Preparation of a New Chiral Stationary Phase Based on Macrocyclic Amide Chiral Selector for the Liquid Chromatographic Chiral Separations

Chirality ◽  
2016 ◽  
Vol 28 (3) ◽  
pp. 253-258 ◽  
Author(s):  
Ji Yeong Sung ◽  
Seung Hyuck Choi ◽  
Myung Ho Hyun
Keyword(s):  
Stationary Phase ◽  
Chiral Stationary Phase ◽  
Chiral Separations ◽  
Chiral Selector ◽  
Liquid Chromatographic

Preparation of chiral stationary phase via activated carbamate intermediate for liquid chromatographic optical resolution

1987 ◽  
Vol 23 (10) ◽  
pp. 727-730 ◽  
Author(s):  
K. Iwaki ◽  
S. Yoshida ◽  
N. Nimura ◽  
T. Kinoshita ◽  
K. Takeda ◽  
...  
Keyword(s):  
Stationary Phase ◽  
Chiral Stationary Phase ◽  
Optical Resolution ◽  
Liquid Chromatographic

Chiral separations of β-blocking drug substances using the Pirkle-type α-Burke 1 chiral stationary phase

1997 ◽  
Vol 757 (1-2) ◽  
pp. 65-71 ◽  
Author(s):  
Poul Vibholm Petersen ◽  
Jens Ekelund ◽  
Lars Olsen ◽  
Sanna Vinding Ovesen
Keyword(s):  
Stationary Phase ◽  
Chiral Stationary Phase ◽  
Chiral Separations ◽  
Blocking Drug ◽  
Drug Substances

scholarly journals Immobilization of Chondroitin Sulfate A onto Monolithic Epoxy Silica Column as a New Chiral Stationary Phase for High-Performance Liquid Chromatographic Enantioseparation

2021 ◽  
Vol 14 (2) ◽  
pp. 98
Author(s):  
Ratih Ratih ◽  
Hermann Wätzig ◽  
Azminah Azminah ◽  
Mufarreh Asmari ◽  
Benjamin Peters ◽  
...  
Keyword(s):  
Stationary Phase ◽  
Chondroitin Sulfate ◽  
High Performance ◽  
Chiral Stationary Phase ◽  
High Performance Liquid Chromatographic ◽  
Schiff Base Formation ◽  
The Individual ◽  
Liquid Chromatographic ◽  
Base Formation ◽  
Chondroitin Sulfate A

Chondroitin sulfate A was covalently immobilized onto a monolithic silica epoxy column involving a Schiff base formation in the presence of ethylenediamine as a spacer and evaluated in terms of its selectivity in enantioseparation. The obtained column was utilized as a chiral stationary phase in enantioseparation of amlodipine and verapamil using a mobile phase consisting of 50 mM phosphate buffer pH 3.5 and UV detection. Sample dilution by organic solvents (preferably 25% v/v acetonitrile-aqueous solution) was applied to achieve baseline enantioresolution (Rs > 3.0) of the individual drug models within 7 min, an excellent linearity (R2 = 0.999) and an interday repeatability of 1.1% to 1.8% RSD. The performance of the immobilized column for quantification of racemate in commercial tablets showed a recovery of 86–98% from tablet matrices. Computational modeling by molecular docking was employed to investigate the feasible complexes between enantiomers and the chiral selector.

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