• 한국식품위생안전성학회지
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• 제35권5호
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• pp.452-458
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• 2020

본 연구는 식물성 식품에 대한 잔류농약의 국내와 코덱스의 residue definition 비교를 통해 국내에서 식이노출 과소평가의 가능성이 있는 농약성분을 파악하고 더 나아가 식이노출 과소평가가 위해성 평가에 미치는 영향에 대해 우선적으로 검토가 필요한 농약성분을 알아내고자 하였다. 연구결과, 국내와 코덱스의 residue definition 정보로부터 식이노출 과소평가의 가능성이 있는 44종의 농약성분이 파악되었다. 이들 성분 중 농약성분의 ADI값, 국내 MRL 정보 및 대사물질의 독성학적 정보에 근거하여 다음의 24종 농약성분이 식이노출 과소평가가 위해성 평가에 미치는 영향에 대해 우선적으로 검토가 필요한 것으로 나타났다: acibensolar-S-methyl, chlorfenapyr, chlorothalonil, cyantraniliprole, cyclaniliprole, cyflumetofen, dithiocarbamates, fenamidone, fenpyroximate, fluazifop-P-butyl, fluopicolide, flupyradifuron, fluxapyroxad, glyphosate, hexythiazox, isoprothiolane, isopyrazam, myclobutanil, penthiopyrad, propiconazole, spinetoram, spiromesifen, spirotetramat, trifloxystrobin. 더 나아가 chlorfenapyr, chlorothalonil, dithiocarbamates, fenamidone은 대사물질의 독성이 더 커서 특히 우선적으로 검토가 요구되는 것으로 판단된다. 본 연구는 식품 중 잔류농약에 대한 국내 위해성 평가방법의 개선을 위해 활용될 수 있을 것으로 기대된다.

• 농약과학회지
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• 제10권4호
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• pp.289-295
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• 2006

살충제 imidacloprid(1-(6-chloro-3-pyridylmethyl)-N-nitroimidazolidin-2-ylideneamine)의 붕어(Carassius auratus L.) 체내 행적과 장기에 미치는 영향을 구명하기 위하여 imidacloprid를 환경추정농도인 0.064 mg $kg^{-1}$로 처리한 시험수에 붕어를 4일간 경시적으로 노출시켰다. 수중의 imidacloprid는 붕어체내에 흡수되어 노출 2일차에 최대 흡수량을 나타내었으며, 다른 장기에 비해 쓸개에서 농도가 가장 높았다. 붕어 사육수에서 미확인 주대사산물과 imidacloprid urea가 대사산물로 검출되었다. 또한 붕어체내에 흡수된 imidacloprid의 주요 배설경로는 담도이었으며, 장기에 대한 조직학적 이상증상은 발견되지 않았다.

• 한국환경농학회지
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• 제42권2호
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• pp.93-103
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• 2023

Persistence and degradation patterns of acequinocyl and its metabolite, hydroxyl-acequinocyl (acequinocyl-OH) and fenpyroximate in butterburs (Petasites japonicus Max.) were investigated after pesticide application. Butterburs, one of the minor crops in South Korea, was planted in two plots (plot A for double and plot B for single application) in a greenhouse. Butterburs samples were also planted in a separate plot without pesticide treatment, as the control. A commercial pesticide containing acequinocyl and fenpyroximate was applied to the foliage of butterburs at hourly intervals after dilution. Recoveries of acequinocyl and acequinocyl-OH were 78.6-84.7% and 83.7-95.5%, respectively; the relative standard deviation of the two compounds were less than 5%. The method limit of quantification was 0.01 mg/kg. The total (Ʃ) acequinocyl residues in butterburs reduced by 96.0% at 14 days and 75.9% at 7 days, in plot A and B, respectively, after final pesticide applications. The biological half-life (DT₅₀) of Ʃ acequinocyl and fenpyroximate, calculated using the dissipation rate, was 3.0 days and 4.0 days, respectively. These data were used to set up maximum residue and safe standard levels when the pesticides are applied to control pests during butterbur cultivation. Risk assessment results showed that the maximum % acceptable daily intake was 7.74% for Ʃ acequinocyl and 0.16% for Ʃ fenpyroximate. The theoretical maximum daily intake of Ʃ acequinocyl and fenpyroximate was 26.3% and 35.8%, respectively. In conclusion, the concentrations of Ʃ acequinocyl and fenpyroximate in butterburs pose no significant health risks to Koreans.

