Negative Surface Charge Research Articles

Antiparasitic effect of biogenic iron nanoparticles against the fish ectoparasite Argulus siamensis: In vitro study

Argulus, an ectoparasite of fish which is ubiquitous in wild and culture ponds, poses a majorchallenge with severe economic losses to the global aquaculture industry. With the increasein intensification of aquaculture practices, there is a dire need to discover new therapeuticoptions in the treatment of argulosis owing to the limited effectiveness of existing drugsand chemicals and their significant side effects. The use of metal nanoparticles hasshown promising results in the management of several parasitic infections. In this prelude,antiparasitic effect of biosynthesised iron nanoparticles was evaluated against Argulussiamensis under in vitro condition. Iron nanoparticles (FeNPs) were biosynthesised usingfresh Bauhinia racemosa leaf extract as a reducing agent and were characterised usingUV-VIS spectrophotometry, dynamic light scattering (DLS) technique, zeta potentialmeasurements, transmission electron microscopy (TEM), scanning electron microscopy(SEM), and fourier transform-infrared spectroscopy (FT-IR). For estimating antiparasiticefficacy of FeNPs under in vitro test, ten adult and juvenile parasites each were challengedfor 6 h separately in 20 ml of five different concentrations of FeNPs test solutions viz. 1.00,1.25, 1.50, 1.75 and 2.00 mg ml-1 in triplicate along with control groups for adults whereas,for juveniles, it was 0.75, 1.00, 1.25, 1.50 and 1.75 mg ml-1. Formation of FeNPs wasmeasured in 370-400 nm UV range. DLS showed an average FeNPs particle size of 119.8 nmwith a polydispersity index of 0.311. Zeta potential measurements showed negative surfacecharges (-11.3 mV) whereas, SEM and TEM micrographs revealed synthesised nanoparticleswere nearly spherical and size ranged from 60-270 nm. Further, FT-IR spectrum showed thepresence of Fe-O, N=O and O-H groups. Argulocidal effectiveness in both cases was foundto be concentration-dependent. The highest argulocidal activity of FeNPs was observed atconcentration of 1.75 mg ml-1 for juveniles and 2.00 mg ml-1 for adult argulids which led to100 and 87% mortality, respectively, in 6 h, however no mortality was recorded in controlgroup up to 16 h. Furthermore, the calculated 6 h-EC50 of biosynthesised FeNPs for juvenileand adult argulid parasites was determined as 0.97 and 1.27 mg ml-1. Results of the presentstudy showed that short term bath treatment with biosynthesised FeNPs is effective againstargulid parasites. However, further research is required to evaluate its therapeutic potentialunder in vivo condition. Keywords:Argulosis, Argulus siamensis, Iron nanoparticles,Parasiticidal activity

Adsorption of phosphorus in water by metal-modified large-size biochar: Realizing the recovery and recycling of phosphorus

Biochar finds extensive use in adsorbing phosphorus (P) from wastewater abundant in P content. Most biochars carry negative surface charges, causing electrostatic repulsion towards anions. However, as P commonly exists as anions in water, the P adsorption capacity of biochar remains limited. Moreover, conventional biochar used for P adsorption presents challenges in recycling due to its small particle size. This study presented a novel approach wherein metal-modified large-size (1–2 mm) walnut shell biochars were created using Fe, Mg, and Ca additives at varying ratios. This innovation aims to enhance P adsorption capacity and recyclability. Experimental findings revealed that unmodified biochar (BC) exhibited minimal P adsorption capacity (0.34 mg/g), while all metal-modified biochars (MBCs) demonstrated elevated P adsorption capabilities (1.06–25.60 mg/g). Among the distinct MBCs, Ca-MBCs displayed the highest P adsorption capacity (25.60 mg/g), trailed by Mg-MBCs (23.58 mg/g) and Fe-MBCs (5.99 mg/g). Furthermore, both isotherm and kinetic adsorption analyses suggested that the P adsorption mechanism for MBCs predominantly involves chemical adsorption. However, desorption studies post-adsorption indicated suboptimal desorption efficiencies for P (19.16–26.07%) in MBCs, posing challenges for their application as fertilizers. Therefore, it is essential to enhance simultaneous P adsorption and desorption capabilities of biochar.

