Determination of GI147211 in human blood by HPLC with fluorescence detection

GI147211 (GG211) is a camptothecin analogue, which exhibits antileukemic and antitumor activity by blocking DNA synthesis. The drug stability considerations and specimen handling were important aspects in method development and validation. This method involves collection of blood at the clinical sit...

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Veröffentlicht in:Journal of pharmaceutical and biomedical analysis 1995-11, Vol.13 (12), p.1521-1530
Hauptverfasser: Selinger, Krzysztof, Smith, Glenn, Depee, Scott, Aureche, Cathy
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container_end_page 1530
container_issue 12
container_start_page 1521
container_title Journal of pharmaceutical and biomedical analysis
container_volume 13
creator Selinger, Krzysztof
Smith, Glenn
Depee, Scott
Aureche, Cathy
description GI147211 (GG211) is a camptothecin analogue, which exhibits antileukemic and antitumor activity by blocking DNA synthesis. The drug stability considerations and specimen handling were important aspects in method development and validation. This method involves collection of blood at the clinical site, immediate freezing, and storage at −70°C. The lactone form is extracted from blood at physiological pH with a mixture of n-butyl chloride and acetonitrile (4:1); the carboxylate is not extracted under these conditions. After evaporation the extract is injected into an HPLC system with a fluorescence detector set at 378/420 nm. The internal standard used is 6,7-dimethoxy-4-methylcoumarin. The main advantages of the procedure are the separation of lactone and carboxylate by means of extraction, simplified specimen collection at clinical sites and the ability to inject almost all of the extracted material (extraction recovery, 60%) into an HPLC system. The method has been validated over the range 0.15–100 ng ml −1 with sufficient precision and accuracy (coefficient of variation below 10%) to support pharmacokinetic studies. Under the conditions of this procedure, the drug is stable in human blood at −70°C for at least 93 days, as well as through two additional freeze-thaw cycles.
doi_str_mv 10.1016/0731-7085(95)01592-2
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The drug stability considerations and specimen handling were important aspects in method development and validation. This method involves collection of blood at the clinical site, immediate freezing, and storage at −70°C. The lactone form is extracted from blood at physiological pH with a mixture of n-butyl chloride and acetonitrile (4:1); the carboxylate is not extracted under these conditions. After evaporation the extract is injected into an HPLC system with a fluorescence detector set at 378/420 nm. The internal standard used is 6,7-dimethoxy-4-methylcoumarin. The main advantages of the procedure are the separation of lactone and carboxylate by means of extraction, simplified specimen collection at clinical sites and the ability to inject almost all of the extracted material (extraction recovery, 60%) into an HPLC system. The method has been validated over the range 0.15–100 ng ml −1 with sufficient precision and accuracy (coefficient of variation below 10%) to support pharmacokinetic studies. 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The method has been validated over the range 0.15–100 ng ml −1 with sufficient precision and accuracy (coefficient of variation below 10%) to support pharmacokinetic studies. 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Drug treatments</topic><topic>Reference Standards</topic><topic>Spectrometry, Fluorescence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Selinger, Krzysztof</creatorcontrib><creatorcontrib>Smith, Glenn</creatorcontrib><creatorcontrib>Depee, Scott</creatorcontrib><creatorcontrib>Aureche, Cathy</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>Journal of pharmaceutical and biomedical analysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Selinger, Krzysztof</au><au>Smith, Glenn</au><au>Depee, Scott</au><au>Aureche, Cathy</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Determination of GI147211 in human blood by HPLC with fluorescence detection</atitle><jtitle>Journal of pharmaceutical and biomedical analysis</jtitle><addtitle>J Pharm Biomed Anal</addtitle><date>1995-11-01</date><risdate>1995</risdate><volume>13</volume><issue>12</issue><spage>1521</spage><epage>1530</epage><pages>1521-1530</pages><issn>0731-7085</issn><eissn>1873-264X</eissn><coden>JPBADA</coden><abstract>GI147211 (GG211) is a camptothecin analogue, which exhibits antileukemic and antitumor activity by blocking DNA synthesis. 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The method has been validated over the range 0.15–100 ng ml −1 with sufficient precision and accuracy (coefficient of variation below 10%) to support pharmacokinetic studies. Under the conditions of this procedure, the drug is stable in human blood at −70°C for at least 93 days, as well as through two additional freeze-thaw cycles.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>8788138</pmid><doi>10.1016/0731-7085(95)01592-2</doi><tpages>10</tpages></addata></record>
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source MEDLINE; Elsevier ScienceDirect Journals Complete
subjects Antineoplastic agents
Antineoplastic Agents - blood
Antineoplastic Agents - pharmacokinetics
Biological and medical sciences
Biotransformation
Calibration
Camptothecin - analogs & derivatives
Camptothecin - blood
Camptothecin - pharmacokinetics
Camptothecin analogue
Chemotherapy
Chromatography, High Pressure Liquid
Drug Stability
Fluorescence detection
GI147211
Half-Life
High-performance liquid chromatography
Human blood
Humans
Hydrolysis
Infusions, Intravenous
Medical sciences
Neoplasms - metabolism
Pharmacology. Drug treatments
Reference Standards
Spectrometry, Fluorescence
title Determination of GI147211 in human blood by HPLC with fluorescence detection
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