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Search Results (3,032)

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Keywords = biocompatible polymer

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17 pages, 6590 KB  
Article
Nanogroove-Induced Enhancement of Neural Spike Activity in Stem Cell-Derived Networks
by Rahman Sabahi-Kaviani, Marina A. Shiryaeva and Regina Luttge
Micromachines 2026, 17(5), 524; https://doi.org/10.3390/mi17050524 (registering DOI) - 25 Apr 2026
Abstract
Nanogrooves provide instructive cues to cells in culture. Several nanofabrication techniques have been developed to create biomimetic substrates, advancing our understanding of cell adhesion. Their integration into nervous system models highlights the critical role of the extracellular matrix (ECM) in developing functional tissue [...] Read more.
Nanogrooves provide instructive cues to cells in culture. Several nanofabrication techniques have been developed to create biomimetic substrates, advancing our understanding of cell adhesion. Their integration into nervous system models highlights the critical role of the extracellular matrix (ECM) in developing functional tissue constructs for in vitro platforms such as Brain-on-Chip (BoC) and Nervous System-on-Chip (NoC). This study presents a nanofabrication approach that integrates photolithography and microtransfer molding (μTM) to pattern nanogrooves using photocurable polymer NOA81 onto microelectrode array (MEA) plates. The resulting nanogrooves exhibited a pattern periodicity of 976 nm and a ridge width of 232 nm, as confirmed by scanning electron microscopy and atomic force microscopy. We assessed the biocompatibility and functional impact of these modified substrates using human induced pluripotent stem cell (hiPSC)-derived neuronal cultures. Neurons cultured on nanogroove-modified MEAs exhibited aligned neural processes due to the anisotropic surface features and expressed vivid spiking behavior and higher burst frequency compared to randomly cultured neuronal networks. In conclusion, the proposed fabrication technique integrates nanogrooves with commercial MEAs using a combination of microtransfer molding and photolithography, resulting in modified culture substrates that enhance spike activity and network organization, aiding in the development of more in vivo-like neural models. Full article
(This article belongs to the Special Issue Microfluidics in Biomedical Research)
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19 pages, 1328 KB  
Article
Evaluation of the Potential of a Fast-Curing Polymer Bioadhesive Hydrogel for Corneal Defect Repair
by Zohreh Arabpour, Soheil Sojdeh, Amirhosein Panjipour, Zahra Bibak Bejandi, Amal Yaghmour, Miranda Castillo, Anwar N. Khandaker, Mohammad Soleimani and Ali R. Djalilian
Gels 2026, 12(5), 357; https://doi.org/10.3390/gels12050357 - 23 Apr 2026
Viewed by 87
Abstract
Corneal defects are a major cause of vision loss and require rapid, biocompatible, and effective sealing methods to restore ocular integrity and prevent infection. Current clinical adhesives, such as cyanoacrylate and fibrin glue, are limited by problems such as poor biocompatibility and inadequate [...] Read more.
Corneal defects are a major cause of vision loss and require rapid, biocompatible, and effective sealing methods to restore ocular integrity and prevent infection. Current clinical adhesives, such as cyanoacrylate and fibrin glue, are limited by problems such as poor biocompatibility and inadequate stability. This study presents the design and evaluation of a fast-curable polymer bioadhesive hydrogel, a corneal glue formulated for efficient sealing of corneal defects. Hydrogels were synthesized from natural and synthetic polymers, including polyvinyl alcohol (PVA), sodium alginate (SA), and carboxymethyl cellulose (CMC), optimized for rapid gelation (~45 s), robust adhesion (~15 kPa), and mechanical strength (tensile strength ~0.35 MPa and storage modulus G′ indicating strong elastic behavior). Physicochemical and rheological properties, including swelling behavior and optical transparency (>90% transmittance across 400–700 nm), were characterized, including gelation time, swelling behavior, and mechanical strength. In vitro biocompatibility was assessed using human corneal epithelial cells to evaluate cytotoxicity and cell adhesion. Ex vivo studies on human cadaveric corneas with full-thickness defects measured adhesive strength and sealing efficacy through burst pressure (~38 mmHg) and leakage tests, with comparisons to commercial fibrin and cyanoacrylate adhesives. The optimized corneal glue exhibited fast curing, robust adhesion, high water retention with minimal swelling, favorable viscoelastic properties, and excellent cytocompatibility effectively sealing corneal defects in ex vivo models. These results highlight its potential as a promising fast-curable bioadhesive for corneal wound repair and ocular surface restoration. Full article
(This article belongs to the Special Issue Biofunctional Hydrogels for Biofabrication in Tissue Engineering)
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19 pages, 1052 KB  
Review
Polymeric Nanogels for Skin Applications
by Sara Silva, Manuela Machado and Eduardo M. Costa
Gels 2026, 12(5), 354; https://doi.org/10.3390/gels12050354 - 23 Apr 2026
Viewed by 80
Abstract
Chronic skin inflammatory diseases including psoriasis and atopic dermatitis affect millions worldwide, imposing substantial physical, psychological, and economic burdens. Despite advances in topical therapies, conventional formulations suffer from poor skin penetration, rapid clearance, local and systemic side effects, and suboptimal patient adherence. Polymeric [...] Read more.
