Table 2.
Application of an external magnetic field in drug-delivery systems with different mechanisms.
mechanism | frequency | drug-delivery system (magnetic particle) | key observations |
---|---|---|---|
heating [139] | 220–260 kHz | poly(N-isopropylacrylamide)-based nanogels | on-demand drug release through on–off mechanism |
heating [140] | 200 kHz | hydrogels composed of magnetic particles | pulsatile release properties over multiple cycles and multiple days |
mechanical deformation [30] | 10 kHz | liposomes attached to chains of magnetic particles | defects on the liposomal walls trigger the release of encapsulated drugs |
mechanical deformation [141] | 0 Hz (static) | core–shell particle with grafted PAA-b-PPEGMA and encapsulated enzymes and therapeutic chemicals | shielded polymer brush barrier is overcome under a weak magnetic field, leading to the merge of enzyme and substrate, namely ‘magnetic field remotely controlled selective biocatalysis’ |
magnetic guidance [31] | 0 Hz | poly(lactic-co-glycolic acid)-based nanoparticles loaded with paclitaxel | eight-fold increase in tumour accumulation and about twofold longer survival time |
magnetic guidance [133] | 0 Hz | iron oxide-coated phosphollipid-polyethylene glycol | disrupting endothelial adherens junctions |
magnetic guidance [10] | 0 Hz | lactoferrin-tethered magnetic double emulsion nanocapsules | high tumour accumulation and efficient suppressing of cancer growth |