Modulation of Innate Immune Toxicity by Silver Nanoparticle Exposure and the Preventive Effects of Pterostilbene

Silver nanoparticles pose a potential risk to ecosystems and living organisms due to their widespread use in various fields and subsequent gradual release into the environment. Only a few studies have investigated the effects of silver nanoparticles (AgNPs) toxicity on immunological functions. Furthermore, these toxic effects have not been fully explored. Recent studies have indicated that zebrafish are considered a good alternative model for testing toxicity and for evaluating immunological toxicity. Therefore, the purpose of this study was to investigate the toxicity effects of AgNPs on innate immunity using a zebrafish model and to investigate whether the natural compound pterostilbene (PTE) could provide protection against AgNPs-induced immunotoxicity. Wild type and neutrophil- and macrophage-transgenic zebrafish lines were used in the experiments. The results indicated that the exposure to AgNPs induced toxic effects including death, malformation and the innate immune toxicity of zebrafish. In addition, AgNPs affect the number and function of neutrophils and macrophages. The expression of immune-related cytokines and chemokines was also affected. Notably, the addition of PTE could activate immune cells and promote their accumulation in injured areas in zebrafish, thereby reducing the damage caused by AgNPs. In conclusion, AgNPs may induce innate immune toxicity and PTE could ameliorate this toxicity.     

Multicolor Layer-by-Layer films using weak polyelectrolyte assisted synthesis of silver nanoparticles

In the present study, we show that silver nanoparticles (AgNPs) with different shape, aggregation state and color (violet, green, orange) have been successfully incorporated into polyelectrolyte multilayer thin films using the layer-by-layer (LbL) assembly. In order to obtain colored thin films based on AgNPs is necessary to maintain the aggregation state of the nanoparticles, a non-trivial aspect in which this work is focused on. The use of Poly(acrylic acid, sodium salt) (PAA) as a protective agent of the AgNPs is the key element to preserve the aggregation state and makes possible the presence of similar aggregates (shape and size) within the LbLcolored films. This approach based on electrostatic interactions of the polymeric chains and the immobilization of AgNPs with different shape and size into the thin films opens up a new interesting perspective to fabricate multicolornanocomposites based on AgNPs.     

Fungus-Mediated Green Synthesis of Silver Nanoparticles Using Aspergillus terreus

The biosynthesis of nanoparticles has received increasing attention due to the growing need to develop safe, cost-effective and environmentally friendly technologies for nano-materials synthesis. In this report, silver nanoparticles (AgNPs) were synthesized using a reduction of aqueous Ag(+) ion with the culture supernatants of Aspergillus terreus. The reaction occurred at ambient temperature and in a few hours. The bioreduction of AgNPs was monitored by ultraviolet-visible spectroscopy, and the AgNPs obtained were characterized by transmission electron microscopy and X-ray diffraction. The synthesized AgNPs were polydispersed spherical particles ranging in size from 1 to 20 nm and stabilized in the solution. Reduced nicotinamide adenine dinucleotide (NADH) was found to be an important reducing agent for the biosynthesis, and the formation of AgNPs might be an enzyme-mediated extracellular reaction process. Furthermore, the antimicrobial potential of AgNPs was systematically evaluated. The synthesized AgNPs could efficiently inhibit various pathogenic organisms, including bacteria and fungi. The current research opens a new avenue for the green synthesis of nano-materials.     

Crosslinked PVA/PVP Supported Silver Nanoparticles: A Reusable and Efficient Heterogeneous Catalyst for the 4-Nitrophenol Degradation

Well-organized and stable silver nanoparticles (AgNPs) were successfully prepared within polymeric film of polyvinyl alcohol and Polyvinylpyrrolidone as supporting matrix. The free-standing film was obtained by using the casting technique. Electron microscopy techniques confirmed the formation of spherical AgNPs of 15 nm size. The prepared AgNPs were crystallized in face-centered cubic structure as indicated by X-ray diffraction. The as-prepared nanocomposite film exhibited good catalytic properties in the complete catalytic degradation of 4-nitrophenol using sodium borohydride as a reducing agent. The AgNPs are tightly held within a polymeric matrix which facilitates their recovery and reuse for several cycles.     

