MHD Equilibrium and Stability of Spherical Tokamak Plasma with Current Hole

The potential characteristics of spherical tokamak configurations with current hole are investigated from the point of view of magnetohydrodynamic (MHD) equilibrium and stability. The effect of the toroidal shear flows is also considered by using a modified Grad-Shafranov equation. Linear and nonlinear stability for low-n kink modes and intermediate-n ballooning mode is analyzed by means of numerical simulations

Dynamics of spherical tokamak plasma on the internal reconnection event

Nonlinear magnetohydrodynamic (MHD) simulations are executed to investigate the dynamical behavior of the relaxation phenomenon observed in spherical tokamak (ST) plasma that is known as the Internal Reconnection Event (IRE). The simulation results successfully reproduce several key features of IRE, and the physical mechanisms are revealed. A sudden collapse of the pressure profile takes place as a result of a nonlinear time development of a pressure-driven instability. A magnetic reconnection induced between the internal and the external magnetic field is found to play a crucial role in determining the nature of the overall process, namely, the rapid expulsion of the plasma heat energy due to the pressure imbalance along the reconnected field lines, and the large distortion in the overall shape. The resultant deformations in overall shape of the plasma are in good agreement with the experimental observations

Simulation Data Analysis by Virtual Reality System

We introduce new software for analysis of time-varying simulation data and new approach for contribution of simulation to experiment by virtual reality (VR) technology. In the new software, the objects of time-varying field are visualized in VR space and the particle trajectories in the time-varying electromagnetic field are also traced. In the new approach, both simulation results and experimental device data are simultaneously visualized in VR space. These developments enhance the study of the phenomena in plasma physics and fusion plasmas

マイクロ波CTマンモグラフィの開発

24個の固定ダイポールアンテナを用いて三次元マイクロ波CT実験を行い，スーパーコンピュータを用いてForward-Backward Time Stepping（FBTS）法によるCT計算を行った．その結果得られた知見は，FBTS法が雑音に強いこと，及び計算の初期設定やキャリブレーション設定が精度向上に重要なことである．また計算モデル化が容易な広帯域平面アンテナの開発も行った．これらの知見を生かし，FBTS法マイクロ波CTマンモグラフィ装置の概念設計を行った

Generation of Tetrafluoroethylene–Propylene Elastomer-Based Microfluidic Devices for Drug Toxicity and Metabolism Studies

フッ素系エラストマー素材を用いた肝臓チップの開発と薬物代謝・毒性試験への応用. 京都大学プレスリリース. 2021-09-16.Drug testing on miniatured livers. 京都大学プレスリリース. 2021-09-17.Polydimethylsiloxane (PDMS) is widely used to fabricate microfluidic organs-on-chips. Using these devices (PDMS-based devices), the mechanical microenvironment of living tissues, such as pulmonary respiration and intestinal peristalsis, can be reproduced in vitro. However, the use of PDMS-based devices in drug discovery research is limited because of their extensive absorption of drugs. In this study, we investigated the feasibility of the tetrafluoroethylene–propylene (FEPM) elastomer to fabricate a hepatocyte-on-a-chip (FEPM-based hepatocyte chip) with lower drug absorption. The FEPM-based hepatocyte chip expressed drug-metabolizing enzymes, drug-conjugating enzymes, and drug transporters. Also, it could produce human albumin. Although the metabolites of midazolam and bufuralol were hardly detected in the PDMS-based hepatocyte chip, they were detected abundantly in the FEPM-based hepatocyte chip. Finally, coumarin-induced hepatocyte cytotoxicity was less severe in the PDMS-based hepatocyte chip than in the FEPM-based hepatocyte chip, reflecting the different drug absorptions of the two chips. In conclusion, the FEPM-based hepatocyte chip could be a useful tool in drug discovery research, including drug metabolism and toxicity studies

Immune Cell Recruitment and Cell-Based System for Cancer Therapy

Immune cells, such as cytotoxic T lymphocytes, natural killer cells, B cells, and dendritic cells, have a central role in cancer immunotherapy. Conventional studies of cancer immunotherapy have focused mainly on the search for an efficient means to prime/activate tumor-associated antigen-specific immunity. A systematic understanding of the molecular basis of the trafficking and biodistribution of immune cells, however, is important for the development of more efficacious cancer immunotherapies. It is well established that the basis and premise of immunotherapy is the accumulation of effective immune cells in tumor tissues. Therefore, it is crucial to control the distribution of immune cells to optimize cancer immunotherapy. Recent characterization of various chemokines and chemokine receptors in the immune system has increased our knowledge of the regulatory mechanisms of the immune response and tolerance based on immune cell localization. Here, we review the immune cell recruitment and cell-based systems that can potentially control the systemic pharmacokinetics of immune cells and, in particular, focus on cell migrating molecules, i.e., chemokines, and their receptors, and their use in cancer immunotherapy