Pb(Mg1/3Nb2/3)-PbTiO3-Based Ultrasonic Transducer for Detecting Infiltrated Water in Pressurized Water Reactor Fuel Rods

In this study, a high-sensitivity Pb( Mg 1 / 3 Nb 2 / 3 ) O 3 - PbTiO 3 (PMN-PT)-based ultrasonic transducer was developed for detecting defective pressurized water reactor (PWR) fuel rods. To apply the PMN-PT substance to nuclear power plant facilities, given the need to guarantee their robustness against radioactive materials, the effects of neutron irradiation on PMN-PT were investigated. As a result, the major piezo-electric constants of PMN-PT, such as the electrical impedance, dielectric constant, and piezo-electric charge constant, were found to vary within acceptable ranges. This means that the PMN-PT could be used as the piezo-electric material in the ultrasonic transducer for nuclear power plants. The newly developed ultrasonic transducer was simulated using a modified KLM model for the through-transmission method and fabricated under the same conditions as in the simulation. The through-transmitted waveforms of normal and defective PWR fuel rods were obtained and compared with simulated results in the time and frequency domains. The response waveforms of the newly developed ultrasonic transducer for pressurized water reactor (PWR) fuel rods showed good agreement with the simulation outcome and could clearly detect defective specimens with high sensitivity

Detection and Classification of Artificial Defects on Stainless Steel Plate for a Liquefied Hydrogen Storage Vessel Using Short-Time Fourier Transform of Ultrasonic Guided Waves and Linear Discriminant Analysis

Liquefied hydrogen storage vessels (LHSVs) are vulnerable to surface-crack initiation, propagation, and fracture on their surfaces because they are under high-pressure, low-temperature conditions. Defects can also occur in the coatings of the storage containers used to prevent hydrogen permeation, and these lead to surface defects such as pitting corrosions. Together, these increase the probability of liquid hydrogen leaks and can cause serious accidents. Therefore, it is important to detect surface defects during periodic surface inspections of LHSVs. Among the candidate non-destructive evaluation (NDE) techniques, testing using guided waves (GWs) is effective for detecting surface defects. Because of the ability of GWs to travel long distances without significant acoustic attenuation, GW testing has attracted much attention as a promising structural monitoring technique for LHSVs. In this study, an ultrasonic NDE method was designed for detecting surface defects of 304SS plate, which is the main material used for fabricating LHSVs. It involves the use of linear discriminant analysis (LDA) based on short-time Fourier transform (STFT) pixel information produced from GW data. To accomplish this, the differences in the number of STFT pixels between sound and defective specimens were used as a major factor in distinguishing the two groups. Consequently, surface defects could be detected and classified with 97% accuracy by the newly developed pixel-based mapping method. This indicates that the newly developed NDE method with LDA can be used to detect defects and classify LHSVs as either sound or defective

Identification of Thiazolo[5,4-b]pyridine Derivatives as c-KIT Inhibitors for Overcoming Imatinib Resistance

c-KIT is a promising therapeutic target against gastrointestinal stromal tumor (GIST). In order to identify novel c-KIT inhibitors capable of overcoming imatinib resistance, we synthesized 31 novel thiazolo[5,4-b]pyridine derivatives and performed SAR studies. We observed that, among these substances, 6r is capable of inhibiting significantly c-KIT and suppressing substantially proliferation of GIST-T1 cancer cells. It is of note that 6r is potent against a c-KIT V560G/D816V double mutant resistant to imatinib. Compared with sunitinib, 6r possesses higher differential cytotoxicity on c-KIT D816V Ba/F3 cells relative to parental Ba/F3 cells. In addition, kinase panel profiling reveals that 6r has reasonable kinase selectivity. It was found that 6r remarkably attenuates proliferation of cancer cells via blockade of c-KIT downstream signaling, and induction of apoptosis and cell cycle arrest. Furthermore, 6r notably suppresses migration and invasion, as well as anchorage-independent growth of GIST-T1 cells. This study provides useful SAR information for the design of novel c-KIT inhibitors overcoming imatinib-resistance

Identification of Thiazolo[5,4-<i>b</i>]pyridine Derivatives as c-KIT Inhibitors for Overcoming Imatinib Resistance

c-KIT is a promising therapeutic target against gastrointestinal stromal tumor (GIST). In order to identify novel c-KIT inhibitors capable of overcoming imatinib resistance, we synthesized 31 novel thiazolo[5,4-b]pyridine derivatives and performed SAR studies. We observed that, among these substances, 6r is capable of inhibiting significantly c-KIT and suppressing substantially proliferation of GIST-T1 cancer cells. It is of note that 6r is potent against a c-KIT V560G/D816V double mutant resistant to imatinib. Compared with sunitinib, 6r possesses higher differential cytotoxicity on c-KIT D816V Ba/F3 cells relative to parental Ba/F3 cells. In addition, kinase panel profiling reveals that 6r has reasonable kinase selectivity. It was found that 6r remarkably attenuates proliferation of cancer cells via blockade of c-KIT downstream signaling, and induction of apoptosis and cell cycle arrest. Furthermore, 6r notably suppresses migration and invasion, as well as anchorage-independent growth of GIST-T1 cells. This study provides useful SAR information for the design of novel c-KIT inhibitors overcoming imatinib-resistance

Affinity‐Directed Site‐Specific Protein Labeling and Its Application to Antibody‐Drug Conjugates

Abstract Chemically modified proteins have diverse applications; however, conventional chemo‐selective methods often yield heterogeneously labeled products. To address this limitation, site‐specific protein labeling holds significant potential, driving extensive research in this area. Nevertheless, site‐specific modification of native proteins remains challenging owing to the complexity of their functional groups. Therefore, a method for site‐selective labeling of intact proteins is aimed to design. In this study, a novel approach to traceless affinity‐directed intact protein labeling is established, which leverages small binding proteins and genetic code expansion technology. By applying this method, a site‐specific antibody labeling with a drug, which leads to the production of highly effective antibody‐drug conjugates specifically targeting breast cancer cell lines is achieved. This approach enables traceless conjugation of intact target proteins, which is a critical advantage in pharmaceutical applications. Furthermore, small helical binding proteins can be easily engineered for various target proteins, thereby expanding their potential applications in diverse fields. This innovative approach represents a significant advancement in site‐specific modification of native proteins, including antibodies. It also bears immense potential for facilitating the development of therapeutic agents for various diseases

Novel SPICE macro modeling for an integrated si schottky barrier diode

Anew and accurate modeling has been performed for an integrated Schottky barrier diode fabricated by 0.18um standard CMOS process. The bulk and distributed effects are considered by adding macro elements to an original SPICE diode model. The resistance and capacitance model parameters have been obtained precisely by a direct extraction method using S-parametersets with various bias points.Thevalidityof this new model andparameter extraction method has been verified by comparing with the measured S-parameters over the wide range of bias up to 10 GHz