Search Results (149)

Chronic obstructive pulmonary disease (COPD) is a progressive respiratory disorder characterized by persistent airflow limitation and chronic airway inflammation. Current therapeutic strategies primarily offer symptomatic relief and are often limited by systemic side effects, inadequate lung deposition, and poor patient compliance. Naringin (NAR), a natural flavonoid with strong antioxidant, anti-inflammatory, and anti-fibrotic activities, has demonstrated potential in mitigating COPD-associated pathophysiology. However, its therapeutic application is restricted by poor water solubility, low bioavailability, and rapid metabolism. Nanotechnology-based drug delivery systems, particularly poly(lactic-co-glycolic acid) (PLGA) nanoparticles, provide an effective approach for lung-targeted therapy. Their nanoscale size promotes deep lung deposition, enhanced cellular uptake, reduced lung clearance, improved therapeutic efficacy, and reduced systemic side effects. The present study aimed to develop NAR-loaded PLGA nanoparticles (NAR PLGA NP) for enhanced cell-targeting in inflammatory lung conditions. NAR PLGA NP were prepared using the emulsion solvent evaporation method, with PLGA in the organic phase and soya lecithin (SL) with poly(vinyl alcohol) (PVA) as surfactants in the aqueous phase. A face-centered central composite design was employed to optimize the formulation. The optimized nanoparticles were characterized for size distribution by dynamic light scattering, entrapment efficiency, Transmission Electron Microscopy (TEM), Fourier Transform Infrared (FTIR), Differential Scanning Calorimetry (DSC), X-Ray Diffraction (XRD), and in vitro drug release. The safety of PLGA and lecithin-coated PLGA nanoparticles (LC PLGA NP) was assessed using an MTT assay on lung epithelial cells, followed by cellular uptake studies, angiogenesis by chick Yolk Sac Membrane (YSM) assay, and in vitro evaluation of reactive oxidative stress (ROS) and anti-inflammatory activity. The optimized PLGA formulation showed a hydrodynamic diameter of 201 ± 1 nm with PDI 0.20 ± 0.03 and EE of 76.11 ± 2.1%, and 81.7 ± 4.9% drug release at 72 h, whereas LC PLGA NP showed a hydrodynamic diameter of 308 ± 3 nm, PDI of 0.21 ± 0.05, entrapment efficiency of 82.45 ± 4.8%, and 71.4 ± 3.2% drug release at 72 h. Both PLGA NP and LC PLGA NP demonstrated good cytocompatibility with lung epithelial cells, efficient cellular uptake, and a significant reduction in intracellular reactive oxygen species (ROS) levels (**** p value < 0.0001). Moreover, the formulations markedly suppressed pro-inflammatory cytokines, including TNF-α, IL-6, and IL-1β, indicating anti-inflammatory activity. The angiogenesis assay further suggested their ability for lung tissue repair and remodeling. These findings support the potential of LC PLGA NP as a promising cell-specific targeting system for naringin in inflammatory lung conditions. Full article

Chronic and infected wounds remain difficult to treat due to persistent microbial burden, biofilm formation, and dysregulated inflammation. As a multifunctional polyphenol, curcumin exhibits broad-spectrum antimicrobial, anti-inflammatory, and antioxidant activities. Nevertheless, the clinical application of curcumin is constrained by its limited solubility in water, inherent instability, and insufficient bioavailability. Chitosan, a cationic polysaccharide, provides complementary advantages including intrinsic antimicrobial activity, mucoadhesion, and the capacity to form versatile delivery platforms such as nanoparticles, hydrogels, and films. This review reframes chitosan–curcumin systems as dual-function bioactive platforms in which both the carrier and payload actively contribute to therapeutic outcomes. Mechanistically, chitosan disrupts microbial membranes, enhances bioadhesion, and supports tissue regeneration, while curcumin modulates intracellular targets including reactive oxygen species, quorum sensing, and inflammatory signaling pathways. Their integration enables multimodal antimicrobial activity, improved biofilm disruption, and coordinated regulation of the wound-healing cascade. This review critically examines the structure–function relationships governing release kinetics, stability, and cytocompatibility, with particular emphasis on chitosan molecular weight, degree of deacetylation, crosslinking strategies, and curcumin loading. Solubility-enhancement strategies for curcumin, including surfactants, nanoparticles, solid dispersions, and chemical derivatives, are evaluated in the context of antimicrobial efficacy and cytotoxicity. Finally, the review highlights translational challenges and future directions, such as antibiotic synergy, antifungal applications, formulation complexity, and the emerging role of artificial intelligence in predictive material design. Collectively, these insights establish design principles for next-generation multifunctional biomaterials that integrate antimicrobial activity with immune modulation and tissue repair. Full article

