Modulation Of Induction Research Articles

The Application of Traditional Chinese Medicine-Derived Formulations in Cancer Immunotherapy: A Review.

Cancer immunotherapy is an advanced therapeutic approach that harnesses the body's immune system to target and eliminate tumor cells. Traditional Chinese medicine (TCM), with a history rooted in centuries of clinical practice, plays a crucial role in enhancing immune responses, alleviating cancer-related symptoms, and reducing the risks of infections and complications in cancer patients. This review systematically examines the current literature on TCM-based formulations in cancer immunotherapy. It explores the mechanisms by which TCM augments immune responses, particularly focusing on how these formulations influence both innate and adaptive immunity. Various TCM herbs and compounds, their active ingredients, and their application in cancer prevention and treatment were analyzed through an integrated review of preclinical studies, clinical trials, and molecular mechanistic investigations. TCM formulations contribute to cancer therapy by modulating the body's internal environment to improve immune defense. They enhance the immune system's ability to detect and destroy cancer cells, promote apoptosis in tumor cells, inhibit tumor growth and metastasis, and augment the effectiveness of conventional cancer treatments. The review highlights specific TCM herbs and formulations that have demonstrated significant anti-cancer properties, including their ability to strengthen immune responses and provide synergistic effects with existing cancer therapies. TCM-derived formulations represent a promising addition to cancer immunotherapy. The mechanisms through which these formulations enhance anti-tumor immunity are multifaceted, involving modulation of immune cell activity, apoptosis induction, and suppression of tumor progression. As cancer immunotherapy evolves, the integration of TCM into conventional treatment regimens may offer enhanced therapeutic efficacy, reduced side effects, and improved overall outcomes for cancer patients. Further clinical research is needed to fully elucidate the therapeutic potential and safety of TCM-based immunotherapeutic strategies in cancer care.

Method for Calculating the Unbalanced Current in Ungrounded Double Wye C-Type Harmonic Filters

This paper presents a methodology to calculate the neutral unbalanced current in C-type filters with an ungrounded double Wye topology; this equipment is widely used in the steel sector to mitigate the harmonic content in electrical installations caused by electric furnaces used in metal smelting processes. A common failure in these filters is the current unbalance caused by the degradation of the capacitor and inductor modules, leading to dangerous surges that affect these components, possible harmonic resonances, and deficient filtering by the equipment. Currently, there are no documented strategies for calculating the neutral current that allow for the proper adjustment of neutral protection in this type of equipment, resulting in catastrophic failures, costly unscheduled shutdowns, and potential harm to plant personnel. In this paper, we propose a methodology for calculating the unbalanced current in double Wye C-type harmonic filters, considering the natural degradation of capacitor and inductor modules and based on on-site measurements of the impedances for each element of the equipment. This allows for the predictive maintenance of these devices and the precise adjustment of neutral overcurrent protection. First, we review the operating principle of C-type harmonic filters and the neutral protection scheme. Then, the calculation methodology is proposed and validated in two practical case studies. In the first case, a 45 Mvar C-type second harmonic filter connected to a 34.5 kV bus is analyzed. In the second case, an 18.5 Mvar C-type second harmonic filter, part of a ±80 Mvar STATCOM system, connected to a 34.5 kV bus is examined. In both cases, these filters reduce the harmonic content in two steel plants: the first connected to a 400 kV bus and the second to a 230 kV bus. The results obtained with the proposed methodology were implemented in the protection device for a neutral current imbalance, considering different degradation values of the capacitors, and compared with the manufacturer’s suggested settings. The discussion highlights the good performance of the proposed methodology, particularly in terms of the protection device’s response speed to a risky unbalanced current.

Simvastatin-Loaded Polymeric Nanoparticles: Targeting Inflammatory Macrophages for Local Adipose Tissue Browning in Obesity Treatment.

