Charge Neutralization Research Articles

Rice proteins – Gum arabic coacervates: Effect of pH and polysaccharide concentration in oil-in-water emulsion stability

In the context of replacing animal proteins in food matrices, rice proteins (RP) become promised because they come from an abundant plant source, are hypoallergenic, and have high digestibility and nutritional value. However, commercial protein isolates obtained by spray drying have low solubility and poor functionality, especially in their isoelectric point. One way to modify these properties is through interaction with polysaccharides, such as gum arabic (GA). Therefore, this work aims to evaluate the effects of pH and GA concentration on the interaction and emulsifying activity of RP:GA coacervates. First, the effects of pH (2.5 to 7.0) and GA concentrations (0.2 to 1.0 wt%, giving rise to RP:GA mass ratios of 1:0.2 to 1:1.0) in RP:GA blends were evaluated. The results demonstrated that biopolymers present opposite net charges at pH between 2.5 and 4.0. At pH 3.0, insoluble coacervates with complete charge neutralization were formed by electrostatic interactions, while at pH 5.0 it was observed that the presence of GA prevented the RP massive aggregation. Second, selected blends with 0.4 or 1.0 wt% of GA (RP:GA mass ratios of 1:0.4 or 1:1.0) at pH 3.0 or 5.0 were tested for their ability to stabilize oil-in-water emulsions. The emulsions were characterized for 21 days. It was observed that the GA increased the stability of RP emulsions, regardless of the pH and polysaccharide concentration. Taken together, our results show that it is possible to combine RP and GA to improve the emulsifying properties of these plant proteins at pH conditions close to their isoelectric point, expanding the possibility of implementation in food systems.

Surface charge-dependent cytokine production using near-infrared emitting silicon quantum dots

Toll-like receptor 9 (TLR-9) is a protein that helps our immune system identify specific DNA types. Upon detection, CpG oligodeoxynucleotides signal the immune system to generate cytokines, essential proteins that contribute to the body’s defence against infectious diseases. Native phosphodiester type B CpG ODNs induce only Interleukin-6 with no effect on interferon-α. We prepared silicon quantum dots containing different surface charges, such as positive, negative, and neutral, using amine, acrylate-modified Plouronic F-127, and Plouronic F-127. Then, class B CpG ODNs are loaded on the surface of the prepared SiQDs. The uptake of ODNs varies based on the surface charge; positively charged SiQDs demonstrate higher adsorption compared to SiQDs with negative and neutral surface charges. The level of cytokine production in peripheral blood mononuclear cells was found to be associated with the surface charge of SiQDs prior to the binding of the CpG ODNs. Significantly higher levels of IL-6 and IFN-α induction were observed compared to neutral and negatively charged SiQDs loaded with CpG ODNs. This observation strongly supports the notion that the surface charge of SiQDs effectively regulates cytokine induction.

Comparative analysis of surface phase diagrams in aqueous environment: Implicit vs explicit solvation models.

Identifying the stable surface phases under a given electrochemical conditions serves as the basis for studying the atomistic mechanism of reactions at solid/water interfaces. In this work, we systematically compare the performance of the two main approaches that are used to capture the impact of an aqueous environment, implicit and explicit solvent, on surface energies and phase diagrams. As a model system, we consider the magnesium/water interface with (i) Ca substitution and (ii) proton and hydroxyl adsorption. We show that while the implicit solvent model is computationally very efficient, it suffers from two shortcomings. First, the choice of the implicit solvent parameters significantly influences the energy landscape in the vicinity of the surface. The default parameters benchmarked on solvation in water underestimate the energy of the dissolved Mg ion and lead to spontaneous dissolution of the surface atom, resulting in large differences in the surface energetics. Second, in systems containing a charged surface and a solvated ion, the implicit solvent model may not converge to the energetically stable ionic charge state but remain in a high-energy metastable configuration, representing the neutral charge state of the ion. When these two issues are addressed, surface phase diagrams that closely match the explicit water results can be obtained. This makes the implicit solvent model highly attractive as a computationally-efficient surrogate model to compute surface energies and phase diagrams.