Efficient removal of fluoride ion by the composite forward osmosis membrane with modified cellulose nanocrystal interlayer

In this paper, the performance of three-layer film composite (TFC) forward osmosis (FO) membrane for the retention of fluoride ions was investigated. A cellulose nanocrystal (CNC) interlayer was introduced on the porous substrate by coating method to enhance the hydrophilicity and retention capacity of the FO membrane. In order to improve the dispersibility of CNC, boric acid (BA) and (3-aminopropyl)triethoxysilane (APTES) were used for chemical modification, respectively. The characterization results demonstrated the successful introduction of CNC, BA/CNC and APTES/CNC–CNC interlayers. The introduction of the interlayer enhanced the hydrophilicity of the membrane and increased the negative surface charge, which facilitated the transport of water molecules and the retention of fluoride ions. The FO tests indicated that the water flux of TFC/CNC membrane was increased by 46.4% compared to the original TFC membrane, and the water flux of TFC/APTES-CNC and TFC/BA-CNC membranes were higher than that of TFC/CNC membranes by 5.9% and 13.0%, respectively. 97.0% and 97.6% of the fluoride ions of TFC/BA-CNC and TFC/APTES-CNC could be retained. Based on the molecular simulation of adsorption, it was demonstrated that BA-CNC interlayer was more favorable for the adsorption of water molecules than CNC and APTES-CNC interlayer. This study contributes to the development of high-performance TFC-FO membrane for the treatment of wastewater containing fluoride.

Biosynthesis of Zinc Oxide Nanoparticles on l-Carnosine Biofunctionalized Polyacrylonitrile Nanofibers; a Biomimetic Wound Healing Material.

Multifunctional biohybrid nanofibers (NFs) that can simultaneously drive various cellular activities and confer antibacterial properties are considered desirable in producing advanced wound healing materials. In this study, a bionanohybrid formulation was processed as a NF wound dressing to stimulate the adhesion and proliferation of fibroblast and endothelial cells that play a major role in wound healing. Polyacrylonitrile (PAN) electrospun NFs were hydrolyzed using NaOH and biofunctionalized with l-carnosine (CAR), a dipeptide which could later biosynthesize zinc oxide (ZnO) nanoparticles (NPs) on the NFs surface. The morphological study verified that ZnO NPs are uniformly distributed on the surface of CAR/PAN NFs. Through EDX and XRD analysis, it was validated that the NPs are composed of ZnO and/or ZnO/Zn(OH)2. The presence of CAR and ZnO NPs brought about a superhydrophilicity effect and notably raised the elastic modulus and tensile strength of Zn-CAR/PAN NFs. While CAR ligands were shown to improve the viability of fibroblast (L929) and endothelial (HUVEC) cells, ZnO NPs lowered the positive impact of CAR, most likely due to their repulsive negative surface charge. A scratch assay verified that CAR/PAN NFs and Zn-CAR/PAN NFs aided HUVEC migration more than PAN NFs. Also, an antibacterial assay implied that CAR/PAN NFs and Zn-CAR/PAN NFs are significantly more effective in inhibiting Staphylococcus aureus (S. aureus) than neat PAN NFs are (1000 and 500%, respectively). Taken together, compared to the neat PAN NFs, CAR/PAN NFs with and without the biosynthesized ZnO NPs can support the cellular activities of relevance for wound healing and inactivate bacteria.

Screening optimal preparation conditions of low-cost metal-modified biochar for phosphate adsorption and unraveling their influence on adsorption performance

