Saci Short Description And Applications

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This is a short presentation that shows the working mechanism and the applications of the new ionization source, for mass spectrometry, named Surface Activated Chemical Ionization (SACI). More informations can be found at the URL: http://www.isbiotechnology.com

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Surface Activated Chemical Surface Activated Chemical Ionization – applications to low Ionization – applications to low molecular weight drugs molecular weight drugs analysisanalysis

Simone CristoniSimone Cristoni

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Surface Activated Chemical Ionization

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Surface Activated Chemical Ionization

Controlled, low

potential

Metal surface

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SACI

High sensitivity

High Versatility (different eluent flow rates, compounds and matrix)

Cost effective (avoid pre purification step working by sample dilution)

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Analysis of addictive drugs

Urine

Hair

Saliva

Sample dilution 1:10

Avoiding pre-concentration step and matrix effect thanks to both high SACI sensitivity and medium High Flow

gradient chromatography

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Analysis of addictive drugs

Mass spectrometer: HCT Ultra Ion Trap (Bruker Daltonics) Acquisition mode: tandem mass spectrometry (MS/MS) Chromatography column: C18 50x4.1 1.8 µm i.d. Eluents: A:H2O + 0.1% FA %B :CH3CN + 0.1% FA Eluent flow: 500 µL/min Gradient: %B: 5 for 5 minutes, from 5 to 40 % in 10 minutes,

from 40 to 5 % in 2 minutes. Sample volume injected: 20 µL

Avoiding pre-concentration step and matrix effect thanks to both high SACI sensitivity and medium High Flow

gradient chromatography

Experimental conditions

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Analysis of addictive drugsUrine 2 ng/mL

APCI

SACI

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Analysis of addictive drugsSaliva

4 Retention time (min)

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a) SACI

Sig

nal

in

ten

sity HCT

0

5.3E+5 12.40

LTQ

4 Retention time (min)

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a) SACI

Sig

nal

in

ten

sity HCT

0

4.1E+4

LTQ

40

Sig

nal

in

ten

sity

3.2E+2

Retention time (min)

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b) APCI

HCT

LTQ

Sig

nal

in

ten

sity

0

1.89E+2

Retention time (min)

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c) ESI

4

HCT

LTQ

0

Sig

nal

in

ten

sity

5.6E+2

Retention time (min)

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b) APCI

4

HCT LTQ

Sig

nal

in

ten

sity

4.2E+3

Retention time (min)

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c) ESI

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LTQHCT 12.20

12.30

10 ng/mL of 6-MAM 1 ng/mL of 6-MAM

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Analysis of pesticides

Water Spinach Sample dilution 1:10

Avoiding pre-concentration step and matrix effect thanks to both high SACI sensitivity and medium High Flow

gradient chromatography

Different matrix

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Analysis of pesticides

Mass spectrometer: ESI-TOF (Bruker Daltonics) Acquisition mode:High mass accuracy full scan MS Chromatography column: C18 50x4.1 3,5 µm i.d. Eluents: A:H2O + 0.1% FA %B :CH3OH + 0.1% FA Eluent flow: 500 µL/min Gradient: %B: 5 for 5 minutes, from 5 to 40 % in 10 minutes,

from 40 to 5 % in 2 minutes. Sample volume injected: 20 µL

Avoiding pre-concentration step and matrix effect thanks to both high SACI sensitivity and medium High Flow

gradient chromatography

Experimental conditions

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Analysis of pesticideswater

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Analysis of pesticidesspinach

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Analysis of toxin in food

Wine Grape Sample dilution 1:10

Avoiding pre-concentration step and matrix effect thanks to both high SACI sensitivity and medium High Flow

gradient chromatography

Different matrix

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Analysis of pesticides

Mass spectrometer: HCT Ultra Ion Trap (Bruker Daltonics) Acquisition mode: tandem mass spectrometry (MS3) Chromatography column: C18 250x4 5 µm i.d. Eluents: A:H2O + 0.1% FA %B :CH3CN + 0.1% FA Eluent flow: 1mL/min. Gradient: %B: 5 for 5 minutes, from 5 to 70 % in 10 minutes,

from 70 to 5 % in 2 minutes. Sample volume injected: 20 µL

Avoiding pre-concentration step and matrix effect thanks to both high SACI sensitivity and medium High Flow

gradient chromatography

Experimental conditions

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Analysis of pesticidesspinach

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Analysis of OTAWine – 10 ng/mL

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Conclusions

High sensitivity (LOD, LOQ, linerity ranges) Cost effecting avoiding matrix effect and pre-concentration step

(e.g. Solid Phase Extraction) Possible to use it in a wide range of chromatographic conditions. High throughput screening of complex mixture if coupled with

high mass accuracy analyzers (e.g TOF or FTICT).

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Future developments

Ion exchange chromatography (low operative voltages employed in SACI makes possible to operate in these chromatographic conditions).

High sensitive quantitation analysis of peptide and protein drugs (ioni monocarica; TOF).

Pesticides (developing high sensitive methods for screening of selected groups of pesticides of interest)

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SACI demo site

Web site: http://www.isbiotechnology.com

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acknowledgment

Dr.ssa Sara Crotti – ISB Milan Dr. Lorenzo Zingaro – ISB Milan Dr.ssa Cristina Canton – ISB Milan Dr.ssa Laura Molin – ISB Milan Dr. Pietro Traldi – CNR Padova Prof. Luigi Rossi Bernardi – University of Milan Dr. Simone Rubini – Bruker Daltonics Dr. Elisa Basso – Bruker Daltonics Dr. Leopoldo Dimiziano – Bruker Daltonics

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