Matrix Layer Research Articles

Mass Spectrometry Imaging with Matrix-Enhanced SIMS: The Influence of Matrix Deposition Rate on Crystal Size and Signal Enhancement.

Matrix-enhanced secondary ion mass spectrometry and matrix-assisted laser desorption/ionization are two mass spectrometry imaging techniques used to image biological molecules in cells and tissues. Both techniques utilize an organic matrix coating to enhance the detection of molecular ions. The homogeneity and crystal size of the matrix coating are critical for obtaining high quality images. Sublimation/deposition is currently widely used to apply a matrix layer onto a sample because of its ability to produce homogeneous layers with small crystal sizes. Additionally, the absence of a solvent during matrix application reduces lateral movement of the analyte. However, vertical migration of the analyte into the matrix coating is required to observe signal enhancement, and the factors that influence this migration are poorly understood. In this work, an in-house built sublimation matrix coater with a Knudsen effusion cell and sample cooling was used for controlled deposition of the matrix alpha-cyano-4-hydroxycinnamic acid onto a section of mouse brain cerebellum. Different deposition rates were used to coat two areas of the brain section with two different crystal sizes. Macro-scan images of the brain and 3D imaging of selected brain regions were performed. The results show differences in migration through the two matrix layers but also differences in analyte migration behavior for the same analyte in different tissue types.

Determining the strength of 3D printed concrete with the modified slant shear test

AbstractThis study deals with the assessment of the load‐bearing capacity of layered 3D printed concrete (3DPC) using a modified slant shear test (MSST) to define a Mohr's envelope. To this aim, the established modified Coulomb yield condition of the concrete is complemented by a Coulomb failure criterion of the layer joints (cold or dry joints). Due to the anisotropy inherent to 3DPC elements, caused by the interlayer of printed concrete, the test setups commonly used for conventional concrete are inadequate to assess the load‐bearing capacity of 3DPC. A total of 45 3DPC specimens with different inclinations of the concrete printed layers, including a cold joint with 30 min time gap were tested using the MSST. The results showed a high strength of the interfaces with two different failure modes, depending on the inclination of the layers: (i) concrete matrix failure and (ii) layer interface failure, where the latter governed for layer inclinations of 60° and 75° with respect to the horizontal plane. The test campaign confirms that the proposed MSST is a highly practical test method that enables determining the parameters governing a Mohr's envelope of layered 3DPC and can thus be used to reliably characterize its load‐bearing capacity.

Catalysis of a LiF-rich SEI by aromatic structure modified porous polyamine for stable all-solid-state lithium metal batteries.

Poly(ethylene oxide) (PEO)-based solid-state polymer electrolyte (SPE) is a promising candidate for the next generation of safer lithium-metal batteries. However, the serious side reaction between PEO and lithium metal and the uneven deposition of lithium ions lead to the growth of lithium dendrites and the rapid decline of battery cycle life. Building a LiF-rich solid electrolyte interface (SEI) layer is considered to be an effective means to solve the above problems. Here, porous organic polymers (POPs) with aromatic structures and non-aromatic structures were synthesized and introduced into the PEO-based SPE as fillers to explore the effect of aromatic structures on LiF-rich SEI formation. The results show that the POPs containing aromatic groups could catalyze the decomposition of LiTFSI to form a stable LiF-rich SEI layer and inhibit the growth of lithium dendrites. The discharge capacity of the LFP/Li battery is 103 mA h g-1 after 500 cycles at 1C (100 °C). It provides a promising way to improve the stability of the solid electrolyte matrix and SEI layer.

Tunicate-specific protein Epi-1 is essential for conferring hydrophilicity to the larval tunic in the ascidian Ciona.

Animals must avoid adhesion to objects in the environment to maintain their mobility and independence. The marine invertebrate chordate ascidians are characterized by an acellular matrix tunic enveloping their entire body for protection and swimming. The tunic of ascidian larvae consists of a surface cuticle layer and inner matrix layer. Hydrophilic substances coat the cuticle; this modification is thought to be for preventing adhesion. However, the molecule responsible for regulating this modification has not been clarified. We here found that the tunicate-specific protein Epi-1 is responsible for preventing adhesiveness of the tunic in the ascidian Ciona intestinalis Type A. Ciona mutants with homozygous knockouts of Epi-1 exhibited adhesion to plastic plates and to other individuals. The cuticle of the Epi-1 mutants was fragile, and it lost the glycosaminoglycans supplied by test cells, the accessory cells that normally attach to the tunic surface. Although it has an apparent signal peptide for membrane trafficking, we showed that the Epi-1 protein is localized to the cytosol of the epidermal cells. Our study suggests that the emergence of the tunicate-specific protein Epi-1 made the tunic less adhesive, providing a selective advantage for the last common tunicate ancestor.

