<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJBIPHY</journal-id><journal-title-group><journal-title>Open Journal of Biophysics</journal-title></journal-title-group><issn pub-type="epub">2164-5388</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojbiphy.2022.122006</article-id><article-id pub-id-type="publisher-id">OJBIPHY-116606</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject><subject> Physics&amp;Mathematics</subject></subj-group></article-categories><title-group><article-title>
 
 
  A Bio-Physical Analysis of Extracellular Ion Mobility and Electric Field Stress
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Xiaodi</surname><given-names>Zhang</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Hui</surname><given-names>Zhang</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>College of Physics &amp;amp; Electronic Engineering, Xianyang Normal University, Xianyang, China</addr-line></aff><pub-date pub-type="epub"><day>21</day><month>03</month><year>2022</year></pub-date><volume>12</volume><issue>02</issue><fpage>153</fpage><lpage>163</lpage><history><date date-type="received"><day>11,</day>	<month>February</month>	<year>2022</year></date><date date-type="rev-recd"><day>16,</day>	<month>April</month>	<year>2022</year>	</date><date date-type="accepted"><day>19,</day>	<month>April</month>	<year>2022</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  The electric field stress applied to the cell in the electric field will cause the biological effects of the cell on electromagnetic field. In this paper, the single-shell spherical cell is equated to dielectric spheres, and a biophysical method is used to solve the boundary value problem, and then Maxwell tensor analysis is used to discuss the electric field stresses affecting the applied electric field applied to the cells. The results of numerical analysis show that the ion mobility decreases nonlinearly with increasing frequency in the lower region of the applied electric field frequency, and increases with increasing equivalent dielectric constant at a certain frequency, and the magnitude of the electric field stress is almost independent of the frequency; as the frequency increases, the ion mobility tends to a minimum value and is almost independent of the equivalent dielectric constant, while the applied electric field frequency and the cell dielectric constant both affect the cell normal and the tangential stresses. Therefore, the frequency applied electric field and cell dielectric constant affect the extracellular ion mobility, electric field stress applied to the cell membrane by the electric field; the extracellular ion mobility caused by the electric field in the low frequency range is more pronounced than that in the high frequency, and electric field stress is the basic cause of cell deformation.
 
</p></abstract><kwd-group><kwd>Mobility</kwd><kwd> Electric Stress</kwd><kwd> Biological Effects of Electromagnetic Field</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Electric fields can regulate cell growth [<xref ref-type="bibr" rid="scirp.116606-ref1">1</xref>], cytoskeleton reorganization [<xref ref-type="bibr" rid="scirp.116606-ref2">2</xref>], activation of intracellular channels [<xref ref-type="bibr" rid="scirp.116606-ref3">3</xref>], protein secretion and gene expression [<xref ref-type="bibr" rid="scirp.116606-ref4">4</xref>] et al. Also experimental studies have revealed that changing electric fields can cause cell deformation, cell fusion, rotation, and cell damage [<xref ref-type="bibr" rid="scirp.116606-ref5">5</xref>]. These phenomena had triggered mechanistic studies on the biological effects of electric fields.