lecture 3 - lc/ms on-line › wp-content › uploads › 2016 › 05 › 304011.pdfratio of signal...
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LECTURE 3
Ionization Techniques for Mass Spectrometry
Jack Henion, Ph.D. Emeritus Professor, Analytical Toxicology
Cornell University Ithaca, NY 14850
Lecture 3, Page 1
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Contents
• Electron ionization (EI) • Electrospray ionization (ESI)
– Nano ESI
• Atmospheric pressure chemical ionization ( APCI) • Atmospheric pressure photoionization ( APPI) • Matrix assisted laser desorption ionization (MALDI) • LAESI • Direct analysis in real time (DART) • Desorption electrospray ionization (DESI) • Atmospheric sampling analysis probe (ASAP) • And there are many more that may or may not mature.
Lecture 3, Page 2
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Many Forms of Ionization have been Reported
• REIMS
• PESI
• LIAD-ESI
• DART
• FAPA
• LAESI/IR-LDESI/MALDESI
• ELDI
• LIAD-ESI
• EI
• APCI
• ESI
• APPI
• ASAP
• MALDI
• DESI
• RADIO
• DAPPI
Lecture 3, Page 3
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Electron Ionization (EI) Source (not yet commercially available for LC/MS)
High vacuum
Lecture 3, Page 4
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Ionization Processes: Electron Ionization (EI) vs. API
• Electron ionization (EI) forms radical cations as shown below: – M + e- M+. + 2 e-
– The radical cation is very reactive and often is the primary director of the ensuing fragmentation
• API techniques generate (M+1)+ ions as shown below:
• Electrospray or APCI:
• (M+H)+ (M+H)+ • (in solution) (ion evaporation or APCI) (gas-phase ion)
But how does this occur?
70 eV electrons
Lecture 3, Page 5
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Positive Ions: Odd-Electron and Even-Electron Ions
Odd Electron Ions
N
HH HN
HH H
EE (8) OE (7)
N
HH HN
HH H
EE (8) EE (8)
Even Electron Ions
H
e2e
OE and EE Ions
H
+
Lecture 3, Page 6
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Electrospray Ionization
Lecture 3, Page 7
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Electrospray Process
“A method by which ions
present in solution can be
transferred to the gas phase”
Classical or Pure ESI or NSI: Droplet Size influenced purely by electrostatic repulsion
High Flow ESI – Gas Assisted: Droplet size influenced by high
velocity gas & electrostatic repulsion
Courtesy ThermoFinnigan Lecture 3, Page 8
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Ink Jet printing
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High-Voltage
Power Supply
electrons electrons
OXIDATION REDUCTION
Taylor Cone
+4 kV
+1 kV
Lecture 3, Page 9
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Maximizing Signal. Minimizing Noise.
Agilent Animation of S/N
Lecture 3, Page 10
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AB SCIEX “Turbo-V “ Gas Entrainment Source High sensitivity at any flow rate.
4. Controlled Entrainment
Background Reduction
1. Increased Thermal Efficiency
of Heater
3. Promote Turbulent Mixing
Improved Heat and Mass Transfer
Maximize Desolvation
2. Second Heater
Double Thermal Load
Signal Enhancement Flow Rate Dependent
5. Reduced Dispersion of Droplets
Lecture 3, Page 11
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• Benefits: Sensitivity across a wider range of
flow rates
–Higher desolvation for >1mL/min flow rates • More heated nitrogen auxiliary gas flow aids
desolvation at high flow rates
–One piece metal needle allows for easy replacement • Available as low flow and regular (high) flow
– Contoured tip for enhanced low flow (micro-spray; 5-25uL) stability • Generates better electrostatic fields enabling spray
stability for lower flow rates
Electrospray Ionization Technology Enhancements: Thermo HESI-II
* Available on all TSQ products Metal Needle Standard
Contoured tip
Higher desolvation
Lecture 3, Page 12
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Synapt HDMS System
Waters Z-Spray
Lecture 3, Page 13
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Agilent Jet Stream Technology
Courtesy of Dr. Alex Mordehai, Agilent Technologies
Lecture 3, Page 14
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Collision Cell
H-SRM Operation – Enhancing Specificity
= only pre-cursor ion transmitted
Lower chemical noise
Lower detection limits
Thermo TSQ Quantum Lecture 3, Page 15
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• No Line of sight – enhanced S/N
• 5x better SRM transmission efficiency
• Argon as collision gas for higher sensitivity
Enhancing Detection Limits – 90º Collision Cell Design
Exit lens
assembly
Entrance lens
assembly
Collision cell
housing
Square quadrupole
collision cell
Lecture 3, Page 16
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A trace of DMSO to Improve Peptide Ionization Reponse
Jesse G. Meyer, Elizabeth A. Komives, Charge State Coalescence During Electrospray Ionization Improves Peptide Identification by Tandem Mass Spectrometry, J. Am. Soc. Mass Spectrom. (2012) 23:1390Y1399.
