High-performance liquid chromatographic analysis of idarubicin and fluorescent metabolites in biological fluids
A specific, sensitive, and reliable high-performance liquid chromatographic (HPLC) method for the determination of idarubicin (IDA) and its known fluorescent metabolites idarubicinol (IDAol) and 4-demethoxy-daunomycinone (AG1) in biological fluids (human plasma and urine) was developed and tested. P...
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Veröffentlicht in: | Cancer chemotherapy and pharmacology 1992, Vol.30 (4), p.303-306 |
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creator | CAMAGGI, C. M CARISI, P STROCCHI, E PANNUTI, F |
description | A specific, sensitive, and reliable high-performance liquid chromatographic (HPLC) method for the determination of idarubicin (IDA) and its known fluorescent metabolites idarubicinol (IDAol) and 4-demethoxy-daunomycinone (AG1) in biological fluids (human plasma and urine) was developed and tested. Plasma samples were solid-phase-extracted (C18 bonded silica cartridges). Complete separation of unchanged drugs and metabolites was achieved on a Cyanopropyl chromatographic column (25 cm x 4.6 mm inside diameter; particle size, 5 microns) using fluorescence detection (excitation wavelength, 470 nm; emission wavelength, 580 nm). Sensitivity was better than 0.2 ng/ml for all analytes; rates of recovery of unchanged drug and metabolites were better than 84.5% (IDA), 80.3% (IDAol), and 83.9% (AG1). The interassay coefficient of variation was 6.5% for IDA, 5.8% for IDAol, and 9.8% for AG1. Mean intra-assay precision was 4.6% for IDA, 5.9% for IDAol, and 5.0% for AG1 at sample concentrations of above 1 ng/ml and 12.1% for IDA, 10.8% for IDAol, and 14.1% for AG1 at sample concentrations of below 1 ng/ml. |
doi_str_mv | 10.1007/BF00686300 |
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M ; CARISI, P ; STROCCHI, E ; PANNUTI, F</creator><creatorcontrib>CAMAGGI, C. M ; CARISI, P ; STROCCHI, E ; PANNUTI, F</creatorcontrib><description>A specific, sensitive, and reliable high-performance liquid chromatographic (HPLC) method for the determination of idarubicin (IDA) and its known fluorescent metabolites idarubicinol (IDAol) and 4-demethoxy-daunomycinone (AG1) in biological fluids (human plasma and urine) was developed and tested. Plasma samples were solid-phase-extracted (C18 bonded silica cartridges). Complete separation of unchanged drugs and metabolites was achieved on a Cyanopropyl chromatographic column (25 cm x 4.6 mm inside diameter; particle size, 5 microns) using fluorescence detection (excitation wavelength, 470 nm; emission wavelength, 580 nm). Sensitivity was better than 0.2 ng/ml for all analytes; rates of recovery of unchanged drug and metabolites were better than 84.5% (IDA), 80.3% (IDAol), and 83.9% (AG1). The interassay coefficient of variation was 6.5% for IDA, 5.8% for IDAol, and 9.8% for AG1. Mean intra-assay precision was 4.6% for IDA, 5.9% for IDAol, and 5.0% for AG1 at sample concentrations of above 1 ng/ml and 12.1% for IDA, 10.8% for IDAol, and 14.1% for AG1 at sample concentrations of below 1 ng/ml.</description><identifier>ISSN: 0344-5704</identifier><identifier>EISSN: 1432-0843</identifier><identifier>DOI: 10.1007/BF00686300</identifier><identifier>PMID: 1643699</identifier><identifier>CODEN: CCPHDZ</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Analysis ; Biological and medical sciences ; Calibration ; Chromatography, High Pressure Liquid - methods ; Daunorubicin - analogs & derivatives ; Daunorubicin - analysis ; Daunorubicin - blood ; Daunorubicin - urine ; Fluorescence ; General pharmacology ; Humans ; Idarubicin - analogs & derivatives ; Idarubicin - analysis ; Idarubicin - blood ; Idarubicin - urine ; Medical sciences ; Pharmacology. Drug treatments ; Reference Standards</subject><ispartof>Cancer chemotherapy and pharmacology, 1992, Vol.30 (4), p.303-306</ispartof><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c311t-cb1491f28e6f3fa8b233737e54f4497cf25eef5e6cc27896138148bc20e9075d3</citedby><cites>FETCH-LOGICAL-c311t-cb1491f28e6f3fa8b233737e54f4497cf25eef5e6cc27896138148bc20e9075d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5459307$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1643699$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>CAMAGGI, C. M</creatorcontrib><creatorcontrib>CARISI, P</creatorcontrib><creatorcontrib>STROCCHI, E</creatorcontrib><creatorcontrib>PANNUTI, F</creatorcontrib><title>High-performance liquid chromatographic analysis of idarubicin and fluorescent metabolites in biological fluids</title><title>Cancer chemotherapy and pharmacology</title><addtitle>Cancer Chemother Pharmacol</addtitle><description>A specific, sensitive, and reliable high-performance liquid chromatographic (HPLC) method for the determination of idarubicin (IDA) and its known fluorescent metabolites idarubicinol (IDAol) and 4-demethoxy-daunomycinone (AG1) in biological fluids (human plasma and urine) was developed and tested. Plasma samples were solid-phase-extracted (C18 bonded silica cartridges). Complete separation of unchanged drugs and metabolites was achieved on a Cyanopropyl chromatographic column (25 cm x 4.6 mm inside diameter; particle size, 5 microns) using fluorescence detection (excitation wavelength, 470 nm; emission wavelength, 580 nm). Sensitivity was better than 0.2 ng/ml for all analytes; rates of recovery of unchanged drug and metabolites were better than 84.5% (IDA), 80.3% (IDAol), and 83.9% (AG1). The interassay coefficient of variation was 6.5% for IDA, 5.8% for IDAol, and 9.8% for AG1. Mean intra-assay precision was 4.6% for IDA, 5.9% for IDAol, and 5.0% for AG1 at sample concentrations of above 1 ng/ml and 12.1% for IDA, 10.8% for IDAol, and 14.1% for AG1 at sample concentrations of below 1 ng/ml.</description><subject>Analysis</subject><subject>Biological and medical sciences</subject><subject>Calibration</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>Daunorubicin - analogs & derivatives</subject><subject>Daunorubicin - analysis</subject><subject>Daunorubicin - blood</subject><subject>Daunorubicin - urine</subject><subject>Fluorescence</subject><subject>General pharmacology</subject><subject>Humans</subject><subject>Idarubicin - analogs & derivatives</subject><subject>Idarubicin - analysis</subject><subject>Idarubicin - blood</subject><subject>Idarubicin - urine</subject><subject>Medical sciences</subject><subject>Pharmacology. Drug treatments</subject><subject>Reference Standards</subject><issn>0344-5704</issn><issn>1432-0843</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkE1LxDAQhoMoun5cvAs9iAehOumkTXvUxXUFwYueS5pOdiNps5u0h_33VnbR08C8Dy8zD2PXHB44gHx8XgAUZYEAR2zGBWYplAKP2QxQiDSXIM7YeYzfACA44ik75YXAoqpmzC_tap1uKBgfOtVrSpzdjrZN9Dr4Tg1-FdRmbXWieuV20cbEm8S2KoyN1baf1m1i3OgDRU39kHQ0qMY7O1BMprix3vmV1cr9UraNl-zEKBfp6jAv2Nfi5XO-TN8_Xt_mT--pRs6HVDdcVNxkJRUGjSqbDFGipFwYISqpTZYTmZwKrTNZVgXHkouy0RlQBTJv8YLd7Xs3wW9HikPd2elC51RPfoy1RCjzqpATeL8HdfAxBjL1JthOhV3Nof61W__bneCbQ-vYdNT-o3udU357yFWcfjZhMmrjH5aLvEKQ-ANyloLT</recordid><startdate>1992</startdate><enddate>1992</enddate><creator>CAMAGGI, C. M</creator><creator>CARISI, P</creator><creator>STROCCHI, E</creator><creator>PANNUTI, F</creator><general>Springer</general><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>1992</creationdate><title>High-performance liquid chromatographic analysis of idarubicin and