Hydrophilic-lipophilic Balance Research Articles

Impact of the hydrophilic-lipophilic balance of free-base and Zn(II) tricationic pyridiniumporphyrins and irradiation wavelength in PDT against the melanoma cell lines

Impact of the hydrophilic-lipophilic balance of free-base and Zn(II) tricationic pyridiniumporphyrins and irradiation wavelength in PDT against the melanoma cell lines

Alkyl polyglycosides derived from α-olefins via Fisher glycosidation and their adsorption and aggregation behavior in aqueous solution

The effective and stable use of α-olefins is a topic of great research interest due to their abundant reserves, and the fact that the hydrolysis and epoxidation reaction of these substances produces hydroxyl group as a key linking group plays an important role in the synthesis of surfactants. Consequently, a series of alkyl polyglycosides (DC08PG, DC10PG, and DC12PG) were synthesized as non-ionic surfactants via the glycosidation reaction of long-chain 1, 2-vicinal diol with different carbon numbers and glucose. The results showed that 1, 2-vicinal diol exhibited increased reactivity in glycosidation due to their unique molecular structure. Furthermore, it was observed that the degree of polymerization (DP) achieved was notably elevated, registering at 1.63, surpassing the DP of 1.37 typically prepared using conventional methods. This enhancement was paralleled by a demonstrable increase in hydrophilicity, as evidenced by the hydrophile-lipophile balance number (HLB), resulting in a substantial improvement in the water solubility of the product, the transmission rate > 90 %. For adsorption and aggregation behavior, DC12PG showed a smaller cross-sectional area (Amin), larger saturation adsorption (Γmax), and could aggregate to form micelles at low concentrations, and short-term dynamic adsorption properties (DST) was prominent. At the same concentration, for foam properties, DC12PG with longer alkyl chains produced higher and more stable foam; for emulsification properties, the emulsification time was 298 s; for wetting properties, the contact angle was 61.59° in 30 s. This analysis will help to reveal the intrinsic connection between the molecular structure and properties of surfactants.

Fully Atom-Efficient Solvent-Mediated Biopolymer Manufacturing: A Base Case Illustrated with Macromolecular Surfactants Tailored to Stable Polymer-Water Interfaces.

This work introduces a novel 1-pot, 0-waste, 0-VOC methodology for synthesizing polymeric surfactants using acrylated epoxidized soybean oil and acrylated glycerol as primary monomers. These macromolecular surfactants are synthesized via reversible addition-fragmentation chain transfer (RAFT) polymerization, allowing for tunable hydrophilic-lipophilic balance (HLB) and ionic properties. We characterize the copolymers' chemical composition and surface-active properties, and evaluate their effectiveness in forming and stabilizing emulsions of semiepoxidized soybean oil and poly(acrylated epoxidized high oleic soybean oil). Comprehensive analyses, including gel permeation chromatography, nuclear magnetic resonance spectroscopy, dynamic light scattering, particle size distribution, zeta potential, and critical micelle concentration, provide detailed insights into the copolymers and the emulsions they form. The results demonstrate that the RAFT-polymerized surfactants offer long-lasting stability and effectively disperse both common oil-in-water emulsions and highly viscous and hydrophobic polymer latexes. These surfactants outperform traditional small molecule surfactants by reducing particle size and preventing phase separation, even over extended storage periods. Stable polymer-water interfaces are achieved through HLB control, tailored by monomer composition, and the final product requires no additional purification since polymerization occurs in liquid surfactants. While small molecules contribute to rapid micelle formation, the polymeric components enhance long-term stability through steric repulsion and slower dynamics. This method enables even the emulsification of polymers with submicron particle size, which ordinarily requires emulsion polymerization. Integrating biobased polymeric surfactants with advanced polymer processing techniques opens new possibilities for transforming highly hydrophobic polymers into latexes, facilitating downstream applications. This innovation enhances the environmental sustainability of surfactant production and broadens the potential for polymer emulsification technologies. Additionally, the integrated solution-processing approach demonstrated here can be applied to other emerging polymers, where judiciously selected nonvolatile solvents facilitate the polymerization and play a role in the final application.