Evaluation an anionic polyacrylamide flocculant with microblock structure in the hematite wastewater treatment: Characterization and flocculation performance

In this study, a template polymer with anionic microblock structure was successfully synthesized through ultrasonic initiated template copolymerization (USTP) by using sodium allylsulfonate (SAS) and acrylamide (AM) as monomers, poly diallyl dimethyl ammonium chloride (polyDADMAC) as template, and 2,2′-azobis [2-(2-imidazolin-2-yl) propane] dihydrochloride (VA-044) as initiator. The anionic polyacrylamide (APAM-T) flocculant was characterized by Fourier transform infrared spectroscopy (FTIR), 1H nuclear magnetic resonance spectroscopy (1H NMR), and scanning electron microscopy (SEM). Furthermore, the X-ray photoelectron spectroscopy (XPS) was conducted to measure the elemental composition. The results of XPS and 1H NMR spectroscopy analysis indicated the existence of anionic microblock structure in APAM-T. Besides, the copolymerization was revealed to follow the self-assembly mechanism by analyzing the association constant (KM). The flocculation performance was evaluated by turbidity and zeta potential in the flocculation tests. The results indicated that the APAM-T with microblock structure enhanced the charge neutralization and bridging adsorption capacity, thus improving the flocculation performance. In the floc particle size distribution and fragmentation and reflocculation experiments, the floc corresponding to APAM-T had the strongest regeneration ability after fragmentation, which further confirmed the criticality of the microblock structure in enhancing the flocculation performance. Compared with existing studies, this study not only demonstrated a novel synthesis method, but also found that the microblock structure could significantly improve its treatment efficiency and effectiveness, providing a new theoretical basis and practical application path for wastewater treatment technology.

Effect of magnetic field coupled magnetic biochar on membrane bioreactor efficiency, membrane fouling mitigation and microbial communities

The excitation by magnetic field was established to mitigate the membrane fouling of magnetic biochar (MB)-supplemented membrane bioreactor (MBR) in this study. The results showed that the transmembrane pressure (TMP) increase rates decreased by about 8 % after introducing the magnetic field compared with the magnetic biochar-MBR (MB-MBR). Membrane characterization suggested that the flocs in the magnetic field-magnetic biochar-MBR (MF-MB-MBR) formed a highly permeable developed cake layer, and a fluffier and more porous deposited layer on membrane surface, which minimized fouling clogging of the membrane pores. Further mechanistic investigation revealed that the decrease in contact angle of fouled membrane surface in MF-MB-MBR, i.e. an enhanced membrane hydrophilicity, is considered important for forming highly permeable layers. Additionally, the magnetic field was demonstrated to have a positive effect on the improvement of the magneto-biological effect, the enhancement of charge neutralization and adsorption bridging between sludge and magnetic biochar, and the reduction of formation of extracellular polymeric substances (EPSs), which all yielded sludge flocs with a large pore structure conducive to form a fluffy and porous deposited layer in the membrane surface. Furthermore, high-throughput sequencing analysis revealed that the magnetic field also led to a reduction in microbial diversity, and that it promoted the enrichment of specific functional microbial communities (e.g. Bacteroidetes and Firmicutes) playing an important role in mitigating membrane fouling. Taken together, this study of magnetic field-enhanced magnetic biochar for MBR membrane fouling mitigation provides insights important new ideas for more effective and sustainable operation strategies.

Dissolution and antioxidant potential of apigenin self nanoemulsifying drug delivery system (SNEDDS) for oral delivery

Self-nanoemulsifying drug delivery systems (SNEDDS) have been used to improve the oral bioavailability of various drugs. In the current study, apigenin was developed as SNEDDS to solve its dissolution problem and enhance oral bioavailability and antioxidant potential. SNEDDS were prepared by mixing Gelucire 44/14, Tween 80, and PEG 400 under controlled conditions. The droplet of diluted SNEDDS demonstrated a spherical shape with a size of less than 100 nm and a neutral charge. The very fast self-emulsification was obtained within 32 s, and the transmittance values exceeded 99%. The highest drug loading was 90.10 ± 0.24% of the initial load with the highest %encapsulation efficiency of 84.20 ± 0.03%. FT-IR and DSC spectra showed no interaction between components. The dissolution in buffer pH 1.2, 4.5, and 6.8 showed significantly higher dissolved apigenin than the apigenin coarse powder. The dissolution profiles were fitted to the Korsmeyer–Peppas kinetics. The cellular antioxidant activities in Caco-2 cells were approximately 52.25–54.64% compared to no treatment and were higher than the apigenin coarse powder (12.70%). Our work highlights the potential of SNEDDS to enhance the dissolution and permeability of apigenin and promote antioxidant efficacy, which has a strong chance of being developed as a bioactive compound for nutraceuticals.

