Determination Of Pesticide Residues Research Articles

Determination of Multiple Pesticide Residues and Dietary Intake Risk Assessment of 35 Pesticides in Beet from Five Provinces of Northern China

Determination of Multiple Pesticide Residues and Dietary Intake Risk Assessment of 35 Pesticides in Beet from Five Provinces of Northern China

Analytical control of residues of the herbicide trifluralin in the assessment of the food safety

Introduction. Trifluralin is a systemic herbicide of the chemical class of dinitroaniline derivatives. During monitoring studies, trifluralin was detected in carrots produced in the Russian Federation. Since trifluralin-based pesticides are not approved for the use in the Russian Federation, residual amounts of the substance are not typical for this crop. To check the contamination of carrots with a pesticide not typical for this crop, confirmatory qualitative and quantitative studies were carried out. Purpose of the work. Increasing the efficiency of identification and reliability of quantitative results when monitoring food products for safety when performing confirmatory analytical studies using the example of determining trifluralin in carrots to assess the safety of food products intended for the consumer. Materials and methods. Gas chromatography coupled with tandem mass spectrometry (GC-MS/MS) was used to identify and quantify trifluralin. Samples were prepared for analysis using the QuEChERS method. Identification was carried out by multiple reaction monitoring (MRM) using a triple quadrupole mass spectrometer using two to four MRM transitions (m/z): 306,1→264,0; 264,0→206,0; 264,0→188,0; 264,0→160,1. Matrix-matched calibration was used for quantitation. Results. The effectiveness of screening studies when monitoring food products using the GC-MS/MS method can be significantly elevated by increasing the number of MRM transitions (at least 3), controlling the reference retention time of the substance, and maintaining the ratio of confirmatory ions. To obtain a reliable quantification of trifluralin content in carrots, the use of a matrix-matched calibration is recommended. Limitation. In the study, only carrots were considered as food products. Conclusion. Confirmation of test results is especially important when determining pesticide residues that are not normally found in a given matrix, or when it is suspected that the maximum permissible level may be exceeded. When conducting a screening study and detecting a food contaminant, contamination of the product can only be reported in advance. Next, a confirmatory analysis is required using a validated quantitative method, including an appropriate calibration procedure. In quantitative analysis, the presence of matrix sample components can cause problems due to sample suppression/enhancement phenomena. Matrix-aware calibration has been shown to be effective in compensating for matrix effects.

Monitoring and Risk Assessment of Multi-Pesticide Residues in Apples: A Focus on Consumer Safety

Pesticide residues in human diets pose significant health hazards, particularly for vulnerable populations such as infants and children. This study aimed to determine pesticide residues in apples and to assess the cumulatively chronic risk posed to adult and child consumers from simultaneous exposure to multiple residues. During the 2022–2023 harvest seasons, 100 apple samples from Turkey were analyzed for the presence of 225 different pesticide residues. Pesticide extraction was performed using the QuEChERS method, followed by detection through liquid chromatography coupled with tandem mass spectrometry. Fifteen distinct pesticides (ten insecticides and five fungicides) were detected in 64 out of the 100 apple samples analyzed. Eleven samples contained pesticide residues that exceeded the maximum residue limit (MRL) set by the Turkish Food Codex and the European Union. Thiophanate-methyl was the most frequently detected pesticide (34%) in apples, with concentrations ranging from 0.012 to 0.108 mg kg−1, all of which were well below the MRL of 0.5 mg kg−1. Other commonly detected residues included chlorantraniliprole (28%), acetamiprid (24%), sulfoxaflor (22%), bifenazate (18%), indoxacarb (13%), diflubenzuron (12%), and carbendazim (10%). Under a worst-case scenario, the hazard index (HI) values for adults and children were 0.85% and 2.60%, respectively, indicating that these values remain significantly below the risk threshold of 100%, suggesting no associated health risks from apple consumption. However, regular monitoring of pesticide residues in fresh fruits and vegetables remains critically important.

