submitted.





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THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:

1. A method of mass spectrometry comprising mass selecting
ions in a first multipole rod set operated at a pressure of at least
approximately 1 millitorr, by applying an auxiliary field to said first rod
~;et
to excite and thereby remove all ions therefrom except for parent ions, and
then transmitting the parent ions into a second multipole rod set operated
at substantially the same pressure as the first multipole rod set, axed
fragmenting parent ions in said second multipole rod set.

2. A method according to claim 1 and including the step of
transmitting fragmented ions from said second multipole rod set into a
further mass spectrometer for mass separation thereof, for detection.

3. A method according to claim 2 wherein said further mass
spectrometer is operated at a lower pressure than said first and second
multipole rod sets and is operated in an RF/DC resolving mode.

4. A method according to claim 2 wherein said further mass
spectrometer is operated at substantially the same pressure as said first and
second multipole rod sets, and ions are mass selected in said further mass
spectrometer using an RF field and an auxiliary field.

5. A method according to any of claims 1 to 4 wherein the first
multipole rod set includes at least two rod pairs, and wherein said
auxiliary field is a dipolar field which is simultaneously applied to both
said rod pairs, with one frequency applied to one rod pair and a second and
different frequency applied to the other rod pair, each frequency being
swept to produce rejection of a range of ion masses, the frequency applied
to said one rod pair being such as to reject ions of mass to charge ratio


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lower than that of ions of interest, and the frequency applied to the other
rod
pair being such as to reject ions of mass to charge ratio higher than that of
ions of interest.

6. A method according to any of claims 1 to 4 and including the steps of
fragmenting ions to produce ion fragments and isolating selected ones of said
ion fragments both in a same multipole rod set, by simultaneously fragmenting
parent ions in said multipole rod set and by applying an auxiliary field to
said
multipole rod set to isolate said selected fragment ions.

7. A method of mass spectrometry comprising providing ions from an ion
source, mass selecting said ions from said ion source to provide first parent
ions, fragmenting said first parent ions to provide first daughter ions, mass
selecting said first daughter ions to isolate said first daughter ions,
fragmenting said first daughter ions to provide second daughter ions, and
transmitting said second daughter ions into a mass spectrometer for mass
separation thereof, for detection; the steps of fragmenting said first parent
ions, selecting said first daughter ions, and fragmenting said first daughter
ions being carried out in at least two multipole rod sets in a chamber at one
pressure, said pressure being at least approximately one millitorr, thereby to
provide MS/MS/MS.

8. A method according to claim 7 wherein the mass selection of a parent
ion and the formation of a daughter ion are both carried out inside the same
multipole rod set.

9. A method according to claim 8 wherein the mass selection of said first
parent ions and the formation of said first daughter ions are both carried out
inside said same multipole rod set.

Description

Note: Descriptions are shown in the official language in which they were submitted.


CA 02236199 1998-04-28
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Title: HIGH PRESSURE MS/MS SYSTEM
FIELD OF THE INVENTION
This invention relates to a high pressure MS/MS system.
BACKGROUND OF THE INVENTION
Triple quadrupole mass spectrometer systems capable of
performing MS/MS usually have two precision quadrupole mass
spectrometers separated by a RF-only quadrupole which is operated as a gas
collision cell. The first mass spectrometer ("Q1") is used to select a
specific
ion mass-to-charge ratio (m/z), and to transmit ions with that m/z ratio
into the RF-only quadrupole or collision cell ("Q2"). The selected ions
(also referred to as the parent ions) are accelerated to an energy of several
tens of electron volts before entering the collision cell.
In the RF-only quadrupole collision cell, some or all of t:he
parent ions are fragmented by collisions with a background gas (which is
commonly argon or nitrogen added to the collision cell at a pressure of up
to several millitorr). The fragment ions, along with any unfragmented
parent ions, are transmitted through Q2 into the second precision
quadrupole ("Q3"), which is operated in a mass resolving mode. The mass
resolving mode of Q3 is normally either to scan over a specified mass
range, or else to transmit selected ion fragments by peak hopping (i.e. by
being rapidly adjusted to select specific ion m/z ratios in sequence). T'he
ions which are transmitted through Q3 are detected by an ion detector, the
signal from which is registered by a data system.
Triple quadrupoles of the kind described are known to be
very sensitive and very specific analytical instruments. The sensitivity is
due in part to the efficient transmission of ions through the quadrupoles,
and to the efficient confinement of ions in the RF-only collision cell. The
high specificity is due to the specific nature of the combination of mass
selection by Q1, fragmentation to create characteristic fragments in Q2, a.nd
mass selection of the fragments in Q3.

