Dissipation pattern and risk assessment of the synthetic pyrethroid Lambda-cyhalothrin applied on tomatoes under dryland conditions, a case study
© The Author(s). 2016
Received: 17 February 2016
Accepted: 8 July 2016
Published: 29 July 2016
The present study was carried out to develop and validate an analytical method for the detection and quantification of lambda-cyhalothrin, a synthetic pyrethroid insecticide, in tomato using gas chromatography-electron capture detector (GC-ECD). The study has meant to ascertain lambda-cyhalothrin dissipation behavior under dry land conditions.
The analytical method was validated using blank tomato spiked at 0.01, 0.1 and 0.5 mg/kg, with satisfactory recoveries ranging between 92.3 to 95.1 % and relative standard deviations (RSDs) < 13.4 %. Good linearity was achieved, with a determination coefficient (R 2) of 0.999 for the 0.005–2.0 mg/L concentration range. The limits of detection and quantification were 0.005 and 0.01 mg/kg, respectively. Dissipation pattern of lambda-cyhalothrin applied on open field grown tomato was also assessed using the same method. Lambda-cyhalothrin residues declined very quickly following first-order rate kinetics with half-life of 3.12 days. At harvest time, 14 days after final application, the remaining residues of lambda-cyhalothrin were below CODEX maximum residue limit (MRL) of 0.05 mg/kg.
Exposure of lambda-cyhalothrin has been assessed and compared to acceptable daily intake (ADI). The assessment of consumers’ exposure was based on the international estimated daily intake (IEDI) compared to acceptable daily intake (ADI). The long-term risk assessment was performed by calculating the hazard quotient (HQ). Since the HQChronic of lambda-cyhalothrin never exceeded 1.2 %, the tomato fruits could be considered safe for human consumption 14 days after application of lambda-cyhalothrin at the recommended dose.
KeywordsLambda-cyhalothrin Residue Risk assessment Degradation pattern
Pesticides are biologically active compounds used worldwide for the protection of food, fiber, and human health (Malhat et al., 2015). After application, pesticides tend to degrade, with their residues remaining not only in the plants but also in various environmental matrices, like water, soil or sediments. Pesticides have been reported to cause toxic effects on humans, ranging from short-term effects such as headaches and nausea to chronic effects like cancer, reproductive damage and endocrine disruption (Berrada et al., 2010; Claeys et al., 2011; Malhat et al. 2014a). Humans main exposure route is via food that contribute five times more than other routes, such as air and drinking water (Claeys et al., 2011; Malhat et al. 2014b).
Pesticides – contaminated food is associated with severe effects on the human health. It is therefore rather important to work out strategies to enhance safe application of pesticides use. Maximum residue levels (MRLs) are useful parameters that promote food safety by restricting the concentration of a pesticide residue permitted on a commodity (Chen et al., 2011; Claeys et al., 2011; Malhat & Hassan, 2011).
Lambda-cyhalothrin [(R,S)-α-cyano-3-phenoxybenzyl (1S)-cis-3-[(Z)-2-chloro-3,3,3-trifluoropropenyl]-2,2-dim ethylcyclopropanecarboxylate], has been widely used to control chewing and sucking insect pests in field crops, beside its wide use in public health (Davey et al., 1992; Roberts et al., 1993; Dikshit et al., 2000; Mathirajan et al., 2000). Information about the dissipation rate of a pesticide after application is a valuable tool for assessing the behavior of residues and estimating the preharvest interval (PHI) (Malhat et al. 2014a). Governments and international organizations are regulating the use of pesticides and are setting the acceptable MRLs in foods. Good knowledge of the pesticide fate in foodstuffs is an important regulatory need to assess human exposure and possible environmental risks. Reliable estimate of long-term dietary intake of pesticide residues are needed to ascertain chronic risk. The consumer is considered to be adequately protected when estimated dietary intake of pesticide residues does not exceed the ADI or the acute reference dose (ARfD) (WHO 1997).
Lambda-cyhalothrin is mainly detected and analyzed via gas chromatography (Bouldin et al., 2006; Hem et al., 2010; Seenivasan and Muraleedharan, 2009). A micro-extraction method followed by GC analysis was reported for lambda- cyhalothrin in vegetables (Vazquez, et al., 2008). However, for field trial and dissipation study, micro-extraction data is sometimes unable to reflect the real field sample due to the sample amount. In turn, an effective simultaneous method is needed for lambda-cyhalothrin to enable handling sufficient representative sample to generate data for regulation.
