The Bioeffects Resulting from Prokaryotic Cells and Yeast Being Exposed to an 18 GHz Electromagnetic Field

The mechanisms by which various biological effects are triggered by exposure to an electromagnetic field are not fully understood and have been the subject of debate. Here, the effects of exposing typical representatives of the major microbial taxa to an 18 GHz microwave electromagnetic field (EMF)were studied. It appeared that the EMF exposure induced cell permeabilisation in all of the bacteria and yeast studied, while the cells remained viable (94% throughout the exposure), independent of the differences in cell membrane fatty acid and phospholipid composition. The resulting cell permeabilisation was confirmed by detection of the uptake of propidium iodine and 23 nm fluorescent silica nanospheres using transmission electron microscopy (TEM) and confocal laser scanning microscopy (CLSM). Upon EMF exposure, the bacterial cell membranes are believed to become permeable through quasi-endocytosis processes. The dosimetry analysis revealed that the EMF threshold level required to induce the uptake of the large (46 nm) nanopsheres was between three and six EMF doses, with a specific absorption rate (SAR) of 3 kW/kg and 5 kW/kg per exposure, respectively, depending on the bacterial taxa being studied. It is suggested that the taxonomic affiliation and lipid composition (e.g. the presence of phosphatidyl-glycerol and/or pentadecanoic fatty acid) may affect the extent of uptake of the large nanospheres (46 nm). Multiple 18 GHz EMF exposures over a one-hour period induced periodic anomalous increases in the cell growth behavior of two Staphylococcus aureus strains, namely ATCC 25923 and CIP 65.8T.


Introduction
An electromagnetic field (EMF) is capable of triggering a variety of biological effects [1][2][3][4] upon genes [5][6][7][8][9], proteins and enzyme kinetics [10][11][12][13][14], depending on the EMF strength, frequency, and time of interaction [15,16]. Despite many studies having been undertaken, the and structure. B. catarrhalis is an aerobic, non-motile Gram-negative diplococcus, opportunistic human pathogen, which is often found in the upper respiratory tract of humans. B. catarrhalis can cause respiratory infections, acute otitis media, sinusitis and infections such as endocarditis, meningitis and bacterial tracheitis [30]. The bacterium can grow well at temperatures as low as 22°C. Cells are kidney bean shaped, with a diameter of 0.6 to 1.0 μm, often appearing in pairs or as tetrads [31]. B. catarrhalis is saccharolytic, DNase, oxidase and catalase-positive with butyrate esterase activity [30]. K. rosea is an aerobic, non-motile, non-encapsulated, non-sporulated Gram-positive coccus, opportunistic human pathogen, which is commonly found on the surface of human skin, mucous membranes, in the oral cavity, and the outer ear canal [29,32]. The bacterium can also be found in freshwater, saltwater, and soil environments [29,32]. Cells have a diameter of approximately 1.0 to 1.8 μm and occur in pairs, tetrads or clusters [29]. Streptomyces griseus is non-motile, aerobic, Gram-positive filamentous, spore forming rod-shaped bacterium, which is a typical inhabitant of soil [33]. Streptomyces griseus is alkaliphilic, produces an aerial mycelium, which has modes of branching that eventually leads the hyphae to form chains of spores called arthospores [33,34]. The optimum temperature for cell growth is in the range 25 to 35°C [33]. Considered relatively harmless to humans, Streptomyces griseus produces many useful secondary metabolites such as enzyme inhibitors, and they comprise 70% of naturally-occurring antibiotics [34]. Saccharomyces cerevisiae is considered to be a "model organism" for scientists because it has a fast rate of growth, being both a unicellular and eukaryotic organism [35]. This yeast has been used since ancient times in fermentation processes that convert sugar into alcohol, and baking processes as a leavening agent [35]. Yeast strains can be isolated from the surfaces of plants, surfaces of insects and warm-blooded animals, soils from all regions of the world and even in aquatic environments [35]. The optimum growth temperature is in the range 30 to 35°C [36]. Saccharomyces cerevisiae cells are round to ovoid, 5 to 10 μm in diameter, grow in either the haploid or diploid form [36]. Pure cultures were stored at -80°C in nutrient broth (NB, Oxoid Ltd., Basingstoke, Hampshire, England) with the addition of 20% (v/v) glycerol. All strains were grown on nutrient agar (NA, Oxoid Ltd., Basingstoke, Hampshire, England), brain-heart infused agar (BHIA, Becton Dickinson, Sparks, NV, USA) or potato dextrose agar (PDA, Becton Dickinson), depending on the requirements of a particular strain. Prior to each experiment, each strain was grown to the stationary phase of growth as confirmed by growth curves (data not shown) at 25°C (B. catarrhalis, K. rosea, Streptomyces griseus), 30°C (Saccharomyces cerevisiae), or 37°C (Staphylococcus aureus). Freshly prepared working suspensions were used for each independent experiment. The bacterial cell density was adjusted to OD 600 0.1 in 10 mM phosphate buffered saline (PBS) at pH 7.4, using a spectrophotometer (Dynamica Halo RB-10 UV-Vis, Precisa Gravimetrics AG, Dietikon, Switzerland). The Streptomyces cerevisiae yeast cell density was adjusted to 7 × 10 5 cells mL -1 using a Neubauer-improved haemocytometer (Paul Marienfeld, Lauda-Königshofen, Germany).

