In this paper, melting and solidification characteristics of composite PCM filled inside the shell and tube heat exchanger were investigated experimentally. ZnO nanoparticles (NPs) were synthesized using the sol–gel method. Myristic acid (MA) considered as the pure PCM and ZnO NPs serving as the supporting material. The morphology and crystal structure of ZnO particles were analyzed using Field Emission Scanning Electron Microscopy (FESEM) and x-ray Diffraction (XRD) techniques. ZnO nanoparticles at concentrations of 0.1, 0.3, and 0.5 wt% were individually dispersed in myristic acid to evaluate the heat transfer characteristics of nanocomposite phase change materials (NCPCMs) through phase change processes. Differential Scanning Calorimetry (DSC) analyses were used to assess the phase change behavior of PCM and nanocomposite PCMs in liquid and solid states. The phase change characteristics of the Myristic acid and nanocomposite PCMs were probed with regard to heat exchanger studies. The results show significant time savings, with a 68.04% reduction in complete melting time and a 42.73% reduction in solidification time when using 0.5 wt% ZnO NPs at a mass flow rate of 5 l min ^−1 . Furthermore, incorporating ZnO NPs at concentrations of 0.1, 0.3, and 0.5 wt% enhanced the thermal conductivity of the NCPCMs by 36.41%, 62.96%, and 82.71%, respectively, compared to pure MA.
Materials of engineering and construction. Mechanics of materials, Chemical technology
Protein-based therapeutics play a pivotal role in modern medicine targeting various diseases. Despite their therapeutic importance, these products can aggregate and form subvisible particles (SvPs), which can compromise their efficacy and trigger immunological responses, emphasizing the critical need for robust monitoring techniques. Flow Imaging Microscopy (FIM) has been a significant advancement in detecting SvPs, evolving from monochrome to more recently incorporating color imaging. Complementing SvP images obtained via FIM, deep learning techniques have recently been employed successfully for stress source identification of monochrome SvPs. In this study, we explore the potential of color FIM to enhance the characterization of stress sources in SvPs. To achieve this, we curate a new dataset comprising 16,000 SvPs from eight commercial monoclonal antibodies subjected to heat and mechanical stress. Using both supervised and self-supervised convolutional neural networks, as well as vision transformers in large-scale experiments, we demonstrate that deep learning with color FIM images consistently outperforms monochrome images, thus highlighting the potential of color FIM in stress source classification compared to its monochrome counterparts.
We present SAM4EM, a novel approach for 3D segmentation of complex neural structures in electron microscopy (EM) data by leveraging the Segment Anything Model (SAM) alongside advanced fine-tuning strategies. Our contributions include the development of a prompt-free adapter for SAM using two stage mask decoding to automatically generate prompt embeddings, a dual-stage fine-tuning method based on Low-Rank Adaptation (LoRA) for enhancing segmentation with limited annotated data, and a 3D memory attention mechanism to ensure segmentation consistency across 3D stacks. We further release a unique benchmark dataset for the segmentation of astrocytic processes and synapses. We evaluated our method on challenging neuroscience segmentation benchmarks, specifically targeting mitochondria, glia, and synapses, with significant accuracy improvements over state-of-the-art (SOTA) methods, including recent SAM-based adapters developed for the medical domain and other vision transformer-based approaches. Experimental results indicate that our approach outperforms existing solutions in the segmentation of complex processes like glia and post-synaptic densities. Our code and models are available at https://github.com/Uzshah/SAM4EM.
Govindhasamy Murugadoss, Nachimuthu Venkatesh, Pandurengan Sakthivel
et al.
