Magnetic nanoparticles with dual functional properties: Drug delivery and magnetic resonance imaging

被引:380
作者
Jain, Tapan K. [1 ]
Richey, John [2 ]
Strand, Michelle [3 ,4 ]
Leslie-Pelecky, Diandra L. [3 ,4 ]
Flask, Chris A. [2 ]
Labhasetwar, Vinod [1 ,5 ]
机构
[1] Cleveland Clin, Dept Biomed Engn, Lerner Res Inst, Cleveland, OH 44195 USA
[2] Case Western Reserve Univ, Case Ctr Imaging Res, Dept Radiol, Cleveland, OH 44106 USA
[3] Univ Nebraska, Dept Phys & Astron, Lincoln, NE 68588 USA
[4] Univ Nebraska, Nebraska Ctr Mat & Nanosci, Lincoln, NE 68588 USA
[5] Cleveland Clin, Taussig Canc Ctr, Cleveland, OH 44195 USA
基金
美国国家卫生研究院;
关键词
iron oxide; anticancer agents; imaging; anti-proliferative effects; tumor;
D O I
10.1016/j.biomaterials.2008.07.004
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
There is significant interest in recent years in developing magnetic nanoparticles (MNPs) having multifunctional characteristics with complimentary roles. In this study, we investigated the drug delivery and magnetic resonance imaging (MRI) properties Of Our novel oleic acid-coated iron-oxide and pluronic-stabilized MNPs. The drug incorporation efficiency of doxorubicin and paclitaxel (alone or in combination) in MNPs was 74-95%; the drug release was Sustained and the incorporated drugs had marginal effects on physical (size and zeta potential) and magnetization properties of the MNPs. The drugs in combination incorporated in MNPs demonstrated highly synergistic anti Proliferative activity in MCF-7 breast cancer cells. The T-2 relaxivity (r(2)) was higher for our MNPs than Feridex IV (TM), whereas the T, relaxivity (r(1)) was better for Feridex IV than for our MNPs, suggesting greater sensitivity of our MNPs than Feridex IV in T-2 weighted imaging. The circulation half-life (17112), determined from the changes in the MRI signal intensity in carotid arteries in mice, was longer for our MNPs than Feridex IV (t(1/2) = 31.2 vs. 6.4 min). MNPs with combined characteristics of MRI and drug delivery could be of high clinical significance in the treatment of various disease conditions. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4012 / 4021
页数:10
相关论文
共 59 条
[1]  
Abramoff MD., 2004, Biophot. Int., V11, P36
[2]  
Alexiou C, 2000, CANCER RES, V60, P6641
[3]   Tegafur loading and release properties of magnetite/poly(alkylcyanoacrylate) (core/shell) nanoparticles [J].
Arias, Jose L. ;
Ruiz, M. Adolfina ;
Gallardo, Visitacion ;
Delgado, Angel V. .
JOURNAL OF CONTROLLED RELEASE, 2008, 125 (01) :50-58
[4]   Magnetodendrimers allow endosomal magnetic labeling and in vivo tracking of stem cells [J].
Bulte, JWM ;
Douglas, T ;
Witwer, B ;
Zhang, SC ;
Strable, E ;
Lewis, BK ;
Zywicke, H ;
Miller, B ;
van Gelderen, P ;
Moskowitz, BM ;
Duncan, ID ;
Frank, JA .
NATURE BIOTECHNOLOGY, 2001, 19 (12) :1141-1147
[5]  
Bulte JWM, 1999, MAGN RESON MED, V42, P379, DOI 10.1002/(SICI)1522-2594(199908)42:2<379::AID-MRM20>3.0.CO
[6]  
2-L
[7]   Supercritical CO2 based production of magnetically responsive micro- and nanoparticles for drug targeting [J].
Chattopadhyay, P ;
Gupta, RB .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2002, 41 (24) :6049-6058
[8]   ANALYSIS OF COMBINED DRUG EFFECTS - A NEW LOOK AT A VERY OLD PROBLEM [J].
CHOU, TC ;
TALALAY, P .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1983, 4 (11) :450-454
[9]   Development of superparamagnetic nanoparticles for MRI: Effect of particle size, charge and surface nature on biodistribution [J].
Chouly, C ;
Pouliquen, D ;
Lucet, I ;
Jeune, JJ ;
Jallet, P .
JOURNAL OF MICROENCAPSULATION, 1996, 13 (03) :245-255
[10]   The drug loading, cytotoxicty and tumor vascular targeting characteristics of magnetite in magnetic drug targeting [J].
Dandamudi, Suman ;
Campbell, Robert B. .
BIOMATERIALS, 2007, 28 (31) :4673-4683