Nanoparticle Size Analyzer Research Articles

ROS responsive nanozyme loaded with STING silencing for the treatment of sepsis-induced acute lung injury

Acute lung injury (ALI) is a common complication of sepsis and a leading cause of mortality in septic patients. Studies indicate that STING may play a crucial role in the pathogenesis of sepsis-induced ALI by interacting with the PARP-1/NLRP3 pathway. Therefore, targeting STING inhibition has potential as a novel therapeutic strategy for ALI. However, effective inhibition remains challenging due to the widespread expression of STING across various tissues. In this study, we developed a nanozyme-based drug delivery system, DSPE-TK-mPEG-MnO2@siSTING (abbreviated as DTmM@siSTING), using DSPE-TK-mPEG-MnO2 as the carrier, and characterized it via scanning electron microscopy, dynamic light scattering, nanoparticle size analysis, and gel electrophoresis. To evaluate the therapeutic effects of DTmM@siSTING, an in vitro ALI cell model and an in vivo ALI mouse model were established, assessing the nanozyme's impact on ROS levels, inflammatory responses, and the PARP-1/NLRP3 pathway in sepsis-induced ALI. Results demonstrated that DTmM@siSTING exhibited good physiological stability. In vitro, DTmM@siSTING significantly reduced ROS levels, myeloperoxidase activity, and expression of inflammatory cytokines, while also inhibiting PARP-1/NLRP3 pathway activation. In vivo experiments further revealed that DTmM@siSTING effectively delivered siSTING to the lungs, mitigating sepsis-induced ALI and associated inflammatory responses. Additionally, DTmM@siSTING displayed excellent biocompatibility. In summary, our findings suggest that DTmM@siSTING significantly enhances the therapeutic efficacy of siSTING, alleviating ALI by inhibiting ROS production, inflammatory responses, and activation of the PARP-1/NLRP3 pathway. This novel approach presents a promising therapeutic avenue for sepsis-induced ALI.

Preparation and properties of fluorinated VAc-VeoVa10 latex emulsified with allyl nonyl phenoxy propyl alcohol polyoxyethylene ether ammonium sulphate

Purpose The traditional VeoVa10-VAc copolymer latex, which prepared via the emulsion polymerization of the mixed monomers of VAc and VeoVa10, has the poor water resistance and thermal stability because of the migration of the conventional emulsifier molecules and the low bond energy of C-C bond. The purpose of this work is that the fluorinated monomer is used to modify the latex. The film of the resultant latex has the C-F bond with high bond energy and low surface energy, which can effectively improve the heat resistance and water resistance of the resultant film. In addition, the reactive emulsifier is used to replace the conventional emulsifier. The drawbacks of the conventional emulsifier molecules migrate and desorb can be avoided when the polymer latex is stored, thereby also improving the water resistance. Design/methodology/approach The modified VAc-VeoVa10 latex has been successfully synthesized via the semi-continuous seeded emulsion polymerization, which VAc and VeoVa10 is used as the main monomers and HFMA was used as the functional monomer. KPS and reactive surfactants of SE-10 were used as the initiator and emulsifier, respectively. The structure of resultant latex film was characterized by Fourier transform infrared spectroscopy (FTIR). The latex films were tested by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and contact angle (CA). The particle size and its distribution of the latex were measured by the nano particle size analyzer. Findings The factors that had an influence on the properties of the latex and the film were investigated in detail. The stability of the resultant latex is good. The average particles of the latex and its distribution are small and uniform, respectively. In comparison with the conventional latex film, the thermal stability and hydrophobicity of the resultant latex film are improved obviously. Practical implications The resultant latex can be used in both the waterborne interior and exterior wall coatings, pickering stabilized waterborne polymer dispersions, polymer powders, environmentally friendly polymer-modified waterproof mortar and other fields, which can be satisfied with the high demand of thermal stability and hydrophobicity. Originality/value The modification of poly (VAc-VeoVa10) by reactive surfactant and fluorinated monomer is seldom reported. In this study, the fluorinated poly (VAC-VeoVa) latex is prepared via the reactive surfactants, which VAc and VeoVa10 is used as the main monomers and hexafluorobutyl methacrylate is used as the functional monomer. Potassium persulfate (KPS) and allyl nonyl phenoxy propyl alcohol polyoxyethylene ether ammonium sulfate are used as the initiator and emulsifier, respectively.

