Field Microscopy Research Articles

Reduced order homogenization of composites with strength difference effects in elastoplasticity coupled to damage

This paper addresses reduced order homogenization of composites with strength difference (SD) effects in elastoplasticity coupled to damage, while containing several well-known plasticity criteria as special cases. We extend two approaches for this purpose: 1. nonuniform transformation field analysis (NTFA by Michel and Suquet, 2003) and 2. a recent variant called cluster-based NTFA (CNTFA by Ri et al., 2021), and conduct a comparative study on them. For the NTFA approach, a space–time decomposition is done separately for volumetric and deviatoric inelastic strain fields. A coupled model is derived for the present case to govern the evolution of resulting reduced variables. For the CNTFA approach, a clustering analysis is additionally performed for a spatial decomposition of the micro-domain. Unlike the NTFA, the online analysis is formulated as a unified minimization problem, which does not require a major adaptation for the present case. For both approaches, localization rules are deduced from the superposition principle and then homogenized to obtain the effective responses. FE-based implementation is presented in detail for both approaches. Numerical results show that both approaches provide a striking acceleration rate against conventional FE computations. The CNTFA predictions are more accurate than the NTFA ones by involving clustered microscopic fields in the online analysis, thus resulting into a slightly increased memory requirement.

Advances in biofilm characterization: utilizing rheology and atomic force microscopy in foods and related fields

Advances in biofilm characterization: utilizing rheology and atomic force microscopy in foods and related fields

Magnetic braneworlds: cosmology and wormholes

We construct 4D flat Big Bang-Big Crunch cosmologies and Anti-de Sitter (AdS) planar eternally traversable wormholes using braneworlds embedded in asymptotically AdS5 spacetimes. The background geometries are the AdS5 magnetic black brane and the magnetically charged AdS5 soliton, respectively. The two setups arise from different analytic continuations of the same saddle of the gravitational Euclidean path integral, in which the braneworld takes the form of a Maldacena-Maoz Euclidean wormhole. We show the existence of a holographic dual description of this setup in terms of a microscopic Euclidean boundary conformal field theory (BCFT) on a strip. By analyzing the BCFT Euclidean path integral, we show that the braneworld cosmology is encoded in a pure excited state of a CFT dual to a black brane microstate, whereas the braneworld wormhole is encoded in the ground state of the BCFT. The latter confines in the IR, and we study its confining properties using holography. We also comment on the properties of bulk reconstruction in the two Lorentzian pictures and their relationship via double analytic continuation. This work can be interpreted as an explicit, doubly-holographic realization of the relationship between cosmology, traversable wormholes, and confinement in holography, first proposed in arXiv:2102.05057, arXiv:2203.11220.

CYTOSKELETON DYNAMICS AND SPATIAL ORGANIZATION DURING EPITHELIAL-TO-MESENCHYMAL TRANSITION

Epithelial-to-mesenchymal transition (EMT) is a crucial process that occurs during normal development, such as embryogenesis and organ formation. If it is inappropriately activated, it can lead to pathological processes like metastasis. Although EMT is well studied at the morphological and transcriptome level, cytoskeleton changes during this process are less understood. In our work we aimed to describe the morphological changes that occurred in MCF-7, A-549 and HaCaT cells after EMT, analyze microtubule dynamics, spatial distribution and its contribution to cell motility, identify changes in actin filament organization and study focal adhesion turnover in the cells after EMT. We hypothesized that the dynamics of microtubules in cells undergoing EMT might change. Cells undergoing EMT were expected to have more dynamic microtubules. Also, cells undergoing EMT are expected to adhere more efficiently to diverse substrates, and therefore spread and move more easily. Focal contacts in cells undergoing EMT were expected to be more pronounced and dynamic than in cells that not undergoing EMT. The research methods used in the study included inducing EMT in modified MCF-7 cells through an inserted inducible Tet-on system and stimulation of EMT in A-549 and HaCaT cells using TGF-β. The cells were observed using bright field microscopy, and immunofluorescence analysis was conducted to visualize microtubules and actin filaments. Transfection with EB-3–RFP protein was done to describe and measure microtubule dynamics, while transduction with Talin-RFP and transient transfection with Ptag-RFP-vinculin was done to visualize focal adhesions. Time-lapse fluorescent microscopy was used to record films, and the Fiji Image J program was used to analyze the data. All statistical analysis was performed using GraphPad Prism (Dotmatics, USA), and a nonparametric Mann-Whitney U test or parametric t-test with Welch correction. The actin filament measurements were completed using Matlab scripts. The major research findings: In all three-cell models after EMT, cell morphology changed. Cells increased in size. MCF-7 and HaCaT became spread out, while A-549 became elongated. Some of the cells lost cell-cell contacts. All three cell models after EMT had alterations in microtubule organization and dynamics. MCF-7 and HaCaT cells showed more frequently individual MTs at cell edges, while A-549 had less covered nucleus by MTs after EMT. Microtubule dynamics (growth velocity) increased, and the length of microtubule growth tracks became longer. The average angle of MT growth trajectories to cell radius decreased. Actin fibers rearranged into more pronounced stress fibers after EMT. Alterations in the focal adhesion behaviors were different in three models used. These results indicate that cytoskeletal changes during EMT mainly include increased microtubule dynamics.