Obesity is defined as chronic, low-grade inflammation within specific tissues. Given the escalating prevalence of obesity among individuals of all ages, obesity has reached epidemic proportions, posing an important public health challenge. Despite significant advancements in treating obesity, conventional approaches remain largely ineffective or involve severe side effects, thus underscoring the pressing need to explore and develop treatment approaches. Targeted and local immunomodulation using nanoparticles (NPs) can influence fat production and utilization processes. Statins, known for their anti-inflammatory properties, show the potential for mitigating obesity-related inflammation. A localized delivery option offers several advantages over oral and parenteral delivery methods. Here, we developed simvastatin (Sim) encapsulated within PLGA NPs (Sim-NP) for localized delivery of Sim to adipose tissues (ATs) for immunomodulation to treat obesity. In vitro experiments revealed the strong anti-inflammatory effects of Sim-NPs, which resulted in enhanced modulation of macrophage (MΦ) polarization and induction of AT browning. We then extended our investigation to an in vivo mouse model of high-fat-diet (HFD)-induced obesity. Sim-NP administration led to the controlled release of Sim within AT, directly impacting MΦ activity and inducing AT browning while inducing weight loss. Our findings demonstrated that Sim-NP administration effectively inhibited the progression of obesity-related inflammation, controlled white fat production, and enhanced AT modulation. These results highlight the potential of Sim-NP as a potent nanotherapy for treating obesity by modulating the immune system.

In vitro assessment of Dracocephalum lindbergii for growth inhibition, apoptosis induction, and cytokine modulation against Leishmaniamajor

Leishmaniasis is a vector-borne disease caused by several species of flagellate protozoan parasites belonging to the genus Leishmania, which are part of the Trypanosomatidae family. This study aims to evaluate the in vitro anti-Leishmania activity of Dracocephalum lindbergii Rech.f (D. lindbergii) on the growth, apoptosis induction, and proliferation of Leishmania major. To conduct this study, the aerial parts of D. lindbergii were collected during the flowering stage in May 2022 from North Khorasan province, Iran. The plant material was extracted using various solvents, starting with those of lower polarity and progressing to those of higher polarity. To assess the impact of the D. lindbergii fraction on L. major promastigotes, amastigotes, and macrophages (THP-1), cell viability was determined using the MTT assay. Additionally, flow cytometry with the Annexin V-PE apoptosis detection kit was employed to distinguish between viable, necrotic, and apoptotic promastigotes in response to treatment with the 100 % methanolic fraction of D. lindbergii (D). The expression levels of TNF-α, IFN-γ, IL-12, IL-10, TGF-β, IL4, iNOS, and GAPDH were quantified using real-time PCR (qPCR) on the macrophage cell line. Each treatment approach exhibited marked anti-leishmanial effects across different concentrations over 24, 48, and 72 h of incubation, showing statistically significant differences compared to the untreated control group (P < 0.001). Different concentrations of D, MAT, and AmpB, both individually and in combination, significantly reduced the total number of intramacrophage amastigotes compared to the untreated control groups at 24, 48, and 72 h. The results also showed time-dependent variations in the anti-Leishmania activity of the fraction. In terms of cellular morphology, treated cells exhibited changes such as shrinkage, cytoplasmic condensation, and reduced mobility, particularly noticeable after 24 h of treatment. Additionally, fraction D demonstrated significant antioxidant properties. This study highlights the potential of D. lindbergii as an anti-Leishmania agent, with the 100 % methanolic fraction emerging as a promising candidate for the development of novel treatments for leishmaniasis.

Biomimetic copper-containing nanogels for imaging-guided tumor chemo-chemodynamic-immunotherapy

