Mastitis, an inflammation of mammary tissue frequently associated with infection, is a prevalent disease among dairy animals. Bacterial intra-mammary infection is identified as a primary cause of bovine mastitis (BM). In dairy cattle, antimicrobials are used for mastitis treatment during the lactating phase and for dry cow therapy. Although self-curing can occur, the success of mastitis treatment depends on several factors, including the type of bacteria responsible for the infection, the effectiveness of the administered antibiotics, and the host's overall immune response. Moreover, the growing resistance of microorganisms to antibiotics has restricted the available treatment options for managing intramammary infections. In addition, the utilization of critically essential antimicrobials in animals raised for food production may elevate the risk of human infections that are challenging to treat. Therefore, it is crucial to have alternative treatments with equivalent or superior effectiveness as part of any stewardship program. These may include the application of nanotechnology, stem cell technology, photodynamic and laser radiation or the use of traditional herbal medical plants, nutraceuticals, antibacterial peptides, bacteriocins, antibodies therapy, bacteriophages, phage lysins, and probiotics as alternatives to antibiotics. This review aims to discuss the potential of vaccination as an indirect strategy, along with nanotechnology, probiotics, stem cell therapy, antimicrobial peptides, photodynamic therapy, laser irradiation, and antibody treatments as direct approaches. These approaches are examined as possible alternative therapeutic options to antibiotic treatment for BM.

Silver nanoparticles (AgNP) are becoming increasingly prevalent in daily life due to their unique properties, which have expanded their application across multiple sectors. This widespread use has led to a marked rise in human exposure to AgNP, raising concerns about their safety and potential health impacts. Studies have demonstrated that AgNP can induce harmful effects, including oxidative stress and pro-inflammatory responses, underscoring the need to identify protective agents to mitigate health risks. Flavonoids, known for their anti-inflammatory and antioxidant properties, hold significant  promise as effective agents in mitigating the toxic effects of AgNP. This review examines the current literature on the protective effects of flavonoids against AgNP toxicity. It highlights the underlying mechanisms by which flavonoids exert protective actions, with a focus on relevant pathways and molecular interactions. The results of in vitro and in vivo studies demonstrated that flavonoids exert protective effects against AgNP-induced damages through their antioxidant and anti-inflammatory activity. This analysis underscores the flavonoids potential as a promising strategy to reduce the negative impacts of AgNP, supporting safer and more sustainable applications of nanotechnology across diverse fields.

The rise in antibiotic resistance has created an urgent need for alternative strategies to combat multidrug-resistant (MDR) bacterial infections. Silver nanoparticles (AgNPs) possess unique antibacterial properties, making them a promising option in biomedical applications. This study explores the green synthesis of silver nanoparticles (AgNPs) using Citrus sinensis peel extract and their synergistic potential with cefotaxime against multidrug-resistant (MDR) clinical isolates. For the optimization of AgNPs synthesis, Plackett-Burman experimental design (PBD) was implemented that demonstrated incubation time, temperature and extract: AgNO3 ratio as significant factors. The UV-Vis spectroscopy analysis revealed a characteristic absorbance peak of CS-AgNPs at 470 nm. The size of biosynthesized AgNPs was analyzed using Scanning Electron Microscopy (SEM), that showed size range of 50-60 nm with spherical shaped morphology. Fourier Transform Infrared Spectroscopy (FTIR) analysis found different functional groups involved in the stabilization and capping of AgNPs, as indicated by the peaks at 2925 cm-1, 1630 cm-1, 1100 cm-1 and 1016 cm-1 revealing -CH stretching aliphatic carbon, the carboxyl group, OH group and C-O-C group, respectively. The cytotoxicity of the synthesized CS-AgNPs and its synergistic effect with cefotaxime (CTX) antibiotic was analyzed with MTT assay. The combination of CS-AgNPs and CTX showed significant decrease in cytotoxicity compared to CS-AgNPs alone. Antibacterial activity of CS-AgNPs against MDR clinical isolates was performed using minimum inhibitory concentration (MIC) method. The MIC of CS-AgNPs was observed within 3.125-12.5 µg/ml range. Synergism assay of CS-AgNPs with CTX was also evaluated to determine the fractional inhibitory concentration (FIC) index. Clinical isolates (E. coli), S-11, S-14, S-16, S-19, and S-20 showed FIC in the range of 0.162-0.402 indicating synergism whereas, S-04, S-06, S-10, S-15 and S-21 showed the FIC in the range of 0.644-0.804 indicating the additive effect. The MDR E. coli clinical isolates S-11, S-16, S14, S-19 and S-20 demonstrated 65-85% biofilm inhibition which was significantly (p ≤ 0.001) high in all tested isolates. Significant (p ≤ 0.001) eradication of preformed biofilm in the range of 60-78% was also observed in S-16 clinical isolate.

The increasing prevalence of engineered nanoparticles (ENPs) in food systems has raised concerns about their toxicity and potential health risks. To provide a comprehensive evaluation, a structured literature search was conducted using databases such as Web of Science and PubMed, focusing on studies published in the past ten years that examine ENP exposure pathways, toxicity mechanisms, contributing factors, and risk assessment strategies. This review first explores the diverse sources of ENPs, including food additives, nanocarriers, packaging, agricultural practices, and environmental contamination. Upon ingestion, ENPs undergo complex transformations within the human gastrointestinal tract (GIT), causing oxidative stress, cellular dysfunction, inflammation, and gut microbiota dysbiosis, potentially leading to systemic toxicity in vital organs. The toxicity of ENPs is influenced by their physicochemical properties, food matrix effects, GIT conditions, and host-specific factors. This review further discusses current toxicity assessment methodologies, including in silico, in vitro, in vivo, and emerging technologies. Finally, we identify critical research gaps, such as the lack of long-term exposure studies and limited evaluations of organic ENPs. By providing a comprehensive analysis of ingested ENP toxicity, this review aims to guide safer ENP applications and mitigate potential health risks.

Upconversion nanoparticles (UCNPs) are emerging as highly promising nanomaterials due to their exceptional optical properties, enabling diverse applications in biosensing, bioimaging, photodynamic therapy, and drug delivery. However, their potential toxicity should be comprehensively investigated for the safe utilization of UCNPs in several biomedical and environmental applications. This review systematically evaluates the current knowledge on UCNP toxicity from 2008 to 2024, focusing on key toxicological pathways, such as oxidative stress, reactive oxygen species (ROS) production, inflammatory responses, and apoptosis/necrosis, alongside their absorption, distribution, metabolism, and excretion processes and kinetics. Distinctively, this review introduces a bibliometric analysis of UCNP toxicity and biodistribution research, providing a quantitative assessment of publication trends, influential authors, leading institutions, funding agencies, and keyword occurrences. This approach offers a macroscopic perspective on the evolution and current landscape of UCNP safety research, a dimension largely unexplored in existing literature. Furthermore, the review combines mechanistic insights into UCNP toxicity with a critical evaluation of surface modifications, physicochemical properties, and administration routes, presenting a holistic framework for understanding UCNP biosafety. By combining bibliometric data with mechanistic insights, this review provides a data-driven perspective on UCNP-associated risks, actionable strategies for enhancing biosafety through surface engineering, and a forward-looking discussion on regulatory challenges and future directions for UCNP-based technologies. These findings bridge existing gaps in the literature and offer a comprehensive resource for researchers, clinicians, and policymakers, facilitating the safe development and utilization of UCNP-based technologies while establishing robust safety guidelines to mitigate adverse effects on human health and the environment.

