Capillary electrophoretic chiral separation of Cinchona alkaloids using a cyclodextrin selector

2008 ◽  
Vol 31 (6-7) ◽  
pp. 1130-1136 ◽  
Author(s):  
Dimitrios Tsimachidis ◽  
Petr Česla ◽  
Tomas Hájek ◽  
Georgios Theodoridis ◽  
Pavel Jandera
2006 ◽  
Vol 27 (5-6) ◽  
pp. 1248-1254 ◽  
Author(s):  
Carmem Dickow Cardoso ◽  
Valquíria A. Polisel Jabor ◽  
Pierina Sueli Bonato

Author(s):  
María Gabriela Vargas Martinez ◽  
Guillermo Ramírez Galicia

<p>A capillary electrophoretic method for the chiral separation of the 3-chiral-1,4-benzodiazepines was developed. Enantiomeric resolution of oxazepam, lorazepam, temazepam, and lormetazepam was achieved using sulfated cyclodextrins (CD's) as chiral selectors. A 3-levels, 4-factors fractional factorial (34-2) design was applied to test 3 different CD's: heptakis-6-sulfato--cyclodextrin (HSCD), heptakis-(2,3-diacetyl-6-sulfato)--cyclodextrin (HDASCD), and heptakis-(2,3-dimethyl-6-sulfato)--cyclodextrin (HDMSCD). The CD type, its concentration, the pH of the electrolyte, and % organic modifier were tested as the factors in the experimental design. The highest resolution values were obtained using a 20 mM borate buffer, pH 9.0 with the addition of 5 % HSCD and 15 % methanol as an organic modifier. At these separation conditions, the equilibrium constants of the benzodiazepine-HSCD complex formation were calculated. A theoretical study of the interaction benzodiazepine-HSCD complex using semiempirical calculations is postulated.</p>


Chirality ◽  
2015 ◽  
Vol 28 (3) ◽  
pp. 199-203 ◽  
Author(s):  
Zoltán-István Szabó ◽  
Levente Szőcs ◽  
Daniela-Lucia Muntean ◽  
Béla NoszáL ◽  
Gergő Tóth

2001 ◽  
Vol 24 (5) ◽  
pp. 402-406 ◽  
Author(s):  
Kyeong Ho Kim ◽  
Joo Hyun Lee ◽  
Mi Young Ko ◽  
Seon-Pyo Hong ◽  
Jeong Rok Youm

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