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DEVELOPMENT AND VALIDATION OF A STABILITY-INDICATING RP-LC METHOD FOR THE DETERMINATION OF ANTICANCER DRUG EPIRUBICIN IN PHARMACEUTICALS
In the present paper, sensitive, rapid, and different analytical methodology was developed for the determination of anticancer drug epirubicin (EPR). The mixture of epirubicin and moxifloxacin as internal standard was separated on a reversed phase Waters Spherisorb ODS1 column (250mm × 4.6mm × 5mm)...
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Published in: | Journal of liquid chromatography & related technologies 2014-07, Vol.37 (11), p.1583-1596 |
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container_start_page | 1583 |
container_title | Journal of liquid chromatography & related technologies |
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creator | Kurbanoglu, Sevinc Palabiyik, Burcin Bozal Gumustas, Mehmet Şanlı, Senem Uslu, Bengi Ozkan, Sibel A. |
description | In the present paper, sensitive, rapid, and different analytical methodology was developed for the determination of anticancer drug epirubicin (EPR). The mixture of epirubicin and moxifloxacin as internal standard was separated on a reversed phase Waters Spherisorb ODS1 column (250mm × 4.6mm × 5mm) using acetonitrile/water (30:70 v/v) mixture containing 15 mM phosphoric acid as mobile phase at 0.6 mL min
−1
flow rate and 30 C. Also degradation studies were conducted as stress conditions of UV light, acidic hydrolysis, alkaline hydrolysis, oxidation, and heat in oven (100°C), to evaluate the ability of the proposed method for the separation of EPR from its degradation products. The validated method suggests routine analysis of EPR in differently equipped laboratories. |
doi_str_mv | 10.1080/10826076.2013.803202 |
format | article |
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−1
flow rate and 30 C. Also degradation studies were conducted as stress conditions of UV light, acidic hydrolysis, alkaline hydrolysis, oxidation, and heat in oven (100°C), to evaluate the ability of the proposed method for the separation of EPR from its degradation products. The validated method suggests routine analysis of EPR in differently equipped laboratories.</description><identifier>ISSN: 1082-6076</identifier><identifier>EISSN: 1520-572X</identifier><identifier>DOI: 10.1080/10826076.2013.803202</identifier><language>eng</language><publisher>Abingdon: Taylor & Francis Group</publisher><subject>determination ; epirubicin ; liquid chromatography ; stability-indicating high-performance ; validation</subject><ispartof>Journal of liquid chromatography & related technologies, 2014-07, Vol.37 (11), p.1583-1596</ispartof><rights>Copyright Taylor & Francis Group, LLC 2014</rights><rights>Copyright Taylor & Francis Group, LLC</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids></links><search><creatorcontrib>Kurbanoglu, Sevinc</creatorcontrib><creatorcontrib>Palabiyik, Burcin Bozal</creatorcontrib><creatorcontrib>Gumustas, Mehmet</creatorcontrib><creatorcontrib>Şanlı, Senem</creatorcontrib><creatorcontrib>Uslu, Bengi</creatorcontrib><creatorcontrib>Ozkan, Sibel A.</creatorcontrib><title>DEVELOPMENT AND VALIDATION OF A STABILITY-INDICATING RP-LC METHOD FOR THE DETERMINATION OF ANTICANCER DRUG EPIRUBICIN IN PHARMACEUTICALS</title><title>Journal of liquid chromatography & related technologies</title><description>In the present paper, sensitive, rapid, and different analytical methodology was developed for the determination of anticancer drug epirubicin (EPR). The mixture of epirubicin and moxifloxacin as internal standard was separated on a reversed phase Waters Spherisorb ODS1 column (250mm × 4.6mm × 5mm) using acetonitrile/water (30:70 v/v) mixture containing 15 mM phosphoric acid as mobile phase at 0.6 mL min
−1
