• Proceedings of the Korean Society of Applied Pharmacology
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• 1996.04a
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• pp.176-176
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• 1996

축산식품중에 잔류하고 있는 sulfamethazine을 검출하기 위하여 sulfamethazine에 대한 단클론항체를 생산하고 이를 이용하여 효소면역측정법을 개발하였다. 면역원은 sulfamethazine에 KLH를 그리고 흡착항원은 BSA를 glutaraldehyde법으로 결합시켰다. 면역원으로 Balb/c mouse를 면역시킨 다음 비장 형질세포률 얻어 myeloma cell과 융합하여 융합잡종세포를 만들었다. Sulfamethazine에 대한 항체를 분비하는 융합잡종세포를 단계회석법과 ELISA를 이용하여 cloning하여 D2, A9, B8, Bl 클론을 얻었다. 이들 클론에서 얻어진 단클론항체를 사용하여 indirect competitive ELISA를 실시하여 표준곡선을 작성하여 본 결과 농도의존성 곡선을 얻을 수 있었다. 4클론중에서 A9 클론을 사용하여 다른 유사한 sulfonamide듣과 p-aminobenzoic acid와 교차반응을 조사한 결과 sulfamerazine에 12.5%의 교차반응을 보였으나 다른 설파제에 대해서는 교차 반응을 보이지 않았다.

• Proceedings of the Korean Society of Precision Engineering Conference
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• 2013.05a
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• pp.305-306
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• 2013

• Korean Journal of Food Science and Technology
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• v.25 no.5
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• pp.565-570
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• 1993

Peroxidase from Jerusalem artichoke tubers, which might be related to browning reaction, was purified by ammonium sulfate precipitation, DEAE-cellulose and Sephacryl S-200 chromatography. The optimum pH of the purified peroxidase was 5.0 and relatively stable at pH $5.0{\sim}6.0$ using substrate of p-phenylenediamine and $H_2O_2$. D-values for thermal inactivation at 60, 70 and $80^{\circ}C$ were 86, 45 and 33 sec, respectively. Activation energy was 4,111 J/mole. The enzyme showed the most sensitive specificity of substrate for p-phenylenediamine. The compounds such as 1mM potassium cyanide, 10mM sodium diethyldithiocarbamate, L-ascorbic acid, sodium hydrosulfite and L-cysteine inhibited completely while 1mM of $Ca^{2+}\;and\;Cu^{2+}$ activated the purified peroxidase.

• Resources Recycling
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• v.17 no.5
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• pp.37-43
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• 2008

Stripping experiments of iron from the loaded Alamine336 by sulfurous, chloric and sulfuric acid solutions have been performed by varying the concentration of acid and stripping conditions. The stripping percentage of iron decreased with the increase of HCl and $H_{2}SO_4$ concentration, while that increased with the increase of $H_{2}SO_3$ concentration up to 3 M. Stripping temperature had adverse effect on the stripping percentage of iron in the stripping by $H_{2}SO_3$ solution, while the stripping percentage of iron by HCl solution increased with the increase of temperature. Stripping isotherm of iron by 0.1 M HCl and 0.1 M $H_{2}SO_4$ solution indicated that three and four stripping stages could result in a solution containing 0.05 M iron at an O/A ratio of 1/10 from the loaded Alamine336 phase where iron concentration was 0.5 M.

• Journal of fish pathology
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• v.22 no.2
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• pp.125-135
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• 2009