Silver nanoparticles (AgNPs) have attracted tremendous attention in recent years due to their unique physicochemical properties, including pronounced surface plasmon resonance, tunable size, and amenability to functionalization. These attributes underpin the growing interest in AgNPs as SMART nanocarriers for targeted drug delivery and as active components in biosensing platforms. In this work, we discuss various synthesis strategies for AgNPs-ranging from conventional chemical methods to green approaches-and highlight their subsequent functionalization with anticancer drugs, notably doxorubicin (DOX). We also examine the potential of AgNPs in biosensor applications, emphasizing electrochemical and optical detection modalities capable of monitoring drug release, oxidative stress, and relevant biomarkers. Our experimental data support the conclusion that AgNPs can effectively improve therapeutic efficacy by exploiting tumor-specific conditions (e.g., lower pH) while also enhancing biosensor sensitivity via surface plasmon resonance and electrochemical signal amplification. We provide a thorough discussion of the results, including mechanistic aspects of reactive oxygen species (ROS) generation, drug release kinetics, and sensor performance metrics. Overall, AgNP-based nanocarriers emerge as a powerful platform to address current challenges in precision oncology and medical diagnostics.

Cancer is a deadly disease and is one of the primary causes of mortality worldwide. Cancer therapy presents significant challenges, such as chemotherapy resistance, high toxicity, recurrence, and metastasis. As a result, the development of novel therapeutic agents for cancer continues to be a top goal to expand the number of efficient treatments available. The advent of nanotechnology is an important turning point in several scientific disciplines. Owing to the increasing difficulty of this problem, researchers have begun to focus their attention on the possibility of employing plants or extracts from plants as a potential tumor treatment. More than 3,000 medicinal plant species have been documented worldwide for their utilization in cancer treatment. Nevertheless, crude plant extracts lack specificity, and their dosages are not clearly specified. To enhance the therapeutic efficacy of these natural substances, researchers have used them in conjunction with silver nanoparticles (AgNPs). Plants possess intricate phytochemical components including sugars, polyphenols, amino acids, flavonoids, terpenoids, alkaloids, and proteins, which can function as reducing and stabilizing agents. In recent years, the application of plant-derived AgNPs has increased significantly, particularly in cancer treatment. These green-synthesized AgNPs are regarded as outstanding tools for the detection of cancer and targeted drug delivery at the tumor site. By leveraging the distinctive characteristics of nanoparticles and the antioxidant and anticancer qualities of plants, these green-synthesized AgNPs selectively eradicate tumor cells while sparing normal healthy cells. This comprehensive review aimed to summarize the key aspects of plant extracts as anticancer agents, biosynthesis of AgNPs, and recent advancements in the antitumor efficacy of green-synthesized AgNPs.

The proliferation of toxigenic fungi in food and the subsequent production of mycotoxins constitute a significant concern in the fields of public health and consumer protection. This review highlights recent strategies and emerging methods aimed at preventing fungal growth and mycotoxin contamination in food matrices as opposed to traditional approaches such as chemical fungicides, which may leave toxic residues and pose risks to human and animal health as well as the environment. The novel methodologies discussed include the use of plant-derived compounds such as essential oils, classified as Generally Recognized as Safe (GRAS), polyphenols, lactic acid bacteria, cold plasma technologies, nanoparticles (particularly metal nanoparticles such as silver or zinc nanoparticles), magnetic materials, and ionizing radiation. Among these, essential oils, polyphenols, and lactic acid bacteria offer eco-friendly and non-toxic alternatives to conventional fungicides while demonstrating strong antimicrobial and antifungal properties; essential oils and polyphenols also possess antioxidant activity. Cold plasma and ionizing radiation enable rapid, non-thermal, and chemical-free decontamination processes. Nanoparticles and magnetic materials contribute advantages such as enhanced stability, controlled release, and ease of separation. Furthermore, this review explores recent advancements in the application of artificial intelligence, particularly machine learning methods, for the identification and classification of fungal species as well as for predicting the growth of toxigenic fungi and subsequent mycotoxin production in food products and culture media.

Due to their unique elemental compositions and interface coupling effects, bimetallic nanoparticles (BNPs), a class of nanoalloys, have attracted significant attention for applications in biomedicine, environmental remediation, and catalysis. BNPs, formed via the combination of two metal ions under light or thermal conditions, exhibit enhanced catalytic properties due to synergistic interactions between constituent metals, which result in optimized electronic structures, increased active sites, and reduced activation energy for catalytic reactions. However, BNPs may pose potential toxicity risks to organisms through bioaccumulation and environmental exposure. In this study, Ag-Pt nanoparticles (AP NPs) with varying molar ratios were synthesized and characterized to elucidate the relationship between composition, catalytic activity, and cytotoxicity. Catalytic assays revealed that AP NPs exhibited remarkable oxidase-like activity. Cytotoxicity tests revealed dose- and composition-dependent effects, with the AP55 (Ag : Pt at 5 : 5 ratio) exhibiting the highest cytotoxicity compared to monometallic counterparts at equivalent concentrations. Notably, the proportion of Ag in the AP NPs was identified as the dominant factor influencing catalytic activity and cytotoxicity. Mechanistic investigations attributed this cytotoxicity to the interplay of peroxidase-like catalytic activity, oxidative stress, and lysosomal ion release, disrupting cellular redox homeostasis and triggering apoptosis. Enzymatic assays further confirmed reductions in antioxidant defenses, including superoxide dismutase (SOD) and catalase (CAT) activities, amplifying reactive oxygen species (ROS) generation and oxidative damage. These findings underscore the critical role of catalytic behavior in mediating biological interactions and cytotoxic effects of BNPs. We establish a relationship between composition, oxidase-like activity, and cytotoxicity, providing insights into their potential biomedical applications and paving the way for the rational design of multifunctional nanomaterials with tunable biological effects.

The escalating concentrations of emerging contaminants in water systems and the possible environmental threats they emphasize the necessity for more sophisticated methods in the evaluation of water quality. Traditional bioassays raise ethical concerns, require intricate procedures, entail significant expenses, and only allow for endpoint measurements. The using of nitrifying bacteria in bioassays has resulted in increased sensitivity to a wide range of toxic substances, making them valuable for the identification of water pollution. This study introduces a novel nitrifying bacteria bioassay kit for detecting heavy metal contaminants in water. This bioassay is specifically designed for expedited analysis of oxygen consumption. This technique enables the identification of a range of toxic metals. Optimization studies indicated that 100 mg ammonia NH4+-N/L, and 1 mL acclimated culture were the ideal conditions facilitating the necessary volume of gas consumption for sensitive data generation. Determined EC50 values of the selected toxic metals were: chromium (Cr6+), 0.51 mg/L; silver (Ag+), 2.90 mg/L; copper (Cu2+), 2.90 mg/L; nickel (Ni2+), 3.60 mg/L; arsenic (As3+), 4.10 mg/L; cadmium (Cd2+), 5.56 mg/L; mercury (Hg2+), 8.06 mg/L; and lead (Pb2+), 19.3 mg/L. Metagenomics analysis found key species in the research included Nitrosomonas eutropha, Nitrosomonas oligotropha, Nitrosomonas europaea, Nitrobacter vulgaris, Nitrobacter winogradskyi, Nitrospira moscoviensis and Nitrospira lenta. In addition, this bioassay is ideal for field screening and real-time monitoring due to its simplicity and reliability. This bioassay provides a precise, economical, and effective substitute for more intricate and ethically problematic techniques, enhancing the effectiveness of water quality monitoring programs.