Quantum dots (QDs) are employed in photocatalytic applications because of their distinctive optical characteristics, such as high absorption coefficients and tunable bandgaps, enabling efficient visible light absorption and charge carrier generation. This study focuses on synthesizing homogeneous bismuth-doped tin sulfide (Bi-doped SnS) QDs for environmental remediation. Bi-doped SnS QDs with varying Bi concentrations are prepared via a facile, cost-effective chemical method, and their structural, optical, and morphological characteristics are analyzed through X-ray diffraction (XRD), UV–Vis spectroscopy, and transmission electron microscopy (TEM). TEM results confirm that the catalysts are highly homogeneous and tiny (<5 nm). Photocatalytic activity is assessed through the breakdown of Crystal Violet (CV) and Methylene Blue (MB) when exposed to visible light. High efficiencies of 89.0 % and 95.8 % are achieved for CV and MB, respectively, outperforming undoped SnS. Kinetic analysis reveals a pseudo-first-order reaction, providing insights into the underlying degradation kinetics. A plausible mechanism is proposed, elucidating how Bi-ion doping enhances photocatalytic performance and facilitates dye degradation. Additionally, toxicity evaluation using Vigna radiata seeds demonstrates the efficacy of the degradation process. Treated dye solutions (D-CV and D-MB) show no significant changes in intracellular ROS levels compared to untreated dye and control solutions, confirming reduced toxicity. These findings highlight the enhanced photocatalytic performance of Bi-doped SnS QDs and their potential in environmental purification, advancing the understanding of QD-based photocatalysts for sustainable applications.
Microbial contamination poses a significant challenge to the management of water resources and biomedical applications. In this study, the development of a biogenic antimicrobial filtration system has been successfully achieved. This system utilizes a plant extract-mediated synthesis approach for in situ formation of silver nanoparticles (AgNPs) within a porous sponge matrix. The fabrication process involved the immersion of a commercial sponge in an aqueous solution of AgNO3 and plant extract, followed by a thermal treatment. The structural and chemical properties of the Ag@Sponge were then confirmed via a range of analytical methods, including scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). These results indicated the successful incorporation of AgNPs within the sponge, with a predominant spherical morphology and an average size of 54 ± 14 nm. Antimicrobial activity tests demonstrated that Ag@Sponge exhibited significant bacterial and fungal inactivation, achieving >99.99999% microbial reduction against Escherichia coli (E. coli), Staphylococcus aureus (S. aureus), and Candida albicans (C. albicans) (R > 7). Furthermore, the results of filtration experiments demonstrated that microbial removal efficiency increased progressively over six cycles, reaching final reductions of 6.2–6.4 log CFU/mL for E. coli, S. aureus, and C. albicans. Mechanical durability tests confirmed that Ag@Sponge retained >6 log CFU/mL reduction after 5000 cm abrasion (down to 6.6 ± 0.5) and 400 bending cycles (down to 6.1 ± 1.2), indicating strong mechanical resilience and in situ nanoparticle stability. These findings highlight the potential of Ag@Sponge as a sustainable and efficient antimicrobial filtration material for practical applications in water purification and medical decontamination.
In recent years, bovine viral diarrhea virus (BVDV) has been associated with increased respiratory and gastrointestinal diseases in cattle. Comprehensive monitoring and investigations into the virus's pathological features are crucial for developing effective prevention strategies. This study investigated BVDV prevalence and pathogenicity in farms undergoing elimination protocols, with a focus on characterizing a novel Cytopathic Bovine Viral Diarrhea Virus (CP-type BVDV) strain (HH839) isolated from a symptomatic calf in Hohhot, Inner Mongolia. During 2021 and 2022, 103 bovine samples were screened for BVDV via nucleic acid detection. Positive cases underwent viral isolation using MDBK cells. The HH839 strain was analyzed for cytopathic effects, ultrastructure (electron microscopy), antigenicity (serum neutralization), and genetic lineage (whole genome sequencing). Pathogenicity of Cytopathic Bovine Viral Diarrhea Virus (CP-type BVDV) infected group, Noncytopathic Bovine Viral Diarrhea Virus (NCP-type BVDV) infected group, and the mixed-infection group of CP-type and NCP-type BVDV was evaluated in New Zealand White rabbits, with viral distribution and histopathological damage assessed in multiple organs. We identified 33 positive BVDV nucleic acid cases, resulting in a positivity rate of 32.04%. Five strains of NCP-type BVDV were isolated, yielding a 15.15% separation rate, alongside one strain of CP-type BVDV with a separation rate of 3.03%. The CP strain HH839 was isolated from a severely symptomatic calf in Hohhot, Inner Mongolia. The HH839 strain demonstrated significant cytopathic effects in MDBK cells, including cellular crumpling and syncytia formation, with a concentration of 5.23 log10TCID50/0.1 mL. Electron microscopy revealed a spherical morphology with a diameter of 40–60 nm. Genetic analysis indicated a close relationship with the BVDV FBS-D8 strain from the BVDV-1d subtype. Pathogenicity trials showed slight fever and minor body weight loss in infected subjects, with BVDV detected in the trachea, lungs, spleen, and small intestines, predominantly in the spleen. The isolation of HH839, a pathogenic CP-type BVDV-1d strain, underscores the coexistence of multiple BVDV biotypes in regional cattle populations. Enhanced pathogenicity observed in mixed infections highlights complex viral interactions. These findings emphasize the necessity for sustained surveillance and biotype-specific control strategies to mitigate BVDV-associated economic losses in livestock industries.
