• 분석과학
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• 제7권3호
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• pp.421-425
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• 1994

A micro-high performance liquid chromatography(Micro-HPLC) techniquie with solid phase extraction was reported which detected carbendazim and carbaryl at picogram levels. They were separated on microbore packed $C_{18}$ column($1.0mm\;I.\;D{\times}150mm$, $d_f=5{\mu}m$) using a 50% methanol mobile phase and detected at UV 220nm(${\alpha}=2.94$, $R_s=4.71$), while they were not resolved on analtical HPLC system(${\alpha}=1.27$, $R_s=0.76$). The detection thresholds of carbendazim and carbaryl were 0.5ng and 0.1ng on Micro-HPLC, therefore Micro-HPLC system was 20~40 told more sensitive than anayltical HPLC system. Sep-Pak $C_{18}$ catridge was found to be efficient in enriching carbendazim and carbaryl from dilute aqueous solution with 97.0% and 97.8% recoveries of them. The Sep-Pak $C_{18}$ catridge followed by the Micro-HPLC had been applied to the quantitative analysis of carbendazim and carbaryl in spiked juices and a commercial drinking water.

• 한국동물위생학회지
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• 제29권3호
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• pp.339-346
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• 2006

Semi-micro-HPLC using a column-switching technique was developed for simultaneous determination of vitamin A and E contents in infant formula. Vitamin A and E were extracted by PDA - HPLC with reversed phase column using organic solvent and their contents in Certified Reference Material (CRM) and infant formula were determined and compared with hydrolysis method and rapid extraction. Developed method has many advantages of simple and rapid sample preparation and simultaneous determination of vitamin A and E by micro-HPLC using reversed phase column.

• 대한화학회지
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• 제45권6호
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• pp.524-531
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• 2001

Microcystin-LR, -YR 및 -RR과 같은 독성 microcystin의 분석에 있어서 정확성을 높이기 우해 고상 추출을 통한 micro-HPLC/IS/MS를 사용하였다. 이러한 microcystin-LR, -YR, -RR를 확인하는데 HPLC/UV로는 238nm에서의 흡광도를 측정하였고, 질량스펙트럼에서는 1 35m/z 및 $[M+H]^+$m/z의 특성 피이크만을 검출하여 왔다. 본 연구에서는 이중 전하에 해당하는 새로운 선들이 LR에서는 507m/z, PR에서는m/z, YR에서는 532m/z에서 추가로 검출되었다. 이 방법을 사용하여 대청호에서 독성 microcystin의 존재성을 조사하였다.

• Asian-Australasian Journal of Animal Sciences
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• 제4권2호
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• pp.161-164
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• 1991

A rapid and accurate method is described for the determination of nucleo-bases in rumen micro-organisms. A procedure to satisfactorily hydrolyse the micro-organisms involving reaction with a mixture of readily volatile organic acids (acetic and formic acids) under high pressure, is proposed, and optimal conditions for an analytical procedure with reversed phase HPLC is described. The following nucleobases contents (mmol/kg DM) of rumen micro-organisms were found: Adenine (Ade), 82.62; Guanine (Gua), 61.34; Cytosine (Cyt), 84.61; Thymine (Thy), 35.74; Uracil (Ura), 68.62; Hypoxanthine (Hxn), 13.06; Xanthine (Xn), 8.35. Total purine-N content (g/kg N) of rumen micro-organisms were 99.60. The nucleic acid N content (g/kg N) of microbial isolates were: RNA-N, 109.9; DNA-N, 50.9.

• 대한약학회:학술대회논문집
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• 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.1
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• pp.276.1-276.1
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• 2003

This study describes a simple and sensitive semi-micro HPLC method with UV detection and direct deproteinization. The plasma protein was precipitated using perchloric acid (60％) and the supernatant was directly injected onto the semi-micro HPLC system. The separation was achieved on a C18 (25 mm ${\times}$ 2.0 mm I.D) analytical column with a mobile phase of sodium acetate buffer (pH 3.5, 50 mmol) - acetonitrile (60:40, V/V). (omitted)

• 한국약용작물학회:학술대회논문집
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• 한국약용작물학회 2010년도 심포지엄 및 추계학술발표회
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• pp.430-430
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• 2010

