• 한국식품위생안전성학회지
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• 제25권2호
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• pp.106-117
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• 2010

2009년 1월부터 12월까지 서울 강북지역에서 유통되고 있는 농산물 109종 3,988건을 대상으로 272종 농약의 잔류량을 분석하였다. 1. 2009년 서울 강북지역에서 유통 중인 3,988건의 농산물을 대상으로 잔류농약 272종에 대한 잔류 실태를 조사한 결과 총 3,988건 중 1,021건에서 농약이 검출되어 25.6%의 검출률을 나타냈으며, 이 중 잔류허용기준을 초과하여 부적합 농산물로 판정된 시료는 89건으로 부적합률은 2.2% 였다. 2. 분석대상 농약 272종 중에서 검출된 농약 성분은 77종으로 프로시미돈 211회, 엔도설판 195회, 클로르훼나피르 122회, 싸이퍼메쓰린 116회, 비펜스린 60회 등의 순으로 나타났다. 이 중 부적합이 발생된 농약은 30종이며 엔도설판 19회, 프로시미돈 12회, 톨크로포스-메칠 10회, 이프로디온 5회, 플로토라닐 4회 등의 순으로 나타났다. 3. 검출농약 77종 중 내분비계 장애 추정농약에 해당되는 농약은 메소밀, 빈클롤졸린, 싸이퍼메쓰린, 엔도설판, 이프로디온, 카벤다짐, 클로로타로닐, 클로르피리포스, 트리풀루라린, 펜디메타린, 펜발러레이트, 프로시미돈, 헥사코나졸의 13종이었고, 이들의 검출 횟수는 688회였다. 검출된 농약 13종 중 8종이 잔류허용기준을 초과하엿다. 4. 검출된 월별 농약 검출률을 살펴 보면, 10.0%의 검출율을 넘는 달은 2월, 3월, 4월, 7월 이었으며, 3월과 7월이 가장 높은 검출률을 나타내었다. 2월, 3월, 4월에 부적합률이 높은 것으로 나타났다.

• 한국축산식품학회지
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• 제41권6호
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• pp.1022-1035
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• 2021

This study estimated the effect of exposure to propiconazole through implementation and residues in finishing pigs. We analyzed the expression of fibrosis-related genes and performed histological analysis of the blood, liver, kidney, muscle, ileum, and fat tissues. The animals were exposed for 28 d to different concentrations of propiconazole (0.09, 0.44, 0.88, 4.41, and 8.82 mg/kg bw/d). Quantitative, gene expression, and histological analyses in tissues were performed using liquid chromatography mass spectrometry, real-time PCR, and Masson's trichrome staining, respectively. Final body weight did not differ among groups. However, genes involved in fibrosis were significantly differentially regulated in response to propiconazole concentrations. Glucose, alanine aminotransferase, and total bilirubin levels were significantly increased compared with those in the control group, while alkaline phosphatase level was decreased (p<0.05) after exposure to propiconazole. The residue limits of propiconazole were increased in the finishing phase at 4.41 and 8.82 mg/kg bw/d. The liver, kidney, and ileum showed blue staining after propiconazole treatment, confirmed by Masson's trichrome staining. In conclusion, these findings suggest that propiconazole exposure disturbs the expression of fibrosis-related genes. This study on dietary propiconazole in pigs can provide a basis for determining maximum residue limits and a better understanding of metabolism in pigs and meat products.

• 대한수의학회지
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• 제60권4호
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• pp.209-213
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• 2020

This study examined the residue of dl-methylephedrine hydrochloride (MEP) on the muscle of pigs administered orally with MEP 12 g/ton feed for seven consecutive days. Twenty healthy cross swine were administered MEP. Four treated animals were selected arbitrarily to be sacrificed at 1, 2, 3, 4, and 5 days after treatment. MEP residue concentrations in the muscle were determined by liquid chromatography coupled with tandem mass spectrometry. The drug was extracted from muscle samples using 10 mM ammonium formate in acetonitrile followed by clean-up with n-hexane. The analyte was separated on an XBridgeTM hydrophilic interaction liquid chromatography column using 10 mM ammonium formate in deionized distilled water and acetonitrile. The correlation coefficient (R2) of the calibration curve was 0.9974, and the limits of detection and quantification were 0.05 and 0.15 ㎍/kg, respectively. The recoveries at three spiking levels were 94.5-101.2%, and the relative Standard Deviations was less than 4.06%. In the MEP-treated group, MEP residues on one day post-treatment were below the maximum residue limit in the muscle. The developed method is sensitive and reliable for the detection of MEP in porcine muscle tissues. Furthermore, it exhibits low quantification limits for animal-derived food products destined for human consumption.

