Search Results (203)

Polyphenols have attracted considerable scientific interest over recent years due to their broad spectrum of biological activities, including antioxidant, cardioprotective, anti-inflammatory, antidiabetic, and anticancer properties. However, their practical application is often limited by unfavorable physicochemical characteristics, particularly low aqueous solubility. Consequently, amorphous solid dispersions (ASDs) have been extensively investigated as a formulation strategy to overcome these limitations. This article represents the first part of a two-part review and presents the current state of the art in amorphous solid dispersions of polyphenols. The available literature is systematically summarized with respect to the investigated polyphenolic compounds, the employed carriers (with particular emphasis on polymeric systems), the preparation methods, and the solid-state characterization techniques used to confirm amorphization. Both single-component systems and binary combinations of polyphenols reported in the literature are considered. The collected data are presented in tabular form and complemented by a heat map illustrating the frequency of reported polyphenol–carrier combinations. The aim of this review is to organize the available knowledge, identify the most extensively studied systems, and highlight research areas that remain underexplored. A detailed discussion of the pharmaceutical benefits and mechanistic aspects of polyphenols in ASD systems will be provided in Part II. Full article

Printed electronics have emerged as a versatile manufacturing platform for next-generation biosensors, enabling on-demand and low-cost fabrication of functional devices on flexible, stretchable, and unconventional substrates. One major challenge in this field lies in the sintering of printed features, as conventional high-temperature processing is incompatible with polymeric substrates and thermally sensitive biological components. Low-temperature sintering inks, typically processed below 200 °C or even at room temperature, have become a critical enabling technology for bio-integrated electronics. This review provides an overview of the current state-of-the-art and key challenges associated with low-temperature sintering inks for printed bioelectronics. We discuss inks based on metal nanoparticles, metal–organic decomposition precursors, metal oxides, chalcogenides, and hybrid material systems. The emphasis is on how ink chemistry, ligand selection, and precursor structure govern rheology, stability, and sintering behavior. In addition, key low-temperature sintering and curing strategies, including thermal, photonic, laser, plasma, microwave, and chemical sintering, are compared in terms of energy delivery, densification mechanisms, and substrate compatibility. Finally, we outline emerging directions towards low temperature and room-temperature sintering inks, and sustainable biobased ink formulations, and discuss their applications for wearable, implantable, and soft biosensing platforms. Full article

The transition from passive containment to active, responsive management is defining the next generation of intelligent packaging. This evolution creates a critical demand for materials that can be precisely engineered to monitor, regulate, and protect. Hydrogen-bonded organic frameworks (HOFs) have emerged as a uniquely versatile platform in this regard, owing to their synthetically tunable porosity, inherent biocompatibility, and exceptional solution processability derived from reversible supramolecular assembly. This review moves beyond cataloging applications to dissect the fundamental mechanisms by which HOFs enable smart packaging functions, including the following: (i) selective gas capture and atmosphere tailoring via molecular recognition within designed pores; (ii) high-sensitivity optical and electrochemical sensing for real-time quality and safety signaling; and (iii) stimuli-responsive release of active agents (e.g., antimicrobials). We further explore the frontier of integrating HOFs as functional fillers or coatings within polymeric matrices, a key step toward practical devices. Despite challenges such as structural stability and maintaining permanent porosity due to relatively weak hydrogen bonds, this work aims to provide a design blueprint for advancing HOFs from laboratory curiosities to core components of sustainable, multifunctional packaging systems. Full article

Extracellular polymeric substances (EPS) facilitate microbiome adhesion on microplastic surfaces and ensure matrix cohesion, playing a crucial role in establishing the structure and function of the plastisphere. Nevertheless, the dynamic alterations in the composition and features of plastisphere EPS and their relationships with biotic and abiotic factors remain poorly understood, especially in soil ecosystems. The study investigated the variations in the EPS secretion behavior of the plastisphere using three types of microplastics across three representative soils with three incubation durations. Results showed that plastisphere EPS had a more complex composition and lower aromaticity, apparent molecular weight, and polarity than natural soil dissolved organic matter did. Continuous changes in EPS composition and features were detected during incubation. The bacterial plastisphere community played a central role in regulating EPS secretion, and other factors (such as soil properties, incubation time and microplastic types) influenced EPS secretion via the bacterial composition of the plastisphere. A decrease in the number of microbial OTUs was significantly correlated with EPS components that governed the dynamics of the EPS composition and features of the plastisphere during incubation, a pattern that was particularly evident for bacteriomes. This study advances our insight into microbiome-EPS interactions within the soil plastisphere and deepens our understanding of its formation mechanisms. Full article

