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Irinotecan Loaded in Eluting Beads: Preclinical Assessment in a Rabbit VX2 Liver Tumor Model

Purpose The purpose of this study was to study the pharmacokinetics of irinotecan injected intravenously, intra-arterially, or loaded onto a delivery platform. Material and Methods Fifty-four New Zealand White rabbits with VX2 liver tumor, divided in 3 groups of 17 rabbits, each received irinotecan...

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Published in:Cardiovascular and interventional radiology 2012-12, Vol.35 (6), p.1448-1459
Main Authors: Rao, Pramod P., Pascale, Florentina, Seck, Atman, Auperin, Anne, Drouard-Troalen, Laurence, Deschamps, Frederic, Teriitheau, Christophe, Paci, Angelo, Denys, Alban, Bize, Pierre, de Baere, Thierry
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Language:English
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Summary:Purpose The purpose of this study was to study the pharmacokinetics of irinotecan injected intravenously, intra-arterially, or loaded onto a delivery platform. Material and Methods Fifty-four New Zealand White rabbits with VX2 liver tumor, divided in 3 groups of 17 rabbits, each received irinotecan either by intravenous (IV) route, intra-arterial hepatic (IA) route, or loaded on drug-eluting beads (DEBIRI). Animals were killed at 1, 6, and 24 h. Irinotecan and SN-38 concentrations were measured at different time points in serum, tumor, and normal liver. Results Twelve milligrams of irinotecan were injected IV and IA, whereas 6–16.5 mg were injected loaded onto DEBIRI. Normalized serum irinotecan reached a peak of 333 ng/ml (range 198.8–502.5) for IV, 327.1 ng/ml (range 277.1–495.6) for IA, and 189.7 ng/ml (range 111.1–261.9) for DEBIRI ( P  
ISSN:0174-1551
1432-086X
DOI:10.1007/s00270-012-0343-y