• 농약과학회지
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• 제15권4호
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• pp.366-373
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• 2011

인삼 중 농약 잔류량 조사 결과 부적합율과 검출 빈도가 높은 boscalid 농약에 대하여 부적합 원인을 구명하기 위해 안전사용기준에 따라 농약을 살포하되, 그 살포방법을 달리하여 잔류량을 분석하였다. 인삼은 4년근과 6년근을 사용하였으며 분석 시 인삼의 뇌두와 몸통을 나누어 분석하였다. 그 결과 boscalid의 잔류량은 몸통부분보다 뇌두부분에서 더 많은 양이 검출되었으며, 랩 처리구의 잔류 결과로부터 boscalid의 흡수이행 경로를 추정할 수 있었다. 또한 인삼의 전체부위에 대한 최대 잔류량은 4년근 인삼의 관행 처리구에서 0.76 mg/kg, 토양 처리구에서 0.69 mg/kg, 랩 처리구에서 0.62 mg/kg으로 나타났으며, 6년근 인삼에서의 전체부위에 대한 최대 잔류량은 관행 처리구에서 0.74 mg/kg, 토양 처리구에서 0.40 mg/kg, 랩 처리구에서 0.28 mg/kg으로 나타나 4년근 인삼에서 6년근 인삼보다 더 많은 잔류량을 나타내었다. 뿐만 아니라, 4년근과 6년근 인삼 모두 식품의약품안전청에서 제시한 잔류허용기준인 0.3 mg/kg을 초과하였다.

• Mass Spectrometry Letters
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• 제10권2호
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• pp.43-49
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• 2019

The aim of this study was conducted to develop an analytical method to determine the concentration of ceftiofur residue in eel, flatfish, and shrimp. For derivatization and extraction, the sample was hydrolyzed with dithioerythritol to produce desfuroylceftiofur, which was then derivatized by iodoacetamide to obtain desfuroylceftiofur acetamide. For purification, the process of solid phase extraction (Oasis HLB) was used. The target analytes were confirmed and quantified in $C_{18}$ column using liquid chromatography-tandem mass spectrometry with 0.1% formic acid in water (A) and 0.1% formic acid in acetonitrile (B) as the mobile phase. The linearity of the standard calibration curve was confirmed by a correlation coefficient, $r^2>0.99$. The limit of quantification for ceftiofur was 0.002 mg/kg; the accuracy (expressed as the average recoveries) was 80.6-105%; the precision (expressed as the coefficient of variation) was below 6.3% at 0.015, 0.03, and 0.06 mg/kg. The validated method demonstrated high accuracy and acceptable sensitivity to meet the Codex guideline requirements. The developed method was tested using market samples. As a results, ceftiofur was detected in one sample. Therefore, it can be applied to the analysis of ceftiofur residues in fishery products.

• 한국환경과학회:학술대회논문집
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• 한국환경과학회 1997년도 가을 학술발표회 프로그램
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• pp.37-39
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• 1997

Pesticide residues were extracted with 70% acetone and transferred to dichloromethane. Extracts were applied to open-column chromatography with florisil and alumina-N, The final extract was analyzed by gas chromatography with electron-capture detector(GC/ECD) and nitrogen-phosphorus detector(GC/NPD). Recoveries of the 17 organochlorine pesticides were ranged from 60.8 to 84.9% and those of 15 organophosphorus pesticides, from 70.5 to 100.0%(except phosmet and azinphos-methyl). The minimum detectable levels of this analytical method were low (0.021-0.058 mg/kg).

• 한국축산식품학회지
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• 제38권5호
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• pp.1055-1063
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• 2018

The aim of study was to investigate the correlation between the level of 17 antibiotic residues and 6 antibiotic resistances of Escherichia coli isolates in chicken meats. A total of 58 chicken meats were collected from retail grocery stores in five provinces in Korea. The total detection rate of antibiotic residues was 45% (26 out of 58). Ten out of 17 antibiotics were detected in chicken meats. None of the antibiotics exceeded the maximum residue level (MRLs) in chicken established by the Ministry of Food and Drug Safety (MFDS). The most detected antibiotics were amoxicillin (15.5%), followed by enrofloxacin (12.1%) and sulfamethoxazole (10.3%). In a total of 58 chicken meats, 51 E. coli strains were isolated. E. coli isolates showed the highest resistance to ampicillin (75%), followed by tetracycline (69%), ciprofloxacin (65%), trimethoprim/sulfamethoxazole (41%), ceftiofur (22%), and amoxicillin/clavulanic acid (12%). The results of study showed basic information on relationship between antibiotic residue and resistance for 6 compounds in 13 chicken samples. Further investigation on the antibiotic resistance patterns of various bacteria species is needed to improve food safety.