Bothersome Back Exchange in MALDI Plume and Its Impact on Hydrogen/Deuterium Exchange Mass Spectrometry Analysis.

One critical issue in hydrogen/deuterium exchange mass spectrometry (HDX MS) analysis is the deleterious back exchange. Herein, we report that when matrix-assisted laser desorption/ionization (MALDI) is used, the MALDI process itself can also cause significant back exchange. The back exchange occurred inside the reactive MALDI plume was investigated by depositing a fully deuterated sample prepared in D2O on top of a preloaded dried layer of matrix. A benzene-1,3,5-tricarboxamide (BTA) compound that can form supramolecular polymer in water and five peptides of angiotensin II (AT), pentaglycine (5G), pentaalanine (5A), cyclohexaglycine (C6G), and cyclohexaalanine (C6A) were selected as the testing compounds. Just like the situation in solution, the back exchange for the side chains and end groups is fast in the MALDI plume, while for the backbone amides, it is slow and dependent on the primary structure of the peptide. For the peptides tested, 5%-15% of D-labels in the backbone amides can be lost during the MALDI process. This degree of back exchange, although not an unbearable problem for most HDX MS applications as 85%-95% of the informative labels would still survive, could seriously limit the use of MALDI in the HDX MS analysis of supramolecular assemblies. For these assemblies, the EX1-like mechanism with two distinct distributions is common, and the back exchange could gravely distort or even merge the distinct isotopic distributions, which are the characteristic symbols of EX1.

"3D channel maze" to control drug release from multiple unit tablets.

Diffusion is defined as general mechanism for drug release from advanced delivery systems, yet dynamic structure of dosage form intrinsically plays an unknown role. The synchrotron radiation X-ray micro-computed tomography (SR-μCT) three-dimensional (3D) imaging and in-depth analysis of 3D structures were applied to readily differentiate materials and accurately capture internal structure changes of multiple unit pellet system (MUPS) and the constituent pellets, visualizing internal 3D structure of a MUPS of theophylline tablets for their 3 levels hierarchy structures: pellets with rapid drug release characteristics, a protective cushion layer and a matrix layer. Drug release pathways were extracted from SR-μCT images and a 3D maze network was constructed using pore network analysis to quantify the internal structural evolution during drug release. In the initial stage of dissolution about 1h, theophylline release from the MUPS is dominated by diffusion from the matrix layer, whilst the second phase of 23h constant release kinetics is dominated by a 3D channel maze architecture with outlets/channels connecting pellets in the remains of the MUPS, which forms the 3D channel maze as pore networks. The random walking of the dissolved theophylline molecules retarded by the tortuous 3D channel maze which led to the observed controlled release profile as a whole. Based on SR-μCT investigations and 3D structure analysis, a new approach to control drug release via a 3D channel maze structure was discovered.

Lamina Propria and GALT: Their Relationship with Different Gastrointestinal Diseases, Including Cancer

The structural integrity of the gastrointestinal tract is important because it dictates the functionality of this system. Regarding this, gut-associated lymphoid tissue (GALT) has a significant role in immunity. Most cancer research focuses on organized lymphoid structures and less on diffuse structures such as the lamina propria (LP). Therefore, this paper aims to investigate the link between the LP and cancer in humans. The interstitial matrix and loose connective tissue layer located directly under the epithelium is known as the LP. In this area, there are a lot of IgA+ plasma cells (PCs), T and B lymphocytes, macrophages, dendritic cells (DCs), and stromal cells (SCs). Antigens from the lumen are picked up by LP DCs and presented directly to B cells, which may cause IgA class switching and differentiation in the presence of T cells. In humans, the GALT of the mucosa has been proposed as the source of a unique malignancy known as “GALT carcinoma”, which is thought to represent the “third pathway of colorectal carcinogenesis”. However, present colorectal cancer classifications do not define GALT carcinoma as a separate histologic category.