</p><p>In the late 1950s, Schwan et al. [<xref ref-type="bibr" rid="scirp.116606-ref6">6</xref>] began a series of studies on the action of electric fields on biological cells, which viewed as simple geometric shells with electromagnetic properties. In the early 1970s [<xref ref-type="bibr" rid="scirp.116606-ref7">7</xref>], Helfrich added the theory of elasticity to the lipid layer to study the action of applied electric fields on phospholipid vesicles, and Peterlin et al., in 2007, viewed the phospholipid layer as an anisotropic medium to discuss the mechanism of cellular deformation under the action of electric fields [<xref ref-type="bibr" rid="scirp.116606-ref8">8</xref>]. So far, the interaction of static fields, time-varying electric fields, and pulsed waves with biological cells has also been studied [<xref ref-type="bibr" rid="scirp.116606-ref9">9</xref>] - [<xref ref-type="bibr" rid="scirp.116606-ref16">16</xref>]. It is generally accepted that the additional electric fields generated by electric fields inside and outside the cell, the electric field forces exerted on the cell, and the changes induced in ion concentrations on both sides of the cell membrane are responsible for the biological effects of cellular electromagnetic fields.</p><p>Under the action of applied electric field, the analysis of the field in cell membrane, inside and outside the membrane is often assumed there is no free charge in the solution region, and the electric field is solved by the method of separation of variables. For the analysis of the forces exerted on the cell by external electric fields, the Maxwell stress tensor method is commonly used [<xref ref-type="bibr" rid="scirp.116606-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.116606-ref17">17</xref>]. These methods are based on the bio-electromagnetic theory and the model of the interaction between the electric field and the target body, by solving boundary value problem to obtain the electric field distribution in the study area, and then to analyze the stresses exerted on the cell by the stress tensor. This method can give the threshold value of the field intensity that causes the effects, but the limitation is that the influence of the thermal motion and the fact that there is a free charge in the study area are not considered.</p><p>Based on this, this paper uses the theory of bio-electromagnetism to discuss the factors that affect the ion mobility outside the cell membrane and the stress of the electric field applied to the cell membrane when an electric charge is present outside the spherical cell.</p></sec><sec id="s2"><title>2. Model</title><p>The spherical cell is usually represented by the single-shell spherical model shown in <xref ref-type="fig" rid="fig1">Figure 1</xref>(a), where R 0 is the outer radius of the cell membrane, d is the thickness of the cell membrane, ε m 1 , ε i , ε e , σ m 1 , σ i and σ e are the dielectric constant and conductivity of the cell membrane, the inner and outer medium of the cell membrane, respectively. Based on the bio-electromagnetic theory, the single-shelled spherical cell can be equated with a homogeneous media sphere with dielectric constant ε p and conductivity σ p as shown in <xref ref-type="fig" rid="fig1">Figure 1</xref>(b), and there is a relationship as Equation (1) and (2) show [<xref ref-type="bibr" rid="scirp.116606-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.116606-ref19">19</xref>].</p><p>ε p = ε m R 0 3 ( ε i + 2 ε m 1 ) + 2 a 3 ( ε i − ε m 1 ) R 0 3 ( ε i + 2 ε m 1 ) − a 3 ( ε i − ε m 1 ) , a = R 0 − d (1)</p><p>σ p = σ m 2 ( 1 − v ′ ) σ m + ( 1 + 2 v ′ ) σ i ( 2 + v ′ ) σ m + ( 1 − v ′ ) σ i , v ′ = ( 1 − d R 0 ) 3 (2)</p><p>In this paper, the equivalent dielectric sphere is used as the study model, as shown in <xref ref-type="fig" rid="fig1">Figure 1</xref>(b). The spherical coordinate system is established with the center of the dielectric sphere as the coordinate origin and the direction of the external electric field as the z-direction, and the applied electric field is E = e z E 0 exp ( − i ω t ) , where E 0 , ω are the amplitude and frequency of the applied electric field, respectively. Assume that the ions in the extracellular medium is charged with &#177; e , and their mobility is &#177; u , and the average values of ion concentrations at zero field is n + = n − = n 0 .