Determination of ceftazidime in plasma by RP‐HPLC and ultraviolet detection
A simple high‐performance liquid chromatography method for the determination of ceftazidime in plasma has been developed. Using an ultrafiltration technique samples were separated by reverse‐phase high‐performance liquid chromatography on a Symmetry C18 4.6 × 250 mm column (5.0 μm) and ultraviolet a...
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Veröffentlicht in: | Biomedical chromatography 2021-07, Vol.35 (7), p.e5104-n/a |
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description | A simple high‐performance liquid chromatography method for the determination of ceftazidime in plasma has been developed. Using an ultrafiltration technique samples were separated by reverse‐phase high‐performance liquid chromatography on a Symmetry C18 4.6 × 250 mm column (5.0 μm) and ultraviolet absorbance was measured at 260 nm. The mobile phase was a mixture of 10 mm potassium phosphate monobasic pH 2.5 with phosphoric acid and acetonitrile (90:10). The standard curve ranged from 0.1 to 100 μg/ml. Intra‐ and inter‐assay variability for ceftazidime was |
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Using an ultrafiltration technique samples were separated by reverse‐phase high‐performance liquid chromatography on a Symmetry C18 4.6 × 250 mm column (5.0 μm) and ultraviolet absorbance was measured at 260 nm. The mobile phase was a mixture of 10 mm potassium phosphate monobasic pH 2.5 with phosphoric acid and acetonitrile (90:10). The standard curve ranged from 0.1 to 100 μg/ml. Intra‐ and inter‐assay variability for ceftazidime was <12%, and the average recovery was 89%. The lower limit of quantification was 0.1 μg/ml. This method has been used successfully to analyze frog plasma samples at this institution and it could be applied to other small volume samples in a clinical or research setting.</description><identifier>ISSN: 0269-3879</identifier><identifier>EISSN: 1099-0801</identifier><identifier>DOI: 10.1002/bmc.5104</identifier><identifier>PMID: 33629742</identifier><language>eng</language><publisher>England</publisher><subject>ceftazidime ; HPLC ; pharmacokinetics</subject><ispartof>Biomedical chromatography, 2021-07, Vol.35 (7), p.e5104-n/a</ispartof><rights>2021 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3214-e7b94263fb5be0aebba07e585a67739a397f71cb51613c243e38042cc5e5bc893</citedby><cites>FETCH-LOGICAL-c3214-e7b94263fb5be0aebba07e585a67739a397f71cb51613c243e38042cc5e5bc893</cites><orcidid>0000-0002-5184-900X ; 0000-0002-0896-6681</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fbmc.5104$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fbmc.5104$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,778,782,1414,27911,27912,45561,45562</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33629742$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bergman, Joan</creatorcontrib><creatorcontrib>Harvill, Lainey</creatorcontrib><creatorcontrib>Hawkins, Shawna</creatorcontrib><creatorcontrib>Sladky, Kurt</creatorcontrib><creatorcontrib>Cox, Sherry</creatorcontrib><title>Determination of ceftazidime in plasma by RP‐HPLC and ultraviolet detection</title><title>Biomedical chromatography</title><addtitle>Biomed Chromatogr</addtitle><description>A simple high‐performance liquid chromatography method for the determination of ceftazidime in plasma has been developed. Using an ultrafiltration technique samples were separated by reverse‐phase high‐performance liquid chromatography on a Symmetry C18 4.6 × 250 mm column (5.0 μm) and ultraviolet absorbance was measured at 260 nm. The mobile phase was a mixture of 10 mm potassium phosphate monobasic pH 2.5 with phosphoric acid and acetonitrile (90:10). The standard curve ranged from 0.1 to 100 μg/ml. Intra‐ and inter‐assay variability for ceftazidime was <12%, and the average recovery was 89%. The lower limit of quantification was 0.1 μg/ml. This method has been used successfully to analyze frog plasma samples at this institution and it could be applied to other small volume samples in a clinical or research setting.