Preparation and performance evaluation of CNF‐enhanced polyether‐modified polysiloxane defoamer

AbstractIn this article, polyether‐modified polysiloxanes were synthesized by the reaction of poly(methyl hydrogen siloxane) (PMHS) with Allyl alcohol polyether B‐400. FT‐IR, laser particle size analysis, hydrophilic–lipophilic balance (HLB) value test, and surface tension measurements were used to characterize its structures and properties. The results show that the control law for the HLB value of polyether‐modified polysiloxanes was obtained as follow: the HLB value increases with increasing hydrogen content of PMHS. When the polyether‐modified polysiloxanes were used to emulsify the polysiloxane, at the HLB value of 10.5, the average particle size of the emulsion was about 0.23 μm with a narrow particle size distribution. The emulsion has good emulsifying and dispersing properties, as well as excellent foam elimination and foam inhibition performance. When the cellulose nanofibrils (CNF) was used as a protective agent for the preparing of the polysiloxane defoamer, the stability of the emulsion does not affect, but its foam elimination and foam inhibition of emulsion can be further improved at the presence of CNF. The lowest surface tension of CNF‐enhanced polyether‐modified polysiloxane defoamer is about 22.4 mN m−1, which has good surface property. When the concentration of CNF‐enhanced polyether‐modified polysiloxane defoamer was 0.1 g L−1, the foam elimination time and foam inhibition time were 5.8 s and 38 min, respectively, at the temperature (80°C) and alkali environment (pH 13).

Revealing protein aggregation behaviour and dispersion properties induced by molecular interactions between sucrose esters and myofibrillar protein in an aqueous phase system

The effects of sucrose esters (SE) with varying hydrophilic-lipophilic balance (HLB) values (SE 11, 13, 15) and different concentrations (0.01, 0.1, 1.0 mM) on the dispersion properties and structure of myofibrillar proteins (MPs) in the aqueous phase were investigated. The results demonstrated that the SE 11 and SE 13 reduced the particle size and enhanced the distribution uniformity of the MPs. All of the SE exhibited a slight reduction in the ζ-potential absolute values of the MPs. Meanwhile, the SE 11 significantly reduced the turbidity of the MPs, especially in the 0.1 mM group. Macroscopic and microscopic images showed that the optimum dispersion state was in the SE 11–0.1 group. Furthermore, the interactions between SE and MPs exerted a significant impact on the proteins structure. The SE 13 and SE 15 caused significant changes, which presented concentration correlation, in the tertiary and secondary spatial structures of the MPs. Nevertheless, slight structural changes were observed in MPs with different SE11 concentrations. The SE did not alter the molecular weight of the MPs, i.e. it did not induce irreversible aggregation, nor degradation of the proteins. These results were verified by the surface hydrophobicity, UV–Vis spectroscopy, intrinsic fluorescence, circular dichroism, and SDS-PAGE. Molecular docking simulation showed that hydrophobic interactions and hydrogen bonds were the main interaction force between SE 11 and MPs. Therefore, our findings provided meaningful insights into the dispersion state of the MPs aqueous containing SEs and contributed to the practical application of non-ionic surfactants in meat protein processing.