Chronic skin inflammatory diseases including psoriasis and atopic dermatitis affect millions worldwide, imposing substantial physical, psychological, and economic burdens. Despite advances in topical therapies, conventional formulations suffer from poor skin penetration, rapid clearance, local and systemic side effects, and suboptimal patient adherence. Polymeric nanogels, internally crosslinked three-dimensional polymer networks with dimensions of 10–200 nm, emerged as promising platforms to overcome these limitations. Their unique properties including high water content, tunable porosity, biocompatibility, deformability, and stimulus-responsive behavior enhance skin penetration allowing for targeted therapeutic action. This review examines nanogel synthesis methods optimized for targeting skin inflammatory diseases, including biopolymer-based approaches utilizing chitosan and hyaluronic acid, offering insights into how different methods and advanced architecture provide multifunctional capacities and bioactivities. Translation challenges including manufacturing scalability, long-term safety assessment, and regulatory compliance are critically discussed alongside emerging opportunities in personalized medicine and smart microneedle integrated systems for adaptive therapy. Full article
42 pages, 3811 KB  
Review
Additive Manufacturing of Ceramics and Ceramic-Based Composites: Processing, Properties, and Engineering Applications
by Subin Antony Jose, John Crosby and Pradeep L. Menezes
Ceramics 2026, 9(5), 43; https://doi.org/10.3390/ceramics9050043 - 22 Apr 2026
Viewed by 281
Abstract
Ceramics are widely evaluated for their extreme hardness, high-temperature stability, and corrosion resistance, which enable applications in harsh service environments. However, these same properties, high melting points, brittleness, and low thermal shock resistance, make conventional manufacturing of complex ceramic components difficult and expensive. [...] Read more.
Ceramics are widely evaluated for their extreme hardness, high-temperature stability, and corrosion resistance, which enable applications in harsh service environments. However, these same properties, high melting points, brittleness, and low thermal shock resistance, make conventional manufacturing of complex ceramic components difficult and expensive. Traditional processes often require costly diamond tooling or energy-intensive sintering and tend to produce only simple geometries, with significant waste material and risk of defects. Additive manufacturing (AM) has recently emerged as a promising route to fabricate intricate, near-net-shape ceramic parts without these drawbacks. By building components layer by layer, AM reduces the need for extensive machining and enables the fabrication of geometrically complex, near-net-shape ceramic structures with reduced material waste, although challenges such as porosity, interlayer defects, and cracking during post-processing remain. Nonetheless, ceramic AM technologies lag behind their metal and polymer counterparts, and significant challenges remain in achieving fully dense parts with reliable mechanical properties. This review provides an in-depth overview of the state of the art in ceramics and ceramic composite additive manufacturing. We detail the most widely used AM processes (stereolithography, binder jetting, material extrusion, powder bed fusion, inkjet printing, and direct energy deposition) and typical feedstock formulations for each technique. We examine the resulting mechanical properties (strength, toughness, hardness, wear resistance) and functional properties (thermal stability, dielectric behavior, biocompatibility) of additively manufactured ceramics, and discuss their current and potential engineering applications in the aerospace, defense, automotive, biomedical, and