The pharmacokinetic properties of oxolinic acid (OA) were studied after oral administration, intraperitoneal injection and dipping to cultured olive flounder, Paralichthys olivaceus (average 90 g, $23{\pm}1{^{\circ}C}$). Plasma samples were taken at 3, 5, 10, 15, 24, 30, 48, 96 and 144 h post-dose. In oral dosage at 15, 30 and 60 ㎎/㎏, the peak plasma concentrations of OA, which attained at 10~15 h post-dose, were 1.92, 2.45 and 3.72 $\mu{g}/m\ell$, respectively. In intraperitoneal injection with 10 and 20 ㎎/㎏, the peak plasma concentrations of OA, which attained at 10 h post-dose, were 4.1 and 4.8 $\mu{g}/m\ell$, respectively. In dipping in 30 and 50 ppm for 1 h, peak concentrations were observed at 5 h and 30 h post-dose, were 0.22 and 0.38 $\mu{g}/m\ell$, respectively. The kinetic profile of absorption, distribution and elimination of OA in plasma were analyzed fitting to a one-compartment model by WinNonlin program. Calculated parameters for a single oral dosage of 15, 30 and 60 ㎎/㎏, respectively, were: AUC (the area under the concentration-time curve)=70.93, 120.0 and 141.86 $\mu{g}$ $h/m\ell$ $T_{max}$ (time for maximum concentration)=16.22, 20.39 and 17.33 h; $C_{max}$ (maximum concentration)=���D1.61, 2.40 and 3.01 $\mu{g}/m\ell$. Following intraperitoneal injection of 10 and 20 ㎎/㎏, these parameters were AUC=184.7 and 315.92 $\mu{g}$ $h/m\ell$ $T_{max}$=5.91 and 6.26 h; $C_{max}$=4.19 and 4.45 $\mu{g}/m\ell$. Following dipping at 30 and 50 ppm, these parameters were AUC=17.58 and 21.69 $\mu{g}$ $h/m\ell$ $T_{max}$=19.08 and 31.43 h; $C_{max}$x=0.22 and 0.25 $\mu{g}/m\ell$.

• Electrical & Electronic Materials
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• v.5 no.4
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• pp.439-445
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• 1992

최근 광자기 기록매체로 주목받고 있는 RE-TM계 비정질 박막을 T $b_{x}$ (F $e_{0.9}$ $Co_{0.1}$)$_{100-x}$ (x=14, 17, 20, 23, 27[at%])의 조성비를 갖는 모합금을 만든후 진공증착방법으로 합금박막을 제작하였다. 각시료의 조성에 따른 자기광학효과를 알아보기 위하여 80K부터 600K에서 포화자화( $M_{s}$ )와 보자력( $H_{c}$)에 대한 온도의존성과 자기이방성상수(Ku), Polar Kerr 이력곡선을 측정하였다. 또한 Curie 온도 근처에서 열처리 시간에 따른 자기 토크 곡선의 변화를 분석 함으로써 합금박막 표면의 산화정도를 정성적으로 평가할 수 있었다. 실험결과 T $b_{22.72}$(F $e_{68.78}$ $Co_{8.5}$)인 시료가 상온에서 8.4KOe의 보자력을 가졌으며 T $b_{x}$(x=23[at%])인 경우가 가장 큰 수직자기이방성을 나타냈다. Polar Kerr 이력곡선은 Tb함량 x=25~26[at%]에서 부호가 반전됨을 알 수 있었다.다.다.다.

• Journal of Korea Water Resources Association
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• v.39 no.6 s.167
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• pp.487-494
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• 2006

The flood discharge on the rising limb of a hydrograph at Hwawon station greatly differs from the flood discharge on the falling limb for the same stage. When there is such a big hysteresis, there can be a significant amount of errors in the rated discharge obtained from a simple rating curve. To reduce errors in rated discharges, a looped rating curve was established for Hwawon station in the Nakdong River. In order to compute the deviation between real discharges and simply rated discharges, a simple rating curve was established using the stage and discharge data from the results of a hydraulic channel routing. The relationship between the discharge deviation ${\Delta}Q$ and a product of B and ${\Delta}h/{\Delta}t$ was analysed, where B is the channel topwidth; ${\Delta}h$ is the stage increment; At is the time increment. Strong relation between ${\Delta}Q$ and $B{\Delta}h/{\Delta}t$ was found. The discharges calculated from the relationship show differences by 10 % or less for the 7 observations out of 11 observations in 1997 whose stages exceeds 7 m. The observed discharges for the stages over 9 m in 1998 also show small difference with the discharges estimated from the loop rating curve. Looped rating curve is recommended, instead of the simple rating curve to reduce the errors of rated discharges for gauging stations like Hwawon, which has relatively large loop width.

