In 2018, media reports raised issues related to radon released from building materials used as finishing materials in apartment houses. Accordingly, related ministries recommended not to use materials with a radiation index value exceeding 1. In order to calculate the radioactivity index, not only 226Ra producing radon (222Rn) but also 232Th and 40K radioactivity concentrations are required. To determine the concentration of the radionuclide, 40K is measured by a single gamma ray of 1,460.8 keV. And the 228Ac used to measure 232Th mainly utilizes gamma rays of 911.2 keV. However, 228Ac does not appear as a single peak unlike 40K, and appears as multiple peaks at various energies. Among them, gamma rays are emitted at a intensity of 0.83% at 1,459.2 keV, which is likely to interfere with 40K. Therefore, what is actually measured at 1,460.8 keV is theoretically a compound peak of 40K and 228Ac. Because the probability of emission at 1,459.2 keV (0.83%) is low, a low concentration of 232Th will result in little 40K radioactivity error. However, samples containing a high concentration of 232Th overestimate the 40K radioactive concentration, so correction is required. In this study, the IAEA standard substance (IAEA-RGTh-1) ontaining 232Th of actual high concentration was analyzed, and the results of the analysis without correction of 40K were compared and verified. As the 40K correction method, the 911.2 keV gamma-ray of 228Ac was used as the reference peak to separate the peak of 228Ac (1,459.2 keV) from the 40K (1,460.8 keV) mixed peaks. And, the coefficient value obtained by subtracting the peak of 228Ac (1,459.2 keV) from the 40K (1,460.8 keV) mixed peak was set to a pure peak of 40K and the radioactivity concentration was calculated therefrom. As a result of calculating the IAEA-RGTh-1 reference material without correction, it was confirmed that the 40K value was overestimated by about 38 times. If a measurement beyond the MDA of 40K is generated by 228Ac radioactivity because the 40K correction constant is not applied, there is an error in determining that there is 40K radioactivity. However, even if 40K radioactivity is overestimated due to the high concentration of 232Th, the degree to which this effect contributes to the radioactivity index is very small. However, as an analyst, 40K radioactivity correction should be made for more accurate analysis.

Cleanroom could be largely classified into industrial cleanroom that can be contaminated by particlesand bio-cleanroom that can be contaminated by biological particles. Electrical manufacturing companies such as precision machines and electrical parts essentially have industrial cleanroom facilities and clean technologies to produce defects free products due to particles.Industrial cleanroom should be controlled in respect of 4M1E to prevent from foreign materials of submicro unit and to keep out contamination sources from outside. In this paper, a concept for a quantitative methodology to measure the particles from running components was suggested by combining both newly making clean booth such as wear tester and laser particle counter.

Hyperacture rejection (HAR) of pig organs, upon xenotransplantation into primates, could partly be overcome by knocking out the alpha-Gal gene. However, xenotransplanted organs may still undergo immunological acture rejection (AR) or acute vascular rejection (AVR). Among several genes involved in AR and AVR, the hCD47 evades the monocyte/ macrophage mediated phagocytosis by identifying the self/non-self signal (CD47-SIRPa) whereas hTFPI participates in the regulation of coagulation pathway by acting upstream of the thrombin. In this study, we investigated hCD47 and hTFPI as two possible candidates for avoiding AR and AVR, respectively upon pig-to-human xenotransplantation. A co-expression vector for hCD47 and hTFPI was constructed using 2A peptides system (F2A) and transfected into the porcine kidney cell line (PK-15). The transfected cells stably expressed both hCD47 and hTFPI mRNA and proteins. Co-culture of non-transfected, hCD47-transfected, hTFPI-transfected or hCD47+hTPFI-transfected PK15 cells with natural killer (NK) cells, monocytes and macrophages confirmed the cytotoxic effect of hCD47 and revealed a synergistic effect of hCD47 and hTFPI co-transfection. There was an attractive survivability of 25～30% on each type of innate immune cell, NK cell and macrophage. These results suggest that transgenic pigs, genetically modified for hCD47 and hTFPI may be useful for overcoming xenograft rejection. Furthermore, cotransfection with hTFPI may enhance the cytotoxic effect of hCD47, possibly by assisting the hCD47-SIRPa binding by an unknown mechanism.

Ultrastructural studies of oocyte degeneration in the oocyte, and the functions of follicle cells during oocyte degeneration are described to clarify the reproductive mechanism on oocyte degeneration of Mactra chinensis using cytological methods. Commonly, the follicle cells are attached to the oocyte. Follicle cells play an important role in oocyte degeneration. In particular, the functions of follicle cells during oocyte degeneration are associated with phagocytosis and the intracellular digestion of products. In this study, morphologically similar degenerated phagosomes (various lysosomes), which were observed in the degenerated oocytes, appeared in the follicle cells. After the spawning of the oocytes, the follicle cells were involved in oocyte degeneration through phagocytosis by phagolysosomes. Therefore, it can be assumed that follicle cells reabsorb phagosomes from degenerated oocytes. In this study, the presence of lipid granules, which occurred from degenerating yolk granules, gradually increased in degenerating oocytes. The function of follicle cells can accumulate reserves of lipid granules and glycogen in the cytoplasm, which can be employed by the vitellogenic oocyte. Based on observations of follicle cells attached to degenerating oocytes after spawning, the follicle cells of this species are involved in the lysosomal induction of oocyte degeneration for the reabsorption of phagosomes (phagolysosomes) in the cytoplasm for nutrient storage, as seen in other bivalves.