• 제목/요약/키워드: chiral column

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Chiral Drugs의 광학분할을 위한 HPLC Column의 응용 (The Application of Chiral HPLC Columns for Enantiomer Separation of Chiral Drugs)

  • 이원재
    • 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.

Coupled Column Chromatography in Chiral Separation of Salmeterol

  • Kim, Kyeong-Ho;Yun, Hyeong-Won;Kim, Hyun-Ju;Park, Hyun-Ji;Choi, Pok-Wha
    • Archives of Pharmacal Research
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    • 제21권2호
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    • pp.212-216
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    • 1998
  • A coupled achiral-chiral high-performance liquid chromatographic system has been developed for the determination of the enantiomers of salmeterol, S-(+)-salmeterol and R-(-)-salmeterol in urine. THe salmeterol was separated from the interfering components in urine and quantified on the silica column, and the enantiomeric composition was determined on a Sumichiral OA-4700 chiral stationary phase. The two columns were connected by a switching valve equipped with a silica precolumn. The two columns wer connected by a switching valve equipped with a silica precolumn. The precolumn was used to concentrate the salmeterol in the eluent from the achiral column before backflushing onto the chiral phase. The coupled system was validated.

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Determination of Terbutaline Enantiomers in Human Plasma by Coupled Achiral-Chiral High Performance Liquid Chromatography

  • Kim, Kyeong-Ho;Kim, Hyun-Ju;Hong, Seon-Pyo;Shin, Sang-Deok
    • Archives of Pharmacal Research
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    • 제23권5호
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    • pp.441-445
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    • 2000
  • Achiral-chiral column switching HPLC assay was developed to allow the separation and quantification of the enantiomers of terbutaline in human plasma by means of fluorescence detection. Plasma samples were prepared by solid-phase extraction with sep-pak silica, followed by HPLC assay. The enantiomers of terbutaline and the internal standard were separated from the biological matrix on a silica column, and the two enantiomers were resolved and quantified on a Sumichiral OA-4900 column. The two columns were connected by a switching valve equipped with silica trap column, The trap column was used to concentrate the terbutaline in the eluent from the achiral column before back flushing onto the chiral phase. For each enantiomers, the assay was linear between 2.5-125 ng/$m\ell$ (r=0.9999) and detection limit was 1.0 ng/$m\ell$ .

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Achiral/Chiral Coupled Column법에 의한 식품 중의 D-아미노산의 정량분석 (Micro-Determination of D-Amino Acids in Food by Using Achirai/Chiral Coupled Column Method)

  • 이선행;장윤희;이광필
    • 분석과학
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    • 제9권1호
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    • pp.52-61
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    • 1996
  • 식품 중의 몇몇 유리 D-아미노산이 column switching method에 의해 검출되었다. D-아미노산과 L-아미노산의 총량의 정량은 $C_{18}$ 컬럼을 사용한 비키랄 분리에 근거한다. L-아미노산에 대한 D-아미노산의 수준은 o-phthalaldehyde로 유도체화된 아미노산의 postcolumn reaction detection을 포함하는 column switching system에 의해 정량되었다. Postcolumn detection system의 키랄 분리는 chiral crown ether 컬럼에 의해 실행되었다. 이 system은 간장과 발효된 콩, 그리고 콩 같은 식품 중에 있는 D-아미노산의 정량에 적용된다. 이 achiral/chiral coupled-column system하에서는 시료 전처리과정이 중요함을 알게 되었다. Phenylalanine은 시판용 간장 속에 242ppm, 재래식 간장 속에는 102ppm, 발효된 콩에는 1g당 8.34mg, 콩에는 1g당 2.87mg이 함유된 것으로 밝혀졌다. D-phenylalanine은 시판용 간장 속에는 0.67%, 재래식 간장에는 0.34%, 발효된 콩에는 1.81% 미만, 콩에는 2.82% 미만이 검출되었다.

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Chiral Separation of the Enantiomers of Metoprolol and Its Metabolites by High Performance Liquid Chromatography

  • Kim, Kyeong-Ho;Shin, Sang-Duk;Lee, Joo-Hyun;Lee, Sang-Cheal;Kang, Jong-Seong;Mar, Woong-chon;Hong, Seon-Pyo;Kim, Hyun-Ju
    • Archives of Pharmacal Research
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    • 제23권3호
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    • pp.230-236
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    • 2000
  • (1'R, 2R)-, (1'R, 2S)-, (1'S, 2R)- and (1'S, 2S)-$\alpha$-hydroxymetoprolol; (2R)- and (2S)-O-des-methylmetoprolol; and (2R)- and (2S)-metoprolol acid are major metabolites of (2R)-and (2S)-metoprolol, $\beta$-adrenergic antagonist. The focus of most chiral separation methods until now has been on determination of the enantiomeric parent drug. However, it is just as important to be able to follow the metabolism of the enantiomers and their possible chiral metabolites. Therefore, for the study of stereoselective metabolism and pharmacokinetics of metoprolol, the chiral separation of the enantiomers of metoprolol and its metabolites has been investigated using four chiral stationary phases, i.e., Chiralcel OD, Chiral-AGP, Cyclobond I and Sumichiral OA-4900 columns. Metoprolol acid was resolved only by Sumichiral OA-4900. Chiralcel OD provided the highest separation factor and resolution value for metoprolol and O-desmethylmetoprolol and partially resolved the four stereoisomers of $\alpha$-hydroxymetoprolol. Diastereomeric $\alpha$-hydroxymetoprolols were resolved using the coupled column chromatographic system of two chiral stationary phases, Sumichiral OA-4900 column and Chiralcel OD column.

