Magnetic fluid hyperthermia: Focus on superparamagnetic iron oxide nanoparticles
Due to their unique magnetic properties, excellent biocompatibility as well as multi-purpose biomedical potential (e.g., applications in cancer therapy and general drug delivery), superparamagnetic iron oxide nanoparticles (SPIONs) are attracting increasing attention in both pharmaceutical and indus...
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Published in: | Advances in colloid and interface science Vol. 166; no. 1; pp. 8 - 23 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
Amsterdam
Elsevier B.V
10-08-2011
Elsevier |
Subjects: | |
Online Access: | Get full text |
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Summary: | Due to their unique magnetic properties, excellent biocompatibility as well as multi-purpose biomedical potential (e.g., applications in cancer therapy and general drug delivery), superparamagnetic iron oxide nanoparticles (SPIONs) are attracting increasing attention in both pharmaceutical and industrial communities. The precise control of the physiochemical properties of these magnetic systems is crucial for hyperthermia applications, as the induced heat is highly dependent on these properties. In this review, the limitations and recent advances in the development of superparamagnetic iron oxide nanoparticles for hyperthermia are presented.
Magnetic fluid hyperthermia has been developed through the testing of different superparamagnetic nanoparticles in vitro and in vivo, and has now reached the stage of clinical trials for the treatment of many different cancer types.
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► Size and surface modified SPIONs enable a safe and reproducible application to the tumor. ► SPIONs can be magnetically targeted and concentrated in the tumor tissue. ► Optimized SPIONs show a heating efficiency sufficient for a hyperthermia tumor therapy. ► Cancer specific binding agents on the SPIONs surface makes this therapy very selective. ► First clinical trials with SPION hyperthermia were carried out and showed promising results. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 ObjectType-Feature-1 |
ISSN: | 0001-8686 1873-3727 |
DOI: | 10.1016/j.cis.2011.04.003 |