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Search Results (1,342)

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Keywords = testing and validation platform

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21 pages, 11490 KiB  
Article
Research on Disturbance Compensation Control and Parameter Identification of a Multiple Air-Bearing Planar Air-Floating Platform Based on ADRC
by Chuanxiao Xu, Guohua Kang, Junfeng Wu, Zhen Li, Xinyong Tao, Jiayi Zhou and Jiaqi Wu
Aerospace 2025, 12(2), 160; https://doi.org/10.3390/aerospace12020160 - 19 Feb 2025
Abstract
The spacecraft microgravity simulation air-bearing platform is a crucial component of the spacecraft ground testing system. Special disturbances, such as the flatness and roughness of the contact surface between the air bearings and the granite platform, increasingly affect the control accuracy of the [...] Read more.
The spacecraft microgravity simulation air-bearing platform is a crucial component of the spacecraft ground testing system. Special disturbances, such as the flatness and roughness of the contact surface between the air bearings and the granite platform, increasingly affect the control accuracy of the simulation experiment as the number of air bearings increases. To address this issue, this paper develops a novel compensation control system based on Active Disturbance Rejection Control (ADRC), which estimates and compensates for the disturbing forces and moments caused by the roughness and levelness of the contact surface, thereby improving the control precision of the spacecraft ground simulation system. A dynamic model of the multi-air-bearing platform under disturbance is established. A cascade ADRC algorithm based on the Linear Extended State Observer (LESO) is designed. The Gauss–Newton iteration method is used to identify the parameters of the sliding friction coefficient and the tilt angle of the air-bearing platform. A full-physics simulation experimental platform for spacecraft with rotor-based propulsion is constructed, and the proposed algorithm is validated. The experimental results show that on a marble surface with a flatness of grade 00, an overall tilt angle of 0–1 degrees, and a surface friction coefficient of 0–0.01, the position control accuracy for the simulated spacecraft can reach 1.5 cm, and the attitude control accuracy can reach 1°. Under ideal conditions, the identification accuracy for the contact surface friction coefficient is 2 × 10−4, and the recognition accuracy for the overall levelness of the marble surface can reach 1 × 10−3, laying the foundation for high-precision ground simulation experiments of spacecraft in multi-air-bearing scenarios. Full article
(This article belongs to the Section Astronautics & Space Science)
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<p>Main structure of this paper.</p>
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<p>Coordinate system representation.</p>
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<p>Conversion of inertial force systems.</p>
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<p>Controller structure.</p>
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<p>Gauss–Newton method solution process.</p>
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<p>Virtual plane friction coefficient distribution.</p>
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<p>Numerical simulation results for circular trajectory tracking.</p>
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<p>Control outputs.</p>
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<p>Friction coefficient calibration results.</p>
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<p>Marble plane inclination calibration results.</p>
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<p>Floating microgravity simulation experiment system structure.</p>
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<p>Spacecraft simulator.</p>
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<p>Experiment platform hardware and software communication flow chart.</p>
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<p>Observer parameter tuning and parameterization results.</p>
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<p>Calibration result of thrust curve.</p>
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<p>Circular trajectory tracking experiment.</p>
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<p>Experimental results of trajectory tracking.</p>
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<p>Position and attitude control errors.</p>
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<p>Parameter identification experiment.</p>
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<p>Three-axis perturbation identification results.</p>
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<p>Friction coefficient identification results.</p>
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<p>Results of marble inclination identification.</p>
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19 pages, 6803 KiB  
Article
Point-of-Care No-Specimen Diagnostic Platform Using Machine Learning and Raman Spectroscopy: Proof-of-Concept Studies for Both COVID-19 and Blood Glucose
by Allen B. Chefitz, Rohit Singh, Thomas Birch, Yongwu Yang, Arib Hussain and Gabriella Chefitz
Spectrosc. J. 2025, 3(1), 6; https://doi.org/10.3390/spectroscj3010006 - 19 Feb 2025
Viewed by 89
Abstract
Significance: We describe a novel, specimen-free diagnostic platform that can immediately detect both a metabolite (glucose) or an infection (COVID-19) by non-invasively using Raman spectroscopy and machine learning. Aim: Current diagnostic testing for infections and glucose monitoring requires specimens, disease-specific reagents and processing, [...] Read more.
Significance: We describe a novel, specimen-free diagnostic platform that can immediately detect both a metabolite (glucose) or an infection (COVID-19) by non-invasively using Raman spectroscopy and machine learning. Aim: Current diagnostic testing for infections and glucose monitoring requires specimens, disease-specific reagents and processing, and it increases environmental waste. We propose a new hardware–software paradigm by designing and constructing a finger-scanning hardware device to acquire Raman spectroscopy readouts which, by varying the machine learning algorithm to interpret the data, allows for diverse diagnoses. Approach: A total of 455 patients were enrolled prospectively in the COVID-19 study; 148 tested positive and 307 tested negative through nasal PCR testing conducted concurrently with testing using our viral detector. The tests were performed on both outpatients (N = 382) and inpatients (N = 73) at Holy Name Medical Center in Teaneck, NJ, between June 2021 and August 2022. Patients’ fingers were scanned using an 830 nm Raman System and then, using machine learning, processed to provide an immediate result. In a separate study between April 2023 and August 2023, measurements using the same device and scanning a finger were used to detect blood glucose levels. Using a Dexcom sensor and an Accu-Chek device as references, a cross-validation-based regression of 205 observations of blood glucose was performed with a machine learning algorithm. Results: In a five-fold cross-validation analysis (including asymptomatic patients), a machine learning classifier using the Raman spectra as input achieved a specificity for COVID-19 of 0.837 at a sensitivity of 0.80 and an area under receiver operating curve (AUROC) of 0.896. However, when the data were split by time, with training data consisting of observations before 1 July 2022 and test data consisting of observations after it, the model achieved an AUROC of 0.67, with 0.863 sensitivity at a specificity of 0.517. This decrease in AUROC may be due to substantial domain shift as the virus evolves. A similar five-fold cross-validation analysis of Raman glucose detection produces an area under precision–recall curve (AUPR) of 0.58. Conclusions: The combination of Raman spectroscopy, AI/ML, and our patient interface admitting only a patient’s finger and using no specimen offers unprecedented flexibility in introducing new diagnostic tests or adapting existing ones. As the ML algorithm can be iteratively re-trained with new data and the software deployed to field devices remotely, it promises to be a valuable tool for detecting rapidly emerging infectious outbreaks and disease-specific biomarkers, such as glucose. Full article
(This article belongs to the Special Issue Feature Papers in Spectroscopy Journal)
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<p>U.S. Patent No. 11,452,454, U.S. Patent No. 11,304,605. Viral Detector—Human interface with attached laser and signal fiberoptic cables. Inserted finger with minimization of ambient light, as employed in a 476 patient study. Interface houses the Raman probe.</p>
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<p>Dimensions of human interface of viral detector used in a 476 patient study.</p>
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<p>Components of human interface for finger insertion with additional laser safety protections. Raman probe connections for laser and signal fiberoptic cables. Cables connect to the laser source and CCD.</p>
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<p>Receiver Operating Curve: From the machine learning data analysis of 455 patients. AUROC = 0.896.</p>
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<p>Average Raman spectrum output from the device (average intensity shown across cases and controls in the training dataset). From a proof-of-concept analysis of initial 216 patients.</p>
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<p>Individual Raman peaks contain information that can distinguish between cases and controls. <span class="html-italic">t</span>-tests on score z: For each individual, wavenumber values (across the 2000 points) were converted to z-scores to control for patient-specific biases. From a proof-of-concept analysis of initial 216 patients.</p>
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<p>The glucose testing precision–recall curve.</p>
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<p>Same patient tested using different fingers.</p>
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<p>COVID-19 negative spectrum (processed (Raman)).</p>
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<p>COVID-19 negative spectrum (raw (includes fluorescence and background signals)).</p>
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<p>COVID-19 positive spectrum (processed).</p>
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<p>COVID-19 positive spectrum (raw).</p>
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<p>AccuChek 52 Dexcom 67.</p>
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<p>AccuChek 260 Dexcom 287.</p>
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15 pages, 4544 KiB  
Article
Utilizing NF-κB Signaling in Porcine Epithelial Cells to Identify a Plant-Based Additive for the Development of a Porcine Epidemic Diarrhea Virus Vaccine
by Nguyen-Thanh Hoa, Haroon Afzal, Thu-Dung Doan, Asad Murtaza, Chia-Hung Yen and Yao-Chi Chung
Vet. Sci. 2025, 12(2), 181; https://doi.org/10.3390/vetsci12020181 - 18 Feb 2025
Viewed by 135
Abstract
The nuclear factor-kappa B (NF-κB) signaling pathway plays a crucial role in regulating immune responses in epithelial cells. In this study, we established a porcine epithelial NF-κB reporter cell line (PK15-KBR) as an in vitro platform to screen plant-based extracts for their potential [...] Read more.