energy sectors. Persistent challenges, including porosity, shrinkage and cracking during sintering, achieving uniform microstructures, high process costs, and scalability issues, are analyzed, and we highlight promising future directions such as multi-material grading, integration of machine learning for process optimization, and sustainable manufacturing approaches. Despite significant progress, challenges remain in achieving fully dense structures, improving process reliability, and scaling ceramic AM for industrial applications, highlighting the need for further research in process optimization, material design, and multi-material integration. Full article
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35 pages, 3267 KB  
Review
Iron-Based Nanoparticles as Delivery Tools
by Keykavous Parang, Rajesh Vadlapatla, Ajoy Koomer, Victoria Moran, Lanie Jackson and Amir Nasrolahi Shirazi
Pharmaceuticals 2026, 19(5), 654; https://doi.org/10.3390/ph19050654 - 22 Apr 2026
Viewed by 230
Abstract
Iron-based nanoparticles, particularly iron oxide nanostructures (IONPs), have emerged as versatile and clinically relevant platforms for drug delivery and theranostic applications. Among these, superparamagnetic iron oxide nanoparticles (SPIONs), including magnetite (Fe3O4) and maghemite (γ-Fe2O3), are [...] Read more.
Iron-based nanoparticles, particularly iron oxide nanostructures (IONPs), have emerged as versatile and clinically relevant platforms for drug delivery and theranostic applications. Among these, superparamagnetic iron oxide nanoparticles (SPIONs), including magnetite (Fe3O4) and maghemite (γ-Fe2O3), are the most extensively investigated due to their biocompatibility, magnetic responsiveness, and established safety profiles. Their unique superparamagnetic behavior enables external magnetic-field-guided targeting, magnetic resonance imaging (MRI) contrast enhancement, and magnetically triggered hyperthermia, enabling simultaneous diagnosis and therapy. Surface functionalization with polymers, silica, lipids, peptides, and biomolecules further improves colloidal stability, circulation time, targeting specificity, and controlled drug release. Core–shell architectures and multifunctional hybrid systems have expanded the therapeutic scope of iron nanoparticles, integrating chemotherapy, gene delivery, photothermal therapy, and Fenton reaction–mediated catalytic therapy. Despite promising preclinical outcomes, challenges remain regarding long-term biosafety, oxidative stress induction, biodistribution, large-scale reproducibility, and regulatory translation. This review summarizes the physicochemical properties, synthesis strategies, surface-engineering approaches, drug-loading mechanisms, and biomedical applications of iron-based nanoparticles, highlighting recent advances in multifunctional and peptide-functionalized systems. Critical considerations for clinical translation and future perspectives in precision nanomedicine are also discussed. Full article
(This article belongs to the Collection Feature Review Collection in Biopharmaceuticals)
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13 pages, 1563 KB  
Review
Preparation and Biomedical Applications of Spherical Cellulose Hydrogels: A Mini-Review
by Kaiqing Yang, Juping Zheng, Shiquan Shen, Chao Li, Yuzhu Song and Yichen Tian
Gels 2026, 12(5), 349; https://doi.org/10.3390/gels12050349 - 22 Apr 2026
Viewed by 235
Abstract
As the most abundant natural polymer on Earth, cellulose offers distinct advantages including renewability, biocompatibility, and modifiability. Among its various morphologies, spherical cellulose hydrogels (SCHs) represent a particularly versatile form ranging from micrometer to millimeter scales. They possess a unique hydrophilic 3D network, [...] Read more.