Viral infections continue to pose a significant challenge to global health, with increasing resistance to conventional antiviral therapies highlighting the urgent need for alternative treatment strategies. Silver nanoparticles (AgNPs) have attracted attention as broad-spectrum antiviral agents due to their unique physicochemical properties and ability to target multiple stages of viral infection. This review provides a comprehensive analysis of the antiviral mechanisms of AgNPs, highlighting their efficacy against clinically relevant enveloped viruses such as influenza, herpes simplex, hepatitis B, and coronaviruses. How key nanoparticle characteristics, including size, shape, surface functionalization, and synthesis methods, influence their antiviral performance is examined. Studies indicate that AgNPs exert their effects through direct interactions with viral particles, inhibition of viral adhesion, and entry into host cells with disruption of viral replication. Furthermore, their potential applications in therapeutic formulations, antiviral coatings, and nanomedicine-based strategies are explored. Despite their promise, challenges regarding cytotoxicity, stability, and large-scale production must be addressed to ensure their safe and effective clinical use. This review highlights the transformative potential of AgNPs in antiviral therapy and highlights the need for further investigation to facilitate their clinical translation in the fight against emerging and drug-resistant viral infections.

Cancer immunotherapy aims to harness the body's own immune system for effective and long-lasting elimination of malignant neoplastic tissues. Owing to the advance in understanding of cancer pathology and immunology, many novel strategies for enhancing immunological responses against various cancers have been successfully developed, and some have translated into excellent clinical outcomes. As one promising strategy for the next generation of immunotherapies, activating the multi-cellular network (MCN) within the tumor microenvironment (TME) to deploy multiple mechanisms of action (MOAs) has attracted significant attention. To achieve this effectively and safely, delivering multiple or pleiotropic therapeutic cargoes to the targeted sites of cancerous tissues, cells, and intracellular organelles is critical, for which numerous nanocarriers have been developed and leveraged. In this review, we first introduce therapeutic payloads categorized according to their predicted functions in cancer immunotherapy and their physicochemical structures and forms. Then, various nanocarriers, along with their unique characteristics, properties, advantages, and limitations, are introduced with notable recent applications in cancer immunotherapy. Following discussions on targeting strategies, a summary of each nanocarrier matching with suitable therapeutic cargoes is provided with comprehensive background information for designing cancer immunotherapy regimens.

Heavy metals and mycotoxins are important contaminants in food pollution. Sensitive, reliable, and rapid detection of heavy metals and mycotoxins is crucial for human health. In this work, imidazole-functionalized aggregation-induced emission (AIE) molecule tetra-(4-pyridylphenyl) ethylene (TPPE) was used as a precise and specific probe for Ag+ detection, with a limit of detection (LOD) of 0.0318 μM. Meanwhile, a large amount of hydrophobic TPPE molecules were loaded into the amphiphilic block copolymer F127 to form ultrabright fluorescent microspheres (TPPENPs). Lateral flow immunochromatography (LFIA) based on immunoprobe (TPPENPs-Ab) has been successfully developed. The LOD of TPPENPs-LFIA for T-2 toxin was 0.13 μg/L, which was 13.31-fold and 8.62-fold more sensitive than that of gold nanoparticles-based LFIA and ordinary fluorescent microspheres-based LFIA, respectively. TPPENPs-LFIA was employed to detect T-2 toxin in actual grain samples, with a spiked recovery rate of 71.69 - 111.13 %. This assay offers a promising strategy and new idea for multi-target detection.

The growing use of silver (Ag) and copper (Cu) nanoparticles (NPs) for their antimicrobial properties has raised environmental health concerns due to their coexistence in aquatic ecosystems. This study assessed the combined physiological and molecular toxicity of AgNPs and CuNPs in rainbow trout (Oncorhynchus mykiss) exposed to sub-lethal concentrations of the NP mixture for 21 days. Fish were exposed to varying concentrations of co-exposure of AgNPs and CuNPs (T1 group 0.2 AgNPs + 0.2 mg/L CuNPs, T2 group 0.8 AgNPs + 0.6 mg/L CuNPs, and T3 group 1.4 AgNPs + 1.0 mg/L CuNPs). Behavioral alterations were evident, accompanied by a significant (p < 0.05) reduction in hemoglobin, red blood cell count, and hematocrit levels, while white blood cell counts increased, indicating immune activation. Serum biochemical analyses revealed metabolic disturbances linked to oxidative stress and physiological imbalance. Enzymatic activities in gills and liver showed a dynamic response, with elevated catalase (CAT) and superoxide dismutase (SOD) levels at T2 and T3 after 14 days, followed by a decline by day 21. Glutathione S-transferase (GST) activity increased in gills at T2 and T3 after 7 days and in the liver at T3 after 14 days, while lipid peroxidation (LPO) significantly increased in gills at T3 after 7 days and in the liver at T2 and T3 after 14 days. Molecular analysis confirmed upregulation of oxidative stress genes (SOD1, CAT) and inflammatory markers (HSP70, IL- 1β). Histopathological examination revealed gill damage, including lamellar fusion and hyperplasia, and liver degeneration, such as hepatocyte vacuolation and necrosis, with the most severe effects observed at T3. These findings highlight dose-dependent toxicity and oxidative damage caused by the AgNPs-CuONPs mixture, emphasizing its potential physiological and molecular impacts on aquatic organisms.

Infections remain a significant challenge in orthopedic settings despite advancements in preventive measures. Antibiotics are the primary defense against infections, but optimal delivery methods to the infection site are still being investigated. This review aims to examine existing approaches for local drug delivery from a basic science perspective.

Achieving adequate antibiotic concentration at the infection site is challenging due to compromised vasculature in ischemic conditions. Local administration methods, including antibiotic-loaded carriers such as impregnated bone grafts and various bone substitutes, are being explored as alternatives to systemic antibiotic use.

Various materials, including polymethyl methacrylate (PMMA), hydroxyapatite, calcium phosphate/sulfate, bone glass, and hydrogel, are being investigated for local antibiotic delivery. Some of these materials possess inherent antibacterial properties due to their chemical interactions. The selection of appropriate antibiotics, their dosage, release kinetics from the carrier material, physical behavior of the material/graft, and biocompatibility are key areas for further investigation in basic science research.

The review investigates the ecotoxicological implications of fungal-synthesized silver nanoparticles (AgNPs), focusing on their behavior, transformations, and impacts across aquatic and terrestrial ecosystems. Advanced techniques, such as Single-Particle ICP-MS and Nanoparticle Tracking Analysis, reveal the persistence and biotransformation of AgNPs, including silver ion (Ag⁺) release and reactive oxygen species (ROS) generation. The review highlights species-specific bio-accumulation pathways in algae, soil microbes, invertebrates, and vertebrates, along with the limited biomagnification potential within trophic levels. Long-term exposure to AgNPs leads to reduced soil fertility, altered microbial communities, and inhibited plant growth, raising significant ecological concerns. Sustainable mitigation strategies, including bioremediation and advanced filtration systems, are proposed to reduce the environmental risks of AgNPs. This comprehensive analysis provides a framework for future ecological studies and regulatory measures, balancing the technological benefits of fungal-synthesized AgNPs with their environmental safety.

