• Bulletin of the Korean Chemical Society
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• 제27권7호
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• pp.1067-1070
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• 2006

• 분석과학
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• 제26권6호
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• pp.353-356
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• 2013

A method on the determination of caffeine in beverage with acridiene orange-${\beta}$-cyclodextrin (CD) inclusion complex was developed. The conditions such as pH of the sample solution and concentration of acridine orange and ${\beta}$-CD were optimized to 12.0(${\pm}0.5$), $1.9{\times}10^{-6}M$ and $1.25{\times}10^{-3}M$, respectively. Under these optimum conditions, the calibration curve of caffeine was obtained over concentration range of $5{\times}10^{-5}{\sim}1.1{\times}10^{-3}M$. The detection limit was $1.0{\times}10^{-5}M$. The relative errors(%) in beverage samples were less than 5.0%.

• Bulletin of the Korean Chemical Society
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• 제30권12호
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• pp.3034-3038
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• 2009

A simple, rapid, practical and sensitive spectofluorimetric method was developed for the determination of trace amount of heparin (Hep). Under the Optimum conditions, we studied the interaction between NFLX-Ce$^{3+}$-Hep complex by using absorption and fluorescence spectra. It was observed that Hep remarkably enhance the fluorescence intensity of the NFLX-Ce$^{3+}$ complex at ${\lambda}$= 356 nm in the buffer solution of pH = 7.60 and the enhancement effect is shown to relate with the concentration of Hep. The linear range and detection limit for the determination of Hep was obtained. By the Rosenthal graphic method, the association constant (K) and binding numbers (N) of Hep with probe were investigated. This method is relatively free of interference from coexisting substances and successfully applied for the determination of heparin in heparin sodium injection samples. A suitable mechanism of fluorescence enhancement between NFLX-Ce$^{3+}$ and the NFLX-Ce$^{3+}$-Hep systems were proposed and discussed.

• 분석과학
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• 제10권6호
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• pp.433-438
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• 1997

Triton X-100 계면할성제 존재하에서, $Eu^{3+}$-thenoyltrifluoroacetone(TTA)계의 형광세기의 n-octanol 영향에 관해 연구하였고, n-octanol의 정량을 위한 최적 조건을 규명하였다. 이 착물계에서 들뜨기 파장을 345nm로 주사했을 때, $Eu^{3+}$ 이온의 최대 형광파장은 619nm에서 나타났다. n-octanol의 검정곡선은 $1{\times}10^{-5}M{\sim}1{\times}10^{-7}M$의 범위에서 직선적인 관계를 얻었고, 검출한계는 $1{\times}10^{-9}M$이었다. 이 방법을 이용하여 합성시료를 분석한 결과 분석오차내에서 기지값과 일치하였으며, 상대표준편차는 약 3.5%였다.

• Bulletin of the Korean Chemical Society
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• 제33권9호
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• pp.3055-3060
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• 2012

A simple, rapid and sensitive spectrofluorometric method was developed for the determination of folic acid (FA), based on its quenching effect on the fluorescence intensity of enoxacin (ENX)-europium ($Eu^{3+}$) complex as a fluorescent probe. Fluorometric interaction between ENX-$Eu^{3+}$ complex and FA was studied using UV-visible and fluorescence spectroscopy. The quenched fluorescence intensity at an emission wavelength of 614 nm was proportional to the concentration of FA. Optimum conditions for the determination of FA were investigated. Under optimal conditions, the reduced fluorescence intensity at 614 nm was responded linearly with the concentration of FA. The linearity was maintained in the range of $1.25{\times}10^{-9}$ to $1.50{\times}10^{-7}$ M (R = 0.9986) with the limit of detection ($3S_b/m$) (where $S_b$ is the standard deviation of blank and m is the slop of linear calibration curve) of $6.94{\times}10^{-10}$ M. The relative standard deviation (RSD) for 9 repeated measurements of $1.0{\times}10^{-9}$ M FA was 1.42%. This method was simple, cost effective, and relatively free of interference from coexisting substances. Successful determinations of FA in pharmaceutical formulation and biological samples with the developed method were demonstrated.

