• 한국환경농학회지
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• 제37권3호
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• pp.213-220
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• 2018

BACKGROUND: This study was carried out to determine characteristics of residual pesticides in time-dependent manner and calculate half-lives of the residual pesticides in fresh and dried Chinese matrimony vine. In addition, processing factors were calculated based on the residual concentrations in them. METHODS AND RESULTS: The test pesticides, etofenprox and fenitrothion, were sprayed onto the Chinese matrimony vine plants at once or twice (at seven-day interval) and then samples were collected at 0 (after 3 hours), 1, 3, 5 and 7 days after the last spraying. Dried samples were prepared in hot-air drying oven at $60^{\circ}C$ for 48 hours until water content of less than 20%. Residual concentrations of etofenprox in fresh and dried samples decreased by 54.0-60.9% after 7 days of the last pesticide-application. In case of fenitrothion, the concentrations were found to have decreased by 69.2-76.5%. Processing factors of etofenprox were 2.6-3.0 for the one-time spraying and 2.5-3.0 for the two-time spraying and those of fenitrothion were found to be 1.5-22 for the one-time spraying and 1.6-2.0 for the two-time spraying. First half-lives of etofenprox and fenitrothion in fresh and dried samples ranged from 5.0 to 6.3 and from 3.4 to 4.0 days, respectively. The third half-lives were found to be 15.0-18.9 and 10.2-12.1 days, respectively. CONCLUSION: Residual concentrations of the tested pesticides in the studied crop decreased, but those in the dried samples appeared to have increased. In addition, processing factor and half life were constant regardless of spraying times.

• Biomolecules & Therapeutics
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• 제8권2호
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• pp.171-178
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• 2000

To evaluate the pharmacokinetic properties and tissue distribution of a newly developed recombinant human erythropoietin (GC-rhEPO), we analyzed the plasma and tissue levels of erythropoietin by an ELISA after intravenous (IV) and subcutaneous (SC) adminstration to the male rats at the doses of 20, 100, 500 or 2,500 unit/kg. After single IV bolus injection of GC-rhEPO, the plasma concentration was rapidly increased and decreased with two phases with half-lives of 13.4 min and 2.94 hours. AUC was increased dose- dependently but plasma half-lives remained constant regardless of GC-rhEPO doses. Following SC administration, the plasma concentration increased slowly with half-life of 9.2 hours and reached peak at 8 hours. Mean residence time and bioavailability were 18.2 hours and 44%, respectively. After single IV dose of 100 unit/kg, tissue GC-rhEPO level was higher in bone marrow and spleen, while the depletion rate was slower in liver and bone marrow, indicating the higher affinity of GC-rhEPO to bone marrow. Taken together, the experimental results indicate that GC-rhEPO contained the typical pharmacokinetic properties and the tissue distribution patterns inherent to human erythropoietin.

• 약학회지
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• 제15권2호
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• pp.41-52
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• 1971

Cu(II) chelates of several sulfanilamide derivatives (Sulfa-Cu) were prepared and their effects on solubility, absorptivity in intestinal lumen, biding tendency with serum protein and erythrocytes, concentration in rabbit blood, and acetylation rate were studied in comparison with their free ligand forms. For solubility concerned, the partition coefficients of Sulfa-Cu are decreased as following order: Sulfadimethoxine Copper chelate (SDM-Cu), Sulfamethoxypyridazine Copper chelate (SD-Cu), Sulfamerazine Copper chelate (SM-Cu), Sulfaisoxazole Copper chelate (SIX-Cu). The partition coefficients of SDM-Cu and ST-Cu were much greater than those of ligands. this phenomenone acounts for the rapid absorption of SDM-Cu and ST-Cu in the rat small intestine (in situ). The Sulfa-Cu were absorbed at the intestinal lumen of a rat in the rate of first order and there was no difference between long acting sulfa drugs and their Cu0chelates in biological half lives. In binding experiments, sulfa-Cu binded with serum protein in lower ratio than their ligands except SIX-Cu. On other hand, acetylation rates of sulfa-Cu were higher than those of free sulfa drugs and the acetylation rate were higher than those of free sulfa drugs and powder. In a experiment on Sulfa-Cu concentration in rabbit blood, the half lives of SD-Cu, SIX-cu, ST-Cu, and SM-Cu were longer than those of their ligands. Above all, the half life of SD-Cu appeared to be approximately 3.5 times logner than that of corresponding ligand, SD. When absorption of sulfa drugs or sulfa-Cu at the small intestinal lumen of a rat and the concentration in rabbit blood after absorption were compared, it was found that there was not always conrrelated.