Page 17
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APPI
Atmospheric Pressure Photoionization
Lecture 3, Page 18
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APPI source configuration employing a VUV light source and orthogonal spray geometry.
Qualitative diagram representing
ionization of nonpolar compounds
by APPI
APPI Source and Compound Strike Zone
APPI
Electrospray
Ionization
Polarity Very PolarNon-Polar
Mo
lec
ula
r W
eig
ht
100
1,000
10,000
100,000
APCI
Lecture 3, Page 19
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Direct APPI
M + hv M+
M+ + S MH+ + S[-H]
Dopant APPI
D + hv D+
D+ + M MH+ + D[-H]
D+ + M M+ + D
Analyte molecule M is ionized to a molecular
ion M+. (If analyte ionization potential is
below photon energy)
In the presence of protic solvents, M+ may
abstract a hydrogen atom to form MH+.
A photoionizable dopant is delivered in large
concentration to yield many D+ ions.
D+ ionizes analyte M by proton or electron
transfer.
This is PI-initiated APCI.
Direct vs. Dopant APPI
Lecture 3, Page 20
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Benefits of APPI
– Ionizes a relatively wide range of compounds
(e.g., non-polars, electronegative cpds, etc.)
– Predominantly parent ion signal (minimum
fragmentation)
– Low noise source (minimum solvent signal)
– Minimum ion suppression
– Large linear dynamic range
– Works for positive and negative ionization
Lecture 3, Page 21
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APPI Is Best For
• Environmental – PAHs – Steroids – Pesticides
• Food Safety – PAHs – Pesticides – Fish Oil Lipids – Vitamins
• Petroleum/Oils/Biofuels – Petroleum – Biofuels – Triacylglycerol Lipids
• Pharmaceuticals/Small Molecules – Steroids – Metabolites (especially lacking functional groups) – Chiral Separations (i.e., normal phase LC)
R2 = 0.9999
0.E+00
5.E+05
1.E+06
2.E+06
2.E+06
0 250 500 750 1000 1250
Inj. Amount (ng)
Peak A
rea
R2 = 0.9995
0
200
400
0 0.1 0.2 0.3
>5-decade linear
response on
the ZQ
Analysis of Lipids: Diarachidin(1:1 Isooctane:IPA @ 100 uL/min)
R2 = 0.9999
0.E+00
5.E+05
1.E+06
2.E+06
2.E+06
0 250 500 750 1000 1250
Inj. Amount (ng)
Peak A
rea
R2 = 0.9995
0
200
400
0 0.1 0.2 0.3
>5-decade linear
response on
the ZQ
Analysis of Lipids: Diarachidin(1:1 Isooctane:IPA @ 100 uL/min)
50 100 150 200 250 300 350 400
Ion m ass
0
100
%
0
100
%
[M+H]+
315.17
APPI
ESI
Progesterone
50 100 150 200 250 300 350 400
Ion m ass
0
100
%
0
100
%
[M+H]+
315.17
APPI
ESI
Progesterone
Dibenzo[a,h]anthracene,
278 > 250
6.1 - 100,000 pg
R2 = 0.9994
0.0E+00
2.0E+04
4.0E+04
6.0E+04
8.0E+04
1.0E+05
1.2E+05
0 20000 40000 60000 80000 100000
Injection Amount (pg)
Peak A
rea
>104 linear response
Lecture 3, Page 22
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APPI Very Resistant to Ion/Matrix Suppression
min 0 0.5 1 1.5 2 2.5 3 3.5
APPI TIC Full Scan - Rat Plasma Extract
APPI
APCI
ESI
Determination of ion suppression susceptibility for
APPI, APCI, and ESI by post-column addition and
detection of fluphenazine while running an LC/MS
chromatogram of rat plasma.
APPI
APCI
ESI
Average deviation
74%
57%
23%
Median deviation
68%
52%
22%
Ratio of signal for FIA/MS vs. LC/MS
Measurement performed on a 29-compound library of unknown purity
These results show minimal ion
suppression by APPI. APCI shows
less ion suppression than ESI, but
APCI signal is noisier than by APPI
Lecture 3, Page 23