Search Results (945)

Background: Pancreatic cancer is an aggressive malignancy with poor survival. Most patients are diagnosed at advanced or metastatic stages because early disease is often asymptomatic and effective screening tools are lacking. We evaluated a three-marker model comprising serum CA19-9 in combination with the plasma proteins ITIH3 and CEACAM1 for pancreatic ductal adenocarcinoma (PDAC) detection. Methods: Matched plasma and serum samples were collected from 649 participants (250 PDAC cases and 399 controls). Plasma proteins were enriched using high-surface area magnetic covalent organic framework (COF) polymers. Serum CA19-9 was measured using the Tosoh Bioscience immunoassay. The marker panel was trained using a radial-based SVM with repeated 10-fold cross-validation using a set-aside training sample set. The derived model along with a fixed cutoff corresponding to 95% sensitivity in training samples were independently validated using a blinded sample set. Results: In the independent blinded validation, the combined panel of serum CA19-9 with plasma ITIH3 and CEACAM1 achieved an AUC of 0.917 indicating that the three-marker panel maintained strong performance in distinguishing PDAC from controls. At the prefixed threshold, the three-marker panel had a specificity of 53.3% (95% CI: 46.8–59.7%), significantly outperforming CA19-9 alone at 14.5% (95% CI: 10.4–19.7%). Conclusions: In independently blinded validation, combining plasma ITIH3 and CEACAM1 with serum CA19-9 substantially improved diagnostic performance for PDAC, achieving high specificity while maintaining 95% sensitivity compared with serum CA19-9 alone. These findings support further validation of this three-marker panel as a potential PDAC monitoring and detection approach in larger, multicenter studies. Full article

Magnesium alloys are promising materials for orthopedic applications due to their biodegradability and mechanical properties compatible with bone. However, their rapid degradation in physiological environments limits clinical use. In this study, WE43B magnesium alloy was coated with a PEO layer followed by a P(L/G/TMC) polymer applied via ultrasonic spraying. The influence of polymer layer number (10, 20, 30) on coating properties was systematically investigated. Scanning electron microscopy (SEM) analysis revealed an approximately fourfold reduction in porosity after polymer deposition, with progressive pore filling at higher layer numbers, while Fourier transform infrared spectroscopy (FT-IR) mapping indicated uniform polymer coverage. Compared to PEO alone, polymer-modified samples exhibited an approximately 7-fold increase in water contact angle, a ~50% reduction in surface roughness, and improved adhesion. Degradation-related analyses, including ion release, post-immersion SEM, and scanning acoustic microscopy (SAM), indicated that increasing polymer thickness effectively limited degradation processes. Ion release decreased by ~40–50% for the 30-layer coating compared to PEO, with the most pronounced reduction observed between the uncoated PEO and polymer-modified samples. These results demonstrate that the number of polymer layers plays a key role in controlling the barrier properties and stability of hybrid PEO/polymer coatings under simulated physiological conditions. Full article

The increasing global demand for oil and gas, together with the depletion of shallow reservoirs, has driven exploration toward deep and ultra-deep formations characterized by high-temperature and high-pressure (HTHP) conditions. In such environments, conventional drill pipes often experience thermal stress, corrosion, and mechanical degradation, which can reduce drilling efficiency and compromise operational reliability. Thermal insulated drilling pipes (TIDPs) have therefore emerged as an effective solution to minimize heat transfer between drilling fluids and the surrounding formation. This review summarizes recent advances in TIDP materials, structural design strategies, fabrication technologies, and critical performance. Relevant studies were collected from major scientific databases, including Web of Science and Google Scholar, with a focus on insulation materials, coating technologies, and thermal management approaches used in drilling systems. The analysis indicates that advanced insulation systems, including polymer-based coatings, silica aerogels, vacuum-insulated layers, and phase-change materials, can significantly enhance thermal management in drilling operations. These technologies can reduce heat loss by approximately 40–60% (i.e., 400–600 W·m⁻²) and maintain drilling-fluid temperature differentials of 10–18 °C under HTHP conditions. In addition, fabrication techniques such as plasma spraying, composite fabrication, and additive manufacturing enable the development of multifunctional insulation systems with improved thermal, mechanical, and corrosion-resistant properties. Hybrid TIDP systems integrating nanocomposites and advanced polymers show strong potential for improving drilling safety and efficiency. However, challenges related to durability, scalability, and cost remain, highlighting the need for further research on multilayer insulation architectures and sustainable materials. Full article

