New validated HPLC methodology for the determination of (−)-trans-paroxetine and its enantiomer in pharmaceutical formulations with use of ovomucoid chiral stationary phase-Reference-Cited by-同舟云学术

New validated HPLC methodology for the determination of (−)-trans-paroxetine and its enantiomer in pharmaceutical formulations with use of ovomucoid chiral stationary phase

Published:2014-01-10 Issue:15 Volume:406 Page:3697-3702
ISSN:1618-2642
Container-title:Analytical and Bioanalytical Chemistry
language:en
Short-container-title:Anal Bioanal Chem

Author:

Lisowska-Kuźmicz Małgorzata,Kantor-Boruta Małgorzata,Jończyk Anna,Jarończyk Małgorzata,Ocios-Bębenek Agnieszka,Mazurek Aleksander P.,Chilmonczyk Zdzisław,Jarosz Maciej

Publisher

Springer Science and Business Media LLC

Subject

Biochemistry,Analytical Chemistry

Link

http://link.springer.com/article/10.1007/s00216-013-7565-y/fulltext.html

Reference14 articles.

1. Bao Z, Su B, Ren Q (2008) Kinetic and equilibrium study of the enantioseparation of paroxetine intermediate on amylose and tartaric acid-based chiral stationary phases. J Sep Sci 31:16–22

2. Segura M, Roura L, de la Torre R, Joglar J (2003) Synthesis of the major metabolites of paroxetine. Bioorg Chem 31:248–258

3. Zukowski J, Brightwell M, De Biasi V (2003) Chiral HPLC method for chiral purity determination of paroxetine drug substance. Chirality 31:600–604

4. Rodríguez Flores J, Berzas Nevado JJ, Contento Salcedo AM, Cabello Díaz MP (2004) Development of capilary zone electrophoretic method to determine six antidepressants in their pharmaceutical preparations. Experimental design for evaluating the ruggedness of method. J Sep Sci 27:33–40

5. Rodríguez Flores J, Berzas Nevado JJ, Contento Salcedo AM, Cabello Díaz MP (2004) Development and validation method for determination of paroxetine and its metabolites by nonaqueos capillary electrophoresis in human urine. Experimental design for evaluating the ruggedness of method. Electrophoresis 25:454–462

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