Multi-functional magnetic nanoparticles for magnetic resonance imaging and cancer therapy

被引:366
作者
Yallapu, Murali M. [1 ]
Othman, Shadi F. [2 ]
Curtis, Evan T. [2 ]
Gupta, Brij K. [1 ]
Jaggi, Meena [1 ,3 ,4 ]
Chauhan, Subhash C. [1 ,3 ,4 ]
机构
[1] Sanford Res Univ S Dakota, Canc Biol Res Ctr, Sioux Falls, SD 57104 USA
[2] Univ Nebraska, Dept Biol Syst Engn, Lincoln, NE 68583 USA
[3] Univ S Dakota, Sanford Sch Med, Basic Biomed Sci Div, Sioux Falls, SD 57104 USA
[4] Univ S Dakota, Sanford Sch Med, Dept OB GYN, Sioux Falls, SD 57104 USA
关键词
Magnetic nanoparticles; Multi-layer coating; MRI; Drug delivery; Hyperthermia; IRON-OXIDE NANOPARTICLES; GUIDED FOCUSED ULTRASOUND; SURFACE MODIFICATION; DRUG-DELIVERY; HYPERTHERMIC TREATMENT; CELL INTERNALIZATION; IN-VIVO; BIOCOMPATIBILITY; CYCLODEXTRIN; MICROSPHERES;
D O I
10.1016/j.biomaterials.2010.11.028
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
We have developed a multi-layer approach for the synthesis of water-dispersible superparamagnetic iron oxide nanoparticles for hyperthermia, magnetic resonance imaging (MRI) and drug delivery applications. In this approach, iron oxide core nanoparticles were obtained by precipitation of iron salts in the presence of ammonia and provided beta-cyclodextrin and pluronic polymer (F127) coatings. This formulation (F127250) was highly water dispersible which allowed encapsulation of the anti-cancer drug(s) in beta-cyclodextrin and pluronic polymer for sustained drug release. The F127250 formulation has exhibited superior hyperthermia effects over time under alternating magnetic field compared to pure magnetic nanoparticles (MNP) and beta-cyclodextrin coated nanoparticles (CD200). Additionally, the improved MRI characteristics were also observed for the F127250 formulation in agar gel and in cisplatin resistant ovarian cancer cells (A12780CP) compared to MNP and CD200 formulations. Furthermore, the drug-loaded formulation of F127250 exhibited many folds of imaging contrast properties. Due to the internalization capacity of the F127250 formulation, its curcumin-loaded formulation (F127250-CUR) exhibited almost equivalent inhibition effects on A2780CP (ovarian), MDA-MB-231 (breast), and PC-3 (prostate) cancer cells even though curcumin release was only 40%. The improved therapeutic effects were verified by examining molecular effects using Western blotting and transmission electron microscopic (TEM) studies. F127250-CUR also exhibited haemocompatibility, suggesting a nanochemotherapuetic agent for cancer therapy. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1890 / 1905
页数:16
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