AFM Images Research Articles

Novel Preparation and Characterization of Zinc Ricinoleate Through Alkali Catalysis

The enhanced thermal and chemical stability of Zinc oxide-based materials make them excellent candidates for the removal of odor-producing pollutants and compounds. The zinc salt of ricinoleic acid, commonly known as zinc ricinoleate, is viewed as the top performer. This article describes an innovative two-step synthesis of zinc ricinoleate, where the first step consists of the preparation of an intermediate compound, methyl ricinoleate, which is synthesized via transesterification of castor oil with methanol and catalyzed by sodium hydroxide. The second step comprises the preparation of zinc ricinoleate through the saponification of methyl ricinoleate in the presence of zinc oxide particles. XRD, FTIR, and NMR spectroscopies confirmed the synthesis of methyl ricinoleate and zinc ricinoleate. HR-SEM and AFM images showed the formation of larger particles, while the thermal stability of the materials was confirmed by TGA.

Near‐Infinite‐Chain Polymers with Ge=Ge Double Bonds

Despite considerable interest in heteroatom‐containing conjugated polymers, there are only few examples with heavier p‐block elements in the conjugation path. The recently reported heavier acyclic diene metathesis (HADMET) allowed for the synthesis of a polymer containing Ge=Ge double bonds – albeit insoluble and with limited degree of polymerization. By incorporation of long alkyl chains, we now obtained soluble representatives, which exhibit degrees of polymerization near infinity according to diffusion‐ordered NMR spectroscopy (DOSY) and dynamic light scattering (DLS). Analyses of the UV/Vis absorption and the NMR spectroscopic data confirm the presence of σ,π‐conjugation across the silylene‐phenylene linkers between the Ge=Ge double bonds. Favorable intermolecular dispersion interactions lead to ladder‐like cylindrical supramolecular assemblies as confirmed by X‐ray diffraction (XRD), small angle X‐ray scattering (SAXS) and DLS. AFM and TEM images of deposited thin films reveal lamellar ordering of extended polymer bundles.

Near-Infinite-Chain Polymers with Ge=Ge Double Bonds.

Despite considerable interest in heteroatom-containing conjugated polymers, there are only few examples with heavier p-block elements in the conjugation path. The recently reported heavier acyclic diene metathesis (HADMET) allowed for the synthesis of a polymer containing Ge=Ge double bonds - albeit insoluble and with limited degree of polymerization. By incorporation of long alkyl chains, we now obtained soluble representatives, which exhibit degrees of polymerization near infinity according to diffusion-ordered NMR spectroscopy (DOSY) and dynamic light scattering (DLS). Analyses of the UV/Vis absorption and the NMR spectroscopic data confirm the presence of σ,π-conjugation across the silylene-phenylene linkers between the Ge=Ge double bonds. Favorable intermolecular dispersion interactions lead to ladder-like cylindrical supramolecular assemblies as confirmed by X-ray diffraction (XRD), small angle X-ray scattering (SAXS) and DLS. AFM and TEM images of deposited thin films reveal lamellar ordering of extended polymer bundles.

Multiferroic properties and local ferroelectricity of polycrystalline LuFeO3 thin films with triangular grains on glass substrates

Polycrystalline LuFeO3 (LFO) thin films were prepared on multilayer Pt/Ta/glass substrates. The ferroelectric hysteresis loop of the LFO thin film exhibited a remanent polarization of about 5.7 μC/cm2. The ferroelectric hysteresis loop of the LFO thin film deposited at a relatively slow rate provides valuable information about its recoverable energy density (8.8 J/cm3) and loss energy density (9.3 J/cm3), resulting in an estimated energy storage efficiency of around 49%. The LFO thin film had triangular grains with a diameter of approximately 90 nm, which well reflects the crystallinity of hexagonal LFO. From the local piezoelectric d33 hysteresis loops of a triangular grain, it was confirmed that the edge of a triangular grain had a remanent d33 value larger than the center of a triangular grain. Additionally, a mosaic domain structure of the LFO thin film was well correlated with the AFM image. By applying the Landau, Lifshitz, and Kittel (LLK) scaling law, it was confirmed that the LFO thin films have a domain wall energy lower than that of PbTiO3 thin films.