• 한국환경농학회지
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• 제41권2호
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• pp.82-94
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• 2022

BACKGROUND: Spiropidion and its metabolite are tetramic acid insecticide and require the establishment of an official analysis method for the safety management because they are newly registered in Korea. Therefore, this study was to determine the analysis method of residual spiropidion and its metabolite for the five representative agricultural products. METHODS AND RESULTS: Three QuEChERS methods (original, AOAC, and EN method) were applied to optimize the extraction method, and the EN method was finally selected by comparing the recovery test and matrix effect results. Various adsorbent agents were applied to establish the clean up method. As a result, the recovery of spiropidion was reduced when using the dispersive-SPE method with MgSO₄, primary secondary amine (PSA), graphitized carbon black (GCB) and octadecyl (C₁₈) in soybean. Color interference was minimized by selecting the case including GCB and C18 in addition to MgSO₄. This method was established as the final analysis method. LC-MS/MS was used for the analysis by considering the selectivity and sensitivity of the target pesticide and the analysis was performed in MRM mode. The results of the recovery test using the established analysis method and inter laboratory validation showed a valid range of 79.4-108.4%, with relative standard deviation and coefficient of variation were less than 7.2% and 14.4%, respectively. CONCLUSION(S): Spiropidion and its metabolite could be analyzed with a modified QuEChERS method, and the established method would be widely available to ensure the safety of residual insecticides in Korea.

• 한국환경보건학회지
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• 제43권4호
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• pp.280-297
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• 2017

Objectives: We assessed pesticide exposure levels according to cultivation and crop type and investigated agricultural factors related to exposure. Methods: The participants, 341 male and 127 female farmers, were divided into three groups by cultivation crop type: chili greenhouse, cucumber greenhouse, and orchard. We collected questionnaires, socioeconomic characteristics and agricultural factors, and spot urine. Pesticide exposure was examined using four organophosphate and four pyrethroids urinary metabolites: dimethylphosphate, dimethylthiophosphate, diethylphosphate, diethylthiophosphate, Cis and Trans-3-(2-2dichlorovinyl)-2, 2-dimethylcyclopropane carboxylic acid, 3-phenoxybenzoic acid (3-PBA), Cis-3-(2-2dibrmovinyl)-2, and 2-dimethylcyclopropane carboxylic acid. Each metabolite was summed ${\Sigma}DAP$ and ${\Sigma}PY$ according to the chemical class. Results: Urinary metabolite detection rates and concentrations were similar between the greenhouse groups, but the orchard group was different. Similar 3-PBA detection rates were found in the three groups, but the geometric mean was very high in the orchard group compared to the two greenhouse groups. 3-PBA concentration in the orchard group was $4.11{\mu}g/g$ creatinine; the chili and cucumber greenhouse groups were 1.27 and $1.16{\mu}g/g$ creatinine, respectively. ${\Sigma}DAP$ was significantly associated with cultivation crop type and seasonal variation, but ${\Sigma}PY$ was not relevant. Conclusions: Our results suggest that cultivation and crop type may be correlated with different pesticide types and exposure levels. Furthermore, seasonal factors were related as potential factors influencing the level of organophosphate metabolites, but not for pyrethroid metabolites.

• 농약과학회지
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• 제18권4호
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• pp.228-235
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• 2014

착색단고추 중 침투성농약 flonicamid의 잔류특성을 구명하기 위하여 flonicamid 및 그 대사물질의 잔류농도를 분석하고 경시적인 잔류량 변화양상을 조사하였다. 플로니카미드 10% 입상수화제를 추천사용농도 및 그의 2배 농도로 경엽처리하고, 살포 후 1, 7, 15, 30, 50, 70, 87일의 총 7회에 걸쳐 과실, 상엽, 하엽을 구분하여 시료를 채취하여 잔류농도를 분석하였고 살포 후 87일간의 잔류량 변화를 조사하였다. 과실, 상엽, 하엽 모두에서 모화합물인 flonicamid의 잔류량은 1일차에 최고치를 나타낸 이후 급격히 감소되는 경향을 보인 반면, 대사물질 TFNG의 잔류량은 지속적으로 증가하여 15-30일차에 최고 잔류량을 나타내었고 살포 후 87일 이후에도 초기 잔류량 보다 높은 농도를 유지하였다. 과실 중 총 flonicamid의 잔류량이 시간 경과에 따라 점차적으로 증가하여 살포 후 87일까지 높은 농도를 유지하는 잔류양상은 착색단고추 잎 중에 높은 농도로 잔류하는 대사물질 TFNG의 이동에 의한 결과로 보여지며, 이러한 잔류량 변화는 기준량 및 2배량 처리구에서 유사한 양상을 나타내었다.

