Hybrid Radiobioconjugated Superparamagnetic Iron Oxide-Based Nanoparticles for Multimodal Cancer Therapy

Superparamagnetic iron oxide nanoparticles (SPIONs) are widely used for biomedical applications for their outstanding properties such as facile functionalization and doping with different metals, high surface-to-volume ratio, superparamagnetism, and biocompatibility. This study was designed to synth...

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Autores principales: Michał Żuk, Weronika Gawęda, Agnieszka Majkowska-Pilip, Magdalena Osial, Marcin Wolski, Aleksander Bilewicz, Paweł Krysiński
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Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/a0b3b353f27143629d999b80b549b0e8
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spelling oai:doaj.org-article:a0b3b353f27143629d999b80b549b0e82021-11-25T18:41:06ZHybrid Radiobioconjugated Superparamagnetic Iron Oxide-Based Nanoparticles for Multimodal Cancer Therapy10.3390/pharmaceutics131118431999-4923https://doaj.org/article/a0b3b353f27143629d999b80b549b0e82021-11-01T00:00:00Zhttps://www.mdpi.com/1999-4923/13/11/1843https://doaj.org/toc/1999-4923Superparamagnetic iron oxide nanoparticles (SPIONs) are widely used for biomedical applications for their outstanding properties such as facile functionalization and doping with different metals, high surface-to-volume ratio, superparamagnetism, and biocompatibility. This study was designed to synthesize and investigate multifunctional nanoparticle conjugate to act as both a magnetic agent, anticancer immunological drug, and radiopharmaceutic for anticancer therapy. The carrier, <sup>166</sup>Ho doped iron oxide, was coated with an Au layer, creating core-shell nanoparticles ([<sup>166</sup>Ho] Fe<sub>3</sub>O<sub>4</sub>@Au. These nanoparticles were subsequently modified with monoclonal antibody trastuzumab (Tmab) to target HER2+ receptors. We describe the radiobioconjugate preparation involving doping of a radioactive agent and attachment of the organic linker and drug to the SPIONs’ surface. The size of the SPIONs coated with an Au shell measured by transmission electron microscopy was about 15 nm. The bioconjugation of trastuzumab onto SPIONs was confirmed by thermogravimetric analysis, and the amount of two molecules per one nanoparticle was estimated with the use of radioiodinated [<sup>131</sup>I]Tmab. The synthesized bioconjugates showed that they are efficient heat mediators and also exhibit a cytotoxic effect toward SKOV-3 ovarian cancer cells expressing HER2 receptors. Prepared radiobioconjugates reveal the high potential for in vivo application of the proposed multimodal hybrid system, combined with magnetic hyperthermia and immunotherapy against cancer tissues.Michał ŻukWeronika GawędaAgnieszka Majkowska-PilipMagdalena OsialMarcin WolskiAleksander BilewiczPaweł KrysińskiMDPI AGarticleSPIONradio-labeled nanoparticlesanticancer therapymagnetic hyperthermiadrug deliverytrastuzumabPharmacy and materia medicaRS1-441ENPharmaceutics, Vol 13, Iss 1843, p 1843 (2021)
institution DOAJ
collection DOAJ
language EN
topic SPION
radio-labeled nanoparticles
anticancer therapy
magnetic hyperthermia
drug delivery
trastuzumab
Pharmacy and materia medica
RS1-441
spellingShingle SPION
radio-labeled nanoparticles
anticancer therapy
magnetic hyperthermia
drug delivery
trastuzumab
Pharmacy and materia medica
RS1-441
Michał Żuk
Weronika Gawęda
Agnieszka Majkowska-Pilip
Magdalena Osial
Marcin Wolski
Aleksander Bilewicz
Paweł Krysiński
Hybrid Radiobioconjugated Superparamagnetic Iron Oxide-Based Nanoparticles for Multimodal Cancer Therapy
description Superparamagnetic iron oxide nanoparticles (SPIONs) are widely used for biomedical applications for their outstanding properties such as facile functionalization and doping with different metals, high surface-to-volume ratio, superparamagnetism, and biocompatibility. This study was designed to synthesize and investigate multifunctional nanoparticle conjugate to act as both a magnetic agent, anticancer immunological drug, and radiopharmaceutic for anticancer therapy. The carrier, <sup>166</sup>Ho doped iron oxide, was coated with an Au layer, creating core-shell nanoparticles ([<sup>166</sup>Ho] Fe<sub>3</sub>O<sub>4</sub>@Au. These nanoparticles were subsequently modified with monoclonal antibody trastuzumab (Tmab) to target HER2+ receptors. We describe the radiobioconjugate preparation involving doping of a radioactive agent and attachment of the organic linker and drug to the SPIONs’ surface. The size of the SPIONs coated with an Au shell measured by transmission electron microscopy was about 15 nm. The bioconjugation of trastuzumab onto SPIONs was confirmed by thermogravimetric analysis, and the amount of two molecules per one nanoparticle was estimated with the use of radioiodinated [<sup>131</sup>I]Tmab. The synthesized bioconjugates showed that they are efficient heat mediators and also exhibit a cytotoxic effect toward SKOV-3 ovarian cancer cells expressing HER2 receptors. Prepared radiobioconjugates reveal the high potential for in vivo application of the proposed multimodal hybrid system, combined with magnetic hyperthermia and immunotherapy against cancer tissues.
format article
author Michał Żuk
Weronika Gawęda
Agnieszka Majkowska-Pilip
Magdalena Osial
Marcin Wolski
Aleksander Bilewicz
Paweł Krysiński
author_facet Michał Żuk
Weronika Gawęda
Agnieszka Majkowska-Pilip
Magdalena Osial
Marcin Wolski
Aleksander Bilewicz
Paweł Krysiński
author_sort Michał Żuk
title Hybrid Radiobioconjugated Superparamagnetic Iron Oxide-Based Nanoparticles for Multimodal Cancer Therapy
title_short Hybrid Radiobioconjugated Superparamagnetic Iron Oxide-Based Nanoparticles for Multimodal Cancer Therapy
title_full Hybrid Radiobioconjugated Superparamagnetic Iron Oxide-Based Nanoparticles for Multimodal Cancer Therapy
title_fullStr Hybrid Radiobioconjugated Superparamagnetic Iron Oxide-Based Nanoparticles for Multimodal Cancer Therapy
title_full_unstemmed Hybrid Radiobioconjugated Superparamagnetic Iron Oxide-Based Nanoparticles for Multimodal Cancer Therapy
title_sort hybrid radiobioconjugated superparamagnetic iron oxide-based nanoparticles for multimodal cancer therapy
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/a0b3b353f27143629d999b80b549b0e8
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