Cell Dimensions Research Articles

Facile Y-type Micro Ag2Se/MgAgSb flexible thermoelectric device based on lift-off technology.

The development of thermoelectric devices provides an ideal solution for self-sustaining Internet of Things (IoT) applications. However, existing thermoelectric devices face issues such as low integration levels and poor stability. To address these challenges, this paper presents a novel method for fabricating flexible thermoelectric devices using Ag2Se/MgAgSb, which combines MEMS lithographic lift-off techniques to achieve precise control over the dimensions of the thermoelectric functional layer while also reducing fabrication costs. The optimal cell dimensions were identified through simulations. The device achieved an open circuit voltage of 0.49 mV at a temperature difference of 50K. Additionally, the output power density of the Ag₂Se/MgAgSb flexible Y-type thermoelectric device reached 3.39 µW/m² at a temperature difference of 5K. The device also demonstrated excellent flexibility; even after being bent 800 times around a glass rod with a diameter of 4mm, its conductivity decreased by only 12%. Furthermore, it maintained stability under high humidity conditions. This work offers a novel strategy for the miniaturization and large-area controllable fabrication of flexible and reliable thermoelectric devices, as well as an enhancement in their reliability.

Measuring Cell Dimensions in Fission Yeast Using Machine Learning.

In fission yeast (Schizosaccharomyces pombe), cell length is a crucial indicator of cell cycle progression. Microscopy screens that examine the effect of agents or genotypes suspected of altering genomic or metabolic stability and thus cell size are crucial for studying disruptions to cell cycle dynamics. This method is based on using an automated cell segmentation algorithm to measure S. pombe cells imaged by brightfield (BF) microscopy methods. PhotoPhenosizer (PP) is a machine learning-based tool designed for automated cell measuring and dimensional analysis of morphology frequency distributions. Integration of this method into large-scale pipelines for tracking cell dimension change streamlines morphological measurements, which facilitates the examination of cellular responses to genomic and metabolic stresses. In this protocol, we use PP to observe the effect of genomic instability on cell size dynamics over a 12-day chronological lifespan assay. Our results show that relative to wild-type cells, a replication stress mutant shows larger cells during chronological aging in excess glucose media. Our results are consistent with activation of checkpoints that regulate cell morphology in response to DNA damage. This method's application highlights the relevance of its incorporation in experimental routines that require large-scale image processing and its adoption by users with routine needs in S. pombe molecular research projects.

Exploring the phase composition and crystal structure of potassium-doped copper sulfide

This study investigates the phase composition, crystal structure, and phase transitions of potassium-substituted copper sulfide (KxCu1.97-xS), focusing on the effects of potassium doping on the material’s properties. Using X-ray diffraction analysis, we identified the structural characteristics of potassium-doped variants, confirming their retention of the monoclinic chalcocite structure (P21/c) with slight modifications in lattice parameters. The incorporation of potassium ions resulted in observable changes in the unit cell dimensions, suggesting enhanced ionic interactions and potential impacts on electronic conductivity. The thermoelectric coefficient, electro-conductivity, and thermoelectric power were also examined, revealing that potassium doping could stabilize certain phases under varying temperature conditions. This work provides valuable insights into the structure-property relationships in copper sulfides, highlighting the potential for tailored materials in thermoelectric applications and other advanced technologies. Future studies will explore the implications of these findings for optimizing the performance of potassium-doped copper sulfides in practical applications.

Hierarchical Multi‐Component Self‐Assembly Involving Alkali and Lanthanide(III) Metal Ions and Water Soluble Sulfonated Calix[4]arene

AbstractSolid state structural studies of three supramolecular coordination complexes establish the formation of hetero‐bimetallic two‐ and three‐dimensional ensembles involving sulfonated calix[4]arene, and sodium ions and low nuclearity lanthanide(III) ions. The interplay of components is altered in response to the addition of different auxiliary molecules during crystallisation which is associated with significant changes in the metal coordination environments and overall molecular packing, as established in comparing the structures of complexes of similar cell dimensions with those available in the literature. The sulfonated calixarene form a common self‐assembly array despite different lanthanides being incorporated, as an isostructural series of complexes. Crystallographic analysis shows a continually decreasing trend in the lanthanide–oxygen bond length as the lanthanide atomic number increases. As smaller molecules are incorporated to the hetero‐bimetallic calixarene system, the self‐assembly and the metal coordination environment are perturbed.