The nuclear factor-kappa B (NF-κB) signaling pathway plays a crucial role in regulating immune responses in epithelial cells. In this study, we established a porcine epithelial NF-κB reporter cell line (PK15-KBR) as an in vitro platform to screen plant-based extracts for their potential use as vaccine adjuvants against porcine epidemic diarrhea virus (PEDV). The NF-κB inducers were further tested for toxicity assessments, either using CCK-8 assays or intramuscular injection in mice, finally followed by vaccination studies to evaluate their adjuvancy. Initial experiments confirmed that TNF-α effectively activated NF-κB signaling in PK15-KBR cells in a dose-dependent manner, validating the platform’s reliability at Z’ value of 0.68. Of the 224 testers, 3 candidates, including chamomile, mulberry and Boerhaavia diffusa, showed induction activity; however, only chamomile induced a dose-dependent response in PK15-KBR cells. As a proof of concept, chamomile, used as an adjuvant in oral vaccination, demonstrated significantly higher IgG levels at an early stage (day 14, p < 0.05) and enhanced IgA titers. These findings highlight the use of the PK15-KBR cell line in identifying mucosal adjuvants and position chamomile extract as a promising candidate for enhancing vaccine-induced immunity. Full article
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<p>The concept of PK-15 reporter cell line based on NF-κB activation screening. (<b>A</b>) Schematic of transfected plasmid pHAGE-NF-κB-luc-GFP (Plasmid #49343). (<b>B</b>) The workflow for the screening of plant extracts using NF-κB driven luciferase assay, toxicity, and immune efficacy analyses.</p>
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<p>Morphology and fluorescence percentages of PK15-KBR cells. (<b>A</b>) The morphology of PK-15 cells without transduction by lenti-NF-κB-luc-GFP was captured using light and fluorescence microscopes at 10× magnification. (<b>B</b>) The morphology of transduced PK-15 cells that were GFP-positive was captured using light and fluorescence microscopes at 10× magnification. (<b>C</b>) The morphology of the sorted GFP-positive cells was captured using light and fluorescence microscopes at 10× magnification. (<b>D</b>) The percentages of GFP-positive PK-15 cells were measured using flow cytometry analysis at different time points. *** indicates significant differences (<span class="html-italic">p</span> ≤ 0.001), ns indicates non-significant.</p>
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<p>NF-ᴋB quantification of transduced PK15-KBR cells after stimulation with a series of TNF-α concentrations. Dose–response analysis of NF-ᴋB activity was measured using luminescence production via Luciferase assay system. (<b>A</b>) The fold-change of NF-ᴋB activity in PK15-KBR cells exposed to varying concentrations of TNF-α (ng/mL). (<b>B</b>) The fold-change of NF-ᴋB activity in PK15-KBR cells exposed to different conditions (cell numbers, drug action time, and concentration of solvent control). (<b>C</b>) The fold-change of NF-ᴋB activity in PK15-KBR cells exposed to varying concentrations of TNF-α (ng/mL) with addition of 1% DMSO as solvent control. The statistical analysis used in this study is detailed in <a href="#sec2dot11-vetsci-12-00181" class="html-sec">Section 2.11</a>. Significant differences are as follows: <span class="html-italic">p</span> ≤ 0.05 (*), <span class="html-italic">p</span> ≤ 0.01 (**), <span class="html-italic">p</span> ≤ 0.001 (***).</p>
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<p>NF-ᴋB quantification of transduced PK15-KBR cells after stimulation with plant extracts. (<b>A</b>) The fold-change of NF-ᴋB activity in PK15-KBR cells exposed to plant extracts at a concentration of 10 μg/mL. DMSO (0.1%) was defined as solvent control and TNF-α (10 ng/mL as positive control. (<b>B</b>) The fold-change of NF-ᴋB activity in PK15-KBR cells exposed to varying concentrations of three extracts: chamomile, <span class="html-italic">Boerhaavia diffusa</span>, and mulberry. The statistical analysis used in this study is detailed in <a href="#sec2dot11-vetsci-12-00181" class="html-sec">Section 2.11</a>. Significant differences are as follows: <span class="html-italic">p</span> ≤ 0.05 (*), <span class="html-italic">p</span> ≤ 0.001 (***), ns (non-significant).</p>
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<p>Cytotoxicity assay. CCK-8 assays were conducted to measure the cytotoxicity effects of PEs in PK-15 cells. The statistical analysis used in this study is detailed in <a href="#sec2dot11-vetsci-12-00181" class="html-sec">Section 2.11</a>. Significant differences are as follows: <span class="html-italic">p</span> ≤ 0.05 (*), <span class="html-italic">p</span> ≤ 0.001 (***).</p>
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<p>Safety test of intramuscular injection in mice. (<b>A</b>) Experimental design for mice study. (<b>B</b>) Observation of the injection site 7 days after the injection of each group of vaccines. The point of arrow is the point of injection.</p>
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<p>Serum IgG antibody level in mice vaccinated with in-house inactivated PEDV and chamomile extracts. Indirect ELISA assays were conducted to measure serum antibody titer using in-house inactivated PEDV as the antigen. (<b>A</b>) Experimental schedule. (<b>B</b>) Serum IgG antibody level in mice intramuscularly injected with different doses of chamomile extracts: IM (0 mg/kg bw), IM 120 (6 mg/kg bw), IM 480 (24 mg/kg bw), and PBS as the control group. (<b>C</b>) Serum IgG antibody level in mice orally fed with different doses of chamomile extracts: OR (0 mg/kg bw), OR 120 (6 mg/kg bw), OR 480 (24 mg/kg bw), and PBS as the control group. The statistical analysis used in this study is detailed in <a href="#sec2dot11-vetsci-12-00181" class="html-sec">Section 2.11</a>. Significant differences are as follows: <span class="html-italic">p</span> ≤ 0.05 (*), <span class="html-italic">p</span> ≤ 0.01(**), <span class="html-italic">p</span> ≤ 0.001 (***), <span class="html-italic">p</span> ≤ 0.0001 (****) and ns (non-significant).</p>
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<p>Intestinal IgA antibody level in mice vaccinated with in-house inactivated PEDV and chamomile extracts. Indirect ELISA assays were conducted to measure IgA antibody titer using in-house inactivated PEDV as coating antigen. The statistical analysis used in this study is detailed in <a href="#sec2dot11-vetsci-12-00181" class="html-sec">Section 2.11</a>.</p>
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19 pages, 3698 KiB  
Article
Synthesis and Characterization of Memantine-Loaded Niosomes for Enhanced Alzheimer’s Disease Targeting
by Hasan Turkez, Sena Oner, Ozge Caglar Yıldırım, Mehmet Enes Arslan, Marilisa Pia Dimmito, Çigdem Yuce Kahraman, Lisa Marinelli, Erdal Sonmez, Özlem Kiki, Abdulgani Tatar, Ivana Cacciatore, Antonio Di Stefano and Adil Mardinoglu
Pharmaceutics 2025, 17(2), 267; https://doi.org/10.3390/pharmaceutics17020267 - 17 Feb 2025
Viewed by 195
Abstract
Background/Objectives: Over the past 25 years, numerous biological molecules, like recombinant lysosomal enzymes, neurotrophins, receptors, and therapeutic antibodies, have been tested in clinical trials for neurological diseases. However, achieving significant success in clinical applications has remained elusive. A primary challenge has been the [...] Read more.
Background/Objectives: Over the past 25 years, numerous biological molecules, like recombinant lysosomal enzymes, neurotrophins, receptors, and therapeutic antibodies, have been tested in clinical trials for neurological diseases. However, achieving significant success in clinical applications has remained elusive. A primary challenge has been the inability of these molecules to traverse the blood–brain barrier (BBB). Recognizing this hurdle, our study aimed to utilize niosomes as delivery vehicles, leveraging the “molecular Trojan horse” technology, to enhance the transport of molecules across the BBB. Methods: Previously synthesized memantine derivatives (MP1–4) were encapsulated into niosomes for improved BBB permeability, hypothesizing that this approach could minimize peripheral drug toxicity while ensuring targeted brain delivery. Using the human neuroblastoma (SH-SY5Y) cell line differentiated into neuron-like structures with retinoic acid and then exposed to amyloid beta 1–42 peptide, we established an in vitro Alzheimer’s disease (AD) model. In this model, the potential usability of MP1–4 was assessed through viability tests (MTT) and toxicological response analysis. The niosomes’ particle size and morphological structures were characterized using scanning electron microscopy (SEM), with their loading and release capacities determined via UV spectroscopy. Crucially, the ability of the niosomes to cross the BBB and their potential anti-Alzheimer efficacy were analyzed in an in vitro transwell system with endothelial cells. Results: The niosomal formulations demonstrated effective drug encapsulation (encapsulation efficiency: 85.3% ± 2.7%), controlled release (72 h release: 38.5% ± 1.2%), and stable morphology (PDI: 0.22 ± 0.03, zeta potential: −31.4 ± 1.5 mV). Among the derivatives, MP1, MP2, and MP4 exhibited significant neuroprotective effects, enhancing cell viability by approximately 40% (p < 0.05) in the presence of Aβ1-42 at a concentration of 47 µg/mL. The niosomal delivery system improved BBB permeability by 2.5-fold compared to free drug derivatives, as confirmed using an in vitro bEnd.3 cell model. Conclusions: Memantine-loaded niosomes provide a promising platform for overcoming BBB limitations and enhancing the therapeutic efficacy of Alzheimer’s disease treatments. This study highlights the potential of nanotechnology-based delivery systems in developing targeted therapies for neurodegenerative diseases. Further in vivo studies are warranted to validate these findings and explore clinical applications. Full article
(This article belongs to the Section Drug Delivery and Controlled Release)
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<p>Synthetic strategies to obtain memantine derivatives (<b>MP1–4</b>). Reagent and conditions: (<b>a</b>) valproic acid, TEA, and ethylchloroformate in dry THF/DMF, 3 h, rt; (<b>b</b>) phenylbutyric acid, TEA, and ethylchloroformate in dry THF/DMF, 3 h, rt; (<b>c</b>) butyric acid, TEA, and ethylchloroformate in dry THF/DMF, 3 h, rt; (<b>d</b>) caffeic acid, TEA, HOBt, and DCC in dry DMF, 15 h, rt.</p>
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<p>Schematic diagram summarizing in vitro BBB permeability analyses.</p>
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<p>Determination of cytotoxic properties of synthesized memantine derivatives (<b>MP1–4</b>) in cultured human fibroblast cells (HDFa) using MTT cell viability assay. Group analyses were performed with the one-way ANOVA procedure, and comparisons were made using Dunnett’s test (against the control).</p>
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<p>Analysis of the genotoxic properties of synthesized memantine derivatives (<b>MP1–4</b>) in cultured human fibroblast cells (HDFa) using Hoechst 33258 fluorescent staining of cell nuclei. (<b>A</b>) <b>MP1</b>, (<b>B</b>) <b>MP2</b>, (<b>C</b>), <b>MP3</b> and (<b>D</b>) <b>MP4</b>.</p>
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<p>Scanning electron microscope (SEM) image showing the surface topography and morphology of niosomes prepared by the thin film method.</p>
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<p>Drug release profile showing the release of <b>MP1–4</b> drugs from niosomal carriers prepared by the thin film hydration technique at certain time intervals for 24 h.</p>
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<p>Morphological cell structures of differentiated SH-SY5Y cells. (<b>A</b>) 20× resolution of undifferentiated cell cultures; (<b>B</b>) 20× resolution of differentiated cell cultures (application of 10 µM all-trans RA to cell culture for 11 days).</p>
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<p>Determination of the cytotoxic properties of <b>MP1–4</b> in the differentiated SH-SY5Y cell cultures resembling mature neurons using the MTT cell viability test. Group analyses were performed with the one-way ANOVA procedure, and comparisons were made using Dunnett’s test (against the control).</p>
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<p>Determination of the neuroprotective properties of <b>MP1–4</b> in an experimental AD model. Group analyses were performed with the one-way ANOVA procedure, and comparisons were made using Dunnett’s test (against the amyloid beta application). The level of significance was set at 5% (<span class="html-italic">p</span> &lt; 0.05). Significant differences compared to the control group are indicated by an asterisk (*).</p>
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<p>Neuroprotective properties of the <b>MP1–4</b> (47 µg/mL) on the experimental AD model for 24 h of application. Group analyses were performed with the one-way ANOVA procedure, and comparisons were made using Dunnett’s test (against the amyloid beta application). The level of significance was set at 5% (<span class="html-italic">p</span> &lt; 0.05). Significant differences compared to the control group are indicated by an asterisk (*).</p>
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<p>The neuroprotective effect of MP1–4 and the drug/carrier system on cell viability in the Alzheimer’s disease model using an in vitro BBB permeability test. Group analyses were performed with the one-way ANOVA procedure, and comparisons were made using Dunnett’s test (against the amyloid beta application). The level of significance was set at 5% (<span class="html-italic">p</span> &lt; 0.05). Significant differences compared to the control group are indicated by an asterisk (*).</p>
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21 pages, 5586 KiB  
Article
Enhanced Detection of Pipeline Leaks Based on Generalized Likelihood Ratio with Ensemble Learning
by Tao Liu, Xiuquan Cai, Wei Zhou, Kuitao Wang and Jinjiang Wang
Processes 2025, 13(2), 558; https://doi.org/10.3390/pr13020558 - 16 Feb 2025
Viewed by 267
Abstract
To address the challenges of insufficient model generalization, high false alarm rates due to the scarcity of leakage data, and frequent minor leakage alarms in traditional weak leakage (the leakage amount is less than 1%) detection methods for gas transmission pipelines, this paper [...] Read more.
