Optimization of integrated extraction-adsorption process for the extraction and purification of total flavonoids from Scutellariae barbatae herba

2017 ◽  
Vol 175 ◽  
pp. 203-212 ◽  
Author(s):  
Peng Huang ◽  
Qing Zhang ◽  
Hongye Pan ◽  
Lianjun Luan ◽  
Xuesong Liu ◽  
...  
2018 ◽  
Vol 33 (20) ◽  
pp. 3025-3028 ◽  
Author(s):  
Yuping Shen ◽  
Minhui Xu ◽  
Yufei Chen ◽  
Haiyan Wang ◽  
Yiying Zhou ◽  
...  

2016 ◽  
Vol 213 ◽  
pp. 514-520 ◽  
Author(s):  
Estefanía Cordisco ◽  
Carla N. Haidar ◽  
Ezequiel R. Coscueta ◽  
Bibiana B. Nerli ◽  
Luciana P. Malpiedi

Molecules ◽  
2021 ◽  
Vol 26 (14) ◽  
pp. 4162
Author(s):  
Xiaoya Wang ◽  
Jianqing Su ◽  
Xiuling Chu ◽  
Xinyu Zhang ◽  
Qibin Kan ◽  
...  

We examined the application of six different resins with the aim of selecting a macroporous resin suitable for purifying Acanthopanax senticosus total flavonoids (ASTFs) from Acanthopanax senticosus crude extract (EAS) by comparing their adsorption/desorption capacities, which led to the selection of HPD-600. Research on the adsorption mechanism showed that the adsorption process had pseudo-second-order kinetics and fit the Freundlich adsorption model. Moreover, the analysis of thermodynamic parameters indicated that the adsorption process is spontaneous and endothermic. The optimal conditions for purification of ASTFs were determined as sample pH of 3, 60% ethanol concentration, and 3 BV·h−1 flow rate, for both adsorption and desorption, using volumes of 2.5 and 4 BV, respectively. The application of macroporous resin HPD-600 to enrich ASTFs resulted in an increase in the purity of total flavonoids, from 28.79% to 50.57%. Additionally, the antioxidant capacity of ASTFs was higher than that of EAS, but both were lower than that of L-ascorbic acid. The changes in ASTFs compositions were determined using ultra-performance liquid chromatography–tandem mass spectrometry (UHPLC–MS/MS), with the results illustrating that the levels of seven major flavonoids of ASTFs were increased compared to that in the crude extract.


1970 ◽  
Vol 63 (2) ◽  
pp. 225-241 ◽  
Author(s):  
B. D. Reeves ◽  
M. L. A. de Souza ◽  
I. E. Thompson ◽  
E. Diczfalusy

ABSTRACT An improved method for the assay of plasma progesterone by competitive protein binding is described. The improvement is based upon rigorous control of the variables, the compensation for and standardisation of interfering factors inherent in the method and the use of a human corticosteroid binding globulin, that meets the requirements for sensitivity at levels of 1.0 ng of progesterone and below. The assessment of the reliability of the individual steps in the method as well as that of the complete method is presented. The sensitivity of the method is around 0.2 ng progesterone per ml plasma. Accuracy was measured by adding progesterone in amounts ranging from 0.0 to 1.0 ng to 1.0 ml plasma. There was a linear relationship between the progesterone added and recovered throughout the entire range of values, with a coefficient of correlation (r) of 0.94. Of 52 related steroids tested, none was found which would remain associated with progesterone following extraction and purification and which would also compete with progesterone for binding sites.


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