Pharmaceutical analysis by supercritical fluid chromatography: Optimization of the mobile phase composition on a 2‐ethylpyridine column
Identifieur interne : 001377 ( Main/Exploration ); précédent : 001376; suivant : 001378Pharmaceutical analysis by supercritical fluid chromatography: Optimization of the mobile phase composition on a 2‐ethylpyridine column
Auteurs : Claudio Brunelli ; Yining Zhao [États-Unis] ; Melissa-Hanna Brown [Royaume-Uni] ; Pat SandraSource :
- Journal of Separation Science [ 1615-9306 ] ; 2008-05.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Médicament.
English descriptors
- KwdEn :
- 2‐Ethylpyridine stationary phase, Chemical analysis, Chemistry Techniques, Analytical (methods), Chemistry, Pharmaceutical (methods), Chromatography, Supercritical Fluid (methods), Clinical Laboratory Techniques, Drug, Formates (chemistry), Methanol (chemistry), Mobile phase, Mobile phase optimization, Models, Chemical, Optimization, Pharmaceutical Preparations (chemistry), Pharmaceuticals, Phase composition, Propylamines (analysis), Propylamines (chemistry), Pyridines (chemistry), Stationary phase, Steroids (chemistry), Supercritical fluid chromatography, Technology, Pharmaceutical (methods).
- MESH :
- chemical , analysis : Propylamines.
- chemical , chemistry : Formates, Methanol, Pharmaceutical Preparations, Propylamines, Pyridines, Steroids.
- methods : Chemistry Techniques, Analytical, Chemistry, Pharmaceutical, Chromatography, Supercritical Fluid, Technology, Pharmaceutical.
- Clinical Laboratory Techniques, Models, Chemical.
Abstract
The separation of neutral, acidic, and basic pharmaceuticals with diverse physicochemical properties by packed column supercritical fluid chromatography (pSFC) on a 2‐ethylpyridine column (25 cm×4.6 mm id, 3 μm particles) is presented. The optimization strategy involved separations at 100% methanol (MeOH) and at 50% MeOH/50% ACN while keeping the peak symmetry additives formic acid (FA) and isopropylamine (IPA) at constant levels of 0.25% v/v. By plotting the adjusted retention times as a function of the MeOH/ACN ratio, an optimal modifier ratio composition of 65% MeOH/35% ACN was found. The total set of 26 neutral, acidic, and basic pharmaceuticals was analyzed and the optimal composition experimentally verified. This mobile phase composition is currently used in pharmaceutical method development and open‐access generic screening environments.
Url:
DOI: 10.1002/jssc.200700555
Affiliations:
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Le document en format XML
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<series><title level="j">Journal of Separation Science</title>
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<term>Chemical analysis</term>
<term>Chemistry Techniques, Analytical (methods)</term>
<term>Chemistry, Pharmaceutical (methods)</term>
<term>Chromatography, Supercritical Fluid (methods)</term>
<term>Clinical Laboratory Techniques</term>
<term>Drug</term>
<term>Formates (chemistry)</term>
<term>Methanol (chemistry)</term>
<term>Mobile phase</term>
<term>Mobile phase optimization</term>
<term>Models, Chemical</term>
<term>Optimization</term>
<term>Pharmaceutical Preparations (chemistry)</term>
<term>Pharmaceuticals</term>
<term>Phase composition</term>
<term>Propylamines (analysis)</term>
<term>Propylamines (chemistry)</term>
<term>Pyridines (chemistry)</term>
<term>Stationary phase</term>
<term>Steroids (chemistry)</term>
<term>Supercritical fluid chromatography</term>
<term>Technology, Pharmaceutical (methods)</term>
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<keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en"><term>Propylamines</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Formates</term>
<term>Methanol</term>
<term>Pharmaceutical Preparations</term>
<term>Propylamines</term>
<term>Pyridines</term>
<term>Steroids</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Chemistry Techniques, Analytical</term>
<term>Chemistry, Pharmaceutical</term>
<term>Chromatography, Supercritical Fluid</term>
<term>Technology, Pharmaceutical</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Clinical Laboratory Techniques</term>
<term>Models, Chemical</term>
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<keywords scheme="Pascal" xml:lang="fr"><term>Analyse chimique</term>
<term>Chromatographie SFC</term>
<term>Composition phase</term>
<term>Composition phase mobile</term>
<term>Médicament</term>
<term>Optimisation</term>
<term>Phase mobile</term>
<term>Phase stationnaire</term>
<term>Pyridine(2-éthyl)</term>
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<front><div type="abstract" xml:lang="en">The separation of neutral, acidic, and basic pharmaceuticals with diverse physicochemical properties by packed column supercritical fluid chromatography (pSFC) on a 2‐ethylpyridine column (25 cm×4.6 mm id, 3 μm particles) is presented. The optimization strategy involved separations at 100% methanol (MeOH) and at 50% MeOH/50% ACN while keeping the peak symmetry additives formic acid (FA) and isopropylamine (IPA) at constant levels of 0.25% v/v. By plotting the adjusted retention times as a function of the MeOH/ACN ratio, an optimal modifier ratio composition of 65% MeOH/35% ACN was found. The total set of 26 neutral, acidic, and basic pharmaceuticals was analyzed and the optimal composition experimentally verified. This mobile phase composition is currently used in pharmaceutical method development and open‐access generic screening environments.</div>
</front>
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<tree><noCountry><name sortKey="Brunelli, Claudio" sort="Brunelli, Claudio" uniqKey="Brunelli C" first="Claudio" last="Brunelli">Claudio Brunelli</name>
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<country name="États-Unis"><region name="Connecticut"><name sortKey="Zhao, Yining" sort="Zhao, Yining" uniqKey="Zhao Y" first="Yining" last="Zhao">Yining Zhao</name>
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<country name="Royaume-Uni"><noRegion><name sortKey="Brown, Melissa Anna" sort="Brown, Melissa Anna" uniqKey="Brown M" first="Melissa-Hanna" last="Brown">Melissa-Hanna Brown</name>
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