Currently, gold nanoparticles are increasingly used in targeted drug delivery nanostructures. However, their intrinsic catalytic activity is often overlooked when using them as a carrier. In this study, the interaction between the sotalol drug from the beta-blocker family and gold nanoparticles was investigated using capillary electrophoresis and high-performance liquid chromatography. Both methods showed that sotalol undergoes catalytic oxidation on the surface of citrate-stabilized gold nanoparticles into three products. Together with a cleavage of the isopropyl group from the nitrogen atom, the oxidation at the hydroxyl group occurs with the formation of a ketone. Analysis of electropherograms showed 100% conversion of sotalol after 48 h of incubation at a surface coverage of 1.2 × 10¹⁹ molecules per m². To examine the role of reactive oxygen species, the experiments were performed in oxygen-saturated and oxygen-deficient gold nanoparticle dispersions. The effects of radical scavenger additives and pH of nanoparticle dispersion were also assessed. The influence of surface ligands on sotalol conversion was studied using gold nanoparticles coated with thiols, surfactants, and polyelectrolytes. Based on comprehensive data, the mechanism of gold-nanoparticle-assisted multicenter oxidation of sotalol is proposed. Full article

Electrokinetic-Permeable Reactive Barrier (EK-PRB) technology can effectively remediate heavy metal-contaminated soil, and the properties of PRB materials play an important role in determining the remediation efficiency. To select a suitable PRB material, montmorillonite (MMT) was modified using cetyltrimethylammonium bromide (CTAB), sodium dodecylbenzenesulfonate (SDBS), and cocamidopropyl betaine (CAB), respectively; their remediation efficiencies for soils co-contaminated with Zn²⁺, Pb²⁺, and Cd²⁺ were then compared within an EK-PRB system. The results indicated that remediation efficacy varied significantly depending on the heavy metal and the surfactant used for modification. After 7 days of remediation, SDBS-modified MMT achieved the highest Zn²⁺ removal efficiency (49.65%), whereas CTAB-modified MMT showed optimal removal performance for both Pb²⁺ (38.03%) and Cd²⁺ (76.02%). When the remediation time was extended to 14 days, SDBS-modified MMT attained the highest removal efficiencies for Zn²⁺ (69.80%) and Pb²⁺ (69.50%), while CTAB-modified MMT maintained superior Cd²⁺ removal performance (86.94%). Energy consumption analysis showed that both CAB- and SDBS-modified MMT reduced energy consumption moderately compared with the unmodified control, whereas CTAB modification resulted in a substantial increase in energy demand. Experimental results confirm that surfactant-modified MMT effectively optimizes the EK-PRB remediation. A comprehensive evaluation considering both removal efficiency and energy consumption identified SDBS-MMT as the optimal material. The optimized EK-PRB parameters established in this study provide theoretical and technical support for the remediation of soils co-contaminated with multiple heavy metals. Full article