</description><subject>ceftazidime</subject><subject>HPLC</subject><subject>pharmacokinetics</subject><issn>0269-3879</issn><issn>1099-0801</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kL1OwzAURi0EoqUg8QTII0vKtR3H8QgpUKRWVAjmyHZuJKP8VEkKChOPwDPyJKQU2Ji-5XxnOIScMpgyAH5hSzeVDMI9MmagdQAxsH0yBh7pQMRKj8hR2z4DgI64OiQjISKuVcjHZDnDDpvSV6bzdUXrnDrMO_PmM18i9RVdF6YtDbU9fVh9vn_MV4uEmiqjm6JrzIuvC-xoNjjc9n9MDnJTtHjysxPydHP9mMyDxf3tXXK5CJzgLAxQWR3ySORWWgSD1hpQKGNpIqWENkKrXDFnJYuYcDwUKGIIuXMSpXWxFhNyvvO6pm7bBvN03fjSNH3KIN0WSYci6bbIgJ7t0PXGlpj9gb8JBiDYAa--wP5fUXq1TL6FXxQWano</recordid><startdate>202107</startdate><enddate>202107</enddate><creator>Bergman, Joan</creator><creator>Harvill, Lainey</creator><creator>Hawkins, Shawna</creator><creator>Sladky, Kurt</creator><creator>Cox, Sherry</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-5184-900X</orcidid><orcidid>https://orcid.org/0000-0002-0896-6681</orcidid></search><sort><creationdate>202107</creationdate><title>Determination of ceftazidime in plasma by RP‐HPLC and ultraviolet detection</title><author>Bergman, Joan ; Harvill, Lainey ; Hawkins, Shawna ; Sladky, Kurt ; Cox, Sherry</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3214-e7b94263fb5be0aebba07e585a67739a397f71cb51613c243e38042cc5e5bc893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>ceftazidime</topic><topic>HPLC</topic><topic>pharmacokinetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bergman, Joan</creatorcontrib><creatorcontrib>Harvill, Lainey</creatorcontrib><creatorcontrib>Hawkins, Shawna</creatorcontrib><creatorcontrib>Sladky, Kurt</creatorcontrib><creatorcontrib>Cox, Sherry</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Biomedical chromatography</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bergman, Joan</au><au>Harvill, Lainey</au><au>Hawkins, Shawna</au><au>Sladky, Kurt</au><au>Cox, Sherry</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Determination of ceftazidime in plasma by RP‐HPLC and ultraviolet detection</atitle><jtitle>Biomedical chromatography</jtitle><addtitle>Biomed Chromatogr</addtitle><date>2021-07</date><risdate>2021</risdate><volume>35</volume><issue>7</issue><spage>e5104</spage><epage>n/a</epage><pages>e5104-n/a</pages><issn>0269-3879</issn><eissn>1099-0801</eissn><abstract>A simple high‐performance liquid chromatography method for the determination of ceftazidime in plasma has been developed. Using an ultrafiltration technique samples were separated by reverse‐phase high‐performance liquid chromatography on a Symmetry C18 4.6 × 250 mm column (5.0 μm) and ultraviolet absorbance was measured at 260 nm. The mobile phase was a mixture of 10 mm potassium phosphate monobasic pH 2.5 with phosphoric acid and acetonitrile (90:10). The standard curve ranged from 0.1 to 100 μg/ml. Intra‐ and inter‐assay variability for ceftazidime was <12%, and the average recovery was 89%. The lower limit of quantification was 0.1 μg/ml. This method has been used successfully to analyze frog plasma samples at this institution and it could be applied to other small volume samples in a clinical or research setting.</abstract><cop>England</cop><pmid>33629742</pmid><doi>10.1002/bmc.5104</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-5184-900X</orcidid><orcidid>https://orcid.org/0000-0002-0896-6681</orcidid></addata></record> |
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subjects | ceftazidime HPLC pharmacokinetics |
title | Determination of ceftazidime in plasma by RP‐HPLC and ultraviolet detection |
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