Polymer films and coatings play an increasingly critical role in extending material functionality across industrial, biomedical, and environmental applications. Recent advances in surface engineering have enabled precise control of interfacial properties, leading to enhanced durability, cleanliness, and protection. This review summarizes state-of-the-art strategies for modifying polymer surfaces, with an emphasis on plasma-based surface modification and plasma-induced polymerization as versatile, solvent-free methods for tailoring wettability, chemical functionality, and adhesion. Furthermore, it examines emerging classes of self-cleaning and self-sterilizing coatings that leverage photocatalytic, hydrophobic, or antimicrobial mechanisms to mitigate contamination, biofouling, and pathogen transmission. Additionally, developments in high-performance barrier films designed to protect food products and electronic devices through improved resistance to gases, moisture, and chemical agents are highlighted. By integrating insights from materials chemistry, surface physics, and nanostructured coating design, this review provides a comprehensive overview of current achievements and future directions in functional polymer films and coatings aimed at anti-pollution, antibacterial, and anti-corrosion performance. Full article

Fracturing flowback fluid is a complex wastewater generated during oil extraction, characterized by high concentrations of organic matter, suspended solids, salts, and various chemical additives, posing substantial risks to both surface water and groundwater if discharged directly. This study investigated the treatment of simulated fracturing flowback fluid prepared with guar gum using low-temperature plasma coupled with hydrogen peroxide technology. The degradation efficacy and preliminary mechanism of the combined system on organic pollutants were explored. Through a systematic optimization of operational parameters in the laboratory, the optimal treatment conditions were determined as a discharge voltage of 18 kV, a hydrogen peroxide addition of 5%, an initial pH of 11, and a treatment time of 110 min. Under these conditions, the synergistic system achieved 89.59 percent degradation of organic pollutants and 92.96 percent chemical oxygen demand removal. The results revealed that the combined action induced breakage of guar gum polymer chains, thereby enhancing degradation efficiency while effectively controlling fluid viscosity. This technology establishes a practical treatment approach for simulated fracturing flowback fluids containing guar gum, thereby facilitating better waste management in the energy sector. Full article

Conducting polymer–metal nanocomposites are widely investigated as tunable photonic and optoelectronic media; however, reported property trends often remain empirical because electronic disorder at the absorption edge, refractive-index dispersion, free carrier dielectric response, and third-order nonlinearity are rarely quantified within a single, composition-controlled film series. This limitation is particularly relevant for electrochemically grown PANI coatings on transparent conductive substrates, where nanoparticle incorporation can simultaneously enhance polarization while introducing aggregation-driven heterogeneity. Here, Ag/PANI nanocomposite thin films were fabricated directly on indium tin oxide (ITO) by potentiostatic electrodeposition from an aniline/camphorsulfonic acid electrolyte containing controlled Ag nanoparticle loadings (5–15 wt.%). This study addresses the research gap by integrating complementary optical-disorder and dispersion formalisms with dielectric and nonlinear analyses to establish a composition structure optics map for device-relevant films. Ag incorporation narrows the indirect optical gap from 1.98 eV (PANI) to 1.81 eV (5 wt.%), 1.38 eV (10 wt.%), and 1.19 eV (15 wt.%), while markedly broadening the Urbach tail (0.377 eV → 1.28–1.64 eV at 5–10 wt.%). Wemple–DiDomenico modeling and Drude-type dielectric dispersion reveal strongly non-monotonic evolution of oscillator energetics and the carrier response, culminating in large bound-electron dielectric constants (ε_∞ up to 469.8) and plasma frequencies (ω_p up to 248 × 10¹² Hz) at 15 wt.% Ag. Third-order nonlinearity is substantially enhanced but composition-sensitive: χ³ increases from 6.73 × 10⁻⁹ esu (PANI) to ~7.6 × 10⁻⁸ esu at 5 and 15 wt.%, whereas the Kerr coefficient peaks at 25.91 × 10⁻⁷ esu for 5 wt.% and is suppressed at intermediate/high loading. These results demonstrate that the optimal nonlinear performance is governed by a disorder–dispersion balance and microstructure-dependent local-field effects rather than the Ag fraction alone. Full article