EMF exposure
Exposure of the samples to the EMF was carried out as described elsewhere [4,20]. In brief, 2 mL of the working suspension was transferred into a micro Petri dish (35 mm diameter, Griener Bio One, Frickenhausen, Germany). The EMF apparatus used for all experiments was a Vari-Wave Model LT 1500 (Lambda Technologies, Morrisville, NC, USA) instrument with a fixed frequency of 18 GHz. The samples were placed onto a ceramic pedestal PD160 (Pacific Ceramics, Sunnyvale, CA, USA, ε' = 160, loss tangent < 10 −3 ) at a position that had been identified, using electric field modelling of CST Microwave Studio 3D Electromagnetic Simulation Software (CST MWS) (CST of America, Framingham, MA, USA), to be the position that provided the most consistent heating environment (Fig 1). The calculated wavelength of the EMF in water was determined to be 2.34 mm, which is greater than the linear dimensions of each bacterial cell. The depth of penetration was calculated to be 1.04 mm, which was greater than the thickness of the bacterial suspension in the Petri dish. Hence, the possibility of subjecting the samples to non-even heating due to the presence of a non-uniform field distribution was considered to be negligible. The temperature of the suspension was constantly monitored during EMF exposures via a built-in temperature probe, a Luxtron Fiber Optic Temperature Unit (LFOTU) (LumaSense Technologies, Santa Clara, CA, USA), and a portable Cyclopes 330S infrared/thermal monitoring camera (Minolta, Osaka, Japan).

Bulk heat treatment
A Peltier plate heating/cooling system (TA Instruments, New Castle, DE, USA) was used to replicate the bulk temperature profiles achieved during the EMF exposure experiments. All Peltier plate heated samples were performed in parallel with the EMF exposure experiments. At least three independent experiments were conducted. Working suspensions that were not subjected to either EMF exposure or Peltier plate heating were used as the negative controls for all experiments.
Cell treatment and viability assays B. catarrhalis, K. rosea, Streptomyces griseus, and Saccharomyces cerevisiae cells were subjected to three consecutive EMF exposures with SAR doses of approximately 5.0 kW kg -1 that resulted in a temperature increase ranging from 20°C to 40°C (at a heating rate of 20°C per min) for 1 min, then the sample was allowed to cool to 20°C on ice (at a rate of 10°C per min) between exposures. The liquid evaporation that took place during the EMF exposures was found to be approximately 1.5%, determined using an analytical balance (Cheetah Scientific, France). This loss of mass was regarded as being negligible.
The counting of viable cells was conducted immediately after EMF exposures and in parallel with those of the control samples by plating 100 μL cell suspensions on the agar plates containing solidified nutrient media: nutrient agar (NA, Oxoid Ltd., Basingstoke, Hampshire, England), brain-heart infused agar (BHIA, Becton Dickinson, Sparks, NV, USA) or potato dextrose agar (PDA, Becton Dickinson), depending on the requirements of a particular strain. Ten plates for each bacterial strain were used. Three technical replicates were carried out to allow a statistical analysis of the results to be performed. Three independent Student t-tests were performed to compare the consistency of the cell viability rates for each set of experimental conditions, exposure trials and test strains.

