Average Particle Size Research Articles

Study on pH dependent ON/OFF fluorescent switching behaviour of hydrothermally synthesised vanadium disulphide quantum dots (VS2-QDs)

It is fascinating to design and develop an inorganic quantum dot (QDs) which exhibit luminescence features with ion concentration, temperature, and pH sensitivity dependence. Vanadium disulphide (VS2) belongs to the family of transition metal dichalcogenides (TMDs), and is extensively studied owing to its layered characteristics features in sensing and filtrations technology, however, its fluorescence features have not been well studied so far. The current work describes a widely adopted eco-friendly hydrothermal approach for the synthesis of VS2-QDs. The average size of particles was determined to be ∼10 nm by transmission electron microscopy (TEM) and Zetasizer analysis. The synthetic approach adopted here facilitates in situ functionalization of QDs, which results in their high stability in aqueous medium and enhanced sensitivity towards their surroundings. As most of the QDs show the sensitivity towards pH, a thorough investigation of VS2 QDs for their pH dependent photoluminescence has been carried out. The VS2-QDs were discovered to exhibit a remarkable luminescence intensity that was found to be about 11 times higher in basic conditions (pH ∼ 13, QY = ∼4.80%) as compared to that in acidic conditions (pH ∼ 1, QY = ∼1.10%). The root cause of this ON/OFF florescence flipping may be related to the functional groups (such as −SO42−, −NH2, OH−, etc.) attached over the surface of QDs, acid etching, and protonation–deprotonation process. This paper highlights the pH dependent switching behaviour of VS2-QDs that could offer valuable information for designing a futuristic pH-based device for biomedical applications.

Microstructures and properties of Al2O3 dispersion-strengthened Cu10Sn oil bearings prepared by solid-liquid doping and reactive synthesis method

To modify the shortcomings of Cu10Sn oil bearing in mechanical performance, this work proposes to prepare the Al2O3 oxide dispersion strengthened (ODS) Cu10Sn oil bearings by reactive synthesis using elemental Sn and Al2O3 ODS-Cu powder, among which the uniformly doped Al2O3 ODS-Cu powder was synthesized through a solid-liquid doping of Al(NO3)3 in CuO powders followed with hydrogen reduction. The effects of Al2O3 content on the microstructure and properties of ODS-Cu powder and ODS-Cu10Sn oil bearings were investigated in details. The results showed that an increase in Al2O3 amount from 0 to 1.5wt.% leads to a decrease in the average particle size of the reduced ODS-Cu powders, and contributes to the significant improvement of radial compressive strength, and Vickers microhardness. The appropriate sintering temperature is approximately 800 °C, which can result in the evenly distributed Al2O3 and well-developed porosity in oil bearing sample after sintering. The corresponding compressive strength and microhardness of ODS1.5-Cu10Sn oil bearing can reach 305MPa and 208 HV respectively.

Fabrication and characterization of methylammonium lead iodide-based perovskite solar cells under ambient conditions

<p>This study investigated the fabrication and characterization of CH<sub>3</sub>NH<sub>3</sub>PbI<sub>3</sub> based perovskite solar cells (PSCs) using the one-step spin coating technique under ambient conditions, eliminating the need for expensive glovebox and thermal evaporation equipment. The perovskite layer was annealed at 65 °C for 30 seconds and 100 °C for 30 seconds, 1 and 2 minutes. The scanning electron microscope (SEM) images show a smooth and uniform surface coverage for the ETL and CH<sub>3</sub>NH<sub>3</sub>PbI<sub>3</sub> layers. SEM results also show an average grain size of 397 nm for CH<sub>3</sub>NH<sub>3</sub>PbI<sub>3</sub> and an average particle size of ~17 nm for TiO<sub>2</sub> was confirmed by transmission electron microscopy (TEM). X-ray diffraction (XRD) results confirmed the formation of tetragonal perovskite (CH<sub>3</sub>NH<sub>3</sub>PbI<sub>3</sub>) phase with high crystallinity with a crystallite size of 19.99 nm for the samples annealed for 30 seconds at 65 °C and 1 min at 100 °C. FTIR results also confirmed the presence of anatase TiO2 at wavenumber 438 cm<sup>-1</sup> and the formation of the adduct of Pb<sub>2</sub> with dimethyl sulfoxide (DMSO) and MAI is confirmed at 1,015 cm<sup>-1</sup> . From the Tauc plot the bandgap energy of TiO2 and Perovskite layers was determined to be 3.52 eV and 2.06 eV respectively. An open-circuit voltage was 0.9057 V and short circuit current density was 12.2185 mA/cm<sup>2</sup> with a fill factor of 48.05 and power conversion efficiency (PCE) of 5.199%.</p>

