Recent advances in magnetic nanocarriers for tumor treatment
Magnetic nanocarriers are nano-platforms that integrate multiple moieties based on magnetic nanoparticles for diagnostic and therapeutic purposes. In recent years, they have become an advanced platform for tumor treatment due to their wide application in magnetic resonance imaging (MRI), biocatalysi...
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Veröffentlicht in: | Biomedicine & pharmacotherapy 2023-03, Vol.159, p.114227, Article 114227 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Magnetic nanocarriers are nano-platforms that integrate multiple moieties based on magnetic nanoparticles for diagnostic and therapeutic purposes. In recent years, they have become an advanced platform for tumor treatment due to their wide application in magnetic resonance imaging (MRI), biocatalysis, magneto-thermal therapy (MHT), and photoresponsive therapy. Drugs loaded into magnetic nanocarriers can efficiently be directed to targeted areas by precisely reshaping their structural properties. Magnetic nanocarriers allow us to track the location of the therapeutic agent, continuously control the therapeutic process and eventually assess the efficacy of the treatment. They are typically used in synergistic therapeutic applications to achieve precise and effective tumor treatment. Here we review their latest applications in tumor treatment, including stimuli-responsive drug delivery, MHT, photoresponsive therapy, immunotherapy, gene therapy, and synergistic therapy. We consider reducing toxicity, improving antitumor efficacy, and the targeting accuracy of magnetic nanocarriers. The challenges of their clinical translation and prospects in cancer therapy are also discussed.
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•Diverse studies are reviewed for potential clinical applications of magnetic nanocarriers in tumor therapy.•The latest design strategies of magnetic nanocarriers for improving antitumor efficacy and targeting accuracy are presented.•Solutions required to move magnetic nanocarriers from bench top to bedside are discussed. |
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ISSN: | 0753-3322 1950-6007 |
DOI: | 10.1016/j.biopha.2023.114227 |