Prediction of Drug Distribution in Subcutaneous Xenografts of Human Tumor Cell Lines and Healthy Tissues in Mouse: Application of the Tissue Composition‐Based Model to Antineoplastic Drugs. Issue 4 (14th January 2015)

• Record Type: Journal Article
• Authors: Poulin, Patrick; Chen, Yung‐Hsiang; Ding, Xiao; Gould, Stephen E.; Hop, Cornelis Eca; Messick, Kirsten; Oeh, Jason; Liederer, Bianca M.
• Is Part Of: Journal of pharmaceutical sciences. Volume 104:Issue 4(2015:Apr.)
• Page Start: 1508
• Page End: 1521
• Publication Date: 2015-01-14
• Subjects: Pharmacy -- Periodicals; 615.1
• DOI: 10.1002/jps.24336
• Languages: English
• ISSNs: 0022-3549

Abstract

<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Advanced tissue composition‐based models can predict the tissue–plasma partition coefficient (<italic>K</italic><sub>p</sub>) values of drugs under <italic>in vivo</italic> conditions on the basis of <italic>in vitro</italic> and physiological input data. These models, however, focus on healthy tissues and do not incorporate data from tumors. The objective of this study was to apply a tissue composition‐based model to six marketed antineoplastic drugs (docetaxel, DOC; doxorubicin, DOX; gemcitabine, GEM; methotrexate, MTX; topotecan, TOP; and fluorouracil, 5‐FU) to predict their <italic>K</italic><sub>p</sub> values in three human tumor xenografts (HCT‐116, H2122, and PC3) as well as in healthy tissues (brain, muscle, lung, and liver) under steady‐state <italic>in vivo</italic> conditions in female NCR nude mice. The mechanisms considered in the tissue/tumor composition‐based model are the binding to lipids and to plasma proteins, but the transporter effect was also investigated. The method consisted of analyzing tissue composition, performing the pharmacokinetics studies in mice, and calculating the corresponding <italic>in vivo K</italic><sub>p</sub> values. Analyses of tumor composition indicated that the tumor xenografts contained no or low amounts of common transporters by contrast to lipids. The predicted <italic>K</italic><sub>p</sub> values were within twofold and threefold of the measured values in 77% and 93% of cases, respectively. However, predictions for brain for each drug, for liver for MTX, and for each tumor xenograft for GEM were disparate from the observed values, and, therefore, not well served by the model. Overall, this study is the first step toward the mechanism‐based prediction of <italic>K</italic><sub>p</sub> values of small molecules in healthy and tumor tissues in mouse when no transporter and permeation limitation effect is evident. This approach will be useful in selecting compounds based on their abilities to penetrate human cancer xenografts with a physiologically based pharmacokinetic (PBPK) model, thereby increasing therapeutic index for chemotherapy in oncology study. © 2015 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 104:1508–1521, 2015</p> </abstract>