Abundant novel metal-modified biochars have been synthesized for phosphate removal under various preparation conditions, but optimal biochar adsorbents with low cost and high removal performance for application in real scenarios are still largely scarce. In this study, the optimal preparation conditions for metal-modified biochar were screened stepwise by determining their phosphate adsorption performance and cost with frequently used preparation conditions, including different feedstocks (total 7 biomass residues), pyrolysis temperatures (400 °C and 600 °C), modification methods (impregnation and coprecipitation), and modifying metals (Fe/La/Mg). Furthermore, the influences of preparation conditions on adsorption capacity and mechanisms were interpreted via multiple characterization methods by compared with the optimal preparation conditions. The results showed that Mg coprecipitated peanut shell biochar at 600 °C (denoted PS–600–C–Mg) was the optimal phosphate adsorbent with a maximum adsorption capacity of 50.58 mg g−1 and a cost benefit ratio (CBR) of 3.24 × 104 RMB t−1 based on adsorption capacity and cost‒benefit analysis via Monte Carlo simulations. The different mesoporous (2–50 nm) and macroporous structures (>50 nm), which were generated under various preparation conditions and favored the development of metal (hydr)oxides, could explain the greater adsorption capacity of this optimal biochar. Furthermore, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), zeta potential and Fourier transform infrared spectroscopy (FTIR) spectra jointly revealed that modification methods and modifying metal types changed adsorption mechanisms with phosphate significantly. The dominant role of electrostatic force in the adsorption of the optimal biochar towards phosphate was interpreted mainly by the unchanged FTIR spectra, negative surface charge, and further confirmed by the interaction region indicator (IRI) and localized orbital locator (LOL) at the molecular level by using density functional theory (DFT).

Performance comparison of photodynamic antimicrobial chemotherapy with visible-light-activated organic dyes: Rose bengal, crystal violet, methylene blue, and toluidine blue O

This study evaluated the photobiocidal performance of four widely distributed visible-light-activated (VLA) dyes against two bacteria (Staphylococcus epidermidis and Escherichia coli) and two bacteriophages (phages MS2 and phi 6): rose bengal (RB), crystal violet, methylene blue, and toluidine blue O (TBO). The photobiocidal performance of each dye depended on the relationship between the type of dye and microorganism. Gram-negative E. coli and the non-enveloped structure of phage MS2 showed more resistance to the photobiocidal reaction than Gram-positive S. epidermidis and the enveloped structure of phage phi 6. RB had the highest potential to yield reactive oxygen species. However, the photobiocidal performance of RB was dependent on the magnitude of the surface charge of the microorganisms; for example, anionic RB induced a negative surface charge and thus electrical repulsion. On the other hand, the photobiocidal performance of TBO was observed to be less affected by the microorganism type. The comparative results presented in our study have significant implications for selecting photodynamic antimicrobial chemotherapy (PACT) dyes suitable for specific situations and purposes. Furthermore, they contribute to the advancement of PACT-related technologies by enhancing their applicability and scalability.

Unleashing the power of capacitive deionization: Advancing ion removal with biomass-derived porous carbonaceous electrodes

Capacitive deionization (CDI) is a promising electrochemical technique for the removal and recycling of ions from micro-polluted wastewater but is still hindered by the co-ion expulsion effect and anode oxidation. In this study, these issues are addressed through optimization of both materials and electrochemical systems. A diverse set of porous carbons are prepared using biomass as a precursor and KOH as the activation agent. It is found that direct carbonization and/or KOH activation induce a negative surface charge, whereas intense nitrogen-doping results in an inverse surface charge for all biomass-derived carbons, characterized by the potential of zero charge (Epzc). Density functional theory calculations suggest that the carboxyl group and quaternary N contribute most among other functional groups to the negative and positive charges, respectively. A Epzc-matching asymmetric CDI system is constructed employing negatively charged and positively charged carbons as the cathode and anode, respectively. This configuration, coupled with precise optimization of the cathode-to-anode mass ratio (m-/m+), unlocks a high adsorption capacity of 17.2 mg g−1 for NaCl, surpassing the symmetric system by 84.7 %. Further fine tuning of the m-/m+ ratio results in a removal capacity of 167.4 mg g−1 for Cu2+ ions, which is the highest reported for carbonaceous materials to date.

Bioremediation of n-alkanes, polycyclic aromatic hydrocarbons, and heavy metals from wastewater using seaweeds

