New, rapid method to measure dissolved silver concentration in silver nanoparticle suspensions by aggregation combined with centrifugation
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It is unclear whether the antimicrobial activities of silver nanoparticles (AgNPs) are exclusively mediated by the release of silver ions (Ag+) or, instead, are due to combined nanoparticle and silver ion effects. Therefore, it is essential to quantify dissolved Ag in nanosilver suspensions for investigations of nanoparticle toxicity. We developed a method to measure dissolved Ag in Ag+/AgNPs mixtures by combining aggregation of AgNPs with centrifugation. We also describe the reproducible synthesis of stable, uncoated AgNPs. Uncoated AgNPs were quickly aggregated by 2 mM Ca2+, forming large clusters that could be sedimented in a low-speed centrifuge. At 20,100g, the sedimentation time of AgNPs was markedly reduced to 30 min due to Ca2+-mediated aggregation, confirmed by the measurements of Ag content in supernatants with graphite furnace atomic absorption spectrometry. No AgNPs were detected in the supernatant by UV–Vis absorption spectra after centrifuging the aggregates. Our approach provides a convenient and inexpensive way to separate dissolved Ag from AgNPs, avoiding long ultracentrifugation times or Ag+ adsorption to ultrafiltration membranes.
KeywordsSilver nanoparticles Sedimentation Aggregation Separation Centrifugation Nanotoxicology Environmental and health effects
Nanomaterials (NMs) have received increasing attention due to their distinctive physicochemical properties at nanosize (Adeleye et al. 2016; Kim et al. 2010; Lohse and Murphy 2012), especially for their medical application potential, as multi-drug resistant pathogens become ever more frequent (Meredith et al. 2015; Morones-Ramirez et al. 2013; Piddock 2012; Sprenger and Fukuda 2016). Silver nanoparticles (AgNPs) are widely used nanomaterials due to their toxic effects on microorganisms (Chaloupka et al. 2010; Eckhardt et al. 2013; Morones-Ramirez et al. 2013). However, the mechanisms involved in their toxicity to microorganisms are still unclear. The antibacterial activities of AgNPs are generally thought to be indirectly mediated by the release of silver ions (Ag+) (Leclerc and Wilkinson 2014; Shen et al. 2015; Xiu et al. 2012), but some studies have suggested nanoparticles themselves can play a direct role in toxicity to bacteria (Ivask et al. 2013; McQuillan and Shaw 2014) because of their potential to directly interact with microbial components (Eckhardt et al. 2013) and their large proportion of reactive surface sites compared to bulk materials (Oberdörster et al. 2005). It is therefore essential to differentiate ionic and nano-Ag and measure the concentrations of different Ag species to understand their bactericidal effects.
Silver nanoparticles become oxidized, releasing Ag+ in aquatic environments, when oxygen is available (Liu and Hurt 2010; Peretyazhko et al. 2014; Zhang et al. 2011). The dissolved Ag usually coexists with nanoparticles during storage (Loza et al. 2014). Quantifying Ag species in AgNP dispersions, however, is quite challenging due to the difficulty of separating dissolved Ag+ from AgNPs. Ultracentrifugation and ultrafiltration are the methods used routinely. Both have their limits. In ultracentrifugation, precipitating the tiny nanoparticles requires large centrifugal forces and long running times (Mostowfi et al. 2009), which might be problematic when AgNPs continuously release Ag+ in an oxic environment. Sorption of Ag+ to membranes may occur when ultrafiltration (Kennedy et al. 2010; Leclerc and Wilkinson 2014) or dialysis is used. Ion-selective electrodes (ISE) can be used to measure free Ag+ concentration in bulk liquid but not the total dissolved Ag+ (Shen et al. 2015). Emerging techniques such as single particle inductively coupled plasma mass spectrometry (SP-ICP-MS) and asymmetrical flow field-flow fractionation coupled with inductively coupled plasma mass spectrometry (AF4-ICP-MS) are complex to operate and standardize (Mitrano et al. 2012; Pace et al. 2012).
In this study, we developed a convenient and reliable method to quantify dissolved Ag in Ag+/AgNP mixtures by combining aggregation with centrifugation. The aggregation of AgNPs in different concentrations of Ca(NO3)2 solutions was investigated to examine how the aggregation mediated by Ca2+ facilitated the sedimentation of AgNPs during centrifugation. By comparing with ultrafiltration, we demonstrated that this new method provided a simple, fast and effective way to monitor dissolved Ag in AgNP suspensions.