Biological soil crusts (BSCs) are critical ecological components in arid lands. Their formation and stability hinge on the assembly and interactive networks of cyanobacteria-led bacterial communities. Yet, how different functional cyanobacteria shape the underlying microbial structure and assembly rules is poorly understood. Here, we cultivated artificial algal crusts using two representative cyanobacteria: the nitrogen-fixing Leptolyngbya sp. and the non-nitrogen-fixing Microcoleus vaginatus (M. vaginatus CM01). A total of six treatments were established based on the presence or absence of spraying with in situ BSCs leachate: a control group without inoculation of algae or bacteria (soil, S); a treatment group sprayed only with bacterial suspension (soil + bacteria, SB); a treatment group sprayed only with M. vaginatus CM01 (soil + M. vaginatus CM01, SM); a treatment group co-inoculated with both BSCs leachate and M. vaginatus CM01 (soil + M. vaginatus CM01 + bacteria, SMB); a treatment group inoculated only with Leptolyngbya sp. CT01 (soil + Leptolyngbya sp. CT01, SL); and a treatment group co-inoculated with Leptolyngbya sp. CT01 and biocrust leachate (soil + Leptolyngbya sp. CT01 + bacteria, SLB). By integrating 16S rRNA gene sequencing, neutral community modeling (NCM), and structural equation modeling (SEM), we dissected differences in Cyano-BSCs development, bacterial community composition, co-occurrence networks, and assembly mechanisms. Inoculation with M. vaginatus CM01 (SM, SMB) superiorly promoted Cyano-BSCs development: the SM group achieved the highest coverage (23.33%), while the SMB group showed marked increases in organic matter (OM, 4.10 g·kg⁻¹) and chlorophyll a (Chla, 13.40 μg·g⁻¹), alongside a >5-fold rise in bacterial, cyanobacterial, and nitrogen-fixation gene abundances versus controls. The mechanism centers on extracellular polymeric substances (EPS) secreted by M. vaginatus, which homogenized the microenvironment, suppressed stochastic bacterial dispersal (NCM, SM: R² = 0.698), and enhanced deterministic selection. This process forged a highly cooperative network (89.74% positive links, average degree 34.71) that directionally enriched Cyanobacteria (relative abundance 40.40%). The Shannon index of Cyano-BSCs from the group (SMB) reached 7.72 ± 0.09, reflecting high microbial community diversity. SEM confirmed M. vaginatus directly regulated bacterial assembly (path coefficient = 0.59, p < 0.05) and indirectly improved the soil environment (path coefficient = 0.64, p < 0.05), establishing a “cyanobacteria-community-environment” feedback loop. Conversely, the Leptolyngbya sp. groups (SL, SLB), despite enriching nitrogen-fixing bacteria and fungi, exhibited low carbon fixation efficiency (notably 1.26 g·kg⁻¹ OM in SL) and lack of EPS; communities remained stochastic (NCM, SL: R² = 0.751) with no effective regulatory pathway—a pattern mirrored in S and SB groups. Our findings demonstrate that M. vaginatus acts as a core engineer of biological soil Cyano-BSCs formation via an “EPS-mediated habitat filtering—functional group enrichment—cooperative network assembly” cascade, enforcing deterministic community construction. Leptolyngbya sp., with limited niche-constructing ability, fails to exert comparable control. This work provides a targeted framework for the artificial restoration of Cyano-BSCs in arid zones. Full article

Organic dyes are critical components in industries ranging from textiles, plastics, and paper to food, cosmetics, and pharmaceuticals. However, their widespread use leads to significant environmental pollution. Consequently, developing efficient methods to treat dye wastewater is urgently needed. In this work, a high-performance composite membrane was developed with a poly(dibenzo-18-crown-6) covalent organic polymer (COP) interlayer. The chemical structure of the COP was verified by FT-IR, and BET analysis indicated that the as-synthesized material possesses a predominantly mesoporous structure with a minor microporous contribution. Subsequently, the membrane was fabricated by depositing a COP colloid on a nylon-66 support via vacuum filtration, followed by the formation of a dense polyamide (PA) active layer through interfacial polymerization (IP) between amine and acyl chloride monomers. Systematic evaluation of dye separation performance using a cross-flow filtration setup identified optimal operating conditions. Under these conditions, the membrane demonstrated effective molecular sieving behavior, achieving both high dye rejection and favorable solvent permeability. In long-term stability tests, the membrane maintained a rejection rate of over 99% for Congo red over 48 h, while sustaining a water flux of 103.2 L m⁻² h⁻¹ bar⁻¹ (LMH/bar). Furthermore, the membrane exhibited promising potential for dye desalination applications, achieving a high Congo red/potassium chloride separation selectivity of 186.8 with a flux of 138.2 LMH/bar. This study confirms that the poly(dibenzo-18-crown-6)-based composite membrane is a reliable and efficient material for molecular separation in wastewater treatment. Full article