Challenges in diagnosis of clinical and subclinical Plasmodium falciparum infections in Ghana and feasibility of reactive interventions to shrink the subclinical reservoir

BackgroundReactive case detection (RCD) aims to reduce malaria transmission stemming from asymptomatic carriers. Symptomatic individuals diagnosed with malaria at a health centre are followed to their households, where members of the index case and neighbouring households are tested and treated for malaria. An RCD programme was tested in the Ashanti region of Ghana in order to study diagnostic accuracy in the hospital and household settings, assess the prevalence of subclinical infections and possible clustering in index case households, and identify operational challenges for future RCD programmes. Currently, transmission in this region is high, but reactive interventions might become an option once transmission is reduced.Methods264 febrile individuals were enrolled at the Mankranso Government Hospital and tested for malaria using rapid diagnostic tests (RDT). From the pool of RDT-positive febrile index cases, 14 successful RCD follow-ups were conducted, and 233 individuals were enrolled from the index case, neighbour, and control households. The sensitivity of diagnostic tools for clinical and subclinical cases was compared, including RDT, expert microscopy by World Health Organization-certified microscopists, field microscopy, and qPCR.ResultsPoor diagnosis and low receptivity to RCD-style follow-ups were major limitations to a successful and effective RCD programme. Field microscopy detected only 49% of clinical infections compared to RDT. 54% of individuals did not agree to a follow-up, and 66% of attempted follow-ups failed. The system effectiveness of RCD, calculated as the product of correctly diagnosed index cases, successful follow-ups, and proportion of asymptomatic infections detected by RDT, was very low at 4.0%.ConclusionsDue to low system effectiveness and the endemic nature of the disease setting in which asymptomatic prevalence is high and infections are not clustered around index case households, RCD is currently not a feasible option for malaria control in this region. The operational challenges identified through this study may help inform future reactive intervention programme designs once transmission is reduced.

Practical guidelines for cell segmentation models under optical aberrations in microscopy

Cell segmentation is essential in biomedical research for analyzing cellular morphology and behavior. Deep learning methods, particularly convolutional neural networks (CNNs), have revolutionized cell segmentation by extracting intricate features from images. However, the robustness of these methods under microscope optical aberrations remains a critical challenge. This study evaluates cell image segmentation models under optical aberrations from fluorescence and bright field microscopy. By simulating different types of aberrations, including astigmatism, coma, spherical aberration, trefoil, and mixed aberrations, we conduct a thorough evaluation of various cell instance segmentation models using the DynamicNuclearNet (DNN) and LIVECell datasets, representing fluorescence and bright field microscopy cell datasets, respectively. We train and test several segmentation models, including the Otsu threshold method and Mask R-CNN with different network heads (FPN, C3) and backbones (ResNet, VGG, Swin Transformer), under aberrated conditions. Additionally, we provide usage recommendations for the Cellpose 2.0 Toolbox on complex cell degradation images. The results indicate that the combination of FPN and SwinS demonstrates superior robustness in handling simple cell images affected by minor aberrations. In contrast, Cellpose 2.0 proves effective for complex cell images under similar conditions. Furthermore, we innovatively propose the Point Spread Function Image Label Classification Model (PLCM). This model can quickly and accurately identify aberration types and amplitudes from PSF images, assisting researchers without optical training. Through PLCM, researchers can better apply our proposed cell segmentation guidelines. This study aims to provide guidance for the effective utilization of cell segmentation models in the presence of minor optical aberrations and pave the way for future research directions.

