Search Results (2,238)

Antimicrobial resistance is a major global health threat, creating an urgent need for effective non-antibiotic antimicrobial strategies. In this study, CS–AgNPs were synthesized by electron-beam radiolysis, providing a clean, dose-controllable route that avoids additional chemical reducing agents. The effects of irradiation dose and chitosan concentration on nanoparticle formation, physicochemical properties, and antibacterial activity were systematically evaluated. Spectroscopic and structural analyses confirmed the formation of highly crystalline, face-centered cubic silver nanoparticles uniformly dispersed within the chitosan matrix, with Ag–polymer coordination involving –NH₂ and –OH functional groups. Under the optimal conditions (8 kGy, 0.06 mmol AgNO₃, and 0.05% w/v chitosan), ultrasmall, well-dispersed CS–AgNPs were obtained, with an average size of 5.30 ± 2.01 nm and high phase purity. Antibacterial evaluation demonstrated potent, concentration-dependent activity against both Gram-positive Staphylococcus aureus and Gram-negative Escherichia coli, with low minimum inhibitory and minimum bactericidal concentrations (MIC/MBC = 1.96 µg/mL). These findings define a clear structure–property–activity relationship and support a synergistic antibacterial effect between nanosilver and chitosan, while maintaining favorable in vitro cytocompatibility and hemocompatibility within the effective concentration range. Overall, electron-beam radiolysis represents a promising scalable platform for producing broad-spectrum antimicrobial nanomaterials with potential utility in addressing antimicrobial resistance. Full article

The crystal structures of the cobalt(II) metal–organic frameworks or coordination networks of [Co(pdb)(DMF)] and [Co₂(pdi)(DMF)₃]·2(DMF)·H₂O (H₂pdb = 3,3′-(phenazine-5,10-diyl)dibenzoic acid; H₄pdi = 5,5′-(phenazine-5,10-diyl)diisophthalic acid; DMF = N,N-dimethylformamide) were synthesized solvothermally from cobalt(II) nitrate and the free acid of the linker in DMF. Systematic solvothermal screening demonstrated strong metal- and counterion-dependent framework formation, as crystalline coordination polymers were obtained exclusively from cobalt(II) nitrate, whereas other metal salts and cobalt(II) chloride or sulfate produced no crystalline materials. In catena-[(N,N-dimethylformamide)-μ₄-3,3′-(phenazine-5,10-diyl)dibenzoate-cobalt(II)], [Co(pdb)(DMF)], the Co₂ units, acting as secondary building units, are coordinated by four carboxylate groups from four linkers in a paddle-wheel arrangement, giving a three-dimensional (3D) network with cds (or CdSO₄) topology, in which the wide openings are filled by two symmetry-related nets to form a threefold interpenetrated structure. In catena-[tris(N,N-dimethylformamide)-μ₈-5,5′-(phenazine-5,10-diyl)diisophthalate-dicobalt(II)] bis(N,N-dimethylformamide) hydrate, [Co₂(pdi)(DMF)₃]·2(DMF)·H₂O, there are two different Co atoms, of which only Co₂ is connected to each of the four carboxylate groups of the tetracarboxylate linker and, thus, is responsible for 3D network formation. The network topology in [Co₂(pdi)(DMF)₃] is pts (or platinum(II) sulfide) when taking the Co₂ atom as a tetrahedral node and the linker as a square-planar fourfold node; however, this arrangement is inverse to the common square-planar metal and tetrahedral linker nodes found in PtS and most pts topologies. Full article

Microplastics (MPs) are a growing environmental concern due to their ubiquitous presence, especially in wastewater treatment plants (WWTPs), where they are transferred and accumulated in sludge and can be reintroduced into the environment through sludge reuse. The persistence of MPs highlights the need for effective and tailored treatment strategies to enhance their removal or management. This study investigates the effects and impacts of ozonation as a pretreatment method for sludge, followed by anaerobic digestion (AD), on low-density polyethylene (LDPE), polypropylene (PP), and polyamide 66 (PA(66)) MPs. Different ozone doses, ranging from 5 to 50 gO₃/gMPs, were tested in both deionized water and synthetic sludge. The study evaluated MPs degradation through mass variation measurements, Fourier Transform Infrared spectroscopy (FTIR), Differential Scanning Calorimetry (DSC), and Carbonyl Index (CI) analysis. Results showed that ozonation induced chemical modifications in MPs, increasing CI values and leading to the formation of oxygen-containing functional groups, particularly carbonyls. FTIR analysis confirmed the development of new absorption peaks at 1716 cm⁻¹ and 1710 cm⁻¹ for LDPE and PP, respectively, while PA(66) exhibited a shift in its carbonyl peak from 1739 cm⁻¹ to 1754 cm⁻¹. DSC analysis revealed a reduction in crystallinity for all tested polymers, suggesting increased structural disorder. However, no significant MPs mass reduction was observed, and AD did not further enhance MPs degradation. These findings highlight ozonation as a promising strategy for modifying MPs surface chemistry and potentially increasing their environmental degradability. Full article