• 농약과학회지
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• 제9권3호
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• pp.231-236
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• 2005

본 연구는 생산단계의 딸기에 4가지 살균제(tolclofos-m, folpet, procymidone, triflumizole)를 수확 10일전 안전사용 기준량으로 처리한 후 잔류량을 파악하였고, 이것을 근거로 6 가지 kinetic models(first order, zero order, second order, power function model, elovich model, parabolic model)에 따른 반감기를 비교하였다. 최적의 모델로 판명된 first order kinetic model로부터 구한 반감기를 이용하여 생산단계잔류허용기준(field tolerance)을 설정, 제시하였다. 잔류분석법의 적합성 판단을 위한 회수율 실험에서는 $85.1{\sim}105.0%$ 범위를 보였으며, 4 가지 약제 모두 약제 처리 5일 후 평균 73% 이상 소실되었다. 잔류량과 시간과의 상관관계는 first order kinetic model에서 가장 높은 결정계수값을 보였으며, 이를 이용하여 산출한 반감기로 생산단계 잔류허용기준(안)을 설정하였다. 이와 같은 결과는 최적의 kinetic model로 반감기를 산출해야 한다는 이론적 근거를 제시하는 것이며, 수확 후 또는 유통 중의 잔류허용기준뿐만 아니라 생산단계에서도 허용기준을 마련하여 부적합 품목을 사전에 차단할 수 있는 기준설정의 예로서 안전 농산물 공급과 농가소득에 크게 기여할 수 있는 기초자료가 될 것이라 사료된다.

• 한국환경농학회지
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• 제31권1호
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• pp.45-51
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• 2012

본 연구는 단감 재배 중 사용되는 살균제인 pyrimethanil과 trifloxystrobin의 생산단계 잔류허용기준 설정을 통하여 안전한 단감 생산에 기여하고자 수행되었다. 먼저 pyrimethanil과 trifloxystrobin을 살포하고, 살포 후 0, 1, 2, 3, 5, 7, 10, 12, 15, 18일에 단감 시료를 채취하여 각각의 농약을 분석하고 생물학적 반감기를 산출한 다음 생산단계 잔류허용기준(PHRL; Pre-Harvest Residue Limit)을 설정하였다. 단감 중 pyrimethanil과 trifloxystrobin은 Acetonitrile을 이용하여 추출하고 $NH_2$ cartridge와 PSA를 이용하여 정제하여 HPLC/DAD를 이용하여 분석하였다. 두 농약에서 검출한계는 모두 0.01 mg/kg이었다. Pyrimethanil의 회수율은 0.1과 0.5 mg/kg 두 수준에서 각각 $81{\pm}1.62%$, $98{\pm}1.58%$ 이었으며, trifloxystrobin의 회수율은 0.1과 0.5 mg/kg 두 수준에서 각각 $91{\pm}2.94%$, $98{\pm}1.25%$이었다. 단감에서 pyrimethanil의 생물학적 반감기는 기준량 살포 시 15.6일, 배량 살포 시 11.6일이었고, trifloxystrobin의 생물학적 반감기는 기준량 살포 시 10.4일, 배량 살포 시 10.3일이었다. 잔류회귀 감소식을 이용한 생산단계 잔류허용기준은 pyrimethanil과 trifloxystrobin은 각각 수확 10일 전 2.69 mg/kg과 0.83 mg/kg으로 제안하였다.

• Journal of Pharmaceutical Investigation
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• 제22권4호
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• pp.281-287
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• 1992

Omeprazole (OMZ) is very unstable in acidic solution, which selectively inhibit the release of the gastric juice in the gastric mucosa, In order to stabilize (OMZ) in oral solid dosage form, the enteric-coated microcapsules and compression-coated OMZ tablets containing lysine or arginine as stabilizer were prepared and their dissolution and stability test were performed. The haif life of OMZ microcapsules containing arginine was 194 days at $30^{\circ}C$ and OMZ was completely released in 60 min. The half-lives of enteric coated and non-coated compression-coated OMZ tablets with lysine were 292 and 95 days at $30^{\circ}C$, respectively. The half-lives of enteric coated and non-coated compression-coated tablets with arginine were 1752 and 293 days at $30^{\circ}C$, respectively, and OMZ were released completely in 20 min in the 2nd fluid of K.P.VI. Consequently, the enteric-coated compression-coated OMZ tablets with arginine as stabilizer provided a good formulation for oral solid dosage form.

• Journal of Pharmaceutical Investigation
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• 제29권1호
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• pp.47-53
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• 1999

Gastrodia elata (GE) is an oriental medicinal herb which has been used traditionally for the treatment of various brain diseases including convulsion and epilepsy. The purpose of this study was to determine pharmacokinetic parameters of 4-hydroxy-3-methoxybenzaldehyde (HMBA) and p-hydroxybenzaldehyde (PHBA), constituents of GE, in rats. Male rats were cannulated in the femoral vein, femoral artery, bile duct and ureter. They received a single i.v. bolus dose of either HMBA or PHBA through the femoral vein. The concentration of HMBA or PHBA in plasma, bile and urine samples were analyzed by reversed-phase HPLC. HMBA and PHBA have very short half-lives, i.e. 4.03 and 2.26 minutes respectively. Most of HMBA and PHBA were thought to be eliminated through metabolism as the metabolized fraction approaches unity. Derivatives of HMBA or PHBA with longer biological half-lives should be designed to develop better anticonvulsants and more complete qualitative and quantitative understanding of the overall pharmacokinetic fate of these compounds awaits further investigation.