Abstract The micromechanical properties of organic matter (OM) and organic pore structures in the over-mature stage are crucial for determining shale reservoir quality and assessing shale gas resource potential. However, there is still debate about the influence of micromechanical properties of OM on the micro-mesopore structures in over-mature shale. In this study, shale cores from the Niutitang Formation have been specifically chosen for OM isolation, adsorption testing, atomic force microscopy examination, and focused ion beam scanning electron microscopy (FIB-SEM) analysis to assess the micromechanical properties of OM and pore structures. The findings indicate that organic micropores and mesopores predominantly exhibit elliptical, circular, or irregular shapes. Organic pores mainly provide pore volume (PV) and specific surface area (SSA) of shale. In the over-mature stage, residual kerogen and pyrobitumen transition towards a graphite structure, increasing Young’s modulus of OM. Additionally, as thermal maturity increases, the absence of a rigid mineral framework and pore fluid pressure results in the compaction of pores, leading to a decrease in PV and SSA. The organic micropores are more vulnerable to collapse and compaction because of the increased brittleness of OM. The organic micropores and mesopores gradually evolve from regular circular and elliptical shapes to irregular shapes during the over-mature stage. The research findings provide valuable insights into the micromechanical mechanism of pore evolution in over-mature marine shale within complex structural regions.
Win Myat Phyo, Danuthida Saket, Marcio A. da Fonseca
et al.
Abstract Background Surface remineralization is recommended for the management of active non-cavitated interproximal carious lesions in primary teeth. According to the American Academy of Pediatric Dentistry, a recently recognized category of materials called bioactive restorative materials can be used for remineralization. This study aimed to evaluate the release of fluoride (F), calcium (Ca) and phosphate (P) ions from Predicta® Bioactive Bulk-fill composite compared with EQUIA Forte® and Filtek™ Z350 and to determine the remineralization effect of these 3 restorative materials on adjacent initial interproximal enamel carious lesions. Methods The release of F, Ca and P ions from 3 groups ((n = 10/group) (Group 1- Predicta®, Group 2- EQUIA Forte® and Group 3- Filtek™ Z350)) was determined at 1st, 4th, 7th and 14th days. After creating artificial carious lesions, human enamel samples were randomly assigned into 3 groups (n = 13/group) which were placed in contact with occluso-proximal restorative materials and exposed to a 14-day pH cycling period. Surface microhardness was determined using a Knoop microhardness assay at baseline, after artificial carious lesions formation and after pH cycling. The difference in the percentage of surface microhardness recovery (%SMHR) among groups was compared. Mineral deposition was analyzed with energy-dispersive x-ray spectroscopy (EDS) and the enamel surface morphology was evaluated with scanning electron microscopy (SEM). Kruskal-Wallis’s test with Dunn’s post hoc test and one-way ANOVA with Tukey’s post hoc test were used for data analysis. Results EQUIA Forte® released the highest cumulative amount of F and P ions, followed by Predicta® and Filtek™ Z350. Predicta® released higher amount of Ca ions than EQUIA Forte® and Filtek™ Z350. Predicta® demonstrated the highest %SMHR, followed by EQUIA Forte® and Filtek™ Z350. There was a significant difference in the %SMHR between Predicta® and Filtek™ Z350 (p < 0.05). However, EQUIA Forte® demonstrated the highest fluoride content, followed by Predicta® and Filtek™ Z350. The SEM images of EQUIA Forte® and Predicta® revealed the greater mineral deposition. Conclusion Predicta® demonstrated a marked increase in surface microhardness and fluoride content of adjacent initial interproximal enamel carious lesions in primary molars compared with Filtek™ Z350. Predicta® is an alternative restorative material to remineralize adjacent initial interproximal enamel carious lesions in primary molars, especially in high-risk caries patients.