Development of biodegradable polymer composites provides a sustainable alternative to conventional plastics. This study systematically investigates the effect of Eucomis autumnalis (EA) cellulose on the morphological, structural, and thermal behavior of polybutylene succinate (PBS) and polycaprolactone (PCL) blends. EA cellulose was extracted via delignification and hemicellulose removal, yielding 38% cellulose from the leaf biomass. A series of PBS/PCL/EA cellulose composites were prepared using a solution-casting method. Fourier-transform infrared spectroscopy (FTIR) confirmed retention of characteristic functional groups, with spectra dominated by PCL features, indicating the absence of new chemical bond formation between EA cellulose and the polymer matrix. X-ray powder diffraction (XRPD) revealed that EA cellulose acted as a nucleating agent, enhancing the crystallinity, especially in PCL, while slightly affecting PBS crystallization. A scanning electron microscopy (SEM) analysis demonstrated preferential localization of EA cellulose within the PBS phase, contributing to improved phase dispersion and interfacial interaction at the morphological level. Differential scanning calorimetry (DSC) showed enhanced crystallization behavior of PCL at higher EA cellulose loading (5 wt.%), with minimal influence on PBS thermal transitions. A thermogravimetric analysis (TGA) indicated that the thermal stability depends on the polymer composition and cellulose content, with higher PCL fractions contributing to an improved stability. This study provides insight into the structure–property relationships governing PBS/PCL/EA cellulose systems and highlights the potential of EA cellulose as a bio-based additive for tailoring morphological and thermal characteristics of biodegradable polymer blends. A mechanical performance evaluation is recommended for future studies to correlate structural modifications with macroscopic properties. Full article

Background/Objectives: The formulation development of Isotretinoin (ISN) is limited by its solubility and stability issues. This study aimed to characterise the BCS class II drug ISN, particularly the possible different solid state and formulate amorphous solid dispersion aiming for a supersaturation state. Methods: ISN’s physical states are investigated in its raw form, quench-cooled form, physical mixture with the polymer and corresponding solid dispersion form. Quench-cooled ISN was prepared in situ using DSC. Carrier stabilisation of ISN was attempted using the solid dispersion technique. Hereby, the solid dispersion of drug-polymer PVPVA at a ratio of 1:3 was prepared using the solvent evaporation method. Solid dispersion, physical mixture and raw ISN were characterised for the saturated solubility. Physical characterisation of the samples was performed using DSC, ATR-FTIR and a light microscope. Results: Two polymorphs of ISN (forms I and II) were found in the raw ISN, with form II being thermodynamically more stable. ISN possesses strong crystallinity and resistance to amorphisation under the applied quench-cooling condition without the presence of a carrier system. The conjugated polyene structure in ISN contributes to the polymorphic transformation and isomerisation. The incorporation of PVPVA in the solid dispersion system successfully improved the water solubility (sixfold) of ISN despite a combination of crystalline and amorphous components being present in the system. Conclusions: ISN is a class II drug crystal molecule. Taking advantage of solubility and possibility in the polymorphic transformation of ISN in a binary system, we concluded that ISN could potentially be formulated into its corresponding crystalline solid dispersion form. Full article

Background/Objectives: 3D printing, particularly fused deposition modeling (FDM), is an emerging technology in pharmaceutical manufacturing, enabling the customization of dose or release rate to individual patient needs. However, finding the appropriate loading method to ensure the stability of the drug and achieve the targeted dose may be challenging. Furthermore, the drug utilization of most loading methods is poor, which results in considerable waste production and increased environmental burden. This study aimed to compare two post-printing drug-loading techniques: electronic syringe deposition and pan coating on FDM-printed polylactic acid (PLA) tablets. PLA is a biodegradable and biocompatible polymer that is widely used in this field due to its mechanical strength and regulatory approval. Methods: Tablets with honeycomb-shaped infill (30% and 60% infill densities) were fabricated using PLA filaments, followed by loading with a 15% paracetamol solution via either electronic syringe deposition or pan coating. The resulting tablets were assessed for drug content, weight variation, friability%, surface morphology (SEM), drug distribution (Raman mapping), solid-state characteristics (DSC and FTIR), and dissolution performance. Results: The results indicated that pan coating and electronic syringe deposition offered drug utilization up to 88% and 91.7%, respectively, which is superior to conventional soaking methods. Nevertheless, there is a significant difference in drug loading and release rate: pan coating yielded up to 10.14% drug loads and fast release (over 80% in 30 min), while electronic syringe deposition showed lower drug loading up to 4.8% and slower release (less than 80% within 60 min), which could be associated with better mechanical film integrity and higher precision. Both methods met USP standards with a weight loss of less than 1% and maintained the drug’s crystalline state and compatibility with PLA. Conclusions: FDM combined with controlled post-printing drug loading presents a rapid, cost-effective, and flexible novel approach for manufacturing personalized immediate-release tablets, with pan coating potentially being more suitable for commercial scalability and electronic syringe offering precise dosing for personalized therapies. Full article