Materials and methods
Synthesis of uncoated AgNPs
Uncoated AgNPs were produced by the solution-phase method (Polte et al. 2012; Van Hyning and Zukoski 1998). Silver nitrate (AgNO3, Sigma-Aldrich) was used as the precursor and reduced by sodium borohydride (NaBH4, Sigma-Aldrich) to form AgNPs at room temperature (19 ± 4 °C). All the glassware for AgNPs synthesis was soaked in 10 % HNO3 overnight and rinsed with copious amounts of deionized (DI) water (18.2 mΩ, Millipore), followed by drying in an ambient environment. The AgNO3 solution (100 mL, 0.12 mM) was poured into the NaBH4 solution (100 mL, 3 mM) in a 500-mL beaker. The NaBH4 concentration was in 25-fold excess. The mixture was homogenized by magnetic stirring (1200 rpm). The NaBH4 solution was freshly prepared to reduce the degradation resulting from its reaction with water to produce H2 and BO4 −. The solution turned to grey within a few seconds after mixing and changed to light yellow after a few minutes. As the reaction continued, the colour slowly changed to dark yellow at ~25 min and back to yellow. After 1 h, the stirring was stopped, and the solution was stored for 24 h in the dark at room temperature. Finally, the stirring bar was removed and the AgNP suspension was transferred into glass bottles (250 mL, Duran) and stored at 4 °C in the dark.
Characterization of uncoated AgNPs
The localized surface plasmon resonance (LSPR) of uncoated AgNP suspensions was measured by UV–Vis spectrometry (UV–Vis 6800, Jenway, Staffordshire, UK). The relationship between LSPR signal and AgNP concentration was obtained by measuring the absorption spectra of a dilution series of AgNP suspensions.
The size distribution of AgNPs was measured by dynamic light scattering (DLS) (Zetasizer Nano, Malvern Instruments, Malvern, UK) and differential centrifugal sedimentation (DCS) (DC24000, CPS Instruments Europe, Oosterhout, Netherlands).
The dissolved Ag fraction in AgNP suspensions was obtained by filtering the suspensions through a 3-kDa membrane filter (Amicon Ultra-15 Centrifugal Filter Unit, Millipore (UK) Limited, Hertfordshire, UK) at a centrifugal force of 4000g for 20 min at 4 °C. The filtrate was collected and stored at 4 °C for future analysis. Total Ag concentration was measured by acidifying 1 mL AgNP suspension with 9 mL 70 % HNO3 (w/w) overnight at room temperature. The digested suspension was diluted with DI H2O (18.2 mΩ, Millipore) to a final HNO3 concentration of 0.2 % (w/v). The silver content was measured by graphite furnace atomic absorption spectrometry (GFAAS) (AAnalyst 600, PerkinElmer Instruments, Massachusetts, USA). A silver concentration series (0–25 μg/L) was obtained by diluting a standard AgNO3 solution (1000 μg/mL Ag, PerkinElmer Life and Analytical Sciences, Shelton, USA) with 0.2 % HNO3 concentration (w/v). Those standards were measured together with samples to obtain a calibration curve for calculating sample concentrations.
The morphology of AgNPs was imaged by transmission electron microscopy (TEM, JEOL 1200EX, Tokyo, Japan). About 20 μL AgNP suspension was loaded onto TEM grids (CF300-Cu Grids, Electron Microscopy Sciences, Pennsylvania, USA), followed by drying at room temperature. In order to reduce aggregation of AgNPs after loading the grids, grids were coated with 20 μL 100 mg/L polylysine, which carries many positive charges while the AgNPs have a negative surface charge. After 1 h, the grids were rinsed with DI water followed by drying. The morphology of AgNPs in Ca(NO3)2 solution was analysed by adding 100 mg/L bovine serum albumin (BSA) to stabilize the aggregates before loading the sample on a TEM grid without polylysine. BSA can be used to preserve the nanoparticle state in electrolyte solutions to avoid artefacts of drying (Michen et al. 2015).
Determining aggregation kinetics of AgNPs in Ca(NO3)2 solutions
The long-term aggregation of AgNPs in Ca(NO3)2 solution was followed for 96 h after mixing 20 mL of a AgNP suspension with the same volume of a 2 mM Ca(NO3)2 solution by vortexing in screw-cap glass vials (Bijou, capacity 46 mL) and allowing the mixture to settle on a laboratory bench at room temperature (17 ± 1 °C). The liquid from the top layer (5 mL) was taken for recording UV–Vis absorption spectra after 0, 1, 6, 24, 48 and 96 h.