In this study ethanol extracts of aerial part of Geranium thunbergii Sieb. et Zucc. was investigated for their ability to inhibit a-glucosidase, and thus was fractionated using two organic solvents, including dichloromethane, ethyl acetate. The ethyl acetate-soluble fraction, which manifested potent enzyme inhibitory properties, was then followed by tracking down the active compound by combining HPLC micro-fractionation to an enzyme assay in 96-well plate. The ${\alpha}$-glucosidase inhibitory activity profile showed that two peaks exhibited potent inhibitory activity, and then the structural analyses of the two peaks were carried out by HPLC-UV-MS. The main ${\alpha}$-glucosidase inhibitory compounds in the ethyl acetate-soluble fractions of ethanol extracts of Geranium thunbergii Sieb. et Zucc. were tentatively identified as geraniin and kaempferol-7-rhamnoside.

• Bulletin of the Korean Chemical Society
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• 제23권7호
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• pp.1014-1016
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• 2002

• 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.

• 한국지하수토양환경학회지:지하수토양환경
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• 제14권6호
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• pp.35-44
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• 2009

나프탈렌과 TNT는 미국 환경청(U.S. EPA)에서 규정한 발암가능성 물질로(Group C), 환경으로 방출될 경우 수생태계와 인체에 심각한 영향을 주는 것으로 알려져 있다. 그러나 지하수 내 두 물질의 미량 분석법에 대한 기존연구는 매우 미비한 실정이다. 이에 본 연구에서는 HPLC-FLD(Fluorescence etector)와 MSD(Mass detector)를 이용한 지하수 내 나프탈렌 및 TNT의 미량분석법을 개발하여, MDL과 LOQ 및 이온영향을 조사하고, 현재 사용되고 있는 HPLC-UV 분석법과 비교 평가하였다. 나프탈렌의 경우, 3D-Fluorescence를 통하여 확인된 최고의 파장(Ex: 270 nM, Em: 330 nM)이 HPLC-FLD에 적용되었고, $0.3\;{\mu}g/L$의 MDL과 $2.0\;{\mu}g/L$의 LOQ가 획득되었다. 이는 현재 방법(HPLC-UV; MDL: $23.3\;{\mu}g/L$, LOQ: $163.1\;{\mu}g/L$)보다 약 80배 우수한 결과이며, U.S. EPA의 음용수 권고기준($700\;{\mu}g/L$)의 약 350배 이하까지 정량분석이 가능한 수치이다. TNT의 경우, 새롭게 제시된 HPLC-MSD로 측정한 방법(MDL: $0.13\;{\mu}g/L$, LOQ: $0.88\;{\mu}g/L$)이 HPLC-UV(MDL: $16.8\;{\mu}g/L$, LOQ: $117.5\;{\mu}g/L$ at 230 nM)보다 약 130 배 우수한 것으로 조사되었고, U.S. EPA의 음용수 권고기준($20\;{\mu}g/L$)보다 약 23배 낮은 농도까지 정량분석이 가능한 것을 확인하였다. 또한 HPLC-UV(230 nM)의 분석법은 ${NO_3}^-$ 농도가 증가할수록(특히 21 mg/L 이상) 크로마토그램의 기준선이 증가하여 정량에 방해를 주었으나, HPLC-MSD 분석법은 국내 지하수 평균 농도보다 약 3.5배인 63.7 mg/L에서도 분석의 영향 없이 안정한 크로마토그램을 보여주었다. 따라서 새롭게 제시된 HPLC-FLD와 MSD에의한 나프탈렌과 TNT 분석법은 지하수 및 음용수 미량분석에 적합하며, 관련분야 연구에 크게 도움이 될 것이다.

• 한국식품영양과학회지
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• 제28권6호
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• pp.1208-1211
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• 1999

Semi HPLC using a column switching technique was used to determine the trace content of vitamin B12 in various foods. Total analytical time required less than 20 mins per sample and the recovery ratio was 99.9, 99.6, 100.1 and 99.8% for 1.0, 10.0, 100.0 and 1,000 g/kg, respectively. The content of vitamin B12 in various foods obtained using column switching method showed higher levels compared to labels in dried milk(0.5 g/100g) and in grain products(0.51~34.36 g/100g). Thus, this column switching method was more sensitive, effective and precise than the microbiological analysis currently used to determine the trace compounds like a vitamin B12.