CA 02236199 1998-04-28
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Operation of a triple quadrupole as described above requires
that the mass resolving quadrupoles Q1 and Q3 operate in a high vacuum
region (less than 10-5 torr), while the collision cell Q2 operates at a
pressure
of up to several millitorr. Efficient transfer of ions in and out of Q2
requires that the entrance and exit apertures of Q2 be as large as possible.
However this results in the need for large vacuum pumps in order to
pump the gas which leaks from Q2 into the vacuum chambers containing
Ql and Q3.
In addition, many modern triple quadrupole systems are used
'LO with atmospheric pressure ionization sources, such as electrospray, or
APCI (atmospheric pressure chemical ionization). The ions which are
created in the ion source at atmospheric pressure must be sampled into the
vacuum chamber through a small orifice. The gas which enters the
vacuum chamber along with the ions to be analyzed, imposes another
load on the vacuum pump system, typically of an amount similar to that
imposed by the gas leaking from the collision cell.
In one typical configuration now on the market, ions which
enter from an APCI or electrospray source are focussed through an RF-
only quadrupole which is in front of Q1. This RF quadrupole ("QO") acts as
an efficient containment device for ions and transmits the ions efficiently
into Q1. Thus the entire system may contain up to four quadrupoles, in
which QO and Q2 are RF-only, both operating at a pressure of a few
millitorr, while Q1 and Q3 are mass resolving, both operating at a pressure
of approximately 10-5 torr.
The configuration described above requires high capacity and
costly pumps. While the configuration described above can be operated as
a single mass spectrometer (with no collision gas in Q2, and Q3 in an RF-
only mode), rather than as an MS/MS system, it still requires substantial
pumping capability.
A known related device, the quadrupole ion trap mass
spectrometer, can also provide single MS and MS/MS capabilities. The
quadrupole ion trap operates at a pressure of about 1 millitorr of helium,

CA 02236199 1998-04-28
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and both mass separation and fragmentation are performed in the sarrte
region of space, separated in time. Thus the ion trap is a sequential-i:n-
time device, while the triple quadrupole is a sequential-in-space device.
BRIEF SUMMARY OF THE INVENTION
It is an object of the present invention in one aspect to
provide a method of operating a triple quadrupole system with lower
pumping requirements, thereby having lower cost. In another aspect the
invention provides methods of operation which provide MS/MS/MS
capability, thereby providing improved specificity over MS/MS operation.
In yet another aspect the invention provides improved methods of
operating a quadrupole in a mass resolving mode at an elevated pressure,
in order to allow operation of a triple quadrupole with fewer pumping
stages.
In one of these aspects the invention provides a method of
mass spectrometry comprising mass selecting ions in a first multipole rod
set operated at a pressure of at least approximately 1 millitorr, by applying
an auxiliary field to said first rod set to excite and thereby remove all ions
therefrom except for parent ions, and then transmitting the parent ions
into a second multipole rod set operated at substantially the same pressure
as the first multipole rod set, and fragmenting parent ions in said second
multipole rod set.
BRIEF DESCRIPTION OF THE DRAWINGS
In the drawings:
Fig. 1 is a diagrammatic view of a prior art triple quadrupole
configuration;
Fig. 2 shows a triple quadrupole configuration according to
the invention;
Fig. 3 shows the connection of certain voltage sources to rods
of a quadrupole of Fig. 2;
Fig. 4 shows the connection of other voltage sources to rods of