The removal of n-alkanes, polycyclic aromatic hydrocarbons, and heavy metals from wastewater using three dried seaweeds Ulva intestinalis Linnaeus (green alga), Sargassum latifolium (Turner) C.Agardh (brown alga), and Corallina officinalis Kützing (red alga) has been shown to evaluate their potential usage as inexpensive adsorbents. Under natural environmental conditions, numerous analytical methods, including zeta potential, energy dispersive X-ray spectroscopy (EDX), SEM, and FT-IR, are used in this study. The results showed that n-alkanes and polycyclic aromatic hydrocarbons adsorption increased with increasing contact time for all three selected algae, with a large removal observed after 15 days, while the optimal contact time for heavy metal removal was 3 h. S. latifolium dry biomass had more potential as bioadsorbent, followed by C. officinalis and then U. intestinalis. S. latifolium attained removal percentages of 65.14%, 72.50%, and 78.92% for light n-alkanes, heavy n-alkanes, and polycyclic aromatic hydrocarbons (PAHs), respectively, after 15 days. Furthermore, it achieved removal percentages of 94.14, 92.62, 89.54, 87.54, 82.76, 80.95, 77.78, 73.02, and 71.62% for Mg, Zn, Cu, Fe, Cr, Pb, Cd, Mn, and Ni, respectively, after 3 h. Carboxyl and hydroxyl from FTIR analysis took part in wastewater treatment. The zeta potentials revealed that algal cells have a negatively charged surface, and the cell surface of S. latifolium has a more negative surface charge than U. intestinalis and C. officinalis. Our study suggests that seaweeds could play an important role in wastewater treatment and thus help as an economical, effective, and ecofriendly bioremediation system for ecological health and life protection.

Obtention, characterization, and herbicide diquat carrier/release properties by nanocomposite hydrogels based on the polysaccharides and zeolite for future use in agriculture

This work aims to develop new hydrogel nanocomposites based on polysaccharides (methylcellulose (MC) or chitosan (CH)) with zeolite, supported by a poly(methacrylic acid)–co-polyacrylamide (PMAA-co-PAAm) network for agriculture applications, such as water decontamination, and released control systems. The incorporation of zeolite on the nanocomposites has been confirmed by the characteristic peaks of zeolite in nanocomposites through Fourier transform infrared spectroscopy (FTIR) spectra and X-ray diffraction (XRD) patterns. Scanning electron microscopy (SEM) analyzes showed a decrease in the pore volume on the nanocomposites and the presence of micropore at the wall porous structure. The chain elasticity and water retention of the hydrogel were affected by changes in pH rate, for example, the MC nanocomposite swelling values growth from 2.6 g/g at pH 1 to 4.4 g/g at pH 5. The sorption and desorption of diquat studies showed that an increase in the interaction sites provided by the zeolite negative surface charges caused an increment in the attraction forces, which afford the interchange between the diquat molecules and the desorption medium ions. These results indicated that intrinsic and extrinsic factors can affect desorption, and a better understanding of these phenomena can be supplemental in a significant way in the more efficient application of these materials in agricultural systems.

Copolymeric Micelles of Poly(ε-caprolactone) and Poly(methacrylic acid) as Carriers for the Oral Delivery of Resveratrol.

In this study, we report the development of a micellar system based on a poly(methacrylic acid)-b-poly(ε-caprolactone)-b-poly(methacrylic acid) triblock copolymer (PMAA16-b-PCL35-b-PMAA16) for the oral delivery of resveratrol. The micellar nanocarriers were designed to comprise a PCL core for solubilizing the poorly water-soluble drug and a hydrated PMAA corona with bioadhesive properties for providing better contact with the gastrointestinal mucosa. The micelles were first formed in an aqueous media via the solvent evaporation method and then loaded with resveratrol (72% encapsulation efficiency). Studies by transmission electron microscopy (TEM) and dynamic and electrophoretic light scattering (DLS and PALS) revealed a spherical shape, nanoscopic size (100 nm) and a negative surface charge (-30 mV) of the nanocarriers. Loading of the drug slightly decreased the hydrodynamic diameter (Dh) and increased the ƺ-potential of micelles. In vitro dissolution tests showed that 80% and 100% of resveratrol were released in 24 h in buffers with pH 1.2 and 6.8, respectively, whereas for the same time, not more than 10% of pure resveratrol was dissolved. A heat-induced albumin denaturation assay demonstrated the advantage of the aqueous micellar formulation of resveratrol, which possessed anti-inflammatory potential as high as that of the pure drug. Further, the micellar resveratrol (5 µM) exerted a strong protective effect and maintained viability of mucosa epithelial HT-29 cells in a co-cultural model, representing the production of inflammatory cytokines. For comparison, the pure resveratrol at the same concentration did not protect the damaged HT-29 cells at all. Thus, the present study revealed that the PMAA-b-PCL-b-PMAA copolymeric micelles might be considered appropriate nanocarriers for the oral delivery of resveratrol.

