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The list of standard abbreviations for JDS is available at adsa.org/jds-abbreviations-24. Nonstandard abbreviations are available in the Notes. The objective of this experiment was to estimate the bioavailability (BA) of rumen-protected (RP) His, RPLys, and 2 RPMet products using 3 in vivo methods: area under the curve (AUC), plasma dose-response (PDR), and fecal free AA (FFAA) methods. We used 8 rumen-cannulated cows in a replicated 4 × 4 Latin square experiment with 16-d periods. Treatments were (1) abomasal infusion of water (control), (2) abomasal infusion of free His, Lys, and Met (FAA), (3) administration of RPHis + RPLys + RPMet1 (rumen-protected methionine protected with ethyl cellulose; RPAA1), and (4) administration of RPHis + RPLys + RPMet2 (rumen-protected methionine protected with a pH-sensitive polymer; RPAA2). On d 7 of each experimental period, a pulse-dose of water (control) or FAA were infused into the abomasum of the cows, or RPAA were placed directly in the rumen, and blood samples were taken from the jugular vein through a catheter 11 times over a 24-h period for the AUC method. Following the AA pulse-dose, infusion lines were installed into the abomasum for continuous infusion of FAA for the PDR method, or RPAA were fed from d 12 to d 16 and cows were fitted with urinary catheters for total collection of feces for the FFAA method. Fecal collection and blood sampling were conducted from d 14 to 16. Due to technical issues likely leading to unrealistic BA estimates, data for the PDR method are reported in the supplemental material. Relative BA based on the AUC method (computed as AUC of RPAA treatment plasma AA concentration divided by AUC of FAA treatment plasma AA concentration) was lower for RPMet1 compared with RPMet2 (43% vs. 61%) and was 45% (SEM = 3.35) and 72% (SEM = 5.99), for RPHis and RPLys, respectively. Rumen escape fractions of RPAA, estimated in a previous study using an in situ method, and digestibility data from the current study were used for calculations of BA for the FFAA method. Bioavailability based on the FFAA method was lower for RPMet1 (67%) compared with RPMet2 (91%) and was 87% (SEM = 0.71) and 75% (SEM = 2.75) for RPHis and RPLys, respectively. The relative differences in estimated BA based on both the AUC and FFAA methods between the RPMet products were as expected, based on literature, and data for all 4 RPAA products corresponded well with previously estimated BA using the FFAA method. The unrealistic data for the PDR method were likely caused by technical deviations from the original method (e.g., once-daily dosing of RPAA and inability to capture representative plasma concentration data with the sampling time points). Therefore, comparison of the PDR method with the AUC and FFAA methods were not possible in this study. Further comparisons are needed without deviations from the original PDR method. Variability in BA data and differences in estimated BA between the in vivo methods highlight the current challenges for accurate measurements of relative in vivo BA of RPAA products. Different protection technologies may call for different methodology to be used for BA estimations. Further research and standardization of in vivo BA methods are warranted. [ABSTRACT FROM AUTHOR]

Lung cancer, as a serious threat to human health and life, necessitating urgent treatment and intervention. In this study, we prepared hyaluronic acid (HA)-targeted topotecan liposomes for site-specific delivery to tumor cells. The encapsulation efficiency, stability, chemical structure, and morphology of HA-targeted topotecan liposomes were studied, and the release properties, cellular uptake capacity, and therapeutic efficacy of topotecan were further investigated. Results found that the coupling efficiency of HA on the surface of PEG-coated liposomes was determined to be 13.65 nmol/mg of lipid. The HA-targeted topotecan liposomes demonstrated a high encapsulation efficiency of 95% for topotecan, with an average particle size of 98.26 nm and excellent storage and dispersion stability. Drug release and cellular experiments indicated that the coating of HA further reduced the release rate of topotecan and decreased the survival rate of A549 cells, respectively. Flow cytometry and fluorescence staining analyses revealed that the HA-targeted topotecan liposomes enhanced the uptake of topotecan and exhibited significant anti-tumor effects on A549 cancer cells transplanted in mice. H&E staining showed that the pathological tissue treated with HA-targeted topotecan liposomes corresponded to Miller-Payne grade IV. Furthermore, these liposomes increased the accumulation of topotecan in tumors and extended the blood circulation time of the drug. Therefore, HA-targeted topotecan liposomes can be used as a new and easily prepared carrier in the field of lung chemotherapy, demonstrating considerable potential for anti-tumor therapy. [ABSTRACT FROM AUTHOR]

In this work, the structures and electromagnetic properties of lithium ferrite ceramics manufactured by the additive method, based on the extrusion deposition of ferrite samples with a binder and their subsequent heating with high-energy electron beam, were studied. Preliminary synthesis of ferrite powder was carried out by a solid-phase method using iron oxide and lithium carbonate. To prepare ferrite paste, a binder based on ethylcellulose and terpineol was used. The printed samples were sintered by heating with 1.4 MeV electron beam using an ELV-6 accelerator. Using X-ray phase analysis, it was established that the sintered ceramic consists mainly of an ordered α−Li 0.5 Fe 2.5 O 4 phase and a certain amount of disordered β−Li 0.5 Fe 2.5 O 4 phase. Ferrite ceramics are characterized by a relative density of 72.6–92.1 %, specific saturation magnetization of 63–65 emu/g, Curie temperature of 628–630 °C, electrical resistivity of 108–106 Ω cm, depending on the thickness of the printed sample (200 and 400 μm) and sintering temperature (1100 and 1200°С). [ABSTRACT FROM AUTHOR]

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ABSTRACT Polystyrene spheres ranging in diameter from 2, 5, 10, to 20 μm were embedded in five different types of thick organic films (> 50 μm) to serve as model systems to evaluate the use of time‐of‐flight secondary ion mass spectrometry for the localization and particle sizing of pharmaceuticals in orodispersible drug delivery films. It was found that certain films, such as gelatin and ethyl cellulose, are prone to developing micron‐scale topography which can affect the linearity of the sputter yield, which can ultimately affect the maximum analyzable depth. Surprisingly, the sputter yield of the film was more of a determining factor for affecting the measurement of spheres. It was possible to more accurately extract the true dimensions of the buried spheres in faster sputtering films, while slower sputtering films were associated with matrix effects and sputtering artifacts that degraded the quality of the reconstructed image. Signal attenuation was also found to be problematic and quite significant for certain film chemistries, which placed a limit on the size of the particles that could be visualized. Overall, visualization of particles embedded in thick organic films is possible, but the extraction of quantitative data such as size and the amount of material is difficult given the influence of sample dependent sputtering artifacts. [ABSTRACT FROM AUTHOR]