High-Cycle Fatigue Fracture Behavior and Stress Prediction of Ni-Based Single-Crystal Superalloy with Film Cooling Hole Drilled Using Femtosecond Laser

A high-temperature, high-cycle fatigue test was conducted on a nickel-based single-crystal superalloy with a pore structure. Optical and scanning electron microscopy were utilized to examine the crack propagation paths and fatigue fracture surfaces at the macro and micro scales. The analysis of crack initiation and propagation related to the pore structure facilitated the development of a crack shape factor reflecting these distinct fracture behaviors. Predictions about the high-cycle fatigue stress experienced by the specimen were made, accompanied by an error analysis, providing critical insights for precise stress calculations and structural optimization in engine blade design. The results reveal that high-cycle fatigue cracks originate from corner cracks at pore edges, with the initial propagation displaying smooth crystallographic plane features. Subsequent stages show clear fatigue arc patterns in the propagation zones. The fracture surface exhibits the significant layering of oxide layers, primarily composed of NiO, with traces of CoO displaying columnar growth. AL2O3 is predominantly found at the interfaces between the matrix and oxide layers. Short and straight dislocations near the oxide layers and within the matrix suggest that dislocation multiplication and planar slip dominate the slip mechanisms in this alloy. The orientation of the fracture surface is mainly perpendicular to the load direction, with minor inclined facets in localized areas. Correlations were established between the plastic zone dimensions at the crack tips and the corresponding fatigue stresses. Without grain boundaries in single-crystal alloys, these dimensions are easily derived as parameters for fatigue stress analysis. The selected crack shape factor, “elliptical corner crack at pore edges”, captures the initiation and propagation traits relevant to porous structures. Subsequent calculations, accounting for the impact of oxide layers on stress assessments, indicated an error ratio ranging from 1.00 to 1.21 compared to nominal stress values.

Supernatant of plant-associated bacteria potency against biofilms formed by foodborne pathogen and food spoilage bacteria

ObjectivesFood products are often contaminated by pathogens and spoilage bacteria. Most of them can form biofilms, a community of cells embedded in protective extracellular matrix layers resistant to harsh conditions, including antibiotics. Therefore, alternative antibiofilm agents are required to overcome biofilm formation. This study aims to determine and quantify the antibiofilm activity of supernatants from plant-associated bacteria against biofilms of foodborne pathogen and food spoilage bacterium, namely Bacillus cereus and Bacillus subtilis.ResultsPlant-associated bacteria (PAB) have shown promising antibiofilm activities against biofilm-forming pathogens in previous studies. Thirteen PAB isolated from Ternate, Indonesia were used in this study. Supernatants of PAB were subjected to antimicrobial activity and quorum quenching detection, both using the well diffusion method. Four supernatants inhibited the growth of B. subtilis, but none affected the growth of B. cereus. Eight supernatants were able to disrupt the quorum sensing system of an indicator bacterium, wild-type Chromobacterium violaceum. Biofilm inhibition and destruction were quantified using 96-well microplates. The highest biofilm inhibition and destruction activities of PAB supernatants against each of B. cereus and B. subtilis biofilms were > 76%, and were later confirmed by light microscope and scanning electron microscope. Brine shrimp lethality assay (BSLA) was conducted and revealed that the selected PAB supernatants were non-toxic. The 16S rRNA gene of PAB were sequenced and they showed similarities to Bacillus, Priestia, and Chryseobacterium. Compounds in the supernatants were determined by GC–MS which revealed contents of fatty acids, ethyl esters, and diketopiperazines. Therefore, PAB supernatants have potential as antibiofilm agents against biofilm formed by Bacillus cereus and Bacillus subtilis.

Efficient Defect-Driven Cation Exchange beyond the Nanoscale Semiconductors toward Antibacterial Functionalization.

