• 제목/요약/키워드: Sep-Pak $C_{18}$ catridge

검색결과 4건 처리시간 0.018초

Micro-HPLC에 의한 Carbendazim과 Carbaryl의 분석 (Analysis of Carbendazim and Carbaryl by Micro-HPLC)

  • 최경숙;이호연;이덕희;변운기
    • 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.

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이온쌍 액체 크로마토그래피에 의한 마주송이풀 중의 Acteoside의 분리와 정량 (Separation and Determination of Acteoside in Pedicularis resupinata var. oppositifolia by Ion Pair Liquid Chromatography)

  • 윤영자;유구용
    • 분석과학
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    • 제8권2호
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    • pp.161-166
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    • 1995
  • 이온쌍 액체크로마토그래피(IP-HPLC)에 의해 마주송이풀 중 acteoside를 분리 정량하였다. 시료를 메탄올 40mL로서 4시간 추출하였다. 추출물에 대한 분리, 정제를 Sep-Pak $C_{18}$ catridge와 메탄올-물(메탄을 50%, 물 50%, 인산 완충용액 pH=8.0)을 사용하였다. HPLC 분리조건은 poly(styrene-divinylbezene) PRP-1 역상컬럼($15cm{\times}4.6mm$ i. d., $5.0{\mu}m$)과 이동상으로 $5.0{\times}10^{-3}M$ tetrabutylammonium bromide가 포함된 메탄올-물(메탄을 60%, 물 40%, 인산 완충용액 pH=8.2)을 사용하였다. 이와 같은 조건으로 강원도 평창군 일대에서 채집한 마주송이풀 중에 함유된 acteoside를 분리 정량한 결과 그 함량 범위가 0.062~0.076%였다.

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2-Bromoacetyltriphenylene 유도체화제를 이용한 카르복실기 함유 성분의 분석법 (II) - 담즙산 혼합물의 HPLC에 의한 분리정량 (HPLC Determination of Carboxyl Group Using 2-Bromoacetyltriphenylene as a Pre-labeling Reagent - Separative determination of bile acids by HPLC)

  • 박만기;정해수;양호길
    • 약학회지
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    • 제31권2호
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    • pp.105-111
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    • 1987
  • A high performance liquid chromatographic method was developed for the simultaneous determination of free and glycine conjugated bile acids. Free and glycine conjugated bile acids were extracted from bear gall bladder by methanol and from serum using a Sep-pak $C_{18}$ catridge. The extracted bile acids were labeled with 2-bromoacetyltriphenylene in acetonitrite using 18-crown-6-ether as a catalyst. Derivatized bile acids were separated from the individual bile acids on a reversedphase column (Chemcosorb 5-ODS-H) using acetonitrile-methanol-water(10:50:30) as a mobile phase and monitored by an UV-detector at 254nm. Linearities of calibration curve were obtained between 4 ng and 24 ng, and recoveries from bear gall bladder sample were higher than 94%.

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고성능 액체크로마토크래피를 이용한 Biotin의 정량 (Determination of Biotin by HPLC)

  • 김동수;이영자;정동윤;이동엽;안문규
    • 분석과학
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    • 제16권6호
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    • pp.499-503
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    • 2003
  • Biotin을 4-bromomethyl-6,7-dimethoxycoumarin (BrMDMC), 18-crown-6와 $K_2CO_3$를 사용하여 형광성 유도체로 만들어 (들뜸 파장 360 nm, 방출파장 410 nm에서) 기울기 용리 HPLC 분석을 하였다. 검정선의 농도범위는 5 ~ 400 ng, 검출한계는 2 ng, 회수율 98.75%, 그리고 상대표준편차는 1.1% 이었다. 시료의 전처리는 Sep-Pak $C_{18}$ catridge를 이용하였고, 유도체 제조의 중탕온도는 $50^{\circ}C$에서 30분간 시행하였다.