CA 02236199 1998-04-28
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a quadrupole of Fig. 2;
Fig. 5 shows auxiliary rods used with a quadrupole of Fig. 2;
Fig. 6 shows the connection of further voltage sources to rods
of a quadrupole of Fig. 2;
Fig. 7 shows another configuration of a triple quadrupole
mass spectrometer system according to the invention;
Fig. 8 shows RF connections for a quadrupole of Fig. 7;
Fig. 9 shows a configuration of a quadrupole system for
performing MS/MS/MS;
.LO Fig. 10 shows a modified quadrupole configuration for
performing MS/MS/MS; and
Fig. 11 shows yet another configuration for performing
MS/MS/MS.
DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS
'l5 Reference is first made to Fig. 1, which shows a typical prior
art triple quadrupole mass spectrometer system 10, of the kind sold for
example by the Sciex Division of MDS Inc. of Concord, Ontario, Canada as
an API 300 (trade mark) instrument. The mass spectrometer system 10
includes an ion source 12, usually at atmospheric pressure, from which
20 ions are directed through an orifice plate 14, a vacuum chamber 16
pumped by a pump 18, and a skimmer 20 into a set of two vacuum
chambers 22, 24. These vacuum chambers contain four quadrupoles Q0,
Q1, Q2 and Q3, separated by orifices 30, 32 and 34. (Quadrupole Q2 is in a
"can" 26 in chamber 24.) Quadrupole Q3 is followed by a detector 36
25 connected to a data system 38.
In operation, vacuum chamber 16 is normally pumped to
about 2 torr by mechanical pump 18, while vacuum chamber 22 is
normally pumped to between about 1 and 7 millitorr, and vacuum
chamber 24 is normally pumped to about 10-5 torr, by high capacity turbo
30 pumps 39a and 39b. Collision gas (from a source 27) injected into can 26
causes the pressure in Q2 to be between about 1 and 7 millitorr, as is

CA 02236199 1998-04-28
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conventional. Ions and gas from the ion source 12 pass through orifice
plate 14, skimmer 20, and are transmitted through RF-only quadrupole QO
into resolving quadrupole Q1, where parent ions are selected. The parent
ions are fragmented in collision cell Q2, and the fragments and any
unfragmented parent ions are transmitted into Q3 for mass analysis and
detection by detector 36.
As indicated, the arrangement shown in Fig. 1 requires high
pumping capacity. The pumps needed are bulky and expensive.
Reference is next made to Fig. 2, which shows a configuration
7.0 according to the invention and in which corresponding reference
numerals are used to indicate parts corresponding to those of Fig. 1. In Fig.
2, Q0, Q1 and Q2 of Fig. 1 are replaced by two quadrupoles Q11 and Q12,
both operating in chamber 40 pumped to a pressure of between 1 and 7
millitorr by a 50 liter per second turbo pump 42. Q13 (which corresponds
:'~5 to Q3 in Fig. 1) is as before a conventional RF/DC quadrupole, operated
in
a resolving mode in a low pressure region (typically 10-5 torr).
As before, ions enter from the ion source 12 through orifice
plate 14 into chamber 16 kept at a pressure of about 2 torr, and are than
focussed through skimmer 20 into vacuum chamber 40. Quadrupole Q 11
:?0 is now operated in an RF-only mode, with an RF voltage applied (from a
conventional RF-only quadrupole power supply 43) so that Q11 transmits
all ions above a selected mass value. In other words, Q11 operates as a
high pass filter, the cut-off on the filter being set to the lowest ion mass
of
interest for the application in question. As shown in Fig. 3, one pole 44 of
:?5 a conventional RF voltage source 46 (which forms part of power supply 4:3)
is connected to one pair of rods A1, A3 of Q11, while the other pole 48 is
connected to the other pair of rods A2, A4 of Q11.
In addition to the RF voltage applied, an AC voltage is
applied by an AC source 50 across opposite rods of one rod pair A2, A4 of
30 Q11 and creates a dipole field. This field consists of a range of
frequencies
which correspond to the secular frequencies of all ions in the mass range
of interest, with a notch or hole in the frequency spectrum. The purpose

