Chiral separation of amino acids by capillary electrophoresis with 3-[(3-cholamidopropyl)-dimethylammonio]-1-propane sulfonate as chiral selector

2003 ◽  
Vol 57 (1-2) ◽  
pp. 81-86 ◽  
Author(s):  
C. D. Tran ◽  
J. Kang



1996 ◽  
Vol 737 (2) ◽  
pp. 263-272 ◽  
Author(s):  
István E. Valkó ◽  
Heli Sirén ◽  
Marja-Liisa Riekkola


2013 ◽  
Vol 36 (9-10) ◽  
pp. 1568-1574 ◽  
Author(s):  
Yongbo Peng ◽  
Tingting Zhang ◽  
Tingting Wang ◽  
Zhenghua Liu ◽  
Jacques Crommen ◽  
...  


2014 ◽  
Vol 99 ◽  
pp. 16-21 ◽  
Author(s):  
Krisztina Németh ◽  
Celesztina Domonkos ◽  
Virág Sarnyai ◽  
Julianna Szemán ◽  
László Jicsinszky ◽  
...  


Molecules ◽  
2020 ◽  
Vol 25 (12) ◽  
pp. 2879
Author(s):  
Pavel Řezanka ◽  
Denisa Macková ◽  
Radek Jurok ◽  
Michal Himl ◽  
Martin Kuchař

Mephedrone, a psychoactive compound derived from cathinone, is widely used as a designer drug. The determination of mephedrone and its metabolites is important for understanding its possible use in medicine. In this work, a method of capillary electrophoresis for the chiral separation of mephedrone and its metabolites was developed. Carboxymethylated β-cyclodextrin was selected as the most effective chiral selector from seven tested cyclodextrin derivates. Based on the simplex method, the optimal composition of the background electrolyte was determined: at pH 2.75 and 7.5 mmol·L−1 carboxymethylated β-cyclodextrin the highest total resolution of a mixture of analytes was achieved. For mephedrone and its metabolites, calibration curves were constructed in a calibration range from 0.2 to 5 mmol·L−1; limits of detection, limits of quantification, precision, and repeatability were calculated, and according to Mandel’s fitting test, the linear calibration ranges were determined.



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