Purpose: To optimize the preparation of hydrogel and creams integrated using nanosponge loaded with palmarosa essential oil. Method: Palmarosa nanosponge essential oil was formulated by oil-in-water (o/w) emulsion solvent diffusion method using various ratios of drug to polymer; ethylcellulose (EC). Polyvinyl alcohol (PVA) and dichloromethane were used to create the aqueous and dispersed phases, respectively. Furthermore, nanosponge (NS) was studied for particle size and zeta potential, followed by integration into cream and hydrogel preparations. The preparations were evaluated for physicochemical characteristics and antifungal activity in vivo in animals induced by Candida albicans. Results: Results showed that the physical testing for optimum preparation of hydrogel had a pH of 6.9 ± 0.10, adhesion of 1.43 ± 0.40 seconds, spreadability of 5.43 ± 0.55 cm and viscosity of 276 ± 25.16 dPa.s. Meanwhile, for cream preparation, pH, adhesion, spreadability and viscosity values were 6.6 ± 0.2, 2.25 ± 0.37 seconds, 7 ± 0.70 cm, and 1500 ± 5 dPa.s, respectively. The in vivo test for antifungal activity in test animals induced with Candida albicans showed that treatment had a significantly different effect on the healing process of candidiasis infection. Conclusion: This study offers new knowledge regarding the development of hydrogel preparations and nanosponge integration cream containing palmarosa essential oil. The preparations had the advantages of efficacious ingredients, with good drug release and spreadability profile through the skin. [ABSTRACT FROM AUTHOR]

Food waste is a global concern with enormous economic, environmental and social impacts that has contributed to active packaging evolution. However, incorporating bioactive substances into the packaging can deteriorate its physicochemical and mechanical characteristics. Thus, the objective of this work was to entrap the natural bioactive compound thymol into microparticles and apply them in the form of pads for the controlled release of bioactivity in food packaging material. The physicochemical characteristics and bioactivity of five different ethyl cellulose-based microparticles were evaluated. Increasing the amount of thymol in the formulation led to higher encapsulation efficiency. Encapsulation resulted in a substantial increase of >10–20 °C in the volatilization temperature of thymol, and the release of thymol occurred following a sustained profile, best described by the Higuchi release kinetic model. Increasing the polymer to thymol ratio in the microparticles resulted in higher thermal stability and a more gradual release profile. While all formulations demonstrated considerable inhibition of E. coli growth, the ones with the highest thymol content maintained their antimicrobial activity for at least one month of microparticle storage. Furthermore, the ability of the microparticles in retaining pH and titratable acidity of cherry tomatoes was evaluated, and it was confirmed that these characteristics were maintained during 21 days of storage. [ABSTRACT FROM AUTHOR]

Inorganic hydrated salts, noted for their high thermal storage density, excellent thermal conductivity, and non‐toxicity, are suitable candidate material for thermal management, particularly in enhancing human living environments when their phase transition points are near room temperature. Herein, we present an efficient and environmentally friendly microencapsulation method for inorganic hydrated salt through organic phase separation method. Eutectic hydrated salt (EHS) consisted of sodium carbonate decahydrate (SCD) and disodium hydrogen phosphate dodecahydrate (DHPD) was prepared as the core material while the mixture of ethyl cellulose (EC) and acrylonitrile‐butadiene‐styrene (ABS) as composite shell materials. Various characterization techniques were used to evaluate the micromorphology, chemical structure, thermal properties and thermal stability of the microcapsules. The resulting microcapsules exhibited a phase change temperature of 22.6 °C with a remarkable enthalpy of 131.4 J/g. Particularly, the enthalpy remained at 117.7 J/g even after 50 thermal cycles, indicating stable cycling thermal reliability. Furthermore, it was confirmed that the EHS was effectively encapsulated within the composite shell, and the microcapsules had a quasi‐spherical shape and core‐shell structure. More importantly, this method of microencapsulation could potentially be extended to other liquid hydrated salts at room temperature, offering a versatile approach for future applications. [ABSTRACT FROM AUTHOR]

This study focuses on the evaluation and the drug release characteristics of a new coated matrix membrane (CMM) system, particularly emphasizing drug delivery from porous systems that offer more precise release control, especially for drugs with narrow therapeutic indexes (NTIs), such as theophylline. The parameters affecting the delivery of theophylline from the CMM were systematically studied. In the study, ethyl cellulose (ETC) served as the coating polymer, while poly (ethylene glycol) (PEG) was selected as the pore-forming agent. Poly (vinyl alcohol) (PVA) was used as the base polymer in the preparation of matrix membranes, and poly (vinyl pyrrolidone) (PVP) was preferred as the hydrophilicity balancing guest polymer. The effects of matrix membrane (MM) thickness, heat treatment temperature (HTT), coating layer thickness, drug loading concentration and coating layer porosity on the release rate of theophylline from CMM systems were all investigated. Additionally, the impacts of pH and temperature on theophylline release from CMM systems were examined. All experiments were conducted in vitro. By the study, 150 °C was determined as optimal HTT temperature. At more acidic pH values greater release rates were obtained. The release mechanism consistent with the Case I (Fickian) diffusion model and the activation energy for the permeation of theophylline through CMM systems was found as 62.355 J mol−1. As a result of the study, it was determined that the optimized CMM system with improved release properties can control the released amount of theophylline and it was proposed as a promising material for the dermal delivery of theophylline in vivo. A new drug delivery coated matrix membrane system for theophylline delivery. [ABSTRACT FROM AUTHOR]

Azo dyes like methyl orange (MO) are very toxic components due to their recalcitrant properties which makes their removal from wastewater of textile industries a significant issue. The present study aimed to study their removal by utilizing aluminum and Ni foam (NiF) as anodes besides Fe foam electrodes as cathodes in an electrocoagulation (EC) system. Primary experiments were conducted using two Al anodes, two NiF anodes, or Al-NiF anodes to predict their advantages and drawbacks. It was concluded that the Al-NiF anodes were very effective in removing MO dye without long time of treatment or Ni leaching at in the case of adopting the Al-Al or NiF-NiF anodes, respectively. The structure and surface morphology of the NiF electrode were investigated by energy dispersive X-ray (EDX), and field emission scanning electron microscopy (FESEM). Response surface methodology was utilized to predict the optimum conditions by considering current density with 4-8 mA/cm² range, NaCl concentration in the range of 0.5-1 g/L, and electrolysis time of 10-30 min as controlling parameters. A very high MO dye removal percentage was achieved (97.74%) at 8 mA/cm², 1 g/L of NaCl within 30 min of electrolysis and consumed energy was 36.299 kWh/kg. This cost-effective EC system with the Al-NiF anodes besides Fe foam as cathode approved its high efficiency in removing MO dye with moderate amounts of NaCl due to the excellent 3D structure of these foam electrodes which highlight foam electrodes as an excellent choice for EC system in an environmentally friendly pathway. [ABSTRACT FROM AUTHOR]

Nanocomposites represent one of the most useful strategies for resolving the pharmaceutical challenge about the dissolution and delivery of poorly water-soluble drugs. Besides the compatibility between the drug and polymeric carriers, the physical shapes of materials also play their important roles on the release behaviors of a guest poorly water-soluble drug from the host polymeric matrices. In this study, three kinds of nanocomposites in the forms of homogeneous nanofibers (E1), spindles-on-a-string (E2), and beads-on-a-string (E3) were prepared using electrospinning with ketoprofen (KET) as the model drug and a mixture of ethylcellulose (EC) and polyvinylpyrrolidone (PVP) as the polymeric matrices. Controllable preparation mechanisms of these morphologies are disclosed based on the results of SEM, TEM, and processes observations. XRD and FTIR data demonstrated that KET was compatible with PVP and EC. In vitro dissolution tests verified that all the three nanocomposites were able to provide the typical bi-stage fast-sustained release profiles of KET. Whereas, the beads-on-a-string E3 had a better functional performance than the spindles-on-a-string E2, and the homogeneous nanofibers E1 in terms of the KET sustained release profiles in the second stage. The protocols reported here pioneered a new way for developing novel functional nanocomposites based on the process-shape-performance relationship. [ABSTRACT FROM AUTHOR]