• 농약과학회지
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• 제15권2호
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• pp.134-139
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• 2011

분석대상 농약의 토양중 잔류분석법에 따른 검출한계는 0.001~0.005 ppm이었으며 2007년에 전국 논토양 150점에 대한 잔류농약 성분을 분석한 결과 살균제 carpropamid 등 4종, 살충제 buprofezin 등 4종, 제초제는 butachlor 등 3종 농약이 검출 되었다. 검출빈도는 oxadiazon 성분이 19.3%로 가장 높았고 살균제 hexaconazole 성분이 8.0%, isoprothiolane 2.7%순이었고 검출된 농도는 oxadiazon 0.836 ppm, isoprothiolane 0.810 ppm과 buprofezin 0.5 ppm 수준으로 최고 농도를 보였으나 그 밖의 성분은 대체로 잔류수준이 낮게 검출되었다. 2008년에 전국 시설재배지 토양 152점에 대한 잔류농약 성분을 조사한 결과 살균제 hexaconazole 등 6종, 살충제 cadusafos 등 16종, 제초제는 butachlor 등 7종 농약이 검출 되었고 검출빈도는 endosulfan 38.8%로 가장 높았으며, oxadiazon 성분이 13.2%, 살균제 hexaconazole 성분이 10.5%, isoprothiolane 7.2% 순이었다. 검출된 농도는 chlorfenapyr 5.087 ppm으로 가장 높았으며, chlorothalonil 2.565 ppm, oxadiazon 0.715 ppm, isoprothiolane 0.208 ppm 수준을 보였으나 그 밖의 성분은 대체로 잔류수준이 낮게 검출되었다.

• 한국환경농학회지
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• 제40권2호
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• pp.118-126
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• 2021

BACKGROUND: It is very important to monitor the residual characteristics of pesticides in pre-harvest fresh ginseng to ensure consumer safety. METHODS AND RESULTS: Forty-eight fresh ginseng samples were collected from 8 ginseng-growing fields 10 days before harvest and pesticide residues in fresh ginseng with and without rhizome (head of ginseng) and rhizome were analyzed for 320 pesticides by using GC-MS/MS and LC-MS/MS. As a result of the pesticide residue analysis, the number of pesticides detected from the fresh ginseng with rhizome, that without rhizome and rhizome were 26, 25, and 40, respectively, indicating that high number of pesticides found in rhizome, compared with the other parts. Pyraclostrobin was detected with the highest frequency in all samples, reaching to 21.2% in fresh ginseng with rhizome, 16.8% in that without rhizome, and 14.8% in rhizome. CONCLUSION: The residue levels of pesticides detected did not exceed their maximum residue limits, in spite of residual data in fresh ginseng before harvest. The amounts of the estimated daily intakes of all the detected pesticides were found to be from 0.018 to 1.818% of their acceptable daily intakes, indicating that concentrations of pesticides detected from fresh ginseng with and without rhizome collected before harvest do not pose the immediate health risks.

• 한국식품위생안전성학회지
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• 제11권2호
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• pp.89-97
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• 1996

This study was carried out to determine the pesticide residues in rice bran, crude rice bran oil and the oil of various stages of refining process. Each samples were analyzed for 41 pesticide residues by multiclass multiresidue methods with GC-ECD, NPD and identified by GC-MSD. Rice bran were detected cypermethrin, diazinon, dichlofluanid, and its level were ranged from 0.01~0.122 ppm. Crude rice bran oil were detected cypermethrin, diazinon, dichlofluanid, dimethoate, etrimfos, flucythrinate, and its level were ranged from 0.015~0.654 ppm Crude rice bran oil has the higher level of pesticide residues and more varieties of pesticides than rice bran. But pesticide residues in the crude rice bran oil was found to be almost removed then pigment was decolorized by absorption using active carbon and clealy removed by thermolysis for deodorization.

