This manuscript is dedicated to Daniel Waldon (1960–2013) in recognition of his critical role in the development of DESI-MS imaging in our lab and for his invaluable advice on this manuscript.
Whole-body tissue distribution study of drugs in neonate mice using desorption electrospray ionization mass spectrometry imaging†
Article first published online: 5 DEC 2013
Copyright © 2013 John Wiley & Sons, Ltd.
Rapid Communications in Mass Spectrometry
Volume 28, Issue 2, pages 185–190, 30 January 2014
How to Cite
Liu, J., Gingras, J., Ganley, K. P., Vismeh, R., Teffera, Y. and Zhao, Z. (2014), Whole-body tissue distribution study of drugs in neonate mice using desorption electrospray ionization mass spectrometry imaging. Rapid Commun. Mass Spectrom., 28: 185–190. doi: 10.1002/rcm.6775
- Issue published online: 5 DEC 2013
- Article first published online: 5 DEC 2013
- Manuscript Accepted: 26 OCT 2013
- Manuscript Revised: 25 OCT 2013
- Manuscript Received: 27 AUG 2013
Although Desorption Electrospray Ionization (DESI) Mass Spectrometry Imaging (MSI) is uniquely suited for whole-body (WB) tissue distribution study of drugs, success in this area has been difficult. Here, we present WB tissue distribution studies using DESI-MSI and a new histological tissue-friendly solvent system.
Neonate pups were dosed subcutaneously (SC) with clozapine, compound 1, compound 2, or compound 3. Following euthanization by hypothermia, neonates underwent a transcardiac perfusion (saline) to remove blood. After cryosectioning, DESI-MSI was conducted for the WB tissue slides, followed sequentially by histological staining.
Whole-body tissue imaging showed that clozapine and its N-oxide metabolite were distributed in significant amounts in the brain, spinal cord, liver, heart (ventricle), and lungs. Compound 1 was distributed mainly in the liver and muscle, and its mono-oxygenated metabolite was detected by DESI-MSI exclusively in the liver. Compound 2 was distributed mainly in the muscle and fatty tissue. Compound 3 was distributed mainly in fatty tissue and its metabolites were also mainly detected in the same tissue.
The results demonstrate the successful application of DESI-MSI in whole-body tissue distribution studies of drugs and metabolites in combination with sequential histology staining for anatomy. The results also identified lipophilicity as the driving force in the tissue distribution of the three Amgen compounds. Copyright © 2013 John Wiley & Sons, Ltd.