Developing multifunctional nanoplatforms to comprehensively modulate the tumor microenvironment and enhance diagnostic and therapeutic outcomes still remains a great challenge. Here, we report the facile construction of a multivariate nanoplatform based on cancer cell membrane (CM)-encapsulated redox-responsive poly(N-vinylcaprolactam) (PVCL) nanogels (NGs) co-loaded with Cu(II) and chemotherapeutic drug toyocamycin (Toy) for magnetic resonance (MR) imaging-guided combination tumor chemodynamic therapy/chemoimmunotherapy. We show that redox-responsive PVCL NGs formed through precipitation polymerization can be aminated, conjugated with 3,4-dihydroxyhydrocinnamic acid for Cu(II) complexation, physically loaded with Toy, and finally camouflaged with CMs. The created ADCT@CM NGs with an average size of 113.0 nm are stable under physiological conditions and can efficiently release Cu(II) and Toy under tumor microenvironment with a high level of glutathione. Meanwhile, the developed NGs are able to enhance cancer cell oxidative stress and endoplasmic reticulum stress by synergizing the effects of chemodynamic therapy mediated by Cu-based Fenton-like reaction and Toy-mediated chemotherapy, thereby triggering significant immunogenic cell death (ICD). In a melanoma mouse model, the NGs show potent immune activation effects to reinforce tumor therapeutic efficacy through ICD induction and immune modulation including high levels of immune cytokine secretion, increased tumor infiltration of CD8+ cytotoxic T cells, and reduced tumor infiltration of regulatory T cells. With the CM coating and Cu(II) loading, the developed NG platform demonstrates homologous tumor targeting and T1-weighted MR imaging, hence providing a general biomimetic NG platform for ICD-facilitated tumor theranostic nanoplatform. Statement of significanceDeveloping multifunctional nanoplatforms to comprehensively modulate the tumor microenvironment (TME) and enhance theranostic outcomes remains a challenge. Here, a cancer cell membrane (CM)-camouflaged nanoplatform based on aminated poly(N-vinylcaprolactam) nanogels (NGs) co-loaded with Cu(II) and toyocamycin (Toy) was prepared for magnetic resonance (MR) imaging-guided combination tumor chemodynamic therapy/chemoimmunotherapy. The tumor targeting specificity and efficient TME-triggered release of Cu(II) and Toy could enhance tumor cell oxidative stress and endoplasmic reticulum stress by synergizing the effects of chemodynamic therapy mediated by Cu-based Fenton-like reaction and Toy-mediated chemotherapy, respectively, thereby leading to significant immunogenic cell death (ICD) and immune response. With the CM coating and Cu(II) loading, the developed NG platform also demonstrates good T1-weighted tumor MR imaging performance. Hence, this study provides a general biomimetic NG platform for ICD-facilitated tumor theranostics.

Design of Intelligent Window Automatic Monitoring System Based on Microcontroller Control

To ensure the safety of residents’ lives and property by using automatic opening and closing of ordinary windows, this article designs an intelligent window automatic monitoring system. The article proposes a software and hardware design scheme for the system, which comprises a microcontroller control module, temperature and humidity detection module, harmful gas detection module, rainfall detection module, human thermal radiation induction module, Organic Light-Emitting Diode (OLED) display module, stepper motor drive module, Wi-Fi communication module, etc. Users use this system to monitor environmental data such as temperature, humidity, rainfall, harmful gas concentrations, and human health. Users can control the opening and closing of windows through manual, microcontroller, and mobile application (app) remote methods, providing users with a more convenient, comfortable, and safe living environment.

Heme Oxygenase-1 Gene (GT)n Polymorphism Linked to Deep White Matter Hyperintensities, Not Periventricular Hyperintensities.

Oxidative stress plays a principal role in the pathogenesis of white matter hyperintensities (WMHs). The induction of heme oxygenase-1 (HO-1) gene in the brain represents 1 of the pivotal mechanisms to counteract the noxious effects of reactive oxygen species, and the transcriptional modulation of HO-1 induction depends on the length of a GT-repeat (GT)n in the promoter region. We investigated whether the HO-1 gene (GT)n polymorphism is associated with the risk of WMHs. A total of 849 subjects from the memory clinic were consecutively enrolled, and the HO-1 (GT)n genotype was determined. WMHs were assessed with the Fazekas scale and further divided into periventricular WMHs and deep WMHs (DWMHs). Allelic HO-1 (GT)n polymorphisms were classified as short (≤24 (GT)n), median (25≤[GT]n<31), or long (31≤[GT]n). Multivariate logistic regression analysis was used to evaluate the effect of the HO-1 (GT)n variants on WMHs. The number of repetitions of the HO-1 gene (GT)n ranged from 15 to 39 with a bimodal distribution at lengths 23 and 30. The proportion of S/S genotypes was higher for moderate/severe DWMHs than none/mild DWMHs (22.22% versus 12.44%; P=0.001), but the association for periventricular WMHs was not statistically significant. Logistic regression suggested that the S/S genotype was significantly associated with moderate/severe DWMHs (S/S versus non-S/S: odds ratio, 2.001 [95% CI, 1.323-3.027]; P<0.001). The HO-1 gene (GT)n S/S genotype and aging synergistically contributed to the progression of DWMHs (relative excess risk attributable to interaction, 6.032 [95% CI, 0.149-11.915]). Short (GT)n variants in the HO-1 gene may confer susceptibility to rather than protection from DWMHs, but not periventricular WMHs. URL: https://www.chictr.org.cn; Unique identifier: ChiCTR2100045869.

