Selective induction hyperthermia following transcatheter arterial embolization with a mixture of nano-sized magnetic particles (ferucarbotran) and embolic materials: feasibility study in rabbits

Purpose To evaluate the possibility of selective hyperthermia following transcatheter arterial embolization (TAE) with ferucarbotran using a newly developed inductive heating (IH) device. Materials and methods Twelve Japanese white rabbits were separated into four groups: those treated with TAE usin...

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Veröffentlicht in:Japanese journal of radiology 2008-05, Vol.26 (4), p.179-187
Hauptverfasser: Takamatsu, Shigeyuki, Matsui, Osamu, Gabata, Toshifumi, Kobayashi, Satoshi, Okuda, Miho, Ougi, Takahiro, Ikehata, Yoshio, Nagano, Isamu, Nagae, Hideo
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Sprache:eng
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Zusammenfassung:Purpose To evaluate the possibility of selective hyperthermia following transcatheter arterial embolization (TAE) with ferucarbotran using a newly developed inductive heating (IH) device. Materials and methods Twelve Japanese white rabbits were separated into four groups: those treated with TAE using a mixture of ferucarbotran and lipiodol (F-L group); those treated with ferucarbotran and gelatin sponge powder; those treated with saline and lipiodol; and a control group. These four groups received IH. Nine rabbits with renal VX2 carcinoma were separated into three groups: IH after TAE (IH-TAE tumor), TAE without IH (TAE tumor), and no treatment (control tumor). The temperature of the tumor was kept at 45°C for 20 min. The therapeutic effect was pathologically evaluated by TUNEL staining. Results In the heating rates of the kidney, the F-L group showed significantly greater values than the group in which iron was not used. In the IH-TAE tumor group, tumors could be selectively heated. In TUNEL staining, the IH-TAE tumor and TAE tumor groups showed significantly greater values of apoptosis rate than in the control tumor group. Conclusion IH following TAE with a mixture of ferucarbotran and lipiodol was capable of inducing selective hyperthermia with our device. However, further investigation is needed to confirm its safety and effectiveness in the treatment of malignant neoplasms in humans.
ISSN:0288-2043
1867-1071
1862-5274
1867-108X
DOI:10.1007/s11604-007-0212-9