• Korean Journal of Soil Science and Fertilizer
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• v.43 no.4
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• pp.407-414
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• 2010

Until now, the pore size distribution, PSD, of soil profile has been calculated from soil moisture characteristic data by water release method or mercury porosimetry using the capillary rise equation. But the current methods are often difficult to use and time consuming. Thus, in this work, theoretical framework for an easy and fast technique was suggested to estimate the PSD from unsaturated hydraulic conductivity data in an undisturbed field soil profile. In this study, unsaturated hydraulic conductivity data were collected and simulated by the variation of soil parameters in the given boundary conditions (Brooks and Corey soil parameters, ${\alpha}_{BC}=1-5L^{-1}$, b = 1 - 10; van Genuchten soil parameters, ${\alpha}_{VG}=0.001-1.0L^{-1}$, m = 0.1 - 0.9). Then, $K_s$ (1.0 cm $h^{-1})$ was used as the fixed input parameter for the simulation of each models. The PSDs were estimated from the collected K(h) data by model simulation. In the simulation of Brooks-Corey parameter, the saturated hydraulic conductivity, $K_s$, played a role of scaling factor for unsaturated hydraulic conductivity, K(h) Changes of parameter b explained the shape of PSD curve of soil intimately, and a ${\alpha}_{BC}$ affected on the sensitivity of PSD curve. In the case of van Genuchten model, $K_s$ and ${\alpha}_{VG}$ played the role of scaling factor for a vertical axis and a horizontal axis, respectively. Parameter m described the shape of PSD curve and K(h) systematically. This study suggests that the new theoretical technique can be applied to the in situ prediction of PSD in undisturbed field soil.

• Journal of the Korean Chemical Society
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• v.19 no.4
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• pp.225-232
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• 1975

The elution behaviour of molybdate and tungstate through anion exchange column has been studied at the various pH. A discussion is made to evaluate the equilibrium constants of the polymerization of these acids comparing with the behaviour of chromate ion and dichromate ion. The eqailibrium constants found at $20^{\circ}$ are $K = 4{\times}10^{53} for 7MoO_4^{2-} + 8H^+ {\longleftrightarrow} Mo7O_{24}^{6- }+ 4H_2O$$ K = 3{\times}10^{54} for 6WO_4^{2-} + 7H^+ {\longleftrightarrow} HW6O_{21}^{5-} + 7H_2O$ referring to this results the conditions of separation of tungstate and molybdate are obtained. iThe quantitative separations of carbonate, molybdate and tungstate from the pregnant solution have been established by anion exchange chromatography, using the $22 cm{\times}44.27 cm^2$ column of Rexyn 201. The optimum eluents for the quantitative separation of those ions are as follows; 0.2M solution of sodium chloride at pH 8 for carbonate, the mixture of 0.5 M ammonium chloride and 0.05 M sodium sulfate at pH 5 for molybdate and 0.5 M solution of ammonium chloride at pH 10 for tungstate. Tungstate is directly recovered from the pregnant solution as a form of ammonium paratungstate, by eluting with ammonium chloride solution.

• Journal of the Korean Chemical Society
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• v.46 no.6
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• pp.509-514
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• 2002

A method to determin Fe(II) and Fe(III) ion in aqueous solution by chemiluminescence method using a stopped flow system has been studied. The method is based on the increased chemiluminescence intensity with the addition of Fe(III) ion to a solution of lucigenin and hydrogen peroxide. The effects of KOH concentration, flow rate of reagents, $H_2O_2$ concentration and citric acid concentration used for the masking of Fe(II) ion on the chemilu-minescence intensity have been investigated. The calibration curve for total Fe was linear over the range from 1.0${\times}$$10^{-6}$ M to 1.0${\times}$$10^{-4}$M, coefficient of correlation was 0.996 and the detection limit was 1.0${\times}$$10^{-7}$M under the optimal exper-imental conditions of 4.0 M, 2.0 M, 3.5 mL/min for the concentration of $H_2O_2,$ KOH and flow rate of reagents, respec-tively. The calibration curve for Fe(Ⅲ) was linear over the range from 1.0${\times}$$10^{-6}$M to 1.0${\times}10^{-4}$ M, the coefficient of correlation was 0.997 and the detection limit was 5.0${\times}$$10^{-7}$M under the optimal experimental conditions.