• 제목/요약/키워드: extraction and clean-up methods

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딸기 시설재배지 토양 및 농산물 중 잔류성유기오염물질(POPs)의 잔류량 - 유기염소계 농약 (Persistent Organic Pollutants (POPs) Residues in Greenhouse Soil and Strawberry Organochlorine Pesticides)

  • 임성진;오영탁;조유성;노진호;최근형;양지연;박병준
    • 한국환경농학회지
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    • 제35권1호
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    • pp.6-14
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    • 2016
  • BACKGROUND: Residual organochlorine pesticides (OCPs) are chemical substances that persist in the environment, bioaccumulate through the food web, and pose a risk of causing adverse effect to human health and the environment. They were designated as persistent organic pollutants (POPs) by Stockholm Convention. Greenhouse strawberry is economic crop in agriculture, and its cultivation area and yield has been increased. Therefore, we tried to investigate the POPs residue in greenhouse soil and strawberry.METHODS AND RESULTS: Extraction and clean-up method for the quantitative analysis of OCPs was developed and validated by gas chromatography (GC) with electron capture detector (ECD). The clean-up method was established using the modified quick, easy, cheap, effective, rugged, and safe(QuEChERS) method for OCPs in soil and strawberry. Limit of quantitation (LOQ) and recovery rates of OCPs in greenhouse soil and strawberry were 0.9-6.0 and 0.6-0.9 μg/kg, 74.4-115.6 and 75.6-88.4%, respectively. The precision was reliable sincerelative standard deviation (RSD) percentage (0.5-3.7 and 2.9-5.2%) was below 20, which was the normal percent value. The residue of OCPs in greenhouse soil was analyzed by the developed method, and dieldrin, β-endosulfan and endosulfan sulfate were detected at 1.6-23, 2.2-28.4 and 1.8-118.6 μg/kg, respectively. Those in strawberry were not detected in all samples.CONCLUSION: Dieldrin, β-endosulfan and endosulfan sulfate in a part of investigated greenhouse soil were detected. But those were not detected in investigated greenhouse strawberry. These results showed that the residue in greenhouse soil were lower level than bioaccumulation occurring.

한약재 중 살충제 Endosulfan의 잔류분석을 위한 Macroporous Diatomaceous Earth 컬럼 적용 (Application of Macroporous Diatomaceous Earth Column for Residue Analysis of Insecticide Endosulfan in Herbal Medicines)

  • 황정인;전영환;김효영;김지환;이윤정;박주영;김도훈;김장억
    • 한국환경농학회지
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    • 제30권1호
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    • pp.60-67
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    • 2011
  • 현재 식품의약품안전청에서 고시하고 있는 한약재 중 잔류 농약 분석법에 따라 강활, 박하, 천궁 및 황기 시료 중 endosulfan과 그 분해산물인 endosulfan sulfate를 분석한 결과 많은 간섭물질의 등장과 낮은 회수율 등의 문제점을 확인하였다. 이에 고시된 시험법의 액-액 분배 과정을 대신하여 MDE column을 적용하여 ${\alpha}$-endosulfan 80.3 ~ 93.5%, ${\beta}$-endosulfan 81.0 ~ 100.3%, endosulfan sulfate 80.6 ~ 95.6%의 회수율과 1.1 ~ 3.4%의 변이계수(CV)를 얻었으며 이러한 결과는 잔류농약 분석기준을 만족하였다. MDE column의 사용으로 액-액 분배 과정을 대신하면서 발암가능 물질인 dichloromethane 사용을 배제할 수 있어 분석자의 안전성 향상, 노동력 및 전처리 시간의 절감, 발생되는 폐액 감소, 액-액 분배시 emulsion 현상의 해소, 분석자간의 재현성 양호 등의 이점도 얻을 수 있었다.