In Egypt, along with most dry countries information about the dissipation of lambda-cyhalothrin insecticides is very limited. Therefore the aim of the present investigation was to develop a simultaneous method for the detection of lambda-cyhalothrin in tomato grown under open field condition using GC-μECD. The data generated from residue determination were used to estimate the dissipation pattern of lambda-cyhalothrin in tomato. Furthermore, the safety constants viz half-life and preharvest interval (PHI) of lambda-cyhalothrin were assessed to the help growers promoting Good Agricultural Practices (GAP).
Certified reference standard of lambda-cyhalothrin (>99 % purity) were purchased from Dr. Ehrenstorfer GmbH (Augsburg, Germany). All solvent used were residue analysis and HPLC grade and were obtained from Scharlau (Barcelona, Spain). Primary secondary amine (PSA, 40 μm, Bondesil), and graphitized carbon black (GCB), were procured from United Chemical Technology (Bristol, PA, USA). Anhydrous sodium sulfate (analytical reagent grade) was purchased from Merck (Germany) and activated by heating at 130 °C for 12 h and kept in desiccators. Sodium chloride of analytical grade was obtained from El Naser Pharmaceutical Chemicals Company (Cairo, Egypt).
Standard stock solution of 100 mg/L lambda-cyhalothrin was prepared in ethyl acetate. These were stored in dark vials at -20 °C. A working standard solution of 1 mg/L was prepared by appropriate dilution of the stock solution, from which the calibration standards (0.005-2.0 mg/L) were prepared by serial dilution with ethyl acetate. A matrix-matched standard calibration was obtained by mixing working standard solutions with blank tomato extracts. All standard solutions were stored at -20 °C in dark amber bottles until further analysis.
Field experiment design
The field trails including the dissipation study and final residue study were conducted in a randomized block design in open field. Each experiment was conducted in four separate plots measuring 20 m2 each where three plots were used for insecticide treatment and the other plot was used as control (blank sample). None of the plots had been treated with lambda-cyhalothrin in the past. There was no rainfall at any time during the experimental period.
Residue dynamic experiments
To investigate the dissipation of lambda-cyhalothrin, tomato had one single spray with lambda-cyhalothrin formulation (Lambda® 5 % EC), using the recommended rate, i.e. 20 g a.i./ha. Tomato fruits were collected at random at 0 (2 h after spraying), 1, 3, 7, 10 and 14 days after the treatment. Immediately after picking, the samples were put into polyethylene bags and transported to the laboratory, where they were chopped and thoroughly mixed. The sample was kept deep-frozen (- 20 °C) until analysis. Control samples were obtained from the control plot.
Final residue experiments
To investigate the final residues of lambda-cyhalothrin in tomato, the commercial formulation of lambda-cyhalothrin was manually sprayed at recommended dosage of 20 g a.i./ha two and three times at an interval of 14 days. Representative tomato samples were collected at 7 and 14 days after last treatment. Collected tomato samples were chopped immediately after harvesting and thoroughly mixed, packed in polyethylene bags, labeled, and stored at - 20 °C until analysis.
A 10 g of the homogenized sample were placed into 50-mL Teflon centrifuge tube to which 10 mL of ethyl acetate was added and vigorously shaken for 1 min using a vortex mixer at maximum speed. Next 10 g sodium sulfate anhydrous was added, and the sample was vortexed for 30 s. The extracts were centrifuged for 5 min at 3800 rpm and 4 °C. An aliquot of 4 mL was transferred from the supernatant to new clean 15-mL centrifuge tube and cleaned up by dispersive solid-phase extraction with 100 mg PSA, 20 mg GCB. The sample was again vortexed for 1 min and then centrifugation was carried out as mentioned above. Then, an aliquot of the supernatant was decanted, filtered through a 0.22-μm PTFE filter (Millipore, Billerica, MA) and transferred into a glass vial for GC analysis.
