Inert Gas Sparge Leads to Alternate Reaction Pathway
The effect of sparging with an inert gas (argon) was evaluated during the investigation of the solution kinetics of an oxidation‐prone amphiphilic drug containing a sulphide moiety. Samples stored with an air headspace in pH 7 and 8 phosphate buffers at elevated temperatures and in the absence of li...
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Veröffentlicht in: | Journal of pharmacy and pharmacology 2000-06, Vol.52 (6), p.629-632 |
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description | The effect of sparging with an inert gas (argon) was evaluated during the investigation of the solution kinetics of an oxidation‐prone amphiphilic drug containing a sulphide moiety.
Samples stored with an air headspace in pH 7 and 8 phosphate buffers at elevated temperatures and in the absence of light degraded to two main products, a sulphoxide and a cinnamic acid analogue. Initially, this appeared to be a sequential mechanism which could be blocked by removing oxygen. Instead, argon‐sparge forced the direct degradation to the cinnamate, which was evidenced by the formation of a strong odour of sulphide. In addition, argon‐sparged samples remained colourless, while those sparged with oxygen or stored with an air headspace turned yellow and had negligible odour. The half‐lives for samples stored in pH 8 buffers at 93°C at an initial drug concentration of 25 mg mL−1 were 128 days (argon sparged), 86 days (air headspace), and 65 days (oxygen sparged).
The results indicated that for the drug under study, sparging with an inert gas affected the mechanism as well as the rate of the reaction at elevated temperatures. |
doi_str_mv | 10.1211/0022357001774453 |
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Samples stored with an air headspace in pH 7 and 8 phosphate buffers at elevated temperatures and in the absence of light degraded to two main products, a sulphoxide and a cinnamic acid analogue. Initially, this appeared to be a sequential mechanism which could be blocked by removing oxygen. Instead, argon‐sparge forced the direct degradation to the cinnamate, which was evidenced by the formation of a strong odour of sulphide. In addition, argon‐sparged samples remained colourless, while those sparged with oxygen or stored with an air headspace turned yellow and had negligible odour. The half‐lives for samples stored in pH 8 buffers at 93°C at an initial drug concentration of 25 mg mL−1 were 128 days (argon sparged), 86 days (air headspace), and 65 days (oxygen sparged).
The results indicated that for the drug under study, sparging with an inert gas affected the mechanism as well as the rate of the reaction at elevated temperatures.</description><identifier>ISSN: 0022-3573</identifier><identifier>EISSN: 2042-7158</identifier><identifier>DOI: 10.1211/0022357001774453</identifier><identifier>PMID: 10875538</identifier><identifier>CODEN: JPPMAB</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Argon - chemistry ; Biological and medical sciences ; General pharmacology ; Hydrogen-Ion Concentration ; Kinetics ; Medical sciences ; Oxidation-Reduction ; Pharmaceutical Preparations ; Pharmaceutical technology. Pharmaceutical industry ; Pharmacology. Drug treatments ; Sulfides - chemistry ; Temperature</subject><ispartof>Journal of pharmacy and pharmacology, 2000-06, Vol.52 (6), p.629-632</ispartof><rights>2000 Royal Pharmaceutical Society of Great Britain</rights><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4036-b346a169f288f0bf41ce4276d0a4085f7bd454faea1f428c767536a1e1a2a53a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1211%2F0022357001774453$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1211%2F0022357001774453$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1395098$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10875538$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>FRANCHINI, MIRIAM K.</creatorcontrib><creatorcontrib>CARSTENSEN, JENS T.</creatorcontrib><title>Inert Gas Sparge Leads to Alternate Reaction Pathway</title><title>Journal of pharmacy and pharmacology</title><addtitle>J Pharm Pharmacol</addtitle><description>The effect of sparging with an inert gas (argon) was evaluated during the investigation of the solution kinetics of an oxidation‐prone amphiphilic drug containing a sulphide moiety.
Samples stored with an air headspace in pH 7 and 8 phosphate buffers at elevated temperatures and in the absence of light degraded to two main products, a sulphoxide and a cinnamic acid analogue. Initially, this appeared to be a sequential mechanism which could be blocked by removing oxygen. Instead, argon‐sparge forced the direct degradation to the cinnamate, which was evidenced by the formation of a strong odour of sulphide. In addition, argon‐sparged samples remained colourless, while those sparged with oxygen or stored with an air headspace turned yellow and had negligible odour. The half‐lives for samples stored in pH 8 buffers at 93°C at an initial drug concentration of 25 mg mL−1 were 128 days (argon sparged), 86 days (air headspace), and 65 days (oxygen sparged).
