• 제목/요약/키워드: Reversed phase chromatography

검색결과 347건 처리시간 0.023초

Isolation of Phytochemicals from Salvia plebeia Using Countercurrent Chromatography Coupled with Reversed-phase HPLC

  • Kil, Hyun Woo;Rho, Taewoong;Seo, Young Ju;Yu, Aram;Yoon, Kee Dong
    • Natural Product Sciences
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    • 제26권3호
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    • pp.236-243
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    • 2020
  • Salvia plebeia R. Br. is a plant which has been used as an edible crop and traditional medicine in Asian countries. In this study, HPLC-PDA analysis and countercurrent chromatography (CCC) coupled with reversed-phase (RP) HPLC method were applied to isolate ten isolates from 3.3 g of n-butanol soluble extract from hot-water extract of S. plebeia. The use of CCC enabled us to efficiently fractionate the starting material with less sample loss and facilitate the isolation of compounds from S. plebeia extract using RP-HPLC. The isolates were determined to be caffeic acid (1), 6-hydroxyluteolin 7-O-β-D-glucoside (2), eudebeiolide B (3), (R)-rosmarinic acid (4), homoplantaginin (5), eudebeiolide D (6), plebeiolide C (7), salpleflavone (8), eupafolin (9) and hispidulin (10) based on the spectroscopic evidence.

다량 시료중 마이크로시스틴의 농축 및 분석 (Application of Reversed-Phase Solid Phase Extraction for the HPLC Analysis of Microcystins in Water)

  • 김명희;김태승;김태근;박선구
    • 분석과학
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    • 제13권3호
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    • pp.399-402
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    • 2000
  • To determine the concentrations of microcystins present in lake water or in tap water using high performance liquid chromatography, it is necessary to concentrate a large volume of water samples (about 20 L) into very small volume (0.1-0.3 mL). Concentration can be conveniently done when disc type solid phase extraction (SPE) apparatus is used. Using this apparatus we have investigated the recovery rates of three kinds of microcystins, RR, YR, LR. The recovery rates were relatively low and the reproducibilities were not good either. It is expected, however, that the appropriate selection of the disc conditioning and eluting solvents and reproducible reconcentration process after SPE will improve both the recovery rates and the reproducibilities.

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역상 액체 크로마토그래피에 의한 금속-2-hydroxy-arylazopyrazolone 유도체 킬레이트의 용리거동에 관한 연구 (II) (The Elution Behaviors of Some Metal-2-Hydroxy-arylazopyrazolone Chelates by Reversed Phase Liquid Chromatography (II))

  • 이원;김인환;강창희;김은경
    • 분석과학
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    • 제7권3호
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    • pp.379-386
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    • 1994
  • Ni(II), Cu(II), Co(III) 및 Cr(III) 이온과 2-hydroxy-arylazopyrazolone 유도체들 사이에 형성하는 킬레이트들에 대한 역상 액체 크로마토그래피에서의 용리 메카니즘을 열역학적인 접근방법으로 고찰하였다. van't Hoff plot에 의해 온도와 용량인자(k')와의 상관관계를 조사한 결과 온도와 용량인자와의 관계는 양호한 직선성을 나타냈으며, 온도 변화와 무관한 동일한 메카니즘에 의해 분리됨을 알 수 있었다. van't Hoff plot으로부터 엔탈피$({\Delta}H)^{\circ}$, 엔트로피$({\Delta}S)^{\circ}$를 구하고, 엔탈피와 용량인자와의 상관관계를 조사한 결과 [pm(2-OH)(5-Cl)PaPz](r=0.787)을 제외한 대부분이 킬레이트들은 비교적 좋은 직선성(r=0.980~0.999)을 보였고, 보정온도(${\beta}$) 역시 일정한 값을 나타내었다. 이것은 금속-2-hydroxy-arylazopyrazolone 킬레이트와 정지상($C_{18}$)과의 상호작용이 등평형 거동을 하고 있음을 의미한다. 또한 엔탈피와 용량인자와의 상관관계로부터 구한 보정온도는 374.63~806.9k 범위의 값을 나타냈고, 이들 결과로부터 역상 액체 크로마토그래피에서 금속 킬레이트들의 머무름 메카니즘은 소수성 효과에 기인하고 있음을 확인할 수 있었다.

