The novel sensitive and high throughput determination of cefepime in mouse plasma by SCX-LC/MS/MS method following off-line [micro]Elution 96-well solid-phase extraction to support systemic antibiotic programs
A sensitive and high throughput off-line [micro]Elution 96-well solid-phase extraction (SPE) followed by strong cation exchange (SCX) liquid chromatography with tandem mass spectrometry (LC/MS/MS) quantification for determination of cefepime has been developed and validated in mouse plasma. Using th...
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Veröffentlicht in: | Journal of chromatography. B, Analytical technologies in the biomedical and life sciences Analytical technologies in the biomedical and life sciences, 2010-06, Vol.878 (19), p.1623-1628 |
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container_title | Journal of chromatography. B, Analytical technologies in the biomedical and life sciences |
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creator | Bu, Wei Sexton, Holly Fan, Xiaoqing Torres, Patricia Houston, Paul Heyman, Irwin Liu, Liang |
description | A sensitive and high throughput off-line [micro]Elution 96-well solid-phase extraction (SPE) followed by strong cation exchange (SCX) liquid chromatography with tandem mass spectrometry (LC/MS/MS) quantification for determination of cefepime has been developed and validated in mouse plasma. Using the chemical analog, ceftazidime as an internal standard (IS), the linear range of the method for the determination of cefepime in mouse plasma was 4-2048 ng/mL with the lower limit of quantitation level (LLOQ) of 4 ng/mL. The inter- and intra-assay precision and accuracy of the method were below 9.05% and ranged from 95.6 to 113%, respectively, determined by quality control (QC) samples at five concentration levels including LLOQ. After [micro]Elution SPE, 71.1% of cefepime was recovered. The application of the validated assay for the determination of cefepime in mouse pharmacokinetics (PK) samples after intravenous (IV) and subcutaneous (SC) doses was demonstrated. |
doi_str_mv | 10.1016/j.jchromb.2010.03.045 |
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Using the chemical analog, ceftazidime as an internal standard (IS), the linear range of the method for the determination of cefepime in mouse plasma was 4-2048 ng/mL with the lower limit of quantitation level (LLOQ) of 4 ng/mL. The inter- and intra-assay precision and accuracy of the method were below 9.05% and ranged from 95.6 to 113%, respectively, determined by quality control (QC) samples at five concentration levels including LLOQ. After [micro]Elution SPE, 71.1% of cefepime was recovered. The application of the validated assay for the determination of cefepime in mouse pharmacokinetics (PK) samples after intravenous (IV) and subcutaneous (SC) doses was demonstrated.</description><identifier>ISSN: 1570-0232</identifier><identifier>DOI: 10.1016/j.jchromb.2010.03.045</identifier><language>eng</language><ispartof>Journal of chromatography. 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B, Analytical technologies in the biomedical and life sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bu, Wei</au><au>Sexton, Holly</au><au>Fan, Xiaoqing</au><au>Torres, Patricia</au><au>Houston, Paul</au><au>Heyman, Irwin</au><au>Liu, Liang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The novel sensitive and high throughput determination of cefepime in mouse plasma by SCX-LC/MS/MS method following off-line [micro]Elution 96-well solid-phase extraction to support systemic antibiotic programs</atitle><jtitle>Journal of chromatography. 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After [micro]Elution SPE, 71.1% of cefepime was recovered. The application of the validated assay for the determination of cefepime in mouse pharmacokinetics (PK) samples after intravenous (IV) and subcutaneous (SC) doses was demonstrated.</abstract><doi>10.1016/j.jchromb.2010.03.045</doi></addata></record> |
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title | The novel sensitive and high throughput determination of cefepime in mouse plasma by SCX-LC/MS/MS method following off-line [micro]Elution 96-well solid-phase extraction to support systemic antibiotic programs |
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