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      A Proof-of-Concept Study on the Therapeutic Potential of Au Nanoparticles Radiolabeled with the Alpha-Emitter Actinium-225

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          Abstract

          Actinium-225 ( 225Ac) is receiving increased attention for its application in targeted radionuclide therapy, due to the short range of its emitted alpha particles in conjunction with their high linear energy transfer, which lead to the eradication of tumor cells while sparing neighboring healthy tissue. The objective of our study was the evaluation of a gold nanoparticle radiolabeled with 225Ac as an injectable radiopharmaceutical form of brachytherapy for local radiation treatment of cancer. Au@TADOTAGA was radiolabeled with 225Ac at pH 5.6 (30 min at 70 °C), and in vitro stability was evaluated. In vitro cytotoxicity was assessed in U-87 MG cancer cells, and in vivo biodistribution was performed by intravenous and intratumoral administration of [ 225Ac] 225Ac-Au@TADOTAGA in U-87 MG tumor-bearing mice. A preliminary study to assess therapeutic efficacy of the intratumorally-injected radio-nanomedicine was performed over a period of 22 days, while the necrotic effect on tumors was evaluated by a histopathology study. We have shown that [ 225Ac] 225Ac-Au@TADOTAGA resulted in the retardation of tumor growth after its intratumoral injection in U87MG tumor-bearing mice, even though very low activities were injected per mouse. This gold nanoparticle radiopharmaceutical could be applied as an unconventional brachytherapy in injectable form for local radiation treatment of cancer.

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          Over the last few decades, colloidal drug delivery systems (CDDS) such as nano-structures have been developed in order to improve the efficiency and the specificity of drug action. Their small size permits them to be injected intravenously in order to reach target tissues. However, it is known that they can be rapidly removed from blood circulation by the immune system. CDDS are removed via the complement system and via the cells of the mononuclear phagocyte system (MPS), after their recognition by opsonins and/or receptors present at the cell surface. This recognition is dependent on the physicochemical characteristics of the CDDS. In this study, we will focus on parameters influencing the interactions of opsonins and the macrophage plasma membrane with the surface of CDDS, whereby parameters of the polymer coating become necessary to provide good protection.
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            Synthesis and reactions of functionalised gold nanoparticles

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              A reexamination of active and passive tumor targeting by using rod-shaped gold nanocrystals and covalently conjugated peptide ligands.

              The targeted delivery of nanoparticles to solid tumors is one of the most important and challenging problems in cancer nanomedicine, but the detailed delivery mechanisms and design principles are still not well understood. Here we report quantitative tumor uptake studies for a class of elongated gold nanocrystals (called nanorods) that are covalently conjugated to tumor-targeting peptides. A major advantage in using gold as a "tracer" is that the accumulated gold in tumors and other organs can be quantitatively determined by elemental mass spectrometry (gold is not a natural element found in animals). Thus, colloidal gold nanorods are stabilized with a layer of polyethylene glycols (PEGs) and are conjugated to three different ligands: (i) a single-chain variable fragment (ScFv) peptide that recognizes the epidermal growth factor receptor (EGFR); (ii) an amino terminal fragment (ATF) peptide that recognizes the urokinase plasminogen activator receptor (uPAR); and (iii) a cyclic RGD peptide that recognizes the a(v)β(3) integrin receptor. Quantitative pharmacokinetic and biodistribution data show that these targeting ligands only marginally improve the total gold accumulation in xenograft tumor models in comparison with nontargeted controls, but their use could greatly alter the intracellular and extracellular nanoparticle distributions. When the gold nanorods are administered via intravenous injection, we also find that active molecular targeting of the tumor microenvironments (e.g., fibroblasts, macrophages, and vasculatures) does not significantly influence the tumor nanoparticle uptake. These results suggest that for photothermal cancer therapy, the preferred route of gold nanorod administration is intratumoral injection instead of intravenous injection.
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                Author and article information

                Journal
                Pharmaceutics
                Pharmaceutics
                pharmaceutics
                Pharmaceutics
                MDPI
                1999-4923
                21 February 2020
                February 2020
                : 12
                : 2
                : 188
                Affiliations
                [1 ]Institute of Nuclear & Radiological Sciences & Technology, Energy & Safety, National Center for Scientific Research “Demokritos”, 15341 Athens, Greece; salvanou@ 123456rrp.demokritos.gr (E.-A.S.); ctsoukal@ 123456rrp.demokritos.gr (C.T.); mparavatou@ 123456rrp.demokritos.gr (M.P.-P.); staxan@ 123456rrp.demokritos.gr (S.X.)
                [2 ]Institute of Chemical Biology, National Hellenic Research Foundation, 11635 Athens, Greece
                [3 ]Institute of Biosciences and Applications, National Center for Scientific Research “Demokritos”, 15341 Athens, Greece; bmavroidi@ 123456bio.demokritos.gr
                [4 ]A’ Pathology Department, 401 General Military Hospital of Athens, 11525 Athens, Greece; dr.nikoskalogeropoulos@ 123456gmail.com
                [5 ]ICMUB, UMR 6302 CNRS-UB, Université Bourgogne Franche-Comté, 21000 Dijon, France; Franck.Denat@ 123456u-bourgogne.fr
                [6 ]Institut UTINAM, UMR 6213 CNRS-UBFC, Université Bourgogne Franche-Comté, 25030 Besançon, France; gautier.laurent@ 123456univ-fcomte.fr (G.L.); rana.bazzi@ 123456univ-fcomte.fr (R.B.); stephane.roux@ 123456univ-fcomte.fr (S.R.)
                Author notes
                [* ]Correspondence: bouzioti@ 123456rrp.demokritos.gr ; Tel.: +30-21-0650-3687
                Author information
                https://orcid.org/0000-0003-1090-3492
                https://orcid.org/0000-0002-9652-4006
                https://orcid.org/0000-0002-8544-1379
                https://orcid.org/0000-0002-5198-1916
                https://orcid.org/0000-0001-6778-2201
                Article
                pharmaceutics-12-00188
                10.3390/pharmaceutics12020188
                7076693
                32098286
                012f2fa1-983e-4c8e-b981-3eb56a7a506f
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 01 December 2019
                : 19 February 2020
                Categories
                Article

                actinium-225,alpha emitters,gold nanoparticles,radiolabeling,brachytherapy,cancer therapy

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