Search Results (180)

This work aims to design versatile hybrids fabricated by poly(hydroxypropyl methacrylate-co-glycidyl methacrylate) gels loaded with pristine montmorillonite, P(HPMA-co-GMA)/Mmt, by varying the clay content. Insights into design of epoxy-functional hybrids were provided by combining in situ copolymerization reactions with solution mixing to evaluate the effect of aluminosilicate addition on structure–property changes in (alkyl)methacrylate-based gels. Comprehensive analyses were conducted regarding the composition and structural properties of hybrids in the presence of Mmt. The hybrids exhibited excellent swelling, salt surfactant tolerance, and pH sensitivity depending on the composition. The higher the Mmt concentration, the lower the swelling ratio; however, the compressive moduli did not change monotonically with increasing Mmt from 0.80 to 2.20% (w/v). Dye adsorption revealed the effects of variables (dye type, pH, contact time, concentration) on adsorptive properties of hybrids towards cationic methylene blue (MB) and anionic sunset yellow, allura red, blue brilliant, carmoisine, and tartrazine dyes. Adsorption kinetics of MB obeyed pseudo-second-order model, and the maximum dye adsorption capacity for hybrids increased from 5.01 mg g⁻¹ to 16.42 mg g⁻¹, while adsorption isotherms were defined by the Freundlich model. The proposed hybrids have emerged as alternative materials that enable multiple uses of same adsorbent for the removal of different types of pollutants. Full article

Objective: This article investigated the structural characteristics, powder properties, and performance variations of co-processed pregelatinized starch (PS) and microcrystalline cellulose (MCC) at varying ratios. Methods: Scanning Electron Microscopy (SEM) revealed the embedding of MCC within the PS matrix. Fourier-transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) analysis indicated no chemical interaction between the starch and MCC during processing. The physical properties of the co-processed materials were evaluated using multiple indicators, such as the Carr index, and their properties in pharmaceutical applications were evaluated using multiple indicators, such as tensile strength and dilution capacity. Results: The absence of new chemical substances during co-processing, as confirmed by FTIR/XRD analyses, coupled with SEM evidence of a physically interlocked MCC-PS architecture, conclusively demonstrates that structural reorganization occurred via physical mechanisms. An increase in the MCC proportion enhanced the tensile strength of the co-processed material while decreasing the Carr’s index, particle size, tapped density, bulk density, swelling, and water-soluble content. A co-processed sample (PS:MCC = 7:3) was selected for application in formulations. The co-processed material exhibited superior compactibility compared to a physical mixture and demonstrated favorable dilution capacity in poorly compactible model drugs, including Linaoxin and Lingzhi spore powder, as well as higher biological inertness. Conclusions: These findings suggest that the co-processed PS and MCC possess excellent compactibility and dilution capacity. The co-processed excipient demonstrates applicability in direct compression manufacturing of oral solid dosage forms (e.g., tablets), offering distinct advantages for high drug-loading formulations. Full article

Repairing large bone defects remains a significant clinical challenge due to the limitations of current treatments, including infection risk, donor site morbidity, and insufficient vascularization. The autograft is still the gold standard for large bone defects. In this study, we developed chitosan-based (CS-based) scaffolds, incorporating with hydroxyapatite (HAp) and fluorapatite (FAp) ceramics, fabricated by UV crosslinking and freeze-drying, and loaded with P28 peptide, alone or in combination with vascular endothelial growth factor (VEGF), to evaluate the effect of dual bioactive factor delivery. We hypothesized that CS-based scaffolds would optimize ceramic composition and co-delivery of P28 and VEGF, and can enhance early-stage osteogenic differentiation and support bone regeneration. The CS-based scaffolds were characterized by their physicochemical properties, including swelling behavior, mechanical strength, porosity, and in vitro degradation. Biological evaluations were performed including cell proliferation assays, ALP activity, ARS staining, and RT-qPCR, to assess osteogenic differentiation. The results showed that the scaffolds had high porosity, excellent swelling behavior, and degraded within 8 weeks. Dual delivery of P28 and VEGF significantly enhanced early osteogenic markers, indicating a complementary effect. These findings demonstrated that CS-based scaffolds with an optimized ceramic ratio and bioactive factor incorporation have the potential to facilitate bone regeneration. Full article

