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Molecular imaging of brain localization of liposomes in mice using MALDI mass spectrometry
Phospholipids have excellent biocompatibility and are therefore often used as main components of liposomal drug carriers. In traditional bioanalytics, the in-vivo distribution of liposomal drug carriers is assessed using radiolabeled liposomal constituents. This study presents matrix-assisted laser...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5030664/ https://www.ncbi.nlm.nih.gov/pubmed/27650487 http://dx.doi.org/10.1038/srep33791 |
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author | Fülöp, Annabelle Sammour, Denis A. Erich, Katrin von Gerichten, Johanna van Hoogevest, Peter Sandhoff, Roger Hopf, Carsten |
author_facet | Fülöp, Annabelle Sammour, Denis A. Erich, Katrin von Gerichten, Johanna van Hoogevest, Peter Sandhoff, Roger Hopf, Carsten |
author_sort | Fülöp, Annabelle |
collection | PubMed |
description | Phospholipids have excellent biocompatibility and are therefore often used as main components of liposomal drug carriers. In traditional bioanalytics, the in-vivo distribution of liposomal drug carriers is assessed using radiolabeled liposomal constituents. This study presents matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI MSI) as an alternative, label-free method for ex-vivo molecular imaging of liposomal drug carriers in mouse tissue. To this end, indocyanine green as cargo and two liposomal markers, 1,2-dipalmitoyl-sn-glycero-3-phosphoglycerol (DPPG) and 1,2-distearoyl-sn-glycero-3-phosphoethanolamine conjugated with monodisperse polyethylene glycol (PEG(36)-DSPE) were incorporated into liposomal carriers and administered to mice. We used MALDI MSI of the two lipid markers in both positive and negative ion mode for visualization of liposome integrity and distribution in mouse organs. Additional MSI of hemoglobin in the same tissue slice and pixel-by-pixel computational analysis of co-occurrence of lipid markers and hemoglobin served as indicator of liposome localization either in parenchyma or in blood vessels. Our proof-of-concept study suggests that liposomal components and indocyanine green distributed into all investigated organs. |
format | Online Article Text |
id | pubmed-5030664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50306642016-09-26 Molecular imaging of brain localization of liposomes in mice using MALDI mass spectrometry Fülöp, Annabelle Sammour, Denis A. Erich, Katrin von Gerichten, Johanna van Hoogevest, Peter Sandhoff, Roger Hopf, Carsten Sci Rep Article Phospholipids have excellent biocompatibility and are therefore often used as main components of liposomal drug carriers. In traditional bioanalytics, the in-vivo distribution of liposomal drug carriers is assessed using radiolabeled liposomal constituents. This study presents matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI MSI) as an alternative, label-free method for ex-vivo molecular imaging of liposomal drug carriers in mouse tissue. To this end, indocyanine green as cargo and two liposomal markers, 1,2-dipalmitoyl-sn-glycero-3-phosphoglycerol (DPPG) and 1,2-distearoyl-sn-glycero-3-phosphoethanolamine conjugated with monodisperse polyethylene glycol (PEG(36)-DSPE) were incorporated into liposomal carriers and administered to mice. We used MALDI MSI of the two lipid markers in both positive and negative ion mode for visualization of liposome integrity and distribution in mouse organs. Additional MSI of hemoglobin in the same tissue slice and pixel-by-pixel computational analysis of co-occurrence of lipid markers and hemoglobin served as indicator of liposome localization either in parenchyma or in blood vessels. Our proof-of-concept study suggests that liposomal components and indocyanine green distributed into all investigated organs. Nature Publishing Group 2016-09-21 /pmc/articles/PMC5030664/ /pubmed/27650487 http://dx.doi.org/10.1038/srep33791 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Fülöp, Annabelle Sammour, Denis A. Erich, Katrin von Gerichten, Johanna van Hoogevest, Peter Sandhoff, Roger Hopf, Carsten Molecular imaging of brain localization of liposomes in mice using MALDI mass spectrometry |
title | Molecular imaging of brain localization of liposomes in mice using MALDI mass spectrometry |
title_full | Molecular imaging of brain localization of liposomes in mice using MALDI mass spectrometry |
title_fullStr | Molecular imaging of brain localization of liposomes in mice using MALDI mass spectrometry |
title_full_unstemmed | Molecular imaging of brain localization of liposomes in mice using MALDI mass spectrometry |
title_short | Molecular imaging of brain localization of liposomes in mice using MALDI mass spectrometry |
title_sort | molecular imaging of brain localization of liposomes in mice using maldi mass spectrometry |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5030664/ https://www.ncbi.nlm.nih.gov/pubmed/27650487 http://dx.doi.org/10.1038/srep33791 |
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