Pesticide Residues in Agricultural Produce in Hubei Province,PR China

Pesticide residues in agricultural produce were examined in two villages of Qianjiang municipality, Hubei province, PR China. Six food groups were sampled from the fields prior to harvesting from the farmers' market and from farmers' homes. Organochlorine residues were detected in almost all examined food groups, with residue levels significantly lower than the national tolerances (MRL). Total BHC residues were on average 31.7?µg/kg and DDT 102.5 (µg/kg. Organophosphorus residues were detected in vegetable samples. Mean residue levels of phoxim and methamidophos in vegetables were 89.9?µg/kg and 36.5?µg/kg, respectively, both exceeding the MRL. Estimated daily intakes (EDIs) of pesticide residues per person, based on the six food groups sampled, were 4.88?mg for total DDT, 2.04 (µg for total BHC, and 19.33 (µg for methamidophos. The overall results show that the increased use and misuse of pesticides for crop protection in Qianjiang municipality, notably in vegetable production, have led to worrisome levels of pesticide contamination of agricultural produce that may carry certain risks for human health.     

韭菜上五种有机磷农药的残留监测与安全性评价

【目的】2013—2016年,在北京、天津、河北和山东采集韭菜样品,采用超高效液相色谱-三重四级杆串联质谱法检测甲胺磷、甲拌磷、甲基对硫磷、对硫磷和毒死蜱的残留量,并对其残留安全性进行评价。【方法】韭菜样品用乙腈提取,石墨碳固相萃取小柱净化,超高效反相液相色谱分离,三重四级杆质谱检测,基质匹配标准溶液的外标法定量,在添加浓度为0.01~5.0 mg/kg时,方法的准确度、灵敏度和精密度满足农药残留检测的要求。【结果】甲胺磷的最高检出浓度由70.51 mg/kg降低到0.03 mg/kg,超标率由38.10%降到2.03%;甲拌磷的最高检出浓度由6.45 mg/kg降低到0.04 mg/kg,超标率由23.81%降到1.35%;甲基对硫磷的最高检出浓度由6.62 mg/kg降低到0.13 mg/kg,超标率由25.40%降到2.70%;毒死蜱的最高检出浓度由3.95 mg/kg降低到0.47 mg/kg,超标率由15.87%降到4.73%;对硫磷的最高检出浓度由22.69mg/kg降低到0.03 mg/kg,超标率由15.08%降到1.35%。【结论】上述农药的最高残留检出浓度和超标率大幅降低,但是韭菜中仍能检出少量残留。应加强安全综合防治技术的研发,加强安全用药的宣传和指导,保障韭菜产品安全。     

Rapid analytical method for the determination of 220 pesticide with their isomers by GCMS-TIC

This paper presents a cost-effective and validated multi residue modified and miniaturized method for the determination of 220 chemically different groups of pesticides and their isomers. This determination method is performed with single Quaid Gas Chromatography Mass Spectrometry -Total Ion Chromatogram GCMS-TIC. Two methods was experimented and modified with different GCMS parameters to analyses most common used pesticide and their residues in the standers solution and can be applied for real environmental samples. The results showed by single Quaid GCMS-TIC it can analyze 220 pesticides including their isomers within 49.6 min and low detection limit by using modified method 2 as described in this research. Limit of detection (LOD) was ranged from 0.78 to 14.74 ng/ml (ppb) with good separation and resolution. Limit of quantification (LOQ) was ranged between 2.34 and 44.22 ng/ml (ppb). Method 2 was more accurate, shorter, and clear separation rather than method 1. This method can be successfully applied in real environmental samples proven to be a good option for routine analysis of pesticide within the maximum residue limits (MRL) referenced to European commission especially with the most common GCMS-TIC which exists in most of labs and low income countries.     