• Bulletin of the Korean Chemical Society
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• 제29권5호
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• pp.985-987
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• 2008

Parathion is an organophosphate pesticide being legally applied for the purpose of agriculture and is being manufactured in Korea. A gas chromatography/mass spectrometric method was developed for the determination of parathion urinary metabolite, p-nitrophenol. p-Nitrophenol was extracted from weak acidic urine, and then measured by gas chromatography-mass spectrometry (selected ion monitoring). The recovery of pnitrophenol in the overall procedure was 88.2%. The detection limit of the assay was 1.0 $\mu$ g/L based upon assayed urine of 2.0 mL. The method was applied to the determination of p-nitrophenol in urine of workers of a parathion industry. Spot urines of workers of a parathion industry were sampled at the end of shift and pnitrophenol was analyzed using above developed method. p-Nitrophenol could be detected in all of the urine samples at concentrations varying from 3.0 to 681 $\mu$ g/L.

• 한국환경농학회지
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• 제34권2호
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• pp.111-119
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• 2015

BACKGROUND: Ethychlozate (ECZ) is a plant growth regulator of synthetic auxin for agricultural commodities (ACs). Accurate and sensitive method to determine ECZ in diverse ACs on global official purpose is required to legal residue regulation. As the current official method is confined to the limited type of crops with poor validation, this study was conducted to improve and extend the ECZ method using high-performance liquid chromatography (HPLC) in all the registered crops with method verification. METHODS AND RESULTS: ECZ and its acidic metabolite (ECZA) were both extracted from acidified samples with acetone and briefly purified by dichloromethane partition. ECZ was hydrolyzed to form ECZA and the combined ECZA was finally purified by ion-associated partition including hexane-washing. The instrumental quantitation was performed using HPLC/ FLD under ion-suppression of ECZA with no interference by sample co-extractives. The average recoveries of intra- and inter-day experiment ranged from 82.0 to 105.2% and 81.7 to 102.8%, respectively. The repeatability and reproducibility for intra- and inter-day measurements expressed as a relative standard deviation was less than 8.7% and 7.4%, respectively. CONCLUSION: Established analytical method for ECZ residue in ACs was applicable to the nation-wide pesticide residues monitoring program with the acceptable level of sensitivity, repeatability and reproducibility.

• 농약과학회지
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• 제20권2호
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• pp.93-103
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• 2016

Isoxaflutole은 isoxazole계 화합물로 광엽잡초의 체내로 흡수되어 plastoquinone의 합성에 관여하는 4-hydroxy-phenylpyruvate dioxygenase (HPPD)를 저해하거나 carotenoid의 생합성을 억제하는 이행성 제초제이다. 본 연구에서는 국내 신규농약 isoxaflutole에 대한 안전관리를 위해 농산물 중 isoxaflutole 및 diketonitrile의 잔류시험법을 개발하였다. 농산물 시료(감귤, 감자, 고추, 현미, 대두) 중 isoxaflutole 및 diketonitrile을 0.1% acetic acid in water/acetonitrile (2/8, v/v)으로 추출한 뒤 dichloromethane을 이용해 분배한 후, LC-MS/MS로 분석하였다. 시험법의 직선성은 농도 대비 피크면적과의 결정계수($r^2$)가 0.997 이상으로 우수하였으며, 검출한계 및 정량한계는 각각 0.003, 0.01 mg/kg으로 높은 감도를 나타냈다. 농산물 시료 중 모든 처리구에서 평균 회수율은 72.9%-107.3% (RSD 9% 이내)였고, 타실험실과의 실험실간 검증 결과에서도 72.4-111.0%를 나타내어 검증 결과는 모두 CODEX 가이드라인(CAC/GL 40, 2003)의 기준이내를 만족하는 값으로 확인되었다. 따라서 개발된 시험법의 낮은 검출한계 및 정량한계, 우수한 직선성, 회수율 시험을 통한 양호한 정밀성 및 재현성 등이 입증되어 농산물 중 isoxaflutole 및 diketonitrile을 분석하기 위한 식품공전 공정시험법으로 활용하고자 한다.

• Journal of Microbiology and Biotechnology
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• 제16권8호
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• pp.1306-1310
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• 2006

Sphingomonas sp. strain SB5 could degrade carbofuran and carbofuran-7-phenol to a hydrolytic product, 2-hydroxy-3-(3-methlypropan-2-o1)phenol, and several red metabolites. However, the chemical structures of the red metabolites have largely remained unidentified. In this study, we identified the structure of one of the red metabolites as 5-(2-hydroxy-2-methyl-propyl)-2,2-dimethyl- 2,3-dihydro-naphtho[2,3-6]furan-4,6,7,9-tetrone by using mass spectrometric and NMR ($^1$H, $^{13}$C) analyses. It is suggested that the red metabolite resulted from condensation of some metabolites in the degradation of 2-hydroxy-3-(3-methlypropan-2-o1)phenol, a hydrolytic product derived from carbofuran. To our knowledge, this is the first paper to report a red metabolite in bacterial degradation of the insecticide carbofuran.