As the most abundant natural polymer on Earth, cellulose offers distinct advantages including renewability, biocompatibility, and modifiability. Among its various morphologies, spherical cellulose hydrogels (SCHs) represent a particularly versatile form ranging from micrometer to millimeter scales. They possess a unique hydrophilic 3D network, excellent flowability, high specific surface area, and outstanding mechanical stability, demonstrating great potential for biomedical applications. This mini-review highlights the primary bottom-up fabrication strategies for SCHs, including dripping, spraying, emulsion, and microfluidics, and the mechanisms by which different fabrication processes regulate their size, morphology, and structure are elucidated. On this basis, the recent advancements in SCHs across key biomedical domains, specifically in chromatographic separation, controlled drug delivery, tissue engineering, and wound healing, are discussed. Finally, the current challenges and future directions in this field are summarized and predicted, aiming to provide a reference for the development and application of high-performance cellulose-based biomaterials. Full article
(This article belongs to the Special Issue Cellulose Gels: Preparation, Properties and Applications)
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24 pages, 5670 KB  
Review
4D Printing in Biomedical Implants and Functional Healthcare Devices
by Muhammad Shafiq and Liaqat Zeb
J. Funct. Biomater. 2026, 17(4), 203; https://doi.org/10.3390/jfb17040203 - 20 Apr 2026
Viewed by 430
Abstract
Four-dimensional (4D) printing integrates additive manufacturing with stimuli-responsive materials to fabricate biomedical implants and functional healthcare devices that undergo programmed, time-dependent changes in shape or function. Unlike static 3D-printed constructs, 4D-printed systems can respond to clinically relevant stimuli such as temperature, hydration, pH, [...] Read more.
Four-dimensional (4D) printing integrates additive manufacturing with stimuli-responsive materials to fabricate biomedical implants and functional healthcare devices that undergo programmed, time-dependent changes in shape or function. Unlike static 3D-printed constructs, 4D-printed systems can respond to clinically relevant stimuli such as temperature, hydration, pH, light (including near-infrared), magnetic fields, or electrical inputs. These triggers drive defined actuation mechanisms, most commonly thermomechanical shape-memory recovery, swelling-induced morphing, and magnetothermal activation. This review synthesizes the principal material platforms used for biomedical 4D printing, including shape-memory polymers and alloys, hydrogels, liquid-crystal elastomers, and responsive composites, and links material choice to device behavior and translational feasibility. Applications are discussed across self-expanding stents, cardiac occluders, tissue-engineered constructs, implantable drug delivery systems, and adaptive wearables. Key translational challenges include sterilization compatibility, manufacturing reproducibility and quality control, safe stimulus delivery, predictable biodegradation and long-term biocompatibility, and regulatory pathway definition. Full article
(This article belongs to the Section Biomaterials and Devices for Healthcare Applications)
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29 pages, 11237 KB  
Article
Binary/Ternary Composites with Applications in Tissue Engineering
by Luminita Nastas, Roxana Cristina Popescu, Sorin Ion Jinga and Cristina Busuioc
Macromol 2026, 6(2), 26; https://doi.org/10.3390/macromol6020026 - 20 Apr 2026
Viewed by 124
Abstract
This study focuses on the development and characterization of advanced composite materials based on poly(ε-caprolactone) (PCL) and poly(vinylidene fluoride) (PVDF), with or without silver nanoparticles (AgNPs), planned for peripheral nerve or bone regeneration. The complementary properties of PCL (biocompatibility and biodegradability) [...] Read more.
This study focuses on the development and characterization of advanced composite materials based on poly(ε-caprolactone) (PCL) and poly(vinylidene fluoride) (PVDF), with or without silver nanoparticles (AgNPs), planned for peripheral nerve or bone regeneration. The complementary properties of PCL (biocompatibility and biodegradability) and PVDF (mechanical stability and piezoelectric functionality) were exploited by blending the polymers in different ratios, resulting in binary (PCL/PVDF) and ternary (PCL/PVDF/AgNPs) composites. Green-synthesized AgNPs were integrated to enhance antimicrobial activity and to support tissue repair through improved signal transmission. Functional thin films and electrospun fibres were obtained and subjected to advanced characterization techniques, including scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and thermal analysis. The results demonstrated appropriate morphology, chemical composition, structural stability, and favourable interactions with simulated physiological media. Preliminary biocompatibility assays confirmed good cell viability, supporting the biomedical applicability of the designed scaffolds. Overall, the obtained results highlight the potential of AgNPs-functionalized PCL/PVDF binary and ternary composites as promising candidates for flexible, durable, and bioactive implants in peripheral nerve or bone regeneration. Full article
26 pages, 19775 KB  
Article
Composite Materials Based on L-Polylactide with Titanium or Titanium Dioxide Nanoparticles: Dark Antibacterial Activity Through ROS Generation
by Dmitriy E. Burmistrov, Pavel A. Ivliev, Dmitriy A. Serov, Ilya V. Baimler, Alexander V. Simakin, Sergei O. Liubimovskii, Maxim E. Astashev, Valeriy A. Kozlov, Alena A. Nastulyavichus, Guliya R. Nizameeva, Fatikh M. Yanbaev and Sergey V. Gudkov
J. Compos. Sci. 2026, 10(4), 214; https://doi.org/10.3390/jcs10040214 - 19 Apr 2026
Viewed by 418
Abstract
Modification of PLA with functional nanoparticles is a promising approach for imparting new properties to the material. In this work, titanium nanoparticles (Ti NPs) and titanium dioxide nanoparticles (TiO2 NPs) were synthesized by laser ablation and characterized by dynamic light scattering, spectrophotometry, [...] Read more.