AbstractAiming at the problem of prolonged formaldehyde release from artificial boards, a green slow-release formaldehyde scavenger was proposed in this study. Tea polyphenol microcapsules (TPM) were prepared by ionic gel-solvent evaporation method using sodium alginate/ethyl cellulose as the wall material and tea polyphenol as the core material. Fourier transform infrared spectroscopy (FTIR) analysis showed that the TPM exhibited the same characteristic absorption peaks as those of tea polyphenol, ethyl cellulose and sodium alginate. This indicates that the TPM was successfully prepared and the thermal stability of TPM meets the requirements of the hot pressing process of man-made boards. The optimal process of TPM was as follows: the mass ratio of tea polyphenol to ethyl cellulose was 2.58, the dosage of emulsifier was 1.01 g, and the mass fraction of sodium alginate was 17.23%, the encapsulation rate of TPM was 78.31%, and the average particle size was 18.69 ± 4.66 μm. After 180 min. After 180 min, the aldehyde reduction efficiency was 61.08%. In conclusion, TPM meets the requirements of the production process of wood-based panels and the need for continuous control of formaldehyde emission from wood-based panels. [ABSTRACT FROM AUTHOR]

Electrohydrodynamic (EHD) jet printing is a well-known advanced manufacturing technique that uses electric fields to generate and control fine jets of fluid for high-precision deposition of materials. This method enables the printing of extremely fine features, making it ideal for applications such as printed electronics. However, little is known about the optimal conditions for achieving consistent jet stability and droplet formation, especially when dealing with complex and volatile fluids laden with two-dimensional (2D) nanoparticles. In this work, we study the electrohydrodynamic printing process of 2D material-based inks using toluene as the main carrier fluid. Adding ethyl cellulose to toluene allows us to increase the stability of the suspensions and establish the steady cone-jet mode of electrospray. A small amount of ethanol increases the fluid conductivity, stabilizing the steady cone-jet mode and reducing the jet diameter. The inks behave as leaky-dielectric, weakly viscoelastic liquids. For this reason, the jet diameter and minimum flow rate obey the scaling laws for electrospray of Newtonian liquids. We determine the optimal parameter conditions for the EHD printing of our inks directly onto a non-conductive substrate. The influence of the substrate's velocity on the width of the printed lines is analyzed. These findings enlarge the knowledge about how to increase the throughput in the EHD jet printing process while controlling the resolution of the printed lines when using volatile solvents, 2D nanomaterials, and non-conductive substrates. [ABSTRACT FROM AUTHOR]

Aim: This research aimed to develop a pulsatile drug delivery system (PDDS) for etoricoxib, selective COX-2 inhibitor analgesic, to address the limitations of conventional formulations by releasing the drug at specific intervals aligned with the circadian rhythm of pain. Method: Core tablets containing Etoricoxib were prepared by direct compression with varied concentrations of croscarmellose sodium as a superdisintegrant. The optimized core tablets were coated using hydrophilic (HPMC K4M) and hydrophobic (ethyl cellulose) polymers in different ratios to create press-coated pulsatile tablets with varying lag times. Physical properties hardness, thickness, friability, and disintegration, drug content uniformity, and in vitro release were evaluated. Results: The core tablets exhibited rapid drug release, with batch C3 showing 98.61% release within 60 minutes. Press-coated formulations with different polymer ratios exhibited varying lag times, with batch F3 achieving the optimal balance--providing a 4-hour lag time and 96.6% drug release over 8 hours. Stability studies confirmed the physical and chemical stability of the optimized formulation (F3) over 6 months under accelerated conditions. Conclusion: The developed press-coated pulsatile tablets of etoricoxib successfully achieved a controlled lag time and sustained drug release profile, making them suitable for chronopharmacological management of pain. [ABSTRACT FROM AUTHOR]

[Display omitted] Cellulose nanocrystals (CNCs) are sustainable rod-like nanoparticles that can be used to stabilize oil-in-water emulsions and can create hydrophilic coatings. Modifying the surface of CNCs can improve emulsion properties and allow for adjustable wettability. This study explores the improvement of Pickering emulsion properties for various oils and the adjustability of coated surfaces through the physical modification of CNCs, without chemical functionalization. Bio-based additives, including antioxidant tannic acid (TA), methyl cellulose (MC), and ethyl cellulose (EC) were used as surface modifiers. The identification of optimal formulations involved varying the weight fraction of the alkyl cellulose derivatives. The findings suggest that, akin to pure CNCs, Pickering emulsions stabilized by TA and/or MC-modified CNCs demonstrate comparably high stability. The introduction of MC at a low weight fraction enhances hydrophilicity, and AFM analysis reveals smooth surfaces, mitigating the potential influence of roughness. In contrast, EC-modified CNCs result in less stable emulsions but exhibit more hydrophobic surfaces. This translates to a broad spectrum of characteristics, ranging from quasi-superhydrophilic to nearly hydrophobic (with contact angles spanning from below 11° up to 68°), all controllable through a straightforward physical coating process. This facile preparation of coated CNCs provides a versatile approach to customizing the wetting and emulsification properties of nanomaterials. [ABSTRACT FROM AUTHOR]

The document titled "Contents list" is from the journal Green Chemistry, published by The Royal Society of Chemistry. The journal focuses on cutting-edge research for a greener and more sustainable future. The document provides a list of articles and papers featured in the journal's latest issue, covering a range of topics such as solar energy, catalysis, and synthesis methods. The journal aims to connect the world with the chemical sciences and reinvest its profits back into the chemistry community. [Extracted from the article]

Developing solid-state ionic conductors with desirable charge-transport efficiency and reasonable durability is a fundamental and long-lasting challenge for solid-oxide fuel cells (SOFCs). Ceria-based electrolytes, as one of the most common types of electrolytes for intermediate-temperature solid-oxide fuel cells (IT-SOFCs), offer a high surface-exchange coefficient and faster kinetics in the triple phase boundaries (TPBs); however, they suffer to some extent of electronic conductivity in the reducing atmosphere and gradual phase transitions. Here in this work, we have reported a novel co-doped IT-SOFC electrolyte composite combining the apatite structure of Lanthanum Silicate (LSO) with the fluorite structure of Gadolinium-doped Ceria (GDC), which showed a high ionic conductivity and a minimal electronic leak. The resulting GDC-LSO composite electrolyte also achieved an OCV (open-circuit voltage) of 1 V at 800 °C, implying a significant improvement in the OCV values reported for the typical ceria-based electrolytes (∼0.75 V). The sample was prepared using 40 wt% GDC and 60 wt% LSO (40GDC-60LSO) showed a maximum electrical conductivity of 25 mS cm−1 at 800 °C with good densification properties (>95 % relative density). The cell electrochemical performance measurement was conducted using a 3.0 vol% humified H 2 stream at the anode side while the cathode side was exposed to the air at 800 °C. The interdiffusion of cations between La3+ in the LSO phase and Ce4+ and Gd3+ in the GDC phase was detected by XRD and EDX results after sintering samples at 1500 °C for 4 h using 0.5 wt% PVA or 0.5 wt% Ethyl cellulose (EC) as the binder. The proposed GDC-LSO composite could help better understand the influence of compositional constituents and processing variables on the densification and electrical properties of the electrolyte materials for the IT-SOFCs. [ABSTRACT FROM AUTHOR]