Timur Yumalin, Timur Salikhov, Biltu Mahato
et al.
The simple scaling of silicon transistors no longer ensures the advantages of high energy efficiency, driving research into nanotechnologies beyond silicon. Specifically, digital circuits based on carbon nanotube (CNT) field-effect transistors promise significant advantages in energy efficiency. However, the inability to perfectly control internal nanoscale defects and the variability of carbon nanotubes hinder the realization of very large-scale integrated systems. In this study, we investigated a novel method for fabricating transistors based on carbon nanotubes (CNTs) using epoxy mixtures, obtained the electrical properties of the transistors, and compared their microstructure and composition via the scanning electron microscopy. The carrier mobility on epoxy-based transistors was 28.87 cm²/V∙s, and the transistor switching frequency was 2.2 MHz. The samples exhibited electrical and physical stability over an extended period of time. The use of carbon nanotubes in epoxy resin as a conducting layer for transistors opens significant prospects in the field of electronics. The CNT-epoxy mixture technology allows for more flexible and rapid fabrication of thin-film transistors compared to classical methods. However, it is not appropriate to speak of a complete replacement; in this study, we present an alternative method for producing thin-film transistors, which may be of interest for specific purposes.
Sutha Paramasivam, Sathishkumar Chidambaram, Palanisamy Karumalaiyan
et al.
<b>Background:</b> Green synthesized nanoparticles (NPs) have gained increasing popularity in recent times due to their broad spectrum of antimicrobial properties. This study aimed to develop a phytofabrication approach for producing cuprous (Cu<sub>2</sub>O) and cupric oxide (CuO) NPs using a simple, non-hazardous process and to examine their antimicrobial properties. <b>Methods:</b> The synthesis employed <i>Bidens pilosa</i> plant extract as a natural reducing and stabilizing agent, alongside copper chloride dihydrate as the precursor. The biosynthesized NPs were characterized through various techniques, including X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier-transform infrared (FT-IR) spectroscopy, ultraviolet–visible (UV-Vis) spectroscopy, scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDS). <b>Results:</b> XRD analysis confirmed that the synthesized CuO and Cu<sub>2</sub>O NPs exhibited a high degree of crystallinity, with crystal structures corresponding to monoclinic and face-centered cubic systems. SEM images revealed that the NPs displayed distinct spherical and sponge-like morphologies. EDS analysis further validated the purity of the synthesized CuO NPs. The antimicrobial activity of the CuO and Cu<sub>2</sub>O NPs was tested against various pathogenic bacterial strains, including <i>Staphylococcus aureus</i>, <i>Pseudomonas aeruginosa</i>, <i>Escherichia coli</i>, and <i>Bacillus cereus</i>, with the minimum inhibitory concentration (MIC) used to gauge their effectiveness. <b>Conclusions:</b> The results showed that the phytosynthesized NPs had promising antibacterial properties, particularly the Cu<sub>2</sub>O NPs, which, with a larger crystal size of 68.19 nm, demonstrated significant inhibitory effects across all tested bacterial species. These findings suggest the potential of CuO and Cu<sub>2</sub>O NPs as effective antimicrobial agents produced via green synthesis.
Barnaby D. A. Levin, Diane Haiber, Qianlang Liu
et al.
The desire to image specimens in liquids has led to the development of open-cell and closed-cell techniques in transmission electron microscopy (TEM). The closed-cell approach is currently more common in TEM and has yielded new insights into a number of biological and materials processes in liquid environments. The open-cell approach, which requires an environmental TEM (ETEM), is technically challenging but may be advantageous in certain circumstances due to fewer restrictions on specimen and detector geometry. Here, we demonstrate a novel approach to open-cell liquid TEM, in which we use salt particles to facilitate the in situ formation of droplets of aqueous solution that envelope specimen particles coloaded with the salt. This is achieved by controlling sample temperature between 1 and 10°C and introducing water vapor to the ETEM chamber above the critical pressure for the formation of liquid water on the salt particles. Our use of in situ hydration enables specimens to be loaded into a microscope in a dry state using standard 3 mm TEM grids, allowing specimens to be prepared using trivial sample preparation techniques. Our future aim will be to combine this technique with an in situ light source to study photocorrosion in aqueous environments.