This study aims to develop high-performance biocomposites for structural applications using kenaf, bagasse, hemp, and softwood fibers bonded with phenol-formaldehyde (PF) and phenol-urea-formaldehyde (PUF) adhesives, commonly used in particleboard manufacturing. A simple, low-cost fiber treatment was applied by adjusting the fiber pH to 11 and 13 using a 33% NaOH solution, following standard protocols to enhance fiber–adhesive interaction. The effects of alkaline treatment on the chemical structure of bagasse, kenaf, and hemp fibers were investigated using Fourier Transform Infrared Spectroscopy (FTIR) and correlated with composite mechanical performance. PF and PUF were applied at 13% (w/w), while polymeric diphenylmethane diisocyanate (pMDI) at 5% (w/w) served as a control for untreated fibers. The fabricated panels were evaluated for mechanical properties; modulus of elasticity (MOE), modulus of rupture (MOR), and internal bond strength (IB), and physical properties such as thickness swelling (TS) and water absorption (WA) after 24 h of immersion. FTIR analysis revealed that treatment at pH 11 increased the intensity of O–H, C–O–C, and C–O bands and led to the disappearance of the C=O band (~1700 cm⁻¹) in all fibers. Bagasse treated at pH 11 showed the most significant spectral changes and the highest IB values with both PF and PUF adhesives, followed by kenaf at pH 13, exceeding EN 312:6 (2010) standards for heavy-duty load-bearing panels in dry conditions. The highest MOE and MOR values were achieved with kenaf at pH 11, meeting EN 312:4 (2010) requirements, followed by bagasse, while softwood and hemp performed less favorably. In terms of thickness swelling, bagasse consistently outperformed all other fibers across pH levels and adhesives, followed by Kenaf and Hemp, surpassing even pMDI-based composites. These results suggest that high-pH treatment enhances the reactivity of PF and PUF adhesives by increasing the nucleophilic character of phenolic rings during polymerization. The performance differences among fibers are also attributed to variations in the aspect ratio and intrinsic structural properties influencing fiber–adhesive interactions under alkaline conditions. Overall, kenaf and bagasse fibers emerge as promising, sustainable alternatives to industrial softwood particles for structural particleboard production. PF and PUF adhesives offer cost-effective and less toxic options compared to pMDI, supporting their use in eco-friendly panel manufacturing. FTIR spectroscopy proved to be a powerful method for identifying structural changes caused by alkaline treatment and provided valuable insights into the resulting mechanical and physical performance of the biocomposites. Full article

Collagen-based biomaterials are increasingly explored in dentistry for their ability to deliver drugs locally and support healing. In this study, we developed chlortetracycline-loaded collagen sponges aimed at preventing postoperative infections. Five formulations were prepared by lyophilization, each with the same collagen-to-drug ratio but different glutaraldehyde (GA) concentrations: 0%, 0.25%, 0.5%, 0.75%, and 1% (w/w) relative to dry collagen. The sponges were characterized using FT-IR and UV–VIS–NIR spectroscopy, and their swelling capacity, enzymatic stability, and drug release kinetics were evaluated. Antibacterial activity was tested against Escherichia coli, Staphylococcus aureus, and Enterococcus faecalis. Statistical differences between formulations were assessed using one-way ANOVA followed by Tukey’s post hoc test (p < 0.05). All sponges released the antibiotic rapidly within the first 60 min, followed by a sustained release for up to 10 h. The non-crosslinked sponge showed the highest antimicrobial effect, while the 0.25% GA formulation offered a good balance between stability and bioactivity. While higher cross-linking enhanced structural stability, it progressively reduced antimicrobial efficacy, highlighting a crucial design trade-off. These findings underline the need to fine-tune cross-linking conditions to achieve both durability and strong antimicrobial action in collagen-based drug delivery systems for dental applications. Full article

This study aimed to enhance the characteristic properties of chickpea proteins enriched with quercetin by incorporating whey proteins. For this, whey proteins were supplemented into the film systems at 10, 20, 30, 40, and 50% of the total protein content, and these formulations were labeled as CWF1, CWF2, CWF3, CWF4, and CWF5, in that order. Negative control (CF) was designed with chickpea protein alone. Essential amino acid content of chickpea protein (16.48%) was higher than that of whey protein (8.09%). FTIR spectra revealed protein–protein interactions occurred within film systems. Raising the whey protein content above 40% led to morphological issues in the films. Differences in moisture content, thickness, color, and opacity were obvious (p < 0.05). As the protein content boasted, a decrease in solubility and an increase in the swelling ratio of the films was detected (p < 0.05). CWF4 exhibited enhanced barriers and mechanical properties, followed by CWF3, CWF2, CWF1, CF, and CWF5 (p < 0.05). Moreover, in food simulators, quercetin release from films was monitored, and the highest release of quercetin occurred in 50% ethanol, followed by water and 95% ethanol. Ultimately, highly functional quercetin-loaded edible films, especially CWF4, stood out in protecting fresh strawberries. Full article

