Autoxidation and Hydrolysis Kinetics of the Sodium Salt of Phenylbutazone in Aqueous Solution
The present investigation offers experimental results concerning the degradation kinetics of the sodium salt of phenylbutazone based on a reliable HPLC procedure. The method allows the simultaneous determination of the parent compound and its main decomposition products. The degradation kinetics at...
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Veröffentlicht in: | Journal of pharmaceutical sciences 1984-12, Vol.73 (12), p.1709-1713 |
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creator | Fabre, H. Hussam-Eddine, N. Mandrou, B. Lerner, D. |
description | The present investigation offers experimental results concerning the degradation kinetics of the sodium salt of phenylbutazone based on a reliable HPLC procedure. The method allows the simultaneous determination of the parent compound and its main decomposition products. The degradation kinetics at 37°C were compared at pH 7.9 and 10.0 and under oxygen and nitrogen atmospheres. Parallel tests were carried out in the dark and under photolytic conditions for the aforementioned conditions. The influence of traces of iron and a chelating agent of iron on the degradation was studied. At pH 7.9 and pH 10.0 the main degradation products are 3-hydroxy-2-oxohexanoic acid 1,2-diphenylhydrazide and 3-carboxy-2-oxohexanoic acid 1,2-diphenylhydrazide. Azobenzene is formed only at pH 10.0. At pH 7.9, in the dark, the degradation proceeds with a lag phase. In contrast, no lag phase is observed under photolytic conditions. The process of autoxidation and hydrolysis is catalyzed by traces of iron both in the dark and under irradiation conditions. An unexpected increase in the degradation is observed in the presence of iron(III) and EDTA in aerobic conditions and under irradiation. |
doi_str_mv | 10.1002/jps.2600731212 |
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The method allows the simultaneous determination of the parent compound and its main decomposition products. The degradation kinetics at 37°C were compared at pH 7.9 and 10.0 and under oxygen and nitrogen atmospheres. Parallel tests were carried out in the dark and under photolytic conditions for the aforementioned conditions. The influence of traces of iron and a chelating agent of iron on the degradation was studied. At pH 7.9 and pH 10.0 the main degradation products are 3-hydroxy-2-oxohexanoic acid 1,2-diphenylhydrazide and 3-carboxy-2-oxohexanoic acid 1,2-diphenylhydrazide. Azobenzene is formed only at pH 10.0. At pH 7.9, in the dark, the degradation proceeds with a lag phase. In contrast, no lag phase is observed under photolytic conditions. The process of autoxidation and hydrolysis is catalyzed by traces of iron both in the dark and under irradiation conditions. An unexpected increase in the degradation is observed in the presence of iron(III) and EDTA in aerobic conditions and under irradiation.</description><identifier>ISSN: 0022-3549</identifier><identifier>EISSN: 1520-6017</identifier><identifier>DOI: 10.1002/jps.2600731212</identifier><identifier>PMID: 6441841</identifier><identifier>CODEN: JPMSAE</identifier><language>eng</language><publisher>Washington: Elsevier Inc</publisher><subject>Anaerobiosis ; Biological and medical sciences ; Chromatography, High Pressure Liquid ; degradation ; degradation products ; Edetic Acid ; effects of light and pH ; General pharmacology ; Hydrogen-Ion Concentration ; Hydrolysis ; Iron ; Kinetics ; Medical sciences ; Oxidation-Reduction ; Pharmacology. Drug treatments ; Phenylbutazone - analysis ; Phenylbutazone-autoxidation ; Phenylbutazone—autoxidation, hydrolysis, degradation, degradation products, effects of light and pH ; Physicochemical properties. Structure-activity relationships ; Solutions ; Time Factors</subject><ispartof>Journal of pharmaceutical sciences, 1984-12, Vol.73 (12), p.1709-1713</ispartof><rights>1984 Wiley‐Liss, Inc., A Wiley Company</rights><rights>Copyright © 1984 Wiley‐Liss, Inc., A Wiley Company</rights><rights>1986 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4562-9c695bc899a318bee9fa7f5de40477754b10001ea967ae0cd36d54a9ea30a98f3</citedby><cites>FETCH-LOGICAL-c4562-9c695bc899a318bee9fa7f5de40477754b10001ea967ae0cd36d54a9ea30a98f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjps.2600731212$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjps.2600731212$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8484683$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6441841$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fabre, H.