By the same authors

From the same journal

In vivo imaging of systemic transport and elimination of xenobiotics and endogenous molecules in mice

Research output: Contribution to journalArticle



Publication details

JournalArchives of toxicology
DateAccepted/In press - 23 Nov 2016
DateE-pub ahead of print - 20 Dec 2016
DatePublished (current) - Mar 2017
Issue number3
Number of pages18
Pages (from-to)1335-1352
Early online date20/12/16
Original languageEnglish


We describe a two-photon microscopy-based method to evaluate the in vivo systemic transport of compounds. This method comprises imaging of the intact liver, kidney and intestine, the main organs responsible for uptake and elimination of xenobiotics and endogenous molecules. The image quality of the acquired movies was sufficient to distinguish subcellular structures like organelles and vesicles. Quantification of the movement of fluorescent dextran and fluorescent cholic acid derivatives in different organs and their sub-compartments over time revealed significant dynamic differences. Calculated half-lives were similar in the capillaries of all investigated organs but differed in the specific sub-compartments, such as parenchymal cells and bile canaliculi of the liver, glomeruli, proximal and distal tubules of the kidney and lymph vessels (lacteals) of the small intestine. Moreover, tools to image immune cells, which can influence transport processes in inflamed tissues, are described. This powerful approach provides new possibilities for the analysis of compound transport in multiple organs and can support physiologically based pharmacokinetic modeling, in order to obtain more precise predictions at the whole body scale.

Bibliographical note

© The Author(s) 2016.

    Research areas

  • Acetaminophen, Animals, Chemical and Drug Induced Liver Injury, Hepatocytes, Intestines, Kidney, Kupffer Cells, Liver, Male, Mice, Transgenic, Microscopy, Video Recording, Xenobiotics, Journal Article

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