Nin Ghigo, Gerardo Ramos-Palacios, Chloé Bourquin
et al.
Ultrasound Localization Microscopy (ULM) relies on the injection of microbubbles (MBs) to obtain highly resolved density maps of blood circulation in vivo, with a resolution that can reach 10 μm ~ λ/10 in the rodent brain. Static mean velocity maps can be extracted but are intrinsically biased by potential significant changes in the number of MBs detected during the cardiac cycle. Dynamic ULM (DULM) is a technique developed for non-invasive pulsatility measurements in the brain of rodents, leading to temporally resolved velocity and density cine-loops. It was previously based on external triggers such as the electrocardiogram (ECG), limiting its use to datasets acquired specifically for DULM applications while also increasing the required acquisition time. This study presents a new motion matching method using tissue Doppler that eliminates the need for ECG-gating in DULM experiments. DULM can now be performed on any ULM datasets, recovering pertinent temporal information, and improving the robustness of the mean velocity estimates.
Fluorescent molecules are versatile nanoscale emitters that enable detailed observations of biophysical processes with nanoscale resolution. Because they are well-approximated as electric dipoles, imaging systems can be designed to visualize their 3D positions and 3D orientations, so-called dipole-spread function (DSF) engineering, for 6D super-resolution single-molecule orientation-localization microscopy (SMOLM). We review fundamental image-formation theory for fluorescent di-poles, as well as how phase and polarization modulation can be used to change the image of a dipole emitter produced by a microscope, called its DSF. We describe several methods for designing these modulations for optimum performance, as well as compare recently developed techniques, including the double-helix, tetrapod, crescent, and DeepSTORM3D learned point-spread functions (PSFs), in addition to the tri-spot, vortex, pixOL, raPol, CHIDO, and MVR DSFs. We also cover common imaging system designs and techniques for implementing engineered DSFs. Finally, we discuss recent biological applications of 6D SMOLM and future challenges for pushing the capabilities and utility of the technology.
Luis Fabián Peña, Justine C. Koepke, J. Houston Dycus
et al.
SiGe heteroepitaxial growth yields pristine host material for quantum dot qubits, but residual interface disorder can lead to qubit-to-qubit variability that might pose an obstacle to reliable SiGe-based quantum computing. We demonstrate a technique to reconstruct 3D interfacial atomic structure spanning multiqubit areas by combining data from two verifiably atomic-resolution microscopy techniques. Utilizing scanning tunneling microscopy (STM) to track molecular beam epitaxy (MBE) growth, we image surface atomic structure following deposition of each heterostructure layer revealing nanosized SiGe undulations, disordered strained-Si atomic steps, and nonconformal uncorrelated roughness between interfaces. Since phenomena such as atomic intermixing during subsequent overgrowth inevitably modify interfaces, we measure post-growth structure via cross-sectional high-angle annular dark field scanning transmission electron microscopy (HAADF-STEM). Features such as nanosized roughness remain intact, but atomic step structure is indiscernible in $1.0\pm 0.4$~nm-wide intermixing at interfaces. Convolving STM and HAADF-STEM data yields 3D structures capturing interface roughness and intermixing. We utilize the structures in an atomistic multivalley effective mass theory to quantify qubit spectral variability. The results indicate (1) appreciable valley splitting (VS) variability of roughly $\pm$ $50\%$ owing to alloy disorder, and (2) roughness-induced double-dot detuning bias energy variability of order $1-10$ meV depending on well thickness. For measured intermixing, atomic steps have negligible influence on VS, and uncorrelated roughness causes spatially fluctuating energy biases in double-dot detunings potentially incorrectly attributed to charge disorder.