Chitosan-Based Grafted Cationic Magnetic Material to Remove Emulsified Oil from Wastewater: Performance and Mechanism

In order to remove high-concentration emulsified oil from wastewater, a chitosan-based magnetic flocculant, denoted as FS@CTS-P(AM-DMC), was employed in this present study. The effects of factors including the magnetic flocculant dose, pH values, and coexisting ions were investigated. A comparative dosing mode with the assistance of polyacrylamide (PAM) was also included. The evolution of floc size was studied using microscopic observation to investigate the properties of flocs under different pH values and dosing modes. Particle image velocimetry (PIV) and extended Deryaguin–Landau–Verwey–Overbeek models were utilized to illustrate the distribution and velocity magnitude of the particle flow fields and to delve into the mechanism of magnetic flocculation. The results showed that FS@CTS-P(AM-DMC) achieved values of 96.4 and 74.5% for both turbidity and COD removal for 3000 mg/L of simulated emulsified oil. In the presence of PAM, the turbidity and COD removal reached 95.7 and 71.6%. In addition, FS@CTS-P(AM-DMC) demonstrated remarkable recycling and reusability performances, maintaining effective removal after eight cycles. The strength and recovery factors of magnetic flocs without PAM reached 69.3 and 76.8%, respectively. However, with the addition of PAM, they decreased to 46.73 and 51.47%, respectively. During the magnetophoretic processes, FS@CTS-P(AM-DMC) and oil droplets continuously collided and aggregated, forming three-dimensional network aggregates. Moreover, the magnetic floc generated a swirling motion, and the residual emulsified oil droplets could be further captured. Emulsified oil droplets were primarily removed through charge neutralization under acidic conditions. Under neutral and alkaline conditions, magnetic interactions played a major role in magnetic flocculation.

Application of coagulation-microfiltration for membrane fouling mitigation in highly saline dyeing wastewater: Anti-fouling modification of membrane and novel insight of salt into regulation of cake layer formation

Cake layer formation is the dominant microfiltration (MF) membrane fouling mechanism after long-term operation. The regulation of cake layer characteristics is less clarified in the coagulation-microfiltration (CMF) technique due to an incomplete understanding of flocculation mechanism; however, gaining such insight will contribute to improving MF efficiency for water purification. Herein, an antifouling MF membrane for high saline textile wastewater was constructed using polydopamine (pDA) co-deposition with sodium p-styrenesulfonate (SS), and methoxypolyethylene glycols (mPEG). Thereafter, the cake layer formation in the CMF technique could be precisely regulated by adjusting salt concentration (NaCl or Na2SO4). Results indicated that the inorganic salt-induced transformation of flocculation mechanism endows a desired regulation of cake layer characteristics, consequently leading an increase in membrane flux. Various properties and formation of flocs were caused via different flocculation mechanisms (from predominant charge neutralization to integrated interaction) in response to a salt variation, giving rise to a directed transition behavior of cake layer formation from compact to porous structure. Particularly, the coagulation mechanism was validated by the experimental analysis and molecular dynamics simulations. Furthermore, the high salt permeation (>90%) and acceptable dye rejection (>98%) of two commercial reactive dyes could be obtained by the proposed CMF technique, exhibiting a satisfactory fractionation behavior of dyes/inorganic salt. A beneficial contribution is the direct reuse dyeing of NaCl from the spent dyeing bath in new dyeing operations. These results could provide a further understanding of the underlying mechanisms of coagulation-enhancing MF behavior and inspire the precise regulation of cake layer characteristics to achieve efficient MF.