Bio-nanocomposites based on poly (vinyl alcohol) (PVA) and cellulosic nanostructures are favorable for active food packaging applications. The current study systematically investigates the mechanical properties, gas permeation, and swelling parameters of PVA composites with cellulose nanocrystals (CNC) or nano lignocellulose (NLC) fibers. Alterations in these macroscopic properties, which are critical for food packaging applications, are correlated with structural information at the molecular level. Strong interactions between the fillers and polymer host matrix were observed, while the PVA crystallinity exhibited a maximum at ~1% loading. Finally, the orientation of the PVA nanocrystals in the uniaxially stretched samples was found to depend non-monotonically on the CNC loading and draw ratio. Concerning the macroscopic properties of the composites, the swelling properties were reduced for the D1 food simulant, while for water, a considerable decrease was observed only when high NLC loadings were involved. Furthermore, although the water vapor transmission rates are roughly similar for all samples, the CO₂, N₂, and O₂ gas permeabilities are low, exhibiting further decrease in the 1% and 1–5% loading for CNC and NLC composites, respectively. The mechanical properties were considerably altered as a consequence of the good dispersion of the filler, increased crystallinity of the polymer matrix, and morphology of the filler. Thus, up to ~50%/~170% enhancement of the Young’s modulus and up to ~20%/~50% enhancement of the tensile strength are observed for the CNC/NLC composites. Interestingly, the elongation at break is also increased by ~20% for CNC composites, while it is reduced by ~40% for the NLC composites, signifying the favorable/unfavorable interactions of cellulose/lignin with the matrix. Full article

To advance seaweed polysaccharide applications in hydrogel wound dressings, five antibacterial composite hydrogels (groups A~E) were synthesized using oxidized κ-carrageenan (OKC), acrylamide (AM), and progressively increasing concentrations of silver-based metal–organic frameworks (Ag-MOFs). Systematic characterization revealed concentration-dependent effects: (1) positive correlations were obtained for the moisture content (MC, maximized at 82.70% in E) and antibacterial efficacy (dose-dependent enhancement); (2) negative impacts were obtained for the swelling ratio (SR, E: 479% vs. A: 808%); and (3) high-dose drawbacks but low-dose benefits in terms of water resistance (WR), tensile strength (TS), elongation at break (EB), and microstructure were obtained. Group B demonstrated optimal Ag-MOFs loading, enhancing TS and EB, while excessive Ag-MOFs loading in C~E significantly degraded them (p < 0.05). Microstructural analysis showed severe 3D spatial damage in D~E. Furthermore, cytocompatibility assessments revealed that all groups maintained a cell viability exceeding 90%, demonstrating excellent biocompatibility. Among them, A~C showed a viability statistically equivalent to the control (p > 0.05) and were significantly higher than D~E (p < 0.05). In conclusion, group B emerged as the optimal Ag-MOFs formulation and exhibited superior WR, enhanced mechanical strength (TS and EB), and potent antibacterial activity while maintaining microstructural integrity and excellent biosafety. This Ag-MOFs/OKC/PAM hydrogel provides dual infection prevention and tissue support, maximizing seaweed polysaccharide benefits with excellent biocompatibility. Full article

Nanostructured drug-delivery systems with enhanced therapeutic potential have gained attention in biomedical applications. Here, flufenamic acid (FFA)-loaded chitosan/poly(vinyl alcohol) (CHS/PVA; CSPA)-based electrospun nanofibers were fabricated and characterized for antibacterial, anticancer, and antioxidant activities. The FFA-loaded CSPA (FCSPA) nanofibers were characterized by scanning electron microscopy, Fourier-transform infrared spectroscopy, X-ray diffraction (XRD), and differential scanning calorimetry to evaluate their formation process, functional group interactions, and crystallinity. Notably, the average diameter of FCSPA nanofibers decreased with increasing CSPA contents (CSPA-1 to CSPA-3), indicating that FFA addition to CSPA-3 significantly decreased its diameter. Additionally, XRD confirmed the dispersion of FFA within the CSPA amorphous matrix, enhancing drug stability. FCSPA nanofibers exhibited a high swelling ratio (significantly higher than that of the CSPA samples). Biodegradation studies revealed that FCSPA exhibited accelerated weight loss after 72 h, indicating its improved degradation compared with those of other formulations. Furthermore, it exhibited a significantly high drug-encapsulation efficiency, ensuring sustained release. FCSPA nanofibers exhibited excellent antibacterial activity, inhibiting Staphylococcus aureus and Escherichia coli. Regarding anticancer activity, FCSPA decreased HCT-116 cell viability, highlighting its controlled drug-delivery potential. Moreover, FCSPA demonstrated superior antioxidation, scavenging DPPH free radicals. These findings highlight FCSPA nanofibers as multifunctional platforms with wound-healing, drug-delivery, and tissue-engineering potential. Full article

