Influence of Size and Shape on the Anatomical Distribution of Endotoxin-Free Gold Nanoparticles

Laura Talamini(Mario Negri Institute for Pharmacological Research), Martina Bruna Violatto(Mario Negri Institute for Pharmacological Research), Qi Cai(University College Dublin), Marco P. Monopoli(University College Dublin), Karsten Kantner(Philipps University of Marburg), Željka Krpetić(University College Dublin), André Perez‐Potti(University College Dublin), Jennifer Cookman(University College Dublin), David Garry(University College Dublin), Camila P. Silveira(University College Dublin), Luca Boselli(University College Dublin), Beatriz Pelaz(Philipps University of Marburg), Tommaso Serchi(Luxembourg Institute of Science and Technology), Sébastien Cambier(Luxembourg Institute of Science and Technology), Arno C. Gutleb(Luxembourg Institute of Science and Technology), Neus Feliu(Philipps University of Marburg), Yan Yan(University College Dublin), Mario Salmona(Mario Negri Institute for Pharmacological Research), Wolfgang J. Parak(Philipps University of Marburg), Kenneth A. Dawson(University College Dublin), Paolo Bigini(Mario Negri Institute for Pharmacological Research)
ACS Nano
May 30, 2017
Cited by 177Open Access
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Abstract

The transport and the delivery of drugs through nanocarriers is a great challenge of pharmacology. Since the production of liposomes to reduce the toxicity of doxorubicin in patients, a plethora of nanomaterials have been produced and characterized. Although it is widely known that elementary properties of nanomaterials influence their in vivo kinetics, such interaction is often poorly investigated in many preclinical studies. The present study aims to evaluate the actual effect of size and shape on the biodistribution of a set of gold nanoparticles (GNPs) after intravenous administration in mice. To this goal, quantitative data achieved by inductively coupled plasma mass spectrometry and observational results emerging from histochemistry (autometallography and enhanced dark-field hyperspectral microscopy) were combined. Since the immune system plays a role in bionano-interaction we used healthy immune-competent mice. To keep the immune surveillance on the physiological levels we synthesized endotoxin-free GNPs to be tested in specific pathogen-free animals. Our study mainly reveals that (a) the size and the shape greatly influence the kinetics of accumulation and excretion of GNPs in filter organs; (b) spherical and star-like GNPs showed the same percentage of accumulation, but a different localization in liver; (c) only star-like GNPs are able to accumulate in lung; (d) changes in the geometry did not improve the passage of the blood brain barrier. Overall, this study can be considered as a reliable starting point to drive the synthesis and the functionalization of potential candidates for theranostic purposes in many fields of research.


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