• 분석과학
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• 제10권3호
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• pp.168-178
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• 1997

기체 크로마토그래피법을 이용하여 제초제인 ethalfluralin의 잔류분석을 위한 최적 측정 조건을 구하고, 토양에서의 잔류량과 반감기를 조사하였다. 토양시료를 methanol과 dichloromethane으로 추출하여 농축하였다. Toluene으로 다시 녹이고, cyanosilica gel 카트리지로 분리하여 전자포착형 검출기가 장착된 기체 크로마토그래프(GC-ECD)로 분석하였다. 0.1과 1.0ppm의 표준물을 첨가하였을 때, 92.8~101.2%의 회수율을 얻었으며, 검출한계는 0.004ppm이었다. Ethalfluraline의 반감기는 토양 (A)의 경우에는 실내에서 35일, 야외에서 7.2일이었으며, 토양 (B)의 경우에는 실내에서 45일, 야외에서 9.7일이었다.

• Biomolecules & Therapeutics
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• 제6권4호
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• pp.400-405
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• 1998

The pharmacokinetics of CJ-50001 (recombinant human granulocyte-colony stimulating factor, developed by R&D center of Cheil Jedang Corp.) were investigated in rats and dogs. The serum concentrations of CJ-50001 were measured by a sandwich enzyme immunoassay. After single intravenous (iv) administration of Cf-50001 to rats at a dose of 5 $\mu$g/kg, the mean terminal half-life and area under the concentration-time curve (AUC) were 0.96 h and 124.497g . h/ml, respectively. After single subcutaneous (sc) administration at the same dose, maximum serum concentration was observed at about 2 hours after administration, and the mean terminal half-life, AUC and the bioavailability were 1.11 h,63.58$\mu$g . h/ml and 51.07%, respectively. In repeated dosing studies, CJ-50001 was administered iv and sc to rats at a daily dose of 5$\mu$g/kg for 7 days. The pharmacokinetic parameters, such as mean AUC and terminal half-life, were no significantly different from those of single administration. Following single iv and sc administration of CJ-50001 to dogs at a dose of 5 $\mu$g/kg, mean AUCs were much higher than those of rats, due to the decreased clearence (CL). After sc administration to dogs, maximum serum concentration was observed at 2~4 hours after administration and the bioavailability was 54.60%.

• Journal of Microbiology and Biotechnology
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• 제18권11호
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• pp.1803-1808
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• 2008

For practical application, the stability of permeabilized Ochrobactrum anthropi SY509 needs to be increased, as its half-life of enzymatic denitrification is only 90 days. As the cells become viable after permeabilization treatment, this can cause decreased activity in a long-term operation and induce breakage of the immobilization matrix. However, the organic solvent concentration causing zero cell viability was 50%, which is too high for industrial application. Thus, whole-cell immobilization using glutaraldehyde was performed, and 0.1% (v/v) glutaraldehyde was determined as the optimum concentration to maintain activity and increase the half-life. It was also found that 0.1% (v/v) glutaraldehyde reacted with 41.9% of the total amine residues on the surface of the cells during the treatment. As a result, the half-life of the permeabilized cells was increased from 90 to 210 days by glutaraldehyde treatment after permeabilization, and no cell viability was detected.

• The Korean Journal of Physiology and Pharmacology
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• 제25권6호
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• pp.545-553
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• 2021

Fixed-dose combinations development requires pharmacokinetic drugdrug interaction (DDI) studies between active ingredients. For some drugs, pharmacokinetic properties such as long half-life or delayed distribution, make it difficult to conduct such clinical trials and to estimate the exact magnitude of DDI. In this study, the conventional (non-compartmental analysis and bioequivalence [BE]) and model-based analyses were compared for their performance to evaluate DDI using amlodipine as an example. Raw data without DDI or simulated data using pharmacokinetic models were compared to the data obtained after concomitant administration. Regardless of the methodology, all the results fell within the classical BE limit. It was shown that the model-based approach may be valid as the conventional approach and reduce the possibility of DDI overestimation. Several advantages (i.e., quantitative changes in parameters and precision of confidence interval) of the model-based approach were demonstrated, and possible application methods were proposed. Therefore, it is expected that the model-based analysis is appropriately utilized according to the situation and purpose.