Confocal Laser Scanning Microscopy (CLSM) analysis
Propidium iodide (1.0 mg mL -1 solution in water; Life Technologies Australia, Mulgrave, Australia) was used at a concentration of 500 nM to directly determine the permeability of the cells being studied [37]. Non-treated cells, cells inactivated by boiling (100°C) and Peltier plate heattreated cells were used as three different types of control. Heat inactivated cells were prepared by boiling the cell suspension for 15 min, followed by cooling in a 25°C water bath for 30 min. PI was added to all the cell suspensions at 1 min and 10 min after EMF exposures. The PI remained in contact with the studied cells throughout the experiment.
Two types of fluorescent, hydrophilic, neutrally charged silica nanospheres, 23.5 ± 0.2 nm (FITC) and 46.3 ± 0.2 nm (Rhodamine B) (Corpuscular, Cold Spring, NY, USA) were used. These silica nanospheres were selected because hydrophilic nanoparticles rarely translocate through a lipid bilayer [38] and neutrally charged nanoparticle surfaces prevent any nonspecific interactions taking place with the membrane [39]. The nanospheres were added to the cell suspensions 1 min after the EMF exposure at a concentration of 25 μg mL -1 , incubated for 10 min then washed twice by centrifugation at 4500 rpm for 5 min. A 100 μL aliquot of each sample was then analyzed using a Fluoview FV10i-W inverted microscope (Olympus, Tokyo, Japan). Approximately 10 CLSM images per EMF exposure group were obtained.

EMF permeability coefficient
The nanosphere loading capacity of the EMF exposed bacterial and yeast cells were quantified according to the fluorescence intensity of any silica nanospheres that were taken into the cells. A POLARstar Omega microplate reader (BMG Labtech, Ortenberg, Germany) was used to measure the fluorescence intensity of nanospheres in each cell suspension. Each sample was prepared according to the method used for CLSM analysis. A calibration curve was constructed to determine the correlation of fluorescent intensity and nanosphere concentration. A total of seven nanosphere concentrations were prepared (0.005, 0.05, 0.5, 1, 5, 19 and 15 μg mL -1 ).
The mass m of a silica nanosphere was determined from the mass density of silica ρ and is the volume of a silica nanosphere V, related to the radius r as V ¼ 4 3 pr 3 . The radii of the 23.5 nm and 46.3 nm nanospheres were 11.75 × 10 −7 cm and 23.15 × 10 −7 cm, (Corpuscular), volume 6.8 × 10 −18 and 5.2 × 10 −17 cm 3 , and mass 1.8 × 10 −17 and 1.38 × 10 −16 g, respectively. The mass of a single nanosphere was used to calculate the number of internalized nanospheres.

EMF permeability dosimetry
The number of viable cells on agar plates was evaluated after subsequent EMF exposures to confirm that at least 85% of the cells survived the exposure under these conditions. For the bacteria that did not survive, the maximum temperature was decreased to 33°C (with a heating rate of 13°C per min for 1 min), allowing the sample to cool to 20°C on ice for 1.3 min (at a rate of 10°C per min) between exposures. The CLSM analysis of the samples was then carried out to study the permeability of the cells. If no uptake of nanospheres was observed, the number of EMF exposures was increased to four, five or six consecutive exposures. SEM was also used to monitor any changes in cell morphology.
The SAR was calculated with the assumption that all the absorbed field energy was transformed into heat, and disregarding any heat dissipation, as: where c is the specific heat capacity of the medium (kJ kg -1°C-1 ), and @T @t jt ¼ 0 is the time derivative of the temperature determined at t = 0 (°C s -1 ).
The SAR of each EMF exposure was calculated using Eq (1) by measuring the temperature change over time under the optimum settings (power, temperature and number of treatments). It was assumed that the specific heat capacity of the cell suspension was the same as that of water at 25°C, which is 4.18 kJ kg -1°C-1 . The SAR was determined experimentally in this work because it has been suggested that it is a more accurate estimation of energy absorption for biological material [40][41][42]. This is because any variation in the specific heat within a sample of biological matter is usually much smaller than the corresponding variation in conductivity, resulting in a much more uniform temperature than determined using an electric field distribution [40][41][42].

