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      Thallium Labeled Citrate-Coated Prussian Blue Nanoparticles as Potential Imaging Agent

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          Abstract

          Background

          The aim of this study was to develop and characterize a nanoparticle-based image-contrast platform which is biocompatible, chemically stable, and accessible for radiolabeling with 201Tl. We explored whether this nanoparticle enhanced the T1 signal which might make it an MRI contrast agent as well.

          Methods

          The physical properties of citrate-coated Prussian blue nanoparticles (PBNPs) (iron(II);iron(III);octadecacyanide) doped with 201Tl isotope were characterized with atomic force microscopy, dynamic light scattering, and zeta potential measurement. PBNP biodistribution was determined by using SPECT and MRI following intravenous administration into C57BL6 mice. Activity concentrations (MBq/cm 3) were calculated from the SPECT scans for each dedicated volume of interest (VOI) of liver, kidneys, salivary glands, heart, lungs, and brain.

          Results

          PBNP accumulation peaked at 2 hours after injection predominantly in the kidneys and the liver followed by a gradual decrease in activity in later time points.

          Conclusion

          We synthetized, characterized, and radiolabeled a Prussian blue-based nanoparticle platform for contrast material applications. Its in vivo radiochemical stability and biodistribution open up the way for further diagnostic applications.

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          Most cited references18

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          Nanoparticle-liver interactions: Cellular uptake and hepatobiliary elimination.

          30-99% of administered nanoparticles will accumulate and sequester in the liver after administration into the body. This results in reduced delivery to the targeted diseased tissue and potentially leads to increased toxicity at the hepatic cellular level. This review article focuses on the inter- and intra-cellular interaction between nanoparticles and hepatic cells, the elimination mechanism of nanoparticles through the hepatobiliary system, and current strategies to manipulate liver sequestration. The ability to solve the "nanoparticle-liver" interaction is critical to the clinical translation of nanotechnology for diagnosing and treating cancer, diabetes, cardiovascular disorders, and other diseases.
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            Research strategies for safety evaluation of nanomaterials. Part VI. Characterization of nanoscale particles for toxicological evaluation.

            To properly assign mechanisms or causes for toxic effects of nanoscale materials, their properties and characteristics both outside and within the biological environment must be well understood. Scientists have many tools for studying the size, shape, and surface properties of particulates outside of the physiological environment; however, it is difficult to measure many of these same properties in situ without perturbing the environment, leading to spurious findings. Characterizing nanoparticle systems in situ can be further complicated by an organism's active clearance, defense, and/or immune responses. As toxicologists begin to examine nanomaterials in a systematic fashion, there is consensus that a series of guidelines or recommended practices is necessary for basic characterization of nanomaterials. These recommended practices should be developed jointly by physical scientists skilled in nano characterization and biological scientists experienced in toxicology research. In this article, basic nanoparticle characterization techniques are discussed, along with the some of the issues and implications associated with measuring nanoparticle properties and their interactions with biological systems. Recommendations regarding how best to approach nanomaterial characterization include using proper sampling and measurement techniques, forming multidisciplinary teams, and making measurements as close to the biological action point as possible.
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              Targeting kidney mesangium by nanoparticles of defined size.

              Nanoparticles are being investigated for numerous medical applications and are showing potential as an emerging class of carriers for drug delivery. Investigations on how the physicochemical properties (e.g., size, surface charge, shape, and density of targeting ligands) of nanoparticles enable their ability to overcome biological barriers and reach designated cellular destinations in sufficient amounts to elicit biological efficacy are of interest. Despite proven success in nanoparticle accumulation at cellular locations and occurrence of downstream therapeutic effects (e.g., target gene inhibition) in a selected few organs such as tumor and liver, reports on effective delivery of engineered nanoparticles to other organs still remain scarce. Here, we show that nanoparticles of ~75 ± 25-nm diameters target the mesangium of the kidney. These data show the effects of particle diameter on targeting the mesangium of the kidney. Because many diseases originate from this area of the kidney, our findings establish design criteria for constructing nanoparticle-based therapeutics for targeting diseases that involve the mesangium of the kidney.
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                Author and article information

                Contributors
                Journal
                Contrast Media Mol Imaging
                Contrast Media Mol Imaging
                CMMI
                Contrast Media & Molecular Imaging
                Hindawi
                1555-4309
                1555-4317
                2018
                26 April 2018
                : 2018
                : 2023604
                Affiliations
                1Department of Biophysics and Radiation Biology, Semmelweis University, Budapest 1094, Hungary
                2Department of Radiology and Oncotherapy, Semmelweis University, Budapest 1094, Hungary
                3CROmed Translational Research Centers, Budapest 1047, Hungary
                4Institute of Materials and Environmental Chemistry, Research Center for Natural Sciences of the Hungarian Academy of Sciences, Budapest, Hungary
                5Mediso Medical Imaging Systems Ltd., Budapest 1022, Hungary
                6Department of Public Health Medicine, Medical School, University of Pécs, Pécs 7624, Hungary
                7Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore
                8Imperial College London, Kensington, London, UK
                Author notes

                Academic Editor: Daniela Haeusler

                Author information
                http://orcid.org/0000-0002-0828-9828
                http://orcid.org/0000-0003-1122-1872
                http://orcid.org/0000-0002-5741-2669
                http://orcid.org/0000-0003-4112-4600
                http://orcid.org/0000-0001-7343-0413
                Article
                10.1155/2018/2023604
                5944205
                ee117f0e-ca8a-4e40-b368-1d2dec48bdf1
                Copyright © 2018 Krisztián Szigeti et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 23 November 2017
                : 15 March 2018
                Funding
                Funded by: Seventh Framework Programme
                Award ID: HEALTH- F2-2011-278850
                Award ID: FP7 HEALTH-305311
                Award ID: TÁMOP-4.2.1./B- 09/1/KMR-2010-0001
                Funded by: National Research, Development and Innovation Office of Hungary
                Award ID: NVKP-16-1-2016-0017
                Award ID: NVKP_0017
                Funded by: Hungarian Academy of Science
                Funded by: Nanyang Technological University
                Categories
                Research Article

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