• Bulletin of the Korean Chemical Society
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• 제31권2호
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• pp.384-388
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• 2010

Human microsomal prostaglandin E synthase-1 (mPGES-1) catalyzes the conversion of prostaglandin $H_2$ ($PGH_2$) into prostaglandin $E_2$ ($PGE_2$). To establish a stable and efficient method to assess the activity of mPGES-1, a coupled enzyme assay system using mPGES-1, 15-hydroxyprostaglandin dehydrogenase (15-PGDH) and phosphomolybdic acid (PMA) was developed. In this assay system, $PGH_2$ was converted to $PGE_2$ by mPGES-1, and then $PGE_2$ was further transformed to the 15-keto-$PGE_2$ by 15-PGDH accompanying the production of NADH, which was easily detected by fluorescence spectrometry in a multi-well plate format. During the reaction, spontaneous oxidation of $PGH_2$ was prevented by PMA. Using this novel assay, the $K_m$ value of mPGES-1 for $PGH_2$ and the $IC_{50}$ value of the previously characterized inhibitor, MK-886, were determined to be 0.150 mM and $2.8\;{\mu}M$, respectively, which were consistent with the previously reported values. In addition, low backgrounds were observed in the multi-wall plate screening of chemical compounds.

• 대한화학회지
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• 제26권5호
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• pp.320-325
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• 1982

황을 분석하기 위하여 준비한 용액을 이용하여 황화광석중 철, 구리, 코발트를 X-선 형광법으로 정량하였다. 시료를 $Br_2$ 와 $HNO_3$의 혼합용액으로 녹인 다음 HF로 처리하여 주성분인 $SiO_2$를 제거한 다음 용액으로 만들었다. 분석결과는 철함량이 20 ~ 50%에서 ${\pm}$1.5%, 구리 함량이 10 ~ 15%에서 ${\pm}$1.0%, 코발트함량이 1 ~ 5% 범위에서 ${\pm}$0.4% 이내로 다른 습식분석법의 data와 일치하고 있으며 재현성에 있어서도 좋은 결과를 얻었다.

• Natural Product Sciences
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• 제27권3호
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• pp.161-168
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• 2021

The chemical investigation of the 90% EtOH extract from Cicadidae Periostracum led to the isolation and identification of seven known N-acetyldopamine dimers (1-7). These compounds were identified by comparing mass spectrometry data and NMR spectroscopic data with those previously reported. In this study, complete interpretation of 1D and 2D NMR data of 1 and 2 were reported for the first time. In addition, compounds 3 and 4 were isolated from this material for the first time. All isolates were obtained as racemic mixtures, as confirmed by chiral HPLC. Furthermore, we evaluated the neuroprotective activities of compounds 1-7 and found that compounds 1, 5, and 6 significantly attenuated rotenone-induced death of SH-SY5Y neuroblastoma cells at a concentration of 100 μM. Parallel to this result, compounds 3 and 6 displayed antioxidant effects in the cytoplasm, as determined by CM-H2DCFDA fluorescence intensity, while compounds 1 and 5 showed antioxidant effects in the mitochondria, as assessed by MitoSox fluorescence intensity. Overall, these results suggest that some of these compounds protect neuroblastoma cells by ameliorating the release of reactive oxygen species. Further studies are warranted to elucidate the underlying mechanisms by which these compounds exhibit antioxidant and neuroprotective actions.

• Journal of Radiation Protection and Research
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• 제42권1호
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• pp.33-41
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• 2017