Investigation of structural, optical, and magnetic properties of NiFe2O4 for efficient photocatalytic degradation of organic pollutants through photo fenton reactions

Nowadays, water pollution generated from textile effluents is one of the major problems for the human race and ecology. Hence, development of sustainable strategies to lower the water pollution level has become a burning need. In this regard, the present study focuses on the preparation of nano catalyst NiFe2O4 to catalyze the chemical reactions on industrial organic dyes for their fast cleansing from water. By sol-gel auto-combustion technique, NiFe2O4 nanoparticles were synthesized and exposed to thermal process at temperatures of 400, 600, and 800 °C. Highly crystalline phase with spinel cubic structured NiFe2O4 was formed with a crystal size of 18.71 nm, which was confirmed by XRD analysis. The FTIR spectra showed two fundamental absorption bands in the range 597.80–412.59 cm−1, which are the characteristics of tetrahedral M − O and octahedral M − O bond in NiFe2O4. The surface morphology of calcined NiFe2O4 was investigated by scanning electron microscope (SEM). The nanoparticle size analyzer exhibited that the synthesized NiFe2O4 nanoparticles had an average particle size of ∼ 291.3 nm. Three stage decomposition patterns were observed for NiFe2O4, which was analyzed by a temperature programmed STA. Zeta potential analyzer showed that the synthesized sample S1 and S2 were stable in the dispersion medium. Also, NiFe2O4 exhibited optical band gap energies for direct band transitions within the visible spectrum measured to be 1.43–1.45 eV, rendering them effective as photocatalysts under sunlight. The samples showed magnetic measurements by VSM with saturation magnetization, coercivity, remnant magnetization value of 66.81 emu/g, 4.13 Oe and 12.94 emu/g, respectively. The synthesized photocatalyst, NiFe2O4, at 400 °C, significantly degraded three toxic organic pollutants—Methylene blue, Rhodamine B, and Congo Red—under visible light through ‘Photo-Fenton’ reaction mechanisms. Among the three dyes, Methylene Blue exhibited the highest degradation percentage with a rate constant of 0.0149 min−1 and followed pseudo-first-order kinetic model.

Environmentally friendly and temperature resistant water-based drilling fluids with highly inhibitory synthetic nanocellulose polymers for deep sea drilling

The ocean is rich in sustainable hydrocarbon. The process of extracting these resources poses challenges such as coexistence of low temperature and high temperature, high pressure of deepwater and unpredictable shale formations. A kind of ionic crosslinking polymer consisting of N, N-dimethylacrylamide (DMA), 2-acrylamido-2-methylpropane sulfonic acid (AMPS), and Cellulose Nanofibers (CNF) (PADC), was synthesized to address these challenges. Cellulose was first oxidized to nanocellulose (CNF) through 2,2,6,6-tetramethylpiperidinyl-1-oxide (TEMPO) oxidation. Subsequently, the ionic crosslinking polymer, consisting of DMA, AMPS, and CNF, was synthesized using ionic crosslinking polymerization. The surface characteristics and morphology were characterized by transmission electron microscopy (TEM), nanoparticle size analysis, and zeta potential analysis. The structural composition was analyzed by Fourier Transform Infrared Spectroscopy (FT-IR). The shale inhibition mechanism was investigated through contact angle and pressure transmission experiments. The results indicated that the average length of PADC is approximately 1450 nm, with an average diameter of less than 100 nm and contains sulfonic acid groups. The shale contact angle increased from 16.75° to 82°, indicating that PADC increased the hydrophobicity of the shale by 390%. Pressure transfer experiments show that PADC can reduce shale permeability by 37%, which means PADC has good hydration inhibition performance. In addition, a drilling fluid system suitable for deep sea drilling was proposed. The drilling fluid system exhibits good rheological properties at 160 °C and 0 °C. The fluid loss after hot rolling at 160 °C is less than 12 mL. The linear expansion of shale core after 16 h is only 0.7%, and the rolling recovery rate at 160 °C is as high as 99.48%. Luminescent bacteria EC50 is 2.0 × 105 mg/L, which means it is non-toxic and environmentally friendly. And drilling fluid conforms to the power law flow model. Therefore, the drilling fluids proposed in this paper can meet the requirements of deep sea drilling in terms of rheological properties and filtration loss properties at 0–160 °C, and can seal shale pores and inhibit shale hydration through the ionic cross-linking PADC. This research offers insights into the utilization of cellulose in well drilling processes and provides references for designing deep sea drilling fluids.

