Magnetic Nanomaterials as Theranostic Platform in Cancer Treatment and Diagnosis

A special issue of Nanomaterials (ISSN 2079-4991).

Deadline for manuscript submissions: closed (20 October 2021) | Viewed by 8366

Special Issue Editors


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Guest Editor
Institute for Advanced Studies in Nanoscience (IMDEA Nanociencia), Madrid, Spain
Interests: nanomedicine; cancer therapy; autophagy; ROS; nanoparticles; chemotherapy
Special Issues, Collections and Topics in MDPI journals

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Guest Editor
Department of Nanomedicine, Madrid Institute for Advanced Study in Nanoscience, 28039 Madrid, Spain
Interests: Magnetic hyperthermia; photothermia; magnetic nanoparticles; plasmonic nanoparticles; nanobiodegradation; multifunctional nanostructures

Special Issue Information

Dear Colleagues,

This multidisciplinary Special Issue of Nanomaterials focuses on the application of magnetic nanomaterials in cancer treatment and diagnosis and encourages basic and translational scientists working in a related field to submit original research articles and review articles. Today, radiotherapy and chemotherapy are the principal medical therapeutic approaches against cancer. However, the efficacy of these treatments is often limited by a number of unwanted side-effects associated with nonselective and unspecific cytotoxicity. In recent years, nanotechnology has attracted significant interests in cancer therapeutics because of its huge potential to offer many innovative tools to overcome the problems arising from present chemotherapy and radiotherapy approaches. The intersection between the fields of chemistry, physics, and material sciences has created theranostics nanomaterials which are defined as the combination of therapeutic and diagnostic agents within a single platform and are expected to improve the efficacy of treatment of many tumors resistant to traditional therapeutic approaches, as well as to provide novel diagnostic tools. In particular, magnetic nanoparticles, because of their unique physical, chemical, mechanical, and optical properties, have intrinsic cytotoxicity and/or enhance the efficacy of standard chemotherapies. Moreover, magnetic nanoparticles are used as nanocarriers, since they can be easily modified in order to deliver therapeutic molecules, such as drugs, proteins, or nucleic acids. Important advantages of these therapeutic nanostructures concern, as well, their external controllability by different stimuli in order to produce a cytotoxic effect through the delivery of local heating by the application of an external magnetic field or optical near infrared radiation depending on their composition and physical properties. These functions can be utilized for therapeutic hyperthermia of cancer but also for controlled release of cancer drugs through the application of an external magnetic field. Finally, magnetic nanomaterials can also be exploited to favor the delivery of immune agents and can represent a valid therapeutic tool to bypass the obstacles currently encountered in cancer immunotherapy. These innovative biomedical applications are currently exploited in a variety of clinical trials and in the near future may represent a major improvement in the therapy of cancer. In this regard, magnetic nanoparticles can be used as platform materials for theranostics application by offering advantages and opportunities as drug delivery systems and nanodiagnostics, decreasing the side-effects of standard therapies. We aim to receive submissions addressed on recent advances in the broad and fascinating field of functional magnetic nanomaterials for therapeutic and diagnostic purposes.

Dr. Marco Cordani
Dr. Ana Espinosa
Guest Editors

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Keywords

  • cancer treatment
  • magnetic nanomaterials for drug delivery in cancer
  • therapeutic nucleic acids
  • magnetic and photothermal therapy in cancer
  • magnetic nanomaterials for diagnostic applications
  • modulation of immune response by magnetic nanoparticles
  • modulation of autophagy
  • regulation of oxidative stress
  • modulation of EMT and fibrosis

Published Papers (2 papers)