To address the challenges of insufficient model generalization, high false alarm rates due to the scarcity of leakage data, and frequent minor leakage alarms in traditional weak leakage (the leakage amount is less than 1%) detection methods for gas transmission pipelines, this paper proposes a real-time weak leakage detection framework for natural gas pipelines based on the combination of the generalized likelihood ratio (GLR) and ensemble learning. Compared to traditional methods, the core innovations of this study include the following: (1) For the first time, GLR statistics are integrated with an ensemble learning strategy to construct a dynamic detection model for pipeline operating states through multi-sensor collaboration, significantly enhancing the model’s robustness in noisy environments by fusing pressure data from the pipeline inlet and outlet, as well as outlet flow data. (2) An adaptive threshold selection mechanism that dynamically optimizes alarm thresholds using the distribution characteristics of GLR statistics is designed, overcoming the sensitivity limitations of traditional fixed thresholds in complex operating conditions. (3) An ensemble decision module is developed based on a voting strategy, effectively reducing the high false alarm rates associated with single models. The model’s leakage detection capability under normal and noisy pipeline conditions was validated using a self-built gas pipeline leakage test platform. The results show that the proposed method can achieve the precise detection of pipeline leakage rates as small as 0.5% under normal and low-noise conditions while reducing the false alarm rate to zero. It can also detect leakage rates of 1.5% under strong noise interference. These findings validate its practical value in complex industrial scenarios. This study provides a high-sensitivity, low-false-alarm, intelligent solution for pipeline safety monitoring, which is particularly suitable for early warning of weak leaks in long-distance pipelines. Full article
(This article belongs to the Special Issue Progress in Design and Optimization of Fault Diagnosis Modelling)
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<p>Schematic diagram of ensemble learning.</p>
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<p>Framework of combined enhanced leakage warning method based on ensemble learning.</p>
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<p>Schematic diagram of time window selection.</p>
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<p>A schematic diagram of the threshold selection method based on the test statistic.</p>
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<p>Pipeline media leakage test rig.</p>
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<p>Schematic diagram of time window selection.</p>
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<p>Schematic diagram of inlet pressure threshold selection.</p>
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<p>Schematic diagram of outlet pressure threshold selection.</p>
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<p>Schematic diagram of outlet flow threshold selection.</p>
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<p>Schematic diagram of inlet pressure alarm.</p>
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<p>Schematic diagram of outlet pressure alarm.</p>
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<p>Schematic diagram of outlet flow alarm.</p>
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<p>Schematic diagram of ensemble learning alarm.</p>
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<p>Comparison of leakage detection of different models.</p>
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25 pages, 8224 KiB  
Article
Evaluating the Spatial and Temporal Transferability of Model Parameters of a Distributed Soil Conservation Service–Soil Moisture Antecedent–Simple Lag and Route Model for South Mediterranean Catchments
by Ahlem Gara, Khouloud Gader, Slaheddine Khlifi, Christophe Bouvier, Mohamed Ouessar, Marnik Vanclooster, Nadhir Al-Ansari, Salah El-Hendawy and Mohamed A. Mattar
Water 2025, 17(4), 569; https://doi.org/10.3390/w17040569 - 16 Feb 2025
Viewed by 196
Abstract
Accurately predicting the impacts of climate change on hydrological fluxes in ungauged basins continues to be a complex task. In this study, we investigated the transferability of the model parameters SCS-SMA-LR, available in the ATHYS platform, to simulate hydrological behavior within catchments of [...] Read more.
Accurately predicting the impacts of climate change on hydrological fluxes in ungauged basins continues to be a complex task. In this study, we investigated the transferability of the model parameters SCS-SMA-LR, available in the ATHYS platform, to simulate hydrological behavior within catchments of a large South Mediterranean transboundary basin, i.e., the Medjerda bordering Tunisia and Algeria, characterized by contrasting climatic and physiographic conditions. A robustness analysis was set up for donor and receptor catchments situated in the Medjerda catchment in Tunisia. The model was initially calibrated for two donor catchments, for the 127 km2 catchment of the Lakhmess watershed situated on the right bank and for the 362 km2 catchment of the Raghay watershed situated on the left bank of the Medjerda basin in Tunisia, using input data from 1990 to 1994. The model performance was evaluated through multiple accuracy criteria based on the Best Linear Unbiased Estimator (BLUE) for the automatic calibration to quantify the model simulation, proving its good performance. The temporal transferability was assessed by evaluating model performance, transferring the calibrated parameters for the two catchments as validation on data for 3-year periods outside the calibration domain to test the robustness of the model through a diachronic analysis from different decades, i.e., for the periods 1994–1997, 2001–2004, and 2014–2017, respectively. The spatial transferability was assessed by transferring the parameters calibrated on the donor catchments to be applied to the receptor catchments based on similarity and data availability. The model was upgraded to a greater catchment for data from 1994 to 2016 for the right bank, the Siliana Upstream catchment, and to the nearest catchment with a similar area for the data from 2008 to 2017 for the left bank of the Medjerda basin, the Bouheurtma catchment. The capacity of the soil reservoir and the flow velocity parameters proved to have an important impact on the modeling implementations at, respectively, 123.03 mm and 1 m/s for Raghay, and 95.05 mm and 2.5 m/s for Lakhmes. The results show that the space–time transfer process of model parameters produces an acceptable simulation of flow volumes and timing. The proposed methodology proved to be a successful way to monitor ungauged catchments and strengthens the robustness of the SCS-SMA-LR model for hydrological modeling and impact studies in ungauged basins of the Southern Mediterranean region. Full article
(This article belongs to the Section Hydrology)
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<p>Map showing the location of the Raghay watershed (1) (situated at the left bank of the Medjerda River), associated with the transferred Bouheurtma catchment (2), and the Lakhmess catchment (3) (situated at the right bank of the Medjerda River) with the associated greater catchment: Siliana Upstream (4).</p>
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<p>The processes of the SCS-SMA runoff model (<b>A</b>) [<a href="#B32-water-17-00569" class="html-bibr">32</a>] and the simple LR Model (<b>B</b>). (<a href="http://www.athys-soft.org" target="_blank">www.athys-soft.org</a>, accessed on 2 February 2024).</p>
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<p>The overall transferability evaluation methodology.</p>
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<p>Scatter plot and timeline presentation of the calibration on the period 1990–1994 for the donor catchments using daily discharge: (<b>A1</b>) the scatter plot of the observed versus simulated daily discharge in the Raghay catchment; (<b>A2</b>) the comparison between the simulated and observed continuous timeline discharge in the Raghay catchment; (<b>B1</b>) the scatter plot of the observed versus simulated daily discharge in the Lakhmess catchment; (<b>B2</b>) the comparison between the simulated and observed continuous timeline discharge in the Lakhmess catchment.</p>
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<p>The scatter plot of the observed versus simulated daily discharge in the two donor catchments for the temporal transferability assessment. The left part of the figure concerns the Raghay catchment, and the right part concerns the Lakhmess catchment. Diachronic analysis is shown for three time intervals: 1994–1997, 2001–2004, and 2014–2017.</p>
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<p>The FITEVAL results for the Bouheurtma catchment (2008–2017).</p>
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<p>The FITEVAL results for the Siliana Upstream catchment (1994–2016).</p>
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<p>Clustered heat map of the accuracy criteria for the spatial and temporal transferability process within the Medjerda catchment.</p>
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<p>The cumulative observed and simulated discharge illustrating the temporal transferability process for the Medjerda catchment (the Lakhmess catchment (upper part of the figure) and the Raghay catchment (lower part of the figure)).</p>
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20 pages, 7145 KiB  
Article
AERQ—A Web-Based Decision Support Tool for Air Quality Assessment
by Pierluigi Cau, Davide Muroni, Guido Satta, Carlo Milesi and Carlino Casari
Appl. Sci. 2025, 15(4), 2045; https://doi.org/10.3390/app15042045 - 15 Feb 2025
Viewed by 379
Abstract
Technological advancements in low-cost devices, the Internet of Things (IoT), numerical models, big data infrastructures, and high-performance computing are revolutionizing urban management, particularly air quality governance. This study examines the application of smart technologies to address urban air quality challenges using integrated sensor [...] Read more.