Synergistic Construction of Superhydrophilic PVDF Membranes by Dual Modification Strategies for Efficient Emulsion Separation.

Solving the problem of oil and water pollution is an important topic in environmental protection. The separation of oil-water emulsion with high efficiency and low consumption has been the direction of social efforts. Membrane separation technology combined with surface wettability and pore size screening is considered to be one of the most promising ways to separate oil-water emulsions. In this paper, the polyvinylidene difluoride (PVDF) membrane is prepared by combining the two methods of blending and coating modification as a double barrier. The prepared PVDF membrane can completely wet water, achieve superhydrophilic in air, and superoleophobic underwater. The separation efficiency and flux are 99.57% and 678 L h-1 m-2 bar-1, respectively, for toluene emulsions containing surfactants with an average particle size of 1.7µm. At the same time, it can also effectively separate different kinds of light/heavy oils. After three cycles of testing still maintain high efficiency of separation. The results show that the prepared PVDF membrane can effectively separate the emulsion containing surfactant with smaller particle size distribution of oil droplets. This method provides a new strategy for the separation of oil-water emulsions and has broad application prospects.

N-doped TiO2/rGO: synthesis, structure, optical characteristics, and humidity sensing applications

In the current study, the effect of rGO ratio on the N-dopped TiO2 has been synthesized through sol–gel method. The prepared N-doped TiO2/rGO composites were examined for humidity sensing applications. The relationship between optical properties and the humidity sensing properties was studied. The structure, morphology, and bonding interaction have been examined using XRD, FT-IR, PL and HRTEM respectively. The average particle size as estimated from XRD and HRTEM was found to be about 9 nm. The optical properties have been studied using UV/ Vis. Spectroscopy. Further, optical parameters including refractive index and optical band gap energy have been estimated. The humidity sensing behavior of the resultant composites were evaluated in a wide range of humidity (7%–97% RH) at different testing frequencies. The optical band gap was found to be decreased as the amount of rGO increase. Among all prepared samples, both the optical parameters and humidity sensing experiments confirmed that the 0.5% rGO@N-dopped TiO2 sample is the best candidate for the humidity sensing applications. The best optimum testing frequency was demonstrated to be 50 Hz. The sensor demonstrates a fast response and recovery times of 13 s and 33 s with low hysteresis and large sensitivity. The humidity sensing mechanism was studied using complex impedance spectroscopy at different RH levels under testing frequency range from 50 Hz to 5 MHz and testing voltage of 1 VAC. The produced structure demonstrated a promising material for humidity measuring devices.

Preparation and characterization of hydrophobic waterborne polyurethane self‐matting coating