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Research

18 pages, 3249 KiB  
Article
Enhanced In Vitro Magnetic Cell Targeting of Doxorubicin-Loaded Magnetic Liposomes for Localized Cancer Therapy
by Eugenio Redolfi Riva, Edoardo Sinibaldi, Agostina Francesca Grillone, Serena Del Turco, Alessio Mondini, Tianshu Li, Shinji Takeoka and Virgilio Mattoli
Nanomaterials 2020, 10(11), 2104; https://doi.org/10.3390/nano10112104 - 23 Oct 2020
Cited by 12 | Viewed by 2701
Abstract
The lack of efficient targeting strategies poses significant limitations on the effectiveness of chemotherapeutic treatments. This issue also affects drug-loaded nanocarriers, reducing nanoparticles cancer cell uptake. We report on the fabrication and in vitro characterization of doxorubicin-loaded magnetic liposomes for localized treatment of [...] Read more.
The lack of efficient targeting strategies poses significant limitations on the effectiveness of chemotherapeutic treatments. This issue also affects drug-loaded nanocarriers, reducing nanoparticles cancer cell uptake. We report on the fabrication and in vitro characterization of doxorubicin-loaded magnetic liposomes for localized treatment of liver malignancies. Colloidal stability, superparamagnetic behavior and efficient drug loading of our formulation were demonstrated. The application of an external magnetic field guaranteed enhanced nanocarriers cell uptake under cell medium flow in correspondence of a specific area, as we reported through in vitro investigation. A numerical model was used to validate experimental data of magnetic targeting, proving the possibility of accurately describing the targeting strategy and predict liposomes accumulation under different environmental conditions. Finally, in vitro studies on HepG2 cancer cells confirmed the cytotoxicity of drug-loaded magnetic liposomes, with cell viability reduction of about 50% and 80% after 24 h and 72 h of incubation, respectively. Conversely, plain nanocarriers showed no anti-proliferative effects, confirming the formulation safety. Overall, these results demonstrated significant targeting efficiency and anticancer activity of our nanocarriers and superparamagnetic nanoparticles entrapment could envision the theranostic potential of the formulation. The proposed magnetic targeting study could represent a valid tool for pre-clinical investigation regarding the effectiveness of magnetic drug targeting. Full article
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23 pages, 3113 KiB  
Article
Hyperthermia, Cytotoxicity, and Cellular Uptake Properties of Manganese and Zinc Ferrite Magnetic Nanoparticles Synthesized by a Polyol-Mediated Process
by Cristian Iacovita, Adrian Florea, Lavinia Scorus, Emoke Pall, Roxana Dudric, Alin Iulian Moldovan, Rares Stiufiuc, Romulus Tetean and Constantin Mihai Lucaciu
Nanomaterials 2019, 9(10), 1489; https://doi.org/10.3390/nano9101489 - 18 Oct 2019
Cited by 65 | Viewed by 5080
Abstract
Manganese and zinc ferrite magnetic nanoparticles (MNPs) were successfully synthesized
using the polyol method in ethylene glycol and were found to have high saturation magnetization
values (90–95 emu/g at 4 K) when formed by ~30-nm crystallites assembled in an ~80-nm multicore
structure. Hyperthermia [...] Read more.
Manganese and zinc ferrite magnetic nanoparticles (MNPs) were successfully synthesized
using the polyol method in ethylene glycol and were found to have high saturation magnetization
values (90–95 emu/g at 4 K) when formed by ~30-nm crystallites assembled in an ~80-nm multicore
structure. Hyperthermia data revealed a sigmoidal dependence of the specific absorption rate (SAR)
on the alternating magnetic field (AMF) amplitude, with remarkable saturation SAR values in water
of ~1200 W/gFe+Mn and ~800 W/gFe+Zn for the Mn and Zn ferrites, respectively. The immobilization
of the MNPs in a solid matrix reduced the maximum SAR values by ~300 W/gFe+Mn, Zn for both
ferrites. The alignment of the MNPs in a uniform static magnetic field, before their immobilization
in a solid matrix, significantly increased their heating performance. Toxicity assays performed in
four cell lines revealed a lower toxicity for the Mn ferrites, while in the case of the Zn ferrites, only
~50% of cells were viable upon their incubation for 24 h with 0.2 mg/mL of MNPs. Cellular uptake
experiments revealed that both MNPs entered the cells in a time-dependent manner, as they were
found initially in endosomes and later in the cytosol. All of the studied cell lines were more sensitive
to the ZnFe2O4 MNPs. Full article
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