Search Results (163)

This study reports a self-assembled ternary delivery system composed of bovine serum albumin (BSA), Fe^(III), and 8-Shogaol (BSA-Fe^(III)-8S) to enhance the stability of this labile ginger-derived bioactive compound. Optimized nanoparticles prepared via one-pot coprecipitation exhibited a particle size of 115.14 nm, polydispersity index (PDI) of 0.084, zeta potential of +52.23 mV, encapsulation efficiency of 94.93%, and loading capacity of 23.73%. Spectroscopic analyses (FT-IR, UV–Vis, XPS) and fluorescence quenching confirmed the formation of a core–shell metal–phenolic network, where Fe^(III) coordinates with 8-Shogaol and BSA forms the outer protein shell. Compared to free 8-Shogaol, the BSA-Fe^(III)-8S MPN nanoparticles demonstrated significantly enhanced thermal, UV, and storage stability. During simulated gastrointestinal digestion, the nanoparticles retained 64.04% of 8-Shogaol, compared to only 51.38% for the free compound. Cytotoxicity assays on HEK293 cells confirmed the biocompatibility of the nanoparticles. This BSA-Fe^(III)-8S delivery system offers a promising strategy for protecting bioactive phenolic compounds, with potential applications in functional foods and nutraceutical formulations. Full article

Mango (Mangifera indica L.), being a climacteric fruit, is highly perishable due to rapid ripening and post-harvest diseases like anthracnose, which significantly shorten its shelf life and limit long-distance sea export. To mitigate these constraints, a chemical-free secondary metabolite-based formulation (SMsF) was developed to delay ripening and control post-harvest anthracnose during storage. The SMsF possesses dual-action properties and is derived from the culture filtrate of Priestia aryabhattai, exhibiting ACC deaminase activity that restricts ethylene formation. It is also rich in antifungal compounds such as vanillic acid, hydroxybenzoic acid, cryptochlorogenic acid, palmitic acid, and BBIT, which inhibit anthracnose development. Additionally, it contains antioxidants including quercetin, coumaryl quinic acid, oleic acid, and acetylglycitin that enhance shelf life and disease resistance. The efficacy of SMsF was evaluated in mango cv. Banganapalli was stored at 12 ± 1 °C and 85–90% relative humidity under simulated reefer conditions (SRC). Integration of gamma irradiation with SMsF provided superior results in disease control and shelf-life extension. The combined treatment maintained higher fruit firmness (0.86 kg cm⁻²), optimal total soluble solids (14.3 °B), desirable acidity (0.22%), and complete suppression of anthracnose (PDI = 0) up to 40 days of storage under SRC compared with the control. The findings conclusively demonstrate that the synergistic application of SMsF and gamma irradiation effectively regulates ripening, enhances fruit quality, and ensures complete disease suppression, thereby significantly extending storage life. This approach holds strong scientific and commercial significance as a sustainable, residue-free, and export-oriented technology capable of improving long-distance transportation, reducing post-harvest losses, and promoting safe mango trade. Full article

Liver fibrosis is driven by persistent oxidative stress and inflammatory signaling, with transforming growth factor-β (TGF-β) acting as a key profibrotic mediator. Rutin (Ru) is a plant-derived flavonoid with antioxidant and anti-inflammatory effects, but its low bioavailability limits therapeutic efficacy. This study investigated whether rutin-phytoreduced gold nanoparticles (RuAuNPs) enhanced rutin delivery leading to antifibrotic and anti-inflammatory effects in a rat model of liver fibrosis. Liver fibrosis was induced by oral administration of thioacetamide (TAA, 150 mg/kg body weight, p.o.) for six weeks. Following fibrosis induction, the animals were treated with free rutin (30 mg/kg body weight), RuAuNPs (0.3 mg/kg body weight), or AuNPs (0.3 mg/kg body weight), both expressed as nanoparticle mass, all administered orally for four weeks. RuAuNPs were synthesized by green rutin-mediated reduction and further characterized by TEM, DLS, and FTIR spectroscopy; they were spherical, showing an average hydrodynamic size of 104.1 nm (PDI 0.345). FTIR confirmed rutin capping. Biological effects were evaluated by liver morphology (H&E histology, TEM), biochemical assessment of liver aminotransferases and glico-lipidic status, ELISA and spectrophotometry measurement of redox biomarkers (lipid peroxidation, glutathione status, antioxidant enzymes), cytokines (TNF-α, IL-1β, IL-6), and TGF-β. TAA-induced hepatic injury and remodeling with increased profibrotic signaling, oxidative stress, and inflammation. Free rutin slightly ameliorated the liver damage, whereas RuAuNP improved histological features, reduced TGF-β and pro-inflammatory cytokines, decreased lipid peroxidation, and supported antioxidant defenses. Overall, RuAuNP may enhance rutin efficacy in TAA-induced liver fibrosis, with novelty stemming from the integrated in vivo evaluation of tissue changes and key profibrotic/oxidative/inflammatory pathway. Full article