Synthesis of Amphiphilic Polyacrylates as Peelable Coatings for Optical Surface Cleaning

Optical instruments require extremely high precision, and even minor surface contamination can severely impact their performance. Peelable coatings offer an effective and non-damaging method for removing contaminants from optical surfaces. In this study, an amphiphilic polyacrylate copolymer (PMLEA) was synthesized via solution radical copolymerization using the lipophilic monomer lauryl acrylate (LA) and hydrophilic monomers ER-10, methyl methacrylate (MMA), and butyl acrylate (BA). The structure and molecular weight of the copolymer were characterized using Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance (NMR), and gel permeation chromatography (GPC). The hydrophilic–lipophilic balance, surface tension, and wettability of the copolymer were analyzed through water titration, the platinum plate method, and liquid contact angle tests. The cleaning performance of the copolymer coating on quartz glass surface contaminants was evaluated using optical microscopy and Ultraviolet-Visible Near-Infrared (UV-Vis-NIR) spectroscopy. The study examined the effect of varying the ratio of LA to ER-10 on the hydrophilicity, lipophilicity, cleaning efficiency, and mechanical properties of the copolymer coating. The results showed that when the mass ratio of LA to ER-10 was 1:2, the synthesized copolymer exhibited optimal performance in removing dust, grease, and fingerprints from quartz glass surfaces. The coating had a tensile strength of 2.57 MPa, an elongation at break of 183%, and a peeling force of 2.07 N m−1.

Synthesis and characterization of chitosan-pectin fabricated nanoemulsion for ethylhexyl triazone topical delivery

This study aimed to investigate the stability of nanoemulsions for the UVB filter, ethylhexyl triazone (EHT) encapsulation followed by fabrication with chitosan and pectin. Four formulations were developed to assess the influence of hydrophile-lipophile balance (HLB) values on nanoemulsion stability for EHT encapsulation, targeting high Sun Protection Factor (SPF) values. The selected nanoemulsion was then subjected to fabrication with chitosan and pectin, followed by physical characterization and rheological behaviour study. Results indicated that all nanoemulsions exhibited particle sizes ranging from 137.7 nm to 206.0 nm and high entrapment efficiency from 88.76 % to 91.98 %. Sample N3, containing 1 % Tween 20 and 2 % polyethylene glycol (PEG) 400 with HLB of 12, demonstrated the highest stability, yielding a significantly elevated SPF value (10.33). Moreover, polymer-coated nanoemulsions with a low concentration of chitosan (0.1 %) showed enhanced stability when combined with different percentages of pectin. Polymer-coated nanoemulsions indicated shear-thinning behaviour at lower shear rates to Newtonian flow at higher shear rate. Furthermore, both polymer-coated and uncoated nanoemulsions exhibited decreased viscosity with increasing temperature. Also, polymer-coated nanoemulsions was found to enhance the sustainable release of EHT. These findings demonstrated the potential of polymer-coated nanoemulsions for skin application, offering enhanced stability and improved flow behaviour. The design of polymer-coated nanoemulsions could potentially minimize the risks of accumulation and toxicity of UV filters by providing a sustainable release behaviour.

Development of amphiphilic hypercrosslinked porous polymers for magnetic extraction of multiple environmental pollutants in water

Under the principle of similar compatibility, researchers have developed various polarity extractants corresponding to a class of chemicals. Separating different polarities chemicals with one extractant effectively has become a novel research trend in separation science. Given the complexity of environmental sample matrices and the significant differences in polarity and solubility of various compounds, the introduction of hydrophilic groups to hydrophobic material skeletons can lead to sorbents with hydrophilic-lipophilic balance (HLB) property and thus improve their extraction performance for substances with different polarities. In this work, a hypercrosslinked polymer (HCPPz-TPB), designated as HLB, was synthesized by incorporating polar pyrazine and nonpolar triphenylbenzene molecules within each other. Subsequently, a core-shell magnetic composite material was obtained by encapsulating magnetic Fe3O4 nanoparticles in HCPPz-TPB. The material was applied as an adsorbent for magnetic solid phase extraction (MSPE) and combined with a high-performance liquid chromatography-photodiode array detector (HPLC-PDA) to enrich, separate, and detect seven polar contaminants in environmental water samples. The proposed approach, Fe3O4@SiO2@HCPPz-TPB−MSPE-HPLC-PDA, is characterized by its outstanding high sensitivity, low detection limits, wide linear range, and good reproducibility. The method demonstrated satisfactory linearity in the range of 0.05–2 μg mL-1 with R2 values between 0.9969 and 0.9997; the limits of detection (LOD) were observed to be within the range of 0.0019–0.016 μg L-1, and limits of quantification (LOQ) was observed to be within the range of 0.0064–0.054 μg L-1 range with good precision. The recoveries of the different contaminants in the environmental samples ranged from 83.61 to 116.46% (RSD≤10.56, n = 5). The new hydrophilic-lipophilic balance extractant is highly efficient, sensitive, and precise for extracting different polar pollutants. The findings demonstrate that the Fe3O4@SiO2@HCPPz-TPB display a remarkable affinity for multiple targets, driven by complex interactions including multi-stackings and hydrogen bonding as a sorbent. The synthesized Fe3O4@SiO2@HCPPz-TPB may be employed in diverse applications, including extraction, removal, and determination of diverse trace multi-target analytes in complex media.

