• Journal of Ginseng Research
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• 제14권3호
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• pp.373-378
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• 1990

Free malonaldehyde was determined in nine kinds of ginseng polyacetylene-treated micro- some by HPLC analysis. Antioxidant activities of some phenolic compounds and ginseng saponin were also drtermined both by a new HVLC method and by THA method. A new HPLC system separaterl malonaldehyde at a retention time 5,6 min and showed a linear relationship between the peak are a and malonaldehyde concentration. Panaxnol showed the strongest activity among nine polyacetylenes and the addition of either chlorine or aletyl group reduced polyacetylene's own activity. Since C14-polyacetylenes such as panaxyne and panaxyne-epoxide had little or no antioxidant activities, S17-structure should be preserved to exert a radical-scvenging or trapping activity. The antioxidant activities of chlorogenic acid, ferulic acid and catechol were much weaker than those of C17-polyacetylenes. Ginseng saponin showed no antioxidant activity. Since TBA reactive substances and malonaldehyde contents were almost the same in peroxiedized microsome. TBA value seems a good indicator for lipid peroxidation in this particular Fe+3 ADP/NADPH system.

• 한국작물학회지
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• 제47권3호
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• pp.236-239
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• 2002

한국산 맥문동과 중국산 소엽맥문동의 성분패턴비교에서 HPLC 분석 결과, 중국산 소엽맥문동(Ophiopogon japonicus)은 RT. 21.2분의 peak는 표준품과 대조결과 spicatoside B인 것으로 확인되었다 반면에 국산 맥문동(Liriope platyphylla)은 spicatoside A와 spicatoside B가 표준품 대조 결과 RT. 6.8분과 21.2분대에서 확인되었다. 따라서 건조된 상태에서 혼용되어 사용하고 있는 한국산 맥문동과 중국산 소엽맥문동은 HPLC 성분패턴상으로 감별이 가능하게 되었다.

• Archives of Pharmacal Research
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• 제17권6호
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• pp.424-427
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• 1994

An acinomycin complex isolated from culture broth of a soil microorganism, SNUS 9305-011 has been examined by High performance liquid chromatography (HPLC). From the analysis of the fractions obtained by column chromatography of the ethyl acetate extract, three actinomycin components are confimed . The HPLC analysis is carried out with a CN-bonded nucleosil column. Comparison of the retention times of the components with those of actinomycin D, C complex, $X_{o{\beta}$, and V and suggests that they are different actinomycins. FBA mass spectra fo the coponents also shows different molecular ions from those of standards and other reported actionbmycins. The present work has demonstrated that actinomycin components can be separated by a CN-bonded HPLC column, and that ocmparison of their HPLC chormatograms with authentic smaples and information on their molecular ions can be successfully employed for indentification of actionmycins.

• 한국환경농학회지
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• 제23권4호
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• pp.245-250
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• 2004

An analytical method was developed to determine monocrotophos residues in apple, citrus, and soil using high-performance liquid chromatography (HPLC) with ultraviolet absorption detection. Monocrotophos was extracted with acetone from apple, citrus and moist soil samples. The extract was concentrated, added with saline water, and subjected to n-hexane washing to remove nonpolar co-extractives. Dichloromethane partition was then followed to recover monocrotophos from the aqueous phase. Silica gel column chromatography was employed to further purify the extract prior to HPLC determination. Reverse-phase HPLC using an oct-adecylsilyl column was successfully applied to separate and quantitate the monocrotophos residue in sample extracts at the wavelength of 230 nm. Overall recoveries of monocrotophos from fortified samples averaged $95.3{\pm}2.1%$ (n=6), $970{\pm}0.7%$ (n=6), and $92.8{\pm}4.3%$ (n=12) for apple, citrus, and soil, respectively. The proposed method was quite reproducible and sensitive enough to replace the troublesome gas-liquid chromatographic analysis for monocrotophos residues.

• KSBB Journal
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• 제23권1호
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• pp.96-100
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• 2008

한국산 녹차로부터 HPLC On-line $ABTS^{+}$ screening기법을 사용하여 catechin compounds의 특성중의 하나인 항산화활성을 빠르게 분석하였으며 녹차로부터 catechin compound의 추출을 다양한 온도와 시간의 추출방법을 적용하였다. 전 처리한 추출액에 포함된 catechin compounds을 분석하고 최적의 추출조건을 실험적으로 모색하였다. 실험결과에 의하면 추출온도 $60^{\circ}C$, 추출시간 3분으로 추출한 시료가 항산화활성이 가장 우수하였다.

• 생약학회지
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• 제42권3호
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• pp.240-245
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• 2011

A high-performance liquid chromatography (HPLC) method was developed for quantitative analysis of liquiritin and glycyrrhizin in Sagunja-tang (SGT, Sijunzi-tang in Chinese), a traditional Korean medicine. HPLC analysis was performed using a Gemini C18 column operating at $40^{\circ}C$, and photodiode array (PDA) detection at 254 nm and 280 nm for quantification of the two components in SGT. The mobile phase using a gradient flow consisted of two solvent systems. Solvent A was 1.0% (v/v) aqueous acetic acid and solvent B was acetonitrile with 1.0% (v/v) acetic acid. Calibration curves were acquired with $r^2$ values > 0.9998, and the relative standard deviations (RSDs, %) for intra- and inter-day precision were not exceed 4.0%. The recovery of each component was in the range of 91.85 - 108.62%, with a RSD less than 4.0%. The contents of the two components in SGT were 7.94 - 13.83 mg/g.