A549 cells are widely used as an in vitro model of alveolar type II (ATII) epithelial cells; however, their phenotype and metabolic state are highly sensitive to culture conditions, cell density, and the duration of static, non-passaged cultivation. Here, we examined how prolonged static culture affects lipid metabolism, mitochondrial bioenergetics, and viability in A549 cells. A549 cultures were maintained without passaging for up to 25 days in DMEM or Ham’s F-12 and analyzed using lipid secretion assays, targeted lipidomics, [¹⁴C]-acetate incorporation, Seahorse bioenergetic profiling, and transcriptional analysis of stress-associated markers. Several surfactant-associated readouts were highest during early culture, peaking on day 7, as evidenced by elevated expression of ABCA3 and SP-A and maximal secretion of surfactant-associated phospholipids. With prolonged cultivation and increasing culture density, cellular phosphatidylglycerol levels declined progressively and became nearly undetectable by day 25, accompanied by reduced anabolic lipid metabolism, lower oxygen consumption, and impaired glycolytic activity. These changes coincided with increased reactive oxygen species, elevated intracellular Ca²⁺ levels, and increased expression of stress-associated transcripts, including CASP1, IL1B, and C3. Later stages were also associated with reduced mitochondrial respiration and decreased viability. Collectively, our findings show that prolonged static culture is associated with metabolic remodeling and reduced bioenergetic capacity in A549 cells. Full article

Dual-fuel combustion is often proposed for diesel engines as a means to partially replace conventional diesel with cleaner and/or more sustainable alternatives, such as those derived from green hydrogen. However, the low reactivity of these fuels (i.e., methane, hydrogen, and ammonia) often leads to prolonged ignition delay (ID) and combustion instability. This challenge could potentially be overcome using nanomaterials, which are additives that could improve reactivity and compensate for autoignition deficiencies. Thus, this study evaluates the effect of carbon nanotubes (CNTs) dispersed in diesel fuel on the autoignition process under dual-fuel operation. CNTs were dispersed at a concentration of 100 mg/L and stabilized with surfactant sodium dodecylbenzene sulfonate (SDBS). The resulting nanofuels were then tested in a constant volume combustion chamber (CVCC) using methane, hydrogen, and ammonia as secondary fuels across various energy substitution ratios and temperatures (535 °C, 590 °C and 650 °C). The results show that the impact of CNTs on ID is negligible, especially at high temperatures. At the lowest tested temperature (535 °C) and 40% methane substitution ratio, only slight reductions in ID were obtained. Nevertheless, this effect is less significant at higher temperatures (590 °C and 650 °C). Regarding pressure gradient, the addition of CNTs and SDBS generally induced a decrease in pressure-peak of up to 15%. This trend is attributed to the trapping of fuel droplets within the CNT structures, which creates a physical barrier that delays vaporization. Results confirm that autoignition, which is expected to be the main phenomenon influenced by CNT addition, is not enhanced. Full article

Asthma is increasingly recognized as a heterogeneous syndrome where traditional management fails, particularly given spirometry’s limitations in assessing small airway dysfunction. This review synthesizes the transition from clinical phenotyping to deep molecular endotyping, establishing a framework for precision medicine. We highlight the insufficiency of absolute eosinophil counts, proposing eosinophil cationic protein (ECP) and eosinophil-derived neurotoxin (EDN) as superior activation metrics. Furthermore, we explore Type 2 drivers (IL-4/IL-13, periostin) and epithelial alarmins like TSLP. Beyond classical immunology, the text describes metabolic dysregulation, specifically asymmetric dimethylarginine (ADMA) in obese-asthma phenotypes where nitric oxide synthase uncoupling promotes oxidative stress. We also analyze YKL-40 and surfactant protein D (SP-D) as markers of remodeling and barrier permeability, alongside microRNAs—specifically miR-21—in corticosteroid resistance. We conclude that managing refractory asthma requires shifting from reactive symptom control to an integrated analysis of multi-omic biomarkers. Establishing this comprehensive molecular profile via specialized centers is fundamental for addressing current diagnostic limitations, selecting biological therapies, and modifying the disease trajectory through an endotype-driven strategy addressing inflammatory, metabolic, and structural pathologies. Full article

