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      Biologically Targeted Magnetic Hyperthermia: Potential and Limitations

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          Abstract

          Hyperthermia, the mild elevation of temperature to 40–43°C, can induce cancer cell death and enhance the effects of radiotherapy and chemotherapy. However, achievement of its full potential as a clinically relevant treatment modality has been restricted by its inability to effectively and preferentially heat malignant cells. The limited spatial resolution may be circumvented by the intravenous administration of cancer-targeting magnetic nanoparticles that accumulate in the tumor, followed by the application of an alternating magnetic field to raise the temperature of the nanoparticles located in the tumor tissue. This targeted approach enables preferential heating of malignant cancer cells whilst sparing the surrounding normal tissue, potentially improving the effectiveness and safety of hyperthermia. Despite promising results in preclinical studies, there are numerous challenges that must be addressed before this technique can progress to the clinic. This review discusses these challenges and highlights the current understanding of targeted magnetic hyperthermia.

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          Progress and challenges towards targeted delivery of cancer therapeutics

          Targeted delivery approaches for cancer therapeutics have shown a steep rise over the past few decades. However, compared to the plethora of successful pre-clinical studies, only 15 passively targeted nanocarriers (NCs) have been approved for clinical use and none of the actively targeted NCs have advanced past clinical trials. Herein, we review the principles behind targeted delivery approaches to determine potential reasons for their limited clinical translation and success. We propose criteria and considerations that must be taken into account for the development of novel actively targeted NCs. We also highlight the possible directions for the development of successful tumor targeting strategies.
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            The heat shock response: life on the verge of death.

            Organisms must survive a variety of stressful conditions, including sudden temperature increases that damage important cellular structures and interfere with essential functions. In response to heat stress, cells activate an ancient signaling pathway leading to the transient expression of heat shock or heat stress proteins (Hsps). Hsps exhibit sophisticated protection mechanisms, and the most conserved Hsps are molecular chaperones that prevent the formation of nonspecific protein aggregates and assist proteins in the acquisition of their native structures. In this Review, we summarize the concepts of the protective Hsp network. Copyright © 2010 Elsevier Inc. All rights reserved.
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              Heating magnetic fluid with alternating magnetic field

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                Author and article information

                Contributors
                Journal
                Front Pharmacol
                Front Pharmacol
                Front. Pharmacol.
                Frontiers in Pharmacology
                Frontiers Media S.A.
                1663-9812
                02 August 2018
                2018
                : 9
                : 831
                Affiliations
                [1] 1Children's Cancer Institute, Lowy Cancer Research Centre, University of New South Wales , Sydney, NSW, Australia
                [2] 2Department of Radiation Oncology, Nelune Comprehensive Cancer Centre, Prince of Wales Hospital , Sydney, NSW, Australia
                [3] 3ARC Centre of Excellence in Convergent Bio-Nano Science and Technology and Australian Centre for Nanomedicine, University of New South Wales , Sydney, NSW, Australia
                [4] 4School of Chemical Engineering, University of New South Wales , Sydney, NSW, Australia
                [5] 5ARC Centre of Excellence in Convergent Bio-Nano Science and Technology, Monash Institute of Pharmaceutical Sciences, Monash University , Melbourne, VIC, Australia
                [6] 6Department of Radiology, Memorial Sloan Kettering Cancer Center , New York, NY, United States
                [7] 7Department of Chemistry, University of Warwick , Coventry, United Kingdom
                Author notes

                Edited by: Susan Hua, University of Newcastle, Australia

                Reviewed by: James Hainfeld, Nanoprobes, United States; Arkadiusz Jozefczak, Adam Mickiewicz University in Poznan, Poland

                *Correspondence: Maria Kavallaris m.kavallaris@ 123456ccia.unsw.edu.au

                This article was submitted to Pharmaceutical Medicine and Outcomes Research, a section of the journal Frontiers in Pharmacology

                Article
                10.3389/fphar.2018.00831
                6083434
                30116191
                f27a619a-6379-4b41-8c41-d745d9e55385
                Copyright © 2018 Chang, Lim, Goos, Qiao, Ng, Mansfeld, Jackson, Davis and Kavallaris.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 16 April 2018
                : 10 July 2018
                Page count
                Figures: 3, Tables: 4, Equations: 2, References: 153, Pages: 20, Words: 15890
                Funding
                Funded by: National Health and Medical Research Council 10.13039/501100000925
                Award ID: APP1119152
                Award ID: APP1091261
                Funded by: Australian Research Council 10.13039/501100000923
                Award ID: CE140100036
                Award ID: FL140100052
                Funded by: Cancer Council NSW 10.13039/501100001102
                Award ID: PG16-01
                Categories
                Pharmacology
                Review

                Pharmacology & Pharmaceutical medicine
                magnetic hyperthermia,targeted therapy,iron oxide nanoparticles,cancer therapy,magnetic nanoparticles

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