</p></sec><sec id="s3"><title>3. Theoretical Analysis</title><sec id="s3_1"><title>3.1. Ion Mobility</title><p>If the external electric field acting on the cell is weak, according to the Poisson equation which the potential of the extracellular region satisfies and the continuity equation the ion density satisfies, the extracellular ion mobility u satisfies Equation (3):</p><p>∇ 2 u ( r ) = γ 2 u ( r ) (3)</p><p>where u ( r ) = u + ( r ) + u − ( r ) , γ 2 = i ω D + χ 2 , χ = ( 2 n 0 e 2 ε 0 ε e K T ) 1 / 2 = ( σ e ε 0 ε e D ) 1 / 2 is</p><p>the reciprocal of the Debye shielding length, D is the ion diffusion coefficient, and the relationship D with the mobility u is: D q = u K T .</p><p>The general solution of Equation (3) is dressed as Equation (4):</p><p>u ( r , θ ) = B exp ( − γ r ) ( 1 γ r + 1 ( γ r ) 2 ) cos θ (4)</p><p>where B is the coefficient to be determined.</p></sec><sec id="s3_2"><title>3.2. The Field Distribution</title><p>Based on the electromagnetic field theory, suppose that the internal and external electrical potential values of the equivalent dielectric sphere are φ p ( r , t ) and φ e ( r , t ) , respectively, then φ p ( r , t ) and φ e ( r , t ) satisfy Equation (5) and (6) [<xref ref-type="bibr" rid="scirp.116606-ref20">20</xref>]:</p><p>∇ 2 φ e ( r , t ) = − e ε 0 ε e [ n + ( r , t ) − n − ( r , t ) ] , r &gt; R (5)</p><p>∇ 2 φ p ( r , t ) = 0 , r &lt; R 0 (6)</p><p>The φ p ( r , t ) and φ e ( r , t ) satisfies the boundary conditions as Equation (7):</p><p>{ r = a :   φ p = φ e         ε p ∂ φ p ∂ r = ε e ∂ φ e ∂ r         σ e ∂ φ e ∂ r + q D ∂ u ∂ r = 0 r → ∞ :   E e = E r → 0 :   φ p islimitedvalue (7)</p><p>Solving the above boundary value problem, then we get Equation (8):</p><p>{ φ e ( r , θ ) = { − E 0 r + A r 2 − q B ε 0 ε e γ 2 exp ( − γ r ) ( 1 γ r + 1 ( γ r ) 2 ) } cos θ φ p ( r , θ ) = − C r cos θ (8)</p><p>where</p><p>{ A = ε p − ( ε g e + ε p R ) ε p + 2 ( ε g e + ε p R ) R 0 3 E 0 B = − 3 ε p R ε p + 2 ( ε g e + ε p R ) ⋅ γ 2 R 0 ε 0 ε e e E 0 R 0 3 exp ( γ R 0 ) ( 1 γ R 0 + 1 ( γ R 0 ) 2 ) − 1 C = − 3 ε g e ε p + 2 ( ε g e + ε p R ) E 0 (9)</p><p>ε g e = ε e + σ e i ω ε 0 , R = σ e i ω ε 0 ε e γ R 0 + 1 ( γ R 0 ) 2 + 2 ( γ R 0 + 1 ) .</p></sec><sec id="s3_3"><title>3.3. The Electric Field and the Electrical Stress on the Cell Membrane</title><p>From the relationship E = − ∇ φ , the electric field strength E e outside the equivalent medium sphere (cell) is E e = E r e r + E t e t , where e r , e t denote the unit vector in the normal and tangential directions of the cell membrane surface, respectively, and we have Equation (10):</p><p>{ E r = [ E 0 + 2 A r 3 − e ε 0 ε e B γ 2 r exp ( − γ r ) ( 1 + 2 γ r + 2 γ 2 r 2 ) ] cos θ E t = [ − E 0 + A r 3 − e ε 0 ε e B γ 2 r exp ( − γ r ) ( 1 γ r + 1 γ 2 r 2 ) ] sin θ (10)</p><p>Since the electromagnetic wave has momentum, it is incident on the equivalent medium sphere (cell surface) and exerts a certain pressure on the cell. From electromagnetic field theory, the momentum flow density tensor is shown as Equation (11):</p><p>T ↔ = − E D − B H + 1 2 I ↔ ( E ⋅ D + B ⋅ H ) (11)</p><p>where E , H denote the electric field and the magnetic field exposed to cell, respectively. If only the electric field effect is considered, the average value of the electric field stress applied to the unit area outside the cell membrane for a varying electric field is calculated as Equation (12):</p><p>P = 〈 − e r ⋅ T ↔ e 〉 = 1 4 R e ( ε e E r ⋅ E r * − ε e E t ⋅ E t * ) e r + 1 4 R e ( ε e E r ⋅ E t * ) e t = P r e r + P t e t (12)</p><p>In the above equation, T ↔ e = − ε e E E + 1 2 I ↔ ε e ( E ⋅ E ) , 〈 ⋯ 〉 represents the average value in one cycle.