Nanotechnology offers promising new avenues for combating drug-resistant pathogens. Given its antioxidant capacity, the water-soluble fraction of Brazilian kefir was hypothesized to serve as an effective reducing agent for the green synthesis of silver nanoparticles (AgNPs). It was further hypothesized that both the entire fraction (WSF) and the < 10 kDa fraction AgNPs would augment the therapeutic effects of kefir, particularly its antimicrobial activity. The successful synthesis was confirmed through the use of UV-Visible spectroscopy and Fourier-transform infrared analyses. WSF-AgNPs demonstrated potent antimicrobial activity, with minimum inhibitory concentrations of 25 µg/mL against A. baumannii (p < 0.0001) and 50 µg/mL against K. pneumoniae (p < 0.0001). Although no toxicity was observed in long-term tests on adult Drosophila melanogaster, AgNPs intake impaired larvae development. Oxidative stress analysis showed mild oxidative imbalance on advanced oxidation protein products (AOPP), sulfhydryl, and reduced glutathione (GSH) contents, with no alterations observed in reactive oxygen species (ROS) quantities, ferric reducing antioxidant power (FRAP), and catalase (CAT) activity. These findings suggest that kefir-derived AgNPs may have potential for combating drug-resistant infections. Future studies should focus on enhancing specificity through compound conjugation and investigating broader applications, including disinfectants, wound healing, and antibiotic development.

To overcome problems associated with surgical site infection and implant loosening, we developed a titanium (Ti)-based material employing a modified alkaline heat treatment that releases strontium (Sr) and silver (Ag) ions (CaSrAg-Ti). In this study, to determine the optimal Ag treatment concentration, we prepared four different materials-commercially pure Ti (cp-Ti) as a negative control, CaSr1mMAg-Ti, CaSr10mMAg-Ti, and CaSr50mMAg-Ti. Ion release test was performed by immersing the prepared disks in fetal bovine serum. With increased loading of Ag ions, the amount of released ions increased. Colony-forming unit count assay was performed using methicillin-susceptible Staphylococcus aureus and Escherichia coli. High antibacterial activity was observed in CaSr10mMAg-Ti and CaSr50mMAg-Ti groups. In vivo experiments were performed using the rat subcutaneous pocket infection model and evaluated by counting the attached bacteria, wound appearance, and histological evaluation. High antibacterial activity value (AAV >2) and anti-inflammatory effects were observed in the CaSr50mMAg-Ti group. However, CaSr10mMAg-Ti did not exhibit consistent antibacterial activity. For in vivo biocompatibility and bone-bonding ability evaluation, rods were implanted into the rat femur. No cytotoxicity was observed at 1 week, and good bone-bonding ability at 4 and 8 weeks was not significantly different from that of CaSr1mMAg-Ti. To evaluate in vivo bioactivity and cytotoxicity, MC3T3-E1 cells were cultured on disks. CaSr10mMAg-Ti and CaSr50mMAg-Ti significantly inhibited the proliferation and differentiation of MC3T3E1 cells, as well as the production of extracellular matrix in vivo, despite showing good biocompatibility in vivo. In conclusion, CaSr50mMAg-Ti, with increased Ag ion loading, exhibited high antibacterial activity in vivo while maintaining the bone-bonding ability and is a promising therapeutic biomaterial. Further research is needed to determine the optimal combination of therapeutic concentrations of Sr and Ag.

Antibiotics represent one of the most significant medical breakthroughs of the twentieth century, playing a critical role in combating bacterial infections. However, the rapid emergence of antibiotic resistance has become a major global health crisis, significantly complicating treatment protocols. This paper provides a narrative review of the current state of antibiotic resistance, synthesizing findings from primary research and comprehensive review articles to examine the various mechanisms bacteria employ to counteract antibiotics. One of the primary sources of antibiotic resistance is the improper use of antibiotics in the livestock industry. The emergence of drug-resistant microorganisms from human activities and industrial livestock production has presented significant environmental and public health concerns. Today, resistant nosocomial infections occur following long-term hospitalization of patients, causing the death of many people, so there is an urgent need for alternative treatments. In response to this crisis, non-antibiotic therapeutic strategies have been proposed, including bacteriophages, probiotics, postbiotics, synbiotics, fecal microbiota transplantation (FMT), nanoparticles (NPs), antimicrobial peptides (AMPs), antibodies, traditional medicines, and the toxin-antitoxin (TA) system. While these approaches offer innovative solutions for addressing bacterial infections and preserving the efficacy of antimicrobial therapies, challenges such as safety, cost-effectiveness, regulatory hurdles, and large-scale implementation remain. This review examines the potential and limitations of these strategies, offering a balanced perspective on their role in managing bacterial infections and mitigating the broader impact of antibiotic resistance.

Silver nanoparticles possess remarkable properties that render them highly beneficial for medical applications in both infectious and non-infectious diseases. Among their most renowned attributes is their antimicrobial activity. They have demonstrated efficacy against a wide range of bacteria, fungi, protozoa, and viruses. Additionally, the antitumor and anti-diabetic properties of silver nanoparticles, along with their ability to promote wound healing and their application as biosensors, underscore their therapeutic potential for various non-infectious conditions. As silver nanoparticles are employed for medical purposes, their potential toxicity must be considered. While silver nanoparticles present a promising alternative in the therapeutic domain, further research is needed to elucidate their precise mechanisms of action, optimize their efficacy, and mitigate any potential health risks associated with their use.

The intestinal epithelium plays a pivotal role as a vital barrier between the external environment and the human body, regulating nutrient absorption and preventing the entry of harmful substances. The human oral exposure to silver nanoparticles (AgNP) raises concerns about their potential toxicity, especially at the intestinal level. The objective of this work was to investigate the potential pro-inflammatory effects of polyvinylpyrrolidone (PVP)-AgNP of two different sizes, 5 and 50 nm, at the intestinal level, while also assessing the protective ability of quercetin against these effects. To address this, an intestinal co-culture model comprising C2BBe1 cells and THP-1 derived macrophages was established, and the effects of 5 or 50 nm PVP-AgNP were studied, alone or in combination with quercetin, over two-time points, 4 and 24 hours. PVP-AgNP, of both sizes, disrupted the barrier integrity within 4 hours of exposure. However, a notable intensification in pro-inflammatory effects was evident only after 24 hours of exposure, especially with smaller PVP-AgNP (5 nm). This resulted in heightened cellular death, increased levels of reactive species, activation of nuclear factor kappa B (NF-кB), and production of interleukin (IL)-8. Quercetin demonstrates the ability to maintain barrier integrity and mitigate oxidative stress, thereby offering protection against the detrimental effects induced by AgNP at the intestinal level.

Silver nanoparticles (AgNPs) have attracted significant interest in veterinary medicine due to their unique properties, including enhanced stability, greater antimicrobial efficacy, and reduced toxicity compared to traditional silver salts. Their applications span various areas of veterinary practice, such as dermatology, wound management, infection prevention, drug delivery, and disinfection. This review explores their use in pigs, highlighting their role as feed additives to prevent diarrhoea, as antibacterial agents in semen extenders, and veterinary dermatology. AgNPs possess broad-spectrum antibacterial activity against both Gram-positive and Gram-negative bacteria, positioning them as a promising alternative to antibiotics in addressing antibiotic resistance. Additionally, AgNPs have shown antiviral potential, though the exact mechanism of action remains unclear. The review examines the antibacterial and antiviral properties of AgNPs, their utility in facility sanitation, and their potential toxicity to pigs. While AgNPs offer significant benefits in veterinary applications, concerns about their toxicity persist. Efforts to reduce this toxicity, such as surface modifications or combining AgNPs with other substances, are under investigation. Further research is essential to fully understand the potential applications and safety of AgNPs in pig medicine.