Technological advancements in low-cost devices, the Internet of Things (IoT), numerical models, big data infrastructures, and high-performance computing are revolutionizing urban management, particularly air quality governance. This study examines the application of smart technologies to address urban air quality challenges using integrated sensor networks and predictive models. The decision support system (DSS), AERQ, incorporates the AERMOD modeling tool, achieving a 10 m spatial and 1 h temporal resolution for air quality predictions. It processes hourly climate and traffic data via a high-performance computing (HPC) platform, significantly enhancing prediction accuracy and decision-making efficiency. AERMOD has been calibrated and validated for NO2, showing a good performance against observations. Tested in Cagliari, Sardinia, Italy, AERQ demonstrated a 99% reduction in computation time compared to modern desktop systems, delivering detailed 5-year scenarios in under 15 h. AERQ equips stakeholders with air quality indices, scenario analyses, and mitigation strategies, combining advanced visualization tools with actionable insights. By enabling data-driven decisions, the system empowers policymakers, urban planners, and citizens to improve air quality and public health. This study underscores the transformative potential of integrating advanced technologies into urban management, providing a scalable model for efficient, informed, and responsive air quality governance. Full article
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<p>This shows (<b>a</b>) the main roads included in the model, color-coded based on the hourly average number of circulating vehicles (treated as linear pollution sources), (<b>b</b>) the categories of vehicles (e.g., motorcycles, trucks, cars) operating in Cagliari, and (<b>c</b>) the types of vehicle emissions (e.g., Euro 0, Euro 1, etc.). The base map is based on OpenStreetMap, displaying its default names and symbols, with streets and squares labeled in Italian.</p>
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<p>The average hourly distribution throughout the day for March and April 2019. The measured data exhibit a regular daily cycle with two peaks and two minima (average: 25.84; standard deviation: 14.78). The high standard deviation indicates significant variability within the sample. The black line represents the measured NO<sub>2</sub> values, the blue line indicates the best run, and the red dotted line corresponds to the first run.</p>
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<p>The AERQ platform integrates robust hardware and software components designed for advanced air quality analysis. Its physical infrastructure consists of a web server for user access, a high-performance computing (HPC) cluster for executing computationally intensive tasks, and a data warehouse that securely stores large datasets, including environmental, meteorological, and traffic data. The platform’s processing stack leverages the HPC environment to efficiently access and process these datasets, enabling the simulation and analysis of complex air quality scenarios. This setup allows for rapid data handling and high-resolution modeling, supporting both real-time and historical scenario execution and analysis. The platform accommodates two types of users with different access privileges. Only authorized users can utilize the job-on-demand interface to prevent unintentional resource wastage or disruption to other users’ tasks. Public users, like citizens, can access the platform to view pre-run scenarios and reports.</p>
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<p>The job-on-demand interface facilitates the design and execution of scenarios of interest. In the figure, the user can control the number of vehicles (Parco auto), distinguishing between short vehicles (leggeri) such as passenger cars, and motorcycles and long vehicles (pesanti) such as trucks, and buses for both working days (Feriali) and holidays (Festivi). Emission loads are then calculated by combining this traffic scenario with the calibrated emission coefficients for the selected parameters (Parametri). Once completed, the scenarios appear in the catalog.</p>
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<p>AERQ entry point.</p>
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<p>Air quality result interface: The split-view option enables the side-by-side comparison of Aermod output maps. Displayed here is the average spatial distribution of NO<sub>2</sub> at 7 pm in January (left) and June (right) 2019, as computed by Aermod. The differences between the two maps reflect seasonal changes in meteorological and traffic conditions. In both months, the prevailing Mistral wind directs pollutant plumes along its path. In June, only a few hot spots exceeded the hourly mean of 40 µg/m³, mainly concentrated at major road intersections. The base map displays names and symbols, with streets and squares labeled in Italian.</p>
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<p>Air quality comparison. The top panel displays the NO<sub>2</sub> concentration map for the AVG scenario in January 2019. In the bottom panel, after selecting a point on the map, the average hourly NO<sub>2</sub> concentrations throughout the day are compared across three scenarios (AVG, MIN, MAX) with measured values from the nearest monitoring station shown as a placeholder (in this case, the CENCA1 located on the left part of the map). In the AVG scenario, AERMOD input (NO<sub>2</sub> emissions) is calculated hourly by combining emission factors with the average vehicle fleet for each road in Cagliari. In the MIN scenario, the input (emission loads) is based on the average vehicle count minus its standard deviation, while the MAX scenario represents the average vehicle count plus the standard deviation, applied to each road and hour. The pink areas highlight Saturdays and Sundays.</p>
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<p>Concentrations by wind direction: This figure presents pollutant concentrations under the three primary wind directions, along with no-wind conditions, for spring 2019. Under strong wind conditions, pollution hot spots appear primarily at major road intersections, where vehicles tend to decelerate or idle, intensifying pollution peaks. In these scenarios, pollutant plumes follow the wind direction. Conversely, pollutants are not dispersed effectively during low-wind conditions and tend to accumulate, lingering within the city and leading to higher pollution levels overall.</p>
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20 pages, 21655 KiB  
Article
Fracture Mechanical Properties of Double-Edge Cracked Flattened Brazilian Disc Samples Under Compressive Loads
by Wen Hua, Wenyu Zhang, Shiming Dong, Jianxiong Li, Jiuzhou Huang, Ping Luo and Zhanyuan Zhu
Materials 2025, 18(4), 850; https://doi.org/10.3390/ma18040850 - 15 Feb 2025
Viewed by 174
Abstract
The shear-based fracturing of deep fractured rocks under compression-shear loading is one of the most prevalent failure modes due to the existence of in situ stress. In order to study the shear fracture mechanical properties of fractured rocks, a double-edge cracked flattened Brazilian [...] Read more.