</p></sec></sec><sec id="s4"><title>4. Numerical Analysis and Discussion</title><p>In the analysis of the mechanism of the bio-effects of electromagnetic fields, the typical values of the cell geometric and the electrical parameters are often used: R 0 = 10   μ m , d = 5   nm , ε m = 4.4 &#215; 10 − 11     F ⋅ m − 1 , ε i = 6.4 &#215; 10 − 10     F ⋅ m − 1 , ε e = 6.4 &#215; 10 − 10     F ⋅ m − 1 , σ m = 3 &#215; 10 − 7     S ⋅ m − 1 , σ i = 0.3   S ⋅ m − 1 , σ e = 1.2   S ⋅ m − 1 . From the equivalent Equations (1), (2), the typical parameter values correspond to ε p = 6.35 &#215; 10 − 10     F ⋅ m − 1 and σ p = 0.0018   S ⋅ m − 1 , respectively. In the following numerical analysis, the equivalent permittivity of the dielectric sphere is taken around the values of these parameters. Consider that for small ions, the diffusion coefficient D is taken as 2 &#215; 10<sup>9</sup> m<sup>2</sup>/s [<xref ref-type="bibr" rid="scirp.116606-ref21">21</xref>] and the Debye length x is taken as 10<sup>8</sup> m<sup>−1</sup> [<xref ref-type="bibr" rid="scirp.116606-ref20">20</xref>].</p><sec id="s4_1"><title>4.1. Effect of the Frequency and the Equivalent Permittivity on Extracellular Ion Mobility</title><p><xref ref-type="fig" rid="fig2">Figure 2</xref> shows the relationship between the ionic mobility of cell membrane surface and the frequency of external electric field, where θ = 0.5 , the curves of data1, data2 and data are corresponding to ε<sub>p</sub> = 0.5, 6.4 &#215; 10<sup>−11</sup> Fm<sup>−1</sup>, 6.35 &#215; 10<sup>−11</sup> Fm<sup>−1</sup> and 9.6 &#215; 10<sup>−11</sup> Fm<sup>−1</sup>, respectively. <xref ref-type="fig" rid="fig2">Figure 2</xref> shows that the ion mobility decreases nonlinearly with increasing frequency in the region of lower frequency of the applied electric field (e.g., frequency less than 5 &#215; 10<sup>6</sup> Hz) and increases with the increasing of the equivalent permittivity at a certain frequency; With the increasing of the frequency, the ion mobility tends to a minimum value and is almost independent of the equivalent permittivity.</p><p>The diffusion coefficient D is a physical quantity that indicates how fast the ions move by diffusion from a high concentration to a low concentration, driven by a concentration gradient. The ion mobility u characterizes how fast the ions</p><p>move under the action of an electric field and it is equal to the drift velocity per unit electric field. From Einstein’s relation, a larger ion mobility u corresponds to a larger diffusion rate of ions from higher to lower concentrations. From <xref ref-type="fig" rid="fig2">Figure 2</xref>, it can also be concluded that, under the action of external electric field, in the lower frequency region, the larger the equivalent permittivity, the faster the ion diffusion rate from high to low concentration; The higher the frequency, the less the effect of the equivalent permittivity and the frequency on the ion mobility.</p><p>In biological cells, there is a defined concentration relationship inside and outside the cell membrane, and the ion migration across the membrane modulated by the external electric field will affect the physiological and living state of the cell. <xref ref-type="fig" rid="fig2">Figure 2</xref> also illustrates that low frequency electric fields will cause strong biological effects on cells compare to high frequency electric fields.</p></sec><sec id="s4_2"><title>4.2. Electric Field Stress on the Cell</title><sec id="s4_2_1"><title>4.2.1. Effect of the Frequency and the Equivalent Permittivity on the Electric Field Stress</title><p><xref ref-type="fig" rid="fig3">Figure 3</xref>(a) and <xref ref-type="fig" rid="fig3">Figure 3</xref>(b) give the curves of the normal force P<sub>r</sub>, tangential force P<sub>t</sub> (tangential force along the cell surface) versus the applied electric field frequency at θ = 0.5 , respectively, where R 0 = 10 − 5     m , the curves data1, data2 and data3 are corresponding to ε p = 6.4 &#215; 10 − 11     F ⋅ m − 1 , ε p = 6.35 &#215; 10 − 10     F ⋅ m − 1 and ε p = 9.6 &#215; 10 − 10     F ⋅ m − 1 , respectively. <xref ref-type="fig" rid="fig3">Figure 