In bulk heterojunction (BHJ) organic solar cells (OSCs) employing perylene diimide (PDI)-based non-fullerene acceptors, excessive intermolecular interactions among PDI units lead to severe aggregation and pronounced donor–acceptor phase separation, both of which critically limit device performance. To address these issues, numerous structurally engineered PDI derivatives have been developed. In particular, twisted multi-PDI architectures designed to suppress intermolecular aggregation have shown improved morphological control; however, such twisted structures are often highly amorphous, which reduces electron-transport efficiency and constrains OSC performance. In this work, we introduce a mixed-acceptor strategy combining a twisted PDI dimer (SF-PDI₂) with a planar monomeric PDI (m-PDI) to balance aggregation and morphological uniformity. Ternary blend OSCs consisting of PTB7-Th as the donor and these two PDI acceptors exhibit systematic performance variations depending on their relative ratios. At the optimized composition (SF-PDI₂:m-PDI = 90:10 by weight), the device outperforms single-acceptor systems, which is attributed to controlled aggregation arising from the complementary structural features of the two PDI acceptors. This study demonstrates that combining mixed PDI acceptors with similar molecular moieties enables precise control of aggregation, improving both morphology and photovoltaic performance. Full article

Antimicrobial resistance represents not only a biological challenge but also a physicochemical limitation associated with antibiotic transport, membrane interaction, and local availability. In this preliminary study, a liposome-encapsulated doxycycline delivery system was developed using egg yolk-derived phospholipids, and its biophysical properties and release behavior were investigated. Phospholipids were isolated from egg yolk and used to prepare doxycycline-loaded liposomes via a thin-film hydration method combined with freeze–thaw processing. Liposome morphology was characterized by atomic force microscopy (AFM), while encapsulation efficiency was quantified by reversed-phase high-performance liquid chromatography (RP-HPLC). In vitro release kinetics were evaluated using a dialysis diffusion method, and antibacterial activity was assessed as a functional indicator of drug availability using minimum inhibitory concentration (MIC) assays against Staphylococcus aureus and methicillin-resistant S. aureus (MRSA). The prepared liposomes exhibited morphology with diameters of approximately 153 nm (PDI = 0.223). The encapsulation efficiency of doxycycline hyclate was 8.41%, and complete drug release was achieved within 48 h. Liposome-encapsulated doxycycline demonstrated a two-fold reduction in MIC values compared with free doxycycline. These findings offer preliminary insight to support further optimization and expanded investigation of liposome-encapsulated antibiotic delivery systems. Full article