Performance assessment of graphene oxide based nano-cutting fluids during sustainable hard turning through synthesis, characterization and machinability investigation

Achieving sustainability in manufacturing necessitates the implementation of eco-friendly solutions by adopting environmentally friendly coolants with cost-effective, energy-efficient and cleaner production processes without posing any risk to the operator's health. In this current work, mineral oil-based graphene oxide (GO) nano-cutting fluids of different concentration (0.05, 0.1, 0.2, 0.3, 0.4, 0.5 % wt.) are synthesized and their characteristics such as rheological, thermo-physical and tribological properties along with their stability and toxicology impact are thoroughly investigated. Further, the influence of nano-cutting fluid concentration on machinability and sustainability aspects during hard turning such as flank wear, surface integrity, power consumption, cutting temperature, carbon and noise emissions are investigated. According to the result an enhancement of 28.83 % and 29.54 % in viscosity and thermal conductivity have been recorded when concentration of nanofluid increases from 0.05 % to 0.5 %. GO nano-cutting fluids shows anti wear and friction reduction properties by providing excellent lubricious properties, as a result coefficient of friction has been reduced up to 28.36 % at 0.5 % wt. GO compared to plane mineral oil. A notable reduction in flank wear, cutting temperature, surface roughness, cutting temperature, power consumption, carbon emission and noise emission were noticed to be 25.96 %, 27.82 %, 23.86 %, 25.22 %, 11.66 % and 2.72 % respectively when the concentration of GO nanoparticles increases from 0.05 % to 0.5 % wt. Smoother surface with minimal defect has been noticed from the SEM and AFM image of machined workpiece at highest concentration (0.5 % wt.) of GO due to the synergetic effect of GO nano-cutting fluid and dual nozzle MQL system.

Development of nano-porous Au thin film at room temperature via ion irradiation in a-Ge/Au bilayer system followed by chemical etching of Ge

The development of nano-porous gold (NPG) via room temperature ion irradiation has been presented in detail. The bilayer thin films of a-Ge/c-Au have been irradiated by 100 MeV Ni ions with the fluence of 5 × 1013 ions cm−2 at room temperature. NPG is obtained by selectively etching Ge off from the Au matrix by dipping the Ge/Au thin film into 10 % H2O2 solution. Diffusion of Ge and Au across the interface under irradiation was confirmed by TRIM simulation and RBS spectra. The SEM image and EDX spectra confirms the formation of NPG with high purity. In addition, the statistical and fractal analysis of AFM image also confirms the formation of NPG. NPG system has been observed to show very good optical properties (low reflectance and high transmittance). The high quality NPG prepared by this method can be useful in the fields like optical sensors, transparent conductive electrodes, anti-reflective coatings, and photo-detector technology.

Influence of d-d transition electrons and thickness variations on the excited-state optical properties: Nonlinear optical characterization of Cr2O3 thin film

The structural, morphological, linear, and nonlinear optical properties of Cr2O3 thin films with different thicknesses deposited by the thermal deposition, were measured. The structural and morphological parameters of films, determined by XRD, FESEM, and AFM images, are compared to the linear and nonlinear optical characteristics of these media. The bandgap of prepared thin films was obtained from DRS spectra. The electron effective mass (me∗/m0), linear refractive index (n0), optical static, and high frequency dielectric constant (ε0 , ε∞) values were calculated by using the band gap energy values. Increasing the thicknesses of thin films causes to decrease the band gap, an increase RMS, increase the size of nanoparticles and the nonlinear responses of thin films. The high magnitude of n2, and β belonged to the Cr2O3 (300 nm-thickness) in the order of 10−5 cm2/W, and 10−1 cm/W respectively. The fluctuations in nonlinear responses observed at different thicknesses are attributed to d-d transitions and intraband scattering of equilibrium electrons influenced by laser radiation, as indicated by the nonlinearity data. The considerably elevated refractive non-linearity values in the analyzed film materials suggest their potential for practical applications in optoelectronic devices.