Defect engineering is an exciting tool for customizing semiconductors' structural and optoelectronic properties. Elaborating programmable methodologies to circumvent energy constraints in multievent inversions expands our understanding of the mechanisms governing the functionalization of nanomaterials. Herein, we introduce a novel strategy based on defect incorporation and solution rationalization, which triggers energetically unfavorable cation exchange reactions in extended solids. Using Sb2X3 + Ag (I) → Ag: Sb2X3 (X= S, Se) as a system to model, we demonstrate that incorporating chalcogen vacancies and AgSbVX complex defects into initial thin films (TFs) is crucial for activating long-range solid-state ion diffusion. Additional regulation of the Lewis acidity of auxiliary chemicals provides an exceptional conversion yield of the Ag precursor into a solid-state product up to 90%, simultaneously transforming upper matrix layers into AgSbX2. The proposed strategy enables tailoring radiative recombination processes, offers efficiency to invert TFs at moderate temperatures quickly, and yields structures of large areas with substantial antibacterial activity in visible light for a particular inversion system. Similar customization can be applied to most sulfides/selenides with controlled reaction yields.

The effect of positive and reverse current cycles on the wettability, morphology, and corrosion behaviour of electrodeposited nickel matrix layer

ABSTRACT In this study, Ni-TiO2 coatings were formed using a multi-step pulse method with positive and, in some cases, reverse current steps. All coatings were produced at a current density of 4 A dm−2 and a frequency and duty cycle of 10 Hz and 10%, respectively with a thickness of 30 µm. The results showed that by applying the reverse current cycle, the codeposition of TiO2 particles in the coating decreased and the morphology of the coating became irregular. It was found that the effect of the wetting angle of the coating is greater than the incorporation of TiO2 particles on the corrosion behaviour of the coating. Thus, a coating was created with a positive 4-step pulse current with the lowest amount of TiO2 particles (7.7 vol.%) having the highest resistance against corrosion. The sample had compact morphology and high wetting angle (82.61o֯).

The Role of Fabricated Coral Shell Powder in the Healing of Mandibular Bone Gap in Dogs

Background: The reconstruction of mandibular bone defects poses a real challenge and difficulty for surgeons; biomaterial bone substitutes are the most used material for reconstructing mandibular bone defects. Objectives: This study explored the role of fabricated hydroxyapatite (HAp) powder from the coral shell in healing critical size mandible gaps in dogs. Methods: HAp was prepared using the hydrothermal method from coral shells. Characterization of the fabricated coral shell was done by x-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), and energy dispersive x-ray spectroscopy (EDX). The designed research was performed on 18 dogs of both sexes (mean weight: 20±0.5 kg, mean age: 2±0.6 years). The samples were divided into two equal groups. Animals underwent experimental defects at the ventral surface of the lower mandible about 14.5 mm. Results: The results of XRD represented high crystallinity, the EDX results indicated the surface morphology of distributed particles of calcium, phosphorous, carbon, and oxygen, respectively, and the FESEM results suggested that the surface morphology of HAp appears as a spherical particle that regularly distributed within the sample. In the HAp group, at 30 days, the FESEM images show that the defective gap completely closed, and the center of the defect was filled with a thick layer of osteoid matrix. Radiographically, the HAp group at 30 days post-surgery indicated a well-defined circular radiolucent bone gap at the caudal portion of the mandible, with a partially sclerosed margin. Macroscopically, at 30 days, the gap appears very small and is invaded by new bone formation. Conclusion: In conclusion, recycling HAp from coral shells has practical value in the reconstitution of the mandibular gap, and the radiological and critical properties of prepared HAp emphasize this outcome.

Magnetorheological and magnetic actuation behaviour of solvent cast 4D printed styrene-ethylene-butylene-styrene block copolymer based magnetorheological elastomeric materials

In this work styrene-ethylene-butylene-styrene (SEBS) block copolymer based smart magnetorheological elastomeric (MREs) materials have been additively manufactured using solvent-cast 4D Printing (SC-4DP) technique. The effect of carbonyl iron powder (CIP) content on the particle distribution, particle–matrix adhesion, surface and layer morphology of the 4D Printed MRE sample was investigated. CIP particles were observed to be well embedded and dispersed up to 60 wt% content. However, at higher CIP content the tendency of the particles to agglomerate increased significantly. Furthermore, samples with CIP content ≥70 wt% showed poor particle–matrix adhesion and possessed inter-layer coalescence defects. Investigations were also performed to evaluate the magnetic properties of MREs at room temperature. Magnetorheological behaviour was studied to evaluate the effect of varying magnetic field on dynamic viscoelastic properties. Magnetorheological effect increased from ∼79 % to ∼211 % with an increase in CIP content. However, the particle–matrix adhesion also significantly affected the magnetorheological effect for higher CIP content samples. Magnetic actuation capability of flexible MRE samples was evaluated for gripper-based application. SC-4D Printed flexible grippers were able to successfully grip, lift, and drop both the soft deformable and rigid freeform profile objects in different media (air and sodium hydroxide solution) suggesting suitability for remotely actuated gripper-based applications.