Suitability of inorganic coagulants for algae-laden water treatment: Trade-off between algae removal and cell viability, aggregate properties and coagulant residue

Inorganic coagulants could effectively precipitate algae cells but might increase the potential risks of cell damage and coagulant residue. This study was conducted to critically investigate the suitability of polyaluminum (PAC), FeCl3 and TiCl4 for algae-laden water treatment in terms of the trade-off between algal substance removal, cell viability, and coagulant residue. The results showed that an appropriate increase in coagulant dosage contributed to better coagulation performance but severe cell damage and a higher risk of intracellular organic matter (IOM) release. TiCl4 was the most destructive, resulting in 60.85% of the algal cells presenting membrane damage after coagulation. Intense hydrolysis reaction of Ti salts was favorable for the formation of larger and more elongated, dendritic structured flocs than Al and Fe coagulants. TiCl4 exhibited the lowest residue level and remained in the effluents mainly in colloidal form. The study also identified charge neutralization, chemisorption, enmeshment, and complexation as the dominant mechanisms for algae water coagulation by metal coagulants. Overall, this study provides the trade-off analyses between maximizing algae substance removal and minimizing potential damage to cell integrity and is practically valuable to develop the most suitable and feasible technique for algae-laden water treatment.

Elucidating the role of ferric chloride on carbon capture from low-strength municipal wastewater in high-rate activated sludge process: Parameter optimization and crucial mechanism

To enhance organics capture efficiency from low-strength municipal wastewater of China, FeCl3 enhanced high-rate activated sludge (FC-HRAS) process was established in this work. Effects of sludge concentration and FeCl3 dosage on carbon capture in FC-HRAS were investigated. The optimum sludge concentration of 2.0 g/L and FeCl3 dosage of 30 mg Fe/L were obtained, with total COD removal efficiency of 76.8%. Carbon balance analysis showed that FC-HRAS increased organics capture proportion by 91.8% while reducing loss from oxidative metabolism compared to HRAS. The potential mechanism of enhanced carbon capture for FC-HRAS was further explored. Adding Fe(III) caused coagulation of organics by increasing the Zeta potential in wastewater. Impacted by charge neutralization “compression” and coagulation floc “encirclement”, sludge particle sizes decreased, leading to increases of internal surface area and adsorption site of sludge for binding with bacteria; it facilitated the biological flocculation of FC-HRAS. Meanwhile, Fe(III) binding with proteins in EPS induced formation of “protein shell – β polysaccharides kernel” sludge structure and reduction of sludge negative charge, which intensified sludge stability and agglomeration. These factors explained the increase in organics capture proportion. The decrease in metabolism loss of organics could be attributed to the increase in organics transfer resistance in sludge EPS and selective elimination of heteromorphic bacteria (e.g., denitrifiers) in sludge. This work provided guidance for energy-neutral and cost-saving wastewater treatment in China.

Additive manufacturing of ultrahigh-resolution Poly(ε-caprolactone) scaffolds using melt electrowriting

Melt electrowriting (MEW) is an advanced additive manufacturing technology that produces high-resolution scaffolds for medical applications. Although there are many valuable parameter groups for MEW, the corresponding principles need to be clarified to improve the success of printing high-fidelity scaffolds. To this end, we investigate the print limit of MEW with respect to the minimum interfiber distance and the maximum print period based on a medical-grade poly(ε-caprolactone) material. The results indicate that relatively large turning loops and low turning speeds improve the print accuracy of the scaffolds; however, excessively large turning loops and low turning speeds result in fiber accumulation on the edge of the scaffolds, resulting in print failure. The turning loops with 500 μm in diameter and turning speeds of 0.625 × CTS (critical translation speed) can achieve well-defined MEW scaffolds with an interfiber distance down to 25 μm. For printing such high-resolution scaffolds, the constant printing process can last one week. Fiber placement gets random when the fiber diameter is larger than 2.5 μm, caused by the melt polymer degradation and shear thinning in the printing process. Additionally, we verify that the method of charge neutralization is not beneficial for improving the fiber overlay. This is a fundamental study clarifying the principles of printing high-resolution MEW scaffolds, being capable of extending the application of the MEW products.

Morphological Transformation and Surface Engineering of Glycovesicles Driven by Bioinspired Hydrogen Bonds of Nucleobases.

