• 분석과학
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• 제17권1호
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• pp.37-44
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• 2004

효모 Hansenula polymorpha 로부터 탄소원으로 0.5% 메탄올을 이용하여 알코올 산화효소를 대량 유도 발현하였다. 발현 유도된 Hansenula polymorpha 알코올 산화효소는 두 단계의 컬럼 크로마토그래피를 통하여 전기영동에서 단일밴드로 정제하였다. 정제한 효소는 주로 일차 지방족 알코올을 산화시키며, 에탄올에 대해 가장 높은 기질특이성을 보였다. 이 효소가 촉매하는 에탄올 산화반응의 최적 pH는 8.5 이였으며, 최적 온도는 $50^{\circ}C$를 나타내었다. 효소의 $T_m$ 값은 약 $52^{\circ}C$ 이었으며, $65^{\circ}C$에서도 완전히 불활성화 되지 않았다. 또한 효소는 변성제와 7주간의 비교적 장기간 보전에 대해서도 안정하였다. 이 효소는 알코올 측정을 위한 효소학적 방법 및 알코올과 알데히드의 공업적 생산에 이용될 수 있다.

• 비파괴검사학회지
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• 제6권2호
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• pp.46-56
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• 1987

The effect of ultrasonic search units on the detectability and size evaluation of planar flaws was studied for thicker ferritic material using the technique of the DAC curve and reference level. Cylindrical holes were used as calibration reflectors. The planar flaws such as disc and band types were machined. They were detected and evaluated with different search units and sizing criteria. The value evaluated was compared with the actual dimension of planar flaws.

• 농촌의학ㆍ지역보건
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• 제11권1호
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• pp.3-11
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• 1986

In order to observe the infestation rate and intensity of C. sinensis in Yeoju Eup, Kyung-gi Do, 9,512 stool specimens were collected from the inhabitants through student's helps. The specimens were examined by cellophane thick smear technique and Stoll's egg dilution technique. The epidemiological status was analysed statistically by the regession equation and catalytic curve with the results obtained from this area. The results are as follows: 1) Collection rate oft he stool samples was 66.5%, 9.512 out of 14,300 inhabintants complied with our survey. 2) The infestation rate of C.sinensis was 5.0%, and for male 7.8%, for female 2.3%. 3) Average E.P.G. by Stoll's egg dilution technique in this area was 1,572, and for male 1,853, for female 676. 4) The degree of the intensity of C. sinensis infection by E.P.G. count was distributed as 65.2% in light infection, 32.0 % in moderate infection, 2.8% in heavy infection and none in very heavy infection. 5) The intensity of endemicity in this area was represented with the regression equation calculated with cumulative percentages of E.P.G. counts. Regression equation was y=3.887+1.695 log x and Cs. $D_{50}$ was 4.54. 6) The two-stage catalytic model was applied and the calculation lead to the equation $y=0.267(e^{-0.004t}-e^{-0.019t})$; a=0.004 < b=0.019. 7) Other helminthic infection rate in this area was 1.4% in A.lumbricoides 2.7% in T. trichiura, 1.6% in M. yokogawai md 0.2% in Taenia sp. respectively.

• 한국자기학회지
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• 제17권3호
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• pp.114-119
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• 2007

[ $bcc-Th_3P_4$ ] 구조를 가지고 있는 단결정 $Nd_3Se_4$를 성장 시킨 후 $4{\sim}300\;K$ 사이의 온도 영역에서 자기감수율을 측정했다. 측정된 자기기감수율을 축퇴된 $Nd^{3+}$ 기저상태가 결정장의 영향을 받아 발생하는 에너지 갈라짐에 의한 이론적인 자기감수율값과 비교했다. 분석 결과 $Nd_3Se_4$ 결정체 안에 있는 $Nd^{3+}$ 이온의 경우에는 결정장에 의한 영향이 거의 없음을 알 수 있었다. 또한 $T_c$가 53 K인 $Nd_3Se_4$의 자발자기화의 온도에 따른 곡선이 J=9/2에 해당하는 Brillouin function과 일치함을 확인했다.

• Biomolecules & Therapeutics
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• 제6권2호
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• pp.219-224
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• 1998