Size and isotope analysis of individual nanoparticles by multi-collector ICP-MS using “event-triggered signal capture” with a high-speed oscilloscope

Accurate quantitative elemental and isotope analysis of nanoparticles at the single-particle level is crucial for better understanding their origin, properties and behaviors. Single particle inductively coupled plasma-mass spectrometry (spICP-MS) has emerged as a promising technique for nanoparticle analysis. However, challenges persist in obtaining accurate and consistent element profiles and ratios for small-sized nanoparticles by conventional quadrupole (QMS) or time-of-flight mass analyzers (TOF-MS) due to their low level and transient nature. In this paper, we present a novel analytical method for single nanoparticle analysis using multiple collector ICP-MS (MC-ICP-MS) combined with a modern high-speed digital oscilloscope. The single particle events are acquired using an “event-triggered signal capture” (ETSC) technique, which enables the simultaneously capture and visualization of multiple isotopes of transient individual particle profiles with nanosecond time resolution. This greatly facilitates precise and efficient analysis of nanoparticles. The minimum detectable particle size is calculated to be as small as 8 nm (∼1 ag 109Ag) for AgNPs. Based on the 109/107Ag ratios obtained from 2000 particles, the precisions of 109/107Ag ratio measurements on 20 nm, 40 nm, 60 nm, 80 nm and 100 nm were approximately 0.086 (SD), 0.063 (SD), 0.051 (SD), 0.040 (SD), and 0.029 (SD), which is limited by counting statistics of the isotopic signals. Furthermore, the achieved standard error of 109/107Ag can be reduced to sub-permil level (0.7 ‰) even for the measurement of 20 nm AgNPs (N = 17,000). These results demonstrate that the ETSC provides a unique method for isotope analysis of single particles, holding great potential for enhancing our understanding of nanoparticles.

Controlled Size Characterization Process for In-Situ TiB2 Particles from Al Matrix Composites Using Nanoparticle Size Analysis.

The wide size range and high tendency to agglomerate of in-situ TiB2 particles in reinforced Al matrix composites introduce great difficulties in their size characterization. In order to use a nanoparticle size analyzer (NSA) to obtain the precise size distribution of TiB2 particles, a controlled size characterization process has been explored. First, the extraction and drying processes for TiB2 particles were optimized. In the extraction process, alternated applications of magnetic stirring and normal ultrasound treatments were proven to accelerate the dissolution of the Al matrix in HCl solution. Furthermore, freeze-drying was found to minimize the agglomeration tendency among TiB2 particles, facilitating the acquisition of pure powders. Such powders were quantitatively made into an initial TiB2 suspension. Second, the chemical and physical dispersion technologies involved in initial TiB2 suspension were put into focus. Chemically, adding PEI (M.W. 10000) at a ratio of mPEI/mTiB2 = 1/30 into the initial suspension can greatly improve the degree of TiB2 dispersion. Physically, the optimum duration for high-energy ultrasound application to achieve TiB2 dispersion was 10 min. Overall, the corresponding underlying dispersion mechanisms were discussed in detail. With the combination of these chemical and physical dispersion specifications for TiB2 suspension, the bimodal size distribution of TiB2 was able to be characterized by NSA for the first time, and its number-average diameter was 111 ± 6 nm, which was reduced by 59.8% over the initial suspension. Indeed, the small-sized and large-sized peaks of the TiB2 particles characterized by NSA mostly match the results obtained from transmission electron microscopy and scanning electron microscopy, respectively.

Effects of caffeic acid on advanced glycation end product formation and emulsion properties in glycosylated perilla seed meal protein

Protein glycosylation is an effective way to enhance the properties of proteins in food systems. However, the negative effects of glycosylation, such as generation of advanced glycation end products (AGEs), have received less attention; these effects are closely related to the occurrence of various chronic metabolic diseases. In this study, a perilla seed meal protein (PSMP)-fructose/dextran (DEX)-caffeic acid (CA) ternary emulsifying system was constructed. Then, AGEs formation and emulsifying properties were characterized, and the optimal emulsifying system for β-carotene (BC) delivery was investigated. The resulting complex was examined using a high-performance liquid chromatography (HPLC)-ultraviolet (UV) detector, ultra-HPLC-tandem mass spectrometry (UHPLC-MS/MS) system, and nanoparticle size analyzer. The results indicated that CA conjugated with glycosylated PSMP significantly reduced the formation of fructosamine (13.5%), methylglyoxal (33.26%), Nε-carboxymethyl lysine, and Nε-carboxyethyl lysine (>80%). Compared with other conjugates, the PSMP-DEX-CA ternary conjugate showed the lowest AGEs content, smaller particle size, better emulsifying active index, lower polydispersity index, and acceptable ζ-potential. The emulsifying system constructed using abovementioned ternary conjugate revealed better UV and thermal stability in BC delivery, which slowed BC degradation. This study provides a novel approach for constructing a low AGEs emulsion system to deliver BC via PSMP with different modifications.

