Source:http://linkedlifedata.com/resource/pubmed/id/21313809
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2011-2-14
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pubmed:abstractText |
A stability-indicating HPLC assay method was developed for the quantitative determination of duloxetine (DLX) in a pharmaceutical dosage form in the presence of its degradation products, and kinetic determinations were evaluated in acid conditions and UV-C radiation exposure. Chromatographic separation was achieved by use of an ACE C18 column (250 x 4.0 mm id, 5 microm particle size). The mobile phase was prepared by mixing aqueous 50 mM potassium phosphate buffer (pH 6.0 containing 0.3% triethylamine) and acetonitrile (60 + 40, v/v). DLX was rapidly degraded in an acid medium and in the presence of hydrogen peroxide and UV-C radiation; it was more stable in alkaline medium. The described method was linear over a range of 4.0-14.0 microg/mL for determination of DLX (r = 0.9998). The precision was demonstrated by the RSD of intraday (0.79-1.07%) and interday (0.85%) studies. The mean recovery was found to be 100.56%. The acid degradation of DLX in 0.1 M HCI solution showed an apparent zero-order kinetics (k = 0.177 microg/mL/min), and the photodegradation demonstrated an apparent first-order kinetics (k = 0.082 microg/mL/min). The developed method was found to be simple, specific, robust, linear, precise, and accurate for the determination of DLX in enteric-coated pellets.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antidepressive Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Capsules,
http://linkedlifedata.com/resource/pubmed/chemical/Indicators and Reagents,
http://linkedlifedata.com/resource/pubmed/chemical/Tablets, Enteric-Coated,
http://linkedlifedata.com/resource/pubmed/chemical/Thiophenes,
http://linkedlifedata.com/resource/pubmed/chemical/duloxetine
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pubmed:status |
MEDLINE
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pubmed:issn |
1060-3271
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
93
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1829-35
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pubmed:meshHeading |
pubmed-meshheading:21313809-Antidepressive Agents,
pubmed-meshheading:21313809-Capsules,
pubmed-meshheading:21313809-Chromatography, High Pressure Liquid,
pubmed-meshheading:21313809-Drug Stability,
pubmed-meshheading:21313809-Half-Life,
pubmed-meshheading:21313809-Hydrogen-Ion Concentration,
pubmed-meshheading:21313809-Indicators and Reagents,
pubmed-meshheading:21313809-Kinetics,
pubmed-meshheading:21313809-Light,
pubmed-meshheading:21313809-Photochemistry,
pubmed-meshheading:21313809-Reference Standards,
pubmed-meshheading:21313809-Reproducibility of Results,
pubmed-meshheading:21313809-Spectrophotometry, Ultraviolet,
pubmed-meshheading:21313809-Tablets, Enteric-Coated,
pubmed-meshheading:21313809-Thiophenes
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pubmed:articleTitle |
Stress degradation studies and kinetic determinations of duloxetine enteric-coated pellets by HPLC.
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pubmed:affiliation |
Universidade Federal do Rio Grande do Sul (UFRGS), Faculdade de Farmácia, Programa de Pós-Graduação em Ciências Farmacêuticas, Porto Alegre, RS, Brazil. patriciagomes0@yahoo.com.br
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pubmed:publicationType |
Journal Article
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