• KOREAN POULTRY JOURNAL
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• v.38 no.3 s.437
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• pp.118-120
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• 2006

정부에서는 축산물의 안전성 확보를 위하여 축산물가공처리법 및 식육중잔류물질 검사요령에 의거하여 항생물질 등 유해잔류물질이 들어있는 육류의 생산, 유통을 방지하기 위해 1991년에 국가잔류검사프로그램을 도입하여 식육에 대한 잔류물질 검사를 실시해 오고 있다. 서울시 보건환경연구원을 비롯한 전국 16개 시ㆍ도 축산물위생검사기관에서 년간 약 10만건 이상의 가축에 의하여 잔류물질 검사를 실시하고 있다.

• Proceeding of EDISON Challenge
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• 2016.03a
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• pp.576-581
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• 2016

해양환경에서 큰문제가 되고 있는 아주 작은 크기의 플라스틱 입자인 미세플라스틱(Microplastic)은 잔류성이 크고 생물축적성이 있는 잔류성 유기오염 물질(POP)을 잘흡착하여 해양환경과 먹이사슬에 지대한 피해를 끼친다. 본 연구에서는 해양에 존재하는 대표적인 미세플라스틱 uPVC와 입자상의 잔류성 유기오염 물질 PAH를 원형 실린더로 가정하여 해양 환경에서 침강하고 있는 미세플라스틱이 잔류성 유기오염 물질에 의해 오염될 가능성을 알아보았다 이를 위해 표층및 심층수 환경에서 반지름에 따른 충돌효율과 접촉 시간을 구하여 두 실린더가 접촉할 시간의 기댓값인 기대 접촉시간을 계산하였다.

• Proceedings of the Korea Air Pollution Research Association Conference
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• 2003.11a
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• pp.291-292
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• 2003

잔류성 유기오염물질(POPs; Persistent Organic Pollutants)은 환경 내에서 분해가 느려 잔류성이 높고, 생체 지질에 축적되는 독성이 강한 특성이 있다. 따라서 스톡홀름 협약(2001년 5월 23일)에서 12종의 POPs 물질에 대해 국제적 사용금지 및 관리가 결정되었다. POPs는 대부분 반휘발성(semi-volatile) 이어서 대기 중 장거리 이동되어 배출지와 다른 곳에 침적되는 것이 보고되어있다. 이러한 물질들의 대기 중 잔류량과 기체상과 입자상의 분포 특성을 살펴서 환경 내 이동성을 파악하는 것은 인체위해성 수준을 알아내는데 중요한 자료이다. (중략)

• Journal of Korean Society of Environmental Engineers
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• v.33 no.6
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• pp.453-479
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• 2011

Residual pharmaceutical compounds have been recognized as emerging environmental pollutants and are widely distributed all over the world. These compounds cause bioaccumulation and biomagnification during present for a long time in the environment: thereby after adversely biota and human bodies. It is difficult to remove residual pharmaceutical compounds using conventional water/wastewater treatment because of resistant property to photodegradation, biodegradation and chemical decomposition. Moreover, domestic literature data on the pollution of residual pharmaceutical compounds in rivers and lakes are limited. In this paper, species, sources, fate and risk of residual pharmaceutical compounds as well as behavior properties in freshwater resources are demonstrated to encourage the domestic concern about residual pharmaceutical compounds. An extensive review of existing data in the form of figures and tables, encompassing many therapeutic classes are presented.

• Journal of the korean veterinary medical association
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• v.29 no.3
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• pp.165-167
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• 1993

1. FDA와 FSIS는 제약회사에서 설정한 잔류 검사 방법의 유효성과 실용성에 대하여 합의한다. 2. FSIS는 식용동물에서 약물이나 살충제, 환경오염물질의 잔류를 조사한다. 3. FSIS에서 불법적인 약물잔류를 발견하면 FDA와 가축생산자 그리고 적절한 주정부기관에 통보한다. 4. FDA나 적절한 주 정부기관은 의심되는 생산자의 현장조사를 할 수도 있다. 만약 중대한 법률의 위반이 발견되거나 불법적인 잔류가 반복된 경우 생산자에게 벌금형이 부과될 수도 있다. 5. 유죄로 판결된 동물약품남용자는 죄과에 따라 벌금형이나 징역형을 받을 수 있다. 6. 출고 보류된 가축에서 불법적인 잔류가 발견되면 FSIS에 의해 폐기되며 이러한 가축의 생산자는 그들이 생산하는 가축이 잔류허용한계에 적합하다는 것이 증명될 때까지 출하를 금지 당할 수 있다.

• Journal of Food Hygiene and Safety
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• v.34 no.1
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• pp.13-21
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• 2019

A method was developed for the simultaneous detection of an antibiotic fungicide, streptomycin, and its metabolite (dihydrostreptomycin) in agricultural products using liquid chromatography-tandem mass spectrometry (LC-MS/MS). The samples were extracted using methanol adjusted to pH 3 using formic acid, and purified with a HLB (Hydrophilic lipophilic balance) cartridge. The matrix-matched calibration curves were constructed using seven concentration levels, from 0.001 to 0.1 mg/kg, and linearity of five agricultural products (hulled rice, potato, soybean, mandarin, green pepper), with coefficients of determination $(R^2){\geq}0.9906$, for streptomycin and dihydrostreptomycin. The mean recoveries at three fortification levels (LOQ, $LOQ{\times}10$, $LOQ{\times}50$, n = 5) were from 72.0~116.5% and from 72.1~116.0%, and relative standard deviations were less than 12.3% and 12.5%, respectively. The limits of quantification (LOQ) were 0.01 mg/kg, which are satisfactory for quantification levels corresponding with the Positive List System. All optimized results satisfied the criteria ranges requested in the Codex guidelines and the Food Safety Evaluation Department guidelines. The present study could serve as a reference for the establishment of maximum residue limits and be used as basic data for detection of streptomycin and dihydrostreptomycin in food.