Development and Investigation of a Nanoemulgel Formulated from Tunisian Opuntia ficus-indica L. Seed Oil for Enhanced Wound Healing Activity.

The aim of this study is to develop a nanoemulgel encapsulating a Tunisian Prickly Pear (Opuntia ficus-indica L.) seed oil (PPSO) to assess, for the first time, the in vivo efficacy of this nanoformulation on wound healing. Phytocompounds of this oil have been reported in the literature as having powerful pharmacological activities. However, it remains poorly exploited due to low bioavailability. A nanoemulsion (NE) was designed by determining the required hydrophilic-lipophilic balance (HLB) and subsequently characterized. The mean droplet size was measured at 56.46 ± 1.12 nm, with a polydispersity index (PDI) of 0.23 ± 0.01 using dynamic light scattering. The zeta potential was -31.4 ± 1.4 mV, and the morphology was confirmed and assessed using transmission electron microscopy (TEM). These characteristics align with the typical properties of nanoemulsions. The gelification process resulted in the formation of a nanoemulgel from the optimum nanoemulsion. The high wound healing efficiency of the nanoemulgel was confirmed compared to that of a medicinally marketed cream. The outcomes of this research contribute valuable insights, for the first time, into the potential therapeutic applications of PPSO and its innovative pharmaceutical formulation for wound healing.

Oil-in-water microemulsion of Arthrospira platensis carotenoid as antiphotooxidation in vitamin C beverages

Arthrospira platensis is a blue-green microalgae that has carotenoid as the main pigments, with the largest content being beta-carotene. Carotenoids are a type of pigment that is water insoluble, unstable, and has a limited bioavailability. One of the efforts to improve its solubility and stability, especially with regard to its anti-photooxidation capabilities, is to make it into a microemulsion. This study aimed to develop the most stable oil-in-water (O/W) microemulsion containing carotenoids from A. platensis for use as an antiphotooxidation agent in vitamin C beverages. Microemulsions consist of three distinct phases: oil, water and surfactant. The oil phase consisted of virgin coconut oil (VCO) or palm oil, with 7.5% and 15% and the aqueous phase was distilled water at a concentration of 65% or 80%. The surfactant used a combination of Tween 80, Tween 20, and Span 80 with a final hydrophilic-lipophilic balance or HLB value of 14.5. All microemulsion formulations were incubated for 24 hrs before being tested for stability by centrifugation at 3000 rpm for 30 mins, heating at 105oC for 5 hrs, and storage for 2 and 4 weeks. The resulting turbidity index was used to test the microemulsion's stability. The most stable microemulsion was chosen as a delivery system for carotenoid compounds. The carotenoid microemulsion was also tested by centrifugation, heating, and stability at different pH (6.5 and 4.2) and in varied ratios (1:1, 1:9 and 1:99). The results revealed that the concentration of oil and water phases in the microemulsion formulation influenced the microemulsion's stability. The best formulation obtained was a microemulsion with 7.5% of virgin coconut oil, 80% of water concentration, and surfactant with a ratio of 92:5.5:2.5 (Tween 80: Span 80:Tween 20). The most stable carotenoid microemulsion was a microemulsion with 100 ppm of carotenoid added. The carotenoid microemulsion was able to inhibit photooxidation at 4000 lux for 4 hrs. The vitamin C beverage model added with 6 ppm carotenoid microemulsion was able to inhibit photooxidation compared to the control and 12 ppm, for up to 6 hrs and there was a significant decrease in vitamin C and antioxidants after 24 hrs of photooxidation. A. platensis carotenoid microemulsion with a concentration of 6 ppm could inhibit photooxidation on vitamin C beverages for up to 6 hrs.

