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Silver-based nanoantimicrobials: Mechanisms, ecosafety, and future perspectives

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Abstract

Silver nanoparticles (AgNPs) are metallic zero-dimensional nanomaterials that have attracted a lot of attention due to their conductivity, chemical resistance, antibacterial, antiviral, antifungal, antiangiogenic, and antiinflammatory properties. Applying Ag as a microbiocidal agent involves oxidation Ag⁰ to the Ag⁺. AgNPs are well-known for their excellent antimicrobial effects against numerous organisms such as bacteria, fungi, and viruses. Direct contact of AgNPs with large surfaces on the cell wall of bacteria can result in damage to the membrane, causing leakage of cell contents and death of cells. When pathogenic cells are exposed to the AgNPs, a significantly large number of ROS was generated. AgNPs can inhibit the production of different kinds of extracellular hydrolytic enzymes as well as germ tube formation of fungi. Also, AgNPs influence the biosynthesis of organic acid in some fungi and alter the profile of extracellular enzyme, although the total enzymatic activity is increased. Furthermore, AgNPs can disturb the integrity of cell wall and cell regulatory mechanisms, leading to pore formation and cell collapse. The antiviral properties of AgNPs have been reported recently. AgNPs are recorded to associate with glycoproteins on the viral surface and have links to the host cells and then introduce their virus behavior through contact with the viral genome.

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... Furthermore, nanoparticles demonstrate the ability to inhibit microbial proliferation by diffusing into the exopolysaccharide matrix of biofilms, downregulating quorum sensing proteins and/or enhancing quorum quenching within biofilm architectures, subsequently leading to degradation of extracellular polymeric substances (EPS) and microbial mortality in natural environments. The antimicrobial efficacy of nanoparticles is controlled by various parameters, including particle dimensions, concentration, pH conditions, exposure time, morphology and surface modification (47,48). ...
... The rationale behind the mortality of second stage juveniles as a result of AgNPs exposure can be explained in a way that metallic nanoparticles could be held responsible for inducing oxidative stress within the cells of nematodes (Touseef et al., 2021). The cuticular disruption in the structure of nematode has been reported to be associated with the disruption caused by AgNPs in the normal functioning mechanism of ATP synthesis, membrane permeability and response to oxidative stress (Ghadam et al., 2021). Taha Lim et al. (2012) demonstrated the mechanism of toxicity in nematode, C. elegans by investigating the oxidative stress in reproduction toxicity. ...
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... For example, it has been shown to have antibacterial, anticancer, antioxidant, and anti-inflammatory properties [25][26][27][28][29]. Another favorable point is that ZnO can be doped (the incorporation of a low concentration of impurities in a semiconductor material) with other materials to enhance its properties [30,31]. Silver is an additional possible dopant for ZnO and an element that has shown antimicrobial, antiseptic, antifungal, and antiviral characteristics [32][33][34]. In this sense, ZnO nanostructures can be doped with elements with strong and proven antimicrobial activity, such as Ag and Cl, to improve its antimicrobial potential [35][36][37]. ...
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Nanoparticles, ranging in the size from 1 to 100 nm possess novel or enhanced properties compared with larger particles of bulk materials, based on their specific characteristics such as size, distribution and morphology. Noble metal nanoparticles are widely used in the nano-medicinal application; especially silver nanoparticles, which exhibit antifungal, antibacterial, anti-plasmodial and anti-mosquito properties due to the unique properties such as chemical stability, good conductivity and catalytic activity. Nanoparticles are largely synthesized by a variety of chemical and physical approaches. These techniques being expensive and potentially hazardous to the environment, can pose various biological risks. This has necessitated for the alternate eco-friendly and innocuous approaches. In recent years, the convergence between the two fields; nanotechnology and biology; has evolved a new field of nanobiotechnology that encompasses a number of biochemical and biophysical processes employing biological entities such as algae, bacteria, fungi, viruses, yeasts, and plants. Focus on green synthesis of nanoparticles without employing toxic and expensive chemicals frequently used in conventional chemical and physical processes, has augmented their applications and safe usage. This chapter describes the different methods to synthesize silver nanoparticles with a major focus on synthesizing nanoparticles via green route i.e., by utilizing biological entities for the facile, eco-friendly and cost-effective synthesis.
