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      Trastuzumab Conjugated Superparamagnetic Iron Oxide Nanoparticles Labeled with 225Ac as a Perspective Tool for Combined α-Radioimmunotherapy and Magnetic Hyperthermia of HER2-Positive Breast Cancer

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          Abstract

          It has been proven and confirmed in numerous repeated tests, that the use of a combination of several therapeutic methods gives much better treatment results than in the case of separate therapies. Particularly promising is the combination of ionizing radiation and magnetic hyperthermia in one drug. To achieve this objective, magnetite nanoparticles have been modified in their core with α emitter 225Ac, in an amount affecting only slightly their magnetic properties. By 3-phosphonopropionic acid (CEPA) linker nanoparticles were conjugated covalently with trastuzumab (Herceptin ®), a monoclonal antibody that recognizes ovarian and breast cancer cells overexpressing the HER2 receptors. The synthesized bioconjugates were characterized by transmission electron microscopy (TEM), Dynamic Light Scattering (DLS) measurement, thermogravimetric analysis (TGA) and application of 131I-labeled trastuzumab for quantification of the bound biomolecule. The obtained results show that one 225Ac@Fe 3O 4-CEPA-trastuzumab bioconjugate contains an average of 8–11 molecules of trastuzumab. The labeled nanoparticles almost quantitatively retain 225Ac (>98%) in phosphate-buffered saline (PBS) and physiological salt, and more than 90% of 221Fr and 213Bi over 10 days. In human serum after 10 days, the fraction of 225Ac released from 225Ac@Fe 3O 4 was still less than 2%, but the retention of 221Fr and 213Bi decreased to 70%. The synthesized 225Ac@Fe 3O 4-CEPA-trastuzumab bioconjugates have shown a high cytotoxic effect toward SKOV-3 ovarian cancer cells expressing HER2 receptor in-vitro. The in-vivo studies indicate that this bioconjugate exhibits properties suitable for the treatment of cancer cells by intratumoral or post-resection injection. The intravenous injection of the 225Ac@Fe 3O 4-CEPA-trastuzumab radiobioconjugate is excluded due to its high accumulation in the liver, lungs and spleen. Additionally, the high value of a specific absorption rate (SAR) allows its use in a new very perspective combination of α radionuclide therapy with magnetic hyperthermia.

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          Thermal ablation of tumours: biological mechanisms and advances in therapy.

          Minimally invasive thermal ablation of tumours has become common since the advent of modern imaging. From the ablation of small, unresectable tumours to experimental therapies, percutaneous radiofrequency ablation, microwave ablation, cryoablation and irreversible electroporation have an increasing role in the treatment of solid neoplasms. This Opinion article examines the mechanisms of tumour cell death that are induced by the most common thermoablative techniques and discusses the rapidly developing areas of research in the field, including combinatorial ablation and immunotherapy, synergy with conventional chemotherapy and radiation, and the development of a new ablation modality in irreversible electroporation.
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            Hyperthermia in combined treatment of cancer.

            Hyperthermia, the procedure of raising the temperature of tumour-loaded tissue to 40-43 degrees C, is applied as an adjunctive therapy with various established cancer treatments such as radiotherapy and chemotherapy. The potential to control power distributions in vivo has been significantly improved lately by the development of planning systems and other modelling tools. This increased understanding has led to the design of multiantenna applicators (including their transforming networks) and implementation of systems for monitoring of E-fields (eg, electro-optical sensors) and temperature (particularly, on-line magnetic resonance tomography). Several phase III trials comparing radiotherapy alone or with hyperthermia have shown a beneficial effect of hyperthermia (with existing standard equipment) in terms of local control (eg, recurrent breast cancer and malignant melanoma) and survival (eg, head and neck lymph-node metastases, glioblastoma, cervical carcinoma). Therefore, further development of existing technology and elucidation of molecular mechanisms are justified. In recent molecular and biological investigations there have been novel applications such as gene therapy or immunotherapy (vaccination) with temperature acting as an enhancer, to trigger or to switch mechanisms on and off. However, for every particular temperature-dependent interaction exploited for clinical purposes, sophisticated control of temperature, spatially as well as temporally, in deep body regions will further improve the potential.
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              Selective inductive heating of lymph nodes.

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                Author and article information

                Contributors
                Role: Academic Editor
                Role: Academic Editor
                Journal
                Molecules
                Molecules
                molecules
                Molecules
                MDPI
                1420-3049
                25 February 2020
                March 2020
                : 25
                : 5
                : 1025
                Affiliations
                [1 ]Institute of Nuclear Chemistry and Technology, Dorodna 16, 03-195 Warsaw, Poland; e.leszczuk@ 123456ichtj.waw.pl (E.C.); w.maliszewska@ 123456ichtj.waw.pl (W.G.)
                [2 ]Faculty of Chemistry, Biological and Chemical Research Centre, University of Warsaw, Żwirki i Wigury 101, 02-089 Warsaw, Poland
                [3 ]Faculty of Chemistry, University of Warsaw, Pasteura 1, 02-093 Warsaw, Poland; mt_zuk@ 123456chem.uw.edu.pl (M.Ż.); pakrys@ 123456chem.uw.edu.pl (P.K.)
                [4 ]Department for Nuclear Safety and Security, Joint Research Centre, European Commission, 76125 Karlsruhe, Germany; Frank.BRUCHERTSEIFER@ 123456ec.europa.eu (F.B.); alfred.morgenstern@ 123456ec.europa.eu (A.M.)
                [5 ]Institute of Nuclear & Radiological Sciences & Technology, Energy & Safety, N.C.S.R. ‘Demokritos’, Aghia Paraskevi, 15341 Athens, Greece; kmargo@ 123456phys.uoa.gr (M.-A.K.); bouzioti@ 123456rrp.demokritos.gr (P.B.)
                [6 ]Department of Physics, National and Kapodistrian University of Athens, Zografou Panepistimioupolis, 15784 Athens, Greece
                Author notes
                [* ]Correspondence: m.pruszynski@ 123456ichtj.waw.pl (M.P.); a.bilewicz@ 123456ichtj.waw.pl (A.B.); Tel.: +48-22-5041357 (A.B.)
                Author information
                https://orcid.org/0000-0001-8835-2462
                https://orcid.org/0000-0001-7121-9569
                https://orcid.org/0000-0001-6778-2201
                https://orcid.org/0000-0003-2490-3303
                Article
                molecules-25-01025
                10.3390/molecules25051025
                7179151
                32106568
                2e2585a0-7840-4970-8b52-b6f9da35bcd9
                © 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
                : 28 January 2020
                : 24 February 2020
                Categories
                Article

                radionuclide therapy,hyperthermia,spion,trastuzumab
                radionuclide therapy, hyperthermia, spion, trastuzumab

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