AbstractA green method to synthesize self‐matting waterborne polyurethane acrylic hybrid emulsion with hydrophobic function is introduced in this study. A reactive waterborne polyurethane (RWPU) dispersion containing unsaturated CC double bonds was prepared from epoxidized soybean oil. Subsequently, the RWPU dispersion was copolymerized with fluorinated monomers of different carbon chain lengths to prepare polyurethane acrylic hybrid emulsion (PUF). The results revealed the gloss levels of PUF films to be as low as 12.4 gloss units at 60°. The morphology of PUF films was observed by scanning electron microscope and three‐dimensional surface profilometer, and the relationship between surface roughness and gloss was discussed in detail. In addition, thermal gravimetric analysis was conducted to determine the thermal stability of the PUF films, and the results denoted that these PUF films exhibited excellent thermal stability. Comprehensive performance tests indicated that the RWPU dispersion, which was copolymerized with hexafluorobutyl methacrylate at a weight of 10%, exhibited a low gloss, a high contact angle of 120°, and a high elongation percentage of 423%. Furthermore, the dynamic light scattering results showed small average particle size, revealing the excellent storage stabilities.

Determination of Trace Cd(II) in Water and Cosmetics based on Au/GO/CuO Nanocomposite Functionalized Electrochemical Sensor

Abstract Cadmium (Cd(II)) is highly toxic to environmental, and while many approaches have been developed to measure cumulative Cd(II) concentration over time, online monitoring of spatiotemporal changes remains challenging. To address this, an electrochemical sensor for determination of ultra-trace Cd(II) was developed, based on gold/graphene oxide/copper oxide (Au/GO/CuO) nanomaterials modifying glassy carbon electrode. CuO nanoparticles were prepared by a green synthesis method using plant extract, and the Au nanoparticles were deposited on the GO/CuO nanosubstrates by an in-situ electrochemical method. The prepared nanocomposites were characterized by field-emission scanning electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. The CuO nanoparticles are layered flower-like with an average particle size of 200-500 nm. Au/GO/CuO nanocomposites with high specific surface area and excellent electronic transmission capability enhanced the electrochemical signal of the sensor. Owing to the synergistic effect of Au/GO/CuO, the sensor exhibited good performance to Cd(II) in the ultra-wide range of 5×10-11 - 5×10-7 M with a detection limit of 2×10-11 M. The sensor was successfully quantified for determining Cd(II) with desirable recovery, displaying outstanding long-term stability, high sensitivity, and reproducibility. After validating its accuracy, this sensor was successfully used for detection of Cd (II) in water and cosmetic samples.

Non-pigmented laser hair removal mediated via Sepia melanin nanoparticles: in vivo study on albino mice

Objectives Melanin is considered the main chromophore for laser hair removal. Due to a lack of laser-absorbing chromophores, removing non-pigmented hair with laser is quite problematic with unsatisfactory outcomes. This problem could be solved by delivering more melanin to the area around the hair follicle and enhancing that area as a target for light absorption. The insolubility of Sepia melanin as an exogenous dye, in most solvents, limits its bioavailability and thus its clinical use. Methods In our study, to overcome the solubility problems and increase the bioavailability of melanin for biomedical and cosmetic applications, natural sepia melanin was loaded in different nano-delivery systems (spanlastics and transfersomes) to be delivered to the hair follicles. The different formulations of melanin were prepared and characterized. In vivo skin deposition and histopathological studies were conducted on albino mice. Results Transmission electron microscopy (TEM) showed the spherical shape of the prepared vesicles with an average particle size of 252 and 262 nm and zeta potential of -22.5 and -35 mV for melanin spanlastics and melanin transfersomes, respectively. Histopathological examination of hair follicles and pilosebaceous glands for the irradiated and non-irradiated albino mice skin was studied post the application of the prepared formulations topically and subcutaneously. Qualitative statistical analysis was conducted and melanin transfersomes and melanin spanlastics showed significant damage to pilosebaceous glands and hair follicles with a p-value of 0.031 and 0.009 respectively. Conclusion Melanin nanovesicles as transfersomes and spanlastics could be considered a promising approach for the removal of non-pigmented hair.

Calcipotriol Nanosuspension-Loaded Trilayer Dissolving Microneedle Patches for the Treatment of Psoriasis: In Vitro Delivery and In Vivo Antipsoriatic Activity Studies.

