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
Hauptverfasser: FRANCHINI, MIRIAM K., CARSTENSEN, JENS T.
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container_title Journal of pharmacy and pharmacology
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creator FRANCHINI, MIRIAM K.
CARSTENSEN, JENS T.
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><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. 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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). 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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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