纳米银的来源及其影响污水和污泥处理的研究进展

近年来随着纳米银生产和使用的逐渐增多,导致环境中纳米银的浓度逐渐升高。物质流分析表明,大部分的纳米银将随污水进入污水处理厂,进而富集到污泥中。鉴于纳米银的抗菌性,其可能会对污水处理系统中的微生物产生影响。本文首先系统介绍了环境水体中纳米银的不同来源(即天然来源和人为来源),着重总结了目前对其影响污水和污泥处理系统的研究,即对污水中碳、氮、磷的去除效率和污泥厌氧消化过程的影响,并进一步分析了其对这一过程中微生物的毒性作用,探讨了其毒性效应的来源及作用机理,最后对该领域的研究进行了展望。综述内容为深入研究纳米银对污水和污泥处理系统的潜在风险提供了一定的理论基础。     

A comparative study of two different approaches for the incorporation of silver nanoparticles into layer-by-layer films

In this work, a comparative study about the incorporation of silver nanoparticles (AgNPs) into thin films is presented using two alternative methods, the in situ synthesis process and the layer-by-layer embedding deposition technique. The influence of several parameters such as color of the films, thickness evolution, thermal post-treatment, or distribution of the AgNPs along the coatings has been studied. Thermal post-treatment was used to induce the formation of hydrogel-like AgNPs-loaded thin films. Cross-sectional transmission electron microscopy micrographs, atomic force microscopy images, and UV-vis spectra reveal significant differences in the size and distribution of the AgNPs into the films as well as the maximal absorbance and wavelength position of the localized surface plasmon resonance absorption bands before and after thermal post-treatment. This work contributes for a better understanding of these two approaches for the incorporation of AgNPs into thin films using wet chemistry.     

基于植物质还原的银纳米颗粒的制备及在织物抗菌整理上的应用

纳米银是以纳米技术为基础研制而成的新型抗菌产品,由于量子效应和尺寸效应具有普通银系抗菌剂无法比拟的抗菌效果。本研究以黄芩、丁香、洋浦桃、芳樟4种植物质提取液制备银纳米颗粒,并借助于UV-Vis、TEM以及XRD对产物进行表征,结果表明增加植物质提取液浓度或增大NaOH加入量,均有利于制得粒径较小的银纳米颗粒。SEM图片表明采用浸渍法可将所得纳米银颗粒负载于纯棉织物上,通过考察浸渍时间、温度、浴比对织物上载银量的影响,确定较优的浸渍条件为时间30 h,温度55℃,浴比为1:25。分别考察了银纳米颗粒粒径和植物质种类对所得载银织物抗菌性能的影响,发现负载到织物上的纳米银粒径越小,织物抑菌效果越好;利用本身具有抑菌效果的黄芩、丁香来制备银纳米颗粒,有利于增强所得载银织物的整体抗菌性能;4种植物质中以黄芩制得的载银织物抗菌效果最优,对金黄色葡萄球菌、大肠杆菌等实验菌株均有强烈的抑制作用。     

无患子提取液制备纳米银及其协同抗菌性研究

以无患子提取液为还原剂,制备了含有纳米银的无患子复合抗菌液,考察了无患子提取液用量、温度、硝酸银摩尔浓度等因素对纳米银形貌和粒径的影响,并借助UV-Vis可见分光光谱、X射线衍射(XRD)以及透射电子显微镜(TEM)对产物进行表征;通过抑菌环法探讨了复合抗菌液对大肠杆菌的抗菌活性。由UV-Vis图谱可知,复合抗菌液等离子体共振吸收峰(SPR)在418 nm左右,说明该复合抗菌液中有纳米银的存在;XRD图表明合成的纳米银为面心立方结构;TEM图表明合成纳米银粒径为10~40 nm。由此获得的含有纳米银的无患子复合抗菌液对大肠杆菌表现出显著协同抗菌活性,抑菌圈直径变大。     

Effects of copper nanoparticle exposure on host defense in a murine pulmonary infection model

Background

The study investigated the distribution of silver after 28 days repeated oral administration of silver nanoparticles (AgNPs) and silver acetate (AgAc) to rats. Oral administration is a relevant route of exposure because of the use of silver nanoparticles in products related to food and food contact materials.