Supplementing broiler diets with bacterial selenium nanoparticles enhancing performance, carcass traits, blood indices, antioxidant status, and caecal microbiota of Eimeria tenella-infected broiler chickens

Nanomedicine is a critical therapeutic approach for treating most poultry illnesses, particularly parasitic infections. Coccidiosis is a severe protozoan infection affecting poultry; the emergence of drug-resistant Eimeria strains demands the development of new, safe therapies. Consequently, the objective of this work was to investigate the efficacy of the biosynthesized selenium nanoparticles (SeNPs) byPaenibacillus polymyxa (P. polymyxa) against Eimeria tenella (E. tenella) experimental infection in broiler chickens. The prepared SeNPs absorbed the UV at 270 nm were spherical with a size of 26 nm, and had a surface negative charge of -25 mV. One hundred and fifty, 1-day-old male broiler chicks were randomly allocated into 5 groups (30 birds/group with triplicates each) as follows: T1: negative control (noninfected and nontreated with SeNPs);T2: delivered SeNPs (500 µg/kg diet) for 35 successive days, T3: E. tenella-infected (positive control birds), T4: E. tenella-infected and treated with SeNPs (500 µg/kg diet) and T5: E. tenella-infected chicks and treated with anticoccidial agent (sulfadimidine, 16% solution 8 mL/L of drinking water) for 5 successive days. At 14 d of age, each bird in infected groups was orally treated with 3×103 sporulated oocyst of E. tenella. SeNPs considerably decreased the number of oocysts in broiler feces compared to positive control and anticoccidial drug, followed by a substantial reduction of parasite phase count in the cecum (15, 10, and 8 for meronts, gamonts, and developing oocysts) when compared with positive control birds. The Eimeria experimental infection lowered the activity of antioxidant enzymes, superoxide dismutase (SOD), glutathione peroxidase (GPx), and reduced glutathione (GSH) while increasing the stress parameters nitric oxide (NO) and malonaldehyde (MDA). Moreover, the production of proinflammatory (TNF-α and IL-6) and apoptotic genes (BcL2 and Cas-3) were significantly elevated. Administrating SeNPs to chicks significantly decreased oxidative stress, inflammation, and apoptotic markers in the cecum tissue. Therefore, growth performance, carcass weights, antioxidant enzymes, and blood properties of infected chicks were enhanced. The findings compared the protecting role of Se-nanoparticles against cecum damages in E. tenella-infected broilers.

Synthesis of two-dimensional triazine covalent organic frameworks at ambient conditions to detect and remove water pollutants

Synthesis of fully triazine frameworks (C3N3) by metal catalyzed reactions at high temperatures results in carbonized and less-defined structures. Moreover, metal impurities affect the physicochemical, optical and electrical properties of the synthesized frameworks, dramatically. In this work, two-dimensional C3N3 (2DC3N3) has been synthesized by in situ catalyst-free copolymerization of sodium cyanide and cyanuric chloride, as cheap and commercially available precursors, at ambient conditions on gram scale. Reaction between sodium cyanide and cyanuric chloride resulted in electron-poor polyfunctional intermediates, which converted to 2DC3N3 with several hundred micrometers lateral size at ambient conditions upon [2 + 2+2] cyclotrimerization. 2DC3N3 sheets, in bulk and individually, showed strong fluorescence with 63% quantum yield and sensitive to small objects such as dyes and metal ions. The sensitivity of 2DC3N3 emission to foreign objects was used to detect low concentration of water impurities. Due to the high negative surface charge (-37.7 mV) and dispersion in aqueous solutions, they demonstrated a high potential to remove positively charged dyes from water, exemplified by excellent removal efficiency (>99%) for methylene blue. Taking advantage of the straightforward production and strong interactions with dyes and metal ions, 2DC3N3 was integrated in filters and used for the fast detection and efficient removal of water impurities.

