• 제목/요약/키워드: MRLs

검색결과 158건 처리시간 0.025초

Production and Characterization of a Monoclonal Antibody Against Enrofloxacin

  • Chusri, Manaspong;Wongphanit, Pitikarn;Palaga, Tanapat;Puthong, Songchan;Sooksai, Sarintip;Komolpis, Kittinan
    • Journal of Microbiology and Biotechnology
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    • 제23권1호
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    • pp.69-75
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    • 2013
  • Enrofloxacin is a fluoroquinolone antibiotic approved for the treatment of infections in animals. Because of the side effects to consumers of animal products, the maximum residue limits (MRLs) of enrofloxacin in animal tissues for consumption are regulated. In this study, a monoclonal antibody (mAb) against enrofloxacin was prepared and characterized for the development of a direct competitive enzyme-linked immunosorbent assay (ELISA). The obtained mAb, Enro44, was highly specific for enrofloxacin and had a 50% inhibition concentration ($IC_{50}$) of 1.99 ng/ml in a competitive ELISA, and the limit of detection (LOD) was 0.50 ng/ml. The cross-reactivity of the mAb with other quinolones and fluoroquinolones was lower than 0.01%. The subclass of the mAb Enro44 was identified as IgG1. The antigen (Ag)-captured direct competitive ELISA using the mAb Enro44 was tested on different spiked samples, including chicken muscle, cattle milk, and cattle urine, and the assay demonstrated recoveries of 82-112%, 80-125%, and 78-124%, respectively. Furthermore, the quantitation of enrofloxacin obtained from the ELISA and from high-performance liquid chromatography (HPLC) was in good agreement, with the linear regression coefficient between 0.933 and 1.056. The cDNAs encoding a heavy-chain Fd fragment (VH and CH1) and a light chain of the mAb Enro44 were cloned and sequenced. Taken together, the results obtained reveal a potential use of this mAb in an ELISA for the detection of enrofloxacin in food samples. The information of amino acid sequence of this mAb will be useful for further modification and production of the mAb in a bioreactor.

군납 농산물 중 카바메이트계 농약의 모니터링 (Monitoring of Carbamate Pesticide Residues in Agricultural Products Supplied for the Army)

  • 박종고;나익주
    • 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.

Determination of Trichlorfon Pesticide Residues in Milk via Gas Chromatography with μ-Electron Capture Detection and GC-MS

  • Hem, Lina;Khay, Sathya;Choi, Jeong-Heui;Morgan, E.D.;El-Aty, A.M. Abd;Shim, Jae-Han
    • Toxicological Research
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    • 제26권2호
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    • pp.149-155
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    • 2010
  • The pesticide trichlorfon is readily degraded under experimental conditions to dichlorvos. A method has therefore been developed by which residues of trichlorfon in milk are determined as dichlorvos, using gas chromatography with ${\mu}$-electron capture detection. The identification of dichlorvos was confirmed by mass spectrometry. Milk was extracted with acetonitrile followed by centrifugation, freezing lipid filtration, and partitioning into dichloromethane. The residue after partitioning of dichloromethane was dissolved in ethyl acetate for gas chromatography. Recovery concentration was determined at 0.5, 1.0, and 2.0 of times the maximum permitted residue limits (MRLs) for trichlorfon in milk. The average recoveries (n = 6) ranged from 92.4 to 103.6%. The repeatability of the measurements was expressed as relative standard deviations (RSDs) ranging from 3.6%, to 6.7%. Limit of detection (LOD) and limit of quantification (LOQ) were 3.7 and $11.1{\mu}g/l$, respectively. The accuracy and precision (expressed as RSD) were estimated at concentrations from 25 to $250{\mu}g/l$. The intra- and inter-day accuracy (n = 6) ranged from 89.2% to 91% and 91.3% to 96.3%, respectively. The intra- and inter-day precisions were lower than 8%. The developed method was applied to determine trichlorfon in real samples collected from the seven major cities in the Republic of Korea. No residual trichlorfon was detected in any samples.