The shear-based fracturing of deep fractured rocks under compression-shear loading is one of the most prevalent failure modes due to the existence of in situ stress. In order to study the shear fracture mechanical properties of fractured rocks, a double-edge cracked flattened Brazilian disc (DCFBD) sample was developed by introducing two platforms into a double-edge cracked Brazilian disc (DCBD). Extensive finite element analyses were conducted on DCFBD samples to determine the stress intensity factors (SIFs) and T-stress. A comprehensive dataset of SIFs and T-stress was obtained, which provided accurate descriptions of the compression-shear fracture tests performed on this specimen. Furthermore, the effects of the load distribution angle γ, dimensionless crack length α, and crack inclination angle θ on dimensionless SIFs YI, YII, and T-stress T* were discussed. It showed that the effect of load distribution angle γ on the dimensionless SIFs YI and YII can be disregarded when the dimensionless crack length α ≥ 0.60 and load distribution angle γ ≤ 20°. However, it should be considered for the T-stress for larger crack inclination angles. Moreover, it was experimentally validated that the DCFBD samples with appropriate crack lengths and load distribution angles can achieve shear (true mode II) fracture, as demonstrated through a series of fracture tests conducted on these specimens. The results will advance the development of rock shear fracture testing technology. Full article
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<p>Schematic diagram of fracture mode of fractured rocks under compression-shear loading [<a href="#B24-materials-18-00850" class="html-bibr">24</a>]. (<b>a</b>) Tensile-based fracture; (<b>b</b>) Shear-based fracture.</p>
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<p>Shear-based (true mode II) fracture samples under compression-shear loading. (<b>a</b>) DST sample, (<b>b</b>) PTS sample, (<b>c</b>) SBT sample, (<b>d</b>) DCBD sample.</p>
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<p>Schematic diagram of DCFBD sample under uniform distribution pressure.</p>
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<p>A representative finite element model of the DCFBD sample.</p>
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<p>Values of <span class="html-italic">Y</span><sub>I</sub> in the DCFBD samples: (<b>a</b>) <span class="html-italic">γ</span> = 5°, (<b>b</b>) <span class="html-italic">γ</span> = 10°, (<b>c</b>) <span class="html-italic">γ</span> = 15°, (<b>d</b>) <span class="html-italic">γ</span> = 20°.</p>
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<p>Values of <span class="html-italic">Y</span><sub>I</sub> in the DCFBD samples: (<b>a</b>) <span class="html-italic">γ</span> = 5°, (<b>b</b>) <span class="html-italic">γ</span> = 10°, (<b>c</b>) <span class="html-italic">γ</span> = 15°, (<b>d</b>) <span class="html-italic">γ</span> = 20°.</p>
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<p>Values of <span class="html-italic">Y</span><sub>I</sub> in the DCFBD samples: (<b>a</b>) <span class="html-italic">α</span> = 0.40, (<b>b</b>) <span class="html-italic">α</span> = 0.6, (<b>c</b>) <span class="html-italic">α</span> = 0.80, (<b>d</b>) <span class="html-italic">θ</span> = 15°, (<b>e</b>) <span class="html-italic">θ</span> = 30°, (<b>f</b>) <span class="html-italic">θ</span> = 45°.</p>
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<p>Absolute values of <span class="html-italic">Y</span><sub>II</sub> in the DCFBD samples: (<b>a</b>) <span class="html-italic">γ =</span> 5°, (<b>b</b>) <span class="html-italic">γ =</span> 10°, (<b>c</b>) <span class="html-italic">γ =</span> 15°, (<b>d</b>) <span class="html-italic">γ =</span> 20°.</p>
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<p>Absolute values of <span class="html-italic">Y</span><sub>II</sub> in the DCFBD samples: (<b>a</b>) <span class="html-italic">α</span> = 0.40, (<b>b</b>) <span class="html-italic">α</span> = 0.6, (<b>c</b>) <span class="html-italic">α</span> = 0.80, (<b>d</b>) <span class="html-italic">θ</span> = 15°, (<b>e</b>) <span class="html-italic">θ</span> = 30°, (<b>f</b>) <span class="html-italic">θ</span> = 45°.</p>
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<p>Dimensionless T-stress <span class="html-italic">T</span>* of the DCFBD samples: (<b>a</b>) <span class="html-italic">γ</span> = 5°, (<b>b</b>) <span class="html-italic">γ</span> = 10°, (<b>c</b>) <span class="html-italic">γ</span> = 15°, (<b>d</b>) <span class="html-italic">γ</span> = 20°.</p>
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<p>Dimensionless T-stress <span class="html-italic">T</span>* of the DCFBD samples: (<b>a</b>) <span class="html-italic">α</span> = 0.40, (<b>b</b>) <span class="html-italic">α</span> = 0.6, (<b>c</b>) <span class="html-italic">α</span> = 0.80, (<b>d</b>) <span class="html-italic">θ</span> = 15°, (<b>e</b>) <span class="html-italic">θ</span> = 30°, (<b>f</b>) <span class="html-italic">θ</span> = 45°.</p>
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<p>The representative loading diagram of DCFBD samples under compression.</p>
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<p>Fracture forms of DCFBD samples with different loading angles and crack lengths. (<b>a</b>) <span class="html-italic">α</span> = 0.80, <span class="html-italic">θ</span> = <span class="html-italic">γ</span> = 10°; (<b>b</b>) <span class="html-italic">α</span> = 0.80, <span class="html-italic">θ</span> = <span class="html-italic">γ</span> = 15°; (<b>c</b>) <span class="html-italic">α</span> = 0.80, <span class="html-italic">θ</span> = <span class="html-italic">γ</span> = 20°; (<b>d</b>) <span class="html-italic">α</span> = 0.80, <span class="html-italic">θ</span> = <span class="html-italic">γ</span> = 25°; (<b>e</b>) <span class="html-italic">α</span> = 0.70, <span class="html-italic">θ</span> = <span class="html-italic">γ</span> = 10°; (<b>f</b>) <span class="html-italic">α</span> = 0.70, <span class="html-italic">θ</span> = <span class="html-italic">γ</span> = 15°; (<b>g</b>) <span class="html-italic">α</span> = 0.70, <span class="html-italic">θ</span> = <span class="html-italic">γ</span> = 20°; (<b>h</b>) <span class="html-italic">α</span> = 0.70, <span class="html-italic">θ</span> = <span class="html-italic">γ</span> = 25°; (<b>i</b>) <span class="html-italic">α</span> = 0.60, <span class="html-italic">θ</span> = <span class="html-italic">γ</span> = 10°; (<b>j</b>) <span class="html-italic">α</span> = 0.60, <span class="html-italic">θ</span> = <span class="html-italic">γ</span> = 15°; (<b>k</b>) <span class="html-italic">α</span> = 0.60, <span class="html-italic">θ</span> = <span class="html-italic">γ</span> = 20°; (<b>l</b>) <span class="html-italic">α</span> = 0.60, <span class="html-italic">θ</span> = <span class="html-italic">γ</span> = 25°.</p>
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<p>Typical load–displacement curves for the shear fractured DCFBD samples.</p>
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<p>Average tested values of DCFBD specimens: (<b>a</b>) peak load <span class="html-italic">P</span>, (<b>b</b>) true mode II fracture toughness <span class="html-italic">K</span><sub>IIC</sub>.</p>
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<p>The SCB sample for determining mode I fracture toughness.</p>
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12 pages, 12642 KiB  
Brief Report
Immunogenic Cell Death Inducers in Cancer Immunotherapy to Turn Cold Tumors into Hot Tumors
by Valeria Lucarini, Ombretta Melaiu, Paula Gragera, Kamila Król, Valentina Scaldaferri, Verena Damiani, Adele De Ninno, Daniela Nardozi, Luca Businaro, Laura Masuelli, Roberto Bei, Loredana Cifaldi and Doriana Fruci
Int. J. Mol. Sci. 2025, 26(4), 1613; https://doi.org/10.3390/ijms26041613 - 14 Feb 2025
Viewed by 352
Abstract
The combination of chemotherapeutic agents with immune checkpoint inhibitors (ICIs) has revolutionized cancer treatment. However, its success is often limited by insufficient immune priming in certain tumors, including pediatric malignancies. In this report, we explore clinical trials currently investigating the use of immunogenic [...] Read more.
The combination of chemotherapeutic agents with immune checkpoint inhibitors (ICIs) has revolutionized cancer treatment. However, its success is often limited by insufficient immune priming in certain tumors, including pediatric malignancies. In this report, we explore clinical trials currently investigating the use of immunogenic cell death (ICD)-inducing chemotherapies in combination with ICIs for both adult and pediatric cancers. Given the limited clinical data available for pediatric tumors, we focused on recent preclinical studies evaluating the efficacy of these combinations in neuroblastoma (NB). Finally, to address this gap, we propose an innovative strategy to assess the impact of ICD-inducing chemotherapies on antitumor immune responses in NB. Using tumor spheroids derived from a transgenic NB mouse model, we validated our previous in vivo findings concerning how anthracyclines, specifically mitoxantrone and doxorubicin, significantly enhance MHC class I surface expression, stimulate IFNγ and granzyme B production by CD8+ T cells and NK cells, and promote immune cell recruitment. Importantly, these anthracyclines also upregulated PD-L1 expression on NB spheroids. This screening platform yielded results similar to in vivo findings, demonstrating that mitoxantrone and doxorubicin are the most potent immunomodulatory agents for NB. These data suggest that the creation of libraries of ICD inducers to be tested on tumor spheroids could reduce the number of combinations to be tested in vivo, in line with the principles of the 3Rs. Furthermore, these results highlight the potential of chemo-immunotherapy regimens to counteract the immunosuppressive tumor microenvironment in NB, paving the way for improved therapeutic strategies in pediatric cancers. They provide compelling evidence to support further clinical investigations of these combinations to enhance outcomes for children with malignancies. Full article
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<p>Chemotherapeutic drugs promote the recruitment and activation of CD8<sup>+</sup> T cells and NK cells in co-cultures of NB spheroids and syngeneic splenocytes. (<b>A</b>) Experimental scheme. NB cells were seeded in ULA plates to form spheroids. The 4-day-old NB spheroids were either treated with the indicated compounds at different concentrations while monitoring their diameter over the next 96 hours or treated for 1 day, and then, after drug removal, were cultured with syngeneic splenocytes in ULA plates or a microfluidic device. (<b>B</b>) Time–course and dose–response curves of drug-treated 9464D and 975A2 NB spheroids. Spheroid’s diameter was evaluated from 0 to 96 hours. Each color corresponds to a tested concentration (e.g., red for 0.5 µM, green for 1 µM, etc.). Spheroid diameter was analyzed using ImageJ software v1.54j, NIH Image, NIH, Bethesda, MD, USA). Data are the mean ± SEM of 3 independent experiments in triplicate. (<b>C</b>,<b>D</b>) Representative flow cytometric analyses of MHC class I (<b>C</b>) and PD-L1 (<b>D</b>) cell surface expression in NB spheroids treated with the indicated drugs for 24 hours. The graphs represent the MFI ± SD of three independent experiments. Significance levels for comparison between samples were determined by two-tailed Student’s <span class="html-italic">t</span> test. (<b>E</b>) Flow cytometric analysis of IFNγ and granzyme B expression of CD8<sup>+</sup> T cells and NK cells from splenocytes co-cultured with drug-treated NB spheroids for 24 hours. Significance levels for comparison between samples were determined by ANOVA. (<b>F</b>) Representative images of migration in microfluidic devices of red-labeled splenocytes recruited from drug-treated and untreated NB spheroids after 24 hours of co-culture (<b>left</b>). The number of splenocytes migrating toward treated and untreated NB spheroids is assessed using ImageJ software v1.54j, NIH Image, NIH, Bethesda, MD, USA). Data are shown as fold change ± SD (<b>right</b>). Significance levels for comparison between samples were determined by Student’s <span class="html-italic">t</span>-test. CTR, control; CDDP, cisplatin; DX, doxorubicin; IRI, irinotecan; MAFO, mafosfamide; MTX, mitoxantrone; OXP, oxaliplatin; TOPO, topotecan; VINC, vincristine; GZMB, granzyme B; IFNγ, interferon gamma.</p>
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19 pages, 10300 KiB  
Article
Research on Simulation Analysis and Joint Diagnosis Algorithm of Transformer Core-Loosening Faults Based on Vibration Characteristics
by Chen Cao, Zheng Li, Jialin Wang, Jiayu Zhang, Ying Li and Qingli Wang
Energies 2025, 18(4), 914; https://doi.org/10.3390/en18040914 - 13 Feb 2025
Viewed by 422
Abstract
The existing methods for transformer core-loosening fault diagnosis primarily focus on fundamental frequency analysis, neglecting higher-frequency components, which limits early detection accuracy. This study proposes a comprehensive approach integrating full-band vibration analysis, including high-order harmonics, to enhance diagnostic precision. A theoretical model coupling [...] Read more.
