Zebrafish Embryos Allow Prediction of Nanoparticle Circulation Times in Mice and Facilitate Quantification of Nanoparticle-Cell Interactions.


Journal

Small (Weinheim an der Bergstrasse, Germany)
ISSN: 1613-6829
Titre abrégé: Small
Pays: Germany
ID NLM: 101235338

Informations de publication

Date de publication:
02 2020
Historique:
received: 02 12 2019
pubmed: 17 1 2020
medline: 5 5 2021
entrez: 17 1 2020
Statut: ppublish

Résumé

The zebrafish embryo is a vertebrate well suited for visualizing nanoparticles at high resolution in live animals. Its optical transparency and genetic versatility allow noninvasive, real-time observations of vascular flow of nanoparticles and their interactions with cells throughout the body. As a consequence, this system enables the acquisition of quantitative data that are difficult to obtain in rodents. Until now, a few studies using the zebrafish model have only described semiquantitative results on key nanoparticle parameters. Here, a MACRO dedicated to automated quantitative methods is described for analyzing important parameters of nanoparticle behavior, such as circulation time and interactions with key target cells, macrophages, and endothelial cells. Direct comparison of four nanoparticle (NP) formulations in zebrafish embryos and mice reveals that data obtained in zebrafish can be used to predict NPs' behavior in the mouse model. NPs having long or short blood circulation in rodents behave similarly in the zebrafish embryo, with low circulation times being a consequence of NP uptake into macrophages or endothelial cells. It is proposed that the zebrafish embryo has the potential to become an important intermediate screening system for nanoparticle research to bridge the gap between cell culture studies and preclinical rodent models such as the mouse.

Identifiants

pubmed: 31943784
doi: 10.1002/smll.201906719
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1906719

Informations de copyright

© 2020 The Authors. Published by WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Auteurs

Nils-Jørgen Knudsen Dal (NK)

Department of Biosciences, University of Oslo, Blindernveien 31, 0371, Oslo, Norway.

Agnese Kocere (A)

Department of Biosciences, University of Oslo, Blindernveien 31, 0371, Oslo, Norway.

Jens Wohlmann (J)

Department of Biosciences, University of Oslo, Blindernveien 31, 0371, Oslo, Norway.

Simon Van Herck (S)

Department of Pharmaceutics, Ghent University, Ottergemsesteenweg 460, 9000, Ghent, Belgium.

Tobias A Bauer (TA)

Institute for Organic Chemistry, Johannes Gutenberg-University Mainz, Duesbergweg 10-14, 55099, Mainz, Germany.

Julien Resseguier (J)

Department of Biosciences, University of Oslo, Blindernveien 31, 0371, Oslo, Norway.

Shahla Bagherifam (S)

Department of Radiation Biology, Institute for Cancer Research, Norwegian Radium Hospital, Montebello, N-0310, Oslo, Norway.

Hilde Hyldmo (H)

Department of Biosciences, University of Oslo, Blindernveien 31, 0371, Oslo, Norway.

Matthias Barz (M)

Institute for Organic Chemistry, Johannes Gutenberg-University Mainz, Duesbergweg 10-14, 55099, Mainz, Germany.

Bruno G De Geest (BG)

Department of Pharmaceutics, Ghent University, Ottergemsesteenweg 460, 9000, Ghent, Belgium.

Federico Fenaroli (F)

Department of Biosciences, University of Oslo, Blindernveien 31, 0371, Oslo, Norway.

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