CA 02236199 1998-04-28
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of the dipole field is to induce a resonant excitation of each of the
unwanted ions in Q11, in order to cause their amplitudes of oscillation to
increase so that they will strike the rods in Q11 before reaching the end of
Q11. Typically the unwanted ions will consist of all ions except one
desired mass to be transmitted into Q12. Thus, by applying a range of
frequencies, with one "notch" in the range corresponding to the mass of
one ion of interest, only that ions of one mass will not be excited, and wall
be transmitted through Q11 to Q12.
The selection of a single mass ion for transmission while
'LO rejecting the other ions is known in connection with ion traps, and is
commonly performed by using either the method known as "filtered noise
field" ("FNF") or the method known as "SWIFT" (stored wavefor:m
inverse Fourier transform), or any of various related methods, all of
which are forms of dipole field and act to eject all ions except the ion
having the m/z value (or more than one m/z value) of interest. The FNF
is usually applied for a period of a few milliseconds, in order to resonate
the unwanted ions from the cell. Then, in ion traps, a second frequency is
commonly applied to excite the ion of interest (which remains in the cell)
to fragment. Finally {still with reference to ion traps), a mass scan is
:?0 performed in order to sequentially eject the fragment ions and form a
mass spectrum. The steps of isolation, fragmentation and ejection are
performed sequentially in time. In contrast, in the device shown in Fig. 2,
these steps are performed sequentially in space, as the ions flow throul;h
the system.
;?5 The technique of applying FNF to a quadrupole device is tlhe
subject of U.S. patent 3,334,225 by Langmuir and U.S. patent 5,187,365 by
Kelly. Langmuir shows how to apply the technique to allow only one ion
to be passed through a quadrupole. Kelly shows how to apply the method
as a mass scanning technique, by "sweeping" the notch through a mass
30 range, or by fixing a notch frequency and sweeping the trapping RF voltage
to move ions sequentially through the notch position. Both these
methods are applied at the typical low pressure at which a quadrupole is

CA 02236199 1998-04-28
_7_
known to operate, i.e. 10-5 torn However both methods suffer from the
problem that typical transit times of ions through a quadrupole without
collisions (i.e. in the low pressure regime of 10-5 torr) are only of the
order
of a few tens to a few hundreds of microseconds. Since the frequencies
applied to eject ions are often in the range of a few tens of KHz, this means
that the ions may experience only a very few number of cycles in the fieJld
before reaching the end of the quadrupole. This is not sufficient to ensure
rejection unless much higher RF and/or FNF amplitudes are used, which
require high power supplies and added cost and complexity. This is
particularly true where a wide range of frequencies are to be applied, since
the power required at each frequency is additive. Experience with this
process in an ion trap shows that several. milliseconds may be required to
eject the ions.
Therefore, according to the invention Q11 may be operated at
.l5 a pressure sufficient that collisions between the ions and the background
gas in Q11 causes the ions to slow down in Q11 so that they experience
more cycles in the dipole field in Q11. In addition, it is known that in tile
presence of a background gas of a few millitorr pressure, ions are
collisionally focussed to the center of the quadrupole. Experience in ion
:?0 traps has shown that a pressure of about 1 millitorr of helium is
advantageous to the ejection process, since under those conditions all ions
begin from near the center of the trap, with little excess energy. Thus the
presence of a background gas is useful both in slowing the ions down, and
in collisionally focussing them toward the center of the device.
:?5 The inventors have found that at a pressure of a few millitorr
in an RF quadrupole of 20 cm length, the transit time of ions may be of the
order of several hundreds of microseconds to greater than 1 millisecond,
i.e. it is increased approximately by a factor of 10 from the transit time in
the low pressure regime. For example, the transit time of m/z 609 from
;30 reserpine, introduced at an energy of approximately 1 eV into a pressure
of
7 millitorr :in a 20 cm RF-only quadrupole, has been measured at 7..5
milliseconds. The longer time spent in the quadrupole due to collisions

