• 보존과학회지
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• 제31권3호
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• pp.299-308
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• 2015

본 연구는 1996년 천안시 유량동에서 출토된 분홍색 단령의 염료 동정을 통해 조선시대에 사용된 적색 염료를 실증하기 위한 것이다. 이를 위해 유물에 사용된 염료를 추출하고 이것을 당시 염색에 사용되었을 것으로 추정되는 적색계 염료(홍화, 소목, 꼭두서니)에서 추출한 염료와 함께 고성능액체크로마토그래피분석을 실시하였다. 그 결과 유물에서 추출한 염료와 홍화염색포의 추출 염료는 같은 시간대인 17.5분에서 피크가 나타났다. 이때 자외/가시선 분광 분석 결과는 두 시료 모두 519nm에서 최대흡수파장이 나타나 기존 홍화의 홍색소 분석 결과와 같은 것으로 조사되었다. 또한 negative ion mode에서 질량분석을 실시한 결과 유물과 홍화 염색포에서 추출한 염료 시료는 carthamin의 분자량인 910을 나타내는 m/z 909에서 같은 시간대의 피크가 확인되었다. 이와 같은 결과로 이 분홍 단령 직물을 염색하는데 사용된 염재는 홍화인 것으로 동정되었다.

• 한국대기환경학회지
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• 제5권1호
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• pp.68-78
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• 1989

The heavy metal of suspended particulates with human health has long been studied in environmental interest concerned. This study was intended to identify harmful heavy metals of the ambient air borne dusts which were related with the respirable sizes in the aerodynamics. Two sampling sites were selected comparatively; one was in the Shinchon area, which is the commercial district with heavy traffic and the other site was in the Bulgwang area which is residential area. The supended particulates were sampled by high volume air sample with 6 cascade impactor stages. The heavy metals in terms of As, Cd, Cr, Cu, Fe, Hg, Mn, Ni, Pb, Se, V and Zn were determined by stomic absorption spectrometry or inductively coupled plasma emission spectrometry. The samples weretaken bimothly for seven consecutive days from May 1987 to March 1988. The annual average concentration of the respirable suspended dust of which diameter is less than 10$\mum$ was 152.59 $\mug/m^3$ of the Shinchon air samples; the respirable dust was equivalent to approximately 85% of the total suspended particulates. The annual average concentration of the respirable suspended dust of the Bulgwang air samples was 112.56 $\mug/m^3$; that was approximately 86% of the total suspended particulates. The concentration of heavy metals was investigated in relation to the particle size. The concentration of Cr, Fe, Mn and V were tended to be much more in the coarse particles than in the fine particles. Cd and Pb in the fine particles were more than in the coarse particles. In the partial correlation coefficients; in the Shinchon area, high correlations among Fe, Se and Mn were determined; it is assumed that those sources would be originated from coal, gasolineand diesel. In Bulgwang area, would be high correlation among Fe, Se, Hg and Mn considered to be originated from coal, Bunker-C and heavy oil as well. From the above results, the hazardous heavy merals in air should be measured and controlled in originally their sources.

• Mass Spectrometry Letters
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• 제7권4호
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• pp.106-110
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• 2016

Ginseng, a traditional herbal drug, has been used in Eastern Asia for more than 2000 years. Various ginsenosides, which are the major bioactive components of ginseng products, have been shown to exert numerous beneficial effects on the human body when co-administered with drugs. However, this may give rise to ginsenoside-drug interactions, which is an important research consideration. In this study, acassette assay was performed the inhibitory effects of 12 ginsenosides on seven cytochrome P450 (CYP) isoforms in human liver microsomes (HLMs) using LC-MS/MS to predict the herb-drug interaction. After incubation of the 12 ginsenosides with seven cocktail CYP probes, the generated specific metabolites were quantified by LC-MS/MS to determine their activities. Ginsenoside Rb1 and F2 showed strong selective inhibitory effect on CYP2C9-catalyzed diclofenac 4'-hydroxylation and CYP2B6-catalyzed bupropion hydroxylation, respectively. Ginsenosides Rd showed weak inhibitory effect on the activities of CYP2B6, 2C9, 2C19, 2D6, 3A4, and compound K, while ginsenoside Rg3 showed weak inhibitory effects on CYP2B6. Other ginsenosides, Rc, Rf, Rg1, Rh1, Rf, and Re did not show significant inhibitory effects on the activities of the seven CYPs in HLM. Owing to the poor absorption of ginsenosides after oral administration in vivo, ginsenosides may not have significant side effects caused by interaction with other drugs.