Modification of PLA with functional nanoparticles is a promising approach for imparting new properties to the material. In this work, titanium nanoparticles (Ti NPs) and titanium dioxide nanoparticles (TiO2 NPs) were synthesized by laser ablation and characterized by dynamic light scattering, spectrophotometry, and transmission electron microscopy. The average hydrodynamic diameter of Ti NPs was 12 nm, while that of TiO2 NPs was 24 nm; both dispersions possessed a positive zeta potential (23–27 mV) and spherical morphology. L-PLA composite films containing 0.1 wt.% Ti NPs or TiO2 NPs were obtained by solution casting. Atomic force and modulation-interference microscopy confirmed the uniform distribution of nanoparticles within the polymer matrix, although partial aggregation was observed. The introduction of TiO2 NPs increased the water contact angle. Mechanical testing revealed a significant reinforcing effect: the addition of 0.1 wt.% NPs increased the Young’s modulus by 62–68% and the ultimate tensile strength by 16–18% while maintaining a ductile fracture pattern with elongation at break up to ~8%. Both types of composites generated reactive oxygen species (ROS) in aqueous solutions: Ti NPs increased H2O2 production by 5.5 times and TiO2 NPs by 4.9 times, and they also induced the formation of hydroxyl radicals. The accumulation of 8-oxoguanine in DNA and long-lived oxidized protein species confirmed the materials’ ability to cause oxidative damage to biomacromolecules. For E. coli, growth inhibition reached 40.5% (for composites with Ti NPs) and 71% (for composites with TiO2 NPs). The effect was even more pronounced for S. aureus, where inhibition levels were approximately 70% and 80%, respectively; flow cytometry confirmed the strong bactericidal effect, showing that materials containing TiO2 NPs increased the proportion of dead cells to 25% for E. coli and ~68% for S. aureus. Cytotoxicity assessment on human fibroblasts (HSF) demonstrated the high biocompatibility of neat L-PLA and composites with Ti NPs (viability > 95%) and with TiO2 NPs (viability ~93%). The obtained results indicate that L-PLA-based composites with Ti NPs and TiO2 NPs exhibit pronounced ROS-mediated antibacterial activity without additional UV irradiation. These findings position these materials as highly promising candidates for active biodegradable food packaging to extend shelf-life and for biomedical devices, such as wound dressings and implants, where reducing the risk of bacterial colonization is critical. Full article
(This article belongs to the Special Issue The Properties and Applications of Advanced Functional Biocomposites)
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14 pages, 1370 KB  
Technical Note
Personalized 3D-Printed Hybrid PDMS and PEEK Implants for Revisional Orbitomaxillary Reconstruction: A Translational Case-Based Technical Note
by Goran Marić, Darko Solter, Blanka Doko Mandić, Jelena Škunca Herman, Zoran Vatavuk, Damir Godec, Davor Vagić and Alan Pegan
J. Funct. Biomater. 2026, 17(4), 197; https://doi.org/10.3390/jfb17040197 - 18 Apr 2026
Viewed by 384
Abstract
The reconstruction of complex orbitomaxillary defects requires biomaterials that can simultaneously provide structural stability, biocompatibility, and accurate restoration of facial volume and contour. While rigid polymers such as polyetheretherketone (PEEK) offer reliable mechanical support, they do not adequately replicate the viscoelastic behavior of [...] Read more.