Scanning Electron Microscopy (SEM) analysis
A field emission scanning electron microscope FeSEM-SUPRA 40VP (Carl Zeiss, Jena, Germany) with a primary beam energy of 3 kV was used to obtain high-resolution images of the cell samples. A 100 μL aliquot of EMF-exposed suspension was placed on a glass cover slip (ProSciTech, Kirwan, Australia) in duplicate for each EMF exposure experiment. After 20 min, the glass cover slips were washed with nanopure H 2 O (with a resistivity of 18.2 MΩ cm -1 ), dried with 99.99% purity nitrogen gas, then subjected to gold sputtering (6 nm thick gold film) using a NeoCoater MP-19020NCTR (JEOL, Frenchs Forest, Australia). Approximately ten SEM images were obtained at 5,000× (yeast) and 70,000× (bacteria) magnifications for subsequent analysis.

Transmission Electron Microscopy (TEM)
The cell suspensions subjected to MW exposure and with the addition of the 23.5 nm nanospheres were pelleted by centrifugation at 4800 rpm for 5 min at 25°C. The cells were then washed twice with phosphate buffer saline (PBS) in order to remove any unbound nanospheres. The pellets were then suspended in 2 mL of 4% glutaraldehyde in PBS (10 mM, pH 7.4) for 30 min, and washed twice in PBS for 5 min. After the final washing step, the cells were mixed thoroughly in 0.5 mL of 5% agarose gel by stirring. The agar was immediately cooled to 4°C by refrigeration for 30 min, then cut into 1 mm 3 cubes and fixed with 1 mL of 1% osmium tetroxide (OsO 4 ) for 1 h. The cubes were washed twice in nanopure H 2 O (with resistivity of 18.2 MΩ cm -1 ) for 15 min. The cells were dehydrated by passing the cubes through a graded ethanol series (20%, 40%, and 60%) (2 mL) for 15 min and stained for 8 h with 2% uranyl acetate in 70% ethanol (2 mL). After staining, the cells were further dehydrated by passing the cubes through another graded ethanol series (80%, 90% and 100%) for 15 min (2 mL) [43,44].
The embedding medium was prepared using Araldite, dodecenyl succinic anhydride (DDSA), and benzyldimethylamine (BDMA) (ProSciTech) and stirred thoroughly [45]. In order to embed the samples, each cube was washed twice with 100% acetone (2 mL) for 20 min, then incubated in 2 mL of acetone and embedding medium (1:1 ratio) for 8 h, followed by transfer to acetone and embedding medium (1:3 ratio) for 8 h and finally transferred into the pure embedding medium for 8 h. The cube was then transferred into an embedding mold containing fresh pure embedding medium, which was then polymerized for 24 h at 60°C [46]. The final block was trimmed, then cut into ultrathin sections (80 nm thickness) using a Leica EM UC7 ultramicrotome (Leica Microsystems, Wetzlar, Germany) with a glass knife. Sections were placed onto 200 mesh copper grids and examined using a JEM 1010 instrument (JEOL).

Multiple EMF exposure experiments
Working suspensions of two strains, Staphylococcus aureus ATCC 25923 and Staphylococcus aureus CIP 65.8 T , were divided into eighteen batches, each of 2 mL volume. Eighteen batches of samples were subjected to a series of EMF exposures ranging in frequency from 1 to 18 GHz. The first batch was exposed to one EMF dose, which resulted in a temperature increase in the samples ranging from 20°C to 40°C (at a heating rate of 20°C per min) for 1 min. Samples were then allowed to cool to 20°C on ice (at a rate of 10°C per min). The second batch was exposed to two consecutive EMF doses, and so on. The working cell suspensions, which were left untreated for the same period of time as those of the EMF exposed samples, were used as untreated controls. All the cell viability tests were conducted immediately after EMF exposure experiments and in parallel with the untreated control. The number of viable bacteria as a function of the number of EMF exposures was identified by a one-way analysis of variance (ANOVA) using the general linear model procedure. Mean values were separated by Tukey's Honestly Significant Differences test (p < 0.05). All statistical analyses were completed using SPSS v.21 (SPSS Inc., Chicago, IL, USA).

