• YAKHAK HOEJI
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• v.37 no.4
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• pp.362-364
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• 1993

The sensitive detection of free fatty acids was investigated by using H$_{2}$O$_{2}$-bis(2,4,6-trichlorophenyl) oxalate chemiluminescence system after monodansyl cadaverine labeling. Because dansvl moiety is well excited by this chemiluminescence system, monodansyl cadaverine was a prominent reagent to this system for the determination of free fatty acids. The cluent of 50mM tris-HCI buffer (pH 7.7)-acetonitrile (1:4, v/v) was run through TSK gel ODS 80 TM column. The reagent solutions were mixed with the eluent containing the monodansyl cadaverine derivative of fatty acids from the column. By this system, linolic acid was detected 50 fmol by injected amount.

• Proceedings of the Korean Information Science Society Conference
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• 2006.06b
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• pp.91-93
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• 2006

사이버커뮤니티의 발전상은 까페, 싸이, 블로그, 휴대폰 등의 형태로 개체화와 나열형 정보에 주력되어, 정보홍수로 인한 역설적 정보빈곤의 부작용 또한 커지고 있다. 이에 본 논문에서는 나열형 정보의 단점을 극복할 수 있는 공유형 정보의 구현방안으로서, '의미소개체화 기반 게임형토론시스템'을 제안한다. 기존에 나열형 정보의 대안이자 웹 2.0의 모델로 주목받아온 위키(wiki)방식의 원론적 공유에서 나아가, 구성개체 간 상호평가가 수치로 교환되고 그에 따른 가중치가 활용되는 방안이다. 이는 시맨틱 웹과 웹2.0의 통합적 논의이며, 인터넷의 자연스런 발전방향이다. 이 시스템이 구현된 인터넷(Internet)을 포럼넷(Forumnet)이라 부를 수 있다. 포럼넷은 현실적, 기술적으로 개인기반평가에서 개체기반평가로 구현되어갈 것이다.

• Journal of Pharmaceutical Investigation
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• v.20 no.2
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• pp.73-78
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• 1990

A sensitive fluorometric method using 9-fluorenylmethyl pentafluorophenyl carbonate (FMPC) as the fluorescent labeling agent was developed to determine D-penicillamine (D-PA). The fluorophore had excitation and emission wavelengths of 260 nm and 313 nm, respectively. After derivatization, the fluorescent product was separated, and quantified by spectrofluorometry. The derivative was highly fluorescent and stable. Optimum condition for the reaction was investigated. A linear response was obtained over the range of $4.0{\times}10^{-7}-5.0{\times}10{-6}\;M$ with the correlation coefficient of 0.999 (n=6). The procedure described was successfully applied to the determination of the dosage forms of capsule with the recovery of $98.62{\pm}0.57%$ (150 mg), $98.36{\pm}0.57%$, (250 mg).

• Korean Journal of Materials Research
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• v.8 no.4
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• pp.362-367
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• 1998

Mg-6Zn-2Cu 및 Mg-6Zn-1.5Si(wt%)합금의 미세조직 및 석출거동을 조사하였다. 합금은 $4 x 10^{-4}$ 의 진공분위기에서 제조하였고 용체화처리는 $435^{\circ}C$에서 8시간 행하였다. Mg-6Zn합금에 1.5wt.%Si를 첨가한 합금에서는 입계 및 입내에 $10\mu\textrm{m}$-2$\mu\textrm{m}$크기의 구형의 $MgZn_{2}$와 $Mg_{2}$Si상이 존재한다. 시효경화거동은 용체화처리된 Mg-6Zn-2Cu 및 Mg-6Zn-1.5Si합금에서 조사되었다. 결정립 미세화에 의한 경도증가효과는 Mg-6Zn-2Cu합금계에서 크게 나타났으나, 시효에 의한 경도증가효과는 Mg-Zn-Si합금계에서 크게 나타났다. 시효처리 후 생성된 석출상들은 투과전자현미경 분석결과 Mg-6Zn-2Cu합금에서는$ Mg_{2}$$Zn_{3}$이었고 Mg-6Zn-1.5Si 합금에서는 $Mg_{2}$$Zn_{11}$ /이었다.

• Proceedings of the Korea Society for Energy Engineering kosee Conference
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• 1999.05a
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• pp.159-164
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• 1999

PTC (Positive Temperature Coefficient of Resistivity) 소자는 티탄산 바륨 (barium titanate) 계열의 페로브스카이트 (perovskite) 구조를 가지는 물질을 반도체화시켰을 때 큐리온도 부근에서 저항이 1,000배 이상 증가하는 물질을 가리킨다. 처음에는 BaTiO$_3$를 대상으로 12$0^{\circ}C$ 부근에서 발생하는 PTC 현상을 연구하였으나, BaTiO$_3$에 SrTiO$_3$, PbTiO$_3$를 첨가하면, 큐리온도를 낮출 수도 있고, 높일 수도 있어서 PTC 소자의 사용 영역이 넓어졌다. PTC 소자의 응용분야는 1) 천연색 텔레비젼 수상기와 모니터에 사용하는 degausser와 같은 스위칭 소자, 2) 냉장고용 컴프레서등에 사용되는 모터 기동용 소자, 3) 자동차 연료조기증발용 히타와 같은 세라믹 히타 소자로 크게 구분된다.(중략)

• YAKHAK HOEJI
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• v.41 no.4
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• pp.414-420
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• 1997

A rapid and sensitive high performance liquid chromatographic method with UV detection for the analysis of polyamines(putrescine, spermidine, spermine) has been developed. The benzoyl chloride derivatives of putrescine, spermidine and spermine are separated on a mc-Bondapak C18 reverse-phase column with 50% methanol as the mobile phase. This method was applied to the analysis of polyamines in the serum of normal human and uterine cancer patients. The results show that the mean level of polyamines in cancer patients serum is much higher than that in normal human serum.