PYE [2-(1-pyrenyl)ethyldimethylsilylated silica] Column HPLC and HR-GC-(micro) ECD in the Accurate Determination of Toxic Co-planar PCBs and Polybrominated Diphenyl Ethers (PBDEs)

  • Kannan, Narayanan;Hong, Sang-Hee;Oh, Jae-Ryoung;Yim, Un-Hyuk;Li, Donghao;Shim, Won-Joon
    • Bulletin of the Korean Chemical Society
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    • 제26권4호
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    • pp.529-536
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    • 2005
  • Measurement of toxicologically relevant polychlorinated biphenyl (PCB) congeners such as non-ortho(IUPAC#) 77, 81, 126, 169 and mono-ortho 105, 114, 118, 123, 156, 157, 189 and di-ortho 170, 180 and polybrominated diphenyl ethers (PBDEs) such as 47, 66, 85, 99, 100, 138, 153, 154 in environmental samples become almost mandatory in several countries now. However, most of the available methods involve expensive instrumentations such as HRGC-HRMS or ECNI-LRMS, apart from expensive extraction and clean-up (with large volume of solvents) steps. A method has been devised combining the analytical separation power of PYE [2-(1-pyrenyl)ethyldimethysilylated silica] column HPLC and high-resolution gas chromatographic techniques including micro-electron capture detection (ECD) and two dimensional gas chromatograpy-ECD techniques to determine these eco-toxic substances at parts-per-trillion (ppt) levels. This combination resolves co-elution of congeners that occur in disproportionate ratios (e.g. CB-110 and -77) and allows accurate congener-specific determination of target compounds. This method is cost effective as it requires only hexane, that in small quantities (10 mL) and GC-ECD. The elution and analysis time are optimized to less man hours. This method is effectively utilized in the analysis of co-planar PCBs and PBDEs from archived solvent extracts of samples previously analyzed for pesticides and PCBs. Structure based separation of contaminant classes improves GCECD determination at ppt levels.

Recent Trend of Residual Pesticides in Korean Feed

  • Jeong, Jin Young;Kim, Minseok;Baek, Youl-Chang;Song, Jaeyong;Lee, Seul;Kim, Ki Hyun;Ji, Sang Yun;Lee, Hyun-Jeong;Oh, Young Kyun;Lee, Sung Dae
    • 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.

Distribution of Seven N-Nitrosamines in Food

  • Park, Jong-eun;Seo, Jung-eun;Lee, Jee-yeon;Kwon, Hoonjeong
    • Toxicological Research
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    • 제31권3호
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    • pp.279-288
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    • 2015
  • N-nitrosamines, which are classified as carcinogens by IARC and US EPA, can be easily found in various foods. They are reaction products between nitrogen oxide and secondary amines, but can also be generated during fermentation. Ever since the 1960s, when nitrite, used as a preservative in processed meats, was suspected to generate N-nitrosamines, the usage of the food additive has been debated. However, the benefit of nitrite in food supply could not be ignored and the risk-benefit analysis has become a key issue in the use of the additive. For a risk analysis, an accurate estimation of the hazardous material is necessary; therefore, analytical methods for nitrosamines have continuously evolved from the 1950s. Solid supported liquid-liquid extraction and solid phase extractions have replaced the distillation for the clean-up steps, and tandem mass spectrometry is employed for higher selectivity and sensitivity. In the present study, for a better estimation of N-nitrosamine intake, the total diet study samples were prepared for the N-nitrosamines analysis. In order to obtain the most sensitive results, a partial preparation procedure was developed and modified for different food matrices. Among seven N-nitrosamines (N-nitrosodimethylamine, N-nitrosomethylethylamine, N-nitrosodiethylamine, N-nitrosodibutylamine, N-nitrosopiperidine, N-nitrosopyrrolidine, and N-nitrosomorpholine) analyzed in the present study, N-nitrosodiethylamine has shown the highest detection rate in agricultural foods, while N-nitrosodimethylamine has appeared most frequently in livestock and fishery food products. The concentration of N-nitrosodimethylamine was the highest in seasoning.