Printed electronics (PE) have emerged as a rapidly growing technology owing to their potential for low-cost fabrication, flexibility, and scalable device manufacturing. The dependence on fossil-based components raises environmental concerns, leading the scientific community toward sustainable solutions, aiming to reduce the accumulation of electronic waste (e-waste) in the environment and the emission of toxic gases, as well as to offer a circular solution in the sector. This review presents an in-depth overview of biobased polymeric materials in printed and organic (bio-)electronics. Firstly, the principal printing techniques are presented in detail. The review proceeds by outlining the various biobased synthetic and natural polymers, along with their blends, that are employed in the fabrication of biobased substrates for printed devices. Finally, the review emphasizes the existing challenges and constraints in the field of PE, along with the promising opportunities for its future advancement. Full article

This study investigates water-based gel and gel-like cleaning treatments on Superficie 553, an oil painting on canvas by Giuseppe Capogrossi, using portable NMR to assess their impact. The objective was to evaluate the effects of four cleaning systems composed of a buffer solution released in free form and combined with xanthan gum, a cross-linked silicone polymer gel, and an agar gel matrix. Two distinct NMR experiments were conducted. The first involved the acquisition of ¹H depth profiles to detect the distribution of the cleaning solution within the painted layer and the thickness variations resulting from cleaning procedures. The second employed the acquisition of relaxation times, facilitating the investigation of molecular mobility within the organic components of the paint layer. NMR results indicated that the agar gel system caused negligible structural changes, whereas the silicone gel induced rigidification, and the other systems permanently increased molecular mobility. These measurements provided insights into alterations in the dynamic behavior of the polymerized oil. A key strength of this investigation lies in the direct application of diagnostic methods on Superficie 553, made possible by the non-invasive nature and portability of the NMR-MOUSE system. Additionally, portable FTIR was used to detect residues and obtain chemical information, confirming that the silicone gel left detectable residues and identifying the agar gel as the most conservative cleaning method. This enabled in situ analysis of the original artwork without sampling or relocation—a crucial advantage given the difficulty of replicating the complex physicochemical conditions of historical paint surfaces under laboratory constraints. Such real-time, on-site monitoring ensured an authentic evaluation of the treatment effects, preserving the integrity of the artwork throughout the conservation process. Full article

Microbial biosurfactants (mBSs) are bioactive molecules with diverse applications, notably as antimicrobial agents against antibiotic-resistant pathogens. Produced by bacteria and yeasts, mBSs are classified as glycolipids, lipopeptides, polymeric, and particulate types. The global rise in multidrug-resistant organisms, such as Escherichia coli, Klebsiella pneumoniae, Salmonella typhimurium, Pseudomonas aeruginosa, and Acinetobacter baumannii, underscores the urgent need for new antimicrobial strategies. mBSs disrupt microbial growth by interacting with the lipid components of pathogens, offering promising alternatives to conventional antibiotics. This review highlights the sources, chemical structures, and properties of mBSs, their antimicrobial activities, synergistic effects with antibiotics, and structure–activity relationships. Special emphasis is placed on surfactant modification, where targeted changes—such as valine substitution in surfactin—significantly lower critical micelle concentrations (CMC) and enhance antimicrobial potency. Such rational engineering demonstrates how biosurfactants can be tailored for improved biomedical performance while minimizing cytotoxicity. In parallel, artificial intelligence (AI) algorithms, including artificial neural networks and genetic algorithms, optimize yields, predict substrate suitability from agricultural residues, and guide microbial strain engineering. AI models can predict interfacial behavior and synchronize fermentation with purification. Advancing the understanding of mBS interactions with microbial membranes, combined with modification strategies and AI-guided optimization, is essential for developing targeted therapies against resistant infections. Future research should integrate these approaches to engineer novel derivatives, reduce costs, and validate clinical potential through comprehensive in vivo studies. Full article