</creatorcontrib><creatorcontrib>Hussam-Eddine, N.</creatorcontrib><creatorcontrib>Mandrou, B.</creatorcontrib><creatorcontrib>Lerner, D.</creatorcontrib><title>Autoxidation and Hydrolysis Kinetics of the Sodium Salt of Phenylbutazone in Aqueous Solution</title><title>Journal of pharmaceutical sciences</title><addtitle>J. Pharm. Sci</addtitle><description>The present investigation offers experimental results concerning the degradation kinetics of the sodium salt of phenylbutazone based on a reliable HPLC procedure. The method allows the simultaneous determination of the parent compound and its main decomposition products. The degradation kinetics at 37°C were compared at pH 7.9 and 10.0 and under oxygen and nitrogen atmospheres. Parallel tests were carried out in the dark and under photolytic conditions for the aforementioned conditions. The influence of traces of iron and a chelating agent of iron on the degradation was studied. At pH 7.9 and pH 10.0 the main degradation products are 3-hydroxy-2-oxohexanoic acid 1,2-diphenylhydrazide and 3-carboxy-2-oxohexanoic acid 1,2-diphenylhydrazide. Azobenzene is formed only at pH 10.0. At pH 7.9, in the dark, the degradation proceeds with a lag phase. In contrast, no lag phase is observed under photolytic conditions. The process of autoxidation and hydrolysis is catalyzed by traces of iron both in the dark and under irradiation conditions. An unexpected increase in the degradation is observed in the presence of iron(III) and EDTA in aerobic conditions and under irradiation.</description><subject>Anaerobiosis</subject><subject>Biological and medical sciences</subject><subject>Chromatography, High Pressure Liquid</subject><subject>degradation</subject><subject>degradation products</subject><subject>Edetic Acid</subject><subject>effects of light and pH</subject><subject>General pharmacology</subject><subject>Hydrogen-Ion Concentration</subject><subject>Hydrolysis</subject><subject>Iron</subject><subject>Kinetics</subject><subject>Medical sciences</subject><subject>Oxidation-Reduction</subject><subject>Pharmacology. Drug treatments</subject><subject>Phenylbutazone - analysis</subject><subject>Phenylbutazone-autoxidation</subject><subject>Phenylbutazone—autoxidation, hydrolysis, degradation, degradation products, effects of light and pH</subject><subject>Physicochemical properties. Structure-activity relationships</subject><subject>Solutions</subject><subject>Time Factors</subject><issn>0022-3549</issn><issn>1520-6017</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM1vEzEQxS0EKmnhyg1pD4jbBnvXn8dQIKVUEBQQJ2Q59qzqslmn9m7p8tfjaKMgDoiTpZnfe37zEHpG8JxgXL262aV5xTEWNalI9QDNCKtwyTERD9EsA1VZM6oeo9OUbjDGHDN2gk44pURSMkPfF0Mf7r0zvQ9dYTpXXIwuhnZMPhUffAe9t6kITdFfQ7EOzg_bYm3afj9aXUM3tpuhN79CB4XvisXtAGFIGWyHveET9KgxbYKnh_cMfX339sv5RXn1afn-fHFVWsp4VSrLFdtYqZSpidwAqMaIhjmgmAohGN3kUzEBo7gwgK2ruWPUKDA1Nko29Rl6OfnuYsgRUq-3PlloW9Pt82jBpBCS0gzOJ9DGkFKERu-i35o4aoL1vk-d-9R_-syC5wfnYbMFd8QPBeb9i8PeJGvaJprO-nTEJJWUyzpjasJ--hbG_3yqL1frvyKUk9anHu6PWhN_aC5qwfS3j0v9-bVS8s3qUi8zLycecuN3HqJO1kNnwfkIttcu-H9d-xvhvLCo</recordid><startdate>198412</startdate><enddate>198412</enddate><creator>Fabre, H.</creator><creator>Hussam-Eddine, N.</creator><creator>Mandrou, B.</creator><creator>Lerner, D.