Bioanalytical Method: Determining pesticide residues in tomatoes and mushrooms by a bioactive membrane-based sensor, enzyme inhibition and UV-Vis Spectrophotometry

Bioanalytical Method: Determining pesticide residues in tomatoes and mushrooms by a bioactive membrane-based sensor, enzyme inhibition and UV-Vis Spectrophotometry

Determination of pesticide residues in beans using QuEChERS technique coupled to gas chromatography-mass spectrometry: Multivariate optimization of CEN and AOAC methods

The use of pesticides has led to environmental pollution and posed a global health risk, since they remain as residues on foods. Beans one of the most widely cultivated crop in Africa, and susceptible to attack by insects both on field and during storage, leading to the application of pesticides to control pests' infestation. However, misuse of these chemicals by farmers on beans has resulted in the rejection of beans exported to European countries, due to the presence of pesticide residues at concentrations higher than the maximum residues levels (MRLs). In this study, the effectiveness of the Association Official Analytical Chemists (AOAC) Official Method and the European Committee of Standardization (CEN) Standard Method, were determined using multivariate approach for the analysis of organochlorine pesticide residues in 6 varieties of beans samples. The significance of factors (mass of sample, volume of acetonitrile, mass of magnesium sulphate, sample pH, centrifugation time and speed) affecting the efficiency of extraction was estimated using Plackett-Burman design, while central composite design was used to optimize the significant factors. The following optimum factors were subsequently used for method validation, recovery tests, and real sample analysis: 4 g of sample sludge (1:1 v/v), 10 mL of acetonitrile, 4.45 g of MgSO4, and 5 min of centrifugation at 5000 rpm. The figure of merit of analytical methodology estimated using matrix-matched internal standard calibration method gave linearity ranging from 0.25 to 500 μg/kg, with correlation coefficient (R2) greater than 0.99, the recovery ranged from 75.55 to 110.41 (RSD = 0.70–16.65), with LOD and LOQ of 0.23–1.77 μg/kg and 0.76–5.88 μg/kg, respectively.

A novel HCR-CRISPR/Cas12a immunosensor for the sensitive detection of pesticide residues in animal-derived foods

Pesticides are widely used in the cultivation and breeding of agricultural products. However, pesticide residue monitoring has focused mainly on fruits and vegetables and has not focused on animal-derived foods. Therefore, a novel approach for determining pesticide residues in animal-derived food products via an immunosensor based on a chain hybridization reaction (HCR) with CRISPR/Cas12a is presented. Triazophos pesticide was used as a research object. This method establishes a competitive immunoreaction system in which OVA-hapten is encapsulated on the surface of the enzyme label plate, competing with pesticide molecules bound to antibodies on the surface of the nanogold composite probe. Integrating the immunoreaction with two signal amplification mechanisms, HCR and CRISPR/Cas12a, ensures heightened method sensitivity while maintaining enhanced convenience and speed. The method's detection range spans from 0.01 to 50 ng/mL, with a remarkably low detection limit of 0.013 ng/mL. Moreover, in practical sample applications, the assay exhibited a robust correlation with GC‒MS. This approach uniquely offers real-time, cost-effective, and onsite data, providing a more comprehensive and timely foundation for establishing standards on pesticide residues in animal-derived foods, bolstering food safety surveillance, and upholding public health. Moreover, the proposed HCR-CRISPR/Cas12a immunosensor effectively improved the sensitivity and accuracy of pesticides detection, offering a promising and versatile platform for food safety detection.

