This document provides an overview of LC/MS/MS technology and applications. It discusses the advantages of LC/MS/MS over other techniques, describes various ionization methods with a focus on electrospray ionization, and explains the process of tandem mass spectrometry using triple quadrupole and ion trap instruments. The document also reviews instrumental parameters and common MS/MS modes such as MRM and product ion scanning.
A tandem mass spectrometry (TANDEM MS), also named as MS/MS, is a two-step technique used to analyze a sample either by using two or more mass spectrometers connected to each other or a single mass spectrometer by several analyzers arranged one after another.
A tandem mass spectrometry (TANDEM MS), also named as MS/MS, is a two-step technique used to analyze a sample either by using two or more mass spectrometers connected to each other or a single mass spectrometer by several analyzers arranged one after another.
It is a multi-element analysis technique where The ICP source converts the atoms of the elements in the sample to ions. These ions are then separated and detected by the mass spectrometer
mass spectrometry for pesticides residue analysis- L3sherif Taha
This is the third lecture in series of lectures on mass spectrometry for pesticides residue analysis. This lecture (3) include: Electrospray ionization and Atmospheric pressure chemical ionization
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Normal labor is also termed spontaneous labor, defined as the natural physiological process through which the fetus, placenta, and membranes are expelled from the uterus through the birth canal at term (37 to 42 weeks
2. Technology Transfer Workshop
LC/MS/MS: A Primer
• Advantages over GC/MS
• Importance of Chromatography
• Atmospheric Pressure Ionization
– Focus on Electrospray
• Tandem Mass Spectrometry
– Focus on QqQ
• Modes of MS/MS analysis
– MRM
– Product ion scan
• 3200 Qtrap Parameters
3. Technology Transfer Workshop
Why LC/MS/MS?
• Why Liquid Chromatography?
– Analysis of labile analytes
– Analysis of more polar compounds without
derivatization.
– Analysis of significantly higher masses
– Reduction of lengthy clean-up
• Why MS/MS?
– Additional structural elucidation
– Further reduction of clean-up (?)
– Specificity
– Useful MS modes
4. Technology Transfer Workshop
System Configuration
Liquid
Chromatography
Ionization Mass Analyzer
Detector/
Data
Collection
• ESI
• APCI
• APPI
•Triple Quadrapoles
•Ion-Traps
•Hybrids
•Very important!
•Many columns
•Many solvent
systems
5. Technology Transfer Workshop
Atmospheric Pressure Ionization
• Revolutionized LC/MS opening it to a wide
array of applications in the forensic laboratory.
• Desolvation and/or ionization of analytes
occurs at atmospheric pressures
• Gas phase ions are sampled by the high
vacuum mass spectrometer.
6. Technology Transfer Workshop
Types of Ionization
• Several common modes differing by method of
ion formation:
– Electrospray (ESI)
– Atmospheric Pressure Chemical Ionization
(APCI)
– Atmospheric Pressure Photo-Ionization (APPI)
– New dual sources (ESI/APCI) or (APCI/APPI)
7. Technology Transfer Workshop
Which is Best?
• It depends on the exact application.
• Increasing polarity and molecular weight and
thermal instability favors electrospray.
• Most drugs of abuse are highly polar and are
easily analyzed using electrospray.
• High molecular weight proteins also require
electrospray
• Lower polarity and molecular weight favors
APCI or APPI.
• Lower background, but compounds must be
more thermally stable.
8. Technology Transfer Workshop
Focus on Electrospray
Electrospray is a method of getting the
solution phase ions into the gas phase so
that they can be sampled by the mass
spectrometer.
9. Technology Transfer Workshop
Electrospray: The Process
Three Fundamental Processes:
1. Production of charged droplets.
2. Droplet size reduction, and fission.
3. Gas phase ion formation.
10. Technology Transfer Workshop
Electrospray: Overview
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To MS
Orifice
Plate
Curtain
Plate
Drying Gas
Curtain Gas
Droplet Formation
Desolvation
& Fission
Gas Phase Ion
Generation
5kV
Nebulizing
Gas
11. Technology Transfer Workshop
ESI: Production of Charged Droplet
1. A large voltage ( up to 6kV) is applied
between the end of a capillary carrying the LC
mobile phase and the mass spectrometer
entrance.
2. Ions (of the same polarity) are drawn out
toward the counter electrode (curtain plate)
pulling the mobile phase along.
3. When the excess charge at the tip of the
capillary overcomes surface tension, a droplet
is formed.