CA 02236199 1998-04-28
_8_
with the background gas allows more time for rejection of unwanted ions,
and thus permits more efficient mass selection.
If the device shown in Fig. 2 is to operate in a single NfS
mode, in order to transmit ions from the ion source without
fragmentation, then Q12 is operated without inducing fragmentation.
Mass selection may be achieved by operating Q11 as a mass selection
device, by scanning or sweeping the notch through the frequency range
corresponding to the mass range of interest. Alternatively, mass selection
may be achieved by operating Q13 in a resolving mode, with no mass
'l0 selection in Q11. In this case, a spectrum is produced by the conventional
means of scanning the RF and DC voltages on Q13, maintaining a constant
DC/RF ratio, using conventional DC and RF source 52.
If the device shown in Fig. 2 is to operate in the MS/NIS
mode, then Q11 is operated in a mass selection mode, by applying the FTdF
field with one or more notches. Mass selected ions reaching Q12 are then
excited to fragment in Q12 by one or more of the following methods.
(1) Ions are accelerated from Q11 into Q12 by applying a lower
rod-offset voltage (which is the conventional DC bias voltage applied tc> all
four rods) to Q12 than is applied to Q11, from DC source 54. This
:?0 establishes an electric field between the two rod sets Q11 and Q12 which
accelerates ions from Q11 into Q12. If the field is strong enough, and the
pressure low enough, then ions are accelerated sufficiently between
collisions to acquire sufficient energy to fragment in Q12. This mode is
similar to the conventional mode of operation of the triple quadrupole 10,
:?5 where ions are accelerated in the low pressure region of Q1 before
entering
the higher pressure region of collision cell Q2.
(2) Ions may be excited radially by applying a weak dipole
field, from source 56 shown in Fig. 4, between one or both pairs of rods L~1,
B2, B3, B4 of Q12 in order to cause the selected ion to increase its amplitude
30 of radial oscillation and to fragment in Q12 by collisions with the
background gas as it passes through Q12. This method is analogous to that
used in an ion trap, where ions are excited to cause them to fragment lby

CA 02236199 1998-04-28
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excitation applied at their secular frequency of oscillation in the trap. This
method requires that the ions be gently excited so that their amplitude of
oscillation does not exceed the space in between the rods, in order that the
ions will not strike the rods.
(3) Ions which enter Q12 may be excited axially by applying an
oscillating axial electric field, as described in copending PCT application
serial no. PC'T/CA 96/00541 filed 09/08/96 and assigned to MDS Inc., the
assignee of this application. The axial excitation is not a resonant proceeds,
so the frequency may be optimized independently of the ion mass. Ions
7.0 passing through Q12 are accelerated forwards and backwards along the axis,
experiencing several oscillations in their transit time. This increases the
total path through the device, and thus the number of collisions and tile
probability of fragmentation. In addition the ions may be accelerated to
higher energies without risking the loss of ions to the rods, since the
'15 acceleration is along the axis. The method chosen for creating the axial
oscillating field may be any of the methods disclosed in said copending
application, including for example providing four segmented auxiliary
rods 60 located between the main rods B1-B4 of Q12 as shown in Fig. 5.
Appropriate DC voltages are applied to the segments 62 of the auxiliary
:?0 rods 60 to create an axial field along the length of the main rods B1-B4.
The frequency, amplitude and duty cycle of the oscillating
axial field a.re chosen to ensure that the ions maintain a constant drift
forward through the rods of Q12, in order that they do not become trapped.
For example ions may be oscillated axially so that the time during which a
:?5 forward accelerating axial field is applied is longer than the time during
which a reverse axial accelerating field is applied, so that the average
motion is forward.
Each of these three methods of fragmentation may be applied
singly or in combination in order to provide the most efficient
30 fragmentation, depending on the pressure regime of operation.
Ions transmitted through Q12 are collisionally focussed to the
center of Q12 (by collisions with the gas which is present), so that they are

CA 02236199 1998-04-28
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efficiently transmitted through the aperture 34 into Q13. Q13 is as before
operated in a conventional RF/DC mode, either being scanned to produce
a mass spectrum of fragment ions, or being stepped to various RF voltages
in order to sequentially transmit only specific fragment ions. (This last
mode is sometimes referred to as the multiple reaction monitoring or
MRM mode..)
With reference to the use of FNF for mass selection in Q11, a
simplified method of operation is made possible by the fact that in a
quadrupole, ions have frequencies of oscillation in both the x-y and the y-z
planes, due to the independent ion motion in the x and y directions. With
no applied resolving DC, the frequencies of motion in the x and y
directions are the same. In order to eject an ion of a particular m/z r;~tio
from the device, a dipole field can be applied between either pair of rods. If
it is desired to reject all ions below and above one particular mass value,
dipole fields can be applied between both pairs of rods, and rather than
applying simultaneously all frequencies corresponding to unwanted ions,
a single frequency may be applied to each pair of rods. The app:lif~d
frequencies may then be swept rapidly through the required range, so that
each ion in sequence comes into resonance and is rejected. Typical such
:?0 sweepable dipole frequency sources are shown at 62, 64 in Fig. 6,
connected
to rods A1, A3 and A2, A4 respectively of Q11. (In practice, source 64 may
be the same device as source 56 of Fig. 4, operated in a different mode.)
Thus, all ions of m/z value lower than that to be transmitted
through Q11 are rejected by sweeping the dipole frequency applied to rods
:?5 A1, A3 using source 62, while all ions of higher m/z value than that to
~be
transmitted are rejected by simultaneously sweeping the frequency applied
to the other set of poles A2, A4, by sweeping source 64. The first frequency
sweep (source 62) covers the range from the lowest mass which is present
from the source, up to but not including the frequency corresponding to
30 that of the ion of interest. The second frequency sweep (source 64) covers
the range from the frequency corresponding to the m/z values just above
the ions of interest, to that corresponding to the highest mass range which

