Hostname: page-component-74656f9884-j7cmm Total loading time: 0 Render date: 2026-11-10T12:52:38.241Z Has data issue: false hasContentIssue false

Deformation of a biconcave-discoid capsule in extensional flow and electric field

Published online by Cambridge University Press:  03 December 2018

Sudip Das
Affiliation:
Department of Chemical Engineering, Indian Institute of Technology Bombay, Mumbai, 400076, India
Shivraj D. Deshmukh
Affiliation:
Department of Chemical Engineering, Indian Institute of Technology Bombay, Mumbai, 400076, India
Rochish M. Thaokar*
Affiliation:
Department of Chemical Engineering, Indian Institute of Technology Bombay, Mumbai, 400076, India
*
†Email address for correspondence: rochish@che.iitb.ac.in

Abstract

Natural (red blood cells) and artificial biconcave-discoid-shaped capsules have immense biological (a cellular component of blood) and technological (as drug carrier) relevance, respectively. Their low reduced volume allows significant shape changes under external fields such as extensional flows (encountered at junctions and size-varying capillaries in biological flows) and electric fields (in applications such as electroporation and dielectrophoresis). This work demonstrates biconcave-discoid to capped-cylindrical and prolate-spheroid shape transitions of a capsule in uniaxial extensional flow as well as in DC and AC electric fields. The shape changes of a stress-free biconcave-discoid capsule in external fields are important in determining the momentum and mass transfer between the capsule and the medium fluid as well as dielectrophoresis and electroporation phenomena of a capsule in an electric field. The biconcave-discoid to capped-cylindrical/prolate-spheroid shape transition is demonstrated for both a capsule (with parameters relevant to drug delivery) as well as for a red blood cell (physiological conditions). However, significant differences are observed in this shape transition depending upon the applied external fields. In an extensional flow, the pressure-driven transition shows the equator being squeezed in and the poles being pulled out to deform into a capped cylinder at low capillary number and a prolate spheroid at high capillary number. On the other hand, in the transition driven by electric fields, the shoulders of the capsule seem to play a significant role in the dynamics. The shape transition in the electric fields depends upon the relative magnitude of the electric and the hydrodynamic response times, particularly relevant for the dynamics of red blood cells in physiological conditions. A new method of analysing the shape transition of red blood cells in AC electric fields is suggested, where a large separation of time scales is observed between the hydrodynamic and electric responses.

Information

Type
JFM Papers
Copyright
© 2018 Cambridge University Press 
Figure 0

Figure 1. Schematic representation of a capsule in (a) extensional flow (curves with arrows represent streamlines) and (b) uniform electric field (arrows represent field lines). (c) Comparison of the shape of an RBC (——) with the oblate spheroids perturbed with a second-degree Legendre mode (— — for $\unicode[STIX]{x1D716}=-0.5$ and — ⋅ — for $\unicode[STIX]{x1D716}=-0.3$). (d) Schematic presentation of a prolate spheroid representing azimuthal ($T_{\unicode[STIX]{x1D719}}$) and meridional ($T_{s}$) elastic tensions. The centre of the spheroid is at the origin of the Cartesian coordinate system.

Figure 1

Table 1. Values of parameters and scaled variables used in boundary integral simulation for the biconcave-discoid capsule and human RBC.

Figure 2

Figure 2. Observed shapes during the evolution of a capsule at (a) $t=10$, (b) $t=40$, (c) $t=\infty$ for $Ca_{f}=0.015$; (d) $t=20$, (e) $t=70$ (f) $t=\infty$ for $Ca_{f}=0.017$; and (g) $t=2$, (h) $t=7$, (i) $t=\infty$ for $Ca_{f}=0.1$, considering the dilatation parameter $C=1$. (j) Equilibrium displacement of the north pole from the initial position of an undeformed biconcave-discoid as a function of $Ca_{f}$ for $C=1$ (——) and $C=10$ (— —).

Figure 3

Figure 3. At $Ca_{f}=0.1$ and $C=1$. (a–c) Pressure profile. (d–f) Variation of the meridional, $T_{s}$ (— —), azimuthal, $T_{\unicode[STIX]{x1D719}}$ (— ⋅ —) and mean, $T_{m}$ (——) elastic tensions along the arclength. (g–i) Streamlines (shown only in the right-hand half) and the velocity profile (relative magnitude of the flow is proportional to the length of the short arrows shown in the left-hand half). From left to right the columns correspond to times $t=2$, $7$ and $\infty$, respectively.

