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Separation of α-amylase inhibitors from Abelmoschus esculentus (L).Moench by on-line two-dimensional high-speed counter-current chromatography target-guided by ultrafiltration-HPLC.
Zeng, Hualiang; Liu, Qi; Yu, Jingang; Wang, Meiling; Chen, Miao; Wang, Ranhao; He, Xi; Gao, Menghuan; Chen, Xiaoqing.
Afiliação
  • Zeng H; College of Chemistry and Chemical Engineering, Central South University, Changsha, China.
  • Liu Q; College of Chemistry and Chemical Engineering, Central South University, Changsha, China.
  • Yu J; China Division of Physical Biology & Bioimaging Center, Shanghai Synchrotron Radiation Facility, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai, China.
  • Wang M; College of Chemistry and Chemical Engineering, Central South University, Changsha, China.
  • Chen M; College of Chemistry and Chemical Engineering, Central South University, Changsha, China.
  • Wang R; College of Chemistry and Chemical Engineering, Central South University, Changsha, China.
  • He X; College of Chemistry and Chemical Engineering, Central South University, Changsha, China.
  • Gao M; College of Chemistry and Chemical Engineering, Central South University, Changsha, China.
  • Chen X; College of Chemistry and Chemical Engineering, Central South University, Changsha, China.
J Sep Sci ; 38(22): 3897-3904, 2015 Nov.
Article em En | MEDLINE | ID: mdl-26337511
ABSTRACT
In this study, an on-line two-dimensional high-speed counter-current chromatography system based on a six-port valve was developed. Target-guided by ultrafiltration with high-performance liquid chromatography, the one-step isolation of three potential α-amylase inhibitors from Abelmoschus esculentus (L).Moench was achieved by employing the developed orthogonal system and extrusion elution mode. The purities of three potential α-amylase inhibitors were all over 95% as determined by high-performance liquid chromatography. Furthermore, UV, mass spectrometry and 1 H NMR spectroscopy were applied to the structural identification of the isolated three target compounds, their structures were assigned as quercetin-3-O-sophoroside (i), 5,7,3',4'-tetrahydroxy flavonol-3-O-[ß-d-rhamnopyranosil-(1→2)]-ß-d-glucopyranoside (ii ) and isoquercitrin (iii), respectively. The Results demonstrated that the proposed method was highly efficient to screen and isolate enzyme inhibitors from complex natural products extracts, and on-line two-dimensional high-speed counter-current chromatography can effectively increase the peak resolution of target compounds.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: J Sep Sci Ano de publicação: 2015 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: J Sep Sci Ano de publicação: 2015 Tipo de documento: Article País de afiliação: China