flow rate and 30 C. Also degradation studies were conducted as stress conditions of UV light, acidic hydrolysis, alkaline hydrolysis, oxidation, and heat in oven (100°C), to evaluate the ability of the proposed method for the separation of EPR from its degradation products. The validated method suggests routine analysis of EPR in differently equipped laboratories.</description><subject>determination</subject><subject>epirubicin</subject><subject>liquid chromatography</subject><subject>stability-indicating high-performance</subject><subject>validation</subject><issn>1082-6076</issn><issn>1520-572X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNpd0d1KwzAUB_AiCur0DbwIeONN58lHl3oltc22QJeOmolelZi2MKmrthviG_jYpkwRhHASyO8cDvw97wLDGEMI166QCfDJmACm4xAoAXLgneCAgB9w8njo3o74gzn2Tvv-BQDzgAQn3lciHkSaLRdCaRSpBD1EqUwiLTOFsimK0L2O7mQq9ZMvVSJj96NmKF_6aYwWQs-zBE2zHOm5QInQIl9I9destGtQschRkq9mSCxlvrqTsVTIneU8yhdRLFYDSu_PvKPaNH11_nOPvNVU6Hjup9lsAP6acLL165DakuDS2JBhzgAs5iWFMsTmpq6spZbVoRM0qGxQchNw4CULGTMWnksMdORd7ee-de37ruq3xeu6t1XTmE3V7voCB8xNDW8YdfTyH31pd93GbecUcMImQLFTt3u13tRt92o-2q4pi635bNqu7szGrvuCYiiGpIrfpIohqWKfFP0GGz961w</recordid><startdate>20140703</startdate><enddate>20140703</enddate><creator>Kurbanoglu, Sevinc</creator><creator>Palabiyik, Burcin Bozal</creator><creator>Gumustas, Mehmet</creator><creator>Şanlı, Senem</creator><creator>Uslu, Bengi</creator><creator>Ozkan, Sibel A.</creator><general>Taylor & Francis Group</general><general>Taylor & Francis Ltd</general><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SE</scope><scope>7SR</scope><scope>7TB</scope><scope>7U5</scope><scope>7U7</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H8G</scope><scope>JG9</scope><scope>KR7</scope><scope>L7M</scope><scope>P64</scope></search><sort><creationdate>20140703</creationdate><title>DEVELOPMENT AND VALIDATION OF A STABILITY-INDICATING RP-LC METHOD FOR THE DETERMINATION OF ANTICANCER DRUG EPIRUBICIN IN PHARMACEUTICALS</title><author>Kurbanoglu, Sevinc ; Palabiyik, Burcin Bozal ; Gumustas, Mehmet ; Şanlı, Senem ; Uslu, Bengi ; Ozkan, Sibel A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i272t-f83cd21dac8417400c17d30d81a9fecc3c4f8cd235ec5d7a5707d4844ac0bd103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>determination</topic><topic>epirubicin</topic><topic>liquid chromatography</topic><topic>stability-indicating high-performance</topic><topic>validation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kurbanoglu, Sevinc</creatorcontrib><creatorcontrib>Palabiyik, Burcin Bozal</creatorcontrib><creatorcontrib>Gumustas, Mehmet</creatorcontrib><creatorcontrib>Şanlı, Senem</creatorcontrib><creatorcontrib>Uslu, Bengi</creatorcontrib><creatorcontrib>Ozkan, Sibel A.</creatorcontrib><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Toxicology Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of liquid chromatography & related technologies</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kurbanoglu, Sevinc</au><au>Palabiyik, Burcin Bozal</au><au>Gumustas, Mehmet</au><au>Şanlı, Senem</au><au>Uslu, Bengi</au><au>Ozkan, Sibel A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>DEVELOPMENT AND VALIDATION OF A STABILITY-INDICATING RP-LC METHOD FOR THE DETERMINATION OF ANTICANCER DRUG EPIRUBICIN IN PHARMACEUTICALS</atitle><jtitle>Journal of liquid chromatography & related technologies</jtitle><date>2014-07-03</date><risdate>2014</risdate><volume>37</volume><issue>11</issue><spage>1583</spage><epage>1596</epage><pages>1583-1596</pages><issn>1082-6076</issn><eissn>1520-572X</eissn><abstract>In the present paper, sensitive, rapid, and different analytical methodology was developed for the determination of anticancer drug epirubicin (EPR). 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−1
flow rate and 30 C. Also degradation studies were conducted as stress conditions of UV light, acidic hydrolysis, alkaline hydrolysis, oxidation, and heat in oven (100°C), to evaluate the ability of the proposed method for the separation of EPR from its degradation products. The validated method suggests routine analysis of EPR in differently equipped laboratories.</abstract><cop>Abingdon</cop><pub>Taylor & Francis Group</pub><doi>10.1080/10826076.2013.803202</doi><tpages>14</tpages></addata></record> |
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subjects | determination epirubicin liquid chromatography stability-indicating high-performance validation |
title | DEVELOPMENT AND VALIDATION OF A STABILITY-INDICATING RP-LC METHOD FOR THE DETERMINATION OF ANTICANCER DRUG EPIRUBICIN IN PHARMACEUTICALS |
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