The GC- ECD system consisted of a Hewlett Packard 6890 network GC system equipped with Ni63 micro electron capture detector (μ-ECD). The analyte was separated on a HP-5MS capillary column (30 m length x 0.32 mm (i.d) x 0.25 μm film thickness, Agilent Technologies, Santa Clara, CA, USA). The injector and detector temperatures were maintained at 280 and 300 °C, respectively. The column oven temperature was held at 160 °C for 2 min, which was raised to 260 °C at 3 °C/min and held for 5 min. Nitrogen was used as carrier gas flow at 4 ml/min. 1 μL injection volume was injected at splitless mode.
The analytical method of lambda-cyhalothrin in tomato was validated for tomato for parameters such as linearity, precision, specificity and assay accuracy by following guidance document on residue analytical methods (SANCO/12571/2013).
The linearity of the method was calculated from the results directly proportional to the concentration of lambda-cyhalothrin in solvent. Linearity was assessed by the correlation coefficient (R 2 ) resulted from the five-point calibration curve.
Where SD is the standard deviation of the replicate, and M is the mean value of the recovery
Where %ME is the matrix effect, and M matrix and M solvent are the slopes of calibration curves in the matrix and in pure solvent, respectively.
Limits of detection (LOD) and quantification (LOQ)
The LOD was calculated as the quantity of lambda-cyhalothrin that generated a response 3 times greater than the noise level according to ICH method (Ermer et al. 2005). The LOQ was defined as the lowest concentration of lambda–cyhalothrin in tomato that has been validated with acceptable trueness (70–120 %) and precision (RSDr ≤ 20 %) by applying the complete analytical method, defined as a signal-to-noise ratio (S/N) of 10:1. According to the document SANCO/12495/2013 (SANCO, 2013) the limit of quantification should be ≤ MRL. The maximum residue level (MRL) for lambda-cyhalothrin is 0.05 mg/kg for tomato (Codex Alimentarius Commission, 2011).
Kinetic curve fitting
Results and discussion
Optimization of sample preparation
Extraction efficiency and stability of lambda-cyhalothrin was optimized through two different organic solvent: acetonitrile and ethyl acetate. Formation of lambda-cyhalothrin isomers was recorded in the chromatogram of tomato extracted with acetonitrile. On the other hand, no isomers appeared in the chromatogram of ethyl acetate extract. Therefore, ethyl acetate was selected as the most suitable solvent for extraction of lambda-cyhalothrin from tomato in this study. In the present study both PSA and GCB purification capabilities were also studied. The tomato extract was acidic due to the naturally high content of organic acids, which have been removed to a great extent by the PSA sorbent. Lambda-cyhalothrin was not retained by GCB, while many interfering matrix compounds were removed. This indicated that PSA and GCB provide sufficient cleanup for the crude extract of tomato.
Recoveries of lambda-cyhalothrin at different fortification levels validated the procedures adopted for extraction and analysis of lambda-cyhalothrin residues in tomato samples. The recovery achieved was 92.6 % at 0.01 mg/kg level of fortification, 95.1 % at 0.1 mg/kg level and 92.3 % at 0.5 mg/kg level of fortification for tomato which was a clear validation of the procedure adopted for extraction and analysis of lambda-cyhalothrin residues in tomato samples. The obtained value confirmed that the ethyl acetate sample preparation coupled with the GC-ECD analysis is quite suitable for the determination of the residues of lambda-cyhalothrin in tomato. Good linearity was achieved for lambda-cyhalothrin over five concentration levels ranging from 0.005 to 2 mg/L, with excellent correlation coefficient of 0.9999. The precision of the method was determined by analyzing the relative standard deviation (RSD < 20 %) in the observed area. It is suggested that lambda-cyhalothrin can be detected with good precision provided the extraction procedure adopted good recoveries. The specificity and selectivity of this method was achieved by obtaining an identical retention time for injected standard as well as spiked samples. The interferences with the analyte were examined by comparing the chromatograms of standard, blank and fortified samples. Results showed that, no interfering endogenous peak appeared, and the matrix dose not significantly suppress or enhance the response of the instrument. The limit of detection and quantification for lambda-cyhalothrin were 0.005 and 0.01 mg/kg, respectively. SANCO/12571/2013 (SANCO, 2013), suggested that the LOQ values are acceptable where LOQ ≤ MRL (0.05 mg/kg for tomato), indicating that the method was sensitive and able to detect and quantify the analyte at very low levels. The obtained results are within acceptable validation criteria for pesticide residue analysis (SANCO/12571/2013) and indicated that the developed method was accurate and reproducible.