• Korean Journal of Food Science and Technology
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• v.45 no.5
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• pp.537-544
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• 2013

This study was performed to establish method of simultaneous determination of fructose, glucose, and sucrose in honey and commercial vitamin drinks by GC and GC/MS. Optimum chromatographic separation of trimethylsilyl-oxime (TMSO) derivatives by GC was achieved on a DB-5 column. Calibration curves for fructose, glucose and sucrose TMSO derivatives by GC were linear in the range of 50-5000 ${\mu}g/mL$, and their $r^2$ values were 0.9999, The limit of detection and limit of quantification of fructose, glucose, and sucrose were 0.68, 0.47, and 0.53 ${\mu}g/mL$, respectively, and 2.27, 1.58, and 1.77 ${\mu}g/mL$, respectively. Average recoveries of fructose, glucose, and sucrose were 100.5, 101.0, and 99.7%, respectively. When the method was applied to 12 honey samples, the average concentrations of fructose, glucose and sucrose were $42.58{\pm}1.97%$, $27.74{\pm}1.16%$, and $0.79{\pm}0.52%$, respectively. The F/G ratio was $1.53{\pm}0.07$. For fructose and glucose contents, results from the GC analysis were similar to those from the HPLC analysis, but the sucrose content was different for each analysis method. We suggest that the GC method is more suitable than other official analytical methods for simultaneous determination of fructose, glucose, and sucrose in honey.

• Analytical Science and Technology
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• v.29 no.1
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• pp.49-55
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• 2016

A ketone body (acetoacetic acid, β-hydroxybutyric acid, and acetone) increases from blood or urine when bio-energy dependence pays more fatty acid than glucose. However, in case oxidation of fat is greater than the capacity of the citric acid cycle the fatty acid oxidation is made from acetoacetyl CoA to acetoacetate then, again form β-hydroxyburytic acid to acetone, the diffusion take place into the blood. Enzymes that oxidize ketone body in the brain and nerve tissue blood ketone dody is increased during prolonged fasting, brain used it as energy. In this study, we developed the rapid two step derivatization method for sensitive detection of the ketone body by GC-MS/SIM. The plasma was deproteinized and then the hydroxy and carboxyl groups of ketone body are subjected to extraction and drying then, keto-group were derivatized with hydoxylamine at 60℃ for 30 min for oximation. Then it was trimetyl-silylated with BSTFA at 80℃ for 30 min and analyzed using a GC-MS. The linear ranges were in between 0.001 μg/mL and 250 μg/mL for β-hydroxy butyrate, and acetoacetate. The method detection limits were below 0.1 pg over each target compound determined. The mean recoveries (%) of target compounds were ranged from 88.2 % to 92.3 % at 1 µg/mL, from 89.5 % to 94.8 % at 10 μg/mL, with RSD of 6.3-9.4 %. This method could be applied to quantification of ketone bodies which are seen in the keto-acidosis in children and adults from a variety of diseases that cause ketones in the blood and urine.

• Journal of the Economic Geographical Society of Korea
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• v.6 no.1
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• pp.61-77
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• 2003

Finns are central economic agents that play an important role in systems of innovation as they take responsibility for generating and diffusing knowledge in both organizational and societal context. They must be considered as learning organizations which interact with other finns and institutions that share their environment. The systems of innovation literature accentuates institutional conditions that influence innovation in sectoral, regional or national levels. Meanwhile, it tends to ignore the complex dimensions of finn practices in relation to learning and innovation activities. In this context, this paper attempts to examine what finns do for sustaining innovation and how they learn to innovate. This is not just critical to know individual finns innovativeness which depends on interactions with environments within and outside the organizational boundary but also to evaluate the regional innovation system potential. In short, it is important to see that finns would attempt to take advantage of distributed knowledge within and across the boundaries of the finn without sticking to particular regional innovation systems. I argue that the more finns of a cluster attempt not only to combine localized sources of knowledge and external sources of knowledge but also to become a learning organization, the more increased regional innovation system potentials can be.

• Journal of Food Hygiene and Safety
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• v.8 no.1
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• pp.9-15
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• 1993

In an attempt to quantitate and qualitate residual antibiotics and antibacterial agents in meat simultaneously, we studied a gas chromatography-mass spectrometry(GC/M8) analysis. For a simultaneous analysis of penicillin G, chloramphenicol and thiamphenicol in meat, a simple and rapid clean-up procedure including extraction with 0.01 M EDTA-2Na Mcilvaine buffer (pH 4.0), defatting with n-hexane, and elution with 0.01M-methanolic oxalic acid from Bond Elute $C_{18}$ cartridge, and quantitation by selected ion monitoring (SIM) mode after derivatization was performed. The recoveries (%) of penicillin G, chloramphenicol and thiamphenicol (CV, %) at 1 ppm fortification level were 63.5 (7.6), 76.3 (8.1) and 84.7 (2.0), and the detection limits of those were 0.6, 0.085 and $0.084\;\mu\textrm{g}$ beef, respectively. This method using 81M mode allows excellent detection and quantitation of residual antibiotics and antibacterial agents in meat. Moreover, confirmation by a full scan electron impact mass spectrum is possible if residual level in the sample in above 1 ppm.