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Experimental Therapeutics |
Department of Otorhinolaryngology, Head and Neck Surgery [C. A., W. A., P. H.], Department of Experimental Oncology and Therapeutic Research [R. J. K., W. E.], and Institute for Medical Statistics and Epidemiology [S. W.], Klinikum rechts der Isar, Technical University of Munich, 81675 Munich; Physics-Department E 17, Technical University of Munich, 81675 Munich [F. G. P.]; Chemicell, 10777 Berlin [C. B.]; and Cecilien-Klinik, 33175 Bad Lippspringe [A. S. L.], Germany
The specific delivery of chemotherapeutic agents to their desired
targets with a minimum of systemic side effects is an important,
ongoing challenge of chemotherapy. One approach, developed in the past
to address this problem, is the i.v. injection of magnetic particles
[ferrofluids (FFs)] bound to anticancer agents that are then
concentrated in the desired area (e.g., the tumor) by an
external magnetic field. In the present study, we treated squamous cell
carcinoma in rabbits with FFs bound to mitoxantrone (FF-MTX) that was
concentrated with a magnetic field. Experimental VX-2 squamous cell
carcinoma was implanted in the median portion of the hind limb of New
Zealand White rabbits (n = 26). When the
tumor had reached a volume of
3500 mm3, FF-MTX was
injected intraarterially (i.a.; femoral artery) or i.v. (ear vein),
whereas an external magnetic field was focused on the tumor. FF-MTX
i.a. application with the external magnetic field resulted in a
significant (P < 0.05), complete, and
permanent remission of the squamous cell carcinoma compared with the
control group (no treatment) and the i.v. FF-MTX group, with no signs
of toxicity. The intratumoral accumulation of FFs was visualized both
histologically and by magnetic resonance imaging. Thus, our data show
that i.a. application of FF-MTX is successful in treating experimental
squamous cell carcinoma. This "magnetic drug targeting" offers a
unique opportunity to treat malignant tumors locoregionally without
systemic toxicity. Furthermore, it may be possible to use these
magnetic particles as a "carrier system" for a variety of
anticancer agents, e.g., radionuclides, cancer-specific
antibodies, and genes.
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