In the present study, lysozyme was purified by the following multi-step methodology: salt (ammonium sulfate) precipitation, dialysis, and ultrafiltration. The lysozyme potential was measured by enzymatic activity after each purification step. However, after ultrafiltration, the resulting material was considered extra purified. It was concentrated in an ultrafiltration centrifuge tube, and the resulting protein/lysozyme was used to determine its bactericidal potential against five bacterial strains, including three gram-positive (<i>Bacillus subtilis</i> 168, <i>Micrococcus luteus</i>, and <i>Bacillus cereus</i>) and two gram-negative (<i>Salmonella typhimurium</i> and <i>Pseudomonas aeruginosa</i>) strains. The results of ZOI and MIC/MBC showed that lysozyme had a higher antimicrobial activity against gram-positive than gram-negative bacterial strains. The results of the antibacterial activity of lysozyme were compared with those of ciprofloxacin (antibiotic). For this purpose, two indices were applied in the present study: antimicrobial index (AMI) and percent activity index (PAI). It was found that the purified lysozyme had a higher antibacterial activity against <i>Bacillus cereus</i> (AMI/PAI; 1.01/101) and <i>Bacillus subtilis</i> 168 (AMI/PAI; 1.03/103), compared to the antibiotic (ciprofloxacin) used in this study. Atomic force microscopy (AFM) was used to determine the bactericidal action of the lysozyme on the bacterial cell. The purified protein was further processed by gel column chromatography and the eluate was collected, its enzymatic activity was 21.93 U/mL, while the eluate was processed by native-PAGE. By this analysis, the un-denatured protein with enzymatic activity of 40.9 U/mL was obtained. This step shows that the protein (lysozyme) has an even higher enzymatic potential. To determine the specific peptides (in lysozyme) that may cause the bactericidal potential and cell lytic/enzymatic activity, the isolated protein (lysozyme) was further processed by the SDS-PAGE technique. SDS-PAGE analysis revealed different bands with sizes of 34 kDa, 24 kDa, and 10 kDa, respectively. To determine the chemical composition of the peptides, the bands (from SDS-PAGE) were cut, enzymatically digested, desalted, and analyzed by LC-MS (liquid chromatography-mass spectrometry). LC-MS analysis showed that the purified lysozyme had the following composition: the number of proteins in the sample was 56, the number of peptides was 124, and the number of PSMs (peptide spectrum matches) was 309. Among them, two peptides related to lysozyme and bactericidal activities were identified as: A0A1Q9G213 (N-acetylmuramoyl-L-alanine amidase) and A0A1Q9FRD3 (D-alanyl-D-alanine carboxypeptidase). The corresponding protein sequence and nucleic acid sequence were determined by comparison with the database.
Luís P. G. Monteiro, João Borges, João M. M. Rodrigues
et al.
Marine-origin polysaccharides, in particular cationic and anionic ones, have been widely explored as building blocks in fully natural or hybrid electrostatic-driven Layer-by-Layer (LbL) assemblies for bioapplications. However, the low chemical versatility imparted by neutral polysaccharides has been limiting their assembly into LbL biodevices, despite their wide availability in sources such as the marine environment, easy functionality, and very appealing features for addressing multiple biomedical and biotechnological applications. In this work, we report the chemical functionalization of laminarin (LAM) and pullulan (PUL) marine polysaccharides with peptides bearing either six lysine (K<sub>6</sub>) or aspartic acid (D<sub>6</sub>) amino acids via Cu(I)-catalyzed azide-alkyne cycloaddition to synthesize positively and negatively charged polysaccharide-peptide conjugates. The successful conjugation of the peptides into the polysaccharide’s backbone was confirmed by proton nuclear magnetic resonance and attenuated total reflectance Fourier-transform infrared spectroscopy, and the positive and negative charges of the LAM-K<sub>6</sub>/PUL-K<sub>6</sub> and LAM-D<sub>6</sub>/PUL-D<sub>6</sub> conjugates, respectively, were assessed by zeta-potential measurements. The electrostatic-driven LbL build-up of either the LAM-D<sub>6</sub>/LAM-K<sub>6</sub> or PUL-D<sub>6</sub>/PUL-K<sub>6</sub> multilayered thin film was monitored in situ by quartz crystal microbalance with dissipation monitoring, revealing the successful multilayered film growth and the enhanced stability of the PUL-based film. The construction of the PUL-peptide multilayered thin film was also assessed by scanning electron microscopy and its biocompatibility was demonstrated in vitro towards L929 mouse fibroblasts. The herein proposed approach could enable the inclusion of virtually any kind of small molecules in the multilayered assemblies, including bioactive moieties, and be translated into more convoluted structures of any size and geometry, thus extending the usefulness of neutral polysaccharides and opening new avenues in the biomedical field, including in controlled drug/therapeutics delivery, tissue engineering, and regenerative medicine strategies.