Background/Objectives: Coated drug pellets enjoy widespread use in hard gelatine capsules. In heterogeneous pellets, the drug substance is layered onto core pellets. Coatings are often applied to generate a retarded release or an enteric coating. Methods: In the present study, the thickness of a polymer coating layer on drug pellets was correlated to the drug release kinetics. Results: The question should be answered whether it is possible to stop the coating process when a layer thickness referring to an intended drug release is achieved. Inert pellets were first coated with sodium benzoate and second with different amounts of water insoluble polyacrylate in a fluidized bed apparatus equipped with a Wurster inlet. The whole process was controlled in-line and at-line with process analytical technology by the measurement of the particle size and the layer thickness. The in-vitro sodium benzoate release was investigated, and the data were linearized by different standard models and compared with the polyacrylate layer thickness. With increasing polyacrylate layer thickness the release rate diminishes. The superposition of several processes influencing the release results in release profiles corresponding approximately to first order kinetics. The coating layer thickness corresponds to a determined drug release profile. Conclusions: The manufacturing of coated drug pellets with intended drug release is possible by coating process control and layer thickness measurement. Preliminary investigations are necessary for different formulations. [ABSTRACT FROM AUTHOR]

Background: Oxiconazole nitrate is a broad spectrum imidazole antifungal agent. Poor solubility of this drug caused low bioavailability that limits the antifungal efficiency. Due to their low efficiency as drug delivery many conventional dosage form such as cream and ointment need high concentration of active ingredient for effective therapy, which may cause side effect. Materials and Methods: In this study nanosponge was prepared using hydroxyl ethyl cellulose and poly vinyl alcohol by emulsion solvent diffusion method. The entrapment efficiency of particle size has found in the range of 100nm-1µm and 55% - 88% respectively. Based on the characterization, nanosponge with least particle size and highest entrapment efficiency was selected for gel formulation. Results and Discussion: Four different formulations of gel were prepared by using carbopol 934 with varying the concentration of penetration enhancer and various evaluation studies were carried out. The in vitro release study showed that the nanosponge loaded gel formulation with higher concentration of penetration enhancer showed greater drug release. Conclusion: while compared with conventional gel. Based on the stability study carried out, it was concluded that formulation was stable at ambient conditions. [ABSTRACT FROM AUTHOR]

The primary goal of this study was to develop and test Clarithromycin and Curcumin-loaded floating microspheres for sustained medication delivery. Microspheres were formed utilizing a modified solvent evaporation process using Eudragit S-100 and Ethyl Cellulose (18-22 cps) as regulating polymers. The formulation was optimized using 32 factorial design factorial Design-Expert® 13 trial version software. The Drug-to-Polymer Ratio (X1) and the Polymer-to-Polymer (EC to ES-100) Ratio (X2) were chosen as independent factors, whereas % Buoyancy (Y1), Percentage Yield (Y2), and% Drug Entrapment Efficiency (%DEE) (Y3) were chosen as dependent variables. The evaluations covered micromeritic characteristics, particle size, PDI, zeta potential, entrapment efficiency, floating capacity, surface morphology (FESEM), in vitro drug release, kinetics, DSC and FTIR compatibility investigations. Microspheres exhibited good flow, with particle sizes of 31.52 µm to 40.64 µm (optical) and 33.42 µm (PCS), PDI 0.374, practical yields of 75.14±0.24% to 95.14±0.38% and buoyancy of 76.12±1.2% to 84.79±0.87%. Drug entrapment efficiencies were 78.92±0.61% to 89.42±0.71% for Clarithromycin and 74.26±0.54% to 89.56% for Curcumin, with drug loading efficiencies of 12.90±0.27% to 21.19±0.49% and 10.30±0.67% to 21.1±0.78%, respectively. For the provided formulas, the ANOVA revealed a p value of less than 0.0500. In pH 0.1N HCl, Batch F6 demonstrated superior drug release for both Clarithromycin and Curcumin, with respective values of 99.67±1.5% and 99.52±2.1%. This data aligns with the Higuchi model of the Non-Fickian release kinetics mechanism. Stability experiments verified formulation F6's effectiveness and stability, indicating its potential for targeted, prolonged release in gastrointestinal settings. [ABSTRACT FROM AUTHOR]

In this study, quercetin in cellulose porous microspheres were prepared by quasi-emulsion solution diffusion method. The formulation of microspheres was optimized by Box-Behnken Design and their antioxidant activity was evaluated. Morphological structures and physicochemical properties of the microspheres were investigated. The findings of porous microspheres particle size ranged from 150 to 200 μm. The encapsulation efficiency and loading capacity were of 90.32% and 20.54%. Respectively, prepared using polyvinyl alcohol (0.16%), ethyl cellulose and quercetin (41:19, w/w), stirred in dichloromethane/ethanol solution (4:1, v/v). The scanning electron microscopy confirmed porous structure of the microsphere surface. Fourier transform infrared spectroscopy revealed structural changes between quercetin and ethyl cellulose. X-ray diffraction and thermal analysis showed that the encapsulated quercetin was amorphous. Compared with free quercetin, the antioxidant capacity and stability of quercetin in porous microspheres were significantly improved. This research reveals the development of porous microsphere carrier that facilitated improved antioxidant activity and stability of quercetin. [ABSTRACT FROM AUTHOR]

Passive radiative cooling is a zero‐energy technology vital for mitigating the energy crisis. However, achieving intelligent thermal management across varying weather conditions (day/night and summer/winter) while maintaining sustainability is a significant challenge. Here, a recyclable biomass film engineered for adaptive, year‐round energy conservation is introduced. This film utilizes porous acetyl cellulose (AC) as a cooling‐side matrix, enabling efficient radiative cooling during hot days (8.5 °C reduction) and minimizing overcooling on cold nights (only 2.5 °C reduction). This performance is facilitated by high solar reflectance (96.3%) and broad‐spectrum infrared emission (95.4%), optimizing atmospheric thermal regulation. The reverse side, coated with carbon black (CB), demonstrates superior solar heating (20.9 °C increase), allowing for effortless switching between cooling and heating by flipping the film. Further, the film employs a solvent‐responsive ethyl cellulose (EC) adhesion, ensuring durability, complete recycling, and reuse. With ultraviolet (UV) resistance, self‐cleaning, and durability, coupled with intelligent thermal management, this work provides new ideas for advanced radiative heat management materials, enabling adaptive control during both daytime/nighttime and summer/winter. [ABSTRACT FROM AUTHOR]

