• Asian-Australasian Journal of Animal Sciences
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• 제14권3호
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• pp.378-381
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• 2001

Sulfamethazine has been widely used in swine for prevention or treatment of infections. Recently, the safety of the drug to consumers has been questioned because of carcinogenic effects. To prevent unwanted drug residues entering the human food chain, both government authorities and industries have established extensive control measures. The demands for reliable, simple, sensitive, rapid and low-cost methods for residue analysis of foods are increasing nowadays. In this study, we established a rapid prediction test for the detection of cattle with violative tissue residues of sulfamethazine. The recommended therapeutic dose of sulfamethazine (withdrawal time, 15 days) was administered to each of 10 cattle. Blood was sampled before drug administration and during the withdrawal period. The concentration of sulfamethazine in plasma, determined by a semi-quantitative ELISA, was compared to that of an internal standard (10 ppb). The absorbance ratio of internal standard to sample (B/Bs) was employed as an index to determine whether drug residues in cattle tissues were negative or positive. That is, a B/Bs ratio less than 1 was considered residue positive and if larger than 1 was considered negative. All 10 plasma samples from non-treated cattle showed negative to sulfamethazine. Sulfamethazine was detected in plasmas of treated cattle until Day 7 of withdrawal period. The present study showed that the semi-quantitative ELISA could be easily adapted in predicting residues of sulfamethazine in live cattle.

• 농업과학연구
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• 제43권4호
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• pp.634-640
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• 2016

The objective of this study was to evaluate the effectiveness of using HR-GC/MS for the rapid screening of dieldrin residues in soils. Persistent organic pollutants (POPs) of organochlorine pesticides such as dieldrin, were analyzed in sedimentary rock and granite rock collected from greenhouses, Niigata, Japan. Dieldrin remains in Japanese farming soils, more than 40 years after their use as insecticides was prohibited. The averages in soil moisture ranged from 2.79% to 7.20% in soils derived from sedimentary rock and from 25.59% to 31.40% in soils derived from granite rock. Mean concentrations of dieldrin residues in sedimentary rock and granite rock were $39.7ng\;g^{-1}$ and $40.51ng\;g^{-1}$, respectively. Dieldrin residue was detected at a slightly higher concentration in granite rock than sedimentary rock samples. There was no consistency between the two soils or between surface and subsurface soils. The coefficients of variation of the two soils were 10.6% and 8.7%, respectively. These results suggest that our high-resolution mass spectrometry detector (HR-GC/MS) is effective at analyzing residual organochlorine pesticides in soil. In order to increase the precision and sensitivity for chemical analysis of POPs, high-resolution gas chromatography coupled with a HR-GC/MS is highly recommended.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2009년도 추계학술대회 논문집
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• pp.511-511
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• 2009

Lignocellulosic biomass is the most abundant organic material on earth and also promising raw material for bioenergy production. Agricultural residues in the process of bio-oil extraction, is an abundant and low-cost lignocellulosic material. The technology for conversion of lignocellulosic biomass resources to fuels and chemicals, such as ethanol, has been under development for decades. One of the well-studied technologies that are currently being commercialized is to use a dilute acid-catalyzed pretreatment followed by enzymatic hydrolysis and fermentation to produce ethanol. In this work, the dilute-acid hydrolysis of agricultural residues was optimized through the utilization of statistical experimental design. Evaluation criteria for optimization of the pretreatment conditions were based on high xylose recovery and low inhibitor contents in the hydrolyzates. The purpose of this study was to gain a more accurate understanding of the quantities of acid required for effective hydrolysis and the reactivity trade-offs with reaction time and temperature that will enable overall process optimization.

• 한국환경보건학회지
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• 제19권1호
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• pp.90-93
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• 1993

Increasing Public Concern : Pesticide residue is probably one of the fastest growing problems in regard to environmental contamination. Pesticide use in agriculture in this century has produced certain benefits, including a decrease in crop waste and an increase in crop yields and food quality. However, pesticide use also creates problems of having effects on the environment and remaining in food chain. The presence of pesticide residue in food, water, and soil has aroused public concern over potential health hazards. Despite information provided by national and private level agencies suggesting that food is safe, consumer groups worldwide are demanding assurance as to the safely of agricultural products.

