possibilities and limitations of recent developments in...
TRANSCRIPT
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Possibilities and Limitations of
Recent Developments
in
Micro Sample Preparation
Techniques
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State-of-the-Art
Chromatographic &
Mass Spectrometric
Instrumentation
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T
SUPER-CRITICAL
FLUID
P
SOLID LIQUID
GAS
Chromatographic Techniques
- Viscosity- Density- Diffusivity
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Throughput
Productivity Resolution
Robustness, Flexibility, Versatility, Sensitivity, …
“21 st Century LC Triangle”
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Pesticides LC/MS/MS method
Jet stream conditions
Drying gas temperature 275 ºCDrying gas flow (nitrogen) 6 L/minNebulizer gas pressure (nitrogen) 35 psigCapillary voltage 4000 VSheath gas temperature 325 ºCSheath gas flow 12 L/minNozzle voltage Off
6460A QQQ settings
MS1 and MS2 resolution Unit Time Filtering peak width = 0.03 minDynamic MRM transitions up to 4000Constant cycle time 373 msDelta EMV 400 V
Column Eclipse Plus-C18, 2.1 x 100 mm, 1.8 µmColumn temperature 35 ºCInjection volume 5.0 µL Autosampler temp 6 ºCNeedle wash flushport (MeOH:H2O 75:25), 5 secsMobile phase A = 0.01% formic acid in water
B =5 mM ammonium formate 0.01% formic acid in 95:5 acetonitrile:waterFlow rate 0.3 mL/minGradient 0 min 6% B
15 min 95% BStop time 20 min 6% BPost time 1 min
Page 5September, 2009LC/MS Pesticide Analysis
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Dynamic MRM of 300 Pesticides
2 Transitions Each
September, 2009 Page 6LC/MS Pesticide Analysis
Run with 1200-SL LC 2.1 x 100 C18 Eclipse PLUS 1.8 µm
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100 Pesticides in 3 min
With FULL SPECTRA because of FAST RUN TIMES
September, 2009 Page 7LC/MS Pesticide Analysis
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GCxGC – FID
September, 2009 Page 8LC/MS Pesticide Analysis
A
B
1
2
4
5
6
3
3
1
4
5
6
2
A
B
1
2
4
5
6
3
3
1
4
5
6
2
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GCxGC – ToF-MS
September, 2009 Page 9LC/MS Pesticide Analysis
A
B S
S
A
B SS
SS
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DAD 1V1 V2
DAD 2
Dim 1 Pump
Dim 1 Column
Dim 2 Pump 2
Dim 2 Pump 1
Dim 2 Column 1
Dim 2 Column 2
Loop 2
Loop 1
Waste
V1 V2
Comprehensive LCxLC
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BSA Tryptic Digest – Contour plot 150 mm x
0 50
0.4
0.5
0.6
0.7
0.8
Dim
ensi
on 2
100
725
150 200 250 300
Dimension 1
min
min
1st dimension: 4 x HALO C18, 150 x 2.1 mm , 2.7 µm at 4 5°Cmobile phase at pH 1.8 and 100 µL/min
2nd dimension 2 parallel Zorbax 300 Extend C18, 50 x 4. 6 mm, 3.5 µmmobile phase at pH 10 and 4 mL/min Loop volume: 50 µL
725 x 35 = 25.375
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Metabolomics Discovery Pipeline
Biological question
Experimental design
Sampling Samplepreparation
Dataacquisition
Dataanalysis
BiologicalInterpretation
Feature extraction
Mass & ret time
alignment
Normaliz-ation
FilteringStatistical analysis
Data recursion Identification
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Metabolomics Discovery Pipeline
Biological question
Experimental design
Sampling Samplepreparation
Dataacquisition
Dataanalysis
BiologicalInterpretation
Feature extraction
Mass & ret time
alignment
Normaliz-ation
FilteringStatistical analysis
Data recursion Identification
?
