Polyvinylpyrrolidone-coated AgNPs Research Articles

Predicting the effect of silver nanoparticles on soil enzyme activity using the machine learning method: type, size, dose and exposure time

In this study, machine learning models predicted the impact of silver nanoparticles (AgNPs) on soil enzymes. Artificial neural network (ANN) optimized with genetic algorithm (GA) (MAE = 0.1174) was more suitable for simulating overall trends, while the gradient boosting machine (GBM) and random forest (RF) were ideal for small-scale analysis. According to partial dependency profile (PDP) analysis, polyvinylpyrrolidone coated AgNPs (PVP-AgNPs) had the most inhibitory effect (average of 49.5%) on soil enzyme activity among the three types of AgNPs at the same dose (0.02–50 mg/kg). The ANN model predicted that enzyme activity first declined and then rose when AgNPs increased in size. Based on predictions from the ANN and RF models, when exposed to uncoated AgNPs, soil enzyme activities continued to decrease before 30 d, but gradually rose from 30 to 90 d, and fell slightly after 90 d. The ANN model indicated the importance order of four factors: dose > type > size > exposure time. The RF model suggested the enzyme was more sensitive when experiments were conducted at doses, sizes, and exposure times of 0.01–1 mg/kg, 50–100 nm, and 30–90 d, respectively. This study presents new insights on the regularity of soil enzyme responses to AgNPs.

Fe3O4–Mg(OH)2 nanocomposite as a scavenger for silver nanoparticles: Rational design, facile synthesis, and enhanced performance

Silver nanoparticles (AgNPs) are considered as emerging contaminants because of their high toxicity and increasing environmental impact. Removal of discharged AgNPs from water is crucial for mitigating the health and environmental risks. However, developing facile, economical, and environment-friendly approaches remains challenging. Herein, an Fe3O4–Mg(OH)2 nanocomposite, as a novel magnetic scavenger for AgNPs, was prepared by loading Fe3O4 nanoparticles on Mg(OH)2 nanoplates in a one-pot synthesis. Batch removal experiments revealed that the maximum removal capacities for the two model AgNPs (citrate- or polyvinylpyrrolidone-coated AgNPs) were 476 and 442 mg/g, respectively, corresponding to partition coefficients 8.03 and 4.89 mg/g/μM. Removal feasibilities over a wide pH range of 5–11 and in real water matrices and scavenger reusability with five cycles were also confirmed. Both Fe3O4 and Mg(OH)2 components contributed to the removal; however, their nanocomposites exhibited an enhanced performance because of the high specific surface area and pore volume. Chemical adsorption and electrostatic attraction between the coatings on the AgNPs and the two components in the nanocomposite was considered to be responsible for the removal. Overall, the facile synthesis, convenient magnetic separation, and high removal performance highlight the great potential of the Fe3O4–Mg(OH)2 nanocomposite for practical applications.

Evaluation of silver nanoparticle acute and chronic effects on freshwater amphipod (Hyalella azteca).

Silver nanoparticles (AgNPs) are known to cause ecotoxic effects, but there are no existing derived ambient water quality criteria (AWQC) for these nanomaterials to protect freshwater aquatic life due to insufficient toxicological data. We exposed Hyalella azteca to silver nitrate, citrate-coated AgNPs (citrate-AgNPs), and polyvinylpyrrolidone-coated AgNPs (PVP-AgNPs) in a 10-day and 28-day water-only static renewal system with clean sand as a substrate for the amphipods and compared their point estimates with the United States Environmental Protection Agency (USEPA) AWQC for silver. We observed that all treatments decreased the survival, growth, and biomass of H. azteca, and the order of toxicity was AgNO3 > citrate-AgNPs > PVP-AgNPs. The LC50s of AgNO3, citrate-AgNPs, and PVP-AgNPs were 3.0, 9.6, and 296.0µg total Ag L-1, respectively, for the acute exposure and 2.4, 3.2, and 61.4µg total Ag L-1, respectively, for the chronic exposure. Acute and chronic EC20s of citrate-AgNPs ranged from 0.5 to 3.5µg total Ag L-1 while that of PVP-AgNPs ranged from 31.2 to 175µg total Ag L-1 for growth and biomass. Both Ag+ released from AgNPs and the nanoparticles contributed to the observed toxicity. The dissolution and toxicity of AgNPs were influenced by surface coating agents, particle size, and surface charge. Most point estimates for AgNPs were above AWQC for silver (4.1µg L-1) and the lowest concentration (0.12µg/L) at which Ag is expected to cause chronic adverse effects to freshwater aquatic life. Our study demonstrates that the current AWQC for silver, in general, is protective of freshwater aquatic life against AgNPs tested in the present study.