• Monthly Korean Chicken
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• v.3 no.1 s.19
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• pp.2-8
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• 1997

도계장 소송용기 세척, 소독시설 지원사업 추진 - 닭고기 외식브랜드 해외진출 활발 - 닭고기 가격조사 발표 - 인도, 닭고기소비 급신장 최근 3년 $35{\%}$늘어 - 식품위해요소 중점관리제 도입 - 연말 닭고기 랜더링처리 - 배합료 영세율 법인은 제외 - 자외선 이용 종란 살모넬라 제거 - 지난해 1인당 육류소비량 29Kg 국내산육류 유해성 잔류물질 검사 - 계열주체, 96년에 $68{\%}$ 계약생산 - 육류중 유해성 잔류물질 공동조사

• Journal of Food Hygiene and Safety
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• v.34 no.3
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• pp.235-241
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• 2019

An analytical method was developed for the determination of an antibiotic fungicide, kasugamycin, in agricultural products (hulled rice, potato, soybean, mandarin and green pepper) using liquid chromatographytandem mass spectrometry (LC-MS/MS). Samples were extracted with methanol adjusted to pH 13 using 1 N sodium hydroxide, and purified with a HLB (hydrophilic lipophilic balance) cartridge. Linearity of a matrix-matched calibration curve using seven concentration levels, from 0.001 to 0.1 mg/kg, was excellent with a correlation coefficient ($R^2$) of more than 0.9998. The limits of detection (LOD) and quantification (LOQ) of instrument were 0.0005 and $0.001{\mu}g/mL$, respectively, and the LOQ of analytical method calculated as 0.01 mg/kg. The average recoveries at three spiking levels (LOQ, $LOQ{\times}10$, $LOQ{\times}50$, n=5) were in the range of 71.2~95.4% with relative standard deviation of less than 12.1%. The developed method was simple and all optimized results was satisfied with the criteria ranges requested in the Codex guidelines and Food Safety Evaluation Department guidelines. The present study could be served as a reference for the establishment of maximum residue limits (MRL) of kasugamycin and be used as basic data for safety management relative to kasugamycin residues in imported and domestic agricultural products.

• Journal of Food Hygiene and Safety
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• v.34 no.1
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• pp.30-39
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• 2019

An analytical method was developed for the determination of sedaxane in agricultural products using liquid chromatograph-tandem mass spectrometry (LC-MS/MS). The samples were extracted with acetonitrile and partitioned with dichloromethane to remove the interference, and then purified by using silica SPE cartridges to clean up. The analytes were quantified and confirmed by using LC-MS/MS in positive ion mode using multiple reaction monitoring (MRM). The matrix-matched calibration curves were linear over the calibration ranges ($0.001-0.25{\mu}g/mL$) into a blank extract with $r^2$>0.99. For validation, recovery tests were carried out at three different concentration levels (LOQ, 10LOQ, and 50LOQ, n=5) with five replicates performed at each level. The recoveries were ranged between 74.5 to 100.8% with relative standard deviations (RSDs) of less than 12.1% for all analytes. All values were consistent with the criteria ranges requested in the Codex guidelines (CAC/GL 40, 2003) and Food Safety Evaluation Department guidelines (2016). The proposed analytical method was accurate, effective and sensitive for sedaxane determination in agricultural commodities.

• Journal of the Korean Chemical Society
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• v.46 no.4
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• pp.317-323
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• 2002

The composition of trace materials in domestic circulated LPG are determined. The sampling points are two cylinders of LPG cylinder re-inspection center, six vaporizer of LPG-supplying group facilities, and the compressed oil from one LPG station. In the trace materials from cylinder of LPG cylinder-reinspection center, alkene and diene derivative (No. of carbon ${\leq}9),$ aromatic compounds, and tarry chemicals(No. of carbon ${\geq}10)$ are 1.5~39.9%, 0.7%, 57.8~96.0%, respectively. While in the trace materials from LPG-supplying group facilities and in the oil from LPG station, tarry chemicals(No. of carbon>10) exceed 96.6%. Nine samples are classified into three clusters. One cluster is the sample of SE company cylinder-reinspection center(Euclidian distance between S company LPG cylinder-reinspection center and SE company cylinder-reinspection center=2.11), the other is the sample of SE company LPG cylinder-reinspection center(Euclidian distance between from samples of LPG-supplying group facilities including compressed oil from LPG station=0.110) the third is the samples of LPG-supplying group facilities(Euclidian distances among them<0.075). The compositions of samples from LPG-supplying group facilities are similar to those of oil from LPG station. Furthermore densities of samples from LPG-supplying group facilities and compressed oil in LPG station are 0.873, 0.873 [0.00798 (99% confidence limits) respectively. It was presumed that tarry chemicals had been leached from the compressed oil of LPG supplying facilities.