• 한국환경농학회지
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• 제21권4호
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• pp.279-285
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• 2002

대전시 노은 도매 시장에서 채취한 과실류와 6종의 농약잔류량을 조사한 후 이에 대한 위해성 평가를 실시하였다. 전체 120건의 분석시료 중 70.8%가 농약 성분이 검출되었고 그중 1.67%가 잔류허용기준치을 초과하여 검출되었다. 검출 비율이 높은 시료는 사과 복숭아, 포도 등이었다. 검출된 성분에서 살충제는 유기인계, 합성 pyrethroid계, 유기염소계가 비슷한 비율로 검출되었고, 살균제에서는 특히 procymidone(dicarboximide계)과 chlorothalonil(유기염소계)의 검출비율이 높았다. 검출빈도가 높은 성분은 chlorothalonil, chlorpyrifos, fenvalerate, pocymidone, deltamethrin EPN의 순이었다. 위해성을 평가하기 위해서 각 농작물에 대한 농약의 추정섭취량과 ADI를 비교한 결과 추정섭취량의 비율이 1.221% 이하로 나타나 그 영향이 매우 낮은 것으로 판단되었다. 이것은 농약 잔류 허용기준치를 초과한 농작물인 복숭아에서 chlorothalonil, EPN에 대해서도 동일한 결과를 나타내었다.

• 농약과학회지
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• 제10권4호
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• pp.266-271
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• 2006

본 연구는 2005년 1월부터 12월까지 경기도와 인천지역에 납품된 14종 농산물 356점 중 카바메이트계 농약 10종 (aldicarb, bendiocarb, carbaryl, carbofuran, ethiofencarb, fenobucarb, methiocarb, mehtomyl, isoprocarb, propoxur)을 분석하였다. 대상 농산물 356점중 카바메이트계 농약이 12건 검출율(2.53%)이 검출되었으며, 그 중 2종류의 농약이 검출된 농산물은 1건으로 0.27% 이었다. 군납 농산물중 methomyl(0.84%)로 가장 많이 검출되었으며, carbofuran(0.56%), ethiofencarb(0.56%), carbaryl(0.28%) 순으로 나타났다. Aldicarb, bendiocarb, fenobucarb, methioarb, isoprocarb, propoxur 은 시료에서 검출되지 않았다. 검출된 농약은 상추에서 ethiofencarb(0.29 ppm), 고추에서 carbofuran(0.24 ppm), 시금치에서 methomyl(0.23 ppm), carbaryl(0.01 ppm), 배추에서 carbofuran(0.20 ppm), 오이에서 methomyl(0.12 ppm), 쑥갓에서 ethiofencarb(0.01 ppm), 파에서 methomyl(0.01 ppm) 이었으나 모두 MRL 미만으로 안전하였다.

• 한국축산식품학회지
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• 제43권5호
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• pp.914-937
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• 2023

The objective of this study was to establish a multi-residue quantitative method for the analysis of anthelmintic and antiprotozoal drugs in various livestock products (beef, pork, and chicken) using ultra-high-performance liquid chromatography-tandem mass spectrometry. Each compound performed validation at three different levels i.e., 0.5, 1, and 2× the maximum residue limit according to the CODEX guidelines (CAC/GL 71-2009). This study was conducted according to the modified quick, easy, cheap, effective, rugged, and safe procedure. The matrix-matched calibrations gave correlation coefficients >0.98, and the obtained recoveries were in the range of 60.2%-119.9%, with coefficients of variation ≤32.0%. Furthermore, the detection and quantification limits of the method were in the ranges of 0.03-3.2 and 0.1-9.7 ㎍/kg, respectively. Moreover, a survey of residual anthelmintic and antiprotozoal drugs was also carried out in 30 samples of beef, pork, and chicken collected in Korea. Toltrazuril sulfone was detected in all three samples. Thus, our results indicated that the developed method is suitable for determining the anthelmintic and antiprotozoal drug contents in livestock products.