• Current Research on Agriculture and Life Sciences
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• 제11권
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• pp.101-110
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• 1993

Tetranactin과 BPMC 혼합유제의 사과 재배 중 살포횟수 및 처리시기에 따른 잔류정도와 토양에 처리한 후의 분해정도를 조사한 결과는 다음과 같다. Tetranactin과 BPMC의 잔류분석시의 회수율은 사과에서 0.5ppm과 1.0ppm의 농도 수준에서 tetranactin은 74.0-77.5% 이었으며 BPMC는 83.6-87.1% 이었다. 토양에서의 회수율은 tetranactin 82.3-84.4%, BPMC 83.6-87.1% 이었다. Tetranactin 및 BPMC의 잔류분석시의 검출한계는 두 약제 모두 사과의 과육 부분에서는 0.01ppm, 사과의 과피 및 토양에서는 0.3ppm 이었다. 사과의 과육 및 과피부분에서 tetranactin 및 BPMC의 잔류량은 수확 3일전 5회 처리에서 잔류량의 96% 정도가 사과의 과피 부분에 잔류되는 것으로 나타났다. 사과에 대한 tetranactin 및 BPMC의 잔류량은 수확 3일전 5회 처리에서 tetranactin은 0.39ppm, BPMC는 0.75ppm이 잔류되어 tetranactin 및 BPMC의 사과에 대한 안전사용기준은 수확 30일전, 2회 이내의 사용으로 추천할 수 있다. Tetranactin 및 BPMC의 토양 중 분해 반감기는 포장시험 조건에서 각각 6.9일과 6.3일 이었으며 실내시험 조건에서는 각각 24.4 및 23.2일로 나타났다.

• 농업과학연구
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• 제32권2호
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• pp.215-221
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• 2005

대전광역시 유성구 노은농수산물도매시장에서 유통되는 농산물의 안전성을 확립하기 위하여 농산물에 대한 잔류농약 모니터링을 실시하기에 앞서 대전지역에서 잔류분석을 시행할 관련기관(충남대학교 농생대 농화학과, 국립농산물품질관리원 충남지원, 대전광역시 보건환경연구원, 충청남도 보건환경연구원)들간의 각각의 경험을 바탕으로 한 기기 안정도 및 회수율 협력 실험을 통하여 분석 결과의 검증 및 신뢰성을 제고하고자 실시하였다. 기기안정도 실험에서는 bifenthrin의 경우 기관별 크로마토그램상의 area 변화의 상대표준편차 범위가 0.684%(기관 D)~1.212%(기관 C), chlorpyfiphos의 경우 0.159%(기관 A)~0.405%(기관 C), diazinon의 경우 0.324%(기관 B)~0.623%(기관 C), 그리고 ethoprophos의 경우 0.274%(기관 B)~0.736%(기관 C)이었다. 정량 분석법에서는 상대 표준편차범위는 10% 정도가 되어야 만족스럽다고 보고하였는데 본 연구의 결과에서 상대 표준편차는 1.212% 이하로 매우 만족스러운 결과를 얻었다. 따라서 각 기관별 기기는 매우 안정적이었음을 알 수 있었다. 회수율 실험의 경우 참깨와 오이의 결과 회수율은 63.4-94.3%이며 이들의 상대표준편차(RSD) 또한 0.32-1.03으로 각 기관별 분석방법은 별다른 문제가 없는 것으로 판단되어지며 추후에 좀 더 많은 Data를 가지고 기관간의 상관관계를 구하여야 할 것으로 사료된다.

• 농약과학회지
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• 제3권2호
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• pp.37-46
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• 1999

침투성 살충제 carbofuran의 작물체중 잔류성과 그 안전성을 평가하기 위하여 carbofuran을 살포했을 것으로 간주되는 감자와 땅콩 및 마늘 시료를 주산지 부근의 대규모 시장에서 수집한 후 carbofuran과 carbofuran의 식물체중의 주 대사산물로 보고된 3-hydroxycarbofuran의 잔류량을 조사하고 carbofuran의 각 작물체내 대사 양상을 구명하기 위하여 각 작물의 phesphate buffer 추출액중 carbofuran의 분해실험을 수행하였다. 여러 지역의 시장으로부터 수집한 총 20 점의 완숙마늘 시료중 2점 (M-12와 M-16)의 시료에서 0.13과 0.07mg/kg의 carbofuran이 검출되어 10%의 검출빈도를 보였으나, 그 잔류량은 잔류허용기준인 0.5 mg/kg 보다 훨씬 작았다. 3-Hydroxycarbofuran은 총 20점의 시료중 1점 (M-12)의 시료에서 0.13 mg/kg이 검출되어 5%의 검출빈도를 보였으며, 풋마늘과 감자 및 땅콩 시료중 carbofuran과 3-hyoxycarbofuran의 잔류량은 분석결과 모든 시료에서 검출한계 미만이었다. 완숙마늘의 1일 섭취량에 근거한 carbofuran의 최대 섭취추정량은 0.0013mg으로 1일 최대섭취허용량인 0.55 mg의 0.24%이었으며, 마늘과 감자 및 땅콩시료에서 carbofuran이 검출되지 않아 마늘과 감자 및 땅콩 경작시 carbofuran을 사용하여도 생산물은 안전한 것으로 평가되었다. Carbofuran은 각 작물의 phosphate buffer 추출액중에서 주로 가수분해에 의하여 주 대사산물인 carbofuran phenol (m/z 164)을 생성하였으며, 그 양은 배양기간에 비례하여 증가하였다.