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Blood/plasmaBlood/plasma
350
Mas
s (D
a)
550
750
950
Retention time (min)
0 9010 30 50 70
A
C,D
E,F
G
H
B
103
105
107
In-source f ragments of cholesterol esters
Blood plasma lipidome complexity revealed
• Feature 2D retention time/mass map (+ mode) Time/mass window
Lipid Class
A Lysophospholipids
B Monoacylglycerols
C Phospholipids
D Sphingomyelins
E Ceramides
F Diacylglycerols
G Cholesterol esters
H Triacylglycerols
10 10 µµL blood plasmaL blood plasmaµµLLELLE
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Insight into the skin ceramides
• 16 common ceramide classes varying in chain length and fatty acid saturation
Non-hydroxy fatty acid (N)
αααα-hydroxy fatty acid (A)
ωωωω-hydroxy fatty acid (O)
Ester linked ωωωω-hydroxy fatty acid (EO)
Dehydrosphingosine (DS)
Sphingosine (S)
Phytosphingosine (P)
Hydroxy-sphingosine (H)
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The analytical variability must be smaller thanthe biological variability …
the key: sampling and sample preparation
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Insight into the skin ceramides
• Sampling on a patch coated with an adhesive layer
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500
Mas
s (D
a)
700
900
1300
Retention time (min)
30 40 50 60
Ester-linked
103
105
107
1100
Non-ester linked
70
Insight into the skin ceramides
• Feature 2D retention time/mass map (- mode)
~1000 ceramide related features detected in 3 out o f 3 samples
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Sampling and
Sample Preparation:
“ the Key “
to Meaningful Analytical Data
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Can we ... produce precise and accurate data ... ?
- PAHs in the air
- Phthalates in water, sediment, etc.
- Bisphenol A in baby bottles
- Organotin compounds in environmental
and foods samples
- Pesticides in baby food
- ...
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Gaseous Samples
- Static Headspace (SHS)
- In-tube Extraction (ITEX)
- Dynamic Headspace (DHS)
- Purge & Trap (P&T)
- Solid-Phase Microextraction (SPME)
- Headspace Sorptive Extraction (HSSE)
- ...
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Solid Samples
- Ultrasonic Extraction (UE)
- Supercritical Fluid Extraction (SFE)
- Accelerated Solvent Extraction (ASE)
- Pressured Liquid Extraction (PLE)
- Microwave Assisted Solvent Extraction (MASE)
- Gas Phase Stripping (GPS)
- Matrix Solid Phase Dispersion (MSPD)
- ...
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Comparison …
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12
4
15
13
12
11
5
6
78
910
1614
3
10 14 18 22 26 30 34
20
40
60
80
100
Abundance (x 104)
Mixed bed tube
10 14 18 22 26 30 34
20
40
60
80
100
Time, min
Direct liquid injection1
2
4
15
13
12
11
5
67 8
910
1614
3
Spike level 1 ng per PAH – 200 L air through the tube before analysis
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Sorptive sampling High Volume sampling
120 mg PDMS – Glass fibre filtre + PUF60 mg Tenax
Spike d-standards
24 h at 100 mL/min 24 h at 0.9 m 3/min
Total: 144 L Total: 1.296 m 3
Thermal desorption Soxhlet Extraction
Spike d-standards
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Hvol (+PUF)
Mixed Bed
Ratio
TEF (*) TEQ (*) TEQ (*)
Component ng/m³ ng/m³
Hvol (+PUF)
PDMS
Naphthalene 3.33 116.49 35.0 0.001 0.003 0.116
Acenaphtylene 3.08 6.11 2.0 0.001 0.003 0.006
Acenaphtene 0.31 7.14 23.0 0.001 0.000 0.007
Fluorene 5.38 7.92 1.5 0.001 0.005 0.008
Phenanthrene 11.74 13.85 1.2 0.001 0.012 0.014
Anthracene 0.72 0.92 1.3 0.01 0.007 0.009
Fluoranthene 3.43 4.50 1.3 0.001 0.003 0.005
Pyrene 1.98 2.90 1.5 0.001 0.002 0.003
Benzo(a)anthracene 0.36 1.01 2.8 0.1 0.036 0.101
Chrysene 0.81 1.96 2.4 0.01 0.008 0.020
Benzo(b)fluoranthene 0.57 1.78 3.1 0.1 0.057 0.178
Benzo(k)fluoranthene 0.29 0.52 1.8 0.1 0.029 0.052
Benzo(e)pyrene NM 1.49
Benzo(a)pyrene 0.48 1.11 2.3 1 0.480 1.110
Indeno(1,2,3-c,d)pyrene 0.30 0.43 1.4 0.1 0.030 0.043
Dibenzo(a,h)anthracene 0.65 1.07 1.6 1 0.650 1.070
Benzo(g,h,i)perylene 0.67 1.24 1.9 0.01 0.007 0.012
sum 34.10 170.44 1.333 2.754
Mean values 52 analyses - April 2005/March 2006
!
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Liquid Samples
- Micro Liquid-Liquid Extraction (µLLE)
- Solid-Phase Microextraction (SPME)
- Stir Bar Sorptive Extraction (SBSE)
- Single Drop Microextraction (SDME)
- Liquid-Phase microextraction (LPME)
- Membrane Assisted Solvent Extraction (MemASE)
- Solid Phase Extraction (SPE)
- Dispersive Liquid-Liquid Microextraction (DLLME)
- ...