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There are alarming reports of the presence of mycotoxins and the induction of mycotoxicoses in the vital organs of humans and animals, as well as economic loss due to reduced crop yields. In light of these problems, mycotoxin detoxification has become mandatory for the production of healthy products. As the potential for prevention can be absent or limited in the field or during long storage periods, other methods based on several protocols have shown potential usefulness for efficient mycotoxin control; however, few are accepted for practical use. Detoxification can be performed by lactic acid bacteria, Bacillus, moulds, actinobacteria, edible fungi and medicinal plants. Another lower-cost method based on nanoparticles has recently been discovered, and its profitability and efficiency have been proven. Keywords: Mycotoxins, detoxification, nanoparticles, nanocontrol method
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Most of current influenza virus vaccines fail to develop a strong immunity at lung mucosae (site of viral entry) due to sub-optimal vaccination protocols (e.g. inactivated virus administered by parenteral injections). Mucosal immunity could be improved by using locally-delivered vaccines containing appropriate adjuvants. Here we show, in a mouse model, that inclusion of silver nanoparticles (AgNPs) in virus-inactivated flu vaccine resulted in reduction of viral loads and prevention of excessive lung inflammation following influenza infection. Concomitantly, AgNPs enhanced specific IgA secreting plasma cells and antibodies titers, a hallmark of successful mucosal immunity. Moreover, vaccination in the presence of AgNPs but not with gold nanoparticles, protected mice from lethal flu. Compared with other commercial adjuvants (squalene/oil-based emulsion) or silver salts, AgNPs stimulated stronger antigen specific IgA production with lower toxicity by promoting bronchus-associated lymphoid tissue (BALT) neogenesis, and acted as a bona fide mucosal adjuvant.
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Particles with the size of 1-100 nm are known as nanoparticles (NPs). The widespread use of silver NPs (AgNPs) makes it familiar in different industries. They have unique properties as a result of their high surface to volume ratio, although aggregation of NPs interferes with their functions. This phenomenon has several side effects on the environment, the amount of which may depend on the stability of AgNPs. Stability of colloids depends on various agents, such as capping agents and environmental conditions, including pH and ionic strength. In this study, the effects of a variety of electrolytes, such as NaCl (10mM), NaNO 3 (10 and 100mM), and Ca (NO 3) 2 (10mM) at different values of pH were investigated on the aggregation of AgNPs synthesized using an aqueous extract of dried Juglans regia green husk. In NaNO 3 10mM pH 9, NPs were more stable than in other media. Therefore, the special optical and electronic properties of AgNPs in such a medium as well as in water were investigated. The UV-visible extinction spectra of AgNPs in both water and NaNO 3 (10 mM, pH 9.0) showed a surface plasmon resonance (SPR) at 445 nm as well as a broad peak at shorter wavelengths (255 nm). The fluorescence emission spectra of AgNPs at different excitation wavelengths in the range of 245-290 nm revealed emission peaks that were red-shifted in the range of 487-580 nm by the increase in the excitation wavelength. This behavior is attributed to the existence of a variety of emission centers with different energy levels.