• 한국대기환경학회지
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• 제5권2호
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• pp.12-20
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• 1989

Distribution of benzo(a)pyrene (BaP) in Seoul surface soils was investigated with a simple micro-analytical method consisting of ultrasonic extraction, one-dimensional dual band thin-layer chromatographic separation (TLC) and spectrofluorometric determination. The TLC was done in the following condition: thin-layer plate; Kieselguhr G/Acetylated cellulose, Developer; 1st; ether, 2nd; methanol-ether-water (4:4:1, V/V). The results thus obtained were as follows; 1. All the samples collected from various areas were contained detectable amount of benzo(a)pyrene. The range and average of benzo(a)pyrene contents in Seoul areas are 0.20 $\sim$5.90ppm and 1.01 ppm, respectively. 2. Benzo(a)pyrene contents in soils obtained from commercial areas were much higher than those in industrial and residential areas. The contents range in commercial, industrial, and residential areas are 0.31 $\sim$ 5.90 ppm, 0.36 $\sim$ 1.22 ppm and 0.20 $\sim$ 0.67 ppm, respectively. 3. Benzo(a)pyrene contents in soils from major roads were far higher than those from side or park roads. The ranges of benzo(a)pyrene contents in major, park and side road are 0.40 $\sim$ 5.9 ppm, 0.20 $\sim$ 0.70 ppm, 0.31 $\sim$ 1.30 ppm, respectively. These findings suggest strongly that surface soils in Seoul city are polluted by benzo(a)pyrene probably emitted automobiles.

• Nuclear Engineering and Technology
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• 제15권2호
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• pp.142-148
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• 1983

핵급물질에 함유된 미량 희토류윈소인 Sm, Eu, Gd, Dy를 개별 분리하기 위해 Dowex50W$\times$8 양이온교환수지와 $\alpha$-hydroxyisobutyric acid ($\alpha$-HIBA) 사이에서 분배계수를 측정하였다. 양이온교환수지를 이용하여 우라늄매질로부터 미량희토류원소를 군분리한 후 0.40M$\alpha$-HIBA용리액의 pH를 3.40에서 3.60까지 변화시키면서 개별분리하였다. Sm, Eu, Dy은 형광분석법으로 Gd은 비색법으로 정량하였으며 실험결과를 토대로하여 magnesium diuranate(yellow cake) 중의 Sm, Eu, Gd, Dy를 각각 정량하였다

• Journal of Pharmaceutical Investigation
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• 제32권2호
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• pp.119-125
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• 2002

A rapid, selective and reproducible high-performance liquid chromatographic method has been developed for the determination of terazocin in human plasma. Terazocin plus the internal standard, prazocin hydrochloride, were extracted from alkalified plasma with tert-butylmethyl ether, back-extracted into 0.05% phosphoric acid. Fifty ${\mu}l-portions$ of extract were injected onto a octadecylsilane column and eluted with a mixture of acetonitrile, water and triethylamine (30 : 70 : 0.1 v/v, adjusted to pH 5.0 with dilute phosphoric acid) at a flow rate of 1.0 ml/min. The fluorescence intensity of column eluents was monitored at excitation wavelength of 250 nm and emission wavelength of 370 nm. No interference peaks were observed. The practical limit of quantitation was 5 ng/ml for terazocin. The average intraday and interday coefficients of variation were 4.15 and 3.54%, respectively. Also intraday and interday precisions over the range $5{\sim}60\;ng/ml$ were $0.49{\sim}2.92\;and\;0.38{\sim}5.12%$, respectively. The bioequivalence of two terazosin tablets, the $Hytrine^{\circledR}$ (Il Yang Pharmaceutical Co., Ltd.) and the $Teratonin^{\circledR}$ (Sam-A Pharmaceutical Co., Ltd.), was evaluated according to the guideline of Korea Food and Drug Administration (KFDA). Sixteen healthy male volunteers $(24.6{\pm}2.0\;years\;old)$ were divided into two groups and a randomized $2{\times}2$ cross-over study was employed. After one tablet containing 2 mg of terazosin was orally administered, blood was taken at predetermined time intervals and the concentration of terazosin in plasma was determined with a HPLC method using spectrofluorometric detector. AUC was calculated by the linear trapezoidal method. $C_{max}\;and\;T_{max}$ were compiled from the plasma drug concentration-time data. Analysis of variance (ANOVA) was utilized for the statistical analysis of the parameters. The results showed that the differences in $AUC_t,\;C_{max}\;and\;T_{max}$ between the two preparations were 0.21 %, 5.53% and 8.82%, respectively. The powers $(1-{\beta})\;for\;AUC_t,\;C_{max}\;and\;T_{max}$ were >99%, 97.49%, and 33.26%, respectively. Minimum detectable differences $({\Delta},\;%)\;at\;{\alpha}=0.1\;and\;1-{\beta}=0.8$ and the 90% confidence intervals were all less than ${\pm}20%$ except for $T_{max}.\;AUC_t\;and\;C_{max}$ met the criteria of KDFA for bioequivalence, indicating that $Teratonin^{circledR}$ tablets are bioequivalent to $Hytrine^{circledR}$ tablets.