EMF-induced cell permeability
In order to investigate the effect of the 18 GHz EMF exposure on the bacterial and yeast cells, the uptake of two sizes of fluorescent, hydrophilic, non-charged silica nanospheres of 23.5 nm and 46.3 nm was measured. Analysis of the TEM micrographs (Fig 2 and S1 Fig) and CLSM imaging (Fig 3 and S2 Fig) confirmed the uptake of 23.5 nm nanospheres in all studied organisms (up to 97% permeabilised cells). The uptake of propidium iodide (Fig 4 and S3 Fig) also reconfirmed that the EMF induced membrane permeability of the studied cells. A statistical analysis of the data did revealed that there was no statistically significant difference between the Peltier heated and untreated cells (B. catarrhalis (p > 0.05), K. rosea (p > 0.05), Streptomyces griseus (p > 0.05) and Saccharomyces cerevisiae (p > 0.05)). There were, however, statistically significant differences between the EMF exposed cells and the control samples (p < 0.05).
This work indicated that three 18 GHz EMF exposures with 1 min SAR doses of approximately 5.0 kW kg -1 (at 40°C) consistently induced cell wall permeabilisation in all of the studied bacterial cells and yeast, regardless of the differences in their cell wall/ membrane structures. A TEM analysis of the ultra-thin (90 nm) cross-sections of the cells confirmed the intracellular location of the 23.5 nm nanospheres. Although the nanospheres were observed entering into the cells themselves, they were also found to be present on the surface of the cell walls (Fig 2). It was observed that the number of nanospheres around the Gram positive bacterial cells and yeast were considerably more than that observed around the Gram negative bacterial cells. It could be speculated that the peptidoglycan layer of the Gram positive bacterial cell walls and mannoprotein/β-glucan layer of the yeast cell wall [47] may have played a role in filtering and/or trapping the nanospheres. Control groups of the untreated and Peltier plate heated cells were found not to have taken up any of the nanospheres (S1 and S2 Figs), highlighting the lack of cell permeability in these samples. Some bacteria such as B. catarrhalis and yeast were not able to take up the larger (46.3 nm) nanospheres. Although the larger nanospheres were detected in the K. rosea and Saccharomyces cerevisiae cells, the viability of these organisms under these SAR doses remained low (62% and 47%, respectively, as shown in Table 1), and therefore the EMF dosages for these bacteria were further optimized (see next section).
It should be noted that it was previously reported that under the same EMF exposure conditions, Staphylococcus epidermidis cells were not able to take up the 46.3 nm-nanospheres, yet Staphylococcus aureus cells were able to do so [20]. A comparative analysis of the phospholipid and fatty acid compositions (Fig 5) indicated that Staphylococcus epidermidis cells have greater proportion of phosphatidyl-glycerol (PG) and less lysyl-PG compared to those levels reported for Staphylococcus aureus [48]. It is likely that the PG head-groups contributed to the membrane fluidity, affecting the uptake of the 46 nm nanospheres. Some variation in the uptake of the large nanospheres was noted for the Gram-positive B. catarrhalis and Gram-negative E. coli bacterial cells. For example, a substantial proportion of PG has been reported to be present in the B. catarrhalis membrane phospholipids; this higher proportion of PG did not allow the internalisation of 46.3 nm nanospheres. The E. coli cell membranes, however, contained a greater proportion of phosphatidyl-ethanolamine (PE) and were able to internalise the 46 nm nanospheres [20]. It is important to note that other components of the cell membrane may also play a role in the permeabilisation of the cell membrane. For example, it appeared that although PG comprises up to 30% of the membrane phospholipids in P. maritimus cells, this bacterium was found to be able to internalise a majority of the 46.3 nm nanospheres. Amongst the strains tested, it is likely that the greater proportion (up to 65% of total fatty acids) of 15:0 fatty acid, which has the lowest melting temperature (33.5°C, S1 Table), might increase the susceptibility of P. maritimus cells to the EMF exposure. Hence, it is suggested that the amount of the phospholipid head-group (PG) and C 15:0 saturated fatty acid present in the cell membrane may play an important role in the destabilisation of lipid bilayer of the membrane by EMF exposure, such that the cells are then able to internalise the 46 nm nanospheres.
It is also believed that the type and extent of these membrane effects would be strongly dependent on the EMF frequencies being used, as higher frequency fields affect smaller molecules to a greater extent [49]. While oscillations of EMF in the GHz frequency range are too fast to move larger molecules such as proteins and other biomolecules, they can induce the rotation of water dipoles [50]. These rotations and reorientations of dipoles are responsible for the energy loss in consequent heating induced by the EMF. The 18 GHz EMF acts directly on water molecules inducing their rotation and reorientation with polarization lag responsible for dissipation of energy and heating. Larger molecules should not be affected by such rapidly alternating fields, since their rotational frequencies are sufficiently lower, while vibrational frequencies of individual groups have low energy compared to kinetic energy [49]. The rotation of water molecules disrupts hydrogen bonding network and affects the water properties. As a result, dielectric constant of water, ε, is decreased with frequency ϖ according to: where ε s and ε 1 are the dielectric constants of water at zero (static) and infinite (optical limit) frequencies. The relaxation time of water molecule t ¼ 4pZa 3 kT depends on temperature T, the radius of the molecule a and the viscosity η. It was reported that the maximum EMF absorption by water at 20°C and 40°C occurred at 18 GHz [51] and 25 GHz [52], respectively. Apart from heating of water, the decreased dielectric constant affected the interaction between charges and Debye (screening) length, which is a measure of the screening of the electrostatic interactions in polarizable and salty media. In the absence of EMF, the Debye length is given by: where e is the elementary charge and ρ is the density of counterions and salt molecules.
The change in the dielectric constant affects the electrostatic interaction between charges in water media and thus, it can affect the stability of charged bilayers composed of polar lipids. This, together with the heating, are believed to change the physicochemical state (i.e., fluidity) of the cell membranes and could render them more sensitive to membrane deformation [24,28,53]. This modulation of the mechanical stimulation in turn changes the membrane tension, causing it to deform, resulting in an enhanced degree of membrane trafficking via exocytosis/ endocytosis, as was previously reported for several bacterial cell types [20,54,55].
Other studies have suggested that the EMF-induced changes in water properties can alter the conformation of proteins, their degree of hydration, and other properties that results a change in their activity [22,[56][57][58][59]. It was demonstrated that exposing bacteria to an EMF of 51.8, 53, 70.6, 73 and 90 GHz frequency resulted in changes in the enzymatic activities and ion (H + and K + ) transport processes through the plasma membrane [56][57][58][59].