Background: Cannabidiol (CBD), a non-psychoactive compound derived from Cannabis sativa, exhibits therapeutic potential for various conditions, including inflammation, pain, and skin disorders, making it a promising candidate for the topical treatment of psoriasis. However, its poor water solubility and instability limit its therapeutic efficacy. This study focuses on the development and characterization of CBD-loaded nanoemulsions using argan oil as the lipid phase, with and without a chitosan coating, which serves as a stabilizing and functional biopolymer. Methods: Nanoemulsions (NE) and chitosan-stabilized nanoemulsions (CS-NE), both without CBD (serving as controls), and CBD-loaded variants (CBD-NE and CBD-CS-NE) were prepared and characterized for their physicochemical properties, including pH, droplet size, polydispersity index (PDI), zeta potential (ζ-potential), and viscosity at various shear rates and temperatures. Stability was assessed over time, and drug release behavior was investigated through in vitro diffusion and ex vivo skin permeation studies, followed by kinetic modeling. Safety was evaluated through in vitro cytotoxicity assays using HaCaT keratinocyte cells, as well as in vivo toxicity studies using Caenorhabditis elegans (C. elegans). Results: The chitosan-coated formulations exhibited enhanced physical stability, nanoscale droplet size, a positive surface charge, and increased viscosity. Release studies demonstrated that CBD-CS-NE enabled controlled and sustained drug release, with a strong correlation to the Higuchi model, indicating diffusion-controlled permeation. Cytotoxicity assays indicated that CBD-CS-NE was non-toxic to cultured cells, while in vivo testing with C. elegans revealed sensitivity to chitosan-coated systems. Conclusions: These findings highlight the potential of CBD-loaded argan oil nanoemulsions, particularly those stabilized with chitosan, as potential topical delivery systems for managing psoriasis. Full article

Background: Nanoparticles are a promise for wound-healing therapies. However, its lack of efficacy/safety represents a real challenge for therapeutic use. Objectives: To overcome these problems, the ethanolic extract of Casimiroa edulis leaves, previously reported for its anti-inflammatory, antibiotic, and antioxidant activities, was characterized by FIA-ESI-FTICR-MS and encapsulated in biodegradable nanoparticles for potential wound-healing therapies. Methods:Casimiroa edulis-loaded nanoparticles (CE-NP) were prepared using the rapid emulsion-diffusion method and characterized by their particle size distribution, molecular interactions, charge, morphology, pH, physical stability, and antioxidant and occlusive effects. Results: A total of 40/34 ions in positive/negative electrospray ionization modes were obtained from the extract exploration analysis and were putatively annotated by accurate mass against databases with an error tolerance ≤10 mDa. The most abundant compounds showed the following order: tetramethylscutellarein > rutin > S-usnate > lactose > eugenol derivative > rotenone. While polyphenols predominated, carbohydrates, depsidones/other phenolics, etc., were also detected. The solid/spherical nanoparticles observed by TEM were obtained with a blend of acetone:methyl ethyl ketone (75:25) as the organic phase, producing a unimodal particle size (169.30 ± 1.30 nm; PdI = 0.08 ± 0.03). The encapsulation/loading percentages were 57 ± 0.74/1.62 ± 0.02%, ensuring an entrapment of half the extract, as observed in the FTIR studies. The light backscatter profiles show minimal differences, indicating physical stability correlated with the Z potential (−9.45 ± 1.73 mV). The antioxidant activity of the extract/nanoparticles at 40 µg/mL was 17.27 ± 2.86/16.73 ± 1.28 μg/mL, two-fold higher than that previously reported for sapote seeds. Conclusions: Biodegradable CE-NP with suitable characteristics were obtained for the first time, representing a preliminary proposal for wound healing. Efficacy studies are required. Full article

This study systematically compared spray drying (SD) and freeze drying (FD) for microencapsulating Idesia polycarpa oil using a soy protein isolate/maltodextrin (SPI/MD) wall system. SD produced predominantly spherical and compact microcapsules with higher solubility (51.33%), encapsulation efficiency (81.9%), and superior oxidative stability (oxidation induction period, 6.05 h), together with improved thermal resistance, indicating its suitability for applications requiring enhanced stability and aroma retention. In contrast, FD yielded irregular and porous microcapsules with significantly higher emulsifying activity (29.12 m² g⁻¹, p < 0.05) but lower solubility and encapsulation efficiency. Integrated physicochemical characterization-including scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), particle size and polydispersity index (PDI), ζ-potential, differential scanning calorimetry (DSC), oxidative stability index (OSI) measurements, and volatile profiling via odor activity value (OAV) analysis—revealed clear process-dependent structure–function relationships. The denser SPI/MD matrix formed during SD restricted lipid molecular mobility and oxygen diffusion, thereby suppressing lipid oxidation and promoting the retention of key lipid-derived odorants. Conversely, the porous structure generated by FD facilitated interfacial functionality but increased molecular diffusion pathways. Overall, this work demonstrates that SPI/MD-based microencapsulation functions as a molecular stabilization platform for highly unsaturated plant oils and provides mechanistic guidance for selecting drying strategies to tailor Idesia polycarpa oil microcapsules for specific food applications. Full article