Psoriasis, affecting 2-3% of the global population, is a chronic inflammatory skin condition without a definitive cure. Current treatments focus on managing symptoms. Recognizing the need for innovative drug delivery methods to enhance patient adherence, this study explores a new approach using calcipotriol monohydrate (CPM), a primary topical treatment for psoriasis. Despite its effectiveness, CPM's therapeutic potential is often limited by factors like the greasiness of topical applications, poor skin permeability, low skin retention, and lack of controlled delivery. To overcome these challenges, the study introduces CPM in the form of nanosuspensions (NSs), characterized by an average particle size of 211 ± 2 nm. These CPM NSs are then incorporated into a trilayer dissolving microneedle patch (MAP) made from poly(vinylpyrrolidone) and w poly(vinyl alcohol) as needle arrays and prefrom 3D printed polylactic acid backing layer. This MAP features rapidly dissolving tips and exhibits good mechanical properties and insertion capability with delivery efficiency compared to the conventional Daivonex ointment. The effectiveness of this novel MAP was tested on Sprague-Dawley rats with imiquimod-induced psoriasis, demonstrating efficacy comparable to the marketed ointment. This innovative trilayer dissolving MAP represents a promising new local delivery system for calcipotriol, potentially revolutionizing psoriasis treatment by enhancing drug delivery and patient compliance.

Tracking success of interaction of green-synthesized Carbopol nanoemulgel (neomycin-decorated Ag/ZnO nanocomposite) with wound-based MDR bacteria

Abstract Multidrug-resistant wound infections are a global health threat and a leading cause of death, persisting despite available treatments due to antibiotic resistance, biofilms, and ineffective drug delivery systems. The aim of this study is to (i) formulate an innovative nano-drug delivery system (NDDS) based on a Carbopol nanoemulgel (NEG) co-loaded with neomycin-silver/zinc oxide nanocomposite (NC) that could fight clinical MDR and treat biofilm-forming wound pathogens through topical application, and (ii) assess its in vivo wound-healing potential. The silver/zinc oxide (Ag/ZnO) NC was synthesized by co-inoculating the metabolites of Aspergillus welwitschiae and Meyerozyma guilliermondii. The synthesized NC was then conjugated with neomycin and loaded into a Carbopol NEG for efficient topical delivery. The resulting Neo-Ag/ZnO NEG was characterized physicochemically (e.g., UV-visible [UV-Vis] spectrophotometry, field emission scanning electron microscopy, X-ray diffraction, and Fourier transform infrared [FTIR] spectroscopy), biologically (e.g., in vitro antimicrobial, antibiofilm, and hemolytic activities), and pharmacologically (e.g., drug content, ex vivo drug release behavior, and in vivo wound-healing potential). The physicochemical analysis confirmed the successful mycosynthesis of the Carbopol NEG-loaded Neo-Ag/ZnO NC. SEM depicted a crystalline polyhedral shape of the small NC (average particle size of 38 nm). FTIR studies showed a slight interaction with the drug and other bioactive moieties in the Carbopol NEG. The Neo content in the Carbopol NEG was as high as 98%, and a maximum release of 81% for Neo, Ag, and ZnO ions was noticed after 12 h. The NDDS appeared hemocompatible and displayed a minimal inhibition concentration of 0.002 µg/mL with the greatest antimicrobial potential against S. aureus (an inhibition zone of 46 mm) compared to other tested wound microbes (p < 0.05). Statistically significant wound-healing activity was found for NDDS (p = 0.0001) in comparison to the control at a concentration of 100 mg/mL. The results showed that this newly developed Carbopol NEG-loaded neo-Ag/ZnO NC appeared promising for controlling resistant skin infections and boosting wound regeneration.

Self-assembly of the porphyrin monomer on the surface of Fe/graphene material: a novel sensing material for the detection of chloramphenicol antibiotic in aqueous solution.

