According to the micrographs, the morphology of the silica/iron oxide nanoparticles is approximately spherical. The mole ratio of silicon to iron is roughly 1:1, and Figure 1 shows the nanoparticles with the dark side being iron oxide and the lighter side being silica. The average particle size was 80 nm. Figure 2 is a micrograph of the gold nanoparticles indicating that they are also spherical in shape. Lastly, the silica nanoparticles were analyzed using TEM, and the results show spherical morphology with an average particle size of 60 nm. Figure 3 is a micrograph of the silica nanoparticles taken in aqueous solution.

The micrographs of E. coli, in the presence of iron oxide composite nanoparticles, indicate that the cells are able to maintain growth, showing no overt signs of toxicity. A mixture of circular and elongated cell cross sections are seen. It should be noted that E. coli is characteristically rod-shaped. The cells were sectioned and thus the shape is a function of the angle of each cell relative to the diamond knife during sectioning. TEM images of cells grown in the absence of nanoparticles also showed a similar distribution of cross section shapes. There appears to be an association of the nanoparticles with the cell membrane, as shown in Figures 4a and 4b for E. coli and composite iron oxide nanoparticles. Based upon the fact that the surfaces of the nanoparticles are either bare or PEG coated, it is likely that the interaction between the particles and the membrane is non-specific rather than specific between the nanoparticles and a particular component of the membrane such as a surface expressed protein.

Nanoparticles have a tendency to agglomerate in solution due, in part, to the characteristics of the liquid medium with the addition of salt. In regards to the nanoparticles and microbial cell interactions, this will greatly affect the behavior of the cells. Non-agglomerated particles suspended in solution are preferable for testing purposes because of the following:

1) free moving, single unit particles have more contact with microbes.

2) translocation through the cell membrane will be accelerated due to size.

LB media contains a high salt concentration (0.2 M) that may contribute to the agglomeration of the nanoparticles. The surface charge on the nanoparticles in solution allows the nanoparticles to attract to one another because of the influence of ions from the salts, therefore resulting in the formation of large agglomerates 8910. As a result, the nanoparticles may fall out of solution and settle to the bottom of the shake flasks.

As time increased, the mean particle radius increased. The agglomerate size for the silica particles ranged between 300–360 nm, as shown in Figure 5. Figure 6 shows DLS measurements for silica/iron oxide, indicating similar behavior in the LB media. In contrast, Figure 7 shows the PEG-coated gold nanoparticles remained stable in LB media, thus retaining their size without forming large agglomerates. DLS measurements were taken over the time frame correlating with the growth measurements to determine how the particles behaved during that process. Figure 8 is a comparison of the Au particles with the composite particles in suspension for a duration of six hours. Again, the Au particles maintain their size and stability.

The overall results indicated that the growth of E. coli exposed to silica, silica/iron oxide, and gold nanoparticles was uninhibited. Growth curves were generated for E. coli growing in 100 mL of LB media containing silica/iron oxide nanoparticles at a concentration of 2.2 × 10^-3 g/mL of solution. Under these growth conditions, there was no evidence that the nanoparticles prevented the microbial cells from growing. Figure 9 illustrates the growth curves for E. coli growing with and without silica/iron oxide nanoparticles. Results indicate that there is little difference between the two curves.

Another experiment was conducted using pure silica nanoparticles at the same volume as the silica/iron oxide experiment. Growth data was taken for 3.3 × 10^-2 g/mL of silica solution in 100 mL of LB media. Figure 10 depicts the growth curves for this experiment.

As with the silica and silica/iron oxide experiments, a toxicity study was performed using the gold nanoparticles at a concentration of 1.1 × 10^-4 g/mL. The gold particles show greater stability in solution due to the coating of PEG on the surface. This allows the particles to stay suspended in solution; also, they are able to sustain their initial radius of 30 nm. Figure 11 indicates that there is little, if any, effect on growth resulting from the presence of the gold nanoparticles.

A final experiment was conducted to test the influence of the composite iron oxide nanoparticles on E. coli at concentrations much higher than the previous experiments. The amount of the composite nanoparticles was increased to 2.2 × 10^-2 g/mL in one flask and 4.4 × 10^-2 g/mL in a separate flask. Optical density measurements, given in Figure 12, showed that E. coli was not inhibited by the increase in nanoparticle concentration.