The present research focused on extraction of bioactive compounds from Woodfordia fruticosa flower (WF) using ethanol, methanol and ethyl acetate as solvents and the development of silver nanoparticles using these extracts for inhibition of Staphylococcus aureus (S. aureus), Klebsiella pneumoniae (K. pneumoniae), Escherichia coli (E. coli), and Bacillus cereus (B. cereus) bacteria. The functional groups of bioactive compounds present in the solvent extracts were characterized using Fourier transform infrared spectroscopy (FT-IR). The morphological features and formation of silver nanoparticles (10-30 nm, by the reduction of solvent extracts) were evaluated using scanning electron microscopy (SEM) and ultraviolet-visible (UV-Vis) spectroscopy, respectively. The elemental compositions of the synthesized nanoparticles were analyzed using energy-dispersive X-ray spectroscopy (EDX). The inhibition efficiency of the alcoholic and ester extracts of WF and the synthesized silver nanoparticles were evaluated and compared to Moxifloxacin. The results revealed that the synthesized silver nanoparticles demonstrated enhanced bacterial inhibition efficiency compared to the unprocessed ethanol, methanol, and ethyl acetate extracts of WF, and Moxifloxacin.

This study explores the green synthesis of silver nanoparticles (AgNPs) using Cymbopogon citratus (lemongrass) extract as a reducing agent. Synthesis was confirmed by a color change (light yellow to dark brown) under optimal conditions: 1.50 mM silver nitrate, 3.5% v/v extract, at 100 °C, with a pH of 9, and for 60 min. The AgNPs exhibited spherical morphology, a hydrodynamic diameter of 135.41 ± 49.30 nm, a zeta potential of -29.9 ± 1.4 mV, crystalline structure, and minimal aggregation. AgNPs showed significant antibacterial activity, particularly at >20 µg/well, with the zones of inhibition varying by bacterial strain. In vitro studies demonstrated anti-inflammatory, antidiabetic (α-glucosidase and α-amylase inhibition), and antioxidant activities, with AgNPs outperforming plant extract and nearing standard efficacy at higher concentrations. Cyto-toxicity studies indicated that AgNPs and plant extract were less toxic than doxorubicin but exhibited concentration-dependent effects on cancerous and non-cancerous cells. Eco-toxicity assays revealed that AgNPs were less acutely toxic than controls but posed risks with prolonged exposure. This work highlights the eco-friendly synthesis of AgNPs and their potential in biomedical applications, demonstrating efficacy in antibacterial and antioxidant activities.

Nanoparticles have been widely used in cancer diagnostics and treatment research due to their unique properties. Magnetic nanoparticles are popular in imaging techniques due to their ability to alter the magnetization field around them. Plasmonic nanoparticles are mainly applied in cancer treatments like photothermal therapy due to their ability to convert light into heat. While these nanoparticles are popular among their respective fields, magnetic-plasmonic core-shell nanoparticles (MPNPs) have gained popularity in recent years due to the combined magnetic and optical properties from the core and shell. MPNPs have stood out in cancer theranostics as a multimodal platform capable of serving as a contrast agent for imaging, a guidable drug carrier, and causing cellular ablation through photothermal energy conversion. In this review, we summarize the different properties of MPNPs and the most common synthesis approaches. We particularly discuss applications of MPNPs in cancer diagnosis and treatment based on different mechanisms using the magnetic and optical properties of the particles. Lastly, we look into current challenges they face for clinical applications and future perspectives using MPNPs for cancer detection and therapy.

The use of silver nanoparticles (AgNPs) has gained importance in agriculture in recent years thanks to their unique characteristics, including their antimicrobial capacity and their ability to promote plant growth. Due to these attributes, AgNPs are considered a promising solution for the future of agriculture, offering significant potential to address the challenges the sector confronts currently. However, it is important to adjust the application conditions, depending on the target and the crop used, to improve AgNP treatment efficiency. This review compiles recent advances in the use of AgNPs for crop production, both in and ex vitro. AgNPs promote growth and alleviate biotic and abiotic stresses through different ex vitro application methods. They are also efficiently used in vitro to improve plant culture and pathogen elimination. In addition, the safety and toxicity associated with their use are discussed. AgNPs are a novel tool with great potential for the agricultural sector, but it is still necessary to continue researching the mechanisms of AgNP action in order to optimize their application in each specific case.

Silver nanoparticles (AgNPs) have gained significant attention in veterinary medicine due to their antimicrobial properties and potential therapeutic applications. Silver has long been recognized for its ability to combat a wide range of pathogens, and when engineered at the nanoscale, silver's surface area and reactivity are greatly enhanced, making it highly effective against bacteria, viruses, and fungi. This narrative review aimed to summarize the evidence on the antimicrobial properties of AgNPs and their current and potential clinical applications in veterinary medicine. The antimicrobial action of AgNPs involves several mechanisms, including, among others, the release of silver ions, disruption of cell membranes and envelopes, induction of oxidative stress, inhibition of pathogens' replication, and DNA damage. Their size, shape, surface charge, and concentration influence their efficacy against bacteria, viruses, and fungi. As a result, the use of AgNPs has been explored in animals for infection prevention and treatment in some areas, such as wound care, coating of surgical implants, animal reproduction, and airway infections. They have also shown promise in preventing biofilm formation, a major challenge in treating chronic bacterial infections. Additionally, AgNPs have been studied for their potential use in animal feed as a supplement to enhance animal health and growth. Research suggested that AgNPs could stimulate immune responses and improve the gut microbiota of livestock, potentially reducing the need for antibiotics in animal husbandry. Despite their promising applications, further research is necessary to fully understand the safety, efficacy, and long-term effects of AgNPs on animals, humans, and the environment.

This study aims to characterize antibiotic resistance (AR) and virulence markers in Salmonella spp. isolated from Romanian outpatients' stool samples.

In 2019, community-acquired Salmonella strains were collected and identified using MALDI-TOF mass spectrometry, antibiotic susceptibility profiles have been determined with the MicroScan system, and soluble virulence factors were evaluated using specific culture media, while biofilm formation was quantified in 96-well plates. Molecular analysis targeted resistance genes for β-lactams (e.g., blaTEM and blaSHV); tetracyclines (e.g., tet(A)); sulphonamides; and quinolones, as well as virulence genes (e.g., invA, spvC, pldA, and held). Whole-genome sequencing (WGS) was performed on 19 selected isolates. A silver nanoparticles (AgNPsol) alternative to conventional antibiotics was tested for effectiveness against multidrug-resistant (MDR) isolates.