Розробка цифрових карт модуля індукції геомагнітного поля для території України

Knowledge of Ukraine`s geomagnetic field is based on magnetic surveys of the geomagnetic field induction module B and its power and angular components, as well as on observations or calculations of their anomalous values. The article describes the methods for constructing a digital map of the induction module of the geomagnetic field B. The map of module B for the epoch of 1969.5 is developed, which is the ground to create the maps of module B and its anomalies ΔB for an arbitrary epoch. The results of the ground absolute magnetic survey of 1969-1972, the analytical model of the main geomagnetic field BIGRF, as well as the map of the anomalous magnetic field on a scale of 1: 1,000,000 were used to construct the map of the geomagnetic field induction module B. The digital map of the module and anomalies of the geomagnetic field induction module B for the 1969.5 epoch was obtained by calculating the correction based on their difference values at the points of the absolute reference network. It was spread by interpolation according to the 1x1km matrix to the entire data array for the territory of Ukraine. The geomagnetic field induction module B for the 2005.5 epoch was calculated by adding to its values in the 1969.5 epoch the calculated values of the field dynamics ВIGRF and the "magnetizing" effect of anomalies of the induction module ΔΔB. The developed map is an approximate representation of the magnetic field modulus, since the amount of remanent magnetization was not taken into account during the calculation, which may cause minor deviations of the calculated and observed field values. The induction module of the geomagnetic field B in the epoch of 1969.5 varies in the range of 46,500÷62,000 nT, and in the epoch of 2005.5 ‒ 47,000÷63000 nT, increasing from the southwest to the northeast of the territory of Ukraine. Its maximum values are observed in the areas of regional and local magnetic anomalies, in particular in the area of the Kryvyi Rih-Kremenchuk anomalous strip and the southeastern edge of the Kursk anomaly. The dynamics of the BIGRF field for the period of 1969.5÷2005.5 is characterized by values from 700 nT in the east of the territory of Ukraine to 950 nT in the west, and the magnitude of the magnetizing effect ΔΔB varies within ±10 nT, reaching maximum values (up to 100-190 nT) in the regions of intense magnetic anomalies. The digital map of the geomagnetic field induction module B, developed in 2005.5, has been verified. This was done by measuring the values of module B in the magnetic observatories of Kyiv, L’viv, and Odesa, as well as in the Repeat Stations of the Ist and IInd classes. The results showed that there was only a small difference (-20 ÷ 40 nT) between the calculated and measured values of modulus B. Their most significant differences are spatially correlated with areas of modern activation of the Earth's crust on the territory of Ukraine and electrical conductivity anomalies.

Development of stability charts for double salience reluctance machine modeled using hill’s equation

The paper presents a novel algorithm for the development of stability charts. The second-order differential homogeneous equation describing a double salient reluctance machine with a capacitance connected to its stator winding is transformed into hill’s equation. The circuit components are the stator coil time-varying inductance of a double salient reluctance machine, capacitance and resistance. All these are modeled by hill’s equation. The double salient reluctance machine acts as an energy conversion system. The maximum and minimum inductance of the energy conversion system is measured in laboratory by inductance, capacitance, and resistance (LCR) meter. These values help to determine the inductance modulation index. The inductance modulation indetx, the characteristic constant and the characteristic parameter obtained from modeling equations are used in the MATLAB/Simulink model. The MATLAB/Simulink simulations generate stable and unstable oscillations to form stability charts. The proposed stability charts are in good agreement with the Ince-Stritt stability chart, which is widely applied in physics, mechanics and in electrical engineering, especially where the state of stability of a system or an electric oscillatory circuit is to be determined.

Proteomic Analysis Reveals Trilaciclib-Induced Senescence

Trilaciclib, a cyclin-dependent kinase 4/6 inhibitor, was approved as a myeloprotective agent for protecting bone marrow from chemotherapy-induced damage in extensive-stage small cell lung cancer. This is achieved through the induction of a temporary halt in the cell cycle of bone marrow cells. While it has been studied in various cancer types, its potential in hematological cancers remains unexplored. This research aimed to investigate the efficacy of trilaciclib in hematological cancers. Utilizing mass spectrometry-based proteomics, we examined the alterations induced by trilaciclib in the chronic myeloid leukemia cell line, K562. Interestingly, trilaciclib promoted senescence in these cells rather than cell death, as observed in acute myeloid leukemia, acute lymphoblastic leukemia, and myeloma cells. In K562 cells, trilaciclib hindered cell cycle progression and proliferation by stabilizing cyclin-dependent kinase 4/6 and downregulating cell cycle–related proteins, along with the concomitant activation of autophagy pathways. Additionally, trilaciclib-induced senescence was also observed in the nonsmall cell lung carcinoma cell line, A549. These findings highlight trilaciclib's potential as a therapeutic option for hematological cancers and underscore the need to carefully balance senescence induction and autophagy modulation in chronic myeloid leukemia treatment, as well as in nonsmall cell lung carcinoma cell line.