Polymeric composites for manipulating the sustained release of an encapsulated active ingredient are highly sought after for many practical applications; particularly, water-insoluble polymers and core–shell structures are frequently explored to manipulate the release behaviors of drug molecules over an extended time period. In this study, electrospun core–shell nanostructures were utilized to develop a brand-new strategy to tailor the spatial distributions of both an insoluble polymer (ethylcellulose, EC) and soluble polymer (polyvinylpyrrolidone, PVP) within the nanofibers, thereby manipulating the extended-release behaviors of the loaded active ingredient, ferulic acid (FA). Scanning electron microscopy and transmission electron microscopy assessments revealed that all the prepared nanofibers had a linear morphology without beads or spindles, and those from the coaxial processes had an obvious core–shell structure. X-ray diffraction and attenuated total reflectance Fourier transform infrared spectroscopic tests confirmed that FA had fine compatibility with EC and PVP, and presented in all the nanofibers in an amorphous state. In vitro dissolution tests indicated that the radical distributions of EC (decreasing from shell to core) and PVP (increasing from shell to core) were able to play their important role in manipulating the release behaviors of FA elaborately. On one hand, the core–shell nanofibers F3 had the advantages of homogeneous composite nanofibers F1 with a higher content of EC prepared from the shell solutions to inhibit the initial burst release and provide a longer time period of sustained release. On the other hand, F3 had the advantages of nanofibers F2 with a higher content of PVP prepared from the core solutions to inhibit the negative tailing-off release. The key element was the water permeation rates, controlled by the ratios of soluble and insoluble polymers. The new strategy based on core–shell structure paves a way for developing a wide variety of polymeric composites with heterogeneous distributions for realizing the desired functional performances. [ABSTRACT FROM AUTHOR]

The trigeminal nerve is the largest craniofacial nerve, responsible for detecting sensory stimuli originating from the cranial and facial areas. Trigeminal neuralgia is a common form of craniofacial neuropathic pain that causes one of the most severe pain episodes a person can endure. The pain attacks would impact quality of life and mental health of patients. Carbamazepine and oxcarbazepine are recommended as first-line treatments to control pain in patients with trigeminal neuralgia. Oral administration of the mentioned drugs requires higher doses and as a result, higher risk of side effects due to the metabolic processes. Local mucosal drug delivery might be a proper alternative for oral systemic therapy in order to localize the treatment and reduce the side effects. The goal of this study was to develop an oral film containing particles of carbamazepine for treatment of trigeminal neuralgia. Particles were prepared by solvent evaporation method using chloroform and dichloromethane as organic solvents and ethyl cellulose and hydroxypropyl methylcellulose as coating polymers. The optimized particle contained equal weight ratios of polymers and was prepared using chloroform. The particles released about 70% of carbamazepine content within an hour. Optimized particles were loaded in an oral film containing 5% acacia, 10% gelatin as the film-forming polymers, and 1% glycerol and 10% PEG 400 as plasticizers. Satisfactory results were obtained from evaluation of physical characteristics of carbamazepine loaded film including: peak load was equal to 1506 mN, average thickness was 0.49 ± 0.003 mm and average weight was 1.53 ± 0.005 g. Film was completely dissolved in water. Also, release of the pure and coated drug from the optimized film was about 55% and 30%, respectively within 1 hour and about 42% and 80%, respectively after 2 hours. These preliminary results indicate that polymeric film containing particles can be a potentially successful system for delivery of carbamazepine to the oral mucosa. [ABSTRACT FROM AUTHOR]

Background: Blackgrm is one of the most important pulse crops majorly cultivated in rainfed conditions of India. Soil moisture deficit, low and erratic rainfall, use of poor quality seeds, poor crop stand and improper crop management resulting in lower productivity in rainfed ecosystem. Reduced crop stand alone leads to 30% deficit in production. Availability of technology to overcome drought stress is one of the way to expand blackgram cultivation in dry tracks. Hydrophilic polymers may have great potential in restoration and reclamation, when used the polymers correctly and an ideal situations will have atleast 95% of their stores water available for plant absorption. There are N number of inorganic polymers available in the market, that can be applied in the form of soil application. Studies on Hydrophilic bio polymer seed coating to mitigate water stress is very megar or nil. Hence, the present study was formulated in blackgram as hydrophilic bio polymer seed coating on seed germination and field emergence. Methods: Seed coating experiment consists of seven hydrophilic biopolymers (Ethyl cellulose, Methyl cellulose, Carboxyl methyl cellulose, Agar, Gum Arabic, Xanthangum and Carrageenan); two coating methods (dry and dry powder concoction). The germination test conducted in sand media with 60% Water Holding Capacity of sand and PEG induced water stress and evaluated for seed quality parameters against uncoated seeds. Field experiments conducted with water stress periods of 10 days, 20 days and 25 days after life irrigation and observed for biometric and yield parameters. Result: Results revealed that blackgram seeds coated with bio polymerconcoctionof xanthan gum : carrageenan : Agar agar (4:1:1) @ 20 g/kg performed better in terms ofall seed quality parameters and withstand water stress upto 20 days after life irrigation with the yield increase of 53% over stressed control (Skipping irrigation for 20 days after life irrigation) and can be recommended as a pre sowing treatment for drought mitigation in blackgram. [ABSTRACT FROM AUTHOR]

Colorants used in security inks are special pigments that radiate in the UV region or IR region. Obtained pigments can be from valuable rare earth elements or they can be organic based. Organic-based pigments are generally insoluble in water, which limits their use. For this purpose, an organicbased UV-radiating pigment was synthesized and made water-soluble by forming its salt. With the obtained salt-formed pigment, inkjet ink that can be used in counterfeiting was applied and its printability and resistance properties were determined. In this study, 1, 3, 6, 8-pyrene sulfonic acid tetrasodium salt was synthesized and water-based inkjet inks with hydroxy ethyl cellulose binder were produced. The prepared inks were printed on the paper surface. The color and gloss of the prints obtained were measured both in the visible region and in the UV region. Its optical properties were detected by UV spectroscopy. Strength properties such as light fastness, nitro resistance, alkali resistance, acid resistance, rub resistance, drying time, adhesion and dry film weight of the prints were determined. As a result; Inkjet ink with 1, 3, 6, 8-pyrene sulfonic acid tetrasodium salt was produced and it was concluded that it has good resistance properties. [ABSTRACT FROM AUTHOR]

Clobetasol propionate (CP) is a potent corticosteroid used for skin conditions but often causes side effects due its systemic absorption. To improve its solubility and reduce it side effects (like skin irritation, skin atrophy, hypopigmentation and steroidal acne), Microsponge (Msg) has been employed as a unique three-dimensional particle that can encapsulate hydrophilic and lipophilic drugs. This study aims to develop and evaluate CP Msg-loaded hydrogels. Two Clobetasol-loaded ethylcellulose-based Msg formulas were prepared using the quasi-emulsion solvent diffusion method, then they were incorporated into Carbopol hydrogel. Two ratios of Carbopol 940 (1% and 1.5% w/w) were used. The prepared hydrogel were assessed for appearance, pH, drug content, spreadability, extrudability, rheology, and in vitro release. The optimum hydrogel was compared to generic CP cream available locally and plain hydrogel. The results showed that both Msg formulas had good product yield, entrapment efficiency and highly porous micron size. The four prepared hydrogels revealed acceptable characterization including; pH ranged between 5.6and 6, drug content (98.8-100%) and % extrudability (80.7-92%) with pseudoplastic flow type. The hydrogel formula (F2Ha 1%) containing (1:1 weight ratio of CP: ethylcellulose) with (1%w\w Carbopol) was chosen as the optimized formula since it showed the highest spreadablility and approximately 43% of CP was released at 8 hours. The ex-vivo data including; the highest deposition in stratum corneum and epidermal/dermis with the flux, permeability coefficient and lag time of F2Ha were low, compared to plain hydrogel and marketed cream. Based on the study's finding, we concluded that CP Msg-loaded Carbopol hydrogel is a proper drug delivery system for topical application with minimized systemic absorption. [ABSTRACT FROM AUTHOR]