From the total of 309 Salmonella isolates (65.05% from children under 4 years of age) belonging to four subtypes and four serovars, 27.86% showed resistance to at least one antibiotic, most frequently to tetracycline, ampicillin, and piperacillin. The strains frequently expressed haemolysin (67%), aesculinase (65%), and gelatinase (62%). Resistance to trimethoprim-sulfamethoxazole was encoded by the sul1 gene in 44.83% of the strains and to tetracyclines by the tet(A) gene (59.52%). The ESBL genes blaTEM, blaSHV, and blaCTX-M were detected by PCR in 16.18%, 2.91%, and 0.65% of the strains, respectively. Additionally, 98.63% of the strains carried the invA marker, with notable positive associations between blaSHV, qnrB, and sul1 with spvC.

The present findings revealed significant patterns in Salmonella isolates, subtypes, serovars, AR, and virulence, emphasising the need for continuous surveillance of Salmonella infections. Additionally, the potential of AgNPs as an alternative treatment option was demonstrated, particularly for paediatric S. enterica infections.

Liver cancer is one of the most common lethal malignancy in the world. To treat liver cancer, new cure options are crucial. The use of natural substances along nanosciences may provide healing with lower toxicity and a smaller amount of side properties. In this research, The three-component selenium-silver-chitosan nanocomposite (Se-Ag-CS NCs) were synthesised with the help of ultrasound in a stepwise manner. The as-synthesised Se-Ag-CS NCs were characterised accordingly by applying powder X-Ray diffraction (PXRD), Fourier transforms infrared spectroscopy (FTIR), field emission scanning electron microscopy (FESEM), energy dispersive x-ray analysis (EDX), transmission electron microscopy (TEM), dynamic light scattering (DLS) and potential. The PXRD demonstrated that the NCs were synthesised successfully and the grain sizes of 27.3 were obtained. The FESEM and TEM analyses have shown the NCs have a nano-sized structure with spherical and rod-like morphologies in a coating of CS. The DLS analysis also revealed that NCs were synthesised in nanoscale particles. The NCs' surface charge was also positive due to the presence of chitosan. Different concentrations of NCs (0, 0.125, 0.250, 0.500, and 1 mg/ml) were tested at different times (24, 48, and 72 h) to measure cytotoxicity against liver cancer cells. The results showed at a concentration of 1 mg/mL in 72 h, the most toxicity effects were applied to liver cancer cells. Moreover, the results indicated NCs can inhibit the growth of cancer cells in a dose-dependent manner, while the toxicity of nanocomposite on normal cells was less. It is important to create nanocomposites derived from natural polymers as a new strategy in cancer treatment that can fight cancer cells while having low toxicity for normal cells. Therefore, the present results can be considered in improving cancer-fighting methods.

The increasing prevalence of silver nanoparticles (AgNP) in various applications has sparked concerns about their potential adverse effects on human health. Hence, it is crucial to devise strategies to minimize their detrimental effects. Quercetin, a naturally occurring flavonoid present in human diet is known for its broad biological effects, including anti-inflammatory properties. Considering this, quercetin could serve as a promising strategy to protect the body against the harmful effects of AgNP. Thus, this study aimed to evaluate the potential protective role of quercetin against the deleterious effects induced by 5 nm polyvinylpyrrolidone (PVP)-AgNP in C57BL/6J mice. Using a novel administration technology (HaPILLness), mice were given a daily oral dose of AgNP at 1 mg/kg body weight (bw) or 10 mg/kg bw for 14 days, combined with daily IP injections of quercetin at 1 mg/kg bw. Our findings demonstrate that quercetin effectively attenuated the AgNP-induced intestinal inflammatory response, as demonstrated by reduced histological vascular and cellular alterations, along with a notable decrease in cytokine production, attributed to the inhibition of the nuclear factor (NF)-кB inflammatory pathway. Quercetin's protective effects extended to the liver and lungs, by reversing changes in the inflammatory and antioxidant markers cluster of differentiation (CD)4, superoxide dismutase 1 (SOD1) and catalase.

Globally, people widely recognize cancer as one of the most lethal diseases due to its high mortality rates and lack of effective treatment options. Ongoing research into cancer therapies remains a critical area of inquiry, holding significant social relevance. Currently used treatment, such as chemotherapy, radiation, or surgery, often suffers from other problems like damaging side effects, inaccuracy, and the lack of ability to clear tumors. Conventional cancer therapies are usually imprecise and ineffective and usually develop resistance to treatments and cancer recurs. Cancer patients need fresh and innovative treatment that can reduce side effects while maximizing effectiveness. In recent decades several breakthroughs in these, and other areas of medical research, have paved the way for new avenues of fighting cancer including more focused and more effective alternatives. This study reviews exciting possibilities for mesenchymal stem cells (MSCs), nanomaterials, and microbial agents in the modern realm of cancer treatment. Nanoparticles (NPs) have demonstrated surprisingly high potential. They improve drug delivery systems (DDS) significantly, enhance imaging techniques remarkably, and target cancer cells selectively while protecting healthy tissues. MSCs play a double role in tissue repair and are a vehicle for novel cancer treatments such as gene treatments or NPs loaded with therapeutic agents. Additionally, therapies utilizing microbial agents, particularly those involving bacteria, offer an inventive approach to cancer treatment. This review investigates the potential of nanomaterials, MSCs, and microbial agents in addressing the shortcomings of conventional cancer therapies. We will also discuss the challenges and limitations of using these therapeutic approaches.

The applicability of nanomaterials has evolved in biomedical domains thanks to advances in biocompatibility strategies and the mitigation of cytotoxic effects, allowing diagnostics, imaging, and therapeutic approaches. The application of nanoparticles (NP), particularly metal nanoparticles (mNPs), such as gold (Au) and silver (Ag), includes inherent challenges related to the material characteristics, surface modification, and bioconjugation techniques. By tailoring the surface properties through appropriate coating with biocompatible molecules or functionalization with active biomolecules, researchers can reach a harmonious interaction with biological systems or samples (mostly fluids or tissues). Thus, this review highlights the mechanisms associated with the obtention of biocompatible mNP and presents a comprehensive overview of methods that facilitate safe and efficient production. Therefore, we consider this review to be a valuable resource for all researchers navigating this dynamic field.

l-cysteine is a versatile amino acid that plays a pivotal role in synthesizing critical molecules, enzymatic catalysis, regulation, and electron transport. It also has tremendous potential to act as an adjuvant for enhancing the biological efficacy of various nanoparticles in vivo. The current study is aimed to evaluate the protective efficacy of silver nanoparticles (AgNPs) decorated with l-cysteine in carbon tetrachloride (CCl4)-induced hepatotoxicity in the Swiss albino rats as an animal model. The rats were divided into four treatment groups: Group 1 (control without any treatments), Group 2 treated with AgNPs and l-cysteine composite (5 mg/kg body weight on every third day), Group 3 (single dose of 1 mL/kg CCl4), and Group 4 treated with AgNPs-l-cysteine composite in the rats pre-administered with CCl4. After treatment for a month, the rats were killed, and their liver and blood samples were subjected to biochemical analysis and histological examination.: Group 2 showed all the parameters comparable to control Group 1. On the contrary, CCl4-treated, Group 3 rats showed abnormally raised liver function markers (AST and ALT) and liver toxicity markers (GGT, LDH, and total bilirubin) concomitant with disturbed oxidative stress parameters (GSH and MDA) compared to the control. However, Group 4 rats demonstrated a significant recovery from CCl4-induced biochemical alteration in the animals as compared to Group 3. In addition, the biochemical measurements were harmonious with the histological analysis of the liver sections of the treated rats. Hence, the proposed AgNPs-l-cysteine composite is a potent hepato-protecting agent in vivo that can be employed in regulating CCl4-induced hepatotoxicity or any drug or potential pharmaceutical compound exerting similar toxicity.