Polymer powder bed fusion (PBF) is strongly influenced by powder chemistry and powder state, yet many studies discuss the materials and processing conditions in isolation. This review synthesises the literature using a powder-centred framework that connects polymer chemistry and powder production history to measurable powder descriptors, and then links these descriptors to processing windows, defect mechanisms, and application outcomes. Key descriptors include crystallinity and thermal transitions, additive packages, particle size distribution, morphology, and surface texture. Environmental sensitivities are also considered, including moisture uptake, temperature effects, and optical response. These factors are related to powder spreading, energy absorption, and melt solidification or sintering to explain how flowability, packing density, and melt dynamics govern porosity, lack of fusion, distortion, and degradation. Powder qualification is discussed together with lot-to-lot variability and lifecycle effects, including ageing, reuse, and refresh, using the indicators commonly reported in laboratory and production settings and supported by emerging in situ monitoring. Application case studies are consolidated to illustrate how powder state and process control translate into repeatable qualification targets as polymer PBF moves toward a predictable and transferable manufacturing practice. Full article

Liquid crystalline poly(ester imide)s (LCPEIs) were synthesized by solution polymerization from 4-hydroxybenzoic acid (4-HBA), 6-hydroxy-2-naphthoic acid (HNA) and N-(3-carboxyphenyl)-4-hydroxyphthalimide (3-CHP), with the capping groups of benzocyclobutene (BCB)-containing compounds (BCB-HP for phenolic hydroxyl group and BCB-CP for aromatic carboxylic acid). Subsequent cross-linking of the BCB capping groups upon hot pressing afforded the cured LCPEI films. Optimal properties of these films were achieved by adjusting the capping BCB-HP/BCB-CP contents.These LCPEIs showed favorable thermal properties with a relatively high glass transition temperature (T_g, 137–167 °C) and low melting temperature (T_m, 186–194 °C). With the increase in BCB capping content, the tensile modulus, tensile strength, and coefficient of thermal expansion (CTE) exhibited a non-linear tendency of first decreasing and then increasing. LCPEI-3.0 (3 mol% BCB) showed optimal performance: a relatively low CTE (20 × 10⁻⁶ K⁻¹), a relatively high storage modulus (2.55 GPa), a moderate tensile modulus (2.65 GPa), a relatively low dielectric constant (Dk = 3.17) with low dielectric loss (Df = 0.0034) at 10 GHz, and excellent hydrophobicity (water contact angle = 133°). This improvement embodies an effective strategy to combine advantages of polyester, polyimide, and benzocyclobutene to achieve favorable and excellent comprehensive properties for convenient processability and practical application prospects. Full article

Laser-induced graphene (LIG) is most often produced from commercial Kapton; the properties of LIG are inherently linked to those of the polymer substrate, which results in a limited field of applications for LIG on Kapton. This study demonstrates that tailored properties of LIG, including nitrogen doping, which is favorable for electronic applications, can be achieved by using synthesized cross-linked polyimides (PIs) as substrates for graphene induction. Three amorphous polyimides containing 4-[(4-aminophenyl)sulfonyl]aniline (PI-APSA), 1,2-diaminoethane (PI-EDA), and urea (PI-Urea), as crosslinkers, were prepared from different diamines and maleic anhydride, and subsequently used as substrates to produce in situ nitrogen-doped LIG. The resulting materials were comprehensively characterized and compared with LIG on Kapton. Raman spectroscopy confirmed lower defect densities and higher crystallinity than in LIG on Kapton, while sheet resistance was up to three times smaller. The LIG with PI-EDA showed the highest nitrogen content and a specific areal capacitance of 3.1 mF/cm², which is more than an order of magnitude higher than that of LIG/on Kapton, highlighting its strong potential for energy storage devices. PI-APSA-based LIG exhibited the best adhesion and lowest sheet resistance, making it suitable for wearable electrodes, whereas PI-urea-based LIG maintained hydrophilicity. Thus, chemically tailored polyimides enable the formation of nitrogen-doped LIG with tunable interfacial properties, higher structural order, and improved electrical and electrochemical performance compared to commercial Kapton. Full article

