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Review
. 2011 Aug 14;63(9):789-808.
doi: 10.1016/j.addr.2011.03.008. Epub 2011 Apr 5.

Magnetic nanomaterials for hyperthermia-based therapy and controlled drug delivery

Affiliations
Review

Magnetic nanomaterials for hyperthermia-based therapy and controlled drug delivery

Challa S S R Kumar et al. Adv Drug Deliv Rev. .

Abstract

Previous attempts to review the literature on magnetic nanomaterials for hyperthermia-based therapy focused primarily on magnetic fluid hyperthermia (MFH) using mono metallic/metal oxide nanoparticles. The term "hyperthermia" in the literature was also confined only to include use of heat for therapeutic applications. Recently, there have been a number of publications demonstrating magnetic nanoparticle-based hyperthermia to generate local heat resulting in the release of drugs either bound to the magnetic nanoparticle or encapsulated within polymeric matrices. In this review article, we present a case for broadening the meaning of the term "hyperthermia" by including thermotherapy as well as magnetically modulated controlled drug delivery. We provide a classification for controlled drug delivery using hyperthermia: Hyperthermia-based controlled drug delivery through bond breaking (DBB) and hyperthermia-based controlled drug delivery through enhanced permeability (DEP). The review also covers, for the first time, core-shell type magnetic nanomaterials, especially nanoshells prepared using layer-by-layer self-assembly, for the application of hyperthermia-based therapy and controlled drug delivery. The highlight of the review article is to portray potential opportunities for the combination of hyperthermia-based therapy and controlled drug release paradigms--towards successful application in personalized medicine.

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Figures

Figure-1
Figure-1
A schematic representation of some of the unique advantages of magnetic nanomaterials for hyperthermia-based therapy and controlled drug delivery
Figure-2
Figure-2
A schematic representation of possible mechanisms for conversion of magnetic energy into heat (Modified based on figure-13 from Ref 57)
Figure-3
Figure-3
Schematic representation of the two types of controlled drug delivery using magnetic nanoparticle-based hyperthermia.
Figure-4
Figure-4
Size-dependent hyperthermia of MNPs (Reproduced from figure-14 in ref 57).
Figure-5
Figure-5
Demonstration of the concept of DBB in vivo (Reproduced from reference 44).
Figure-6
Figure-6
Stimulus-responsive membrane triggering in vitro (Reproduced from reference 88)
Figure-7
Figure-7
A schematic representation of the principles of ion channel stimulation using nanoparticle heating and local temperature sensing (Reproduced from reference 103).
Figure-8
Figure-8
A schematic representation of “Active drug-elution technology.” (Reproduced from the web site http://www.biophan.com)
Figure-9
Figure-9
Different architectures of nanomaterials.
Figure-10
Figure-10
Solvent dependent SPL values for SPIONs@Au (Reproduced from the reference 131)
Figure-11
Figure-11
Variation in heating rates for FeCo MNPs with change in anisotropy constant (Reproduced from the reference 135).
Figure-12
Figure-12
Scheme of the layer-by-layer sel-assembly and permeability test for microcapsules embedded with Co@Au NPs under an oscillating magnetic field (Reproduced from the reference 19).
Figure 13
Figure 13
A sechematic representation of three different types of nanoconstructs for hyperthermia-based drug delivery type DEP.

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