Film-forming Research Articles

Preparation and Properties of Polyaniline/Hydroxypropyl Methylcellulose Composite Conductive Thin Films.

In this work, a chemical grafting polymerization method was employed to synthesize EHPMC-g-PANI self-supporting films. Polyaniline (PANI) was grafted onto hydroxypropyl methylcellulose (HPMC) modified with epichlorohydrin (EPHMC) to obtain an EHPMC-g-PANI aqueous dispersion, which was subsequently dried to form the self-supporting films. The introduction of HPMC, with its excellent film-forming ability and mechanical strength, successfully addressed the poor film-forming ability and mechanical properties intrinsic to PANI. Compared to in situ polymerized HPMC/PANI, the EHPMC-g-PANI exhibited significantly improved storage stability. Moreover, the fabricated EHPMC-g-PANI films displayed a more uniform and smoother morphology. The conductivity of all the films ranged from 10-2 to 10-1 S/cm, and their tensile strength reached up to 36.1 MPa. These results demonstrate that the prepared EHPMC-g-PANI holds promising potential for applications in various fields, including conductive paper, sensors, and conductive inks.

Investigation on PFAS Sources and Removal in a Municipal Wastewater Treatment Plant

PFAS (per- and poly-fluoroalkyl substances) is a complex family of manmade highly fluorinated aliphatic organic chemicals including thousands of chemical structures identified. PFASs were first synthesized in the 1940s and their physical and chemical properties such as oil and water repellency, temperature resistance, and friction reduction were then used in a wide range of products and industrial applications. Awareness about the possible health and environmental risks related to exposure to these substances has only risen in recent years and is resulting in the inclusion of such compounds in the Proposal for the recast of the Directive of the European Parliament and of the Council concerning urban wastewater treatment.A research was carried out at a municipal wastewater treatment plant (MWWTP) in Northern Italy to define the inflowing load of PFAS, the main load sources and the removal efficiency of the treatment processes.First, the contribution of the water supplied to the local population was excluded by means of specific chemical analyses. Then, the 100 industrial settlements served by the MWWTP were examined for the raw materials used, the final products and the productive cycle and 8 of them were selected as potential sources. A sampling campaign was carried out and the specific PFAS load was calculated. The total PFAS load entering the MWWTP was calculated from the analytical results and the flow. The percent contribution of each of the selected settlements to the total PFAS load was then calculated. 40% derives from a textile dyeing industry and 32% from a waste platform receiving also landfill leachates. 89% of the total PFAS load comes from the sum of such contributions and two other activities: the processing of slaughterhouse wastes and the production of chemicals for agriculture.Specific investigations lead to attribute an important role also to fire drills and fire extinguishing, using Aqueous Film Forming Foams (AFFF) containing PFAS. So, domestic contribution can be held as negligible.The removal in the WWTP was null and, in some cases, negative. As also reported in the literature some precursors can be transformed in PFAS during the biological process and some sludge accumulated compounds can be released.

Development of an innovative eugenol and borax-based orodispersible film for enhanced treatment of mouth ulcers

Orodispersible films (ODFs) have emerged as an advanced and patient-friendly delivery system due to ease of administration, improved patient compliance, quick release and taste-masking of active pharmaceutical ingredients. This research reports the preparation of the ODF containing eugenol and borax (EB-ODF) by a solvent casting technique for treating mouth ulcers. The EB-ODF consisted of vinyl pyrrolidone/vinyl acetate copolymer (Kollidon® VA64, VA64) and hydroxypropyl methylcellulose (HPMC-K250) as the film formers where eugenol and borax were loaded. The thickness of the EB-ODF obtained was 0.119 ± 0.001 mm and the tensile strength was 13.1 ± 1.1 N/mm2 (p > 0.05). The prepared films disintegrated in the oral cavity within 30 s and over 90% of the eugenol was released from the film in the first 5 min. Furthermore, the combined application of eugenol and borax, loaded in EB-ODF, displayed notable synergetic antibacterial property against both gram-negative and gram-positive bacteria. In an in-vivo study on a rat model with chemical burn-induced oral ulcers, the EB-ODF treatment group had a 100% reduction in ulcer area (p > 0.05) after 10 days of treatment and demonstrated a 38.7% higher reduction in oral ulcer area compared to the Dingpeng Cream treatment group (p < 0.0001). The EB-ODF treatment group showed minimal oral irritation, scoring only 1 point and a 65% preference in the taste tests (p < 0.0001). In summary, EB-ODF had successfully overcome the poor palatability of commercially available formulation and provided notable potential for further ulcer treatment product development.