Photothermal therapeutic potency of plasmonic silver nanoparticles for apoptosis and anti-angiogenesis in testosterone induced benign prostate hyperplasia in rats

AimsIn this study, we used a near-infrared laser (NIR) to increase the potency of silver nanoparticles (AgNPs) to develop a novel, less invasive, and simple photothermal therapy technique for benign prostate hyperplasia (BPH). Materials and methodsThe shape, particle size, and zeta-potential of polyvinylpyrrolidone coated-AgNPs (PVP-AgNPs) were determined using transmission electron microscopy (TEM), Zeta-potential, and Particle size analyzer (ELSZ). To induce BPH, thirty-six male Sprague-Dawley (SD) rats were given intramuscular (i.m) injections of testosterone propionate (TP) at 5 mg/kg body weight (b.w)/day suspended in 0.1 ml of olive oil for 14 days. Photothermal therapy with AgNPs-NIR for 14 days was carried out. Prostate size, prostate index (PI), dihydrotestosterone (DHT), prostate-specific antigen (PSA), gross, hepatic, and renal toxicity, as well as antioxidant activity, apoptosis, and angiogenesis markers in prostatic tissues were measured. Histological examinations of prostates and biocompatibility of NIR-AgNPs on vital organs were also performed. Key findingsThe aggregated spherical AgNPs with a mean size of 50–90 nm and a Zeta potential of −53.22 mV displayed high effectiveness in the NIR (532 nm–1 W) region by decreasing prostate size, PI, DHT, and PSA in BPH rats with no signs of gross, hepatic, or renal damage. As compared to alternative therapies, hyperthermia therapy increased antioxidant activities, induced apoptosis, inhibited angiogenesis, reduced histological alterations in the prostates of BPH rats, and improved biocompatibility of the vital organs. SignificanceThe current study demonstrated the effectiveness of plasmonic AgNPs photothermal therapy in the treatment of BPH.

New insights into the enhanced transport of uncoated and polyvinylpyrrolidone-coated silver nanoparticles in saturated porous media by dissolved black carbons

Silver nanoparticles (AgNPs) are among the most applied nanomaterials and have great potential to be present in the environment. Dissolved black carbon (DBC) is ubiquitous in soil as a result of large-scale application of biomass-derived black carbon as soil amendments, while its impacts on the transport of AgNPs remain unclear. In this study, two DBCs with different functional groups were prepared at 300 and 500 °C (DBC300 and DBC500), and their impacts on the transport of uncoated AgNPs (Bare-AgNP) and polyvinylpyrrolidone-coated AgNPs (PVP–AgNP) in saturated quartz sand were investigated. The transport of PVP-AgNP was much higher than Bare-AgNP under the same conditions because of the increased steric hindrance provided by PVP surface coating. The transport of two kinds of AgNPs was both enhanced by the DBCs under all the experimental conditions. DBC500 displayed a stronger enhancement effect than DBC300 on PVP-AgNP transport, but DBC300 facilitated the migration of Bare-AgNP more significantly than DBC500. The higher aromaticity and stronger hydrophobicity of DBC500 drove it to be adsorbed on the surface of PVP-AgNP, thus providing stronger steric hindrance and promotion effect on PVP-AgNP transport. However, DBC300 contained surface sulfhydryl groups, which bound with the Bare-AgNP tightly, therefore it greatly promoted Bare-AgNP transport via enhanced steric hindrance. (X)DLVO calculations indicated DBCs generally increased the energy barrier between the AgNPs and sand grains. The results shed light on the vital roles of both the properties of AgNPs and DBCs on the fate and environmental behaviors of silver nanomaterials in complex environments.

