Liposome-nanoparticle hybrids for multimodal diagnostic and therapeutic applications

被引:128
作者
T Al-Jamal, Wafa' [1 ]
Kostarelos, Kostas [1 ]
机构
[1] Univ London, Sch Pharm, Ctr Drug Delivery Res, Nanomed Lab, London WC1N 1AX, England
关键词
double liposomes; liposome; polystyrene; nanospheres; quantum dot; silica; superparamagnetic iron; oxides; vesosomes;
D O I
10.2217/17435889.2.1.85
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Liposomes have a decade-long clinical presence as nanoscale delivery systems of encapsulated anthracycline molecules. However, their use as delivery systems of nanoparticles is still in the preclinical development stages. Liposome-nanoparticle hybrid constructs present great opportunities in terms of nanoscale delivery system engineering for combinatory therapeutic-imaging modalities. Moreover, many novel materials are being developed in nanotechnology laboratories that often require methodologies to enhance their compatibility with the biological milieu in vitro and in vivo. Liposomes are structurally suitable to make nanoparticles biocompatible and offer a clinically proven, versatile platform for the further enhancement of pharmacological efficacy. Small iron oxide nanoparticles, quantum dots, liposomes, silica and polystyrene nanoparticles have been incorporated into liposomes for a variety of different applications. In this review, all such liposome-nanoparticle hybrid systems are described, both in terms of their structural characteristics and the potential they offer as diagnostic and therapeutic multimodality agents.
引用
收藏
页码:85 / 98
页数:14
相关论文
共 93 条
[11]   Preparation, relaxometry, and biokinetics of PEGylated magnetoliposomes as MR contrast agent [J].
Bulte, JWM ;
de Cuyper, M ;
Despres, D ;
Frank, JA .
JOURNAL OF MAGNETISM AND MAGNETIC MATERIALS, 1999, 194 (1-3) :204-209
[12]   Nanocapsules: lipid-coated aggregates of cisplatin with high cytotoxicity [J].
Burger, KNJ ;
Staffhorst, RWHM ;
de Vijlder, HC ;
Velinova, MJ ;
Bomans, PH ;
Frederik, PM ;
de Kruijff, B .
NATURE MEDICINE, 2002, 8 (01) :81-84
[13]   Bilayer vesicles and liposomes as interface agents [J].
Carmona-Ribeiro, AM .
CHEMICAL SOCIETY REVIEWS, 2001, 30 (04) :241-247
[14]   Interactions between bilayer membranes and latex [J].
Carmona-Ribeiro, AM ;
Lessa, MD .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 1999, 153 (1-3) :355-361
[15]   Interactions between cationic liposomes and drugs or biomolecules [J].
Carmona-Ribeiro, AM .
ANAIS DA ACADEMIA BRASILEIRA DE CIENCIAS, 2000, 72 (01) :39-43
[16]   SYNTHETIC BILAYER ADSORPTION ONTO POLYSTYRENE MICROSPHERES [J].
CARMONARIBEIRO, AM ;
MIDMORE, BR .
LANGMUIR, 1992, 8 (03) :801-806
[17]   PHOSPHOLIPID ADSORPTION ONTO POLYSTYRENE MICROSPHERES [J].
CARMONARIBEIRO, AM ;
HERRINGTON, TM .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1993, 156 (01) :19-23
[18]  
CHAN WC, 2006, CURR OPIN BIOTECH, V13, P40
[19]   Magnetically-responsive polymerized liposomes as potential oral delivery vehicles [J].
Chen, HM ;
Langer, R .
PHARMACEUTICAL RESEARCH, 1997, 14 (04) :537-540
[20]   Preparation of AgBr quantum dots via electroporation of vesicles [J].
Correa, NM ;
Zhang, HG ;
Schelly, ZA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (27) :6432-6434