Currently, electrochemical sensors are in the process of being developed and widely used in various fields, and new materials are being explored to enhance the precision and selectivity of the sensors.The Fe/graphene nanoparticles were synthesized utilizing a green approach, wherein leaf extract was employed as the reducing agent. The resulting materials underwent comprehensive characterization utilizing a range of contemporary techniques, including scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and Raman spectroscopy. The findings of the study revealed that the nanocomposites of Fe/graphene/porphyrin comprised zero-valent iron nanoparticles, exhibiting an average particle size ranging from 15 to 60 nm. These nanoparticles were seen to be evenly dispersed across the graphene sheets. The presence of nanostructure porphyrin nanofibers, measuring 20 nm in diameter, was also shown to exhibit strong integration with the surface of the Fe/graphene nanomaterials. The electrochemical properties of the Fe/graphene/porphyrin nanocomposite were also investigated, demonstrating that the prepared material could be effectively employed as a sensing electrode in the electrochemical sensor for detecting Chloramphenicol (CAP) through CV, EIS, and DPV techniques using a three-electrode electrochemical system. Under optimal conditions, Fe/graphene/porphyrin exhibited a high current response when detecting CAPs.

N-Doping CQDs as an Efficient Fluorescence Probe Based on Dynamic Quenching for Determination of Copper Ions and Alcohol Sensing in Baijiu.

To address an accurate detection of heavy metal ions in Baijiu production, a nitrogen-doping carbon quantum dots (N-CQDs) was prepared by hydrothermal method from citric acid and urea. The as-prepared N-CQDs had an average particle size of 2.74 nm, and a large number of functional groups (amino, carbonyl group, etc.) attached on its surface, which obtained a 9.6% of quantum yield (QY) with relatively high and stable fluorescence performance. As a fluorescent sensor, the fluorescence of N-CQDs at 380 nm excitation wavelength could be quenched quantitatively by adding Cu2+, due to the dynamic quenching of electron transfer caused by the binding of amine groups and Cu2+, which showed excellent sensitivity and selectivity to Cu2+ in the range of 0.5-5 μM with a detection limit (LOD) of 0.032 μM. In addition, the N-CQDs as well as could be applied to quantitative determine alcohol content in the range of 10-80 V/V% depending on the fluorescence enhancement. Upon the experiment, the fluorescent mechanism was studied by Molecular dynamics (MD) simulations, which demonstrated that solvent effect played an influential role on sensing alcohol content in Baijiu. Overall, the work provided a theoretically guide for the design of fluorescence sensors to monitor heavy metal ion in liquid drinks and sense alcohol content.

Parameters Optimization and Physicochemical Properties Characterization of Nanobiochar Prepared from Apple Branches by Ball Milling

Nanobiochar exhibits promising applications across a spectrum of fields due to its exceptional physicochemical properties. Ball milling, a prominent nanobiochar synthesis method, is influenced by process factors and biochar pretreatments, yet dominant controls still remain uncertain. In this study, the apple branch bulk biochar (pyrolyzed under 350[Formula: see text] C) was ball milled under different milling speeds, ball-to-powder mass ratios, and milling durations to investigate the optimal process parameter combinations for ball milling method. Then, we evaluated the impact of pyrolysis temperature and pretreatment temperature of bulk biochar on ball milling effect using optimized parameter combinations. Subsequently, the physicochemical properties of the bulk biochar and nanobiochar were measured. The results showed that high speed with low ball-to-powder mass ratio, low speed with high ball-to-powder mass ratio, and high pyrolysis temperature could significantly decrease the particle sizes of nanobiochar. Ball milling duration and pretreatment temperature had no significant effect on the particle sizes of biochar. The optimal combination of the rotational speed, ball-to-powder mass ratio and milling duration was 400 RPM, 100:1, 2 h and 700 RPM, 20:1, 2 h. The bulk biochar pyrolyzed at 550[Formula: see text] C could be milled into biochar nanoparticles with an average particle size smaller than 100 nm via above parameters. Nanobiochar shows improved properties such as specific surface area, cation exchange capacity, and surface functional groups over bulk biochar. This study provides a scientific basis for the widespread application of ball milling in the field of preparing nanobiochar.