Controllable Current Diversion of GaAs PCSS Array Based on Inductance Modulation

Controllable Current Diversion of GaAs PCSS Array Based on Inductance Modulation

Exploring the combined anti-cancer effects of sodium butyrate and celastrol in glioblastoma cell lines: a novel therapeutic approach

Glioblastoma, a highly aggressive and lethal brain cancer, lacks effective treatment options and has a poor prognosis. In our study, we explored the potential anti-cancer effects of sodium butyrate (SB) and celastrol (CEL) in two glioblastoma cell lines. SB, a histone deacetylase inhibitor, and CEL, derived from the tripterygium wilfordii plant, act as mTOR and proteasome inhibitors. Both can cross the blood–brain barrier, and they exhibit chemo- and radiosensitive properties in various cancer models. GB cell lines LN-405 and T98G were treated with SB and CEL. Cell viability was assessed by MTT assay and IC50 values were obtained. Gene expression of DNA repair, apoptosis, and autophagy-related genes was analyzed by RT-PCR. Cell cycle distribution was determined using flow cytometry. Viability assays using MTT assay revealed IC50 values of 26 mM and 22.7 mM for SB and 6.77 μM, and 9.11 μM for CEL in LN-405 and T98G cells, respectively. Furthermore, we examined the expression levels of DNA repair genes (MGMT, MLH-1, MSH-2, MSH-6), apoptosis genes (caspase-3, caspase-8, caspase-9), and an autophagy gene (ATG-6) using real-time polymerase chain reaction. Additionally, flow cytometry analysis revealed alterations in cell cycle distribution following treatment with SB, CEL and their combination. These findings indicate that SB and CEL may act through multiple mechanisms, including DNA repair inhibition, apoptosis induction, and autophagy modulation, to exert their anti-cancer effects in glioblastoma cells. This is the first study providing novel insights into the potential therapeutic effects of SB and CEL in glioblastoma.

The Janus-faced functions of Apolipoproteins L in membrane dynamics

The functions of human Apolipoproteins L (APOLs) are poorly understood, but involve diverse activities like lysis of bloodstream trypanosomes and intracellular bacteria, modulation of viral infection and induction of apoptosis, autophagy, and chronic kidney disease. Based on recent work, I propose that the basic function of APOLs is the control of membrane dynamics, at least in the Golgi and mitochondrion. Together with neuronal calcium sensor-1 (NCS1) and calneuron-1 (CALN1), APOL3 controls the activity of phosphatidylinositol-4-kinase-IIIB (PI4KB), involved in both Golgi and mitochondrion membrane fission. Whereas secreted APOL1 induces African trypanosome lysis through membrane permeabilization of the parasite mitochondrion, intracellular APOL1 conditions non-muscular myosin-2A (NM2A)-mediated transfer of PI4KB and APOL3 from the Golgi to the mitochondrion under conditions interfering with PI4KB-APOL3 interaction, such as APOL1 C-terminal variant expression or virus-induced inflammatory signalling. APOL3 controls mitophagy through complementary interactions with the membrane fission factor PI4KB and the membrane fusion factor vesicle-associated membrane protein-8 (VAMP8). In mice, the basic APOL1 and APOL3 activities could be exerted by mAPOL9 and mAPOL8, respectively. Perspectives regarding the mechanism and treatment of APOL1-related kidney disease are discussed, as well as speculations on additional APOLs functions, such as APOL6 involvement in adipocyte membrane dynamics through interaction with myosin-10 (MYH10).