Dissolution of Ag Nanoparticles in Agricultural Soils and Effects on Soil Exoenzyme Activities

To assess environmental risks related to the mobility and toxicity of AgNPs, the chemical availability of AgNPs and polyvinylpyrrolidone-coated AgNPs (PVP-AgNPs) in three agricultural soils was quantified in a pot experiment. Porewater collection and soil extractions with 0.01 M CaCl2, 0.4 M Glycine (pH 1.5) and 0.05 M NH4-EDTA were performed. The effect on soil exoenzyme activities was also assessed. Porewater concentration was low (<0.4% and <0.04% of dosed Ag, for AgNPs and PVP-AgNPs, respectively) and only detected in acidic soils (pH 4.4 and 4.9). The PVP-coating reduced the downward mobility of AgNPs in soil and possibly also their dissolution rate (and subsequent release of dissolved Ag+ ions into porewater). The effect of variation in organic matter on soil enzymatic activity was larger than that of AgNPs, as no significant additional inhibitory effect from Ag could be observed. Only at low pH and in the presence of complexing ligands that form very stable Ag complexes (0.4 M Glycine extraction at pH 1.5) up to 58% of the Ag added to soil was released (independently of PVP coating). An extraction with glycine is proposed as a useful indicator of potentially available Ag in soils.

Surface coatings alter transcriptional responses to silver nanoparticles following oral exposure

Silver nanoparticles (AgNPs) are used in food packaging materials, dental care products and other consumer goods and can result in oral exposure. To determine whether AgNP coatings modulate transcriptional responses to AgNP exposure, we exposed mice orally to 20 nm citrate (cit)-coated AgNPs (cit-AgNPs) or polyvinylpyrrolidone (PVP)-coated AgNPs (PVP-AgNPs) at a 4 mg/kg dose for 7 consecutive days and analyzed changes in the expression of protein-coding genes and long noncoding RNAs (lncRNAs), a new class of regulatory RNAs, in the liver. We identified unique and common expression signatures of protein-coding and lncRNA genes, altered biological processes and signaling pathways, and coding-non-coding gene interactions for cit-AgNPs and PVP-AgNPs. Commonly regulated genes comprised only about 10 and 20% of all differentially expressed genes in PVP-AgNP and cit-AgNP exposed mice, respectively. Commonly regulated biological processes included glutathione metabolic process and cellular oxidant detoxification. Commonly regulated pathways included Keap-Nrf2, PPAR, MAPK and IL-6 signaling pathways. The coding-non-coding gene co-expression analysis revealed that protein-coding genes were co-expressed with a variable number of lncRNAs ranging from one to twenty three and may share functional roles with the protein-coding genes. PVP-AgNP exposure induced a more robust transcriptional response than cit-AgNP exposure characterized by more than two-fold higher number of differentially expressed both protein-coding and lncRNA genes. Our data demonstrate that the surface coating strongly modulates the spectrum and the number of differentially expressed genes after oral AgNP exposure. On the other hand, our data suggest that AgNP exposure can alter drug and chemical sensitivity, metabolic homeostasis and cancer risk irrespective of the coating type, warranting further investigations.

Dissolution of Silver Nanoparticles in Colloidal Consumer Products: Effects of Particle Size and Capping Agent.