Robust branched Poly(p-terphenyl isatin) anion exchange membranes with enhanced microphase separation structure for fuel cells

Anion exchange membrane fuel cells (AEMFCs) are gradually becoming the focus of sustainable hydrogen energy research due to the advantages of clean by-products, faster oxidation-reduction dynamics and allowing cheap platinum-free base materials. As the key components of AEMFCs, anion exchange membranes (AEMs) are required to have high ionic conductivity and dimensional stability. This study focused on the design and preparation of branched AEMs for AEMFCs. The b-PTIN-x membranes were generated by incorporating 1,3,5-triphenylbenzene (TPB) units into rigid poly(p-terphenyl isatin) (PTI) polymer backbones. This innovative approach aimed to induce microphase separation structures by exploiting TPB with high FFV, as well as to enhance the tensile strength of AEMs with the help of branched structures. SAXS and AFM images revealed that the AEMs achieved enhanced microphase separation structures, resulting in the formation of ion transport channels with dimensions in the range of a few nanometers (3.36–3.70 nm). The branched b-PTIN-11 membranes displayed significant OH− conductivity (153.9 mS cm−1 at 80 °C) while having a low ion exchange capacity (IEC) (1.73 mmol g−1). The b-PTIN-11 membranes displayed improved tensile strength (56.69 MPa) and exceptional dimensional stability, with swelling ratio (SR) of 18.5 % at 80 °C. They also showed great chemical stability with 89.64 % conductivity remaining, lasting for more than 1200 h in 3 M NaOH solution at 80 °C. Ultimately, the b-PTIN-11 membrane underwent testing to evaluate its performance in a fuel cell using H2–O2. It demonstrated a peak power density (PPD) of 566 mW cm−2 when subjected to a current density of 1339 mA cm−2.

Modeling Conformational Transitions of Biomolecules from Atomic Force Microscopy Images using Normal Mode Analysis.

Observing a single biomolecule performing its function is fundamental in biophysics as it provides important information for elucidating the mechanism. High-speed atomic force microscopy (HS-AFM) is a unique and powerful technique that allows the observation of biomolecular motion in a near-native environment. However, the spatial resolution of HS-AFM is limited by the physical size of the cantilever tip, which restricts the ability to obtain atomic details of molecules. In this study, we propose a novel computational algorithm designed to derive atomistic models of conformational dynamics from AFM images. Our method uses normal-mode analysis to describe the expected motions of the molecule, allowing these motions to be represented with a limited number of coordinates. This approach mitigates the problem of overinterpretation inherent in the analysis of AFM images with limited resolution. We demonstrate the effectiveness of our algorithm, NMFF-AFM, using synthetic data sets for three proteins that undergo significant conformational changes. NMFF-AFM is a fast and user-friendly program that requires minimal setup and has the potential to be a valuable tool for biophysical studies using HS-AFM.

Self-powered high performance UV photodetectors based on spin coated n-ZnO/p-Si heterostructure

Self-powered photodetectors with high responsivity and external quantum efficiency (EQE) are in great demand for various practical applications. This paper reports the fabrication and evaluation of self-powered, high-performing ultraviolet photodetectors with fast switching action. A p-n junction was formed by spin coating n-type ZnO on p-silicon substrates. The photodetector showed a responsivity of 0.15 A/W and an EQE of 52 %. The switching speed of devices was as low as 250 ms, even under zero bias. XRD analysis revealed the hexagonal wurtzite structure and AFM images confirmed the good quality of the films with roughness values as low as 2 nm. Defect analysis was done by photoluminescence studies. The molarity of the precursor solution and the annealing temperature were varied to optimize the performance. Sample with molarity 0.5 M annealed at 500 °C showed the best results.

Epitaxial growth and characterization of copper gallate (CuGa2O4) thin films by pulsed laser deposition

High-quality crystalline copper gallate (CuGa2O4) thin films were grown on c-plane sapphire substrates using the pulsed laser deposition (PLD) technique by optimizing the growth parameters (i.e., temperature, oxygen chamber pressure, and laser energy density). The obtained XRD patterns validated that the preferred orientation of the crystalline CuGa2O4 thin film is along the [111] direction, and the crystallinity of the films improved with increasing substrate temperature while maintaining a constant O2 pressure, as assessed by measuring the full width at half maximum (FWHM) of the prominent (222) plane. Reducing the oxygen pressure leads to the emergence of β-Ga2O3 peaks rather than the CuGa2O4 peaks due to the incomplete oxidation of copper (Cu). Subsequent XRD phi (φ) scans revealed a sixfold rotational symmetry of CuGa2O4 and a 30° epitaxial relationship between the film and the sapphire substrate. X-ray photoelectron spectroscopy (XPS) spectra confirmed the presence of Cu1+, Cu2+, and Ga3+ oxidation states in the films. Increasing laser energy density resulted in the complete oxidation of Cu and an increase in the film thickness from 51.8 nm to 183.4 nm. The direct bandgap of CuGa2O4 films was determined to be approximately 4.50 eV by analyzing the UV–Vis absorbance spectra using the Tauc equation. The refractive index was found to be approximately 2.05 ± 0.01 based on the spectroscopic ellipsometry data. While the impact of increasing laser energy density was negligible on the parameters such as crystal structure, rotational symmetry, oxidation states of gallium (Ga), oxygen (O), bandgap, and refractive index of CuGa2O4 thin film, notable alterations in the oxidation state of Cu and film thickness were observed. The surface roughness (Rrms) measured from AFM images showed a strong correlation with the values derived from ellipsometry analysis.