Backgrounds: Antibody–drug conjugates (ADCs) combine the specificity of monoclonal antibodies with the cytotoxic potency of drugs, representing a significant class of targeted cancer therapeutics. Despite their clinical success, formulation-related instability, rather than biological inefficacy, is a major contributing factor to setbacks in ADC development. This review examines the biochemical, physicochemical, and formulation factors that contribute to ADC stability, with a focus on excipient selection, conjugation site heterogeneity, and linker–payload reactivity. Methods: This comprehensive review was based on a selection of peer-reviewed mechanistic, analytical, and manufacturability studies on ADC stability. Our goal was to highlight formulation strategies, degradation pathways, and solid-state stabilization principles that affect the pharmacokinetics and therapeutic efficacy of ADC. Results: Results demonstrate how formulation variability including buffer composition, excipient choice, ionic strength, and lyophilization can directly affect payload release, linker cleavage, kinetics, and antibody conformation. It has been demonstrated that techniques, such as lyophilization with glass-forming matrices and the addition of surfactants, enhance stability against hydrolysis, oxidation, and aggregation. Developments in analytical characterization, such as real-time kinetic modeling and multi-attribute techniques based on mass spectrometry, have made quantification of degradation and bioactivity losses more predictable in ADC formulations. The connection between chemical stability and formulation outcomes is being redefined by new techniques, such as model-informed optimization and AI-driven design. Conclusions: ADC formulation is now a key component of molecular stability, clinical reliability, and regulatory compliance rather than a secondary consideration. By guaranteeing long-term stability, better pharmacokinetics, and improved therapeutic indices across next-generation designs, these approaches have the potential to revolutionize ADC development. Full article

The review critically discusses the methodological approach used to characterize the mechanism and to assess kinetic parameters in catalytic processes promoted by surfactant-based nanozymes. Using the hydrolysis of carboxylic and phosphoric esters as model reactions, it quantitatively analyzes several examples in which the catalytic system consists either of aggregates formed by non-functional surfactants or of surfactants bearing one or more reactive functions, ranging from classical nucleophiles to transition metal ions. This analysis highlights both the importance of the design of the kinetic experiments and of the selection of the appropriate experimental conditions, and the need to apply the correct model and set of kinetic equations in the interpretation of the data, in order to obtain kinetic parameters with true chemical significance. Improper kinetic modeling may lead to misleading rate enhancements and false claims of very high activity of the system studied. The aim of the review is not to provide a general overview of micelle and liposome-promoted catalysis, but rather to offer methodological tools to correctly assess rate accelerations with these systems. Full article

As the core abrasive in chemical mechanical polishing (CMP) processes, the morphology, size uniformity, and chemical reactivity of CeO₂ nanoparticles (NPs) are crucial factors determining the surface precision and yield of devices. In this work, a KNO₃–LiNO₃ eutectic molten salt was used as the reaction medium. By systematically adjusting key processing parameters (such as the type of cerium source, the species and dosage of surfactants, and calcination conditions), the regulatory effects of these factors on particle growth mechanisms were clarified. This adjustment enabled the controlled synthesis of spherical CeO₂ NPs with customized morphology, particle size, and surface defect states. The multi-stage reaction process of the precursor during calcination was identified by applying thermal analysis techniques, including TG-DSC and TG-FTIR. This process includes dehydration, ion exchange, and thermal decomposition. Microstructural analysis shows that the type and dosage of the cerium source and template agent significantly affect the uniformity of particle size and spherical morphology. Moreover, by using an optimized process with a heating rate of 6 °C/min and maintaining at 400 °C for 3 h, spherical CeO₂ NPs with an average particle size of 60 nm, uniform size distribution, and high sphericity were successfully synthesized via a single-step calcination process. Based on these findings, a further proposal was put forward regarding a crystal growth mechanism mediated by micelle-directed assembly and oriented attachment. This method only requires a single calcination step, has mild reaction conditions, and involves a simple process without the need for specialized equipment—features that show great potential for scalable production. It provides both a theoretical basis and experimental support for the controlled preparation of high-performance CeO₂ abrasives. Full article