The utilization of silver nanoparticles (AgNPs) in consumer products has significantly increased in recent years, primarily due to their antimicrobial properties. Increased use of AgNPs has raised ecological concerns. Once released into an aquatic environment, AgNPs may undergo oxidative dissolution leading to the generation of toxic Ag+. Therefore, it is critical to investigate the ecotoxicological potential of AgNPs and determine the physicochemical parameters that control their dissolution in aquatic environments. We have investigated the dissolution trends of aqueous colloidal AgNPs in five products, marketed as dietary supplements and surface sanitizers. The dissolution trends of AgNPs in studied products were compared to the dissolution trends of AgNPs in well-characterized laboratory-synthesized nanomaterials: citrate-coated AgNPs, polyvinylpyrrolidone-coated AgNPs, and branched polyethyleneimine-coated AgNPs. The characterization of the studied AgNPs included: particle size, anion content, metal content, silver speciation, and capping agent identification. There were small differences in the dissolved masses of Ag+ between products, but we did not observe any significant differences in the dissolution trends obtained for deionized water and tap water. The decrease of the dissolved mass of Ag+ in tap water could be due to the reaction between Ag+ and Cl-, forming AgCl and affecting their dissolution. We observed a rapid initial Ag+ release and particle size decrease for all AgNP suspensions due to the desorption of Ag+ from the nanoparticles surfaces. The observed differences in dissolution trends between AgNPs in products and laboratory-synthesized AgNPs could be caused by variances in capping agent, particle size, and total AgNP surface area in suspensions.

Toxicity responses of different organs of zebrafish (Danio rerio) to silver nanoparticles with different particle sizes and surface coatings

Silver nanoparticles (AgNPs) in aquatic ecosystems are toxic to aquatic organisms. In this study, we aimed to investigate the toxicities and molecular mechanisms of AgNPs with different surface coatings (sodium citrate and polyvinylpyrrolidone) and particle sizes (20 nm and 100 nm) in the gills, intestines, and muscles of zebrafish after 96 h of exposure. Our results indicated that the contribution of particle size to AgNP toxicity was greater than that of the surface coating. Citrate-coated AgNPs were more toxic than polyvinylpyrrolidone-coated AgNPs, and 20-nm AgNPs were more toxic than 100-nm AgNPs. The toxic effects of AgNPs to the tissues were in the order intestines > gills > muscles. Differential expression of genes with the different AgNPs confirmed that they had toxic effects in the zebrafish tissues at the molecular level. Our comprehensive comparison of the toxicities of different AgNPs to aquatic ecosystems will be helpful for further risk assessments of AgNPs.

Involvement of telomerase activity inhibition and telomere dysfunction in silver nanoparticles anticancer effects.

To investigate the possible mechanisms of telomerase and telomere underlying the anticancer effects of silver nanoparticles (AgNPs). 25nm polyvinylpyrrolidone-coated AgNPs were used. The telomerase activity and telomere function were evaluated. The anticancer effects of AgNPs were gauged with cell viability assay under different statement of telomerase and telomere. AgNPs could inhibit telomerase activity and lead to telomere shortening and dysfunction. Overexpression of telomerase attenuated the anticancer activity of AgNPs, whereas downregulation of telomerase activity or dysfunction of the telomere enhanced the cytotoxicity of AgNPs in HeLa cells. Our findings provided strong evidence that the anticancer effects of AgNPs were mediated via interference with the telomerase/telomere.

Simultaneous determination of the size and concentration of AgNPs in water samples by UV–vis spectrophotometry and chemometrics tools

The combination of UV–vis spectrophotometry with a chemometric calibration tool based on partial least squares (PLS) has allowed us the development of a multivariate analytical method that simultaneously estimates the concentration and size of mixtures of silver nanoparticles (AgNPs) in environmental water samples. The method is based on changes in the surface plasmon resonance band (SPRB) of AgNPs when they form aggregated/assembled structures with L-cysteine (L-cys). Measurementts were performed by employed a fixed-time kinetics method that implies that the final spectra (response) are obtained by subtstracting the solutions spectra at fixed times. Optimization of experimental conditions affecting aggregation such as time, temperature, pH and concentration of aggregating substance was performed by experimental design and response surface methodologies (RSM). A multivariate calibration model using AgNPs of known diameter size ((20 ± 3), (41 ± 3), (59 ± 5) and (79 ± 7) nm) within a concentration range between 0.62 and 2.5 mg L−1 was constructed by using a mixture experimental design and PLS. The method was finally applied to estimate size and concentration of AgNPs in AgNPs-spiked river and tap water samples. Water samples were spiked with individual, binary and ternary mixtures of AgNPs of different sizes and by using two types of AgNPs: citrate-coated AgNPs (cit-AgNPs) and polyvinylpyrrolidone-coated AgNPs (PVP-AgNPs). A good correspondence was obtained between predicted values and the total amount of AgNPs added with recovery values ranged within 80–160% for the individual mixtures, 68–108% for the binary mixtures and 60–64% for the ternary mixtures of AgNPs. Finally, transmission electron microscopy (TEM) measurements were performed for those cases where discrepancies between the expected and the obtained values were observed. TEM micrographs evidenced the presence of agglomerates or aggregates of AgNPs in some of the mixtures or water tested.