CA 02236199 1998-04-28
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is present. Thus all ions except those having the m/z value of interest will
be rejected. The frequencies may be swept through the ranges several
times during the transit time of ions through Q11 in order to ensu:re
effective removal of all unwanted ions.
Reference is next made to Fig. 7, where corresponding
reference numerals indicate parts corresponding to those of Figs. 1 and 2.
In Fig. 7, all three quadrupoles Q21, Q22 and Q23 are operated at the same
pressure as Q11 and Q12 described in connection with Fig. 2, i.e. at a
pressure in the range between 1 and 7 millitorr. Q21, Q22 and Q:?3
7.0 correspond 1:o Q11, Q12 and Q13 respectively of Fig. 3. Q21 and Q22 are
operated in the same way as Q11, Q12. Q23 is now operated in a mass
selection mode similar to that described for Q11, i.e. in an RF-only mode
with FNF as previously described, or with another mode of mass selection
which is effective at a higher pressure. This configuration allov~~s
:~5 pumping of the single vacuum chamber 66 in which all three quadrupoles
are contained by one turbo vacuum pump 68 (for example at 50 liters per
second to maintain the entire vacuum region at 8 millitorr pressure). It
will be realized that the ion detector 36 must also operate at this pressure,
or else must be in a separately pumped region (not shown) at lower
:?0 pressure.
A further cost advantage can be achieved by operating one or
both resolving quadrupoles (Q21 and Q23) at a low q value (hence a low RF
amplitude value), and scanning the position of the notch. For example, if
the RF voltage is kept at less than 500 volts, then solid state amplifiers can
:?5 be used, rather than the more common tank coil. For quadrupole rods of
3/8" diameter, an operating frequency of 816 KHz, and a maximum mass
range of 2000 amu, an upper limit of 500 volts RF would result in a
maximum q value for the highest mass ion of 0.1. This results in a saving
in both space and power consumption.
30 Another cost saving method of operating the triple
quadrupole shown in Fig. 7 is to use only one RF power supply (part of
quadrupole power supply 43), connected for example to Q22, and to

CA 02236199 1998-04-28
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capacitively couple the other two quadrupoles (e.g. Q21 and Q23), e.g. by
capacitors C21, C23. This results in the RF level on all three quadrupoles
being in a fixed ratio. Mass selection in Q21 and Q23 is achieved by
applying different notch frequencies to these two quadrupoles. However
in order to achieve the full mass range on both Q21 and Q23, the RF levels
on these two quadrupoles need to be virtually identical. As shown in Fig.
8, this can be achieved by driving Q21 and Q23 from separate identical
secondary coils 72, 74 of transformer 76 (in power supply 43), where the
primary coil 78 is connected as shown to Q22.
'l0 Another configuration according to the invention is showm
in Fig. 9. Here a mass selecting quadrupole Q31 in a chamber 82 pumped
to 10-5 torr i.s followed by short quadrupoles Q32, Q33 and Q34, all in a
single vacuum chamber 84 which is pumped to a pressure of 1 to 7
millitorr, followed by another mass selecting quadrupole Q35 in a vacuum
.L5 chamber 86 pumped to 10-5 torr, followed by detector 36. This arrangemient
allows MS/MS/MS, in which one ion is selected in Q31 as a parent or a
precursor ion and is then fragmented in Q32, which acts as a collision cell.
The fragments and any unfragmented precursor ions are then mass
selected in Q33 (using the methods described) to provide second precursor
:?0 ions. The second parent or precursor ions are fragmented in Q34 (which
also acts as a collision cell), and are then transmitted to Q35 which mass
selects from the fragments and any unfragmented second parent or
precursor ions.
The technique of MS/MS/MS, which is also performed in ion
;?5 traps by a series of sequential-in-time steps, is useful for very specific
analysis of compounds in the presence of many interferences, and is also
useful in order to elucidate the structure of unknown compounds, by
analyzing the fragmentation pattern of each of the main fragments of tile
parent.
:30 The technique of MS/MS/MS using five quadrupoles in
series has been shown by Beaugrand et al. at the 1986 ASMS Conference.
However these workers used the conventional configuration of an RF/F~C

