RATIONALE Cyanobacteria are a small group of photosynthetic planktonic bacteria, producing a large group of strong hepatotoxins called microcystins (MCs). Many studies have been conducted to evaluate the presence of MCs and nodularin (NOD) in water or in marine organisms, but little research has been done on the atmospheric environment. Waterborne toxins can be found in the aerosol phase due to bubble-bursting processes. METHODS The aim of this study was to obtain a sensitive method for the simultaneous determination of trace concentrations of individual cyanotoxins in aerosol samples, using liquid chromatography coupled with a triple quadrupole (HPLC/MS/MS). During method development improved electrospray ionization was found in negative ion mode. In contrast with other authors, we have developed a chromatographic separation using alkaline conditions, thus achieving good resolution, improved electrospray ionization and therefore better sensitivity. RESULTS A sensitive analytical method was set up to simultaneously measure trace concentrations of cyanotoxins in aerosol samples in a single chromatographic analysis using the internal standard method. The limit of detection for all the toxins was determined to be between 1 fg/?L (MC LA and LF) and 9 fg/?L (NOD). CONCLUSIONS The method was applied to ten aerosol samples from the Venice Lagoon. In these samples, trace concentrations of MC-LA ranging between 90 fg m -3 and 706 fg m -3, MC-LF between n.d. and 369 fg m -3 and MC-LW between n.d. and 262 fg m -3. This is the first study to quantify the cyanotoxins in Venetian aerosol samples using the HPLC/(-)ESI-MS/MS. Copyright

Simultaneous quantification of microcystins and nodularin in aerosol samples using high-performance liquid chromatography/negative electrospray ionization tandem mass spectrometry

Gambaro A;Barbaro E;Zangrando R;Barbante;
2012

Abstract

RATIONALE Cyanobacteria are a small group of photosynthetic planktonic bacteria, producing a large group of strong hepatotoxins called microcystins (MCs). Many studies have been conducted to evaluate the presence of MCs and nodularin (NOD) in water or in marine organisms, but little research has been done on the atmospheric environment. Waterborne toxins can be found in the aerosol phase due to bubble-bursting processes. METHODS The aim of this study was to obtain a sensitive method for the simultaneous determination of trace concentrations of individual cyanotoxins in aerosol samples, using liquid chromatography coupled with a triple quadrupole (HPLC/MS/MS). During method development improved electrospray ionization was found in negative ion mode. In contrast with other authors, we have developed a chromatographic separation using alkaline conditions, thus achieving good resolution, improved electrospray ionization and therefore better sensitivity. RESULTS A sensitive analytical method was set up to simultaneously measure trace concentrations of cyanotoxins in aerosol samples in a single chromatographic analysis using the internal standard method. The limit of detection for all the toxins was determined to be between 1 fg/?L (MC LA and LF) and 9 fg/?L (NOD). CONCLUSIONS The method was applied to ten aerosol samples from the Venice Lagoon. In these samples, trace concentrations of MC-LA ranging between 90 fg m -3 and 706 fg m -3, MC-LF between n.d. and 369 fg m -3 and MC-LW between n.d. and 262 fg m -3. This is the first study to quantify the cyanotoxins in Venetian aerosol samples using the HPLC/(-)ESI-MS/MS. Copyright
2012
Istituto per la Dinamica dei Processi Ambientali - IDPA - Sede Venezia
bacterial toxin
cyclopeptide
marine toxin
microcystin
nodularin
aerosol
article
chemistry
electrospray mass spectrometry
high performance liquid chromatography
isolation and purification
Italy
limit of detection
methodology
pH
reproducibility
tandem mass spectrometry
Aerosols
Bacterial Toxins
Chromatography
High Pressure Liquid
Hydrogen-Ion Concentration
Italy
Limit of Detection
Marine Toxins
Microcystins
Peptides
Cyclic
Reproducibility of Results
Spectrometry
Mass
Electrospray Ionization
Tandem Mass Spectrometry
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/261019
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