Kin-Wai Tam, Cheuk-Yin Wong, Kenneth Lap-Kei Wu
et al.
The in vitro derivation of Schwann cells from human bone marrow stromal cells (hBMSCs) opens avenues for autologous transplantation to achieve remyelination therapy for post-traumatic neural regeneration. Towards this end, we exploited human induced pluripotent stem-cell-derived sensory neurons to direct Schwann-cell-like cells derived from among the hBMSC-neurosphere cells into lineage-committed Schwann cells (hBMSC-dSCs). These cells were seeded into synthetic conduits for bridging critical gaps in a rat model of sciatic nerve injury. With improvement in gait by 12-week post-bridging, evoked signals were also detectable across the bridged nerve. Confocal microscopy revealed axially aligned axons in association with MBP-positive myelin layers across the bridge in contrast to null in non-seeded controls. Myelinating hBMSC-dSCs within the conduit were positive for both MBP and human nucleus marker HuN. We then implanted hBMSC-dSCs into the contused thoracic cord of rats. By 12-week post-implantation, significant improvement in hindlimb motor function was detectable if chondroitinase ABC was co-delivered to the injured site; such cord segments showed axons myelinated by hBMSC-dSCs. Results support translation into a protocol by which lineage-committed hBMSC-dSCs become available for motor function recovery after traumatic injury to both peripheral and central nervous systems.
The diffusion growth of intermetallic compounds in Al-Er alloys are closely related to the properties of the alloys. The current work aims at explaining the dominance of Al3Er in the Al-Er alloys precipitation phases and the interface thin layer phenomenon by diffusion couple technique, estimating the parabolic growth constant and diffusion activation energy of intermetallic compound in Al-Er diffusion couples to provide theoretical guidance for the design of new Al-Er alloys. In this work, Al-Er diffusion couples were successfully prepared by casting-cladding method in the atmosphere. The growth of Al-Er intermetallic compounds at diffusion couple interface during annealing were observed and recorded by High-Temperature Laser-Scanning Confocal Microscopy at 673, 698, 723 and 748 K respectively. The results show that the growth characteristics of Al-Er intermetallic compounds were accord with layer-terraced growth during annealing. The thickness of intermetallic compound was linear with the square root of time at experimental temperature. The intermetallic compound layer was composed of Al3Er and a very thin AlEr phase. The parabolic growth constants of Al3Er phase at 673, 698, 723 and 748 K were 1.017 × 10−14, 1.609 × 10−14, 3.111 × 10−14 and 4.76 × 10−14 respectively. The activation energy of Al3Er phase was (88.4 ± 5.3) kJ/mol and the pre-exponential factor was 7.126 × 10−8 m2/s.
Materials of engineering and construction. Mechanics of materials
Fluorescence lifetime imaging microscopy (FLIM) systems are limited by their slow processing speed, low signal-to-noise ratio (SNR), and expensive and challenging hardware setups. In this work, we demonstrate applying a denoising convolutional network to improve FLIM SNR. The network will be integrated with an instant FLIM system with fast data acquisition based on analog signal processing, high SNR using high-efficiency pulse-modulation, and cost-effective implementation utilizing off-the-shelf radio-frequency components. Our instant FLIM system simultaneously provides the intensity, lifetime, and phasor plots \textit{in vivo} and \textit{ex vivo}. By integrating image denoising using the trained deep learning model on the FLIM data, provide accurate FLIM phasor measurements are obtained. The enhanced phasor is then passed through the K-means clustering segmentation method, an unbiased and unsupervised machine learning technique to separate different fluorophores accurately. Our experimental \textit{in vivo} mouse kidney results indicate that introducing the deep learning image denoising model before the segmentation effectively removes the noise in the phasor compared to existing methods and provides clearer segments. Hence, the proposed deep learning-based workflow provides fast and accurate automatic segmentation of fluorescence images using instant FLIM. The denoising operation is effective for the segmentation if the FLIM measurements are noisy. The clustering can effectively enhance the detection of biological structures of interest in biomedical imaging applications.