• KSBB Journal
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• 제29권2호
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• pp.124-130
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• 2014

Acer tegmentosum was a traditional Korean herbal medicine showing various pharmacological activities. In this work, A. tegmentosum were extracted with boiling water and then successively partitioned with dichloromethane, ethyl acetate, n-butyl alcohol (n-BuOH), and water. Salidoside, the target compound, was purified in n-BuOH phase using a chromatography method. For the analysis of salidoside, TLC and LC-MS were used as well as on-line screening $HPLC-ABTS^+$ assay with three different wavelength of 254, 280, and 320 nm. An amount of 1.34 g of salidoside were obtained in n-BuOH phase fromAcer tegmentosum was a traditional Korean herbal medicine showing various pharmacological activities. In this work, A. tegmentosum were extracted with boiling water and then successively partitioned with dichloromethane, ethyl acetate, n-butyl alcohol (n-BuOH), and water. Salidoside, the target compound, was purified in n-BuOH phase using a chromatography method. For the analysis of salidoside, TLC and LC-MS were used as well as online screening $HPLC-ABTS^+$ assay with three different wavelength of 254, 280, and 320 nm. An amount of 1.34 g of salidoside were obtained in n-BuOH phase from 3 kg of dry biomass. The on-line screening $HPLC-ABTS^+$ assay is rapid and efficient tool to search bioactivity from A. tegmentosum. 3 kg of dry biomass. The on-line screening $HPLC-ABTS^+$ assay is rapid and efficient tool to search bioactivity from A. tegmentosum.

• 해양환경안전학회지
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• 제12권2호
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• pp.99-106
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• 2006

해양환경에서 오염물질의 거동은 화학적 특성뿐 아니라 부유물질 표면의 정전하, pH 및 염분과 같은 환경 인자에 크게 영향을 받을 것이다. 이 연구는 해산어 양식장에서 빈번히 사용하고 있는 항생제인 옥소린산의 거동이 여러 종류의 부유물질, 염분 및 pH에 따라 어떻게 변동하는가를 HPLC에 의한 화학적 분석과 bioassay 분석으로 검토하였다. 부유물질의 농도가 증가할수록 옥소린산은 HPLC 분석에 의해서도 저농도로 검출되었고, 생물활성에 의한 bioassay 분석으로도 현저히 감소하는 것으로 나타났다. 이 결과는 부유물질이 옥소린산을 흡착하여 수서환경에서 제거하는 역할을 한다는 것을 알 수 있다. 그리고 옥소린산은 염분 40%o과 pH 7에서 bioassay 분석에 의해 생물활성이 약간 저해되지만 HPLC 분석은 조금 다른 양상을 보였다.

• 한국응용과학기술학회지
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• 제34권4호
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• pp.1076-1084
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• 2017

석유제품 내의 식별제를 정성 정량분석하기 위해 HPLC의 적용가능성을 연구하였다. 등유와 자동차용 경유에 함유된 식별제의 정성분석을 위해 HPLC에서 최적의 분석조건(이동상 용매의 비율, 유속 등)을 선정하고, 이를 바탕으로 식별제의 정량분석을 위한 검량곡선을 작성하였다. 특히, 일정 농도 범위에서의 등유는 4.75분에서, 그리고 자동차용 경유는 4.17분의 머무름시간(retention time)을 나타내었고, 등유와 자동차용 경유의 검량곡선 상관계수($R^2$)가 0.999 이상을 나타내어 정량분석에 적용 가능할 것으로 나타났다. 현행 식별제의 분석방법인 UV/Vis 분광광도계를 이용한 분석결과와 비교분석을 실시하였고, 등유의경우 약 7 %의 낮은 편차를 보였으며, 자동차용 경유의 경우 약 20 %의 다소 큰 편차를 확인하였다.

• 대한본초학회지
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• 제26권1호
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• pp.13-19
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• 2011

Objective : This study was to compare antioxidant activity and HPLC pattern analysis from 4 species of changpo(ch$\={a}$ngp$\'{u}$). Methods : To compare the antioxidant activity and HPLC pattern analysis from the 4 species of changpo, we performed the in vitro anti-oxidative activity assays and HPLC analysis from 70% ethanol extracts of Acorus gramineus Sol. (=AG), A. tatarinowii Schott (=AT), A. calamus L. (=AC) and Anemone altaica Fisch. ex C.A.Mey (=AA) taken in the herbal medicine market of Korea. Results : AG has the most effective anti-oxidative activity among 4 species of changpo. As the HPLC pattern analysis, AT was detected the unknown peak at retention time 14.9 min whereas AG was not showed any peak at the same retention time. These results suggest that AG could be used rather than AT when it need to be prescribed as anti-oxidative medicine. Conclusions : This result can be used as the basic data contributing to the stability of AG according to an appropriate clinical application.