New sterically stabilized vesicles based on nonionic surfactant, cholesterol, and poly(ethylene glycol)-cholesterol conjugates

被引:49
作者
Beugin, S
Edwards, K
Karlsson, G
Ollivon, M
Lesieur, S
机构
[1] Univ Paris Sud, Equipe Physicochim Syst Polyphases, CNRS, URA 1218, F-92296 Chatenay Malabry, France
[2] Uppsala Univ, Dept Phys Chem, S-75121 Uppsala, Sweden
关键词
D O I
10.1016/S0006-3495(98)78026-9
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Monomethoxypoly(ethylene glycol) cholesteryl carbonates (M-PEG-Chol) with polymer chain molecular weights of 1000 (M-PEG1000-Chol) and 2000 (M-PEG2000-Chol) have been newly synthesized and characterized. Their aggregation behavior in mixture with diglycerol hexadecyl ether (C(16)G(2)) and cholesterol has been examined by cryotransmission electron microscopy, high-performance gel exclusion chromatography, and quasielastic light scattering. Nonaggregated, stable, unilamellar vesicles were obtained at low polymer levels with optimal shape and size homogeneity at cholesteryl conjugate/ lipids ratios of 10 mol% M-PEG1000-Chol or 5 mol% M-PEG2000-Chol, corresponding to the theoretically predicted brush conformational state of the PEG chains. At 20 mol% M-PEG1000-Chol or 10 mol% M-PEG2000-Chol, the saturation threshold of the C(16)G(2)/cholesterol membrane in polymer is exceeded, and open disk-shaped aggregates are seen in coexistence with closed vesicles. Higher levels up to 30 mol% lead to the complete solubilization of the vesicles into disk-like structures of decreasing size with increasing PEG content. This study underlines the bivalent role of M-PEG-Chol derivatives: while behaving as solubilizing surfactants, they provide an efficient steric barrier, preventing the vesicles from aggregation and fusion over a period of at least 2 weeks.
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收藏
页码:3198 / 3210
页数:13
相关论文
共 87 条
[1]  
AKIYOSHI K, 1992, ORG SOLUTIONS SURFAC, P290
[2]   ADSORPTION OF CHAIN MOLECULES WITH A POLAR HEAD A-SCALING DESCRIPTION [J].
ALEXANDER, S .
JOURNAL DE PHYSIQUE, 1977, 38 (08) :983-987
[3]  
Allen T.M., 2008, J LIPOSOME RES, V2, P289, DOI [10.3109/08982109209010210, DOI 10.3109/08982109209010210]
[4]   THE USE OF GLYCOLIPIDS AND HYDROPHILIC POLYMERS IN AVOIDING RAPID UPTAKE OF LIPOSOMES BY THE MONONUCLEAR PHAGOCYTE SYSTEM [J].
ALLEN, TM .
ADVANCED DRUG DELIVERY REVIEWS, 1994, 13 (03) :285-309
[5]   LONG-CIRCULATING (STERICALLY STABILIZED) LIPOSOMES FOR TARGETED DRUG-DELIVERY [J].
ALLEN, TM .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1994, 15 (07) :215-220
[6]   LIPOSOMES CONTAINING SYNTHETIC LIPID DERIVATIVES OF POLY(ETHYLENE GLYCOL) SHOW PROLONGED CIRCULATION HALF-LIVES INVIVO [J].
ALLEN, TM ;
HANSEN, C ;
MARTIN, F ;
REDEMANN, C ;
YAUYOUNG, A .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1066 (01) :29-36
[7]  
ALLEN TM, 1995, LIPOSOMES NEW SYSTEM, P123
[8]  
ALLEN TM, 1993, LIPOSOME TECHNOLOGY, P59
[9]  
Azmin M N, 1986, J Microencapsul, V3, P95, DOI 10.3109/02652048609031563
[10]   THE EFFECT OF NON-IONIC SURFACTANT VESICLE (NIOSOME) ENTRAPMENT ON THE ABSORPTION AND DISTRIBUTION OF METHOTREXATE IN MICE [J].
AZMIN, MN ;
FLORENCE, AT ;
HANDJANIVILA, RM ;
STUART, JFB ;
VANLERBERGHE, G ;
WHITTAKER, JS .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1985, 37 (04) :237-242