Oral exposure to silver nanoparticles increases oxidative stress markers in the liver of male rats and deregulates the insulin signalling pathway and p53 and cleaved caspase 3 protein expression

The present study was aimed at assessing the impact of AgNPs on the liver of male rats orally exposed to 0, 50, 100 and 200 mg/kg/day of polyvinyl pyrrolidone coated AgNPs (PVP-AgNPs) for 90 days. The induction of apoptotic cell death -by measuring the protein levels of the active form of caspase 3- and the levels of the microtubule-associated protein 1A/1B-light chain (LC3) protein were measured as a marker of the induction of autophagy. PVP-AgNPs caused an increase of the activity of superoxide dismutase (SOD) and catalase (CAT) in the liver of male rats. However, the activity decreased after exposure to high amounts of PVP-AgNPs. Increased protein levels of IRS-1, AKT, GSK3β and mTOR proteins were observed in a dose-dependent manner. However, these proteins showed a decrease at 200 mg/kg/day. The same pattern was observed for the p53, p21 and cleaved caspase 3 protein levels. The current results suggest that the increase of ROS production by PVP-AgNPs stimulated SOD and CAT activity, as well as IRS-1, AKT, mTOR, p53, p21 and caspase 3 as protective mechanisms of cell survival and preserve DNA fidelity. However, cellular damage by excessive ROS production might induce the depletion of these survival mechanisms at 200 mg/kg/day.

Partitioning of nanoparticle-originated dissolved silver in natural and artificial sediments.

Sediments are believed to be a major sink for silver nanoparticles (AgNPs) in the aquatic environment, but there is a lack of knowledge about the environmental effects and behavior of AgNPs in sediments. The release of highly toxic Ag+ through dissolution of AgNPs is one mechanism leading to toxic effects in sediments. We applied an ultrasound-assisted sequential extraction method to evaluate the dissolution of AgNPs and to study the partitioning of dissolved Ag in sediments. Silver was spiked into artificial and 2 natural sediments (Lake Höytiäinen sediment and Lake Kuorinka sediment) as silver nitrate (AgNO3 ), uncoated AgNPs, or polyvinylpyrrolidone-coated AgNPs (PVP-AgNPs). In addition, the total body burdens of Ag in the sediment-dwelling oligochaete Lumbriculus variegatus were assessed over a 28-d exposure period. The dissolution rate was found to be similar between the uncoated AgNP and PVP-AgNP groups. In all sediments, dissolved Ag was mainly bound to the residual fraction of the sediment, followed by iron and manganese oxides or natural organic matter. In Lake Kuorinka sediment, dissolved Ag that originated from PVP-AgNPs was relatively more bioaccessible, also resulting in higher total body burden in L. variegatus than that from uncoated AgNPs or AgNO3 . In artificial sediment and Lake Höytiäinen sediment, AgNO3 was significantly more bioaccessible than AgNPs. Our results highlight the importance of sediment properties and AgNP surface chemistry when evaluating the environmental exposure of AgNPs. Environ Toxicol Chem 2017;36:2593-2601. © 2017 SETAC.

