Isolation of -Amylase Inhibitors from Kadsura longipedunculata Using a High-Speed Counter-Current Chromatography Target Guided by Centrifugal Ultrafiltration with LC-MS

被引:15
作者
Cen, Yin [1 ]
Xiao, Aiping [2 ]
Chen, Xiaoqing [1 ]
Liu, Liangliang [2 ]
机构
[1] Cent South Univ, Coll Chem & Chem Engn, Changsha 410083, Hunan, Peoples R China
[2] Chinese Acad Agr Sci, Inst Bast Fiber Crops, Changsha 410205, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
alpha-amylase; HSCCC; Kadsura; longipedunculata; ultrafiltration; ALPHA-GLUCOSIDASE; ANTIOXIDANT ACTIVITY; LONICERA-JAPONICA; IDENTIFICATION; SEPARATION; SPECTROMETRY; COMPONENTS; EXTRACTS; BINDING; MILLET;
D O I
10.3390/molecules21091190
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this study, a high-speed counter-current chromatography (HSCCC) separation method target guided by centrifugal ultrafiltration with high-performance liquid chromatography-mass spectrometry (CU-LC-MS) was proposed. This method was used to analyze -amylase inhibitors from Kadsuralongipedunculata extract. According to previous screening with CU-LC-MS, two screened potential -amylase inhibitors was successfully isolated from Kadsuralongipedunculata extract using HSCCC under the optimized experimental conditions. The isolated two target compounds (with purities of 92.3% and 94.6%) were, respectively, identified as quercetin-3-O-rhamnoside (1) and protocatechuic acid (2) based on the MS, UV, and H-1-NMR spectrometry data. To verify the inhibition of screened compounds, the inhibitory activities of quercetin-3-O-rhamnoside (1) and protocatechuic acid (2) on -amylase were tested, and it demonstrated that the experimental IC50 values of quercetin-3-O-rhamnoside (1) and protocatechuic acid (2) were 28.8 and 12.5 mol/L. These results proved that the hyphenated technique using CU-LC-MS and HSCCC was a rapid, competent, and reproductive method to screen and separate potential active compounds, like enzyme inhibitors from the extract of herbal medicines.
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页数:10
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