Propellant Free Pressurized Spray System of Etodolac to Manage Acute Pain Conditions: In Vitro and In Vivo Evaluation.

This study aimed to develop a propellant-free topical spray formulation of Etodolac (BCS-II), a potent NSAID, which could be beneficial in the medical field for the effective treatment of pain and inflammation conditions. The developed novel propellant-free spray formulation is user-friendly, cost-effective, propellant-free, eco-friendly, enhances the penetration of Etodolac through the skin, and has a quick onset of action.Various formulations were developed by adjusting the concentrations of different components, including lecithin, buffering agents, film-forming agents, plasticizers, and permeation enhancers. The prepared propellant-free spray formulations were then extensively characterized and evaluated through various in vitro, ex vivo, and in vivo parameters. The optimized formulation exhibits an average shot weight of 0.24 ± 0.30ml and an average drug content or content uniformity of 87.3 ± 1.01% per spray. Additionally, the optimized formulation exhibits an evaporation time of 3 ± 0.24min. The skin permeation study demonstrated that the permeability coefficients of the optimized spray formulation were 21.42cm/h for rat skin, 13.64cm/h for mice skin, and 18.97cm/h for the Strat-M membrane. When assessing its potential for drug deposition using rat skin, mice skin, and the Strat-M membrane, the enhancement ratios for the optimized formulation were 1.88, 2.46, and 1.92, respectively against pure drug solution. The findings from our study suggest that the propellant-free Etodolac spray is a reliable and safe topical formulation. It demonstrates enhanced skin deposition, and improved effectiveness, and is free from any skin irritation concerns.

Polyvinyl Alcohol/Zr-based Metal Organic Framework Mixed-matrix Membranes Synthesis and Application for Hydrogen Separation

Membrane gas separation is an environmentally friendly and economical method used to separate valuable gases, industrial process gas wastes, and carbon dioxide from mixed gases. The most important part of this method is the membranes. Gas separation membranes are expected to have high separation and permeability performance, high mechanical strength, easy and fast production capability, and low prices. Polymer-based membranes are mostly preferred depending on the ease of modification capability. In this study, a zirconium-based metal organic framework (Zr-MOF, MIL-140 A) was synthesized and used as a filler within polyvinyl alcohol (PVA) matrix for the selective separation of hydrogen (H2) from carbon dioxide (CO2). The effect of MIL-140 A addition on the mechanical, structural, and morphological properties of PVA was evaluated. The MIL-140 A significantly improved the mechanical strength of the membrane. According to the gas separation results, the increasing concentration of MIL-140 A increased the selective separation performance of the nanocomposite membrane. The highest mechanical strength (43.1 MPa) and best film-forming ability were obtained with 3 wt% MIL-140 A loaded membrane. The ideal H2/CO2 selectivity and hydrogen permeability were obtained as 5.6 and 944 Barrer, respectively at 2 bar feed pressure and room temperature. The highest ideal H2/CO2 selectivity was obtained as 6.3 with the H2 permeability of 959 Barrer when the MIL-140 A ratio was 4 wt%.