• International Journal of Internet, Broadcasting and Communication
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• 제15권2호
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• pp.181-186
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• 2023

With the development of VR technology, the visual immersion of VR games has been greatly enhanced nowadays. There has been an issue that has been troubling players in previous VR games, which is motion sickness. Therefore, VR games have been limited in terms of game mechanics, game duration, and game scale, greatly reducing the immersive experience of visual immersion. However, <Half-Life: Alyx> is different from previous VR games in that players can actually perform spatial displacement in the game scene, rather than being fixed in one place for 360-degree observation and interaction. At the same time, compared to traditional games, VR games no longer need to rely on screens, and the complete visual immersion enhances the fun and playability of the game. This research focuses on the VR game <Half-Life: Alyx> to explore its immersive factors in terms of visual perception. Through in-depth analysis of elements such as color, texture mapping, lighting, etc. in VR games, it was found that the game creates a strong sense of visual immersion in these aspects. Through analysis, it is helpful to gain a deeper understanding of the factors that contribute to visual immersion in VR games, which has certain reference value for game developers and related professionals.

• 방사성폐기물학회지
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• 제21권4호
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• pp.465-479
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• 2023

To ensure the safety of disposal facilities for radioactive waste, it is essential to quantitatively evaluate the performance of the waste disposal facilities by using safety assessment models. This paper addresses the development of the safety assessment model for the underground silo of Wolseong Low-and Immediate-Level Waste (LILW) disposal facility in Korea. As the simulated result, the nuclides diffused from the waste were kept inside the silo without the leakage of those while the integrity of the concrete is maintained. After the degradation of concrete, radionuclides migrate in the same direction as the groundwater flow by mainly advection mechanism. The release of radionuclides has a positive linear relationship with a half-life in the range of medium half-life. Additionally, the solidified waste form delays and reduces the migration of radionuclides through the interaction between the nuclides and the solidified medium. Herein, the phenomenon of this delay was implemented with the mass transfer coefficient of the flux node at numerical modeling. The solidification effects, which are delaying and reducing the leakage of nuclides, were maintained the integrity of the nuclides. This effect was decreased by increasing the half-life and the mass transfer coefficient of radionuclides.

• 한국간호교육학회지
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• 제17권1호
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• pp.120-128
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• 2011

Purpose: The purpose of this study was to test the validity and reliability of a life respect instrument for elementary school students. Method: The study was conducted as follows: identification of the tentative content domains, items generation, test of content validity, and data collecting with a preliminary questionnaire. Descriptive statistics, factor analysis, Cronbach's alpha, Guttman split-half, and Pearson correlation coefficients were used to analyze the data. Results: Two factors were extracted through factor analysis: 'Value about life respect', and 'Attitude about life respect.' These factors explained 58.82% of all factors. A total of 16 items belonging to 2 domains were generated. Cronbach's alpha and Guttman split-half coefficient were .82, and .84 respectively. Conclusion: The life respect instrument modified in this study will be useful for evaluating the effect of life respect education for elementary school students.

• 한국환경농학회지
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• 제28권3호
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• pp.281-288
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• 2009

Azoxystrobin과 kresoxim-methyl의 참외 중 반감기와 잔류양상을 조사하였다. Azoxystrobin의 참외 중 0일차 잔류량은 기준량 및 배량 처리구에서 각각 0.09 및 0.14 mg/kg으로 나타났으며 농약의 반감기 소실곡선식은 y=0.0766e$^{-0.138x}$ ($r^2$=0.9424) 및 y=0.1143e$^{-0.0890x}$ ($r^2$=0.9310) 이었으며 생물학적 반감기는 각각 5.0일 및 7.8일 이었다. Kresoxim-methyl의 참외 중 0일차 잔류량은 기준량 및 배량 처리구에서 각각 0.10 및 0.23 mg/kg으로 나타났으며 농약의 소실곡선식은 y=0.0896e$^{-0.1672x}$ ($r^2$=0.9428) 및 y=0.1504e$^{-0.1446x}$ ($r^2$=0.9040) 이었고 생물학적인 반감기는 각각 4.1일 및 4.8일 이었다. 재배기간 중 참외의 무게증가에 농약희석효과를 배제한 절대잔류농도는 약제 살포 후 14일 경과시 azoxystrobin은 기준량 및 배량에서 0.01 및 0.05 mg/kg으로서 각각 83.6 및 67%의 농약이 분해되었다. Kresoxim-methyl은 각각 0.01 및 0.03 mg/kg 으로서 86.2 및 87.8% 정도의 농약 분해율을 보였다.