This study is focused to design a colon specific pellet formulation of rifaximin based on the combination of time-dependent and pH sensitive delivery system using Quality-by-Design (QbD) approach for better and promising treatment of inflammatory bowel disease (IBD). An extrusion/spheronization process was utilized for the preparation of core macroparticles using ethyl cellulose (EC) as matrix former and microcrystalline cellulose (MCC) as a spheronizing aid. Two critical process parameters (CPPs) i.e., spheronization time and spheronizer speed were taken as independent factors while aspect ratio, sphericity, carr's index, and particle size were taken as dependent responses to optimize the composition of the core macroparticles. To regulate the drug release, core macroparticles were coated with Eudragit NE40D and Eudragit FS30D to impart time-dependent and pH sensitive release of drug. The optimized coated macroparticles were characterized for drug content and in vitrodrug release in different pH media of stomach and intestine. The coating levels of the inner and outer polymers were further optimized for the time required for 10 %, 50 % and 90 % drug release. The result showed that the 90% of drug of P3 and P4 formulation were found to be released in 10.87 and 13.19hrs respectively. When exposed to Scanning Electron Microscopy the images of coated macroparticles suggested a uniform and smooth coat of polymers over the surface of macroparticles. This formulation reduces the dose and the side effects due to its specific targeting at the site of inflammation makes it a better choice over the tablets. The result indicates that the developed formulation may possibly reduce the dosing frequency and side effects associated with the conventional tablet formulation for the site-specific targeting at inflammation site. [ABSTRACT FROM AUTHOR]

The permeability of triamcinolone acetonide (TA), from bilayer mucoadhesive buccal films, through a biomimetic membrane, Permeapad™, was investigated employing Franz diffusion cell. The delivery systems composition and ethyl cellulose (EC) backing layer, on drug permeability, were assessed. Three TA-loaded films were tested; hydroxypropyl methylcellulose (HPMC K4M; bilayer [F1] and monolayer), HPMC K4M/Polyvinylpyrrolidone (PVP): 90/10 [F2], and HPMC K15M film [F3]. All films contained propylene glycol (PG-plasticiser). TA solution alone was used as a control. TA permeability via a Permeapad™ barrier, simulating buccal mucosa, was assessed over 8 h using a Franz diffusion cell. TA permeated into the receptor compartment, released in the donor compartment, and located on/within the Permeapad™ barrier were analysed using UV-spectrophotometer. 45.7 % drug retention within the Permeapad™ barrier was delivered from F1 (highest). F1, F2, and F3 significantly improved the TA's permeability through Permeapad™, compared to TA solution alone (e.g., 8.5 % TA-solution, 21.5 %-F1), attributed to the synergy effect of HPMC and propylene glycol acting as penetration enhancers. F1 displayed a significant increase in drug permeability (receptor compartment; 21.5 %) compared to F3 (17.0 %). PVP significantly enhanced drug permeability (27.5 %). Impermeable EC backing layer controlled unidirectional drug release and reduced drug loss into the donor compartment (e.g., ∼28 % for monolayer film to ∼10 % for bilayer film, F1). The mucoadhesive films demonstrated improved TA permeability via Permeapad™. The findings suggest that these bilayer mucoadhesive films, particularly F1, hold promise for the effective topical treatment of oral mucosa disorders, such as recurrent aphthous stomatitis and oral lichen planus. • Bilayer mucoadhesive buccal films to enhance TA permeability through Permeapad™. • F1-highest TA retention in Permeapad™ for potentially treating oral mucosa disorders. • EC backing layer minimized the loss of TA into the donor compartment. • The biomimetic membrane, Permeapad™ was successfully used for TA permeation assay. • Franz cell was used to predict the amount of drug permeating across Permeapad™. [ABSTRACT FROM AUTHOR]

Purpose: The formalin-ethyl acetate (FEA) concentration method is commonly used in routine clinical practice to detect parasite eggs in feces. This procedure involves extraction of oil with the organic solvent ethyl acetate (EA), which reduces fecal sediment and provides a cleaner background for microscopic analysis. However, clinically, some sediment failed to float after EA treatment. Methods: Hexane, commonly used in the food oil extraction from oilseeds did not float the feces. Gas chromatography–mass spectrometry (GC–MS) analysis showed that neither the amount of the oil nor the classes of the oil determined was differed whether hexane or EA was used to float the feces. Oil red, Bodipy and Calcofluor staining showed that the unabsorbed oil droplets in the fecal sediment were trapped within the leaf structure. HCl or acetic acid was added to see if the acid residue could dissolve the cellulose of the leaf to promote the bulk float. Results: Our result showed that the fecal bulk contained the loosened mesophyll cell wall. The addition of acid residues improved fecal bulk float. The proximity of cellulose fiber to EA, but not hexane, may enhance the efficacy of oil extraction from cellulose. Conclusion: This is the first report that the interaction of cellulose with ethyl acetate in fecal solution has an effect on bulk float. This study improves the understanding of fecal bulk flotation and may assist in the visualization of parasite eggs in clinical practice with non-floating fecal samples in the FEA concentration method. [ABSTRACT FROM AUTHOR]

The development of efficient therapeutic agents with low side effects for inflammatory bowel disease management is a longstanding challenge. Recently, hydrogen molecule (H2) is identified as an emerging spectrum‐wide, effective, and biosafe anti‐inflammatory agent, but intestine‐targeted H2 delivery is still challenging. Here, an intestine‐targeted controlled hydrogen‐releasing microcapsule (MgH2@EC@ES) is developed by confining abundant MgH2 microparticles in the hydrophobic network of ethyl cellulose (EC) before being encapsulated with Eudragit S100 (ES) by a multistep microemulsion method. The pH‐responsive swelling feature of ES enables MgH2@EC@ES microcapsules to escape from the stomach after oral administration and to hydrolytically produce a high amount of H2 in the intestinal tract in a sustained way. High‐dose oral administration of MgH2@EC@ES microcapsules exhibits a high outcome of colitis prevention, which is comparable to the first‐line drug 5‐aminosalicylic acid (5‐ASA) in the changes of body/spleen weights and disease activity and even better in the recovery of colon length and the improvement of histopathological change in the colon than 5‐ASA in a colitis mouse model. Mechanically, it is innovatively revealed that H2 released from MgH2@EC@ES microcapsules protects the complexes in the mitochondrial electron transfer chain from oxidative damage to enhance the energy metabolism of intestinal cells in support of mucosal restoration in colitis. [ABSTRACT FROM AUTHOR]