• 한국국제농업개발학회지
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• 제30권4호
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• pp.339-346
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• 2018

본 연구는 HPLC-DAD/MS를 이용하여 농산물 중 triazine계 제초제인 cyanazine의 잔류 분석법을 확립하였다. 대표 농산물은 사과, 배추, 고추, 현미 및 콩을 선정하였고, 아세톤을 첨가하여 추출된 cyanazine 성분을 dichloromethane 액-액 분배법과 florisil 흡착크로마토그래피법으로 정제하여 HPLC-DAD/MS 분석대상의 시료로 사용하였다. Cyanazine의 정량적 분석을 위한 최적 HPLC-DAD/MS 분석조건을 확립하였으며, 정량한계(LOQ)는 0.02 mg/kg 이었다. 각 대표 농산물에 대해 정량한계, 정량한계의 10배 및 50배 수준에서 회수율을 검토한 결과, 모든 처리농도에서 83.6~93.3% 수준을 나타내었으며, 반복 간 변이계수(CV)는 최대 2.8%를 나타내어 잔류분석 기준인 회수율 70~120% 및 분석오차 10% 이내를 충족시키는 만족한 결과를 도출하였고, 또한 LC/MS SIM을 이용하여 실제 농산물 시료에 적용하여 재확인 하였다. 이상의 결과로 신규 cyanazine의 HPLC-DAD/MS 분석법은 검출한계, 회수율 및 분석오차 면에서 국제적 분석기준을 만족하는 신뢰성이 확보된 정량 분석법으로 사용 가능할 것이다.

• Journal of Biosystems Engineering
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• 제33권2호
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• pp.136-141
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• 2008

Fecal contaminations on poultry carcasses, not easily discemable by human eyes, are potential harbor sites of pathogenic Escherichia Coli (E. coli O157:H7). Development of sensitive detection methods for fecal contamination is essential to ensure safe production of poultry products. Fluorescence has been shown to be very sensitive in detecting fecal and other biological substances that can harbor pathogens. In this study, fluorescence excitation-emission spectra of poultry fecal matter were compared with spectra for poultry skin and meat. Results indicated that the combinations of fluorescence intensities at the wavelength of 520 nm, 579 nm, 625 nm, and 635 nm with 411 nm excitation showed above 97% accuracy for differentiation of the contaminants from poultry tissues. Excitation and emission bands determined could be used for constructing a real-time fluorescence imaging device for detection of harmful residues on poultry carcasses.

• 한국환경농학회지
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• 제38권4호
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• pp.321-331
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• 2019

BACKGROUND: Pinoxaden is the phenylpyrazoline herbicide developed by Syngenta Crop Protection, Inc. and marketed on 2006. The maximum residue levels for wheat and barley were set by import tolerance. Thus, Ministry of Food and Drug Safety (MFDS) official analytical method determining Pinoxaden residue was necessary in various food matrixes. Satisfaction of international guideline of CODEX (Codex Alimentarius Commission CAC/GL 40) and National Institute of Food and Drug Safety Evaluation-MFDS (2017) are additional pre-requirements for analytical method. In this study, liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was investigated to analyze residue of Pinoxaden (M4), which is defined as pesticide residue in Korea, in foods. METHODS AND RESULTS: Pinoxaden (M4) was extracted followed by acid digestion (2hr reflux with 1N HCl) and pH adjusting (pH 4-5 with 3% ammonium solution). To remove oil, additional clean-up step with hexane saturated with acetonitrile was required to high oil contained sample before purification. HLB cartridge and nylon syringe filter were used for purification. Then, samples were analyzed by LC-MS/MS using reserve phase column C₁₈. Five agricultural group representative commodities (mandarin, potato, soybean, hulled rice, and red pepper) were used to verify the method in this study. The liner matrix-matched calibration curves were confirmed with coefficient of determination (r²) > 0.99 at calibration range 0.002-0.2 mg/kg. The limits of detection and quantitation were 0.004 and 0.01 mg/kg, respectively, which were suitable to apply Positive List System (PLS). Mean average accuracies of pinoxaden (M4) were shown to be 74.0-105.7%. The precision of pinoxaden and its metabolites were also shown less than 14.5% for all five samples. CONCLUSION: The method investigated in this study was suitable to CODEX (CAC/GL 40) and National Institute of Food and Drug Safety Evaluation-MFDS (2017) guideline for residue analysis. Thus, this method can be useful for determining the residue in various food matrixes in routine analysis.