본 연구에서는 농산물 시료 중 GC-ECD/MS 분석법을 이용 하여 국내에서 사용금지된 잔류성 유기염소계 살충제 19종 (aldrin, α-BHC, β-BHC, γ-BHC, δ-BHC, cis-chlordane, trans-chlordane, p,p'-DDT, o,p'-DDT, p,p'-DDE, p,p'-DDD, dieldrin, endrin, δ-keto-endrin, heptachlor, heptachlor epoxide, α-endosulfan, β-endosulfan 및 endosulfan sulfate)에 대해 동시분석법을 확립하였다. 농산물 시료에 acetone을 가하여 추출된 대상농약 19종의 잔류분은 n-hexane 분배법과 florisil 흡착 크로마토그래피법으로 정제하여 분석대상 시료로 하였다. DB- 5 capillary column을 이용한 GC-ECD 분석 시 불순물의 간섭은 없었으며, 사과, 고추, 배추, 현미 및 콩을 포함한 5종의 대표 농산물 중 대상농약 19종 각각의 정량한계(LOQ)는 각 0.003~0.01 mg/kg 수준이었다. 5종의 대표 농산물에 대한 대상농약 전체의 회수율은 76.5~116.0%를 나타내었으며, 농산물 시료 및 처리수준에 관계없이 10% 미만의 분석오차를 나타내어 잔류분석기준 이내를 만족하였다. 본 연구에서 확립된 국내 사용금지 잔류성 유기염소계 살충제 19종의 동시분석법은 검출한계, 회수율 및 분석오차 면에서 국제적 분석기준을 만족할 뿐만 아니라, GC/MS SIM을 이용한 잔류분의 재확인 과정의 결과를 종합해 볼 때 분석과정의 편이성 및 신뢰성이 확보된 동시분석법으로 국내·외 수출입 및 유통 농산물의 잔류농약 검사에 사용 가능할 것이다.

This experiment was conducted to establish a simultaneous analytical method for 19 kinds of organochlorine insecticides (aldrin, α-BHC, β-BHC, γ-BHC, δ-BHC, cis-chlordane, transchlordane, p,p'-DDT, o,p'-DDT, p,p'-DDE, p,p'-DDD, dieldrin, endrin, δ-keto-endrin, heptachlor, heptachlor epoxide, α-endosulfan, β-endosulfan, and endosulfan sulfate) forbidden in Korea using GC-ECD/MS. These insecticide residues were extracted with acetone from representative samples of five raw products which comprised hulled rice, soybean, apple, green pepper, and Chinese cabbage. The extract was diluted with large volume of saline water and directly partitioned into n-hexane to remove polar co-extractives in the aqueous phase. For the hulled rice and soybean samples, n-hexane/acetonitrile partition was additionally employed to remove non-polar lipids. The extract was finally purified by optimized florisil column chromatography. The analytes were quantitated by GLC-ECD/MS, using a DB-5 capillary column. The crops were fortified with each insecticide at 3 levels per crop. Mean recovery ratio were ranged from 76.5% to 116.0% in five representative agricultural commodities. The coefficients of variation were all less than 10%, irrespective of sample types and fortification levels. Quantitative limits of 19 kinds of organochlorine insecticides were ranged 0.003~0.01 mg/kg in crop samples. A GC-ECD/MS with selected-ion monitoring method was also provided to confirm the suspected residues. The proposed simultaneous analysis method was reproducible and sensitive enough to determine the residues of 19 kinds of organochlorine insecticides forbidden in Korea.

ABSTRACT
 서 언
 재료 및 방법
  시약 및 기구
  농산물 시료
  GC-ECD/MS 기기분석 조건
  표준검량선 및 분석정량한계(Limit of quantitation, LOQ)
  시료 추출 및 분배
  Florisil 흡착크로마토그래피
  대표 농산물에 대한 잔류성 유기염소계 농약 19종의 회수율 검정
 결과 및 고찰
  GC-ECD 분석조건의 확립
  시료 추출 및 분배과정의 확립
  Florisil 흡착 크로마토그래피 정제조건의 최적화
  4. 농산물 시료 중 잔류성 유기염소계 농약 19종의 분석정량한계 및 회수율
  GC/MS를 이용한 잔류분의 재확인
 적 요
 REFERENCES

• 정명근(강원대학교 생약자원개발학과) | Myoung-Gun Choung (Department of Herbal Medicine Resource, Kangwon National University) Corresponding author