Silver nanoparticles exhibit coating and dose-dependent neurotoxicity in glutamatergic neurons derived from human embryonic stem cells

Silver nanoparticles (AgNPs) are used extensively as anti-microbial agents in various products, but little is known about their potential neurotoxic effects. In this study, we used glutamatergic neurons derived from human embryonic stem cells as a cellular model to study 20nm citrate-coated AgNPs (AgSCs) and Polyvinylpyrrolidone-coated AgNPs (AgSPs) induced neurotoxicity. AgSCs significantly damaged neurite outgrowths; increased the production of reactive oxygen species and Ca2+ influxes; reduced the expression of MAP2, PSD95, vGlut1 and NMDA receptor proteins at concentrations as low as 0.1μg/ml. In contrast, AgSPs exhibited neurotoxicity only at higher concentration. Furthermore, our results showed that AgSCs induced glutamate excitotoxicity by the activation of calmodulin and the induction of nitric oxide synthase; increased the phosphorylation of glycogen synthase kinase-3 α/β at Tyr216 and Tau at Ser396 and reduced the expression of Tau46, which are typically observed in Alzheimer’s disease. This study indicated that stem cells can provide an excellent platform for studying nanoparticle induced neurotoxicity.

Oral subchronic exposure to silver nanoparticles in rats

Because of their extremely small size, silver nanoparticles (AgNPs) show unique physical and chemical properties, with specific biological effects, which make them particularly attractive for being used in a number of consumer applications. However, these properties also influence the potential toxicity of AgNPs. In this study, we assessed the potential toxic effects of an in vivo oral sub-chronic exposure to polyvinyl pyrrolidone coated AgNPs (PVP-AgNPs) in adult male rats. We also assessed if oral PVP-AgNPs exposure could alter the levels of various metals (Fe, Mg, Zn and Cu) in tissues. Rats were orally given 0, 50, 100 and 200 mg/kg/day of PVP-AgNPs. Silver (Ag) accumulation in tissues, Ag excretion, biochemical and hematological parameters, metal levels, as well as histopathological changes and subcellular distribution following PVP-AgNPs exposure, were also investigated. After 90 days of treatment, AgNPs were found within hepatic and ileum cells. The major tissue concentration of Ag was found in ileum of treated animals. However, all tissues of PVP-AgNPs-exposed animals showed increased levels of Ag in comparison with those of rats in the control group. No harmful effects in liver and kidney, as well as in biochemical markers were noted at any treatment dose. In addition, no hematological or histopathological changes were found in treated animals. However, significant differences in Cu and Zn levels were found in thymus and brain of PVP-AgNPs-treated rats.

Anaerobic toxicity of cationic silver nanoparticles

The microbial toxicity of silver nanoparticles (AgNPs) stabilized with different capping agents was compared to that of Ag+ under anaerobic conditions. Three AgNPs were investigated: (1) negatively charged citrate-coated AgNPs (citrate-AgNPs), (2) minimally charged polyvinylpyrrolidone coated AgNPs (PVP-AgNPs) and (3) positively charged branched polyethyleneimine coated AgNPs (BPEI-AgNPs). The AgNPs investigated in this experiment were similar in size (10–15nm), spherical in shape, but varied in surface charge which ranged from highly negative to highly positive. While, at AgNPs concentrations lower than 5mgL−1, the anaerobic decomposition process was not influenced by the presence of the nanoparticles, there was an observed impact on the diversity of the microbial community. At elevated concentrations (100mgL−1 as silver), only the cationic BPEI-AgNPs demonstrated toxicity similar in magnitude to that of Ag+. Both citrate and PVP-AgNPs did not exhibit toxicity at the 100mgL−1 as measured by biogas evolution. These findings further indicate the varying modes of action for nanoparticle toxicity and represent one of the few studies that evaluate end-of-life management concerns with regards to the increasing use of nanomaterials in our everyday life. These findings also highlight some of the concerns with a one size fits all approach to the evaluation of environmental health and safety concerns associated with the use of nanoparticles.

