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

Journal
Journal of Colloid and Interface Science
Journal Volume
322
Journal Issue
1
Pages
263-273
Date Issued
2008
Author(s)
LIN-CHAU CHANG  
Chang Y.-Y.
Gau C.-S.
DOI
10.1016/j.jcis.2008.02.051
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-43049138311&doi=10.1016%2fj.jcis.2008.02.051&partnerID=40&md5=19d4d92405315b4d53e0bd76f7fb6dbd
https://scholars.lib.ntu.edu.tw/handle/123456789/569912
Abstract
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 3beta-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.
SDGs

[SDGs]SDG6

Type
journal article

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