This review highlights recent progress in the sustainable extraction, production and application of plant fiber-reinforced biopolymer composites. The review mainly focuses on properties of these materials—mechanical, thermal, and interfacial—and explores how factors such as fiber type, extraction methods, and surface treatments (e.g., enzymatic retting, deep eutectic solvents, steam explosion) affect fiber morphology and bonding with the polymer matrix. The work also discusses strategies to select and modify biopolymer matrices (e.g., PLA, PHA) for better compatibility, recyclability, and long-term performance, addressing challenges like fire resistance and environmental impact. Special attention is given to cellulose surface modification, which improves wettability and interfacial adhesion, while highlighting alternatives to conventional chemical treatments due to cellulose’s high crystallinity and strong hydrogen bonding. Despite advances in surface treatments and manufacturing, persistent challenges include moisture sensitivity, processing reproducibility, and standardization. Future research should prioritize application-tailored extraction, scalable eco-friendly modifications, and standardized testing to optimize durability and circular economy alignment. These fiber-reinforced biopolymer composites offer a viable path to fossil-free, high-performance materials. Overall, this review provides a comprehensive perspective that bridges sustainability and industrial applicability, offering practical guidance for developing high-performance, eco-friendly composites. Full article

PEEK (polyetheretherketone) is a semi-crystalline thermoplastic polymer which, thanks to its excellent mechanical properties, chemical resistance, and high biocompatibility, is widely used in medicine, especially in biomedical engineering. The dynamic development of additive technologies, especially FFF (Fused Filament Fabrication), has enabled the production of personalized medical implants from PEEK, such as skull implants, dental implant components, and orthopedic implants like spine, knee and hip implants. Therefore, the aim of the study was to evaluate the polymer as an alternative material for orthopedic applications and to analyze the effect of annealing and soaking in PBS solution on its strength properties. Heat treatment improves the strength properties of the material. On the other hand, prolonged soaking in PBS solution, which simulates physiological conditions, can lead to changes in the interlayer bonds of the filament layers, which in turn affects the strength properties of the material. Full article

Polyethylene glycol (PEG) is a widely used water-soluble polymer (WSP) whose properties such as crystallinity depend on molecular weight. This study explores whether Raman spectroscopy, combined with supervised machine learning, can differentiate PEG samples of defined molecular weights within the investigated molecular weight range. Eight PEG materials with molecular weights ranging from 1000 to 35,000 g/mol were analyzed by confocal Raman microscopy under standardized conditions. A Support Vector Machine (SVM) classifier achieved 93.4% accuracy in five-fold cross-validation and 72.6% on an independent test set, confirming that molecular-weight-dependent vibrational signatures are present in the Raman spectra. Principal component analysis followed by linear discriminant analysis (PCA–LDA) models supported these findings, revealing that discriminative information arises mainly from line-shape and shoulder regions rather than from peak centers, consistent with gradual increases in conformational order. Although sample morphology and drying behavior introduce variability, the results demonstrate that Raman spectroscopy provides a reproducible, non-destructive means of distinguishing between PEG samples of different molecular weights. The established workflow provides a foundation for future quantitative evaluations of spectral trends, cross-polymer generalization, and adaptation to variable measurement conditions to enhance applicability in analytical and industrial contexts. Full article

To improve the quality of additive manufacturing of PEEK parts, copolymers with varying 4,4′-dichlorodiphenylsulfone (DCDPS) contents were synthesized. A study of the thermophysical properties of the resulting copolymers revealed that increasing the DCDPS content leads to lower melting temperatures, crystallization temperatures, and degree of crystallinity, while simultaneously increasing the glass transition temperature. It was found that structural amorphization leads to a predictable decrease in the strength and elastic modulus of both cast and printed samples. However, at a DCDPS concentration of 15%, the decrease in mechanical properties is offset by an increase in polymer chain rigidity. The practical result of this study was the successful adaptation of the material to FDM printing: copolymers with DCDPS contents in the range of 5–20% ensured stable molding without deformation or delamination, demonstrating an optimal balance between processability and performance. Full article