Bio‐active ethylcellulose (EC) polymeric films have been obtained by incorporating curcumin (curc) and Ag(I)‐based compounds, known for their antioxidant and antimicrobial activity, respectively, within the polymeric matrix. The recently reported Ag(I) coordination polymer, in both its structural forms (α‐[(bpy)Ag(OTf)]∞ and β‐{[(bpy)Ag][OTf]}∞), and the [(bpy)Ag(OTf)]∞‐curc polymeric co‐crystal (bpy=2,2′‐bipyridine; OTf=trifluoromethanesulfonate) have been selected as Ag(I) species. The hybrid composite films have been prepared through the simple solvent casting method and characterized through Powder X‐Ray Diffraction (PXRD), Differential Scanning Calorimetry (DSC) and Fourier Transform Infrared (FTIR) spectroscopy, Scanning Electron Microscope (SEM), UV‐vis spectroscopy. The deep investigation of the film samples highlighted the non‐inert behaviour of EC towards these specific active ingredients. Antimicrobial tests showed that EC films embedding the Ag(I)‐based compounds present good antimicrobial performance, in particular against Staphylococcus aureus, used as a model of Gram‐positive bacteria. In addition, Silver migration tests, performed on the Ag(I)‐incorporating EC films, evidenced low values of silver release particularly in the case of the EC films incorporating [(bpy)Ag(OTf)]∞‐curc. [ABSTRACT FROM AUTHOR]

UV spectrophotometric determination of salicylic acid in several multicomponent drugs using an ethylcellulose-based sorbent for solid-phase extraction (SPE) for sample preparation was shown to be selective. Selective binding of the analyte to sorbent active sites and stepwise elution successively with purified water and NaOH solution (0.1 M) during SPE eliminated interference of other active pharmaceutical ingredients of multicomponent drugs during identification and quantitation of salicylic acid by UV spectrophotometry. Use of the ethylcellulose sorbent made it possible to improve the metrological parameters and decrease systematic error of the quantitative procedure by an average of 47%. [ABSTRACT FROM AUTHOR]

The goal of this research was to analyse the synergistic effect between selected plant extracts with zinc oxide particles, and zinc stearate. The influence of ZnO on the antimicrobial effectiveness of the selected extracts was confirmed in previous research carried out by the authors. However, the impact of zinc stearate on extract activity has yet to be analysed. The aim was to cover PLA films with active coatings based on hydroxy-propyl-methyl-cellulose (HPMC), or/and ethyl cellulose (EC) containing plant extracts and ZnO which has a synergistic effect. An additional aim was to use a CO2 extract of raspberry seed (RSE) with zinc stearate as active additives within the coatings. An examination of the antimicrobial properties (against Staphylococcus aureus, Escherichia coli, Bacillus subtilis, Pseudomonas syringae and Φ6 bacteriophage) of the covered films, as well as an investigation of layer presence with regards to PLA morphology (SEM, ATR-FTIR analysis) was carried out. The research work that was performed indicated that black chokeberry extract (ChE) and zinc oxide particles were effective against S. aureus, P. syringae and B. subtilis strains. In addition, the ChE with zinc stearate (ZnSt) was active against all analysed strains. The HPMC with ChE and ZnO as additives had antimicrobial properties against S. aureus, P. syringae and E. coli strains. The ChE was found to inhibit the growth of all of the analysed bacterial strains. When considering the coatings based on EC with the CO2 extract of raspberry seed (RSE) and ZnO, it was noted that they were only active against Gram-negative bacteria. The results of the experiments confirmed that AC1 (EC with RSE with ZnO) and AC2 (EC with RSE with ZnSt) coatings were not active against a phi6 bacteriophage. The HPMC coating containing the AC3 layer (ChE and ZnO) eliminated Φ6 particles, confirming its antiviral properties. In addition, the presence of the active (AC1, AC2 and AC3) coatings was confirmed by SEM and FTIR analysis. [ABSTRACT FROM AUTHOR]

BACKGROUND: Allergic conjunctivitis is one of the most common eye disorders. Different drugs are used for its treatment. Hesperidin is an active substance isolated from Citrus sinensis L. (Rutaceae) fruit peels, with known anti‐inflammatory activity but low solubility. It was complexed with cyclodextrin and encapsulated in situ gel to extend its duration in the eye. RESULTS: The optimized formulation comprised 1% hesperidin, 1.5% hydroxyethyl cellulose, and 16% poloxamer 407. The viscosity at 25 °C was 492 ± 82 cP, and at 35 °C it was 8875 ± 248 cP, the pH was 7.01 ± 0.03, gelation temperature was 34 ± 1.3 °C, and gelation time was 33 ± 1.2 s. There was a 66% in vitro release in the initial 2 h, with a burst effect. A lipoxygenase (LOX) inhibition test determined that hesperidin was active at high doses on leukotyrens seen in the body in allergic diseases. In cell‐culture studies, the hesperidin cyclodextrin complex loaded in situ gel, BRN9‐CD (poloxamer 16%, hydroxy ethyl cellulose (HEC) 1.5%), enhanced cell viability in comparison with the hesperidin solution. It was determined that BRN9‐CD did not cause any irritation in the ocular tissues in the Draize test. CONCLUSION: The findings of this study demonstrate the potential of the in situ gel formulation of hesperidin in terms of ease of application and residence time on the ocular surface. Due to its notable LOX inhibition activity and positive outcomes in the in vivo Draize test, it appears promising for incorporation into pharmaceutical formulations. © 2024 The Authors. Journal of The Science of Food and Agriculture published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

This study investigated the potential enhancement of proton conductivity in Nafion membranes through the incorporation of sulfo ethyl cellulose (SEC) at varying weight ratios (5 and 10 wt.%). Results indicated that increasing the weight ratio of SEC led to improvements in water absorption, activation energy, and proton conductivity within the composite membranes. Specifically, the composite membrane exhibited a significant increase in proton conductivity, reaching up to 170 mS cm−1, in contrast to the pristine Nafion membrane which recorded 40.08 mS cm−1, particularly at temperatures exceeding 120°C. At the sub‐molecular level, Fourier transfer inferred spectroscopy (FTIR) analysis of Nafion/SEC membranes unveiled cross‐linking interactions occurring between the sulfo acid groups of Nafion chains and the hydroxyls within the SEC matrix. Moreover, X‐ray diffraction (XRD) findings of the composite membranes were instrumental in identifying crystalline phases, orientation, and structural features. The results indicated variations in atomic radius and alterations in lattice parameters at the nanoscale, induced by heightened surface forces resulting from the inclusion of SEC in the Nafion matrix. This phenomenon leads to a reduction in crystallite size, accompanied by an increase in peak broadening and surface area within the composite membranes. Such changes signify a clear interaction between SEC and Nafion, as confirmed by both scanning electron microscopy and thermal gravimetry analyses. Taken together, these findings strongly indicate that the cross‐linked composite membranes utilizing SEC‐Nafion hold significant promise as proton exchange membranes. [ABSTRACT FROM AUTHOR]