Curcumin/Fusidic Acid Bitherapy Loaded Mixed Micellar Nanogel for Acne Vulgaris Treatment: In Vitro and In Vivo Studies

The combination of herbal drugs with a topical antibacterial for managing a chronic disease like acne vulgaris has emerged lately to settle side effects and bacterial multidrug resistance. Mixed micelles (MMs) incorporated into nanogel were explored for hybrid delivery of curcumin (Cur) and fusidic acid (FA) combination presenting a multi-strategic treatment. Curcumin-fusidic acid–loaded mixed micelles (Cur-FA-MMs) were assessed for size, surface charge, compatibility, in vitro release, and encapsulation. The selected formula was further loaded into nanogel and investigated for viscosity, ex vivo permeation, and in vivo potential. Cur-FA-MMs exhibited uniform nanosized spherical morphology, and negative surface charge affording high encapsulation for both drugs with a biphasic in vitro release over a period of 48h and good colloidal stability. The attained Cur-FA-MM-loaded nanogel had optimum viscosity with remarkable permeation coefficient values nearly 2-fold that related to plain nanogel. The pharmacodynamic effect of Cur on FA was pronounced by the significant improvement of the skin’s degree of inflammation, epidermal hypertrophy, and congestion in animals treated with Cur-FA-MM-loaded nanogel. In conclusion, micellar nanogel could enable the progressive effect of Cur (an antioxidant with reported antibiotic activity) on FA (antibiotic) and decrease the risk of emerging antibiotic resistance by enhancing the solubility and permeation of Cur.Graphical

The impact of non-deproteinization on physicochemical and biological properties of natural rubber latex for biomedical applications

Latex is a colloidal suspension derived from the Hevea brasiliensis tree, derived from natural rubber, poly(isoprene), and assorted constituents including proteins and phospholipids. These constituents are inherent to both natural rubber and latex serum. This investigation was undertaken to examine the impact of the deproteinization process on chemical and biological dynamics of natural rubber latex. Natural Rubber (NR) extracted from the pure latex (LNCP) was obtained through centrifugation, followed by six rounds of solvent purification (LP6). The structure was characterized using Fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), swelling test, surface zeta potential (ζ), scanning electron microscopy (SEM) and in vitro assay. The results revealed that the LP6 group presented decreased swelling kinetics, reduced cell adhesion and proliferation, and a smoother surface with decreased negative surface charge. Conversely, the LNCP group shown accelerated swelling, heightened adhesion and cellular growth, and a more negatively charged and rougher surface. As such, the attributes of latex serum and proteins have potential usage across numerous biomedical applications.

Formulation, characterization, and physical stability of encapsulated walnut green husk (Juglans regia L.) extract in phosphatidylcholine liposomes

This study aimed to optimize a liposomal formulation to enhance the stability of a phenolic-rich extract from green walnut husk. Liposomes were prepared using varying concentrations of phosphatidylcholine (0.15–2% w/v), extract (0–1.3% v/v), and sodium laurate (0–0.2% w/v) via ethanol injection and sonication. Characterization included visual appearance, particle size, polydispersity index, surface charge, encapsulation efficiency, and morphology. Stable liposomes were achieved at 0.15% and 0.3% w/v phosphatidylcholine, although with low encapsulation efficiency (<40%). The addition of 0.2% (w/v) sodium laurate improved the stability, especially at higher phosphatidylcholine concentrations, enhancing the electrostatic repulsion. Optimal concentrations of 2% w/v phosphatidylcholine, 0.2% w/v sodium laurate, and 0.6% v/v extract were determined. The liposomes exhibited a spherical unilamellar morphology with a size of 97.5 ± 0.9 nm and a negative surface charge of –39.8 ± 0.9 mV. These nanoliposomes showed 79.7 ± 0.7% encapsulation efficiency and remained stable under pH, temperature, ionic strength, and storage time variations. Overall, the liposomes proved effective in preserving the natural phenolics of walnut husks under challenging environmental conditions.

Fused silica as an anti-fouling material for oil sands optical instruments

Optical instruments have application in many chemical industries for use in inline observation, measurement, and process control for product and waste streams. Typically, these instruments are fitted with sapphire windows which offer extreme hardness, optical transparency and inertness but can be susceptible to fouling with hydrocarbons in the streams. This work explored the potential of fused silica as an alternative anti-fouling material for optical instrument windows for use in aqueous streams containing hydrocarbons. The advantage of fused silica is that it offers adequate hardness and transparency while retaining chemically reactive silanol groups on its surface. Closed loop experiments conducted with oil sands mature fine tailings (MFT) containing residual bitumen, a hydrocarbon known to cause severe fouling of optical windows, demonstrated no fouling issue on fused silica. The hydrophilicity of the optical surface increased following exposure to the mildly alkaline MFT. We hypothesized that in alkaline aqueous streams the silanol groups are deprotonated to create a negatively charged surface, thereby introducing a repulsive force between the surface and the negatively charged hydrocarbon droplets and increasing the hydrophilicity of both materials. Contrarily, the relatively inert sapphire is limited in its capacity to form negative surface charges and consistently fouled with bitumen. When silanol groups on the fused silica were removed via fluoro-functionalization, it resulted in complete fouling of the optical surface. Finally, bitumen fouling was observed on both fused silica and sapphire surfaces in neutral aqueous environments compared to none on the fused silica in an alkaline environment.