육류가공식품의 조리방법에 따른 PAHs 발생 특성에 관한 연구 (Characteristics of PAH Occurrence during Meat Cooking)

  • 이병호;안유진;박동윤;변기영;김경동;이미림;서정범;박은영;박흥재
    • 한국환경과학회지
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    • 제25권11호
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    • pp.1459-1466
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    • 2016
  • In this study, the concentrations of polycyclic aromatic hydrocarbons (PAHs) were investigated in meat process food and for cooking methods (pan-frying and charcoal fire). The methodology involved liquid-liquid extraction, silica gel cartridge clean-up and determination by gas chromatography/mass spectrometry (GC/MS). The recovery of 17 PAHs spiked into these samples ranged from 66.6 % to 98.0% and the coefficient of variation was less than 10%, but that of dibenz(a,h)anthracene was 16.39%. The mean concentration of total PAHs in processed samples was ND~7.2 ng/g, whereas that pan-fried and charcoal-fired samples were ND~22.1 ng/g and, 12.7~367.8 ng/g, respectively. Therefore, the concentrations of total PAHs in cooked samples were higher than in original samples and charcoal-fired samples had the highest total PAH levels.

기체크로마토그래피/동위원소 희석 질량분석법을 이용한 토양 중 폴리브롬화 디페닐에테르의 분석법 (Determination of Polybrominated Diphenyl Ethers(PBDEs) in Soil using Gas Chromatography/Isotope Dilution Mass Spectrometry)

  • 나윤철;장윤석;김해동;홍종기
    • 분석과학
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    • 제17권1호
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    • pp.29-36
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    • 2004
  • 본 연구에서는 토양중에 존재하는 폴리브롬화 디페닐에테르 (polybrominated diphenyl ethers, PBDEs)를 동위원소희석법을 이용한 기체크로마토그래피/질량분석기-선택이온검색법에 의해 검출하는 분석방법을 소개하였다. 토양 중 PBDEs는 속실렛 장치로 추출하고 실리카와 플로리실 흡착제를 이용한 고체상 추출법을 비교하였다. 정제 후 추출물은 기체크로마토그래피/질량분석기-선택이온검색방법으로 분석하였으며, 동위원소로 치환된 4종의 PBDEs를 내부표준물질로 이용한 동위원소 희석법으로 8종의 PBDEs를 정량하였다. 속실렛추출 후 플로리실과 실리카 카트리지를 통한 회수율은 각각 30.8~110.8%, 44.4~110.7%이었다. 이 분석법의 검출한계는 0.04~0.3 ng/g로 나타났다.

해양생물독소 예소톡신: 원인조류와 수산물 오염 (Yessotoxins: Causative Organisms and Seafood Contaminations)

  • 김문기;백승호;홍성진
    • 한국식품위생안전성학회지
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    • 제35권5호
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    • pp.411-418
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    • 2020
  • 본 연구에서는 제외국 관리 해양생물독소인 YTXs의 원인조류, 독화생물, 국내·외 관리현황 및 분석법에 대해 리뷰하였다. 현재까지 YTXs에 의한 국내 수산물 오염이 보고된 사례는 없지만 기후변화로 인한 국내 연안 해역의 아열대화로 독성조류의 국내 유입 가능성이 있을 뿐 아니라 외국의 경우 YTXs에 의한 오염이 빈번하게 발생하고 있기 때문에 해당 국가로부터 수입되는 수산물의 경우 잠재적인 오염가능성이 있어 이에 대한 선제적 대응이 필요하다. YTXs는 와편모조류인 Protecratium reticulatum, Gonyaulax polygramma, Gonyaulax spinifera과 Lingulodinium polyedrum에 의해 생성되는 것으로 알려져 있으며, 이들은 국내 연안에도 출현한다. 현재 패류 내 YTXs는 메탄올 추출, SPE 카트리지 정제 후 LC-MS/MS를 이용하여 분석하고 있다. YTXs, pectenotoxins, azaspiracids와 같은 지용성 패독은 추출 및 정제 등의 전처리 과정이 유사하여 동시분석이 가능할 것으로 보이며, 이에 대한 분석법 최적화가 필요하다. 향후 국내 해역의 YTXs의 원인조류 출현 및 국내 유통(국내산 및 수입산) 수산물의 오염에 대한 지속적인 모니터링이 필요하다.

