• 한국어병학회지
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• 제23권1호
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• pp.57-67
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• 2010

퀴놀론계 항균제인 nalidixic acid(OA), piromidic acid(PA), oxolinic acid(OA)를 사육수온($13{\pm}1.5^{\circ}C$, $23{\pm}1.5^{\circ}C$)에 따라서 넙치(평균체중 700 g)에 60 mg/kg의 농도로 1회 경구 투여한 다음, 경시적인 혈청내 잔류농도를 분석하였다. 수온이 $23{\pm}1.5^{\circ}C$의 경우, 투여 후 NA는 10시간째 ($11.55{\mu}g/m\ell$), PA는 24시간째($3.79{\mu}g/m\ell$), OA는 30시간째($1.12{\mu}g/m\ell$)에 각각 최대혈중농도에 도달하였다. 수온이 $13{\pm}1.5^{\circ}C$의 경우, 투여 후 NA는 10시간째($6.36{\mu}g/m\ell$), PA는 15시간째($1.4{\mu}g/m\ell$), OA는 30시간째($1.01{\mu}g/m\ell$)에 각각 최대혈중농도에 도달하였다. NA와 PA의 넙치 혈중내 흡수정도는 수온 $13{\pm}1.5^{\circ}C$보다 수온 $23{\pm}1.5^{\circ}C$에서 매우 높게 나타났으며, NA의 넙치 혈중내 소실정도는 수온 $13{\pm}1.5^{\circ}C$보다 수온 $23{\pm}1.5^{\circ}C$에서 두드러지게 빨랐다. 한편 OA의 넙치 혈중내 흡수 및 소실정도는 사육수온에 크게 영향을 받지 않는 것으로 나타났다. NA 및 PA는 one-compartment model, OA는 two-compartment model로 해석하여 WinNonlin program을 이용, 약물동태학적 매개변수(parameter)를 조사하였다. 수온이 $23{\pm}1.5^{\circ}C$의 경우, 혈장농도-시간곡선하 면적(AUC)은 NA, PA, OA가 각각 258.26, 248.12 및 $138.20{\mu}g{\cdot}h/m\ell$, 혈중최고농도의 도달시간($T_{max}$)은 10.67, 21.15 및 23.95 h, 혈중최고농도($C_{max}$)는 8.91, 3.09 및 $1.06{\mu}g/m\ell$로 계산되었다. 수온이 $13{\pm}1.5^{\circ}C$의 경우, AUC는 NA, PA, OA가 각각 341.45, 103.89 및 $159.10{\mu}g{\cdot}h/m\ell$, 혈중최고농도의 도달시간은 7.72, 12.89 및 28.03 h, 혈중최고농도는 6.23, 1.22 및 $1.02{\mu}g/m\ell$로 계산되었다.

• 천문학회지
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• 제31권2호
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• pp.117-125
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• 1998

We have observed the 10-9 transitions of $HC_3N$ and its $^{13}C$ substitutes ($H^{13}CCCN,\;HC^{13}CCN$, and $HCC^{13}CN$), and the vibration ally excited 12-11 ($v_r=1$) $HC_3N$ transition toward the Sgr B2 molecular cloud. The observed $HC_3N$ emission shows an elongated shape around the Principal Cloud ($\~$4.5 pc in R.A. $\times$ 7.4 pc in Decl.). The optically thin $H^{13}CCCN$ line peaks around the (N) core and we derive the total column density $N(H^{13}CCCN) = 4 {\times}10^{13} cm^{-2}$ at this position. Toward the 2' N cloud which shows the peculiar chemistry, the $HC_3N$ lines show enhancements compared to the extended envelope. The shocks of the 2' N may have resulted in the enhancement of $HC_3N$. The hot component of $HC_3N$ is strongly concentrated around the (N) core and its HPW is $\~$0.9 pc in diameter. We derive the lower limit of the abundance ratio $N(HC_3N)/N(H^{13}CCCN)$ to be larger than 40 in most regions except the (M) and (N) cores. The fractionation processes of $^{13}C $at this region may not be as effective as previously reported.

• Bulletin of the Korean Chemical Society
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• 제13권4호
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• pp.375-381
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• 1992

In this study we have synthesized two spiro orthocarbonates, which can be polymerized with volume expansion, and determined their crystal structures. The crystal data are as follows; 3,4,10,11-Di(9,10-dihydro-9,10-ethanoanthracenyl)- 1,6,8,13-tetraoxa-6.6-tridecane 5: a = 16.898 (1), b = 9.299 (1), c = 24.359 (2) ${\AA}$, $\beta$ = 123.73 $(7)^{\circ}$, space group P21/c and R = 0.073 for 2954 reflections; compound 8: a = 15.244 (4), b = 15.293 (3), c = 10.772 (3) $\AA$, ${\beta}$ = 99.45 $(2)^{\circ}$, space group P21/c and R = 0.082 for 2346 reflections. The seven-membered rings of compound 5 are chair forms and all the six-membered rings are boat shaped. For a six-membered spiro orthocarbonate, 3,9-Di(9-fluorenylidenyl)-1,4,6,9-tetraoxa-5,5-und ecane 8, fluorene groups [C(1) atom through C(13) atom] are planar within ${\pm}0.09{\AA}$ and the six-membered rings have chair conformations. The whole molecule has pseudo-C2 symmetry. The water molecules in the crystal are linked with each other through the hydrogen bond with distance of 2.790 (20) ${\AA}$.