A screen-printed, amperometric biosensor array incorporated into a novel automated system for the simultaneous determination of organophosphate pesticides

Organophosphate pesticides present serious risks to human and environmental health. A rapid reliable, economical and portable analytical system will be of great benefit in the detection and prevention of contamination. A biosensor array based on six acetylcholinesterase enzymes for use in a novel automated instrument incorporating a neural network program is described. Electrochemical analysis was carried out using chronoamperometry and the measurement was taken 10s after applying a potential of 0 V vs. Ag/AgCl. The total analysis time for the complete assay was less than 6 min. The array was used to produce calibration data with six organophosphate pesticides (OPs) in the concentration range of 10(-5) M to 10(-9) M to train a neural network. The output of the neural network was subsequently evaluated using different sample matrices. There were no detrimental matrix effects observed from water, phosphate buffer, food or vegetable extracts. Furthermore, the sensor system was not detrimentally affected by the contents of water samples taken from each stage of the water treatment process. The biosensor system successfully identified and quantified all samples where an OP was present in water, food and vegetable extracts containing different OPs. There were no false positives or false negatives observed during the evaluation of the analytical system. The biosensor arrays and automated instrument were evaluated in situ in field experiments where the instrument was successfully applied to the analysis of a range of environmental samples. It is envisaged that the analytical system could provide a rapid detection system for the early warning of contamination in water and food.     

Risk assessment of oncogenic potency of pesticide residues in fruits and vegetables

Pesticides are used in agriculture to improve food security by assuring good harvest, however, they can have harmful effects in human beings and animals. One of the harmful effects of pesticides is their carcinogenicity. Exposure to oncogenic compounds may result in cancer to the exposed animal or person. In this paper, exposure assessment of oncogenic potency of pesticides was performed from raw and processed fruits and vegetables. The oncogenic risk was calculated by multiplying the estimated daily intake (EDI) of the pesticide residue with the oncogenic potency factor (Q*) of the concerned pesticide. The total potential oncogenic risk was calculated to be 2.76 x 10(-3) before processing and 8.97 x 10(-4) after processing. The risk was higher than the EPA acceptable limit of 1 x10(-6). Despite the calculated levels exceeding the EPA acceptable limit, food processing activities reduced the dietary oncogenic risk to an average 33.8%.     

Screen-printed bienzymatic sensor based on sol-gel immobilized Nippostrongylusbrasiliensis acetylcholinesterase and a cytochrome P450 BM-3 (CYP102-A1) mutant

Here, we describe the development of a bi-enzymatic biosensor that simplifies the sample pretreatment steps for insecticide detection, and opens the way for a highly sensitive detection of phosphorothionates in food. These compounds evolve their inhibitory activity towards acetylcholinesterases (AChEs) only after oxidation, which is performed in vivo by P450 monooxygenases. Consequently, phosphorothionates require a suitable sample pretreatment by selective oxidation to be detectable in AChE based systems. In this study, enzymatic phosphorothionate activation and AChE inhibition were integrated in a single biosensor unit. A triple mutant of cytochrome P450 BM-3 (CYP 102-A1) and Nippostrongylus brasiliensis AChE (NbAChE) was immobilized using a fluoride catalyzed sol-gel process. Different sol-gel types were fabricated and characterized regarding enzyme loading capacity and enzyme activity containment. The enzyme sol-gel itself already proved to be suitable for the highly sensitive detection of paraoxon and parathion in a spectrometric assay. A method for screen-printing of this enzyme sol-gel on thick film electrodes was developed. Finally, amperometric biosensors containing coimmobilized NbAChE and the cytochrome P450 BM-3 mutant were produced and characterized with respect to signal stability, organophosphate detection, and storage stability. The detection limits achieved were 1 microg/L for paraoxon and 10 microg/L for parathion, which is according to EC regulations the highest tolerable pesticide concentration in infant food.     

