Interfacial interactions between amphiphilic cyclodextrins and physiologically relevant cations

被引:10
作者
Dubes, A
Parrot-Lopez, H
Shahgaldian, P
Coleman, AW
机构
[1] CNRS, Inst Biol & Chim Prot, UMR 5086, F-69367 Lyon 07, France
[2] Univ Lyon 1, CNRS, Synth Reconnaissance Org Mol & Biomol UMR 5078, F-69622 Villeurbanne, France
关键词
amphiphilic cyclodextrins; self-assembly; monolayers; Langmuir isotherm; solid lipid nanoparticles; AFM;
D O I
10.1016/S0021-9797(02)00067-X
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 compression isotherms of a series of amphiphilic cyclodextrins, formed (a) by acylation at the secondary hydroxyl face and (b) by acylation accompanied by varying degrees of sulfatation (DS) at the primary hydroxyl face (DS = 0, 4, and 7), have been studied on subphases of pure water and of water containing NaCl, KCl, MgCl2, and CaCl2 at inter- and extracellular concentrations. The formation of solid lipid nanoparticles (SLNs) by two of the molecules has been observed, while these do not aggregate at concentrations of monovalent salts up to 150 mM for the sulfated derivative. In the presence of divalent salts one of these with a DS = 0 for sultatation degree flocculates at divalent salt concentrations below 0.1 mM while the other with a DS = 4 flocculates at Mg2+ concentration above 5 mM and a Ca2+ concentration above 3 mM. AFM noncontact mode imaging has been carried out, in air, for the SLNs deposited on mica. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:103 / 111
页数:9
相关论文
共 54 条
[11]   Cyclodextrins in targeting -: Application to nanoparticles [J].
Duchêne, D ;
Ponchel, G ;
Wouessidjewe, D .
ADVANCED DRUG DELIVERY REVIEWS, 1999, 36 (01) :29-40
[12]   DIVALENT-CATION CYCLODEXTRIN INTERACTIONS AT THE AIR-WATER-INTERFACE - A 3-STAGE PROCESS [J].
EDDAOUDI, M ;
BASZKIN, A ;
PARROTLOPEZ, H ;
BOISSONNADE, MM ;
COLEMAN, AW .
LANGMUIR, 1995, 11 (01) :13-15
[13]   Chemical switching of vesicle bilayer membrane disruption by bis(crown ether) bolaamphiphiles [J].
Fyles, TM ;
Zeng, B .
JOURNAL OF ORGANIC CHEMISTRY, 1998, 63 (23) :8337-8345
[14]   Ellipsometry, Brewster angle microscopy, and thermodynamic studies of monomolecular films of cryptophanes at the air-water interface [J].
Gambut, L ;
Chauvet, JP ;
Garcia, C ;
Berge, B ;
Renault, A ;
Riviere, S ;
Meunier, J ;
Collet, A .
LANGMUIR, 1996, 12 (22) :5407-5412
[15]  
GOKEL GW, 1989, MONOGRAPHS SUPRAMOLE
[16]   MONOLAYER AND MULTILAYER FILMS OF CYCLODEXTRINS SUBSTITUTED WITH 2 AND 3 ALKYL CHAINS [J].
GREENHALL, MH ;
LUKES, P ;
KATAKY, R ;
AGBOR, NE ;
BADYAL, JPS ;
YARWOOD, J ;
PARKER, D ;
PETTY, MC .
LANGMUIR, 1995, 11 (10) :3997-4000
[17]  
Gregoriadis G., 1993, LIPOSOMES DRUG DELIV
[18]   Structural properties of several amphiphile cyclodextrins and some related nanospheres. An X-ray scattering and freeze-fracture electron microscopy study [J].
Gulik, A ;
Delacroix, H ;
Wouessidjewe, D ;
Skiba, M .
LANGMUIR, 1998, 14 (05) :1050-1057
[19]  
HABIB MJ, 1991, J PARENT SCI TECHN, V45, P124
[20]  
Hamelin B, 1999, CHEM-EUR J, V5, P546, DOI 10.1002/(SICI)1521-3765(19990201)5:2<546::AID-CHEM546>3.0.CO