Application of non-ionic liquids-based modified dielectrics during electric discharge machining (EDM) of Ti6Al4V alloy to enhance machining efficiency and process optimization

The non-conventional manufacturing technologies are notorious when it comes to productivity and processing time in production-related industries. However, the aerospace and other high-end sectors enjoy another quality matrix of these processes and compromise on the processing time. For instance, the machinability of hard-to-cut materials such as Ti6Al4V aerospace alloy for micro-impressions is challenging and commonly carried out through non-conventional processes. Among these processes, the electric discharge machining (EDM) is famous for machining Ti6Al4V. In the current study, the EDM process is enhanced through modified dielectrics such as kerosene with non-ionic liquids (span 20, 60, and 80) and cryogenically treated tool electrodes (aluminum and graphite), and is compared to the conventional kerosene-based process. A three-phase experimental campaign is deployed to explore parametric effects including modified dielectric conditions (non-ionic liquid type and concentration), tool material, and machine parameter pulse ON:OFF time. A total of 60 experiments (54 modified dielectrics and 6 as baseline) were performed to explore process physics. The statistical analyses show that the unmodified process (kerosene dielectric-based) results in the least favorable results 0.58 mm3/min against cryo-graphite and 1.2 mm3/min against cryo-aluminum electrodes. However, the modified dielectrics outperform and improve process dynamics by altering dielectric conditions through hydrophilic-lipophilic balance. Surface morphological analysis shows significantly shallow craters on the machined surface showing evidence of effective flushing through a modified dielectric (S-20) as compared to a kerosene-based dielectric. A thorough microscopical, statistical, and scanning electron-based analysis is carried out to explain the process and correlate significant improvements.

Novel non-fluorinated surfactants for emulsion polymerization of fluorinated monomers

In order to replace toxic fluorinated surfactants such as PFOA and GenX, herein we report a series of non-fluorinated surfactants (NFS) for the emulsion polymerization of fluorinated monomers. The surfactant is a statistic copolymer synthesized from free radical polymerization of poly(ethylene oxide) methacrylate (PEGMA) as hydrophilic monomer with methyl methacrylate (MMA) or tert-butyl methacrylate (TBMA) as hydrophobic comonomer. With properly designed hydrophile lipophile balance (HLB), monomer ratio, and the length of PEG segments, the polymeric NFS form unimolecular micelles in water, which facilitates the emulsion polymerization of fluorinated monomers including vinyl difluoride (VDF) where the solid content of emulsion can be higher than 25 wt% without the occurrence of significant coagulation. The optimized loading ratio of NFS is as low as 88 ppm which is ten times lower than that of fluorinated surfactants. The results demonstrate that the statistic copolymers construct unimolecular micelles to be powerful NFS for the emulsion polymerization of fluorinated monomers.

Data-Driven Design of Novel Polymer Excipients for Pharmaceutical Amorphous Solid Dispersions.