Simultaneous enumeration of yeast and bacterial cells in the context of industrial bioprocesses

Abstract In scenarios where yeast and bacterial cells coexist, it is of interest to simultaneously quantify the concentrations of both cell types, since traditional methods used to determine these concentrations individually take more time and resources. Here, we compared different methods for quantifying the fuel ethanol Saccharomyces cerevisiae PE-2 yeast strain and cells from the probiotic Lactiplantibacillus plantarum strain in microbial suspensions. Individual suspensions were prepared, mixed in 1:1 or 100:1 yeast-to-bacteria ratios, covering the range typically encountered in sugarcane biorefineries, and analyzed using bright field microscopy, manual and automatic Spread-plate and Drop-plate counting, flow cytometry (at 1:1 and 100:1 ratios), and a Coulter counter (at 1:1 and 100:1 ratios). We observed that for yeast cell counts in the mixture (1:1 and 100:1 ratios), flow cytometry, the Coulter counter, and both Spread-plate options (manual and automatic CFU counting) yielded statistically similar results, while the Drop-plate and microscopy-based methods gave statistically different results. For bacterial cell quantification, the microscopy-based method, Drop-plate, and both Spread-plate plating options and flow cytometry (1:1 ratio) produced no significantly different results (P > 0.05). In contrast, the Coulter counter (1:1 ratio) and flow cytometry (100:1 ratio) presented results statistically different (P < 0.05). Additionally, quantifying bacterial cells in a mixed suspension at a 100:1 ratio wasn't possible due to an overlap between yeast cell debris and bacterial cells. We conclude that each method has limitations, advantages, and disadvantages.

Haploinsufficiency of intraflagellar transport protein 172 causes autism-like behavioral phenotypes in mice through BDNF

IntroductionPrimary cilia are hair-like solitary organelles growing on most mammalian cells that play fundamental roles in embryonic patterning and organogenesis. Defective cilia often cause a suite of inherited diseases called ciliopathies with multifaceted manifestations. Intraflagellar transport (IFT), a bidirectional protein trafficking along the cilium, actively facilitates the formation and absorption of primary cilia. IFT172 is the largest component of the IFT-B complex, and its roles in Bardet-Biedl Syndrome (BBS) have been appreciated with unclear mechanisms. ObjectivesWe performed a battery of behavioral tests with Ift172 haploinsufficiency (Ift172+/-) and WT littermates. We use RNA sequencing to identify the genes and signaling pathways that are differentially expressed and enriched in the hippocampus of Ift172+/- mice. Using AAV-mediated sparse labeling, electron microscopic examination, patch clamp and local field potential recording, western blot, luciferase reporter assay, chromatin immunoprecipitation, and neuropharmacological approach, we investigated the underlying mechanisms for the aberrant phenotypes presented by Ift172+/- mice. ResultsIft172+/- mice displayed excessive self-grooming, elevated anxiety, and impaired cognition. RNA sequencing revealed enrichment of differentially expressed genes in pathways relevant to axonogenesis and synaptic plasticity, which were further confirmed by less spine density and synaptic number. Ift172+/- mice demonstrated fewer parvalbumin-expressing neurons, decreased inhibitory synaptic transmission, augmented theta oscillation, and sharp-wave ripples in the CA1 region. Moreover, Ift172 haploinsufficiency caused less BDNF production and less activated BDNF-TrkB signaling pathway through transcription factor Gli3. Application of 7,8-Dihydroxyflavone, a potent small molecular TrkB agonist, fully restored BDNF-TrkB signaling activity and abnormal behavioral phenotypes presented by Ift172+/- mice. With luciferase and chip assays, we provided further evidence that Gli3 may physically interact with BDNF promoter I and regulate BDNF expression. ConclusionsOur data suggest that Ift172 per se drives neurotrophic effects and, when defective, could cause neurodevelopmental disorders reminiscent of autism-like disorders.