This study aimed to biosynthesize silver nanoparticles (AgNPs) using aqueous leaf extract of Galega officinalis and to evaluate their insecticidal activity against key stored-product pests. AgNP formation was confirmed through UV–vis spectroscopy, which showed a surface plasmon resonance peak at 380 nm. FTIR analysis indicated the presence of plant-derived functional groups likely involved in the reduction and stabilization of Ag⁺ ions. Dynamic light scattering revealed an average hydrodynamic diameter of 25.07 nm, a PDI of 0.39, and a zeta potential of −22 mV, while TEM images showed predominantly spherical and polydisperse particles ranging from 4.3 to 42.4 nm. Insecticidal bioassays performed on Sitophilus granarius, Tribolium confusum, Plodia interpunctella, and Ephestia kuehniella revealed concentration-dependent mortality. The highest mortality rates were recorded at 1000 ppm, reaching 100% in T. confusum, 83.33% in P. interpunctella, and 76.67% in both S. granarius and E. kuehniella. These findings demonstrate the potent insecticidal activity of G. officinalis-mediated AgNPs and support their potential as environmentally friendly alternatives for stored-product pest management, warranting further studies on safety, large-scale synthesis, and integration into pest-control programs. Full article

This study reports the fabrication of chitosan/carboxymethyl cellulose (C/M) nanocomposites by electrolyte gelation–spray drying and the evaluation of their antibacterial performance as carriers for the antibiotic ampicillin. Chitosan (C), a cationic biopolymer derived from chitin, was combined with the anionic polysaccharide carboxymethyl cellulose (M) at different mass ratios to form stable nanocomposites via electrostatic interactions and then collected in a spray dryer. The resulting particles exhibited mean diameters ranging from 800 to 1500 nm and zeta potentials varying from +90 to −40 mV, depending on the C/M ratio. The optimal formulation (C/M = 2:1 ratio) achieved a high recovery yield (71.1%), lower PDI (0.52), and ampicillin encapsulation efficiency EE (82.4%). Fourier transform infrared spectroscopy (FTIR) confirmed the presence of hydrogen bonding and ionic interactions among C/M, and ampicillin within the nanocomposite matrix. The nanocomposites demonstrated controlled ampicillin release and pronounced antibacterial activity against Staphylococcus aureus, with minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) values of 3.2 µg/mL and 5.3 µg/mL, respectively, which were lower than those of free ampicillin. These results indicate that the chitosan/carboxymethyl cellulose nanocomposites are promising, eco-friendly carriers for antibiotic delivery and antibacterial applications. Full article

Saccharomyces cerevisiae was cultured under the influence of static magnetic fields (SMFs) to assess their impact on the biosynthesis of silver nanoparticles (AgNPs). Cell-free media derived from SMF-exposed cultures facilitated the formation of AgNPs, with a significant reduction in nanoparticle size observed at an optimal field strength of 7 mT. AgNPs synthesized under SMF conditions exhibited smaller crystalline structures than those produced in control media, as evidenced by dynamic light scattering (DLS) and transmission electron microscopy (TEM) measurements. Over a 75-day period, SMF-exposed AgNPs demonstrated enhanced stability, as determined by DLS and polydispersity index (PDI) assessments. Further analysis through sodium dodecyl-sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and Fourier transform infrared spectroscopy (FTIR) suggested the formation of a protein corona on the AgNPs in SMF-treated samples, which likely inhibits agglomeration and enhances long-term stability. These findings indicate that SMF-induced stress in S. cerevisiae triggers the secretion of specific proteins that contribute to the stabilization of AgNPs, providing a novel approach to controlling nanoparticle synthesis and stability through magnetic field exposure. Full article