Design of dual peak star shaped metamaterial absorber for S and C band sensing applications

This paper presents the detailed design configuration and investigation of a small-scale dual-band metamaterial absorber (MTMA) for solid and liquid sensing applications. The overall dimension of the MTMA unit cell is 10 × 10 × 1.57 mm3 and constitutes an affordable FR-4 substrate. The absorber exhibits dual absorption peaks at 3.470 GHz for the S-band and 7.219 GHz for the C-band, respectively. Both absorption characteristics have been validated through comprehensive simulation and experimental procedures. The dual-band absorption rate exceeded 99% during simulations, and experimental validation showed an absorption rate above 98%. For sensing applications, various solid materials, including different Rogers substrates ( RT 5880, RT 5870, RT 4003 and RT 4835) and liquids such as sunflower and crown oil, were utilized. Our findings indicate that the proposed MTMA achieves a maximum Q-factor of 191 and a sensitivity of up to 2.5 for both solid and liquid sensing applications compared to previous studies. The simulation and experimental validation of the result indicate that suggested MTMA can be effectively used in different sensing applications such as the medical and communications industry.

Crystallographic Characterization of Gypsum Synthesized from Marine Wastes: Babylonia japonica, Olive sayana, and Conasprella bermudensis

The study synthesized gypsum nanocrystals using conventional wet chemical precipitation methods from marine mollusks like Babylonia Japonica, Olive Sayana, and Conasprella bermudensis. Different characterization techniques like Thermogravimetric Analysis (TGA), X-ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscopy (SEM), and Energy Dispersive X-ray Spectroscopy (EDX) were used to confirm the formation of the nanocrystals. XRD data assessed various structural parameters, including the dimension of the unit cell, crystallinity index, specific surface area, lattice parameters, dislocation density, and macrostrain. The Rietveld refinement study did not reveal the formation of alternate phases, and the predicted lattice parameters, Full Width at Half Maximum (FWHM), and X-ray density contradicted the actual data. The synthesized gypsum displays crystallite dimension within the acceptable range of < 200 nm, as calculated using various XRD model equations. Additionally, the values for strain (2× 10-4 to 4 × 10-4), stress (-1×107 to 2×107 N/m2), and energy density (2.87 × 102 to 2.16× 103 J/m3) were also estimated for the synthesized samples. The preferential growth calculation indicates stable phase formation of gypsum along the (020) and (040) plane. Furthermore, The study compared the properties of gypsum, including pH, conductivity, and potential difference (PD), in soil extraction and an aqueous medium.

Synthesis, Structure And Thermogravimetric Analysis Of Copper(II) Complex Derived From N1 ,N3 -Bis(1-(Pyridin2-Yl)Ethylidene)Propane-1,3-Diamine

Cu(II) complex derived from ligand, (N 1 ,N3 -bis(1-(pyridin-2-yl)ethylidene)propane-1,3-diamine (L) which was synthetized in situ, is reported. The isolated Cu(II) complex was characterized by elemental analyses, IR, and UV-Vis spectroscopies, and Thermogravimetric analyze (TGA). Additionally, the structure of the complex was determined by single crystal X-ray diffraction study. The diimine ligand was coordinated to Cu(II) ion through two azomethine nitrogen atoms and two pyridine nitrogen atom. One bromide ion complete the coordination sphere yielding a distorted square pyramidal geometry. The structure of the copper(II) complex is confirmed by X-ray diffraction. The complex crystallizes in the monoclinic space group P21/c with unit cell dimensions a = 8.3433 (3) Å, b = 13.2605 (3) Å, c = 18.838 (6) Å,  = 97.522 (16)°, V = 2066.2 (6) Å3 , Z = 4, R1 = 0.048 and wR2 = 0.081. The Cu(II)cation in N4Br inner is situated in a distorted square pyramidal environment. Thermogravimetric analyze of the complex were carried out at 20–800 °C and showed that the complex were decomposed into three steps.