Figure 4

Figure 4. Observed shapes during the evolution of a biconcave-discoid capsule at (a) $t=26$ and (b) $t=\infty$ for $Ca_{e}=0.02$ and $\unicode[STIX]{x1D70E}_{r}=0.1$. Corresponding streamlines (shown only in the right-hand half), velocity profile (relative magnitude of the flow is proportional to the length of the short arrows shown in left-hand half) and electric stress distribution (shown by short arrows from the interface) are shown in (c) and (d), respectively. Observed shapes during deformation at (e) $t=0$ and (f) $t=15$ at $Ca_{e}=0.05$ and $\unicode[STIX]{x1D70E}_{r}=0.1$. Streamlines, velocity profile and electric stress distribution are shown in (g) corresponding to the shape shown in (e). The variation of the meridional, $T_{s}$ (— —), azimuthal, $T_{\unicode[STIX]{x1D719}}$ (— ⋅ —) and mean, $T_{m}$ (——) membrane tensions along the arclength are shown in the inset of (g).

Figure 5

Figure 5. Observed shapes during the evolution of a biconcave-discoid capsule at (a) $t=20$, (b) $t=85$ and (c) $t=\infty$ for $Ca_{e}=0.3$ and $\unicode[STIX]{x1D70E}_{r}=10$. Corresponding streamlines (shown only in the right-hand half), velocity profile (relative magnitude of the flow is proportional to the length of the short arrows shown in the left-hand half) and electric stress distribution (shown by short arrows from the interface) are shown in (d), (e) and (f), respectively. The variation of meridional, $T_{s}$ (— —), azimuthal, $T_{\unicode[STIX]{x1D719}}$ (— ⋅ —) and mean, $T_{m}$ (——) membrane tensions along the arclength are shown in the insets.

Figure 6

Figure 6. Observed shapes during the evolution of a biconcave-discoid capsule at (a) $t=10$, (b) $t=23$, (c) $t=29$, (d) $t=37$ and (e) $t=\infty$ for $Ca_{e}=0.5$ and $\unicode[STIX]{x1D70E}_{r}=10$. Corresponding streamlines (shown only in the right-hand half), velocity profile (relative magnitude of the flow is proportional to the length of the short arrows shown in the left-hand half) and electric stress distribution (shown by short arrows from the interface) are shown in (f), (g), (h), (i) and (j), respectively. The variation of meridional, $T_{s}$ (— —), azimuthal, $T_{\unicode[STIX]{x1D719}}$ (— ⋅ —) and mean, $T_{m}$ (——) membrane tensions along the arclength are shown in the insets.

Figure 7

Figure 7. Transmembrane potential at the interface during the shape evolution of a biconcave-discoid capsule at $(\cdots \,)$ $t=5$, (— —) $t=20$, (— ⋅ —) $t=35$, (– ⋅ ⋅) $t=55$, (– – ⋅) $t=85$ and (——) $t=\infty$ for $Ca_{e}=0.3$ (a), and at $(\cdots \,)$ $t=10$, (— —) $t=23$, (— ⋅ —) $t=29$, (– ⋅ ⋅) $t=37$, (– – ⋅) $t=50$ and (——) $t=\infty$ for $Ca_{e}=0.5$ (b).

Figure 8

Figure 8. Observed shapes during the deformation of a biconcave-discoid capsule for $Ca_{e}=0.4$ and $\unicode[STIX]{x1D70E}_{r}=10$ at (a) $t=0$, (b) $20$, (c) $42$, (d) $52$ and (e) $\infty$, considering $k_{f}=1$ and at (f) $t=0$, (g) $500$, (h) $1500$, (i) $5000$ and (j) $\infty$, considering $k_{f}=0.01$.

Figure 9

Figure 9. Transmembrane potential of the static shape of an RBC as a function of frequency. Marker point ○ represents $t_{cap}^{-1}$.