Background: Diabetic nephropathy (DN) is largely driven by transforming growth factor-β1 (TGF-β1)-mediated fibrosis. Clustered regularly interspaced short palindromic repeats (CRISPR)-associated protein 9 (Cas9) ribonucleoprotein (RNP) complexes offer precise gene disruption, yet effective non-viral delivery remains a challenge. This study developed cationic lipid-based hybrid nanostructured lipid carriers (NLCs) for intracellular delivery of TGFB1-targeting RNP as an early-stage platform for DN gene modulation. Methods: A single-guide RNA (sgRNA) targeting human TGFB1 was assembled with Cas9 protein (1:1 and 1:2 molar ratios). Hybrid NLCs comprising squalene, glyceryl trimyristate, and the cationic lipid 1,2-dioleoyl-3-trimethylammonium-propane (DOTAP) were formulated via optimized emulsification–sonication to achieve sub-100 nm particles. Physicochemical properties, including polydispersity index (PDI), were assessed via dynamic light scattering (DLS), while silencing efficacy in HEK293T cells was quantified using quantitative reverse transcription PCR (RT-qPCR) and enzyme-linked immunosorbent assay (ELISA). Results: Optimized NLCs achieved hydrodynamic diameters of 65–99 nm (PDI < 0.5) with successful RNP complexation. The 1:2 Cas9:sgRNA formulation produced the strongest gene-editing response, reducing TGFB1 mRNA by 67% (p < 0.01) compared with 39% for the 1:1 ratio. This translated to a significant reduction in TGF-β1 protein (p < 0.05) within 24 h. Conclusions: DOTAP-based hybrid NLCs enable efficient delivery of CRISPR–Cas9 RNP and achieve significant suppression of TGFB1 expression at both transcriptional and protein levels. These findings establish a promising non-viral platform for upstream modulation of profibrotic signaling in DN and support further evaluation in kidney-derived cells and in vivo renal models. Full article

Background: Tumor-lysate vaccines can capture tumor heterogeneity; however, their effectiveness may be reduced by antigen instability and short antigen presentation. Here, we aimed to improve antigen protection and prolong presentation by using a slow-degrading polymeric nanocarrier and an approved adjuvant. Methods: We encapsulated breast cancer cell lysates (MCF-7 and MDA-MB-231) in poly(ε-caprolactone) (PCL) nanoparticles using a double-emulsion (w/o/w) method and co-administered them with alum. We then characterized particle size, PDI, zeta potential, morphology, and in vitro release. Next, we evaluated nitric oxide (NO), TNF-α/IL-10 responses, and cytocompatibility in J774 macrophages. Finally, we quantified serum antibody titers in Balb/c mice after six biweekly immunizations, generated hybridomas, purified IgG, and tested antibody-mediated cytotoxicity alone and together with doxorubicin. Results: PCL nanoparticles were ~220–255 nm (PDI 0.10–0.19; ζ −2 to −3 mV) and released ~90–95% of encapsulated lysate by 800 h (~33 days). Encapsulated lysate (40 μg/mL) modestly increased NO versus control and increased further with alum (p < 0.05). TNF-α increased 7.4–9.72-fold, whereas IL-10 rose 2.82–3.11-fold. Importantly, encapsulated antigen + alum produced the highest ELISA responses after the sixth dose (6.36-fold for MCF-7 and 7.00-fold for MDA-MB-231 versus control; p < 0.05). Hybridoma-derived antibody signals increased through day 42, and Protein G purification yielded up to ~395 μg and ~318 μg IgG. Purified antibodies reduced cell viability, and viability decreased further when antibodies were combined with doxorubicin (to ~31.6% in MCF-7 and ~40.3% in MDA-MB-231). Conclusions: Overall, sustained PCL-mediated antigen release combined with alum strengthened humoral responses to tumor lysate and enabled recovery of functional antibodies with diagnostic capture and in vitro cytotoxic activity. In future work, key mechanistic steps such as lymph-node trafficking and cross-presentation should be tested directly. Full article