The bioequivalence of two clarithromvcin products was evaluated with 16 normal male volunteers (age 23-28 yr, body weight 57.5-75.517g) following single oral dose. Test product was ReYon Clarithromycin tablets (ReYon Pharm. Corp., Korea) and reference product was Klarici $d_{R}$ tablets (Abbott Korea). Both products contain 250 mg of clarithromucin. One tablet of the test or the reference product was administered to the volunteers, respectively, by randomized two period cross-over study (2$\times$2 Latin square method). The determination of clarithromycin was accomplished using a modified agar well diffusion bioassay. As a result of the assay validation, the quantification of clarithromycin in human serum by this technique was possible down to 0.03$\mu$g/ml using 100$\mu$l of serum. The coefficient of variation (C.V.) was less than 10%. Average drug concentrations at each sampling time and pharmacokinetic parameters calculated were not significantly different between two products P>0.05); the area under the curve to last sampling time (24 hr) (AU $Co_{24hr}$ (8.10$\pm$ 1.26 vs 8.22$\pm$ 1.627g . hr/ml), AUC from time zero to infinite (AU $Co_{\infty}$) (8.61 $\pm$ 1.28 vs 8.84$\pm$ 1.71 $\mu$g . hr/ml), maximum plasma concentration ( $C_{msx}$) (0.87$\pm$0.22 vs 0.88$\pm$0.19 $\mu$g/ml) and time to maximum plasma concentration ( $T_{max}$) (2.69 $\pm$0.48 vs 2.56$\pm$ 0.51 hr). The differences of mean AU $Co_{24h}$, $C_{msx}$ and $T_{msx}$ between the two products (1.44, 1.39, and 4.65%, respectively) were less than 20%. The power (1-$\beta$) and treatment difference ($\Delta$) for AU $Co_{24hr}$, and $C_{max}$ were more than 0.8 and less than 0.2, respectivly. Although the power for $T_{max}$ was under 0.8, $T_{max}$. of the two products was not significantly different each other (p>0.05). These results suggest that the bioavailability of ReYon Clarithromycin tablets is not significantly different from that of Klarici $d_{R}$ tablets. Therefore, two products are bioequivalent based on the current results. results.sults.sults.s.s.s.s.s.s.s.

• Journal of Pharmaceutical Investigation
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• 제33권4호
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• pp.299-304
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• 2003

The purpose of this study was to investigate the effect of coadministration (2.5, 10, 20 mg/kg) and 3 or 7 days-pretreatment (10 mg/kg) of diltiazem on the pharmacokinetic parameters of paclitaxel (50 mg/kg) given orally in rats. The plasma concentrations of paclitaxel coadministered or pretreated with diltiazem were significantly (p<0.05 at 20 mg/kg coadmin., p<0.05 at pretreat.) increased compared to that of control, from 0.5 hr to 24 hr. Area under the plasma concentration-time curve (AUC) of paclitaxel coadministered or pretreated with diltiazem was significantly (p<0.05 at 20 mg/kg coadmin., p<0.01 at pretreat.) higher than that of control. Peak concentrations $(C_{max})$ of paclitaxel with diltiazem were significantly (p<0.05 at 20 mg/kg coadmn. and pretreat.) increased compared to that of control. Elimination rate constants $(K_{el})$ of paclitaxel with diltiazem were significantly (p<0.05 at 20 mg/kg and 7 days-pretreat.) reduced compared to those of control. Half-life $(t_{1/2})$ and mean residence time (MRT) of paclitaxel with diltiazem was significantly (p<0.05 at 20 mg/kg ad 7 days-pretreat.) prolonged compared to those of control. Absolute bioavailability (AB%) of paclitaxel with diltiazem was significantly (p<0.05 at 20 mg/kg and 3 days-pretreat, p<0.01 at 7 days -pretreat.) increased compared to that of control. Based on these results, it might be considered that diltiazem may inhibit cytochrome $P_{450}$ and P-glycoprotein, which are respectively engaged in paclitaxel absorption and metabolism in liver and gastrointestinal mucosa.

• 한국재료학회지
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• 제18권6호
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• pp.318-325
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• 2008

Single crystal $ZnIn_2S_4$ layers were grown on thoroughly etched semi-insulating GaAs(100) substrate at $450^{\circ}C$ with hot wall epitaxy (HWE) system by evaporating $ZnIn_2S_4$ source at $610^{\circ}C$. The crystalline structure of the single crystal thin films was investigated by the photoluminescence (PL) and double crystal X-ray rocking curve (DCRC). The temperature dependence of the energy band gap of the $ZnIn_2S_4$ obtained from the absorption spectra was well described by the Varshni's relation, $E_g(T)=2.9514\;eV-(7.24{\times}10^{-4}\;eV/K)T^2/(T＋489\;K)$. After the as-grown $ZnIn_2S_4$ single crystal thin films were annealed in Zn-, S-, and In-atmospheres, the origin of point defects of $ZnIn_2S_4$ single crystal thin films has been investigated by the photoluminescence (PL) at 10 K. The native defects of $V_{Zn}$, $V_S$, $Zn_{int}$, and $S_{int}$ obtained by PL measurements were classified as a donors or acceptors type. And we concluded that the heat-treatment in the S-atmosphere converted $ZnIn_2S_4$ single crystal thin films to an optical p-type. Also, we confirmed that In in $ZnIn_2S_4$/GaAs did not form the native defects because In in $ZnIn_2S_4$ single crystal thin films existed in the form of stable bonds.