The reconstruction of complex orbitomaxillary defects requires biomaterials that can simultaneously provide structural stability, biocompatibility, and accurate restoration of facial volume and contour. While rigid polymers such as polyetheretherketone (PEEK) offer reliable mechanical support, they do not adequately replicate the viscoelastic behavior of soft tissues. This report presents a translational revision case employing a personalized hybrid biomaterial approach that combines a 3D-printed PEEK implant for structural orbital floor support with a patient-specific polydimethylsiloxane (PDMS) implant for malar volumetric augmentation. Reconstruction was planned using CT segmentation and contralateral mirroring. Patient-specific implants were subsequently designed using CAD/CAM techniques, combining a rigid PEEK implant for structural orbital support with a flexible PDMS implant for malar volumetric augmentation with complementary mechanical properties. Revision surgery included the removal of inadequately positioned titanium hardware, the release of incarcerated extraocular muscles, and the restoration of orbital anatomy and facial symmetry. Postoperative imaging demonstrated stable implant positioning and sustained orbitomaxillary stability. Despite successful anatomical reconstruction, residual functional sequelae, including strabismus related to the severity of the initial orbital trauma, persisted and were addressed separately in a staged manner, resulting in satisfactory ocular alignment and resolution of diplopia in primary gaze. This case underscores the complementary functional roles of rigid and elastic polymers and highlights the translational potential of PDMS as a permanent, patient-specific implant material for volumetric and contour restoration in craniofacial reconstruction. Full article
(This article belongs to the Special Issue Three-Dimensional Printing and Biomaterials for Medical Applications)
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19 pages, 3835 KB  
Article
Reinforcement of Thermo-Compressed Sodium Alginate Films with Calcium Alginate Powder
by Prasong Srihanam, Wilaiwan Simchuer, Vanseng Chounlamany, Kesiny Phomkeona, Phengxay Deevanhxay and Yodthong Baimark
Mar. Drugs 2026, 24(4), 142; https://doi.org/10.3390/md24040142 - 17 Apr 2026
Viewed by 434
Abstract
Alginate is a biocompatible and biodegradable polymer derived from seaweed. It has been extensively researched and developed for various applications. However, its poor mechanical properties present a significant drawback that limits its use in multiple fields. Furthermore, the fabrication of reinforced alginate films [...] Read more.
Alginate is a biocompatible and biodegradable polymer derived from seaweed. It has been extensively researched and developed for various applications. However, its poor mechanical properties present a significant drawback that limits its use in multiple fields. Furthermore, the fabrication of reinforced alginate films using conventional melt processing has the potential for scaling up production. This study aimed to enhance the mechanical properties of sodium alginate (SA) films by incorporating calcium alginate (CA) powder. The SA/CA biocomposite films were created using a thermo-compression technique, with glycerol acting as a plasticizer for the SA matrix. Various CA contents—2.5, 5, 10, and 20 wt%—were investigated. Scanning electron microscopy and energy dispersive spectroscopy revealed good interfacial adhesion between the SA film matrix and the CA powder. As the CA content increased, the moisture content of SA/CA biocomposite films decreased. The addition of CA powder significantly improved the tensile properties of the SA films. Based on the tensile test, SA/CA biocomposite films with 20 wt% CA powder exhibited a maximum tensile strength of 11.7 MPa and a Young’s modulus of 234.7 MPa. These results indicate a substantial increase of 208% in maximum tensile strength and 907% in Young’s modulus compared to SA films without CA. These findings indicated that the CA powder serves as an effective reinforcing filler for thermo-compressed SA films, which could lead to the development of high-strength alginate-based products for potential use in various applications, including biomedical, agricultural, and packaging applications. Full article
(This article belongs to the Special Issue Marine Polysaccharides-Based Biomaterials)
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32 pages, 1953 KB  
Review
Electrospinning of Natural Polymeric Fibers with Essential Oils for the Control of Multidrug-Resistant Pathogens
by Deysi Alejandrina Cabrera Segura, Verónica Santacruz Vázquez, Sandra Mendoza, Santa Toxqui-López, Paulina Arellanes-Lozada and Claudia Santacruz Vázquez
Polymers 2026, 18(8), 972; https://doi.org/10.3390/polym18080972 - 16 Apr 2026
Viewed by 406
Abstract
Antimicrobial resistance (AMR) represents one of the major threats to global health, driven by the indiscriminate use of antibiotics and decline in the development of new therapeutic agents. In this context, essential oils (EOs) have emerged as innovative natural alternatives due to their [...] Read more.