Agricultural biomass has potential as a renewable and versatile carbon feedstock for developing eco-friendly and biodegradable polymers capable of replacing conventional petrochemical plastics. To address the growing environmental concerns associated with plastic waste and carbon emissions, lignocellulosic residues, edible crop by-products, and algal biomass were utilized as sustainable raw materials. These biomasses provided carbohydrate-, lipid-, and lignin-rich fractions that were deconstructed through optimised physical, chemical, and enzymatic pretreatments to yield fermentable intermediates, such as reducing sugars, organic acids, and fatty acids. The intermediates were subsequently converted through tailored microbial fermentation processes into biopolymer precursors, primarily polyhydroxyalkanoates (PHAs) and lactate-based monomers. The resulting monomers underwent polymerization via polycondensation and ring-opening reactions to produce high-performance biodegradable plastics with tunable structural and mechanical properties. Additionally, the direct extraction and modification of naturally occurring polymers, such as starch, cellulose, and lignin, were explored to develop blended and functionalized bioplastic formulations. Comparative evaluation revealed that these biomass-derived polymers possess favourable physical strength, thermal stability, and biodegradability under composting conditions. Life-cycle evaluation further indicated a significant reduction in greenhouse gas emissions and improved carbon recycling compared to fossil-derived counterparts. The study demonstrates that integrating agricultural residues into bioplastic production not only enhances waste valorization and rural bioeconomy but also supports sustainable material innovation for packaging, farming, and consumer goods industries. These findings position agriculture-based biodegradable polymers as a critical component of circular bioeconomy strategies, contributing to reduced plastic pollution and improved environmental sustainability. Full article

Granular copper oxide nanoparticles (CopOx NPs), synthesized via laser ablation (100 nm, ζ-potential +30 mV), were introduced into photolithographic polymethyl methacrylate (PMMA) resin at concentrations of 0.001–0.1%. The resulting composite material enables the fabrication of high-resolution (up to 50 μm) parts with a high degree of surface quality after polishing using the MSLA method. CopOx NPs increased the degree of resin polymerization (decrease by almost 4× in unpolymerized components at 0.1% CopOx NPs) and induced the in situ formation of self-organized periodic structures visible under a modulation interference microscope. The composite samples exhibit pronounced oxidative activity: they intensify the generation of hydrogen peroxide and hydroxyl radicals and cause the oxidative modification of biomolecules (formation of 8-oxoguanine in DNA and long-lived reactive forms of proteins). A key property of the materials is their selective biological activity. While lacking cytotoxicity for human fibroblasts, they exhibit a strong antibacterial effect against E. coli, leading to cell death within 24 h. Thus, the developed composite photolithographic resin combines improved technological characteristics (high printing resolution, degree of polymerization) with functional properties (selective antibacterial activity) and holds promise for application in biomedicine, as well as in the food and agricultural industries. Full article

The emergence of electrically conductive polymeric materials has revolutionized the landscape of sustainable energy technologies, presenting unprecedented opportunities for advancing both photovoltaic conversion systems and electrochemical energy-storage platforms. These remarkable macromolecular materials exhibit distinctive characteristics including adjustable electronic band structures, exceptional mechanical adaptability, solution-phase processability, and cost-effective manufacturing potential. This extensive review provides an in-depth examination of the fundamental principles governing charge carrier mobility in conjugated polymer systems, explores diverse synthetic methodologies for tailoring molecular architectures, and analyzes their transformative applications across multiple energy technology domains. In photovoltaic technologies, electrically conductive polymers have driven major advancements in organic solar cells and photoelectrochemical systems, significantly improving energy conversion efficiency while reducing manufacturing costs. In electrochemical energy storage, their integration into supercapacitors and rechargeable lithium-based batteries has enhanced charge storage capability, accelerated charge–discharge processes, and extended operational lifespan compared with conventional electrode materials. This comprehensive analysis emphasizes emerging developments in hybrid composite architectures that combine conductive polymers with carbon-based nanomaterials, metal oxides, and other functional components to create next-generation flexible, lightweight, and wearable energy systems. By synthesizing fundamental materials chemistry with device engineering perspectives, this review illuminates the transformative potential of electrically conductive polymers in establishing sustainable, efficient, and resilient energy infrastructures for future technological landscapes. Full article

