Determination of cationic polar pesticides in cereals using ion chromatography and tandem mass spectroscopy
Applications | 2022 | Thermo Fisher ScientificInstrumentation
The presence of ionic pesticides in cereal based foods raises health and regulatory concerns. Quaternary amine compounds such as chlormequat mepiquat paraquat and diquat are widely used as plant growth regulators herbicides and desiccants but require sensitive selective analysis due to their polar non volatile and often toxic nature. Reliable quantitation supports food safety monitoring and compliance with maximum residue levels set by agencies in the EU US and Canada.
This study applied ion exchange chromatography coupled to tandem mass spectrometry to quantify four cationic polar pesticides in oat based cereal samples. The key aims were to achieve chromatographic resolution of structurally similar quaternary ions to separate them from common matrix cations and to demonstrate method sensitivity reproducibility and recovery in real cereal matrices using modified polar pesticide extraction protocols.
This analysis employed a weak cation exchange column functionalized with carboxylic acid groups operated at forty degrees under an electrolytically generated methanesulfonic acid gradient. A triple quadrupole mass spectrometer with heated electrospray ionization performed selective reaction monitoring for quantitation. Suppressed conductivity detection was used in parallel to characterize elution windows. Key instrumental components included
The optimized method achieved baseline separation of monovalent and divalent quaternary amines including paraquat and diquat within a fifteen minute gradient. Calibration was linear from one to one hundred micrograms per liter with r2 values exceeding 0.9999 and detection limits below 0.1 micrograms per liter. Method reproducibility was demonstrated with retention time RSDs below 0.2 percent and peak area RSDs under two percent. Recoveries of spiked cereal extracts ranged from eighty six to one hundred eighteen percent. Oatmeal samples showed trace pesticide levels below 0.001 milligrams per kilogram. Toasted oat cereal extractions required an extended wash to prevent matrix interference but yielded consistent results with concentrations below regulatory limits.
Continued expansion of IC MS technology will focus on high resolution accurate mass capabilities to resolve isobaric species further and reduce carryover. Automation of extraction and cleanup using online solid phase cartridges will streamline workflows. The method can be extended to a wider range of ionic pesticides and degradates across diverse food and environmental matrices. Emerging regulatory requirements may drive the need for multi residue approaches combining anionic and cationic polar analytes in single runs.
An ion exchange chromatography tandem mass spectrometry method was successfully developed for fast accurate quantitation of four quaternary amine polar pesticides in cereal products. The approach delivers excellent separation sensitivity and robustness even in complex matrices and meets stringent recovery and detection criteria. It provides a powerful tool for food safety laboratories to monitor cationic pesticide residues and ensure regulatory compliance.
IC-MS, IC/MS/MS
IndustriesFood & Agriculture
ManufacturerThermo Fisher Scientific
Summary
Importance of the Topic
The presence of ionic pesticides in cereal based foods raises health and regulatory concerns. Quaternary amine compounds such as chlormequat mepiquat paraquat and diquat are widely used as plant growth regulators herbicides and desiccants but require sensitive selective analysis due to their polar non volatile and often toxic nature. Reliable quantitation supports food safety monitoring and compliance with maximum residue levels set by agencies in the EU US and Canada.
Objectives and Study Overview
This study applied ion exchange chromatography coupled to tandem mass spectrometry to quantify four cationic polar pesticides in oat based cereal samples. The key aims were to achieve chromatographic resolution of structurally similar quaternary ions to separate them from common matrix cations and to demonstrate method sensitivity reproducibility and recovery in real cereal matrices using modified polar pesticide extraction protocols.
Methodology and Instrumentation
This analysis employed a weak cation exchange column functionalized with carboxylic acid groups operated at forty degrees under an electrolytically generated methanesulfonic acid gradient. A triple quadrupole mass spectrometer with heated electrospray ionization performed selective reaction monitoring for quantitation. Suppressed conductivity detection was used in parallel to characterize elution windows. Key instrumental components included
- Reagent Free IC system with eluent generator and electrolytic trap column
- Dionex IonPac CS21 Fast four micron guard and analytical columns
- Electrolytic suppressed conductivity detector
- TSQ Altis Plus triple quadrupole mass spectrometer with HESI II source
- Autosampler with online dilution and diverter valve for MS protection
Main Results and Discussion
The optimized method achieved baseline separation of monovalent and divalent quaternary amines including paraquat and diquat within a fifteen minute gradient. Calibration was linear from one to one hundred micrograms per liter with r2 values exceeding 0.9999 and detection limits below 0.1 micrograms per liter. Method reproducibility was demonstrated with retention time RSDs below 0.2 percent and peak area RSDs under two percent. Recoveries of spiked cereal extracts ranged from eighty six to one hundred eighteen percent. Oatmeal samples showed trace pesticide levels below 0.001 milligrams per kilogram. Toasted oat cereal extractions required an extended wash to prevent matrix interference but yielded consistent results with concentrations below regulatory limits.
Method Benefits and Practical Applications
- Fast selective separation of challenging quaternary amines
- Low detection limits suitable for trace compliance testing
- Combined conductivity and MS detection increases confidence in elution profiling and quantitation
- Adaptable extraction protocols ensure accurate recoveries in complex cereal matrices
- Supports routine QA QC and regulatory monitoring for polar pesticides
Future Trends and Potential Applications
Continued expansion of IC MS technology will focus on high resolution accurate mass capabilities to resolve isobaric species further and reduce carryover. Automation of extraction and cleanup using online solid phase cartridges will streamline workflows. The method can be extended to a wider range of ionic pesticides and degradates across diverse food and environmental matrices. Emerging regulatory requirements may drive the need for multi residue approaches combining anionic and cationic polar analytes in single runs.
Conclusion
An ion exchange chromatography tandem mass spectrometry method was successfully developed for fast accurate quantitation of four quaternary amine polar pesticides in cereal products. The approach delivers excellent separation sensitivity and robustness even in complex matrices and meets stringent recovery and detection criteria. It provides a powerful tool for food safety laboratories to monitor cationic pesticide residues and ensure regulatory compliance.
Reference
- Application note 000607 Thermo Fisher Scientific Determination of cationic polar pesticides in cereals using ion chromatography and tandem mass spectrometry
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