Dissipation of lambda-cyhalothrin in tomato
Regression equation, correlation coefficient, and half-life of lambda-cyhalothrin in tomatoes
Correlation coefficient (R 2 )
C t = 0.5908e -0.222t
The dissipation half-life of lambda-cyhalothrin in tomato was 3.12 days. In this context, Jayakrishnan et al. (2005) found that lambda-cyhalothrin residues followed first order kinetics with half-life of 3.6-4.5 days and 3.7-3.9 days from first and second spray, respectively, whereas the reported concentration declined with time and reached non-detectable after 7-10 days of treatment in tomato from first year trial.
Final residue levels and safety evaluation
Terminal residue of lambda-cyhalothrin in tomatoes
Number of times sprayed
Days after spraying
Residues in tomatoes (mg/kg)
(20 g a.i/ha)
Long term dietary intake and chronic risk assessment
Long-term consumer exposure to lambda-cyhalothrin residues is estimated according to the WHO/FAO method (WHO 1997). Residues data are combined with cultural dietary information (GEMS Cluster Diets) to estimate residue intake by consumers. The consumer is considered to be adequately protected providing the calculated intake of residues does not exceed the acceptable daily intake or the acute reference dose. Based on supervised trial value, the supervised trial median residue (STMR) in tomatoes was 0.069 mg/kg (Table 2).
The IEDI is a prediction of the long-term daily intake of a pesticides residues on the basis of the assumptions of average daily food consumption per person and median residues from supervised trials. The IEDI calculation reported here considers potential residues from use of lambda-cyhalothrin on tomato. The IEDI is calculated using food consumption data from the GEMS/Food Cluster Diet (cluster diet G06) (GEMS/FOOD 2014), together with lambda-cyhalothrin residues represented by STMR value calculated. The IEDI is compared to the relevant toxicological end-point, the acceptable daily intake (ADI). The ADI of lambda-cyhalothrin was established as 0.02 mg/kg bw based on its non observed adverse effect level (NOAEL) of 2 mg/kg bw per day and a 100-fold coefficient of safety factor. The body weights assumed in the IEDI calculation are 60 kg (cluster diet G06).
Where 0.214 kg/Egyptian adult was the daily dietary intake of tomatoes according to GEMS/Food regional diet, (GEMS/FOOD 2014). IEDI of lambda-cyhalothrin in tomato was 2.46 x10-4 mg/kg bw.
The calculated percent IEDI and ADI ratios was HQChronic = 1.2 % for Egyptian adults.
When HQChronic % ˃ 100 %, then the chronic risk of lambda-cyhalothrin is unacceptable; the higher the HQChronic %, the greater the chronic risk. The result indicates that, there is no unacceptable chronic risk to human health from the consumption of tomato treated with lambda-cyhalothrin according to the use considered.
Residues of lambda-cyhalothrin were successfully extracted from tomato samples using the QuEChERS method with slightly modification. The developed method demonstrated acceptable accuracy and precision and was successfully applied to the dissipation kinetics of lambda-cyhalothrin in tomato from the field. This study is the first record about the dissipation behaviour of lambda-cyhalothrin in tomato under Egyptian field condition, usually known as dry conditions. The present results suggested that it is safe to harvest lambda-cyhalothrin treated tomatoes 14 days after treatment. This finding would help the government to provide guidance on the proper and safe use, and establishing local maximum residue levels (MRL) for lambda- cyhalothrin. The present study has portrayed the dietary intake of lambda- cyhalothrin, based on tomato consumption. Nevertheless, the dietary intake study is not necessarily inclusive of vulnerable consumers specially children. Moreover, the study has not included the effect of tomato washing as the standard procedure before consumption of tomato and how such practice would affect residue level. With such shortcoming in mind, the present pilot study is a prelude to a more comprehensive study that would delineate on the full spectrum of risk assessment.
The authors would like to acknowledge the support provided by the Suez Canal University, Central Pesticides Laboratory-Agriculture Research Centre, for providing the facilities, chemicals, instrumentation used in the present study.
The authors would like to thank the anonymous reviewers for their valuable suggestions.
FM has designed the experimental setting, performed the analytical work, and helped in the writing up. NL contributed in results analysis, determining risk assessment and dissipation rate. TA has helped in data interpretation, and writing up. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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