Ultrasound assisted upper critical solution temperature type switchable deep eutectic solvent based liquid-liquid microextraction for the determination of triazole in water

BackgroundThe use of pesticides to protect crops has long been an important measure to provide healthy and safe agricultural products, but excess pesticides flow into fields and rivers, causing environmental pollution. Earlier methods utilizing organic solvent liquid-liquid microextraction for pesticide residue detection were not environmentally friendly. Therefore, it is significant to find a greener and more convenient detection method to determine pesticide residues. ResultsA new method was established to detect three triazole fungicides (TFs), including myclobutanil, epoxiconazole and tebuconazole, in environmental water samples. And the determination was conducted using a high-performance liquid chromatography with the ultraviolet detector (HPLC-UV). The switchable deep eutectic solvent (SDES) can be reversibly switched between hydrophilic and hydrophobic states through temperature modulation. Additionally, the method exhibited excellent linearity for all target analytes within the concentration range of 10–2000 μg L−1, with satisfactory R2 values (≥0.9975). The limits of detection (LODs) ranged from 2.3 to 2.6 μg L−1, and the limits of quantification (LOQs) ranged from 7.8 to 8.7 μg L−1. The accuracy of the method was assessed through intra-day and inter-day precision tests, yielding relative standard deviations (RSDs) in the ranges of 2.8%–6.7% and 2.2%–7.5%, respectively. Density functional theory (DFT) results indicated that hydrogen bonding is a significant factor affecting the binding of DES with triazoles. Three different green assessment tools were used to prove that the SDES-HLLME method had good greenness and broad applicability. SignificanceThis is a homogeneous liquid-liquid microextraction (HLLME) method based on the upper critical solution temperature (UCST) type switchable deep eutectic solvent program, which can complete the extraction within a few minutes without dispersant. In terms of pesticide detection, the analytical method is simple and more conducive to environmental protection.

Safety evaluation of Indocalamus Iatifolius McClure leaves based on acute toxicity, harmful metals, and 9 organochlorine residue determination

To investigate the safety of Indocalamu Iatifolius McClur leaves sold in the market, a study was conducted using Indocalamu Iatifolius McClur leaves randomly collected from an online store and a large supermarket. Acute toxicity experiments were performed on mice, and their body weight was monitored for 14 days after administration. After the observation period, blood samples were collected for biochemical analysis, and organ pathology was examined. Then, the content of copper (Cu), lead (Pb), cadmium (Cd), mercury (Hg), arsenic (As), and the residues of nine organochlorine pesticides in Indocalamu Iatifolius McClur leaves were measured according to the National Food Safety Standard (GB/T5009-2003) and the pesticide residue determination methods in the 2020 edition of the Chinese Pharmacopoeia. The results showed that the mice in the Indocalamu Iatifolius McClur leaves (online store) group experienced mortality and severe liver and lung damage. The levels of lead, cadmium, mercury, arsenic, and the nine organochlorine pesticides met the relevant standards and regulations. However, the copper content in the Indocalamu Iatifolius McClur leaves (online store) group was nearly 80 times higher than that in the supermarket group. Mice in the Indocalamu Iatifolius McClur leaves (supermarket) group remained healthy without any abnormalities, and the levels of harmful metals and organochlorine pesticides complied with the standards and regulations. The study suggests the need for regulatory policies and safety standards for the sale of Indocalamu Iatifolius McClur leaves.

Dynamics of degradation of residual amounts of propineb and its metabolite propyleneurea in apple fruits

The behavior of propineb and propylentiourea (PTU) in apples was studied in dynamics after treatment withAnthracol, water-dispersible granules (WDG) in 3 regions.The determination of pesticide residues was carried out according to developed and optimized methods.It was found that after 3-fold treatment with the fungicide propineb andPTUdecompose quickly and evenly in fruits in various regions of cultivation. 28 days after the last treatment, the content of the active substance of the drug and its metabolite are at a level below the corresponding of the maximum allowable level (MAL).At the time of harvesting, the studied substances in apples were not found in any of the climatic zones, as well as they were absent in the juice.Based on the data obtained on the decomposition of propineb in apple fruits, the nature of dissipation was established.The half-life ranged from 3 to 8 days.

Advances on multiclass pesticide residue determination in citrus fruits and citrus-derived products - A critical review.