Exploring the Mechanism of 4-Hydroxy-1,3,5-triazine-6-thiol Collector on Depressant-Free Flotation Separation of Galena from Sphalerite.

The flotation separation of galena from sphalerite was commonly implemented under pH > 10.5, which led to the consumption of lime. In this paper, 2-diethylamine-4-hydroxy-1,3,5-triazine-6-thiol (DEHTT) was synthesized and introduced as a highly selective collector to perform the depressant-free flotation separation of Pb/Zn sulfide minerals. The microflotation results indicated that 8.0 × 10-7 mol/L DEHTT recovered 94.17% galena and 26.67% sphalerite from their mixture at pH 8.5 regulated by Na2CO3, and under the same conditions, sodium isobutyl xanthate (SIBX) floated out 94.94% galena and 50.41% sphalerite, deducing a superior flotation selectivity of DEHTT in comparison to SIBX. In situ AFM images displayed the more preferable adsorption of DEHTT on galena in comparison to that on sphalerite. The results of adsorption thermodynamics and kinetics inferred that the adsorption of DEHTT onto the galena surface was a spontaneous endothermic chemical process. XPS further indicated that DEHTT combined with interface Pb atoms to form the -S-Pb and -O-Pb bonds. The special affinity of DEHTT to galena achieved the selective flotation separation of galena from sphalerite without the addition of lime and depressants.

Response of the distribution and molecular transition of gluten proteins and quality of Chinese steamed bread to different hydration levels

This study systematically explored how different hydration levels (45 %, 50 %, and 55 % water addition) affect the evolution of gluten network morphology, distribution, conformational and molecular transition, and moisture migration during the processing of Chinse steamed bread (CSB), and their impact on quality formation. Higher hydration levels resulted in a more uniform distribution and fibrous structure of the gluten network during mixing. However, excessive hydration (55 %) caused gluten fibers to rupture during fermentation. This increased the specific volume but decreased the chewiness and stickiness of CSB. MRI results highlighted that differences in moisture migration and internal structure among samples with different hydration levels were enlarged after steaming. AFM images revealed the increase in both protein molecular chain height and width with increasing hydration level, particularly after steaming. Moreover, high hydration levels promoted the depolymerization of glutenin macropolymers during mixing, fermentation, as well as repolymerization during cooking. These results indicated that both macroscopic qualities and molecular structure of gluten protein became more sensitive to the physical and biochemical processes during CSB processing. These dynamic transitions play a crucial role in determining dough rheological properties and CSB's overall quality. This research offers theoretical insights for precise dough product regulation and understanding underlying mechanisms.

Electroless ZnO Deposition on Mg-Al Alloy for Improved Corrosion Resistance to Marine Environments

Electroless ZnO (≈900 nm) was deposited on the surface of an Mg-Al alloy (AM60) to reduce its degradation in the marine environment. Uncoated and coated ZnO samples were exposed to an SME simulated marine solution for up to 30 days. The AFM and optical images revealed that the corrosion attack on the ZnO-AM60 surface was reduced due to an increase in the surface hydrophobicity of the ZnO coating (contact angle of ≈91.6°). The change in pH to more alkaline values over time was less pronounced for ZnO-AM60 (by ≈13%), whereas the release of Mg2+ ions was reduced by 34 times, attributed to the decrease in active sites on the Mg-matrix provided by the electroless ZnO coating. The OCP (free corrosion potential) of ZnO-AM60 shifted towards less negative values of ≈100 mV, indicating that electroless ZnO may serve as a good barrier for AM60 in a marine environment. The calculated polarization resistance (Rp), based on EIS data, was ≈3 times greater for ZnO-AM60 than that of the uncoated substrate.