In this work, we demonstrate a functional and previously insufficiently explored route for converting cyclic olefin copolymer (COC) TOPAS^® thin films into antibacterial hybrid materials through a combination of solvent casting, plasma activation, noble-metal sputtering, and subsequent thermal or laser treatment. While COC is already well-known as a transparent, chemically resistant material for pharmaceutical and optical applications, its coupling with post-treated noble-metal nanostructures for antibacterial functionality has not been systematically described. The main contribution of this study lies in showing that COC can serve not only as a passive packaging substrate, but also as an active platform for the formation of biologically relevant surface nanostructures. Compared with previously reported metal/polymer systems, the present work provides clear evidence that noble-metal layers on COC undergo substantial structural evolution after thermal and excimer-laser treatment, resulting in regular nanoclustered morphologies. A particularly important finding is the detection of Au particle implantation below the COC surface during sputtering, as revealed by Rutherford backscattering spectrometry, which distinguishes this system from conventional surface-only metal coatings. Furthermore, we show that laser and thermal processing do not merely reshape the deposited layer, but significantly influence the final biological response of the material. Ag-based structures showed strong bactericidal behavior against both Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus. The prepared samples were comprehensively characterized by AFM, DSC, RBS, SEM, and TGA, and their roughness and wettability were also evaluated, enabling direct correlation between physicochemical changes and antibacterial performance. These results introduce a new strategy for upgrading conventionally used pharmaceutical COC materials into multifunctional surfaces with added antibacterial value. Full article

Ultrasound patches represent a transformative advancement beyond conventional ultrasonography, evolving into intelligent theranostic systems for personalized healthcare. This evolution is propelled by synergistic innovations in flexible piezoelectric materials and integrated designs. The development of piezoelectric polymers, lead-free ceramics, and bio-composite materials has laid the foundation for long-term, conformal, and biosafe interfacing with the human body. Structurally, miniaturized transducer arrays (e.g., CMOS-integrated arrays achieving ~200 μm focal spots and 100 kPa focal pressure), multimodal integration, and bioinspired interfaces have enabled high-precision deep-tissue sensing and spatiotemporally controlled energy delivery—exemplified by strain-sensing feedback improving the signal-to-noise ratio by 5 dB for precise neuromodulation. These capabilities are converging to create closed-loop platforms, as demonstrated in continuous cardiovascular monitoring (up to 164 mm depth for 12 h), image-guided neuromodulation for neurological disorders, on-demand drug delivery (achieving 100% higher plasma concentration than ultrasound alone), and integrated tumor therapy with real-time feedback. Despite persistent challenges in material biocompatibility, energy efficiency, and clinical standardization, the future of ultrasound patches lies in their deep integration with multimodal sensing, machine learning, and adaptive control algorithms. This path will ultimately realize their potential for intelligent, closed-loop theranostics in chronic disease management, telemedicine, and personalized therapy. Full article

Polyvinyl alcohol/carboxymethyl cellulose (PVA/CMC) blend nanocomposites reinforced with plasma-assisted synthesized zinc oxide–gold (ZnO–Au) nanoparticles were prepared via casting at varying nanoparticle concentrations. Structural and interfacial modifications were analyzed using XRD, FTIR, Raman spectroscopy, and XPS. XRD analysis confirmed the nanocomposite crystallinity, showing an average crystallite size of 24.48 nm and a lattice strain of 4.32 × 10⁻³ for the 0.15 wt% ZnO–Au composite. FTIR and Raman spectra revealed band shifts and broadening, indicating strong interactions between ZnO–AuNPs and the polymer matrix. XPS analysis further verified Zn and Au incorporation and changes in C 1s and O 1s intensities, reflecting modified surface chemistry. Optical analysis revealed a reduction in the band gap from 4.60 eV (pure PVA/CMC) to 3.52 eV for the 0.15 wt% ZnO–Au nanocomposite, accompanied by an increase in refractive index from 2.058 to 2.244, along with enhanced UV-shielding the performance due to reduced UV transmittance and increased film opacity. Thermogravimetric analysis demonstrated enhanced thermal stability, while antibacterial tests against E. coli and S. aureus confirmed strong antimicrobial activity. These findings demonstrate that PVA/CMC/ZnO–Au nanocomposites are a promising candidate for antibacterial, UV-blocking, food packaging, and optoelectronic applications. Full article