About 90% of active pharmaceutical ingredients (APIs) in the oral drug delivery system pipeline have poor aqueous solubility and low bioavailability. To address this problem, amorphous solid dispersions (ASDs) embed hydrophobic APIs within polymer excipients to prevent drug crystallization, improve solubility, and increase bioavailability. There are a limited number of commercial polymer excipients, and the structure-function relationships which lead to successful ASD formulations are not well-documented. There are, however, certain solid-state ASD characteristics that inform ASD performance. One characteristic shared by successful ASDs is a high glass transition temperature (Tg), which correlates with higher shelf stability and decreased drug crystallization. We aim to identify how polymer features such as side chain geometry, backbone methylation, and hydrophilic-lipophilic balance impact Tg to design copolymers capable of forming high-Tg ASDs. We tested a library of 50 ASD formulations (18 previously studied and 32 newly synthesized) of the model drug probucol with copolymers synthesized through automated photoinduced electron/energy transfer-reversible addition-fragmentation chain-transfer (PET-RAFT) polymerization. A machine learning (ML) algorithm was trained on the Tg data to identify the major factors influencing Tg, including backbone methylation and nonlinear side chain geometry. In both polymer alone and probucol-loaded ASDs, a Random Forest Regressor captured structure-function trends in the data set and accurately predicted Tg with an average R2 > 0.83 across a 10-fold cross validation. This ML model will be used to predict novel copolymers to design ASDs with high Tg, a crucial factor in predicting ASD success.

On-site extraction of benzophenones from swimming pool water using hybrid tapes based on the integration of hydrophilic-lipophilic balance microparticles and an outer magnetic nanometric domain

An on-site extraction device is presented consisting of scotch tape modified with concentric domains of micrometric hydrophilic-lipophilic balance (HLB) particles surrounded by a ring of nanometric magnetic ones. On the one hand, HLB microparticles are readily available at the surface of the tape, exposed to interact with the target analytes, being responsible for the extraction capacity of the sorptive phase. On the other hand, the presence of magnetic nanoparticles enables the attachment of the modified tape onto a metallic screw via a magnet, which is then coupled to a wireless drill, enabling the stirring of the microextraction device. Both are simply fixed to the cost-effective, flexible, and versatile support, i.e., scotch tape, owing to their adhesive properties. The microextraction device has been applied to the determination of six benzophenones in swimming pool water samples. The variables that may affect the extraction process have been evaluated. Under the optimum conditions and using liquid chromatography-tandem mass spectrometry as the instrumental technique, the method provided a limit of detection of 0.03 µg L−1. The intra-day precision, evaluated at three different concentration levels and expressed as relative standard deviation, was lower than 10%, which also comprises the variability within single-use sorptive tapes. The accuracy, calculated with spiked samples and expressed as relative recovery, ranged from 71 to 138%. The method was applied to the analysis of swimming pool water, revealing the presence of such compounds.Graphical

Covalent organic polymer-based sodium alginate composite beads: Decontamination of ciprofloxacin micro-polluted groundwater in a PRB system

The ecological threat posed by ciprofloxacin (CIP) contaminated groundwater could be settled by permeable reactive barriers (PRB) technology. However, exploiting proper and recyclable backfill medium was a major challenge for a PRB system. Herein, a novel three-component covalent organic polymer (SLEL-7) was synthesized by a solvothermal method for the adsorptive purification of CIP in groundwater, followed by the successful introduction into sodium alginate to acquire excellent recyclable beads (SLEL-7@SA beads) achieving enhanced adsorption behaviors. Plausible adsorption mechanisms were proposed through characterizations and adsorption studies in addition to the main controlling factors, including pore filling effect, hydrogen bonding and π-π EDA interaction, of course, hydrophilic-lipophilic balance and electrostatic interaction also took part in. Aside from that, a laboratory PRB column loading SLEL-7@SA beads as backfill medium was established which could continuously treat 60 bed volumes (BVs) of CIP (500 μg·L–1). And to be more specific, the Thomas, Yoon-Nelson and Adams-Bohart models were applied to predict the dynamic behaviors of CIP adsorption in the column. Overall, this work emphasized the structural and functional design of three-component COPs and the great potential of macroscopic COP@SA composite beads for in-situ remediation of CIP micro-polluted groundwater.