Cleaning Oil-Based Drilling Cuttings with Synthetic Gemini Surfactants.

The chemical cleaning method is the simplest approach for degreasing oil-based drilling cuttings (ODCs), with the effectiveness of the treatment relying mainly on the selection of the surfactant and the cleaning conditions. However, achieving the standard treatment of ODCs directly using conventional surfactants proves challenging. In light of this, this study introduces a synthesized and purified Gemini surfactant named DCY-1. The structure of DCY-1 was confirmed through Fourier transform infrared (FTIR) and nuclear magnetic resonance (NMR) analyses. The characterization in this article encompasses the use of an interface tension meter, nanoparticle size analysis, scanning electron microscopy, and infrared oil measurement. The critical micelle concentration (CMC) of DCY-1 was determined to be 3.37 × 10-3 mol/L, with a corresponding γcmc value of 37.97 mN/m. In comparison to conventional surfactants, DCY-1 exhibited a larger micelle size of 4.52 nm, approximately 24.52% larger than that of SDS. Moreover, the residual oil rate of 3.96% achieved by DCY-1 was the lowest among the chemical cleaning experimental results. Through a single-factor experiment, the optimal cleaning ability of DCY-1 for ODCs was determined as follows: a surfactant concentration of 3 mmol/L, a temperature of 60 °C, an ODC/liquid mass ratio of 1:4, a cleaning duration of 40 min, and a stirring speed of 1000 rad/min. Under these optimal conditions and after merely two cleaning procedures, the residual oil content of ODCs was reduced to 1.64%, accompanied by a smooth and loose surface structure.

New materials-based on gelatin coordinated with zirconium or aluminum for ecological retanning

Ecological retanning agent is an effective way to solve the pollution source of leather manufacturing industry. In this study, the gelatin from chrome-containing leather shavings in the leather industry was used to realize sustainable leather post-tanning. The gelatin hydrolysate (GH) coordinated with Zr4+ or Al3+ to prepare eco-friendly retanning agents GH-Zr and GH-Al. The successful coordination between GH and metal ions was characterized by FTIR and XPS. The retanning agents were characterized by FTIR curve-fitting and circular dichroism spectroscopy. The results showed that the conformation of the secondary structure of the polypeptide became ordered and stable after coordinating with the metal ions. The particle size and weight average molecular weight of the retanning agents were ~1700 nm and ~2100, respectively, measured by nanoparticle size analyzer and gel permeation chromatography (GPC). The retanning agents were applied to retanning of chrome tanned leather and glutaraldehyde tanned leather. The abundant free amino from retanning agents can consume the free formaldehyde. Meanwhile, retanning agents can effectively improve the multiple binding sites, resulting in favorable thickening rate (>110 %) and excellent dye and fatliquor absorption rate with ~99.91 % and ~93.18 %. Thus, this strategy can provide a viable choice for solid leather waste and sustainable development of the leather industry.

Exploration of properties (crystallographic, morphological, optical) of nano cobalt aluminate synthesized by facile sol–gel method: Effects of sintering temperature

The present work reports on the facile sol–gel synthesis of CoAl2O4 nanoparticles using cobalt nitrate and aluminum nitrate as the metal salts and citric acid and glycerol as chelating agents. The consequence of sintering temperature on the structure, particle size, morphology, composition, zeta potential, color, and reflectance spectra at neutral pH condition were explored with various instrumental techniques. The CoAl2O4 nanoparticles were characterized with Powder X-ray diffraction (PXRD), Fourier-transform infrared spectroscopy (FT-IR), Field emission scanning electron microscopy (FESEM), Energy dispersive spectroscopy (EDS), Nanoparticle size analyzer, Ultraviolet–Visible Diffuse Reflectance Spectroscopy (UV–Vis-DRS) and CIE-Lab colorimetric method. From the data of PXRD, the crystallite size and peak profile analysis were investigated by four different models. It was found that the average crystallite size varied in the range of 28.01–320.97 nm and single-phase cubic CoAl2O4 was formed without any impurity. The average particle size of CoAl2O4 nanoparticles was discerned from the FESEM images using ImageJ software and from a nanoparticle size analyzer. The average particle sizes were increased with the increasing sintering temperature. The values of zeta potential found in all of the samples represented high dispersion stability. From the colorimetry of CoAl2O4 nanoparticles, the CIE-La*b* output illustrated high purity and brightness and the spectra.

