The multi-electrode current source (MECS) interstitial hyperthermia system, which is used for treatment of cancer, employs segmented electrodes inserted in plastic tubes implanted in the treatment volume. The mean power deposition of the individual electrodes is controlled by varying the duty cycle of the RF signal applied to the electrodes, using thermocouples inside the electrodes for thermometry.A non-zero loss angle results in self-heating of the catheter. The thermal influence of selfheating was investigated and an analysis of the measurement of temperatures inside the catheter during and after heating is presented. Analytical models and a high-resolution numerical model were used for the calculation of steady state and transient distributions, respectively. The model results are compared with experimental data obtained in a muscle equivalent phantom.Results indicate that there is no difference between temperature inside and outside the catheter when using lossless catheter materials (e.g. PE and PTFE). Self-heating in the catheter wall has an adverse effect on the uniformity of the stationary temperature distribution and the reliability of temperature measurement with internal thermometry. These problems remain within acceptable limits for mildly lossy materials; the difference between the temperature inside and outside is only 6% when using low-loss Nylon.Analysis of the thermal decay after power-off shows that low-loss materials allow more time to obtain an accurate estimate of the tissue temperature at the catheter wall during power-on. This effect is enhanced by the presence of minute air layers in the applicator.Distortion of temperature gradients along the catheter was also investigated. Key factors are the thermal conduction across the catheter wall, and especially the presence of minute layers of air between consecutive layers of the probe. The distortion extends less than two millimetres, which is acceptable.The simulation results are compatible with measurements in phantoms and show that, if the proper choice of materials is made, the MECS applicator answers our expectations and that the temperature measurement inside the catheter can be used for direct feedback treatment control.

No abstract

No abstract

A convenient and practical methodology for the preparation of various spiro-β-amino alcohols has been elaborated. The approach involves allylboration and ring-closing methathesis to prepare spirobicyclic compounds and their subsequent modification to spiro-β-amino alcohols containing four-to six-membered azacycles. N-Boc-protected azaspirocyclic olefins reacted with NBS in solvent under reflux to give tricyclic bromocyclocarbamates. The structure of one of the bromides was established by single-crystal X-ray analysis. The dehydrobromination of the tricyclic bromides with tBuOK

Reactions of the [K]+ salts of the [nido-7,9-C2B9H12]- anion (2) and its C-phenylated derivative [7-Ph-nido-7,9-C2B9H11]- (4) with [OsCl2(PPh3)3] (3) proceed in benzene at ambient temperature with the formation of 16-electron chlorohydrido-Os(IV) exo-nido complexes, [exo-nido-10,11-{(Ph3P)2OsHCl}-10,11-(mu-H)2-7-R-7,9-C2B9H8] (5: R = H; 6: R = Ph), along with the small amounts of the charge-compensated nido-carboranes [nido-7,9-C2B9H11PPh3] (7) and [7-Ph-nido-7,9-C2B9H10PPh3] (8) as byproducts. However, when carried out under mild heating in ethanol, the reaction of 2 with 3 selectively afforded a 16-electron dihydrido-Os(IV) exo-nido complex [exo-nido-10,11-{(Ph3P)2OsH2}-10,11-(mu-H)2-7,9-C2B9H9] (9). Structures of both complexes 5 and 9 have been confirmed by single-crystal X-ray diffraction studies, which revealed that nido-carboranes in these species function as a bidentate dicarbollide ligands [7-R-nido-7,9-C2B9H10]2- linked to the Os(IV) center via two B-H...Os bonds involving adjacent B-H vertices in the upper CBCBB belt of the carborane cage. Thus, compounds 5 and 9 represent the first structurally characterized exo-nido-metallacarboranes based on meta-dicarbollide-type ligands. Variable-temperature 1H and 31P{1H} NMR experiments indicate that complex 9 is fluxional in solution and shows an unusual exchange between terminal Os-(H)2 and bridging {B-H}2...Os hydrogen atoms. Upon heating in d8-THF at 65 degrees C, complex 9 converts irreversibly to its closo isomer [2,2-(PPh3)2-2,2-H2-closo-2,1,7-OsC2B9H11] (13), which could thus be obtained as a pure crystalline solid. The structure of 13 has been established on the basis of analytical and multinuclear NMR data and a single-crystal X-ray diffraction study.