Interfacial properties of Pluronics and the interactions between Pluronics and cholesterol/DPPC mixed monolayers

被引:42
作者
Chang, Lin-Chau [1 ]
Chang, Yao-Yu [1 ]
Gau, Churn-Shiouh [1 ]
机构
[1] Natl Taiwan Univ, Coll Med, Sch Pharm, Taipei 10764, Taiwan
关键词
Pluronics; cholesterol; monolayer technique; cell membrane; hydrophobicity;
D O I
10.1016/j.jcis.2008.02.051
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 [物理化学]; 081704 [应用化学];
摘要
Pluronics are triblock copolymers of poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) (PEO-PPO-PEO) with wide range of hydrophilic-lipophilic balance. In order to investigate the relationship between the chemical structures of Pluronics and the interfacial properties at the air-water interface by monolayer techniques, Pluronics L61, P65, F68, P84, P123, L35, and P105 were selected. Since cholesterol influenced substantially the molecular packing stage and the characteristics of cell membranes, the interactions between Pluronics and model cell membranes in the absence and presence of cholesterol were compared. The results of pi-A isotherms and surface elasticities of Pluronic monolayers indicated that the first and second transition like stage were mainly affected by the numbers of EO and PO monomers, respectively. Pluronics with higher hydrophobicities demonstrated larger surface activities and penetration abilities to dipalmitoylphosphatidylcholine (DPPC) monolayers, which might be due to hydrophobic interactions and van der Waals forces. In the presence of cholesterol, hydrogen bonding effects was supposed to exist between the 3 beta-hydroxy group of cholesterol and ether oxygen of PEO chains, which led Pluronic F68, with the longest PEO chain herein, to exhibit significantly higher penetration ability. Our findings proposed a theoretical basis for selection of optimized drug carriers and the starting point for further investigations. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:263 / 273
页数:11
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