2024
DOI: 10.1016/j.ijpx.2024.100231
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Magnetic nanosystem a tool for targeted delivery and diagnostic application: Current challenges and recent advancement

Nilesh Rarokar,
Sakshi Yadav,
Suprit Saoji
et al.
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Cited by 10 publications
(3 citation statements)
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“…Developed by Stephanie Huth and coworkers [ 125 ] magnetofection was first used for MNP–naked DNA complexes or MNP–viral vector complexes that were attracted to the bottom by a magnet, placed close below the bottom of a dish. Subsequently, nucleic acid-bound MNPs could be introduced into the cells after their exposition to AMF [ 126 ].…”
Section: Combination Therapies Using Np-based Mhtmentioning
confidence: 99%
“…Developed by Stephanie Huth and coworkers [ 125 ] magnetofection was first used for MNP–naked DNA complexes or MNP–viral vector complexes that were attracted to the bottom by a magnet, placed close below the bottom of a dish. Subsequently, nucleic acid-bound MNPs could be introduced into the cells after their exposition to AMF [ 126 ].…”
Section: Combination Therapies Using Np-based Mhtmentioning
confidence: 99%
“…The most commonly synthesized magnetic nanoparticles for biomedical applications are iron oxide nanoparticles (IONPs) consisting of magnetite (Fe 3 O 4 ), maghemite (γ-Fe 2 O 3 ), hematite (α-Fe 2 O 3 ), or mixed ferrites [ 144 ]. The popularity of IONPs as drug carriers comes from their biocompatibility, non-toxicity, ease of preparation, and stability [ 145 , 146 , 147 ].…”
Section: Magnetic Nanoparticles As a Platform For Tumor-homing Peptidesmentioning
confidence: 99%
“…When synchronized with an external magnetic field and magnetizable implants, magnetic nanosystems enhance the precision of particle delivery to specific areas and exert localized effects. 55 Subsequently, the plasma stability and distribution of the nanosystem in different organs after systemic administration in the presence or absence of magnetic field were investigated utilizing ICP-MS. As shown in Figure 6a, the blood circulation of IONPs was significantly prolonged by NV-IONP-Lapa owing to the coupling of more biocompatible NVs, resulting in slightly greater accumulation in tumor tissues (P > 0.05), probably through the homing effect of NVs originating from normal ovarian epithelial cells and the enhanced permeability and retention (EPR) effect. 56 However, this prolonged blood circulation was attenuated by application of a magnet due to magnetic field-guided rebiodistribution of drugs (Figure 6a), resulting in significantly boosted (approximately 10-fold enhanced) accumulation of NV-IONP-Lapa in tumor site as indicated by fluorescence imaging (Figures 6b and S26).…”
Section: Efficient Tumor Cells Killing Of Nv-ionp-lapa In Vitromentioning
confidence: 99%