Enhancing photodynamic immunotherapy by reprograming the immunosuppressive tumor microenvironment with hypoxia relief

Tumor hypoxia impairs the generation of reactive oxygen species and the induction of immunogenic cell death (ICD) for photodynamic therapy (PDT), thus impeding its efficacy and the subsequent immunotherapy. In addition, hypoxia plays a critical role in forming immunosuppressive tumor microenvironments (TME) by regulating the infiltration of immunosuppressive tumor-associated macrophages (TAMs) and the expression of programmed death ligand 1 (PD-L1). To simultaneously tackle these issues, a MnO2-containing albumin nanoplatform co-delivering IR780, NLG919, and a paclitaxel (PTX) dimer is designed to boost photodynamic immunotherapy. The MnO2-catalyzed oxygen supply bolsters the efficacy of PDT and PTX-mediated chemotherapy, collectively amplifying the induction of ICD and the expansion of tumor-specific cytotoxic T lymphocytes (CTLs). More importantly, hypoxia releif reshapes the immunosuppressive TME via down-regulating the intratumoral infiltration of M2-type TAMs and the PD-L1 expression of tumor cells to enhance the infiltration and efficacy of CTLs in combination with immune checkpoint blockade (ICB) by NLG919, consequently eradicating primary tumors and almost completely preventing tumor relapse and metastasis. This study sets an example of enhanced immunotherapy for breast cancers through dual ICD induction and simultaneous immunosuppression modulation via both hypoxia relief and ICB, providing a strategy for the treatment of other hypoxic and immunosuppressive cancers.

The transcriptional landscape of Populus pattern/effector-triggered immunity and how PagWRKY18 involved in it.

Plants trigger a robust immune response by activating massive transcriptome reprogramming through crosstalk between PTI and ETI. However, how PTI and ETI contribute to the quantitative or/and qualitative output of immunity and how they work together when both are being activated were unclear. In this study, we performed a comprehensive overview of pathogen-triggered transcriptomic reprogramming by analyzing temporal changes in the transcriptome up to 144 h after Colletotrichum gloeosporioides inoculated in Populus. Moreover, we constructed a hierarchical gene regulatory network of PagWRKY18 and its potential target genes to explore the underlying regulatory mechanisms of PagWRKY18 that are not yet clear. Interestingly, we confirmed that PagWRKY18 protein can directly bind the W-box elements in the promoter of a transmembrane leucine-rich repeat receptor-like kinase, PagSOBIR1 gene, to trigger PTI. At the same time, PagWRKY18 functions in disease tolerance by modulation of ROS homeostasis and induction of cell death via directly targeting PagGSTU7 and PagPR4 respectively. Furthermore, PagPR4 can interact with PagWRKY18 to inhibit the expression of PagPR4 genes, forming a negative feedback loop. Taken together, these results suggest that PagWRKY18 may be involved in regulating crosstalk between PTI and ETI to activate a robust immune response and maintain intracellular homeostasis.

Comparative Analysis of Water Isotopic Compositions: Evaluating Isotope Analyzer for Soil and Extraction Method for Stem Water

Stable isotopes of water (δ2H and δ18O) are reliable tracers for the investigation of plant–soil–water interactions in forest ecosystems. However, variations in isotopic compositions may arise due to differences in analytical instruments and water extraction methods. In this study, we conducted three different experiments to identify isotopic differences caused by analytical and methodological variations. First, we analyzed soil water by using the two most commonly applied methods: isotope ratio mass spectrometry (IRMS) and cavity ring-down spectroscopy (CRDS). Second, we compared the isotopes in xylem water extracted from the stems of nine tree species using cryogenic vacuum distillation (CVD) with different heating times. Third, we compared the compositions in xylem water extracted with three different methods: mechanical squeezing using a pressure chamber (PC), an induction module (IM), and CVD. The differences in isotopic composition between IRMS and CRDS were significant but minimal. Soil properties were not significant factors contributing to differences between the two instruments. For the xylem water extraction with CVD, each of the nine tree species required heating for more than three hours. Significant differences were observed in δ2H among the three extraction methods for xylem water. Xylem water extracted by CVD showed more depleted values compared to those obtained by PC and IM. Our results highlight the importance of considering analytical and methodological variations in stable isotope analysis.

Modified Seasonal Decomposition Variations of Earth Magnetic Field Induction Module

In this paper, we present a modification of the classic method of seasonal decomposition of the time series, in particular its application for the analysis of geomagnetic data. Seasonal decomposition is a powerful tool for time series analysis, but its classic implementation does not always provide accurate results when the time series contains amplitude outliers and prolonged gaps. We propose a modified approach to solve this task of seasonal decomposition, by applying an average daily profile. This ensures the extraction of various anomalies in the residual component of the decomposition, in particular, global and contextual outliers, as well as disturbances due to magnetic storms in the variations of geomagnetic field induction module. Keywords: geomagnetic field, seasonal decomposition, data gaps, autocorrelation function, residual component, outliers, magnetic storm, DST index