우리나라 연안해역 생산 패류 중 다환방향족탄화수소 분석 (Analysis of Polycyclic Aromatic Hydrocarbons (PAHs) in Shellfishes from Korean Coastal Area)

  • 홍도희;강은혜;윤민철;조미라;손광태;이가정
    • 한국수산과학회지
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    • 제54권4호
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    • pp.397-403
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    • 2021
  • Polycyclic Aromatic Hydrocarbons (PAHs) were analyzed and safety evaluation was carried out in Korean coastal area. The target congeners were benzo[a]pyrene, benzo[a]anthracene, benzo[b]fluoranthene, and chrysene. The method of analysis was significant. The highest PAHs 4 congener concentrations (12.2 ㎍/kg) was found in the mussel of Gangwon area. Comparison among the average concentration of PAHs for each congener showed that, benzo[a] anthracene was found in mussel (0.276 ㎍/kg), oyster (0.463 ㎍/kg), ark shell clam (1.92 ㎍/kg), and chrysene was found in mussel (0.848 ㎍/kg), oyster (1.36 ㎍/kg), scallop (0.489 ㎍/kg), sea squirt (3.07 ㎍/kg), and ark shell clam (0.449 ㎍/kg). In addition, benzo[b]fluoranthene was found in mussel (0.253 ㎍/kg), scallop (0.244 ㎍/kg), and sea squirt (1.64 ㎍/kg). The most hazardous benzo[a]pyrene was found in mussel (0.147 ㎍/kg), and scallop (0.244 ㎍/kg), it was not detected in the other shellfishes. However, all the PAHs levels recorded in this study did not exceed international MRLs. There was no significant difference among the PAHs concentration in shellfish based on sampling area or species. Body exposure was calculated based on PAHs concentration and intake rate. The results of this study indicated that PAHs in shellfish were within acceptable safe levels.

Probabilistic exposure assessment, a risk-based sampling plan and food safety performance evaluation of common vegetables (tomato and brinjal) in Bangladesh

  • Mazumder, Mohammad Nurun-Nabi;Bo, Aung Bo;Shin, Seung Chul;Jacxsens, Liesbeth;Akter, Tahmina;Bir, Md. Shahidul Haque;Aktar, Most Mohshina;Rahman, Md. Habibur;WeiQiang, Jia;Park, Kee Woong
    • 농업과학연구
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    • 제48권1호
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    • pp.33-43
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    • 2021
  • Along with the widespread use of pesticides in the world, concerns over human health impacts are rapidly growing. There is a large body of evidence on the relationship between the exposure to pesticides and the elevated rate of chronic diseases such as different types of cancers, diabetes, neurodegenerative disorders like Parkinson, Alzheimer, and amyotrophic lateral sclerosis (ALS), birth defects, and reproductive disorders. This research assessed the health risk of pesticide residues by the dietary intake of vegetables collected from the agro-based markets of Dhaka, Bangladesh. As some of the banned pesticides were also found in vegetable samples, they may pose a higher risk because of cheaper availability and hence the government of Bangladesh should take strong measures to control these banned pesticides. Five organo phosphorus (chlorpyrifos, parathion, ethion, acephate, fenthion) and two carbamate (carbaryl and carbofuran) pesticide residues were identified in twenty four samples of two common vegetables (tomato and brinjal). The pesticide residues ranged from below a detectable limit (< 0.01) to 0.36 mg·kg-1. Acephate, chlorpyrifos, ethion, and carbaryl were detected in only one sample, while co-occurrence occurred twice for parathion. Continuous monitoring and strict regulation should be enforced regarding the control of pesticide residues in fresh vegetables and other food commodities in Bangladesh.

유통 한약재의 잔류농약 및 잔류이산화황의 함량 분석 (The analysis of Residual Pesticides and Sulfur Dioxide in Commercial Medicinal Plants)

  • 김태희;장설;이아름;이아영;최고야;김호경
    • 대한본초학회지
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    • 제27권6호
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    • pp.43-48
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    • 2012
  • Objectives : This study was investigated to determine the contents of pesticide residues and sulfur dioxide residues in commercial herbal medicines in Korea. Methods : Chromatographic test was performed on 100 samples consisted with 10 kinds of medicinal plants including improted and domestic products. To establish 19 pesticide residues (DDE, DDD, DDT, Dieldrin, Methoxychlor, BHC isomers, Aldrin, Endosulfan isomers, Endrin, Captan, Procymidone, Chlorpyrifos and Imidacloprid) in commercial herbal medicines, chromatographic equipments were used with the gas chromatography-mass detector and gas chromatography-electron capture detector for qualitative analysis. The imidacloprid analysis was performed by high performance liquid chromatograpgy-ultraviolet detector at 270 nm UV wavelength. The contents of sulfur dioxides were analyzed by modified Monnier-Williams method. All methods were based on notification procedure of Korea Food & Drug Administration (KFDA). Results : The residual pesticides were not founded in improted and domestic samples. Among 100 samples, the residues of sulfur dioxide in 73 samples were not detected and 25 samples showed contents in the range of 0~21.90 mg/kg. The excess samples of MRLs were 2 samples (30 mg/kg to medicinal herbs), Asiasari Radix et Rhizoma (Imported product) and the average amount of sulfur dioxide in 2 unsuitable samples were 14.83 mg/kg. These samples were found to transgress KFDA regulatory guidance of residual sulfur dioxide. Conclusion : These results are able to use as basic data to improve the reliability and value of commercial medicinal herbs.

