Table 6-1 Characteristics of 133Xe implanted stent
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As a therapeutic method for myocardial infarction caused by arteriosclerosis
in coronary arteries, a balloon is introduced into the blood vessel
to expand it, or a mesh cylinder called a stent is implanted in
the vessel to prevent its narrowing or stenosis (Fig. 6-15). However,
restenosis occurs in about 30% of patients if only such angioplastic
methods are applied. This might be caused by quick proliferation
of intimal cells. In order to avoid this, it is thought that endovascular
irradiation would be effective in suppressing the proliferation
of the cells, by inserting a radioactive micro-source in the blood
vessel. Techniques are under development using radioisotopes such
as 90Sr, 90Y, 32P, 186Re and 192Ir emitting beta-ray or low energy gamma-ray, which are temporarily
inserted, or using permanently implanted radioactive stents. In JAERI, a novel technique was developed to produce radioactive stents by the implantation of xenon-133 (133Xe) ions using an on-line isotope separator (ISOL) (Fig. 6-16). It was reported that 32P (half-life 14.3 day, maximum energy 1.71 MeV) was used as a beta-ray source on the surface of stent. The 133Xe gives shorter endovascular irradiation time corresponding to its short half-life of 5.25 day, avoiding a disturbance in the recovery of the intima. Further, due to the maximum beta-ray energy of as low as 0.346 MeV, the risk to surrounding nontarget tissues can be reduced (Table 6-1). In order to realize the homogenious implantation of 133Xe ion beam on the surface of cylindrical stents, an up-down driven rotary target holder was designed for irradiation. Using this apparatus, up to 8 stents with radioactivity of a maximum of 98 kBq can be simultaneously processed. Through animal experiments the inhibitive effects on restenosis have been shown. |
Reference
S. Watanabe et al., Production of Radioactive Endovascular Stents by Implantation of 133Xe Ions, Appl. Radiat. Isot. 51 (2), 197 (1999). |
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