</creator><general>Elsevier Inc</general><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><general>American Pharmaceutical Association</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>198412</creationdate><title>Autoxidation and Hydrolysis Kinetics of the Sodium Salt of Phenylbutazone in Aqueous Solution</title><author>Fabre, H. ; Hussam-Eddine, N. ; Mandrou, B. ; Lerner, D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4562-9c695bc899a318bee9fa7f5de40477754b10001ea967ae0cd36d54a9ea30a98f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1984</creationdate><topic>Anaerobiosis</topic><topic>Biological and medical sciences</topic><topic>Chromatography, High Pressure Liquid</topic><topic>degradation</topic><topic>degradation products</topic><topic>Edetic Acid</topic><topic>effects of light and pH</topic><topic>General pharmacology</topic><topic>Hydrogen-Ion Concentration</topic><topic>Hydrolysis</topic><topic>Iron</topic><topic>Kinetics</topic><topic>Medical sciences</topic><topic>Oxidation-Reduction</topic><topic>Pharmacology. Drug treatments</topic><topic>Phenylbutazone - analysis</topic><topic>Phenylbutazone-autoxidation</topic><topic>Phenylbutazone—autoxidation, hydrolysis, degradation, degradation products, effects of light and pH</topic><topic>Physicochemical properties. Structure-activity relationships</topic><topic>Solutions</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fabre, H.</creatorcontrib><creatorcontrib>Hussam-Eddine, N.</creatorcontrib><creatorcontrib>Mandrou, B.</creatorcontrib><creatorcontrib>Lerner, D.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pharmaceutical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fabre, H.</au><au>Hussam-Eddine, N.</au><au>Mandrou, B.</au><au>Lerner, D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Autoxidation and Hydrolysis Kinetics of the Sodium Salt of Phenylbutazone in Aqueous Solution</atitle><jtitle>Journal of pharmaceutical sciences</jtitle><addtitle>J. Pharm. Sci</addtitle><date>1984-12</date><risdate>1984</risdate><volume>73</volume><issue>12</issue><spage>1709</spage><epage>1713</epage><pages>1709-1713</pages><issn>0022-3549</issn><eissn>1520-6017</eissn><coden>JPMSAE</coden><abstract>The present investigation offers experimental results concerning the degradation kinetics of the sodium salt of phenylbutazone based on a reliable HPLC procedure. The method allows the simultaneous determination of the parent compound and its main decomposition products. The degradation kinetics at 37°C were compared at pH 7.9 and 10.0 and under oxygen and nitrogen atmospheres. Parallel tests were carried out in the dark and under photolytic conditions for the aforementioned conditions. The influence of traces of iron and a chelating agent of iron on the degradation was studied. At pH 7.9 and pH 10.0 the main degradation products are 3-hydroxy-2-oxohexanoic acid 1,2-diphenylhydrazide and 3-carboxy-2-oxohexanoic acid 1,2-diphenylhydrazide. Azobenzene is formed only at pH 10.0. At pH 7.9, in the dark, the degradation proceeds with a lag phase. In contrast, no lag phase is observed under photolytic conditions. The process of autoxidation and hydrolysis is catalyzed by traces of iron both in the dark and under irradiation conditions. An unexpected increase in the degradation is observed in the presence of iron(III) and EDTA in aerobic conditions and under irradiation.</abstract><cop>Washington</cop><pub>Elsevier Inc</pub><pmid>6441841</pmid><doi>10.1002/jps.2600731212</doi><tpages>5</tpages></addata></record> |
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subjects | Anaerobiosis Biological and medical sciences Chromatography, High Pressure Liquid degradation degradation products Edetic Acid effects of light and pH General pharmacology Hydrogen-Ion Concentration Hydrolysis Iron Kinetics Medical sciences Oxidation-Reduction Pharmacology. Drug treatments Phenylbutazone - analysis Phenylbutazone-autoxidation Phenylbutazone—autoxidation, hydrolysis, degradation, degradation products, effects of light and pH Physicochemical properties. Structure-activity relationships Solutions Time Factors |
title | Autoxidation and Hydrolysis Kinetics of the Sodium Salt of Phenylbutazone in Aqueous Solution |
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