• 보존과학회지
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• 제12권1호
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• pp.1-14
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• 2003

조선시대 관요가 위치한 경기도 광주의 백자에 대한 화학적인 특성을 살펴보기 위하여 백자요지에서 출토된 백자를 대상으로 X-선 회절 분석, 유도결합 플라즈마 원자방출 분광분석, 에너지분산 X-선 분광분석의 자연과학적인 방법을 이용하여 연구하였다. 백자요지에서 출토된 백자는 출토된 유구에 관계없이 유사한 태토로 제조되었으며, 태토의 제조에는 광물학적으로 같은 계통의 원료로 장석광물이 사용되지 않은 점이 특징적이다. 폐기물의 퇴적 1에서 출토된 백자는 백자요지의 다른 유구에서 출토된 백자와는 $Fe_2O_3$를 포함한 태토의 조성 및 광물학적인 특성에 차이가 있었다. 폐기물의 퇴적 떼서는 백자요지의 다른 유구와 성격을 달리하는 유물이 출토되었다는 발굴조사의 결과와 백자의 과학적인 분석결과와 일치하였다. 백자에는 유약성분의 특성상 라임계열과 알칼리-라임계열의 유약이 사용되었으며, 전반적으로 유약조성의 범위는 넓었다.

• Journal of Pharmaceutical Investigation
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• 제39권5호
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• pp.321-325
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• 2009

5-HT$_{2C}$ receptors have been considered as therapeutic targets for the treatment of various central nervous system disorders such as depression, anxiety, epilepsy, schizophrenia and sleep disorders. We chemically synthesized KKHQ80114 (K14) and KKHQ80109 (K09), selective 5-HT$_{2C}$ agonists, with the purpose of developing therapeutic agents for the treatment of obesity. The objective of this work is to investigate analytical methods of these compounds in the plasma and urine of rats by gas chromatography/mass spectrometry. In this experiment, K14 was determined in plasma and urine by using K09 as internal standard. Calibration curves give a good linearity in plasma (r$^2$=0.9993) and urine (r$^2$=0.9988). Among hexane, ethyl acetate and diethyl ether, the highest peak was observed in diethyl ether. However, ethyl acetate was used since more interfering peaks were observed with diethyl ether. Inter-day precision and accuracy were determined in the ranges of 50-500 ng/mL for plasma and 10-500 ng/ml for urine. Quantitation limits were 50 ng/mL plasma and 25 ng/ mL urine. These data may be applicable for further studies of these compounds including absorption and metabolism due to no pharmacokinetic or analytical data available.

• 한국재료학회지
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• 제23권1호
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• pp.7-12
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• 2013

The $Cu_2ZnSnS_4$ (CZTS) thin film solar cell is a candidate next generation thin film solar cell. For the application of an absorption layer in solar cells, CZTS thin films were deposited by pulsed laser deposition (PLD) at substrate temperature of $300^{\circ}C$ without post annealing process. Deposition time was carefully adjusted as the main experimental variable. Regardless of deposition time, single phase CZTS thin films are obtained with no existence of secondary phases. Irregularly-shaped grains are densely formed on the surface of CZTS thin films. With increasing deposition time, the grain size increases and the thickness of the CZTS thin films increases from 0.16 to $1{\mu}m$. The variation of the surface morphology and thickness of the CZTS thin films depends on the deposition time. The stoichiometry of all CZTS thin films shows a Cu-rich and S-poor state. Sn content gradually increases as deposition time increases. Secondary ion mass spectrometry was carried out to evaluate the elemental depth distribution in CZTS thin films. The optimal deposition time to grow CZTS thin films is 150 min. In this study, we show the effect of deposition time on the structural properties of CZTS thin film deposited on soda lime glass (SLG) substrate using PLD. We present a comprehensive evaluation of CZTS thin films.