This study reports the development of peptide-based hydrogels for the encapsulation and controlled release of peptide nucleic acids in drug delivery applications. Ultrashort aromatic peptides, such as Fmoc-FF, self-assemble into biocompatible hydrogels with nanostructured architectures. The functionalization of tripeptides (Fmoc-FFK and Fmoc-FFC) with lysine (K) or cysteine (C) enables electrostatic or covalent interactions with model PNAs engineered with glutamic acid or cysteine residues, respectively. Hydrogels were polymerized in situ in the presence of PNAs, and component ratios were systematically varied to optimize mechanical properties, loading efficiency, and release kinetics. The formulations obtained with a 1/10 ratio of Fmoc-FF(K or C)/Fmoc-FF provided an optimal balance between structural integrity and delivery performance. All hydrogel formulations demonstrated high stiffness (G′ > 19,000 Pa), excellent water retention, and minimal swelling under physiological conditions (ΔW < 4%). The release studies over 10 days showed that electrostatic loading enabled faster and higher release (up to 90%), while covalent bonding resulted in slower, sustained delivery (~15%). These findings highlight the tunability of the hydrogel system for diverse therapeutic applications. Full article

Drug-loaded hydrogels are promising for modern medicine due to their physical modifiability. However, most hydrogels suffer from poor swelling, which limits their drug encapsulation and release capabilities. In this study, Poly (N-(2-hydroxyethyl) acrylamide-co-acrylic acid) (Poly (HEAA-co-AA)) hydrogels with high swelling properties are synthesized via free radical polymerization of neutralized acrylic monomers. The effects of the material ratio and acrylic acid neutralization degree on the swelling properties of hydrogels in water are investigated, and the swelling properties of hydrogels prepared with different monomer ratios in different pH buffer solutions are systematically studied. The results show that the swelling degree is sensitive to the monomer ratio and pH. The maximum equilibrium swelling degree of the hydrogels occurs at an HEAA to AA molar ratio of 2:2, with values of 11.36 g g⁻¹ at pH 1.68 and 112.79 g g⁻¹ at pH 9.18. Finally, the mechanical properties of PHA hydrogels under different HEAA/AA molar ratios are investigated, showing that the mechanical properties of PHA improved compared to those of PAA. The mechanical properties of the hydrogels are best and show good stability in rheological tests when the molar ratio of HEAA to AA is 2:2. This work has major potential applications in drug carrier systems. Full article

Hydrogels with tunable properties are of great interest for the development of advanced drug delivery systems. In this study, novel hydrogels with an interpenetrating polymer network (IPN) structure were obtained from the pH-responsive poly(methacrylic acid) (PMAA) and the neutral poly(N,N-dimethylacrylamide) (PDMAM). The newly synthesized IPN hydrogels were shown to be pH responsive with a 1.5 to 2.5 fold increase in their equilibrium swelling ratio at a pH above 5 which makes them appropriate for targeted intestine drug delivery. Moreover, their pH responsiveness was found to be strongly influenced by the IPN’s composition. The IPN hydrogels were loaded with PMH via swelling and the drug entrapment efficiency was found to depend on their swelling characteristic varying with the IPN’s composition from 20% to 60%. The drug release profiles were investigated under conditions resembling the oral route of drug application. The PMH release profiles appeared to follow Fickian diffusion at a stomach-like pH = 1.2 and sub-diffusion mechanism at an intestine-like pH = 6.8. The results from this study reveal that IPN hydrogels of PMAA and PDMAM are promising candidates for oral delivery of promethazine hydrochloridee demonstrating pH responsiveness and controllable swelling dependent on their composition. Further investigations are planned to fully reveal their potential as smart drug delivery systems. Full article