The short-term aggregation kinetics were monitored for 0.5–2 h after mixing AgNP and Ca(NO3)2 solutions by recording the hydrodynamic size of aggregates by DLS in real time. The AgNP suspension (0.5 mL, total Ag 5012 ± 75 μg/L, dissolved Ag 28 ± 0.5 μg/L) was mixed with 0.5 mL of different concentrations of Ca(NO3)2 in a disposable plastic cuvette and immediately placed in the Zetasizer Nano to record the Z-average diameter. Temperature was controlled at 25 °C. Different concentrations of AgNPs that were obtained by diluting the AgNP stock by DI H2O were mixed with 0.5 mL of 2 or 20 mM Ca(NO3)2 in the same way to investigate the aggregation of dilute AgNP suspensions.
Centrifugation of AgNPs in Ca(NO3)2
The sedimentation speeds of AgNPs with or without Ca2+-mediated aggregation were compared at the same centrifugal force. AgNPs were aggregated by mixing 10 mL AgNP suspension with 10 mL Ca(NO3)2 solution (2 mM). After 10 min, the AgNPs/Ca(NO3)2 mixture was aliquoted into several centrifuge tubes (1 mL for each tube). Diluting 10 mL of the same AgNP suspension in 10 mL DI H2O was used as control. Centrifugation was undertaken to sediment aggregates or individual AgNPs at a centrifugal force of 20,100g (Centrifuge 5417 C, Eppendorf, Engelsdorf, Germany), leaving dissolved Ag in the supernatant. To investigate the extent to which pre-aggregation can reduce centrifugation time, one tube from each treatment was taken to measure the Ag content in the supernatant (0.4–0.5 mL) at 0, 0.5, 1, 1.5, 2, 2.5, 3 and 4 h. The supernatants were acidified to 1 % HNO3 (w/v) overnight (more than 12 h) at 80 °C, and further diluted to a final HNO3 concentration of 0.2 % (w/v) for Ag concentration measurement by GFAAS.
Measurement of AgNP content in supernatant after centrifugation of AgNPs in Ca(NO3)2
Suspensions of AgNPs (0.5 mL) were mixed with Ca(NO3)2 (0.5 mL) in 1.5-mL microcentrifuge tubes (safe-lock microcentrifuge tubes, Eppendorf, Germany) to form large aggregates. After reacting for 10 min, aggregates were centrifuged at 20,100g for 30 min. Ten aliquots were processed in parallel. The amount of AgNPs in the supernatant was measured by UV–Vis absorption spectroscopy. The supernatants (0.5 mL) from those ten aliquots were pooled into one tube since 4 mL was the minimum volume required for a UV–Vis absorption measurement with a 10-cm path length quartz cuvette. Although the UV–Vis absorption of nanoparticles depends on their size, shape, surface coating, aggregation states and surrounding environmental conditions, it can still be used for concentration measurement as long as the particles and surrounding environmental conditions are similar (Hendel et al. 2014). A low concentration of AgNPs (<10 μg/L) can be detected by UV–Vis spectrometry using a 10-cm path length quartz cuvette. The peak absorbance, typically between 390 and 400 nm, was used to quantify the AgNPs, and the absorbance at longer wavelengths (500–700 nm) was used to monitor the aggregates (Gorham et al. 2014).
Measuring dissolved Ag in AgNPs suspension with aggregation–centrifugation or ultrafiltration
Different concentrations of AgNPs were prepared by diluting the AgNP stock with DI H2O. The total Ag concentration of the AgNP stock was 5012 ± 75 μg/L, and it contained around 10 % dissolved Ag. Those diluted AgNP suspensions were aggregated in 2 mM Ca(NO3) for 10 min and then centrifuged (20,100g, 30 min). The supernatant (0.4–0.5 mL) was collected carefully and stored at −20 °C for dissolved Ag analysis. Each concentration was assayed in duplicate. Ultrafiltration was carried out by filtering the same AgNP suspensions through 3-kDa membrane filters (Amicon Ultra-15 Centrifugal Filter Unit, Millipore (UK) Limited, Hertfordshire, UK). The filtrates were stored at −20 °C. The dissolved Ag concentrations were always analysed by GFAAS.
