Mass Spectrometry for the Analysis of Pesticide Residues and their Metabolites

Despina Tsipi, Helen Botitsi, Anastasios Economou

• Publisher: Wiley
• Year: 2015
• Print ISBN:
  9781118500170
• eBook ISBN:
  9781119070009
• Edition: 1
• Topic: Sciences physiques
• Subtopic: Spectroscopie et analyse du spectre

Provides an overview of the use of mass spectrometry (MS) for the analysis of pesticide residues and their metabolites.

• Presents state of the-art MS techniques for the identification of pesticides and their transformation products in food and environment
• Covers important advances in MS techniques including MS instrumentation and chromatographic separations (e.g. UPLC, HILIC, comprehensive GCxGC) and applications
• Illustrates the main sample preparation techniques (SPE, QuEChERS, microextraction) used in combination with MS for the analysis of pesticides
• Describes various established and new ionization techniques as well as the main MS platforms, software tools and mass spectral libraries

1
PESTICIDE CHEMISTRY AND RISK ASSESSMENT

Despina Tsipi,¹ Helen Botitsi,¹ and Anastasios Economou²

¹ Pesticide Residues Laboratory, General Chemical State Laboratory, Athens, Greece

² Laboratory of Analytical Chemistry, Department of Chemistry, National and Kapodistrian University of Athens, Athens, Greece

1.1 INTRODUCTION

And he gave it for his opinion that whoever could make two ears of corn or two blades of grass to grow upon a spot of ground where only one grew before, would deserve better of mankind, and do more essential service to his country, than the whole race of politicians put together.

Jonathan Swift, 1667–1745

Plant protection, worldwide, has a very important role in the food production. One of the most important ways of protecting plants and plant products against harmful organisms, including weeds, and of improving agricultural production is the use of plant protection products (pesticides). Pesticides have brought to the world the most abundant, safe, and cheap food in its history. Pesticides, like pharmaceuticals, are the most thoroughly tested chemicals in the world, and only those that pass strict government testing are authorized for use. Active substances (pesticides) should only be included in plant protection products where it has been demonstrated that they present a clear benefit for plant production and they are not expected to have any harmful effect on human or animal health or any unacceptable effects on the environment, especially if placed on the market without having been officially tested and authorized or if incorrectly used.

Human exposure to pesticides and their metabolites through the food chain could be direct, through the consumption of treated foods, or indirect, through the transfer of residues into products of animal origin from treated feed items. Regulatory agencies, internationally, have provided pesticide regulations increasingly stringent in terms of establishment of the maximum residue limits (MRLs) for pesticides in food of plant and animal origin. Monitoring studies are organized annually by national authorities to enforce compliance with MRLs and to ensure food safety for consumers.

The unlimited number of pesticides and their metabolites, in conjunction with their low concentration levels in various food commodities and environmental matrices, makes the analysis of pesticide residues one of the most challenging and complex areas of analytical chemistry. Pesticide residue methods have been developed worldwide using hyphenated confirmatory techniques, such as gas chromatography–mass spectrometry (GC–MS) and liquid chromatography–mass spectrometry (LC–MS) for the determination of trace concentration levels.

Mass spectrometry (MS) platforms are widely applied in pesticide residues for (i) the determination of pesticide residues and their metabolites in food to ensure safety of the food supply, (ii) the investigation of the contamination of water resources from pesticides and their relevant metabolites, and (iii) the structure elucidation of unknown metabolites or degradation/transformation products (TPs) that sometimes can be more toxic than the parent pesticides.

This chapter provides information regarding the chemistry and toxicity of pesticides, their metabolites, and TPs. Risk assessment topics are discussed. Definitions and explanations in various topics of pesticides are also included.