• 한국축산식품학회지
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• 제42권4호
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• pp.712-722
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• 2022

In this study, we investigated the residual properties of tebuconazole-treated pigs. Twenty pigs were treated with different concentrations (0.25, 1.25, 2.5, 12.5, and 25 mg/kg bw/d) of tebuconazole for 28 d. Blood biochemistry, histology, and residual levels were analyzed using the VetTest analyzer, Masson's trichrome staining kit, and liquid chromatography-mass spectrometry, respectively. The final body weights were not significantly different between the control and treatment groups. Alkaline phosphatase, blood urea nitrogen, cholesterol, and gamma-glutamyl transpeptidase levels were significantly different from those of the control after exposure for 14 d. However, alanine aminotransferase levels showed changes only after exposure to pesticides for 28 d. The biochemical parameters were separated during the experimental period (14 d versus 28 d) by principal component analysis. Based on variable importance plots, blood urea nitrogen/creatinine ratio, blood urea nitrogen, glucose, and gamma-glutamyl transpeptidase are candidate biomarkers for tebuconazole exposure. The residual levels were observed at T4 (12.5 mg/kg bw/d) and T5 (25 mg/kg bw/d) in the liver and fat tissues, respectively. Fibrosis increased in the liver, kidney, and fat tissues, depending on the tebuconazole concentration. In conclusion, the residue limits of tebuconazole and the physiological changes caused by dietary tebuconazole in pigs provide important information for establishing maximum residue limits of pork and pork products.

• 한국식품과학회지
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• 제39권5호
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• pp.575-579
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• 2007

본 연구는 홍삼 및 농축액의 합리적인 농약잔류허용기준 개정을 위한 과학적인 자료를 얻고자 수행하였다. 인삼 재배 시에 사용 등록된 농약 3종(azoxystrobia, fenhexamid, cyprodinil)을 인삼포에 직접 살포하여 수확한 수삼을 홍삼과 농축액으로 직접 제조하였다. 수확한 수삼에 azoxystrobin 0.12 ppm, fenhexamid 0.19 ppm, cyprodinil 1.78 ppm이 잔류하였으며 농약이 잔류된 수삼을 원료로 홍삼 및 농축액으로 가공하여 각 제품의 농약 잔류량을 조사한 결과 fenhexamid의 경우 홍삼에 0.54 ppm, 홍삼농축액에서 1.93 ppm이 잔류하였다. Azoxysoobin은 홍삼에서 0.24 ppm, 홍삼농축액에서 0.81 ppm이 잔류하여 가공단계를 거치면서 증가하였다. 그러나 cyprodinil의 경우 1.78 ppm이 잔류된 수삼이 홍삼으로 가공되면서 1.49 ppm으로 감소하였으나 홍삼농축액에서는 3.66 ppm으로 증가하였다. 농약이 잔류된 수삼을 이용하여 홍삼과 농축액 제조시 azoxystrobin, fenhexamid, cyprodinil의 감소계수(dry base)는 홍삼에서 0.66, 0.94, 0.28, 홍삼농축액에서 3.25, 4.94, 1.01이였다.

• 농약과학회지
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• 제18권1호
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• pp.1-7
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• 2014

본 연구는 참외에 대한 살균제 metalaxyl-M과 flusilazole의 잔류량 변화를 측정하여 약제별 잔류특성을 파악하고, 반감기를 산출함으로써 생산단계 잔류허용기준(PHRL, Pre-Harvest Residue Limit) 설정을 위한 기초자료로서 활용하고자 수행하였다. 공시 약제인 metalaxyl-M과 flusilazole은 안전사용기준에 준하여 7일 간격으로 1회, 2회살포하였으며, 살포 2시간 후를 0일차로 하여 0, 1, 2, 3, 5, 7, 9, 11일차에 수확하였고, 잔류량의 경시변화 결과를 토대로 생물학적 반감기를 산출하였다. 시료는 QuEChERS방법을 이용하여 전처리하였으며, metalaxyl-M의 경우 GC/NPD를 이용하여 분석하였으며, flusilazole은 LC/MS/MS를 이용하여 분석하였다. 참외 중 metalaxyl-M과 flusilazole의 LOQ (Limit of quantitation)는 각각 0.02 mg/kg, 0.01 mg/kg이었으며, metalaxyl-M 회수율은 95.7-103.2%이었고, flusilazole은 100.2-106.8%이었으며, 표준편차는 모두 10% 미만이었다. 참외 중 각 농약에 대한 생물학적 반감기는 flusilazole의 경우 1, 2회 처리구에서 12일이었으며, metalaxyl-M의 경우 23일이었다. 본 연구결과, metalaxyl-M 및 flusilazole의 수확 10일 전 PHRL은 각각 1.5, 0.3 mg/kg로 나타났으며, 수확 시 metalaxyl-M, flusilazole의 잔류농도는 MRL을 초과하지 않을 것으로 예측되었다.

