Impact of cyclofructan derivatives as efficient chiral selector in chiral analysis: An overview

Chirality ◽  
2021 ◽  
Author(s):  
Hassan Y. Aboul‐Enein ◽  
Valliappan Kannappan ◽  
Selvakumar Kanthiah

Author(s):  
Seung Il Cho ◽  
Jiyeon Shim ◽  
Min-Su Kim ◽  
Doo Soo Chung ◽  
Yong-Kweon Kim


Molecules ◽  
2021 ◽  
Vol 26 (8) ◽  
pp. 2261
Author(s):  
Gabriel Hancu ◽  
Lajos Attila Papp ◽  
Gergő Tóth ◽  
Hajnal Kelemen

Cyclodextrin (CD) derivatives are the most efficient and frequently used chiral selectors (CSs) in capillary electrophoresis (CE). There are situations when the use of a single CD as CS is not enough to obtain efficient chiral discrimination of the enantiomers; in these cases, sometimes this problem can be resolved using a dual CD system. The use of dual CD systems can often dramatically enhance enantioseparation selectivity and can be applied for the separation of many analytes of pharmaceutical interest for which enantioseparation by CE with another CS systems can be problematic. Usually in a dual CD system an anionic CD is used together with a neutral one, but there are situations when the use of a cationic CD with a neutral one or the use of two neutral CDs or even two ionized CDs can be an efficient solution. In the current review we present general aspects of the use of dual CD systems in the analysis of pharmaceutical substances. Several examples of applications of the use of dual CD systems in the analysis of pharmaceuticals are selected and discussed. Theoretical aspects regarding the separation of enantiomers through simultaneous interaction with the two CSs are also explained. Finally, advantages, disadvantages, potential and new direction in this chiral analysis field are highlighted.



1998 ◽  
Vol 807 (1) ◽  
pp. 37-56 ◽  
Author(s):  
Claudia Desiderio ◽  
Salvatore Fanali


2007 ◽  
Vol 65 (9-10) ◽  
pp. 575-579
Author(s):  
R WANG ◽  
Z JIA ◽  
J FAN ◽  
L CHEN ◽  
H XIE ◽  
...  
Keyword(s):  




Author(s):  
Anna Krin ◽  
Juan Lopez ◽  
Susana Blanco ◽  
Pablo Pinacho ◽  
Juan Avilés-Moreno ◽  
...  


2019 ◽  
Vol 6 (1) ◽  
pp. 18-23
Author(s):  
Sema Salgın ◽  
◽  
Seda Öner ◽  
Uğur Salgın
Keyword(s):  


Molecules ◽  
2021 ◽  
Vol 26 (12) ◽  
pp. 3527
Author(s):  
Ali Fouad ◽  
Adel A. Marzouk ◽  
Montaser Sh. A. Shaykoon ◽  
Samy M. Ibrahim ◽  
Sobhy M. El-Adl ◽  
...  

Daptomycin, a macrocyclic antibiotic, is here used as a new chiral selector in preparation of chiral stationary phase (CSP) in a recently prepared polymer monolithic capillary. The latter is prepared using the copolymerization of the monomers glycidyl methacrylate (GMA) and ethylene glycol dimethacrylate (EGDMA) in the presence of daptomycin in water. Under reversed phase conditions (RP), the prepared capillaries were tested for the enantioselective nanoliquid chromatographic separation of fifty of the racemic drugs of different pharmacological groups, such as adrenergic blockers, H1-blockers, NSAIDs, antifungal drugs, and others. Baseline separation was attained for many drugs under RP-HPLC. Daptomycin expands the horizon of chiral selectors in HPLC.



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