Nanoporous impedemetric biosensor for detection of trace atrazine from water samples

Trace contamination of ground water sources has been a problem ever since the introduction of high-soil-mobility pesticides, one such example is atrazine. In this paper we present a novel nanoporous portable bio-sensing device that can identify trace contamination of atrazine through a label-free assay. We have designed a pesticide sensor comprising of a nanoporous alumina membrane integrated with printed circuit board platform. Nanoporous alumina in the biosensor device generates a high density array of nanoscale confined spaces. By leveraging the size based immobilization of atrazine small molecules we have designed electrochemical impedance spectroscopy based biosensor to detect trace amounts of atrazine. We have calibrated the sensor using phosphate buffered saline and demonstrated trace detection from river and bottled drinking water samples. The limit of detection in all the three cases was in the femtogram/mL (fg/mL) (parts-per-trillion) regime with a dynamic range of detection spanning from 10 fg/mL to 1 ng/mL (0.01 ppt to 1 ppm). The selectivity of the device was tested using a competing pesticide; malathion and selectivity in detection was observed in the fg/mL regime in all the three cases.     

A sensitive and regenerable biosensor for organophosphate pesticide based on self‐assembled multilayer film with CdTe as fluorescence probe

A fluorescence biosensor for organophosphorus pesticides was developed. A pH indicator, CdTe quantum dots, were used as an optical transducer of the inhibition of enzyme by analyte. Through the intervening agency of chitosan, the recognition elements (acetylcholinesterase and CdTe) were immobilized onto the surface of quartz by electrostatic attraction to form a self‐assembled multilayer film. In the absence of pesticide, acetylcholine was biocatalytically hydrolysed to yield acetic acid and choline. The released acid resulted in pH decrease, which was sensed by the immobilized pH indicator (CdTe). In the presence of pesticide, the action of acetylcholine was reduced; the fluorescence intensity of the film changed and was related to the concentration of pesticide. This multilayer film could be used as the biosensor for monocrotophos, with a detection limit of 3.20 × 10^?8 mol/L; the sensitivity was 100 times higher than that of CdTe in aqueous solution. The sensor was easily regenerated, and had good stability and selectivity for organophosphorus pesticides. Copyright © 2011 John Wiley & Sons, Ltd.     

基于酶生物传感器法检测果蔬中毒死蜱残留的提取工艺研究

使用自主研制的酶生物传感器型农残检测仪进行农药残留检测,通过筛选可测果蔬种类、调整优化样品处理大小、样品加标后静置时间、样品与提取液比例和振荡提取速度,提高检测用酶对农药的抑制敏感性,从而达到降低农药检出限、提高回收率的目的。主要设置的参数如下:样品处理方式分为打碎、切碎(切成1 cm×1 cm和1. 5 cm×3 cm大小);加标后静置时间为5 min、15min、30 min、60 min和90 min;料液比为1∶1、1∶2. 5、1∶5、1∶7. 5和1∶10;振荡提取速度为0 r/min、110 r/min、190 r/min和225 r/min;主要测定的农药为毒死蜱。结果发现,不同果蔬品种对固定化酶的抑制率影响小,样品大小为1 cm×1 cm、加标后静置时间为5 min、料液比为1∶1、加入提取剂后的振荡速度为190 r/min为最佳前处理方式组合。酶生物传感器农残检测仪能够满足快速检测果蔬中有机磷农药残留的需要。     

Occurrence and distribution of pesticides in soil at agrichemical facilities in Illinois

Detectable concentrations of pesticides were found in soil samples collected from 49 agrichemical facilities located throughout Illinois. Analysis of 822 soil samples resulted in the detection of 53 pesticides and nitrate; 20 pesticides were found in fewer than 1% of the samples. Most frequently detected were alachlor, atrazine, metolachlor, trifluralin, pendimethalin, cyanazine, metribuzin, metribuzin DA, butylate, and α‐BHC. Chlordane, dieldrin, and DDT, although not distributed at the facilities in recent years, were found in soil samples from more than one third of the sites. Approximately 24% of the pesticide detections occurred in a concentration range between the detection limit and 50 μg/kg, and 79% of all detections were less than 1000 μg/kg.