QuEChERS 기반 동시분석법을 이용한 국내 유통 축산물 중 Imidacloprid 총잔류량 평가 (Evaluation of Total Residues of Imidacloprid in Livestock Products from Domestic Markets by using a Simultaneous Analytical Method Based on QuEChERS)

  • 이승원;윤지현;김지유;임다정;조형욱;문준관;곽혜민;장희라;김인선
    • 한국환경농학회지
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    • 제42권3호
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    • pp.220-230
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    • 2023
  • Imidacloprid is a neonicotinoid insecticide widely used for insect control in a variety of crops. The evaluation of imidacloprid total residues in animal feeds derived from crop by-products is required to ensure the safety of livestock products. We performed simultaneous LC/MS/MS analyses of imidacloprid and its metabolites in five different livestock products including beef, pork, chicken, milk and egg from domestic markets. The methods for sample preparation and instrumental analysis were established by modifying QuEChERS method to meet the Codex guidelines. The methods generated 0.0035 mg/kg of the limit of determination (LOD), 0.01 mg/kg of the limit of quantitation (LOQ) and standard calibration linearity with >0.983 of the coefficients of determination (R2). The methods exhibited the recovery values of imidacloprid and its metabolites ranging from 65.66 to 119.27% without any interference between matrices. Imidacloprid total residues in the livestock products were found as values lower than the LOQ and maximum residue limits (MRLs). This study suggests that the methods are successfully applicable for the safety evaluation of imidacloprid total residues in livestock products from domestic markets.

쑥갓 및 참나물 중 Lufenuron의 생산단계 잔류허용기준 설정을 위한 잔류 특성 연구 (Residual Characteristics of Lufenuron in Crown Daisy and Chamnamul for Establishing Pre-Harvest Residue Limit)

  • 오아연;반선우;장희라
    • 한국환경농학회지
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    • 제42권1호
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    • pp.21-27
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    • 2023
  • Pre-harvest residue limits (PHRLs) have been proposed as criteria for a proactive role to exceed the maximum residue limit (MRL) of pesticides in agricultural products at harvest. However, PHRL numbers are significantly less than those of established MRLs. This study was performed to determine the dissipation constants and residual concentrations of lufenuron after application on crown daisy and chamnamul under green house conditions. Two residue field trials for each crown daisy and chamnamul were selected to consider a different geographical site at least 20 km far from one another. The pesticide was treated according to critical GAP. After samples were sprayed with lufenuron, they were collected at 0, 1, 3, 5, 7, 10, and 14 days and analyzed using HPLC-DAD. The mean recoveries of crown daisy and chamnamul were within the range of 70-120% with below 20% coefficient variation, which is within the acceptable limits specified by the manual of pre-harvest residue study for pesticides (MFDS, 2014). The biological half-lives in field I and field II were 7.0 and 4.6 days for crown daisy and 2.7 and 2.8 days for chamnamul, respectively. The lower bounds of 95% confidence intervals of dissipation rate constants of lufenuron in crown daisy were determined to be 0.0692 and 0.1298 for field I and field II, respectively, and in chamnamul were 0.2067 for both field I and field II. After applying lufenuron 5% EC, the lufenuron residues on crown daisy and chamnamul at the pre-harvest intervals (14 days for crown daisy and 7 days for chamnamul) were below the safe levels. The dissipation rates of lufenuron in crown daisy and chamnamul were evaluated for similarities with leafy vegetables based on a 95% confidence interval.