From silicon to silica: a green chemistry approach for hollow sphere nanoparticle formation.

Herein we report on an environmentally friendly and scalable production route for hollow silica spheres (HSSs). The process is based on close to 100% conversion of non-crystalline solid Si nanoparticles (D̄ = 40 ± 9 nm) in mild alkaline solutions (pH ≤ 9.0) at ambient temperature. The Si nanoparticles are prepared using the centrifugal chemical vapor deposition (cCVD) method. Combining transmission electron microscopy (TEM) imaging and nanoparticle size analysis with hydrogen evolution data, elemental mapping, and nitrogen adsorption for surface area measurement, we show for the first time experimental data that document a Kirkendall type Si-to-HSS formation process. Our understanding is that the Si nanoparticles exposed to air form a SiO2 film, which is stable in the mild alkaline environment. Silicon from the Si nanoparticles is transported through the thin SiO2 film and is reacting with H2O/OH- species on the particle surface or in the already thickened SiO2 shell to form silicic acid that in turn rapidly gets converted to a sol-gel to continue the growing of the silica shell. We foresee that this green chemistry approach can be utilized for HSS preparation for use in batteries, insulation materials and drug delivery.

Development of Polymeric Micelles for Combined Delivery of Luteolin and Doxorubicin for Cancer Therapy.

Background: Luteolin (LUT) is a bioactive compound with several pharmacological activities including anticancer effect. Doxorubicin (DOX) is an anthracycline chemotherapeutic drug that have proven to be effective in treating various types of cancers. Polymeric micelles (PMs) containing biologically active materials have emerged as prospective dosage forms with high drug-loading, which can add therapeutic benefit to the poorly water-soluble compounds and novel chemical entities. PMs are effective in delivering several drugs, such as anticancer drugs, antifungal drugs, flavonoids and drugs targeting the brain. The aim of the current study is to develop PMs for LUT and DOX as a combined delivery system for cancer therapy. Methods: PMs were prepared using 2.5% of each of LUT and DOX with varying compositions of Poloxamer 188, Poloxamer 407, Vitamin E (TPGS), Poloxamer 123 and Gellucire 44/14 at room temperature. Particle size, polydispersity index, zeta potential, were achieved using Zetasizer Nano particle size analyzer and the sizes were further confirmed with transmission electron microscopy (TEM). Prepared PMs were further characterized using powder X-ray diffraction (PXRD) and fourier transform infrared spectroscopy (FTIR). An MTT assay was performed on breast cancer (MCF-7) cells and liver cancer (HepG2) cells to determine the cytotoxic effect of the different PMs formulations. Results: PMs were successfully developed and optimized using 74.3% Poloxamer 407 with 20.7% Vitamin E (TPGS), and 70% Poloxamer 407 with 25% Gellucire 44/14, respectively. The droplet size and polydispersity index were found to be 62.03 ± 3.99 nm, 91.96 ± 5.80 nm and 0.33 ± 0.05, 0.59± 0.03, respectively for PMs containing TPGS and Gellucire 44/14. Zeta potentials of the PMs containing TPGS and Gellucire 44/14 were recorded as -2.27 ±0.11mV and -7.78 ± 0.10 mV, respectively. The PMs showed a spherical structure with approximately 50-90 nm range evident by TEM analysis. The PXRD spectra of PMs powder presented the amorphization of LUT and DOX. The FTIR spectra of LUT-loaded and DOX-loaded PMs were identical, suggesting consistent PMs composition. The MTT assay showed that the representative combined drug loaded PMs treatment led to a reduction in the viability of MCF-7 and HepG2 cells compared to drug free PMs and pure LUT, DOX alone. Conclusions: PMs with LUT and DOX exhibited significant cytotoxic effects against breast and liver cancer cells and could thus be an important new pharmaceutical formulation to treat cancer.