Glycopolymer-based supramolecular glycoassemblies with signal-driven cascade morphological deformation and accessible surface engineering toward bioinspired functional glycomaterials have attracted much attention due to their diverse applications in fundamental and practical scenarios. Herein, we achieved the cascade morphological transformation and surface engineering of a nucleobase-containing polymeric glycovesicle through exploiting the bioinspired complementary multiple hydrogen bonds of complementary nucleobases. First, the synthesized thymine-containing glycopolymers (PGal30-b-PTAm249) are capable of self-assembling into well-defined glycovesicles. Several kinds of amphiphilic adenine-containing block copolymers with neutral, positive, and negative charges were synthesized to engineer the glycovesicles through the multiple hydrogen bonds between adenine and thymine. A cascade of morphological transformations from vesicles to ruptured vesicles with tails, to worm-like micelles, and finally to spherical micelles were observed via continuously adding the adenine-containing polymer into the thymine-containing glycovesicles. Furthermore, the surface charge properties of these glyconano-objects can be facilely regulated through incorporating various adenine-containing polymers. This work demonstrates the potential application of a unique bioinspired approach to precisely engineer the morphology and surface properties of glycovesicles for boosting their biological applications.

Bioflocculant Producing Bacillus megaterium from Poultry Slaughterhouse Wastewater: Elucidation of Flocculation Efficacy and Mechanism

The study focused on isolating bioflocculant-producing microorganisms from poultry slaughterhouse wastewater (PSW). Microorganisms (n = 20) were isolated, and the D2 isolate, identified as Bacillus megaterium using 16S rDNA and RpoD (sigma 70), had maximum flocculation activity. Furthermore, characteristics of the bioflocculant produced by B. megaterium were determined, and the optimum storage conditions, including the flocculation mechanism, were identified. The bioflocculant was composed mainly of polysaccharides and proteins and was better stored frozen in a crude form. Furthermore, the flocculation efficacy was assessed using response surface methodology at pH 4 (min) and 9 (max), bioflocculant dosage of 1% (min) and 3% (max, v/v), indicating pH 6.5 and dosage of 2% (v/v) as optimum flocculation conditions for floc formation under ambient temperature. These results were further confirmed with microscopy assessments with zeta potential measurements confirming that the bioflocculant was ionic, albeit charge neutralization was not the primary mechanism for floc agglomeration. Hydrogen bonding was predominant, indicative of a neutralization-bridging mechanism, an assertion also based on the functional groups prevalent in the isolate-B. megaterium. The results obtained indicate that bioflocculants can be used to treat isolates that are sourced from wastewater.

SYBR Green I and DNA-modulated charge neutralization assembly of naked AuNPs for fast colorimetric sensing of Cd2+ in cosmetics

The involvement of cadmium in cosmetics results in inevitable exposure to our daily life. Therefore, it is of great significance to develop a simple and rapid method for fast screening of cadmium in cosmetics. Gold nanoparticles (AuNPs)-based colorimetric sensing offers a simple strategy for analytical detection, but the typical surface functionalization of AuNPs adds complexity to the overall detection. Nucleic acid dye-based charge neutralization offered a truly simple and fast approach for the assembly of AuNPs over the conventional salt-induced strategy. Herein, we developed a simple colorimetric sensing system for Cd2+, based on nucleic acid dye SYBR Green I (SG) and Cd2+ aptamer (Cd-2-1)-modulated charge neutralization assembly of naked AuNPs. The method rationale was based on the higher affinity of Cd2+ to Cd-2-1 DNA over SG, as well as the stable and fast charge neutralization-induced assembly of AuNPs by SG. The limit of detection (LOD) of the proposed method was 0.27 μM, which was substantially lower than the maximum permitted amount of Cd2+ in cosmetics regulated by the Chinese Food and Drug Administration (CFDA, 5 mg/kg, equivalent to 4.45 µM in our assay). Successful exploration of the proposed method was demonstrated for the detection of Cd2+ in cosmetics.