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PAHs in water10 ng/L
LLE SPE DLLME SBSE
Sample size (mL) 500 100 5 5
Solvent A3 x 25 mL
DCM 5 mL 8 µL DCM none
Solvent B 1 mL hexane500 µL
acetone noneconcentration (evaporation) yes yes no no
Final volume 1 mL hexane 0,2 mL 8 µL TCE
Final concentration (*) 5 ng/mL 1 ng/200 µL 50 pg/8µL 5 0 pg/stir barInjection volume 2 µL 2 µL 2 µL TD
Amount injected (pg) 10 pg 10 pg 12,5 pg 50 pg
PAHs in Water at the 10 ppt Level (ng/L)
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On-line SPE - LC-MS/MS
Load Pump
(SPE)
SPE 1-6WASTE
In-line filter
External
V
Analysis Pump 1
(Elute)
Analytical column
and QQQ
Injection valve
Loop sizes > 1 mL
Inject
Column switching valve
6 port / 2 positions
Load or Elute
Column selector valve
Multi-position
Select SPE cartridge
Inject and Load
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On-line SPE - LC-MS/MS
Load Pump
(SPE)
SPE 1-6WASTE
In-line filter
External
V
Analysis Pump 1
(Elute)
Analysis Pump 2
(Add)
Analytical column
and QQQ
Injection valve
Loop sizes > 1 mL
Inject
Column switching valve
6 port / 2 positions
Load or Elute
Column selector valve
Multi-position
Select SPE cartridge
Elute and Detect
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Endocrine Disrupting Chemicals
– Problem = low sensitivity even in MS
– 20 µL direct analysis vs 10 mL SPE > x50044x10x10
0.50.5
11
1.51.5
22
2.52.5
33
3.53.5
44
4.54.5
Acquisition Time (min)Acquisition Time (min)Acquisition Time (min)Acquisition Time (min)Acquisition Time (min)Acquisition Time (min)Acquisition Time (min)Acquisition Time (min)1.51.5 22 2.52.5 33 3.53.5 44 4.54.5 55 5.55.5 66 6.56.5 77 7.57.5 88 8.58.5 99 9.59.5 1010 10.510.5 1111
Direct analysisDirect analysis
100 ppb, 20 100 ppb, 20 µµLL
11 22
OnOn--line SPE analysisline SPE analysis
0.2 ppb, 10 mL0.2 ppb, 10 mL
∆∆∆∆∆∆∆∆tR= 4.5 min tR= 4.5 min
= SPE load time= SPE load time
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PPCPs
– 23 compounds, 46 transitions (Only Q is shown)
– 1.5 mL SPE
3x10
0
0.2
0.4
0.6
0.8
1
1.2
1.4
1.6
1.8
2
2.2
2.4
Acquisition Time (min)Acquisition Time (min)Acquisition Time (min)Acquisition Time (min)3.4 3.6 3.8 4 4.2 4.4 4.6 4.8 5 5.2 5.4 5.6 5.8 6 6.2 6.4 6.6 6.8 7 7.2 7.4 7.6 7.8 8 8.2 8.4 8.6 8.8
PPCP LOD (ppt)
Diclofenac (Na) 0.25
Promethazin (HCl) <0.20
Propranolol <0.20
Clemastin (fumarate) 0.25
Metoclopramide (HCl) <0.20
Lidocaine (HCl.H2O) <0.20
Bupivacaine (HCl) 0.25
Fluticasone propionate 0.50
Acetominophen 0.50
Carbamazepin <0.20
Penicillin V (K) 0.50
Caffein 0.25
Ranitidine (HCl) 1.00
Sulfamethoxazole 0.25
Sulfachloropyridazine 0.25
Sulfadiazine 0.50
Sulfadimethoxine <0.20
Sulfamerazine <0.20
Sulfamethazine <0.20
Sulfamethizole 0.50
Sulfanilamide 0.25
Sulfathiazole 0.25
Standard 2.5 ppt (ng/L)Standard 2.5 ppt (ng/L)
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Multipurpose Samplers
for Automated Sample Preparation/Injection
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Solutions … endless
• Static (SHS) and dynamic headspace (DHS)
• Thermal desorption (ALEX and ATEX)
• Solid phase microextraction (SPME)
• Solid phase extraction (SPE)
• Twister thermal and liquid desorption
• Membrane solvent extraction
• Agitate/heat/ultrasonic extraction
• Matrix solid phase dispersion (DPX)
• Derivatization
• Fractionation
• Large volumne injection with evaporation
• LC-GC transfer
• ….