Effects of carboxymethyl cellulose concentration on mechanical, viscoelastic properties, and thermal properties of starch/plant fiber foaming tableware materials with foam structure

In this study, a novel bio-based composite of starch/plant fiber foaming tableware material was prepared by the hot-pressing foaming method. The influence of the content of carboxymethyl cellulos (CMC) as a new type of film-forming agent filler on the properties of foam materials was systematically investigated. The results showed that the foam material with 10 wt% CMC had excellent cell morphology and uniform cell size (the average cell size reached the minimum value of 465.7 μm), relatively high porosity (57.01%), and excellent thermal insulation properties (thermal conductivity: 0.0541 W/m·K). The tensile strength of foam increased from 4.289 MPa for 0 wt% CMC to 5.714 MPa for 10 wt% CMC loading. Similarly, the flexural strength also increased from 11.609 MPa to 15.719 MPa for the foam material with 10 wt% CMC. The thermal stability and viscoelastic properties of the foam material reached the highest after adding 10 wt% CMC. In addition, the increase of CMC content is beneficial to improve the oil resistance and biodegradability of the material. The research shows that CMC is an effective filler to improve the properties of starch/plant fiber foaming tableware materials, which can greatly promote the development of bio-based polymer foam materials.

A comparison between solvent casting and electrospinning methods for the fabrication of HPMC fast-dissolving films: investigation of the physicochemical, mechanical and drug release characteristics

The fast-dissolving film is an innovative dosage form that rapidly delivers the loaded drug upon contact with saliva. Many studies have been conducted on the fabrication of fast-dissolving films using hydroxy propyl methyl cellulose (HPMC) as a common film-forming agent with solvent-casting method or sometimes with electrospinning. However, there is no comparison of these two methods on the physicochemical, mechanical, and drug-release behavior of HPMC films. This paper aims to compare bisoprolol-containing fast-dissolving films composed of HPMC and polyethylene glycol (PEG) as plasticizer constructed by solvent-casting and electrospinning methods. Given the formulation parameters (e.g., plasticizer and polymer concentrations) and process parameters (e.g., tip-to-needle distance, voltage, and feed rate), various solvent-casting films and nanofiber mats were prepared. Films were characterized in terms of disintegration time, folding endurance, thermal behavior (using DSC), crystallin structure (using XRD), drug content, and drug release. The size and morphology of nanofibers were also evaluated by SEM. Solvent-casting film composed of 6% w/v HPMC and 6% v/v PEG400, as well as nanofiber mat composed of 13% w/v HPMC and 3% w/v PEG2000 were successfully constructed. DSC and XRD analysis revealed that the crystalline structure of bisoprolol converted into the amorphous structure in the polymeric films. Nanofibers were smooth and free of beads with a mean size of 0.66 ± 0.19 μm. In terms of flexibility, the nanofiber mats outperformed the solvent-casting films. The disintegration time of the nanofiber mat was less than that of the solvent-casting film (3 s versus 30 s). Besides, nanofibers indicated faster release. The superior performance of nanofiber mats can be attributed to their nanostructure. The results showed that the characteristics of the fast-dissolving films fabricated of HPMC, including disintegration time, release rate, and flexibility could be improved through the electrospinning process.

Preparation and High-Temperature Resistance Properties of Phenolic Resin/Phosphate Hybrid Coatings.

In this study, a novel fabrication method was used to synthesize phenolic resin/phosphate hybrid coatings using aluminum dihydrogen phosphate (Al(H2PO4)3, hereafter denoted as Al), SC101 silica sol (Si) as the primary film-forming agent, and phenolic resin (PF) as the organic matrix. This approach culminated in the formation of Al+Si+PF organo-inorganic hybrid coatings. Fourier-transform infrared spectroscopy (FT-IR) and X-ray photoelectron spectroscopy (XPS) results confirmed the successful integration of hybrid structures within these coatings. The crystalline structure of the coatings post-cured at various temperatures was elucidated using X-ray diffraction (XRD). Additionally, the surface and cross-sectional morphologies were meticulously analyzed using scanning electron microscopy (SEM), offering insights into the microstructural properties of the coatings. The coatings' porosities under diverse thermal and temporal regimes were quantitatively evaluated using advanced image processing techniques, revealing a significant reduction in porosity to a minimum of 5.88% following a thermal oxidation process at 600 °C for 10 h. The antioxidant efficacy of the phosphate coatings was rigorously assessed through cyclic oxidation tests, which revealed their outstanding performance. Specifically, at 300 °C across 300 h of cyclic oxidation, the weight losses recorded for phosphate varnish and the phenolic resin-infused phosphate coatings were 0.15 mg·cm-2 and 0.09 mg·cm-2, respectively. Furthermore, at 600 °C and over an identical period, the weight reduction was noted as 0.21 mg·cm-2 for phosphate varnish and 0.085 mg·cm-2 for the hybrid coatings, thereby substantiating the superior antioxidation capabilities of the phenolic resin hybrid coatings in comparison to the pure phosphate varnish.

