Search Results (17,929)

The CRISPR-Cas9 technology, one of the groundbreaking genome editing methods for addressing genetic disorders, has emerged as a powerful, precise, and efficient tool. However, its clinical translation remains hindered by challenges in delivery efficiency and targeting specificity. This review provides a comprehensive analysis of the structural features, advantages, and potential applications of various non-viral and stimuli-responsive systems, examining recent progress to emphasize the potential to address these limitations and advance CRISPR-Cas9 therapeutics. We describe how recent reports emphasize that nonviral vectors, including lipid-based nanoparticles, extracellular vesicles, polymeric nanoparticles, gold nanoparticles, and mesoporous silica nanoparticles, can offer diverse advantages to enhance stability, cellular uptake, and biocompatibility, based on their structures and physio-chemical stability. We also summarize recent progress on stimuli-responsive nanoformulations, a type of non-viral vector, to introduce precision and control in CRISPR-Cas9 delivery. Stimuli-responsive nanoformulations are designed to respond to pH, redox states, and external triggers, facilitate controlled and targeted delivery, and minimize off-target effects. The insights in our review suggest future challenges for clinical applications of gene therapy technologies and highlight the potential of delivery systems to enhance CRISPR-Cas9’s clinical efficacy, positioning them as pivotal tools for future gene-editing therapies. Full article

Surface acoustic wave-based (SAW) sensors are of great interest due to their high sensibility and fast and stable responses. They can be obtained at an overall low cost and with an intuitive and easy-to-use method. The chemical sensitization of a piezoelectric transducer plays a key role in defining the properties of SAW sensors. In this study, we investigate the structural and adhesion properties of a new class of coating material based on polyurethane polymeric composites. We used dark-field microscopy (DFM) and scanning electron microscopy (SEM) to observe the microstructure of polyurethane composite coatings on piezoelectric sensor elements and to analyze the effects of the chemical resistance and adhesion test (CAT) on the coating layers obtained with the polyurethane polymeric composites. The results of the microscopy showed that all polyurethane composite coatings exhibited excellent uniformity and stability after chemical adherence testing (CAT). All of the observations were correlated with the results of the ultrasonic analysis, which demonstrated the role of polyurethane as a binder to form the stable structure of the composites and, at the same time, as an adhesion promoter, increasing the chemical resistance and the adherence of the coating layer to the complex surface of the piezoelectric sensor element. Full article

Carbon nitrides are polymeric materials with a broad range of applications, including photocatalysis. Among them, graphitic carbon nitride (g-C₃N₄), a low-cost material, is an excellent photocatalyst under visible light irradiation owing to its features such as correct band positions, high stability and non-toxicity. g-C₃N₄ is a metal-free material that is easily synthesized by polymerizing nitrogen-rich compounds and is an efficient heterogeneous catalyst for many reaction procedures due to its distinctive electronic structure and the benefits of the mesoporous texture. In addition, in situ or post-modification of g-C₃N₄ can further improve catalytic performance or expand its application for remediating environmental pollution. Water pollution from organic compounds such as pesticides and pharmaceuticals is increasing dramatically and is becoming a serious problem around the world. These pollutants enter water supplies in a variety of ways, including industrial and hospital wastewater, agricultural runoff, and chemical use. To solve this problem, photocatalysis is a promising technology. Without the use of other oxidative chemicals, g-C₃N₄ uses renewable solar energy to transform harmful pollutants into harmless products. As a result, much recent research has focused on the photocatalytic activity of g-C₃N₄ for wastewater treatment. For this reason, the main objective of this paper is to contribute a chronological overview of the bibliometrics on g-C₃N₄ for the removal of pesticides and pharmaceuticals from water using the tools BibExcel, Bibliometrix and R-Studio IDE. A bibliometric analysis was performed using the Science Citation Index Expanded (WoS^©) database to analyze the scientific literature published in the field over the last 10 years. The results were used to identify limitations and guide future research. Full article