Structural analysis and theoretical studies of 2-(2-chlorobenzylidene) malononitrile (CS) “a riot controlling agent”

In solvent methanol, malononitrile and 2-chlorobenzaldehyde were stirred in the presence of base piperidine to synthesise the target chemical 2-(2-chlorobenzylidene) malononitrile (CS). The crystal structure of the target compound C10H5ClN2 has been elucidated through X-ray crystallographic analysis. It crystallises in the monoclinic crystal system within the P21 space group, containing four molecules per asymmetric unit. The unit cell dimensions are a = 3.8825(3) Å, b = 21.0202(18) Å, c = 21.3481(18) Å, and β = 95.096(4)°. The phenyl and malononitrile groups, which make up the molecular components, are each planar but slanted towards one another at a dihedral angle of 12.7° (4). Besides this, target molecule is also stabilized by hydrogen bonding, halogen bonding and π stacking interactions. Solid-state structure has been analysed through Hirshfeld surface analysis, including the evaluation of the different energy frameworks, indicating that the molecular sheets are primarily formed by hydrogen bonds and halogen bonds and the stabilization is dominated via the electrostatic energy contribution. Fingerprint plots were carried out to study the relative contribution of noncovalent interactions in the target compound CS. Further, the density functional theory calculations were employed using B3LYP hybrid functional with 6-311++G level basic set to optimize the structural coordinates in gas phase and in different solvents (chloroform, water, and methanol). The chemically active regions of the target compound were identified by the analysis of molecular electrostatic potential surface. Further, from PASS analysis and literature reports, molecular docking of title compounds was carried out with human transient receptor potential ankyrin 1 ion channel (hTRPA1) (PDB-ID 6PQO). ΔGb (docking energy) and inhibition constant was calculated to be −7.53 kcal/mol and 3.33 μM respectively, with the target ion channel.

AtZAT10/STZ1 improves drought tolerance and increases fiber yield in cotton.

Drought poses a significant challenge to global crop productivity, necessitating innovative approaches to bolster plant resilience. Leveraging transgenic technology to bolster drought tolerance in crops emerges as a promising strategy for addressing the demands of a rapidly growing global populace. AtZAT10/STZ1, a C2H2-type zinc finger protein transcription factor has shown to significantly improve Arabidopsis' tolerance to various abiotic stresses. In this study, we reports that AtSTZ1 confers notable drought resistance in upland cotton (Gossypium hirsutum), amplifying cotton fiber yield under varying conditions, including irrigated and water-limited environments, in field trials. Notably, AtSTZ1-overexpressing transgenic cotton showcases enhanced drought resilience across critical growth stages, including seed germination, seedling establishment, and reproductive phases. Morphological analysis reveals an expanded root system characterized by an elongated taproot system, increased lateral roots, augmented root biomass, and enlarged cell dimensions from transgenic cotton plants. Additionally, higher contents of proline, chlorophyll, soluble sugars, and enhanced ROS-scavenging enzyme activities are observed in leaves of transgenic plants subjected to drought, underscoring improved physiological adaptations. Furthermore, transgenic lines exhibit heightened photosynthetic rate, increased water use efficiency, and larger stomatal and epidermal cell sizes, coupled with a decline in leaf stomatal conductance and density, as well as diminished transpiration rates compared to the wild type counterparts. Transcriptome profiling unveils 106 differentially expressed genes in transgenic cotton leaves post-drought treatment, including protein kinases, transcription factors, aquaporins, and heat shock proteins, indicative of an orchestrated stress response. Collectively, these findings underscore the capacity of AtSTZ1 to augment the expression of abiotic stress-related genes in cotton following drought conditions, thus presenting a compelling candidate for genetic manipulation aimed at enhancing crop resilience.

Crystal Structure and Li-Fe Order in Synthetic Mg(2-2x)LixFe3+x(SiO4) Olivine Structure.