Nanocelluloses and Their Applications in Conservation and Restoration of Historical Documents.

Nanocelluloses have gained significant attention in recent years due to their singular properties (good biocompatibility, high optical transparency and mechanical strength, large specific surface area, and good film-forming ability) and wide-ranging applications (paper, food packaging, textiles, electronics, and biomedical). This article is a comprehensive review of the applications of nanocelluloses (cellulose nanocrystals, cellulose nanofibrils, and bacterial nanocellulose) in the conservation and restoration of historical paper documents, including their preparation methods and main properties. The novelty lies in the information collected about nanocelluloses as renewable, environmentally friendly, and sustainable materials in the field of cultural heritage preservation as an alternative to conventional methods. Several studies have demonstrated that nanocelluloses, with or without other particles, may impart to the paper documents excellent optical and mechanical properties, very good stability against temperature and humidity aging, higher antibacterial and antifungal activity, high protection from UV light, and may be applied without requiring additional adhesive.

Development of robust polysesquioxane/polymer dual-network hybrid membranes for flue gas carbon capture

In the present study, robust organic/inorganic dual-network membranes were designed by combining the advantages of polysesquioxane with superior thermal and structural stabilities, and polyether with outstanding CO2-philic and film-forming abilities. Specifically, a typical polysesquioxane precursor, bis(triethoxysilyl)ethane (BTESE), was selected to generate the inorganic-based amorphous network via a hydrolysis and condensation process, during which polyethylene glycol (PEG) was introduced to form the organic network. The Si-O-Si network derived from BTESE could provide excellent mechanical stability, while the repeat polar ethylene oxide units contained in PEG were expected to furnish a strong affinity toward CO2 through dipolar-dipolar interactions. In comparison to individual membranes, the dual-network membranes presented both attractive CO2/N2 separation performance and improved structural stability. These dual-network membranes proposed in this work hold great potential in industrial flue gas carbon capture and the strategies for designing such inorganic–organic dual-network membranes could be extended to other robust inorganic–organic hybrid films/materials.

Perylene Diimide‐Based Low‐Cost and Thickness‐Tolerant Electron Transport Layer Enables Polymer Solar Cells Approaching 19% Efficiency

AbstractThe materials for electron transport layers (ETLs) play a significant role in the performance of polymer solar cells (PSCs) but face challenges, such as low electron transport mobility and conductivity, low solution processibility, and extreme thickness sensitivity, which will undermine the photovoltaic performance and hinder compatibility of large‐scale fabrication technique. To address these challenges, a new n‐type perylene diimide‐based molecule (PDINB) with two special amine‐anchored long‐side chains is designed and synthesized feasibly. PDINB shows very high solubility in common organic solvents, such as dichloromethane (&gt;75 mg ml−1) and methanol with acetic acid as an additive (&gt;37 mg ml−1), which leads to excellent film formability when deposited on active layers. With PDINB as ETLs, the photovoltaic performance of the PSCs is boosted comprehensively, leading to power conversion efficiency (PCE) up to 18.81%. Thanks to the strong self‐doping effect and high conductivity of PDINB, it displays an appreciable thickness‐tolerant property as ETLs, where the devices remain consistently high PCE values with the thickness varying from 5 to 30 nm. Interestingly, PDINB can be used as a generic ETL in different types of PSCs including non‐fullerene PSCs and all‐polymer PSCs. Therefore, PDINB can be a potentially competitive candidate as an efficient ETL for PSCs.