PET biodegradation remains limited due to its intrinsic properties—high crystallinity, hydrophobicity, and strong chemical stability. These characteristics lead to extremely slow degradation rates and contribute to PET’s persistence in the environment. Understanding how microorganisms respond at the molecular level when exposed to such a recalcitrant polymer is therefore essential. Living organisms express genes in response to their needs during development. When microbes are under critical conditions, such as when contaminants are present, they express genes encoding specific enzymes that attack the pollutant. In this study, a fungus isolated from the infected fruit of the plant Randia monantha was identified as Aspergillus terreus. It was tested for polyethylene terephthalate (PET) degradation, and the fungus Aspergillus nidulans was evaluated due to its previously reported recombinant cutinases for PET degradation. A microplastic polyethylene terephthalate (PET-MP) particle size of <355 μm for degradation was established, and a PET weight loss of 1.62% for A. nidulans and 1.01% for A. terreus was found. Additionally, the degradation of PET was confirmed by FTIR and SEM. This study also compares the transcriptomic profiles of Aspergillus nidulans and Aspergillus terreus during cultivation with PET-MP residues, which serve as a replacement for the carbon source. We present the first evidence of chitinase overexpression during direct exposure of PET to Aspergillus fungi. Interestingly, chitinase expression was detected in the crude extracts of A. nidulans and A. terreus during culture in the presence of PET residues, which replaced the carbon source. The chitinase produced by each fungus has a similar molecular weight of approximately 44 kDa. Chitinase activity was monitored over a 14-day cultivation period; from day 2, chitinase activity was detected in both cultures and continued to increase until day 14, when the highest values reported in this work were 24.88 ± 4.17 U mg⁻¹ and 10.41 ± 0.47 U mg⁻¹ for A. nidulans and A. terreus, respectively. Finally, we proposed a pathway for PET degradation by Aspergillus fungi that involves mycelial adherence and the secretion of hydrophobins, followed by the production of intermediates and monomers via esterase hydrolysis, and ultimately, the entry of monomers to the ethylene glycol (EG) and terephthalic acid (TPA) pathways, further suggesting these Aspergillus as candidates to produce valuable compounds under these conditions, such as muconic acid, gallic acid, and vanillic acid. Full article

Background: Reconstruction of the proximal humerus after wide tumor resection is technically demanding, and traditional methods such as allograft–prosthetic composites, reverse shoulder arthroplasty, and metal implants are limited by graft unavailability, pediatric size mismatch, their high cost, and metal-related stress shielding. Polyether ether ketone (PEEK), with its modulus closer to cortical bone and radiolucency, offers a promising alternative. Building upon the success in craniomaxillofacial surgery and its favorable physical characteristics, we applied personalized 3D-printed PEEK implants for proximal humerus reconstruction. This study reports the first evidence of applying patient-specific 3D-printed PEEK implants in the proximal humerus. Methods: A retrospective cohort study was conducted on seven patients who underwent wide resection of primary malignant bone tumors of the proximal humerus, followed by reconstruction using patient-specific 3D-printed PEEK implants. Implant design was based on preoperative computed tomography (CT) imaging, incorporating contralateral humeral mirroring and computer-aided design. The implants were fabricated using fused deposition modeling (FDM) with medical-grade PEEK under stringent thermal control (nozzle temperature > 400 °C and heated build chamber), followed by a controlled annealing process to minimize internal stress, optimize polymer crystallinity, and enhance mechanical durability. Outcomes assessed included implant survival, oncologic control, shoulder range of motion, and functional outcomes measured using the Musculoskeletal Tumor Society (MSTS) score. The mean follow-up duration was 56.3 months. Results: All patient-specific PEEK implants were successfully manufactured and implanted with satisfactory geometric accuracy. Mechanical implant survival was 85.7% at final follow-up, with one implant fracture occurring at 28 months. No cases of deep infection, dislocation, loosening, or permanent neurovascular injury were observed. Local soft-tissue recurrence occurred in two patients (28.6%), without distant metastasis or tumor-related mortality. The limb-salvage rate was 100%. At final follow-up, the mean MSTS score was 23.0 ± 1.6. Shoulder motion was limited but comparable to outcomes reported for conventional anatomic megaprosthetic reconstructions. Conclusions: Patient-specific 3D-printed PEEK implants provide a feasible and oncologically safe option for proximal humerus reconstruction after tumor resection, with acceptable midterm implant survival and functional outcomes. The favorable elastic modulus and radiolucency of PEEK offer distinct biomechanical and imaging advantages over metallic implants. Further design optimization and larger prospective studies are warranted to enhance mechanical durability and functional restoration. Full article