Single-run reversed-phase HPLC method for determining sertraline content, enantiomeric purity, and related substances in drug substance and finished product

[1]  S. Fanali,et al.  Further study on enantiomer resolving ability of amylose tris(3-chloro-5-methylphenylcarbamate) covalently immobilized onto silica in nano-liquid chromatography and capillary electrochromatography. , 2020, Journal of chromatography. A.

[2]  S. Fanali,et al.  Comparative study on enantiomer resolving ability of amylose tris(3-chloro-5-methylphenylcarbamate) covalently immobilized onto silica in nano-liquid chromatography and capillary electrochromatography. , 2019, Journal of chromatography. A.

[3]  C. Castells,et al.  Enantioseparation of the racemates of a number of pesticides on a silica-based column with immobilized amylose tris(3-chloro-5-methylphenylcarbamate) , 2019, Microchemical Journal.

[4]  R. Cirilli,et al.  Temperature and eluent composition effects on enantiomer separation of carvedilol by high-performance liquid chromatography on immobilized amylose-based chiral stationary phases , 2019, Journal of pharmaceutical analysis.

[5]  S. Carradori,et al.  A chromatographic study on the retention behavior of the amylose tris(3-chloro-5-methylphenylcarbamate) chiral stationary phase under aqueous conditions. , 2018, Journal of separation science.

[6]  R. Cirilli,et al.  Unusual retention behavior of omeprazole and its chiral impurities B and E on the amylose tris (3-chloro-5-methylphenylcarbamate) chiral stationary phase in polar organic mode , 2018, Journal of pharmaceutical analysis.

[7]  R. Cirilli,et al.  Development of a high-performance liquid chromatography method for the simultaneous determination of chiral impurities and assay of (S)-clopidogrel using a cellulose-based chiral stationary phase in methanol/water mode. , 2018, Journal of separation science.

[8]  A. Calcaterra,et al.  The market of chiral drugs: Chiral switches versus de novo enantiomerically pure compounds , 2018, Journal of pharmaceutical and biomedical analysis.

[9]  D. Muntean,et al.  Chirality of Modern Antidepressants: An Overview , 2017, Advanced pharmaceutical bulletin.

[10]  A. Coluccia,et al.  Heterocyclic pharmacochemistry of new rhinovirus antiviral agents: A combined computational and experimental study. , 2017, European journal of medicinal chemistry.

[11]  S. Carradori,et al.  The sodium salt of the enantiomers of ricobendazole: Preparation, solubility and chiroptical properties , 2017, Journal of pharmaceutical and biomedical analysis.

[12]  R. N. Rao,et al.  Determination of rat plasma levels of sertraline enantiomers using direct injection with achiral-chiral column switching by LC-ESI/MS/MS. , 2010, Journal of pharmaceutical and biomedical analysis.

[13]  A. Kalali,et al.  Generic penetration in the retail antidepressant market. , 2010, Psychiatry (Edgmont (Pa. : Township)).

[14]  M. Lämmerhofer.  Chiral recognition by enantioselective liquid chromatography: mechanisms and modern chiral stationary phases. , 2010, Journal of chromatography. A.

[15]  R. N. Rao,et al.  Separation of stereoisomers of sertraline and its related enantiomeric impurities on a dimethylated beta-cyclodextrin stationary phase by HPLC. , 2009, Journal of pharmaceutical and biomedical analysis.

[16]  F. Gasparrini,et al.  Study of mechanisms of chiral discrimination of amino acids and their derivatives on a teicoplanin-based chiral stationary phase. , 2004, Journal of chromatography. A.

[17]  A. Ohnishi,et al.  Reversed-phase liquid chromatographic separation of enantiomers on polysaccharide type chiral stationary phases. , 2001, Journal of chromatography. A.

[18]  E. Yashima,et al.  3-Fluoro-, 3-chloro- and 3-bromo-5-methylphenylcarbamates of cellulose and amylose as chiral stationary phases for high-performance liquid chromatographic enantioseparation , 1997 .