• 한국환경보건학회지
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• 제45권6호
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• pp.594-604
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• 2019

Objectives: This study developed and validated an analysis method of urinary metals and metalloids that can be applied inductively with coupled plasma mass spectrometry (ICP-MS). Methods: 0.3 mL of urine was used to analyze 25 metal and metalloid compounds using ICP-MS. The validation of the analytical method included linearity, accuracy, precision, and the calculation of detection limits. In addition, a comparison test was performed with the graphite furnace atomic absorption spectrometry (GF-AAS) method, which is the current standard method, with urine samples of 66 healthy subjects. Results: The linearities (R²) of calibration curves of all 25 compounds were ≥ 0.999. Of the 25 compounds, the intra-day and inter-day accuracy% of 17 and 20 met ≤15%, respectively. In addition, fifteen compounds showed ≤15% recovery% for certificated reference materials. Intraclass correlation coefficients of the comparison between the current methods and new methods in this study were 0.952 (p-value<0.001) and 0.911 (p-value<0.001) for urinary cadmium and mercury, respectively. Conclusion: This study proposes an efficient simultaneous methodology that can analyze multi elements in smaller sample amounts. More reproduction experiments are needed in the future.

• 분석과학
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• 제18권5호
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• pp.396-402
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• 2005

수소화물 발생법-원자흡수 분광계를 이용한 무기비소의 분석 시 예비환원제로써 L-Cysteine, KI, $FeSO_4$의 최적 조건을 찾고자 하였으며, 이들이 분석에 미치는 영향을 서로 비교 연구하였다. 이와 더불어 $H_2SO_4$-trap에 의하여 시료 중 공존 가능성이 있는 유기비소인 MMA(monomethylarsonate)와 DMA(dimethylarsinate)를 제거하여 무기비소만을 분리 분석하였다. 1.8 M 염산과 0.08 M 질산의 혼합산에서 비소 표준용액 20 ppb는 산을 넣지 않았을 때보다도, 높은 흡광도를 나타내었다. L-Cysteine의 경우 0.5 g 정도를 취하고 약 0.07 M의 질산이나 염산의 약 산성 조건에서 30 분 이상을 반응시켰을 경우에 완전히 As(V)는 As(III)로 환원되었다. KI의 경우, 3 g 정도를 취하고 약 0.8 M의 질산 조건에서 1시간 이상 반응시켰을 경우에 완전히 As(V)는 As(III)로 환원되었다. $FeSO_4$의 경우에는, 다른 예비환원제와 비교하여 NaBH4와 $Fe^{2+}$의 반응으로 인한 침전물의 생성으로 튜브내부가 막히게 되어, As(V)가 As(III)로 환원되는 효율의 재현성이 없었다. 분석결과의 정확도를 확인하기 위하여, NIST SRM 1643C Trace Elements in Water ($82.1{\pm}1.2ng/mL$)를 사용하였으며 그 결과는 KI를 예비환원제로 사용하였을 경우에는 97.5%의 회수율이고 L-Cysteine를 예비환원제로 사용하였을 경우에는 101.9%의 회수율로서 두 경우 모두 만족할 만한 수준이였다.