Transport and Model Calculation of Microplastics Under the Influence of Ionic Type, Strength, and Iron Oxide

Microplastics (MPs) in soil have attracted extensive attention as an emerging pollutant, and the transport of MPs is affected by their own physical and chemical properties, the chemical composition of soil solutions, and soil minerals. However, in the presence of oxides, the underlying mechanism for the transport of MPs in different ionic types and ionic strengths is still not fully understood. In this study, the effects of ionic type, ionic strength, and iron oxide on the transport of polystyrene microplastics (PSMPs) with different functional groups were investigated through stability experiments and transport experiments. The colloid transport model, CD-MUSIC model, and DLVO theory were used to explore the transport mechanism. The results showed that normalized concentrations (c/c0) of PSMPs were 0.99 in the NaH2PO4 background and 0.94 in the CaCl2 background, respectively, which indicated that the strongest stability of PSMPs was observed in the former and the weakest in the latter. Different ionic types had different effects on the transport of PSMPs. For the cations Na+ and Ca2+, Ca2+ strongly inhibited PSMPs transport in pure quartz sand because of the bridging effect and strong charge neutralization effect; the recovery rate of the PSMPs in the effluent was (43.83±1.71)%, and a first-order retention coefficient on the second kinetic Site-2 (k2a) was 1.54 min-1. The presence of iron oxide enhanced the inhibition, the recovery rate of the PSMPs in the effluent decreased to (6.04±0.40)%, and k2a increased to 5.33 min-1. For the anions Cl- and PO43-, the transport of PSMPs in pure quartz sand was dominated by surface electronegativity of PSMPs, and PSMPs exhibited lower electronegativity under Cl- background and thus showed higher recovery[(92.95±0.63)%] and lower k2a (0.19 min-1). However, in the presence of iron oxides, the Zeta potential of the quartz sand surface was the controlling factor for PSMPs transport. According to results of the CD-MUSIC model, PO43- could be easily adsorbed on the iron oxide surface to form innersphere complexes, which reduced the surface electronegativity of the iron-loaded quartz sand and enhanced the transport of PSMPs, higher recovery[(76.22±1.39)%], and lower k2a (0.66 min-1). Moreover, the species of the formed innersphere complex was controlled by the PO43- concentration, and different species of innersphere complexes had distinct negative surface charges. Higher surface electronegativity of the iron-loaded quartz sand was observed under higher PO43- concentration, which was not conducive to the transport of PSMPs. Further, the transport ability of PSMPs decreased with the increase in ionic strength. Finally, the Derjaguin-Landau-Verwey-Overbeek (DLVO) theory was used to calculate the variation in the primary barrier between PSMPs and the collector under the conducted experimental conditions, which helped better elucidate the transport behavior of PSMPs. The variation in the primary barrier was consistent with the transport ability of PSMPs, and a higher primary barrier indicated a larger repulsion between PSMPs and the collector, which was in favor of PSMPs transport.

Unravelling the anthocyanin-binding capacity of native starches from different botanical origins

In this study, the cyanidin-3-O-glucoside (C3G)-binding capacities of three native starches were investigated. While potato starch had the largest binding capacity of 0.34 mg/100 mg, corn and pea starch had binding capacities of 0.17 and 0.06 mg/100 mg. Confocal microscopy confirmed the binding results and revealed close associations between the surface properties and binding capacities. These findings were further substantiated with wettability and gelatinization results. The morphological observations showed that corn starch had advantageous particle sizes and more surface gullies, providing more opportunities to bind C3G. The zeta potential results, however, indicated that potato starch had the highest negative surface charges (−24 mV). These favorable electronic characteristics were believed to be responsible for the strongest electrostatic interactions. Hydrogen bonds, however, had a negligible effect on the formation of complexes. Overall, the negative surface charges and specific surface areas of the native starches were the most important factors determining C3G-binding capacities.