A Simple Method for Visualization and Quantitative Evaluation of Single and Collective Cell Migration in Bright Field Microscopy Images

A Simple Method for Visualization and Quantitative Evaluation of Single and Collective Cell Migration in Bright Field Microscopy Images

Additive manufacturing of quartz glass using coaxial wire feeding technology

This study explores the process of coaxial wire feeding and melting for quartz additive manufacturing using Direct Energy Deposition (DED). Quartz glass, valued for its excellent mechanical, optical, and thermal properties, is widely used in semiconductor, aerospace, and optical communication industries. Additive manufacturing offers advantages such as cost-effective materials, rapid formation, and customization of structures. However, current methods for additive manufacturing of quartz glass often result in low quality or require complex post-processing, particularly for optical components. In optics, there is a demand for high-quality, straightforward processes, and custom-shaped quartz glass. This article presents a coaxial wire feeding mechanism wherein quartz wire is fed vertically downward along the optical axis into the melting zone created by a CO2 laser, facilitating smooth material deposition onto the molten zone’s surface. Laser power, wire feeding speed, substrate movement speed, and defocusing distance are key factors influencing the quality of single-layer quartz glass formation. Positive defocusing was found to have a beneficial impact on single-layer quartz glass additive manufacturing. Subsequently, optimized process parameters enabled the production of uniformly cross-sectional single-layer quartz glass. Microscopic morphology analysis and temperature field simulation were conducted on the experimental results before and after optimization. Finally, complex quartz glass structures were additively manufactured using the optimized experimental parameters. Results demonstrate that coaxial wire feeding technology has significant potential for achieving uniform dimensions and complex structures in quartz glass additive manufacturing.

Crack/Cl− - triggered design and tensile self-healing mechanism of epoxy coatings on offshore steel bars

The double-walled microcapsules triggered under the crack/Cl− condition were prepared by using isocyanate and 1,6-diaminohexane respectively as the internal and external core material, and polyurea as the wall material. During the synthesis process, lead sulfate was added to the wall material to trap chloride ions. The morphology and dispersion of the microcapsules embedded in the epoxy composite were characterized, using the scanning electron microscope (SEM) and super depth of field microscope. Self-healing coatings containing 0.0 wt%, 3.0 wt%, 5.0 wt%, and 8.0 wt% of composite double-walled microcapsules were subjected to tensile tests. The digital speckle correlation method (DSCM) and pull-out test were applied to analyze the mechanical properties and crack-triggering principle of the coating. The toughening effect and self-healing behavior of the epoxy resin with varying dosages of microcapsules were studied. The self-healing efficiency and mechanism of the composite coating were obtained during the process of stretching, crack expansion, and micro-capsule triggering.

Electrical characterization of freeze-thaw damage in saturated concrete and its interfacial transition zones

Determining the freeze-thaw (F-T) damage of the interfacial transition zone (ITZ) is crucial to understanding the mechanism of F-T in concrete and improving its frost resistance. In this paper, the F-T damage of saturated concrete/mortar and ITZ is characterized using AC impedance spectroscopy, and the micro-mechanisms of F-T damage in cement-based materials (CBMs) are summarized. Firstly, the damage factor was defined by the effective resistivity of the CBMs, and a correlation between the damage factor and the compressive strength loss was established. The F-T damage process was divided into a damage development stage and a damage stabilization stage based on the damage factor and fractal dimension. Then, the effective resistivity separation formula was proposed to calculate the ITZ effective resistivity, and the ITZ damage factor was calculated for non-destructive quantitative characterization of the F-T damage in the ITZ. Finally, the microscopic mechanism of F-T damage in CBMs and their ITZs was summarized based on damage factor, fractal dimension, super depth of field microscopy, and nanoindentation. The results showed a linear relationship between the damage factor and compressive strength loss (Lc = 0.176Er+0.030); the ITZ had damage factors of 80 % and 70 %, which were 1.6 and 1.4 times higher than those of the matrix, respectively; F-T cycles produce micro-damage, part of which connects with the disconnected pores to form connected pores, the micro-damage extends and accumulates along the surface of the aggregates, leading to ITZ debonding from aggregate and deterioration of the mechanical properties.

