A fickian diffusion transport process with features of transport catalysis: Doxorubicin transport in human red blood cells

140Citations
Citations of this article
24Readers
Mendeley users who have this article in their library.

Abstract

The transport of the antineoplastic drug doxorubicin (Adriamycin) in human red blood cells was investigated by measuring the net efflux from loaded cells. Previous data indicated that doxorubicin transport was a Fickian diffusion transport process of the electrically neutral molecule through the lipid domain of the cell membrane (Dalmark, 1981 [In press]). However, doxorubicin transport showed saturation kinetics and a concentration-dependent temperature dependence with nonlinear Arrhenius plots. The two phenomena were related to the doxorubicin partition coefficient between 1-octanol and a water phase. This relationship indicated that the two phenomena were caused by changes in the physicochemical properties of doxorubicin in the aqueous phase and were not caused by interaction of doxorubicin with cell membrane components. The physicochemical properties of doxorubicin varied with concentration and temperature because of the ability of doxorubicin to form polymers by self-association in aqueous solution like other planar aromatic molecules through pi-electron orbital interaction. The hypothesis is proposed that doxorubicin transport across cell membranes takes place by simple Fickian diffusion. © 1981, Rockefeller University Press., All rights reserved.

Cite

CITATION STYLE

APA

Dalmark, M., & Storm, H. H. (1981). A fickian diffusion transport process with features of transport catalysis: Doxorubicin transport in human red blood cells. Journal of General Physiology, 78(4), 349–364. https://doi.org/10.1085/jgp.78.4.349

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free