Copper‐graphene coatings for improving thermal shielding of CFRPs through electrodeposition techniques

AbstractToday, carbon fiber reinforced plastics (CFRPs) are materials of interest several industrial sectors because of their mechanical properties and low weight. However, applications in high‐temperature areas are limited because of thermal degradation. Thus, thin coatings acting as thermal shielding and ensuring the upkeep of CFRP structural stiffness are of high interest. This work presents an innovative approach to produce copper/graphene bilayer coatings through electrodeposition and electrophoretic deposition; it consists of laser pre‐treatment of the composite surface to remove the matrix layer exposing the carbon fibers, enabling the subsequent deposition. Bi‐layer graphene/copper coatings exhibit an enhancement in copper electrodeposition efficiency of more than 59% resulting in a 97% stiffness improvement compared to the single layer copper electroplating. All the obtained coatings were able to act as a thermal shield of the CFRPs, reducing the maximum temperature of the composite by more than 60%. In particular, due to the synergistic effect of copper and graphene, the GNPs‐Cu coating achieved the highest maximum temperature reduction (81%). Cross‐sectional analysis indicates severe delamination in uncoated CFRPs, whereas double‐layer coatings maintain structural integrity and prevent delamination even under high‐energy exposure. In addition, the coated composites exhibit a higher electrical conductivity compared to the laser cleaned CFRP, with the GNPs‐Cu coating that obtained a 90% enhancement because of the outstanding electrical properties of copper and graphene.Highlights The laser cleaning pretreatment allows the electrodepositions on CFRPs. The GNP‐Cu scenario achieves the highest deposition efficiency. A 97% stiffness improvement was achieved by GNPs‐Cu scenario. GNPs‐Cu coatings exhibit the utmost reduction in resistivity (98%). The GNPs‐Cu coating achieves the highest thermal shielding performance (81%).

Development of dual drug loaded-hydrogel scaffold combining microfluidics and coaxial 3D-printing for intravitreal implantation

Treating diabetic retinopathy (DR) effectively is challenging, aiming for high efficacy with minimal discomfort. While intravitreal injection is the current standard, it has several disadvantages. Implantable systems offer an alternative, less invasive, with long-lasting effects drug delivery system (DDS). The current study aims to develop a soft, minimally invasive, biodegradable, and bioadhesive material-based hydrogel scaffold to prevent common issues with implants. A grid-shaped scaffold was created using coaxial 3D printing (3DP) to extrude two bioinks in a single filament. The scaffold comprises an inner core of curcumin-loaded liposomes (CUR-LPs) that prepared by microfluidics (MFs) embedded in a hydrogel of hydroxyethyl cellulose (HEC), and an outer layer of hyaluronic acid-chitosan matrix with free resveratrol (RSV), delivering two Sirt1 agonists synergistically activating Sirt1 downregulated in DR. Optimized liposomes, prepared via MFs, exhibit suitable properties for retinal delivery in terms of size (<200 nm), polydispersity index (PDI) (<0.3), neutral zeta potential (ZP), encapsulation efficiency (∼97 %), and stability up to 4 weeks. Mechanical studies confirm scaffold elasticity for easy implantation. The release profiles show sustained release of both molecules, with different patterns related to different localization of the molecules. RSV released initially after 30 min with a total release more than 90 % at 336 h. CUR release starts after 24 h with only 4.78 % of CUR released before and gradually released thanks to its internal localization in the scaffold. Liposomes and hydrogels can generate dual drug-loaded 3D structures with sustained release. Microscopic analysis confirms optimal distribution of liposomes within the hydrogel scaffold. The latter resulted compatible in vitro with human retinal microvascular endothelial cells up to 72 h of exposition. The hydrogel scaffold, composed of hyaluronic acid and chitosan, shows promise for prolonged treatment and minimally invasive surgery.