• 한국방사선학회논문지
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• 제14권4호
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• pp.447-453
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• 2020

본 연구는 한국원자력연구원에 있는 고에너지 양성자 선형가속기에서 발생된 100 MeV 양성자와 HPGe 감마선 측정시스템을 이용하여 ¹⁷⁹Re 방사성동위원소의 반감기를 정확하게 측정하였다. 결과적으로 얻어진 반감기는 19.64 ± 0.26 min이다. 현재까지 알려진 ¹⁷⁹Re 방사성동위원소의 반감기에 대한 과거 결과들과 비교했을 때 1960년도 발표한 B. Harmatz와 1975년도에 발표한 B. J. Meijer의 결과들은 중심값 자체가 본 연구에서 얻어진 결과보다 높게 측정되었다. 1966년에 발표된 K. J. Hofstetter의 경우 오차가 매우 큰이 특징이라고 할 수 있다. 이 결과는 본 연구의 결과와 오차범위 내에서 중심값은 매우 일치하는 경향을 보였다. 2009년도에 발표된 Coral M. Baglin의 19.5 min의 값과 오차범위 내에서 매우 일치하는 결과를 보여주고 있다. 얻어진 측정된 결과는 ENSDF(Evaluated Nuclear Structure Data File)의 결과와 비교하였다. 본 연구를 통하여 기존에 부정확했던 ¹⁷⁹Re의 반감기의 결과를 보다 신뢰성 있게 나타났고 비교적 최근에 발표된 Coral M. Baglin의 결과의 타당성을 확인 할 수 있었다.

• 대한핵의학회지
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• 제9권1호
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• pp.59-71
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• 1975

53 patients with hyperthyroidism have been analyzed with special reference to therapeutic response to radioactive iodine ($^{131}I$) treatment. Mean effective half-life, 24 hour uptake rate and radiation dose of $^{131}I$ in hyperthyroid patients included in this study were respectively. 1. Mean effective half-life of $^{131}I\;was\;4.7{\pm}1.5$ days in the tracer dose and $5.0{\pm}1.5$ days in the therapeutic dose. 2. Mean 24 hour uptake rate of $^{131}I\;was\;72.7{\pm}11.1%$ in the tracer dose and $73.4{\pm}12.3%$ in the theapeutic dose. 3. Mean radiation dose of $^{131}I\;was\;5,319{\pm}2,648$ RAD as predicted and $5,692{\pm}2,843$ RAD as actual. A single dose of radioactive iodine treatment was satisfactory in 34 patients (radioiodine sensitive) and multiple doses of radioactive iodine treatments were required in 19 patients (radioiodine resistant). A radioiodine resistant group of patients with hyperthyroidism was distinctively characteristic in the following aspects. 1. Mean thyroid weight calculated in the resistant group ($63.9{\pm}14.0gm$) was significantly (p<0.01) greater than that of the sensitive group ($46.6{\pm}13.3gm$). 2. Mean 24 hour uptake rate of the tracer dose in the resistant group ($67.3{\pm}10.7%$) was significantly (p<0.01) lower than that of the sensitive group ($75.7{\pm}10.5%$). 3. Mean 24 hour uptake rate of the therapeutic dose in the resistant group ($68.5{\pm}13.7%$) was significantly (p<0.05) lower than that of the sensitive group ($76.1{\pm}10.9%$). 4. Mean predicted radiation dose, of $^{131}I$ in the resistant group ($3,684{\pm}1,745$ RAD) was significantly (p<0.01) lower than that of the sensitive group ($6,232{\pm}2,683$ RAD). 5. Mean actual radiation dose of $^{131}I$ in the resistant group ($4,100{\pm}1,691$ RAD) was significantly (p<0.01) lower than that of the sensitive group ($6,582{\pm}3,024$ RAD). 6. No significant difference was detected in terms of effective half-life of $^{131}I$ among the groups (p>0.05). 7. The average mean % difference of effective half-life, uptake rate and radiation dose measured following the tracer and therapeutic dose of $^{131}I$ were not statistically significant (p>0.05). Therefore effective half-life, uptake rate and radiation dose of the therapeutic dose of $^{131}I$ were readily predictable following the tracer dose of $^{131}I$. 8. It is concluded that the possibility of resistance to radioactive iodine treatment may be anticipated in patients with thyroid gland large in size and compromised $^{131}I$ uptake rate.