The existing methods for transformer core-loosening fault diagnosis primarily focus on fundamental frequency analysis, neglecting higher-frequency components, which limits early detection accuracy. This study proposes a comprehensive approach integrating full-band vibration analysis, including high-order harmonics, to enhance diagnostic precision. A theoretical model coupling magnetostriction and thermodynamics was developed, combined with empirical mode decomposition (EMD) and Pearson’s correlation coefficient for fault characterization. A 10 kV transformer core vibration test platform was constructed, capturing signals under normal, partially loose, and completely loose states. The simulation results aligned with the experimental data, showing vibration accelerations of 0.01 m/s2 (Phase A) and 0.023 m/s2 (Phase B). A multi-physics coupling model incorporating Young’s modulus variations simulated core loosening, revealing increased high-frequency components (up to 1000 Hz) and vibration amplitudes (0.2757 m/s2 for complete loosening). The joint EMD–Pearson method quantified fault severity, yielding correlation values of 0.0007 (normal), 0.0044 (partial loosening), and 0.0116 (complete loosening), demonstrating a clear positive correlation with fault progression. Experimental validation confirmed the model’s reliability, with the simulations matching the test results. This approach addresses the limitations of traditional methods by incorporating high-frequency analysis and multi-physics modeling, significantly improving early fault detection accuracy and providing a quantifiable diagnostic framework for transformer core health monitoring. Full article
(This article belongs to the Special Issue Design and Optimization of Power Transformer Diagnostics: 3rd Edition)
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<p>Three-dimensional view of the transformer.</p>
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<p>A simplified transformer model.</p>
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<p>Transformer mesh profiling model.</p>
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<p>Low-side three-phase power frequency voltage.</p>
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<p>Flux density distribution of core.</p>
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<p>The diagram of point selection.</p>
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<p>Vibration diagrams of acceleration at various points of the transformer: (<b>a</b>) time-domain plot of vibrational acceleration in three directions at point A; (<b>b</b>) frequency-domain plot of vibrational acceleration in three directions at point A; (<b>c</b>) time-domain plot of vibrational acceleration in three directions at point B; (<b>d</b>) frequency-domain plot of vibrational acceleration in three directions at point B; (<b>e</b>) time-domain plot of vibrational acceleration in three directions at point C; and (<b>f</b>) frequency-domain plot of vibrational acceleration in three directions at point C.</p>
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<p>Distribution of experimental measurement points.</p>
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<p>Phase A top vibration acceleration of the core.</p>
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<p>Phase B top vibration acceleration of the core.</p>
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<p>Phase A and C top frequency histogram.</p>
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<p>Frequency-domain diagram of the transformer core: (<b>a</b>) phase A of the transformer core and (<b>b</b>) phase C of the transformer core.</p>
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<p>Time-domain comparison between simulation results and test results: (<b>a</b>) comparison of transformer phase A simulation results and test results and (<b>b</b>) comparison of transformer phase B simulation results and test results.</p>
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<p>Schematic diagram of transformer core loosening: (<b>a</b>) complete loosening of transformer core and (<b>b</b>) partial loosening of transformer core.</p>
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<p>Time-domain diagram of normal core.</p>
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<p>Time-domain diagram of partially loosened core.</p>
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<p>Time-domain diagram of completely loosened core.</p>
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<p>Spectrum of different loosening states.</p>
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<p>EMD decomposition results for different loosening states of the transformer core: (<b>a</b>) empirical mode decomposition diagram of normalcy; (<b>b</b>) empirical mode decomposition diagram of partial loosening; and (<b>c</b>) empirical mode decomposition diagram of complete loosening.</p>
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44 pages, 12626 KiB  
Article
Hyperspectral Image Segmentation for Optimal Satellite Operations: In-Orbit Deployment of 1D-CNN
by Jon Alvarez Justo, Dennis D. Langer, Simen Berg, Jens Nieke, Radu Tudor Ionescu, Per Gunnar Kjeldsberg and Tor Arne Johansen
Remote Sens. 2025, 17(4), 642; https://doi.org/10.3390/rs17040642 - 13 Feb 2025
Viewed by 308
Abstract
AI on spaceborne platforms optimizes operations and increases automation, crucial for satellites with limited downlink capacity. It can ensure that only valuable information is transmitted, minimizing resources spent on unnecessary data, which is especially important in hyperspectral Earth Observation missions, producing large data [...] Read more.
AI on spaceborne platforms optimizes operations and increases automation, crucial for satellites with limited downlink capacity. It can ensure that only valuable information is transmitted, minimizing resources spent on unnecessary data, which is especially important in hyperspectral Earth Observation missions, producing large data volumes. Our previous work showed that the 1D-CNN, 1D-Justo-LiuNet, outperformed 2D-CNNs and Vision Transformers for hyperspectral segmentation with an accuracy of 0.93 and 4563 parameters, making our model the best choice for in-orbit deployment. While the state of the art has deployed 1D-CNNs on low-power platforms, such as Unmanned Aerial Vehicles, they have still not been deployed in space before. In this work, we mark the first deployment and testing of a 1D-CNN in a satellite. We implement a C version of the 1D-Justo-LiuNet and, after ground validation, we deploy it on board the HYPSO-1 satellite. We demonstrate in-flight segmentation of hyperspectral images via the 1D-CNN to classify pixels into sea, land, and cloud categories. We show how in-orbit segmentation improves satellite operations, increases automation, and optimizes downlink. We give examples of how in-orbit segmentation addresses mission challenges in HYPSO-1, such as incomplete data reception, incorrect satellite pointing, and cloud cover, helping to decide whether to transmit or discard data on board. An additional CNN autonomously interprets the segmented images, enabling on-board decisions on data downlink. Full article
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<p>HYPSO-1 system architecture general pipeline.</p>
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<p>Architecture of <span class="html-italic">1D-Justo-LiuNet</span> for feature extraction and classification proposed in our previous work in [<a href="#B39-remotesensing-17-00642" class="html-bibr">39</a>].</p>
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<p>Sliding process with stride <math display="inline"><semantics> <mrow> <mi>S</mi> <mo>=</mo> <mn>1</mn> </mrow> </semantics></math> over <math display="inline"><semantics> <mrow> <mi>x</mi> <mo>[</mo> <mi>λ</mi> <mo>]</mo> </mrow> </semantics></math>.</p>
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<p>Flow diagram of operations in the convolution layer (Implementation 1).</p>
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<p>Flow diagram of operations in the convolution layer (Implementation 2).</p>
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<p>Venice, Italy, Europe, on 22 June 2024 at 09:44 UTC+00. Coordinates: 45.3° latitude and 12.5° longitude. Solar zenith angle: 28.7°; exposure time: 35 ms. (<b>a</b>) Planned geographical area. (<b>b</b>) Segmented image in orbit. (<b>c</b>) RGB composite from cube.</p>
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<p>Venice, Italy, Europe, on 22 June 2024 at 09:44 UTC-retransmitted. (<b>a</b>) RGB composite from cube. (<b>b</b>) Segmented image overlaid.</p>
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<p>Trondheim, Norway, Europe, on 17 May 2024 at 10:54 UTC. Coordinates: 63.6° latitude and 9.84° longitude. Solar zenith angle: 44.9°; exposure time: 50 ms. (<b>a</b>) Planned geographical area. (<b>b</b>) Segmented image in orbit. (<b>c</b>) RGB composite from cube.</p>
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<p>Namib desert close to Gobabeb, Namibia, Africa, on 25 June 2024 at 08:51 UTC. Coordinates: −23.6° latitude and 15.0° longitude. Exposure time: 20 ms. (<b>a</b>) Planned geographical area. (<b>b</b>) Segmented image in orbit. (<b>c</b>) RGB composite from cube.</p>
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<p>Grad-CAM explanations for classification of segmented images. (<b>a</b>) Segmented image (<span class="html-italic">no mispointing</span>). (<b>b</b>) Grad-CAM explanation. (<b>c</b>) Segmented image (<span class="html-italic">mispointing</span>). (<b>d</b>) Grad-CAM explanation.</p>
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<p>Bermuda Archipelago, British Overseas, Atlantic Ocean, on 16 July 2024 at 14:27 UTC. Coordinates: 32.4° latitude and −64.8° longitude. Solar zenith angle: 32.6°; exposure time: 30 ms. (<b>a</b>) Planned geographical area. (<b>b</b>) Segmented image in orbit. (<b>c</b>) RGB composite from cube.</p>