This paper presents a simple, post-synthesis treatment of carbon dots (C-dots) that relies on the oxidizing activity of sodium hypochlorite to induce surface oxidation, etching and pronounced structural rearrangements. The thus treated C-dots (ox-C-dots) exhibit up to six-fold enhancement in quantum yield compared to non-oxidised analogues, while maintaining low levels of cytotoxicity against HeLa and U87 cell lines. In addition, we demonstrate that a range of polymeric materials (polyurethane sponge, polyvinylidene fluoride membrane, polyester fabric) impregnated with ox-C-dots show advanced antifungal properties against Talaromyces pinophilus, while their untreated counterparts fail to do so. Full article

Step emulsification (SE) is renowned for its robustness in generating monodisperse emulsion droplets at arrayed nozzles. However, few studies have explored poly(dimethylsiloxane) (PDMS)-based SE devices for producing monodisperse oil-in-water (O/W) droplets and polymeric microspheres with diameters below 20 µm—materials with broad applicability. In this study, we present a PDMS-based microfluidic SE device designed to achieve this goal. Two devices with 264 nozzles each were fabricated, featuring straight and triangular nozzle configurations, both with a height of 4 µm and a minimum width of 10 µm. The devices were rendered hydrophilic via oxygen plasma treatment. A photocurable acrylate monomer served as the dispersed phase, while an aqueous polyvinyl alcohol solution acted as the continuous phase. The straight nozzles produced polydisperse droplets with diameters exceeding 30 µm and coefficient-of-variation (CV) values above 10%. In contrast, the triangular nozzles, with an opening width of 38 µm, consistently generated monodisperse droplets with diameters below 20 µm, CVs below 4%, and a maximum throughput of 0.5 mL h⁻¹. Off-chip photopolymerization of these droplets yielded monodisperse acrylic microspheres. The low-cost, disposable, and scalable PDMS-based SE device offers significant potential for applications spanning from laboratory-scale research to industrial-scale particle manufacturing. Full article

This study investigates the synthesis and application of acrylic–urethane hybrid polymer dispersions as advanced binders for leather finishing. Two polymerization techniques—seeded emulsion and miniemulsion—were used to produce hybrid polymer dispersions by varying the ratios of polyurethane (PU) and acrylic (AC). The synthesized dispersions, i.e., the hybrid polyurethanes, showed stable, uniform particle sizes, inferring good compatibility and interaction between the PU and AC phases, as confirmed by particle sizes, FTIR, and DSC analyses. The performance of the coating on leather surfaces was assessed by using standard physical tests, including rubbing fastness, flexing endurance, water spot resistance, and grain strength. The results showed that the hybrid polymers outperformed their individual PU and AC counterparts, particularly in terms of abrasion resistance and mechanical integrity. Of the two polymerization techniques, the seeded emulsion hybrids exhibited superior coating properties, providing greater resistance to cracking and abrasion under stress, improved grain strength, and better color retention during rubbing tests. These findings highlight the potential of acrylic–urethane hybrids, particularly those prepared via seeded emulsion polymerization, to address the limitations of traditional binders in high-performance leather applications. Full article

