Determination of irinotecan (CPT-11) and SN-38 in human whole blood and red blood cells by liquid chromatography with fluorescence detection

FA (Floris) de Jong, RHJ Mathijssen, Peter de Bruijn, Walter Loos, Jaap Verweij, A Sparreboom*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

40 Citations (Scopus)

Abstract

An analytical method was developed for the anticancer agent irinotecan (CPT-11) and its main metabolite SN-38 in human whole blood and in red blood cells (RBCs). Sample pretreatment involved deproteinization of whole blood or plasma-diluted RBCs isolated by MESED instruments, with a mixture of aqueous perchloric acid and methanol (1:1, v/v). Separation was carried out using isocratic elution on a Hypersil ODS stationary phase, with detection at excitation and emission wavelengths of 355 and 515 nm, respectively. The lower limit of quantitation (LLQ) in blood was established at 5.00 ng/ml for both compounds, with values for within-run precision (WRP) and between-run precision (BRP) of less than 10%. The method is currently being applied to investigate the blood distribution of CPT-11 and SN-38 in cancer patients.

Original languageEnglish
Pages (from-to)383-388
Number of pages6
JournalJournal of Chromatography B-Biomedical Applications
Volume795
Issue number2
DOIs
Publication statusPublished - 5 Oct 2003

Research programs

  • EMC MM-03-86-08

Fingerprint

Dive into the research topics of 'Determination of irinotecan (CPT-11) and SN-38 in human whole blood and red blood cells by liquid chromatography with fluorescence detection'. Together they form a unique fingerprint.

Cite this