Temperature dependence of the interaction of prazosin with lipid Langmuir monolayers

被引:14
|
作者
Gzyl-Malcher, Barbara [1 ]
Handzlik, Jadwiga [2 ]
Klekowska, Ewelina [1 ]
机构
[1] Jagiellonian Univ, Fac Chem, Dept Phys Chem & Electrochem, PL-30060 Krakow, Poland
[2] Jagiellonian Univ, Coll Med, Dept Technol & Biotechnol Drugs, PL-30688 Krakow, Poland
关键词
Langmuir monolayer; Phospholipid; Cholesterol; Drug; Compressibility; SURFACE-PROPERTIES; MODEL MEMBRANE; BRAIN; MODULATION; PROSTATE; SUBTYPES; BINDING; PLASMA; DNA;
D O I
10.1016/j.colsurfb.2013.07.030
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The influence of temperature on membrane prazosin interactions was studied. Prazosin, a quinazoline derivative of 2-furoylpiperazine, is a classic antihypertensive and antiarrhythmic drug. A mixed cholesterol/phospholipid monolayer at the water/air interface was employed as a simplified biomembrane model. Brewster angle microscopy (BAM) was used to visualize the monolayer morphology. It was found that prazosin penetrates Langmuir monolayers and modifies the interactions between membrane components, causing monolayer fluidization. An increase in temperature facilitates penetration of prazosin into the monolayers. Prazosin interacts preferentially with phosphatidylcholine and modifies the morphology of the condensed phase domains of DPPC. In the presence of prazosin, monolayers collapse at lower surface pressures. The difference between the collapse pressures of monolayers on water with and without prazosin increases with temperature. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:171 / 176
页数:6
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