Protein tyrosine kinase 7 (PTK7), a catalytically defective receptor protein tyrosine kinase, is frequently upregulated in various cancers, including triple-negative breast cancer (TNBC), and is associated with poor clinical outcomes. Analysis of The Cancer Genome Atlas (TCGA) data confirmed that PTK7 mRNA expression is significantly higher in TNBC tumor tissues compared with adjacent normal tissues and non-TNBC breast cancer subtypes. Kaplan–Meier survival analysis demonstrated a strong correlation between high PTK7 expression and worse relapse-free survival in TNBC patients (HR = 1.46, p = 0.015). In vitro, anti-PTK7 monoclonal antibodies (mAbs) significantly reduced proliferation, wound healing, migration, and invasion in TNBC MDA-MB-231 cells. Ki-67 immunofluorescence assays revealed substantial decreases in cell proliferation following treatment with PTK7 mAbs (32-m, 43-m, 50-m, and 52-m). Moreover, actin polymerization, a critical process in cell migration and invasion, was markedly impaired upon PTK7 mAb treatment. In vivo, PTK7 mAbs significantly reduced tumor volume and weight in a TNBC xenograft mouse model compared with controls. Treated tumors exhibited decreased expression of Ki-67 and vimentin, indicating reduced proliferation and epithelial-to-mesenchymal transition. These findings highlight PTK7 as a promising therapeutic target in TNBC and demonstrate the potent anti-cancer effects of PTK7-neutralizing mAbs both in vitro and in vivo. Further exploration of PTK7-targeted therapies, including humanized mAbs and antibody-drug conjugates, is warranted to advance treatment strategies for PTK7-positive TNBC. Full article

Making transparent aromatic polymers with high T_g and low thermal expansion behavior, like glass, is challenging. We report transparent and soluble poly(amide-imide)s (PAIs) with high dimensional stability synthesized from the new monomer, trifluoromethylated trimellitic anhydride. Insertion of trifluoromethyl (CF₃) groups into polymer chains enhanced solubility and the optical properties of polymers without sacrificing high thermal stability. Model reactions were utilized to study how the CF₃ group in trimellitic anhydride affects the polymerization reaction with aromatic diamine monomers, and a series of new PAIs were synthesized. All the polymers were soluble in polar organic solvents and can be solution-cast into nearly colorless and flexible freestanding films. The obtained PAI films possessed high thermal stability (T_d5: 437–452 °C in N₂) and high transparency (84~87% transmittance at 550 nm). Interestingly, PAIs prepared in this study exhibited high thermodimensional stability with low CTE values from 9 to 26 ppm/°C. The transparent poly(amide-imide) film with low CTE value finds its application in display and optical devices that require flexible and transparent form factors. Full article

This study investigates the effects of the debranching time of waxy potato starch using pullulanase and recrystallization on particle morphology, debranching degree, and crystal structure. The results demonstrated that after gelatinization and debranching, the surface of the starch crystals became rough and uneven due to hydrolysis, with most particles showing a fragmented surface. The crystalline state was not significantly changed with debranching time. X-ray diffraction analysis revealed no significant differences in the patterns of recrystallized linear dextrin (LD) after various debranching times. Notably, the short-range ordered structure of LD after debranching and recrystallization was more organized than that of the original or gelatinized starch. Additionally, polarized light microscopy showed that the birefringent pattern disappeared as a result of debranching and recrystallization, indicating the breakdown of particle structure, although the overall particle morphology did not change significantly with varying debranching times. Furthermore, linear dextrin derived from starch debranched for 6 h (with pullulanase at 15 μg/g) successfully embedded stearic acid, oleic acid, and linoleic acid, forming a VI-type starch–fatty acid complex. Full article

Biodegradable and biocompatible polymeric materials and stimulus-responsive hydrogels are widely used in the pharmaceutical, agricultural, biomedical, and consumer sectors. The effectiveness of these formulations depends significantly on the appropriate selection of polymer support. Through chemical or enzymatic hydrolysis, these materials can gradually release bioactive agents, enabling controlled drug release. The objective of this work is to synthesize, characterize, and apply two controlled-release polymeric systems, focusing on the release of a phyto-pharmaceutical agent (herbicide) at varying pH levels. The copolymers were synthesized via free radical polymerization in solution, utilizing tetrahydrofuran (THF) as the organic solvent and benzoyl peroxide (BPO) as the initiator, without the use of a cross-linking agent. Initially, the herbicide was grafted onto the polymeric chains, and its release was subsequently tested across different pH environments in a heterogeneous phase using an ultrafiltration (UF) system. The development of these two controlled-release polymer systems aimed to measure the herbicide’s release across different pH levels. The goal is to adapt these materials for agricultural use, enhancing soil quality and promoting efficient water usage in farming practices. The results indicate that the release of the herbicide from the conjugate systems exceeded 90% of the bioactive compound after 8 days at pH 10 for both systems. Furthermore, the two polymeric systems demonstrated first-order kinetics for herbicide release in aqueous solutions at different pH levels. The kinetic constant was found to be higher at pH 7 and 10 compared to pH 3. These synthetic hydrogels are recognized as functional polymers suitable for the sustained release of herbicides in agricultural applications. Full article

