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Development of Analytical Method for Detection of Fungicide Validamycin A Residues in Agricultural Products Using LC-MS/MS

LC-MS/MS를 이용한 농산물 중 살균제 Validamycin A의 시험법 개발

  • Park, Ji-Su (Pesticide and Veterinary Drug Residues Division, Food Safety Evaluation Department, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety) ;
  • Do, Jung-Ah (Pesticide and Veterinary Drug Residues Division, Food Safety Evaluation Department, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety) ;
  • Lee, Han Sol (Pesticide and Veterinary Drug Residues Division, Food Safety Evaluation Department, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety) ;
  • Park, Shin-min (Pesticide and Veterinary Drug Residues Division, Food Safety Evaluation Department, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety) ;
  • Cho, Sung Min (Pesticide and Veterinary Drug Residues Division, Food Safety Evaluation Department, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety) ;
  • Shin, Hye-Sun (Pesticide and Veterinary Drug Residues Division, Food Safety Evaluation Department, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety) ;
  • Jang, Dong Eun (Pesticide and Veterinary Drug Residues Division, Food Safety Evaluation Department, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety) ;
  • Cho, Myong-Shik ;
  • Jung, Yong-hyun (Pesticide and Veterinary Drug Residues Division, Food Safety Evaluation Department, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety) ;
  • Lee, Kangbong (Pesticide and Veterinary Drug Residues Division, Food Safety Evaluation Department, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety)
  • 박지수 (식품의약품안전처 식품의약품안전평가원 식품위해평가부 잔류물질과) ;
  • 도정아 (식품의약품안전처 식품의약품안전평가원 식품위해평가부 잔류물질과) ;
  • 이한솔 (식품의약품안전처 식품의약품안전평가원 식품위해평가부 잔류물질과) ;
  • 박신민 (식품의약품안전처 식품의약품안전평가원 식품위해평가부 잔류물질과) ;
  • 조성민 (식품의약품안전처 식품의약품안전평가원 식품위해평가부 잔류물질과) ;
  • 신혜선 (식품의약품안전처 식품의약품안전평가원 식품위해평가부 잔류물질과) ;
  • 장동은 (식품의약품안전처 식품의약품안전평가원 식품위해평가부 잔류물질과) ;
  • 조명식 (광주지방식품의약품안전청 유해물질분석과) ;
  • 정용현 (식품의약품안전처 식품의약품안전평가원 식품위해평가부 잔류물질과) ;
  • 이강봉 (식품의약품안전처 식품의약품안전평가원 식품위해평가부 잔류물질과)
  • Received : 2018.11.15
  • Accepted : 2018.12.25
  • Published : 2019.02.28

Abstract

Validamycin A is an aminoglycoside fungicide produced by Streptomyces hygroscopicus that inhibits trehalase. The purpose of this study was to develop a method for detecting validamycin A in agricultural samples to establish MRL values for use in Korea. The validamycin A residues in samples were extracted using methanol/water (50/50, v/v) and purified with a hydrophilic-lipophilic balance (HLB) cartridges. The analyte was quantified and confirmed by liquid chromatograph-tandem mass spectrometer (LC-MS/MS) in positive ion mode using multiple reaction monitoring (MRM). Matrix-matched calibration curves were linear over the calibration ranges (0.005~0.5 ng) into a blank extract with $R^2$ > 0.99. The limits of detection and quantification were 0.005 and 0.01 mg/kg, respectively. For validation validamycin A, recovery studies were carried out three different concentration levels (LOQ, $LOQ{\times}10$, $LOQ{\times}50$, n = 5) with five replicates at each level. The average recovery range was from 72.5~118.3%, with relative standard deviation (RSD) less than 10.3%. All values were consistent with the criteria ranges requested in the Codex guidelines (CAC/GL 40-1993, 2003) and the NIFDS (National Institute of Food and Drug Safety) guideline (2016). Therefore, the proposed analytical method is accurate, effective and sensitive for validamycin A determination in agricultural commodities.

발리다마이신 에이는 아미노글리코사이드계 항생물질로 이탄당인 균당을 2개의 포도당으로 분해하는 효소(trehalase)의 작용을 저해하여 균 증식을 억제한다. 우리나라에서는 벼, 고추, 복숭아, 마늘, 양파, 참다래 등에 세균성 병해를 방제하기 위해 농약으로 등록되어 있다. 국외의 경우 일본에 잔류허용기준(MRLs)이 감자 포함 43품목에서 0.05-0.06 mg/kg으로 기준이 설정되어 있고, 유럽은 0.01 mg/kg 일률 기준을 적용하고 있으며 국내의 경우 기준이 설정될 예정이다. 축산물의 경우 잔류물의 정의를 설정하고 있지 않으나 농산물의 경우 잔류물의 정의는 일본에서 모화합물로 설정되어 있으며 국내에서도 모화합물로 규정할 예정이다. 따라서 발리다마이신 에이의 잔류허용기준 신설에 따른 안전관리를 위하여 공정시험법을 개발하였다. 분석기기는 발리다마이신 에이의 물리 화학적 특성을 고려하여 선택성과 감도가 우수한 LC-MS/MS를 분석기기로 선정하였고 메탄올/물(50/50, v/v)을 이용하여 진탕 추출 후 HLB 카트리지를 이용한 정제 조건을 확립하여 시험법을 개발하였다. 발리다마이신 에이의 직선성은 결정계수($r^2$)가 0.99이상으로 우수하였으며, 검출한계 및 정량한계는 각각 0.005, 0.01 mg/kg으로 높은 감도를 나타내었다. 대표 농산물 5종(현미, 감자, 대두, 감귤, 고추)에 대하여 정량한계, 정량한계 10배, 정량한계 50배 수준으로 회수율 실험한 결과 평균 회수율(5반복)은 72.5-118.3%이었으며 분석오차는 10.3% 이하로 정확성 및 재현성이 우수함을 확인할 수 있었다. 검증 결과 각 농도별 발리다마이신 에이의 평균 회수율은 70.9~117.7%이었고, 상대표준편차(RSD)는 7.9% 이하로 조사되었다. 두 실험실간 회수율 결과에 따른 평균값은 75.9~112.7%이며 RSD는 18%미만으로 본 연구는 국제식품규격위원회 가이드라인(Codex Alimentarius Commission, CAC/GL 40)의 잔류농약 분석기준 및 식품의약품안전평가원의 '식품등 시험법 마련 표준절차에 관한 가이드라인(2016)'에 적합한 수준임을 검증하였다. 따라서 본 연구에서 개발한 시험법은 농산물 중 발리다마이신 에이의 잔류검사를 위한 공정시험법으로 활용할 수 있으며 유사 농산물에 대한 적용도 가능하리라 판단되어 향후 국내 농산물 중 농약의 잔류허용기준 신설 및 잔류농약 검사의 기초자료로 활용 가능할 것이다.

Keywords

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