1.2 PESTICIDE CHEMISTRY

1.2.1 Historical Perspective

The International Union of Pure and Applied Chemistry (IUPAC) defines a pesticide as any substance or mixture of substances intended for preventing, destroying, or controlling any pest (Holland, 1996). Looking back over the years, the modern pesticide history begins in 1939 with the synthesis of dichlorodiphenyltrichloroethane (DDT) from Paul Muller in Geigy (Switzerland). In 1948, after the successful widespread use of DDT as insecticide to protect human health from diseases (like malaria) and also in agriculture practice, Paul Muller was awarded the Nobel Prize (The History of Pesticides, 2008).

After the synthesis of DDT, a plethora of organic chemical compounds with insecticide, herbicide, and fungicide action started to be synthesized. Later in the 1960s, laboratory studies in the United States proved that some chemical compounds belonging to the class of organochlorine insecticides such as dieldrin, endrin, and aldrin are not degraded in the environment and bioaccumulate in living organisms. In the same time period, DDT residues have been detected in river waters in the United States, while in 1963, the phenomenon of dead fish in Mississippi was attributed to the presence of aldrin in river water (Delaplane, 2000). In 1972, mainly due to their high environmental persistence and bioaccumulation, organochlorine insecticides were banned first in the United States and later in Europe.

Nowadays, more than 1600 pesticides belonging to more than 100 chemical classes are in use worldwide for food production. Information on synthetic and commercially available pesticides is readily found at “The Pesticide Manual” (The Pesticide Manual, 2012). Furthermore, the electronic Compendium of Pesticide Common Names (http://alanwood.net/pesticides/) contains data sheets for more than 1700 different active ingredients and for more than 350 ester and salt derivatives used in pesticide formulations.

The challenge of providing new molecules to control pests is a straightforward task with high rates of scientific success and considerable commercial reward. In no other field of chemistry has been such a diversity of structures arising from the application of the principles of chemistry to the mechanisms of action in pests to develop selectivity and sensitivity in agents toward certain species while reducing toxicity to other forms of life. The dramatic advances and the rapid changes in pesticide chemistry are presented, over the past 50 years, in the conferences in pesticide chemistry of the IUPAC taking place at 4-year intervals.

1.2.2 Identity and...

Table of contents

• COVER
• TITLE PAGE
• TABLE OF CONTENTS
• LIST OF CONTRIBUTORS
• FOREWORD
• PREFACE
• 1 PESTICIDE CHEMISTRY AND RISK ASSESSMENT
• 2 LEGISLATION, MONITORING, AND ANALYTICAL QUALITY CONTROL FOR PESTICIDE RESIDUES
• 3 ADVANCED SAMPLE PREPARATION TECHNIQUES FOR MS ANALYSIS
• 4 RECENT DEVELOPMENTS IN GAS CHROMATOGRAPHY–MASS SPECTROMETRY
• 5 RECENT DEVELOPMENTS IN LIQUID CHROMATOGRAPHY–MASS SPECTROMETRY: ADVANCES IN LIQUID CHROMATOGRAPHIC SEPARATIONS AND IONIZATION TECHNIQUES/INTERFACES
• 6 RECENT DEVELOPMENTS IN LIQUID CHROMATOGRAPHY–MASS SPECTROMETRY: MASS DETECTORS
• 7 MATRIX EFFECTS IN LIQUID CHROMATOGRAPHY–ELECTROSPRAY IONIZATION–MASS SPECTROMETRY
• 8 LIQUID CHROMATOGRAPHY–MASS SPECTROMETRY ANALYSIS OF PESTICIDE RESIDUES AND THEIR METABOLITES IN FOOD SAMPLES
• 9 APPLICATION OF LC–MS/MS AND LC–TOF-MS FOR THE IDENTIFICATION OF PESTICIDE RESIDUES AND THEIR METABOLITES IN ENVIRONMENTAL SAMPLES
• 10 MASS SPECTROMETRIC TECHNIQUES FOR THE DETERMINATION OF PESTICIDE TRANSFORMATION PRODUCTS FORMED BY ADVANCED OXIDATION PROCESSES
• INDEX
• WILEY SERIES ON MASS SPECTROMETRY
• END USER LICENSE AGREEMENT