Quinoa, in addition to its nutritional benefits, is adaptable to, and tolerant of, high-altitude and Mediterranean environmental conditions. However, its largely cross-compatible free-living ancestor, pitseed goosefoot, possesses expansive adaptive variation as its ecotypes are found on arid or well-drained soils throughout temperate and subtropical North America. In this context, the objective of this study was to characterize F7:10 lines from quinoa × pitseed goosefoot hybrids to identify promising lines with desirable agronomic traits and adaptation to hyper-arid production environments. The agro-morphological characterization of 14 interspecific experimental lines plus wild parents (5), checks (3, including one derived from a much earlier wide cross), and an F2 population was performed for 25 quantitative and 26 qualitative descriptors, along with calculation of the selection index. Among the morphological variables, the average number of primary branches per plant (NPB) was six (CV = 78%), the average plant height (PH) was 143.5 cm (CV = 40%), and the average panicle diameter (PDI) was 17.9 cm (CV = 62%). With regard to the yield component variables, the average harvest index (HI) was 39% (CV = 36%), the average weight of 1000 grains (W1000G) was 2.59 g (CV = 42%), and the average yield per hectare (HYP) was 4.68 t ha⁻¹ (CV = 65%). Regarding the correlations between variables, it was observed that all phenological phases showed positive correlations with plant height (PH) and negative correlations with yield components, specifically with DG, DT, HI, and W1000G. The highest-yielding lines were GR10 (8.16 t ha⁻¹), GR07 (7.53 t ha⁻¹), GR11 (7.27 t ha⁻¹), and GR01 (7.02 t ha⁻¹). Multivariate and cluster analyses identified four groups of lines, with groups II and IV standing out for their desirable agronomic traits. However, based on the selection index, lines RL08, RL07, ER06, GR03, and GR11 were identified as the most promising. In terms of quality, 18 out of the 23 lines were classified as sweet (<0.11% saponin) and 5 as bitter (>0.11 saponin). In conclusion, the selection index identified pitseed goosefoot cross-derived quinoa lines having superior yield potential, short plant height, large grain size, early maturity, and low saponin content. Full article

Background/Objectives: Neuroblastoma (NB) is the most common extracranial solid tumor in children and accounts for 12–15% of pediatric cancer-related deaths. Current multimodal therapies lack specific cellular targets, causing systemic toxicity and drug resistance. The development of innovative tumor-targeted nanoformulations might represent a promising approach to enhance NB diagnosis and antitumor efficacy, while decreasing off targets side effects. Fibronectin extra-domain B (FN-EDB) is upregulated in the tumor microenvironment. Methods: FN-EDB expression was evaluated by immunohistochemical staining in cell line-derived and tumor patient-derived animal models of NB. A gold nanoparticle, decorated with an antibody (Ab) recognizing FN-EDB (L19-AuNP) was developed by the company Nano Flow and its tumor binding was tested by ELISA in vitro and in patient-derived xenograft (PDX) models of NB by photoacoustic imaging in vivo. Results: All animal models of NB used have been shown to express FN-EDB. L19 Ab demonstrated excellent binding specificity to FN-EDB both when used in free form and after conjugation to AuNP. Compared to the non-functionalized (no Ab L19-coupled) AuNP, which showed an increase in PDI and zeta potential over time, making them unsuitable for use in in vivo studies, L19-AuNP demonstrated good stability. In vivo, L19-AuNP specifically homed into PDX models of NB, accumulating better in tumors expressing higher levels of FN-EDB. Negligible distribution to healthy organs occurred. Conclusions: In this preliminary study, L19-AuNP was shown to be a novel diagnostic tool specifically for binding NB expressing FN-EDB, paving the way for the development of theranostic nanoformulations co-encapsulating gold moiety and standard-of-care therapy for NB. Full article