14. Technology Transfer Workshop
ESI: Gas Phase Ion Formation
• Several models of bare ion formation; all seem
to play some role.
• Charge Residue Model
• All the solvent evaporates, leaving a bare gas
phase ion.
• Ion Evaporation Model
• As the droplet shrinks the charges (analyte) that
reside on the surface get just enough energy to
jump into the gas phase.
• Ion Emission Model
• The high voltage case some ion formation
directly from the LC capillary.
15. Technology Transfer Workshop
ESI: Types of Ions Formed
• Electrospray can operate in either positive or
negative mode.
• Positive mode:
– Best suited to basic drugs that form a stable
HCl salt.
• [M+H]+ is the primary ion formed
• [M+nH]n+ and [M+Na+]+ can also be formed.
• Negative mode:
– Best suited to acidic drugs that form stable Na
salts.
• [M-H]-, [M-nH]n- and [M+I-]-
16. Technology Transfer Workshop
ESI: Ionization Efficiency
• Enhanced by the production of smaller droplets.
– Lower mobile phase flow rate yield smaller droplets.
– Nebulizing gas promotes droplet formation
– Use of volatile mobile phases promotes desolvation and
droplet fission
• Enhanced by increasing the concentration of analyte
ions at the end of the capillary tip.
– Matrix modifiers to promote solution ion formation.
– Chromatography to produce narrow highly concentrated
bands of analyte.
17. Technology Transfer Workshop
ESI: Pros and Cons
Pros
• Soft ionization technique, resulting in little
decomposition of labile analytes.
• Generally produces only molecular ions.
• Multi charged analytes easily produced,
allowing proteins to be analyzed.
• Wide range of analytes
• Highly efficient ion production.
18. Technology Transfer Workshop
ESI: Pros and Cons
Cons
• Lower flow rates
– concentration dependent
– nL/min (nanospray)
• Analyte must form solution phase ion.
– HCl or Na salt good indicator of suitability
•Ion Suppression
19. Technology Transfer Workshop
ESI: Ion Suppression
• The bogeyman of electrospray!
• Often results from inefficient droplet formation.
• Causes:
– Nonvolatile buffers or salts (phosphates)
– Nonvolatile materials in mobile phase Ion pairing
– Reported that higher molecular weight analyte ions can
suppress smaller analytes.
• Generally more prominent early in an RP-LC run, but
can occur at anytime.
• Underscores the need for good chromatography!
20. Technology Transfer Workshop
ESI: Ion Supression
~90%reduction
Ion Suppression Study
Oxycodone Infusion with solvent
flow.
Negative control injected at ~0.1min
21. Technology Transfer Workshop
ESI: Keys to Remember
1. Electrospray is a soft ionization technique generally
producing [M+H]+ ions in positive mode.
2. Most drugs that form an HCl salt will be analyzable by
positive mode electrospray.
3. Volatile buffers and mobile phases will increase
generally ionization efficiency.
4. Good chromatography producing concentrated bands
of analyte at the nebulizer tip will increase ionization
efficiency.
5. Poor clean-up can lead to significant ion suppression
usually at the beginning of the LC run.
23. Technology Transfer Workshop
Tandem Mass Spectrometry
• Triple Quadrupole (QqQ)
– Two mass filtering quadrupoles bracket an Rf
only collision cell.
• Ion Trap (IT)
– A single ion trap serves as mass analyzer and
collision cell.
• Hybrids (e.g. LIT)
– Instrument is in the QqQ geometry, but one
quadrupole can also trap and store ions.
24. Technology Transfer Workshop
Triple Quads v. Ion Traps
• Advantages
– Very sensitive. (SIM)
– Good for quantitation
– Some useful MS scanning
modes
• Limitations
– No MSn
– Expensive
– Limited to unit mass
resolution.
– Less sensitive in full scan
mode.
• Advantages
– Higher full scan sensitivity
– Higher mass resolution
– MSn
• Limitations
– Not as good for
quantitations.
– Space Charge Effects
– 1/3 cut-off rule.
– Cannot perform certain
MS experiments.
Triple Quadrupole Ion Trap
25. Technology Transfer Workshop
Triple Quad Configuration
Q1 Q2 Q3
Q0
RF only
Collision Cell
Scanning
RF/DC
Scanning
RF/DC
RF only
• Q1 and Q3 are standard mass filter quadrupoles.
– The can scan masses sequentially (e.g. 50 to 500 amu)
– The can be used to select a single mass.
• Q2 is an RF only quadrupole that is in a gas filled chamber.
– Q2 is the “collision cell” where mass fragmentation occurs.