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Micro-LLE-LVI-GC-MS/MS10 ng/L Organotins
upper arm
10 µL syringe
lower arm
1 mL syringe
heated tray
(Peltier)
agitator
DHSTrays
(2 mL and 20 mL vials)
SFSTDU
5 x 10 mL
wash station
3 x 100 mL
wash station
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Stir Bar Sorptive Extraction (SBSE)
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SBSE procedure for vegetables and fruit
Ultra-Turrax + ultrason (15 min)
SBSE: 60 min
1 mL extract
+ 10 mL water
TD-RTL-CGC-MS
15 g sample + 15 mL ACN
P. Sandra, B. Tienpont and F. DavidJ. Chromatogr., 1000 (2003) 299-309
Modified ratio ACN/waterMulti-Twister extractionN. Ochiai, K. Sasamoto, H. Kanda, T. Yamagami, F. David, B. Tienpont and P. SandraJ. Sep. Sci 28 (2005) 1083-1092
(=QuEChERS)
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Analysis of Baby Food
(mixed vegetables, rice, chicken).
Detection of piperonylbutoxide
Time (min)
Abundance (*10-1)
5.00 7.00 9.00 11.00 13.00 15.00 17.00 19.00 21.00 23.00 25.00 27.00 29.00
0
400
200
600
800
1000
1200
31.00 33.00 35.00
1
1(00
A O
O
OO
O
Non-spiked
Spiked - 2 ppb
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QuEChERS:
d-SPE method for pesticides
Quick Easy Cheap Effective Rugged and Safe
QuEChERS (Catchers)
M. Anastassiades et al, J. AOAC Int., 86 (2003) 412
Cryo-milling + water
Shake with Acetonitrile
Add MgSO4 + NaCl
GC - MS or LC - MS
Centrifugation
(Dispersive SPE)
Centrifugation
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Automated Liner Exchange (ALEX) on MPS2
Detailed view of ALEX system1. PTV Injector, 2. ALEX support head,3. Transport adaptor, 4. Electrical gripper,5. Inlet liner tray, 6. Auto-sampler tower
QuEChERS sample prep5-10 µL LVI
PTV solvent vent mode
Automated LinerExchange System (ALEX)
QuEChERS extraction is not very selective –extracts are not clean !!
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New: dispersive SPE by DPX
Disposable Pipette Extraction
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Classical Luke QuEChERS SBSE
Sample size 15 g 15 g 15 g
Solvent A 30 mL acetone 15 mL acetonitrile 15 mL aceto nitrile
Solvent B 30 mL DCM dilute 1/10 in water
Solvent C 30 mL petroleum ether
extraction LLE LLE PDMS extraction
Clean-up (GPC + SPE optional) d-SPE none
Concentration yes (25 mL to 5 mL) yes (1 mL to 100 µL ) none
Final concentration 62,5 ng/5mL 50 pg/µL 5 ng on stir bar
Injection volume 1,5 µL 1 µL TD
Injected 18,75 pg 50 pg 5 ng
Pesticides in Food (non-fatty matrices) at 10 µg/kg
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SBSE procedures for biological samples
Urine 5 (1) mL Blood/bile 1mL, 1g stomach content
Acetylation:
0.5 g K2CO3 + 0.5 mL AA
1mL NH4OAc + 10 µL β-glucuronidase, 90 min @ 37°C
Ethylchloroformate:
2.5 mL EtOH/PYR (2:1) + 0.1 mL ECF
+ 10 mL water
SBSE: 60 min
TD-CGC-MS
+ 1 mL MeOH+ 10 mL water
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Insert vialInsert vial
PyroVial
1717
1010Pt filamentPt filament
BodyBody
Bottom part with ring Bottom part with ring electrodeselectrodes
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Possibilities for Automated Analysis
BEFORE PYROLYSIS AFTER PYROLYSIS
Exchange of headspace gas
Addition of reagents/catalysts
Addition of IS or marker
Fraction collection in PyroVial
Gas phase recovery * HS injection
Liquid desorption * of pyrolysate
Addition of reagents
Addition of IS
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PyroVial – (HT) LC / SFC Set-up
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Pyrolysate Carcio-mutagens
500°C
700°C
900°C
Trp-P-13-amino-1,4-dimethyl-5H-pyrido[4,3-b)indole
NH
N
NH2
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Multipurpose Samplers
for Automated Sample Preparation/Injection