In this study, we report the synthesis of amphiphilic hyperbranched poly[(2-dimethylaminoethyl methacrylate)-co-(benzyl methacrylate)] statistical copolymers with two different stoichiometric compositions using the reversible addition–fragmentation chain transfer polymerization (RAFT) technique. The selection of monomers was made to incorporate a pH and thermoresponsive polyelectrolyte (DMAEMA) component and a hydrophobic component (BzMA) to achieve amphiphilicity and study the effects of architecture and environmental factors on the behavior of the novel branched copolymers. Molecular characterization was performed through size exclusion chromatography (SEC) and spectroscopic characterization techniques (¹H-NMR and FT-IR). The self-assembly behavior of the hyperbranched copolymers in aqueous media, in response to variations in pH, temperature, and ionic strength, was studied using dynamic light scattering (DLS), electrophoretic light scattering (ELS), and fluorescence spectroscopy (FS). Finally, the efficacy of the two novel copolymers to encapsulate curcumin (CUR), a hydrophobic, polyphenolic drug with proven anti-inflammatory and fluorescence properties, was established. Its encapsulation was evaluated through DLS, UV–Vis, and fluorescence measurements, investigating the change of hydrodynamic radius of the produced mixed copolymer–CUR nanoparticles in each case and their fluorescence emission properties. Full article

This study investigates the stability and application of trithiocarbonate-based chain transfer agents (CTAs) in reversible addition–fragmentation chain transfer (RAFT) radical polymerization under harsh conditions. We evaluated the stability of 4-cyano-4-(2-carboxyethylthiothioxomethylthio) pentanoic acid (Rtt-17) and 4-cyano-4-(dodecylsulfanylthiocarbonyl) sulfanylpentanoic acid (Rtt-05) at 60 °C under basic conditions using ¹H NMR and UV–vis absorption spectra, showing that Rtt-05 is more stable than Rtt-17. The greater stability of Rtt-05 is attributed to the hydrophobic dodecyl group, which allows it to form micelles in water, thereby protecting the trithiocarbonate group from the surrounding aqueous phase. In contrast, hydrophilic Rtt-17, without long alkyl chains, cannot form micelles in water. Following the stability assessment, Rtt-17 and Rtt-05 were employed for RAFT polymerization of hydrophilic monomers, such as N,N-dimethylacrylamide (DMA) and 2-(methacryloyloxy)ethyl phosphorylcholine (MPC). DMA can dissolve in both water and organic solvents, and MPC can dissolve in water and polar solvents. Both CTAs successfully controlled the polymerization of DMA, producing polymers with narrow molecular weight distributions (M_w/M_n) less than 1.2. Also, Rtt-17 demonstrated effective control of MPC polymerization, yielding M_w/M_n values of around 1.2. However, during the polymerization of MPC, Rtt-05 failed to maintain control, resulting in a broad M_w/M_n (≥1.9). The inability of Rtt-05 to control MPC polymerization is due to the formation of micelles, which disrupts the interaction between the hydrophilic MPC propagating radicals and the trithiocarbonate group in the hydrophobic core of Rtt-05 micelles. The findings provide critical insights into designing CTAs for specific applications, particularly for biomedical and industrial uses of hydrophilic polymers, highlighting the potential for precise molecular weight control and tailored polymer properties. Full article