Nanosized Tungsten Powder Synthesized Using the Nitridation–Decomposition Method

A facile, one-step nitridation–decomposition method was developed for the synthesis of nanosized tungsten powder with a high surface area. This approach involved the nitridation of WO3 in NH3 to form mesoporous tungsten nitride (W2N), followed by in situ decomposition of W2N to directly yield single-phase W particles. The phase and morphology evolution during the synthesis were systematically investigated and compared with the carbothermal reduction of WO3. It was revealed that powdered tungsten product with single-phase particles was obtained after nitridation at 800 °C combined with in situ decomposition at 1000 °C, displaying an average particle size of 15 nm and a large specific surface area of 6.52 m2/g. Furthermore, the proposed method avoided the limitations associated with intermediate phase formation and coarsening observed in carbothermal reduction, which resulted in the growth of W particles up to ~4.4 μm in size. This work demonstrates the potential of the nitridation–decomposition approach for the scalable and efficient synthesis of high-quality, fine-grained tungsten powder.

Quantitative characterization of microstructure and research on spatial variation characteristics of loess of different strata in Luochuan, Shaanxi, China.

The complete sequence of loess strata in Luochuan has become a typical section in loess strata, and is the main focus of research for many scholars studying loess. We were based on the theory of aeolian loess and established a set of quantitative index parameters for loess microstructure through our previous research, such as equivalent diameter, sphericity, morphology ratio, orientation angle Phi, orientation angle Theta, pore Eq-Radius, throat Eq-Radius and throat channelLength. Through the quantitative characterization of various index parameters of the Luochuan loess, we found that the probability density of each index parameter meets a specific distribution well, and in terms of spatial dimension, it shows that as the depth of the strata increases, the average particle size and the mode of pore Eq-Radius, throat Eq-Radius and throat channelLength generally increase, while the mode of particle morphology ratio generally decreases. In addition, loess particles in deeper strata are less prone to vertical sedimentation and tend to deposit gently or horizontally. Most particles in different strata are distributed in a northwest or southwest direction. During the formation period of strata, the main cause for spatial differences is the material carrying force. We conducted a statistical analysis on the correlation between the macroscopic physical properties of loess and its microstructure index parameters. Specifically, we found a positive correlation between loess density and the average particle size and the mode of particle equivalent diameter, Additionally, we found a negative correlation between loess liquid limit and plastic limit, and the mode of particle morphology ratio. Furthermore, there was a negative correlation between permeability coefficient and the mode of pore Eq-Radius, throat Eq-Radius, and throat channelLength.

Cadmium oxide nanoparticles from new organometallic Cd(II)-Schiff base complex and in vitro biological potentials: dual S. aureus and E. coli DNA gyrase inhibition by the precursors via in silico binding modes’ study

AbstractAt the nanoscale level, several biological processes take place, owing to the potential that engineered nanomaterials might interrelate with bio-molecules and cellular procedures. This study aimed to synthesize cadmium oxide nanoparticles via a one-step calcination process of tetradentate Schiff base-Cd(II) complex at different temperature ranges. The as-synthesized compounds were carried out via a viz UV–visible, elemental analysis, 1H NMR, molar conductivity, transmission electron microscopy (TEM), FT-IR spectroscopy, and X-ray diffraction (PXRD). The band gap energy and average particle sizes of the CdO particles are respectively (2.69 eV, 3.54 eV), 26.88 nm for CdO@250, and (3.20 eV, 3.57 eV), 25.67 nm for CdO@300, while CdO@350 exhibited the 3.78 eV and 28.42 nm values. The antioxidant accomplishments of the test samples through the scavenging activity of DPPH radicals showed CdO@300 to possess (IC50 = 5.18 ± 0.56 µg/mL). Similarly, the as-synthesized CdO nanoparticles exhibited higher antibacterial activities against S. aureus and E. coli as compared to the corresponding Cd-HMB and ligand (HMB), while ciprofloxacin acted as a standard antibiotic. Furthermore, HMB and its complex Cd-HMB were docked against the DNA gyrase enzymes of S. aureus (PDB IDs: 5CDQ) and E. coli (PDB IDs: 6F86) as receptors. The binding sites docking results showed that the binding energies of HMB and Cd-HMB to 5CDQ ranged from − 3.44 to − 4.99 kcal/mol and from − 6.45 to − 6.64 kcal/mol, while the binding energies related to the target 6F86 are in the ranges of (− 3.64, − 4.76) kcal/mol and (− 6.08, − 6.09) kcal/mol respectively. Therefore, the significant antioxidant and antibacterial activities of the ligand (HMB), Cd-HMB, and CdO NPs review the broad application prospects of these compounds as therapeutic agents for wide-ranging biomedical applications.

