수출입 농산물의 잔류농약 검사를 위한 유기인계 농약 8종의 동시 분석 (Simultaneous Analysis of Eight Kinds of Organophosphorus Pesticides for Inspection of Residual Pesticides in Import-Export Agricultural Products)

서지정보

· 발행기관 : 한국국제농업개발학회
· 수록지 정보 : 한국국제농업개발학회지 / 31권 / 2호 / 150 ~ 163페이지
· 저자명 : 정명근

초록

본 연구에서는 농산물 시료 중 GC-NPD/MS 분석법을 이용하여 물리화학적 특성이 유사한 유기인계 살충제 chlorpyrifosmethyl, mecarbam, parathion-methyl, phenthoate, prothiofos, tebupirimfos, 유기인계 살균제 iprobenfos 및 유기인계 제초제anilofos를 포함하는 8종의 유기인계 농약에 대해 동시 분석법을 확립하였다. 농산물 시료에 acetone을 가하여 추출된 대상농약 8종의 잔류분은 n-hexane 분배법과 florisil 흡착 크로마토그래피법으로 정제하여 분석대상 시료로 하였다. DB-17 capillary column을 이용한 GC-NPD 분석 시 불순물의 간섭은 없었으며, 감귤, 고추, 배추, 현미 및 콩을 포함한 5종의대표 농산물 중 대상농약 8종 각각의 정량한계(LOQ)는tebupirimfos, chlorpyrifos-methyl 및 parathion-methyl은 0.004 mg/kg, 그 외 iprobenfos, mecarbam, prothiofos, phenthoate 및 anilofos는 0.008 mg/kg이었다. 5종의 대표 농산물에 대한 대상농약 전체의 회수율은 80.5~105.0%를 나타내었으며, 농산물 시료 및 처리수준에 관계없이 10% 미만의 분석오차를 나타내어 잔류분석기준 이내를 만족하였다. 본 연구에서확립된 유기인계 농약 8종(anilofos, chlorpyrifos-methyl, iprobenfos, mecarbam, parathion-methyl, phenthoate, prothiofos 및 tebupirimfos)의 동시 분석법은 검출한계, 회수율 및 분석오차 면에서 국제적 분석기준을 만족할 뿐만 아니라, GC/ MS SIM을 이용한 잔류분의 재확인 과정의 결과를 종합해볼 때 분석과정의 편이성 및 신뢰성이 확보된 계열별 동시분석법으로 국내·외 수출입 농산물 잔류농약 검사에 사용 가능할 것이다.

영어초록

This experiment was conducted to establish a simultaneous analytical method for 8 kinds of organophosphorus pesticides of 3 different purposes with similar physicochemical characteristics as insecticide(chlorpyrifos-methyl, mecarbam, parathion- methyl, phenthoate, prothiofos and tebupirimfos), fungicide(iprobenfos), and herbicide (anilofos) in crops using GC-NPD/MS. All the pesticides residues were extracted with acetone from representative samples of five raw products which comprised mandarin, green pepper, kimchi cabbage, hulled rice and soybean. 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 separated and quantitated by GLC with NPD using a DB-17 capillary column. Accuracy and precision of the proposed method was validated by the recovery experiment on every crop samples fortified with anilofos, chlorpyrifos-methyl, iprobenfos, mecarbam, parathion-methyl, phenthoate, prothiofos and tebupirimfos at 3 concentration levels per crop in each triplication. Mean recoveries ranged from 80.5 to 105.0% in five representative agricultural commodities. The coefficients of variation were all less than 10%, irrespective of sample types and fortification levels. Limit of quantitation(LOQ) of the analytes were 0.004(tebupirimfos, chlorpyrifos-methyl and parathion-methyl) and 0.008(iprobenfos, mecarbam, prothiofos, phenthoate and anilofos) mg/kg as verified by the recovery experiment. A confirmatory technique using GC/MS with selected-ion monitoring was also provided to clearly identify the suspected residues. Therefore, this analytical method was reproducible and sensitive enough to determine the residues of anilofos, chlorpyrifos-methyl, iprobenfos, mecarbam, parathion-methyl, phenthoate, prothiofos, and tebupirimfos in import-export agricultural products.

참고자료

· 없음