Insight into the role of chitosan in rapid recovery and re-stabilization of disintegrated aerobic granular sludge

The disintegration and instability of aerobic granular sludge (AGS) systems during long-term operation pose significant challenges to its practical implementation, and rapid recovery strategies for disintegrated AGS are gaining more attention. In this study, the recovery and re-stabilization of disintegrated AGS was investigated by adding chitosan to a sequencing batch reactor and simultaneously adjusting the pH to slightly acidic condition. Within 7 days, chitosan addition under slight acidity led to the re-aggregation of disintegrated granules, increasing the average particle size from 166.4 μm to 485.9 μm. Notably, sludge volume indexes at 5 min (SVI5) and 30 min (SVI30) decreased remarkably from 404.6 mL/g and 215.1 mL/g (SVI30/SVI5 = 0.53) to 49.1 mL/g and 47.6 mL/g (SVI30/SVI5 = 0.97), respectively. Subsequent operation for 43 days successfully re-stabilized previous collapsed AGS system, resulting in an average particle size of 750.2 μm. These mature and re-stabilized granules exhibited characteristics of large particle size, excellent settleability, compact structure, and high biomass retention. Furthermore, chitosan facilitated the recovery of COD and nitrogen removal performances within 17–23 days of operation. It effectively facilitated the rapid aggregation of disintegrated granules by charge neutralization and bridging effects under a slightly acidic environment. Moreover, the precipitated chitosan acted as carriers, promoting the adhesion of microorganisms once pH control was discontinued. The results of batch tests and microbial community analysis confirmed that chitosan addition increased sludge retention time, enriching slow-growing microorganisms and enhancing the stability and pollutant removal efficiency of the AGS system.

Aggregation of graphene oxide upon the stripping of oxidized debris: An experimental and molecular dynamics simulation study

The most recent structural study of graphene oxide (GO) indicates that the oxidized debris (ODs) adhered to as-prepared GO will strip in certain aquatic settings. The impact of ODs stripping on the characteristics of GO has been widely reported, but its effects on GO aggregation have received less attention. Here, the influence of OD stripping on the GO aggregation property was identified, and the aggregation of as-prepared GO and GO upon OD stripping was compared. Upon ODs stripping, the pKa values of GO shifted from 3.91, 6.25, and 9.84 to 4.54, 6.65, and 10.21, respectively. Further analysis indicated the removal of ODs reduced the net negative charge and improved the hydrophobicity of GO, hence promoting the aggregation of GO. The acceleration of GO-Ca2+-OD aggregate formation was facilitated by the collective effects of ODs stripping, functional group deprotonation, double layer compression, OD bridging, and charge neutralization. The metal ions and stripped ODs attach to GO edges and link GO, which perform like bridges and contribute to further aggregation. In general, the existence of ODs adds complexity to the constructions and characteristics of GO, and it is important to take this into account while evaluating the aggregation characteristic of GO-based materials.

Cationic etherified starch-acrylamide-DMDAAC graft flocculant: Synthesis, flocculation performance, metal ion synergistic effect and cost-effectiveness

The flocculants based on naturally derived polymers are promising due to their wide availability and biodegradability. However, the flocculation performance and cost-effectiveness are less than satisfactory. This study developed novel flocculants with cationic etherified starch-acrylamide-dimethyl diallyl ammonium chloride (CAD), specifically designed for the efficient removal of anionic dyes. The synthesis conditions were optimized through the flocculation efficiency of anionic acid black-172 (AB) dye. Experimental results showed that CAD achieved a removal ratio of 91.6±1.8% with a flocculant dosage of 150 mg/L and maintained excellent decolorization efficiency across different pH, environmental temperatures, and ionic strengths. Most importantly, the synergistic effect with the presence of metal ions, particularly Fe3+, on the decolorization efficacy of CAD was observed. In the presence of Fe3+ (0.02 mol/L), the required flocculant dosage was reduced by two-thirds, while the maximum dye removal ratio reached 94.2±1.9%. The study indicates that the high efficiency of CAD primarily originates from dual mechanisms of charge neutralization and bridging. Furthermore, the operation cost of removing an equivalent amount of AB dye with CAD is about 40% of that incurred using commercial cationic polyacrylamide, highlighting its economic advantage in industrial applications. In summary, the CAD flocculant shows great promise for complex wastewater treatment.