Combined helical-blade-strengthened co-flow focusing and high-throughput screening for the synthesis of highly homogeneous nanoliposomes

Nanoliposomes have been widely employed as promising drug delivery vehicles for the treatment of various diseases. However, the large-scale synthesis of drug-loaded nanoliposomes manifesting a highly uniform particle size is impeded by several unmet challenges. Herein a novel helical-blade-strengthened co-flow focusing (HBSCF) device was developed by installing multiple parallel helical blades in a commonly used co-flow focusing microfluidic device. This transformation in the microchannel structure may accelerate the mixing of aqueous and lipid streams in a radial direction, thereby affording the production of nanoliposomes with a significantly lower polydispersity index (PDI) value in terms of particle size. Moreover, a high-throughput experimental platform was developed by employing HBSCF device alongside its integration with various automation modules, which afforded 672 distinct experimental schemes for the synthesis and size characterization of drug-loaded nanoliposomes within 40 h. Afterwards, based on the above obtained large data set of nanoliposomes, a typical machine learning (ML) model pertaining to particle size was established to predict candidate synthesis schemes for the desired average particle size. Therefore, by narrowing the screening ranges through ML, the final synthesis scheme capable of producing liposomes with the desired particle size along with minimum PDI value can be precisely and rapidly obtained using automated experiments based on the same platform. Taken together, an effective integration of the HBSCF synthesis along with an automated high-throughput experimental platform may have broad implications for the industrialization and clinical application of nanomedicine.

Environmentally Friendly Synthesis of Polymer Nanoparticles in a Packed Reactor Using Glass Beads

AbstractPolymeric particles less than 100 nm in size (polymer nanoparticles), which are useful in the fields of medicine and so on, are synthesized through emulsion polymerization, wherein surfactants are essential for maintaining their dispersion stability, contaminating particle surfaces and causing high environmental pollution. The soap‐free emulsion polymerization (SFEP) of styrene in a packed reactor using microglass beads enables the synthesis of polymer nanoparticles without surfactants. Ultraviolet irradiation is used for radical polymerization using an initiator during the SFEP of styrene. The reaction space in the packed reactor is controlled by the size of glass beads to be filled in the reactor. A decrease in the size of the glass beads narrows the reaction space, causing the average polystyrene particle size to reach 27.3 nm and suppress convection flow by the wall of the glass beads, thereby limiting particle motion and preventing particle growth through particle collisions.This article is protected by copyright. All rights reserved