Recent botulinum neurotoxin type A (BoNT/A) formulations have shifted towards the use of polysorbate 20 (PS20) and polysorbate 80 (PS80) as a non-human-derived excipient to enhance product stability. Polysorbates are a distinct class of synthetic non-ionic surfactants with high heterogeneity in chemical structure and properties. Accumulating mechanistic and clinical evidence suggests that they may trigger immunological reactions, including hypersensitivity and immunogenicity. Such risks are largely associated with their susceptibility to degradation via hydrolysis and oxidation, forming reactive byproducts that can interact with proteins and immune pathways. Despite these mechanistic insights, data on the association between polysorbate excipients and observed immune outcomes in practice is relatively sparse and excipient-related immunogenicity and hypersensitivity is often underrecognized in practice. This review provides a summary of polysorbate excipients in BoNT/A formulations, focusing on their chemical properties and degradation pathways, characterizing downstream immune effects and appraising available clinical data of polysorbate-containing BoNT/A formulations. Finally, we discuss potential risk mitigation strategies including process modifications that could prevent degradation, and consideration of alternative excipients, such as human serum albumin, that has been shown to be immunologically inert and has an established safety profile. By integrating chemical, mechanistic, and clinical perspectives, this review seeks to clarify the implications of polysorbate use in BoNT/A formulations and inform both clinical practice and future formulation strategies. Full article

N-chlorotaurine (Tau-Cl) is a mild oxidizing haloamine formed from the reaction of hypochlorous acid (HOCl) with taurine (2-amino-ethanesulfonic acid). It is widely used as a topical antiseptic. In this study, we investigated haloamines derived from the neurotransmitter γ-aminobutyric acid, specifically GABA chloramine and bromamine (GABA-Cl, GABA-Br), as well as their halogenated γ-aminobutyric acid ethyl esters (GABAet-Cl, GABAet-Br). Due to their higher hydrophobicity, the esterified haloamines were more potent oxidants in the presence of lyophilic surfactant micelles, demonstrating their greater ability to access hydrophobic environments. By using fluorescent azapentalenes as molecular targets incorporated into sodium dodecyl sulfate (SDS) micelles, the second-order oxidation rate constants (k₂) resulted in 1.15 × 10² and 1.10 × 10⁴ M⁻¹min⁻¹ for GABA-Cl and GABAet-Cl, respectively. As expected, due to the presence of a bromine atom, GABAet-Br was even more reactive (4.50 × 10⁶ M⁻¹min⁻¹). The ability of GABAet-Br to access hydrophobic sites was demonstrated by comparing the reaction rate using micelles generated by different surfactants such as SDS (4.5 × 10⁶ M⁻¹min⁻¹), cetyltrimethylammonium chloride (CTAC, 2.5 × 10⁴ M⁻¹min⁻¹), and triton X-100 (TX-100, 3.9 × 10³ M⁻¹min⁻¹). GABAet-Cl and GABAet-Br exhibited higher bactericidal activity against Staphylococcus aureus and Escherichia coli, probably due to their increased lipophilicity and improved penetration into microorganisms compared to GABA-Cl and GABA-Br. The enhancement of the oxidation capacity by GABAet-Cl and GABAet-Br represents a new direction in the exploration and application of haloamines as antiseptic agents. Full article