Pesticides were detected at sampling depths to 4.5 m. However, approximately 50% of all pesticide detections were found in the gravel fill that serves as the parking lot/road base for each facility. No predictable pattern in pesticide occurrence in relation to sampling depth could be determined on the basis of the mobility or persistence of the pesticide.     

A survey of pesticide residues in pollen loads collected by honey bees in France

In 2002, a field survey was initiated on French apiaries to monitor weakness of honey bee, Apis mellifera L., colonies. Apiaries were evenly distributed in five sites located on continental France. Five colonies were randomly selected in each apiary, leading to a total of 125 studied honey bee colonies. For 3 yr (starting in autumn 2002), colonies were visited four times per year: after winter, before summer, during summer, and before winter. Pollen loads from traps were collected at each visit. Multiresidue analyses were performed in pollen to search residues of 36 different molecules. Specific analyses were conducted to search fipronil and metabolites and also imidacloprid and metabolites. Residues of 19 searched compounds were found in samples. Contamination by pesticides ranged from 50 to 0%. Coumaphos and tau-fluvalinate residues were the most concentrated of all residues (mean concentrations were 925.0 and 487.2 microg/kg, respectively). Fipronil and metabolite contents were superior to the limit of detection in 16 samples. Residues of fipronil were found in 10 samples. Nine samples contained the sulfone compound, and three samples contained the desulfinyl compound. Residues of imidacloprid and 6-chloronicotinic acid were found in 69% of samples. Imidacloprid contents were quantified in 11 samples with values ranging from 1.1 to 5.7 microg/kg. 6-Chloronicotinic acid content was superior to the limit of quantification in 28 samples with values ranging from 0.6 to 9.3 microg/kg. Statistical tests showed no difference between places of sampling with the exception of fipronil. Possible origins of these contaminations, concentration and toxicity of pesticides, and the possible consequences for bees are discussed.     

喷施农药对银耳生长的影响及膳食暴露风险评估

为制订银耳(Tremella fuciformis)栽培中农药合理使用的建议,以我国银耳主栽菌株Tr01为对象,研究8组常用农药对其生长的影响,采用食品安全指数法评估长期膳食银耳导致的农药残留慢性暴露健康风险.结果表明,除咪鲜胺乳油和哒螨灵、啶虫脒微乳剂的部分处理外,其余6组农药对银耳子实体生长并无显著影响.银耳中的农...     

The impact of flucycloxuron on eggs weight kinetic and hematological parameters of chicken (Gallus domesticus)

The struggle against the harmful bugs of culture is intensified, and several products are appeared every year without the knowledge how to control their effects on environment and especially on being life. The introduced chemical products in nature are generally, the synthesis products witch are the pesticides. Our study consist the impact mechanism of a pesticides (FCX) on other biological model than harmful bugs, this biological model is a vertebrate model witch is the domestic chicken eggs (Gaollus domesticus). The toxicity of Flucycloxuron reviewed across the eggs weight kinetic accompanied with embryonic hematological parameters, in ovo and after hatching. The tested concentrations of pesticide are 1, 10 and 20 microg/egg injected at first day of incubation. Eggs treatment by three concentrations of pesticides, disturbs the studied parameters, where we observe that the pesticide inhibit the nutriment transformation, translated by eggs decreased weight kinetic according to the control, also the FCX affect the shell weight and cause the alteration of shell integrity. Hematological parameters show a clear impact of the pesticide at the lowest concentration (1 microg/egg). The obtained results confirm that the chosen biological model is good bio-indicator for eventual pollution and they are not far from pesticides toxicity.     