Machine learning-guided reconstruction of cytoskeleton network from live-cell AFM images

How actin filaments (F-actins) are dynamically reorganized in motile cells at the level of individual filaments is an open question. To find the answer, a high-speed atomic force microscopy (HS-AFM) system has been developed to live-imagine intracellular dynamics of the individual F-actins. However, noise and low resolution made it difficult to fully recognize individual F-actins in the HS-AFM images. To tackle this problem, we developed a new machine learning method that quantitatively recognizes individual F-actins. The method estimates F-actin orientation from the image while improving the resolution. We found that F-actins were oriented at±35° toward the membrane in the lamellipodia, which is consistent with Arp2/3 complex-induced branching. Furthermore, in the cell cortex our results showed non-random orientation at four specific angles, suggesting a new mechanism for F-actin organization demonstrating the potential of our newly developed method to fundamentally improve our understanding of the structural dynamics of F-actin networks.

Surface Migration of Fatty Acid to Improve Sliding Properties of Hypromellose-Based Coatings

Hypromellose (HM) is a cellulose-derived polymer of pharmaceutical grade that forms easily from thin films and coatings. As few studies concern HM-formulated systems, this study focuses on the formulation of HM films by incorporating a fatty acid additive, making it possible to control surface properties such as wetting and slip behavior for pharmaceutical or medical applications. The results show that the addition of a very small amount (from 0.1 to 1% w/w) of fatty acid additive reduces HM film affinity for water and water vapor transmission rate, while film appearance and gloss are rather preserved. Surface properties were probed using wettability measurements, Tapping Mode AFM, ATR-FTIR spectrometry, and friction measurements. Tapping Mode AFM images show that the surface roughness reduces by up to 65%. Wettability results show that the surface energy decreases from 43 to 31 mJ.m−2, whereas surface FTIR spectrometry measurements demonstrate that fatty acid molecules migrate on the surface of the formulated films, the driving force being the microphase separation between the polar HM macromolecules and the hydrophobic additive, leading to the formation of a weak boundary layer with poor cohesion. As a consequence, the surface coefficient of friction significantly reduces from 0.38 to 0.08, and fatty acid molecules thus act as a lubricant, improving the sliding properties of HM-based coatings.

Influence of annealing temperature on 3D surface stereometric analysis in C-Ni films

PurposeThe purpose of this paper is to study the correlation between the thicknesses of the C–Ni films that have been prepared by RF-magnetron sputtering on quartz substrates and their three-dimensional (3D) micro morphology. In this work by AFM images, this paper studied stereo metric analysis of these films.Design/methodology/approachThe C–Ni films have been prepared by RF-magnetron sputtering on quartz substrates using a mosaic target consisting of pure graphite and strips of pure nickel approximately 2 cm2 attached to the graphite race track. The field emission scanning electronic microscopy (FESEM) images were used for the morphological characterization.FindingsThe histogram peaks are zero for all samples and the histograms are almost symmetric around zero. Temperature did not have much effect on the degree of isolation, so all four diagrams have similar results. The qualitative observations through statistical parameters of the 3D surface texture revealed that the smoothest surface has been obtained for C-Ni films annealed at 500 °C (Sa, Sq, Sz and Sv have the lower values), while the most irregular topography has been found for C-Ni films annealed at 300 °C (the fractal dimension D = 2.01 ± 0.131).Originality/valueAs shown in FESEM images, the size of the particles was increased for films deposited from 300 ºC to 800ºC; however, at 1000ºC, it decreased significantly. The histogram peaks are zero for all samples and the histograms were almost symmetric around zero. Also, the largest and lowest root mean heights (Sq) belong to films at 300 °C and 500 °C. Furthermore, the more irregular surface was found at 300 °C, and the more regular surface was found at 500 °C. As the temperature was increased to 800 °C, the values of the IAPSD function increased systematically, and then the values of the IAPSD function was decreased in the fourth sample. The surface skewness of samples annealed at 1000 °C was positive which confirms the lack of dominance of cavities on their surface with the highest amount of C-Ni films at 800 °C.

