天然产物研究与开发
天然產物研究與開髮
천연산물연구여개발
NATURAL PRODUCT RESEARCH AND DEVELOPMENT
2009年
2期
267-270,295
,共5页
曹丽华%藏利国%张金娥%崔官伟%唐波
曹麗華%藏利國%張金娥%崔官偉%唐波
조려화%장리국%장금아%최관위%당파
有机磷农药%残留%银杏叶%气相色谱-质谱
有機燐農藥%殘留%銀杏葉%氣相色譜-質譜
유궤린농약%잔류%은행협%기상색보-질보
organophosphorus pesticide%multiresidue%Ginkgo biloba%gas chromatography-mass spectrometry
采用振荡离心法提取、柱层析法净化技术,成功建立了气相色谱-质谱法同时测定银杏叶中五种有机磷农药残留量的方法.结果表明,采用程序升温,所测定的五种有机磷农药在HP-5MS柱上得到了很好的分离,且方法简单、快速、灵敏,完全符合实际需要.方法回收率在88.8%~102%之间,相对标准偏差为1.6%~4.7%,最低定量检出浓度在0.01~0.05 mg/kg之间.
採用振盪離心法提取、柱層析法淨化技術,成功建立瞭氣相色譜-質譜法同時測定銀杏葉中五種有機燐農藥殘留量的方法.結果錶明,採用程序升溫,所測定的五種有機燐農藥在HP-5MS柱上得到瞭很好的分離,且方法簡單、快速、靈敏,完全符閤實際需要.方法迴收率在88.8%~102%之間,相對標準偏差為1.6%~4.7%,最低定量檢齣濃度在0.01~0.05 mg/kg之間.
채용진탕리심법제취、주층석법정화기술,성공건립료기상색보-질보법동시측정은행협중오충유궤린농약잔류량적방법.결과표명,채용정서승온,소측정적오충유궤린농약재HP-5MS주상득도료흔호적분리,차방법간단、쾌속、령민,완전부합실제수요.방법회수솔재88.8%~102%지간,상대표준편차위1.6%~4.7%,최저정량검출농도재0.01~0.05 mg/kg지간.
A simple and rapid method based on gas chromatography-mass spectrometry (GC-MS) for simultaneous determination of pesticides' multiresidues in Ginkgo biloba leaves is developed.It shows that the organophosphorus pesticides are separated well on a HP-5MS column by the optimized temperature program.The recovery for fortified sample is between 88.8% and 102%,with the relative standard deviation (RSD) from 1.6% to 4.7%,and the concentration limit of detection is in the range of 0.01 -0.05 mg/kg.