3</xref> shows that at a certain position on the cell surface ( θ = 0.5 ) and within a certain frequency range (e.g., frequency less than 5 &#215; 10<sup>6</sup> Hz), the normal and tangential forces acting on the cell surface hardly change with the increasing frequency; With further increase in frequency, the normal force on the cell decreases slowly, and when the frequency reaches a certain value, e.g., the frequency is 8.41 &#215; 10<sup>6</sup> Hz, the normal force</p><p>starts to increase, and the normal force is always expressed as pressure on the cell in the whole frequency range; For a certain frequency, the size of the normal force decreases and the size of the tangential force increases with the increase of the equivalent dielectric constant; For the cells with different equivalent permittivity, the threshold value of the change of the direction of the tangential force acting on the cell membrane surface is at same value, such as the frequency is 1.48 &#215; 10<sup>7</sup> Hz.</p></sec><sec id="s4_2_2"><title>4.2.2. Distribution of Electric Field Stress on the Cell Membrane Surface</title><p>To analyze the effect of the frequency on the electric field stress distribution acting on the cell surface, <xref ref-type="fig" rid="fig4">Figure 4</xref>(a) and <xref ref-type="fig" rid="fig4">Figure 4</xref>(b) give the electric field stress distribution on the intersection formed the spherical cell surface and the x-o-z plane, where ε p = 6.35 &#215; 10 − 10     F ⋅ m − 1 , the curves of data1, data2 and data3 is the P<sub>r</sub>, P<sub>t</sub> and P, respectively. The frequency of applied electric field in <xref ref-type="fig" rid="fig4">Figure 4</xref>(a) and <xref ref-type="fig" rid="fig4">Figure 4</xref>(b) is 1.5 &#215; 10<sup>6</sup> Hz and 6.7 &#215; 10<sup>7</sup> Hz, respectively. It is show that the normal and tangential electric field stresses are smaller near the same direction as the external electric field, i.e. near θ = 0˚, 180˚; Near the vertical direction, the maximum normal force and the minimum tangential force are exhibited, and the maximum value of the tangential force is approximately near θ = 45˚ and −45˚; Within a certain angle range, the electric field stresses are exhibited as the pull force on the cell membrane, i.e. for the frequency is 6.7 &#215; 10<sup>7</sup> Hz, when − 12 ∘ &lt; Δ θ &lt; 1 2 ∘ and 168 ∘ &lt; Δ θ &lt; 1 9 2 ∘ , then P r &gt; 0 .</p><p><xref ref-type="fig" rid="fig4">Figure 4</xref>(c) shows the variation of P<sub>r</sub>, P<sub>t</sub> and P with θ, where the external field frequency is 6.7 &#215; 10<sup>7</sup> Hz and ε p = 9.6 &#215; 10 − 10     F ⋅ m − 1 . Comparing <xref ref-type="fig" rid="fig4">Figure 4</xref>(b) and <xref ref-type="fig" rid="fig4">Figure 4</xref>(c), it can be seen that with the increase of ε p , the maximum value of P<sub>r</sub>, P is in decreases, but the value of Δ θ is increases gradually.</p><p>The force exerted by the electric field on the cell membrane is decomposed into normal force perpendicular to the membrane surface (pressure or tension) and tangential force along the surface. The action of electric field force can cause the cell deformation. The frequency of the applied electric field and the change of the cell electrical parameters will lead to the cell deformation.</p></sec></sec></sec><sec id="s5"><title>5. Conclusions</title><p>1) In a certain frequency range, the changes in frequency and cellular electrical parameters affect the extracellular ion mobility. In the lower frequency range (e.g., less than 5 &#215; 10<sup>6</sup> Hz), the ion mobility decreases rapidly with the increasing frequency; At the same frequency, the mobility increases with increasing equivalent dielectric constant; With further increase of external electric field frequency, the ion mobility tends to the minimum value and is almost independent of the dielectric constant. It can be seen that the ion mobility caused by high equivalent permittivity in the low frequency electric field region is more pronounced compared to the lower equivalent permittivity and the high frequency region.