• 한국식품영양과학회지
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• 제22권5호
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• pp.581-585
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• 1993

참죽나무(Cedrela sinensis A. Juss.) 잎의 ethyl acetate분획으로부터 분리한 5종의 flavonoid성분들은 HPLC에 의한 용매계 THF-dioxane-MeOH-HOAc-5% $H_3PO_4-H_2O$(145 : 125 : 50 : 20 : 2 : 658)에서 양호한 분리능을 나타내었다. 또한 주성분인 quercitrin의 함량은 MeOH엑스 및 EtOAc 분획에서 각각 9.48%(w/w) 및 37.06%(w/w) 함유되어 있음을 알 수 있었다.

• 분석과학
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• 제16권1호
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• pp.78-81
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• 2003

Peptides separation in high performance liquid chromatography (HPLC) is very important for the analysis of total proteins using mass spectrometry rather than two-dimensional polyacrylamide gel electrophoresis (2D-PAGE). In this study, we investigated the optimal HPLC condition of peptides for the use of mass fingerprinting. As a result of pursuing a combination of solvent additives for HPLC, water and acetonitile containing both 0.1% trifluoroacetic acid and 0.1% acetic acid respectively showed the most efficient resolution and sensitivity.

• 한국식품과학회지
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• 제28권2호
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• pp.360-365
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• 1996

벼(Oryza sativa L.)의 가식부인 쌀의 brassinosteroid 활성물질의 존재를 구명하기 위하여 벼를 도정하여 미강과 백미를 얻고 이들을 각각 MeOH로 추출하여 얻어진 추출물을 rice inclination test의 생물검정법으로 검정한 결과 활성이 인정되었다. 각각의 추출물을 생물검정법을 지표로 용매분획, silica gel adsorption chromatography, Sephadex LH-20 column chromatography, charcoal adsorption chromatography 등의 수법으로 brassinosteroid 활성물질을 정제하고, silica gel adsorption chromatography, TLC 등에 의해 활성본체를 분리하고 각 활성획분을 HPLC에 의해 활성본체 구명을 시도한 결과 미강의 활성획분에서는 castasterone과 teasterone이 동정되었다. 완숙된 쌀에서 brassinosteroid 활성물질의 확인 및 동정은 본 연구가 최초로 생각되며, brassinosteroid 활성물질은 주로 미강에 존재하였으며, 그 함량은 g중량당 castasterone이 0.15 ng 이고 teasterone은 0.37 ng 수준이었다.

• Applied Biological Chemistry
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• 제39권1호
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• pp.95-98
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• 1996

• 약학회지
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• 제53권2호
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• pp.60-68
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• 2009

In terms of chiral issue, two enantiomers of chiral drugs often differ significantly in their pharmacological, toxicological and pharmacokinetic profile. Chiral switches of racemic drugs have been redeveloped as single enantiomers. Several chiral resolution techniques in chirotechnology are introduced and the most used chiral HPLC chromatographic method among several chiral analysis techniques is described with its several advantages. Several types of chiral HPLC columns derived from their chiral selectors are discussed with their property and applications for enantiomer separation.

• Biotechnology and Bioprocess Engineering:BBE
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• 제9권4호
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• pp.285-291
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• 2004

A simulated moving bed (SMB) chromatography system is a powerful tool for preparative scale separation, which can be applied to the separation of chiral compound. We have de-signed our own lab-scale SMB chromatography using 5 HPLC pumps, 6 stainless steel columns and 4 multi-position valves, to separate a racemic mixture of ketoprofen in to its enantiomers. Our design has the characteristics of the low cost for assembly for the SMB chromatography and easy repair of the unit, which differs from the designs suggested by other investigators. It is possible for the flow path through each column to be independently changed by computer control, using 4 multi-position rotary valves and 5 HPLC solvent delivery pumps. In order to prove the operability of our SMB system, attempts were made to separate the (S)-ketoprofen enantiomer from a ketoprofen racemic mixture. The operating parameters of the SMB chromatography were calculated for ketoprofen separation from a batch chromatography experiment as well as by the triangle theory. With a feed concentration of 1 mg/mL, (S)-ketoprofen was obtained with a purity of 96% under the calculated operating conditions.

• Archives of Pharmacal Research
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• 제29권9호
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• pp.808-813
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• 2006

Two methods for the chiral purity determination of bevantolol were developed, namely capillary electrophoresis (CE) using carboxymethyl-${\beta}$-cyclodextrin (CM-${\beta}$-CD) as a chiral selector and high-perfomance liquid chromatography (HPLC) using a chiral stationary phase. In the HPLC method, the separation of bevantolol enantiomers was performed on a Chiralpak AD-H column by isocratic elution with n-hexane-ethanol-diethylamine (10:90:0.1, v/v/v) as mobile phase. In the CE method, bevantolol enantiomers were separated on an uncoated fused silica capillary with 50 mM amonium phosphate dibasic adjusted to a pH 6.5 with phosphoric acid containing 15 mM CM-${\beta}$-CD as running buffer. Validation data such as linearity, recovery, detection limit, and precision of the two methods are presented. The detection limits of S-(-)-bevantolol were 0.1% and 0.05% for CE and HPLC method, respectively and R-(+)-bevantolol were 0.15% and 0.05% for CE and HPLC method, respectively. There was generally good agreement between the HPLC and CE results.

• KSBB Journal
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• 제22권2호
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• pp.119-122
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• 2007

RP-HPLC에서 주요 변수인 이동상의 조성과 컬럼의 종류를 변화시켜 난백 단백질을 실험하였다. C4, C8 C18 컬럼을 비교 실험하여 C18 컬럼에서 가장 많은 피크를 보여 C18 컬럼을 선택하였다. 등용매 용리에서 ACN : water의 조성이 50 : 50에서 가장 많은 피크를 보여 이 결과를 토대로 기울기 용리를 하여 실험하였다. 기울기 용리에서 얻어진 4가지 피크를 확인하기 위하여 단일성분인 lysozyme와 ovalbumin의 체류시간을 측정하여 확인하였고 논문을 통해 2가지 피크를 예측할 수 있었다.

• 분석과학
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• 제7권3호
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• pp.403-411
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• 1994

본 실험은 알팔파의 Allelopathy와 Autotoxicity에 관련되는 생리활성 물질의 분리, 정제, 동정하기 위하여 실시되었다. 알팔파 생잎 1kg을 80% MeOH로 추출하여 silica gel TLC와 DCCC의 분리와 정제과정을 거쳐 HPLC로 동정하였다. HLPC 분석결과 4개의 phenolic 물질(salicylic acid, rutin, quercetin, scopoletin) 등이 동정되었다. 이들 물질을 이용한 발아실험에서도 모두 알팔파의 발아와 생육에 억제적으로 작용하였으며, 이 중 quercetin의 처리가 가장 억제적이었다. 따라서 최소한 이들 물질이 알팔파의 Allelopathy와 Autotoxicity에 관련하는 것으로 생각되었다.

• 한국환경과학회지
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• 제7권6호
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• pp.811-815
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• 1998

Currently in Korea, standard operating procedure for the analyses of phenolic compounds in water is the spectrometric comparison of colors developed by 4-amino antipyrin with phenolic compounds. It is however that this method cannot identify individual compound and that some phenolic compounds do not react with 4-amino antipyrin. Spectrometric determinations of phenolic compounds were compared with chromatographic analyses of gas chromatography (GC) and high pressure liquid chromatography (HPLC) of various phenolic compounds. Individual phenolic compounds could be determined by both chromatographic methods but HPLC methods were more precise with lower detection levels in general.