• 대한화학회지
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• 제44권3호
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• pp.212-219
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• 2000

산성조건에서 HCr$O_4^-$이온과 $H_2O_2$사이의 산화-환원반응의 생성물인 $CrO(O_2)_2$의흡광도의 측정에 근거를 두어 개발된 흡수분광분석법에 FIA기법을 접목하여 $Cr_2O_7^{2-}$이온과 Mn$O_4^-$이온을 함유하는 혼합시료에 대한 새로운 분석법을 개발하였다. 새로운 분석법은 혼합물 시료의 분석과정에서 두 번에 걸친 주입분석을 수행해야 하고 $Cr_2O_7^{2-}$이온의 분석에 앞서 Mn$O_4^-$이온의 제거를 위한 별도의 작업을 선행해야 한다는 번거로움을 내포하지만, 두 가지의 분석파장들을 사용해야 하는 기존의 흡수분광분석법에 비해 단일분석파장(570 nm)를 사용할 수 있다는 장점을 가진다. 또한, 새로운 분석법은 주어진 분석파장(570 nm)에서 넓은 농도범위($Cr_2O_7^{2-}$이온:$2.0{\times}10^{-6}$M∼$8.0 {\times}10^{-3}$M,Mn$O_4^-$이온:$2.0{\times}10^{-6}$M∼$4.0{\times}10^{-3}$M)에 걸쳐 Beer의 법칙을 정확히 따르는 검정선의 작성이 가능하다는 점에 있어서 기존의 흡수분광분석법에 비해 $Cr_2O_7^{2-}$이온과 Mn$O_4^-$이온의 분석의 용이성을 더욱 증대시킬 수 있다는 장점도 가진다.

• 대한수의학회지
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• 제24권2호
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• pp.149-162
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• 1984

The research was conducted(1) to confirm the agent(s) responsible for the antimicrobial activity contained in the fermented tomato juice with L. acidophilus(2) to extract and purify the antimicrobial agent(s)(3) to find the biological, physical and chemical properties of the agent(s). The following results were obtained and summarized as followings; 1. The agent responsible for the inhibitory activity was confirmed by both well assay method using fermented tomato juice with L. acidophilus and turbidimetric technique using the cell-free filtrate or neutralized filtrate of tomato acidohilus culture and found exerted antimicrobial agent other than lactic acid. 2. The procedures of purification : The isolation and purification of antimicrobial agent from the lyophilized acidophilus tomato culture were carried out by (1) methanol extraction (2) acetone extraction, (3) Sephadex G-50 gel filtration (4) paper chromatography and (5) thin layer chromatography. 3. The biological, physical and chemical properties of antimicrobial agent: The biological, physical, chemical properties of the purified antimicrobial agent were: (1) The antimicrobial activity was strong against test organisms; Bacillus subtilis(ATCC 6633), Escheichia coli(ATCC 25922), Staphylococcus aureus(ATCC 167), Pseudomonas fluorescens(KFCC 32394), Proteus vulgaris and Shigella dysenteriae. (2) The pH value of the agent was 2.0 and the inhibitory activity was lost when it was neutralized at 7.0 of pH and the agent was heat stable at $121^{\circ}C$ for 60 minutes. (3) The ultraviolet light absorption spectra of methanol-acetone extract and TLC fraction exhibited a maximum absorption at 260nm and 224nm respectively. (4) The most purified agent from TLC plate increased about 130-fold in activity. (5) The agent isolated from TLC plate was free from $H_2O_2$ or lactic acid. 4. Bioautographic assy: By means of bioautography of the agent on silica gel of TLC plate a strong inhibitory activity against B. subtilis was demonstrated. 5. Mass spectrometry: The agent obtained from TLC plate was analyzed by mass spectrometry which show the parent peak at m/e 264 suggesting the molecular weight of the compound and molecular group such as [$C_2H{^+}_4$], [CO], [CH=NH], [$C_3{H^}4_7$], [$\begin{array}{rcl}O\\{\parallel}\\CH_3-C\\\end{array}$], [$C_6-H{^+}_{11}$], [$C_5H{^+}_{11}$], [$\begin{array}{rcl}O\\{\parallel}\\C_5H_7-C^+\\\end{array}$] were suggested.