A 100 ml suspension of cells placed on a glass slide were taken from a cell suspension growing with 2.2 × 10^-3 g/ml silica-iron oxide nanoparticles. A cylindrical neodymium-iron-boron permanent magnet (Arbor Scientific, Ann Arbor, MI) was placed two inches away on the right hand side of a glass slide sitting on a digital confocal microscope for imaging. Figure 13 depicts the movement of E. coli as a result of the external magnet positioned next to the slide. Some cells exhibited motion along the magnetic field lines (indicated by the square in Figure 13), but not all of the cells moved in the direction of the field (cells highlighted with circles). This suggests that not all cells were in contact with nanoparticles, and also that the cells were not being swept along by bulk fluid motion resulting from motion of magnetic nanoparticles alone.

Table I gives the specifications for each type of nanoparticle (silica, silica/iron oxide, and gold) used in this study. The silica nanoparticles were made by base catalyzed hydrolysis of TEOS 11. Silica/iron oxide nanoparticles were flame-generated from iron pentacarbonyl and hexamethyldisiloxane in a premixed methane/oxygen/nitrogen flame 12. Each particle contains both gamma-Fe₂O₃ and silica in a 1:1 molar ratio. Lastly, the gold particles were produced via sodium citrate reaction with HAuCl₄ in water followed by the addition of polyethylene glycol (PEG) to coat the surface 13.

For rapid growth of the microbial cells, Luria Bertani (LB) medium was prepared and sterilized for each experiment. A set of 250 mL shake flasks were also sterilized before experimentation. 100 mL of LB medium was transferred to each flask. Various concentrations of nanoparticles were carefully placed into each flask, leaving one as a control to track the normal growth of the microbial cells without nanoparticles. Experiments were performed using both a negative control (flask containing cells plus media) and a positive control (flask containing nanoparticles plus media). Both of the negative and positive control values obtained from optical density measurements were subtracted from the experimental values (flasks containing cells, media, and nanoparticles). The growth curves represent the difference between the controls and the experimental values.

Each flask was then inoculated with 1 mL of E. coli (pBR322 JM105) grown in liquid LB medium. The flasks were shaken at 180 rpm and 37°C in a shaking water bath. Optical density measurements from each flask were taken every thirty minutes to record the growth of the microbes from inoculation through late exponential phase using a spectrophotometer set at 600 nm. The growth rate of microbial cells interacting with the nanoparticles was determined from a plot of the log of the optical density versus time.

Transmission electron microscopy (TEM) was used to obtain images of the nanoparticles. Silica/iron oxide samples were prepared for TEM imaging by inserting a TEM grid (copper coated with formvar) into dry powder using tweezers to hold the grid. The sample grid was then lightly tapped to remove any excess particles, and the grid was placed in the TEM for imaging. The silica and gold nanoparticles were in suspension, and samples were prepared by inserting the TEM grid into each liquid sample. The sample grids were then allowed to air dry overnight.

One of the more common methods employed to characterize pharmaceutical colloids is dynamic light scattering (DLS). Analysis of the size distribution of the nanoparticles was performed using a DLS autocorrelation tool known as Photocor^®. DLS measurements were taken of the nanoparticles in distilled water and in LB growth media. With this procedure, the difference between the behavior of the nanoparticles in solutions with and without salt was compared.

After characterizing the various nanoparticles, experiments were conducted to observe the relationship between the iron oxide composite nanoparticles and E. coli in LB media. Cell/nanoparticle interactions were observed using a Zeiss EM10 CA transmission electron microscope at the University of Maryland Biological Ultrastructure Facility. Samples of E. coli were withdrawn at points during late exponential phase (optical density ~0.6). After collection, they were centrifuged and suspended at room temperature in 0.12 M Millonig's phosphate buffer at pH 7.3 and later with 2% glutaraldehyde. The cell pellets were then washed again with buffer, and then secondary fixed with 1% OsO₄. At this point, they were washed with distilled water and then postfixed with 2% uranyl acetate, rinsed in buffer and double distilled water, dehydrated in a series of ethanol and propylene oxide immersions, and embedded in Spurr's resin. A diamond knife was used to section the embedded cells. The sections were post-stained with 2.5% aqueous uranyl acetate and 0.2% aqueous lead citrate.