Synthesis of uncoated AgNPs
Characteristics of uncoated AgNP suspensions
Zeta potential in DI water (mV)
9.6 ± 0.3
17 ± 4.5
27 ± 4.2
13 ± 0.5
−40 ± 17
AgNPs aggregate in Ca(NO3)2 solutions
Concentration dependence of aggregation of AgNPs in Ca(NO3)2
Time required to sediment AgNPs after aggregation
Sedimentation of Ca2+-aggregated AgNPs is complete
We investigated the efficiency of combining aggregation with centrifugation to precipitate different concentrations of AgNPs (100, 10 and 2 % of the concentration of the AgNP stock suspensions). Supernatants did not show any absorption from 350 to 700 nm after aggregating those concentrations of AgNPs in 2 mM Ca(NO3)2. Instead, 21–50 % of AgNPs remained in the supernatant without Ca2+ (Fig. 6b). Therefore, 2 mM Ca(NO3)2 was sufficient to aggregate even the very dilute AgNPs.
Measuring dissolved Ag in AgNP suspensions by aggregation or ultrafiltration
Formation of stable, uncapped AgNPs
Our study demonstrated the successful synthesis of monodispersed uncoated AgNPs (Fig. 1; Table 1). The formation of uncoated AgNPs is controlled by the aggregative growth of small AgNPs (Polte et al. 2012; Van Hyning et al. 2001), but aggregation of the NPs can lead to the failure of synthesis (Mulfinger et al. 2007). Frequently, the electrolyte with highest ionic strength contributes most to the aggregation (Huynh and Chen 2011; Li et al. 2012). As expected, by decreasing initial AgNO3 and NaBH4 concentrations to reduce the ionic strength and increasing the NaBH4/AgNO3 concentration ratio so more BH4 − is available to stabilize uncoated AgNPs (Van Hyning and Zukoski 1998), we managed to produce stable uncoated AgNPs. The process was reproducible, and the three batches of AgNPs did not differ significantly in their aggregation in Ca(NO3)2 or sedimentation by centrifugation.
Aggregation of AgNPs in Ca(NO3)2 solution
According to classic colloidal theory, interactions between nanoparticles are determined by van der Waals forces, electrostatic repulsive forces and steric effects due to surface stabilizers and solvation effects (Nel et al. 2009). For uncoated AgNPs, negatively charged ions such as BH4 − adsorb on the nanoparticles with counter ions enriched near the surface (Mulfinger et al. 2007; Pfeiffer et al. 2014). Positively charged Ca2+ ions screen the negative surface charge of AgNPs, thus decreasing surface energy. Aggregation of AgNPs occurs when the kinetic energy of Brownian motion overcomes the nanoparticle–nanoparticle energy barrier, which is reduced in Ca(NO3)2 solution (Zhang et al. 2012). The structure of aggregates formed, such as configuration and monomer numbers, depends on nanoparticle concentration, size distribution, surface coating and conditions in the surrounding liquid (Baalousha et al. 2013; El Badawy et al. 2010). The gap between clustered nanoparticles can be as narrow as a few nanometres (Silvera Batista et al. 2015). Under normal gravitational force, small metallic nanoparticles take days or weeks to settle a few millimetres (Alexander et al. 2013). In contrast, the AgNPs completely sedimented to the bottom in 2 mM Ca(NO3)2 solution within 4 days (Fig. 2), suggesting that aggregation facilitates sedimentation of AgNPs.
The aggregation rate of AgNPs increased markedly when the Ca(NO3)2 concentration was increased from 0.1 to 0.2 mM, reaching a maximum rate at 0.5 mM (Fig. 3a, b). This suggests that ~0.2 mM was the concentration separating the slow and fast aggregation regimes, which is known as the critical coagulation concentration (CCC). The aggregation rate was proportional to AgNP concentration in both 2 and 20 mM Ca(NO3)2 solutions (Fig. 3c, d). Increasing AgNP concentration will increase the number of AgNPs with high enough kinetic energy to overcome the energy barrier upon collision and thereby increase the aggregation rate. Notably, 2 and 20 mM Ca(NO3)2 aggregated equivalent concentrations of AgNPs equally fast (Fig. 3d), suggesting that any concentration above the CCC is sufficient to ensure optimum aggregation of AgNPs.
Efficiency of AgNP sedimentation in Ca(NO3)2 solution by centrifugation
It is predicable that centrifugation will shorten the sedimentation time of AgNP aggregates. As the sedimentation velocity is proportional to the square of nanoparticle diameter, the sedimentation distance declines dramatically with decreasing size (Bonaccorso et al. 2013). Consequently, it takes exceedingly long times to sediment small AgNPs completely (Fig. S3). Therefore, centrifugation of monodispersed AgNPs in H2O will especially increase the sedimentation of the larger AgNPs, leading to a steep initial decrease in Ag content in the upper layer of the suspension and a slowdown afterwards (Fig. 5). In Ca(NO3)2 solutions, complete sedimentation was achieved in half an hour (Fig. 5). As TEM graphs showed, individual AgNPs assembled into compact clusters that sedimented much faster due to their larger sizes (Fig. 4).