Results

AgNPs were synthesized with a size distribution of 14 ± 4 nm in diameter (90% of the nanoparticle volume) and stabilized in aqueous suspension by the polymer polyvinylpyrrolidone (PVP). The AgNPs remained stable throughout the duration of the 28-day oral toxicity study in rats. The organ distribution pattern of silver following administration of AgNPs and AgAc was similar. However the absolute silver concentrations in tissues were lower following oral exposure to AgNPs. This was in agreement with an indication of a higher fecal excretion following administration of AgNPs. Besides the intestinal system, the largest silver concentrations were detected in the liver and kidneys. Silver was also found in the lungs and brain. Autometallographic (AMG) staining revealed a similar cellular localization of silver in ileum, liver, and kidney tissue in rats exposed to AgNPs or AgAc. Using transmission electron microscopy (TEM), nanosized granules were detected in the ileum of animals exposed to AgNPs or AgAc and were mainly located in the basal lamina of the ileal epithelium and in lysosomes of macrophages within the lamina propria. Using energy dispersive x-ray spectroscopy it was shown that the granules in lysosomes consisted of silver, selenium, and sulfur for both AgNP and AgAc exposed rats. The diameter of the deposited granules was in the same size range as that of the administered AgNPs. No silver granules were detected by TEM in the liver.

Conclusions

The results of the present study demonstrate that the organ distribution of silver was similar when AgNPs or AgAc were administered orally to rats. The presence of silver granules containing selenium and sulfur in the intestinal wall of rats exposed to either of the silver forms suggests a common mechanism of their formation. Additional studies however, are needed to gain further insight into the underlying mechanisms of the granule formation, and to clarify whether AgNPs dissolve in the gastrointestinal system and/or become absorbed and translocate as intact nanoparticles to organs and tissues.     

Preparation of AgNPs/PS composite via reverse microemulsion polymerization

Silver nanoparticles (AgNPs) were synthesized in reverse microemulsions using silver nitrate as silver source, hydrazine hydrate as reducing agent, n‐heptane as oil phase, cetyl trimethyl ammonium bromide (CTAB) as surfactant, and isoamyl alcohol as cosurfactant. A uniform silver nanoparticles/polystyrene (AgNPs/PS) composite was further prepared by a reverse microemulsion polymerization method. The morphologies and structures of the AgNPs and the AgNPs/PS composite were characterized by UV‐visible spectroscopy (UV–vis), X‐ray diffraction (XRD), fourier transform infrared spectra (FTIR), and transmission electron microscopy (TEM). Furthermore, the molecular weight of the AgNPs/PS composite was measured by gel permeation chromatography (GPC), and the thermal stability of the AgNPs/PS composite was determined by thermal gravimetric (TG) analysis. Results show that the AgNPs have a particle size of 3–10 nm, and are almost spherical, uniform, and monodisperse both in a AgNPs colloid and in the AgNPs/PS composite. There are no characteristic peaks of silver oxide in the synthetic AgNPs and AgNPs/PS composite. The AgNPs/PS composite has a better thermal stability and a higher molecular weight than virgin PS. POLYM. COMPOS., 35:1325–1329, 2014. © 2013 Society of Plastics Engineers     

In situ assembly of well-dispersed Ag nanoparticles (AgNPs) on electrospun carbon nanofibers (CNFs) for catalytic reduction of 4-nitrophenol