• 한국환경농학회지
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• 제36권1호
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• pp.50-56
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• 2017

본 연구는 수박 중 pyridalyl 및 fluopicolide의 경시적 잔류양상을 살펴보고 생산단계 잔류허용기준 설정을 위한 생물학적 반감기를 산출하고자 수행되었다. 두 시험약제를 안전사용기준에 따라 두 포장지역에서 각각 살포한 후 포장 1에서는 10일간 포장 2에서는 20일간 일자별 수박 시료를 채취하여 각각의 잔류분을 HPLC/UVD로 분석하였다. 두 시험농약의 분석정량한계는 각각 0.05 mg/kg, 0.02 mg/kg이었으며, 회수율은 81.2~90.5% 수준이었고 시료 중 시험농약은 43~47일간 안정하였다. 수박 중 초기 잔류량은 pyridalyl이 0.12~0.16 mg/kg, fluopicolide은 0.23~0.24 mg/kg이었으며, 모든 포장내에서 농약잔류허용기준보다 낮은 수준이었다. 수박 중 pyridalyl의 생물학적 반감기는 포장 1에서 26.9일, 포장 2에서 17.9일 이었으며, fluopicolide의 생물학적 반감기는 포장 1에서 16.6일, 포장 2에서 94.2일이었다. 수박의 pyridalyl 및 fluopicolide의 수확 10일 전 생산단계 잔류허용기준은 각각 0.21 mg/kg, 1.03 mg/kg이었으며 재배기간 중 두 시험약제 모두 매우 낮은 잔류소실 경향을 보였다.

• 한국초지조사료학회지
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• 제38권3호
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• pp.156-164
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• 2018

Pesticide application in agriculture provides significant benefits such as protection from disease, prevention of harmful insects, and increased crop yields. However, accurate toxicological tests and risk assessments are necessary because of many related adverse effects associated with pesticide use. In this review, we discuss and analyze residual pesticides contained in livestock feed in Korea. A pesticide residue tolerance standard for livestock feed has not been precisely established; so, risk assessments are required to ensure safety. Standards and approaches for animal criteria and appropriate methods for evaluating residual pesticides are discussed and analyzed based on technology related to animal product safety in Korea. The safety of livestock feed containing pesticides is assessed to establish maximum residue limits relative to pesticides. Analysis of residual pesticides in milk, muscle, brain, and fat was performed with a livestock residue test and safety evaluation of the detected pesticide was performed. Efficacy of organic solvent extraction and clean-up of feed was verified, and suitability of the instrument was examined to establish if they are effective, rapid, and safe. This review discussed extensively how pesticide residue tolerance in livestock feed and hazard evaluation may be applied in future studies.

• 한국환경농학회지
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• 제38권1호
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• pp.1-9
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• 2019

BACKGROUND: Accurate and simple analytical method determining Fluxametamid residue was necessary in various food matrices. Additionally, fulfilment of the international guideline of Codex (Codex Alimentarius Commission CAC/GL 40) was required for the analytical method. In this study, we developed Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS) method to determine the Fluxametamid residue in foods. METHODS AND RESULTS: Fluxametamid was extracted with acetonitrile, partitioned and concentrated with dichloromethane. To remove the interferences, silica SPE cartridge was used before LC-MS/MS (Liquid Chromatography-Tandem Mass Spectrometry) analysis with $C_{18}$ column. Five agricultural commodities (mandarin, potato, soybean, hulled rice, and red pepper) were used as a group representative to verify the method. The liner matrix-matched calibration curves were confirmed with coefficient of determination ($r^2$) greater than 0.99 at calibration range of 0.001-0.25 mg/kg. The limits of detection and quantification were 0.001 and 0.005 mg/kg, respectively. Mean average accuracies were shown to be 82.24-115.27%. The precision was also shown to be less than 10% for all five samples. CONCLUSION: The method investigated in this study was suitable to the Codex guideline for the residue analysis. Thus, this method can be useful for determining the residue in various food matrices as routine analysis.

• 한국환경농학회지
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• 제42권3호
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• pp.193-202
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• 2023

Residue monitoring of propiconazole (PCZ) in cabbage, shallot, and spinach was conducted under multi-trial greenhouse conditions. This study aimed to understand the fate of the applied fungicide in these vegetables. Furthermore, the associated health risk of PCZ in leafy vegetables was assessed through dietary risk assessment. Commercially available PCZ (22% suspension concentrate) was administered thrice according to the OECD fungicide application interval guideline. The plant samples were extracted using a slightly modified QuEChERS technique and analyzed using gas chromatography-tandem mass spectrometry. The average PCZ recovery was between 84.5% and 117.6%, with a <5% coefficient of variance. The dissipation of PCZ residue in cabbage, shallot, and spinach after 14 days was 96%, 90%, and 99%, respectively, with half-lives of <5 days. Meanwhile, dietary risk assessments of PCZ residues in the studied vegetables using the risk quotient (RQ) were significant < 100 (RQ < 100). Thus, the population groups considered in this study were not at substantial risk from consuming leafy vegetables sprayed with PCZ following critical, good agricultural practices.