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Development of a Simultaneous Analysis Method for DDT (DDD & DDE) in Ginseng  

Kim, Sung-Dan (Pesticides Analysis Team, Kangbuk Agro-Fishery Products Inspection Center Seoul Metropolitan Government Research Institute of Public Health and Environment)
Cho, Tae-Hee (Pesticides Analysis Team, Kangbuk Agro-Fishery Products Inspection Center Seoul Metropolitan Government Research Institute of Public Health and Environment)
Han, Eun-Jung (Pesticides Analysis Team, Kangbuk Agro-Fishery Products Inspection Center Seoul Metropolitan Government Research Institute of Public Health and Environment)
Park, Seoung-Gyu (Pesticides Analysis Team, Kangbuk Agro-Fishery Products Inspection Center Seoul Metropolitan Government Research Institute of Public Health and Environment)
Han, Chang-Ho (Pesticides Analysis Team, Kangbuk Agro-Fishery Products Inspection Center Seoul Metropolitan Government Research Institute of Public Health and Environment)
Jo, Han-Bin (Pesticides Analysis Team, Kangbuk Agro-Fishery Products Inspection Center Seoul Metropolitan Government Research Institute of Public Health and Environment)
Choi, Byung-Hyun (Pesticides Analysis Team, Kangbuk Agro-Fishery Products Inspection Center Seoul Metropolitan Government Research Institute of Public Health and Environment)
Publication Information
Korean Journal of Food Science and Technology / v.40, no.2, 2008 , pp. 123-128 More about this Journal
Abstract
The MRLs (maximum residue limits) of DDT (DDD and DDE) in fresh ginseng, dried ginseng, and steamed red ginseng are set as low as 0.01 mg/kg, 0.05 mg/kg, and 0.05 mg/kg, respectively. Therefore, this study was undertaken to develop a simple and highly sensitive analysis method, as well as to reduce interfering ginseng matrix peaks, for the determination of DDT isomers (o,p'-DDE, p,p'-DDE, o,p'-DDD, p,p'-DDD, o,p'-DDT, and p,p'-DDT) in fresh ginseng, dried ginseng, and steamed red ginseng at the 0.01 mg/kg level. The method used acetonitrile extraction according to simultaneous analysis, followed by normal-phase Florisil solid-phase extraction column clean-up. The purification method entailed the following steps: (1) dissolve the concentrated sample extract in 7 mL hexane; (2) add 3 mL of $H_2SO_4$; (3) vigorously shake on avortex mixer; (4) cetrifuge at 2000 rpm for 5 min; (5) transfer 3.5 mL of the supernatant to the Florisil-SPE (500 mg/6 mL);and (6) elute the SPE column with 1.5 mL of hexane and 10 mL of ether/hexane (6:94). The determination of DDT isomers was carried out by a gas chromatography-electron capture detector (GC-${\mu}$ECD). The hexane and ether/hexane (6:94) eluate significantly removed chromatographic interferences, and the addition of 30% $H_2SO_4$ to the acetonitrile extract effectively reduced many interfering ginseng matrix peaks, to allow for the determination of the DDT isomers at the 0.01 mg/kg level. The recoveries of the 6 fortified (most at 0.01 mg/kg) DDT isomers from fresh ginseng, dried ginseng, and steamed red ginseng ranged from 87.9 to 99.6%. The MDLs (method detection limits) ranged from 0.003 to 0.009 mg/kg. Finally, the application of this method for the determination of DDT isomers is sensitive, rapid, simple, and inexpensive.
Keywords
DDT (DDD & DDE); ginseng; simultaneous analysis;
Citations & Related Records
Times Cited By KSCI : 4  (Citation Analysis)
Times Cited By SCOPUS : 0
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