오비트랩 고분해능 질량분석기를 이용한 폐사 조류 중 다성분 잔류 농약 스크리닝 기법 (Residual Multi Pesticides Screening of Dead Birds by Orbitrap High Resolution Mass Spectrometry)

  • 이두희;김보경;왕승준;손기동;정현미;최종우
    • 한국환경농학회지
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    • 제36권4호
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    • pp.269-278
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    • 2017
  • BACKGROUND: The objective of this study was to evaluate screening method of residual multi pesticides in dead birds by Orbitrap high resolution mass spectrometry (HRMS) to identify the cause of death for birds. METHODS AND RESULTS: Extraction and clean-up method of residual pesticides in liver of dead birds was used QuEChERS (Quick Easy Cheap Effective Rugged and Safe) and method validations was conducted using liquid chromatography and gas chroamtography with triple-quadrupole mass spectrometer (LC/MS/MS and GC/MS/MS) Also, we were evaluated screening method for the determination of residual pesticides in liver of dead birds by LC and GC Orbitrap Mass Spectrometry. Results of method validations, Correlation coefficients of the matrix matched calibration curves were >0.978, and the method detection limits (MDLs) and limits of quantitation (LOQ) were 2.8~72.1 ng/g (18.4 ng/g on average) and 9.0~230 ng/g (58.5 ng/g on average). The accuracy ranged from 69.1%to 130% (103% on average), and the precision values were less than 14.8%(3.8%on average). The screening of residual pesticides in liver of dead birds by LC and GC Orbitrap HRMS was detected monocrotophos, carbofuran, carbosulfan, deltametrin, benfuracarb, carbofuran, phosphamidon, prochloraz in investigated samples. CONCLUSION: This results showed that accurate mass were extraction of residual pesticides in dead birds by Orbitrap HRMS. It suggested that this screening method is applicable to the residual pesticide analysis for the cause of death as a main tool.

농산물 중 살균제 Isopyrazam의 개별 잔류분석법 확립 (Method Development and Validation for Analysis of Isopyrazam Residues in Agricultural Products)

  • 김지윤;김자영;함헌주;도정아;오재호;이영득;허장현
    • 농약과학회지
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    • 제17권2호
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    • pp.84-93
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    • 2013
  • Isopyrazam은 신규 농약으로 현재 국내에는 공정분석법이 확립되어 있지 않아 농산물 중 잔류농약 분석을 위한 개별 분석법 개발이 필요하다. 본 연구는 현미, 대두, 고추, 감귤, 참외, 오이를 대표 농산물로 선정하여 isopyrazam에 대한 공정 개별 분석법을 확립하고자 수행되었다. Isopyrazam의 syn과 anti 이성질체를 분석하기 위해 여러 가지 추출, 분배 및 정제방법을 비교하면서 최적의 조건을 충족해 가며 분석법을 확립하였다. 대표 농산물 시료 중 함유된 isopyrazam은 acetonitrile로 추출한 후 n-hexane으로 액-액 분배하였으며, florisil을 이용하여 정제한 후 HPLC/UVD로 최종 분석하였다. 시료 중 현미와 대두는 n-hexane/acetonitrile을 이용한 유지제거 과정을 추가하였다. 본 분석법의 isopyrazam에 대한 정량한계는 1.0 ng (S/N > 10)이었고, 분석정량한계는 0.04 mg $kg^{-1}$이었다. 회수율은 isopyrazam syn과 anti-isomer에서 각각 81.0~105.4%, 80.8~105.6%이었으며, 반복 간 분석오차는 10% 미만이었다. 분석성분에 대한 확인을 위하여 LC/MS SIM을 이용하였다. 본 연구에서 확립된 isopyrazam의 분석법은 우수한 정량성 및 재현성, 분석과정의 편의성을 고려할 때 농산물 중 잔류농약에 대한 검사 및 안전성 평가를 위한 공정 분석법으로 활용될 수 있을 것으로 사료된다.