The application of agrochemicals in citrus fruits is widely used to improve the quality of crops, increase production yields, and prolong post-harvest life. However, these substances are potentially toxic for humans and the ecosystem due to their widespread use, high stability, and bioaccumulation. Conventional techniques for determining pesticide residues in citrus fruits are chromatographic methods coupled with different detectors. However, in recent years, the need for analytical strategies that are less polluting for the environment has encouraged the appearance of new alternatives, such as sensors and biosensors, which allow selective and sensitive detection of pesticide residues in real time. A comprehensive overview of the analytical platforms used to determine pesticide residues in citrus fruits and citrus-derived products is presented herein. The review focuses on the evolution of these methods since 2015, their limitations, and possible future perspectives for improving pesticide residue determination and reducing environmental contamination.

Determination of pesticide residues in five different corn-based products using a single and simple solid–liquid extraction without clean-up steps followed by comprehensive two-dimensional liquid chromatography coupled to tandem mass spectrometry

Pesticide residues in food products are a critical issue concerning food safety. Recent studies have increasingly focused on developing selective, rapid, innovative, and environmentally friendly analytical methods for detecting pesticides in foodstuffs. This study presents a novel analytical method utilizing comprehensive two-dimensional liquid chromatography-tandem mass spectrometry for the simultaneous determination of one hundred and thirteen multiclass pesticides in corn products. The method simplifies the process with a single-step solid–liquid extraction and benefits from two-dimensional separation to enhance resolution and minimize matrix effects. The methodology was validated according to European Commission DG-SANTE (SANTE/11312/2021) and European Committee for Standardization (EN 15662, 2018) guidelines, obtaining acceptable analytical parameters. Limits of detection ranged from 0.2 µg/L to 30.2 µg/L and limits of quantification from 0.3 to 91.6 μg/L, all bellow regulatory limits. Accuracy, ranged from 60 to 120 % and precision, estimated by relative standard deviation, was consistently below 15.1 % in all cases. The applicability of the method was demonstrated by analyzing pesticides in five representative corn products (tortilla, corn flakes, corn cake, starch, and polenta). Sixteen pesticides were detected, all within the regulatory residue limits. Three metric tools were applied to assess the analytical process. Environmental sustainability was evaluated using the AGREE metric, while analytical performance and method applicability were assessed with the Red-Green-Blue and Blue Applicability Grade Index models, respectively, yielding promising scores (0.5, ≥ 0.55, and 0.65). These findings and the comparison to previous methods indicated that this approach represents a promising, alternative and user-friendly strategy for pesticide determination, offering effective productivity and reliable analytical performance.

Multirezidualna metoda za določanje ostankov fitofarmacevtskih sredstev v medu s plinsko kromatografijo sklopljeno s tandemsko masno spektrometrijo

In our laboratory we introduced and validated a new analytical method for determination of environmental pesticide residues in honey. The extraction was conducted using acetone, petroleum ether and dichlorometane. The determination was conducted using gas chromatography coupled with tandem mass spectrometry. Practical usage of method was analyses of 31 samples of Slovenian honey. 33 active substances (pesticides) were sought. The insecticide cypermethrin was the only active substance found in three samples. The active substances sought were not found in 90.3 % of the samples analysed. The risk assessment showed that no unacceptable risk is expected for consumers. The results were compared with those from the literature. We revealed that honey from Slovenia contained a lower portion of positive samples per active substance sought as in Italy, comparable as in Estonia and Spain, comparable to higher as in Poland and higher as in Egypt.