</p><p>2) The electric fields exert the electric field forces on the cell surface. In the small frequency range, the frequency hardly affects the magnitude of electric field stress; With the increase of frequency, the frequency and the changes of the cell equivalent dielectric constant will affect the electric field stress applied to the cell. The electric field stress is the fundamental cause of the cell deformation.</p><p>The study of the biological effects of electromagnetic fields has always been a hot topic in bio-electromagnetics research. The content of this paper can be used as the basic analysis theory of the biological effects of the electromagnetic field.</p></sec><sec id="s6"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s7"><title>Cite this paper</title><p>Zhang, X.D. and Zhang, H. (2022) A Bio-Physical Analysis of Extracellular Ion Mobility and Electric Field Stress. Open Journal of Biophysics, 12, 153-163. https://doi.org/10.4236/ojbiphy.2022.122006</p></sec></body><back><ref-list><title>References</title><ref id="scirp.116606-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Radisic, M., Park, H., Shing, H., et al. (2004) Functional Assembly of Engineered Myocardium by Electrical Stimulation of Cardiac Myocytes Cultured on Scaffolds. PNAS, 101, 18129-18134. https://doi.org/10.1073/pnas.0407817101</mixed-citation></ref><ref id="scirp.116606-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Sheikh, A.Q., Taghian, T., Hemingway, B., et al. (2013) Regulation of Endothelial MAPK/ERK Signalling and Capillary Morphogenesis by Low-Amplitude Electric Field. Journal of the Royal Society Interface, 10, Article ID: 20120548. https://doi.org/10.1098/rsif.2012.0548</mixed-citation></ref><ref id="scirp.116606-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Rackauskas, G., Saygili, E., Rana, O.R., et al. (2015) Sub-Threshold High Frequency Electrical Field Stimulation Induces VEGF Expression in Cardiomyocytes. Cell Transplantation, 24, 1653-1659. https://doi.org/10.3727/096368914X682783</mixed-citation></ref><ref id="scirp.116606-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Llucia-Valldeperas, A., Sanchez, B., Soler-Botija, G., et al. (2014) Physiological Conditioning by Electric Field Stimulation Promotes Cardiomyogenic Gene Expression in Human Cardiomyocyte Progenitor Cells. Stem Cell Research &amp; Therapy, 5, 93. https://doi.org/10.1186/scrt482</mixed-citation></ref><ref id="scirp.116606-ref5"><label>5</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>Schwan</surname><given-names> H.P. </given-names></name>,<etal>et al</etal>. (<year>1982</year>)<article-title>Nonthermal Cellular Effects of Electromagnetic Fields: AC-Field Induced Ponderomotoric Forces</article-title><source> British Journal of Cancer</source><volume> 5</volume>,<fpage> 220</fpage>-<lpage>224</lpage>.<pub-id pub-id-type="doi"></pub-id></mixed-citation></ref><ref id="scirp.116606-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Schaw, H.P. (1957) Electrical Properties of Tissue and Cell Suspensions. Advances in Biological and Medical Physics, 5, 147-209. https://doi.org/10.1016/B978-1-4832-3111-2.50008-0</mixed-citation></ref><ref id="scirp.116606-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Helfrich, W. (1973) Elastic Properties of Lipid Bilayers: Theory and Possible Experiments. Zeitschrift für Naturforschung, 28C, 693-703. https://doi.org/10.1515/znc-1973-11-1209</mixed-citation></ref><ref id="scirp.116606-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Peterlin, P., Svetina, S. and &amp;#381;eks, B. (2007) The Prolate-to-Oblate Shape Transition of Phospholipid of an AC Electric Field Can Be Explained by the Dielectric Anisotropy of a Phospholipid Bilayer. Journal of Physics: Condensed Matter, 16, Article ID: 