• 센서학회지
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• 제17권6호
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• pp.437-446
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• 2008

Single crystalline ${ZnIn_2}{Se_4}$ layers were grown on thoroughly etched semi-insulating GaAs (100) substrate at $400^{\circ}C$ with hot wall epitaxy (HWE) system by evaporating ${ZnIn_2}{Se_4}$ source at $630^{\circ}C$. The crystalline structure of the single crystalline thick films was investigated by the photoluminescence (PL) and Double crystalline X-ray rocking curve (DCRC). The carrier density and mobility of ${ZnIn_2}{Se_4}$ single crystalline thick films measured from Hall effect by van der Pauw method are $9.41{\times}10^{16}cm^{-3}$ and $292cm^2/V{\cdot}s$ at 293 K, respectively. The temperature dependence of the energy band gap of the ${ZnIn_2}{Se_4}$ obtained from the absorption spectra was well described by the Varshni's relation, $E_g(T)$=1.8622 eV-$(5.23{\times}10^{-4}eV/K)T^2$/(T+775.5 K). After the as-grown ${ZnIn_2}{Se_4}$ single crystalline thick films was annealed in Zn-, Se-, and In-atmospheres, the origin of point defects of ${ZnIn_2}{Se_4}$ single crystalline thick films has been investigated by the photoluminescence (PL) at 10 K. The native defects of $V_{Zn}$, $V_{Se}$, $Zn_{int}$, and $Se_{int}$ obtained by PL measurements were classified as a donors or acceptors type. And we concluded that the heat-treatment in the Se-atmosphere converted ${ZnIn_2}{Se_4}$ single crystalline thick films to an optical p-type. Also, we confirmed that In in ${ZnIn_2}{Se_4}$/GaAs did not form the native defects because In in ${ZnIn_2}{Se_4}$ single crystalline thick films existed in the form of stable bonds.

• 약학회지
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• 제30권1호
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• pp.14-23
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• 1986

This study was conducted to investigate the correlation between the dissolution rates and the bioavailabilities of commercial phenytoin products, and also the correlation between their biovailabilities in rabbits and those in humans. Dissolution test was conducted in pH 9. 0 alkaline borate buffer (0.2M) using basket method with seven phenytoin products commercially available. According to the dissolution rate, the phenytoin products were divided into three groups, such as rapid, intermediate and slow group. Three phenytoin products from each group were selected for the bioavailability test in rabbits and humans. The bioavailability test was carried out in rabbits and normal volunteers using cross over design. Single doses of 20mg/kg and 300mg/man were orally administered to rabbits and normal volunteers respectively. Average $C_{max}$, $t_{max}$ and AUC of three phenytoin products were determined from the serum concentration-time curve in rabbit and human experiments. The relative bioavailability evaluation was conducted using AUC of three phenytoin products. The correlations between the dissolution rate constants and bioavailabilities (AUC) of three phenytoin products in rabbits as well as those in humans were not found. Whereas, there was significant correlation between average AUC of three phenytoin products in humans and those in rabbits (r=0.993, p<0.1). From the results of this experiment, it can be concluded that the bioavailability of phenytoin products in humans may be predicted from the results of the rabbit experiment. Also it is assumed that the prediction of the bioavailability of phenytoin products in humans may be difficult from the only results of in vitro dissolution test.

• 수산해양기술연구
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• 제21권1호
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• pp.28-34
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• 1985

액체식 자기컴퍼스 방위지시부의 제진특성을 인공자장발생장치내에서 수평자장의 세기에 따라, 컴퍼스종류 및 컴퍼스액의 점성계수별로 측정한 결과는 다음과 같다. 1. 컴퍼스종류별 제진특성은, 실험용 컴퍼스(A, B, C, D, E) 모두 수평자장의 세기가 강할수록 주기는 짧으며, 과행각은 커지는 경향을 나타내었다. 2. 실험용 컴퍼스 모두 지자기의 수평자장이 0.39 gauss인 적도부근에 가까울수록 자기컴퍼스 카아드는 비교적 빨리 안정되고, 평균자장이 아주 약한 극지인 0.03 gauss에서는 주기는 45초 이상으로 길어져 불안정하였다. 3. 컴퍼스종류별 제요소를 ISO의 성능기준과 비교한 결과, A컴퍼스가 그 성능이 가장 양호하여, 자침의 자기능률과 카아드의 직경이 자기컴퍼스 방위 지시부의 제진특성에 큰 영향을 미침을 알 수 있었다. 4. 컴퍼스액의 점성계수별 제진특성은 점성계수가 크고 수평자장이 강할수록 진폭은 커지며, 주기는 짧아지는 경향을 나타내었다. 5. 컴퍼스종류별 제진곡선의 주요점까지의 경과시간(t 하(i))은 수평자장(H)의 -0.71승에, 과행각(P 하(i))은 0.22승에 비례하였으며, 컴퍼스액의 점성계수에 따른 제진곡선의 주요점까지의 경과시간(t 하(i))은 수평자장(H)의 -0.80승에, 과행각(P 하(i))은 0.13~1.08승에 비례하였다.