This study was performed to study the removal efficiency of residual organophosphorus pesticides with process for making Perilla Jangachi. Two organophosphorus pesticides(chlorpyrifos-methyl and fenitrothion) were artificially attached to Perilla leaves. Then Perilla leaves were washed with detergent solution for 1minute and rinsed 2 times each for 1 minutes. After washing with neutral detergent solution, Perilla Jangachi was made with 2 steps of optimal condition. As a pretreatment, when soaked with 2% salt concentration solution for 42hours, the removal rate of residual pesticides was 81.75% of chlorpyrifos-methyl and 76.82% of fenitrothion. When Perilla leaves were steamed for 72 seconds after soaking, it became 88.94% and 82.19%, respectively. Finally, after making optimal Perilla Jangachi with 27% onion contents, removal rate was 89.12% of chlorpyrifos-methyl and 82.76% of fenitrothion. Consequently, it appeared that the process for making Perilla Jangachi effectively removed the residual pesticides of Perilla leaves.

The simultaneous determination of residual pesticides was developed using a gas chromatography. In this study, a simple and reliable methodology was improved to detect 175 kinds of residual pesticides by a liquid-liquid extraction procedure, followed by chromatographic analysis by gas chromatography. The 175 kinds of residual pesticides was classified into 4 groups according to the chemical structure, column type, resolution and sensitivity. The soybean sample selected for recovery experiment was not detected any pesticides. The recovery rates were ranged from 70.6% to 119.7% in most pesticides. The relative standard deviation (RSD 0.3~5.6%) was lower than 5.6% in all cases. The limits of detection (LOD) was lower than the maximum residue levels established by Korean legislations. The method has been successfully applied to the analysis of approximately 130 real samples.

To obtain the risk assessment of hazardous materials in Rehmanniae Radix Preparata, the residual pesticides and heavy metals in samples on the Korea and China are surveyed. Group Ⅰ(BHC-δ, BHC-β, Fenitrothion, Penthoate, Endosulfan-α, Dieldrin, Endosulfan-β and Endosulfan-sulfate), Group Ⅱ(BHC-γ, Aldrin, DDD, DDT-p,p Permethrin and Fenvalerate), Group Ⅲ(BHC-α, Chlorpyrifos, Tolyfluanid, Captan and DDT-o,p) and Group Ⅳ(Quintozene, Vinclozolin, DDE and Chlorfenapyr) could analysed on gas chromatography-ECD for evaluation of residual pesticides. Qualified detection concentration on the GC-ECD are 0.45 ng/g～2.50 ng/g. Group Ⅰ, Group Ⅱ, Group Ⅲ and Group Ⅳ are not detected in Rehmanniae Radix Preparata on the Korea and China. Concentration of As, Cd and Pb in Rehmanniae Radix Preparat. on the Korea are 3.06%, 7.00% and 5.78% for Korea Food & Drug Administration(KFDA). Concentration of As, Cd and Pb in Rehmanniae Radix Preparata. on the China are 5.16%, 5.33% and 6.50% for Korea Food & Drug Administration(KFDA). The hazardous materials in Rehmanniae Radix Preparata on the Korea and China were verified the safety of the residual heavy metals and pesticides compare with Korea Food & Drug Administration (KFDA) advisory level.

양상추(Lactuca Sativa L.)의 정식 후 42일 경과한 결구 초기부터 결구가 형성(정식 후 67일 경과)되어 제품으로 출하될 때까지의 품질 변화와 잔류농약에 대해 알아보았다. 양상추의 정식 후 결구가 형성되면서부터 전체 중량과 가식부 중량이 모두 증가하였는데, 결구 형성 초기에는 전체중량의 약 40% 정도가 가식부였지만 제품 출하 시점에서는 약 80%까지 큰 증가추세를 보였다. PH, 당도, 수분의 경우는 양상추 결구과정 중 약간의 증

The simultaneous analysis of multi-residual pesticides was developed using a gas chromatography (GC) method. In this study, a simple and reliable methodology was improved to detect 154 kinds of pesticides in ginseng extract sample by using a liquid-liquid extraction procedure, open column chromagraphy and chromatographic analysis by GC electron capture detector (ECD) and GC nitrogen-phosphorus detector (NPD). The 154 kinds of pesticides were classified in 4 groups according to the chemical structure. The extraction of pesticides was experimented with 70% acetone and dichloromethane/petroleum ether in order, and cleaned up via open column chromatography (3×30㎝) packed with florisil (30g, 130℃, 12hrs). The final extract was concentrated in a rotator evaporator at 40℃ until dryness. Then the residue was redissolved to 2㎖ with acetone, and analyzed by GC-ECD and GC-NPD. The applied concentration of pesticides was over 1~10㎍/㎖. The recovery tests were ranged from 70.7% to 115.2% with standard deviations between 0.3 and 5.7% of the standard spiked to the ginseng extract sample (Group Ⅰ~Ⅳ). The limit of detection (LOD) ranged from 0.001 to 0.099㎍/㎖ (Group Ⅰ~Ⅳ). The 9 kinds of pesticides were not detected. The developed method was applied satisfactory to the determination of the 154 kinds of pesticides in the ginseng extract with good reproducibility and accuracy.

Pesticides were extracted from samples with 70% acetone and methylene chloride in order, and then cleaned up via open-column chromatography apparatus packed with florisil, and finally analyzed simultaneously the organophosphorus pesticides using GC/NPD. Ultra-2 and Ultra-1 fused silica capillary columns were used to separate and identify the products. Recovery of most analytes from soybean sample, taken from pesticide residues well, was greater than(80%) for all except(6) analytes. This method can simultaneously determine multiple pesticides with a high degree of accuracy and precision.

A method for the simultaneous analysis of 31 residual organic chloride pesticides was studied using gas chromatography. Prepared analytical samples were injected to gas chromatography (HP 5890 Series II plus) on the Ultra-2 column with ECD. The packing materials for column were changed as the following reagents ; florisil and alumina N. The residual solution was loaded to column and was eluted with elution solvents ; ether : benzene (2 : 8) solution, hexane : benzene (1:1) solution, dichloromethane, acetone, and methanol. The analytical results showed that 6 kinds of organic chlorides were not detected when florisil (first condition) was used as the column packing material. The nondetected 6 kinds of organic chlorides in the first analytical condition were detected and the recoveries of thrin-pesticides were increased, in particular, captan and captafol, but the recoveries of benzene hexachloride compounds were decreased when dichloromethane and methanol were added as elution solvents (packing material was florisil as in the first condition). The recoveries of dichlorfluanid, chlorofenvinfos, folpet, and dicofol were increased and that of aldrin was increased, but those of captan and captafol were not good when alumina N was used as the packing material. To detect simultaneously thrin-pesticides, captan, and captafol, florisil and alumina N were used as the packing materials. The elution result showed that captan and captafol were not detected. This was because the column was activated insufficiently. The analytical method was the best (31 kinds of organic chlorides in the residual pesticides were detected sharply and showed high sensitivity) when the column (packing materials were florisil and alumina N, together) was fully activated and the impurities were removed using various elution solvents.