Low-Salinity Water Flooding (LSWF) has gained attention for its cost-effectiveness and environmental advantages, yet its underlying mechanisms remain not fully understood. Oil recovery in LSWF is primarily governed by interfacial dynamics and formation wettability. This research investigates the effects of seawater dilution in carbonate reservoirs through laboratory analyses and displacement experiments. Results show that oil recovery efficiency is largely driven by rock–fluid interactions rather than fluid–fluid interactions, with optimal brine concentrations enhancing wettability alteration, boundary flexibility, and mineral leaching. These findings highlight the importance of considering both fluid–rock interactions and mineral reactivity, rather than attributing recovery to a single mechanism. Molecular dynamics simulations further supported the experimental observations. Overall, the study emphasizes that early and well-designed low-salinity injection strategies can maximize LSWF performance. The results elucidate the key interaction mechanisms between surfactants and the various components of heavy oil through atomic-scale precision modeling and dynamic process tracking. These simulations clarify, at the microscopic level, the differences in displacement dynamics and efficiency of organic solvent systems toward different hydrocarbon components. Full article

Among different formations, inorganic/inorganic assemblies can be considered “two in one” systems offering collective and/or new physical-chemical properties and substantial activity. Herein, a post-synthetic approach involving the assembly through Van der Waals forces and/or hydrogen bonding of the preformed ZnO@OAm NPs and Ca(OH)₂@OAm NPs of non-uniform sizes (9 nm and 27 nm, respectively), albeit coated with the same surfactant (oleylamine-OAm), is reported. The resulting semiconductor hetero-nanostructure (named CaZnO) has been physicochemically characterized. The X-ray diffraction (XRD) peaks correspond to both ZnO and Ca(OH)₂, confirming the successful formation of a dual-phase system. Field emission scanning electron microscopy coupled with energy-dispersive spectroscopy (FESEM-EDS) of CaZnO indicated the formation of Ca(OH)₂ NPs decorated with irregular-shaped ZnO NPs. The synthesized hetero-nanostructure was evaluated by assessing any negative effects on the photosynthetic function of tomato plants as well as for the generation of reactive oxygen species (ROS). The impact of the CaZnO hetero-nanostructure on photosystem II (PSII) photochemistry was evaluated under both the growth light intensity (GLI) and a high light intensity (HLI) at a short (90 min) and long (96 h) duration exposure. An enhancement of photosystem II (PSII) function of tomato plants by 15 mg L⁻¹ CaZnO hetero-nanostructure right after 90 min was evidenced, indicating its potential to be used as a photosynthetic biostimulant, improving photosynthetic efficiency and crop yield, but pending further testing across various plant species and cultivation conditions. Full article

Intracerebral hemorrhage (ICH) remains the least treatable form of stroke, with inflammation implicated as a major pathophysiological feature. Hence, this study sought to associate serum proteins and hormones associated with inflammation and ICH outcomes. Patients presenting to Duke University Hospital with computed tomography-verified spontaneous, supratentorial, non-traumatic ICH within 24 h of symptom onset were prospectively recruited. In this pilot study, equal numbers of men and women and Black and White individuals were included and matched by a 6-month modified Rankin Score (mRS). The primary analyses were the correlation of L-ratios (LR; Log2(Day 2/Day 1 concentrations)) of serum gonadal hormones and neuroinflammatory proteins with mRS > 3 at 6 months. A total of 40 participants were included in this pilot study. LRs were significantly higher for C-reactive protein (CRP; p = 0.013) and lower for interleukin-6 (IL-6; p = 0.026) and surfactant protein-D (p = 0.036) in participants with unfavorable outcomes at 6 months after ICH. Further, higher CRP (p = 0.02) and lower IL-6 (p = 0.035) and surfactant protein-D (p = 0.041) LRs were associated with mRS > 3 at 6 months after ICH in multiple logistic regression analyses, adjusted for race and sex. The relationship amongst gonadal hormones, neuroinflammatory proteins, and ICH outcome is complex. In this pilot study, unfavorable outcomes after ICH may have been associated with selected inflammatory biomarkers. A larger scale study is warranted to define interactions between hormones, proteins, and their effects on ICH outcomes. Full article