곡물류 중 잔류농약 다성분 분석을 위한 개선된 QuEChERS 시료 정제법의 개발 (Multi-residue Pesticide Analysis in Cereal using Modified QuEChERS Samloe Preparation Method)

  • 양인철;홍수명;권혜영;김택겸;김두호
    • 농약과학회지
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    • 제17권4호
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    • pp.314-334
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    • 2013
  • 곡물류 모니터링 시료인 현미, 보리, 옥수수 3가지 작물을 대상으로 보편적으로 많이 사용되고 등록된 농약을 조사, 76종을 선정하여 QuEChERS AOAC Official 2007. 01. 법과 변형된 QuEChERS 법으로 LC-MS/MS를 이용하여 회수율 시험을 비교하였다. 1% acetic acid를 사용하여 추출하는 QuEChERS AOAC Official 2007. 01. 법의 0.05, 0.2 mg/kg 회수율 결과는 현미 32.4~139.0%, 보리 24.2~123.7%, 옥수수 29.0~117.2%였고, 그 중 sulfonylurea 계통인 azimsulfuron, ethoxysulfuron, flucetosulfuron, imazosulfuron에 대해 회수율이 낮게 나오는 문제가 있었으며, 이들 농약의 평균 회수율은 53.3%였다. 이런 문제를 해결하기 위해 QuEChERS 법의 추출용매를 1% formic acid가 함유된 acetonitrile 용매로 바꾼 결과, 0.05, 0.2 mg/kg 수준의 회수율은 현미 73.2~132.2%, 보리 80.9~136.8%, 옥수수 66.6~143.5%였으며 변이계수는 모두 10% 미만이었다. 문제시 되었던 sulfonylurea 계통의 농약의 회수율도 53.3%에서 90.5%로 증가하였다. 검출한계(limits of detection, LOD)와 정량한계(limits of quantification, LOQ)는 현미 0.24~1.92, 0.79~65.74 ng/g, 보리 0.12~21.12, 0.36~63.36 ng/g, 옥수수 0.28~100.8, 0.86~302.4 ng/g이었다. 변형한 QuEChERS 법을 모니터링 시료 현미, 보리, 옥수수에 적용하여 98개 시료를 분석한 결과 36개의 시료에서 26종의 농약이 검출되었다. 검출 농도가 가장 높은 농약은 tricyclazole로 1.17 mg/kg로 조사되었다. 변형한 QuEChERS법으로 전처리를 하여 질량분석기 뿐만 아니라 현재 많이 보급된 검출기인 ECD, NPD 및 UPLC에서도 분석이 가능한지 실험하였고, 현미, 보리, 옥수수의 평균 회수율은 ECD는 65.3~130.3%, NPD는 61.6~133.0%로 대부분의 농약들이 잔류농약 검색용을 목적으로 하는 다성분 분석의 기준인 70~130% 이내의 회수율과 30%의 미만의 변이계수 조건을 만족하였다.

경기 북부 내 직거래 농산물의 잔류농약 실태조사 및 위해성 평가 (Monitoring and Risk Assessment of Pesticide Residues Farmers' Market Produce in Northern Gyeonggi-do)

  • 임정화;박포현;임부건;유경신;강민성;송서현;강남희;유나영;김정은;강충원;김윤호;서정화;최옥경;윤미혜
    • 한국식품위생안전성학회지
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    • 제35권3호
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    • pp.243-251
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    • 2020
  • 경기 북부 내 직거래 매장에서 유통 되는 농산물 207건을 수거하여 잔류농약의 실태를 조사하였다. 로컬푸드와 소비자생활협동조합(생협) 매장을 대상으로 일반농산물 94건, 친환경농산물 113건의 다소비 채소류를 수거하여 다종농약다성분 분석법으로 GC/ECD, GC/NPD, GC-MS/MS, LC/PDA, LC/FLD, LC-MS/MS를 이용하여 263종의 농약을 분석하였다. 잔류농약이 검출된 검체는 모두 로컬푸드 매장에서 수거한 일반 농산물로 14건의(6.8%) 시료에서 잔류농약이 검출되었고, 그 중 1건에서(0.5%) 잔류농약허용기준을 초과하였다. 총 16개 농약성분이 검출되었고 검출된 작물은 시금치, 얼갈이, 깻잎, 아욱, 오이, 부추, 미나리였다. 농약 검출량을 바탕으로 일일섭취추정량(EDI)과 일일섭취허용량(ADI)을 이용하여 위해성 평가를 하였으며, %ADI 값의 범위는 0.0134-61.6259%로 안전한 수준이었다.