The rise in demand for iron- and steel-based products globally has resulted in the depletion of high-grade iron ores, high energy consumption, and CO2 emissions. The world is rich in low-grade ores that have not been exploited, and this study aims to develop a feed for cast iron production, goethite ore–carbon composite pellets. A pelletizing disc was used to make the pellets followed by induration in a muffle furnace at 1373 K for 25 min, and the results showed that goethite–carbon composite pellets with the desired physical properties of a drop index greater than 4, dry compression strength greater than 2.2 kg/pellet, and an indurated compression strength above 250 kg/pellet could be produced by controlling the coal, limestone, and ethyl hydroxyethyl cellulose, avoiding the addition of impurities from bentonite. About 0.4 wt.% ethyl hydroxyethyl cellulose could be added to achieve the optimum strength in the composite pellets with a binary basicity of 0.27 and coal addition of 2.5 wt.%. A total metal recovery of 48.46% was achieved from the preliminary smelting experiments on the furnace burden, with a binary basicity of 1.3 at 1673 K with 25 min holding time and a carbon-to-oxygen ratio (wt.%) of 1.4 using an induction furnace. These composite pellets can potentially be used as a raw material for cast iron production towards the decarbonization of the steel industry. [ABSTRACT FROM AUTHOR]

Biodegradable polymers (BPs)‐based triboelectric nanogenerators (TENGs) have advantages, including biocompatibility and biodegradability. However, biodegradable TENGs (BD‐TENGs) possess relatively low output performance, limiting their application due to the small differences in triboelectric polarities for most BPs. Molecular doping is a simple and effective method in altering the triboelectric polarity of triboelectric materials and improving the output performance of BD‐TENGs. However, there is a lack of laws and mechanism about the differences in triboelectric polarities of different doped molecules, especially of molecules with biodegradability and biocompatibility. Here, kinds of doping molecules are selected for doping in tribopositive and tribonegative materials, respectively, and their triboelectric polarities and related laws are researched. In particular, the output performance of BD‐TENG is improved several times by doping small amounts of poly (propylene glycol) (PPG) and ethyl cellulose (EC), with enhanced resolution in abnormal respiratory signal monitoring. This work not only provides theoretical guidance for the selection of triboelectric molecules but also conducts in‐depth research in molecular‐level triboelectric mechanisms. [ABSTRACT FROM AUTHOR]

Background: Miconazole nitrate, a BCS class II drug which is used for treatment of fungal infections. To minimize the disadvantages of sticky creams and ointments and their tendency to rub off, an intelligent dosage regimen needs to be designed as a film-forming spray formulation. The aim of this investigation was to develop a film-forming spray formulation containing 0.5% Miconazole nitrate for the treatment of fungal infections on the skin. Materials and Methods: The Miconazole nitrate film-forming spray formulation was prepared using different concentrations of Eudragit RL-100, Ethylcellulose, Camphor and Menthol crystals (Eutectic mixture), Polyethene glycol 400 and Ethanol by simple solvent dissolving method using a statistical tool, 23 full factorial design to optimize the film forming spray formulation. The film-forming spray underwent thorough testing to evaluate its formulation characteristics, including pH, viscosity, evaporation time, density, drug release and container-related factors such as spray angle, spray diameter and amount of spray solutions released per actuation at valve assembly. To carry out an antifungal activity test on an optimized spray formulation and compare it with a commercially available cream. Results and Discussion: From the study, the ethyl cellulose concentration has a greater influence on the viscosity and density, 45 cps and 0.8472 g/mL of the spray formulation respectively. Eudragit RL-100 and the eutectic mixture have a higher impact on the drug release 92.44% at 8 hr in pH 6.8 phosphate buffer. Conclusion: The topical treatment of fungal infections proved to be suitable for the Miconazole nitrate film-forming spray formulation. Longer, continuous medication administration is facilitated by the skin's longer retention period. The medication exhibits good antifungal effectiveness in preventing fungal infections, according to antifungal investigations. The Miconazole nitrate film-forming spray is a considerably better alternative to current dosage forms for treating topical fungal infections, as evidenced by its good stability, simplicity of administration and action. [ABSTRACT FROM AUTHOR]

A sodium bentonite product (nanoclay) was added to a polyhydroxybutyrate/ethyl cellulose (PHB/EC) blend coating agent, and the impact of the nanoclay content on the properties of the coated paper was investigated. The organically treated nanoclay exhibited enhanced compatibility with the PHB/EC blend, ensuring uniform dispersion within the coating layer and improving the barrier properties of the coated paper. The mechanical properties of the PHB/EC blend-coated paper with nanoclay demonstrated ductile behavior, reducing the tensile strength and increasing the elongation. However, at higher nanoclay loadings, specifically up to 25%, aggregation among nanoclay particles occurred. This hindered the enhancement of barrier properties, thereby decreasing the degree of elongation. Incorporating nanoclay as a filler in the PHB/EC blend at suitable levels showed potential for further enhancing the barrier properties and ensuring economic feasibility in the production of packaging paper. [ABSTRACT FROM AUTHOR]

The structure and electromagnetic properties of a lithium ferrite, Li0.5Fe2.5O4, fabricated by an additive manufacturing process based on extrusion printing of ferrite samples with a binder substance followed by hightemperature sintering are studied. A preliminary ferrite-powder synthesis is carried out by the solid-phase method using iron oxide and lithium carbonate. The ferrite paste for printing is prepared using a binder based on ethyl cellulose and terpineol. The samples measuring 100 and 500 μm are fabricated by extrusion in a Voltera V-one 3D printer. The samples are sintered in a laboratory furnace at 1100°C. The microstructure and properties of the resulting ferrites depend on the printed layer thickness. The samples are characterized by a relative density of 72 and 76%, a specific saturation magnetization of 50 and 62 emu/g, a Curie temperature of 625 and 630°C, and a specific electric resistivity of 1.1·1010 and 1.6·109 Ω·cm for the 100 and 500 μm-thick samples, respectively. [ABSTRACT FROM AUTHOR]

BACKGROUND: The inherent properties of coconut oil (CO), including its elevated saturated fatty acid content and low melting point, make it suitable for application in plastic fat processing. The present study explores the physicochemical characteristics, micromorphology and oxidative stability of oleogels produced from CO using various gelators [ethylcellulose (EC), β‐sitosterol/γ‐oryzanol (PS) and glyceryl monostearate (MG)] to elucidate the formation mechanisms of coconut oleogels (EC‐COO, PS‐COO and MG‐COO). RESULTS: Three oleogel systems exhibited a solid‐like behavior, with the formation of crystalline forms dominated by β and β′. Among them, PS‐COO exhibited enhanced capability with respect to immobilizing liquid oils, resulting in solidification with high oil‐binding capacity, moderate hardness and good elasticity. By contrast, MG‐COO demonstrated inferior stability compared to PS‐COO and EC‐COO. Furthermore, MG‐COO and PS‐COO demonstrated antioxidant properties against CO oxidation, whereas EC‐COO exhibited the opposite effect. PS‐COO and EC‐COO exhibited superior thermodynamic behavior compared to MG‐COO. CONCLUSION: Three oleogels based on CO were successfully prepared. The mechanical strength, storage modulus and thermodynamic stability of the CO oleogel exhibited concentration dependence with increasing gelling agent addition. PS‐COO demonstrated relatively robust oil‐binding capacity and oxidative stability, particularly with a 15% PS addition. This information contributes to a deeper understanding of CO‐based oleogels and offers theoretical insights for their application in food products. © 2024 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]