136220. https://doi.org/10.1088/0953-8984/19/13/136220</mixed-citation></ref><ref id="scirp.116606-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Vlahovska, P.M., Gracià, R.S., Aranda-Espinoza, S., et al. (2009) Electrohydrodynamic Model of Vesicle Deformation in Alternating Electric Fields. Biophysical Journal, 96, 4789-4803. https://doi.org/10.1016/j.bpj.2009.03.054</mixed-citation></ref><ref id="scirp.116606-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Yamamoto, T., Espinoza, S., Dimova, R., et al. (2010) Stability of Spherical Vesicle in Electric Fields. Langmuir, 26, 12390-12407. https://doi.org/10.1021/la1011132</mixed-citation></ref><ref id="scirp.116606-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Peterlin, P. (2010) Frequency Dependent Electrodeformation of Giant Phospholipid Vesicles in AC Electric Field. Journal of Biological Physics, 36, 339-354. https://doi.org/10.1007/s10867-010-9187-3</mixed-citation></ref><ref id="scirp.116606-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Salipante, P.F. and Vlahovska, P.M. (2014) Vesicle Deformation in DC Pulses. Soft Matter, 10, 3386-3393. https://doi.org/10.1039/C3SM52870G</mixed-citation></ref><ref id="scirp.116606-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Mcconnell, L., Vlahovska, P.M., Miksis, M.J., et al. (2015) Vesicle Dynamics in Uniform Electric Fields: Squaring and Breathing. Soft Matter, 11, 4840-4846. https://doi.org/10.1039/C5SM00585J</mixed-citation></ref><ref id="scirp.116606-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Sinhaa, K.P. and Thaokarb, R.M. (2019) Shape Deformation of a Vesicle under Axisymmetric Non-Uniform Alternating Electric Field. Journal of Physics Condensed Matter, 31, Article ID: 035101. https://doi.org/10.1088/1361-648X/aaef15</mixed-citation></ref><ref id="scirp.116606-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Zhang, H., Wang, L.Y., Zhang, P.J., et al. (2018) Modulation of Membrane Potential and Ion Concentration of Isolate Ellipsoidal Cell Exposed to Static Electric Field. Scientia Sinica (Technologica), 48, 783-790. https://doi.org/10.1360/N092017-00266</mixed-citation></ref><ref id="scirp.116606-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Zhang, H., Wang, Y.L., Zhang, X.D., et al. (2017) The Effect of Impulse Wave on Ion Migration across Cell Membrane. Journal of Northwest University (Natural Science Edition), 47, 481-486.</mixed-citation></ref><ref id="scirp.116606-ref17"><label>17</label><mixed-citation publication-type="other" xlink:type="simple">Zhang, H., Wang, Y., Zhang, P.J., et al. (2021) Estimation of Biophysical Properties of Cell Exposed to Electric Field. Chinese Physics B, 30, 038702-038709. https://doi.org/10.1088/1674-1056/abc543</mixed-citation></ref><ref id="scirp.116606-ref18"><label>18</label><mixed-citation publication-type="other" xlink:type="simple">Zhao, C.X. (2018) Analysis of Equivalent Dielectric Constant of Double-Layer Ellipsoid and Design of Related Artificial Electromagnetic Materials. Lanzhou University, Lanzhou.</mixed-citation></ref><ref id="scirp.116606-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">Qin, Y.R. (2005) Modeling of Cell Membrane Voltage Changes in Suspension under External Electric Field. South China University of Technology, Guangzhou.</mixed-citation></ref><ref id="scirp.116606-ref20"><label>20</label><mixed-citation publication-type="other" xlink:type="simple">Garcia, A., Grosse, C. and Brito, P. (1985) On the Effect of Volume Charge Distribution on the Maxwell-Wagner Relaxation. Journal of Physics D: Applied Physics, 18, 739-745. https://doi.org/10.1088/0022-3727/18/4/018</mixed-citation></ref><ref id="scirp.116606-ref21"><label>21</label><mixed-citation publication-type="other" xlink:type="simple">Grosse, C. and Schwan, H.P. (1992) Cellular Membrane Potentials Induced by Alternating Fields. Biophysical Journal, 63, 1632-1642. https://doi.org/10.1016/S0006-3495(92)81740-X</mixed-citation></ref></ref-list></back></article>