Ws. Price et al., A MODEL FOR DIFFUSIVE TRANSPORT THROUGH A SPHERICAL INTERFACE PROBED BY PULSED-FIELD GRADIENT NMR, Biophysical journal, 74(5), 1998, pp. 2259-2271
In biological systems, because of higher intracellular viscosity and/o
r the restriction of the diffusion space inside cells, the (apparent)
diffusion coefficient of an intracellular species (e.g., water) is gen
erally smaller than when it is in the extracellular medium. This diffe
rence affects the spin-echo signal attenuation in the pulsed field gra
dient NMR experiment and thus affords a means of separating the intrac
ellular from the extracellular species, thereby providing a basis for
studying transmembrane transport. Such experiments have commonly been
analyzed using the macroscopic model of Karger (see Adv. Magn. Reson.
21:1-89(1998)). In our previous study, we considered a microscopic mod
el of diffusive transport through a spherical interface using the shor
t gradient pulse approximation (J. Magn. Reson. A114:39-46 (1995)). Th
e spins in the external medium were modeled with the ''partially absor
bing wall'' condition or as having a small but finite lifetime. In the
present paper, we extend our treatment to the case in which there is
no limitation upon the lifetime in either medium. We also consider a s
imple modification of Karger's model that more properly accounts for t
he restricted intracellular diffusion. Importantly, it was found that
the exact solution within the short gradient pulse approximation devel
oped here and the modified Karger model are in close agreement in the
(experimentally revealed) long-time limit. The results of this study s
how that when there is no limitation upon the lifetime of the transpor
ted species in either phase, the spin-echo attenuation curve is very s
ensitive to transport.