Celecoxib-Loaded Cubosomal Nanoparticles as a Therapeutic Approach for Staphylococcus aureus In Vivo Infection.

There is a great need for novel approaches to treating bacterial infections, due to the vast dissemination of resistance among pathogenic bacteria. Staphylococcus aureus are ubiquitous Gram-positive pathogenic bacteria and are rapidly acquiring antibiotic resistance. Here, celecoxib was encapsulated into cubosomal nanoparticles, and the particle morphology, size distribution, zeta potential, entrapment efficiency, and celecoxib release were evaluated in vitro. Also, a systemic infection model in mice elucidated the in vivo antibacterial action of the celecoxib cubosomes. Cubosomes are a nanotechnology-based delivery system which can adhere to the external peptidoglycan layers of Gram-positive bacteria and penetrate them. The size distribution investigation revealed that the prepared celecoxib-loaded cubosomes had a mean particle size of 128.15 ± 3.04 nm with a low polydispersity index of 0.235 ± 0.023. The zeta potential measurement showed that the prepared cubosomes had a negative surface charge of -17.50 ± 0.45, indicating a highly stable nanodispersion formation with little susceptibility to particle aggregation. The cubosomal dispersion exhibited an entrapment efficiency of 88.57 ± 2.36%. The transmission electron micrograph for the prepared celecoxib-loaded cubosomes showed a narrow size distribution for the cubosomal nanoparticles, which had a spherical shape and were non-aggregated. The tested cubosomes diminished the inflammation in the treated mice's liver and spleen tissues, as revealed by hematoxylin and eosin stain and Masson's trichrome stain. The immunostained tissues with nuclear factor kappa B and caspase-3 monoclonal antibodies revealed a marked decrease in these markers in the celecoxib-treated group, as it resulted in negative or weak immunostaining in liver and spleen that ranged from 4.54% to 17.43%. This indicates their inhibitory effect on the inflammatory pathway and apoptosis, respectively. Furthermore, they reduced the bacterial burden in the studied tissues. This is alongside a decrease in the inflammatory markers (interleukin-1 beta, interleukin-6, cyclooxygenase-2, and tumor necrosis factor-alpha) determined by ELISA and qRT-PCR. The IL-1β levels were 16.66 ± 0.5 pg/mg and 17 ± 0.9 pg/mg in liver and spleen, respectively. Also, IL-6 levels were 85 ± 3.2 pg/mg and 84 ± 2.4 pg/mg in liver and spleen, respectively. In conclusion, the current study introduced cubosomes as an approach for the formulation of celecoxib to enhance its in vivo antibacterial action by improving its oral bioavailability.

Preparation of Janus film for fog water collection via layer-by-layer assembling of nanocellulose and nanochitin on PLA

In order to explore the possibility of natural carbohydrate polymers as a biodegradable and sustainable fog water harvesting material, this work proposed an efficient substrate (hydrophobic)-transition layer (amphoteric)-coating (hydrophilic) sandwich spin-coating strategy to form all biomass-based Janus film. The oxalic acid hydrolyzed nanochitin (OAChN) was applied as a transition layer that enabled successful spin-coating of the hydrophilic nanocellulose (TEMPO-oxidized cellulose nanofiber, TOCN) and nanochitin (partially deacetylated chitin nanofibers, DEChN) on the hydrophobic polylactic acid (PLA) film substrate. In which a layer-by-layer (LBL) assembling of TOCN (carboxyl-rich negative surface charge) and DEChN (amino-rich positive surface charge) was designed to form a thickness and surface property controllable polysaccharide coating on PLA. The finally formed PLA-OAChN-TOCN/DEChN (LBL) film showed hydrophilic and hydrophobic heteromeric faces at the opposite sides and thus had improved fog water collection capacity of 90.85 mg·cm−2·h−1 (30 layers of TOCN/DEChN spin-coated on PLA), which was 276 % higher than the pure PLA film. The transition layer engaged sandwich spin-coating strategy, together with LBL assembling method proposed in this study provided a feasible fabrication of all biomass-based fog water collectors (FWC) that could contribute to alleviating water shortage.