Carbon nanofibers/silver nanoparticles (CNFs/AgNPs) composite nanofibers were fabricated by two steps consisting of the preparation of the CNFs by electrospinning and the hydrothermal growth of the AgNPs on the CNFs. The as-prepared nanofibers were characterized by scanning electron microscopy, energy dispersive spectroscopy, transmission electron microscopy, X-ray diffraction, resonant Raman spectra, thermal gravimetric and differential thermal analysis, and X-ray photoelectron spectroscopy, respectively. The results indicated that not only were AgNPs (25-50 nm) successfully grown on the CNFs but also the AgNPs were distributed without aggregation on the CNFs. Further more, by adjusting the parameters in hydrothermal processing, the content of silver supported on the CNFs could be easily controlled. The catalytic activities of the CNFs/AgNPs composite nanofibers to the reduction of 4-nitrophenol (4-NP) with NaBH(4) were tracked by UV-visible spectroscopy. It was suggested that the CNFs/AgNPs composite nanofibers exhibited high catalytic activity in the reduction of 4-NP, which might be attributed to the high surface areas of AgNPs and synergistic effect on delivery of electrons between CNFs and AgNPs. And, the catalytic efficiency was enhanced with the increasing of the content of silver on the CNFs/AgNPs composite nanofibers. Notably, the CNFs/AgNPs composite nanofibers could be easily recycled due to their one-dimensional nanostructural property.     

Silver Nanoparticles Mediate Differential Responses in Keratinocytes and Fibroblasts during Skin Wound Healing

With advances in nanotechnology, pure silver has been recently engineered into nanometer‐sized particles (diameter <100 nm) for use in the treatment of wounds. In conjunction with other studies, we previously demonstrated that the topical application of silver nanoparticles (AgNPs) can promote wound healing through the modulation of cytokines. Nonetheless, the question as to whether AgNPs can affect various skin cell types—keratinocytes and fibroblasts—during the wound‐healing process still remains. Therefore, the aim of this study was to focus on the cellular response and events of dermal contraction and epidermal re‐epithelialization during wound healing under the influence of AgNPs; for this we used a full‐thickness excisional wound model in mice. The wounds were treated with either AgNPs or control with silver sulfadiazine, and the proliferation and biological events of keratinocytes and fibroblasts during healing were studied. Our results confirm that AgNPs can increase the rate of wound closure. On one hand, this was achieved through the promotion of proliferation and migration of keratinocytes. On the other hand, AgNPs can drive the differentiation of fibroblasts into myofibroblasts, thereby promoting wound contraction. These findings further extend our current knowledge of AgNPs in biological and cellular events and also have significant implications for the treatment of wounds in the clinical setting.     

Preparation of modified sodium lignosulfonate hydrogel–silver nanocomposites

In this article, modified sodium lignosulfonate (MSLS) hydrogel particles were prepared using sodium lignosulfonate as starting material. The hydrogel particles exhibit a reversible property transformed between the two states of macrohydrogel and microhydrogel by ultrasonic dispersion and vacuum drying. Using this property, highly stable and uniformly dispersed silver nanoparticles (AgNPs) have been prepared via in situ reduction of silver ions (silver nitrate) in the microhydrogel aqueous dispersion with sodium borhydride. The hybrid microhydrogel with AgNPs was transformed into MSLS hydrogel–silver nanocomposites by drying under vacuum at 40°C. X‐ray diffraction, ultraviolet–visible (UV–vis) spectrophotometry, Fourier transform infrared spectra, atomic absorption spectroscopy, transmission electron microscopy, and scanning electron microscopy were used to characterize the composite system. The results show that the size of spherical silver nanoparticles incorporated in the hydrogel framework is about 10 nm. POLYM. COMPOS., 34:860–866, 2013. © 2013 Society of Plastics Engineers     

Double‐hydrophobic siloxane diblock copolymers: Synthesis,micellization behavior,and application as a stabilizer for silver nanoparticles