Antimicrobial resistance (AMR) represents one of the major threats to global health, driven by the indiscriminate use of antibiotics and decline in the development of new therapeutic agents. In this context, essential oils (EOs) have emerged as innovative natural alternatives due to their broad-spectrum antimicrobial activity and low potential to induce bacterial resistance. However, their clinical application is limited by their volatility, low chemical stability, and rapid degradation. The incorporation of EOs into electrospun natural polymer fibers has emerged as an effective strategy to overcome these limitations, improving their stability, enabling controlled release, and enhancing their antimicrobial efficiency. This review focuses on the use of electrospun natural polymers for biomedical applications, highlighting their biocompatibility, biodegradability, and ability to mimic the extracellular matrix, thereby promoting cell interaction. Additionally, their high surface area and porous structure facilitate efficient encapsulation and controlled release of bioactive compounds. Recent advances in the development of these systems against clinically relevant multidrug-resistant pathogens are analyzed, along with the antimicrobial mechanisms of EOs. Finally, the factors influencing encapsulation and release efficiency, as well as the main challenges and future perspectives for clinical translation, are discussed. Full article
(This article belongs to the Special Issue Recent Advances in Electrospun Polymer Nanofibers)
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22 pages, 3994 KB  
Article
Aromatic Tricyanoethylenes a New Class of ‘Compact’ Photoinitiators for One- and Two-Photon Photopolymerization
by Elnara R. Zhiganshina, Tatyana S. Lyubova, Anastasia E. Tarakanova, Maxim V. Arsenyev, Roman S. Kovylin, Natalia D. Anisimova, Yuri V. Polushtaytsev, Konstantin A. Kozhanov, Anastasia V. Pisarenko, Diana Ya. Aleynik, Marfa N. Egorikhina, Alexei Vitukhnovsky, Larisa G. Klapshina and Sergey A. Chesnokov
Polymers 2026, 18(8), 958; https://doi.org/10.3390/polym18080958 - 14 Apr 2026
Viewed by 429
Abstract
In this paper, we consider a series of new compact A-π-D photoinitiators consisting of donor aromatic fragments (naphthalene, anthracene, phenanthrene, pyrene and perylene) and a strong acceptor tricyanoethylene group—aryltricyanoethylenes (ArTCNEs). Spectral, photophysical, and electrochemical characteristics of ArTCNEs are studied. One-photon (with LED@405 nm) [...] Read more.