Dietary Intake of Pesticides Based on Vegetable Consumption in Ismailia,Egypt: A Case Study

The objective of this study was to assess pesticide residues in tomatoes, cucumbers, peppers, strawberries, and potatoes collected from local markets in Ismailia, Egypt, and to assess dietary intake and health risk implications of pesticide residues through food consumption. Vegetable selection was based on their popularity and consumption. Selection of pesticides was based on their impact on humans, and on their heavy use. The majority of the analyzed samples contained detectable levels of pesticides. Residues of some organophosphorus pesticides, including malathion, ethion, and profenofos and some pyrethroid pesticides such as fenpropathrin and cypermethrin were found in some samples at concentration equal to or exceeding their European Union's maximum residue limits (EU-MRLs). The fungicide bupirimate detected in potato samples exceeded the EU-MRL by 1500%. Phentohate and profenofos were the most frequently detected pesticides in 30 and 27% of analyzed samples, respectively. Data were used to estimate the potential health risks associated with exposure to these pesticides by ingestion of food. Estimated daily intakes (EDIs) of pesticides ranged from 0.03% to 40% of the acceptable daily intakes (ADIs), depending on pesticide concentration and vegetable consumption. Overall, the EDIs of the different pesticides from vegetable consumption are not considered a public health problem.     

Toxicological evaluation of multi-class pesticide residues in vegetables and associated human health risk study for adults and children

This article describes, for the first time in 10 years, the toxicological evaluation of pesticide residues in highly consumed vegetables (35 commodities) and health risk studies. Among 1075 vegetable samples consisting mainly of tuber, root, fruiting, and Brassica, 20% of samples contained 38 pesticides in the range of 0.005–18.7 mg/kg and 1% > maximum residue limits (MRLs). Organophosphates and chloronitrile were most frequently found (20%) in the pesticide class. The highest concentration of 18.7 mg/kg was noted for dichlofluanid. Fruiting vegetables (8%), especially tomatoes (5%), were the most contaminated, while multi-residues were determined in 5% of the samples. Risk assessment was performed by analytical results and consumption on the 97.5 percentile expressed as hazard index (HI) and hazard quotient (HQ). The highest chronic HI was calculated for diazinon in lettuce (32% Acceptable Daily Intake (ADI) adults and 36% children) and for forbidden dieldrin in carrots (26%, 62% ADI). The highest acute HI was estimated for dichlofluanid in lettuce (69% Acute Reference Dose (ARfD)) for adults, whereas for children it was above the acceptance values of ARfD (168%). Organophosphate insecticides with common mode of action showed the greatest HQ (108% ADI). Vegetables may not be a serious problem for consumers, but investigations on pesticide residues are necessary to ensure food safety and the protection of human health, especially toward children who are more highly exposed to pesticides than adults.     

Gold immunochromatographic assay for simultaneous detection of carbofuran and triazophos in water samples

Using a simple test for rapid identification and quantification of pesticide multiresidues in food and environmental samples is a long-cherished approach for practical monitoring purposes. Here two gold-based lateral-flow strips (strip A and strip B) were investigated for simultaneous detection of carbofuran and triazophos. For the strip A format, a bispecific monoclonal antibody (BsMcAb) against both carbofuran and triazophos was employed to prepare the immunogold probe. For the strip B format, anti-carbofuran monoclonal antibody (McAb) and anti-triazophos McAb separately labeled with colloidal gold were combined as detector reagents. By comparison of visual results from pesticide standard tests between the two formats, the strip B assay manifested higher sensitivities for both pesticides. Analysis of spiked water samples by the preferable strip indicated that the detection limits for carbofuran and triazophos were 32 and 4 μg/L, respectively. The strength of the portable one-step strip assay was in the simultaneous screening for two pesticides within a short time (8-10 min) without any equipment.     

