Adhesion characteristics and stability assessment of lectin-modified liposomes for site-specific drug delivery

被引:56
作者
Bakowsky, Heike [1 ]
Richter, Thomas [2 ]
Kneuer, Carsten [3 ]
Hoekstra, Dick [4 ]
Rothe, Ulrich [1 ]
Bendas, Gerd [3 ,5 ]
Ehrhardt, Carsten [6 ]
Bakowsky, Udo [2 ]
机构
[1] Univ Halle Wittenberg, Fac Med, Dept Phys Chem, D-06114 Halle, Germany
[2] Univ Marburg, Dept Pharmaceut Technol & Biopham, D-35037 Marburg, Germany
[3] Univ Leipzig, Inst Pharmacol Pharm & Toxicol, D-04103 Leipzig, Germany
[4] Univ Groningen, Dept Cell Biol, NL-9713 AV Groningen, Netherlands
[5] Univ Bonn, Dept Pharm, D-53121 Bonn, Germany
[6] Trinity Coll Dublin, Sch Pharm & Pharmacal Sci, Dublin 2, Ireland
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2008年 / 1778卷 / 01期
关键词
concanavalin A; quartz crystal microbalance; atomic force microscopy; drug targeting; PEGylation; Glycocalyx;
D O I
10.1016/j.bbamem.2007.09.033
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Carbohydrate moieties of the cellular glycocalyx have been suggested to play an important role in biological recognition processes during pathologic conditions, such as inflammation and cancer. Herein, we describe lectin-modified liposomes which might have potential for site-specific drug delivery during the therapy of such diseases. Specific interactions of plain (i.e., unmodified) and PEGylated, lectin-grafted liposomes with model membranes were investigated under real-time flow conditions using a quartz crystal microbalance. In addition, the morphology of the liposomal systems was assessed by atomic force microscopy. Plain liposomes exhibited only unspecific adhesion to glycolipid membranes and had a tendency to coalesce. The degree of membrane interaction was significantly increased when plain liposomes were modified with the lectin, Concanavalin A. However, vesicle fusion also markedly increased as a result of lectin modification. Additional PEGylation of liposomes reduced unspecific adhesion phenomena, as well as coalescence. Moreover, our studies enabled us to establish quartz crystal microbalance and atomic force microscopy as powerful and complementary methods to characterize adhesion properties of targeted drug delivery systems. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:242 / 249
页数:8
相关论文
共 37 条
[1]   Assessing transferrin modification of liposomes by atomic force microscopy and transmission electron microscopy [J].
Anabousi, S ;
Laue, M ;
Lehr, CM ;
Bakowsky, U ;
Ehrhardt, C .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2005, 60 (02) :295-303
[2]   Characterization of the interactions between various hexadecylmannoside-phospholipid model membranes with the lectin Concanavalin A [J].
Bakowsky, U ;
Rettig, W ;
Bendas, G ;
Vogel, J ;
Bakowsky, H ;
Harnagea, C ;
Rothe, U .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2000, 2 (20) :4609-4614
[3]   The influence of repeated injections on phan-nacokinetics and biodistribution of different types of sterically stabilized immunoliposomes [J].
Bendas, G ;
Rothe, U ;
Scherphof, GL ;
Kamps, JAAM .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2003, 1609 (01) :63-70
[4]   Targetability of novel immunoliposomes prepared by a new antibody conjugation technique [J].
Bendas, G ;
Krause, A ;
Bakowsky, U ;
Vogel, J ;
Rothe, U .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 181 (01) :79-93
[5]   A liposome-based model system for the simulation of lectin-induced cell adhesion [J].
Bendas, G ;
Vogel, J ;
Bakowski, U ;
Krause, A ;
Muller, J ;
Rothe, U .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1997, 1325 (02) :297-308
[6]   Lectin-mediated drug targeting: history and applications [J].
Bies, C ;
Lehr, CM ;
Woodley, JF .
ADVANCED DRUG DELIVERY REVIEWS, 2004, 56 (04) :425-435
[7]   SPECIFIC TARGETING WITH POLY(ETHYLENE GLYCOL)-MODIFIED LIPOSOMES - COUPLING OF HOMING DEVICES TO THE ENDS OF THE POLYMERIC CHAINS COMBINES EFFECTIVE TARGET BINDING WITH LONG CIRCULATION TIMES [J].
BLUME, G ;
CEVC, G ;
CROMMELIN, MDJA ;
BAKKERWOUDENBERG, IAJM ;
KLUFT, C ;
STORM, G .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1149 (01) :180-184
[8]   LIPOSOMES FOR THE SUSTAINED DRUG RELEASE INVIVO [J].
BLUME, G ;
CEVC, G .
BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1029 (01) :91-97
[9]  
CHUA MM, 1984, BIOCHIM BIOPHYS ACTA, V800, P291
[10]   A KINETIC-STUDY OF CONCANAVALIN-A BINDING TO GLYCOLIPID MONOLAYERS BY USING A QUARTZ-CRYSTAL MICROBALANCE [J].
EBARA, Y ;
OKAHATA, Y .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1994, 116 (25) :11209-11212