Oligo(ethylene glycol) methacrylate-based molecular bottlebrushes: Correlations between composition and phase transition temperatures in aqueous solutions

Correlations between phase transition temperatures (Tpt) in aqueous solutions and quantitative amphiphilic characteristics of a large array of thermoresponsive molecular bottlebrushes, polymethacrylates containing oligoethylene glycol (OEG), oligopropylene glycol (OPG), higher n-alkyl blocks of different lengths in their side chains, have been systematically studied for the first time. The estimated hydrophilic-lipophilic balance (HLBp) of the polymers calculated from the HLBm of the starting monomers using the Davis group number method was used for the amphiphilic characterization. The adequacy of this approach was confirmed by analyzing experimental data on the distribution of monomers and polymers in hexane-water heterophase system. Depending on the mutual arrangement of OEG-, OPG- and n-alkyl blocks in macromolecules, 107 considered molecular brushes considered were divided into 5 types and specific correlations between Tpt and HLBp values were determined for each type. The correlations found can be used to predict the phase transition temperatures of promising thermoresponsive polymethacrylic molecular brushes containing OEG-, OPG- and higher n-alkyl blocks in the side chains when varying the length of the blocks and their ratio in the macromolecules.

Formulation and evaluation of nanoemulgel loaded with essential oils with mosquito repellent activities

The mosquito repellent potential of plant materials, including essential oils, has been exploited for centuries. However, due to the volatility of essential oils, the protection against mosquitoes is short-lived. This study aimed to formulate citronella oil (CO) (Cymbopogon nardus) and palmarosa oil (PO) (C. martini) in the form of nanoemulgel (NEG) to delay their volatility and prolong protection time against mosquitoes. Nanoemulsions (NE) of both essential oils were prepared using ultrasonication after suitable hydrophilic-lipophilic balance (HLB) selection and phase diagram development. NEGs were formulated by mixing NEs and Carbopol 934 gel. Physicochemical characterizations, including in vitro release and permeation studies were conducted. Tween 80, Transcutol P and distilled water with 40 % glycerol were selected as surfactant, co-surfactant and aqueous components of the NEs, respectively. HLB values of 11 and 12 were found to be appropriate for CO and PO NEs preparation, respectively. The NEGs were kinetically stable and the formulation components were chemically compatible with each other. The NEG formulations prolonged the release of both essential oils for 24 h and significantly reduced the percentage permeation via cellulose acetate membrane as compared to NEs. Consequently, NEG could be a potential formulation to prolong the mosquito repellent activity of essential oils.

Optimization and characterization of essential oil-loaded nanoemulsions for enhanced antiviral activity against tobacco mosaic virus (TMV) in tobacco plants

Tobacco mosaic virus (TMV) is a significant viral pathogen that infects various economically important crops, including tobacco, tomatoes, and cucumbers. The current study aimed to develop and optimize essential oil-loaded nanoemulsions using Response Surface Methodology (RSM) to enhance antiviral activity against TMV in Nicotiana tabacum plants. Essential oils from tea tree (Melaleuca alternifolia) and lime peel (Citrus latifolia) were chemically analyzed using gas chromatography-mass spectrometry (GC-MS). Terpinene-4-ol (70.92 %) and trans-isolimonene (33.82 %) were identified as the major components in tea tree and lime peel oils, respectively. RSM was used to optimize the nanoemulsion formulations based on oil concentration, hydrophilic-lipophilic balance (HLB), and stirring speed. Optimal tea tree oil (TTEO) and lime peel oil (LPEO) nanoemulsions were developed and characterized using Fourier-transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), and particle size analysis. The antiviral efficacy of the optimized formulations was tested against TMV using RT-qPCR analysis and physiological measurements. TTEO nanoemulsions significantly inhibited TMV expression by 89.78 %, while LPEO nanoemulsions achieved a 42.22 % reduction after six days. Additionally, these essential oils (EOs) enhanced plant defense mechanisms by modulating the activities of phenylalanine ammonia-lyase (PAL) and peroxidase (POD), along with maintaining chlorophyll levels. This study demonstrates that TTEO and LPEO nanoemulsions offer promising eco-friendly antiviral agents for TMV management in tobacco plants. The research underscores the potential of essential oil-based formulations in mitigating viral infections in crops, providing a sustainable alternative to synthetic chemicals.