• 한국광학회지
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• 제14권6호
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• pp.674-679
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• 2003

본 연구에서는 C-밴드와 L-밴드 파장(1525 nm-1625 nm)에서 파장 변화가 가능한 광섬유 링 레이저를 제작하고, 이를 이용하여 아세틸렌 분자 전이선에 대한 분광연구를 수행하였다. 제작된 광섬유 링 레이저는 공진기 내부에 FFP-TF(Fiber Fabry-Perot Tunable Filter)를 이용하여 약 102 nm(1510.4-1612.6 nm)의 범위에서 파장을 연속 가변할 수 있었다. 광섬유 링 레이저의 파장가변특성을 이용하여 C-밴드(1525-1565 nm)에서 흡수선이 많은 아세틸렌($^{13}$C$_2$H$_2$)분자에서 50개 이상의 전이선에 대하여 높은 신호대 잡음비를 갖는 흡수 스펙트럼을 측정하였다.

• Biomolecules & Therapeutics
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• 제6권4호
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• pp.406-411
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• 1998

The pre-mixed $_{13}C$-urea powder preparation in ${Helikit}_{TM}$ for test of Helicobacter pylori was evaluated for pharmacological properties. The oral doses of the preparation used in mice were 30-fold as compared to human doses. The results obtained in the present study demonstrate that spontaneous movement, hexobarbital-induced hypnosis, rotarod performance, body temperature, acetic acid-induced writhing syndrome, chemical and electroshock convulsion, pupil size and intestinal propulsion had not been affected at the oral doses of 230, 700 and 2100 mg/kg in mice. The blood pressure was slightly elevated as given intravenously in rats at a dose of 5 mg/kg of the preparation, but respiration was not influenced at the dose. In isolated guinea pig ileum and rat fundus preparation, the preparation at a concentration of $1{\times}10^{4}$ g/ml neither caused any direct effect nor inhibited the contraction produced by acetylcholine, histamine or 5-hydroxytryptamine. These results reported here provide evidence that pre-mixed $^{13}C$ 13/C-urea powder preparation is free of general pharmacological properties performed in oral administration.

• Bulletin of the Korean Chemical Society
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• 제19권8호
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• pp.847-851
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• 1998

13C, 15N, and 29Si NMR chemical shifts have been computed for selected X-substituted silatranes (X=Cl, F, H, CH3) using Gauge-Including Atomic Orbitals (GIAO) and Continuous Set of Gauge Transformations (CSGT) at the Hartree-Fock level of theory. The isotropic 13C chemical shifts are largely insensitive to substituent-induced structural changes. In this study, the isotropic 13C chemical shifts GIAO and CSGT calculations at the HF/6-31G and HF/6-31G* levels are sufficiently accurate to aid in experimental peak assignments. The isotropic 13C chemical shifts X-substituted silatranes at HF/6-31G* level are approximately 4 ppm different from the experimental values. In contrast, the isotropic 15N and 29Si chemical shifts and the chemical shielding tensors are quite sensitive to substituent-induced structural changes. These trends are consistent with those of the experiment. The 15N chemical shift parameters demonstrate a very clear correlation with Si-N distance, especially when we use the polarization function. Changes in anisotropy, 3a as well as in the 15N isotropic chemical shifts are due primarily to changes in the value of a.. But in case of "Si the correlations are not as clean as for the 15N chemical shift.

• Communications for Statistical Applications and Methods
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• 제13권1호
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• pp.135-140
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• 2006

The paper by Paik (1985) introduced a structural property of the designs which was related to the concordance matrix $NN^{t}$ of the design. This special property was termed Property-C. The designs which have Property-C need not calculation of the generalize inverse of C matrix for solution of reduced normal equation. Paik also mentioned that some block designs belong to Property-C. This paper show the Extended Group Divisible designs defined by Hinkelmann (1964) are included in Property-C.

• 약학회지
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• 제32권3호
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• pp.164-169
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• 1988

$^{13}C$ NMR chemical shifts for 18 ${\alpha}-susbstituted$ toluenes at high dilution in $CCl_4$ solution have been determined. Substituents are as follows: H, Me, Et, n-Pr, iso-Pr, Ph, F, Cl, Br, $NH_2$, NHMe, $NMe_2$, OH, OMe, OCOMe, $CO_2Me$, $CO_2Et$, CN. Those chemical shifts of the methylene carbon of the toluene and the ${\alpha}-carbon$ of the n-butane systems are correlated well. (r=.975, slope=.962)

• 생약학회지
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• 제8권1호
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• pp.23-29
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• 1977

The $^{13}C-chemical\;shifts$ of the phenolic coumarine derivatives, aesculetin, daphnetin and herniarin were studied on the basis of my previous report. All spectral data found in this report could be utilized to the structure elucidation of the unknown phenolic coumarine derivatives and other phenolic compounds. In addition, it is suggested that a long range coupling may occur in the following structure as represented by arrow.

• Journal of Ginseng Research
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• 제19권1호
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• pp.45-50
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• 1995

(20S)- and (20R)-protopanaxadiol were prepared from crude ginseng saponin by chemical treatment. The $^{1}H$- and $^{13}C$-NMR signals of these compounds were fully assigned by various NMR techniques such as DEPT, 1H-1H COSY, HMQC, HMBC and NOESY.