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Analysis of malachite green and leuco-malachite green in sea food

수산식품 중 말라카이트그린 및 류코말라카이트그린의 분석

  • Choi, Dongmi (Center for Food Evaluation, Korea Food & Drug Administration) ;
  • Hong, Soongun (Center for Food Evaluation, Korea Food & Drug Administration) ;
  • Im, Moohyeog (Center for Food Evaluation, Korea Food & Drug Administration) ;
  • Jeong, Jiyoon (Center for Food Evaluation, Korea Food & Drug Administration) ;
  • Chang, Moonik (Center for Food Evaluation, Korea Food & Drug Administration) ;
  • Park, Kunsang (Center for Food Evaluation, Korea Food & Drug Administration) ;
  • Hong, Mooki (Center for Food Evaluation, Korea Food & Drug Administration) ;
  • Woo, Gunjo (Center for Food Evaluation, Korea Food & Drug Administration)
  • 최동미 (식품의약품안전청, 식품평가부) ;
  • 홍순근 (식품의약품안전청, 식품평가부) ;
  • 임무혁 (식품의약품안전청, 식품평가부) ;
  • 정지윤 (식품의약품안전청, 식품평가부) ;
  • 장문익 (식품의약품안전청, 식품평가부) ;
  • 박건상 (식품의약품안전청, 식품평가부) ;
  • 홍무기 (식품의약품안전청, 식품평가부) ;
  • 우건조 (식품의약품안전청, 식품평가부)
  • Received : 2005.01.06
  • Accepted : 2006.02.13
  • Published : 2006.04.27

Abstract

To determine malachite green and leuco-malachite green residues in sea food, a liquid chromatographic method has been optimized. The target compounds were extracted in the homogenized edible tissues with a mixture of McIlvaine buffer-acetonitrile and partitioned against dichloromethane. After concentrating the lower layer, the resulting residues were re-dissolved in methanol and analyzed by the HPLC with visible detector at 620 nm using acetonitrile-acetate buffer. For the analysis of leuco-malachite green with malachite green simultaneously, post-column packed with lead(IV) oxide was used for oxidizing leuco-malachite green to malachite green. The correlation coefficients($r^2$) was 0.9989 for malachite green, and 0.9995 for leuco-malachite green. The limit of detection was 0.005 mg/kg for the combined of malachite green and leuco-malachite green at signal/noise${\geq}3$. The recovery rate was within a reliable range of 84~98% (CV 3~16%). Leuco-malachite green were detected in carp and crusian carp.

고속액체크로마토그라피를 이용하여 어류 중 말라카이트그린 및 류코말라카이트그린의 최적 분석조건을 확립하고 국내유통 수산식품을 분석하였다. 균질화한 시료를 아세토니트릴로 추출하고 디클로로메탄에 분산시켜 농축 후 메탄올에 용해하여 분석하였다. 이동상으로는 아세토니트릴과 아세테이트 완충용액의 혼합용액을 사용하였으며, 검출파장은 620 nm이었다. 류코말라카이트그린을 말라카이트그린과 동시에 분석하기 위하여 산화납(IV) 컬럼을 분석컬럼 뒤에 연결하여 류코말라카이트그린을 말라카이트그린으로 산화하였다. 상관계수($r^2$)는 말라카이트그린이 0.9989, 류코말라카이트그린이 0.9995이었으며, 검출한계는 신호대 잡음비 3 이상에서 말라카이트그린과 류코말라카이트그린의 합으로서 0.005 mg/kg이었다. 회수율은 84~98%(CV는 3~16%)로 만족할 만한 수준이었다. 분석결과 잉어 및 붕어 서료에서 류코말라카이트그린이 검출되었다.

Keywords

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