Protonation Kinetics Compromise Liposomal Fluorescence Assay of Membrane Permeation

被引:13
作者
Sezer, Deniz [1 ]
Oruc, Tugce [1 ]
机构
[1] Sabanci Univ, Fac Engn & Nat Sci, TR-34956 Istanbul, Turkey
关键词
MOLECULAR-DYNAMICS SIMULATIONS; PH-PARTITION HYPOTHESIS; LIPID-BILAYERS; FATTY-ACIDS; PERMEABILITY; TRANSPORT; DRUGS; MECHANISM; MODEL; WATER;
D O I
10.1021/acs.jpcb.7b01881
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The membrane permeation of weak acids and bases couples to the ambient pH and can be studied using pH-sensitive dyes as reporters. Such fluorescence measurements with aliphatic amine drugs have revealed biexponential kinetics of permeation into liposomes (Eyer et al. J. Controlled Release 2014, 173, 102). Permeability coefficients have been obtained using the faster of the two kinetic components. Here, the origin of the biexponential kinetics is studied with a kinetic rate model that in addition to drug permeation accounts for the protonation of the drug and the dye. Surprisingly, the experimental readout is found to strongly depend on the rates of protonation. The analysis demonstrates that fluorescence studies of drug permeation relying on pH-sensitive proxies should be accompanied by comprehensive modeling of the relevant kinetic processes.
引用
收藏
页码:5218 / 5227
页数:10
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