Olivines are naturally occurring silicates consisting of isolated (SiO4)4- tetrahedra linked through M1O6 and M2O6 octahedra. In this study, we report the structural and crystal-chemical characterization of synthetic olivine crystals containing up to 25% Li-Fe3+ synthesized using the flux growth technique. Based on site scattering, <M1-O> and <M2-O> mean bond lengths, and charge neutrality of the chemical formula, we found a perfect ordering of Li and Fe3+ at the two distinct M1 and M2 sites. Unrestrained linear extrapolation to a hypothetical isostructural LiFe3+(SiO4) composition aligns well with the tabulated ionic radii of Li and Fe3+. Comparison made with the isostructural LiSc(SiO4) reveals that the Li-centered M2O6 octahedron has a significant capacity to distort in order to accommodate structural stresses, due to the relatively weak Li-O bond, while still achieving a bond valence sum that closely matches the formal charge of Li+. This behavior suggests the potential feasibility of an extended Li + Fe3+ for 2 Mg coupled substitution within the olivine structure. The reported structure of the LiFe3+(SiO4) endmember in the literature, despite its apparent matching of cell dimensions and space group with olivine, exhibits extremely unconventional crystal chemical features, raising questions about its validity. Given the importance of the suitability of Li-insertion in LiFeSiO4 as electrodes in rechargeable Li-ion batteries, further studies are needed to investigate its crystal structure and crystal chemistry.

A Plasma Membrane Intrinsic Protein Gene OfPIP2 Involved in Promoting Petal Expansion and Drought Resistance in Osmanthus fragrans

Osmanthus fragrans, a native to China, is renowned as a highly popular gardening plant. However, this plant faces significant challenges from drought stress, which can adversely affect its flowering. In this study, we found that the plasma membrane-localized gene OfPIP2 exhibited a substantial upregulation during the flowering stages and in response to drought stress. GUS staining has illustrated that the OfPIP2 promoter can drive GUS activity under drought conditions. The overexpression of OfPIP2 was found to enhance petal size by modulating epidermal cell dimensions in Petunia and tobacco. Moreover, this overexpression also bolstered drought tolerance, as evidenced by a reduction in stomatal aperture in both species. Furthermore, yeast one-hybrid (Y1H) and dual-luciferase (Dual-LUC) assays have indicated that the transcription factor OfMYB28 directly binds to the OfPIP2 promoter, thereby regulating its expression. Together, we speculated that a module of OfMYB28-OfPIP2 was not only involved in the enhancement of petal size but also conferred the improvement of drought tolerance in O. fragrans. These results contribute valuable insights into the molecular function of the OfPIP2 gene and lay a foundation for molecular breeding strategies in O. fragrans.

Synthesis, Characterization and Identification of Mononuclear Transition Metals Complexes 1, 3-Bis-((5-methyl-1H-Imidazol-4-yl) Methyleneamino) Propan-2-ol Ligand

The ligand 1,3-bis-((5-methyl-1H-imidazol-4-yl)methyleneamino)propan-2-ol (H3L) derived from 1,3-diaminopropan-2-ol and 5-methyl-1H-imidazole-4-carbaldehyde has been synthetized and used to prepare five complexes in which the ligand acts in tetradentate fashion. Complexes formulated as [Mn(H3L)(H2O)2].2SCN (1), [(Co(H3L)].2SCN (2), [(Ni(H3L)].2SCN (3), [(Cu(H3L)(NO3)].(NO3).2H2O (4), and [(Zn(H3L)].2SCN (5) were synthesized by mixing an equimolar amount of an methanol solution containing the appropriate nitrate salt and KSCN, in 1:2 ratio, in the case of 1, 2, 3 and 5 and an ethanol solution containing the appropriate ligand H3L. The complex 4 has been synthetized in the absence of KSCN. In all the complexes the ligand acts in its neutral form and in tetradentate fashion, its hydroxy group remaining free and non-deprotonated. The ligand is coordinated to metal ion through two azomethine nitrogen atoms and two pyrazole sp2 nitrogen atoms. The complexes are characterized by elemental analysis, conductance and room temperature magnetic moments measurements, UV–Vis and IR spectroscopic studies. The structure of the copper(II) complex 4 is confirmed by X-ray diffraction. 4 crystallizes in the monoclinic space group P21/c with unit cell dimensions a = 8.5459 (3) Å, b = 10.9177 (3) Å, c = 22.4562 (6) Å, b = 96.954 (3)°, V = 2079.79 (11) Å3, Z = 4, R1 = 0.050 and wR2 = 0.131. The CuII cation in N4O inner is situated in a distorted square pyramidal environment.