Iron(III) Monoglycerolate: A Potential Hemostatic Agent for Topical Application

Background: Glycerolates of biogenic elements are of interest because of their pharmacological activity. Some of them are used as active substances in agents for topical application and as biocompatible precursors in sol-gel synthesis of bioactive materials. Objective: In this work, morphostructural feature, ability to hydrolyze, and the pharmacological activity of previously synthesized iron(III) monoglycerate were studied. Methods: Analytical techniques, including SEM, TEM, XRD, TGA, IR spectroscopy, DLS and ELS, were used. Hemostatic activity was studied in vivo, and primary toxicological studies were carried out on experimental animals. Antimicrobial activity was studied using the agar diffusion method. Results: When dispersed in glycerol, solid crystalline iron(III) monoglycerolate transforms into an amorphous state, forming aggregates with an average particle size of 250 nm (according to DLS data). It slowly hydrolyzes in water at room temperature, while hydrolysis does not take place in an aqueous glycerol media. Iron(III) monoglycerolate is nontoxic and exhibits pronounced hemostatic activity and low antibacterial activity (relative to the strain S. аureus). Conclusion: Iron(III) monoglycerolate can be considered a potential hemostatic agent, showing promise for topical application in medical and veterinary practice, as well as a novel biocompatible precursor in the sol-gel synthesis of practically useful substances.

Exploring non-cytotoxic, antioxidant, and anti-inflammatory properties of selenium nanoparticles synthesized from Gymnema sylvestre and Cinnamon cassia extracts for herbal nanomedicine

The increasing need for pharmaceutical agents that possess attributes such as safety, cost-effectiveness, environmental sustainability, and absence of side effects has driven the advancement of nanomedicine research, which lies at the convergence of nanotechnology and medicine. Aims and objectivesThe study aimed to synthesize non-toxic selenium nanoparticles (SeNPs) using Gymnema sylvestre (G. sylvestre) and Cinnamon cassia (C. cassia) extracts. It also sought to develop and evaluate versatile nanomedicine formulations i.e. selenium nanoparticles of G. sylvestre and C. cassia (SeNPs), drug (lupeol) loaded SeNPs (DLSeNPs), drug-loaded and coated (PEG) SeNPs (DLCSeNPs) without side effects. MethodsThe SeNPs formulations were hydrothermally synthesized, loaded with lupeol to improve efficacy, coated with polyethylene glycol (PEG) for targeted delivery, and characterized using UV–Vis spectrophotometry, Fourier-transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), zeta potential analysis, size distribution analysis, and X-ray diffraction (XRD). Hemolytic cytotoxicity, 2,2-Diphenyl-1-picrylhydzayl (DPPH), total Reducing power, and total antioxidant capacity (TAC) antioxidant assays, carrageenan-induced paw edema, and histological studies were used to estimate the acute anti-inflammatory activity of the synthesized SeNPs. ResultsThe final form of PEGylated and drug (lupeol)-loaded selenium nanoparticles (DLCSeNPs) exhibited an average particle size ranging from 100 to 500 nm as evidenced by SEM, and Zeta potential results. These nanoparticles demonstrated no cytotoxic effects and displayed remarkable antioxidant (IC50 values 19.29) and anti-inflammatory capabilities. These results were fed into Graph-pad Prism 5 software and analyzed by one-way ANOVA, followed by Tukey's post hoc test (p < 0.001). All nano-formulations exhibited significant overall antioxidant activity, with IC50 values ≤ 386 (p < 0.05) as analyzed by ANOVA. The study's results suggest that G. sylvestre outperformed C. cassia in terms of reducing 2,2-diphenyl-1-picryl-hydrazyl-hydrate (DPPH) free radical, potassium ferricyanide, and ammonium molybdate in respective antioxidant assays. As far as anti-inflammatory activities are concerned drug (lupeol)-loaded and PEG-coated G. sylvestre SeNPs exhibited the highest anti-inflammatory potential from all other nano-formulations including drug (lupeol)-loaded and PEG-coated C. cassia SeNPs, as exhibited to reduce the release of pro-inflammatory signals i.e. cytokines and NF-kB, making them innovative anti-inflammatory nanomedicine. ConclusionThe study synthesized lupeol-loaded and PEG-coated SeNPs, showcasing the potential for biocompatible, cost-effective anti-inflammatory nanomedicines. G. Sylvester's superior antioxidant and anti-inflammatory performance than Cinnamon cassia emphasizes medicinal plant versatility.