Strategies to Determine and Mitigate Pesticide Residues in Food
Abstract
1. Introduction
2. Historical Evolution of Pesticides and Regulations at EU and Global Level
3. Methods to Determine Pesticide Residues in Food
4. Processing Factors
5. Classification of Pesticides
6. Factors That Most Influence Contamination of Food with Pesticide Residues
6.1. Physicochemical Properties of the Pesticide and Its Formulation
6.2. Application Practices and Compliance with Good Agricultural Practice (GAP)
6.3. Crop Morphology
6.4. Environmental and Edaphic Conditions
6.5. Post-Harvest Treatments and Storage
6.6. Household Preparation and Processing
6.7. Regulatory Oversight and Socio-Economic Drivers
6.8. Global Supply Chain and Trade Patterns
7. Strategies for the Mitigation of Pesticide Residues in Food Through Household and Processing Practices
7.1. Washing
7.2. Peeling, Milling, and Polishing
7.3. Drying and Dehydration
7.4. Juicing and Oil Extraction
7.5. Jam-Making
7.6. Blanching
7.7. Thermal Processing Techniques
7.8. Fermentation
7.9. Innovative Approaches for Pesticide Residue Removal
8. Artificial Intelligence (AI) Applied to the Mitigation of Pesticide Residues in Food
8.1. Precision Agriculture and Smart Pesticide Application
8.2. Predictive Modeling of Pesticide Residue Dynamics
8.3. AI-Assisted Food Sorting and Screening
8.4. Consumer-Level Guidance and Smart Processing Recommendations
8.5. Regulatory Analytics and Policy Development
8.6. Key Challenges in Implementing AI Systems
9. Conclusions and Future Perspectives
Author Contributions
Funding
Data Availability Statement
Conflicts of Interest
Abbreviations
| 3-CA | 3-Chloroaniline |
| AI | Artificial Intelligence |
| ANN | Artificial Neural Networks |
| BHC | Benzenehexachloride |
| CAC | Codex Alimentarius Commission |
| CNN | Convolutional Neural Networks |
| DDT | Dichlorodiphenyltrichloroethane |
| DL | Deep Learning |
| DOMs | Degrees of Milling |
| DTs | Digital Twins |
| EFSA | European Food Safety Authority |
| EPA | United States Environmental Protection Agency |
| EU | European Union |
| EWDs | Electrolyzed Water Devices |
| FAO | Food and Agriculture Organization of the United Nations |
| GAP | Good Agricultural Practices |
| GC-MS/MS | Gas Chromatography coupled with tandem Mass Spectrometry |
| IPM | Integrated Pest Management |
| IRAC | Insecticide Resistance Action Committee |
| JMRP | Joint FAO/WHO Meeting on Pesticide Residues |
| LAB | Lactic Acid Bacteria |
| LC-MS/MS | Liquid Chromatography coupled with tandem Mass Spectrometry |
| Log Kow | Octanol-Water Partition Coefficient |
| LOQ | Limit of Quantification |
| ML | Machine Learning |
| MRLs | Maximum Residue Limits |
| NIPH | Mexican National Institute of Public Health |
| OD600 | Optical Density at 600 nm |
| PAN | Pesticide Action Network |
| PFAS | Per- and polyfluoroalkyl subs |
| PFs | Processing Factors |
| PHI | Pre-harvest Interval |
| PRIMo | Pesticide Residues Intake Model |
| PVPP | Polyvinylpolypyrrolidone |
| SUD | Sustainable Use of pesticides Directive |
| SVM | Support Vector Machine |
| UAVs | Unmanned Aerial Vehicles |
| UV | Ultraviolet |
| WHO | World Health |
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| Report | EFSA 2021 Report [8] | EFSA 2022 Report [9] | EFSA 2023 Report [10] | |||
| Date of Publication | 26th April 2023 | 23rd May 2024 | 14th May 2025 | |||
| Control Program | National control programme | EU-coordinated control program | National control programme | EU-coordinated control program | National control programme | EU-coordinated control program |
| Number of samples | 87.863 | 13.845 | 110.829 | 11.727 | 132.793 | 13.246 |
| Compliant | 96.1% | 98.7% | 96.3% | 99.1% | 98% | 99% |
| Non-Compliant | 3.9% | 1.3% | 3.7% | 0.9% | 2% | 1% |
| Food Material | Pesticide | Processing Conditions | Percentage of Reduction | Reference |
|---|---|---|---|---|
| Lettuce | Chlorfenapyr | Rinsed under running tap water for 5 min | 82.5 ± 1.3 | [78] |
| Perilla Leaves | Pyraclostrobin | 76.3 ± 4.5 | ||
| Spinach | Chlorantraniliprole | 87.2 ± 2.1 | ||
| Crown Daisy | Azoxystrobin | 78.5 ± 0.8 | ||
| Ssamchoo | Fludioxonil | 59.7 ± 4.1 | ||
| Cadusafos | Washed with mineral water and soaked for 20 min | 65.8 | [79] | |
| Long-grain Rice | Fenamidone | 65.9 | ||
| Pirimiphos-methyl | 73.0 | |||
| Bupirimate | 40.7 | |||
| Brown Rice | Carbaryl | 56.8 | ||
| Fenpropidin | 47.8 | |||
| Ethoprophos | 63.5 | |||
| Basmati Rice | SpinosadA | 51.3 | ||
| Tetraconazole | 53.1 | |||
| Tomato | Difenoconazole metabolite CGA205375 | Washed with tap water for 5 min | 82.05 | [80] |
| Lettuce | Thiamethoxam | Soaked in water with vegetable detergent for 5 min | 57.5 ± 2.3 | [78] |
| Perilla Leaves | Indoxacarb | 45.8 ± 5.1 | ||
| Spinach | Lufenuron | 43.9 ± 8.3 | ||
| Crown Daisy | Diniconazole | 38.6 ± 4.5 | ||
| Ssamchoo | Imidacloprid | 32.6 ± 2.7 | ||
| Bupirimate | Washed with mineral water and soaked in water and vinegar for 20 min | 67.1 | [79] | |
| Long-grain Rice | Difenoconazole | 68.4 | ||
| Spiroxamine | 76.6 | |||
| Cadusafos | 69.7 | |||
| Brown Rice | Fenthion sulfoxide | 65.8 | ||
| Phoxim | 70.2 | |||
| Prothioconazole desthio | 58.6 | |||