Copper-induced pro-apoptotic response and its alleviation by Quercetin through autophagic modulation in HEPG2 cells

BackgroundRecent studies indicated that the liver is susceptible to Cu-induced stress as it stores and distributes the metal to other cellular organelles. To counteract the hepatocytic damage, a known polyphenol, quercetin, was employed for its remarkable antioxidant properties. Thus, the study aimed to assess quercetin’s potency against Cu-induced toxicity in HEPG2 cells. MethodsThe cellular viability of HEPG2 cells was carried out by MTT assay. All the cellular experiments were divided into control, Cu 100 µM, Cu 100 µM (with Q μM), Cu 300 µM, Cu 300 µM (with Q 50 nM), and only quercetin (50 nM). Following this, reactive oxygen species (ROS) levels and mitochondrial membrane potential (MMP) were evaluated in co-exposure studies. Moreover, rhodamine-123, Hoechst stain, monodansylcadaverine (MDC), and acridine orange (AO) stain were used to visualize the morphological changes under bright field and fluorescent microscopy. Subsequently, western blotting was adopted to determine the expression level of apoptotic and autophagic marker proteins. ResultsCopper increased intracellular ROS, resulted in morphological abnormalities, nuclear condensation, and disrupted MMP. Moreover, Cu caused apoptotic cell deaths characterized by overexpressed pro-apoptotic proteins such as poly (ADP-ribose) polymerase (PARP), cysteine-dependent aspartate-specific proteases 3 (Caspase 3), and Bcl-2-associated X protein (Bax) and downregulated anti-apoptotic proteins such as B-cell lymphoma 2 (Bcl-2), respectively. However, quercetin restored overexpressed pro-apoptotic proteins and induced autophagosome-bound microtubule-associated protein light chain-3 (LC3II) conversion from LC3I. Furthermore, Cu-modulated autophagy marker proteins, including sequestosome-1 (p62), heat shock cognate proteins (Hsc 70, Hsc 90), lysosome-associated membrane protein (LAMP-2A), and AMP-associated protein kinase (AMPK). ConclusionThis study promotes the nutraceutical ability of quercetin to combat Cu-induced hepatotoxicity by understanding the intricate biological signaling pathways within cells.

Fourier Raman light field microscopy based on surface-enhanced Raman scattering.

Raman scattering, as a vibrational spectrum that carries material information, has no photobleaching that enables long-duration imaging. Raman spectra have very narrow emission peaks, and multiplex Raman imaging can be achieved by using different Raman scattering peak signals. These advantages make Raman imaging widely used in biology, cytology, and medicine, which has a wider range of application scenarios. However, obtaining a three-dimensional (3D) Raman image requires scanning for tens of minutes to several hours at present. Therefore, a fast non-scanning 3D Raman imaging method is greatly needed. In this article, we propose a Fourier Raman light field microscopy based on surface-enhanced Raman scattering (sers-FRLFM). Using flower-like gap-enhanced Raman nanoparticles (F-GERNs) to enhance Raman scattering signals, a Fourier-configured light field microscope (LFM) is capable of recording complete four-dimensional Raman field information in a single frame, facilitating the 3D reconstruction of the Raman image without generating reconstruction artifacts at the native object plan. Moreover, F-GERNs can mark specific locations and have the potential to become a new tracing method to achieve specific imaging. This imaging method has great potential in the 3D real-time Raman imaging of cells, microorganisms, and tissues with the lateral resolution of 2.40 µm and an axial resolution of 4.02 µm.

Human Enteroid Monolayers: A Novel, Functionally-Stable Model for Investigating Oral Drug Disposition.