Antioxidant and flexible bioplastics based on microwave-assisted extracted coffee fruit cascara pectic polysaccharides

Pectic polysaccharides with film-forming ability are often recovered from renewable agrifood by-products through solid-liquid extraction (SLE). Targeting an organic solvent-free approach, in this work, it is hypothesized that pectic polysaccharides of interest for bioplastics development can be recovered by microwave-assisted extraction (MAE) and purified by ultrafiltration. Coffee fruit cascara (CFC) was used as raw material. MAE of CFC-derived pectic polysaccharides was carried out at 120 °C at different times (2 min, 5 min, and 10 min). A 3-times (1 h each) sequential SLE with 2% acetic acid under reflux at atmospheric pressure was also performed. High molecular weight (HMW) extracts obtained by MAE for 2 min (HMW_MAE 2′) and by SLE for 1 h (HMW_SLE1), composed of 60 mol% and 54 mol% uronic acids with 18% and 17% methyl-esterification, and 7% and 8% acetylation, respectively, were selected for bioplastics development. HMW_MAE 2’ originated slightly transparent, dark brown, hydrophilic (ca. 32° water contact angle), and antioxidant (90% ABTS•+ inhibition after 5 min) bioplastics, similar to HMW_SLE1-derived materials, but 10-fold more stretchable (20% and 2% elongation at break, respectively). Therefore, MAE followed by ultrafiltration showed to be a fast and clean strategy to recover low methyl-esterified CFC pectic polysaccharides with the ability to develop antioxidant and flexible bioplastics.

The Influence of the Heat Transfer Mode on the Stability of Foam Extinguishing Agents

The mass loss mechanisms of an aqueous film-forming foam (AF foam), an AR/AFFF water-soluble film-forming foam extinguishing agent (AR foam), and a Class A foam extinguishing agent (A foam) at different levels of thermal radiation, thermal convection, and heat conduction intensity were studied. At a relatively low thermal radiation intensity, the liquid separation rate of the AF, AR, and A foams is related to the properties of the foam itself, such as viscosity and surface/interface tension, which are relatively independent of the external radiation heat flux of the foam. At low radiation intensity (15 kW/m2 and 25 kW/m2), the liquid separation rate of the AF and A foams is relatively stable. When the heat flux intensity is 35 kW/m2, the liquid separation rate of the AF and A foams increases notably, which may be mainly due to the rapid decrease in foam viscosity. And the mass loss behavior is dominated by liquid separation in the AF, AR, and A foams under the influence of thermal radiation and thermal convection. Under the same experimental conditions, the liquid separation rate of AF is the fastest. There is no significant difference in the evaporation rates of the three kinds of foam in the same heat conduction condition. In addition, the AR and A foams usually have a 25% longer liquid separation time (t) under thermal radiation and thermal convection, and the thermal stability is better than AF foam. The temperature reached by the AF foam layer under thermal convection was lower than that of the AR and A foams, and the time for the foam layer to reach the highest temperature under heat conduction was longer than that of the AR and A foams.

Molecular Dynamics Simulations of the Short-Chain Fluorocarbon Surfactant PFHXA and the Anionic Surfactant SDS at the Air/Water Interface.

The research and development of alternatives to long-chain fluorocarbon surfactants are desperately needed because they are extremely toxic, difficult to break down, seriously harm the environment, and limit the use of conventional aqueous film-forming foam fire extinguishing agents. In this study, mixed surfactant systems containing the short-chain fluorocarbon surfactant perfluorohexanoic acid (PFHXA) and the hydrocarbon surfactant sodium dodecyl sulfate (SDS) were investigated by molecular dynamics simulation to investigate the microscopic properties at the air/water interface at different molar ratios. Some representative parameters, such as surface tension, degree of order, density distribution, radial distribution function, number of hydrogen bonds, and solvent-accessible surface area, were calculated. Molecular dynamics simulations show that compared with a single type of surfactant, mixtures of surfactants provide superior performance in improving the interfacial properties of the gas-liquid interface. A dense monolayer film is formed by the strong synergistic impact of the two surfactants. Compared to the pure SDS system, the addition of PFHXA caused SDS to be more vertically oriented at the air/water interface with a reduced tilt angle, and a more ordered structure of the mixed surfactants was observed. Hydrogen bonding between SDS headgroups and water molecules is enhanced with the increasing PFHXA. The surface activity is arranged in the following order: PFHXA/SDS = 1:1 > PFHXA/SDS = 3:1 > PFHXA/SDS = 1:3. These results indicate that a degree of synergistic relationship exists between PFHXA and SDS at the air/water interface.