| Basmati Rice | Fenamidone | 60.6 | ||
| Azoxystrobin | 50.4 |
| Food Material | Pesticide | Processing Conditions | Percentage of Reduction | Reference |
|---|---|---|---|---|
| Spinach | Propamocarb | 2 min at 80–100 °C | 41.0 | [96] |
| Chlorantraniliprole | 30.0 | |||
| Cowpeas | Cyromazine | 67.6 | [97] | |
| Acetamiprid | 60.9 | |||
| Chinese Kale | Carbofuran | 69.0 | [98] | |
| Deltamethrin | 45.0 | |||
| Yard Long Bean | Captan | 80.0 | ||
| Flumethrin | 59.0 |
| Method | Principle | Advantages | Limitations | References |
|---|---|---|---|---|
| Ozonated Water Washing | Ozone (O3) is a powerful oxidizing agent that breaks down pesticide molecules into less toxic or inert compounds | Leaves no chemical residues and also disinfects microbial contaminants | Ozone is short-lived in solution and must be continuously generated High concentrations may damage produce quality (discoloration, off-flavors) Careful control needed to avoid worker respiratory exposure | [103] |
| Ultrasonification | High-frequency sound waves generate cavitation bubbles in water, which collapses and create localized heat and turbulence, which disrupts surface pesticide films | Eco-friendly, non thermal, improves cleaning without damaging texture | Efficacy depends on duration, ultrasonic frequency, and pesticide type Equipment cost and scale-up in domestic settings is a barrier | [104] |
| Electrolyzed Water Devices (EWDs) | Generate electrolyzed water solutions (acidic, neutral, or alkaline) by passing an electric current through water containing a small amount of salt. The process produces: Hypochlorous acid (HOCl) and free chlorine (in acidic electrolyzed water, AEW); Sodium hydroxide (NaOH) (in alkaline electrolyzed water, AIEW) | Effective residue removal Non-toxic Quick and scalable Also disinfects | Limited penetration Sensitive to pH and temperature Equipment must be corrosion-resistant due to free chlorine Not effective for all pesticides classes, especially highly lipophilic or systemic compounds | [105] |
| Cold Plasma | Plasma (ionized gas) produces reactive oxygen and nitrogen species that degrade pesticide residue on food surfaces | Non-thermal, minimal quality impact, and high removal efficiency | Some pesticides (e.g., chlorpyrifos) show resistance under typical plasma conditions Potential formation of unknown degradation by products: safety and regulatory approval remain challenging Scaling up and process standardization is still under development | [99] |
| Enzymatic Degradation | Use of specific enzymes (e.g., organophosphorus hydrolases, laccases) that target and degrade pesticide molecule | High specificity: enzymes like organophosphorus hydrolases can break down particular pesticide classes Biodegradable process producing minimal toxicity | Enzyme production is costly; activity can be sensitive to pH and temperature Delivery in practical food processing systems remains under exploration | [106] |
| Photocatalysis (TiO2-UV Treatment) | Photocatalytic materials like titanium dioxide (TiO2) generate reactive radicals under UV light, degrading pesticides molecules on the surface | Can be implemented in washing units or grain surface treatment | UV exposure may damage some foods or degrade nutrients Only surface residues are affected, penetration in negligible | [107] |
| Edible Coatings with Detoxifying Agents | Active edible coatings (e.g., made from chitosan, alginate) enriched with detoxifying agents like activated carbon, plant extracts, or enzymes | Active coatings can absorb or degrade residual pesticides during storage Can concurrently extend shelf-life and reduce residue exposure | Effectiveness depends on coating uniformity and interaction time Regulatory hurdles for introduction of new coating formulas | [108] |
| Microbial Bioremediation | Use of non-pathogenic bacteria or fungi capable of metabolizing or biding pesticides residues | Certain non pathogenic bacteria or fungal species can metabolize or bind pesticide molecules into inert forms Potentially scalable in fermentative or wash treatments | Specificity to pesticide types, potential biocontrol or spoilage risk if not carefully selected Regulatory and safety evaluations needed for live microbial agents Mostly applied to environmental remediation, limited food use | [109] |
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Oliveira, A.R.; Barros, S.C.; Torres, D.; Sanches Silva, A. Strategies to Determine and Mitigate Pesticide Residues in Food. Molecules 2026, 31, 63. https://doi.org/10.3390/molecules31010063
Oliveira AR, Barros SC, Torres D, Sanches Silva A. Strategies to Determine and Mitigate Pesticide Residues in Food. Molecules. 2026; 31(1):63. https://doi.org/10.3390/molecules31010063
Chicago/Turabian StyleOliveira, Ana Rita, Sílvia Cruz Barros, Duarte Torres, and Ana Sanches Silva. 2026. "Strategies to Determine and Mitigate Pesticide Residues in Food" Molecules 31, no. 1: 63. https://doi.org/10.3390/molecules31010063
APA StyleOliveira, A. R., Barros, S. C., Torres, D., & Sanches Silva, A. (2026). Strategies to Determine and Mitigate Pesticide Residues in Food. Molecules, 31(1), 63. https://doi.org/10.3390/molecules31010063