Exploring the potential of tomato juice (Solanum lycopersicum L.) patch for tooth bleaching.

Tomato, renowned for its tooth-whitening properties due to its hydrogen peroxide and peroxidase enzyme content, requires formulation for enhanced applicability. This study assessed the dental whitening efficacy of a patch containing tomato juice as the active ingredient. Tomato juice patches were formulated at concentrations of 55%, 60%, and 65%. A control group (C) containing a 12% hydrogen peroxide patch was also included. A matrix layer of the patches was prepared using the solvent casting method at 40 for 18 h, with TegadermTM applied as the backing layer. For the dental whitening procedure, each group of patches was applied to the labial surface of anterior stained teeth (n=6/group) for 3 h, repeated 14 times. Tooth brightness was evaluated qualitatively and quantitatively using digital dental photo CIEL*a*b* analysis. Meanwhile, enamel surfaces were examined under a scanning electron microscope (SEM). Repeated-measures analysis of variance (ANOVA) was employed for statistical analysis. The application of tomato juice patches led to enhanced tooth brightness. The patch containing 65% tomato juice significantly improved stained tooth brightness (P<0.05). SEM analysis revealed less enamel erosion with the 65% tomato juice patch compared to the 12% hydrogen peroxide patch. Tomato juice patches effectively increased tooth brightness while minimizing demineralization. Further research is needed to optimize formulation and explore its potential.

A tough Janus poly(vinyl alcohol)-based hydrogel for wound closure and anti postoperative adhesion

Traditional adhesive hydrogels perform well in tissue adhesion but they fail to prevent postoperative tissue adhesion. To address this challenge, a biodegradable Janus adhesive hydrogel (J-AH) was designed and fabricated by the assembly of three different functional layers including anti-adhesive layer, reinforceable layer, and wet tissue adhesive layer. Each layer of J-AH serves a specific function: the top zwitterionic polymeric anti-adhesive layer shows superior resistance to cell/protein and tissue adhesion; the middle poly(vinyl alcohol)/tannic acid reinforceable matrix layer endows the hydrogel with good mechanical toughness of ∼2.700 MJ/m3; the bottom poly(acrylic acid)/polyethyleneimine adhesive layer imparts tough adhesion (∼382.93 J/m2 of interfacial toughness) to wet tissues. In the rat liver and femoral injury models, J-AH could firmly adhere to the bleeding tissues to seal the wounds and exhibit impressive hemostatic efficiency. Moreover, in the in vivo adhesion/anti-adhesion assay of J-AH between the defected cecum and peritoneal walls, the top anti-adhesive layer can effectively inhibit undesired postoperative abdominal adhesion and inflammatory reaction. Therefore, this research may present a new strategy for the design of advanced bio-absorbable Janus adhesive hydrogels with multi-functions including tissue adhesion, anti-postoperative adhesion and biodegradation. Statement of significanceDespite many adhesive hydrogels with tough tissue adhesion capability have been reported, their proclivity for undesired postoperative adhesion remains a serious problem. The postoperative adhesion may lead to major complications and even endanger the lives of patients. The injectable hydrogels can cover the irregular wound and suppress the formation of postoperative adhesion. However, due to the lack of adhesive properties with tissue, it is difficult for the hydrogels to maintain on the wound surface, resulting in poor anti-postoperative adhesion effect. Herein, we design a Janus adhesive hydrogel (J-AH). J-AH integrates together robust wet tissue adhesion and anti-postoperative adhesion. Therefore, this research may present a new strategy for the design of advanced bio-absorbable Janus adhesive hydrogels.

The Effect of Synthetic Polyamine BPA-C8 on the Fertilization Process of Intact and Denuded Sea Urchin Eggs.