In Situ Chemical Modulation of Graphitization Degree of Carbon Fibers and Its Potassium Storage Mechanism.

Graphite is considered to be the most auspicious anode candidate for potassium ion batteries. However, the inferior rate performances and cycling stability restrict its practical applications. Few studies have investigated the modulating the graphitization degree of graphitic materials. Herein, a nitrogen-doped carbon-coated carbon fiber composite with tunable graphitization (CNF@NC) through etching growth, in-situ oxidative polymerization, and subsequent carbonization process is reported. The prepared CNF@NC with abundant electrochemical active sites and a rapid K+/electron transfer pathway, can effectively shorten the K+ transfer distance and promote the rapid insertion/removal of K+. Amorphous domains and short-range curved graphite layers can provide ample mitigation spaces for K+ storage, alleviating the volume expansion of the highly graphitized CNF during repeated K+ insertion/de-intercalation. As expected, the CNF@NC-5 electrode presents a high initial coulombic efficiency (ICE) of 69.3%, an unprecedented reversible volumetric capacity of 510.2 mA h cm-3 at 0.1 A g-1 after 100 cycles with the mass-capacity of 294.9 mA h g-1. The K+ storage mechanism and reaction kinetic analysis are studied by combining in-situ analysis and first-principles calculation. It manifests that the K+ storage mechanism in CNF@NC-5 is an adsorption-insertion-insertion mechanism (i.e., the "1+2" model). The solid electrolyte interphase (SEI) film forming is also detected.

Low-cost dopant-free fluoranthene-based branched hole transporting materials for efficient and stable n-i-p perovskite solar cells

It has been widely recognized that hole transporting materials (HTMs) play a key role in the rapid progress of perovskite solar cells (PVSCs). However, common organic HTMs such as spiro-OMeTAD not only suffer from high synthetic costs, but also usually require the additional chemical doping process to improve their hole transport ability, which unfortunately induces the terrible stability issue. Therefore, it is urgent to develop low-cost dopant-free HTMs for efficient and stable PVSCs. In this work, we have successfully developed a new class of efficient dopant-free fluoranthene-based HTMs (TPF1–5) with quite low lab synthetic costs by combining donor-acceptor and branched structure designs. The detailed structure-property study revealed that tuning the twisted arms at different substitution sites would regulate the intermolecular interactions and film-forming ability, thereby significantly affecting the performance of the HTMs. By applying these HTMs in conventional PVSCs, the dopant-free TPF1-based devices not only achieved the best efficiency of 21.76%, which is comparable to that of the doped spiro-OMeTAD control devices, but also showed much better operational stability, which maintained over 87% of the initial efficiency under maximum power point tracking after 1038 h.

Analysis of fire extinguishing performance and mechanisms in transformer oil pool fires by large-scale compressed nitrogen foam: Impact of different nozzle pressures

This article investigates the suppression of transformer oil pool fires using compressed nitrogen aqueous film-forming foam extinguishing agents with varying nozzle pressures (0.1–0.4 MPa), and a comprehensive analysis of fire extinguishing behavior and resistance to re-ignition was conducted. The research findings indicate that at a nozzle pressure of 0.4 MPa, there is a significant enhancement in fire extinguishing efficiency, with a reduction in extinguishing time by 15.0%–29.2%, and an increase in resistance to re-ignition by 32.2%–48.2%, making it the optimal choice. In comparison to the 0.1 MPa condition, the maximum instantaneous emissions of CO and SO2 at 0.4 MPa are only 66.7%. The interaction of various effects, such as atomization, results in a significant enhancement of flame intensification and fire extinguishing effects when compressed nitrogen aqueous film-forming foam is sprayed at high nozzle pressures. The study provides valuable insights for firefighters in the practical use of foam extinguishing agents.