The results indicated that for the drug under study, sparging with an inert gas affected the mechanism as well as the rate of the reaction at elevated temperatures.</description><subject>Argon - chemistry</subject><subject>Biological and medical sciences</subject><subject>General pharmacology</subject><subject>Hydrogen-Ion Concentration</subject><subject>Kinetics</subject><subject>Medical sciences</subject><subject>Oxidation-Reduction</subject><subject>Pharmaceutical Preparations</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>Sulfides - chemistry</subject><subject>Temperature</subject><issn>0022-3573</issn><issn>2042-7158</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtP20AUhUcVFUmBfVeVF4id6Z23s0QRJEBEI15Zjm6cO8WtY4cZR2n-fR05gqobVndxvu9c6TD2lcM5F5x_BxBCagvArVVKy0-sL0CJ1HKdHbD-Lk7bXPbYlxh_AYA1xhyyHofMai2zPlPXFYUmGWFMHlYYflIyIVzEpKmTi7KhUGFDyT1h3hR1lUyxedng9ph99lhGOtnfI_Z0dfk4HKeTH6Pr4cUkzRVIk86lMsjNwIss8zD3iuekhDULQAWZ9na-UFp5JOReiSy3xmrZGsRRoJYoj9hZ17sK9euaYuOWRcypLLGieh2d5UJwK6AFoQPzUMcYyLtVKJYYto6D2y3l_l-qVb7tu9fzJS3-EbppWuB0D2DMsfQBq7yI75wcaBjsMN1hm6Kk7Yd_3c10PDUD03pp5xWxoT9vHobfzlhptZvdjdxM3N8Orx7BPcu_2cSLxA</recordid><startdate>200006</startdate><enddate>200006</enddate><creator>FRANCHINI, MIRIAM K.</creator><creator>CARSTENSEN, JENS T.</creator><general>Blackwell Publishing Ltd</general><general>Pharmaceutical Press</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>200006</creationdate><title>Inert Gas Sparge Leads to Alternate Reaction Pathway</title><author>FRANCHINI, MIRIAM K. ; CARSTENSEN, JENS T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4036-b346a169f288f0bf41ce4276d0a4085f7bd454faea1f428c767536a1e1a2a53a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Argon - chemistry</topic><topic>Biological and medical sciences</topic><topic>General pharmacology</topic><topic>Hydrogen-Ion Concentration</topic><topic>Kinetics</topic><topic>Medical sciences</topic><topic>Oxidation-Reduction</topic><topic>Pharmaceutical Preparations</topic><topic>Pharmaceutical technology. Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>Sulfides - chemistry</topic><topic>Temperature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>FRANCHINI, MIRIAM K.</creatorcontrib><creatorcontrib>CARSTENSEN, JENS T.</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 pharmacy and pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>FRANCHINI, MIRIAM K.</au><au>CARSTENSEN, JENS T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inert Gas Sparge Leads to Alternate Reaction Pathway</atitle><jtitle>Journal of pharmacy and pharmacology</jtitle><addtitle>J Pharm Pharmacol</addtitle><date>2000-06</date><risdate>2000</risdate><volume>52</volume><issue>6</issue><spage>629</spage><epage>632</epage><pages>629-632</pages><issn>0022-3573</issn><eissn>2042-7158</eissn><coden>JPPMAB</coden><abstract>The effect of sparging with an inert gas (argon) was evaluated during the investigation of the solution kinetics of an oxidation‐prone amphiphilic drug containing a sulphide moiety.
Samples stored with an air headspace in pH 7 and 8 phosphate buffers at elevated temperatures and in the absence of light degraded to two main products, a sulphoxide and a cinnamic acid analogue. Initially, this appeared to be a sequential mechanism which could be blocked by removing oxygen. Instead, argon‐sparge forced the direct degradation to the cinnamate, which was evidenced by the formation of a strong odour of sulphide. In addition, argon‐sparged samples remained colourless, while those sparged with oxygen or stored with an air headspace turned yellow and had negligible odour. The half‐lives for samples stored in pH 8 buffers at 93°C at an initial drug concentration of 25 mg mL−1 were 128 days (argon sparged), 86 days (air headspace), and 65 days (oxygen sparged).
The results indicated that for the drug under study, sparging with an inert gas affected the mechanism as well as the rate of the reaction at elevated temperatures.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>10875538</pmid><doi>10.1211/0022357001774453</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current); MEDLINE; Wiley Online Library Journals Frontfile Complete |
subjects | Argon - chemistry Biological and medical sciences General pharmacology Hydrogen-Ion Concentration Kinetics Medical sciences Oxidation-Reduction Pharmaceutical Preparations Pharmaceutical technology. Pharmaceutical industry Pharmacology. Drug treatments Sulfides - chemistry Temperature |
title | Inert Gas Sparge Leads to Alternate Reaction Pathway |
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