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Global Translational Medicine                                               SPION for cancer theranostics




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            Figure 6. (A and B) Transmission electron microscopy micrographs. (B) Absorbance spectra of magnetic iron oxide nanocubes (IONCs). (C) Schematic of
            the experimental setup for combined hyperthermia experiments. (D) Temperature elevation curves of IONCs at the same iron concentrations ([Fe]  = 12
            or 25 mM), measured inside the coil setup magnetic hyperthermia (MHT) at 520 kHz, 25 mT; laser at 0.3 W/cm . (E) MHT at 520 kHz. (F) Laser at
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            0.3 W/cm . (G) Dual mode heating capacity of IONCs. (H) Specific loss power (SLP) as a function of frequency with a magnetic field of 2 Mt. (I) Near-
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            infrared spectroscopy laser power in dual mode. (J) Heating capacity of 9 nm IONPs in dual mode. Reproduced with permission from Espinosa et al.
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            Copyright 2016 American Chemical Society.
            in vitro studies on MHT have been conducted, the therapy   for improved tumor specificity and extends the circulation
            remains in the pre-clinical stage, with only a few reports   time of SPIONs in the bloodstream, thereby increasing
            involving human patients. 64                       their half-life. A  variety of anticancer drugs, including
                                                               cisplatin,  methotrexate, daunorubicin, DOX, and
            4.3. Drug delivery applications                    paclitaxel, have been successfully loaded onto the organic
            One of the major challenges in drug delivery is the poor   or inorganic scaffolds of surface-modified SPIONs for drug
            absorption of hydrophobic drugs, while another challenge   delivery applications. In magnetic drug delivery systems,
            involves achieving site-specific targeting of drugs to diseased   the  application of  an  external magnetic  field  allows  the
            sites. Magnetic drug delivery using NP-based techniques   magnetic nanocarriers to bypass the reticuloendothelial
            offers a promising solution to these issues by enhancing the   system, ensuring targeted delivery of anticancer drugs to
            therapeutic efficacy and biocompatibility of drugs.  The   the desired site. Magnetic targeting refers to the targeting
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            concept of “magnetic drug delivery” using SPIONs as drug   of SPIONs to a specific tumor site by applying an external
            carriers  was  first  proposed  in  the  late  1970s  by  Widder   magnetic field, which can be achieved using either passive
            et  al.   and  Senyei  et al.   In  this  approach,  therapeutic   or active strategies. 68,69  Passive targeting is considered one
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            agents are either encapsulated within or attached to   of the key targeting techniques for targeting, where the
            SPIONs using a protective polymeric layer. These NPs are   free accumulation of nanoformulations at the tumor site
            then guided to the diseased site using an external magnetic   enhances both cancer diagnosis and MRI detection. 70,71
            field. The core of the NPs is typically superparamagnetic   Angiogenesis, or the formation of new blood vessels, is
            to ensure responsiveness to the magnetic field, while the   a most common phenomenon in cancer cells, leading to
            surrounding polymeric layer provides stability, protection,   the formation of abnormal, leaky vessels. Passive targeting
            and suitability for  in vivo applications. This polymeric   does not use specific ligands for tumor-specific receptors.
            coating also facilitates conjugation with biological ligands   As a result, the distribution of the nanoformulations is


            Volume 4 Issue 2 (2025)                         43                              doi: 10.36922/gtm.8464
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