Composites based on rPE and OPEFB waste are considered sustainable materials. However, their performance is limited by hydrophobic–hydrophilic incompatibility, which weakens interfacial adhesion. This study investigated the atmospheric-pressure air plasma treatment of rPE to enhance its compatibility with OPEFB fibers and evaluated its role as a compatibilizer. Atmospheric plasma treatment for 120 s introduced oxygen-containing groups onto the rPE surface, as evidenced by C-O and OH peaks in the FTIR spectra and the higher O/C ratio in the XPS analysis. Consequently, the water contact angle decreased, reducing the difference in surface tension between rPE and OPEFB from 45.61% to 7.80%. Composites containing 20 wt.% OPEFB were fabricated by varying the proportion of untreated rPE with p-rPE. All p-rPE-based composites exhibited fewer interfacial voids than untreated rPE composites, indicating improved fiber–matrix adhesion. The tensile strength and elastic modulus increased with the p-rPE content, whereas the elongation at break remained higher than that of the untreated composite. Therefore, p-rPE shows potential as a compatibilizer, enabling agricultural and plastic waste value enhancement. Full article

Melatonin, an indoleamine crucial for regulating circadian rhythms, sleep–wake cycles, and immune–endocrine homeostasis, is present in biological fluids at extremely low concentrations, making its quantification analytically challenging. This narrative review provides a critical comparative assessment of current methodologies for melatonin determination across various biological matrices—plasma, urine, saliva, breast milk, and hair. The discussed techniques include immunoassays, colorimetric and spectrophotometric methods, chromatographic–mass spectrometric platforms (LC–MS/MS, UHPLC–MS/MS), and emerging biosensors. Each approach is evaluated regarding analytical sensitivity, specificity, reproducibility, cost, and clinical applicability. While immunoenzymatic and colorimetric techniques offer accessible, low-cost solutions for large-scale or preliminary studies, LC–MS/MS remains the benchmark for reference analysis, providing sub-picogram detection limits and multiplexing capability. However, its high cost, procedural complexity, and inter-laboratory variability limit routine implementation. New developments, including molecularly imprinted polymers, dispersive microextraction, and nanomaterial-based biosensors, suggest a shift toward hybrid, sustainable, and portable analytical platforms. By synthesizing recent methodological advances and identifying key limitations, this review aims to guide researchers and clinicians in selecting the most appropriate analytical approach for clinical, pharmacological, and circadian biomonitoring applications. Full article

Background/Objectives: Current clinical evidence suggests that cannabidiol (CBD) demonstrates therapeutic potential in the management of chronic pain, particularly in conditions involving inflammation. However, its therapeutic potential is severely limited by poor oral bioavailability, extensive first-pass metabolism, and the need for frequent high-dose administration, which compromises patient adherence and tolerability. Long-acting injectable (LAI) delivery systems offer a strategy to overcome these limitations by providing sustained plasma concentrations and reducing dosing frequency. This study aimed to develop and optimise CBD-loaded poly (lactic-co-glycolic acid) (PLGA) microspheres for LAI delivery and to evaluate poly(2-ethyl-2-oxazoline) (POx) as a functional and biocompatible alternative to the conventionally used poly (ethylene glycol) (PEG). Methods: CBD-loaded microspheres were prepared using emulsion–solvent evaporation technique. The formulations were optimised based on entrapment efficiency (EE), drug loading (DL), particle size distribution, surface morphology, thermal behaviour, in vitro release kinetics, and cytocompatibility using NIH 3T3 fibroblasts. Multiple in vitro release methodologies, including dialysis bag, shaking-flask, and USP Apparatus IV, were evaluated to identify the most discriminative and practical approach for long-term release assessment. Results: The optimised POx-based microspheres demonstrated superior control over particle size, yielding significantly smaller and more uniform particles compared with PEG-based microspheres (124 ± 1.47 µm vs. 218 ± 13.5 µm, respectively). Differential scanning calorimetry (DSC) confirmed molecular dispersion of CBD within the polymer matrix. In vitro release studies demonstrated sustained drug release over 20 days. Conclusions: POx represents a promising alternative to PEG for the formulation of CBD-loaded PLGA microspheres, offering enhanced physicochemical stability and biological compatibility. This platform supports the development of safe and effective long-acting injectable CBD therapies and consideration of POx as an alternative to PEG. Full article