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<p>Dahlak Archipelago, Eritrea, Africa, on 16 June 2024 at 07:28 UTC. Coordinates: 16.0° latitude and 40.4° longitude. Solar zenith angle: 16.0°; exposure time: 25 ms. (<b>a</b>) Planned geographical area. (<b>b</b>) Segmented image in orbit. (<b>c</b>) RGB composite from cube.</p>
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<p>Aegean Archipelago, Greece, Europe, on 2 May 2024 at 08:44 UTC. Coordinates: 38.5° latitude and 25.2° longitude. Solar zenith angle: 39.0°; exposure time: 30 ms. (<b>a</b>) Planned geographical area. (<b>b</b>) Segmented image in orbit. (<b>c</b>) RGB composite from cube.</p>
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<p>Abu Dhabi and Dubai, United Arab Emirates, Asia, on 9 May 2024 at 06:12 UTC. Coordinates: 25.3° latitude and 54.7° longitude. Solar zenith angle: 29.5°; exposure time: 40 ms. (<b>a</b>) Planned geographical area. (<b>b</b>) Segmented image in orbit. (<b>c</b>) RGB composite from cube.</p>
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<p>Abu Dhabi and Dubai, United Arab Emirates, Asia, on 27 June 2024 at 06:17 UTC. Coordinates: 25.1° latitude and 55.0° longitude. Solar zenith angle: 28.9°; exposure time: 40 ms. (<b>a</b>) Segmented image in orbit. (<b>b</b>) RGB composite from cube.</p>
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<p>Namib desert close to Gobabeb, Namibia, Africa, on 13 June 2024 at 08:49 UTC. Coordinates: −23.6° latitude and 15.0° longitude. Solar zenith angle: 56.8°; exposure time: 20 ms. (<b>a</b>) Planned geographical area. (<b>b</b>) Segmented image in orbit. (<b>c</b>) RGB composite from cube.</p>
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<p>Mojave Desert, USA, North America, on 28 May 2024 at 17:52 UTC. Coordinates: 38.7° latitude and −116.1° longitude. Solar zenith angle: 28.9°; exposure time: 20 ms. (<b>a</b>) Planned geographical area. (<b>b</b>) Segmented image in orbit. (<b>c</b>) RGB composite from cube.</p>
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<p>Lake Assal near Gulf of Tadjoura and the Red Sea, Djibouti, Africa, on 28 May 2024 at 06:57 UTC. Coordinates: 11.6° latitude and 42.8° longitude. Solar zenith angle: 32.6°; exposure time: 20 ms. (<b>a</b>) Planned geographical area. (<b>b</b>) Segmented image in orbit. (<b>c</b>) RGB composite from cube.</p>
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<p>Cape Town, South Africa, Africa, on 13 April 2024 at 08:06 UTC. Coordinates: −34.3° latitude and 18.2° longitude. Solar zenith angle: 58.1°; exposure time: 30 ms. (<b>a</b>) Planned geographical area. (<b>b</b>) Segmented image in orbit. (<b>c</b>) RGB composite from cube.</p>
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<p>Vancouver Island, Canada, North America, on 13 July 2024 at 18:43 UTC. Coordinates: 50.4° latitude and −126.0° longitude. Solar zenith angle: 35.2°; exposure time: 30 ms. (<b>a</b>) Planned geographical area. (<b>b</b>) Segmented image in orbit. (<b>c</b>) RGB composite from cube.</p>
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<p>Caspian Sea, Asia, on 7 July 2024 at 06:58 UTC. Coordinates: 46.2° latitude and 50.4° longitude. Solar zenith angle: 31.4°; exposure time: 30 ms. (<b>a</b>) Planned geographical area. (<b>b</b>) image in orbit. (<b>c</b>) RGB composite from cube.</p>
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<p>New Orleans (Gulf of Mexico), USA, North America, on 14 June 2024 at 16:04 UTC. Coordinates: 30.6° latitude and −89.4° longitude. Solar zenith angle: 25.8°; exposure time: 30 ms. (<b>a</b>) Planned geographical area. (<b>b</b>) Segmented image in orbit. (<b>c</b>) RGB composite from cube.</p>
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<p>Trondheim, Norway, Europe, on 26 April 2024 at 10:49 UTC. Coordinates: 64.3° latitude and 9.42° longitude. Solar zenith angle: 50.5°; exposure time: 40 ms. (<b>a</b>) Planned geographical area. (<b>b</b>) Segmented image in orbit. (<b>c</b>) RGB composite from cube.</p>
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<p>Long Island - New York, USA, North America, on 16 June 2024 at 15:14 UTC. Coordinates: 41.3° latitude and −73.4° longitude. Solar zenith angle: 27.1°; exposure time: 35 ms. (<b>a</b>) Planned geographical area. (<b>b</b>) Segmented image in orbit. (<b>c</b>) RGB composite from cube.</p>
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<p>Alaska, USA, North America, on 15 April 2024 at 21:08 UTC. Coordinates: 61.3° latitude and −147.1° longitude. Solar zenith angle: 51.1°; exposure time: 25 ms. (<b>a</b>) Planned geographical area. (<b>b</b>) Segmented image in orbit. (<b>c</b>) RGB composite from cube.</p>
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<p>Svalbard, Norway, Europe, on 3 May 2024 at 19:07 UTC. Coordinates: 78.2° latitude and 13.6° longitude. Solar zenith angle: 80.2°; exposure time: 35 ms. (<b>a</b>) Planned geographical area. (<b>b</b>) Segmented image in orbit. (<b>c</b>) RGB composite from cube.</p>
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<p>Finnmark, Norway, Europe, on 21 July 2024 at 18:24 UTC. Coordinates: 70.2° latitude and 22.8° longitude. Solar zenith angle: 79.5°; exposure time: 35 ms. (<b>a</b>) Planned geographical area. (<b>b</b>) Segmented image in orbit. (<b>c</b>) RGB composite from cube.</p>
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<p>Florida, USA, North America, on 21 May 2024 at 15:51 UTC. Coordinates: 27.2° latitude and −82.6° longitude. Solar zenith angle: 22.1°; exposure time: 30 ms. (<b>a</b>) Planned geographical area. (<b>b</b>) Segmented image in orbit. (<b>c</b>) RGB composite from cube.</p>
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<p>Comparative analysis of timing and MAC operations across <span class="html-italic">1D-Justo-LiuNet</span>. (<b>a</b>) Processing times in miliseconds. (<b>b</b>) Number of MAC operations.</p>
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15 pages, 5122 KiB  
Article
A Sub-Pixel Measurement Platform Using Twist-Angle Analysis in Two-Dimensional Planes
by Jiangbo Lyu, Wenchao Kong, Yan Zhou, Yazhi Pi and Zizheng Cao
Sensors 2025, 25(4), 1081; https://doi.org/10.3390/s25041081 - 11 Feb 2025
Viewed by 323
Abstract
Arrayed ultraviolet (UV) LED light sources have been widely applied in various semiconductor processes, ranging from photopolymerization to lithography. In practical cases, based on data provided by manufacturers, calibration of individual UV LEDs is often needed before their real usage in high-precision applications. [...] Read more.
Arrayed ultraviolet (UV) LED light sources have been widely applied in various semiconductor processes, ranging from photopolymerization to lithography. In practical cases, based on data provided by manufacturers, calibration of individual UV LEDs is often needed before their real usage in high-precision applications. In this paper, we present a high-precision, automated light source measurement platform, which can be applied to the performance evaluation of various types of light sources. In order to minimize errors introduced by the automated measurement system, the platform employs a sub-pixel measurement technique, along with a twist-angle method, to perform multiple measurements and analyses of the spatial intensity distribution of the light source on a given plane. Through noise analysis of repeated measurements, the platform’s effectiveness and reliability are validated within a certain tolerance range. The high-precision automated light source measurement platform demonstrates excellent performance in the precise control and data acquisition of complex light sources. The light source dataset derived from the test results can provide guidance for the optimization of light sources in fields such as lighting, imaging, and lithography. Full article
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<p>Schematic of the light source testing setup.</p>
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<p>(<b>a</b>) Schematic of the UV LED array light source. (<b>b</b>) Polar luminous intensity distribution curve.</p>
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<p>Workflow of the light source control and driving algorithm. (<b>a</b>) Spatial intensity distribution measurement process. (<b>b</b>) Temporal response measurement process.</p>
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<p>Schematic diagram of measurement method. (<b>a</b>) Grid sampling. (<b>b</b>) Sub-pixel sampling. (<b>c</b>) Multi-frame superposition.</p>
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<p>Spatial intensity distribution results. (<b>a</b>) Grid sampling. (<b>b</b>) Sub-pixel sampling. (<b>c</b>) Multi-frame superposition. (<b>d</b>) Three-dimensional irradiance data distribution. (<b>e</b>) Irradiance data distribution of a specific cross-section. (<b>f</b>) Super-resolution reconstruction analyzed using the Fourier method.</p>
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<p>Grid sampling spatial intensity distribution results of 16 LEDs.</p>
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<p>Sub-pixel sampling spatial intensity distribution results of 16 LEDs.</p>
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<p>Multi-frame superposition spatial intensity distribution results of 16 LEDs.</p>
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<p>Super-resolution reconstruction results of 16 LEDs analyzed using the Fourier method.</p>
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<p>The rising edge of the response time waveform.</p>
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21 pages, 3599 KiB  
Article
Using Deep Learning to Identify Deepfakes Created Using Generative Adversarial Networks
by Jhanvi Jheelan and Sameerchand Pudaruth
Computers 2025, 14(2), 60; https://doi.org/10.3390/computers14020060 - 10 Feb 2025
Viewed by 327
Abstract
Generative adversarial networks (GANs) have revolutionised various fields by creating highly realistic images, videos, and audio, thus enhancing applications such as video game development and data augmentation. However, this technology has also given rise to deepfakes, which pose serious challenges due to their [...] Read more.