Deciphering the Mechanism of Action of the Antimicrobial Peptide BP100.

The linear undecapeptide KKLFKKILKYL-NH2 (BP100) highlights for its antibacterial activity against Gram-negative bacteria and its low toxicity. These excellent biological properties prompted the investigation of its mechanism of action, which were undertaken using spectroscopic techniques, biophysical analysis, microscopy, and molecular dynamic simulations. Studies were conducted in different membrane environments, such as anionic, zwitterionic, and mixed membranes, as well as in vesicles (LUVs and GUVs) and bacteria. The findings suggest that BP100 exhibits a preference for anionic membranes, and its mechanism of action involves charge neutralization and membrane permeabilization. In these membranes, BP100 transitions from an unstructured state in water to an α-helix with the axis parallel to the surface. MD simulations suggest that after electrostatic interaction with the membrane, BP100 flips, facilitating the insertion of its hydrophobic face into the membrane bilayer. Thus, BP100 adopts an almost vertical transmembrane orientation with lysine side chains snorkelling on both sides of the membrane. As a result of the rotation, BP100 induces membrane thinning and slow lipid diffusion and promotes water penetration, particularly in anionic lipid membranes. These investigations pointed towards a carpet-like mechanism and are aligned with the biological activity profile described for BP100. This review covers all the studies carried out on the mechanism of action of BP100 published between 2009 and 2023.

Excellent coagulation performance of polysilicate aluminum ferric for treating oily wastewater from Daqing gasfield: Responses to polymer properties and coagulation mechanism

The polysilicate aluminum ferric (PSAF) was synthesized via copolymerization of polysilicic acid (PSi), AlCl3 and FeCl3 for treating oily wastewater from Daqing gas field. This study investigated the effects of key preparation factors such as the degree of PSi's preactivation and the ratio of (Fe + Al)/Si and Al/Fe on both polymerization and coagulation performance exhibited by PSAF. To determine the optimal timing for introducing Al3+ and Fe3+, zeta potential, viscosity and particle size were investigated. Additionally, infrared spectroscopy, X-ray powder diffraction, polarizing microscopy and scanning electron microscope analysis were employed to investigate the structure and morphology of PSAF. The results indicate that under conditions characterized by a SiO2 mass fraction of 2.5% and pH = 4.5, an optimal timing for introducing Al3+ and Fe3+ is at 100 min when PSi exhibits moderate polymerization along with sufficient stability. When considering molar ratios such as (Al + Fe)/Si being 6:4 and Al/Fe being 5:5, respectively, PSAF falls within a “stable zone” enabling storage period up to 32 days. Moreover, Jar test results demonstrate that at a dosage of 200 mg/L PSAF for oily wastewater treatment in gas fields could reach the maximum turbidity removal efficiency up to 99.5% while oil removal efficiency reach 88.6% without pH adjustment. The copolymerization facilitates the formation of larger PSAF aggregates with positive potential, thereby augmenting the coagulants' adsorption bridging and charge neutralization capabilities. As a result, PSAF has great potential as a practical coagulant for treating oil-containing wastewater in industrial settings.

Evaluating a targeted Palbociclib-Trastuzumab loaded smart niosome platform for treating HER2 positive breast cancer cells

In this study, we present a targeted and pH-sensitive niosomal (pHSN) formulation, incorporating quantum dot (QD)-labeled Trastuzumab (Trz) molecules for the specific delivery of Palbociclib (Pal) to cells overexpressing human epidermal growth factor receptor 2 (HER2). FTIR analyses confirmed the successful preparation of the pHSNs and their bioconjugation. The labeled Trz-conjugated Pal-pHSNs (Trz-Pal-pHSNs) exhibited a size of approximately 170 nm, displaying a spherical shape with a neutral surface charge of −1.2 mV. Pal encapsulation reached ∼86%, and the release pattern followed a two-phase pH-dependent mechanism. MTT assessments demonstrated enhanced apoptosis induction, particularly in HER2-positive cells, by Trz-Pal-pHSNs. Fluorescence imaging further validated the internalization of particles into cells. In conclusion, Trz-Pal-pHSNs emerge as a promising platform for personalized medicine in the treatment of HER2-positive breast cancer.