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Determination of Paroxetine in Pharmaceutical Preparations Using HPLC with Electrochemical Detection
dc.contributor.author | Agrawal, Nitasha | |
dc.contributor.author | Esteve-Romero, Josep | |
dc.contributor.author | Dubey, Neeti Prakash | |
dc.contributor.author | Durgbanshi, Abhilasha | |
dc.contributor.author | Bose, Devasish | |
dc.contributor.author | Vives-Peris, Vicente | |
dc.contributor.author | Carda-Broch, Samuel | |
dc.date.accessioned | 2014-03-07T19:44:26Z | |
dc.date.available | 2014-03-07T19:44:26Z | |
dc.date.issued | 2013 | |
dc.identifier.issn | 1874-0650 | |
dc.identifier.uri | http://hdl.handle.net/10234/86109 | |
dc.description.abstract | A reliable and sensitive high performance liquid chromatographic method for the determination of widely prescribed antidepressant has been developed. Paroxetine is a potent selective serotonin reuptake inhibitor used for the treatment of depression and various mood disorders. The optimum mobile phase was prepared using a combination of 40% acetonitrile and phosphate buffer 0.01 M to pH 3 and running under isocratic mode at a flow rate of 1.0 ml/min. with electrochemical detection at 0.9V. The applicability of the developed method is in the field of quality control as well as for monitoring the level of drug at various concentrations during synthesis of the parent drug. The suggested methodology was validated following the guidelines of the FDA in terms of: sensitivity (LOD and LOQ, 0.005 and 0.01 ng/mL, respectively), linearity between 0.5 - 50 ng/mL (r2 > 0.9999), inter- and intraday precision (< 0.259% and < 0.538%), robustness (less than 5.0%) and recovery (99.7 - 100.7%). The developed method is specific, rapid (less than 10 min), precise, reliable, accurate, cheap and suitable for routine analysis for the determination of paroxetine in pharmaceutical preparations. | ca_CA |
dc.format.extent | 5 p. | ca_CA |
dc.format.mimetype | application/pdf | ca_CA |
dc.language.iso | eng | ca_CA |
dc.publisher | Bentham Open | ca_CA |
dc.relation.isPartOf | The Open Analytical Chemistry Journal, 2013, Volume 7 | ca_CA |
dc.rights | © Agrawal et al. Licensee Bentham Open This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited. | ca_CA |
dc.rights | Attribution-NonCommercial 4.0 Spain | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc/4.0/ | * |
dc.subject | Paroxetine | ca_CA |
dc.subject | HPLC | ca_CA |
dc.subject | electrochemical detection | ca_CA |
dc.subject | pharmaceutical | ca_CA |
dc.title | Determination of Paroxetine in Pharmaceutical Preparations Using HPLC with Electrochemical Detection | ca_CA |
dc.type | info:eu-repo/semantics/article | ca_CA |
dc.identifier.doi | http://dx.doi.org/10.2174/1874065001307010001 | |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | ca_CA |
dc.relation.publisherVersion | http://www.benthamscience.com/open/toacj/articles/V007/1TOACJ.pdf | ca_CA |
dc.type.version | info:eu-repo/semantics/publishedVersion | ca_CA |
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This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.