Generative adversarial networks (GANs) have revolutionised various fields by creating highly realistic images, videos, and audio, thus enhancing applications such as video game development and data augmentation. However, this technology has also given rise to deepfakes, which pose serious challenges due to their potential to create deceptive content. Thousands of media reports have informed us of such occurrences, highlighting the urgent need for reliable detection methods. This study addresses the issue by developing a deep learning (DL) model capable of distinguishing between real and fake face images generated by StyleGAN. Using a subset of the 140K real and fake face dataset, we explored five different models: a custom CNN, ResNet50, DenseNet121, MobileNet, and InceptionV3. We leveraged the pre-trained models to utilise their robust feature extraction and computational efficiency, which are essential for distinguishing between real and fake features. Through extensive experimentation with various dataset sizes, preprocessing techniques, and split ratios, we identified the optimal ones. The 20k_gan_8_1_1 dataset produced the best results, with MobileNet achieving a test accuracy of 98.5%, followed by InceptionV3 at 98.0%, DenseNet121 at 97.3%, ResNet50 at 96.1%, and the custom CNN at 86.2%. All of these models were trained on only 16,000 images and validated and tested on 2000 images each. The custom CNN model was built with a simpler architecture of two convolutional layers and, hence, lagged in accuracy due to its limited feature extraction capabilities compared with deeper networks. This research work also included the development of a user-friendly web interface that allows deepfake detection by uploading images. The web interface backend was developed using Flask, enabling real-time deepfake detection, allowing users to upload images for analysis and demonstrating a practical use for platforms in need of quick, user-friendly verification. This application demonstrates significant potential for practical applications, such as on social media platforms, where the model can help prevent the spread of fake content by flagging suspicious images for review. This study makes important contributions by comparing different deep learning models, including a custom CNN, to understand the balance between model complexity and accuracy in deepfake detection. It also identifies the best dataset setup that improves detection while keeping computational costs low. Additionally, it introduces a user-friendly web tool that allows real-time deepfake detection, making the research useful for social media moderation, security, and content verification. Nevertheless, identifying specific features of GAN-generated deepfakes remains challenging due to their high realism. Future works will aim to expand the dataset by using all 140,000 images, refine the custom CNN model to increase its accuracy, and incorporate more advanced techniques, such as Vision Transformers and diffusion models. The outcomes of this study contribute to the ongoing efforts to counteract the negative impacts of GAN-generated images. Full article
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<p>Example of a GAN [<a href="#B12-computers-14-00060" class="html-bibr">12</a>].</p>
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<p>Fake images generated by StyleGAN from [<a href="#B10-computers-14-00060" class="html-bibr">10</a>].</p>
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<p>Examples of images of faces in the 140K real and fake face dataset [<a href="#B9-computers-14-00060" class="html-bibr">9</a>].</p>
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<p>Cropping operation on an image.</p>
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<p>Detailed architecture of the system.</p>
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<p>Website interacting with the server.</p>
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<p>Web interface of the application showing that a correct prediction has been made.</p>
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<p>Flowchart showing the image prediction process for the user.</p>
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<p>Graph for the analysis of the results of gan_8_1_1.</p>
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<p>Bar chart comparing the accuracy of all models.</p>
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17 pages, 460 KiB  
Article
The Creation and Evaluation of an AI Assistant (GPT) for Educational Experience Design
by Antonio Julio López-Galisteo and Oriol Borrás-Gené
Information 2025, 16(2), 117; https://doi.org/10.3390/info16020117 - 7 Feb 2025
Viewed by 1332
Abstract
The emergence of generative artificial intelligence (GAI) has revolutionized numerous aspects of our lives and presents significant opportunities in education. However, specific digital competencies are essential to effectively leverage this technology’s potential. Notably, prompt engineering proficiency presents a significant barrier to achieving optimal [...] Read more.
The emergence of generative artificial intelligence (GAI) has revolutionized numerous aspects of our lives and presents significant opportunities in education. However, specific digital competencies are essential to effectively leverage this technology’s potential. Notably, prompt engineering proficiency presents a significant barrier to achieving optimal outcomes. In response, various solutions are being developed, including custom GPTs available through OpenAI’s ChatGPT platform. This study validates ‘GamifIcA Edu’, a specialized GPT-based assistant for gamification and serious games, designed to enable educators to implement these pedagogical approaches without requiring advanced prompt engineering expertise. This is achieved through the utilization of pre-designed instructional frameworks. The assistant’s effectiveness was evaluated using a comprehensive rubric across five distinct use-case scenarios. Each scenario underwent four different tests, representing varied learning contexts across multiple academic disciplines. The validation methodology involved a systematic assessment of the assistant’s performance in diverse educational settings. The findings demonstrate the successful implementation of this custom-designed GPT, which generated contextually appropriate responses through natural language interactions, thus eliminating the need for complex prompt structures. This research highlights the potential of instruction-based design in the development of AI assistants that empower users with limited prompt engineering knowledge to achieve expert-level results. These findings have significant implications for the democratization of AI-enhanced educational tools. Full article
(This article belongs to the Special Issue Artificial Intelligence and Games Science in Education)
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<p>A flowchart illustrating the methodology developed for the design and validation of the ‘GamifIcA Edu’ assistant.</p>
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22 pages, 3646 KiB  
Article
Determining Ligand Binding and Specificity Within the β2-Integrin Family with a Novel Assay Platform
by Carla Johanna Sommer-Plüss, Céline Leiggener, Elira Nikci, Riccardo Vincenzo Mancuso, Said Rabbani, Christina Lamers and Daniel Ricklin
Biomolecules 2025, 15(2), 238; https://doi.org/10.3390/biom15020238 - 7 Feb 2025
Viewed by 460
Abstract
The family of the β2-integrin receptors is critically involved in host defense and homeostasis, by mediating immune cell adhesion, migration, and phagocytosis. Due to their key roles in immune surveillance and inflammation, their modulation has been recognized as an attractive drug [...] Read more.
The family of the β2-integrin receptors is critically involved in host defense and homeostasis, by mediating immune cell adhesion, migration, and phagocytosis. Due to their key roles in immune surveillance and inflammation, their modulation has been recognized as an attractive drug target. However, the development of therapeutics has been limited, partly due to the high promiscuity of endogenous ligands, their functional responses, and gaps in our understanding of their disease-related molecular mechanisms. The delineation of the molecular role of β2 integrins and their ligands has been hampered by a shortage of validated assay systems. To facilitate molecular and functional studies on the β2-integrin family, and to enable screening of modulators, this study provides a uniform and validated assay platform. For this purpose, the major ligand-binding domains (αI) of all four β2 integrins were recombinantly expressed in both low- and high-affinity states. By optimizing the expression parameters and selecting appropriate purification tags, all αI-domain variants could be produced with high yield and purity. Direct binding studies using surface plasmon resonance (SPR) confirmed the expected activity and selectivity profiles of the recombinant αI domains towards their reported ligands, validating our approach. In addition, the SPR studies provided additional insights into ligand binding, especially for the scarcely described family member CD11d. Alongside characterizing endogenous ligands, the platform can be employed to test pharmacologically active compounds, such as the reported β2-integrin antagonist simvastatin. In addition, we established a bead-based adhesion assay using the recombinant αI domains, and a cell-based adhesion assay underlining most findings generated with the isolated αI domains. Interestingly, the binding of ligands to the recombinant αDI is not dependent on divalent cation, in contrast to the full integrin CD11d/CD18, suggesting a binding mode distinct of the metal ion-dependent adhesion site (MIDAS). The setup highlights the applicability of recombinant αI domains for first screenings and direct or competitive interaction studies, while the full integrin is needed to validate those findings. Full article
(This article belongs to the Special Issue New Insights into Integrins)
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<p>SDS-PAGE analysis of purified recombinant αI domains of four β<sub>2</sub> integrins in their wild-type (WT) and high-affinity (HA) variants. The gel visualized after Coomassie blue staining. Molecular weight marker (lanes 1, 10), α<sub>D</sub>I (lanes 2, 3), α<sub>L</sub>I (lanes 4, 5), α<sub>M</sub>I (lanes 6, 7), and α<sub>X</sub>I (lanes 8, 9). The image shows His-fused proteins under non-reducing conditions. The original uncropped image can be found in the <a href="#app1-biomolecules-15-00238" class="html-app">Supplementary Material as Figure S5</a>.</p>
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<p>Ligand interaction profile of the high-affinity (HA) variants of recombinant β<sub>2</sub>-integrin αI domains for C3-derived opsonins as measured by SPR in Mg<sup>2+</sup>-containing buffer. The assay was performed as described in <a href="#sec2-biomolecules-15-00238" class="html-sec">Section 2</a>.</p>
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<p>Ligand interaction profile of the wild-type (WT) form of recombinant β<sub>2</sub>-integrin αI domains for C3-derived opsonins as measured by SPR in Mg<sup>2+</sup> containing buffer. The assay was performed as described in the <a href="#sec2-biomolecules-15-00238" class="html-sec">Section 2</a>.</p>
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<p>SPR sensorgrams of the β<sub>2</sub>-integrin αI-domain high-affinity (HA) and wild-type (WT) variants binding to immobilized ICAM-1 in MgCl<sub>2</sub> supplemented HBST. The assay was performed as described in the <a href="#sec2-biomolecules-15-00238" class="html-sec">Section 2</a>.</p>
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<p>Interference of simvastatin in ligand binding to β<sub>2</sub>-integrin αI domains measured by a competitive SPR assay. The αI domains were preincubated at a fixed concentration of 5 µM with a dilution series of simvastatin (3–100 µM) in HBST supplemented with 1 mM MgCl<sub>2</sub> and 5% DMSO. (<b>A</b>) Representative sensorgram of CR3 α<sub>M</sub>I binding to iC3b in absence and presence of simvastatin. (<b>B</b>) Concentration-dependent inhibition of ligand binding by simvastatin for all three tested αI domains, shown as percentage of non-inhibited binding signal, as mean and standard deviation; <span class="html-italic">p</span> ≥ 0.05 = ns, 0.01 &gt; <span class="html-italic">p</span> &gt; 0.05 = *.</p>
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<p>Schematic presentation of the V-well adhesion assay.</p>
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<p>Adhesion assays based on αI domain-coated beads (<b>A</b>) or β<sub>2</sub>-integrin-transfected HEK293 cells (<b>B</b>). iC3b-coated wells were used to measure CR3- and CR4-mediated adhesion, and ICAM-1-coated wells for LFA-1 and CD11d-/CD18-mediated adhesion. Inhibition by EDTA or domain-specific blocking antibodies was determined in comparison to non-ligand coated wells. Statistical analysis has been calculated with GraphPad Prism 10.2.0, with an unpaired <span class="html-italic">t</span>-test from mean and standard deviation, with <span class="html-italic">p</span> ≥ 0.05 = ns, 0.01 &gt; <span class="html-italic">p</span> &gt; 0.05 = *, 0.001 &gt; <span class="html-italic">p</span> &gt; 0.01 = **, 0.0001 &gt; <span class="html-italic">p</span> &gt; 0.001 = *** and &lt;0.0001 = ****.</p>
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