Investigation of the Enantioseparation of Basic Drugs with Erythromycin Lactobionate as a Chiral Selector in CE

2010 ◽  
Vol 72 (3-4) ◽  
pp. 289-295 ◽  
Author(s):  
Guangfu Xu ◽  
Yingxiang Du ◽  
Bin Chen ◽  
Jiaquan Chen
2008 ◽  
Vol 31 (14) ◽  
pp. 2701-2706 ◽  
Author(s):  
Nerissa L. Deñola ◽  
Noel S. Quiming ◽  
Alicia P. Catabay ◽  
Yoshihiro Saito ◽  
Kiyokatsu Jinno
Keyword(s):  

2006 ◽  
Vol 27 (12) ◽  
pp. 2367-2375 ◽  
Author(s):  
Nerissa L. Deñola ◽  
Noel S. Quiming ◽  
Alicia P. Catabay ◽  
Yoshihiro Saito ◽  
Kiyokatsu Jinno

2006 ◽  
Vol 27 (21) ◽  
pp. 4364-4374 ◽  
Author(s):  
Maria A. Martínez-Gómez ◽  
R. M. Villanueva-Camañas ◽  
Salvador Sagrado ◽  
Maria J. Medina-Hernández

2021 ◽  
Vol 2021 ◽  
pp. 1-6
Author(s):  
Jin Xu ◽  
Xuecheng Sun ◽  
Xiaodong Sun ◽  
Ye Lu

In this paper, a capillary coated with poly(glycidyl methacrylate) nanoparticles (PGMA NPs) was prepared and applied to construct a capillary electrophoresis (CE) enantioseparation system with glucosyl-β-cyclodextrin (Glu-β-CD) as a chiral selector. The PGMA NP coating can be easily introduced through a simple ring-opening reaction. Two basic drugs were used as models to evaluate the separation performance of the PGMA coating. Under the optimal conditions selected, the separation of the two enantiomers was obtained.


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