• 한국응용약물학회:학술대회논문집
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• 한국응용약물학회 2001년도 추계학술대회 및 정기총회
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• pp.88-88
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• 2001

The effects of pH and temperature on the degradation of prokidn in various buffered aqueous solutions(pH 1.32~9.66) and temperatures (35, 45 and 6$0^{\circ}C$ were investigated. The effect of ionic strength on the degradation of prokidin was also measured by varying ionic strength (0.0466~1.5) at pH 1.35 and 45$^{\circ}C$ The effect of metal ions on the degradation of prokidin at pH 7.35 and 3.98 was observed. The degradation of prokidin followed the pseudo- first- order kinetics. The degradation rate of prokidin showed pH-dependent and temperature-dependent patterns. Prokidin was very stable at the pH below 3.95, where half-lives at 35, 45 and 6$0^{\circ}C$were 294, 206 and 107 day, respectively. However, it degraded very rapidly at pH above 6.49; the half-lives at 35, 45 and 6$0^{\circ}C$were 60, 25 and 13 day, respectively. As ionic strength increased, the degradation rate of prokidin increased. Some metal ions increased the degradation rate in the rank order of Mn > Fe > Cu >Fe On the other hand. other metal ions such as Bi, Ba. Zn, Ni, Co did not show unfavorable effect.

• 한국비블리아학회지
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• 제2권1호
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• pp.266-295
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• 1974

The purpose of this study is to make a contribution to the effective management of medical literature in Korean libraries and specifically to help to select medical books and periodicals by determining the value and life of medical literature by means of citation counting and analysis. This report will present methods of calculation and data collection to measure the importance, half life of medical literature and the authority of author for Korean medical libraries. The writer conducted comparative studies based on data covering a two-year period, 1970-1971, using about 16,899 citations in 1,032 articles of the above journals. The references and citations are counted and analyzed by the number of authors, periodicals. books and publication dates. By the following ratio. calculated by the citation counting and analysis, we can decide the rates of medical periodicals to books, foreign literature to domestic literature and literature of the most numerously cited. authors, for the selecting method of Korean Medical libraries. (1) It is disclosed that 61 main authors are cited 9 times. Most of them are Western authors, they are cited 14,374 times which represents 88.6 % of the total citations. (2) The cited medical literature is classified as follows: The ratio of cited medical periodicals to the cited medical books is 82.0%. (The books at a rate of 18.0%.) Therefore, the wnter concentrated the efforts on the analysis of periodicals. (3) Classification of the periodicals by countries indicates that about 11.2% of total citations are made from Korean medical literature. The medical activities in Korea are dependent on the advanced foreign countries at ratio of 88.8%. Of the foreign medical periodicals cited, Japanese literature represents only 4.5% while literature of European countries and America constitutes 84.3%. (4) If medical journals are arranged in order of decreasing productivity of articles on a given subject, they may be revealed that it is necessary to have 98 titles of key journals to cover 60% of information in the field of medical science and 60 titles for an average of 50%. (5) For the purpose of measuring the life of medical literature in Korea, the writer has calculated the half lives of periodicals and books as follows: Kinds of Literature 1. Periodicals 2. Books 3. Whole literature Half-lives 7.75 years 4.11 years 6.37 years (6) The half lives of domestic and Japanese literature in the medical science are comparatively short.

• 한국환경농학회지
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• 제36권1호
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• pp.50-56
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• 2017

본 연구는 수박 중 pyridalyl 및 fluopicolide의 경시적 잔류양상을 살펴보고 생산단계 잔류허용기준 설정을 위한 생물학적 반감기를 산출하고자 수행되었다. 두 시험약제를 안전사용기준에 따라 두 포장지역에서 각각 살포한 후 포장 1에서는 10일간 포장 2에서는 20일간 일자별 수박 시료를 채취하여 각각의 잔류분을 HPLC/UVD로 분석하였다. 두 시험농약의 분석정량한계는 각각 0.05 mg/kg, 0.02 mg/kg이었으며, 회수율은 81.2~90.5% 수준이었고 시료 중 시험농약은 43~47일간 안정하였다. 수박 중 초기 잔류량은 pyridalyl이 0.12~0.16 mg/kg, fluopicolide은 0.23~0.24 mg/kg이었으며, 모든 포장내에서 농약잔류허용기준보다 낮은 수준이었다. 수박 중 pyridalyl의 생물학적 반감기는 포장 1에서 26.9일, 포장 2에서 17.9일 이었으며, fluopicolide의 생물학적 반감기는 포장 1에서 16.6일, 포장 2에서 94.2일이었다. 수박의 pyridalyl 및 fluopicolide의 수확 10일 전 생산단계 잔류허용기준은 각각 0.21 mg/kg, 1.03 mg/kg이었으며 재배기간 중 두 시험약제 모두 매우 낮은 잔류소실 경향을 보였다.