EMF permeability dosage requirements
Cell viability experiments and CLSM analysis of the EMF exposed K. rosea and Saccharomyces cerevisiae cells revealed that three and six exposures with 1 min SAR doses at of approximately 3.0 kW kg -1 (at 33°C) were sufficient to induce cell permeability of the viable cells. In the case of B. catarrhalis and Streptomyces griseus cells, only three exposure doses at 40°C were required to induce membrane permeability ( Table 1, Figs 1 and 2). This dose specific permeabilisation implies that 18 GHz EMF can be used to target a specific type of cells and hence a new drug delivery/release method. The lack of permeabilisation of young yeast cells (Fig 3) was observed, however due to the lack of data pertaining to the composition of the young yeast cell wall, the reason of this phenomenon remains unclear. Certain biological effects were previously attributed to the EMF of SAR dose of 4.0 kW kg -1 at 8.53 GHz, 4.85 kW kg -1 at 2.45 GHz, e.g., threedimensional conformational changes in green fluorescent protein (GFP) [60] and increased citrate synthase binding efficiency [10].  Fig 6).
The periodic increases in cell number (inferred from the direct counting of viable cells) throughout the multiple 18 GHz EMF exposures is a notable phenomenon which, to the best our knowledge, has not been previously reported. Copty et al. suggested that the enzyme kinetics could be changed by heating the water molecules that are attached to the cellular proteins [60]. This perhaps may attribute to the increases in cell number.

Conclusion
A fundamental understanding of the phenomenon of permeabilisation of prokaryotic and yeast cells by exposing them to 18 GHz EMF radiation is important. The results of this study have demonstrated that exposure to 18 GHz EMF induced cell permeability in all of the organisms being studied in a manner that could not be duplicated using conventional heating methods under similar temperature conditions, regardless of the differences in cell wall/ membrane structures of each type of cell. It was established that the threshold level of EMF exposure that was required to induce cell permeability to allow the passage of large nanospheres (46 nm) through the cell membrane was in the range of three and six EMF exposure doses with specific absorption rate (SAR) of 3 kW/kg and 5 kW/kg per exposure, depending on the type of cell.
In addition, it was found that multiple 18 GHz EMF exposures could induce notable periodic increases in the cell number of Staphylococcus aureus CIP 65.8 T and ATCC 25923. Further study of the effect of EMF exposure has on multicellular eukaryotes and liposomes (with or without proteins) is required in order to fully evaluate the effects of such multiple EMF exposures have on biological systems and its applicability as a new drug delivery/release technique due to its non-invasive nature, local application, and cost-effectiveness.