Judging from the similar shapes of UV–Vis absorption spectra of supernatant and monodispersed AgNP suspensions, coupled with negligible absorption in the long wavelength region that is characteristic for aggregates (Fig. 6), we can conclude that aggregates but not all individual AgNPs were sedimented by centrifugation. Increasing Ca(NO3)2 concentrations enhanced the aggregation rate and therefore the sedimentation rate of AgNPs (Fig. 6a). When the Ca(NO3)2 concentration was larger than the CCC, the fast aggregation regime was obtained and virtually all AgNPs precipitated, making this pre-aggregation approach applicable to a broad range of AgNPs concentrations (Fig. 6b). Furthermore, this approach should be extendable to other AgNPs such as citrate- and PVP-capped AgNPs since they also aggregate in Ca2+ and other electrolyte solutions but may require higher concentrations of Ca2+ (Huynh and Chen 2011).
Comparing the aggregation–centrifugation method with ultrafiltration
Both the aggregation–centrifugation method and ultrafiltration enabled measurement of the dissolved Ag concentration in AgNP suspensions. Larger dissolved Ag concentrations were obtained by aggregation–centrifugation than by ultrafiltration (Fig. 7). This suggests that some of the dissolved Ag is not effectively separated from the AgNPs by ultrafiltration. The various Ag species in AgNP suspensions include nanoparticulate Ag, free Ag+ in the bulk liquid (Kennedy et al. 2010), Ag bound to ions or organic groups in the bulk liquid (Levard et al. 2013; Liu et al. 2010; Ostermeyer et al. 2013) and Ag+ attached to the nanoparticle surface (Pfeiffer et al. 2014). During ultrafiltration, nano-Ag together with any attached Ag+ would presumably be retained by the membrane. Silver loss also occurs due to the adsorption of Ag+ to the filter units during ultrafiltration. Silver ion adsorption by the same brand of ultrafiltration units has been reported in several studies (Kennedy et al. 2010; Leclerc and Wilkinson 2014; Shen et al. 2015). In the aggregation–centrifugation method, Ag loss by adsorption is minimized. Presumably, all free Ag+ in the bulk liquid will remain in the supernatant. Once individual AgNPs aggregate into compact clusters by Ca2+ bridging, the dissolved Ag+ ions that acted as counter ions to balance the negative charges on AgNP surfaces might become released from the AgNPs. Additionally, Ca2+ could replace the surface-attached Ag+ in the diffuse and Stern layer, releasing Ag+ into the bulk liquid. Therefore, more dissolved Ag can be collected by centrifugation after aggregation. Since both of these pools of Ag+ species contribute to the toxicity of AgNPs, it is advantageous to include their concentration in measurements of dissolved Ag in AgNP suspensions.
In this study, a new method to measure dissolved Ag in AgNP suspensions was developed. By combining aggregation with centrifugation, only half an hour was required to separate dissolved Ag from AgNPs. Uncoated AgNPs were aggregated by Ca(NO3)2, and a concentration of 2 mM was sufficient to induce the formation of large AgNPs clusters. This pre-aggregation facilitated the sedimentation of a wide range of AgNP concentrations by centrifugation. The combined aggregation–centrifugation method avoided the loss of Ag in ultrafiltration. That more dissolved Ag was obtained by the new method has significant implications for the study of AgNPs toxicity. Since the combined aggregation–centrifugation method significantly reduces centrifugation time to separate nanoparticles from ions, it will be especially helpful for real-time toxicity assays where speed and the convenience of table top centrifugation represent a major methodological improvement. The method may also be applicable for separating ions from other nanoparticles.
We are grateful for a studentship from the Darwin Trust of Edinburgh for Feng Dong and support from the Facility for Environmental Nanoscience Analysis and Characterisation (FENAC) at the University of Birmingham. We thank Dr. Christine Elgy and M. F. Belinga for their technical support in dynamic light scattering and graphite furnace atomic absorption spectrometry. We thank the Centre for Electron Microscopy for help with transmission electron microscopy.
Compliance with ethical standards
Conflict of interest
The authors declare that they have no conflict of interest.
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