Thiolated-2-methacryloyloxyethyl phosphorylcholine protected silver nanoparticles as novel photo-induced cell-killing agents

Event Abstract Back to Event Thiolated-2-methacryloyloxyethyl phosphorylcholine protected silver nanoparticles as novel photo-induced cell-killing agents Arunee Sangsuwan1, Hideya Kawasaki2, 3 and Yasuhiko Iwasaki2, 3 1 Kansai university, Graduate School of Science and Engineering, Japan 2 Kansai university, Faculty of Chemistry, Materials and Bioengineering, Japan 3 Kansai university, ORDIST, Japan Introduction: The usefulness of silver nanoparticles is well known due to their various advantages and extensive applications. Thus, the synthesis of metal nanoparticles with predictable and well-defined structures is of interest in medical and diagnostic applications[1]. However, AgNPs are of limited use in medicine because of their toxicity, which may damage healthy surrounding tissue. Research is continuously being conducted to resolve this issue. In this study, thiolated-2-methacryloyloxyethyl phosphorylcholine (MPC-SH) protected silver nanoparticles (MPC-AgNPs) were prepared as cell-killing agents under UV irradiation. The viability of cells in contact with MPC-AgNPs was relatively high and MPC-AgNPs also exhibit a cell-killing effect under UV irradiation. Materials and Methods: Thiol-terminated MPC (MPC-SH) was synthesized from the modified method of Goda and co-workers[2]. MPC-SH was mixed with silver nitrate and formic acid in deionized water. The solution was stirred at 70 °C for 3 hours. The reaction mixture was dialyzed to purify MPC-AgNPs. MPC-AgNPs were then centrifuged at 6,000 rpm for 15 minutes and lyophilized. The cytotoxicity of MPC-AgNPs was detemined by using HeLa cells and half maximal inhibitory concentration (LC50) of the nanoparticles was determined. Moreover, photo-induced toxicity of MPC-AgNPs was investigated under 356 nm photo irradiation. Results: The MPC-AgNPs can be prepared via strong thiolmetal coordination. Immobilized MPC on AgNPs was confirmed by XPS and IR analyses. The presence of AgNPs in the form of Ag0 was verified by XRD, and the average diameter of particles was determined as 13.4 ± 2.2 nm by TEM and 18.4 nm (PDI 0.18) by DLS. MPC-AgNPs showed toxicity at concentrations of 5 μg/mL or higher as shown in Fig.1. The LC50 of MPC-AgNPs was about 14.7 μg/mL, which shows a greater biocompatibility than AgNO3, bare AgNPs, chitosan-coated AgNTs, and polyvinylpyrrolidone-coated AgNPs, as determined by previous studies[3],[4]. Photo-induced toxicity of MPC-AgNPs on HeLa cells significantly decreased the cell viability to about 50% in a particle concentration at 0.5 μg/mL, and at a higher concentration of 1 μg/mL, the HeLa cells died completely from the photo-induced toxicity of MPC-AgNPs as shown in Fig.2. Discussion: MPC improves both biocompatibility and dispersity of nanoparticles. MPC-AgNPs used in our research were small size particles, which are conducive to high cytotoxicity, in accordance with the results of previous studies. In addition, the particles exhibit a highly potent cell-killing effect under UV irradiation; they lost SPR after irradiation, resulting in a decreasing SPR band and particle size, as measured by UV-visible spectrophotometry and DLS, respectively. Conclusion: The present study demonstrates that MPC-AgNPs can be prepared via strong thiolmetal coordination and the average diameter of particles was determined as 13.4 ± 2.2 nm by TEM and 18.4 nm (PDI 0.18) by DLS. MPC improves both biocompatibility and dispersity of nanoparticles. Our findings suggest that the cell death mechanism is possible because particles lose areas of their surface and particles losing MPC are toxic. Finally, biocompatible MPC-AgNPs are exhibited after activation by light, which makes them potentially useful as photo-induced cell-killing agents. Grant-in-Aid for Scientific Research on Innovative Areas ‘‘Nanomedicine Molecular Science’’ (No. 2306) from the Ministry of Education, Culture, Sports, Science, and Technology of Japan.