To further the development of an in vitro model which faithfully recapitulates drug disposition of orally administered drugs, we investigated the utility of human enteroid monolayers to simultaneously assess intestinal drug absorption and first-pass metabolism processes. We cultured human enteroid monolayers from three donors, derived via biopsies containing duodenal stem cells that were propagated and then differentiated atop permeable Transwell® inserts, and confirmed transformation into a largely enterocyte population via RNA-seq analysis and immunocytochemical (ICC) assays. Proper cell morphology was assessed and confirmed via bright field microscopy and ICC imaging of tight junction proteins and other apically and basolaterally localized proteins. Enteroid monolayer barrier integrity was demonstrated by elevated transepithelial electrical resistance (TEER) that stabilized after 10 days in culture and persisted for 42 days. These results were corroborated by low paracellular transport probe permeability at 7 and 21 days in culture. The activity of a prominent drug metabolizing enzyme, CYP3A, was confirmed at 7, 21, and 42 days culture under basal, 1α,25(OH)2 vitamin D3-induced, and 6',7'-dihydroxybergamottin-inhibited conditions. The duration of these experiments is particularly noteworthy, as this is the first study assessing drug metabolizing enzymes and transporters (DMET) expression/function for enteroids cultured for greater than 12 days. The sum of these results suggests enteroid monolayers are a promising ex vivo model to investigate and quantitatively predict an orally administered drug's intestinal absorption and/or metabolism. Significance Statement This study presents a novel ex vivo model of the human intestine, human intestinal organoid (enteroid) monolayers, that maintain barrier function and metabolic functionality for up to 42-days in culture. The incorporation of both barrier integrity and metabolic function over an extended period within the same model is an advancement over historically used in vitro systems, which either lack one or both of these attributes or have limited viability.

A novel kit for enrichment of fecal helminth eggs.

We developed a new concentration kit, called the ParaEgg (PE), for easy detection trematode eggs from fecal samples in endemic areas of clonorchiasis and metagonimiasis in Korea. To create a standard of detection efficiency, 120 fecal samples were examined using the water-ether concentration method (WECM). The PE kit and Mini ParaSep (PS) kit were used to compare the detection sensitivity of 100 egg-positive and 20 egg-negative samples in WECM. Additionally, stool samples, which were intentionally spiked with 10, 20, and 30 Clonorchis sinensis eggs, were evaluated to assess the sensitivity in lowinfection cases. The PE and PS kits showed detection rates of 100% and 92%, respectively, from 100 egg-positive samples in WECM. Meanwhile, eggs were detected in 3 (PE) and 2 (PS) out of 20 egg-negative samples in WECM. The PE kit detected the highest number of eggs per gram of feces (727 on average), followed by the WECM (524) and PS kit (432). In fecal samples that were intentionally spiked with 10, 20, and 30 C. sinensis eggs, PE only detected eggs 2 out of 5 samples in 10 eggs spiked (40%), and the detection rates were 80% and 100%, respectively. The PE kit enabled a more accurate identification of trematode eggs because of the clearance of small fecal debris in the microscopic field. In conclusion, the PE kit is obviously helpful to detect and identify trematode eggs in stool examinations especially in endemic areas of clonorchiasis and metagonimiasis.

Multi-Focus Images Fusion for Fluorescence Imaging Based on Local Maximum Luminosity and Intensity Variance.

Due to the limitations on the depth of field of high-resolution fluorescence microscope, it is difficult to obtain an image with all objects in focus. The existing image fusion methods suffer from blocking effects or out-of-focus fluorescence. The proposed multi-focus image fusion method based on local maximum luminosity, intensity variance and the information filling method can reconstruct the all-in-focus image. Moreover, the depth of tissue's surface can be estimated to reconstruct the 3D surface model.

Negative Regulators, TUP1, NRG1, and TOR1: Possible Molecular Targets of Antibiofilm Activity of Nano-Fe3 O4 in Candida albicans

