Surface modified superparamagnetic nanoparticles for drug delivery: Interaction studies with human fibroblasts in culture

被引:357
作者
Gupta, AK [1 ]
Curtis, ASG [1 ]
机构
[1] Univ Glasgow, Inst Biomed & Life Sci, Ctr Cell Engn, Glasgow G12 8QQ, Lanark, Scotland
关键词
Iron Oxide; Magnetic Nanoparticles; Protein Adsorption; Dermal Fibroblast; Iron Oxide Nanoparticles;
D O I
10.1023/B:JMSM.0000021126.32934.20
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The concept of drug delivery using magnetic nanoparticles greatly benefit from the fact that nanotechnology has developed to a stage that it makes possible not only to produce magnetic nanoparticles in a very narrow size distribution range with superparamagnetic properties but also to engineer particle surfaces to provide site specific delivery of drugs. The size and surface characteristics of the nanoparticles are crucial factors that determine the success of the particles when used in vivo. The aim of this study was to modify the surfaces of the magnetic nanoparticles with PEG to improve the biocompatibility of the nanoparticles by resisting protein adsorption and increasing their intracellular uptake. In this study, the poly(ethyleneglycol) (PEG) modified superparamagnetic iron oxide nanoparticles have been prepared and their influence on human dermal fibroblasts is assessed in terms of cell adhesion/viability, morphology, particle uptake and cytoskeletal organisation studies. Various techniques have been used to determine nanoparticle-cell interactions including light, fluorescence, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The modification of nanoparticle surface induced alterations in cell behaviour distinct from the unmodified particles, suggesting that cell response can be directed via specifically engineered particle surfaces. (C) 2004 Kluwer Academic Publishers.
引用
收藏
页码:493 / 496
页数:4
相关论文
共 13 条
[1]   PROTEIN ADSORPTION TO POLYMER PARTICLES - ROLE OF SURFACE-PROPERTIES [J].
ABSOLOM, DR ;
ZINGG, W ;
NEUMANN, AW .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1987, 21 (02) :161-171
[2]   Actin assembly plays a variable, but not obligatory role in receptor-mediated endocytosis in mammalian cells [J].
Fujimoto, LM ;
Roth, R ;
Heuser, JE ;
Schmid, SL .
TRAFFIC, 2000, 1 (02) :161-171
[3]  
GUPTA AK, 2004, IN PRESS IEEE TRANSC
[4]   INTEGRIN LIGAND INTERACTIONS - A YEAR IN REVIEW [J].
HAAS, TA ;
PLOW, EF .
CURRENT OPINION IN CELL BIOLOGY, 1994, 6 (05) :656-662
[5]   REGULATING THE FATE OF MESSENGER-RNA - THE CONTROL OF CELLULAR IRON-METABOLISM [J].
KLAUSNER, RD ;
ROUAULT, TA ;
HARFORD, JB .
CELL, 1993, 72 (01) :19-28
[6]  
Moghimi SM, 2001, PHARMACOL REV, V53, P283
[7]   Development and experimental application of receptor-specific MR contrast media [J].
Reimer, P ;
Weissleder, R .
RADIOLOGE, 1996, 36 (02) :153-163
[8]   LONG CIRCULATING MICROPARTICULATE DRUG CARRIERS [J].
STOLNIK, S ;
ILLUM, L ;
DAVIS, SS .
ADVANCED DRUG DELIVERY REVIEWS, 1995, 16 (2-3) :195-214
[9]   SURFACE MODIFICATION OF NANOPARTICLES TO OPPOSE UPTAKE BY THE MONONUCLEAR PHAGOCYTE SYSTEM [J].
STORM, G ;
BELLIOT, SO ;
DAEMEN, T ;
LASIC, DD .
ADVANCED DRUG DELIVERY REVIEWS, 1995, 17 (01) :31-48
[10]   ANTIMYOSIN-LABELED MONOCRYSTALLINE IRON-OXIDE ALLOWS DETECTION OF MYOCARDIAL INFARCT - MR ANTIBODY IMAGING [J].
WEISSLEDER, R ;
LEE, AS ;
KHAW, BA ;
SHEN, T ;
BRADY, TJ .
RADIOLOGY, 1992, 182 (02) :381-385