– Q2 does not filter ions. It accepts all ion sent to it by Q1 and
passes all ions formed by collision to Q3 to be sorted.
26. Technology Transfer Workshop
Triple Quads…
• In scanning mode 99% ions lost between the rods.
– Poorer full scan sensitivity
• In SIM mode 100% of selected ion reaches detector.
– Makes them highly sensitive and great for quantitation!
• Mass resolution typically limited to “unit” (+/- 0.2 amu)
• Fragmentation is controlled by the energy ions have
when they enter the collision cell.
– Higher energy >> greater fragmentation.
27. Technology Transfer Workshop
Collision Cell
• LINAC (linear accelerator) Collision Cell
– Filled with N2 gas at roughly 3x10-5 torr.
– Drives ions out, reducing “cross-talk”
• The analyte molecules undergo collision
activated disassociation by energetic collision
with the N2 molecules.
• The N2 also acts to “cool” fragments,
facilitating transport to the detector.
28. Technology Transfer Workshop
Ion Traps
• Ions fill the space between a ring electrode and
a pair of end-cap electrodes.
• Mass analysis and fragmentation occur in the
same space.
Ring Electrode
Ring Electrode
Entrance
Endcap
Electrode
Exit Endcap
Electrode
29. Technology Transfer Workshop
Ion Traps…
• In full scan mode: Ions fill and are trapped in space
then masses are scanned out of the trap sequentially.
– Ions are not lost, so full scan sensitivity is better, but
filling/closing cycles make them poorer at quantitation.
• Mass resolution is controlled by the “speed” at which
masses are scanned out of the trap.
– slower scanning = better mass resolution.
• In MS/MS mode: Ions trapped. Fragmentation occurs
when the selected ion is excited by a so called “tickle”
voltage and collides with bath gas (He). This process
can occur recursively thus MS/MS/MS/MS….
30. Technology Transfer Workshop
Hybrid Instruments
• Typically in the same configuration as a triple
quadrupole instrument.
• On the Qtrap Q3 is the hybrid quadrupole
dubbed a “linear ion trap” or LIT.
• Q3 can function as a quadrupole OR an LIT.
Q0 Q1 Q2 Q3
Applied Biosystems 3200 Qtrap System
31. Technology Transfer Workshop
LIT Scanning
Radial Trapping
Axial
Trapping
Auxiliary RF
Ramped….
Exit Lens
with Grid
Main RF
Ramped…
Q2
…simultaneously
Ramp EXB
Radial Trapping
32. Technology Transfer Workshop
Advantages of LIT vs. IT
• Has a larger “volume” so it can be filled with
more ions before exhibiting space charge
effects.
• Ions are formed outside the trap, so it is not
limited by the 1/3 rule.
• Can perform MS/MS/MS experiments by
selecting an ion and fragmenting it using the
spillover collision gas. (1/3 rule applies here…)
33. Technology Transfer Workshop
Modes of Operation
• Triple Quads and Ion Traps
– Full Scan (LC/MS)
– MRM (Multiple Reaction Monitoring)
– Product Ion Scan (PI)
• Exclusively Triple Quad
– Constant Neutral Loss
– Precursor Ion Scan
• Exclusively Ion Trap
– MSn
H
Y
B
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D
S
34. Technology Transfer Workshop
Multiple Reaction Monitoring (MRM)
• Q1 Selects an [M+H]+
• Q2 fragments the selected ion.
• Q3 monitors only one daughter ion
Q0 Q1 Q2 Q3
N2 CAD Gas
Precursor ion
selection
Ion accumulation
Fragmentation
Exit lens
Steps MS2: 1 2 3 &4
35. Technology Transfer Workshop
MRM
• Only the daughter ion reaches the detector.
• Sensitivity of MRM is a function of how much of the
daughter ion is produced.
• The parent ion fragmentation to daughter ion is
commonly referred to as a “transition”
Q0 Q1 Q2 Q3
N2 CAD Gas
Precursor ion
selection
Ion accumulation
Fragmentation
Exit lens
Steps MS2: 1 2 3 &4
36. Technology Transfer Workshop
Example MRM Data
• Many transitions can be stacked together in a method.
• The instrument will monitor each pair for a short time.
• MRM is analogous to SIM on a GC/MS only more
compound specific.
Oxycodone: (316.2241)
Parent : 316.2
Daughter : 241
Result of one MRM cycle of 130 drugs.
37. Technology Transfer Workshop
Product Ion Scanning
• Q1 selects a parent ion.
• Q2 fragments the selected ion
• Q3 traps then scans out all fragment ions.