This research evaluated the effect of fermentation with Lactobacillus plantarum 11122, Lactobacillus casei 23184, and Lactobacillus lactis 1011 on structure, pasting, and in vitro digestion properties of glutinous rice starch varying in TN and HY genotype, respectively. The results showed that fermentation decreased the weight-average molecular weight and increased the radius of gyration. The short chain was increased by degrading the medium chain (B₂, DP 24−35) of amorphous in starch, which directly led to the increase of branching degree and rearrangement of the starch chain. LAB fermentation increases the short-range ordered structure, helix structure, and crystallinity by polymerization or interactions of short chains between intermolecular and intramolecular. Furthermore, the pasting characteristic of the fermented starch sample obtained obvious improvement in terms of hydration capacity, including breakdown and setback value. Fermentation facilitated the forming of both slowly digestible starch (17.1–30.79%) and resistant starch (32.3–46.8%) in TN but caused a decline in the content of rapidly digestible starch (25.47–43.6% in TN, 9.36–17.8% in HY). The result of Pearson’s correlation tests and PCA showed the variety of structural and physicochemical of fermentation-treated starch depend highly on the starter culture and starch resources. These results provided new data support for the potential application of modified starch by fermentation with LABs. Full article

Group 11 metals form with pyrazolate ligand complexes with a general formula of [MPz]_n. The value of “n” varies depending on the type of substituent in the ligand and the metal atom. Copper(I) and silver(I) ions mainly form cyclic di-, tri-, and tetra-nuclear complexes or polymeric structures. Cyclic trinuclear d¹⁰ metal pyrazolates [MPz^m]₃ (M = Cu(I) and Ag(I); Pz = substituted pyrazolate ligand) are of particular interest because their planar structure allows them to form supramolecular aggregates via noncovalent metal–metal, metal–π, and metal–electron donor interactions. Designing complexes based on these interactions has been a focus of research for the last two decades. The ability of cyclic trinuclear copper(I) and silver(I) pyrazolates to form coordination and supramolecular structures determines their properties and potential applications in catalysis, gas sensing, molecular recognition, and photoluminescence. In this review, we discuss noncovalent interactions between cyclic trinuclear silver(I) and copper(I) complexes with various types of ligands. Full article

This study evaluated the strength, hardness, and color stability of 3D-printed denture base resins and compared the outcome with conventional heat-cured denture base resins after aging by thermocycling. A total of 72 specimens from conventional and 3D-printed materials were fabricated in different shapes and dimensions based on the mechanical and color tests performed. The specimens were divided into five groups: flexural, tensile, and compressive strengths (n = 20), hardness, and color stability (n = 6). In all these groups, half of the specimens were stored in a distilled water bath at 37 °C for 24 h, and the remaining half of the specimens were subjected to aging by thermocycling. The 3D-printed specimens demonstrated the highest means of tensile strength (32.20 ± 3.8 MPa), compressive strength (106.31 ± 4.07 MPa), and Vickers hardness number (24.51 ± 0.36), and the lowest means of flexural strength (54.29 ± 13.17 MPa) and color difference (ΔE = 2.18 ± 1.09). Conventional heat-cured specimens demonstrated the highest means of flexural strength (59.96 ± 8.39 MPa) and color difference (ΔE = 4.74 ± 2.37) and the lowest means of tensile strength (32.17 ± 9.06 MPa), compressive strength (46.05 ± 4.98 MPa), and Vickers hardness number (10.42 ± 1.05). Aging significantly reduced the flexural strength (−27%), tensile strength (−44%), and hardness (−7%) of 3D-printed resins in contrast to the conventional resin’s compressive strength (−15%) and color stability (p < 0.05). The 3D-printed resin had comparable flexural and tensile strength and significantly superior compressive strength, hardness, and color stability compared with conventional resins. Aging significantly and negatively affected the flexural strength, tensile strength, and hardness of 3D-printed resin. Full article