Background: Phosphate rock and its by-product are widely used in various industries to produce phosphoric acid, gypsum, gypsum board, and fertilizer. Owing to its high level of natural radioactive nuclides (e.g., $^{238}U$ and $^{226}Ra$), the radiological safety of workers who work with phosphate rock should be systematically managed. In this study, $^{238}U$, $^{232}Th$, $^{226}Ra$, and $^{40}K$ levels were measured to analyze the transport characteristics of these radionuclides in the production cycle of phosphate rock. Materials and Methods: Energy dispersive X-ray fluorescence and gamma spectrometry were used to determine the activity of $^{238}U$, $^{232}Th$, $^{226}Ra$, and $^{40}K$. To evaluate the extent of secular disequilibrium, the analytical results were compared using statistical methods. Finally, the distribution of radioactivity across different stages of the phosphate rock production cycle was evaluated. Results and Discussion: The concentration ratios of $^{226}Ra$ and $^{238}U$ in phosphate rock were close to 1.0, while those found in gypsum and fertilizer were extremely different, reflecting disequilibrium after the chemical reaction process. The nuclide with the highest activity level in the production cycle of phosphate rock was $^{40}K$, and the median $^{40}K$ activity was $8.972Bq{\cdot}g^{-1}$ and $1.496Bq{\cdot}g^{-1}$, respectively. For the $^{238}U$ series, the activity of $^{238}U$ and $^{226}Ra$ was greatest in phosphate rock, and the distribution of activity values clearly showed the transport characteristics of the radionuclides, both for the byproducts of the decay sequences and for their final products. Conclusion: Although the activity of $^{40}K$ in k-related fertilizer was relatively high, it made a relatively low contribution to the total radiological effect. However, the activity levels of $^{226}Ra$ and $^{238}U$ in phosphate rock were found to be relatively high, near the upper end of the acceptable limits. Therefore, it is necessary to systematically manage the radiological safety of workers engaged in phosphate rock processing.

• 한국식품과학회지
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• 제52권2호
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• pp.125-129
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• 2020

본 연구는 무기성분을 활용하여 국산 콩과 외국산 콩의 원산지 판별법을 개발하기 위해 수행하였다. 2018년도에 수집한 국산 100점, 미국, 중국, 베트남, 태국으로 구성된 외국산 97점에 대하여 ED-XRF를 이용하여 총 26종 무기성분의 농도를 산출하였다. T-test, ANOVA, CDA 분석을 통해 원산지판별에 영향을 주는 주요 변수로 5종(P, Ni, Br, Zn, Mn)의 무기성분을 선발하였다. 원산지 판별식을 설정한 결과 감응도 91.0%, 선택성 95.9%, 효율성 93.4%를 나타냈다. 2019년도에 수집한 국산 30점, 외국산 30점으로 원산지 판별식을 검증한 결과 국산 예측률 93.3%, 외국산 예측률 100.0%를 나타냈다. 복잡한 전처리 없이 ED-XRF와 통계처리를 통해 국산 콩과 외국산 콩을 판별할 수 있는 실용적인 판별 체계를 구축하였으며 부정유통 단속을 위한 과학적인 근거자료로서 활용이 가능할 것으로 판단된다.

• Journal of Plant Biotechnology
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• 제37권2호
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• pp.196-204
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• 2010

With the completion of genome sequencing of several organisms, attention has been focused to determine the function and functional network of proteins by proteome analysis. The recent techniques of proteomics have been advanced quickly so that the high-throughput and systematic analyses of cellular proteins are enabled in combination with bioinformatics tools. Furthermore, the development of proteomic techniques helps to elucidate the functions of proteins under stress or diseased condition, resulting in the discovery of biomarkers responsible for the biological stimuli. Ultimate goal of proteomics orients toward the entire proteome of life, subcellular localization, biochemical activities, and their regulation. Comprehensive analysis strategies of proteomics can be classified as three categories: (i) protein separation by 2-dimensional gel electrophoresis (2-DE) or liquid chromatography (LC), (ii) protein identification by either Edman sequencing or mass spectrometry (MS), and (iii) quanitation of proteome. Currently MS-based proteomics turns shiftly from qualitative proteome analysis by 2-DE or 2D-LC coupled with off-line matrix assisted laser desorption ionization (MALDI) and on-line electrospray ionization (ESI) MS, respectively, to quantitative proteome analysis. Some new techniques which include top-down mass spectrometry and tandem affinity purification have emerged. The in vitro quantitative proteomic techniques include differential gel electrophoresis with fluorescence dyes, protein-labeling tagging with isotope-coded affinity tag, and peptide-labeling tagging with isobaric tags for relative and absolute quantitation. In addition, stable isotope labeled amino acid can be in vivo labeled into live culture cells through metabolic incorporation. MS-based proteomics extends to detect the phosphopeptide mapping of biologically crucial protein known as one of post-translational modification. These complementary proteomic techniques contribute to not only the understanding of basic biological function but also the application to the applied sciences for industry.