Influence of natural organic matter on transport and retention of polymer coated silver nanoparticles in porous media

Interactions between organic matter (OM) and engineered polymer coatings as they affect the retention of polyvinylpyrrolidone (PVP) polymer-coated silver nanoparticles (AgNPs) were studied. Two distinct types of OM—cysteine representing low molecular weight multivalent functional groups, and Suwannee River Humic Acid (HA) representing high molecular weight polymers, were investigated with respect to their effects on particle stability in aggregation and deposition. Aggregation of the PVP coated AgNPs (PVP-AgNPs) was enhanced by cysteine addition at high ionic strengths, which was attributed to cysteine binding to the AgNPs and replacing the otherwise steric stabilizing agent PVP. In contrast the addition of HA did not increase aggregation rates and decreased PVP-AgNP deposition to the silica porous medium, consistent with enhanced electrosteric stabilization by the HA. Although cysteine also reduced deposition in the porous medium, the mechanisms of reduced deposition appear to be enhanced electric double layer (EDL) interaction at low ionic strengths. At higher ionic strengths, aggregation was favored leading to lower deposition due to smaller diffusion coefficients and single collector efficiencies despite the reduced EDL interactions.

Key Factors Controlling the Transport of Silver Nanoparticles in Porous Media

The current study investigated the mobility of four silver nanoparticles (AgNPs) stabilized using different capping agents and represent the common stabilization mechanisms as well as surface charging scenarios in reactive and nonreactive porous media. The AgNPs were (1) uncoated H2-AgNPs (electrostatically stabilized) and (2) citrate coated AgNPs (Citrate-AgNPs) (electrostatically stabilized), (3) polyvinylpyrrolidone coated AgNPs (PVP-AgNPs) (sterically stabilized), and (4) branched polyethyleneimine coated AgNPs (BPEI-AgNPs) (electrosterically stabilized). The porous media were (1) quartz sand (QS), (2) ferrihydrite-coated sand (FcS), and (3) kaolin-coated sand (KcS). The H2-AgNPs and Citrate-AgNPs were readily mobile in QS but significantly retained in FcS and KcS with more deposition achieved in the KcS media. The deposition of the H2-AgNPs and Citrate-AgNPs followed the order of KcS > FcS > QS. The PVP-AgNPs breakthrough occurred more rapid as compared to the H2-AgNPs and Citrate-AgNPs but the deposition of PVP-AgNPs followed the same order of the electrostatically stabilized AgNPs (KcS > FcS > QS). The BPEI-AgNPs were readily mobile regardless of the porous media reactivity. Physicochemical interactions were the dominant filtration mechanism in the majority of the investigated cases but straining played the major role in the deposition of the electrostatically stabilized H2-AgNPs and Citrate-AgNPs in the KcS media. The results highlight the importance of both the stabilization mechanism and capping agent chemistry as key factors governing the transport of AgNPs in the environment.

Effect of silver nanoparticles on human primary keratinocytes

Silver nanoparticles (AgNPs) have many biological applications in biomedicine, biotechnology and other life sciences. Depending on the size, shape and the type of carrier, AgNPs demonstrate different physical and chemical properties. AgNPs have strong antimicrobial, antiviral and antifungal activity, thus they are used extensively in a range of medical settings, particularly in wound dressings but also in cosmetics. This study was undertaken to examine the potential toxic effects of 15 nm polyvinylpyrrolidone-coated AgNPs on primary normal human epidermal keratinocytes (NHEK). Cells were treated with different concentrations of AgNPs and then cell viability, metabolic activity and other biological and biochemical aspects of keratinocytes functioning were studied. We observed that AgNPs decrease keratinocyte viability, metabolism and also proliferatory and migratory potential of these cells. Moreover, longer exposure resulted in activation of caspase 3/7 and DNA damage. Our studies show for the first time, that AgNPs may present possible danger for primary keratinocytes, concerning activation of genotoxic and cytotoxic processes depending on the concentration.