This work investigates the reciprocal adhesion of Polybenzoxazole (PBO) and silicon nitride (SiN) with a focus on the combined effects of surface chemistry and environmental conditions, i.e., temperature (T) and relative humidity (RH). A set of six samples, including standard and silicon-rich SiN substrates treated with oxygen (O₂) or carbon tetrafluoride (CF₄) plasma, was fabricated and characterized by AFM, XPS, and TEM/EDX to quantify surface roughness and interfacial chemical modifications. Adhesion with PBO was then assessed through nanoindentation both in situ, during ambient control, and ex situ, after aging in a climatic chamber. Compared to PBO adhesion with as-deposited standard and silicon-rich SiN, O₂ plasma treatment was shown to improve adhesion by 13% and 24%, respectively, whereas CF₄ plasma treatment was still beneficial but more limited, improving adhesion by 8% for both substrates. The different effects were ascribed to the formation of a surface oxide layer after O₂ plasma, enhancing chemical affinity and substantially equalizing the adhesion on the two SiN substrates, while CF₄ plasma was impacting adhesion by reducing the substrates’ activity and, thus, increasing the efficiency of the PBO curing procedure. Notably, the adhesion loss with increasing dew point of the ambient (dependent on temperature and relative humidity) was observed across all samples regardless of surface treatment, reinforcing the critical role of absorbed moisture on polymeric film adhesion. However, this trend was observed for all samples only for in situ testing, with a loss of 25% in the critical load of delamination for the most critical environment, while ex situ tests showed a marked recovery of adhesion properties, leading to measurements no longer reflecting the actual state of the samples inside the altered environment. The results presented in this paper highlight the effect of substrate preparation on the adhesion of an organic compound and a substantial difference in environmental control methods for adhesion testing, providing an alternative approach to classical aging treatments and subsequent characterization for qualifying polymer/inorganic interfaces exposed to stressful operational conditions. Full article

Biocompatible thin films are essential for advancing biomedical devices, as they enhance integration with biological tissues, improve device longevity, and reduce complications. The rapid evolution of both medical needs and materials science has led to a diverse array of deposition techniques, each offering unique advantages and challenges for tailoring surface properties without compromising the bulk characteristics of implants and sensors. While laser-based methods—such as pulsed laser deposition (PLD) and Matrix-Assisted Pulsed Laser Evaporation (MAPLE)—are renowned for their precision, ability to preserve complex material stoichiometry, and suitability for low-temperature processing, the broader landscape includes several other important approaches. Physical Vapor Deposition (PVD) techniques, including magnetron sputtering and pulsed electron deposition, are widely used for their ability to create uniform, adherent coatings with controlled thickness and composition, making them suitable for both hard and soft biomedical substrates. Chemical Vapor Deposition (CVD) and its plasma-enhanced variant (PECVD) offer conformal coatings and excellent control over film chemistry, which is particularly valuable for functional polymer and ceramic films. Other methods, such as sol–gel processing, ion beam deposition, and electrophoretic deposition, provide additional flexibility in terms of coating composition, adhesion, and processing temperature, allowing for the fabrication of films with tailored mechanical, chemical, and biological properties. Despite these advances, the field faces ongoing challenges in optimizing film properties for specific clinical applications, ensuring reproducibility, and scaling up production for widespread use. The necessity of this review lies in its comprehensive comparison of laser-based techniques with alternative deposition methods, providing critical insights into their respective strengths, limitations, and suitability for different biomedical scenarios. By synthesizing recent developments and highlighting current gaps, this review aims to guide researchers and clinicians in selecting the most appropriate thin-film deposition strategies to meet the evolving demands of next-generation biomedical devices. Full article

Plasma regeneration was investigated as a means of regenerating microstructures on biosensors for repeated use. These microstructures were based on the deposition of suspensions containing polymer microspheres. While this method provides a simple way to structure surfaces, obtaining regular structures in a reproducible way remains a challenge. Therefore, it would be advantageous to be able to reuse regular structures, which requires regeneration. To investigate this concept, surface acoustic wave (SAW) resonators were structured using 5 µm and 20 µm polystyrene microspheres and coated with parylene C to stabilize the particle structures. After use in bioanalytical experiments, the biological residues and the parylene C cover layer were removed with plasma, and a new parylene C layer was added. Both atmospheric and low-pressure plasma were tested for regeneration. As a result, the low-pressure plasma was to be preferred because it did not damage the transducer structures on the SAW resonators, unlike the atmospheric plasma. Water contact angle measurements and transmission spectra recorded with a network analyzer confirmed that freshly prepared and regenerated structured SAW resonators coated with parylene C exhibited similar wetting properties and resonance parameters. Therefore, plasma regeneration is an effective way to enable the reuse of perfectly structured SAW resonators. Full article