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pH 区域精制离心分配色谱法用于从茄属植物中制备分离和纯化甾体糖苷生物碱。

pH-Zone-refining centrifugal partition chromatography for preparative isolation and purification of steroidal glycoalkaloids from Solanum xanthocarpum.

机构信息

Analytical Chemistry Division, Central Institute of Medicinal and Aromatic Plants, Lucknow, India.

出版信息

J Sep Sci. 2009 Sep;32(18):3126-32. doi: 10.1002/jssc.200900323.

Abstract

pH-Zone-refining centrifugal-partition chromatography (CPC) was successfully applied in the separation of complex polar steroidal glycoalkaloids of close Rf values, directly from a crude extract of Solanum xanthocarpum. The experiment was performed with a two phase solvent system composed of ethyl acetate/butanol/water (1:4:5 by volume) where triethylamine (5 mM) was added to the upper organic mobile phase as an eluter and TFA (10 mM) to the aqueous stationary phase as a retainer. Separation of 1 g of crude extract over CPC resulted in two distinct pH-zones. The fractions collected in pH-zone i afforded 72 mg of solasonine while the fractions collected in pH-zone ii were slightly impure, hence were purified over medium pressure LC, which afforded 30 mg of solasonine and further 15 mg of solamargine (SM). The steroidal glycoalkaloids, SM and solasonine were isolated in 93.3 and 91.6% purity, respectively. The isolated alkaloids were characterized on the basis of their (1)H, (13)C-NMR, and ESI-MS data.

摘要

pH 区域精制离心分配色谱 (CPC) 成功地应用于从茄属植物粗提物中直接分离具有相近 Rf 值的复杂极性甾体糖苷生物碱。实验采用由乙酸乙酯/正丁醇/水(体积比 1:4:5)组成的两相溶剂系统,在上层有机流动相中添加三乙胺(5 mM)作为洗脱剂,在水相固定相中添加 TFA(10 mM)作为保留剂。通过 CPC 对 1 g 粗提物进行分离,得到两个明显的 pH 区域。在 pH 区域 i 收集的馏分中得到 72 mg 的茄碱,而在 pH 区域 ii 收集的馏分稍微不纯,因此通过中压 LC 进行纯化,得到 30 mg 的茄碱和进一步的 15 mg 的澳洲茄碱(SM)。甾体糖苷生物碱 SM 和茄碱的纯度分别为 93.3%和 91.6%。分离得到的生物碱基于其(1)H、(13)C-NMR 和 ESI-MS 数据进行表征。

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