Sea urchin eggs are covered with layers of extracellular matrix, namely, the vitelline layer (VL) and jelly coat (JC). It has been shown that sea urchin eggs' JC components serve as chemoattractants or ligands for the receptor on the fertilizing sperm to promote the acrosome reaction. Moreover, the egg's VL provides receptors for conspecific sperm to bind, and, to date, at least two sperm receptors have been identified on the surface of sea urchin eggs. Interestingly, however, according to our previous work, denuded sea urchin eggs devoid of the JC and VL do not fail to become fertilized by sperm. Instead, they are bound and penetratedby multiple sperm, raising the possibility that an alternative pathway independent of the VL-residing sperm receptor may be at work. In this research, we studied the roles of the JC and VL using intact and denuded eggs and the synthetic polyamine BPA-C8. BPA-C8 is known to bind to the negatively charged macromolecular complexes in the cells, such as the JC, VL, and the plasma membrane of echinoderm eggs, as well as to the actin filaments in fibroblasts. Our results showed that, when added to seawater, BPA-C8 significantly repressed the Ca2+ wave in the intact P. lividus eggs at fertilization. In eggs deprived of the VL and JC, BPA-C8 binds to the plasma membrane and increases fibrous structures connecting microvilli, thereby allowing the denuded eggs to revert towards monospermy at fertilization. However, the reduced Ca2+ signal in denuded eggs was nullified compared to the intact eggs because removing the JC and VL already decreased the Ca2+ wave. BPA-C8 does not cross the VL and the cell membrane of unfertilized sea urchin eggs to diffuse into the cytoplasm at variance with the fibroblasts. Indeed, the jasplakinolide-induced polymerization of subplasmalemmal actin filaments was inhibited in the eggs microinjected with BPA-C8, but not in the ones bath-incubated with the same dose of BPA-C8.

Investigation on 2D SiCf/SiC composite scribing mechanism by single- and double-grit

To validate the proposed removal mechanism of 2D SiCf/SiC composite, single- and double-grit scribing experiments were conducted on the fiber woven surface (WS) and stacking surface (SS) along the 0°, 45°, and 90°. The results indicate that transverse fibers mainly undergo shear, tensile, and bending fractures. The removal modes of normal fibers are shear and bending fractures. The longitudinal fibers are damaged by tensile (cut-in side) and bending (cut-off side) fractures, accompanied by fiber peel-off. The removal forms of the matrix include crack propagation, ductile scratch, powdery removal, and brittle peel-off. The order of scribing force is FSS0 > FWS45 > FSS90 > FWS0. The maximum and minimum scribing force occur on SS0 and WS0, respectively, due to the powdery removal of matrix and fibers + matrix peel-off. The 2nd grit scribes the matrix layer and fiber tip in a very low depth to cause powdery and ductile removal, which exhibit the different material removal mechanism with the 1st grit. The scribing damage formed by 1st grit greatly reduces the force required by the 2nd grit for the same material removal volume. The coupling effect among grits in multi-grit scribing and grinding cannot be ignored.

A comparison of physical, morphological, and mechanical properties of bio‐polyester hybrid nanocomposites

AbstractIt is imperative to improve the physical, morphological, and mechanical properties of biodegradable polymers like polylactic acid (PLA), poly (butylene adipate‐co‐terephthalate) (PBAT), and polycaprolactone (PCL) in order to employ them on a larger scale. The development of hybrid nanocomposite materials using nano inclusions can improve desired qualities. Here we introduced an interactive nano reinforcement approach to improve the properties by combining graphene oxide (GO) and carboxyl functionalized MWCNT (f‐MWCNT), to provide for their chemical bonding for synergic reinforcement. A constant filler 2 wt.% was added to the biopolyesters by melt blending process and examined the different physical properties like water absorption, intrinsic viscosity, and hardness. To completely evaluate the functionalization of the nanofillers, wide‐angle X‐ray diffraction (WAXD), Raman spectroscopy and Fourier transform infrared radiation (FTIR) analyses were used. The paired nanoparticles and polymer matrix appear to mix well together, as shown by electron microscopy, which also reveals good dispersion and the creation of a reinforcing network microstructure across the matrix layer. A thorough analysis of the results showed that effective stress transmission, delaying the start of faults and generating microcracks, and dissipating additional mechanical energy all contributed to efficient hybrid network formation, which improved the mechanical properties of hybrid filler nanocomposites except some nanocomposites. These findings offer a viable technique for chemically altering biodegradable polymers, like PLA, PBAT, and PCL for use in biomedical, wastewater management, and agricultural applications.