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Column-Switching System을 이용한 우유속의 D-아미노산의 미량정량 (Micro-Determination of D-Amino Acids in Milk by using Column Switching System)

  • 이선행;김경희;이영철;김상태
    • 대한화학회지
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    • 제39권4호
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    • pp.257-265
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    • 1995
  • 시중에 시판되고 있는 우유를 전처리하여 이 우유에 포함된 유리 아미노산을 dansyl-chloride로 유도체화시켜 C-18 컬럼을 이용한 역상 LC법으로 분리한 다음 표준물 첨가법으로 정량했다. 미량의 D-아미노산의 분리에서는 LC의 Column-Switching System을 이용하였으며 비키랄 컬럼을 통과한 단실 D/L-아미노산에 $Cu(N-benzyl-L-proline)_2$를 이동상에 첨가한 키랄 분리를 수행하여 L-아미노산에서 D-아미노산을 분리 정량했다. 이 방법은 우유시료 중에 존재하는 16가지 아미노산의 정량이 가능하며 이중에 12가지의 D-아미노산이 column switching 방법을 통한 키랄 분리로 정량이 가능하다. 우유 100 mL에 총 유리 아미노선이 41.00 mg 포함되어 있음을 확인했으며, D-아미노산은 D-glutamic acid가 2.05%, D-alanine 2.93%만이 포함되어 있음을 확인했다.

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키랄 크로마토그래피에 의한 시판되는 나프록센의 광학순도 측정 (Measurement of optical purity for commercial naproxen by chiral HPLC)

  • 유정재;이원두;류재정
    • 분석과학
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    • 제24권5호
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    • pp.360-367
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    • 2011
  • 8개의 제약회사에서 제조되어 현재 시판되고 있는 10개의 나프록센에 대한 광학순도를 최적조건의 키랄 HPLC로 조사하였다. Chiralcel OD-H 칼럼과 ChiralHyun-LE(S)-1 칼럼을 키랄정지상으로 사용하였고, hexane:isopropanol:acetic acid 이 100:2.85:0.1로 혼합된 용액을 전개용매로 사용하였다. 대부분 시료의 광학순도는 97% 이상이었고, 하나는 95% 수준으로 나타났다. 이 값들에 대한 상대표준편차 평균은 0.034%로 매우 작게 나타났다.

Development and Application of Crown Ether-based HPLC Chiral Stationary Phases

  • Hyun, Myung-Ho
    • Bulletin of the Korean Chemical Society
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    • 제26권8호
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    • pp.1153-1163
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    • 2005
  • Crown ether-based HPLC chiral stationary phases (CSPs) have been successfully utilized in the resolution of various racemic compounds containing a primary amino group. Especially, CSPs based on chiral crown ethers incorporating chiral binaphthyl unit or tartaric acid unit and based on phenolic pseudo chiral crown ethers have shown high chiral recognition efficiency. In this account paper, a review on the development of crown etherbased HPLC CSPs, their structural characteristics and applications to the resolution of racemic compounds including chiral drugs containing a primary or secondary amino group with the variation of the type and the content of mobile phase components and with the variation of the column temperature is presented.

역상 크로마토그래피에서 다당유도체로 공유결합된 키랄 컬럼을 이용한 거울상 이성질체의 광학분리 (Enantiomer separation using a covalently immobilized chiral column derived from polysaccharide derivative by reversed phase liquid chromatography)

  • 황호;김경옥;백채선;이원재
    • 분석과학
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    • 제22권2호
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    • pp.148-151
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    • 2009
  • 역상 액체 크로마토그래피에서 다당유도체 선택자가 공유결합된 키랄 컬럼인 Chiralpak IB을 사용하여 N-FMOC $\alpha$-amino acid의 광학 이성질체의 분리를 수행하였다. 공유결합된 키랄 컬럼인 Chiralpak IB에서 여러 역상 이동상 조건들이 광학분할의 선택성과 분리인자, 머무름시간에 미치는 영향을 보여주었다. 또한 역상 액체 크로마토그래피에서 N-FMOC $\alpha$-amino acid의 광학 이성질체의 분리 결과를 순상 액체 크로마토그래피 결과와 비교하였는데 순상이동상을 사용한 것보다는 대체적으로 낮은 광학분할을 보여주었다.

Comparison of liquid chromatographic enantiomer resolution of racemic amino compounds on chiral stationary phases of crown ether type

  • Lee, Won-Jae;Baek, Chae-Sun;Kim, Ji-Yeon
    • 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.285.1-285.1
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    • 2003
  • ChiroSil RCA(+) and SCA(-) HPLC chiral stationary phases (CSPs) developed by covalently bonding (+)- and (-)-(18-crown-6)-2,3,11,12-tetracarboxylic acid (18-C-6-T A) to silica gel were employed for enantioresolution of racemic amino compounds, respectively. Also, these 18-C-6-TA covalently bonded CSPs were compared to a commercially available Crownpak CR CSP prepared by coating chiral crown ether as a chiral selector on ODS column. (omitted)

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