In this paper, we consider a series of new compact A-π-D photoinitiators consisting of donor aromatic fragments (naphthalene, anthracene, phenanthrene, pyrene and perylene) and a strong acceptor tricyanoethylene group—aryltricyanoethylenes (ArTCNEs). Spectral, photophysical, and electrochemical characteristics of ArTCNEs are studied. One-photon (with LED@405 nm) and two-photon (λ = 780 nm, impulse duration of 100 fs) photopolymerization of PETA can be effectively initiated by ArTCNEs with the tertiary amine N,N-dimethylcyclohexylamine DMCHA and/or the iodonium salt diphenyliodonium chloride Iod. Based on results of experiments on photodegradation, photopolymerization and EPR spectroscopy, a photoinitiation mechanism of radical photopolymerization was proposed for two-component (AntTCNE/DMCHA) and three-component (AntTCNE/DMCHA/Iod) initiating systems. The composition containing PerTCNE/DMCHA as a photoinitiator demonstrated the best reactivity under two-photon nanolithography conditions: the polymerization threshold was 2 mW at a laser beam scanning speed of 100 μm/s, and the widest fabrication window of 11 mW was typical for it. As an example, 3D “cage” structures were fabricated using the AntTCNE-based composition, and the test structure resolution parameters, such as the minimum line width and the distance between lines of 80 and 400 nm, respectively, were achieved. MTT experiments with human dermal fibroblasts showed promising preliminary biocompatibility of the resulting polymers, which opens up possibilities for using the obtained materials in biological applications. Full article
(This article belongs to the Special Issue Photopolymerization: Materials, Applications and Challenges)
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21 pages, 1322 KB  
Review
Synthetic-Polymer-Based Cardiac Patches for MI-Induced Heart Failure Treatment: A Review
by Ahmed Eliwa, Mohamed K. Abbas, Maryam Al-Ejji, Khadija Zadeh and Hamda Aboujassoum
Biomolecules 2026, 16(4), 580; https://doi.org/10.3390/biom16040580 - 14 Apr 2026
Viewed by 442
Abstract
Myocardial infarction (MI) is one of the prevalent cardiovascular diseases, which is caused by obstruction of one or more coronary arteries, leading to cardiac tissue ischemia and death. One of the main consequences of MI is heart failure, which is defined as dysfunction [...] Read more.
Myocardial infarction (MI) is one of the prevalent cardiovascular diseases, which is caused by obstruction of one or more coronary arteries, leading to cardiac tissue ischemia and death. One of the main consequences of MI is heart failure, which is defined as dysfunction of the heart muscle to pump blood into peripheral organs. Cardiac patches have drawn a lot of interest as a potentially effective way to restore damaged cardiac tissue and enhance its functionality. They are polymer-based scaffolds designed to be implanted on the heart surface, and they have shown a significant therapeutic effect in the treatment of MI by improving cardiac function and providing mechanical support for the infarction site by the delivery of various bioactive substances or cells. Several biomaterials with specific mechanical and chemical characteristics have been widely used as a scaffold in the process of fabricating cardiac patches. In this study, we focus on the latest developments in the manufacturing of synthetic-polymer-based cardiac patches used to treat heart failure induced by myocardial infarction. We describe the mechanical and chemical characteristics of several synthetic polymers and highlight the main benefits and drawbacks of each type. An overview of the major challenges and the future development directions in the field of cardiac patches is also highlighted. Full article
(This article belongs to the Section Bio-Engineered Materials)
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37 pages, 8993 KB  
Review
Self-Assembling Short Peptide Carriers for Gene Delivery
by Longyu An, Zhanyao Xu and Xiaoming Zhang
Int. J. Mol. Sci. 2026, 27(8), 3464; https://doi.org/10.3390/ijms27083464 - 12 Apr 2026
Viewed by 827
Abstract
Gene therapy relies on safe and efficient delivery systems, yet traditional viral vectors and synthetic polymers often fail to meet these requirements due to immunogenicity and biocompatibility concerns. This review highlights self-assembling short peptides as a highly programmable and biocompatible non-viral platform uniquely [...] Read more.
Gene therapy relies on safe and efficient delivery systems, yet traditional viral vectors and synthetic polymers often fail to meet these requirements due to immunogenicity and biocompatibility concerns. This review highlights self-assembling short peptides as a highly programmable and biocompatible non-viral platform uniquely positioned to overcome these translational bottlenecks. To provide a comprehensive overview of next-generation gene delivery, we systematically trace the trajectory from fundamental chemistry to clinical applications. First, we elucidate the supramolecular interactions and mechanisms driving peptide–nucleic acid co-assembly. Second, we outline concrete design strategies, detailing how sequence engineering and environmental responsiveness dictate the formation of optimized nanomorphologies. Third, we critically analyze how these nanocarriers navigate critical physiological and intracellular barriers, with a specific focus on cellular uptake, endosomal escape, and cargo release. Finally, we demonstrate the platform’s versatility in emerging frontiers, particularly mRNA vaccines and CRISPR/Cas9 gene editing. We conclude by identifying current obstacles to clinical translation and proposing future directions centered on multifunctional integration and stimuli-responsive design. Full article
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