Metallic nanoparticles (MNPs) have attracted great interest among scientists and researchers for years due to their unique optical, physiochemical, biological, and magnetic properties. As a result, MNPs have been widely utilized across a variety of scientific fields, including biomedicine, agriculture, electronics, food, cosmetics, and the environment. In this regard, the current review article offers a comprehensive overview of recent studies on the synthesis of MNPs (metal and metal oxide nanoparticles), outlining the benefits and drawbacks of chemical, physical, and biological methods. However, the biological synthesis of MNPs is of great importance considering the biocompatibility and biological activity of certain MNPs. A variety of characterization techniques, including X-ray diffraction, transmission electron microscopy, UV-visible spectroscopy, scanning electron microscopy, dynamic light scattering, atomic force microscopy, Fourier transform infrared spectroscopy, and others, have been discussed in depth to gain deeper insights into the unique structural and spectroscopic properties of MNPs. Furthermore, their unique properties and applications in the fields of medicine, agriculture, and the environment are summarized and deeply discussed. Finally, the main challenges and limitations of MNPs synthesis and applications, as well as their future prospects have also been discussed.

Recently, gold nanoparticles (Au Nps) have gained tremendous attention for its unique properties as a safe nanocarrier for delivering drugs that are used in different disease diagnoses. Although silver nanoparticles (Ag NPs) have been generally applied due to their strong antibacterial, antiviral, antifungal, and antimicrobial properties, their toxicity is a subject of sustained debate, thus requiring further studies. The present study aims to evaluate the potential protective effect of gold nanoparticles and phthalocyanine-gold nanoconjugates (Pc-Au NCs) against the hepatorenal toxicity of silver nanoparticles in male rats. Herein, 60 adult male Rattus norvegicus rats were divided into six equal groups (n = 10/group); the first group was kept as control, the second received gold nanoparticles (Au NPs) intraperitoneally (10 µg/kg) daily for 3 weeks, the third group is gold-phthalocyanine (Pc-Au) group where rats were injected intraperitoneally with gold-phthalocyanine for 3 weeks (10 µg/kg), the fourth group received silver nanoparticles (Ag NPs) (4 mg/kg) daily intraperitoneally for 3 weeks, the fifth group is silver + gold nanoparticles group (Ag + Au), and the sixth is silver + gold-phthalocyanine nanoconjugates (Ag + Pc-Au) group in which rats were intraperitoneally injected firstly with Ag NPs (4 mg/kg) for 3 weeks then with gold or gold-phthalocyanine for another 3 weeks (10 µg/kg). Our results revealed that Ag NPs could increase the serum AST, ALT, ALP, urea, creatinine, and lipid profile and significantly decreased the total protein and albumin. Moreover, histopathological alterations detected in the kidney and the liver of the Ag NPs group included vascular congestion, inflammatory cell infiltration, and tissue distortion. Alongside, exposure to Ag NPs induces hepatic and renal oxidative stress by suppressing the antioxidant-related genes including glutathione peroxidase 1 (gpx1), superoxide dismutase (sod), and catalase (cat). Ag NPs also upregulated the hepatic and renal genes involved in inflammation such as the interleukin-6 (il-6) and tumor necrosis factor-α (tnf-α), nuclear factor kappa B (nf-κβ), apoptosis such as the BCL2 associated X (bax), casp3, and other related to metabolism including asparagine synthetase (asns), suppressor of cytokine signaling 3 (socs3), MYC proto-oncogene (myc), and C-C motif chemokine ligand 2 (ccl2). On the other hand, treatment with Au NPs and Pc-Au NCs could effectively ameliorate the hepatorenal damages induced by Ag NPs and improve liver and kidney architecture and function, especially in the Pc-Au NCs group. Briefly, our study revealed the underlined mechanism of Ag NPs hepatotoxic and nephrotoxic effects and that Pc-Au NCs could alleviate these adverse impacts via their anti-oxidative, anti-apoptotic, and anti-inflammatory activities.

The synthesis of silver nanoparticles with controlled physicochemical properties is essential for governing their intended functionalities and safety profiles. However, synthesis process involves multiple parameters that could influence the resulting properties. This challenge could be addressed with the development of predictive models that forecast endpoints based on key synthesis parameters. In this study, we manually extracted synthesis-related data from the literature and leveraged various machine learning algorithms. Data extraction included parameters such as reactant concentrations, experimental conditions, as well as physicochemical properties. The antibacterial efficiencies and toxicological profiles of the synthesized nanoparticles were also extracted. In a second step, based on data completeness, we employed regression algorithms to establish relationships between synthesis parameters and desired endpoints and to build predictive models. The models for core size and antibacterial efficiency were trained and validated using a cross-validation approach. Finally, the features' impact was evaluated via Shapley values to provide insights into the contribution of features to the predictions. Factors such as synthesis duration, scale of synthesis and the choice of capping agents emerged as the most significant predictors. This study demonstrated the potential of machine learning to aid in the rational design of synthesis process and paves the way for the safe-by-design principles development by providing insights into the optimization of the synthesis process to achieve the desired properties. Finally, this study provides a valuable dataset compiled from literature sources with significant time and effort from multiple researchers. Access to such datasets notably aids computational advances in the field of nanotechnology.

The widespread use of silver nanoparticles in many industries is increasing every year. Along with this use, there is growing concern about the potential unintentional exposure of human and animal organisms to these nanomaterials. It has been shown that AgNPs have the ability to penetrate organisms and can have harmful effects on cells and organs in the body. In order to reduce the effects of AgNPs on living organisms, newer solutions are being investigated, such as particle stabilization or other methods of synthesizing these particles. The physical synthesis of AgNPs using high-voltage arc discharge (HVAD) may be one of these alternatives. To determine the effect of silver nanoparticles obtained by this method, cytogenetic analysis was performed on domestic dog somatic cells using a cytokinesis-blocking micronucleus assay. In the experiments performed, peripheral blood cells of the domestic dog were exposed in vitro for 3 and 24 h to three tested colloidal silver compounds (unstable AgNP-HVAD, sodium citrate-stabilized silver nanoparticles-AgNP+C, and silver nitrate). The toxicity of these compounds was evaluated at concentrations of 5, 10, and 20 µg/L, and the presence of the following cellular abnormalities was analyzed: micronuclei, nuclear buds, nucleoplasmic bridges, or multinucleated cells. The study showed a significant increase in the number of micronuclei compared to the control sample, as well as the presence of nuclear buds and nucleoplasmic bridges in somatic cells of the domestic dog, confirming the genotoxic nature of the particles. However, there was no cytotoxic effect due to the lower number of multinucleated cells and the absence of apoptotic or necrotic cells in the samples analyzed. Further studies are needed to better understand the mechanisms of toxicity of AgNPs produced by the HVAD method and the extent of their effects on mammalian somatic cells.