Leveraging Machine Learning for Size and Shape Analysis of Nanoparticles: A Shortcut to Electron Microscopy.

Characterizing nanoparticles (NPs) is crucial in nanoscience due to the direct influence of their physiochemical properties on their behavior. Various experimental techniques exist to analyze the size and shape of NPs, each with advantages, limitations, proneness to uncertainty, and resource requirements. One of them is electron microscopy (EM), often considered the gold standard, which offers visualization of the primary particles. However, despite its advantages, EM can be expensive, less accessible, and difficult to apply during dynamic processes. Therefore, using EM for specific experimental conditions, such as observing dynamic processes or visualizing low-contrast particles, is challenging. This study showcases the potential of machine learning in deriving EM parameters by utilizing cost-effective and dynamic techniques such as dynamic light scattering (DLS) and UV-vis spectroscopy. Our developed model successfully predicts the size and shape parameters of gold NPs based on DLS and UV-vis results. Furthermore, we demonstrate the practicality of our model in situations in which conducting EM measurements presents a challenge: Tracking in situ the synthesis of 100 nm gold NPs.

Chitosan nanoparticles loaded with Eucommia ulmoides seed essential oil: Preparation, characterization, antioxidant and antibacterial properties

Eucommia ulmoides seed essential oil (EUSO) is a natural plant oil rich in various nutrients, which has been widely used due to its unique medicinal effects. However, it is prone to oxidation and rancidity under many adverse environmental influences. Nanoencapsulation technology can protect and slow down the loss of its biological activity. In this study, chitosan nanoparticles (CSNPs) loaded with EUSO were prepared by emulsification and ionic gel technology. EUSO-CSNPs were characterized by Fourier transform infrared (FTIR) spectroscopy, Thermogravimetric analysis (TGA) and X-ray diffraction (XRD). The results confirmed the success of EUSO encapsulation and the encapsulation rate ranged from 36.95 % to 67.80 %. Nanoparticle size analyzer, Scanning electron microscope (SEM) and Transmission electron microscopy (TEM) showed that CSNPs were spherical particles with a range of 200.6–276.0 nm. The results of in vitro release study indicated that the release of EUSO was phased, and EUSO-CSNPS had certain sustained-release properties. Furthermore, EUSO-CSNPs had higher antioxidant and antibacterial abilities than pure EUSO and chitosan, which was verified through free radical scavenging experiments and bacteria biofilm experiments, respectively. This technology can enhance the medicinal value of EUSO in biomedical and other fields, and will provide support for in vivo research of EUSO-CSNPs in the future.

Hydrogel loaded with exosomes from Wharton's Jelly-derived mesenchymal stem cells enhances wound healing in mice.

To explore the effect of hydrogel loaded with exosomes from Wharton's Jelly-derived mesenchymal stem cell (WJMSC) on wound healing. Exosomes were extracted from WJMSC, and the morphology and size of WJMSC-derived exosomes (WEX) were analyzed by transmission electron microscopy and nanoparticle size analyzer, respectively. The surface markers CD9, CD81, and Calnexin of WEX were detected by Western blotting. Exosome-loaded alginate hydrogel (WEX-gel) was prepared; its morphology was studied by scanning electron microscope, and its rheological behavior was examined by a rheometer. The in vitro drug release performance of WEX-gel was investigated by BCA method. RAW264.7 cells were treated with alginate hydrogel, WEX and WEX-gel, respectively; and the expression of CD86 and CD206 in macrophages was detected by flow cytometry. A full-thickness skin wound model was established in mice; the model mice were randomly divided into blank control group, WEX control group and WEX-gel group, and PBS, WEX and WEX-gel were applied to the wound area of mice, respectively. On day 3, the skin tissue of mice was excised, and the antibacterial effect of WEX hydrogel was evaluated by plate counting. On day 15, the mice were euthanized and the percentage of residual wounds was calculated. The histological changes of the skin wound were observed after hematoxylin and eosin (HE) and Masson stainings. The expression of CD86, CD206, CD31 and vascular endothelial growth factor (VEGF) in the skin wound tissue was detected by immunohistochemistry. Exosomes were successfully extracted from WJMSC. WEX-gel presented a regular three-dimensional network structure, good rheology and controlled drug release performance. WEX-gel promoted the polarization of RAW264.7 cells from the M1 phenotype to M2 phenotype in vitro. The residual wound percentage in blank control group, WEX control group and WEX-gel group were (27.5±3.4)%, (15.3±1.2)% and (7.6±1.1)%, respectively (P<0.05). The antibacterial property of WEX-gel is better than that of WEX (P<0.05). The dermis thickness, the number of new hair follicles, and the rate of collagen deposition in the WEX-gel group were significantly higher than those in the other two groups (all P<0.05). The expression of CD206, CD31 and VEGF in skin wound tissue was higher and the expression of CD86 was lower in WEX-gel group than those in other two groups (all P<0.05). WEX-gel can significantly promote wound healing in mice by regulating the polarization of macrophages.