Conventional petroleum-based protective coatings release high levels of volatile organic compounds (VOCs) and contribute to resource depletion, urging the development of environmentally responsible alternatives. Among the bio-based candidates, microalgae and Cyanobacteriophyta have recently gained attention for their ability to produce diverse biopolymers and pigments with intrinsic protective functionalities. However, existing literature has focused mainly on algal biofuels and general biopolymers, leaving a major gap in understanding their application as sustainable coating materials. This review addresses that gap by providing the first integrated assessment of algae-based protective coatings. It begins by defining abiotic and biotic surface degradation mechanisms, including microbiologically influenced corrosion, to establish performance benchmarks. The review then synthesizes recent findings on key algal components, including alginate, extracellular polymeric substances (EPS), and phycocyanin, linking biochemical composition to functional performance, techno-economic feasibility, and industrial scalability. It evaluates their roles in adhesion strength, UV stability, corrosion resistance, and antifouling activity. Reported performance metrics include adhesion strengths of 2.5–3.8 MPa, UV retention above 85% after 2000 h, and corrosion rate reductions of up to 40% compared with polyurethane systems. Furthermore, this study introduces the concept of carbon-negative, multifunctional coatings that simultaneously protect infrastructure and mitigate environmental impacts through CO₂ sequestration and pollutant degradation. Challenges involving biomass variability, processing costs (>USD 500/ton), and regulatory barriers are critically discussed, with proposed solutions through hybrid cultivation and biorefinery integration. By bridging materials science, environmental engineering, and sustainability frameworks, this review establishes a foundation for transforming algae-based coatings from laboratory research to scalable, industrially viable technologies. Full article

Recent advances in 3D printing of silica glass have highlighted the limitations of conventional stereolithography (SLA), which requires high-temperature sintering (≈1000 °C) and often uses slurry-based materials. To address these limitations, a sinterless approach using polyhedral oligomeric silsesquioxane (POSS)-based resin has gained attention, as it can form transparent fused silica at only 650 °C. However, previous POSS-based systems suffered from high shrinkage owing to the addition of organic monomers. In this study, a novel low-viscosity polymerizable POSS resin was synthesized without additional monomers, maintaining its sinterless properties while reducing shrinkage. Experimental results showed that our POSS resin has a silica content of 41%, with a shrinkage rate of only 36 ± 1%, which effectively reduced cracking and warping when calcinating large-volume models. It was demonstrated that this resin can be applied not only to high-resolution glass 3D printing with sub-200 nm line widths using two-photon polymerization, but also to low-cost glass 3D printing using single-photon polymerization. The 3D-printed objects can be converted into silica glass structures at significantly lower temperatures than traditional sintering, offering a promising route for efficient and precise glass manufacturing. Potential applications of our POSS resin include the production of multi-scale devices, such as microfluidic devices and optical components, and hybrid processing with semiconductors and MEMS and photonic devices. Full article

Methodological fusion of materials chemistry, which enables us to create materials, with nanotechnology, which enables us to control nanostructures, could enable us to create advanced functional materials with well controlled nanostructures. Positioned as a post-nanotechnology concept, nanoarchitectonics will enable this purpose. This review paper highlights the broad scope of applications of the new concept of nanoarchitectonics, selecting and discussing recent papers that contain the term ‘nanoarchitectonics’ in their titles. Topics include controls of dopant atoms in solid electrolytes, transforming the framework of carbon materials, single-atom catalysts, nanorobots and microrobots, functional nanoparticles, nanotubular materials, 2D-organic nanosheets and MXene nanosheets, nanosheet assemblies, nitrogen-doped carbon, nanoporous and mesoporous materials, nanozymes, polymeric materials, covalent organic frameworks, vesicle structures from synthetic polymers, chirality- and topology-controlled structures, chiral helices, Langmuir monolayers, LB films, LbL assembly, nanocellulose, DNA, peptides bacterial cell components, biomimetic nanoparticles, lipid membranes of protocells, organization of living cells, and the encapsulation of living cells with exogenous substances. Not limited to these examples selected in this review article, the concept of nanoarchitectonics is applicable to diverse materials systems. Nanoarchitectonics represents a conceptual framework for creating materials at all levels and can be likened to a method for everything in materials science. Developing technology that can universally create materials with unexpected functions could represent the final frontier of materials science. Nanoarchitectonics will play a significant part in achieving this final frontier in materials science. Full article