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The potential use of nanotechnology in the control of toxigenic fungi and mycotoxin production has been little explored. In this report, engineered silver nanoparticles (AgNPs) were synthesized and characterized by single particle Inductively Coupled Plasma Mass Spectrometry. Then, their effectiveness in the control of the growth of the main aflatoxigenic and ochratoxigenic species affecting foods and aflatoxins (AFs) and ochratoxin A (OTA) production was studied. The target species and their associated mycotoxins were Aspergillus flavus (AFB 1 and AFB 2 ), A. parasiticus (AFB 1 , AFB 2 , AFG 1 and AFG 2 ), A. carbonarius, A. niger, A. ochraceus, A. steynii, A. westerdijkiae and Penicillium verrucosum (OTA). Spore suspensions supplemented with AgNPs (average diameter size 30 nm, range 14–100 nm) at doses 0–45 μg/mL were incubated for 2–30 h. At selected exposure times aliquots were removed and cultured on maize-based medium (MBM) for 10 days. In these cultures, percentage of viable spores, effective doses (EDs) to inhibit the number of viable spores to 50%, 90% and 100%, colony lag phases, colony growth rates (GR), EDs to inhibit the colony GR to 50%, 90% and 100% were estimated. AF and OTA levels were determined by UPLC-MS/MS. Under the assayed conditions, effective doses of the AgNPs against all the studied fungal species could be estimated. These doses generally decreased with increasing exposure time and were higher for A. flavus and A. parasiticus than for ochratoxigenic species. Colonies from spores treated at high exposure times (20–30 h) and variable AgNP doses showed long lag phases or even did not occur depending on the fungal species. Colony GR, as well as AF and OTA levels in MBM cultures decreased when AgNP dose and contact period increased. The factors species, AgNP dose, exposure time and their interactions significantly affect fungal growth and AF and OTA accumulation in MBM. The results suggest that AgNPs only or as active ingredient hosted in paints, films or other polymers could be a good strategy in the management of the main aflatoxigenic and ocratoxigenic species affecting food and AF and OTA contamination.
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The cell-free culture filtrate (CFF) of the fungi Fusarium chlamydosporum NG30 and Penicillium chrysogenum NG85 was tested to synthesize silver nanoparticles (AgNPs). The synthesized AgNPs were further characterized by means of transmission electron microscopy (TEM), dynamic light scattering (DLS) and Fourier transform infra-red (FTIR) spectroscopy. TEM revealed their spherical shape, homogeneity and a size range between 6 and 26 nm for F. chlamydosporum AgNPs (FAgNPs) and from 9 to 17.5 nm for P. chrysogenum AgNPs (PAgNPs). DLS showed that the diameter of FAgNPs was narrower than that of PAgNPs. FTIR spectroscopy indicated that the functional groups present in the CFF might be responsible for the reduction of silver ions to form stabilized protein-capped AgNPs. In addition, the AgNPs showed notable antifungal activity and potency in thwarting mycotoxin production. Thus, using Aspergillus flavus as a test microorganism the minimum inhibitory concentration (MIC) was 48, 45 and 50 μg/mL for FAgNPs, PAgNPs and the antifungal compound itraconazole, respectively. Also, when testing Aspergillus ochraceus FAgNPs, PAgNPs and itraconazole led to MIC values of 51, 47 and 49 μg/mL, respectively. The statistical MIC values to inhibit completely the total aflatoxin production by A. flavus were 5.9 and 5.6 μg/mL for FAgNPs and PAgNPs, respectively, and to inhibit the ochratoxin A production by A. ochraceus 6.3 and 6.1 μg/mL for FAgNPs and PAgNPs, respectively. The cytotoxicity assay of the AgNPs on human normal melanocytes (HFB 4) revealed a cell survival of 80% and 75% at a concentration of 6 μg/mL for FAgNPs and PAgNPs, respectively.
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The nonradiative conversion of light energy into heat (photothermal therapy, PTT) or sound energy (photoacoustic imaging, PAI) has been intensively investigated for the treatment and diagnosis of cancer, respectively. By taking advantage of nanocarriers, both imaging and therapeutic functions together with enhanced tumour accumulation have been thoroughly studied to improve the pre-clinical efficiency of PAI and PTT. In this review, we first summarize the development of inorganic and organic nano photothermal transduction agents (PTAs) and strategies for improving the PTT outcomes, including applying appropriate laser dosage, guiding the treatment via imaging techniques, developing PTAs with absorption in the second NIR window, increasing photothermal conversion efficiency (PCE), and also increasing the accumulation of PTAs in tumours. Second, we introduce the advantages of combining PTT with other therapies in cancer treatment. Third, the emerging applications of PAI in cancer-related research are exemplified. Finally, the perspectives and challenges of PTT and PAI for combating cancer, especially regarding their clinical translation, are discussed. We believe that PTT and PAI having noteworthy features would become promising next-generation non-invasive cancer theranostic techniques and improve our ability to combat cancers.