Q0 Q1 Q2 Q3
N2 CAD Gas linear ion trap
3x10-5 Torr
Precursor ion
selection
Ion accumulation
Fragmentation
Exit lens
Steps MS2: 1 2 3 &4
38. Technology Transfer Workshop
Product Ion Scan
• Selection of a single parent ion by Q1 allows
separate product ion scans for coeluting
compounds to be easily generated.
– Provided they don’t have the same mass…
Q0 Q1 Q2 Q3
N2 CAD Gas linear ion trap
3x10-5 Torr
Precursor ion
selection
Ion accumulation
Fragmentation
Exit lens
Steps MS2: 1 2 3 &4
39. Technology Transfer Workshop
Example EPI Data
• Oxycodone (316.2) is selected by Q1.
• Q2 fragments oxycodone
• Q3 operating as an LIT traps all the fragments,
and the scans them out.
• “Enhanced” means using the LIT.
40. Technology Transfer Workshop
Linking MRM and EPI
• MRM is an excellent survey method.
– Allows for stacking of many transitions
– Relatively fast* cycle time
• EPI is an excellent for qualitative identification
– Parent ion linked fragmentation pattern
– Many fragments that can be library matched.
• An ideal qualitative method would use MRM to
look for drugs, and EPI to confirm them.
41. Technology Transfer Workshop
3200 Qtrap Overview: The Source
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GS1 IS
TEM &GS2
ihe
Orifice
Plate
Voltage, Temperature
& Gas Parameters
42. Technology Transfer Workshop
Source Parameters
• IonSpray Voltage (IS) [5000]
– The voltage applied between the needle and
orifice plate that “ionizes” and nebulizes the
liquid flow. Polarity determines what type of ions
will reach MS. In positive mode typically 4000
and 5500V; In negative mode –3000 to –4000V.
• Ion Source Gas 1 (GS1) [50]
– The nebulizer gas pressure. Facilitates droplet
formation. Higher flow, higher GS1.
43. Technology Transfer Workshop
Source Parameters
• Temperature (TEM) [400]
– The temperature of the heater gas (“the hairdryer”). It
promotes desolvation. The setting is optimized based on
mobile phase flow rate and composition.
• Ion Source Gas 2 (GS2) [55]
– The heater gas pressure. Aids in solvent evaporation,
increasing ion efficiency. Heated gas stream intersects
nebulized liquid stream at about 90o right in front of the
curtain plate.
• Higher liquid flow, and/or higher aqueous mobile phase
composition, higher TEM and GS2 required. Needs to
be optimized.
44. Technology Transfer Workshop
Source Parameters
• Curtain Gas (CUR) [35]
– High purity N2 that flows between the orifice and
the curtain plate. It repulses large droplets and
neutrals keeping the Q0 clean.
• Interface Heater (ihe) [ON]
– Orifice plate heater. I am sure it is important, but
I cannot tell you why.
45. Technology Transfer Workshop
3200 Qtrap: Potentials
• Most potentials are relative to the entrance
potential (EP).
• As ions move from the source to the detector
they see increasingly negative volatage.
Q0 Q1 Q2 Q3
EP CEP CXP
DP
CE CEM
46. Technology Transfer Workshop
More Potentials
• Declustering Potential (DP) [45]*
– The voltage applied to the orifice plate.
– Used to break up ion clusters e.g.( [M+H3O+]+) and
reduce chemical noise (increase sensitivity).
• HOWEVER high DP values can induce fragmentation
prior to mass analysis. Generally called “In source CID”.
Great for LC/MS. Bad for LC/MS/MS.
• Entrance Potential (EP) [10]*
– The voltage between the skimmer (ground) and the
entrance to Q0. Typically set to -10V in positive mode.
• Collision Cell Entrance Potential (CEP) [10]*
– The potential difference between Q0 and IQ2.
– Facilitates ion transmission to the collision cell.
– Most mass dependent parameter
47. Technology Transfer Workshop
Still More Potentials
• Collision Energy (CE) [20]*
– The potential difference between the Q0 and Q2.
– Determines the degree of fragmentation in Q2.
– Greater CE is usually structurally elucidating unless so
high it obliterates the parent molecule into small
common mass fragments.
• (CE = EP – RO2; CE = -5V – (-25V) = 20V)
• Collision Energy Spread (CES) [30]
– Since different analytes need different CE for optimized
fragmentation
• Collision Cell Exit Potential (CXP) [4]
– The potential difference between Q2 and IQ3.
– Always 4V.