Stable diesel and bio-oil emulsion through solvent extraction and ultrasonic aided emulsification

Fast pyrolysis bio-oil is considered a highly preferable supplement to conventional fossil fuels. However, the direct application of pyrolysis bio-oil is limited due to poor fuel properties. Emulsification of bio-oil with diesel using a solvent is considered a relatively straightforward technique for utilizing bio-oil directly with diesel. In this study, new solvents were studied with the aid of sonication to produce a stable emulsion of diesel and bio-oil. 2-Octanol, 2-Heptanol and 2-Octanone were selected as solvents based on computer-aided molecular design (CAMD) method. Bio-oil was blended with 5, 10, 15 and 20 wt% of 2-Octanol using sonication. The solvent-oil blends with different solvents (2-Heptanol and 2-Octanone) at 20 wt% were also investigated for extracting organics from bio-oil. Subsequently, sonication-assisted emulsification of the solvent-extracted bio-oil with diesel was conducted with the aid of a composite surfactant with a hydrophilic-lipophilic balance (HLB) value of 7. Extraction of bio-oil with 20 wt% of 2-Octanol provided a maximum organic yield of 37.9 ± 1.3 % with a Higher Heating Value (HHV) of 31.9 MJ/kg. The desired ratio for emulsification was found to be 80: 15: 5 (diesel: surfactant: solvent-extracted bio-oil). The emulsion samples showed promising quality with an HHV of 44.0 MJ/kg and a pH of 8.0 ± 0.1. Moreover, no phase separation was observed even after the accelerated ageing process at 80 ºC for 24 hours. The results showed that all three solvents had an overall positive effect on the extraction of organics from bio-oil and aided in emulsification with diesel in which 2-Octanol was the most effective solvent for achieving a stable diesel – bio-oil emulsion.

Tailoring lyotropic liquid crystals for skin barrier penetration: Exploring composition and structure–function relationships

Lyotropic liquid crystals (LLCs) have garnered attention as a promising nanocarrier delivery system for enhancing skin permeation owing to their unique structural properties, such as improved drug loading and controlled drug release and versatility. LLCs are greatly explored for topical drug delivery owing to their strong bio-adhesive nature and structural similarity to the biological membranes when applied topically, which improves skin retention and permeation of the drugs. This review explores the functionality of structural design, especially the optimization of micellar systems, hexagonal and lamellar phases, and bicontinuous cubic and sponge phases, to achieve efficient skin permeation of therapeutic loaded LLCs. Furthermore, customization of surfactant to achieve skin compatibility and permeation is explored along with incorporating molecular modifications, functionalization, and the influence of surfactant hydrophilic–lipophilic balance. Additionally, the review illuminates the impact of LLCs curvature and the engineering of ordered and disordered phases for optimal drug release. Emerging advanced techniques such as surface modification with various ligands, stimuli-responsive LLCs for on-demand drug release, and combination therapies with multifunctional LLCs for synergistic effects that can promote targeted and site-specific drug delivery have also been discussed. The detailed findings have been discussed in this review with appropriate case studies. Challenges and future perspectives in designing and formulating LLCs for skin permeation are addressed to ignite future research. The knowledge and advancements presented in this review pave the way for developing next-generation LLCs-based systems, enabling enhanced permeation through the skin and opening new possibilities in the treatment of various dermatological conditions.