PH-dependent synthesis of CeO2-ZnO nanocomposite for enhanced environmental remediation of endosulfan and dimethoate pesticides

This research aims to tackle significant challenges related to the synthesis and utilization of advanced nanocomposite materials in environmental remediation, specifically focusing on pesticide degradation. The synthesis of CeO2-ZnO nanocomposites employs both co-precipitation and hydrothermal methods, with the inclusion of the zwitterionic surfactant (SB-12) as a surface modifier. The modulation of pH levels during the synthesis of CeO2-ZnO nanocomposites allows for the optimization of crucial reaction parameters. Notably, it is observed that nanocomposites prepared at pH 9 exhibit the smallest average particle size. To comprehensively characterize these prepared nanocomposites, various analytical techniques such as FTIR, XRD, DR-UV/Vis, TEM/EDS, and Nano particle size analysis are employed. The FTIR results reveal a reduced presence of impurities at higher pH levels. Notably, the CeO2-ZnO nanocomposites synthesized via the hydrothermal method at pH 9 exhibit polyhedral nanostructures. The research's significant contribution lies in the practical application of these nanocomposites for the degradation of highly toxic and persistent organochlorine and organophosphorus pesticides, particularly Endosulfan and Dimethoate. These nanoparticles demonstrate remarkable pesticide degradation capabilities, with a particular emphasis on their high effectiveness against Endosulfan. The potential implications of this work extend to areas such as environmental protection, sustainable agriculture, and the remediation of pesticide-contaminated ecosystems.

Multifunctional electrospun nanofibrous scaffold enriched with alendronate and hydroxyapatite for balancing osteogenic and osteoclast activity to promote bone regeneration.

Electrospun composite nanofiber scaffolds are well known for their bone and tissue regeneration applications. This research is focused on the development of PVP and PVA nanofiber composite scaffolds enriched with hydroxyapatite (HA) nanoparticles and alendronate (ALN) using the electrospinning technique. The developed nanofiber scaffolds were investigated for their physicochemical as well as bone regeneration potential. The results obtained from particle size, zeta potential, SEM and EDX analysis of HA nanoparticles confirmed their successful fabrication. Further, SEM analysis verified nanofiber's diameters within 200-250nm, while EDX analysis confirmed the successful incorporation of HA and ALN into the scaffolds. XRD and TGA analysis revealed the amorphous and thermally stable nature of the nanofiber composite scaffolds. Contact angle, FTIR analysis, Swelling and biodegradability studies revealed the hydrophilicity, chemical compatibility, suitable water uptake capacity and increased in-vitro degradation making it appropriate for tissue regeneration. The addition of HA into nanofiber scaffolds enhanced the physiochemical properties. Additionally, hemolysis cell viability, cell adhesion and proliferation by SEM as well as confocal microscopy and live/dead assay results demonstrated the non-toxic and biocompatibility behavior of nanofiber scaffolds. Alkaline phosphatase (ALP) and tartrate-resistant acid phosphatase (TRAP) assays demonstrated osteoblast promotion and osteoclast inhibition, respectively. These findings suggest that developed HA and ALN-loaded PVP/PVA-ALN-HA nanofiber composite scaffolds hold significant promise for bone regeneration applications.

