With the advent of therapeutic radiation treatment machines with photon end point energies of several MeV, a new channel is available to transfer the photon energy to biological material, namely, pair production. This process has a photon threshold energy of 1.02 MeV. The probability of pair production, which depends on the square of the atomic number (Z) of the interacting material, increases markedly as the photon energy is further increased. As the goal of treatment planning in radiation therapy is to locally maximize the absorbed dose in abnormal cells and minimize the dose in surrounding normal cells, in this study the authors measured the dose enhancement which could be expected if a high-Z material such as gold was present adjacent to tumor sites during irradiation. The authors used photon beams produced by electron accelerators with energies ranging from 6 to 25 MV. They chose either gold or lead foils as high-Z materials, the measurements being repeated using the same geometry but replacing the high-Z materials with a low-Z material (aluminum). The comparison of the experimental results using low- and high-Z materials verified the theoretical prediction of the expected dose enhancement. The effect of finite range of the electron-positron pairs was also studied by varying the spacing between two foils placed parallel or orthogonal to the incident photon beam. Using an 18 MV photon beam, the authors observed a maximum dose enhancement of 44%. They intend therefore to proceed from these phantom studies to animal measurements.

Thin sections of deep-frozen unfixed muscle were studied in a scanning electron microscope modified for transmission imaging and equipped with a "cryostage" for vacuum compatibility of hydrated tissue.With an energy-dispersive x-ray analysis system, intracellular atomic species in the scan beam path were identified by their fluorescent x-rays and spatially localized in correlation with the electron optical image of the microstructure. Marked differences are noted between the ultrastructure of deep-frozen hydrated muscle and that of fixed dehydrated muscle. In frozen muscle, myofibrils appear to be composed of previously undescribed longitudinal structures between 400-1000 A wide ("macromyofilaments"). The usual myofilaments, mitochondria, and sarcoplasmic reticulum were not seen unless the tissue was "fixed" before examination. Fluorescent x-ray analysis of the spatial location of constituent elements clearly identified all elements heavier than Na. Intracellular Cl was relatively higher than expected.The present body of knowledge relating the microstructure and physiologic function of muscle is based primarily on (1) electron microscope studies of fixed tissue, dehydrated so as to be compatible with the vacuum required for electron optical imaging and (2) (Fig. 1).To obtain sufficient contrast in the electron optical images of a thin section of tissue, the normal reflected electron imaging operation of the SEM was converted to transmission imaging-causing it to function as a transmission scanning electron microscope. The contrast obtained in unstained unfixed tissue was enhanced by partial dark-field techniques that were developed for this purpose. A detailed description of the cryostage and transfer system and transmission imaging technique will be reported separately (16).X-Ray Analysis. In the SEM, a 20 keV electron beam focused to a small spot, about 75 A in diameter, is scanned 3423

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The authors demonstrated that the nMAG PGD with MRI could be used to measure the 3D dosimetric structures at the mm-scale in the vicinity of the foil. The current study provided more accurate 3D spatial dose distribution than the previous studies. Furthermore, the measurements were validated by the MC simulation.