Directed Differentiation of Adipose-Derived Stem Cells Using Imprinted Cell-Like Topographies as a Growth Factor-Free Approach.

The influence of surface topography on stem cell behavior and differentiation has garnered significant attention in regenerative medicine and tissue engineering. The cell-imprinting method has been introduced as a promising approach to mimic the geometry and topography of cells. The cell-imprinted substrates are designed to replicate the topographies and dimensions of target cells, enabling tailored interactions that promote the differentiation of stem cells towards desired specialized cell types. In fact, by replicating the size and shape of cells, biomimetic substrates provide physical cues that profoundly impact stem cell differentiation. These cues play a pivotal role in directing cell morphology, cytoskeletal organization, and gene expression, ultimately influencing lineage commitment. The biomimetic substrates' ability to emulate the native cellular microenvironment supports the creation of platforms capable of steering stem cell fate with high precision. This review discusses the role of mechanical factors that impact stem cell fate. It also provides an overview of the design and fabrication principles of cell-imprinted substrates. Furthermore, the paper delves into the use of cell-imprinted polydimethylsiloxane (PDMS) substrates to direct adipose-derived stem cells (ADSCs) differentiation into a variety of specialized cells for tissue engineering and regenerative medicine applications. Additionally, the review discusses the limitations of cell-imprinted PDMS substrates and highlights the efforts made to overcome these limitations.

Structure, morphology and surface properties of α-lactose monohydrate in relation to its powder properties

The particulate properties of α-lactose monohydrate (αLMH), an excipient and carrier for pharmaceuticals, is important for the design, formulation and performance of a wide range of drug products. Here an integrated multi-scale workflow provides a detailed molecular and inter-molecular (synthonic) analysis of its crystal morphology, surface chemistry and surface energy. Predicted morphologies are validated in 3D through X-ray diffraction contrast tomography. Interestingly, from aqueous solution fastest growth is found to lie along the b-axis, i.e. the longest unit cell dimension of the αLMH crystal structure reflecting the greater opportunities for solvation on the prism compared to the capping faces leading to their slower relative growth rates. The tomahawk morphology reflects the presence of β-lactose which asymmetrically binds to the capping surfaces creating a polar morphology. The crystal lattice energy is dominated by van der Waals interactions (between lactose molecules) with electrostatic interactions contributing the remainder. Predicted total surface energies are in good agreement with those measured at high surface coverage by inverse gas chromatography, albeit their dispersive contributions are found to be higher than those measured. The calculated surface energies of crystal habit surfaces are not found to be significantly different between different crystal surfaces, consistent with αLMH's known homogeneous binding to drug molecules when formulated. Surface energies for different morphologies reveals crystals with the elongated crystal morphologies have lower surface energies compared to those with a triangular or tomahawk morphologies, correlating well with literature data that the surface energies of the lactose carriers are inversely proportional to their aerosol dispersion performance.

Decomposition of Charge Loss Mechanisms in 3-D Nand Flash Memory: Impact of Cell Dimension via High-Temperature Long-Term Retention Characteristics

Decomposition of Charge Loss Mechanisms in 3-D Nand Flash Memory: Impact of Cell Dimension via High-Temperature Long-Term Retention Characteristics

Development and Characterization of a Flexible Soundproofing Metapanel for Noise Reduction