In-Situ Measurement of Thermal Barrier Coating Properties Via Induction Phase Radiometry: Methodology Development

Abstract This research introduces a new method for accurately measuring the thermal resistance of thermal barrier coatings (TBCs), as typically used in gas turbine engines. The proposed method involves periodic internal heat generation inside the airfoil in the vicinity of the TBC-alloy boundary using low-frequency modulated induction heating through a coil. The phase lag between the radiation flux emitted to the surroundings from the exposed side of the TBC and the recorded voltage input to the modulated induction coil is proportional to the thermal resistance (L2/α) of the thin film. A simplified analytical model is developed to quantify the relationship between the lag as a function of the thermal resistance and induction modulation frequency. Numerical experiments are conducted to solve the full physics. Comparing the output with the simplified model, precision of 0.8% under ideal conditions can be observed. Moreover, the robustness of the methodology to recover properties is characterized by differing levels and types of noise levels, including Gaussian and constant-lag biases. For the relevant application, it is found that the suggested approach maintains a recovery error bound to range of 1–10%, dependent on input noise level.

Self-assembled fructo-oligosaccharide conjugated ferulic acid microparticle: Anticancer, anti-inflammatory and immunomodulatory effects

Fructo-oligosaccharide ferulic acid conjugate was synthesized, which self-assembles into disc shaped amorphous microparticles (FA FOS I), that could be used for targeted delivery to the colon. It is accessed for its ability to ameliorate colorectal cancer and inflammation. The microparticle exhibited selective cytotoxicity and apoptosis induction in colon cancer cells. The microparticle arrested the cell cycle in the G0-G1 phase. In-vivo anti-colorectal cancer activity were evaluated in colitis associated colon cancer mice model. There was a reduction in 60.83% of tumour lesions and 48.27% reduction in the malignant cells. The immunohistochemistry (IHC) revealed the suppression of inflammation and related inflammatory cytokines in the colon. The inhibition of cell proliferation, up-regulation of tumour suppressor protein and induction of apoptosis in the malignant cells were observed. The evaluation of immune modulation by FA FOS I microparticle revealed a 9% increase in WBC count and an increase in the infiltration of T-helper cells and cytotoxic T-cells into the tumour microenvironment. There was a considerable decrease in the expression of immune suppressing PD-L1 by the tumour cells on treatment with FA FOS I microparticle. All these data implicate better efficacy of the FA FOS I microparticle delivery to colon and amelioration of colitis associated colorectal cancer through multimodal route of inflammation reduction, apoptosis induction and positive modulation of immune system in the tumour microenvironment. FA FOS I was proposed to be a candidate drug which is physiologically and metabolically stable under gastro-intestinal condition and potentiating its effect in the target site large intestine; without being absorbed or transported to other tissue nor causing any adverse cytotoxicity to the neighbouring normal tissue.

The interaction of Suk-Saiyasna remedy with GABAA and CB1 receptor-targeting drugs: Enhancing hypnotic and sedative effects in in vivo models.

The Suk-Saiyasna remedy, an herbal treatment, was historically used but ceased due to its cannabis content. After a relaxation of drug control laws in Thailand, its use re-emerged. This study examines the Suk-Saiyasna remedy's impact on rodent behavior and its receptor effects. This study was conducted to assess the sedative-like effects of the remedy on mice. The mice were divided into groups receiving 0.6, 3, 30, and 60 mg/kg extracts, with negative controls for comparison. We also investigated the impact on receptors, utilizing negative controls and pretreatment with receptor blockers, followed by either a negative control or a 60 mg/kg extract. Furthermore, this study investigated the behavioral aspects of mice, including anxiolytic effects, antidepressant-like effects, and motor coordination, utilizing the elevated plus-maze, open-field, and rotarod performance tests. The Suk-Saiyasna remedy (P < 0.05) decreased significantly in the latent period and increased sleeping time in the treated groups. Moreover, the Suk-Saiyasna remedy also showed efficacy in reaction to GABAA receptors and cannabinoid CB1 receptors (P < 0.05). In addition, positive effects were observed regarding the animal behavior in the arena, as the animal activity, behavior, and muscle coordination were reduced (P < 0.05). The Suk-Saiyasna remedy may be involved in a sedative-hypnotic-like effect in rodents under normal conditions through the modulation of GABAergic neurons and induction of the cannabinoid CB1 receptor mechanism.