Currently, acne therapy relies not only on specific drugs but also on complementary treatments, such as dermocosmetics. Several studies have reported the use of chitosan and alginate in scaffolds for drug delivery systems. These materials can be loaded with a product that exhibits anti-acne properties such as silk sericin, a protein with antioxidant, photoprotective, and moisturizing properties. Therefore, this study proposes the development of a chitosan/alginate scaffold, loaded with sericin, to serve as a dermocosmetic platform complementing the pharmacological treatment of acne. The moisture content of the alginate and chitosan was determined as 14.7 and 21%, respectively; the ash content, which is similar for both polymers, was approximately 5%. The employed chitosan had a deacetylation degree of 82%, as determined by infrared spectrometry and corroborated by potentiometry. This technique was also used to determine the mannuronic/guluronic ratio of the alginate [M/G = 1.3] and confirm the identity of each one of the polymers in the raw materials and the resulting scaffolds. The molecular weights of alginate, chitosan, and sericin were 85, 5.1, and 57.4 kDa, respectively. The pH [6.31] and total protein concentration of the sericin solution [c(SER) = 6.1 mg/mL] were determined using UV-visible spectrophotometry. Swelling and release studies indicated that, although there were varying degrees of cross-linking and certain variables to control, the mechanism that defines the nature of both processes (otherwise complementary) is the relaxation of the polymer chains. Full article

Background/Objectives: Even with improvements in surgical techniques and the application of appropriate antibiotic prophylaxis, wound infections are still major public health problems in low- and middle-income countries. This study proposes the design of new particulate polymeric matrices based on chitosan (CS) for the controlled release of Metronidazole (MTZ), in order for it to be used for the treatment of Clostridium perfringens infections. Methods: The nanoparticles were prepared via inverse emulsion using tannic acid (TA) and sodium tripolyphosphate (TPP) as cross-linking agents. The ratio of CS to TPP, the concentration of CS solution, and the ratio of CS to TA were varied to optimize the synthesis procedure. Nanoparticles have been characterized based on several points of view in order to correctly correlate their properties with synthesis parameters. Results: The FTIR spectra of the analyzed nanoparticles confirmed both the formation of hydrogen bonds between CS and TA and the ionic cross-linking of CS with TPP. The average diameters of the nanoparticles ranged from 70 to 170 nm, whereas the zeta potential values were around 8 mV. Their swelling degree in a weak basic environment, as well as the drug loading/release capacity was influenced, as expected, by the synthesis parameters. The obtained nanoparticles were tested in vitro to evaluate their behavior in the blood environment, the cytotoxic effect, and the antimicrobial activity of nanoparticles loaded with MTZ against Clostridium perfringens cultures. Conclusions: The in vitro obtained results demonstrate that these non-hemolytic and non-cytotoxic particles can be efficient drug delivery systems for the treatment of Clostridium perfringens in wound infections. Full article

Variability and relationship between phenological traits and leaf, acorn, and tree size morphometric traits were examined in early and late bud-flushing groups of the pedunculate oak population in the vicinity of Sremska Mitrovica, Serbia. According to the obtained three-year results, there were no significant differences in tree size and leaf morphometric characteristics between the early and late group. The effect of trees within phenological groups was statistically significant and considerable, especially in leaf blade width (lbw) and leaf area (la). Acorn length (acl) and acorn index (acinx) were significantly influenced by phenological group, achieving moderate contribution of phenological group to the total variation. There was a clear effect of phenological group on variation of examined phenological traits. The effect of year of monitoring on the same traits was not significant, but there was a clear effect of interaction between phenological group and year, especially in case of traits describing the period from bud swelling until the emergence of wrinkled leaves (f12a), unfolded leaves (f12b), and fully developed leaves (f12g) and their ratio with the period from 8 March until the emergence of wrinkled leaves: f12b/f02a and f12g/f02a ratio. Earlier phenology in warmer years is clearer in the early bud-flushing group than in the late one. Periods between different bud swelling and f12a, f12b, and f12g phenological phases were significantly shorter in 2017 (with a warm April) than in 2015 (with moderate temperatures in March and April) in the early group, but significantly longer in the late group. Examined traits were classified in six groups based on their factorial loadings with the first six principal components rotated by Varimax method, revealing strict distinction between traits by their original nature. In that sense, all examined groups of traits could be considered as informative in variability studies of pedunculate oak. The tree size traits (tree height and diameter at breast height) formed the separate, fifth group, suggesting no close relationship of these traits with any other examined characteristic. Both cluster analysis and PCA suggest distinct classification by trees’ phenology, but also considerable differences by the second principal component which is closely related to leaf size characteristics. The research should be continued on variability between populations and progenies, especially with respect to phenological and acorn morphometric traits. Understanding the phenological variations between early and late oaks could be essential for designing robust forest adaptation management strategies. Full article