fluorescent metabolites in biological fluids</title><author>CAMAGGI, C. M ; CARISI, P ; STROCCHI, E ; PANNUTI, F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c311t-cb1491f28e6f3fa8b233737e54f4497cf25eef5e6cc27896138148bc20e9075d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Analysis</topic><topic>Biological and medical sciences</topic><topic>Calibration</topic><topic>Chromatography, High Pressure Liquid - methods</topic><topic>Daunorubicin - analogs & derivatives</topic><topic>Daunorubicin - analysis</topic><topic>Daunorubicin - blood</topic><topic>Daunorubicin - urine</topic><topic>Fluorescence</topic><topic>General pharmacology</topic><topic>Humans</topic><topic>Idarubicin - analogs & derivatives</topic><topic>Idarubicin - analysis</topic><topic>Idarubicin - blood</topic><topic>Idarubicin - urine</topic><topic>Medical sciences</topic><topic>Pharmacology. Drug treatments</topic><topic>Reference Standards</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CAMAGGI, C. M</creatorcontrib><creatorcontrib>CARISI, P</creatorcontrib><creatorcontrib>STROCCHI, E</creatorcontrib><creatorcontrib>PANNUTI, F</creatorcontrib><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>Cancer chemotherapy and pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>CAMAGGI, C. M</au><au>CARISI, P</au><au>STROCCHI, E</au><au>PANNUTI, F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High-performance liquid chromatographic analysis of idarubicin and fluorescent metabolites in biological fluids</atitle><jtitle>Cancer chemotherapy and pharmacology</jtitle><addtitle>Cancer Chemother Pharmacol</addtitle><date>1992</date><risdate>1992</risdate><volume>30</volume><issue>4</issue><spage>303</spage><epage>306</epage><pages>303-306</pages><issn>0344-5704</issn><eissn>1432-0843</eissn><coden>CCPHDZ</coden><abstract>A specific, sensitive, and reliable high-performance liquid chromatographic (HPLC) method for the determination of idarubicin (IDA) and its known fluorescent metabolites idarubicinol (IDAol) and 4-demethoxy-daunomycinone (AG1) in biological fluids (human plasma and urine) was developed and tested. Plasma samples were solid-phase-extracted (C18 bonded silica cartridges). Complete separation of unchanged drugs and metabolites was achieved on a Cyanopropyl chromatographic column (25 cm x 4.6 mm inside diameter; particle size, 5 microns) using fluorescence detection (excitation wavelength, 470 nm; emission wavelength, 580 nm). Sensitivity was better than 0.2 ng/ml for all analytes; rates of recovery of unchanged drug and metabolites were better than 84.5% (IDA), 80.3% (IDAol), and 83.9% (AG1). The interassay coefficient of variation was 6.5% for IDA, 5.8% for IDAol, and 9.8% for AG1. Mean intra-assay precision was 4.6% for IDA, 5.9% for IDAol, and 5.0% for AG1 at sample concentrations of above 1 ng/ml and 12.1% for IDA, 10.8% for IDAol, and 14.1% for AG1 at sample concentrations of below 1 ng/ml.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>1643699</pmid><doi>10.1007/BF00686300</doi><tpages>4</tpages></addata></record> |
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subjects | Analysis Biological and medical sciences Calibration Chromatography, High Pressure Liquid - methods Daunorubicin - analogs & derivatives Daunorubicin - analysis Daunorubicin - blood Daunorubicin - urine Fluorescence General pharmacology Humans Idarubicin - analogs & derivatives Idarubicin - analysis Idarubicin - blood Idarubicin - urine Medical sciences Pharmacology. Drug treatments Reference Standards |
title | High-performance liquid chromatographic analysis of idarubicin and fluorescent metabolites in biological fluids |
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