This study addresses the critical challenge of developing lightweight, flexible soundproofing materials for contemporary applications by introducing an innovative Flexible Soundproofing Metapanel (FSM). The FSM represents a significant advancement in acoustic metamaterial design, engineered to attenuate noise within the 2000–5000 Hz range—a frequency band associated with significant human auditory discomfort. The FSM’s novel structure, comprising a box-shaped frame and vibrating membrane, was optimized through rigorous finite element analysis and subsequently validated via comprehensive open field tests for enclosure-type soundproofing. Our results demonstrate that the FSM, featuring an optimized configuration of urethane rubber (Young’s modulus 6.5 MPa) and precisely tuned unit cell dimensions, significantly outperforms conventional mass-law-based materials in sound insulation efficacy across target frequencies. The FSM exhibited superior soundproofing performance across a broad spectrum of frequency bands, with particularly remarkable results in the crucial 2000–5000 Hz range. Its inherent flexibility enables applications to diverse surface geometries, substantially enhancing its practical utility. This research contributes substantially to the rapidly evolving field of acoustic metamaterials, offering a promising solution for noise control in applications where weight and spatial constraints are critical factors.

Change in the qualitative composition of non-metallic mineral raw materials as a result of blasting operations

Purpose. The research purpose is to study the change in the qualitative composition of granite before and after blasting operations to determine its compliance with the criteria of marketable products. Methods. X-ray phase and X-ray structural research methods are used to study changes in the mineral composition of granites before and after blasting operations. To separate magnetic and non-magnetic fractions of the selected granite samples, a three-roller RST magnetic separator is used. X-ray phase research is conducted using a DRON-3 diffractometer. Additionally, an analysis of the unit cell dimensions of the quartz crystal lattice was conducted, and the dislocation density along the corresponding crystallographic planes was studied. Findings. It has been determined that after blasting operations, granite mass is redistributed from coarse fractions of 1-20 mm to small fractions of 0-1 mm with an increase in the latter by 4.2%. It has been found that the biotite content decrea-ses naturally and consistently, and the quartz content increases correspondingly in products in the following series: magnetic separator drum (90%, 2%) → lower roller (72%, 14%) → upper roller (55%, 31%) → non-magnetic product (48%, 34%) before blasting operations. Therefore, despite significant differences in the magnetic favorability of these two mineral phases, they are present in all magnetic separation products (with the exception of quartz in the non-magnetic product): magnetic separator drum → lower roller → upper roller. Originality. It has been established that along the crystallographic directions 101 and 211, the maximum gradient of dislocation density increase in the quartz crystal lattice in granite samples before blasting operations is observed during the transition from the lower roller product to the upper roller product, amounting to 1.55·1010 and 6.63·1010 cm-2, respectively. After blasting operations, in granite samples along the same directions, the maximum gradient of dislocation density increase is observed between the upper roller product and the non-magnetic product, amounting to 3.01·1010 and 4.67·1010cm-2. As a result of the thermodynamic impact of blasting operations, the weighted average dislocation density value along crystallographic planes 101 and 211 in the quartz crystal lattice increases by 47.21 and 25.72%, respectively. Practical implications. Understanding the quality characteristics of marketable products after blasting operations will contribute to optimizing the stages of further processing of non-metallic mineral raw materials (two-, three- or four-stage crushing) and expanding the scope of granite applications. This increases its competitiveness in the building materials market by reducing the costs for additional processing with a reduction in the labor intensity of the process.

Scanning electron microscopy and light microscopy of tongue, fingers, toes, nuptial pad, and humeral gland in Sylvirana nigrovittata (Anura: Ranidae)

