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HPLC/UV/MS method application for the separation of obeticholic acid and its related compounds in development process and quality control.
Dousa, Michal; Slavíková, Markéta; Kubelka, Tomás; Cerný, Josef; Gibala, Petr; Zezula, Josef.
Afiliación
  • Dousa M; Zentiva, k.s. Praha, A Sanofi Company, U Kabelovny 130, 102 37 Praha 10, Czech Republic. Electronic address: michal.dousa@seznam.cz.
  • Slavíková M; Zentiva, k.s. Praha, A Sanofi Company, U Kabelovny 130, 102 37 Praha 10, Czech Republic.
  • Kubelka T; Zentiva, k.s. Praha, A Sanofi Company, U Kabelovny 130, 102 37 Praha 10, Czech Republic.
  • Cerný J; Zentiva, k.s. Praha, A Sanofi Company, U Kabelovny 130, 102 37 Praha 10, Czech Republic.
  • Gibala P; Zentiva, k.s. Praha, A Sanofi Company, U Kabelovny 130, 102 37 Praha 10, Czech Republic.
  • Zezula J; Zentiva, k.s. Praha, A Sanofi Company, U Kabelovny 130, 102 37 Praha 10, Czech Republic.
J Pharm Biomed Anal ; 149: 214-224, 2018 Feb 05.
Article en En | MEDLINE | ID: mdl-29126083
ABSTRACT
An HPLC method with UV and electrospray ionization - mass spectrometry (ESI-MS) detection was developed for the separation and determination of obeticholic acid (OBE) and its related compounds in development process and quality control. OBE and its related compounds were classified into three major group based on the mass spectra profiles (A) those containing a hydroxyl group at position 3 and 7, (B) those containing a hydroxyl group and/or carbonyl group at position 3, hydrogen, ethyl or ethylidene group at position 6 and a hydroxyl group and/or carbonyl group at position 7, and (C) those containing carbonyl groups at position 3 and 7. ESI-MS ionization of OBE and its related compounds often produced intense adduct ions [M+H+98]+ and/or [M+H+196]+ that were identified as the adduct ions of phosphoric acid ([M+H+H3PO4]+ and [M+H+2H3PO4]+) originating from the mobile phase. The separation on HPLC system was accomplished using stationary phase based on XSelect CSH C18 (3.0×150mm×2.5µm) and a linear gradient elution using acetonitrile and 0.05% of o-phosphoric acid. The condition of chromatographic system was set as follows flow rate 0.7mL/min, temperature 45°C and UV detection at 192nm. The separation of the 19 compounds was finished in less than 18min (including equilibration time). The HPLC/UV method was partially validated according to International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines in terms of repeatability, selectivity, linearity and limit of quantification and detection.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Control de Calidad / Ácido Quenodesoxicólico / Contaminación de Medicamentos / Composición de Medicamentos / Fraccionamiento Químico Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: J Pharm Biomed Anal Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Control de Calidad / Ácido Quenodesoxicólico / Contaminación de Medicamentos / Composición de Medicamentos / Fraccionamiento Químico Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: J Pharm Biomed Anal Año: 2018 Tipo del documento: Article