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Separation and Purification of Lipase Inhibitory Peptide from Fermented Milk by Lactobacillus plantarum Q180

  • Kim, Seulki;Lim, Sang-Dong
    • 한국축산식품학회지
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    • 제40권1호
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    • pp.87-95
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    • 2020
  • In this study, we separated and purified lipase inhibitory peptide from fermented milk by Lactobacillus plantarum Q180 with the aim of developing a new functional anti-lipase activity yogurt product. L. plantarum 180 was inoculated into 10% reconstituted skimmed milk and incubated at 37℃ until the pH of the culture reached pH 4.4. The lipase activity was measured using porcine pancreatic lipase. The lipase inhibitory peptides were gradually isolated by ultrafiltration, reversed phase column chromatography (RPC), reversed phase high-performance liquid chromatography (RP-HPLC), and gel permeation high-performance liquid chromatography (GP-HPLC) from the fermented milk by L. plantarum Q180. An ODS-AQ column was used for the RPC, a Vydac C18 column for the RP-HPLC, and a Superdex Peptide HR column for the GP-HPLC. The peptide was composed of Asp, Thr, Ile, Ser, Ala, and Gln, and the anti-lipase activity (IC50) was 2,817 ㎍/mL.

소수성 파라메터를 적용한 알킬벤젠류의 역상컬럼내의 용출거동 예측 (Prediction of Retention Behavior of Alkyl Benzenes by Hydrophobicity Parameters in Reversed-Phase Column)

  • 이창영;박명용;이용문
    • 약학회지
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    • 제53권5호
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    • pp.281-285
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    • 2009
  • The retention of solutes in reversed-phase high-performance liquid chromatography depends on their hydrophobicity. Although the retention behaviors of alkyl benzenes have been reported so far, quite a few authors have mentioned the retention behavior of alkyl benzenes with plural hydrophobicity parameters. In this sense, we were interested in the retention behaviors of alkyl benzenes having benzene moiety and increasing alkyl chain. In this study, we therefore investigated the retention behavior of alkyl benzenes in reversed-phase high-performance liquid chromatography in order to obtain information concerning the effects of the aromatic moiety and the carbon chain on the retention mechanism by comparing their capacity factor (k') in relation to the carbon chain length. The eluent acetonitrile ($CH_3CN$) showed high selectivity on alkyl benzenes, showing the high difference of capacity factor (${\Delta}log\;k'$) between toluene and octyl benzene. Indeed, the ${\Delta}log\;k'$ of 80% $CH_3CN$ represented 1.42- and 4.25-times longer than 90% MeOH and 60% THF, respectively. The hydrophobicity parameters, van der Waals volume, bond constant, partition constant, $\pi$-energy effect and enthalpy were evaluated with the capacity factor (k') of alkyl benzenes eluted on 80% CH3CN, 90% MeOH and 60% THF, respectively. The best eluent for predicting retention behavior of alkyl benzenes was 90% MeOH ($R^2$ 0.999). The three parameters, van der Waals volume, bond constant and partition constant were well coincident to log k' by increasing alkyl benzenes. However, $\pi$-energy effect and enthalpy were severely disagreeable. Taken together, van der Waals volume, bond constant and partition constant were a reliable parameters to predict the retention behaviors of alkyl benzenes on reversed-phase column.

Optical Resolution of Dabsyl Amino Acids in Reversed-Phase Liquid Chromatography

  • Lee, Sun-Haing;Oh, Tae-Sub;Lee, Young-Cheal
    • Bulletin of the Korean Chemical Society
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    • 제11권5호
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    • pp.411-415
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    • 1990
  • The dabsylation of amino acids has been applied to resolve their optical isomers with the use of chiral mobile phase in high performance liquid chromatography. The dabsyl amino acids were successfully separated on reversed phase column($C_{18}$) by adding a chiral L-benzylproline-Cu(II) chelate to the mobile phase. The separation selectivity of the dabsyl amino acid enantiomers was not less than that of dansyl amino acids. The retention order of the dabsyl amino acid enantiomers was as those of the dansyl amino acid enantiomers except dabsyl threonine. The optical selectivity of the dabsyl amino acids increase with pH of the mobile phase and concentration of the chelate, but slightly decreases with concentration of buffer and organic solvent composition. However serine, methionine, valine, and leucine showed a slight decrease in the optical selectivity with increase in pH. The retention times of the dabsyl amino acids decreases with increasing pH and acetonitrile concentration but increases with the concentration of the chiral chelate added. The mechanism of the optical resolution is based on a stereospecific interaction including a intramolecular hydrophobic effect and SN-2 reactivity of the ligand exchange chromatography.It is advantageous to detect absorption at 436 nm, which is less interferent them the other detection systems. The derivatized dabsyl amino acids are stable for a month.