Synthesis, characterization and photoelectrochemical performance of Bi2Fe4O9 thin films

Mullite-type Bi2Fe4O9 has been little explored in thin film form as a photoanode for photoelectrochemical water splitting. In this study, Bi2Fe4O9 thin films have been prepared using the sol-gel technique from a simple precursor solution based on the corresponding metal salts, acetic acid, and polyvinyl alcohol. The films were deposited by dip-coating onto fluorine-doped tin oxide substrates and dried at 350 °C, repeating the dipping-drying cycle six times, and finally sintered at 600 °C. The films were characterized by GIXRD, revealing the formation of the material in its orthorhombic phase. Raman spectroscopy showed the Ag and B1g vibrational modes, validating the formation of the bismuth iron oxide. UV–Vis transmittance measurements revealed that the material exhibits two optical transitions: a direct band gap of 2.86 eV and an indirect band gap of 1.98 eV. FESEM micrographs and AFM images showed a uniform nanostructured surface morphology. The photoelectrochemical properties of the Bi2Fe4O9 films were studied using cyclic voltammetry and chronoamperometry with front side illumination, demonstrating the stability of the material in aqueous media and the generation of photocurrent in the presence of H2O2. Furthermore, results from intensity-modulated photocurrent spectroscopy (IMPS) revealed that the photocurrent is limited by both bulk and surface recombination and a short hole diffusion length.

SO3 removal by submicron absorbents synthesized via inhibition method: The product layer grows like parallel peaks

Injecting calcium hydroxide powder into the flue gas is an effective strategy for SO3 removal. However, commercial calcium hydroxide has several disadvantages, including large particle size, low efficiency, and unsuitability for excessive grinding. In this work, sub-micron calcium hydroxide was synthesized by an inhibition method and its performance for SO3 removal from flue gas was investigated on a pilot-scale platform (120 Nm3/h). When the concentration of sodium alginate solution was 100 mg/L, the average particle size of calcium hydroxide decreased from 13.66 µm to 0.84 µm, which improved the SO3 removal (92.1 %) and conversion of the absorbent. The results of the fixed-bed experiments indicate that the absorption kinetics of the reaction is consistent with the Bangham model. In addition, density functional theory verifies that calcium hydroxide captures SO3 by chemisorption. The AFM image shows that the calcium sulfate whiskers produced during the reaction grow like parallel peaks on the adsorbent surface. The calculations suggest that the driving force for SO3 adsorption originates from Ca-p orbital (Ca(OH)2) and O-s orbital (SO3) hybridization. This study complements the island growth mechanism for gas-solid two-phase reactions and provides an effective method for removing SO3 from flue gas in coal-fired power plants. In addition, it will provide an important reference for the development of submicron adsorbents.

Chitosan based extruded nanofibrous bioscaffold for local delivery of mesenchymal stem cells to improve diabetic wound healing

BackgroundMesenchymal stem cells (MSCs)-based treatment strategy has shown promise in bolstering the healing process of chronic wounds in diabetic patients, who are at risk of amputation and mortality. To overcome the drawbacks of suboptimal cell retention and diminished cell viability at the injury site, a novel nanofibrous biomaterial-based scaffold was developed by using a controlled extrusion of a polymeric solution to deliver the cells (human adipose-derived MSCs (ADMSCs) and placenta-derived MSCs (PLMSCs)) locally to the animal model of diabetic ulcers.MethodsThe physicochemical and biological properties of the nano-bioscaffold were characterized in terms of microscopic images, FTIR spectroscopy, tensile testing, degradation and swelling tests, contact angle measurements, MTT assay, and cell attachment evaluation. To evaluate the therapeutic efficacy, a study using an excisional wound model was conducted on diabetic rats.ResultsThe SEM and AFM images of scaffolds revealed a network of uniform nanofibers with narrow diameters between 100-130 nm and surface roughness less than 5 nm, respectively. ADMSCs and PLMSCs had a typical spindle-shaped or fibroblast-like morphology when attached to the scaffold. Desired characteristics in terms of swelling, hydrophilicity, biodegradation rate, and biocompatibility were achieved with the CS70 formulation. The wound healing process was accelerated according to wound closure rate assay upon treatment with MSCs loaded scaffold resulting in increased re-epithelialization, neovascularization, and less inflammatory reaction. Our findings unequivocally demonstrated that the cell-loaded nano-bioscaffold exhibited more efficacy compared with its acellular counterpart. In summation, our study underscores the potential of this innovative cellular scaffold as a viable solution for enhancing the healing of diabetic ulcers.ConclusionThe utilization of MSCs in a nanofibrous biomaterial framework demonstrates significant promise, providing a novel avenue for advancing wound care and diabetic ulcer management.Graphical