CA 02236199 1998-04-28
-13-
quadrupole at low pressure, followed by an RF-only collision cell at higher
pressure, followed by an RF/DC quadrupole at low pressure, followed by
an RF-only collision cell at higher pressure, followed by a final RF/DC
quadrupole at low pressure. This configuration imposes significant
complexity and cost of vacuum pumps, since each collision cell is an
additional gas load. The configuration in which Q32, Q33 and Q34 are all
at the same relatively high pressure as shown, means that the pumping
requirements are no greater than for a conventional triple quadrupole
which performs MS/MS.
If Q31 is operated as a high pressure mass selection device
rather than as a low pressure RF/DC quadrupole, then this provides
MS/MS/MS at even lower cost. This version is shown in Fig. 10, in which
primed reference numerals indicate parts corresponding to those of Fig. 9.
In Fig. 10, Q31 is an RF-only quadrupole in which ions are mass selected
='~5 using FNF or another appropriate technique, as previously described.
Another method of providing triple MS is to combine mass
selection and fragmentation in the same device, as shown in Fig. 11. Here,
ions are mass selected by Q41, which is either a conventional RF/D~C
quadrupole at low pressure, or a higher pressure RF-only quadrupo~le
:?0 using FNF mass selection or other suitable form of mass selection ;as
described above.
Q41 is followed by quadrupoles Q42 and Q43, which are both
operated at relatively high pressure (1 to 7 millitorr or higher). Parent ions
mass selected by Q41 are accelerated into Q42, to cause the parent ions to
:?5 fragment in Q42. Simultaneously a notched filtered noise field from
source 50 is. applied to Q42 to cause all fragments except one selected
fragment to be rejected. The amplitude of the excitation of the FN:F is
selected so that the parent ions are not rejected before they have a chance
to fragment in Q42.
;30 The selected fragments are transmitted through Q42 to Q43,, a
second RF collision cell, where they are fragmented to form second
fragments, by any of the available means (e.g. radial or axial excitation). A

CA 02236199 1998-04-28
-14-
radial or dipole source is for example shown at 88, connected to two rods of
Q43. The resulting second fragments are then mass analyzed in Q44,
which is an RF/DC quadrupole operated at low pressure (10-5 torr). This
provides MS/MS/MS capability with only four quadrupoles.
It will be appreciated that the methods of operating the mass
spectrometers as described above can be applied with other mass selection
devices or methods in place of the final quadrupole. For example, the
final quadrupole may be replaced by a time-of-flight mass spectrometer,
where the output from the preceding quadrupole is focussed into an
7.0 extraction region, and is then accelerated orthogonally into the flight
tube
of the time-of-flight mass spectrometer. Alternatively, ions may be
trapped in the preceding mass spectrometer and then pulsed radially
through a slot in the rod into a time-of-flight device, as described in
copending provisional application of Charles Jolliffe, Bruce Thomson and
~'~5 John Barry French filed concurrently herewith.
Alternatively, the final quadrupole may be replaced by an ion
trap for mass analysis or for further processing using methods which are
well understood for ion traps. In general, the advantages which accrue
from providing a mass selection device and an ion fragmentation device
:?0 as described in this application may be similarly realized with any
following device which is used for ion reaction, processing or mass
analysis. Improvements are due to lower costs associated with reduced
pumping requirements and potentially shorter quadrupole devices.
It will also be appreciated by those skilled in the art that
:?5 wherever dipolar fields have been described as a method of exciting the
ions in a quadrupole, quadrupolar fields may be used instead. In cases
where the ions are not exactly on the center axis of the quadrupole, a
quadrupolar field (or a combination of quadrupolar and dipolar fields)
may be more efficient than using only a dipolar field. In addition, in any
30 place where a quadrupole is used simply to provide ion confinement, and
is not used to provide mass resolution, then a hexapole or octopole could
equally be used, since the ion containment in them is at least as good as in




Image

Representative Drawing
A single figure which represents the drawing illustrating the invention.
Administrative Status

For a clearer understanding of the status of the application/patent presented on this page, the site Disclaimer , as well as the definitions for Patent , Administrative Status , Maintenance Fee  and Payment History  should be consulted.