The double‐hydrophobic well‐defined polydimethylsiloxane‐block‐poly(methyl methacrylate) (PDMS‐b‐PMMA) diblock copolymers were synthesized via atom transfer radical polymerization (ATRP). Their chemical compositions and the structure were investigated. The micellization behavior of the double‐hydrophobic diblock copolymers with equal block length was thoroughly studied. The results showed that their self‐assembly behavior was analogous to the star‐like micelles. Furthermore, the effect of temperature on the aggregates was investigated to verify that the resulting copolymer (PDMS‐b‐PMMA) was to some extent temperature sensitive. Till date, there have been few reports on the utilization of nonamphiphilic block copolymers to synthesize and confine metal nanoparticles in aggregates. In this study, we explored the role of double‐hydrophobic block copolymers as a mediator for organically dispersible silver nanoparticles (AgNPs) and it offered to be an effective stabilizer for preparing AgNPs. Besides, AgNPs generated in organic solvent is an important addition to the hitherto predominantly water‐based processes for producing nanoparticles inside the polymer surfactant. POLYM. ENG. SCI., 2013. © 2012 Society of Plastics Engineers     

Effect of nanoparticle shape on the conductivity of Ag nanoparticle poly(vinyl alcohol) composite films

In this work, the shape effect of silver nanoparticles (AgNPs) on photocatalysis and electrical conductivity was investigated. Different shapes of AgNPs achieved using various concentrations of NaBH₄ were characterized using particle size analysis, UV–visible spectroscopy and high‐resolution transmission electron microscopy. The colours of colloidal solutions were found to be influenced by the shape of the nanoparticles. Yellow and blue AgNPs were spherical and triangular in shape, respectively, whereas distorted spherical particles showed a red colour and the presence of both particles in one solution resulted in a green colloidal solution. The AgNPs were used to prepare Ag/poly(vinyl alcohol) (PVA) composite films and their electrical conductivity was investigated. Owing to their better charge carrier generation, uniform distribution in the PVA matrix and enhanced surface plasmon resonance, blue AgNPs (triangular shaped) exhibited superior conductivity performance compared to the other nanoparticles. The values for maximum conductivity for the blue and yellow AgNPs were 3.45 × 10^?4 Ω^?1 cm^?1 and 2.67 × 10^?4 Ω^?1 cm^?1respectively. © 2019 Society of Chemical Industry     

Biofilm-inactivating activity of silver nanoparticles: A comparison with silver ions

The antimicrobial activity of silver nanoparticles (AgNPs) against Pseudomonas aeruginosa PA01 planktonic and biofilm bacteria was examined; their activity was compared with that of silver ions. The inactivation of biofilms by AgNPs was greatly influenced by stirring, which caused an increased AgNP biosorption. Although the activity of AgNPs against planktonic cells was ca. 10% that of silver ions, their activity against biofilm cells was comparable to the silver ions’ activity at the same concentration after 90 min under stirring (ca. 3.5 log inactivation). AgNPs inactivated biofilms in a biosorption-dependent manner, whereas this was not the case for silver ions.     

Physicochemical and antimicrobial properties of sodium alginate/gelatin-based silver nanoformulations

In the present investigation, synthesis of silver nanoparticles (AgNPs) has been successfully carried out in a very simple and cost-effective manner by reducing Ag⁺ ions in sodium alginate solution and further stabilizing the colloidal mixture with gelatin solution. The ultraviolet–visible (UV–vis) spectra were in excellent agreement with the nanostructure morphology obtained from dynamic light scattering transmission electron microscopy and their size distributions. Increase in precursor concentration was found to promote agglomeration of AgNPs. Antibacterial assays revealed that the nanoformulations were more active against Gram-negative bacteria. Swelling studies of the hydrogel films demonstrated a rapid increase in water uptake. However, an increase in swelling % was observed with decreasing AgNP content. The use of biocompatible materials such as sodium alginate and gelatin not only provides green and economic attributes to this piece of research work but, at the same time, also opens up possibilities of using the nanoformulations in wound dressings, active packaging and several other biomedical applications.     