Background: Candida albicans is an opportunistic pathobiont that manifests as candidiasis. Drug-resistant biofilms hinder current treatment of candidiasis. The morphological control of filamentous growth and biofilm formation is vital for the pathogenicity of C. albicans. This study aimed to investigate the antifungal activity of magnetic iron oxide nanoparticles (nano-Fe3 O4 ) against C. albicans, their ability to inhibit pre-formed biofilms, and to examine the expression levels of negative regulators, transcriptional repressors thymidine uptake 1 (TUP1), the negative transcriptional regulator of glucose repressed genes (NRG1), and target of rapamycin (TOR1) in C. albicans pre-formed biofilms after treatment with nano-Fe3 O4 . Methods: This study examines the antifungal activity of nano-Fe3 O4 against C. albicans, its ability to inhibit pre-formed biofilms, and investigates the expression levels of negative regulators, TUP1, NRG1, and TOR1 in C. albicans pre-formed biofilms after treatment with nano-Fe3 O4 . Results: Nano-Fe3 O4 at concentrations of 2× minimum inhibitory concentration (MIC), 1× MIC, and ½× MIC showed significant inhibitory effects on C. albicans pre-formed biofilm formation by 2,3-bis (2-methoxy-4-nitro-5 sulfophenyl)-5-[(phenylamino) carbonyl])-2H-tetrazolium hydroxide (XTT), crystal violet staining and light field microscopy with a MIC of 50 μg/mL. Gene expression profiling showed that nano-Fe3 O4 upregulates targets TUP1, NRG1, and TOR1 in C. albicans pre-formed biofilms. Conclusion: Our results suggest that nano-Fe3 O4 diminishes pre-formed biofilms and may subsequently reduce the pathogenicity of C. albicans, which can be responsible for biofilm-associated infections. TUP1, NRG1, and TOR1 may be possible molecular targets in C. albicans pre-formed biofilms after treatment with nano-Fe3 O4.

Reinforced protection of fragile bronze cultural relics based on nano-cuprammonium fiber material

Bronze artifacts often suffer from “bronze disease” due to the presence of chloride ions, which result from copper chlorides forming on their surfaces during storage. Therefore, reinforced protection is essential for these unearthed cultural artifacts, and new materials for the reinforced protection of fragile bronzes are urgently needed. In this study, cuprammonium solvent and nanocellulose (CNC) were utilized as reinforcement materials to protect fragile bronzes. The chemical and aesthetic properties before and after reinforcement were analyzed using ultra-depth field microscopes, SEM-EDX, XRD, and Raman spectroscopy. The results indicated that at a nano-cuprammonium reinforcer concentration of 2.5 mol/L, the optimal reinforcement effect on simulated bronze powdery rust samples was achieved.Mechanical strength increased by an average of 77.59%. The mass growth rate reached 84.8%, while the color difference ΔE\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\Delta E$$\\end{document} remained below 4.0. Additionally, aging resistance significantly improved, aligning with cultural artifact protection standards.Meanwhile, a compact and stable protective membrane formed on the surface of the bronzes, isolating the bronze matrix from direct contact with the external environment, which delayed bronze corrosion and contributed to long-term stable preservation.Graphical

PCL reinforced nano strontium hydroxyapatite-Butea monosperma-scaffold for bone regeneration

Biocomposite materials, composed of biodegradable polymers and supplements, are promising for bone regenerative matrices due to their mechanical strength and excellent osteoconductivity. This study focuses on fabricating electrospun composite scaffolds using the bark extract of Butea monosperma (BM), nano strontium hydroxyapatite (nSrHA), and polycaprolactone (PCL). Four types of scaffolds were prepared: PCL (control), BM-PCL, nSrHA-PCL, and BM-nSrHA-PCL. The scaffolds were evaluated through various techniques: bright field microscopy for standardization, SEM for structural evaluation, and SEM-EDX for elemental analysis. Additionally, mechanical strength, release study, degradation, and protein adsorption were assessed. Furthermore, cytotoxicity, proliferation, and cytocompatibility of the scaffolds were evaluated using rat adipose-derived mesenchymal stem cells (rADMSCs) through SEM, MTT assay, LDH assay, DAPI staining, and Direct contact assay. SEM analysis confirmed that all four fabricated scaffolds were nano-fibrous in nature. The incorporation of phytochemicals and nSrHA was confirmed via SEM-EDX. Mechanical testing revealed that the BM-nSrHA-PCL scaffolds had superior mechanical properties compared to the control PCL scaffolds. Protein adsorption studies indicated enhanced protein binding in BM-nSrHA-PCL scaffolds. Degradation studies showed that BM-nSrHA-PCL scaffolds had a controlled degradation rate suitable for tissue engineering applications. Cytotoxicity tests confirmed that all scaffolds were noncytotoxic. Proliferation and cytocompatibility assays demonstrated that BM-nSrHA-PCL scaffolds significantly promoted cell proliferation compared to other scaffold types. These results suggest that the BM-nSrHA-PCL scaffolds exhibit improved mechanical properties, protein adsorption, controlled degradation, and enhanced cell proliferation, making them promising candidates for bone tissue engineering applications.