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      A review of bismuth‐based nanoparticles and their applications in radiosensitising and dose enhancement for cancer radiation therapy

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          Abstract

          About 50% of cancer patients receive radiation therapy. Despite the therapeutic benefits of this method, the toxicity of radiation in the normal tissues is unavoidable To improve the quality of radiation therapy, in addition to other methods such as IMRT, IGRT, and high radiation dose, nanoparticles have shown excellent potential when ionising radiation is applied to the target volume. Recently, bismuth‐based nanoparticles (BiNPs) have become particularly popular in radiation therapy due to their high atomic numbers (Z), high X‐ray attenuation coefficient, low toxicity, and low cost. Moreover, it is easy to synthesise in a variety of sizes and shapes. This study aimed to review the effects of the bismuth‐based NP and its combination with other compounds, and their potential synergies in radiotherapy, discussed based on their physical, chemical, and biological interactions. Targeted and non‐targeted bismuth‐based NPs used in radiotherapy as radiosensitizers and dose enhancement effects are described. The results reported in the literature were categorised into various groups. Also, this review has highlighted the importance of bismuth‐based NPs in different forms of cancer treatment to find the highest efficiency for applying them as a suitable candidate for various cancer therapy and future clinical applications.

          Abstract

          This review has highlighted the importance of bismuth‐based nanoparticles in different forms for cancer treatment to find the highest efficiency for applying them as a suitable candidate for various commercial and future clinical applications due to their dose enhancement properties, radiosensitisation, and superior biocompatibility.

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          PEGylation as a strategy for improving nanoparticle-based drug and gene delivery.

          Coating the surface of nanoparticles with polyethylene glycol (PEG), or "PEGylation", is a commonly used approach for improving the efficiency of drug and gene delivery to target cells and tissues. Building from the success of PEGylating proteins to improve systemic circulation time and decrease immunogenicity, the impact of PEG coatings on the fate of systemically administered nanoparticle formulations has, and continues to be, widely studied. PEG coatings on nanoparticles shield the surface from aggregation, opsonization, and phagocytosis, prolonging systemic circulation time. Here, we briefly describe the history of the development of PEGylated nanoparticle formulations for systemic administration, including how factors such as PEG molecular weight, PEG surface density, nanoparticle core properties, and repeated administration impact circulation time. A less frequently discussed topic, we then describe how PEG coatings on nanoparticles have also been utilized for overcoming various biological barriers to efficient drug and gene delivery associated with other modes of administration, ranging from gastrointestinal to ocular. Finally, we describe both methods for PEGylating nanoparticles and methods for characterizing PEG surface density, a key factor in the effectiveness of the PEG surface coating for improving drug and gene delivery.
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            Animal Communication: When I’m Calling You, Will You Answer Too?

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              Transferrin-functionalized nanoparticles lose their targeting capabilities when a biomolecule corona adsorbs on the surface.

              Nanoparticles have been proposed as carriers for drugs, genes and therapies to treat various diseases. Many strategies have been developed to target nanomaterials to specific or over-expressed receptors in diseased cells, and these typically involve functionalizing the surface of nanoparticles with proteins, antibodies or other biomolecules. Here, we show that the targeting ability of such functionalized nanoparticles may disappear when they are placed in a biological environment. Using transferrin-conjugated nanoparticles, we found that proteins in the media can shield transferrin from binding to both its targeted receptors on cells and soluble transferrin receptors. Although nanoparticles continue to enter cells, the targeting specificity of transferrin is lost. Our results suggest that when nanoparticles are placed in a complex biological environment, interaction with other proteins in the medium and the formation of a protein corona can 'screen' the targeting molecules on the surface of nanoparticles and cause loss of specificity in targeting.
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                Author and article information

                Contributors
                shahbazi@med.mui.ac.ir
                Journal
                IET Nanobiotechnol
                IET Nanobiotechnol
                10.1049/(ISSN)1751-875X
                NBT2
                IET Nanobiotechnology
                John Wiley and Sons Inc. (Hoboken )
                1751-8741
                1751-875X
                04 May 2023
                June 2023
                : 17
                : 4 ( doiID: 10.1049/nbt2.v17.4 )
                : 302-311
                Affiliations
                [ 1 ] Department of Medical Physics School of Medicine Isfahan University of Medical Sciences Isfahan Iran
                [ 2 ] School of Medicine Isfahan University of Medical Sciences Isfahan Iran
                Author notes
                [*] [* ] Correspondence

                Daryoush Shahbazi‐Gahrouei, Department of Medical Physics, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

                Email: shahbazi@ 123456med.mui.ac.ir

                Author information
                https://orcid.org/0000-0002-8538-1898
                https://orcid.org/0000-0002-8289-0152
                https://orcid.org/0000-0002-0479-3410
                https://orcid.org/0000-0002-3424-7277
                Article
                NBT212134
                10.1049/nbt2.12134
                10288357
                37139612
                3a2ef5cb-99ad-4a6d-9f57-5de12344fbe5
                © 2023 The Authors. IET Nanobiotechnology published by John Wiley & Sons Ltd on behalf of The Institution of Engineering and Technology.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 10 April 2023
                : 15 March 2023
                : 15 April 2023
                Page count
                Figures: 2, Tables: 2, Pages: 10, Words: 7742
                Categories
                Review
                Review
                Custom metadata
                2.0
                June 2023
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.9 mode:remove_FC converted:23.06.2023

                nanomedicine,nanoparticles,radiation therapy
                nanomedicine, nanoparticles, radiation therapy

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