The micromorphology and histology of anuran skin, particularly in Thai species, remain relatively understudied. Anurans use their tongues for prey capture and their hands and feet for adhesion and mating, suggesting a close relationship between micro-surface features and histological structure. Information on Sylvirana nigrovittata is particularly limited. This study provides a detailed examination of the micro-surface and histological characteristics of the tongue, fingers, toes, nuptial pad, and humeral gland in S. nigrovittata. Specimens collected from Phu Luang Wildlife Sanctuary in Loei province, northeastern Thailand, were studied using scanning electron microscopy (SEM) for micro-surface features and H&amp;E staining for histological details. SEM micrographs revealed that the tongue was cordate-shaped, with about 75% of its surface covered by filiform papillae and 25% by fungiform papillae housing taste buds. Filiform papillae were trapezoidal, averaging 23.88±5.68 µm in width and 38.83±6.57 µm in length, while fungiform papillae were disc-like, averaging 52.95±14.64 µm in width and 66.70±15.88 µm in length. Digital pads on fingers and toes presented prismatic cells, with fingertip cells averaging 7.09±0.97 µm in width and 11.81±1.24 µm in length, and toe cells averaging 8.40±1.37 µm in width and 11.28±1.63 µm in length. Subdigital surfaces were smoother, containing squamous cells with dimensions of 10.65±3.21 µm in width and 21.29±4.35 µm in length. Subarticular tubercles were composed of prismatic cells with hexagonal or pentagonal surfaces, averaging 10.02±2.85 µm in width and 13.08±1.94 µm in length. Nuptial pad displayed cylindrical structures with dome-like tips, averaging 24.01±3.96 µm in width and 21.16±4.37 µm in length, and feature mucous openings. They consisted of a thick keratinized stratified squamous epithelium and a dense dermis with specialized mucous glands. Humeral gland exhibited rough surfaces with squamous cells and microridges, showing both small and large mucous openings, with average cell dimensions of 16.23±1.70 µm in width and 19.11±2.05 µm in length. Histological analysis confirmed that these structures were predominantly composed of keratinized stratified squamous epithelium, with variations in dermal collagen density and mucous gland distribution. This study enhances our understanding of the skin and gland morphology in S. nigrovittata, highlighting on its anatomical and functional adaptations.

Integrating simulated and experimental studies on novel single crystal bis(guanidininium) n-carboxylatephenylalanine towards enhanced antitumor effect

A novel organic crystal bis(guanidininium) n-carboxylatephenylalanine (GUPA) was synthesized and X-ray diffraction outcomes exposed P21, triclinic space group with cell dimensions a = 6.6492(3) Å, b = 16.2440(7) Å, c = 7.8985(3) Å, β = 0.127(2) °, V = 853.11(6) Å3, Z = 2 and possess good agreement with experimental data. Intermolecular interactions were revealed through hirshfeld and major contribution from O-H interaction confirms the presence of intermolecular hydrogen bonds. Through B3LYP algorithm with set 6–311++ G (d, p), chemical reactivity forms and molecular structure of GUPA was investigated, confirming a good stability and hard electrophilic nature. While first order hyperpolarizability value (35.37 × 10−31 esu) was indicative of good nonlinear optical material and hyperconjugate interactions and charge delocalization was further confirmed by natural bond orbitals. To further investigate the electronic properties theoretical (TD-DFT) and experimental absorption wavelengths were compared and excitation energies, oscillator strength and type of electronic transition with contributions have also been studied. The topological properties were evaluated using ELF/LOL maps and RDG with NCI were used to establish the type of interaction present in the GUPA molecular system. The anti-breast cancer effect of GUPA was computationally studied through molecular docking against p53 gene and was further investigated through in vitro MDA-MB-231 cell line studies and GUPA showed better inhibition of cancer cells and their expression.

Understanding error rejection of differential impedance spectroscopy for the in situ characterization of highly conductive fluids

Abstract Differential impedance spectroscopy (DIS) can offer distinct advantages over conventional impedance spectroscopy (IS), particularly for the in situ characterization of highly conductive, corrosive fluids. To enhance the understanding of DIS and determine the conditions under which this method is preferable over conventional IS with fixed electrode positions, error calculations were performed. Two scenarios were analyzed, one accounting solely for random instrument errors and the other including random errors as well as systematic errors from a serial offset impedance. Our analyses reveal that while permittivity measurements of highly conductive media remain challenging regardless of whether a conventional or differential impedance approach is used, DIS enables highly accurate conductivity measurements across a wide frequency and conductivity range. Studying different cell dimensions with equal cell constants revealed that despite the increased influence of systematic errors at small scales, conductivity can still be accurately measured, underscoring the applicability of DIS for microfluidic applications. Other potential parasitic effects, such as those arising from the electromagnetic skin effect, stray capacitances, electrode size, and temperature gradients, are discussed, providing a comprehensive framework for sample characterization with DIS.