Sampling-rate calibration vs. equilibrium calibration for in vivo solid-phase microextraction: Analysis of neonicotinoids in bananas

In vivo solid-phase microextraction (in vivo SPME) is an emerging fascinating sample pretreatment technique, but its quantitative correction method is different from the traditional correction methods, which has become a bottleneck limiting its development. At present, the sampling-rate calibration and equilibrium calibration are mainly used, however, their characteristics and applicability are not clear. In this study, the sampling-rate calibration and equilibrium calibration were evaluated in the case of the determination of neonicotinoids in bananas by in vivo SPME. The factors that affect the sampling rate (Rs), such as the matrix states, sampling durations, and individual differences were studied, and they all had impacts on Rs. Conversely, the equilibrium distribution coefficient (Kfs) remained constant after extraction equilibrium and the individual differences were smaller. The highest accuracy and precision were achieved by equilibrium calibration, and the relative recoveries were in the range of 83.2 %-104.3 % with the relative standard deviations below 8.1 % compared to a standard QuEChERS-based method. The lower limits of quantification for 4 neonicotinoids in bananas were below 5 ng g−1, lower than the standard method and the maximum residue levels in China and the European Union. This work clarifies the characteristics, rules and performance of the sampling-rate calibration and equilibrium calibration, which is of crucial importance for the development and application of in vivo SPME. The developed method is convenient, sensitive, and accurate for the determination of pesticide residues, which is of great significance to guide the safe use of pesticides in the field and prevent products with excessive pesticide residues from entering the market.

Comparison of nitrogen and helium as carrier gases for determination of pesticide residues in foods via gas chromatography–tandem mass spectrometry with atmospheric pressure chemical ionization

The applicability of nitrogen as an alternative carrier gas to helium for the multiresidue analysis of pesticides using gas chromatography–tandem mass spectrometry with atmospheric pressure chemical ionization (GC–(APCI)MS/MS) was examined. The methods using both carrier gases were validated for 151 pesticides in foods at a spiking level of 0.01 ppm, maintaining identical conditions for both gases, including the GC column and carrier gas flow rate. The use of nitrogen resulted in slightly broader peaks and lower peak intensities that those observed upon using helium. However, sufficient sensitivity was achieved for all target compounds because of the high sensitivity of the GC–(APCI)MS/MS method. Further, target-compound separation was not significantly affected by the carrier gas type, and no interfering peaks were observed, demonstrating the high selectivity of the nitrogen-based method, even beyond the optimum linear velocity. Finally, the analytical performance of the nitrogen-based method was comparable to those of the helium-based method. Considering cost-effectiveness of nitrogen, this method is highly valuable in the event of helium shortages and for routine pesticide residue monitoring.

Determination of pesticide residues in urine by chromatography-mass spectrometry: methods and applications.

Pollution has emerged as a significant threat to humanity, necessitating a thorough evaluation of its impacts. As a result, various methods for human biomonitoring have been proposed as vital tools for assessing, managing, and mitigating exposure risks. Among these methods, urine stands out as the most commonly analyzed biological sample and the primary matrix for biomonitoring studies. This review concentrates on exploring the literature concerning residual pesticide determination in urine, utilizing liquid and gas chromatography coupled with mass spectrometry, and its practical applications. The examination focused on methods developed since 2010. Additionally, applications reported between 2015 and 2022 were thoroughly reviewed, utilizing Web of Science as a primary resource. Recent advancements in chromatography-mass spectrometry technology have significantly enhanced the development of multi-residue methods. These determinations are now capable of simultaneously detecting numerous pesticide residues from various chemical and use classes. Furthermore, these methods encompass analytes from a variety of environmental contaminants, offering a comprehensive approach to biomonitoring. These methodologies have been employed across diverse perspectives, including toxicological studies, assessing pesticide exposure in the general population, occupational exposure among farmers, pest control workers, horticulturists, and florists, as well as investigating consequences during pregnancy and childhood, neurodevelopmental impacts, and reproductive disorders. Such strategies were essential in examining the health risks associated with exposure to complex mixtures, including pesticides and other relevant compounds, thereby painting a broader and more accurate picture of human exposure. Moreover, the implementation of integrated strategies, involving international research initiatives and biomonitoring programs, is crucial to optimize resource utilization, enhancing efficiency in health risk assessment.