The rising resistance of various pathogens and the demand for materials that prevent infections drive the need to develop broad-spectrum antimicrobial membranes capable of combating a range of microorganisms, thereby enhancing safety in biomedical and industrial applications. Herein, we introduce a simple and efficient technique to engineer membranes composed of polylactic acid (PLA) and polybutylene adipate terephthalate (PBAT) biopolymers and α-Ag2WO4 particles using an electrospinning technique. The corresponding structural, thermal, mechanical, and antimicrobial properties were characterized. X-ray diffraction (XRD) patterns confirmed the integration of crystalline α-Ag2WO4 within the polymer matrix. Scanning electron microscopy (SEM) and Raman confocal microscopy revealed uniformly dispersed α-Ag2WO4 particles in the electrospun fibers, influencing their diameter and surface roughness. Thermal analysis indicated adjustments in the thermal stability and crystallinity of the composites with an increasing α-Ag2WO4 content. Dynamic mechanical analysis (DMA) highlighted variations in storage modulus and glass transition temperatures due to interactions between α-Ag2WO4 and polymer chains, with tensile tests showing an increase in elastic modulus and ultimate tensile strength as the α-Ag2WO4 content increased. Antimicrobial assessments revealed that PLA/PBAT membranes with α-Ag2WO4 showed pronounced antibacterial activity, forming inhibition halos across all samples against Pseudomonas aeruginosa, methicillin-resistant Staphylococcus aureus, and Mycobacterium smegmatis (a surrogate for Mycobacterium tuberculosis). These membranes also exhibited potent antiviral activity against bacteriophage phi 6, a surrogate for SARS-CoV-2, suggesting potential applications in combating infections caused by enveloped viruses. The antimicrobial activities are attributed to the generation of reactive oxygen species (ROS) and the controlled release of Ag+ ions. This work underscores the multifaceted capabilities of α-Ag2WO4-enhanced PLA/PBAT membranes in combating bacterial and viral growth, where both durability and microbial resistance are critical. Taken together, our findings provide a solution for obtaining advanced materials to be applied in a wide range of industrial applications, such as filtration systems, food preservation, antimicrobial coatings, protective textiles, and cleaning products.

Silver nanomaterials have been widely proven to have antifungal effects against Trichosporon asahii. However, the antifungal mechanism of silver nanomaterials with different morphologies still needs to be explored.

Herein, the antifungal effect of silver nanomaterials against fungus was comparative investigated via silver nanowires and silver nanoparticles with a similar size (30 nm).

The optimal antifungal concentration of silver nanowires is 6.24 μg/mL, meanwhile the antifungal concentration of silver nanoparticles is 100 μg/mL. The silver nanowires are significantly superior to the silver nanoparticles. SEM and TEM results indicated that both silver nanoparticles and silver nanowires showed significant morphological changes in the mycelium of the strain, compared with the control. The lower MFC value of silver nanowires indicates good sterilization effect and suitability for eradication treatment, which is slower than that of silver nanoparticles. Moreover, we also investigated the toxicological effects of silver nanoparticles and silver nanowires.

We comparative studied and transcriptomic analyzed the antifungal mechanism of Ag nanoparticles and nanowires against Trichosporon asahii. The antifungal effects of silver nanowires were better than the silver nanoparticles, especially in the metabolic processes and oxidative phosphorylation. RNA sequencing results indicated that 15 key targets were selected for experimental verification to interpret the potential antifungal mechanism of Ag nanomaterials against fungus. This work proves that silver nanomaterials with different morphologies have potential applications in fungus therapy such as T. asahii.

The aim of this systematic review was to assess the antimicrobial effectiveness of silver nanoparticles (AgNPs) incorporated to different orthodontic bonding systems. Additionally, the review investigated the impact of AgNPs on the bonding properties of these materials. The hypothesis posed that the addition of AgNPs would enhance the antimicrobial efficacy of orthodontic bonding systems while maintaining their bonding properties. The systematic review employed a PICO-based search strategy, targeting in vitro studies focusing on the integration of nano silver particles into orthodontic bonding systems with potential antimicrobial activity. The intervention involved the use of nano silver in orthodontic bonding systems, with a comparison to systems lacking nano silver. The primary outcomes assessed were antimicrobial activity and shear bond strength (SBS). The search process, conducted without publication date restrictions, yielded 551 potential articles: 34 from PubMed, 360 from PubMed Central, 42 from Embase, 54 from Scopus, and 61 from Web of Science. Ultimately, a qualitative synthesis was conducted on 13 papers. The PRISMA diagram, visually represented the search strategy, screening process, and inclusion criteria. The study protocol was registered in PROSPERO CRD42023487656 to enhance transparency and adherence to systematic review guidelines. Quality assessment of the included studies was performed using the Newcastle-Ottawa Scale, revealing that the 13 articles meeting the inclusion criteria demonstrated a high level of evidence. Seven studies were included in the meta-analysis regarding shear bond strength. In summary, the synthesized findings from these studies strongly underscore the promising potential of orthodontic materials modified with AgNPs. These materials exhibit effective resistance against cariogenic bacteria without compromising bonding properties below clinical acceptability. Such innovative materials hold significant implications for advancing oral health within the realm of orthodontics.

The growing threat of viral infections requires innovative therapeutic approaches to safeguard human health. Nanomaterials emerge as a promising solution to overcome the limitations associated with conventional therapies. The eco-friendly synthesis of silver nanoparticles (AgNPs) currently represents a method that guarantees antimicrobial efficacy, safety, and cost-effectiveness. This study explores the use of AgNPs derived from the peel (Lp-AgNPs) and juice (Lj-AgNPs) Citrus limon "Ovale di Sorrento", cultivars of the Campania region. The antiviral potential was tested against viruses belonging to the Coronaviridae and Herpesviridae. AgNPs were synthesized by reduction method using silver nitrate solution mixed with aqueous extract of C. limon peel and juice. The formation of Lp-AgNPs and Lj-AgNPs was assessed using a UV-Vis spectrophotometer. The size, ζ-potential, concentration, and morphology of AgNPs were evaluated by dynamic light scattering (DLS), nanoparticle tracking analysis (NTA), and field emission-scanning electron microscopy (FE-SEM). Cytotoxicity was evaluated in a concentration range between 500 and 7.8 µg/mL on VERO-76 and HaCaT cells, with the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium test bromide (MTT). Antiviral activity consisted of virus pre-treatment, co-treatment, cellular pre-treatment, and post-infection tests versus HSV-1 and SARS-CoV-2 at a multiplicity of infections (MOI) of 0.01. Plaque reduction assays and real-time PCR provided data on the antiviral potential of tested compounds. Lp-AgNPs and Lj-AgNPs exhibited spherical morphology with respective diameters of 60 and 92 nm with concentrations of 4.22 and 4.84 × 1010 particles/mL, respectively. The MTT data demonstrated minimal cytotoxicity, with 50 % cytotoxic concentrations (CC50) of Lp-AgNPs and Lj-AgNPs against VERO cells of 754.6 and 486.7 µg/mL. Similarly, CC50 values against HaCaT were 457.3 µg/mL for Lp-AgNPs and 339.6 µg/mL for Lj-AgNPs, respectively. In the virus pre-treatment assay, 90 % inhibitory concentrations of HSV-1 and SARS-CoV-2 were 8.54-135.04 µg/mL for Lp-AgNPs and 6.13-186.77 µg/mL for Lj-AgNPs, respectively. The molecular investigation confirmed the antiviral data, recording a reduction in the UL54 and UL27 genes for HSV-1 and in the Spike (S) gene for SARS-CoV-2, following AgNP exposure. The results of this study suggest that Lp-AgNPs and Lj-AgNPs derived from C. Limon could offer a valid ecological, natural, local and safe strategy against viral infections.