Применение комплекса биологически активных веществ из Аronia melanocarpa в парафармацевтических фитоплёнках

The article presents the results of using non-pharmacopoeial plant raw material – dried leaves of the perennial cultivated chokeberry shrub Aronia melanocarpa (Michx.) Elliott. as a source of substances with anti-inflammatory and wound-healing effect. The development of a parapharmaceutical phytofilm based on a complex of biologically active substances from A. melanocarpa is described. The results of preclinical evaluation of the developed phytofilm in an experimental model of skin wound on outbred white rats are presented. The developed phytofilm is environmentally safe compared to synthetic analogues which production is accompanied by a negative environmental impact. Substances with antioxidant properties which can play the role of a medicinal base were found in the composition of aqueous extracts from chokeberry leaves: polyphenols – 7.4±0.7, tannins – 4.6±0.5 mg/cm3. The safety of using A. melanocarpa leaves as raw material for phytofilm has been confirmed in heavy metal tests. The composition and film-forming ability of chokeberry leaves aqueous extract, including polyvinyl alcohol (098-15(G)) (6%), food grade gelatin P-11 (0.5%), glycerin (GOST 6259-75) (0.4%), colloidal silver solution 200 mg/dm3 (1%) has been established. A. melanocarpa leaves extract application to the film-forming solution increases the final vapor permeability by 48% and solubility by 14%. The model experiment shows the effect of using the created phytofilm in the reparation of linear wounds, manifested as significant decrease in their length by 30% by the fifth day, by 25% by the seventh day compared with the control, as well as normalization of the skin histological structure by the tenth day.

Precision-Engineered Medium-Sized Molecular Host and Emitter for Ensuring Consistent Performance in Solution-Processed Narrowband OLEDs.

In this study, two novel multiple resonance (MR) emitters, DtCzBN and Cy-DtCzBN, were designed based on the well-known BCzBN structure and synthesized for narrowband solution-processed organic light-emitting diodes (OLEDs). Cy-DtCzBN possesses a dimeric V-shaped structure formed by coupling two individual DtCzBN units via a nonconjugated cyclohexane linker. When compared with DtCzBN, Cy-DtCzBN, as a medium-sized molecule, was found to maintain the optical and photophysical properties of the corresponding monomeric unit, DtCzBN, but exhibits high thermal stability, excellent solubility, and good film-forming ability. Additionally, solution-processed OLEDs were fabricated by using two sets of molecules: one set of small molecular hosts and emitters (i.e., mCP and DtCzBN) and the other set of medium-sized molecular hosts and emitters (i.e., Cy-mCP and Cy-DtCzBN). Notably, devices using medium-sized molecular hosts and emitters exhibited similar optical and photophysical properties but showed significantly improved reproducibility and thermal stability compared with those based on small molecular hosts and emitters. Our current study provides some insights into molecular design strategies for thermally stable hosts and emitters, which are highly suitable for solution-processed OLEDs.

Spray: Film Forming System Promising as Transdermal Drug Delivery System

Transdermal drug delivery systems offer numerous advantages over conventional routes, including improved patient compliance and reduced systemic side effects. Spray-on film forming systems (SFFS) have emerged as a novel and versatile approach for delivering drugs through the skin. This abstract presents an overview of SFFS technology, highlighting its potential in transdermal drug delivery. SFFS formulations consist of a solution or suspension of drug molecules and polymers, which upon spraying onto the skin, form a thin, uniform film that adheres to the application site. This film acts as a reservoir for drug release, providing controlled and sustained delivery over time. The versatility of SFFS allows for the incorporation of various drugs, including small molecules, peptides, and proteins, catering to a wide range of therapeutic needs. Moreover, SFFS offers advantages such as ease of application, improved bioavailability, and enhanced skin permeation compared to traditional dosage forms. This abstract summarizes recent advancements in SFFS technology, including formulation strategies, characterization methods, and in vitro/in vivo evaluations. Additionally, challenges such as skin irritation, film integrity, and scalability are discussed, along with potential solutions. Overall, SFFS holds great promise as a transdermal drug delivery system, offering opportunities for enhanced therapeutic outcomes and patient convenience.