Preparation and Utilization of a Comb‐Like Polycarboxylate Dispersant for Organic Pigment

AbstractAs a novel form of carboxylate comb‐like copolymers, SAM‐(m)PEG was prepared by polymerizing styrene (S), acrylic (A), and maleic anhydride (M) to obtain a random copolymer labeled SAM. SAM was then esterified using either polyethylene glycol (PEG) or methyl PEG (mPEG), a waterborne polymer dispersant for dispersing and stabilizing C.I. Pigment Yellow 180 (PY 180). The structures of SAM‐(m)PEG and the ground suspension of PY 180 were characterized by Fourier transform infrared (FT‐IR) spectroscopy, nuclear magnetic resonance (NMR) spectroscopy, scanning electron microscopy (SEM), a nanoparticle size analysis, and viscometry. The effects of different branch chains, synthetic formulas, and grinding conditions on the dispersibility of SAM‐(m)PEG were evaluated. In addition, the optical properties of the pigments were investigated after ultrafine grinding. The adsorption mechanism between the SAM‐(m)PEG dispersants and PY 180 particles is also discussed. SAM‐PEG6002 outperformed the other SAM‐(m)PEG dispersants owing to its excellent dispersion and stability. When used as the dispersant, the average particle size (Z‐average) of PY 180 after grinding was 264.6 nm, and the particle size distribution became narrow (PDI=0.089). Moreover, SAM‐PEG6002 effectively maintained the color performance of the pigment, and the product was successfully applied to the pigment coating. Therefore, SAM‐PEG6002 is an effective waterborne polymer dispersant for organic pigments.

Effect of chemical species and temperature on the stability of air nanobubbles

The colloidal stability of air nanobubbles (NBs) was studied at different temperatures (0–30 °C) and in the presence of sulfates, typically found in mining effluents, in a wide range of Na2SO4 concentrations (0.001 to 1 M), along with the effect of surfactants (sodium dodecyl sulfate), chloride salts (NaCl), and acid/base reagents at a pH range from 4 to 9. Using a nanobubble generator based on hydrodynamic cavitation, 1.2 × 108 bubbles/mL with a typical radius of 84.66 ± 7.88 nm were generated in deionized water. Multiple evidence is provided to prove their presence in suspension, including the Tyndall effect, dynamic light scattering, and nanoparticle size analysis. Zeta potential measurements revealed that NBs are negatively charged even after two months (from − 19.48 ± 1.89 to − 10.13 ± 1.71 mV), suggesting that their stability is due to the negative charge on their surface. NBs were found to be more stable in alkaline solutions compared to acidic ones. Further, low amounts of both chloride and sulfate dissolved salts led to a reduction of the size of NBs. However, when high amounts of dissolved salts are present, NBs are more likely to coalesce, and their size to be increased. Finally, the investigation of the stability of air NBs at low temperatures revealed a non-monotonic relationship between temperature and NBs upon considering water self-ionization and ion mobility. This research aims to open a new frontier towards the application of the highly innovative NBs technology on the treatment of mining, mineral, and metal processing effluents, which are challenging aqueous solutions containing chloride and sulfate species.

Development of Anti-aging Cosmetics Using Chitosan/ γ-Cyclodextrin/Fucoidan Nanoparticles (Nanogel) Based on the Drug Delivery System

Purpose: This study aimed to develop MARINAVI-FD, a cosmetic material containing γ-cyclodextrin/chitosan/fucoidan nanoparticles, i.e., CH-γ-CD-Fu (Nanogel) based on the DDS system, and anti-aging cosmetics that have proven antioxidant and moisturizing effects.Methods: CH-γ-CD-Fu (nanogel) was identified through electron microscope (scanning electron microscope) analysis and nanoparticle size analysis (dynamic light scattering). Radical scavenging DPPH and ABTS assays were performed. Skin keratinocytes (HaCat cells) was assessed by the MTT assay, and the moisturizing effect was evaluated through enzyme-linked immunosorbent assay. Temperature and storage conditions were checked for the stability of the formulation. In the human body application test, Moisture Meter D Compact device was used.Results: The CH-γ-CD-Fu (Nanogel) has confirmed particle size of approximately 500 nm. In the DPPH and ABTS assays, compared with Fu (foucoidan), the CH-γ-CD-Fu (nanogel) showed higher scavenging ability at treatment concentration of 15.625–500 μg/mL. CH-γ-CD-Fu (Nanogel) showed a survival rate of &gt;80% in skin keratinocytes (HaCat cells) up to a concentration of 5,000 μg/mL. In the measurement of hyaluronic acid production, CH-γ-CD-Fu (Nanogel) showed better production at 194.87 ng/mL than at 121.47 ng/mL at a concentration of 200 μg/mL in the control group. The stability of skin and cream formulations of anti-aging cosmetics containing MARINAVI-FD was confirmed. The moisturizing effect was observed 2.5 mm depth of skin human application.Conclusion: In this study, CH-γ-CD-Fu (nanogel) was used to materialize into anti-aging cosmetics.