Figure 10

Figure 10. Shapes observed during the deformation of an RBC at (a) $t=10$ and (b) $t=\infty$ for $Ca_{e}=0.5$ and at (g) $t=20$ and (h) $t=\infty$ for $Ca_{e}=1$ in an AC field with $\unicode[STIX]{x1D714}=2.5$, considering $C=1$. Variation of the meridional, $T_{s}$ (— —), azimuthal, $T_{\unicode[STIX]{x1D719}}$ (— ⋅ —) and mean, $T_{m}$ (——) elastic tensions along the arclength for the corresponding cases are shown in (c,d) and (i,j), respectively. Shapes observed during the deformation of an RBC at (e) $t=24$ and (f) $t=\infty$ for $Ca_{e}=0.5$ and at (k) $t=20$ and (l) $t=\infty$ for $Ca_{e}=1$, considering $C=10$.

Figure 11

Figure 11. At $Ca_{e}=0.5$. (a) Transmembrane potential at the north pole in a single cycle of the applied electric field during the calculation of average electric stress at (– –) $t=10$ and (——) $t=\infty$. (b) Variation of the transmembrane potential at the end of the particular cycle of the applied field over the arclength at (– –) $t=10$ and (——) $t=\infty$, corresponding to figure 10(a,b), respectively.

Figure 12

Figure 12. At $Ca_{e}=1$. (a) Transmembrane potential at the north pole in a single cycle of the applied electric field during the calculation of average electric stress at (– –) $t=20$ and (——) $t=\infty$. (b) Variation of the transmembrane potential at the end of the particular cycle of the applied field over the arclength at (– –) $t=20$ and (——) $t=\infty$, corresponding to figure 10(g,h), respectively.

Figure 13

Figure 13. Shapes observed during the deformation of an RBC at (a) $t=10$, (b) $t=70$ and (c) $t=\infty$ for $Ca_{e}=0.5$ in an AC field with $\unicode[STIX]{x1D714}=2.5$, considering $C=1$ and $\unicode[STIX]{x1D70E}_{r}=10$.

Figure 14

Figure 14. At $Ca_{e}=0.5$ and $\unicode[STIX]{x1D70E}_{r}=10$. (a) Transmembrane potential at the north pole in a single cycle of the applied electric field during the calculation of the average electric stress at (– –) $t=10$, (— ⋅ —) $t=70$ and (——) $t=\infty$. (b) Variation of the transmembrane potential at the end of the particular cycle of the applied field over the arclength at (– –) $t=10$, (— ⋅ —) $t=70$ and (——) $t=\infty$, corresponding to figure 13(a–c), respectively.

Figure 15

Figure 15. Comparison of boundary integral simulations at $k_{s}=30$ and the reported (Pozrikidis 1990) evolution at $k=10$ of an oblate-spheroid shape perturbed with a second-degree Legendre mode ($\unicode[STIX]{x1D716}=-0.3$). In each panel (——) $t=0$, (— —) $t=0.095$, (— ⋅ —) $t=0.235$, (– ⋅ ⋅) $t=0.540$ and (— — ⋅) $t=\infty$. Boundary integral simulation results (a–c) and reported (Pozrikidis 1990) shape evolution (d).

Figure 16

Figure 16. Comparison of boundary integral simulations at $k_{s}=60$ and the reported (Pozrikidis 1990) evolution at $k=20$ of an oblate-spheroid shape perturbed with a second-degree Legendre mode ($\unicode[STIX]{x1D716}=-0.3$). In each panel (——) $t=0$, (— —) $t=0.1$, (— ⋅ —) $t=0.3$ and (— — ⋅) $t=\infty$. Boundary integral simulation results (a–c) and reported (Pozrikidis 1990) shape evolution (d).

Figure 17

Figure 17. Comparison of boundary integral simulations at $k_{s}=15$ and the reported (Pozrikidis 1990) evolution at $k=5$ of an oblate-spheroid shape perturbed with second-degree Legendre mode ($\unicode[STIX]{x1D716}=-0.5$). In each panel (——) $t=0$, (— —) $t=0.15$, (— ⋅ —) $t=0.375$, (– ⋅ ⋅) $t=0.682$ and (— — ⋅) $t=\infty$. Boundary integral simulation results (a–c) and reported (Pozrikidis 1990) shape evolution (d).

Figure 18

Table 2. Percentage change in area at different membrane parameter $C$ for $\unicode[STIX]{x1D716}=-0.3$ and $k_{s}=30$.

Figure 19

Table 3. Percentage change in area at different membrane parameter $C$ for $\unicode[STIX]{x1D716}=-0.3$ and $k_{s}=60$.

Figure 20

Table 4. Percentage change in area at different membrane parameter $C$ for $\unicode[STIX]{x1D716}=-0.5$ and $k_{s}=15$.