Pesticide detection with a liposome-based nano-biosensor

Monitoring of the organophosphorus pesticides dichlorvos and paraoxon at very low levels has been achieved with liposome-based nano-biosensors. The enzyme acetylcholinesterase was effectively stabilized within the internal nano-environment of the liposomes. Within the liposomes, the pH sensitive fluorescent indicator pyranine was also immobilized for the optical transduction of the enzymatic activity. Increasing amounts of pesticides lead to the decrease of the enzymatic activity for the hydrolysis of the acetylcholine and thus to a decrease in the fluorescent signal of the pH indicator. The decrease of the liposome biosensors signal is relative to the concentration of dichlorvos and paraoxon down to 10⁻¹⁰ M levels. This biosensor system has been applied successfully to the detection of total toxicity in drinking water samples. Also a colorimetric screening device for pesticide analysis has been evaluated.     

An impedimetric immunosensor based on interdigitated microelectrodes (IDmicroE) for the determination of atrazine residues in food samples

A novel impedimetric immunosensor for atrazine detection has been developed. The immunosensor is based on an array of interdigitated micro-electrodes (IDmicroE) and immunoreagents specifically developed to detect this pesticide. Immunochemical determination of atrazine is possible without the use of any label. An atrazine-haptenized protein was covalently immobilized on the surface of the interdigitated mu-electrodes area (interdigits space) previously activated with (3-glycidoxypropyl)trimethoxysilane. Before, the gold electrodes were blocked using N-acetylcysteamine to prevent non-specific adsorptions. All biofunctionalization steps were characterized by chemical affinity methods and impedance spectroscopy. Immunosensors measures are made by exposing the sensor to solutions containing a mixture of the analyte and the specific antibody. With this configuration, the immunosensor detects atrazine with a limit of detection of 0.04 microg L(-1) without the use of any label. The potential of the immunosensor to analyze pesticide residues in complex sample matrices, such as red wine, has been evaluated. The results shown that after solid-phase extraction atrazine can be determined in this type of sample with a limit of detection of 0.19 microg L(-1), far below the Maximum Residue Level (MRL) established by EC for residues of this herbicide in wine.     

Report on the levels of cadmium, lead, and mercury in imported rice grain samples

In an attempt to know whether highly consumed food might contribute to metal exposure, we analyzed cadmium, lead, and mercury in 27 rice grain samples commonly consumed in Saudi Arabia by atomic absorption spectrometry after acid digestion. The mean concentrations and ranges of cadmium, lead, and mercury in tested rice samples were 20.261 (range <DL-178.026 μg/kg), 134.819 (range 23.1–1529.0 μg/kg), and 3.186 (range <DL-43.573 μg/kg), respectively. The results showed high concentrations of metals and in some cases exceeded the Provisional Tolerance Weekly Intake (PTWI) recommended by FAO/WHO. It was also noted that different rice grain samples had varying concentrations of these metals. Because the bulk of literature warns against the cumulative effects of prolonged heavy metal exposure, regular consumption of rice by local populations might pose potential health problems.     

RAPID DETECTION OF SALMONELLA TYPHIMURIUM IN FOOD SAMPLES USING A BIENZYME ELECTROCHEMICAL BIOSENSOR WITH FLOW INJECTION

A bienzyme (tyrosinase and horseradish peroxidase) electrochemical biosensor was developed for detection of Salmonella typhimurium, and evaluated for application in a flow injection system coupled with immunomagnetic separation for food samples. Parameters for immunomagnetic separation, enzymatic reaction, flow injection and electrochemical detection were determined using pure culture samples. The selectivity was tested in the presence of Listeria monocytogenes, Campylobacter jejuni and E. coli 0157:H7. The results showed a linear relationship for logarithmic values between peak current ratio and the cell number of S. typhimurium in the range of 10³ 10⁵ cfu/mL, with R²= 0.99. The detection limit of this method was 1.09 × 10³ cfu/mL for S. typhimurium and the detection time was 2.5 h. Samples of chicken carcass wash water and ground beef were used to evaluate the biosensor. The results demonstrated that this biosensor has a potential for rapid detection of different pathogens in various food samples.