• 한국환경보건학회지
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• 제47권5호
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• pp.496-503
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• 2021

Background: Considering the expenses of and difficulties in arsenic speciation by high performance liquid chromatography-inductively coupled plasma-mass spectrometry (HPLC-ICP-MS), alternative measurement methods should be useful, especially for large-scale research and projects. Objectives: A measurement method was developed for arsenic speciation using HPLC-atomic fluorescence spectrometry (HPLC-AFS) as an alternative to HPLC-ICP-MS. Methods: Total arsenic and toxic arsenic species in some seafoods were determined by atomic absorption spectrometry coupled with hydride vapor generation (AAS-HVG) and HPLC-AFS, respectively. Recovery rate of arsenic species in seafood was evaluated by ultra sonication, microwave and enzyme (pepsin) for the optimal extraction method. Results: Limits of detection of HPLC-AFS for As³⁺, dimethylarsinate (DMA), monomethylarsonate (MMA) and As⁵⁺ were 0.39, 0.53, 0.60 and 0.64 ㎍/L, respectively. The average accuracy ranged from 97.5 to 108.7%, and the coefficient of variation was in the range of 1.2~16.7%. As³⁺, DMA, MMA and As⁵⁺ were detected in kelp, the sum of toxic arsenic in kelp was 40.4 mg/kg. As³⁺, DMA, MMA and As⁵⁺ were not detected in shrimp and squid, but total arsenic (iAS and oAS) content in shrimp and squid analyzed by AAS-HVG were 18.1 and 24.7 mg/kg, respectively. Conclusions: HPLC-AFS was recommendable for the quantitative analysis method of arsenic species. As toxic arsenic species are detected in seaweeds, further researches are needed for the contribution degree of seafood in arsenic exposure.

• 분석과학
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• 제9권1호
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• pp.20-25
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• 1996

암석 및 토양 등의 지질시료에 미량으로 존재하는 우라늄과 토륨을 파장분산형 X-선 형광분석법을 사용하여 정량하였다. X-선관의 target 물질로 사용되는 Rh의 산란선을 내부 표준물질로 사용하였다. 토륨의 경우는 50초, 그리고 우라늄의 경우는 400초 동안 측정하였을 때, 우라늄과 토륨의 X-선 형광분석결과는 중성자방사화분석 및 유도결합플라즈마 원자방출분광분석의 결과와 큰 차이를 보이지 않았으며 10% 이내의 정밀도와 15% 이내의 정확도를 보여 주었다.

• 한국식품과학회지
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• 제48권5호
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• pp.418-423
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• 2016

근적외선분광분석기와 에너지 분산형 X선 형광분석기를 이용한 분석방법을 개발하여 각각 97.5, 98.0%의 높은 정확도의 판별식을 확립하였고, 시중 유통 시료를 분석하여 검증한 결과 각각 96.3, 95.0%의 판별 정확도를 확인하였다. 이상의 연구 결과를 통하여 근적외선분광분석기와 에너지 분산형 X선 형광분석기를 이용하여 청국장 원산지 판별이 가능함을 확인하였고 이는 유기성분 함량에 따른 근적외선 흡광도와 무기성분 함량에 따른 X선 형광에너지 강도가 국내산과 수입산 간에 차이가 있기 때문으로 사료된다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2014년도 제46회 동계 정기학술대회 초록집
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• pp.206.2-206.2
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• 2014

Recently, particle induced X-ray emission (PIXE) analysis system was installed at the 2MV ion acceleration system in Korea institute science and technology (KIST). This installation is for complement to low atomic resolution of heavy atoms at Rutherford backscattering spectrometry (RBS) system. For quantitative analysis, a mass calibration of the PIXE set-up has been done with thin film standards and. The GUPIX software package has been used to process the PIXE spectra and the results are compared with the values from RBS system. Therefore, the instrumental constant H (solid angle and correction factor) is determined relying completely on the GUPIX data base (cross-sections, fluorescence and Coster-Kronig probabilities, stopping powers and attenuation coefficients) for a large set of elements. These H values can be used in future analysis.