Determination and health risk assessment of carbamate pesticide residues in date palm fruits (Phoenix dactylifera) using QuEChERS method and UHPLC-MS/MS

This study aimed to investigate carbamate pesticide residues in different varieties of date palm fruits in the UAE, utilizing UHPLC-MS/MS. For sample preparation and clean-up, the efficiency and performance of different QuEChERS dispersive solid-phase extraction kits were compared. Precision and recovery were assessed at 10 μg kg−1 for the three kits, revealing that Kit 2 demonstrated the best performance. The selected QuEChERS method was validated to detect 14 carbamate residues in 55 date samples. The method exhibited strong linearity with R2 > 0.999 and low LOD (0.01–0.005 μg kg−1) and LOQ (0.003–0.04 μg kg−1). Excellent accuracy (recovery: 88–106%) and precision (RSD: 1–11%) were observed, with negligible matrix effect (− 4.98–13.26%). All samples contained at least one carbamate residue. While most detected residues were below their MRLs, carbosulfan was found in 21 samples, propoxur in 2 samples, and carbofuran in 1 sample above their MRLs. The hazard index (HI) was calculated for carbosulfan, phenmedipham, carbaryl, propoxur, carbofuran, and methomyl to assess potential health risks for date consumers. All HI values were below the safety limit of 1.0, indicating that the consumption of dates does not pose a non-carcinogenic health risk for adults and children.

Determination of pesticide residues in oat flour using low-temperature partition extraction and GC-MS analysis.

The online version contains supplementary material available at 10.1007/s13197-024-06006-z.

Effectiveness of Water Hyacinth Biochar as a Potential Adsorbent in Solid-Phase Extraction Together with Liquid Chromatography-Mass Spectrometry for Determination of Pesticide Residues in Lager Beer

Effectiveness of Water Hyacinth Biochar as a Potential Adsorbent in Solid-Phase Extraction Together with Liquid Chromatography-Mass Spectrometry for Determination of Pesticide Residues in Lager Beer

Quantitative determination of residue amounts of pesticide active ingredients used in grapes by LC-MS/MS and GC-MS/MS devices and evaluation of these pesticides in terms of public health.

The aim of this study was to quantitatively determine pesticide residues in grapes, one of the most produced and consumed fruits in Turkey and in the world. A total of 226 active ingredients were analyzed in 21 samples collected from Southeastern and Eastern Anatolia regions using QuEChERS (quick, easy, cheap, effective, rugged, and safe) extraction method and multiple residue analysis technique and LC-MS/MS and GC-MS/MS devices. In 11 out of 21 samples (52.4%), no active ingredient was detected, while at least one active ingredient was detected in 10 samples (47.6%). Thirteen different active substances (Ametoctradin, Azoxystrobin, Boscalid, Diphenoconazole, Dimethomorph, Fenhexamid, Fluopyram, Flutriafol, Metalaxyl- Metalaxyl-M, Metrafenone, Tebuconazole, Trifloxystrobin) were detected in the samples. The top 3 most detected active substances were Boscalid-Azoxystrobin and Fluopyram, respectively. The active ingredients were found between 0.015 and 0.499 mg kğ-1 values.

Determination of pesticide residues and heavy metals in Adhatoda Vasaka Linn.

Heavy metals and pesticide residue analysis plays an important role in the quality control of medicinal plants like Vasaka (Adhatoda vasica). Hence a study was conducted to determine heavy metals and pesticide residues in this medicinal herb, which is a highly useful commodity in the health system. The reliable, rapid and nontoxic sample preparation method like QuEChERS and analytical methods like GC-MS were proposed for the simultaneous determination of pesticide residues and Heavy metal detection was carried out by ICP-MS. In this study, the presence of organophosphorus and organochlorine pesticides like alachlor, heptachlor, heptachlor epoxide, aldrin, dieldrin, endrin, etc was checked but not detected. Heavy metals like Arsenic (As), Cadmium (Cd), Mercury (Hg) and Lead (Pb) are traced in samples about 2.3005 ppb, 0.799 ppb, 2.290 ppb and 10.204 ppb respectively in the present study.