Volume 80, Issue 4, Pages (April 2001)

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Volume 80, Issue 4, Pages 1670-1690 (April 2001) An Electrochemical Model of the Transport of Charged Molecules through the Capillary Glycocalyx  T.M. Stace, E.R. Damiano  Biophysical Journal  Volume 80, Issue 4, Pages 1670-1690 (April 2001) DOI: 10.1016/S0006-3495(01)76139-5 Copyright © 2001 The Biophysical Society Terms and Conditions

Figure 1 The assumed form of the cF distribution, as in Eq. 22, showing the parameters rg, Δrg, rec, and Δrec. Not to scale. Biophysical Journal 2001 80, 1670-1690DOI: (10.1016/S0006-3495(01)76139-5) Copyright © 2001 The Biophysical Society Terms and Conditions

Figure 2 The dependence of the exclusion factor, Eq. 34, on ξ0 for several different values of m. Biophysical Journal 2001 80, 1670-1690DOI: (10.1016/S0006-3495(01)76139-5) Copyright © 2001 The Biophysical Society Terms and Conditions

Figure 3 (a) Time variation of anionic molecular tracer concentration, cL(r, t), for F/m=1 and B/m=1. Note that the initial distribution for cL follows a hyperbolic tangent. (b) Time variation of δ(r, t) corresponding to the instantaneous cL distributions shown in (a). Note that δ varies significantly with time. (c) Time variation of anionic molecular tracer concentration for F/m=285 and B/m=800. In this case, the initial cL distribution follows a Gaussian. (d) Time variation of δ(r, t) corresponding to the instantaneous cL distributions shown in (c). Note that the instantaneous δ distributions are indistinguishable, which is consistent with a quasi-static approximation for δ. In all panels, m=5, Q=72314, and the geometric parameters are rg=0.86, Δrg=0.02, and rec=1 such that there is no leakage into the extravascular space. Biophysical Journal 2001 80, 1670-1690DOI: (10.1016/S0006-3495(01)76139-5) Copyright © 2001 The Biophysical Society Terms and Conditions

Figure 4 (a) Graphical representation of R′(1; λ), corresponding to the left-hand side of the characteristic equation associated with the eigenvalue problem. As λ varies, so does R′(1; λ). The eigenvalues, corresponding to the roots of the characteristic equation (dots), occur where R′(1; λ) vanishes. (b) The first five eigenfunctions, Rn(r). To within a constant multiplicative factor, the eigenfunction, R0(r), corresponds to the equilibrium distribution of cL. (c) Comparison of the solutions obtained by the finite-difference method versus the eigenfunction expansion (truncated after the first 15 terms); cF is also shown. For all panels, F=4744, B=4000, Q=200871, m=5, rg=0.52, Δrg=0.2, rec=0.6, and Δrec=0.03. Biophysical Journal 2001 80, 1670-1690DOI: (10.1016/S0006-3495(01)76139-5) Copyright © 2001 The Biophysical Society Terms and Conditions

Figure 5 Plots of cL(r, t) at various times assuming a box-shaped distribution for cF with F=235,200, B=4000, and m=3. The cF distribution is shown (dot-dash) as the rectangle extending from rg=0.42 to rec=0.5. Biophysical Journal 2001 80, 1670-1690DOI: (10.1016/S0006-3495(01)76139-5) Copyright © 2001 The Biophysical Society Terms and Conditions

Figure 6 Dependence of λ1 on ξ0 for different values of anionic molecular valence magnitude, m. The solid lines correspond to λ1 found by numerically solving the eigenvalue problem for rg=0.4, Δrg=0.1, rec=0.5, and Δrec=0.03. The dashed lines are the results for the corresponding box-shaped distribution, and the dotted lines show the asymptotic approximation of λ1 for the box-shaped distribution. Agreement for the last two is excellent for λ1<2. It should be noted that the asymptotic approximations in all cases converge to λ1=8.244 as ξ0 → 0, whereas the correct limit is λ1=3.8317, as can be seen from the solutions to the eigenvalue problem. Thus the asymptotic formula given by Eq. 72 is not valid for λ1>∼2. The two right-hand axes show the exclusion factor given by Eq. 34 and the diffusion time, τ1, given by Eq. 74. Whereas λ1 and the exclusion factor are independent of either the diffusion coefficient or the geometric parameters of the system, τ1 depends on both. In computing τ1, the diffusion coefficient, DL, was taken to be 2.4×10−11 m2/s and the system radius, R, was taken to be 5μm. Biophysical Journal 2001 80, 1670-1690DOI: (10.1016/S0006-3495(01)76139-5) Copyright © 2001 The Biophysical Society Terms and Conditions

Figure 7 Dependence of λ1 on the valence magnitude, m, of the anionic molecular tracer for different values of ξ0. The solid lines correspond to λ1 found by numerically solving the eigenvalue problem for a smoothly varying cF distribution with rg=0.4, Δrg=0.1, rec=0.5, and Δrec=0.03. The dotted lines are the results for the corresponding box-shaped distribution and the dashed lines show the asymptotic approximation of λ1 for the box-shaped distribution. Agreement is excellent for λ1<2. The linearity of the results on the log-linear plot illustrates well the exponential dependence of λ1 on the valence magnitude, m, for λ1<2. It should be noted that, as in Fig. 6, the asymptotic approximations in all cases converge to λ1=8.244 as ξ0 → 0, whereas the correct limit is λ1=3.8317. The two right-hand axes show the exclusion factor given by Eq. 34 and the diffusion time, τ1, given by Eq. 74. In computing τ1, the parameters used were the same as in Fig. 6. Biophysical Journal 2001 80, 1670-1690DOI: (10.1016/S0006-3495(01)76139-5) Copyright © 2001 The Biophysical Society Terms and Conditions

Figure 8 (a) Dependence of λ1 on rec for ξ0=11.9 and m=5. The geometric parameters are fixed relative to rec such that rg=0.75 rec, Δrg=0.5 rec=0.03, and Δrec=0.5 rec. This result may be interpreted as the variation of λ1 with changing cavity size, but fixed capillary diameter and glycocalyx shape. The solid curve is calculated for a smoothly varying cF, while the dashed curve is the corresponding solution for the box-shaped distribution. (b) Dependence of λ1 on rg for a smooth distribution of cF (solid curve), and for the box-shaped distribution (dotted curve). Other parameters are fixed at ξ0=11.9, m=5, rec=0.6, and Δrec=0.03. The unusual behavior of the solid curve for small rec−rg occurs because the value of Δrg is large enough relative to rec−rg to cause the distribution to be sharply peaked, rather than flat near the endothelial-cell wall. Biophysical Journal 2001 80, 1670-1690DOI: (10.1016/S0006-3495(01)76139-5) Copyright © 2001 The Biophysical Society Terms and Conditions