Administrative Status

Title Date
Forecasted Issue Date 2006-10-03
(22) Filed 1998-04-28
(41) Open to Public Inspection 1999-10-28
Examination Requested 2003-01-31
(45) Issued 2006-10-03
Deemed Expired 2013-04-29

Abandonment History

There is no abandonment history.

Payment History

Fee Type Anniversary Year Due Date Amount Paid Paid Date
Registration of a document - section 124 $100.00 1998-04-28
Application Fee $300.00 1998-04-28
Maintenance Fee - Application - New Act 2 2000-04-28 $100.00 2000-04-27
Maintenance Fee - Application - New Act 3 2001-04-30 $100.00 2001-04-11
Maintenance Fee - Application - New Act 4 2002-04-29 $100.00 2002-04-15
Request for Examination $400.00 2003-01-31
Maintenance Fee - Application - New Act 5 2003-04-28 $150.00 2003-04-24
Maintenance Fee - Application - New Act 6 2004-04-28 $200.00 2004-03-25
Maintenance Fee - Application - New Act 7 2005-04-28 $200.00 2005-03-16
Maintenance Fee - Application - New Act 8 2006-04-28 $200.00 2006-03-17
Final Fee $300.00 2006-07-12
Maintenance Fee - Patent - New Act 9 2007-04-30 $200.00 2007-03-21
Maintenance Fee - Patent - New Act 10 2008-04-28 $250.00 2008-03-07
Maintenance Fee - Patent - New Act 11 2009-04-28 $250.00 2009-03-16
Maintenance Fee - Patent - New Act 12 2010-04-28 $250.00 2010-03-19
Registration of a document - section 124 $100.00 2010-03-25
Registration of a document - section 124 $100.00 2010-03-25
Registration of a document - section 124 $100.00 2010-03-25
Maintenance Fee - Patent - New Act 13 2011-04-28 $250.00 2011-03-09
Owners on Record

Note: Records showing the ownership history in alphabetical order.

Current Owners on Record
DH TECHNOLOGIES DEVELOPMENT PTE. LTD.
Past Owners on Record
APPLIED BIOSYSTEMS (CANADA) LIMITED
JAVAHERY, GHOLAMREZA
JOLLIFFE, CHARLES
MDS INC.
THOMSON, BRUCE
Past Owners that do not appear in the "Owners on Record" listing will appear in other documentation within the application.
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Document
Description 
Date
(yyyy-mm-dd) 
Number of pages   Size of Image (KB) 
Representative Drawing 1999-10-13 1 6
Cover Page 1999-10-13 1 27
Abstract 1998-04-28 1 14
Description 1998-04-28 15 729
Claims 1998-04-28 2 87
Drawings 1998-04-28 3 48
Drawings 2005-07-26 3 56
Claims 2005-07-26 2 84
Claims 2005-07-27 2 87
Drawings 2005-07-27 3 50
Claims 2005-09-29 2 85
Representative Drawing 2006-08-30 1 9
Cover Page 2006-08-30 1 34
Prosecution-Amendment 2005-09-29 2 74
Correspondence 2011-06-07 1 12
Assignment 1998-04-28 4 165
Prosecution-Amendment 2003-01-31 1 43
Fees 2003-04-24 1 33
Fees 2001-04-11 1 32
Fees 2002-04-15 1 31
Fees 2000-04-27 1 48
Prosecution-Amendment 2005-01-26 2 59
Prosecution-Amendment 2005-07-26 6 170
Prosecution-Amendment 2005-07-27 7 199
Correspondence 2006-07-12 1 38
Assignment 2010-03-25 22 640
Assignment 2010-03-25 3 78
Correspondence 2011-05-25 1 17