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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of pharmaceutical sciences 1984-12, Vol.73 (12), p.1709-1713
Hauptverfasser: Fabre, H., Hussam-Eddine, N., Mandrou, B., Lerner, D.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1713
container_issue 12
container_start_page 1709
container_title Journal of pharmaceutical sciences
container_volume 73
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
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_75877844</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0022354915465190</els_id><sourcerecordid>75877844</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4562-9c695bc899a318bee9fa7f5de40477754b10001ea967ae0cd36d54a9ea30a98f3</originalsourceid><addsrcrecordid>eNqFkM1vEzEQxS0EKmnhyg1pD4jbBnvXn8dQIKVUEBQQJ2Q59qzqslmn9m7p8tfjaKMgDoiTpZnfe37zEHpG8JxgXL262aV5xTEWNalI9QDNCKtwyTERD9EsA1VZM6oeo9OUbjDGHDN2gk44pURSMkPfF0Mf7r0zvQ9dYTpXXIwuhnZMPhUffAe9t6kITdFfQ7EOzg_bYm3afj9aXUM3tpuhN79CB4XvisXtAGFIGWyHveET9KgxbYKnh_cMfX339sv5RXn1afn-fHFVWsp4VSrLFdtYqZSpidwAqMaIhjmgmAohGN3kUzEBo7gwgK2ruWPUKDA1Nko29Rl6OfnuYsgRUq-3PlloW9Pt82jBpBCS0gzOJ9DGkFKERu-i35o4aoL1vk-d-9R_-syC5wfnYbMFd8QPBeb9i8PeJGvaJprO-nTEJJWUyzpjasJ--hbG_3yqL1frvyKUk9anHu6PWhN_aC5qwfS3j0v9-bVS8s3qUi8zLycecuN3HqJO1kNnwfkIttcu-H9d-xvhvLCo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>75877844</pqid></control><display><type>article</type><title>Autoxidation and Hydrolysis Kinetics of the Sodium Salt of Phenylbutazone in Aqueous Solution</title><source>MEDLINE</source><source>Access via Wiley Online Library</source><source>Alma/SFX Local Collection</source><creator>Fabre, H. ; Hussam-Eddine, N. ; Mandrou, B. ; Lerner, D.</creator><creatorcontrib>Fabre, H. ; Hussam-Eddine, N. ; Mandrou, B. ; Lerner, D.</creatorcontrib><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><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&amp;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>
fulltext fulltext
identifier ISSN: 0022-3549
ispartof Journal of pharmaceutical sciences, 1984-12, Vol.73 (12), p.1709-1713
issn 0022-3549
1520-6017
language eng
recordid cdi_proquest_miscellaneous_75877844
source MEDLINE; Access via Wiley Online Library; Alma/SFX Local Collection
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-22T20%3A47%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Autoxidation%20and%20Hydrolysis%20Kinetics%20of%20the%20Sodium%20Salt%20of%20Phenylbutazone%20in%20Aqueous%20Solution&rft.jtitle=Journal%20of%20pharmaceutical%20sciences&rft.au=Fabre,%20H.&rft.date=1984-12&rft.volume=73&rft.issue=12&rft.spage=1709&rft.epage=1713&rft.pages=1709-1713&rft.issn=0022-3549&rft.eissn=1520-6017&rft.coden=JPMSAE&rft_id=info:doi/10.1002/jps.2600731212&rft_dat=%3Cproquest_cross%3E75877844%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=75877844&rft_id=info:pmid/6441841&rft_els_id=S0022354915465190&rfr_iscdi=true