HILIC 분석법 개발을 위한 지능형 솔루션 (Hydrophilic Interaction Liquid Chromatography)

  • Matt James;Colin Pipe;Mark Fever;Jen Field;Seungho Chae
    • FOCUS: LIFE SCIENCE
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    • 제1호
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    • pp.6.1-6.9
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    • 2024
  • The document is a white paper on Hydrophilic Interaction Liquid Chromatography (HILIC) analysis method development. HILIC is a type of chromatography that uses an organic/aqueous mobile phase and a polar stationary phase. In HILIC, water is a strong solvent, and unlike in Reversed Phase Liquid Chromatography (RPLC), increasing the proportion of water in the mobile phase reduces the retention time of the analyte. The paper discusses when to consider HILIC analysis methods, the advantages of HILIC, and the challenges often encountered due to the lack of understanding of HILIC mechanisms compared to RPLC. It also provides a systematic flowchart for intelligent solutions for HILIC analysis method development, which includes a three-step approach for chromatography analysis method development. The first step involves gathering as much information as possible about the analyte (e.g., pKa, log P, log D). The second step involves analyzing the sample under different pH conditions using three HILIC columns in either isocratic or gradient mode to identify the suitable column/pH combination for the analyte. The third step involves optimizing the separation by investigating other parameters such as temperature and ionic strength, and assessing the robustness of the method. The paper emphasizes that the selection of the appropriate stationary/mobile phase combination, based on the differences between the HILIC stationary phases and the mobile phase pH, can provide high selectivity in the analysis. This step-by-step approach can help users develop an efficient analysis method.

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방향족 슬폰산들의 역상 이온쌍 크로마토그래피 (Reversed-Phase Ion-Pair Chromatography of Aromatic Sulfonic Acids)

  • 강삼우;오해범;이승석
    • 대한화학회지
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    • 제30권2호
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    • pp.224-230
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    • 1986
  • 알킬처리된 실리카(ODS)칼럼을 이용하여 역상 이온쌍 크로마토그래피방법으로 방향족 술폰산들의 분리 인자를 조사하였으며 또한 분리를 시도하였다. 반대이온으로서 브롬화 도데실 트리메틸암모늄(DTAB)을 사용하였으며, 시료의 분리인자는 반대이온의 농도, 메탄올의 농도, 전해질의 종류 및 농도, 시료 분자에 붙어있는 작용기의 종류 및 위치등에 의하여 영향을 받았다. 최적 조건하에서 몇 가지 혼합시료를 분리할 수 있었다.

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Separation of Optical Isomers of Amino Acids with Addition of Benzyl-L-proline Copper (II) Chelate by Reversed Phase Liquid Chromatography

  • Lee, Sun-Haing;Oh, Dae-Sub;Kim, Byoung-Eog
    • Bulletin of the Korean Chemical Society
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    • 제9권6호
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    • pp.341-345
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    • 1988
  • Separation of optical isomers of dansyl amino acids by a reversed phase liquid chromatography has been accomplished by adding a copper (II) chelate of N-benzyl-L-proline to the mobile phase. The pH, the eluent composition and the concentration of copper (II) chelate all affect the optical separations. The elution orders between D and L DNS-amino acids were consistant except dansyl phenylalanine showing that D forms of DNS-amino acids elute earlier than L forms. These behaviors are different from the results obtained by the use of copper (II) proline. The retention mechanism for the optical separation of the dansyl amino acids can be explained by the equilibrium of liqand exchange and by hydrophobic interaction.