Facile modification of thin-film composite nanofiltration membrane with silver nanoparticles for anti-biofouling

This study focuses on the modification of a commercial nanofiltration (NF) membrane by an in-situ reaction to load silver nanoparticles (AgNPs) for anti-biofouling. Poly (vinyl alcohol) (PVA) was coated onto the NF membrane firstly, and silver salt was then deposited on the surface of PVA layer. Through thermal reduction, AgNPs with 10–20 nm in diameter were formed and immobilized onto the membrane surface by the interaction between AgNPs and PVA, as confirmed by UV–vis absorption spectrum, SEM and XPS analysis. Compared to the pristine NF90 membrane, the PVA composite membranes (NF90-PVA) and AgNPs (NF90-PVA-AgNPs) modified membranes exhibit lower water flux and slightly higher salt rejection. Release of silver ion experiments were assessed via batch method, and the results indicate silver ion can be released from the AgNPs modified membrane continuously and steadily, which may be responsible for the improved and long-time antibacterial ability of the membrane. Due to the simplicity of the method, the ability to immobilize the AgNPs to avoid leaching out, and the strong antibacterial activity, this NF90-PVA-AgNPs composite membrane displays potential applications in industrial water-treatment.     

Mangrove-mediated synthesis of silver nanoparticles using native Avicennia marina plant extract from southern Iran

The development of eco-friendly and nontoxic processes for the synthesis of nanoparticles is one of the most important discussed issues in nanotechnology science. This study reports the green synthesis of silver nanoparticles (AgNPs) using aqueous extract of leaf, stem, and root of Avicennia marina, the native and dominant mangrove plant in southern Iran. Among the different plant parts, the extract of leaves yielded the maximum synthesis of AgNPs. Synthesized AgNPs were investigated using UV–visible spectrophotometry, transmission electron microscopy (TEM), field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), energy-dispersive spectroscopy (EDS), and Fourier transform infrared (FTIR) spectroscopy. Absorption spectrum in 420?nm confirmed the synthesis of AgNPs. TEM images revealed that the synthesized AgNPs had the same spherical morphology with a size range between 0 and 75?nm. The distribution size histogram indicated that the most frequent particles were in the range of 10–15?nm and the mean size of nanoparticles was 17.30?nm. The results of SEM image showed nanoparticles with a size range between 15 and 43?nm. XRD pattern indicated the crystalline nature of synthesized nanoparticles. EDS results confirmed the presence of elements like silver, carbon, chlorine, nitrogen, and oxygen in the nanoparticles produced from leaf extract. Silver had the maximum percentage of formation, 51.6%. FTIR indicated the presence of different functional groups such as amines, alcohol, alkanes, phenol, alkyl halides, and aromatic loops in the synthesis process. Green biosynthesis of AgNPs using aqueous extract of native A. marina appears rapid, reliable, nontoxic, and eco-friendly.     

Green synthesis of silver nanoparticles using plant extracts

The strategy for design of new nanometals was developed due to their wide applications in many fields. One of the most important nanometals is silver nanoparticles (AgNPs) because of their extensive applications in biotechnology and biomedical fields. AgNPs were usually synthesized by using chemical and physical methods. In the chemical methods, various toxic chemicals are used, which are harmful to the health of living organisms. Therefore, the AgNPs were synthesized by using biological methods based on green chemistry for reducing the toxic chemicals. There are various resources for green synthesis of AgNPs, such as bacteria, fungi, enzyme and plant extracts. The green synthesis of AgNPs involves three main steps: the selection of the solvent medium, the selection of environmentally reducing agents, and the selection of non-toxic substances for the stability of AgNPs. The biosynthesis of AgNPs using plant extracts is more favorable than other biological methods because of removing the elaborate process of maintaining cell cultures. It can be also suitably scaled up for large scale production of AgNPs. This review focuses on green synthesis of AgNPs using various plant extracts.