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In the present study, microalgae Chlorococcum humicola and Chlorella vulgaris were grown in different concentrations of NaCl (25-1000 mM) to elucidate its impact on morphology, lipid synthesis, minerals status and antioxidative responses. Scanning Electron microscopy showed distorted cell morphology and increased cell size by 33.52% (C. humicola) and 27.79% (C. vulgaris) at 100 mM NaCl. Energy Dispersive Spectroscopy data revealed reduction in mineral contents (C, S, Fe, Mg, Si, Mn and Zn) by 14-54% in both algae. Further, C. humicola was found to have high lipid content than C. vulgaris under NaCl regime. The activities of superoxide dismutase, catalase and glutathione reductase were increased by 2.5-5 folds in both algae as compared to control. The increased level of ascorbate, cysteine and proline in both algae indicated tolerance against salinity. Thus, C. humicola and C. vulgaris may exhibit dual benefits viz., high lipid production and reclamation of sodic soil.
Article
Silver nanoparticles (AgNPs) have attracted the attention of researchers due to their properties. Biological synthesis of AgNPs is eco-friendly and cost-effective preferred to physical and chemical methods, which utilize environmentally harmful agents and large amounts of energy. Microorganisms have been explored as potential biofactories to synthesize AgNPs. Bacterial NP synthesis is affected by Ag salt concentration, pH, temperature and bacterial species. In this study, Bacillus spp., isolated from soil, were screened for AgNP synthesis at pH 12 with 5 mM Ag nitrate (AgNO3) final concentration at room temperature. The isolate with fastest color change and the best ultraviolet-visible spectrum in width and height were chosen as premier one. AgNO3 and citrate salts were compared in terms of their influence on NP synthesis. Spherical Ag chloride (AgCl) NPs with a size range of 35-40 nm were synthesized in 1.5 mM Ag citrate solution. Fourier transform infrared analysis demonstrated that protein and carbohydrates were capping agents for NPs. In this study, antimicrobial and antitumor properties of the AgNP were investigated. The resulting AgCl NPs had bacteriostatic activity against four standard spp. And multi-drug resistant strain of Pseudomonas aeruginosa. These NPs are also cytotoxic to cancer cell lines MCF-7, U87MG and T293.
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Background: CD19-specific chimeric antigen receptor (CAR) T cells induce high rates of initial response among patients with relapsed B-cell acute lymphoblastic leukemia (ALL) and long-term remissions in a subgroup of patients. Methods: We conducted a phase 1 trial involving adults with relapsed B-cell ALL who received an infusion of autologous T cells expressing the 19-28z CAR at the Memorial Sloan Kettering Cancer Center (MSKCC). Safety and long-term outcomes were assessed, as were their associations with demographic, clinical, and disease characteristics. Results: A total of 53 adults received 19-28z CAR T cells that were manufactured at MSKCC. After infusion, severe cytokine release syndrome occurred in 14 of 53 patients (26%; 95% confidence interval [CI], 15 to 40); 1 patient died. Complete remission was observed in 83% of the patients. At a median follow-up of 29 months (range, 1 to 65), the median event-free survival was 6.1 months (95% CI, 5.0 to 11.5), and the median overall survival was 12.9 months (95% CI, 8.7 to 23.4). Patients with a low disease burden (<5% bone marrow blasts) before treatment had markedly enhanced remission duration and survival, with a median event-free survival of 10.6 months (95% CI, 5.9 to not reached) and a median overall survival of 20.1 months (95% CI, 8.7 to not reached). Patients with a higher burden of disease (≥5% bone marrow blasts or extramedullary disease) had a greater incidence of the cytokine release syndrome and neurotoxic events and shorter long-term survival than did patients with a low disease burden. Conclusions: In the entire cohort, the median overall survival was 12.9 months. Among patients with a low disease burden, the median overall survival was 20.1 months and was accompanied by a markedly lower incidence of the cytokine release syndrome and neurotoxic events after 19-28z CAR T-cell infusion than was observed among patients with a higher disease burden. (Funded by the Commonwealth Foundation for Cancer Research and others; ClinicalTrials.gov number, NCT01044069 .).